| geneid | 80205 |
|---|---|
| ensemblid | ENSG00000177200.18 |
| hgncid | 25701 |
| symbol | CHD9 |
| name | chromodomain helicase DNA binding protein 9 |
| refseq_nuc | NM_001308319.2 |
| refseq_prot | NP_001295248.1 |
| ensembl_nuc | ENST00000447540.6 |
| ensembl_prot | ENSP00000396345.2 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 53054991 |
| end | 53327497 |
| strand | + |
| ver | v1.2 |
| region | chr16:53054991-53327497 |
| region5000 | chr16:53049991-53332497 |
| regionname0 | CHD9_chr16_53054991_53327497 |
| regionname5000 | CHD9_chr16_53049991_53332497 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 2897 | 147 | 63 | 13 | 50 | 5 | 15 | 35 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| a0002 | 0/0 | 2897 | 49 | 8 | 9 | 19 | 4 | 9 | 13 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| a0003 | 1/0 | 2897 | 34 | 5 | 4 | 19 | 1 | 4 | 15 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| a0004 | 0/0 | 2897 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| a0005 | 0/0 | 2897 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| a0006 | 0/0 | 2897 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| a0007 | 0/0 | 2897 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| a0008 | 0/0 | 2897 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| a0009 | 0/0 | 2897 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 8694 | 81 | 41 | 5 | 23 | 4 | 7 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| c0002 | 0/0 | 8694 | 48 | 8 | 8 | 19 | 4 | 9 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| c0003 | 0/0 | 8694 | 37 | 3 | 5 | 23 | 1 | 5 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| c0004 | 1/0 | 8694 | 34 | 5 | 4 | 19 | 1 | 4 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| c0005 | 0/0 | 8694 | 22 | 16 | 1 | 3 | 0 | 2 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| c0006 | 0/0 | 8694 | 3 | 0 | 0 | 3 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| c0007 | 0/0 | 8694 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| c0008 | 0/0 | 8694 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| c0009 | 0/0 | 8694 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| c0010 | 0/0 | 8694 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| c0011 | 0/0 | 8694 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| c0012 | 0/0 | 8694 | 1 | 0 | 0 | 0 | 0 | 1 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| c0013 | 0/0 | 8694 | 1 | 0 | 1 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| c0014 | 0/0 | 8694 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| c0015 | 0/0 | 8694 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| c0016 | 0/0 | 8694 | 1 | 0 | 1 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| c0017 | 0/0 | 8694 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| c0018 | 0/0 | 8694 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| c0019 | 0/0 | 8694 | 1 | 0 | 1 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 2854 | 141 | 31 | 19 | 59 | 9 | 21 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| t0002 | 0/0 | 2852 | 35 | 6 | 4 | 20 | 1 | 4 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| t0003 | 0/0 | 2852 | 21 | 21 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| t0004 | 0/0 | 2854 | 12 | 12 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| t0005 | 0/0 | 2853 | 8 | 3 | 0 | 3 | 0 | 2 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| t0006 | 0/0 | 2854 | 3 | 0 | 0 | 3 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| t0007 | 0/0 | 2854 | 2 | 2 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| t0008 | 0/0 | 2854 | 2 | 0 | 0 | 2 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| t0009 | 0/0 | 2854 | 2 | 0 | 0 | 2 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| t0010 | 0/0 | 2852 | 2 | 0 | 0 | 2 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| t0011 | 0/0 | 2853 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| t0012 | 0/0 | 2854 | 1 | 0 | 1 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| t0013 | 0/0 | 2852 | 1 | 0 | 1 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| t0014 | 0/0 | 2853 | 1 | 0 | 1 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| t0015 | 0/0 | 2854 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| t0016 | 0/0 | 2851 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| t0017 | 0/0 | 2852 | 1 | 0 | 0 | 0 | 0 | 1 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| t0018 | 0/0 | 2854 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| t0019 | 0/0 | 2864 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| t0020 | 0/0 | 2854 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0057 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0119 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 8694 | 81 | 41 | 5 | 23 | 4 | 7 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| a0001c0003 | 0/0 | 8694 | 37 | 3 | 5 | 23 | 1 | 5 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| a0001c0005 | 0/0 | 8694 | 22 | 16 | 1 | 3 | 0 | 2 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| a0001c0008 | 0/0 | 8694 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| a0001c0012 | 0/0 | 8694 | 1 | 0 | 0 | 0 | 0 | 1 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| a0001c0013 | 0/0 | 8694 | 1 | 0 | 1 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| a0001c0014 | 0/0 | 8694 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| a0001c0015 | 0/0 | 8694 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| a0001c0016 | 0/0 | 8694 | 1 | 0 | 1 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| a0001c0017 | 0/0 | 8694 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| a0002c0002 | 0/0 | 8694 | 48 | 8 | 8 | 19 | 4 | 9 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| a0002c0019 | 0/0 | 8694 | 1 | 0 | 1 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| a0003c0004 | 1/0 | 8694 | 34 | 5 | 4 | 19 | 1 | 4 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| a0004c0006 | 0/0 | 8694 | 3 | 0 | 0 | 3 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| a0005c0007 | 0/0 | 8694 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| a0006c0009 | 0/0 | 8694 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| a0007c0010 | 0/0 | 8694 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| a0008c0011 | 0/0 | 8694 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| a0009c0018 | 0/0 | 8694 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 11547 | 54 | 16 | 5 | 21 | 4 | 7 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| a0001c0001t0002 | 0/0 | 11545 | 2 | 2 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| a0001c0001t0003 | 0/0 | 11545 | 20 | 20 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| a0001c0001t0007 | 0/0 | 11547 | 2 | 2 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| a0001c0001t0009 | 0/0 | 11547 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| a0001c0001t0015 | 0/0 | 11547 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| a0001c0001t0020 | 0/0 | 11547 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| a0001c0003t0001 | 0/0 | 11547 | 1 | 0 | 1 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| a0001c0003t0002 | 0/0 | 11545 | 30 | 3 | 3 | 19 | 1 | 4 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| a0001c0003t0010 | 0/0 | 11545 | 2 | 0 | 0 | 2 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| a0001c0003t0013 | 0/0 | 11545 | 1 | 0 | 1 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| a0001c0003t0016 | 0/0 | 11544 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| a0001c0003t0017 | 0/0 | 11545 | 1 | 0 | 0 | 0 | 0 | 1 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| a0001c0003t0019 | 0/0 | 11557 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| a0001c0005t0001 | 0/0 | 11547 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| a0001c0005t0004 | 0/0 | 11547 | 11 | 11 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| a0001c0005t0005 | 0/0 | 11546 | 7 | 3 | 0 | 2 | 0 | 2 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| a0001c0005t0011 | 0/0 | 11546 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| a0001c0005t0012 | 0/0 | 11547 | 1 | 0 | 1 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| a0001c0005t0018 | 0/0 | 11547 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| a0001c0008t0001 | 0/0 | 11547 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| a0001c0012t0001 | 0/0 | 11547 | 1 | 0 | 0 | 0 | 0 | 1 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| a0001c0013t0001 | 0/0 | 11547 | 1 | 0 | 1 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| a0001c0014t0001 | 0/0 | 11547 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| a0001c0015t0002 | 0/0 | 11545 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| a0001c0016t0002 | 0/0 | 11545 | 1 | 0 | 1 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| a0001c0017t0002 | 0/0 | 11545 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| a0002c0002t0001 | 0/0 | 11547 | 45 | 8 | 7 | 17 | 4 | 9 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| a0002c0002t0008 | 0/0 | 11547 | 2 | 0 | 0 | 2 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| a0002c0002t0014 | 0/0 | 11546 | 1 | 0 | 1 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| a0002c0019t0001 | 0/0 | 11547 | 1 | 0 | 1 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| a0003c0004t0001 | 1/0 | 11547 | 31 | 5 | 4 | 16 | 1 | 4 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| a0003c0004t0006 | 0/0 | 11547 | 3 | 0 | 0 | 3 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| a0004c0006t0001 | 0/0 | 11547 | 3 | 0 | 0 | 3 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| a0005c0007t0009 | 0/0 | 11547 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| a0006c0009t0004 | 0/0 | 11547 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| a0007c0010t0001 | 0/0 | 11547 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| a0008c0011t0003 | 0/0 | 11545 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| a0009c0018t0005 | 0/0 | 11546 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | copy fasta | chr16 | 53049991 | 53332497 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0001t0001g0119 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0001t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0001t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0001t0003g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0001t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0001t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0001t0003g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0001t0003g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0001t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0001t0003g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0001t0003g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0001t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0001t0003g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0001t0003g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0001t0003g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0001t0003g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0001t0003g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0001t0003g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0001t0003g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0001t0003g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0001t0003g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0001t0003g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0001t0003g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0001t0007g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0001t0007g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0001t0009g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0001t0015g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0001t0020g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0003t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0003t0002g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0003t0002g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0003t0002g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0003t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0003t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0003t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0003t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0003t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0003t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0003t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0003t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0003t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0003t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0003t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0003t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0003t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0003t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0003t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0003t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0003t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0003t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0003t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0003t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0003t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0003t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0003t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0003t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0003t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0003t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0003t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0003t0010g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0003t0010g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0003t0013g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0003t0016g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0003t0017g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0003t0019g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0005t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0005t0004g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0005t0004g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0005t0004g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0005t0004g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0005t0004g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0005t0004g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0005t0004g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0005t0004g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0005t0004g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0005t0004g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0005t0004g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0005t0005g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0005t0005g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0005t0005g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0005t0005g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0005t0005g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0005t0005g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0005t0005g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0005t0011g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0005t0012g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0005t0018g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0008t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0012t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0013t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0014t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0015t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0016t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0001c0017t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0002c0002t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0002c0002t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0002c0002t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0002c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0002c0002t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0002c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0002c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0002c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0002c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0002c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0002c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0002c0002t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0002c0002t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0002c0002t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0002c0002t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0002c0002t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0002c0002t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0002c0002t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0002c0002t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0002c0002t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0002c0002t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0002c0002t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0002c0002t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0002c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0002c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0002c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0002c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0002c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0002c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0002c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0002c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0002c0002t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0002c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0002c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0002c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0002c0002t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0002c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0002c0002t0008g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0002c0002t0008g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0002c0002t0014g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0002c0019t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0003c0004t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0003c0004t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0003c0004t0001g0057 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0003c0004t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0003c0004t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0003c0004t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0003c0004t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0003c0004t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0003c0004t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0003c0004t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0003c0004t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0003c0004t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0003c0004t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0003c0004t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0003c0004t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0003c0004t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0003c0004t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0003c0004t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0003c0004t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0003c0004t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0003c0004t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0003c0004t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0003c0004t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0003c0004t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0003c0004t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0003c0004t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0003c0004t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0003c0004t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0003c0004t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0003c0004t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0003c0004t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0003c0004t0006g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0003c0004t0006g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0003c0004t0006g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0004c0006t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0004c0006t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0004c0006t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0005c0007t0009g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0006c0009t0004g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0007c0010t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0008c0011t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| a0009c0018t0005g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0160 | EUR | GBR | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG00099 | hp2 | a0002 | c0002 | t0001 | g0150 | EUR | GBR | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0210 | EUR | GBR | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG00140 | hp2 | a0001 | c0003 | t0002 | g0041 | EUR | GBR | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG00323 | hp1 | a0002 | c0002 | t0001 | g0129 | EUR | FIN | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0206 | EUR | FIN | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG00408 | hp1 | a0002 | c0002 | t0008 | g0137 | EAS | CHS | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | CHS | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | CHS | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG00558 | hp2 | a0001 | c0001 | t0015 | g0166 | EAS | CHS | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG00597 | hp1 | a0005 | c0007 | t0009 | g0076 | EAS | CHS | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG00597 | hp2 | a0003 | c0004 | t0001 | g0007 | EAS | CHS | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG00609 | hp1 | a0002 | c0002 | t0001 | g0010 | EAS | CHS | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | CHS | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | CHS | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG00621 | hp2 | a0001 | c0003 | t0002 | g0003 | EAS | CHS | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG00733 | hp1 | a0001 | c0013 | t0001 | g0055 | AMR | PUR | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG00733 | hp2 | a0002 | c0002 | t0001 | g0208 | AMR | PUR | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG00735 | hp1 | a0001 | c0016 | t0002 | g0156 | AMR | PUR | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG00735 | hp2 | a0002 | c0002 | t0001 | g0054 | AMR | PUR | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG01074 | hp1 | a0001 | c0003 | t0002 | g0202 | AMR | PUR | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG01099 | hp1 | a0001 | c0003 | t0013 | g0186 | AMR | PUR | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG01099 | hp2 | a0002 | c0002 | t0001 | g0048 | AMR | PUR | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG01109 | hp1 | a0001 | c0003 | t0001 | g0158 | AMR | PUR | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG01167 | hp1 | a0002 | c0002 | t0014 | g0011 | AMR | PUR | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG01167 | hp2 | a0001 | c0005 | t0012 | g0229 | AMR | PUR | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG01168 | hp1 | a0003 | c0004 | t0001 | g0216 | AMR | PUR | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG01168 | hp2 | a0002 | c0002 | t0001 | g0049 | AMR | PUR | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG01169 | hp1 | a0003 | c0004 | t0001 | g0203 | AMR | PUR | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG01169 | hp2 | a0002 | c0002 | t0001 | g0012 | AMR | PUR | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG01243 | hp1 | a0001 | c0003 | t0002 | g0153 | AMR | PUR | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG01255 | hp1 | a0003 | c0004 | t0001 | g0207 | AMR | CLM | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG01255 | hp2 | a0002 | c0002 | t0001 | g0088 | AMR | CLM | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG01257 | hp1 | a0002 | c0019 | t0001 | g0180 | AMR | CLM | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | CLM | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG01433 | hp1 | a0002 | c0002 | t0001 | g0087 | AMR | CLM | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG01433 | hp2 | a0003 | c0004 | t0001 | g0123 | AMR | CLM | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0130 | EUR | IBS | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG01515 | hp2 | a0003 | c0004 | t0001 | g0100 | EUR | IBS | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG01884 | hp1 | a0001 | c0005 | t0004 | g0097 | AFR | ACB | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG01884 | hp2 | a0001 | c0005 | t0004 | g0078 | AFR | ACB | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0131 | AFR | ACB | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG02015 | hp1 | a0001 | c0003 | t0002 | g0154 | EAS | KHV | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG02015 | hp2 | a0003 | c0004 | t0001 | g0195 | EAS | KHV | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | KHV | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG02027 | hp2 | a0001 | c0003 | t0002 | g0033 | EAS | KHV | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG02040 | hp2 | a0002 | c0002 | t0001 | g0024 | EAS | KHV | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0220 | AFR | ACB | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG02055 | hp2 | a0001 | c0017 | t0002 | g0237 | AFR | ACB | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG02080 | hp1 | a0002 | c0002 | t0008 | g0065 | EAS | KHV | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG02080 | hp2 | a0001 | c0003 | t0002 | g0070 | EAS | KHV | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG02129 | hp1 | a0001 | c0003 | t0002 | g0028 | EAS | KHV | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | KHV | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | KHV | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG02135 | hp2 | a0002 | c0002 | t0001 | g0164 | EAS | KHV | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG02155 | hp1 | a0003 | c0004 | t0001 | g0214 | EAS | CDX | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG02155 | hp2 | a0001 | c0003 | t0002 | g0036 | EAS | CDX | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG02165 | hp1 | a0003 | c0004 | t0001 | g0194 | EAS | CDX | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG02165 | hp2 | a0002 | c0002 | t0001 | g0144 | EAS | CDX | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0172 | AFR | ACB | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG02257 | hp2 | a0001 | c0005 | t0005 | g0017 | AFR | ACB | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0079 | AFR | ACB | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG02280 | hp2 | a0001 | c0001 | t0007 | g0122 | AFR | ACB | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG02300 | hp1 | a0001 | c0003 | t0002 | g0161 | AMR | PEL | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0171 | AFR | ACB | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | ACB | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0063 | SAS | PJL | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG02602 | hp2 | a0001 | c0012 | t0001 | g0132 | SAS | PJL | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG02615 | hp2 | a0001 | c0005 | t0004 | g0232 | AFR | GWD | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0175 | AFR | GWD | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG02622 | hp2 | a0001 | c0005 | t0011 | g0228 | AFR | GWD | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG02630 | hp1 | a0001 | c0001 | t0020 | g0101 | AFR | GWD | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | GWD | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG02683 | hp1 | a0001 | c0003 | t0002 | g0094 | SAS | PJL | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG02717 | hp1 | a0002 | c0002 | t0001 | g0109 | AFR | GWD | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG02717 | hp2 | a0001 | c0003 | t0002 | g0059 | AFR | GWD | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG02738 | hp1 | a0001 | c0003 | t0002 | g0086 | SAS | PJL | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0211 | SAS | PJL | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0133 | AFR | GWD | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG02809 | hp2 | a0001 | c0014 | t0001 | g0115 | AFR | GWD | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG02886 | hp1 | a0001 | c0001 | t0007 | g0103 | AFR | GWD | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0105 | AFR | GWD | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG02895 | hp1 | a0002 | c0002 | t0001 | g0163 | AFR | GWD | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG02895 | hp2 | a0003 | c0004 | t0001 | g0141 | AFR | GWD | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG02897 | hp1 | a0001 | c0005 | t0004 | g0238 | AFR | GWD | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG02897 | hp2 | a0002 | c0002 | t0001 | g0120 | AFR | GWD | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0139 | AFR | ESN | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG02922 | hp2 | a0001 | c0005 | t0004 | g0236 | AFR | ESN | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0016 | AFR | ESN | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG02965 | hp2 | a0003 | c0004 | t0001 | g0148 | AFR | ESN | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG02970 | hp1 | a0001 | c0005 | t0005 | g0032 | AFR | ESN | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | ESN | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG02976 | hp1 | a0001 | c0008 | t0001 | g0077 | AFR | ESN | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG02976 | hp2 | a0001 | c0005 | t0004 | g0233 | AFR | ESN | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG03017 | hp1 | a0002 | c0002 | t0001 | g0140 | SAS | PJL | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG03017 | hp2 | a0001 | c0003 | t0002 | g0083 | SAS | PJL | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0227 | AFR | GWD | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0112 | AFR | MSL | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | MSL | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG03130 | hp1 | a0002 | c0002 | t0001 | g0102 | AFR | ESN | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG03130 | hp2 | a0003 | c0004 | t0001 | g0177 | AFR | ESN | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG03139 | hp1 | a0001 | c0005 | t0004 | g0169 | AFR | ESN | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0183 | AFR | ESN | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG03195 | hp2 | a0001 | c0005 | t0004 | g0234 | AFR | ESN | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | MSL | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG03225 | hp2 | a0002 | c0002 | t0001 | g0113 | AFR | MSL | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG03239 | hp1 | a0003 | c0004 | t0001 | g0209 | SAS | PJL | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG03239 | hp2 | a0002 | c0002 | t0001 | g0136 | SAS | PJL | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG03453 | hp1 | a0003 | c0004 | t0001 | g0134 | AFR | MSL | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | MSL | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG03486 | hp1 | a0002 | c0002 | t0001 | g0114 | AFR | MSL | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | MSL | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG03492 | hp1 | a0002 | c0002 | t0001 | g0126 | SAS | PJL | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0022 | AFR | ESN | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG03516 | hp2 | a0006 | c0009 | t0004 | g0107 | AFR | ESN | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0223 | AFR | GWD | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG03579 | hp1 | a0001 | c0005 | t0018 | g0001 | AFR | MSL | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0222 | AFR | MSL | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG03669 | hp1 | a0002 | c0002 | t0001 | g0219 | SAS | PJL | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG03688 | hp1 | a0002 | c0002 | t0001 | g0138 | SAS | STU | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG03688 | hp2 | a0001 | c0005 | t0005 | g0061 | SAS | STU | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG03831 | hp1 | a0003 | c0004 | t0001 | g0162 | SAS | BEB | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0205 | SAS | BEB | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG03942 | hp1 | a0001 | c0003 | t0017 | g0181 | SAS | BEB | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG03942 | hp2 | a0003 | c0004 | t0001 | g0204 | SAS | BEB | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | STU | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG04115 | hp2 | a0001 | c0003 | t0002 | g0152 | SAS | STU | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0218 | SAS | BEB | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG04184 | hp2 | a0001 | c0005 | t0005 | g0089 | SAS | BEB | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG04199 | hp1 | a0002 | c0002 | t0001 | g0042 | SAS | STU | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | STU | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG04204 | hp1 | a0002 | c0002 | t0001 | g0108 | SAS | STU | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG04204 | hp2 | a0003 | c0004 | t0001 | g0157 | SAS | STU | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | YRI | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0221 | AFR | YRI | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| NA18939 | hp2 | a0002 | c0002 | t0001 | g0020 | EAS | JPT | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| NA18946 | hp2 | a0001 | c0003 | t0002 | g0073 | EAS | JPT | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| NA18950 | hp1 | a0001 | c0003 | t0010 | g0013 | EAS | JPT | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| NA18950 | hp2 | a0003 | c0004 | t0006 | g0074 | EAS | JPT | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| NA18952 | hp1 | a0004 | c0006 | t0001 | g0127 | EAS | JPT | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| NA18952 | hp2 | a0001 | c0001 | t0009 | g0050 | EAS | JPT | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| NA18961 | hp1 | a0001 | c0015 | t0002 | g0053 | EAS | JPT | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| NA18961 | hp2 | a0003 | c0004 | t0001 | g0198 | EAS | JPT | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| NA18962 | hp2 | a0002 | c0002 | t0001 | g0147 | EAS | JPT | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| NA18963 | hp2 | a0002 | c0002 | t0001 | g0037 | EAS | JPT | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| NA18964 | hp2 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| NA18966 | hp1 | a0001 | c0003 | t0002 | g0040 | EAS | JPT | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| NA18966 | hp2 | a0003 | c0004 | t0001 | g0200 | EAS | JPT | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| NA18970 | hp1 | a0003 | c0004 | t0001 | g0197 | EAS | JPT | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| NA18970 | hp2 | a0001 | c0003 | t0002 | g0002 | EAS | JPT | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| NA18972 | hp2 | a0001 | c0003 | t0002 | g0191 | EAS | JPT | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| NA18974 | hp1 | a0001 | c0003 | t0002 | g0023 | EAS | JPT | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| NA18974 | hp2 | a0003 | c0004 | t0001 | g0213 | EAS | JPT | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| NA18981 | hp1 | a0001 | c0003 | t0002 | g0046 | EAS | JPT | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| NA18981 | hp2 | a0009 | c0018 | t0005 | g0155 | EAS | JPT | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| NA18982 | hp1 | a0001 | c0003 | t0002 | g0142 | EAS | JPT | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| NA18982 | hp2 | a0003 | c0004 | t0001 | g0196 | EAS | JPT | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| NA18989 | hp1 | a0004 | c0006 | t0001 | g0121 | EAS | JPT | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| NA18989 | hp2 | a0001 | c0005 | t0001 | g0215 | EAS | JPT | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| NA18992 | hp2 | a0002 | c0002 | t0001 | g0082 | EAS | JPT | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| NA18993 | hp1 | a0001 | c0003 | t0002 | g0080 | EAS | JPT | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| NA18993 | hp2 | a0003 | c0004 | t0001 | g0192 | EAS | JPT | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| NA18995 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| NA18999 | hp1 | a0003 | c0004 | t0006 | g0190 | EAS | JPT | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| NA18999 | hp2 | a0001 | c0003 | t0010 | g0006 | EAS | JPT | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| NA19009 | hp1 | a0002 | c0002 | t0001 | g0146 | EAS | JPT | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| NA19010 | hp2 | a0002 | c0002 | t0001 | g0145 | EAS | JPT | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| NA19011 | hp1 | a0003 | c0004 | t0001 | g0093 | EAS | JPT | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| NA19011 | hp2 | a0004 | c0006 | t0001 | g0128 | EAS | JPT | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| NA19012 | hp2 | a0001 | c0003 | t0002 | g0005 | EAS | JPT | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0096 | AFR | LWK | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| NA19043 | hp2 | a0001 | c0005 | t0004 | g0104 | AFR | LWK | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| NA19062 | hp1 | a0003 | c0004 | t0006 | g0199 | EAS | JPT | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| NA19062 | hp2 | a0001 | c0003 | t0019 | g0004 | EAS | JPT | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| NA19063 | hp1 | a0003 | c0004 | t0001 | g0030 | EAS | JPT | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| NA19063 | hp2 | a0002 | c0002 | t0001 | g0149 | EAS | JPT | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| NA19064 | hp1 | a0003 | c0004 | t0001 | g0217 | EAS | JPT | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| NA19064 | hp2 | a0002 | c0002 | t0001 | g0118 | EAS | JPT | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| NA19066 | hp1 | a0002 | c0002 | t0001 | g0034 | EAS | JPT | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| NA19066 | hp2 | a0003 | c0004 | t0001 | g0187 | EAS | JPT | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| NA19068 | hp1 | a0001 | c0005 | t0005 | g0151 | EAS | JPT | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| NA19068 | hp2 | a0001 | c0003 | t0016 | g0039 | EAS | JPT | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| NA19070 | hp2 | a0002 | c0002 | t0001 | g0193 | EAS | JPT | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| NA19074 | hp1 | a0002 | c0002 | t0001 | g0035 | EAS | JPT | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| NA19074 | hp2 | a0001 | c0003 | t0002 | g0125 | EAS | JPT | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| NA19084 | hp1 | a0003 | c0004 | t0001 | g0201 | EAS | JPT | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| NA19084 | hp2 | a0001 | c0003 | t0002 | g0015 | EAS | JPT | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| NA19087 | hp2 | a0007 | c0010 | t0001 | g0212 | EAS | JPT | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| NA19088 | hp1 | a0001 | c0005 | t0005 | g0135 | EAS | JPT | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| NA19088 | hp2 | a0001 | c0003 | t0002 | g0047 | EAS | JPT | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| NA19240 | hp1 | a0001 | c0005 | t0004 | g0231 | AFR | YRI | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| NA19240 | hp2 | a0001 | c0005 | t0005 | g0018 | AFR | YRI | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0226 | AFR | ASW | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | ASW | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0185 | EUR | TSI | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| NA20805 | hp2 | a0002 | c0002 | t0001 | g0044 | EUR | TSI | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG02109 | hp1 | a0008 | c0011 | t0003 | g0062 | AFR | ACB | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0184 | AFR | ACB | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | ACB | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0176 | AFR | ACB | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0167 | AFR | ACB | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG02559 | hp2 | a0003 | c0004 | t0001 | g0143 | AFR | ACB | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | MSL | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG03471 | hp2 | a0002 | c0002 | t0001 | g0106 | AFR | MSL | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG06807 | hp1 | a0001 | c0003 | t0002 | g0170 | AFR | USA | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| HG06807 | hp2 | a0002 | c0002 | t0001 | g0095 | AFR | USA | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| NA18955 | hp1 | a0001 | c0003 | t0002 | g0029 | EAS | JPT | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| NA18955 | hp2 | a0003 | c0004 | t0001 | g0189 | EAS | JPT | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| NA20300 | hp1 | a0001 | c0005 | t0004 | g0235 | AFR | USA | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| NA20300 | hp2 | a0001 | c0003 | t0002 | g0224 | AFR | USA | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0119 | REF | REF | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| homoSapiens_grch38 | hp1 | a0003 | c0004 | t0001 | g0057 | REF | REF | CHD9_chr16_53049991_53332497 | CHD9 | chr16 | 53049991 | 53332497 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:53157040
|
C | G | 1 | a0009 | 1 | NA18981.hp2 | missense_variant | MODERATE | c.951C>G | p.Ile317Met | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/39 | 1202/11547 | 951/8694 | 317/2897 | chr16 | 53157040 | ||
| chr16:53227453
|
G | A | 1 | a0005 | 1 | HG00597.hp1 | missense_variant | MODERATE | c.2101G>A | p.Val701Ile | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 6/39 | 2352/11547 | 2101/8694 | 701/2897 | chr16 | 53227453 | ||
| chr16:53229065
|
T | A | 1 | a0004 | 3 | NA18952.hp1 NA18989.hp1 NA19011.hp2 |
missense_variant | MODERATE | c.2251T>A | p.Leu751Met | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 8/39 | 2502/11547 | 2251/8694 | 751/2897 | chr16 | 53229065 | ||
| chr16:53255612
|
T | A | 1 | a0008 | 1 | HG02109.hp1 | missense_variant | MODERATE | c.4042T>A | p.Ser1348Thr | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 19/39 | 4293/11547 | 4042/8694 | 1348/2897 | chr16 | 53255612 | ||
| chr16:53303737
|
A | G | 1 | a0007 | 1 | NA19087.hp2 | missense_variant | MODERATE | c.5731A>G | p.Ile1911Val | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 31/39 | 5982/11547 | 5731/8694 | 1911/2897 | chr16 | 53303737 | ||
| chr16:53307765
|
G | C | 1 | a0006 | 1 | HG03516.hp2 | missense_variant | MODERATE | c.6865G>C | p.Ala2289Pro | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 33/39 | 7116/11547 | 6865/8694 | 2289/2897 | chr16 | 53307765 | ||
| chr16:53307836
|
T | G | 8 | a0001a0002a0004others(5): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
missense_variant | MODERATE | c.6936T>G | p.Asp2312Glu | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 33/39 | 7187/11547 | 6936/8694 | 2312/2897 | chr16 | 53307836 | ||
| chr16:53324527
|
A | G | 3 | a0002a0004a0007 | 53 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(50): Show |
missense_variant | MODERATE | c.8326A>G | p.Thr2776Ala | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 39/39 | 8577/11547 | 8326/8694 | 2776/2897 | chr16 | 53324527 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:53156545
|
A | G | 1 | a0002c0019 | 1 | HG01257.hp1 | synonymous_variant | LOW | c.456A>G | p.Gln152Gln | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/39 | 707/11547 | 456/8694 | 152/2897 | chr16 | 53156545 | ||
| chr16:53229052
|
C | T | 4 | a0001c0003a0001c0015a0001c0016others(1): Show | 40 | HG00140.hp2 HG00621.hp2 HG00735.hp1 others(37): Show |
synonymous_variant | LOW | c.2238C>T | p.Ile746Ile | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 8/39 | 2489/11547 | 2238/8694 | 746/2897 | chr16 | 53229052 | ||
| chr16:53245666
|
G | A | 1 | a0001c0008 | 1 | HG02976.hp1 | synonymous_variant | LOW | c.3270G>A | p.Leu1090Leu | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 15/39 | 3521/11547 | 3270/8694 | 1090/2897 | chr16 | 53245666 | ||
| chr16:53245837
|
A | G | 1 | a0001c0014 | 1 | HG02809.hp2 | synonymous_variant | LOW | c.3441A>G | p.Pro1147Pro | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 15/39 | 3692/11547 | 3441/8694 | 1147/2897 | chr16 | 53245837 | ||
| chr16:53250054
|
G | A | 7 | a0001c0005a0002c0002a0002c0019others(4): Show | 77 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(74): Show |
synonymous_variant | LOW | c.3849G>A | p.Gln1283Gln | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 17/39 | 4100/11547 | 3849/8694 | 1283/2897 | chr16 | 53250054 | ||
| chr16:53255635
|
G | A | 1 | a0001c0015 | 1 | NA18961.hp1 | synonymous_variant | LOW | c.4065G>A | p.Leu1355Leu | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 19/39 | 4316/11547 | 4065/8694 | 1355/2897 | chr16 | 53255635 | ||
| chr16:53274237
|
G | A | 1 | a0001c0012 | 1 | HG02602.hp2 | synonymous_variant | LOW | c.4902G>A | p.Leu1634Leu | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 24/39 | 5153/11547 | 4902/8694 | 1634/2897 | chr16 | 53274237 | ||
| chr16:53292948
|
G | A | 7 | a0001c0005a0002c0002a0002c0019others(4): Show | 77 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(74): Show |
synonymous_variant | LOW | c.5406G>A | p.Gln1802Gln | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 29/39 | 5657/11547 | 5406/8694 | 1802/2897 | chr16 | 53292948 | ||
| chr16:53314879
|
C | G | 1 | a0001c0017 | 1 | HG02055.hp2 | synonymous_variant | LOW | c.7419C>G | p.Ser2473Ser | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 36/39 | 7670/11547 | 7419/8694 | 2473/2897 | chr16 | 53314879 | ||
| chr16:53324082
|
A | G | 1 | a0001c0016 | 1 | HG00735.hp1 | synonymous_variant | LOW | c.7881A>G | p.Val2627Val | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 39/39 | 8132/11547 | 7881/8694 | 2627/2897 | chr16 | 53324082 | ||
| chr16:53324577
|
T | C | 1 | a0001c0013 | 1 | HG00733.hp1 | synonymous_variant | LOW | c.8376T>C | p.Ala2792Ala | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 39/39 | 8627/11547 | 8376/8694 | 2792/2897 | chr16 | 53324577 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:53156028
|
A | C | 1 | a0001c0001t0020 | 1 | HG02630.hp1 | 5_prime_UTR_variant | MODIFIER | c.-62A>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/39 | 62 | chr16 | 53156028 | |||||
| chr16:53156029
|
T | C | 3 | a0001c0005t0005a0001c0005t0011a0009c0018t0005 | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-61T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/39 | 61 | chr16 | 53156029 | |||||
| chr16:53324922
|
A | C | 1 | a0001c0003t0010 | 2 | NA18950.hp1 NA18999.hp2 |
3_prime_UTR_variant | MODIFIER | c.*27A>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 39/39 | 27 | chr16 | 53324922 | |||||
| chr16:53324977
|
G | A | 1 | a0001c0005t0012 | 1 | HG01167.hp2 | 3_prime_UTR_variant | MODIFIER | c.*82G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 39/39 | 82 | chr16 | 53324977 | |||||
| chr16:53325165
|
A | AATTATGC others(5): Show |
1 | a0001c0003t0019 | 1 | NA19062.hp2 | 3_prime_UTR_variant | MODIFIER | c.*272_*283dupTTATGC others(6): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 39/39 | 284 | INFO_REALIGN_3_PRIME | chr16 | 53325165 | ||||
| chr16:53325426
|
T | C | 1 | a0001c0001t0007 | 2 | HG02280.hp2 HG02886.hp1 |
3_prime_UTR_variant | MODIFIER | c.*531T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 39/39 | 531 | chr16 | 53325426 | |||||
| chr16:53325514
|
G | A | 1 | a0001c0003t0013 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*619G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 39/39 | 619 | chr16 | 53325514 | |||||
| chr16:53325617
|
A | G | 1 | a0001c0005t0018 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*722A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 39/39 | 722 | chr16 | 53325617 | |||||
| chr16:53325618
|
T | A | 3 | a0001c0005t0005a0001c0005t0011a0009c0018t0005 | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*723T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 39/39 | 723 | chr16 | 53325618 | |||||
| chr16:53325672
|
A | G | 4 | a0001c0005t0004a0001c0005t0012a0001c0005t0018others(1): Show | 14 | HG01167.hp2 HG01884.hp1 HG01884.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*777A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 39/39 | 777 | chr16 | 53325672 | |||||
| chr16:53326024
|
C | T | 1 | a0001c0003t0017 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1129C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 39/39 | 1129 | chr16 | 53326024 | |||||
| chr16:53326150
|
A | G | 2 | a0001c0001t0009a0005c0007t0009 | 2 | HG00597.hp1 NA18952.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1255A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 39/39 | 1255 | chr16 | 53326150 | |||||
| chr16:53326361
|
G | T | 11 | a0001c0001t0002a0001c0001t0015a0001c0003t0002others(8): Show | 42 | HG00140.hp2 HG00558.hp2 HG00621.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*1466G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 39/39 | 1466 | chr16 | 53326361 | |||||
| chr16:53326407
|
A | G | 1 | a0003c0004t0006 | 3 | NA18950.hp2 NA18999.hp1 NA19062.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1512A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 39/39 | 1512 | chr16 | 53326407 | |||||
| chr16:53326765
|
AAC | A | 12 | a0001c0001t0002a0001c0001t0003a0001c0003t0002others(9): Show | 62 | HG00140.hp2 HG00621.hp2 HG00735.hp1 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*1874_*1875delCA | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 39/39 | 1874 | INFO_REALIGN_3_PRIME | chr16 | 53326765 | ||||
| chr16:53326770
|
A | C | 3 | a0001c0005t0005a0001c0005t0011a0009c0018t0005 | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1875A>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 39/39 | 1875 | chr16 | 53326770 | |||||
| chr16:53326812
|
A | G | 1 | a0002c0002t0008 | 2 | HG00408.hp1 HG02080.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1917A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 39/39 | 1917 | chr16 | 53326812 | |||||
| chr16:53326870
|
TA | T | 5 | a0001c0003t0016a0001c0005t0005a0001c0005t0011others(2): Show | 11 | HG01167.hp1 HG02257.hp2 HG02622.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1989delA | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 39/39 | 1989 | INFO_REALIGN_3_PRIME | chr16 | 53326870 | ||||
| chr16:53327007
|
A | G | 1 | a0001c0005t0011 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2112A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 39/39 | 2112 | chr16 | 53327007 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:53055283
|
C | A | 18 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0003g0016others(15): Show | 18 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(15): Show |
intron_variant | MODIFIER | c.-165+206C>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53055283 | ||||||
| chr16:53055349
|
C | T | 19 | a0001c0001t0001g0225a0001c0001t0001g0230a0001c0001t0003g0220others(16): Show | 19 | HG01167.hp2 HG02055.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.-165+272C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53055349 | ||||||
| chr16:53055494
|
G | GC | 48 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0168others(45): Show | 48 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.-165+426dupC | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53055494 | |||||
| chr16:53055494
|
G | GCCC | 24 | a0001c0001t0001g0185a0001c0001t0001g0188a0001c0001t0001g0206others(21): Show | 24 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.-165+424_-165+426d others(5): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53055494 | |||||
| chr16:53055494
|
G | GCCCC | 12 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0218others(9): Show | 12 | HG00140.hp1 HG00733.hp2 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.-165+423_-165+426d others(6): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53055494 | |||||
| chr16:53055636
|
G | T | 1 | a0001c0001t0015g0166 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-165+559G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53055636 | ||||||
| chr16:53055692
|
C | T | 122 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0116others(119): Show | 122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.-165+615C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53055692 | ||||||
| chr16:53055783
|
C | T | 1 | a0003c0004t0001g0100 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-165+706C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53055783 | ||||||
| chr16:53056003
|
CCTTTTTT others(11): Show |
C | 20 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0003g0016others(17): Show | 20 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(17): Show |
intron_variant | MODIFIER | c.-165+927_-165+944d others(20): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53056003 | ||||||
| chr16:53056064
|
T | C | 5 | a0001c0001t0003g0220a0001c0001t0003g0221a0001c0001t0003g0222others(2): Show | 5 | HG02055.hp1 HG03540.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.-165+987T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53056064 | ||||||
| chr16:53056100
|
A | G | 1 | a0001c0001t0001g0099 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-165+1023A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53056100 | ||||||
| chr16:53056408
|
G | A | 1 | a0001c0001t0020g0101 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-165+1331G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53056408 | ||||||
| chr16:53056644
|
C | T | 1 | a0001c0001t0001g0098 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-165+1567C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53056644 | ||||||
| chr16:53056922
|
A | C | 5 | a0001c0001t0003g0220a0001c0001t0003g0221a0001c0001t0003g0222others(2): Show | 5 | HG02055.hp1 HG03540.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.-165+1845A>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53056922 | ||||||
| chr16:53056927
|
C | T | 1 | a0001c0005t0004g0097 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-165+1850C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53056927 | ||||||
| chr16:53057019
|
A | T | 36 | a0001c0001t0001g0165a0001c0001t0001g0185a0001c0001t0001g0188others(33): Show | 36 | HG00140.hp1 HG00323.hp2 HG00733.hp2 others(33): Show |
intron_variant | MODIFIER | c.-165+1942A>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53057019 | ||||||
| chr16:53057025
|
T | C | 1 | a0002c0002t0001g0102 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-165+1948T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53057025 | ||||||
| chr16:53057139
|
T | C | 58 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0165others(55): Show | 58 | HG00140.hp1 HG00323.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.-165+2062T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53057139 | ||||||
| chr16:53057179
|
A | T | 1 | a0001c0001t0003g0096 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-165+2102A>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53057179 | ||||||
| chr16:53057432
|
T | C | 1 | a0001c0001t0001g0021 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-165+2355T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53057432 | ||||||
| chr16:53057451
|
G | A | 3 | a0001c0001t0003g0105a0002c0002t0001g0106a0006c0009t0004g0107 | 3 | HG02886.hp2 HG03471.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-165+2374G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53057451 | ||||||
| chr16:53057452
|
A | G | 36 | a0001c0001t0001g0165a0001c0001t0001g0185a0001c0001t0001g0188others(33): Show | 36 | HG00140.hp1 HG00323.hp2 HG00733.hp2 others(33): Show |
intron_variant | MODIFIER | c.-165+2375A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53057452 | ||||||
| chr16:53057523
|
A | G | 17 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0003g0016others(14): Show | 17 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(14): Show |
intron_variant | MODIFIER | c.-165+2446A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53057523 | ||||||
| chr16:53057813
|
G | A | 17 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0003g0016others(14): Show | 17 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(14): Show |
intron_variant | MODIFIER | c.-165+2736G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53057813 | ||||||
| chr16:53058430
|
T | C | 1 | a0002c0002t0001g0108 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-165+3353T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53058430 | ||||||
| chr16:53058445
|
A | T | 51 | a0001c0001t0001g0119a0001c0001t0001g0124a0001c0001t0001g0159others(48): Show | 51 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.-165+3368A>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53058445 | ||||||
| chr16:53058530
|
G | A | 1 | a0001c0001t0003g0022 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-165+3453G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53058530 | ||||||
| chr16:53058704
|
T | C | 5 | a0001c0001t0003g0220a0001c0001t0003g0221a0001c0001t0003g0222others(2): Show | 5 | HG02055.hp1 HG03540.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.-165+3627T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53058704 | ||||||
| chr16:53058844
|
G | T | 37 | a0001c0001t0001g0165a0001c0001t0001g0185a0001c0001t0001g0188others(34): Show | 37 | HG00140.hp1 HG00323.hp2 HG00733.hp2 others(34): Show |
intron_variant | MODIFIER | c.-165+3767G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53058844 | ||||||
| chr16:53058998
|
G | A | 1 | a0002c0002t0001g0118 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-165+3921G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53058998 | ||||||
| chr16:53059068
|
T | C | 38 | a0001c0001t0001g0165a0001c0001t0001g0185a0001c0001t0001g0188others(35): Show | 38 | HG00140.hp1 HG00323.hp2 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.-165+3991T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53059068 | ||||||
| chr16:53059128
|
A | G | 1 | a0001c0001t0007g0103 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-165+4051A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53059128 | ||||||
| chr16:53059201
|
G | T | 1 | a0001c0005t0004g0238 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-165+4124G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53059201 | ||||||
| chr16:53059292
|
T | C | 27 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0116others(24): Show | 27 | HG01884.hp1 HG01891.hp2 HG02257.hp1 others(24): Show |
intron_variant | MODIFIER | c.-165+4215T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53059292 | ||||||
| chr16:53059334
|
TG | T | 17 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0003g0016others(14): Show | 17 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(14): Show |
intron_variant | MODIFIER | c.-165+4259delG | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53059334 | |||||
| chr16:53059428
|
A | T | 1 | a0001c0003t0002g0094 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-165+4351A>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53059428 | ||||||
| chr16:53059632
|
G | A | 1 | a0002c0002t0001g0208 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-165+4555G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53059632 | ||||||
| chr16:53059808
|
G | A | 53 | a0001c0001t0001g0119a0001c0001t0001g0124a0001c0001t0001g0159others(50): Show | 53 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(50): Show |
intron_variant | MODIFIER | c.-165+4731G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53059808 | ||||||
| chr16:53060514
|
T | C | 1 | a0001c0001t0003g0167 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-165+5437T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53060514 | ||||||
| chr16:53060920
|
C | CT | 26 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0092others(23): Show | 26 | HG00323.hp2 HG01109.hp2 HG01255.hp1 others(23): Show |
intron_variant | MODIFIER | c.-165+5866dupT | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53060920 | |||||
| chr16:53060920
|
CT | C | 24 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0025others(21): Show | 24 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.-165+5866delT | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53060920 | |||||
| chr16:53061595
|
T | C | 1 | a0001c0005t0004g0169 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-165+6518T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53061595 | ||||||
| chr16:53061652
|
C | T | 1 | a0001c0001t0001g0225 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-165+6575C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53061652 | ||||||
| chr16:53061860
|
G | C | 36 | a0001c0001t0001g0165a0001c0001t0001g0185a0001c0001t0001g0188others(33): Show | 36 | HG00140.hp1 HG00323.hp2 HG00733.hp2 others(33): Show |
intron_variant | MODIFIER | c.-165+6783G>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53061860 | ||||||
| chr16:53062024
|
C | T | 2 | a0001c0001t0001g0084a0001c0001t0001g0085 | 2 | HG00621.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.-165+6947C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53062024 | ||||||
| chr16:53062032
|
A | G | 9 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0116others(6): Show | 9 | HG02486.hp1 HG02615.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.-165+6955A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53062032 | ||||||
| chr16:53062166
|
A | C | 1 | a0001c0001t0003g0184 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-165+7089A>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53062166 | ||||||
| chr16:53062200
|
A | G | 1 | a0003c0004t0001g0093 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-165+7123A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53062200 | ||||||
| chr16:53062517
|
A | G | 1 | a0001c0001t0003g0184 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-165+7440A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53062517 | ||||||
| chr16:53062753
|
G | A | 1 | a0001c0001t0003g0105 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-165+7676G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53062753 | ||||||
| chr16:53062800
|
G | A | 17 | a0001c0001t0001g0008a0001c0001t0020g0101a0001c0003t0002g0002others(14): Show | 17 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(14): Show |
intron_variant | MODIFIER | c.-165+7723G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53062800 | ||||||
| chr16:53062962
|
G | A | 2 | a0001c0003t0002g0028a0001c0003t0002g0029 | 2 | HG02129.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.-165+7885G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53062962 | ||||||
| chr16:53063200
|
CT | C | 52 | a0001c0001t0001g0014a0001c0001t0001g0119a0001c0001t0001g0124others(49): Show | 52 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.-165+8126delT | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53063200 | |||||
| chr16:53063228
|
A | C | 29 | a0001c0001t0001g0008a0001c0001t0001g0225a0001c0001t0001g0230others(26): Show | 29 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.-165+8151A>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53063228 | ||||||
| chr16:53063240
|
G | T | 1 | a0001c0001t0002g0175 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-165+8163G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53063240 | ||||||
| chr16:53063250
|
G | A | 1 | a0001c0001t0003g0184 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-165+8173G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53063250 | ||||||
| chr16:53063266
|
A | T | 1 | a0001c0003t0002g0161 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-165+8189A>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53063266 | ||||||
| chr16:53063358
|
T | TCA | 19 | a0001c0001t0001g0069a0001c0001t0001g0071a0001c0001t0001g0072others(16): Show | 19 | HG00558.hp2 HG00621.hp1 HG01074.hp2 others(16): Show |
intron_variant | MODIFIER | c.-165+8324_-165+832 others(6): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53063358 | |||||
| chr16:53063358
|
T | TCACA | 20 | a0001c0001t0001g0081a0001c0001t0001g0091a0001c0001t0001g0206others(17): Show | 20 | HG00323.hp2 HG01884.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.-165+8322_-165+832 others(8): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53063358 | |||||
| chr16:53063358
|
T | TCACACA | 22 | a0001c0001t0001g0092a0001c0001t0001g0165a0001c0001t0002g0175others(19): Show | 22 | HG00621.hp2 HG00733.hp2 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.-165+8320_-165+832 others(10): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53063358 | |||||
| chr16:53063358
|
T | TCACACAC others(1): Show |
13 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0173others(10): Show | 13 | HG00597.hp2 HG01255.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.-165+8318_-165+832 others(12): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53063358 | |||||
| chr16:53063358
|
T | TCACACAC others(3): Show |
3 | a0001c0001t0001g0178a0001c0003t0002g0202a0003c0004t0001g0201 | 3 | HG01074.hp1 HG02630.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.-165+8316_-165+832 others(14): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53063358 | |||||
| chr16:53063358
|
T | TCACACAC others(5): Show |
7 | a0002c0002t0001g0010a0002c0002t0001g0012a0002c0002t0001g0219others(4): Show | 7 | HG00609.hp1 HG01167.hp1 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.-165+8314_-165+832 others(16): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53063358 | |||||
| chr16:53063358
|
T | TCACACAC others(7): Show |
1 | a0001c0003t0002g0029 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-165+8312_-165+832 others(18): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53063358 | |||||
| chr16:53063358
|
TCA | T | 23 | a0001c0001t0001g0110a0001c0001t0001g0182a0001c0003t0002g0033others(20): Show | 23 | HG00099.hp2 HG00735.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.-165+8324_-165+832 others(6): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53063358 | |||||
| chr16:53063358
|
TCACA | T | 41 | a0001c0001t0001g0031a0001c0001t0001g0119a0001c0001t0001g0124others(38): Show | 41 | HG00323.hp1 HG00408.hp1 HG01257.hp2 others(38): Show |
intron_variant | MODIFIER | c.-165+8322_-165+832 others(8): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53063358 | |||||
| chr16:53063358
|
TCACACA | T | 7 | a0001c0001t0003g0220a0001c0001t0003g0221a0001c0001t0003g0222others(4): Show | 7 | HG02055.hp1 HG03041.hp1 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.-165+8320_-165+832 others(10): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53063358 | |||||
| chr16:53063358
|
TCACACAC others(1): Show |
T | 13 | a0001c0001t0001g0225a0001c0001t0001g0230a0001c0001t0002g0171others(10): Show | 13 | HG01167.hp2 HG02055.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.-165+8318_-165+832 others(12): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53063358 | |||||
| chr16:53063358
|
TCACACAC others(5): Show |
T | 1 | a0001c0001t0020g0101 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-165+8314_-165+832 others(16): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53063358 | |||||
| chr16:53063402
|
A | AC | 5 | a0001c0001t0001g0075a0001c0003t0002g0094a0003c0004t0001g0162others(2): Show | 5 | HG00597.hp1 HG02683.hp1 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.-165+8325_-165+832 others(5): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53063402 | ||||||
| chr16:53063402
|
A | ACACACAC others(4): Show |
1 | a0001c0003t0010g0013 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-165+8325_-165+832 others(15): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53063402 | ||||||
| chr16:53063466
|
T | A | 7 | a0001c0001t0003g0220a0001c0001t0003g0221a0001c0001t0003g0222others(4): Show | 7 | HG02055.hp1 HG03041.hp1 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.-165+8389T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53063466 | ||||||
| chr16:53063594
|
G | A | 1 | a0001c0003t0002g0036 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-165+8517G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53063594 | ||||||
| chr16:53063618
|
C | T | 14 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0031others(11): Show | 14 | HG00408.hp2 HG00621.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.-165+8541C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53063618 | ||||||
| chr16:53063830
|
C | CT | 65 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0119others(62): Show | 65 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(62): Show |
intron_variant | MODIFIER | c.-165+8771dupT | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53063830 | |||||
| chr16:53063840
|
T | G | 1 | a0002c0002t0001g0208 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-165+8763T>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53063840 | ||||||
| chr16:53063844
|
T | G | 35 | a0001c0001t0001g0165a0001c0001t0001g0185a0001c0001t0001g0188others(32): Show | 35 | HG00140.hp1 HG00323.hp2 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.-165+8767T>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53063844 | ||||||
| chr16:53064173
|
T | C | 1 | a0001c0005t0005g0061 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-165+9096T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53064173 | ||||||
| chr16:53064262
|
T | C | 1 | a0001c0005t0005g0032 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-165+9185T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53064262 | ||||||
| chr16:53064286
|
T | G | 10 | a0001c0001t0001g0218a0003c0004t0001g0187a0003c0004t0001g0194others(7): Show | 10 | HG02015.hp2 HG02155.hp1 HG02165.hp1 others(7): Show |
intron_variant | MODIFIER | c.-165+9209T>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53064286 | ||||||
| chr16:53064536
|
C | G | 1 | a0003c0004t0001g0157 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-165+9459C>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53064536 | ||||||
| chr16:53064948
|
G | A | 2 | a0001c0001t0001g0185a0001c0001t0001g0188 | 2 | HG03492.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-165+9871G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53064948 | ||||||
| chr16:53064983
|
G | A | 42 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0165others(39): Show | 42 | HG00140.hp1 HG00323.hp2 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.-165+9906G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53064983 | ||||||
| chr16:53065003
|
AAGAG | A | 5 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0002g0171others(2): Show | 5 | HG02451.hp1 HG02486.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-165+9929_-165+993 others(8): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53065003 | |||||
| chr16:53065508
|
A | G | 154 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0110others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.-165+10431A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53065508 | ||||||
| chr16:53065544
|
G | A | 1 | a0002c0002t0001g0037 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-165+10467G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53065544 | ||||||
| chr16:53065638
|
T | TAAA | 8 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0002g0171others(5): Show | 8 | HG01167.hp1 HG01169.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.-165+10579_-165+10 others(9): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53065638 | |||||
| chr16:53065638
|
T | TAAAA | 29 | a0001c0001t0001g0008a0001c0001t0001g0185a0001c0001t0001g0225others(26): Show | 29 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.-165+10578_-165+10 others(10): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53065638 | |||||
| chr16:53065638
|
T | TAAAAA | 110 | a0001c0001t0001g0014a0001c0001t0001g0110a0001c0001t0001g0119others(107): Show | 110 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(107): Show |
intron_variant | MODIFIER | c.-165+10577_-165+10 others(11): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53065638 | |||||
| chr16:53065638
|
T | TAAAAAA | 7 | a0001c0001t0001g0111a0001c0001t0003g0220a0001c0001t0007g0122others(4): Show | 7 | HG02055.hp1 HG02280.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.-165+10576_-165+10 others(12): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53065638 | |||||
| chr16:53065943
|
T | A | 1 | a0003c0004t0001g0201 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-165+10866T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53065943 | ||||||
| chr16:53066043
|
G | A | 3 | a0001c0001t0002g0175a0002c0002t0001g0106a0006c0009t0004g0107 | 3 | HG02622.hp1 HG03471.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-165+10966G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53066043 | ||||||
| chr16:53066224
|
A | G | 60 | a0001c0001t0001g0014a0001c0001t0001g0116a0001c0001t0001g0117others(57): Show | 60 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.-165+11147A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53066224 | ||||||
| chr16:53066299
|
A | C | 49 | a0001c0001t0001g0165a0001c0001t0001g0168a0001c0001t0001g0173others(46): Show | 49 | HG00140.hp1 HG00323.hp2 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.-165+11222A>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53066299 | ||||||
| chr16:53066564
|
C | G | 7 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0182others(4): Show | 7 | HG01884.hp1 HG02615.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-165+11487C>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53066564 | ||||||
| chr16:53066568
|
C | G | 1 | a0001c0001t0001g0111 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-165+11491C>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53066568 | ||||||
| chr16:53066606
|
C | T | 1 | a0005c0007t0009g0076 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-165+11529C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53066606 | ||||||
| chr16:53066659
|
CCATA | C | 7 | a0001c0001t0001g0168a0001c0001t0001g0173a0001c0001t0001g0174others(4): Show | 7 | HG01891.hp2 HG02257.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.-165+11585_-165+11 others(10): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53066659 | |||||
| chr16:53066662
|
T | G | 12 | a0001c0001t0003g0096a0001c0001t0003g0220a0001c0001t0003g0221others(9): Show | 12 | HG02055.hp1 HG02257.hp2 HG03041.hp1 others(9): Show |
intron_variant | MODIFIER | c.-165+11585T>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53066662 | ||||||
| chr16:53066734
|
A | G | 7 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0182others(4): Show | 7 | HG01884.hp1 HG02615.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-165+11657A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53066734 | ||||||
| chr16:53066778
|
T | C | 66 | a0001c0001t0001g0008a0001c0001t0001g0185a0001c0001t0001g0188others(63): Show | 66 | HG00140.hp1 HG00323.hp2 HG00597.hp2 others(63): Show |
intron_variant | MODIFIER | c.-165+11701T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53066778 | ||||||
| chr16:53066910
|
T | A | 2 | a0002c0002t0001g0012a0002c0002t0014g0011 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-165+11833T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53066910 | ||||||
| chr16:53066973
|
T | G | 35 | a0001c0001t0001g0185a0001c0001t0001g0188a0001c0001t0001g0206others(32): Show | 35 | HG00140.hp1 HG00323.hp2 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.-165+11896T>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53066973 | ||||||
| chr16:53067172
|
G | A | 130 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0119others(127): Show | 130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.-165+12095G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53067172 | ||||||
| chr16:53067400
|
G | A | 9 | a0001c0001t0003g0096a0001c0001t0003g0220a0001c0001t0003g0221others(6): Show | 9 | HG02055.hp1 HG03041.hp1 HG03225.hp2 others(6): Show |
intron_variant | MODIFIER | c.-165+12323G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53067400 | ||||||
| chr16:53067457
|
A | G | 1 | a0002c0002t0001g0147 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-165+12380A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53067457 | ||||||
| chr16:53067688
|
A | G | 6 | a0001c0001t0003g0220a0001c0001t0003g0222a0001c0001t0003g0223others(3): Show | 6 | HG02055.hp1 HG03041.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.-165+12611A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53067688 | ||||||
| chr16:53067755
|
G | A | 7 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0182others(4): Show | 7 | HG01884.hp1 HG02615.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-165+12678G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53067755 | ||||||
| chr16:53067866
|
G | A | 7 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0182others(4): Show | 7 | HG01884.hp1 HG02615.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-165+12789G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53067866 | ||||||
| chr16:53067878
|
T | G | 1 | a0001c0001t0001g0038 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-165+12801T>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53067878 | ||||||
| chr16:53067900
|
G | GA | 5 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0002g0171others(2): Show | 5 | HG02451.hp1 HG02486.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-165+12832dupA | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53067900 | |||||
| chr16:53067960
|
G | A | 2 | a0002c0002t0001g0019a0002c0002t0001g0020 | 2 | NA18939.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.-165+12883G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53067960 | ||||||
| chr16:53068005
|
G | C | 2 | a0001c0003t0002g0033a0002c0002t0001g0024 | 2 | HG02027.hp2 HG02040.hp2 |
intron_variant | MODIFIER | c.-165+12928G>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53068005 | ||||||
| chr16:53068372
|
G | A | 2 | a0001c0005t0005g0017a0001c0005t0005g0018 | 2 | HG02257.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-165+13295G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53068372 | ||||||
| chr16:53068375
|
T | C | 5 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0003g0079others(2): Show | 5 | HG01884.hp2 HG02280.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-165+13298T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53068375 | ||||||
| chr16:53068409
|
G | A | 9 | a0001c0001t0003g0096a0001c0001t0003g0220a0001c0001t0003g0221others(6): Show | 9 | HG02055.hp1 HG03041.hp1 HG03225.hp2 others(6): Show |
intron_variant | MODIFIER | c.-165+13332G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53068409 | ||||||
| chr16:53068431
|
C | G | 2 | a0001c0001t0007g0103a0002c0002t0001g0102 | 2 | HG02886.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-165+13354C>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53068431 | ||||||
| chr16:53068620
|
T | C | 1 | a0003c0004t0001g0177 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-165+13543T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53068620 | ||||||
| chr16:53068737
|
A | C | 7 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0182others(4): Show | 7 | HG01884.hp1 HG02615.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-165+13660A>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53068737 | ||||||
| chr16:53068849
|
G | A | 1 | a0001c0003t0016g0039 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-165+13772G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53068849 | ||||||
| chr16:53068992
|
C | CTTTTATT others(3): Show |
6 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0182others(3): Show | 6 | HG02615.hp1 HG02717.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.-165+13935_-165+13 others(16): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53068992 | |||||
| chr16:53068992
|
C | CTTTTATT others(8): Show |
1 | a0001c0005t0004g0097 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-165+13930_-165+13 others(21): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53068992 | |||||
| chr16:53069130
|
G | A | 2 | a0001c0001t0003g0184a0001c0005t0011g0228 | 2 | HG02109.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-165+14053G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53069130 | ||||||
| chr16:53069322
|
A | G | 3 | a0001c0001t0001g0014a0001c0001t0003g0016a0001c0005t0004g0104 | 3 | HG02965.hp1 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-165+14245A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53069322 | ||||||
| chr16:53069559
|
C | T | 3 | a0002c0002t0001g0145a0002c0002t0001g0146a0002c0002t0001g0149 | 3 | NA19009.hp1 NA19010.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.-165+14482C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53069559 | ||||||
| chr16:53069610
|
TG | T | 7 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0182others(4): Show | 7 | HG01884.hp1 HG02615.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-165+14534delG | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53069610 | ||||||
| chr16:53069638
|
T | C | 9 | a0001c0001t0001g0168a0001c0001t0001g0173a0001c0001t0001g0174others(6): Show | 9 | HG01891.hp2 HG02257.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.-165+14561T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53069638 | ||||||
| chr16:53069656
|
A | G | 133 | a0001c0001t0001g0014a0001c0001t0001g0110a0001c0001t0001g0111others(130): Show | 133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
intron_variant | MODIFIER | c.-165+14579A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53069656 | ||||||
| chr16:53069923
|
G | GT | 133 | a0001c0001t0001g0014a0001c0001t0001g0110a0001c0001t0001g0111others(130): Show | 133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
intron_variant | MODIFIER | c.-165+14854dupT | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53069923 | |||||
| chr16:53069937
|
T | G | 1 | a0003c0004t0001g0157 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-165+14860T>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53069937 | ||||||
| chr16:53070485
|
T | TTTCCTTC others(9): Show |
1 | a0001c0001t0007g0103 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-165+15411_-165+15 others(22): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53070485 | |||||
| chr16:53070485
|
T | TTTCCTTC others(13): Show |
1 | a0002c0002t0001g0102 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-165+15411_-165+15 others(26): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53070485 | |||||
| chr16:53070485
|
TTTCTTTC others(1): Show |
T | 4 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0014t0001g0115others(1): Show | 4 | HG02486.hp1 HG02809.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-165+15412_-165+15 others(14): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53070485 | |||||
| chr16:53070489
|
T | C | 3 | a0001c0001t0002g0171a0001c0001t0007g0103a0002c0002t0001g0102 | 3 | HG02451.hp1 HG02886.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-165+15412T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53070489 | ||||||
| chr16:53070489
|
T | TTTCC | 11 | a0001c0001t0001g0026a0001c0001t0001g0058a0001c0001t0001g0060others(8): Show | 11 | HG00621.hp1 HG01109.hp2 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.-165+15454_-165+15 others(10): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53070489 | |||||
| chr16:53070489
|
TTTCC | T | 14 | a0001c0001t0001g0027a0001c0001t0001g0043a0001c0001t0001g0064others(11): Show | 14 | HG00140.hp2 HG02027.hp1 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.-165+15454_-165+15 others(10): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53070489 | |||||
| chr16:53070489
|
TTTCCTTC others(9): Show |
T | 1 | a0002c0002t0001g0145 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-165+15442_-165+15 others(22): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53070489 | |||||
| chr16:53070493
|
C | T | 1 | a0002c0002t0001g0144 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-165+15416C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53070493 | ||||||
| chr16:53070512
|
CCTTCCTT others(15): Show |
C | 5 | a0001c0001t0020g0101a0001c0003t0002g0170a0002c0002t0001g0012others(2): Show | 5 | HG01167.hp1 HG01169.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-165+15438_-165+15 others(28): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53070512 | |||||
| chr16:53070516
|
CCTTCCTT others(11): Show |
C | 124 | a0001c0001t0001g0014a0001c0001t0001g0110a0001c0001t0001g0111others(121): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.-165+15442_-165+15 others(24): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53070516 | |||||
| chr16:53070520
|
CCTTCCTT others(7): Show |
C | 3 | a0002c0002t0001g0144a0003c0004t0001g0207a0006c0009t0004g0107 | 3 | HG01255.hp1 HG02165.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-165+15446_-165+15 others(20): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53070520 | |||||
| chr16:53070650
|
G | A | 133 | a0001c0001t0001g0014a0001c0001t0001g0110a0001c0001t0001g0111others(130): Show | 133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
intron_variant | MODIFIER | c.-165+15573G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53070650 | ||||||
| chr16:53071151
|
T | A | 124 | a0001c0001t0001g0014a0001c0001t0001g0110a0001c0001t0001g0111others(121): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.-165+16074T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53071151 | ||||||
| chr16:53071702
|
G | C | 7 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0002g0171others(4): Show | 7 | HG02451.hp1 HG02486.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.-165+16625G>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53071702 | ||||||
| chr16:53071773
|
C | T | 2 | a0001c0001t0003g0184a0001c0005t0011g0228 | 2 | HG02109.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-165+16696C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53071773 | ||||||
| chr16:53071872
|
T | C | 1 | a0001c0003t0002g0040 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-165+16795T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53071872 | ||||||
| chr16:53071963
|
G | T | 7 | a0001c0001t0003g0220a0001c0001t0003g0221a0001c0001t0003g0222others(4): Show | 7 | HG02055.hp1 HG03041.hp1 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.-165+16886G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53071963 | ||||||
| chr16:53071983
|
C | T | 1 | a0001c0005t0005g0032 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-165+16906C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53071983 | ||||||
| chr16:53072311
|
G | C | 214 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0021others(211): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.-165+17234G>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53072311 | ||||||
| chr16:53072320
|
C | CT | 129 | a0001c0001t0001g0014a0001c0001t0001g0110a0001c0001t0001g0111others(126): Show | 129 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(126): Show |
intron_variant | MODIFIER | c.-165+17256dupT | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53072320 | |||||
| chr16:53072399
|
CT | C | 225 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0021others(222): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.-165+17340delT | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53072399 | |||||
| chr16:53072426
|
G | A | 3 | a0001c0001t0001g0230a0001c0005t0012g0229a0001c0017t0002g0237 | 3 | HG01167.hp2 HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-165+17349G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53072426 | ||||||
| chr16:53072461
|
G | A | 2 | a0001c0001t0003g0184a0001c0005t0011g0228 | 2 | HG02109.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-165+17384G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53072461 | ||||||
| chr16:53072560
|
T | C | 124 | a0001c0001t0001g0014a0001c0001t0001g0110a0001c0001t0001g0111others(121): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.-165+17483T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53072560 | ||||||
| chr16:53072695
|
A | AT | 7 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0002g0171others(4): Show | 7 | HG02451.hp1 HG02486.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.-165+17626dupT | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53072695 | |||||
| chr16:53072704
|
A | AT | 7 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0182others(4): Show | 7 | HG01884.hp1 HG02615.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-165+17636dupT | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53072704 | |||||
| chr16:53072884
|
G | A | 117 | a0001c0001t0001g0014a0001c0001t0001g0119a0001c0001t0001g0124others(114): Show | 117 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(114): Show |
intron_variant | MODIFIER | c.-165+17807G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53072884 | ||||||
| chr16:53072941
|
C | T | 14 | a0001c0001t0001g0026a0001c0001t0001g0038a0001c0001t0001g0071others(11): Show | 14 | HG00609.hp2 HG01074.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.-165+17864C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53072941 | ||||||
| chr16:53072946
|
C | T | 5 | a0001c0001t0001g0085a0001c0001t0020g0101a0001c0003t0002g0170others(2): Show | 5 | HG00621.hp1 HG01167.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.-165+17869C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53072946 | ||||||
| chr16:53073603
|
G | A | 1 | a0001c0005t0005g0017 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-165+18526G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53073603 | ||||||
| chr16:53073920
|
G | A | 2 | a0002c0002t0001g0150a0003c0004t0001g0123 | 2 | HG00099.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.-165+18843G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53073920 | ||||||
| chr16:53074100
|
A | G | 133 | a0001c0001t0001g0014a0001c0001t0001g0110a0001c0001t0001g0111others(130): Show | 133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
intron_variant | MODIFIER | c.-165+19023A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53074100 | ||||||
| chr16:53074462
|
G | A | 1 | a0001c0005t0004g0238 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-165+19385G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53074462 | ||||||
| chr16:53074625
|
A | G | 7 | a0001c0001t0003g0220a0001c0001t0003g0221a0001c0001t0003g0222others(4): Show | 7 | HG02055.hp1 HG03041.hp1 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.-165+19548A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53074625 | ||||||
| chr16:53074649
|
G | A | 141 | a0001c0001t0001g0014a0001c0001t0001g0110a0001c0001t0001g0111others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.-165+19572G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53074649 | ||||||
| chr16:53074955
|
G | A | 34 | a0001c0001t0001g0185a0001c0001t0001g0188a0001c0001t0001g0206others(31): Show | 34 | HG00140.hp1 HG00323.hp2 HG00733.hp2 others(31): Show |
intron_variant | MODIFIER | c.-165+19878G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53074955 | ||||||
| chr16:53074970
|
C | T | 1 | a0001c0001t0001g0165 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-165+19893C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53074970 | ||||||
| chr16:53075212
|
A | G | 7 | a0001c0001t0003g0220a0001c0001t0003g0221a0001c0001t0003g0222others(4): Show | 7 | HG02055.hp1 HG03041.hp1 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.-165+20135A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53075212 | ||||||
| chr16:53075321
|
G | A | 2 | a0001c0001t0002g0171a0001c0001t0007g0103 | 2 | HG02451.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-165+20244G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53075321 | ||||||
| chr16:53075385
|
A | T | 140 | a0001c0001t0001g0014a0001c0001t0001g0110a0001c0001t0001g0111others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.-165+20308A>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53075385 | ||||||
| chr16:53075407
|
T | G | 140 | a0001c0001t0001g0014a0001c0001t0001g0110a0001c0001t0001g0111others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.-165+20330T>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53075407 | ||||||
| chr16:53075433
|
G | A | 1 | a0001c0005t0004g0231 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-165+20356G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53075433 | ||||||
| chr16:53075467
|
A | C | 1 | a0001c0005t0001g0215 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-165+20390A>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53075467 | ||||||
| chr16:53075589
|
C | T | 2 | a0001c0001t0001g0014a0001c0001t0003g0016 | 2 | HG02965.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-165+20512C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53075589 | ||||||
| chr16:53075593
|
A | T | 1 | a0001c0001t0003g0176 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-165+20516A>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53075593 | ||||||
| chr16:53075665
|
A | G | 140 | a0001c0001t0001g0014a0001c0001t0001g0110a0001c0001t0001g0111others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.-165+20588A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53075665 | ||||||
| chr16:53075761
|
C | T | 8 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0002g0171others(5): Show | 8 | HG02451.hp1 HG02486.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.-165+20684C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53075761 | ||||||
| chr16:53075909
|
G | A | 10 | a0001c0001t0001g0168a0001c0001t0001g0173a0001c0001t0001g0174others(7): Show | 10 | HG01891.hp2 HG02257.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.-165+20832G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53075909 | ||||||
| chr16:53075921
|
A | G | 1 | a0002c0002t0001g0037 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-165+20844A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53075921 | ||||||
| chr16:53076013
|
C | T | 2 | a0001c0001t0003g0184a0001c0005t0011g0228 | 2 | HG02109.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-165+20936C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53076013 | ||||||
| chr16:53076191
|
T | A | 1 | a0001c0001t0003g0176 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-165+21114T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53076191 | ||||||
| chr16:53076280
|
A | T | 2 | a0002c0002t0001g0012a0002c0002t0014g0011 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-165+21203A>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53076280 | ||||||
| chr16:53076377
|
C | T | 2 | a0001c0001t0001g0014a0001c0001t0003g0016 | 2 | HG02965.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-165+21300C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53076377 | ||||||
| chr16:53076406
|
C | T | 4 | a0001c0001t0020g0101a0001c0003t0002g0170a0002c0002t0001g0012others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.-165+21329C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53076406 | ||||||
| chr16:53076459
|
C | T | 45 | a0001c0001t0001g0119a0001c0001t0001g0159a0001c0001t0001g0160others(42): Show | 45 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.-165+21382C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53076459 | ||||||
| chr16:53076523
|
C | T | 1 | a0001c0001t0002g0171 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-165+21446C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53076523 | ||||||
| chr16:53076596
|
A | C | 7 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0182others(4): Show | 7 | HG01884.hp1 HG02615.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-165+21519A>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53076596 | ||||||
| chr16:53076605
|
A | T | 1 | a0001c0001t0003g0105 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-165+21528A>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53076605 | ||||||
| chr16:53076754
|
C | T | 1 | a0003c0004t0001g0148 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-165+21677C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53076754 | ||||||
| chr16:53076789
|
G | A | 140 | a0001c0001t0001g0014a0001c0001t0001g0110a0001c0001t0001g0111others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.-165+21712G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53076789 | ||||||
| chr16:53076832
|
G | T | 140 | a0001c0001t0001g0014a0001c0001t0001g0110a0001c0001t0001g0111others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.-165+21755G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53076832 | ||||||
| chr16:53076980
|
A | C | 106 | a0001c0001t0001g0014a0001c0001t0001g0119a0001c0001t0001g0124others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.-165+21903A>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53076980 | ||||||
| chr16:53077144
|
C | T | 104 | a0001c0001t0001g0014a0001c0001t0001g0119a0001c0001t0001g0124others(101): Show | 104 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(101): Show |
intron_variant | MODIFIER | c.-165+22067C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53077144 | ||||||
| chr16:53077363
|
G | A | 11 | a0001c0001t0001g0225a0001c0001t0001g0230a0001c0005t0004g0231others(8): Show | 11 | HG01167.hp2 HG02055.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-165+22286G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53077363 | ||||||
| chr16:53077438
|
C | G | 114 | a0001c0001t0001g0014a0001c0001t0001g0110a0001c0001t0001g0111others(111): Show | 114 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(111): Show |
intron_variant | MODIFIER | c.-165+22361C>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53077438 | ||||||
| chr16:53077480
|
C | T | 1 | a0001c0001t0003g0105 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-165+22403C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53077480 | ||||||
| chr16:53077618
|
C | T | 1 | a0001c0001t0003g0112 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-165+22541C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53077618 | ||||||
| chr16:53077769
|
G | A | 7 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0182others(4): Show | 7 | HG01884.hp1 HG02615.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-165+22692G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53077769 | ||||||
| chr16:53077852
|
T | C | 8 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0002g0171others(5): Show | 8 | HG02451.hp1 HG02486.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.-165+22775T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53077852 | ||||||
| chr16:53077902
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.-165+22825C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53077902 | ||||||
| chr16:53077996
|
C | T | 1 | a0002c0002t0001g0106 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-165+22919C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53077996 | ||||||
| chr16:53078043
|
C | T | 35 | a0001c0001t0001g0185a0001c0001t0001g0188a0001c0001t0001g0206others(32): Show | 35 | HG00140.hp1 HG00323.hp2 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.-165+22966C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53078043 | ||||||
| chr16:53078085
|
A | C | 7 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0182others(4): Show | 7 | HG01884.hp1 HG02615.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-165+23008A>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53078085 | ||||||
| chr16:53078097
|
T | A | 10 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0182others(7): Show | 10 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.-165+23020T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53078097 | ||||||
| chr16:53078285
|
G | T | 1 | a0003c0004t0006g0199 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-165+23208G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53078285 | ||||||
| chr16:53078590
|
T | G | 1 | a0003c0004t0001g0200 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-165+23513T>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53078590 | ||||||
| chr16:53078628
|
C | A | 1 | a0006c0009t0004g0107 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-165+23551C>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53078628 | ||||||
| chr16:53078740
|
C | T | 1 | a0001c0001t0007g0103 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-165+23663C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53078740 | ||||||
| chr16:53078943
|
C | T | 5 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0002g0171others(2): Show | 5 | HG02451.hp1 HG02486.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-165+23866C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53078943 | ||||||
| chr16:53078981
|
G | A | 2 | a0001c0001t0003g0022a0001c0001t0003g0167 | 2 | HG02559.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-165+23904G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53078981 | ||||||
| chr16:53079131
|
A | G | 8 | a0001c0001t0001g0008a0001c0003t0002g0005a0001c0003t0019g0004others(5): Show | 8 | HG00597.hp2 HG00609.hp1 NA18939.hp2 others(5): Show |
intron_variant | MODIFIER | c.-165+24054A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53079131 | ||||||
| chr16:53079142
|
C | T | 1 | a0001c0001t0001g0225 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-165+24065C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53079142 | ||||||
| chr16:53079232
|
G | A | 4 | a0001c0003t0002g0033a0002c0002t0001g0024a0002c0002t0001g0034others(1): Show | 4 | HG02027.hp2 HG02040.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.-165+24155G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53079232 | ||||||
| chr16:53079360
|
C | G | 1 | a0001c0003t0002g0036 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-165+24283C>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53079360 | ||||||
| chr16:53079577
|
A | C | 8 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0002g0171others(5): Show | 8 | HG02451.hp1 HG02486.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.-165+24500A>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53079577 | ||||||
| chr16:53079686
|
C | T | 9 | a0001c0001t0003g0096a0001c0001t0003g0220a0001c0001t0003g0221others(6): Show | 9 | HG02055.hp1 HG03041.hp1 HG03225.hp2 others(6): Show |
intron_variant | MODIFIER | c.-165+24609C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53079686 | ||||||
| chr16:53079752
|
G | A | 11 | a0001c0001t0001g0225a0001c0001t0001g0230a0001c0005t0004g0231others(8): Show | 11 | HG01167.hp2 HG02055.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-165+24675G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53079752 | ||||||
| chr16:53079785
|
T | C | 2 | a0001c0001t0001g0124a0003c0004t0001g0148 | 2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-165+24708T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53079785 | ||||||
| chr16:53079801
|
G | T | 1 | a0003c0004t0001g0100 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-165+24724G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53079801 | ||||||
| chr16:53080229
|
A | G | 7 | a0001c0001t0003g0220a0001c0001t0003g0221a0001c0001t0003g0222others(4): Show | 7 | HG02055.hp1 HG03041.hp1 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.-165+25152A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53080229 | ||||||
| chr16:53080344
|
G | A | 140 | a0001c0001t0001g0014a0001c0001t0001g0110a0001c0001t0001g0111others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.-165+25267G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53080344 | ||||||
| chr16:53080606
|
A | G | 1 | a0001c0001t0001g0092 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-165+25529A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53080606 | ||||||
| chr16:53081314
|
G | C | 2 | a0002c0002t0001g0019a0002c0002t0001g0020 | 2 | NA18939.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.-165+26237G>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53081314 | ||||||
| chr16:53081659
|
T | A | 35 | a0001c0001t0001g0185a0001c0001t0001g0188a0001c0001t0001g0206others(32): Show | 35 | HG00140.hp1 HG00323.hp2 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.-165+26582T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53081659 | ||||||
| chr16:53081765
|
AT | A | 96 | a0001c0001t0001g0014a0001c0001t0001g0110a0001c0001t0001g0111others(93): Show | 96 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.-165+26697delT | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53081765 | |||||
| chr16:53081776
|
T | G | 36 | a0001c0001t0001g0008a0001c0001t0001g0045a0001c0001t0001g0058others(33): Show | 36 | HG00140.hp2 HG00558.hp2 HG00597.hp2 others(33): Show |
intron_variant | MODIFIER | c.-165+26699T>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53081776 | ||||||
| chr16:53081839
|
G | GTGAA | 48 | a0001c0001t0001g0025a0001c0001t0001g0038a0001c0001t0001g0051others(45): Show | 48 | HG00558.hp1 HG00597.hp1 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.-165+26792_-165+26 others(10): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53081839 | |||||
| chr16:53081839
|
G | GTGAATGA others(1): Show |
88 | a0001c0001t0001g0008a0001c0001t0001g0021a0001c0001t0001g0026others(85): Show | 88 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.-165+26788_-165+26 others(14): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53081839 | |||||
| chr16:53081839
|
G | GTGAATGA others(5): Show |
31 | a0001c0001t0001g0045a0001c0001t0001g0064a0001c0001t0001g0067others(28): Show | 31 | HG00621.hp2 HG01074.hp1 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.-165+26784_-165+26 others(18): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53081839 | |||||
| chr16:53081839
|
G | GTGAATGA others(9): Show |
2 | a0001c0001t0001g0090a0001c0001t0001g0099 | 2 | HG01109.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.-165+26780_-165+26 others(22): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53081839 | |||||
| chr16:53081839
|
GTGAA | G | 5 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0002g0171others(2): Show | 5 | HG02451.hp1 HG02486.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-165+26792_-165+26 others(10): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53081839 | |||||
| chr16:53081873
|
A | G | 4 | a0001c0001t0003g0105a0001c0001t0003g0176a0001c0003t0002g0041others(1): Show | 4 | HG00140.hp2 HG02486.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-165+26796A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53081873 | ||||||
| chr16:53081992
|
T | C | 1 | a0002c0002t0001g0205 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-165+26915T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53081992 | ||||||
| chr16:53082200
|
T | TTTTA | 18 | a0001c0001t0001g0098a0001c0001t0003g0022a0001c0001t0003g0079others(15): Show | 18 | HG00609.hp1 HG02129.hp2 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.-165+27170_-165+27 others(10): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53082200 | |||||
| chr16:53082200
|
TTTTA | T | 105 | a0001c0001t0001g0014a0001c0001t0001g0031a0001c0001t0001g0043others(102): Show | 105 | HG00323.hp2 HG00558.hp1 HG00621.hp1 others(102): Show |
intron_variant | MODIFIER | c.-165+27170_-165+27 others(10): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53082200 | |||||
| chr16:53082200
|
TTTTATTT others(1): Show |
T | 48 | a0001c0001t0001g0119a0001c0001t0001g0159a0001c0001t0001g0160others(45): Show | 48 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.-165+27166_-165+27 others(14): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53082200 | |||||
| chr16:53082200
|
TTTTATTT others(5): Show |
T | 4 | a0001c0001t0003g0112a0001c0003t0002g0170a0001c0005t0018g0001others(1): Show | 4 | HG03098.hp1 HG03130.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-165+27162_-165+27 others(18): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53082200 | |||||
| chr16:53082200
|
TTTTATTT others(9): Show |
T | 1 | a0003c0004t0001g0177 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-165+27158_-165+27 others(22): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53082200 | |||||
| chr16:53082200
|
TTTTATTT others(13): Show |
T | 2 | a0001c0001t0002g0175a0002c0002t0001g0106 | 2 | HG02622.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-165+27154_-165+27 others(26): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53082200 | |||||
| chr16:53082268
|
T | C | 7 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0182others(4): Show | 7 | HG01884.hp1 HG02615.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-165+27191T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53082268 | ||||||
| chr16:53082374
|
A | T | 1 | a0001c0005t0018g0001 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-165+27297A>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53082374 | ||||||
| chr16:53082786
|
G | A | 2 | a0001c0003t0002g0125a0001c0003t0002g0142 | 2 | NA18982.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.-165+27709G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53082786 | ||||||
| chr16:53082864
|
G | A | 5 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0002g0171others(2): Show | 5 | HG02451.hp1 HG02486.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-165+27787G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53082864 | ||||||
| chr16:53082990
|
G | C | 1 | a0002c0002t0001g0102 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-165+27913G>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53082990 | ||||||
| chr16:53083080
|
G | A | 1 | a0001c0001t0003g0079 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-165+28003G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53083080 | ||||||
| chr16:53083225
|
G | A | 1 | a0002c0002t0001g0024 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-165+28148G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53083225 | ||||||
| chr16:53083309
|
C | T | 2 | a0001c0001t0003g0096a0002c0002t0001g0113 | 2 | HG03225.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-165+28232C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53083309 | ||||||
| chr16:53083437
|
G | A | 1 | a0003c0004t0001g0207 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-165+28360G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53083437 | ||||||
| chr16:53083885
|
G | A | 5 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0002g0171others(2): Show | 5 | HG02451.hp1 HG02486.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-165+28808G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53083885 | ||||||
| chr16:53083902
|
C | T | 5 | a0001c0001t0007g0122a0001c0001t0020g0101a0001c0003t0002g0170others(2): Show | 5 | HG01167.hp1 HG01169.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.-165+28825C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53083902 | ||||||
| chr16:53083928
|
T | A | 2 | a0001c0001t0003g0184a0001c0005t0011g0228 | 2 | HG02109.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-165+28851T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53083928 | ||||||
| chr16:53083928
|
T | C | 3 | a0001c0001t0001g0081a0002c0002t0001g0037a0002c0002t0001g0082 | 3 | NA18963.hp1 NA18963.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.-165+28851T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53083928 | ||||||
| chr16:53083997
|
G | A | 2 | a0001c0001t0001g0124a0003c0004t0001g0148 | 2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-165+28920G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53083997 | ||||||
| chr16:53084050
|
C | T | 2 | a0001c0001t0001g0117a0002c0002t0001g0114 | 2 | HG03486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-165+28973C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53084050 | ||||||
| chr16:53084064
|
G | C | 2 | a0002c0002t0001g0019a0002c0002t0001g0020 | 2 | NA18939.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.-165+28987G>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53084064 | ||||||
| chr16:53084077
|
G | C | 5 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0002g0171others(2): Show | 5 | HG02451.hp1 HG02486.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-165+29000G>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53084077 | ||||||
| chr16:53084585
|
T | G | 1 | a0001c0001t0007g0122 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-165+29508T>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53084585 | ||||||
| chr16:53084782
|
C | G | 1 | a0002c0002t0001g0219 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-165+29705C>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53084782 | ||||||
| chr16:53084845
|
G | A | 1 | a0002c0002t0001g0063 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-165+29768G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53084845 | ||||||
| chr16:53084850
|
T | C | 5 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0002g0171others(2): Show | 5 | HG02451.hp1 HG02486.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-165+29773T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53084850 | ||||||
| chr16:53084852
|
G | A | 1 | a0002c0002t0001g0113 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-165+29775G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53084852 | ||||||
| chr16:53084939
|
G | T | 1 | a0003c0004t0001g0148 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-165+29862G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53084939 | ||||||
| chr16:53084959
|
C | T | 1 | a0002c0002t0001g0113 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-165+29882C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53084959 | ||||||
| chr16:53085121
|
G | A | 3 | a0001c0001t0001g0230a0001c0005t0012g0229a0001c0017t0002g0237 | 3 | HG01167.hp2 HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-165+30044G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53085121 | ||||||
| chr16:53085237
|
T | A | 2 | a0001c0001t0001g0014a0001c0001t0003g0016 | 2 | HG02965.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-165+30160T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53085237 | ||||||
| chr16:53085241
|
T | A | 237 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0021others(234): Show | 237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.-165+30164T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53085241 | ||||||
| chr16:53085424
|
G | T | 1 | a0002c0002t0001g0113 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-165+30347G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53085424 | ||||||
| chr16:53085444
|
C | T | 1 | a0002c0002t0001g0113 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-165+30367C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53085444 | ||||||
| chr16:53085731
|
C | T | 52 | a0001c0001t0001g0014a0001c0001t0001g0119a0001c0001t0001g0124others(49): Show | 52 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.-165+30654C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53085731 | ||||||
| chr16:53085821
|
G | T | 51 | a0001c0001t0001g0014a0001c0001t0001g0119a0001c0001t0001g0124others(48): Show | 51 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.-165+30744G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53085821 | ||||||
| chr16:53085850
|
T | C | 237 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0021others(234): Show | 237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.-165+30773T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53085850 | ||||||
| chr16:53086038
|
G | A | 1 | a0001c0005t0018g0001 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-165+30961G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53086038 | ||||||
| chr16:53086110
|
T | C | 194 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0021others(191): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.-165+31033T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53086110 | ||||||
| chr16:53086428
|
G | A | 1 | a0002c0002t0001g0044 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-165+31351G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53086428 | ||||||
| chr16:53086452
|
C | G | 64 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0021others(61): Show | 64 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.-165+31375C>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53086452 | ||||||
| chr16:53086527
|
G | A | 64 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0021others(61): Show | 64 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.-165+31450G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53086527 | ||||||
| chr16:53086688
|
A | T | 3 | a0001c0001t0001g0031a0001c0001t0001g0067a0001c0001t0001g0068 | 3 | HG02135.hp1 NA19009.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.-165+31611A>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53086688 | ||||||
| chr16:53086757
|
C | G | 13 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0116others(10): Show | 13 | HG01884.hp1 HG02451.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.-165+31680C>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53086757 | ||||||
| chr16:53087443
|
C | T | 2 | a0001c0001t0003g0096a0002c0002t0001g0113 | 2 | HG03225.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-165+32366C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53087443 | ||||||
| chr16:53087603
|
T | C | 1 | a0003c0004t0001g0007 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-165+32526T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53087603 | ||||||
| chr16:53087947
|
CA | C | 27 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0116others(24): Show | 27 | HG01167.hp2 HG01884.hp1 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.-165+32885delA | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53087947 | |||||
| chr16:53088007
|
G | C | 1 | a0002c0002t0001g0126 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-165+32930G>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53088007 | ||||||
| chr16:53088078
|
C | T | 1 | a0003c0004t0001g0157 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-165+33001C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53088078 | ||||||
| chr16:53088211
|
G | A | 1 | a0001c0003t0002g0070 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-165+33134G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53088211 | ||||||
| chr16:53088275
|
C | CT | 115 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0021others(112): Show | 115 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(112): Show |
intron_variant | MODIFIER | c.-165+33201dupT | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53088275 | |||||
| chr16:53088275
|
C | CTT | 19 | a0001c0001t0001g0174a0001c0001t0001g0178a0001c0001t0003g0022others(16): Show | 19 | HG00735.hp1 HG01167.hp1 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.-165+33200_-165+33 others(8): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53088275 | |||||
| chr16:53088275
|
C | CTTT | 35 | a0001c0001t0001g0168a0001c0001t0001g0185a0001c0001t0001g0188others(32): Show | 35 | HG00140.hp1 HG00323.hp2 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.-165+33199_-165+33 others(9): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53088275 | |||||
| chr16:53088278
|
TG | T | 14 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0116others(11): Show | 14 | HG01884.hp1 HG02109.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.-165+33202delG | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53088278 | ||||||
| chr16:53088279
|
G | T | 179 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0021others(176): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.-165+33202G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53088279 | ||||||
| chr16:53088284
|
T | G | 1 | a0002c0019t0001g0180 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-165+33207T>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53088284 | ||||||
| chr16:53088304
|
G | T | 1 | a0001c0001t0001g0051 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-165+33227G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53088304 | ||||||
| chr16:53088315
|
T | C | 1 | a0001c0001t0001g0119 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-165+33238T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53088315 | ||||||
| chr16:53088338
|
C | T | 2 | a0001c0001t0001g0160a0001c0003t0001g0158 | 2 | HG00099.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.-165+33261C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53088338 | ||||||
| chr16:53088391
|
C | T | 10 | a0001c0001t0001g0168a0001c0001t0001g0173a0001c0001t0001g0174others(7): Show | 10 | HG01891.hp2 HG02257.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.-165+33314C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53088391 | ||||||
| chr16:53088394
|
T | C | 10 | a0001c0001t0001g0168a0001c0001t0001g0173a0001c0001t0001g0174others(7): Show | 10 | HG01891.hp2 HG02257.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.-165+33317T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53088394 | ||||||
| chr16:53088401
|
C | G | 10 | a0001c0001t0001g0168a0001c0001t0001g0173a0001c0001t0001g0174others(7): Show | 10 | HG01891.hp2 HG02257.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.-165+33324C>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53088401 | ||||||
| chr16:53088520
|
C | T | 7 | a0001c0001t0003g0220a0001c0001t0003g0221a0001c0001t0003g0222others(4): Show | 7 | HG02055.hp1 HG03041.hp1 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.-165+33443C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53088520 | ||||||
| chr16:53088574
|
G | A | 36 | a0001c0001t0001g0185a0001c0001t0001g0188a0001c0001t0001g0206others(33): Show | 36 | HG00140.hp1 HG00323.hp2 HG00733.hp2 others(33): Show |
intron_variant | MODIFIER | c.-165+33497G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53088574 | ||||||
| chr16:53088694
|
G | A | 1 | a0001c0001t0003g0112 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-165+33617G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53088694 | ||||||
| chr16:53088798
|
A | C | 1 | a0001c0003t0002g0003 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-165+33721A>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53088798 | ||||||
| chr16:53088888
|
C | T | 2 | a0001c0003t0002g0047a0001c0003t0016g0039 | 2 | NA19068.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.-165+33811C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53088888 | ||||||
| chr16:53088924
|
C | T | 13 | a0001c0001t0001g0225a0001c0001t0001g0230a0001c0001t0007g0103others(10): Show | 13 | HG01167.hp2 HG02055.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.-165+33847C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53088924 | ||||||
| chr16:53089047
|
G | A | 1 | a0001c0005t0004g0104 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-165+33970G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53089047 | ||||||
| chr16:53089119
|
A | T | 9 | a0001c0001t0003g0220a0001c0001t0003g0221a0001c0001t0003g0222others(6): Show | 9 | HG02055.hp1 HG03041.hp1 HG03239.hp1 others(6): Show |
intron_variant | MODIFIER | c.-165+34042A>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53089119 | ||||||
| chr16:53089122
|
A | T | 227 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0021others(224): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.-165+34045A>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53089122 | ||||||
| chr16:53089308
|
G | C | 13 | a0001c0001t0001g0225a0001c0001t0001g0230a0001c0001t0007g0103others(10): Show | 13 | HG01167.hp2 HG02055.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.-165+34231G>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53089308 | ||||||
| chr16:53089471
|
A | C | 193 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0021others(190): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.-165+34394A>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53089471 | ||||||
| chr16:53089703
|
G | A | 1 | a0003c0004t0006g0199 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-165+34626G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53089703 | ||||||
| chr16:53089849
|
G | A | 6 | a0002c0002t0001g0095a0002c0002t0001g0126a0002c0002t0001g0129others(3): Show | 6 | HG00099.hp2 HG00323.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.-165+34772G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53089849 | ||||||
| chr16:53090147
|
G | A | 1 | a0001c0003t0002g0002 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-165+35070G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53090147 | ||||||
| chr16:53090281
|
C | G | 123 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0021others(120): Show | 123 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(120): Show |
intron_variant | MODIFIER | c.-165+35204C>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53090281 | ||||||
| chr16:53090282
|
T | A | 1 | a0001c0001t0001g0064 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-165+35205T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53090282 | ||||||
| chr16:53090290
|
C | G | 1 | a0003c0004t0001g0189 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-165+35213C>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53090290 | ||||||
| chr16:53090290
|
C | T | 7 | a0001c0001t0003g0220a0001c0001t0003g0221a0001c0001t0003g0222others(4): Show | 7 | HG02055.hp1 HG03041.hp1 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.-165+35213C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53090290 | ||||||
| chr16:53090889
|
T | C | 1 | a0001c0013t0001g0055 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-165+35812T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53090889 | ||||||
| chr16:53090931
|
T | TGCAGGGA others(8): Show |
185 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0021others(182): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.-165+35856_-165+35 others(21): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53090931 | |||||
| chr16:53090974
|
T | C | 1 | a0001c0001t0001g0067 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-165+35897T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53090974 | ||||||
| chr16:53091001
|
A | AC | 34 | a0001c0001t0001g0026a0001c0001t0001g0185a0001c0001t0001g0188others(31): Show | 34 | HG00140.hp1 HG00323.hp2 HG00733.hp2 others(31): Show |
intron_variant | MODIFIER | c.-165+35933dupC | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53091001 | |||||
| chr16:53091001
|
ACC | A | 12 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0116others(9): Show | 12 | HG01884.hp1 HG02451.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.-165+35932_-165+35 others(8): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53091001 | |||||
| chr16:53091006
|
C | G | 1 | a0001c0001t0001g0064 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-165+35929C>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53091006 | ||||||
| chr16:53091008
|
C | A | 1 | a0001c0003t0002g0086 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-165+35931C>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53091008 | ||||||
| chr16:53091008
|
C | G | 137 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0021others(134): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.-165+35931C>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53091008 | ||||||
| chr16:53091013
|
C | A | 137 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0021others(134): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.-165+35936C>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53091013 | ||||||
| chr16:53091121
|
G | T | 13 | a0001c0001t0001g0225a0001c0001t0001g0230a0001c0001t0007g0103others(10): Show | 13 | HG01167.hp2 HG02055.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.-165+36044G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53091121 | ||||||
| chr16:53091157
|
C | T | 1 | a0001c0003t0016g0039 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-165+36080C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53091157 | ||||||
| chr16:53091246
|
A | G | 2 | a0002c0002t0001g0012a0002c0002t0014g0011 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-165+36169A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53091246 | ||||||
| chr16:53091907
|
T | C | 137 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0021others(134): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.-165+36830T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53091907 | ||||||
| chr16:53092201
|
C | G | 65 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0021others(62): Show | 65 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.-165+37124C>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53092201 | ||||||
| chr16:53092293
|
C | CT | 193 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0021others(190): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.-165+37216_-165+37 others(7): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53092293 | ||||||
| chr16:53092426
|
C | T | 124 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0021others(121): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.-165+37349C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53092426 | ||||||
| chr16:53092646
|
C | A | 1 | a0006c0009t0004g0107 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-165+37569C>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53092646 | ||||||
| chr16:53092769
|
A | ATTAT | 10 | a0001c0001t0003g0184a0001c0001t0007g0122a0001c0001t0020g0101others(7): Show | 10 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.-165+37716_-165+37 others(10): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53092769 | |||||
| chr16:53092903
|
C | T | 2 | a0001c0005t0004g0097a0001c0005t0004g0169 | 2 | HG01884.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-165+37826C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53092903 | ||||||
| chr16:53093110
|
A | G | 1 | a0006c0009t0004g0107 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-165+38033A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53093110 | ||||||
| chr16:53093145
|
A | G | 1 | a0001c0005t0005g0032 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-165+38068A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53093145 | ||||||
| chr16:53093378
|
A | G | 1 | a0001c0001t0001g0043 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-165+38301A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53093378 | ||||||
| chr16:53093388
|
C | T | 7 | a0001c0001t0003g0184a0001c0001t0007g0122a0001c0001t0020g0101others(4): Show | 7 | HG01167.hp1 HG01169.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.-165+38311C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53093388 | ||||||
| chr16:53093475
|
C | A | 1 | a0003c0004t0001g0162 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-165+38398C>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53093475 | ||||||
| chr16:53093682
|
G | A | 10 | a0001c0001t0001g0014a0001c0001t0001g0124a0001c0001t0001g0168others(7): Show | 10 | HG01891.hp2 HG02257.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.-165+38605G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53093682 | ||||||
| chr16:53093696
|
C | A | 2 | a0002c0002t0001g0087a0002c0002t0001g0088 | 2 | HG01255.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.-165+38619C>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53093696 | ||||||
| chr16:53093934
|
G | T | 107 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0021others(104): Show | 107 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.-165+38857G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53093934 | ||||||
| chr16:53093935
|
T | A | 107 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0021others(104): Show | 107 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.-165+38858T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53093935 | ||||||
| chr16:53094144
|
G | A | 86 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0116others(83): Show | 86 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.-165+39067G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53094144 | ||||||
| chr16:53094167
|
A | G | 1 | a0001c0001t0001g0025 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-165+39090A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53094167 | ||||||
| chr16:53094641
|
C | CT | 34 | a0001c0001t0001g0064a0001c0001t0001g0185a0001c0001t0001g0188others(31): Show | 34 | HG00140.hp1 HG00323.hp2 HG00733.hp2 others(31): Show |
intron_variant | MODIFIER | c.-165+39580dupT | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53094641 | |||||
| chr16:53094705
|
T | C | 3 | a0001c0001t0001g0230a0001c0005t0012g0229a0001c0017t0002g0237 | 3 | HG01167.hp2 HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-165+39628T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53094705 | ||||||
| chr16:53094799
|
C | T | 142 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0021others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.-165+39722C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53094799 | ||||||
| chr16:53094825
|
T | C | 1 | a0001c0001t0007g0103 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-165+39748T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53094825 | ||||||
| chr16:53094980
|
A | G | 142 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0021others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.-165+39903A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53094980 | ||||||
| chr16:53094985
|
A | C | 192 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0021others(189): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.-165+39908A>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53094985 | ||||||
| chr16:53095060
|
T | C | 13 | a0001c0001t0001g0225a0001c0001t0001g0230a0001c0001t0007g0103others(10): Show | 13 | HG01167.hp2 HG02055.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.-165+39983T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53095060 | ||||||
| chr16:53095122
|
T | C | 185 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0021others(182): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.-165+40045T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53095122 | ||||||
| chr16:53095187
|
C | A | 142 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0021others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.-165+40110C>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53095187 | ||||||
| chr16:53095585
|
TC | T | 12 | a0001c0001t0001g0225a0001c0001t0001g0230a0001c0001t0007g0103others(9): Show | 12 | HG01167.hp2 HG02055.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.-165+40510delC | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53095585 | |||||
| chr16:53095590
|
C | T | 61 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0027others(58): Show | 61 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.-165+40513C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53095590 | ||||||
| chr16:53095753
|
T | C | 141 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0027others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.-165+40676T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53095753 | ||||||
| chr16:53096055
|
G | T | 7 | a0001c0001t0003g0220a0001c0001t0003g0221a0001c0001t0003g0222others(4): Show | 7 | HG02055.hp1 HG03041.hp1 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.-165+40978G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53096055 | ||||||
| chr16:53096056
|
AT | A | 22 | a0001c0001t0001g0008a0001c0001t0001g0026a0001c0001t0001g0038others(19): Show | 22 | HG00609.hp2 HG01099.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.-165+40997delT | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53096056 | |||||
| chr16:53096057
|
T | TA | 3 | a0001c0001t0001g0211a0001c0001t0001g0218a0002c0002t0001g0205 | 3 | HG02738.hp2 HG03831.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.-165+40980_-165+40 others(7): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53096057 | ||||||
| chr16:53096058
|
T | A | 34 | a0001c0001t0001g0021a0001c0001t0001g0185a0001c0001t0001g0188others(31): Show | 34 | HG00323.hp2 HG00733.hp2 HG01074.hp1 others(31): Show |
intron_variant | MODIFIER | c.-165+40981T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53096058 | ||||||
| chr16:53096295
|
T | C | 59 | a0001c0001t0001g0014a0001c0001t0001g0027a0001c0001t0001g0031others(56): Show | 59 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.-165+41218T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53096295 | ||||||
| chr16:53096347
|
T | C | 214 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0021others(211): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.-165+41270T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53096347 | ||||||
| chr16:53096434
|
C | T | 12 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0116others(9): Show | 12 | HG01884.hp1 HG02451.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.-165+41357C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53096434 | ||||||
| chr16:53096600
|
C | T | 1 | a0001c0001t0001g0058 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-165+41523C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53096600 | ||||||
| chr16:53097133
|
T | C | 140 | a0001c0001t0001g0014a0001c0001t0001g0027a0001c0001t0001g0031others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.-165+42056T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53097133 | ||||||
| chr16:53097156
|
T | C | 1 | a0001c0003t0002g0059 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-165+42079T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53097156 | ||||||
| chr16:53097174
|
T | TG | 140 | a0001c0001t0001g0014a0001c0001t0001g0027a0001c0001t0001g0031others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.-165+42097_-165+42 others(7): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53097174 | ||||||
| chr16:53097212
|
G | T | 8 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0182others(5): Show | 8 | HG01884.hp1 HG02451.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.-165+42135G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53097212 | ||||||
| chr16:53097354
|
C | CCCTT | 7 | a0001c0001t0001g0098a0001c0001t0003g0184a0001c0001t0003g0221others(4): Show | 7 | HG02109.hp2 HG02129.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.-165+42327_-165+42 others(10): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53097354 | |||||
| chr16:53097354
|
C | CCCTTCCT others(1): Show |
4 | a0001c0001t0003g0220a0001c0003t0002g0170a0001c0003t0002g0224others(1): Show | 4 | HG02055.hp1 HG06807.hp1 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.-165+42323_-165+42 others(14): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53097354 | |||||
| chr16:53097354
|
C | CCCTTCCT others(5): Show |
1 | a0001c0005t0011g0228 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-165+42319_-165+42 others(18): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53097354 | |||||
| chr16:53097354
|
C | CCCTTCCT others(13): Show |
1 | a0001c0001t0003g0222 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-165+42311_-165+42 others(26): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53097354 | |||||
| chr16:53097354
|
CCCTT | C | 42 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0060others(39): Show | 42 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.-165+42327_-165+42 others(10): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53097354 | |||||
| chr16:53097354
|
CCCTTCCT others(1): Show |
C | 147 | a0001c0001t0001g0014a0001c0001t0001g0025a0001c0001t0001g0027others(144): Show | 147 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.-165+42323_-165+42 others(14): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53097354 | |||||
| chr16:53097354
|
CCCTTCCT others(5): Show |
C | 2 | a0001c0001t0001g0111a0002c0002t0001g0044 | 2 | HG03471.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.-165+42319_-165+42 others(18): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53097354 | |||||
| chr16:53097354
|
CCCTTCCT others(9): Show |
C | 1 | a0001c0005t0005g0032 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-165+42315_-165+42 others(22): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53097354 | |||||
| chr16:53097388
|
C | T | 139 | a0001c0001t0001g0014a0001c0001t0001g0027a0001c0001t0001g0031others(136): Show | 139 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.-165+42311C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53097388 | ||||||
| chr16:53097462
|
C | T | 140 | a0001c0001t0001g0014a0001c0001t0001g0027a0001c0001t0001g0031others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.-165+42385C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53097462 | ||||||
| chr16:53097493
|
A | C | 1 | a0002c0002t0001g0113 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-165+42416A>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53097493 | ||||||
| chr16:53097494
|
G | A | 139 | a0001c0001t0001g0014a0001c0001t0001g0027a0001c0001t0001g0031others(136): Show | 139 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.-165+42417G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53097494 | ||||||
| chr16:53097545
|
A | G | 5 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0003t0002g0041others(2): Show | 5 | HG00140.hp2 HG01074.hp2 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.-165+42468A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53097545 | ||||||
| chr16:53097740
|
G | A | 59 | a0001c0001t0001g0014a0001c0001t0001g0027a0001c0001t0001g0031others(56): Show | 59 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.-165+42663G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53097740 | ||||||
| chr16:53097809
|
A | G | 54 | a0001c0001t0001g0043a0001c0001t0001g0119a0001c0001t0001g0159others(51): Show | 54 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(51): Show |
intron_variant | MODIFIER | c.-165+42732A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53097809 | ||||||
| chr16:53097853
|
G | A | 3 | a0001c0003t0002g0083a0001c0003t0017g0181a0001c0005t0005g0061 | 3 | HG03017.hp2 HG03688.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.-165+42776G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53097853 | ||||||
| chr16:53097856
|
C | T | 1 | a0002c0002t0001g0102 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-165+42779C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53097856 | ||||||
| chr16:53097918
|
G | A | 1 | a0001c0001t0020g0101 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-165+42841G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53097918 | ||||||
| chr16:53097945
|
C | T | 1 | a0002c0002t0001g0102 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-165+42868C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53097945 | ||||||
| chr16:53097946
|
C | T | 1 | a0002c0002t0001g0102 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-165+42869C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53097946 | ||||||
| chr16:53097953
|
C | G | 1 | a0002c0002t0001g0102 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-165+42876C>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53097953 | ||||||
| chr16:53097967
|
A | G | 2 | a0003c0004t0001g0213a0003c0004t0001g0217 | 2 | NA18974.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.-165+42890A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53097967 | ||||||
| chr16:53098246
|
C | T | 1 | a0003c0004t0001g0157 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-165+43169C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53098246 | ||||||
| chr16:53098303
|
T | C | 137 | a0001c0001t0001g0014a0001c0001t0001g0027a0001c0001t0001g0031others(134): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.-165+43226T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53098303 | ||||||
| chr16:53098304
|
C | T | 137 | a0001c0001t0001g0014a0001c0001t0001g0027a0001c0001t0001g0031others(134): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.-165+43227C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53098304 | ||||||
| chr16:53098406
|
G | A | 39 | a0001c0001t0001g0021a0001c0001t0001g0071a0001c0001t0001g0072others(36): Show | 39 | HG00323.hp2 HG00733.hp2 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.-165+43329G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53098406 | ||||||
| chr16:53098453
|
G | C | 1 | a0001c0001t0001g0071 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-165+43376G>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53098453 | ||||||
| chr16:53098475
|
C | CA | 6 | a0001c0001t0001g0210a0001c0001t0003g0131a0002c0002t0001g0034others(3): Show | 6 | HG00140.hp1 HG01891.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.-165+43415dupA | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53098475 | |||||
| chr16:53098475
|
CA | C | 43 | a0001c0001t0001g0008a0001c0001t0001g0021a0001c0001t0001g0071others(40): Show | 43 | HG00323.hp2 HG00733.hp2 HG01074.hp1 others(40): Show |
intron_variant | MODIFIER | c.-165+43415delA | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53098475 | |||||
| chr16:53098492
|
AG | A | 2 | a0001c0003t0002g0142a0002c0002t0001g0149 | 2 | NA18982.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.-165+43416delG | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53098492 | ||||||
| chr16:53098493
|
G | A | 47 | a0001c0001t0001g0043a0001c0001t0001g0119a0001c0001t0001g0159others(44): Show | 47 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(44): Show |
intron_variant | MODIFIER | c.-165+43416G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53098493 | ||||||
| chr16:53098521
|
A | G | 1 | a0002c0002t0001g0102 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-165+43444A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53098521 | ||||||
| chr16:53098658
|
G | A | 1 | a0001c0013t0001g0055 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-165+43581G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53098658 | ||||||
| chr16:53098839
|
A | G | 1 | a0001c0001t0001g0179 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-165+43762A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53098839 | ||||||
| chr16:53098892
|
G | A | 56 | a0001c0001t0001g0014a0001c0001t0001g0027a0001c0001t0001g0031others(53): Show | 56 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.-165+43815G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53098892 | ||||||
| chr16:53099087
|
G | T | 1 | a0002c0002t0001g0102 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-165+44010G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53099087 | ||||||
| chr16:53099649
|
A | G | 1 | a0009c0018t0005g0155 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.-165+44572A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53099649 | ||||||
| chr16:53099995
|
C | G | 55 | a0001c0001t0001g0014a0001c0001t0001g0027a0001c0001t0001g0031others(52): Show | 55 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.-165+44918C>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53099995 | ||||||
| chr16:53100453
|
C | CTTTTTTT others(1): Show |
39 | a0001c0001t0001g0021a0001c0001t0001g0071a0001c0001t0001g0072others(36): Show | 39 | HG00323.hp2 HG00733.hp2 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.-165+45386_-165+45 others(14): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53100453 | |||||
| chr16:53100453
|
CT | C | 45 | a0001c0001t0001g0038a0001c0001t0001g0081a0001c0001t0001g0091others(42): Show | 45 | HG00609.hp2 HG01884.hp2 HG02040.hp2 others(42): Show |
intron_variant | MODIFIER | c.-165+45393delT | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53100453 | |||||
| chr16:53100527
|
T | A | 1 | a0001c0003t0010g0006 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-165+45450T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53100527 | ||||||
| chr16:53100811
|
G | A | 1 | a0002c0002t0001g0063 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-165+45734G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53100811 | ||||||
| chr16:53100923
|
C | T | 1 | a0001c0001t0007g0103 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-165+45846C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53100923 | ||||||
| chr16:53101120
|
C | T | 134 | a0001c0001t0001g0014a0001c0001t0001g0027a0001c0001t0001g0031others(131): Show | 134 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.-165+46043C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53101120 | ||||||
| chr16:53101137
|
T | G | 1 | a0001c0001t0003g0133 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-165+46060T>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53101137 | ||||||
| chr16:53101213
|
G | T | 2 | a0001c0001t0001g0071a0001c0001t0001g0072 | 2 | HG01074.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.-165+46136G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53101213 | ||||||
| chr16:53101215
|
T | A | 3 | a0004c0006t0001g0121a0004c0006t0001g0127a0004c0006t0001g0128 | 3 | NA18952.hp1 NA18989.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.-165+46138T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53101215 | ||||||
| chr16:53101217
|
A | G | 3 | a0004c0006t0001g0121a0004c0006t0001g0127a0004c0006t0001g0128 | 3 | NA18952.hp1 NA18989.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.-165+46140A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53101217 | ||||||
| chr16:53101273
|
C | CT | 63 | a0001c0001t0001g0008a0001c0001t0001g0021a0001c0001t0001g0026others(60): Show | 63 | HG00323.hp2 HG00609.hp2 HG00733.hp2 others(60): Show |
intron_variant | MODIFIER | c.-165+46215dupT | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53101273 | |||||
| chr16:53101518
|
T | C | 32 | a0001c0001t0001g0045a0001c0001t0001g0058a0001c0001t0001g0099others(29): Show | 32 | HG00140.hp2 HG00558.hp2 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.-165+46441T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53101518 | ||||||
| chr16:53101529
|
C | T | 1 | a0002c0019t0001g0180 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-165+46452C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53101529 | ||||||
| chr16:53101911
|
T | C | 1 | a0001c0001t0007g0103 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-165+46834T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53101911 | ||||||
| chr16:53101959
|
G | A | 5 | a0001c0001t0001g0031a0001c0001t0001g0067a0001c0001t0001g0068others(2): Show | 5 | HG01109.hp2 HG01257.hp2 HG02135.hp1 others(2): Show |
intron_variant | MODIFIER | c.-165+46882G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53101959 | ||||||
| chr16:53102256
|
G | A | 40 | a0001c0001t0001g0021a0001c0001t0001g0071a0001c0001t0001g0072others(37): Show | 40 | HG00323.hp2 HG00733.hp2 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.-165+47179G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53102256 | ||||||
| chr16:53102280
|
C | T | 1 | a0001c0001t0001g0085 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-165+47203C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53102280 | ||||||
| chr16:53102538
|
C | A | 1 | a0001c0001t0001g0008 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-165+47461C>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53102538 | ||||||
| chr16:53102546
|
A | T | 1 | a0003c0004t0001g0207 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-165+47469A>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53102546 | ||||||
| chr16:53102647
|
C | T | 1 | a0001c0001t0001g0075 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-165+47570C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53102647 | ||||||
| chr16:53102681
|
C | G | 1 | a0001c0003t0002g0041 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-165+47604C>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53102681 | ||||||
| chr16:53102694
|
T | TA | 54 | a0001c0001t0001g0043a0001c0001t0001g0084a0001c0001t0001g0119others(51): Show | 54 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.-165+47623dupA | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53102694 | |||||
| chr16:53102842
|
C | A | 1 | a0001c0001t0002g0171 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-165+47765C>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53102842 | ||||||
| chr16:53103006
|
T | C | 170 | a0001c0001t0001g0014a0001c0001t0001g0021a0001c0001t0001g0027others(167): Show | 170 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.-165+47929T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53103006 | ||||||
| chr16:53103088
|
G | T | 55 | a0001c0001t0001g0014a0001c0001t0001g0027a0001c0001t0001g0031others(52): Show | 55 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.-165+48011G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53103088 | ||||||
| chr16:53103098
|
G | T | 134 | a0001c0001t0001g0014a0001c0001t0001g0027a0001c0001t0001g0031others(131): Show | 134 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.-165+48021G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53103098 | ||||||
| chr16:53103157
|
CT | C | 110 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0026others(107): Show | 110 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.-165+48083delT | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53103157 | |||||
| chr16:53103159
|
TTA | T | 86 | a0001c0001t0001g0021a0001c0001t0001g0071a0001c0001t0001g0072others(83): Show | 86 | HG00323.hp2 HG00408.hp1 HG00733.hp2 others(83): Show |
intron_variant | MODIFIER | c.-165+48083_-165+48 others(8): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53103159 | ||||||
| chr16:53103159
|
TTAA | T | 7 | a0001c0001t0001g0043a0002c0002t0001g0095a0002c0002t0001g0126others(4): Show | 7 | HG00099.hp2 HG00323.hp1 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.-165+48083_-165+48 others(9): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53103159 | ||||||
| chr16:53103160
|
T | A | 2 | a0001c0001t0003g0096a0003c0004t0001g0162 | 2 | HG03831.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-165+48083T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53103160 | ||||||
| chr16:53103190
|
G | GT | 133 | a0001c0001t0001g0014a0001c0001t0001g0027a0001c0001t0001g0031others(130): Show | 133 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.-165+48123dupT | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53103190 | |||||
| chr16:53103220
|
A | T | 1 | a0001c0003t0002g0170 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-165+48143A>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53103220 | ||||||
| chr16:53103370
|
G | A | 173 | a0001c0001t0001g0014a0001c0001t0001g0021a0001c0001t0001g0027others(170): Show | 173 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.-165+48293G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53103370 | ||||||
| chr16:53103512
|
T | G | 1 | a0001c0003t0002g0047 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-165+48435T>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53103512 | ||||||
| chr16:53103607
|
G | C | 1 | a0001c0003t0002g0003 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-165+48530G>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53103607 | ||||||
| chr16:53103680
|
T | C | 1 | a0001c0001t0003g0112 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-165+48603T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53103680 | ||||||
| chr16:53103807
|
C | G | 5 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0005t0004g0104others(2): Show | 5 | HG02486.hp1 HG02809.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-165+48730C>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53103807 | ||||||
| chr16:53104098
|
G | A | 39 | a0001c0001t0001g0021a0001c0001t0001g0071a0001c0001t0001g0072others(36): Show | 39 | HG00323.hp2 HG00733.hp2 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.-165+49021G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53104098 | ||||||
| chr16:53104139
|
C | A | 1 | a0008c0011t0003g0062 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-165+49062C>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53104139 | ||||||
| chr16:53104140
|
T | C | 54 | a0001c0001t0001g0014a0001c0001t0001g0027a0001c0001t0001g0031others(51): Show | 54 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.-165+49063T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53104140 | ||||||
| chr16:53104196
|
G | A | 1 | a0001c0001t0003g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-165+49119G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53104196 | ||||||
| chr16:53104198
|
A | G | 1 | a0001c0001t0003g0139 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-165+49121A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53104198 | ||||||
| chr16:53104248
|
C | T | 1 | a0001c0003t0002g0073 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-165+49171C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53104248 | ||||||
| chr16:53104265
|
G | C | 1 | a0001c0001t0020g0101 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-165+49188G>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53104265 | ||||||
| chr16:53104811
|
C | CA | 93 | a0001c0001t0001g0008a0001c0001t0001g0026a0001c0001t0001g0038others(90): Show | 93 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.-165+49751dupA | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53104811 | |||||
| chr16:53104828
|
A | AG | 3 | a0001c0001t0001g0211a0001c0003t0002g0191a0003c0004t0006g0190 | 3 | HG02738.hp2 NA18972.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.-165+49752dupG | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53104828 | |||||
| chr16:53104828
|
A | G | 36 | a0001c0001t0001g0021a0001c0001t0001g0071a0001c0001t0001g0072others(33): Show | 36 | HG00323.hp2 HG00733.hp2 HG01074.hp1 others(33): Show |
intron_variant | MODIFIER | c.-165+49751A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53104828 | ||||||
| chr16:53104995
|
A | AC | 39 | a0001c0001t0001g0021a0001c0001t0001g0071a0001c0001t0001g0072others(36): Show | 39 | HG00323.hp2 HG00733.hp2 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.-165+49919dupC | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53104995 | |||||
| chr16:53104999
|
A | C | 39 | a0001c0001t0001g0021a0001c0001t0001g0071a0001c0001t0001g0072others(36): Show | 39 | HG00323.hp2 HG00733.hp2 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.-165+49922A>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53104999 | ||||||
| chr16:53105013
|
C | A | 39 | a0001c0001t0001g0021a0001c0001t0001g0071a0001c0001t0001g0072others(36): Show | 39 | HG00323.hp2 HG00733.hp2 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.-165+49936C>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53105013 | ||||||
| chr16:53105041
|
G | A | 3 | a0004c0006t0001g0121a0004c0006t0001g0127a0004c0006t0001g0128 | 3 | NA18952.hp1 NA18989.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.-165+49964G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53105041 | ||||||
| chr16:53105077
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-165+50000G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53105077 | ||||||
| chr16:53105221
|
G | A | 39 | a0001c0001t0001g0021a0001c0001t0001g0071a0001c0001t0001g0072others(36): Show | 39 | HG00323.hp2 HG00733.hp2 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.-165+50144G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53105221 | ||||||
| chr16:53105267
|
G | T | 1 | a0006c0009t0004g0107 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-165+50190G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53105267 | ||||||
| chr16:53105339
|
T | A | 8 | a0001c0003t0002g0005a0001c0003t0019g0004a0002c0002t0001g0009others(5): Show | 8 | HG00597.hp2 HG00609.hp1 NA18939.hp2 others(5): Show |
intron_variant | MODIFIER | c.-165+50262T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53105339 | ||||||
| chr16:53105523
|
A | G | 8 | a0001c0001t0003g0220a0001c0001t0003g0221a0001c0001t0003g0222others(5): Show | 8 | HG02055.hp1 HG03041.hp1 HG03540.hp1 others(5): Show |
intron_variant | MODIFIER | c.-164-50403A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53105523 | ||||||
| chr16:53105523
|
A | T | 6 | a0001c0005t0004g0232a0001c0005t0004g0233a0001c0005t0004g0234others(3): Show | 6 | HG02615.hp2 HG02897.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-164-50403A>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53105523 | ||||||
| chr16:53105671
|
T | G | 1 | a0001c0001t0001g0072 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-164-50255T>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53105671 | ||||||
| chr16:53105694
|
G | A | 37 | a0001c0001t0001g0021a0001c0001t0001g0071a0001c0001t0001g0072others(34): Show | 37 | HG00323.hp2 HG00733.hp2 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.-164-50232G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53105694 | ||||||
| chr16:53105822
|
CT | C | 12 | a0001c0001t0001g0008a0001c0001t0001g0021a0001c0001t0001g0051others(9): Show | 12 | HG00323.hp1 HG00558.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.-164-50086delT | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53105822 | |||||
| chr16:53105876
|
T | C | 2 | a0002c0002t0001g0102a0008c0011t0003g0062 | 2 | HG02109.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-164-50050T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53105876 | ||||||
| chr16:53106009
|
A | G | 1 | a0003c0004t0006g0190 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-164-49917A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53106009 | ||||||
| chr16:53106033
|
A | G | 37 | a0001c0001t0001g0043a0001c0001t0001g0119a0001c0001t0001g0159others(34): Show | 37 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(34): Show |
intron_variant | MODIFIER | c.-164-49893A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53106033 | ||||||
| chr16:53106112
|
A | G | 37 | a0001c0001t0001g0021a0001c0001t0001g0071a0001c0001t0001g0072others(34): Show | 37 | HG00323.hp2 HG00733.hp2 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.-164-49814A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53106112 | ||||||
| chr16:53106456
|
G | A | 2 | a0001c0001t0003g0096a0003c0004t0001g0177 | 2 | HG03130.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-164-49470G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53106456 | ||||||
| chr16:53106540
|
G | T | 37 | a0001c0001t0001g0021a0001c0001t0001g0071a0001c0001t0001g0072others(34): Show | 37 | HG00323.hp2 HG00733.hp2 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.-164-49386G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53106540 | ||||||
| chr16:53106653
|
T | C | 1 | a0001c0001t0002g0171 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-164-49273T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53106653 | ||||||
| chr16:53106657
|
T | TAC | 38 | a0001c0001t0001g0021a0001c0001t0001g0071a0001c0001t0001g0072others(35): Show | 38 | HG00323.hp2 HG00733.hp2 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.-164-49247_-164-49 others(8): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53106657 | |||||
| chr16:53106657
|
T | TACACAC | 2 | a0002c0002t0001g0102a0008c0011t0003g0062 | 2 | HG02109.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-164-49251_-164-49 others(12): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53106657 | |||||
| chr16:53106657
|
T | TATAC | 23 | a0001c0001t0001g0026a0001c0001t0001g0038a0001c0001t0001g0081others(20): Show | 23 | HG00609.hp2 HG01884.hp2 HG02040.hp2 others(20): Show |
intron_variant | MODIFIER | c.-164-49268_-164-49 others(10): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53106657 | |||||
| chr16:53106657
|
T | TATACAC | 3 | a0001c0001t0001g0008a0001c0001t0003g0016a0001c0005t0004g0104 | 3 | HG02965.hp1 NA18992.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-164-49268_-164-49 others(12): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53106657 | |||||
| chr16:53106657
|
TAC | T | 130 | a0001c0001t0001g0014a0001c0001t0001g0027a0001c0001t0001g0031others(127): Show | 130 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.-164-49247_-164-49 others(8): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53106657 | |||||
| chr16:53106685
|
G | A | 1 | a0001c0001t0003g0112 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-164-49241G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53106685 | ||||||
| chr16:53106687
|
T | C | 21 | a0001c0001t0001g0008a0001c0001t0001g0026a0001c0001t0001g0038others(18): Show | 21 | HG00609.hp2 HG01884.hp2 HG02040.hp2 others(18): Show |
intron_variant | MODIFIER | c.-164-49239T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53106687 | ||||||
| chr16:53106850
|
G | A | 4 | a0001c0001t0001g0225a0001c0001t0001g0230a0001c0001t0007g0103others(1): Show | 4 | HG02055.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-164-49076G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53106850 | ||||||
| chr16:53107024
|
C | T | 2 | a0002c0002t0001g0102a0008c0011t0003g0062 | 2 | HG02109.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-164-48902C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53107024 | ||||||
| chr16:53107096
|
A | T | 39 | a0001c0001t0001g0021a0001c0001t0001g0071a0001c0001t0001g0072others(36): Show | 39 | HG00323.hp2 HG00733.hp2 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.-164-48830A>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53107096 | ||||||
| chr16:53107239
|
C | T | 37 | a0001c0001t0001g0021a0001c0001t0001g0071a0001c0001t0001g0072others(34): Show | 37 | HG00323.hp2 HG00733.hp2 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.-164-48687C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53107239 | ||||||
| chr16:53107240
|
G | A | 2 | a0001c0001t0001g0045a0001c0001t0001g0099 | 2 | NA19087.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-164-48686G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53107240 | ||||||
| chr16:53107291
|
C | A | 1 | a0002c0002t0001g0113 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-164-48635C>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53107291 | ||||||
| chr16:53107403
|
T | G | 1 | a0001c0001t0001g0067 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-164-48523T>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53107403 | ||||||
| chr16:53107405
|
A | G | 1 | a0001c0001t0001g0067 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-164-48521A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53107405 | ||||||
| chr16:53107459
|
C | CAAAAT | 105 | a0001c0001t0001g0027a0001c0001t0001g0043a0001c0001t0001g0045others(102): Show | 105 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.-164-48438_-164-48 others(11): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53107459 | |||||
| chr16:53107459
|
C | CAAAATAA others(3): Show |
31 | a0001c0001t0001g0014a0001c0001t0001g0026a0001c0001t0001g0038others(28): Show | 31 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.-164-48443_-164-48 others(16): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53107459 | |||||
| chr16:53107459
|
C | CAAAATAA others(8): Show |
7 | a0001c0001t0001g0008a0001c0001t0001g0081a0001c0001t0001g0230others(4): Show | 7 | HG01167.hp2 HG02055.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-164-48448_-164-48 others(21): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53107459 | |||||
| chr16:53107470
|
AAAATAAA others(12): Show |
A | 7 | a0001c0001t0003g0220a0001c0001t0003g0221a0001c0001t0003g0222others(4): Show | 7 | HG02055.hp1 HG03041.hp1 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.-164-48433_-164-48 others(25): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53107470 | |||||
| chr16:53107489
|
T | TAAATA | 37 | a0001c0001t0001g0021a0001c0001t0001g0071a0001c0001t0001g0072others(34): Show | 37 | HG00323.hp2 HG00733.hp2 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.-164-48416_-164-48 others(11): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53107489 | |||||
| chr16:53107676
|
C | T | 24 | a0001c0001t0001g0008a0001c0001t0001g0026a0001c0001t0001g0038others(21): Show | 24 | HG00597.hp1 HG00609.hp2 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.-164-48250C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53107676 | ||||||
| chr16:53107815
|
G | A | 1 | a0001c0003t0013g0186 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-164-48111G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53107815 | ||||||
| chr16:53107845
|
C | A | 1 | a0002c0019t0001g0180 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-164-48081C>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53107845 | ||||||
| chr16:53107950
|
A | G | 2 | a0002c0002t0001g0102a0008c0011t0003g0062 | 2 | HG02109.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-164-47976A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53107950 | ||||||
| chr16:53108287
|
A | G | 1 | a0002c0002t0001g0024 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-164-47639A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53108287 | ||||||
| chr16:53108335
|
CTACAAAA others(2): Show |
C | 39 | a0001c0001t0001g0021a0001c0001t0001g0071a0001c0001t0001g0072others(36): Show | 39 | HG00323.hp2 HG00733.hp2 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.-164-47581_-164-47 others(15): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53108335 | |||||
| chr16:53108368
|
G | T | 70 | a0001c0001t0001g0043a0001c0001t0001g0110a0001c0001t0001g0111others(67): Show | 70 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(67): Show |
intron_variant | MODIFIER | c.-164-47558G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53108368 | ||||||
| chr16:53108511
|
TATAG | T | 97 | a0001c0001t0001g0026a0001c0001t0001g0038a0001c0001t0001g0043others(94): Show | 97 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.-164-47368_-164-47 others(10): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53108511 | |||||
| chr16:53108511
|
TATAGATA others(1): Show |
T | 30 | a0001c0001t0001g0014a0001c0001t0001g0045a0001c0001t0001g0067others(27): Show | 30 | HG00408.hp1 HG00597.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.-164-47372_-164-47 others(14): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53108511 | |||||
| chr16:53108511
|
TATAGATA others(5): Show |
T | 3 | a0001c0003t0002g0040a0001c0003t0002g0070a0001c0013t0001g0055 | 3 | HG00733.hp1 HG02080.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.-164-47376_-164-47 others(18): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53108511 | |||||
| chr16:53108511
|
TATAGATA others(9): Show |
T | 2 | a0001c0001t0001g0098a0003c0004t0006g0190 | 2 | HG02129.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.-164-47380_-164-47 others(22): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53108511 | |||||
| chr16:53108511
|
TATAGATA others(17): Show |
T | 7 | a0001c0005t0004g0231a0001c0005t0004g0232a0001c0005t0004g0233others(4): Show | 7 | HG02615.hp2 HG02897.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.-164-47388_-164-47 others(30): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53108511 | |||||
| chr16:53108638
|
A | G | 39 | a0001c0001t0001g0021a0001c0001t0001g0071a0001c0001t0001g0072others(36): Show | 39 | HG00323.hp2 HG00733.hp2 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.-164-47288A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53108638 | ||||||
| chr16:53108676
|
A | G | 2 | a0002c0002t0001g0102a0008c0011t0003g0062 | 2 | HG02109.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-164-47250A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53108676 | ||||||
| chr16:53108823
|
T | C | 39 | a0001c0001t0001g0021a0001c0001t0001g0071a0001c0001t0001g0072others(36): Show | 39 | HG00323.hp2 HG00733.hp2 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.-164-47103T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53108823 | ||||||
| chr16:53108834
|
C | T | 37 | a0001c0001t0001g0021a0001c0001t0001g0071a0001c0001t0001g0072others(34): Show | 37 | HG00323.hp2 HG00733.hp2 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.-164-47092C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53108834 | ||||||
| chr16:53108893
|
A | AAAAAT | 5 | a0001c0001t0001g0225a0001c0001t0001g0230a0001c0001t0007g0103others(2): Show | 5 | HG01167.hp2 HG02055.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.-164-47009_-164-47 others(11): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53108893 | |||||
| chr16:53108942
|
A | C | 1 | a0001c0001t0015g0166 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-164-46984A>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53108942 | ||||||
| chr16:53109035
|
C | T | 4 | a0001c0001t0003g0096a0002c0002t0001g0102a0003c0004t0001g0177others(1): Show | 4 | HG02109.hp1 HG03130.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-164-46891C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53109035 | ||||||
| chr16:53109211
|
GC | G | 14 | a0001c0001t0003g0220a0001c0001t0003g0221a0001c0001t0003g0222others(11): Show | 14 | HG02055.hp1 HG02615.hp2 HG02897.hp1 others(11): Show |
intron_variant | MODIFIER | c.-164-46714delC | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53109211 | ||||||
| chr16:53109268
|
T | C | 37 | a0001c0001t0001g0021a0001c0001t0001g0071a0001c0001t0001g0072others(34): Show | 37 | HG00323.hp2 HG00733.hp2 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.-164-46658T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53109268 | ||||||
| chr16:53109458
|
A | G | 1 | a0002c0002t0001g0219 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-164-46468A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53109458 | ||||||
| chr16:53109481
|
C | T | 37 | a0001c0001t0001g0021a0001c0001t0001g0071a0001c0001t0001g0072others(34): Show | 37 | HG00323.hp2 HG00733.hp2 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.-164-46445C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53109481 | ||||||
| chr16:53109498
|
T | C | 14 | a0001c0001t0003g0220a0001c0001t0003g0221a0001c0001t0003g0222others(11): Show | 14 | HG02055.hp1 HG02615.hp2 HG02897.hp1 others(11): Show |
intron_variant | MODIFIER | c.-164-46428T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53109498 | ||||||
| chr16:53109630
|
C | T | 1 | a0001c0001t0001g0021 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-164-46296C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53109630 | ||||||
| chr16:53109677
|
C | CT | 23 | a0001c0001t0001g0027a0001c0001t0001g0064a0001c0001t0001g0067others(20): Show | 23 | HG00597.hp2 HG00609.hp1 HG02027.hp1 others(20): Show |
intron_variant | MODIFIER | c.-164-46224dupT | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53109677 | |||||
| chr16:53109677
|
C | CTT | 7 | a0001c0001t0001g0069a0001c0001t0003g0184a0001c0001t0003g0220others(4): Show | 7 | HG02055.hp1 HG02109.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.-164-46225_-164-46 others(8): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53109677 | |||||
| chr16:53109677
|
C | CTTT | 11 | a0001c0001t0003g0096a0001c0001t0003g0221a0001c0003t0002g0224others(8): Show | 11 | HG01168.hp1 HG02615.hp2 HG02897.hp1 others(8): Show |
intron_variant | MODIFIER | c.-164-46226_-164-46 others(9): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53109677 | |||||
| chr16:53109677
|
C | CTTTT | 27 | a0001c0001t0001g0021a0001c0001t0001g0072a0001c0001t0001g0206others(24): Show | 27 | HG00323.hp2 HG00733.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.-164-46227_-164-46 others(10): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53109677 | |||||
| chr16:53109677
|
C | CTTTTT | 9 | a0001c0001t0001g0071a0001c0001t0001g0211a0001c0001t0001g0218others(6): Show | 9 | HG01243.hp2 HG02738.hp2 HG03669.hp1 others(6): Show |
intron_variant | MODIFIER | c.-164-46228_-164-46 others(11): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53109677 | |||||
| chr16:53109691
|
T | TTTC | 6 | a0001c0001t0001g0225a0001c0001t0001g0230a0001c0001t0007g0103others(3): Show | 6 | HG01167.hp2 HG02055.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-164-46233_-164-46 others(9): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53109691 | |||||
| chr16:53109691
|
T | TTTTC | 59 | a0001c0001t0001g0043a0001c0001t0001g0110a0001c0001t0001g0111others(56): Show | 59 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(56): Show |
intron_variant | MODIFIER | c.-164-46232_-164-46 others(10): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53109691 | |||||
| chr16:53109691
|
T | TTTTTC | 25 | a0001c0001t0001g0008a0001c0001t0001g0026a0001c0001t0001g0081others(22): Show | 25 | HG00597.hp1 HG01884.hp2 HG02040.hp2 others(22): Show |
intron_variant | MODIFIER | c.-164-46231_-164-46 others(11): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53109691 | |||||
| chr16:53109754
|
G | A | 2 | a0003c0004t0001g0187a0003c0004t0001g0194 | 2 | HG02165.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.-164-46172G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53109754 | ||||||
| chr16:53110150
|
C | T | 3 | a0001c0005t0004g0232a0001c0005t0004g0235a0001c0005t0004g0238 | 3 | HG02615.hp2 HG02897.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-164-45776C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53110150 | ||||||
| chr16:53110279
|
G | A | 46 | a0001c0001t0001g0043a0001c0001t0001g0119a0001c0001t0001g0159others(43): Show | 46 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(43): Show |
intron_variant | MODIFIER | c.-164-45647G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53110279 | ||||||
| chr16:53110392
|
T | A | 14 | a0001c0001t0003g0220a0001c0001t0003g0221a0001c0001t0003g0222others(11): Show | 14 | HG02055.hp1 HG02615.hp2 HG02897.hp1 others(11): Show |
intron_variant | MODIFIER | c.-164-45534T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53110392 | ||||||
| chr16:53110738
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-164-45188G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53110738 | ||||||
| chr16:53110748
|
A | G | 21 | a0001c0001t0001g0008a0001c0001t0001g0026a0001c0001t0001g0038others(18): Show | 21 | HG00609.hp2 HG01884.hp2 HG02040.hp2 others(18): Show |
intron_variant | MODIFIER | c.-164-45178A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53110748 | ||||||
| chr16:53110791
|
A | T | 2 | a0001c0003t0002g0152a0001c0005t0005g0061 | 2 | HG03688.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.-164-45135A>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53110791 | ||||||
| chr16:53110885
|
G | A | 1 | a0002c0002t0001g0095 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-164-45041G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53110885 | ||||||
| chr16:53110973
|
T | G | 1 | a0001c0001t0001g0124 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-164-44953T>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53110973 | ||||||
| chr16:53110975
|
G | A | 2 | a0001c0001t0003g0096a0003c0004t0001g0177 | 2 | HG03130.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-164-44951G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53110975 | ||||||
| chr16:53111010
|
A | G | 1 | a0001c0001t0003g0096 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-164-44916A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53111010 | ||||||
| chr16:53111073
|
G | A | 25 | a0001c0001t0001g0008a0001c0001t0001g0026a0001c0001t0001g0038others(22): Show | 25 | HG00609.hp2 HG01884.hp2 HG02040.hp2 others(22): Show |
intron_variant | MODIFIER | c.-164-44853G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53111073 | ||||||
| chr16:53111101
|
C | T | 37 | a0001c0001t0001g0021a0001c0001t0001g0071a0001c0001t0001g0072others(34): Show | 37 | HG00323.hp2 HG00733.hp2 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.-164-44825C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53111101 | ||||||
| chr16:53111137
|
C | T | 3 | a0001c0003t0002g0047a0001c0003t0002g0191a0001c0003t0016g0039 | 3 | NA18972.hp2 NA19068.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.-164-44789C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53111137 | ||||||
| chr16:53111183
|
T | G | 2 | a0001c0003t0002g0028a0001c0003t0002g0029 | 2 | HG02129.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.-164-44743T>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53111183 | ||||||
| chr16:53111317
|
T | G | 5 | a0001c0001t0001g0225a0001c0001t0001g0230a0001c0001t0007g0103others(2): Show | 5 | HG01167.hp2 HG02055.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.-164-44609T>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53111317 | ||||||
| chr16:53111416
|
A | C | 3 | a0001c0003t0002g0047a0001c0003t0002g0191a0001c0003t0016g0039 | 3 | NA18972.hp2 NA19068.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.-164-44510A>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53111416 | ||||||
| chr16:53111673
|
A | T | 1 | a0001c0001t0003g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-164-44253A>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53111673 | ||||||
| chr16:53111858
|
G | A | 38 | a0001c0001t0001g0021a0001c0001t0001g0071a0001c0001t0001g0072others(35): Show | 38 | HG00323.hp2 HG00733.hp2 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.-164-44068G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53111858 | ||||||
| chr16:53111900
|
G | A | 2 | a0001c0001t0003g0096a0003c0004t0001g0177 | 2 | HG03130.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-164-44026G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53111900 | ||||||
| chr16:53111901
|
C | T | 25 | a0001c0001t0001g0008a0001c0001t0001g0026a0001c0001t0001g0038others(22): Show | 25 | HG00609.hp2 HG01884.hp2 HG02040.hp2 others(22): Show |
intron_variant | MODIFIER | c.-164-44025C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53111901 | ||||||
| chr16:53112086
|
T | G | 2 | a0001c0003t0002g0083a0001c0003t0017g0181 | 2 | HG03017.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.-164-43840T>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53112086 | ||||||
| chr16:53112094
|
G | A | 6 | a0001c0001t0003g0220a0001c0001t0003g0222a0001c0001t0003g0223others(3): Show | 6 | HG02055.hp1 HG03041.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.-164-43832G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53112094 | ||||||
| chr16:53112271
|
G | A | 25 | a0001c0001t0001g0008a0001c0001t0001g0026a0001c0001t0001g0038others(22): Show | 25 | HG00609.hp2 HG01884.hp2 HG02040.hp2 others(22): Show |
intron_variant | MODIFIER | c.-164-43655G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53112271 | ||||||
| chr16:53112569
|
G | T | 2 | a0002c0002t0001g0102a0008c0011t0003g0062 | 2 | HG02109.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-164-43357G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53112569 | ||||||
| chr16:53112678
|
A | G | 2 | a0002c0002t0001g0102a0008c0011t0003g0062 | 2 | HG02109.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-164-43248A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53112678 | ||||||
| chr16:53112927
|
A | G | 4 | a0001c0001t0003g0131a0001c0001t0003g0139a0001c0001t0003g0172others(1): Show | 4 | HG01891.hp1 HG02257.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-164-42999A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53112927 | ||||||
| chr16:53113117
|
G | A | 3 | a0001c0001t0001g0218a0003c0004t0001g0187a0003c0004t0001g0194 | 3 | HG02165.hp1 HG04184.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.-164-42809G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53113117 | ||||||
| chr16:53113209
|
T | C | 1 | a0001c0001t0002g0171 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-164-42717T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53113209 | ||||||
| chr16:53113355
|
A | G | 2 | a0002c0002t0001g0102a0008c0011t0003g0062 | 2 | HG02109.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-164-42571A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53113355 | ||||||
| chr16:53113364
|
C | CT | 52 | a0001c0001t0001g0026a0001c0001t0001g0043a0001c0001t0001g0091others(49): Show | 52 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(49): Show |
intron_variant | MODIFIER | c.-164-42542dupT | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53113364 | |||||
| chr16:53113364
|
C | CTT | 25 | a0001c0001t0001g0021a0001c0001t0001g0072a0001c0001t0001g0206others(22): Show | 25 | HG00323.hp2 HG00733.hp2 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.-164-42543_-164-42 others(8): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53113364 | |||||
| chr16:53113364
|
C | CTTT | 15 | a0001c0001t0001g0071a0001c0001t0001g0218a0002c0002t0001g0102others(12): Show | 15 | HG01243.hp2 HG02015.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.-164-42544_-164-42 others(9): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53113364 | |||||
| chr16:53113461
|
T | C | 7 | a0001c0001t0003g0220a0001c0001t0003g0221a0001c0001t0003g0222others(4): Show | 7 | HG02055.hp1 HG03041.hp1 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.-164-42465T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53113461 | ||||||
| chr16:53113501
|
C | T | 47 | a0001c0001t0001g0043a0001c0001t0001g0119a0001c0001t0001g0159others(44): Show | 47 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(44): Show |
intron_variant | MODIFIER | c.-164-42425C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53113501 | ||||||
| chr16:53113502
|
G | A | 2 | a0002c0002t0001g0102a0008c0011t0003g0062 | 2 | HG02109.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-164-42424G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53113502 | ||||||
| chr16:53113557
|
C | T | 37 | a0001c0001t0001g0021a0001c0001t0001g0071a0001c0001t0001g0072others(34): Show | 37 | HG00323.hp2 HG00733.hp2 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.-164-42369C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53113557 | ||||||
| chr16:53113593
|
G | C | 1 | a0001c0014t0001g0115 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-164-42333G>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53113593 | ||||||
| chr16:53113661
|
C | T | 26 | a0001c0001t0001g0008a0001c0001t0001g0026a0001c0001t0001g0038others(23): Show | 26 | HG00609.hp2 HG01884.hp2 HG02040.hp2 others(23): Show |
intron_variant | MODIFIER | c.-164-42265C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53113661 | ||||||
| chr16:53113802
|
C | T | 2 | a0001c0001t0003g0096a0003c0004t0001g0177 | 2 | HG03130.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-164-42124C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53113802 | ||||||
| chr16:53113990
|
C | T | 12 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0116others(9): Show | 12 | HG01884.hp1 HG02451.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.-164-41936C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53113990 | ||||||
| chr16:53114086
|
TA | T | 12 | a0001c0001t0001g0008a0001c0001t0001g0058a0001c0001t0001g0091others(9): Show | 12 | HG01167.hp1 HG01167.hp2 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.-164-41827delA | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53114086 | |||||
| chr16:53114148
|
A | G | 26 | a0001c0001t0001g0008a0001c0001t0001g0026a0001c0001t0001g0038others(23): Show | 26 | HG00609.hp2 HG01884.hp2 HG02040.hp2 others(23): Show |
intron_variant | MODIFIER | c.-164-41778A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53114148 | ||||||
| chr16:53114218
|
T | A | 1 | a0001c0001t0001g0091 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-164-41708T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53114218 | ||||||
| chr16:53114288
|
C | T | 1 | a0001c0001t0001g0069 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-164-41638C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53114288 | ||||||
| chr16:53114420
|
G | C | 1 | a0006c0009t0004g0107 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-164-41506G>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53114420 | ||||||
| chr16:53114424
|
AT | A | 7 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0003g0079others(4): Show | 7 | HG01884.hp2 HG02280.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.-164-41497delT | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53114424 | |||||
| chr16:53114440
|
T | C | 7 | a0001c0001t0003g0220a0001c0001t0003g0221a0001c0001t0003g0222others(4): Show | 7 | HG02055.hp1 HG03041.hp1 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.-164-41486T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53114440 | ||||||
| chr16:53114447
|
G | A | 1 | a0001c0001t0001g0067 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-164-41479G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53114447 | ||||||
| chr16:53114515
|
C | T | 47 | a0001c0001t0001g0043a0001c0001t0001g0119a0001c0001t0001g0159others(44): Show | 47 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(44): Show |
intron_variant | MODIFIER | c.-164-41411C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53114515 | ||||||
| chr16:53114528
|
G | A | 1 | a0003c0004t0001g0148 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-164-41398G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53114528 | ||||||
| chr16:53114560
|
C | CATTATTT others(3): Show |
1 | a0001c0003t0010g0006 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-164-41352_-164-41 others(16): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53114560 | |||||
| chr16:53114777
|
C | T | 1 | a0001c0001t0003g0112 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-164-41149C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53114777 | ||||||
| chr16:53114853
|
C | T | 1 | a0001c0003t0016g0039 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-164-41073C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53114853 | ||||||
| chr16:53114922
|
T | TTTGA | 17 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0116others(14): Show | 17 | HG01884.hp1 HG02109.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.-164-40980_-164-40 others(10): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53114922 | |||||
| chr16:53114922
|
TTTGA | T | 37 | a0001c0001t0001g0021a0001c0001t0001g0071a0001c0001t0001g0072others(34): Show | 37 | HG00323.hp2 HG00733.hp2 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.-164-40980_-164-40 others(10): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53114922 | |||||
| chr16:53114957
|
C | A | 13 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0116others(10): Show | 13 | HG01884.hp1 HG02451.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.-164-40969C>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53114957 | ||||||
| chr16:53114960
|
C | T | 60 | a0001c0001t0001g0043a0001c0001t0001g0110a0001c0001t0001g0111others(57): Show | 60 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(57): Show |
intron_variant | MODIFIER | c.-164-40966C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53114960 | ||||||
| chr16:53115078
|
C | T | 7 | a0001c0001t0003g0220a0001c0001t0003g0221a0001c0001t0003g0222others(4): Show | 7 | HG02055.hp1 HG03041.hp1 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.-164-40848C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53115078 | ||||||
| chr16:53115342
|
A | C | 1 | a0001c0003t0002g0170 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-164-40584A>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53115342 | ||||||
| chr16:53115504
|
A | C | 37 | a0001c0001t0001g0021a0001c0001t0001g0071a0001c0001t0001g0072others(34): Show | 37 | HG00323.hp2 HG00733.hp2 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.-164-40422A>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53115504 | ||||||
| chr16:53115655
|
G | A | 1 | a0001c0001t0001g0211 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-164-40271G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53115655 | ||||||
| chr16:53115845
|
T | A | 1 | a0003c0004t0001g0177 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-164-40081T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53115845 | ||||||
| chr16:53115854
|
G | T | 1 | a0001c0001t0003g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-164-40072G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53115854 | ||||||
| chr16:53115861
|
A | G | 26 | a0001c0001t0001g0008a0001c0001t0001g0026a0001c0001t0001g0038others(23): Show | 26 | HG00609.hp2 HG01884.hp2 HG02040.hp2 others(23): Show |
intron_variant | MODIFIER | c.-164-40065A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53115861 | ||||||
| chr16:53115996
|
T | G | 2 | a0001c0001t0003g0096a0003c0004t0001g0177 | 2 | HG03130.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-164-39930T>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53115996 | ||||||
| chr16:53116184
|
C | G | 7 | a0001c0001t0003g0220a0001c0001t0003g0221a0001c0001t0003g0222others(4): Show | 7 | HG02055.hp1 HG03041.hp1 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.-164-39742C>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53116184 | ||||||
| chr16:53116551
|
G | A | 1 | a0001c0001t0003g0096 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-164-39375G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53116551 | ||||||
| chr16:53116608
|
G | A | 1 | a0002c0002t0001g0106 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-164-39318G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53116608 | ||||||
| chr16:53116823
|
G | A | 37 | a0001c0001t0001g0021a0001c0001t0001g0071a0001c0001t0001g0072others(34): Show | 37 | HG00323.hp2 HG00733.hp2 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.-164-39103G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53116823 | ||||||
| chr16:53117014
|
G | A | 37 | a0001c0001t0001g0021a0001c0001t0001g0071a0001c0001t0001g0072others(34): Show | 37 | HG00323.hp2 HG00733.hp2 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.-164-38912G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53117014 | ||||||
| chr16:53117237
|
T | A | 3 | a0001c0005t0005g0135a0002c0002t0008g0065a0002c0002t0008g0137 | 3 | HG00408.hp1 HG02080.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.-164-38689T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53117237 | ||||||
| chr16:53117246
|
T | A | 1 | a0001c0001t0003g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-164-38680T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53117246 | ||||||
| chr16:53117264
|
G | A | 4 | a0001c0001t0003g0131a0001c0001t0003g0139a0001c0001t0003g0172others(1): Show | 4 | HG01891.hp1 HG02257.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-164-38662G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53117264 | ||||||
| chr16:53117407
|
A | AAT | 69 | a0001c0001t0001g0043a0001c0001t0001g0084a0001c0001t0001g0110others(66): Show | 69 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(66): Show |
intron_variant | MODIFIER | c.-164-38500_-164-38 others(8): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53117407 | |||||
| chr16:53117407
|
A | AATAT | 6 | a0001c0001t0003g0133a0001c0005t0004g0235a0003c0004t0001g0134others(3): Show | 6 | HG02559.hp2 HG02809.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-164-38502_-164-38 others(10): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53117407 | |||||
| chr16:53117407
|
A | AATATAT | 2 | a0001c0005t0004g0097a0001c0005t0004g0169 | 2 | HG01884.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-164-38504_-164-38 others(12): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53117407 | |||||
| chr16:53117407
|
AAT | A | 37 | a0001c0001t0001g0021a0001c0001t0001g0071a0001c0001t0001g0072others(34): Show | 37 | HG00323.hp2 HG00733.hp2 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.-164-38500_-164-38 others(8): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53117407 | |||||
| chr16:53117413
|
T | C | 1 | a0001c0001t0001g0091 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-164-38513T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53117413 | ||||||
| chr16:53117831
|
C | CT | 71 | a0001c0001t0001g0043a0001c0001t0001g0110a0001c0001t0001g0111others(68): Show | 71 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(68): Show |
intron_variant | MODIFIER | c.-164-38083dupT | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53117831 | |||||
| chr16:53117989
|
C | T | 37 | a0001c0001t0001g0021a0001c0001t0001g0071a0001c0001t0001g0072others(34): Show | 37 | HG00323.hp2 HG00733.hp2 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.-164-37937C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53117989 | ||||||
| chr16:53118049
|
G | A | 37 | a0001c0001t0001g0021a0001c0001t0001g0071a0001c0001t0001g0072others(34): Show | 37 | HG00323.hp2 HG00733.hp2 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.-164-37877G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53118049 | ||||||
| chr16:53118127
|
A | G | 1 | a0001c0001t0001g0173 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-164-37799A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53118127 | ||||||
| chr16:53118217
|
G | A | 1 | a0002c0002t0001g0063 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-164-37709G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53118217 | ||||||
| chr16:53118218
|
A | G | 1 | a0001c0005t0005g0089 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-164-37708A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53118218 | ||||||
| chr16:53118233
|
A | C | 1 | a0002c0002t0001g0144 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-164-37693A>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53118233 | ||||||
| chr16:53118236
|
G | A | 37 | a0001c0001t0001g0021a0001c0001t0001g0071a0001c0001t0001g0072others(34): Show | 37 | HG00323.hp2 HG00733.hp2 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.-164-37690G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53118236 | ||||||
| chr16:53118336
|
G | A | 36 | a0001c0001t0001g0021a0001c0001t0001g0071a0001c0001t0001g0072others(33): Show | 36 | HG00323.hp2 HG00733.hp2 HG01074.hp1 others(33): Show |
intron_variant | MODIFIER | c.-164-37590G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53118336 | ||||||
| chr16:53118386
|
C | T | 1 | a0001c0001t0007g0122 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-164-37540C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53118386 | ||||||
| chr16:53118467
|
G | A | 12 | a0001c0001t0001g0225a0001c0001t0001g0230a0001c0001t0007g0103others(9): Show | 12 | HG01167.hp2 HG02055.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.-164-37459G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53118467 | ||||||
| chr16:53118541
|
T | G | 37 | a0001c0001t0001g0021a0001c0001t0001g0071a0001c0001t0001g0072others(34): Show | 37 | HG00323.hp2 HG00733.hp2 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.-164-37385T>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53118541 | ||||||
| chr16:53118680
|
G | A | 2 | a0002c0002t0001g0102a0008c0011t0003g0062 | 2 | HG02109.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-164-37246G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53118680 | ||||||
| chr16:53118759
|
T | A | 37 | a0001c0001t0001g0021a0001c0001t0001g0071a0001c0001t0001g0072others(34): Show | 37 | HG00323.hp2 HG00733.hp2 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.-164-37167T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53118759 | ||||||
| chr16:53118776
|
A | G | 2 | a0002c0002t0001g0150a0003c0004t0001g0123 | 2 | HG00099.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.-164-37150A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53118776 | ||||||
| chr16:53118793
|
C | CT | 10 | a0001c0001t0001g0008a0001c0001t0001g0110a0001c0001t0001g0111others(7): Show | 10 | HG00099.hp2 HG02055.hp2 HG02080.hp2 others(7): Show |
intron_variant | MODIFIER | c.-164-37114dupT | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53118793 | |||||
| chr16:53118793
|
C | CTT | 31 | a0001c0001t0001g0021a0001c0001t0001g0071a0001c0001t0001g0072others(28): Show | 31 | HG00323.hp2 HG00733.hp2 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.-164-37115_-164-37 others(8): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53118793 | |||||
| chr16:53118793
|
C | CTTT | 6 | a0001c0001t0001g0211a0002c0002t0001g0042a0003c0004t0001g0192others(3): Show | 6 | HG02738.hp2 HG04199.hp1 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.-164-37116_-164-37 others(9): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53118793 | |||||
| chr16:53118863
|
G | T | 1 | a0001c0003t0002g0083 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-164-37063G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53118863 | ||||||
| chr16:53118877
|
T | C | 39 | a0001c0001t0001g0021a0001c0001t0001g0071a0001c0001t0001g0072others(36): Show | 39 | HG00323.hp2 HG00733.hp2 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.-164-37049T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53118877 | ||||||
| chr16:53119012
|
G | A | 1 | a0001c0003t0002g0086 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-164-36914G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53119012 | ||||||
| chr16:53119373
|
T | TA | 40 | a0001c0001t0001g0021a0001c0001t0001g0071a0001c0001t0001g0072others(37): Show | 40 | HG00323.hp2 HG00733.hp2 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.-164-36543dupA | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53119373 | |||||
| chr16:53119386
|
A | C | 11 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0116others(8): Show | 11 | HG01884.hp1 HG02451.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.-164-36540A>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53119386 | ||||||
| chr16:53119438
|
A | G | 207 | a0001c0001t0001g0008a0001c0001t0001g0021a0001c0001t0001g0026others(204): Show | 207 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.-164-36488A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53119438 | ||||||
| chr16:53119560
|
T | C | 154 | a0001c0001t0001g0008a0001c0001t0001g0021a0001c0001t0001g0026others(151): Show | 154 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.-164-36366T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53119560 | ||||||
| chr16:53119618
|
A | C | 4 | a0001c0001t0002g0175a0001c0005t0018g0001a0002c0002t0001g0106others(1): Show | 4 | HG02622.hp1 HG03471.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-164-36308A>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53119618 | ||||||
| chr16:53119620
|
A | G | 93 | a0001c0001t0001g0021a0001c0001t0001g0043a0001c0001t0001g0071others(90): Show | 93 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.-164-36306A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53119620 | ||||||
| chr16:53119693
|
G | A | 2 | a0001c0001t0001g0084a0001c0001t0001g0085 | 2 | HG00621.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.-164-36233G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53119693 | ||||||
| chr16:53119989
|
G | C | 222 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0021others(219): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.-164-35937G>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53119989 | ||||||
| chr16:53120062
|
C | CA | 40 | a0001c0001t0001g0021a0001c0001t0001g0071a0001c0001t0001g0072others(37): Show | 40 | HG00323.hp2 HG00733.hp2 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.-164-35851dupA | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53120062 | |||||
| chr16:53120252
|
A | T | 18 | a0001c0001t0001g0027a0001c0001t0001g0031a0001c0001t0001g0045others(15): Show | 18 | HG00408.hp2 HG00621.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.-164-35674A>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53120252 | ||||||
| chr16:53120253
|
A | T | 214 | a0001c0001t0001g0008a0001c0001t0001g0021a0001c0001t0001g0026others(211): Show | 214 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.-164-35673A>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53120253 | ||||||
| chr16:53120260
|
T | A | 214 | a0001c0001t0001g0008a0001c0001t0001g0021a0001c0001t0001g0026others(211): Show | 214 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.-164-35666T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53120260 | ||||||
| chr16:53120325
|
T | G | 1 | a0001c0001t0003g0222 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-164-35601T>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53120325 | ||||||
| chr16:53120449
|
A | G | 75 | a0001c0001t0001g0056a0001c0001t0001g0060a0001c0001t0001g0110others(72): Show | 75 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.-164-35477A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53120449 | ||||||
| chr16:53120482
|
G | A | 2 | a0001c0001t0003g0016a0001c0005t0004g0104 | 2 | HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-164-35444G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53120482 | ||||||
| chr16:53120527
|
C | T | 2 | a0001c0003t0017g0181a0002c0002t0001g0164 | 2 | HG02135.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.-164-35399C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53120527 | ||||||
| chr16:53120620
|
T | A | 49 | a0001c0001t0001g0056a0001c0001t0001g0119a0001c0001t0001g0124others(46): Show | 49 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.-164-35306T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53120620 | ||||||
| chr16:53120676
|
C | T | 44 | a0001c0001t0001g0056a0001c0001t0001g0211a0001c0001t0003g0131others(41): Show | 44 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(41): Show |
intron_variant | MODIFIER | c.-164-35250C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53120676 | ||||||
| chr16:53120687
|
G | A | 1 | a0003c0004t0001g0207 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-164-35239G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53120687 | ||||||
| chr16:53120748
|
T | C | 3 | a0004c0006t0001g0121a0004c0006t0001g0127a0004c0006t0001g0128 | 3 | NA18952.hp1 NA18989.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.-164-35178T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53120748 | ||||||
| chr16:53120794
|
C | T | 46 | a0001c0001t0001g0056a0001c0001t0001g0211a0001c0001t0003g0131others(43): Show | 46 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(43): Show |
intron_variant | MODIFIER | c.-164-35132C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53120794 | ||||||
| chr16:53120920
|
C | T | 47 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0025others(44): Show | 47 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.-164-35006C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53120920 | ||||||
| chr16:53120960
|
C | T | 49 | a0001c0001t0001g0027a0001c0001t0001g0031a0001c0001t0001g0058others(46): Show | 49 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(46): Show |
intron_variant | MODIFIER | c.-164-34966C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53120960 | ||||||
| chr16:53121534
|
G | T | 1 | a0001c0005t0004g0097 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-164-34392G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53121534 | ||||||
| chr16:53122165
|
GT | G | 80 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0025others(77): Show | 80 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.-164-33760delT | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53122165 | ||||||
| chr16:53122415
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-164-33511G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53122415 | ||||||
| chr16:53122544
|
CT | C | 95 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0025others(92): Show | 95 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(92): Show |
intron_variant | MODIFIER | c.-164-33364delT | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53122544 | |||||
| chr16:53122630
|
C | T | 1 | a0001c0001t0007g0122 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-164-33296C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53122630 | ||||||
| chr16:53122638
|
A | G | 1 | a0001c0001t0015g0166 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-164-33288A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53122638 | ||||||
| chr16:53122737
|
C | T | 1 | a0001c0001t0007g0122 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-164-33189C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53122737 | ||||||
| chr16:53122746
|
G | A | 1 | a0001c0001t0002g0175 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-164-33180G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53122746 | ||||||
| chr16:53122807
|
T | C | 22 | a0001c0001t0001g0091a0001c0001t0001g0168a0001c0001t0001g0173others(19): Show | 22 | HG01891.hp2 HG02055.hp1 HG02451.hp2 others(19): Show |
intron_variant | MODIFIER | c.-164-33119T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53122807 | ||||||
| chr16:53122835
|
T | A | 1 | a0001c0008t0001g0077 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-164-33091T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53122835 | ||||||
| chr16:53122867
|
C | T | 1 | a0001c0003t0002g0202 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-164-33059C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53122867 | ||||||
| chr16:53122873
|
AT | A | 62 | a0001c0001t0001g0027a0001c0001t0001g0031a0001c0001t0001g0058others(59): Show | 62 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.-164-33037delT | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53122873 | |||||
| chr16:53122935
|
T | C | 1 | a0002c0002t0001g0102 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-164-32991T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53122935 | ||||||
| chr16:53123007
|
G | A | 1 | a0001c0005t0004g0097 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-164-32919G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53123007 | ||||||
| chr16:53123028
|
A | G | 2 | a0001c0001t0002g0171a0001c0001t0002g0175 | 2 | HG02451.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.-164-32898A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53123028 | ||||||
| chr16:53123083
|
G | A | 41 | a0001c0001t0001g0056a0001c0001t0001g0159a0001c0001t0001g0211others(38): Show | 41 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(38): Show |
intron_variant | MODIFIER | c.-164-32843G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53123083 | ||||||
| chr16:53123171
|
C | CT | 120 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0021others(117): Show | 120 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(117): Show |
intron_variant | MODIFIER | c.-164-32741dupT | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53123171 | |||||
| chr16:53123244
|
G | A | 3 | a0001c0001t0002g0171a0001c0001t0002g0175a0002c0002t0001g0102 | 3 | HG02451.hp1 HG02622.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-164-32682G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53123244 | ||||||
| chr16:53123264
|
G | A | 3 | a0001c0001t0002g0171a0001c0001t0002g0175a0002c0002t0001g0102 | 3 | HG02451.hp1 HG02622.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-164-32662G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53123264 | ||||||
| chr16:53123473
|
T | C | 2 | a0002c0002t0001g0019a0002c0002t0001g0020 | 2 | NA18939.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.-164-32453T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53123473 | ||||||
| chr16:53123493
|
T | G | 1 | a0001c0003t0002g0036 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-164-32433T>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53123493 | ||||||
| chr16:53123526
|
C | T | 1 | a0002c0002t0001g0044 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-164-32400C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53123526 | ||||||
| chr16:53123713
|
G | A | 52 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0021others(49): Show | 52 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(49): Show |
intron_variant | MODIFIER | c.-164-32213G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53123713 | ||||||
| chr16:53123811
|
T | A | 60 | a0001c0001t0001g0026a0001c0001t0001g0081a0001c0001t0001g0119others(57): Show | 60 | HG00140.hp2 HG00558.hp2 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.-164-32115T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53123811 | ||||||
| chr16:53123953
|
T | C | 3 | a0003c0004t0001g0134a0003c0004t0001g0141a0003c0004t0001g0143 | 3 | HG02559.hp2 HG02895.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-164-31973T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53123953 | ||||||
| chr16:53124307
|
A | G | 68 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0182others(65): Show | 68 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.-164-31619A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53124307 | ||||||
| chr16:53124403
|
C | T | 1 | a0001c0003t0002g0041 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-164-31523C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53124403 | ||||||
| chr16:53124467
|
A | AT | 72 | a0001c0001t0001g0084a0001c0001t0001g0092a0001c0001t0001g0124others(69): Show | 72 | HG00099.hp2 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.-164-31432dupT | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53124467 | |||||
| chr16:53124467
|
A | ATT | 17 | a0001c0001t0001g0110a0001c0001t0001g0182a0001c0001t0001g0225others(14): Show | 17 | HG00408.hp1 HG00733.hp2 HG02080.hp1 others(14): Show |
intron_variant | MODIFIER | c.-164-31433_-164-31 others(8): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53124467 | |||||
| chr16:53124467
|
AT | A | 8 | a0001c0001t0001g0066a0001c0001t0003g0096a0001c0003t0002g0125others(5): Show | 8 | HG00408.hp2 HG01099.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.-164-31432delT | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53124467 | |||||
| chr16:53124467
|
ATTTTTTT others(1): Show |
A | 9 | a0001c0005t0004g0104a0001c0005t0004g0231a0001c0005t0004g0232others(6): Show | 9 | HG02615.hp2 HG02897.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.-164-31439_-164-31 others(14): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53124467 | |||||
| chr16:53124467
|
ATTTTTTT others(3): Show |
A | 1 | a0001c0008t0001g0077 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-164-31441_-164-31 others(16): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53124467 | |||||
| chr16:53124508
|
C | T | 1 | a0003c0004t0006g0074 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-164-31418C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53124508 | ||||||
| chr16:53124514
|
G | A | 3 | a0001c0001t0001g0043a0001c0001t0001g0185a0001c0001t0001g0188 | 3 | HG02683.hp2 HG03492.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-164-31412G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53124514 | ||||||
| chr16:53124567
|
C | G | 1 | a0001c0001t0001g0025 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-164-31359C>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53124567 | ||||||
| chr16:53124798
|
C | T | 6 | a0002c0002t0001g0106a0002c0002t0001g0109a0002c0002t0001g0113others(3): Show | 6 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-164-31128C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53124798 | ||||||
| chr16:53124851
|
GC | G | 11 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0231others(8): Show | 11 | HG01167.hp2 HG01884.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-164-31072delC | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53124851 | |||||
| chr16:53124857
|
C | T | 11 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0231others(8): Show | 11 | HG01167.hp2 HG01884.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-164-31069C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53124857 | ||||||
| chr16:53124891
|
G | A | 5 | a0002c0002t0001g0109a0002c0002t0001g0113a0002c0002t0001g0114others(2): Show | 5 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.-164-31035G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53124891 | ||||||
| chr16:53124949
|
A | G | 1 | a0001c0003t0002g0015 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-164-30977A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53124949 | ||||||
| chr16:53125016
|
C | G | 1 | a0001c0005t0001g0215 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-164-30910C>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53125016 | ||||||
| chr16:53125142
|
G | C | 1 | a0001c0005t0004g0097 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-164-30784G>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53125142 | ||||||
| chr16:53125218
|
A | AT | 96 | a0001c0001t0001g0008a0001c0001t0001g0025a0001c0001t0001g0043others(93): Show | 96 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.-164-30685dupT | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53125218 | |||||
| chr16:53125218
|
A | ATT | 8 | a0001c0001t0001g0185a0001c0003t0002g0029a0001c0005t0005g0017others(5): Show | 8 | HG02109.hp1 HG02135.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.-164-30686_-164-30 others(8): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53125218 | |||||
| chr16:53125218
|
AT | A | 9 | a0001c0001t0003g0226a0001c0005t0004g0078a0001c0005t0004g0104others(6): Show | 9 | HG01167.hp2 HG01884.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.-164-30685delT | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53125218 | |||||
| chr16:53125222
|
T | A | 14 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0031others(11): Show | 14 | HG00408.hp2 HG00621.hp1 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.-164-30704T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53125222 | ||||||
| chr16:53125226
|
T | A | 2 | a0001c0001t0001g0031a0001c0001t0001g0179 | 2 | HG01257.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.-164-30700T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53125226 | ||||||
| chr16:53125230
|
T | A | 1 | a0001c0001t0001g0031 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-164-30696T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53125230 | ||||||
| chr16:53125413
|
G | T | 19 | a0001c0001t0003g0022a0001c0001t0003g0079a0001c0001t0003g0096others(16): Show | 19 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.-164-30513G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53125413 | ||||||
| chr16:53125493
|
T | C | 76 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0182others(73): Show | 76 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.-164-30433T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53125493 | ||||||
| chr16:53125528
|
G | A | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.-164-30398G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53125528 | ||||||
| chr16:53125713
|
A | G | 3 | a0002c0002t0001g0109a0002c0002t0001g0113a0002c0002t0001g0114 | 3 | HG02717.hp1 HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-164-30213A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53125713 | ||||||
| chr16:53125911
|
A | T | 68 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0182others(65): Show | 68 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.-164-30015A>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53125911 | ||||||
| chr16:53126099
|
G | GTCATATG others(9): Show |
1 | a0001c0003t0019g0004 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-164-29826_-164-29 others(22): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53126099 | |||||
| chr16:53126112
|
A | G | 1 | a0003c0004t0001g0200 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-164-29814A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53126112 | ||||||
| chr16:53126149
|
T | C | 1 | a0003c0004t0006g0190 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-164-29777T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53126149 | ||||||
| chr16:53126405
|
T | C | 1 | a0002c0002t0001g0054 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-164-29521T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53126405 | ||||||
| chr16:53126586
|
C | CT | 15 | a0001c0001t0001g0165a0001c0005t0001g0215a0001c0005t0004g0078others(12): Show | 15 | HG01167.hp2 HG01884.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.-164-29321dupT | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53126586 | |||||
| chr16:53126586
|
C | CTT | 18 | a0001c0005t0004g0097a0001c0005t0005g0017a0001c0005t0005g0018others(15): Show | 18 | HG00323.hp1 HG00609.hp1 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.-164-29322_-164-29 others(8): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53126586 | |||||
| chr16:53126586
|
C | CTTT | 44 | a0001c0001t0001g0111a0001c0001t0001g0182a0001c0005t0005g0032others(41): Show | 44 | HG00099.hp2 HG00408.hp1 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.-164-29323_-164-29 others(9): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53126586 | |||||
| chr16:53126586
|
CT | C | 46 | a0001c0001t0001g0060a0001c0001t0003g0022a0001c0001t0003g0079others(43): Show | 46 | HG00140.hp2 HG00558.hp2 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.-164-29321delT | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53126586 | |||||
| chr16:53126741
|
C | G | 1 | a0006c0009t0004g0107 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-164-29185C>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53126741 | ||||||
| chr16:53126969
|
G | A | 1 | a0001c0005t0004g0097 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-164-28957G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53126969 | ||||||
| chr16:53127037
|
C | T | 2 | a0002c0002t0001g0019a0002c0002t0001g0020 | 2 | NA18939.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.-164-28889C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53127037 | ||||||
| chr16:53127862
|
T | G | 78 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0182others(75): Show | 78 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.-164-28064T>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53127862 | ||||||
| chr16:53127922
|
G | A | 1 | a0001c0001t0002g0171 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-164-28004G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53127922 | ||||||
| chr16:53127940
|
C | CA | 43 | a0001c0001t0001g0008a0001c0001t0001g0021a0001c0001t0001g0025others(40): Show | 43 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.-164-27967dupA | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53127940 | |||||
| chr16:53127940
|
C | CAA | 67 | a0001c0001t0001g0052a0001c0001t0001g0067a0001c0001t0001g0075others(64): Show | 67 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.-164-27968_-164-27 others(8): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53127940 | |||||
| chr16:53128110
|
T | C | 1 | a0001c0001t0003g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-164-27816T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53128110 | ||||||
| chr16:53128184
|
AT | A | 68 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0182others(65): Show | 68 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.-164-27731delT | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53128184 | |||||
| chr16:53128187
|
T | C | 1 | a0002c0002t0001g0118 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-164-27739T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53128187 | ||||||
| chr16:53128286
|
G | A | 1 | a0001c0005t0001g0215 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-164-27640G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53128286 | ||||||
| chr16:53128540
|
C | T | 2 | a0001c0001t0009g0050a0005c0007t0009g0076 | 2 | HG00597.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.-164-27386C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53128540 | ||||||
| chr16:53128554
|
C | G | 1 | a0002c0002t0001g0106 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-164-27372C>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53128554 | ||||||
| chr16:53128596
|
T | A | 1 | a0001c0005t0004g0097 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-164-27330T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53128596 | ||||||
| chr16:53128732
|
C | T | 1 | a0002c0002t0001g0130 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-164-27194C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53128732 | ||||||
| chr16:53128838
|
A | G | 12 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(9): Show | 12 | HG01167.hp2 HG01884.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.-164-27088A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53128838 | ||||||
| chr16:53128990
|
T | C | 1 | a0003c0004t0001g0141 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-164-26936T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53128990 | ||||||
| chr16:53129350
|
G | C | 1 | a0001c0008t0001g0077 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-164-26576G>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53129350 | ||||||
| chr16:53129420
|
T | C | 1 | a0001c0005t0005g0061 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-164-26506T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53129420 | ||||||
| chr16:53129884
|
T | C | 54 | a0001c0005t0005g0089a0002c0002t0001g0009a0002c0002t0001g0010others(51): Show | 54 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.-164-26042T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53129884 | ||||||
| chr16:53129914
|
C | G | 1 | a0001c0005t0004g0097 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-164-26012C>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53129914 | ||||||
| chr16:53130239
|
G | A | 2 | a0001c0005t0005g0017a0001c0005t0005g0018 | 2 | HG02257.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-164-25687G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53130239 | ||||||
| chr16:53130309
|
C | T | 1 | a0002c0002t0001g0106 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-164-25617C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53130309 | ||||||
| chr16:53130366
|
G | A | 8 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(5): Show | 8 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.-164-25560G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53130366 | ||||||
| chr16:53130412
|
C | T | 2 | a0001c0003t0002g0125a0001c0003t0002g0142 | 2 | NA18982.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.-164-25514C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53130412 | ||||||
| chr16:53130486
|
C | A | 43 | a0001c0001t0001g0159a0001c0001t0002g0171a0001c0001t0002g0175others(40): Show | 43 | HG00140.hp2 HG00558.hp2 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.-164-25440C>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53130486 | ||||||
| chr16:53130546
|
G | A | 1 | a0001c0001t0001g0185 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-164-25380G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53130546 | ||||||
| chr16:53130549
|
T | G | 74 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(71): Show | 74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.-164-25377T>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53130549 | ||||||
| chr16:53130559
|
G | T | 1 | a0001c0005t0005g0089 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-164-25367G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53130559 | ||||||
| chr16:53130567
|
C | G | 1 | a0002c0002t0001g0164 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-164-25359C>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53130567 | ||||||
| chr16:53130721
|
G | C | 53 | a0001c0005t0005g0089a0002c0002t0001g0009a0002c0002t0001g0010others(50): Show | 53 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.-164-25205G>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53130721 | ||||||
| chr16:53130771
|
G | C | 8 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(5): Show | 8 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.-164-25155G>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53130771 | ||||||
| chr16:53130794
|
C | G | 19 | a0001c0001t0003g0022a0001c0001t0003g0079a0001c0001t0003g0096others(16): Show | 19 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.-164-25132C>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53130794 | ||||||
| chr16:53130824
|
G | A | 1 | a0001c0005t0004g0097 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-164-25102G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53130824 | ||||||
| chr16:53130858
|
T | C | 1 | a0001c0001t0001g0098 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-164-25068T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53130858 | ||||||
| chr16:53130981
|
G | C | 1 | a0002c0002t0001g0118 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-164-24945G>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53130981 | ||||||
| chr16:53131074
|
G | GCCGCCGC others(13): Show |
235 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0021others(232): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.-164-24850_-164-24 others(26): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53131074 | |||||
| chr16:53131074
|
G | GCCGCCGC others(33): Show |
1 | a0001c0001t0015g0166 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-164-24831_-164-24 others(46): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53131074 | |||||
| chr16:53131074
|
G | GCTGCCGC others(13): Show |
1 | a0001c0005t0004g0097 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-164-24851_-164-24 others(26): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53131074 | |||||
| chr16:53131123
|
A | G | 54 | a0001c0005t0005g0089a0002c0002t0001g0009a0002c0002t0001g0010others(51): Show | 54 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.-164-24803A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53131123 | ||||||
| chr16:53131191
|
C | T | 2 | a0001c0005t0005g0017a0001c0005t0005g0018 | 2 | HG02257.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-164-24735C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53131191 | ||||||
| chr16:53131213
|
G | A | 1 | a0003c0004t0001g0148 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-164-24713G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53131213 | ||||||
| chr16:53131221
|
C | T | 1 | a0001c0001t0001g0043 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-164-24705C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53131221 | ||||||
| chr16:53131382
|
C | T | 1 | a0003c0004t0001g0177 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-164-24544C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53131382 | ||||||
| chr16:53131383
|
C | A | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.-164-24543C>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53131383 | ||||||
| chr16:53131385
|
C | T | 1 | a0001c0001t0001g0168 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-164-24541C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53131385 | ||||||
| chr16:53131462
|
T | C | 141 | a0001c0001t0001g0159a0001c0001t0002g0171a0001c0001t0002g0175others(138): Show | 141 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.-164-24464T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53131462 | ||||||
| chr16:53131517
|
C | T | 1 | a0001c0005t0001g0215 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-164-24409C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53131517 | ||||||
| chr16:53131548
|
C | T | 1 | a0001c0001t0001g0091 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-164-24378C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53131548 | ||||||
| chr16:53131562
|
G | A | 7 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0168others(4): Show | 7 | HG01891.hp2 HG02451.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-164-24364G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53131562 | ||||||
| chr16:53131573
|
C | T | 2 | a0001c0003t0002g0083a0001c0003t0017g0181 | 2 | HG03017.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.-164-24353C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53131573 | ||||||
| chr16:53131600
|
G | T | 1 | a0001c0001t0001g0025 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-164-24326G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53131600 | ||||||
| chr16:53131721
|
C | A | 64 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(61): Show | 64 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(61): Show |
intron_variant | MODIFIER | c.-164-24205C>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53131721 | ||||||
| chr16:53131763
|
C | A | 1 | a0001c0001t0001g0124 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-164-24163C>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53131763 | ||||||
| chr16:53131783
|
G | A | 1 | a0001c0003t0002g0070 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-164-24143G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53131783 | ||||||
| chr16:53132090
|
A | T | 75 | a0001c0005t0001g0215a0001c0005t0004g0078a0001c0005t0004g0097others(72): Show | 75 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.-164-23836A>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53132090 | ||||||
| chr16:53132105
|
TG | T | 64 | a0001c0001t0020g0101a0001c0005t0004g0078a0001c0005t0004g0104others(61): Show | 64 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(61): Show |
intron_variant | MODIFIER | c.-164-23813delG | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53132105 | |||||
| chr16:53132275
|
C | T | 73 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(70): Show | 73 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.-164-23651C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53132275 | ||||||
| chr16:53132327
|
G | A | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.-164-23599G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53132327 | ||||||
| chr16:53132352
|
T | C | 64 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(61): Show | 64 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(61): Show |
intron_variant | MODIFIER | c.-164-23574T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53132352 | ||||||
| chr16:53132404
|
A | G | 3 | a0003c0004t0001g0093a0003c0004t0001g0189a0003c0004t0001g0192 | 3 | NA18955.hp2 NA18993.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.-164-23522A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53132404 | ||||||
| chr16:53132429
|
A | G | 1 | a0001c0005t0004g0097 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-164-23497A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53132429 | ||||||
| chr16:53132517
|
A | G | 1 | a0001c0001t0003g0221 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-164-23409A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53132517 | ||||||
| chr16:53132599
|
A | C | 1 | a0001c0001t0003g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-164-23327A>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53132599 | ||||||
| chr16:53132793
|
C | CT | 78 | a0001c0001t0001g0025a0001c0001t0001g0051a0001c0001t0001g0060others(75): Show | 78 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.-164-23106dupT | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53132793 | |||||
| chr16:53132793
|
C | CTT | 14 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0117others(11): Show | 14 | HG02040.hp1 HG02080.hp1 HG02135.hp2 others(11): Show |
intron_variant | MODIFIER | c.-164-23107_-164-23 others(8): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53132793 | |||||
| chr16:53132793
|
CT | C | 5 | a0001c0003t0002g0015a0001c0005t0001g0215a0001c0005t0005g0061others(2): Show | 5 | HG02895.hp2 HG03688.hp2 HG04204.hp2 others(2): Show |
intron_variant | MODIFIER | c.-164-23106delT | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53132793 | |||||
| chr16:53132793
|
CTT | C | 8 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(5): Show | 8 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.-164-23107_-164-23 others(8): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53132793 | |||||
| chr16:53132794
|
T | C | 1 | a0001c0001t0003g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-164-23132T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53132794 | ||||||
| chr16:53132822
|
G | A | 1 | a0001c0003t0002g0023 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-164-23104G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53132822 | ||||||
| chr16:53132853
|
G | A | 1 | a0001c0001t0003g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-164-23073G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53132853 | ||||||
| chr16:53132896
|
C | T | 1 | a0001c0005t0004g0097 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-164-23030C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53132896 | ||||||
| chr16:53132904
|
G | A | 3 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0182 | 3 | HG02615.hp1 HG02970.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-164-23022G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53132904 | ||||||
| chr16:53132983
|
A | G | 1 | a0003c0004t0001g0201 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-164-22943A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53132983 | ||||||
| chr16:53133494
|
G | T | 1 | a0001c0005t0004g0097 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-164-22432G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53133494 | ||||||
| chr16:53133610
|
G | C | 2 | a0001c0001t0001g0124a0001c0001t0001g0225 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-164-22316G>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53133610 | ||||||
| chr16:53133649
|
A | G | 1 | a0001c0003t0002g0005 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-164-22277A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53133649 | ||||||
| chr16:53133788
|
T | C | 1 | a0001c0001t0001g0099 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-164-22138T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53133788 | ||||||
| chr16:53133847
|
C | A | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.-164-22079C>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53133847 | ||||||
| chr16:53134039
|
A | G | 1 | a0002c0002t0001g0219 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-164-21887A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53134039 | ||||||
| chr16:53134047
|
G | A | 1 | a0001c0005t0004g0097 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-164-21879G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53134047 | ||||||
| chr16:53134146
|
A | G | 1 | a0002c0002t0001g0219 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-164-21780A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53134146 | ||||||
| chr16:53134275
|
G | A | 1 | a0001c0017t0002g0237 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-164-21651G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53134275 | ||||||
| chr16:53134402
|
A | C | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.-164-21524A>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53134402 | ||||||
| chr16:53134469
|
CCTTA | C | 19 | a0001c0001t0003g0016a0001c0001t0003g0079a0001c0001t0003g0096others(16): Show | 19 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.-164-21453_-164-21 others(10): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53134469 | |||||
| chr16:53134493
|
T | G | 2 | a0001c0001t0001g0045a0001c0001t0001g0051 | 2 | HG00558.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-164-21433T>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53134493 | ||||||
| chr16:53134619
|
G | A | 63 | a0001c0005t0004g0169a0001c0005t0005g0017a0001c0005t0005g0018others(60): Show | 63 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.-164-21307G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53134619 | ||||||
| chr16:53134955
|
C | T | 1 | a0002c0002t0001g0063 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-164-20971C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53134955 | ||||||
| chr16:53134989
|
T | C | 2 | a0001c0003t0002g0040a0001c0003t0002g0070 | 2 | HG02080.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.-164-20937T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53134989 | ||||||
| chr16:53135478
|
T | C | 5 | a0001c0001t0003g0022a0001c0001t0003g0079a0001c0001t0003g0105others(2): Show | 5 | HG02280.hp1 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-164-20448T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53135478 | ||||||
| chr16:53136157
|
A | G | 53 | a0002c0002t0001g0009a0002c0002t0001g0010a0002c0002t0001g0012others(50): Show | 53 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.-164-19769A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53136157 | ||||||
| chr16:53136167
|
A | G | 1 | a0001c0001t0015g0166 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-164-19759A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53136167 | ||||||
| chr16:53136217
|
A | G | 12 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(9): Show | 12 | HG01167.hp2 HG01884.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.-164-19709A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53136217 | ||||||
| chr16:53136311
|
C | G | 2 | a0001c0001t0002g0171a0001c0001t0002g0175 | 2 | HG02451.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.-164-19615C>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53136311 | ||||||
| chr16:53136366
|
T | C | 2 | a0001c0001t0001g0092a0001c0008t0001g0077 | 2 | HG02976.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-164-19560T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53136366 | ||||||
| chr16:53136453
|
A | G | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.-164-19473A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53136453 | ||||||
| chr16:53136556
|
T | TA | 69 | a0001c0001t0001g0159a0001c0001t0001g0211a0001c0001t0003g0220others(66): Show | 69 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(66): Show |
intron_variant | MODIFIER | c.-164-19354dupA | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53136556 | |||||
| chr16:53136557
|
A | G | 1 | a0001c0003t0002g0005 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-164-19369A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53136557 | ||||||
| chr16:53136573
|
T | A | 1 | a0001c0003t0013g0186 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-164-19353T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53136573 | ||||||
| chr16:53136626
|
C | T | 20 | a0001c0001t0003g0016a0001c0001t0003g0022a0001c0001t0003g0079others(17): Show | 20 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.-164-19300C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53136626 | ||||||
| chr16:53136821
|
C | T | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.-164-19105C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53136821 | ||||||
| chr16:53136885
|
A | T | 1 | a0001c0005t0004g0097 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-164-19041A>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53136885 | ||||||
| chr16:53136892
|
G | C | 76 | a0001c0005t0001g0215a0001c0005t0004g0078a0001c0005t0004g0097others(73): Show | 76 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.-164-19034G>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53136892 | ||||||
| chr16:53136960
|
G | A | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.-164-18966G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53136960 | ||||||
| chr16:53137212
|
C | T | 75 | a0001c0005t0001g0215a0001c0005t0004g0078a0001c0005t0004g0097others(72): Show | 75 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.-164-18714C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53137212 | ||||||
| chr16:53137260
|
C | T | 1 | a0001c0017t0002g0237 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-164-18666C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53137260 | ||||||
| chr16:53137522
|
C | T | 3 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0012g0229 | 3 | HG01167.hp2 HG01884.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-164-18404C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53137522 | ||||||
| chr16:53137549
|
G | C | 19 | a0001c0001t0003g0022a0001c0001t0003g0079a0001c0001t0003g0096others(16): Show | 19 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.-164-18377G>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53137549 | ||||||
| chr16:53137752
|
C | T | 45 | a0002c0002t0001g0009a0002c0002t0001g0010a0002c0002t0001g0012others(42): Show | 45 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(42): Show |
intron_variant | MODIFIER | c.-164-18174C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53137752 | ||||||
| chr16:53138241
|
A | G | 53 | a0002c0002t0001g0009a0002c0002t0001g0010a0002c0002t0001g0012others(50): Show | 53 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.-164-17685A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53138241 | ||||||
| chr16:53138327
|
T | C | 2 | a0001c0001t0001g0038a0001c0001t0001g0098 | 2 | HG00609.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.-164-17599T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53138327 | ||||||
| chr16:53138473
|
A | T | 1 | a0003c0004t0001g0100 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-164-17453A>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53138473 | ||||||
| chr16:53138608
|
T | C | 1 | a0001c0005t0004g0078 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-164-17318T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53138608 | ||||||
| chr16:53138731
|
G | T | 64 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(61): Show | 64 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(61): Show |
intron_variant | MODIFIER | c.-164-17195G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53138731 | ||||||
| chr16:53138778
|
G | A | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.-164-17148G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53138778 | ||||||
| chr16:53139009
|
C | T | 1 | a0001c0005t0005g0061 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-164-16917C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53139009 | ||||||
| chr16:53139121
|
GAT | G | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.-164-16803_-164-16 others(8): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53139121 | |||||
| chr16:53139242
|
G | A | 65 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.-164-16684G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53139242 | ||||||
| chr16:53139321
|
A | G | 53 | a0002c0002t0001g0009a0002c0002t0001g0010a0002c0002t0001g0012others(50): Show | 53 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.-164-16605A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53139321 | ||||||
| chr16:53139336
|
G | A | 1 | a0001c0003t0002g0003 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-164-16590G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53139336 | ||||||
| chr16:53139540
|
T | C | 2 | a0002c0002t0001g0087a0002c0002t0001g0088 | 2 | HG01255.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.-164-16386T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53139540 | ||||||
| chr16:53139677
|
A | C | 1 | a0001c0005t0004g0097 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-164-16249A>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53139677 | ||||||
| chr16:53139691
|
T | A | 1 | a0002c0002t0001g0082 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.-164-16235T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53139691 | ||||||
| chr16:53139734
|
A | G | 1 | a0001c0017t0002g0237 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-164-16192A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53139734 | ||||||
| chr16:53139880
|
A | T | 139 | a0001c0001t0002g0171a0001c0001t0002g0175a0001c0001t0003g0016others(136): Show | 139 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.-164-16046A>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53139880 | ||||||
| chr16:53139982
|
C | G | 1 | a0001c0005t0004g0097 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-164-15944C>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53139982 | ||||||
| chr16:53140359
|
A | G | 53 | a0002c0002t0001g0009a0002c0002t0001g0010a0002c0002t0001g0012others(50): Show | 53 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.-164-15567A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53140359 | ||||||
| chr16:53140416
|
C | CAA | 22 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(19): Show | 22 | HG00323.hp1 HG01167.hp2 HG01515.hp1 others(19): Show |
intron_variant | MODIFIER | c.-164-15494_-164-15 others(8): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53140416 | |||||
| chr16:53140416
|
C | CAAA | 51 | a0001c0005t0005g0018a0002c0002t0001g0009a0002c0002t0001g0010others(48): Show | 51 | HG00099.hp2 HG00408.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.-164-15495_-164-15 others(9): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53140416 | |||||
| chr16:53140416
|
CA | C | 23 | a0001c0001t0001g0021a0001c0001t0003g0022a0001c0001t0003g0079others(20): Show | 23 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.-164-15493delA | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53140416 | |||||
| chr16:53140460
|
G | T | 1 | a0003c0004t0001g0148 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-164-15466G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53140460 | ||||||
| chr16:53140954
|
C | G | 73 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(70): Show | 73 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.-164-14972C>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53140954 | ||||||
| chr16:53141024
|
T | C | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.-164-14902T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53141024 | ||||||
| chr16:53141227
|
A | G | 1 | a0001c0005t0005g0089 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-164-14699A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53141227 | ||||||
| chr16:53141338
|
A | G | 1 | a0001c0001t0003g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-164-14588A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53141338 | ||||||
| chr16:53141635
|
T | C | 1 | a0001c0008t0001g0077 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-164-14291T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53141635 | ||||||
| chr16:53141923
|
A | T | 1 | a0001c0001t0001g0091 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-164-14003A>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53141923 | ||||||
| chr16:53141944
|
A | G | 1 | a0008c0011t0003g0062 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-164-13982A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53141944 | ||||||
| chr16:53142018
|
A | G | 1 | a0001c0003t0002g0073 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-164-13908A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53142018 | ||||||
| chr16:53142146
|
A | G | 3 | a0003c0004t0001g0134a0003c0004t0001g0141a0003c0004t0001g0143 | 3 | HG02559.hp2 HG02895.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-164-13780A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53142146 | ||||||
| chr16:53142403
|
G | A | 1 | a0001c0005t0005g0135 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-164-13523G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53142403 | ||||||
| chr16:53142519
|
C | T | 1 | a0008c0011t0003g0062 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-164-13407C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53142519 | ||||||
| chr16:53142535
|
G | A | 1 | a0003c0004t0001g0196 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-164-13391G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53142535 | ||||||
| chr16:53142583
|
A | C | 1 | a0001c0003t0002g0003 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-164-13343A>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53142583 | ||||||
| chr16:53142748
|
TAATTTAT others(6): Show |
T | 1 | a0001c0001t0001g0052 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.-164-13176_-164-13 others(19): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53142748 | |||||
| chr16:53143295
|
C | T | 12 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(9): Show | 12 | HG01167.hp2 HG01884.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.-164-12631C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53143295 | ||||||
| chr16:53143358
|
T | TTTTA | 53 | a0001c0001t0001g0008a0001c0001t0001g0043a0001c0001t0001g0045others(50): Show | 53 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.-164-12526_-164-12 others(10): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53143358 | |||||
| chr16:53143358
|
T | TTTTATTT others(1): Show |
58 | a0001c0001t0001g0014a0001c0001t0001g0021a0001c0001t0001g0025others(55): Show | 58 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.-164-12530_-164-12 others(14): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53143358 | |||||
| chr16:53143358
|
T | TTTTATTT others(5): Show |
6 | a0001c0001t0001g0173a0001c0001t0001g0178a0001c0001t0003g0227others(3): Show | 6 | HG02630.hp1 HG02630.hp2 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.-164-12534_-164-12 others(18): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53143358 | |||||
| chr16:53143358
|
TTTTA | T | 12 | a0001c0001t0001g0091a0001c0003t0002g0059a0001c0003t0002g0224others(9): Show | 12 | HG02257.hp2 HG02717.hp2 HG02965.hp2 others(9): Show |
intron_variant | MODIFIER | c.-164-12526_-164-12 others(10): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53143358 | |||||
| chr16:53143358
|
TTTTATTT others(1): Show |
T | 13 | a0001c0005t0001g0215a0001c0005t0004g0078a0001c0005t0004g0097others(10): Show | 13 | HG01167.hp2 HG01884.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.-164-12530_-164-12 others(14): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53143358 | |||||
| chr16:53143358
|
TTTTATTT others(5): Show |
T | 56 | a0001c0005t0011g0228a0002c0002t0001g0009a0002c0002t0001g0010others(53): Show | 56 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(53): Show |
intron_variant | MODIFIER | c.-164-12534_-164-12 others(18): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53143358 | |||||
| chr16:53143358
|
TTTTATTT others(9): Show |
T | 1 | a0001c0005t0004g0232 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-164-12538_-164-12 others(22): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53143358 | |||||
| chr16:53143358
|
TTTTATTT others(13): Show |
T | 2 | a0001c0001t0002g0171a0001c0001t0002g0175 | 2 | HG02451.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.-164-12542_-164-12 others(26): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53143358 | |||||
| chr16:53143376
|
T | A | 1 | a0001c0005t0004g0097 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-164-12550T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53143376 | ||||||
| chr16:53143387
|
T | TTTATTTA others(9): Show |
1 | a0006c0009t0004g0107 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-164-12524_-164-12 others(22): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53143387 | |||||
| chr16:53143629
|
C | T | 1 | a0001c0001t0003g0139 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-164-12297C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53143629 | ||||||
| chr16:53143641
|
C | T | 2 | a0001c0003t0002g0023a0001c0003t0002g0080 | 2 | NA18974.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.-164-12285C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53143641 | ||||||
| chr16:53144338
|
G | A | 73 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(70): Show | 73 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.-164-11588G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53144338 | ||||||
| chr16:53144339
|
G | A | 1 | a0001c0013t0001g0055 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-164-11587G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53144339 | ||||||
| chr16:53144445
|
C | T | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.-164-11481C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53144445 | ||||||
| chr16:53144645
|
C | T | 1 | a0001c0003t0002g0033 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-164-11281C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53144645 | ||||||
| chr16:53144653
|
C | T | 1 | a0001c0005t0004g0097 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-164-11273C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53144653 | ||||||
| chr16:53144655
|
A | T | 2 | a0001c0001t0001g0026a0001c0001t0001g0081 | 2 | NA18963.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.-164-11271A>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53144655 | ||||||
| chr16:53144756
|
C | A | 1 | a0001c0001t0001g0052 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.-164-11170C>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53144756 | ||||||
| chr16:53144759
|
C | T | 1 | a0001c0001t0001g0230 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-164-11167C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53144759 | ||||||
| chr16:53144808
|
G | A | 1 | a0001c0001t0003g0112 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-164-11118G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53144808 | ||||||
| chr16:53144831
|
T | A | 1 | a0001c0001t0001g0052 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.-164-11095T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53144831 | ||||||
| chr16:53144832
|
A | T | 1 | a0001c0001t0001g0052 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.-164-11094A>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53144832 | ||||||
| chr16:53144853
|
A | T | 1 | a0001c0001t0001g0052 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.-164-11073A>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53144853 | ||||||
| chr16:53144866
|
C | A | 1 | a0001c0001t0003g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-164-11060C>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53144866 | ||||||
| chr16:53144923
|
T | C | 2 | a0001c0001t0002g0171a0001c0001t0002g0175 | 2 | HG02451.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.-164-11003T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53144923 | ||||||
| chr16:53144994
|
C | CA | 63 | a0001c0001t0001g0159a0001c0001t0002g0175a0001c0001t0003g0016others(60): Show | 63 | HG00140.hp2 HG00558.hp2 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.-164-10915dupA | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53144994 | |||||
| chr16:53144994
|
C | CAA | 10 | a0001c0001t0003g0221a0001c0005t0004g0097a0001c0005t0005g0017others(7): Show | 10 | HG01884.hp1 HG02257.hp2 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.-164-10916_-164-10 others(8): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53144994 | |||||
| chr16:53144994
|
CA | C | 63 | a0001c0001t0001g0060a0001c0001t0001g0160a0001c0005t0004g0078others(60): Show | 63 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.-164-10915delA | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53144994 | |||||
| chr16:53145074
|
G | T | 142 | a0001c0001t0001g0159a0001c0001t0002g0171a0001c0001t0002g0175others(139): Show | 142 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.-164-10852G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53145074 | ||||||
| chr16:53145393
|
T | C | 1 | a0001c0001t0001g0085 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-164-10533T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53145393 | ||||||
| chr16:53145580
|
C | A | 64 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(61): Show | 64 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(61): Show |
intron_variant | MODIFIER | c.-164-10346C>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53145580 | ||||||
| chr16:53145599
|
A | G | 1 | a0001c0005t0001g0215 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-164-10327A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53145599 | ||||||
| chr16:53145655
|
G | A | 11 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(8): Show | 11 | HG01167.hp2 HG01884.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-164-10271G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53145655 | ||||||
| chr16:53145837
|
C | A | 1 | a0001c0001t0001g0052 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.-164-10089C>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53145837 | ||||||
| chr16:53145843
|
T | C | 1 | a0006c0009t0004g0107 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-164-10083T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53145843 | ||||||
| chr16:53145846
|
G | A | 2 | a0002c0002t0001g0048a0002c0002t0001g0049 | 2 | HG01099.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.-164-10080G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53145846 | ||||||
| chr16:53145865
|
T | C | 1 | a0001c0013t0001g0055 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-164-10061T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53145865 | ||||||
| chr16:53145870
|
G | T | 7 | a0001c0005t0004g0231a0001c0005t0004g0232a0001c0005t0004g0233others(4): Show | 7 | HG02615.hp2 HG02897.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.-164-10056G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53145870 | ||||||
| chr16:53145961
|
G | A | 1 | a0001c0005t0004g0097 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-164-9965G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53145961 | ||||||
| chr16:53146215
|
G | T | 1 | a0001c0001t0001g0052 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.-164-9711G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53146215 | ||||||
| chr16:53146223
|
T | TAA | 61 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(58): Show | 61 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.-164-9684_-164-968 others(6): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53146223 | |||||
| chr16:53146250
|
G | A | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.-164-9676G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53146250 | ||||||
| chr16:53146263
|
G | A | 1 | a0002c0002t0001g0082 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.-164-9663G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53146263 | ||||||
| chr16:53146265
|
C | T | 1 | a0001c0001t0002g0175 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-164-9661C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53146265 | ||||||
| chr16:53146286
|
G | A | 76 | a0001c0005t0001g0215a0001c0005t0004g0078a0001c0005t0004g0097others(73): Show | 76 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.-164-9640G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53146286 | ||||||
| chr16:53146413
|
G | GTATATAT others(5): Show |
2 | a0001c0005t0005g0017a0001c0005t0005g0018 | 2 | HG02257.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-164-9512_-164-951 others(16): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53146413 | |||||
| chr16:53146413
|
G | GTATATAT others(13): Show |
1 | a0001c0005t0005g0061 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-164-9512_-164-951 others(24): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53146413 | |||||
| chr16:53146413
|
G | GTATATAT others(15): Show |
1 | a0001c0005t0011g0228 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-164-9512_-164-951 others(26): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53146413 | |||||
| chr16:53146413
|
G | GTATATAT others(21): Show |
3 | a0001c0005t0005g0135a0001c0005t0005g0151a0009c0018t0005g0155 | 3 | NA18981.hp2 NA19068.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.-164-9512_-164-951 others(32): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53146413 | |||||
| chr16:53146413
|
G | GTATATAT others(25): Show |
1 | a0001c0005t0005g0032 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-164-9512_-164-951 others(36): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53146413 | |||||
| chr16:53146413
|
G | GTATATAT others(27): Show |
1 | a0001c0005t0005g0089 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-164-9512_-164-951 others(38): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53146413 | |||||
| chr16:53146415
|
G | A | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.-164-9511G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53146415 | ||||||
| chr16:53146415
|
G | GTGTA | 10 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0231others(7): Show | 10 | HG01167.hp2 HG01884.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.-164-9510_-164-950 others(8): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53146415 | |||||
| chr16:53146415
|
G | GTGTATA | 2 | a0001c0005t0004g0169a0001c0005t0018g0001 | 2 | HG03139.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-164-9510_-164-950 others(10): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53146415 | |||||
| chr16:53146415
|
G | GTGTATAT others(1): Show |
48 | a0002c0002t0001g0009a0002c0002t0001g0010a0002c0002t0001g0012others(45): Show | 48 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(45): Show |
intron_variant | MODIFIER | c.-164-9510_-164-950 others(12): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53146415 | |||||
| chr16:53146415
|
G | GTGTATAT others(3): Show |
4 | a0002c0002t0001g0087a0002c0002t0001g0088a0002c0002t0001g0120others(1): Show | 4 | HG01255.hp2 HG01433.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-164-9510_-164-950 others(14): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53146415 | |||||
| chr16:53146415
|
G | GTGTGTAT others(49): Show |
1 | a0001c0005t0004g0097 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-164-9510_-164-950 others(60): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53146415 | |||||
| chr16:53146419
|
G | A | 75 | a0001c0005t0004g0078a0001c0005t0004g0097a0001c0005t0004g0104others(72): Show | 75 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.-164-9507G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53146419 | ||||||
| chr16:53146419
|
G | GTATATA | 7 | a0001c0001t0001g0026a0001c0001t0001g0038a0001c0001t0001g0081others(4): Show | 7 | HG00099.hp1 HG00609.hp2 HG02129.hp2 others(4): Show |
intron_variant | MODIFIER | c.-164-9494_-164-948 others(10): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53146419 | |||||
| chr16:53146419
|
G | GTATATAT others(11): Show |
1 | a0001c0001t0001g0188 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.-164-9506_-164-948 others(22): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53146419 | |||||
| chr16:53146419
|
G | GTATATAT others(15): Show |
2 | a0001c0001t0001g0091a0001c0001t0007g0103 | 2 | HG02886.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-164-9489_-164-948 others(26): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53146419 | |||||
| chr16:53146419
|
G | GTATATAT others(17): Show |
2 | a0001c0001t0001g0045a0001c0001t0007g0122 | 2 | HG02280.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-164-9489_-164-948 others(28): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53146419 | |||||
| chr16:53146419
|
G | GTATATAT others(19): Show |
4 | a0001c0001t0001g0043a0001c0001t0001g0119a0003c0004t0001g0143others(1): Show | 4 | HG02559.hp2 HG02683.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-164-9489_-164-948 others(30): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53146419 | |||||
| chr16:53146419
|
G | GTATATAT others(21): Show |
11 | a0001c0001t0001g0056a0001c0001t0001g0071a0001c0001t0001g0072others(8): Show | 11 | HG00140.hp1 HG00323.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.-164-9489_-164-948 others(32): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53146419 | |||||
| chr16:53146419
|
G | GTATATAT others(23): Show |
4 | a0001c0001t0001g0068a0001c0001t0001g0178a0001c0012t0001g0132others(1): Show | 4 | HG02602.hp2 HG02630.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.-164-9489_-164-948 others(34): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53146419 | |||||
| chr16:53146419
|
G | GTATATAT others(24): Show |
1 | a0001c0001t0001g0052 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.-164-9489_-164-948 others(35): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53146419 | |||||
| chr16:53146419
|
G | GTATATAT others(25): Show |
4 | a0001c0001t0001g0008a0001c0001t0001g0051a0001c0008t0001g0077others(1): Show | 4 | HG00558.hp1 HG02976.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-164-9489_-164-948 others(36): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53146419 | |||||
| chr16:53146419
|
G | GTATATAT others(29): Show |
3 | a0001c0001t0001g0025a0001c0001t0009g0050a0001c0013t0001g0055 | 3 | HG00733.hp1 HG02300.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.-164-9489_-164-948 others(40): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53146419 | |||||
| chr16:53146419
|
G | GTATATAT others(31): Show |
1 | a0001c0001t0001g0092 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-164-9489_-164-948 others(42): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53146419 | |||||
| chr16:53146419
|
G | GTATGTAT others(11): Show |
1 | a0008c0011t0003g0062 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-164-9504_-164-950 others(22): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53146419 | |||||
| chr16:53146419
|
G | GTATGTAT others(17): Show |
2 | a0001c0001t0001g0064a0001c0001t0001g0085 | 2 | HG00621.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.-164-9504_-164-950 others(28): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53146419 | |||||
| chr16:53146419
|
G | GTATGTAT others(19): Show |
3 | a0001c0001t0001g0179a0001c0003t0002g0002a0001c0003t0002g0015 | 3 | HG01257.hp2 NA18970.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.-164-9504_-164-950 others(30): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53146419 | |||||
| chr16:53146419
|
G | GTATGTAT others(21): Show |
15 | a0001c0001t0001g0031a0001c0001t0001g0058a0001c0001t0001g0066others(12): Show | 15 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(12): Show |
intron_variant | MODIFIER | c.-164-9504_-164-950 others(32): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53146419 | |||||
| chr16:53146419
|
G | GTATGTAT others(23): Show |
17 | a0001c0001t0001g0075a0001c0001t0001g0099a0001c0001t0003g0016others(14): Show | 17 | HG01243.hp1 HG02015.hp1 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.-164-9504_-164-950 others(34): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53146419 | |||||
| chr16:53146419
|
G | GTATGTAT others(25): Show |
12 | a0001c0001t0001g0021a0001c0001t0001g0211a0001c0003t0001g0158others(9): Show | 12 | HG00735.hp1 HG01109.hp1 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.-164-9504_-164-950 others(36): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53146419 | |||||
| chr16:53146419
|
G | GTATGTAT others(27): Show |
2 | a0001c0001t0001g0069a0001c0001t0003g0176 | 2 | HG02486.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.-164-9504_-164-950 others(38): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53146419 | |||||
| chr16:53146419
|
G | GTATGTAT others(29): Show |
3 | a0001c0001t0002g0171a0001c0003t0002g0202a0001c0003t0010g0013 | 3 | HG01074.hp1 HG02451.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.-164-9504_-164-950 others(40): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53146419 | |||||
| chr16:53146419
|
G | GTATGTAT others(31): Show |
4 | a0001c0001t0001g0110a0001c0003t0002g0029a0001c0003t0010g0006others(1): Show | 4 | HG01099.hp1 HG02970.hp2 NA18955.hp1 others(1): Show |
intron_variant | MODIFIER | c.-164-9504_-164-950 others(42): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53146419 | |||||
| chr16:53146419
|
G | GTATGTAT others(33): Show |
3 | a0001c0003t0002g0028a0001c0003t0002g0036a0001c0017t0002g0237 | 3 | HG02055.hp2 HG02129.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.-164-9504_-164-950 others(44): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53146419 | |||||
| chr16:53146419
|
G | GTATGTAT others(35): Show |
3 | a0001c0001t0003g0167a0001c0003t0002g0170a0006c0009t0004g0107 | 3 | HG02559.hp1 HG03516.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-164-9504_-164-950 others(46): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53146419 | |||||
| chr16:53146419
|
G | GTATGTAT others(37): Show |
1 | a0001c0001t0001g0225 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-164-9504_-164-950 others(48): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53146419 | |||||
| chr16:53146419
|
G | GTATGTAT others(45): Show |
1 | a0001c0001t0001g0111 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-164-9504_-164-950 others(56): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53146419 | |||||
| chr16:53146419
|
G | GTATGTAT others(29): Show |
1 | a0001c0001t0002g0175 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-164-9504_-164-950 others(40): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53146419 | |||||
| chr16:53146419
|
G | GTATGTGT others(19): Show |
1 | a0001c0001t0001g0027 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-164-9504_-164-950 others(30): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53146419 | |||||
| chr16:53146419
|
G | GTATGTGT others(37): Show |
1 | a0001c0001t0001g0182 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-164-9504_-164-950 others(48): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53146419 | |||||
| chr16:53146419
|
G | GTGTATAT others(11): Show |
1 | a0001c0001t0001g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-164-9506_-164-950 others(22): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53146419 | |||||
| chr16:53146419
|
G | GTGTATAT others(21): Show |
3 | a0001c0001t0001g0117a0001c0001t0003g0112a0001c0001t0020g0101 | 3 | HG02630.hp1 HG03098.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-164-9506_-164-950 others(32): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53146419 | |||||
| chr16:53146419
|
G | GTGTATAT others(27): Show |
3 | a0001c0001t0001g0124a0001c0001t0001g0174a0003c0004t0001g0177 | 3 | HG01891.hp2 HG03130.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-164-9506_-164-950 others(38): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53146419 | |||||
| chr16:53146419
|
G | GTGTATAT others(29): Show |
1 | a0001c0001t0003g0220 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-164-9506_-164-950 others(40): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53146419 | |||||
| chr16:53146419
|
G | GTGTATAT others(31): Show |
3 | a0001c0001t0003g0096a0001c0001t0003g0222a0005c0007t0009g0076 | 3 | HG00597.hp1 HG03579.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-164-9506_-164-950 others(42): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53146419 | |||||
| chr16:53146419
|
G | GTGTATAT others(33): Show |
2 | a0001c0001t0003g0221a0001c0001t0003g0223 | 2 | HG03540.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-164-9506_-164-950 others(44): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53146419 | |||||
| chr16:53146419
|
G | GTGTATAT others(35): Show |
2 | a0001c0001t0003g0226a0001c0001t0003g0227 | 2 | HG03041.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-164-9506_-164-950 others(46): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53146419 | |||||
| chr16:53146419
|
G | GTGTATAT others(37): Show |
1 | a0001c0001t0003g0184 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-164-9506_-164-950 others(48): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53146419 | |||||
| chr16:53146419
|
G | GTGTATAT others(41): Show |
1 | a0001c0001t0003g0133 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-164-9506_-164-950 others(52): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53146419 | |||||
| chr16:53146419
|
G | GTGTGTGT others(13): Show |
1 | a0001c0005t0001g0215 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-164-9506_-164-950 others(24): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53146419 | |||||
| chr16:53146436
|
T | A | 5 | a0001c0001t0003g0022a0001c0001t0003g0079a0001c0001t0003g0105others(2): Show | 5 | HG02280.hp1 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-164-9490T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53146436 | ||||||
| chr16:53146436
|
T | TATATATA others(19): Show |
2 | a0001c0001t0003g0172a0001c0001t0003g0183 | 2 | HG02257.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-164-9489_-164-948 others(30): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53146436 | |||||
| chr16:53146436
|
T | TATATATA others(21): Show |
1 | a0001c0001t0003g0131 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-164-9489_-164-948 others(32): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53146436 | |||||
| chr16:53146436
|
T | TATATATA others(25): Show |
1 | a0001c0001t0003g0139 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-164-9489_-164-948 others(36): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53146436 | |||||
| chr16:53146437
|
A | ATATATAT others(24): Show |
1 | a0001c0001t0001g0060 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-164-9489_-164-948 others(35): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53146437 | ||||||
| chr16:53146438
|
A | T | 7 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0168others(4): Show | 7 | HG01891.hp2 HG02451.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-164-9488A>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53146438 | ||||||
| chr16:53146563
|
C | T | 74 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(71): Show | 74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.-164-9363C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53146563 | ||||||
| chr16:53146656
|
A | G | 45 | a0001c0001t0002g0171a0001c0001t0002g0175a0001c0001t0015g0166others(42): Show | 45 | HG00140.hp2 HG00558.hp2 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.-164-9270A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53146656 | ||||||
| chr16:53146673
|
C | G | 1 | a0001c0001t0001g0052 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.-164-9253C>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53146673 | ||||||
| chr16:53146754
|
G | A | 19 | a0001c0001t0003g0022a0001c0001t0003g0079a0001c0001t0003g0096others(16): Show | 19 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.-164-9172G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53146754 | ||||||
| chr16:53146796
|
CA | C | 74 | a0001c0001t0001g0021a0001c0005t0004g0078a0001c0005t0004g0104others(71): Show | 74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.-164-9115delA | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53146796 | |||||
| chr16:53146837
|
G | A | 1 | a0003c0004t0001g0007 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-164-9089G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53146837 | ||||||
| chr16:53147107
|
A | G | 1 | a0001c0005t0004g0097 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-164-8819A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53147107 | ||||||
| chr16:53147114
|
A | C | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.-164-8812A>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53147114 | ||||||
| chr16:53147168
|
G | C | 1 | a0006c0009t0004g0107 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-164-8758G>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53147168 | ||||||
| chr16:53147335
|
C | T | 65 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.-164-8591C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53147335 | ||||||
| chr16:53147421
|
C | A | 1 | a0001c0003t0002g0142 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-164-8505C>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53147421 | ||||||
| chr16:53147579
|
A | G | 1 | a0001c0001t0003g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-164-8347A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53147579 | ||||||
| chr16:53147719
|
A | G | 2 | a0001c0001t0001g0092a0001c0008t0001g0077 | 2 | HG02976.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-164-8207A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53147719 | ||||||
| chr16:53147877
|
A | G | 1 | a0001c0001t0001g0168 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-164-8049A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53147877 | ||||||
| chr16:53147966
|
G | A | 1 | a0002c0002t0001g0102 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-164-7960G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53147966 | ||||||
| chr16:53148062
|
C | T | 2 | a0001c0001t0001g0045a0001c0001t0001g0051 | 2 | HG00558.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-164-7864C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53148062 | ||||||
| chr16:53148110
|
G | A | 1 | a0003c0004t0001g0197 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-164-7816G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53148110 | ||||||
| chr16:53148132
|
A | G | 74 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(71): Show | 74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.-164-7794A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53148132 | ||||||
| chr16:53148292
|
G | A | 1 | a0001c0001t0003g0112 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-164-7634G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53148292 | ||||||
| chr16:53148731
|
G | T | 1 | a0001c0017t0002g0237 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-164-7195G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53148731 | ||||||
| chr16:53148733
|
A | G | 1 | a0001c0005t0004g0097 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-164-7193A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53148733 | ||||||
| chr16:53148822
|
T | C | 1 | a0001c0005t0004g0097 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-164-7104T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53148822 | ||||||
| chr16:53148920
|
G | A | 3 | a0003c0004t0001g0203a0003c0004t0001g0204a0003c0004t0001g0216 | 3 | HG01168.hp1 HG01169.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.-164-7006G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53148920 | ||||||
| chr16:53149187
|
C | G | 2 | a0001c0005t0004g0233a0001c0005t0004g0234 | 2 | HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-164-6739C>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53149187 | ||||||
| chr16:53149212
|
G | A | 1 | a0006c0009t0004g0107 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-164-6714G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53149212 | ||||||
| chr16:53149287
|
G | T | 1 | a0001c0001t0001g0056 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-164-6639G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53149287 | ||||||
| chr16:53149307
|
T | C | 7 | a0001c0005t0004g0231a0001c0005t0004g0232a0001c0005t0004g0233others(4): Show | 7 | HG02615.hp2 HG02897.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.-164-6619T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53149307 | ||||||
| chr16:53149334
|
A | G | 6 | a0002c0002t0001g0106a0002c0002t0001g0109a0002c0002t0001g0113others(3): Show | 6 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-164-6592A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53149334 | ||||||
| chr16:53149362
|
C | T | 1 | a0001c0005t0004g0097 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-164-6564C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53149362 | ||||||
| chr16:53149488
|
A | C | 1 | a0002c0002t0001g0102 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-164-6438A>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53149488 | ||||||
| chr16:53149576
|
A | AT | 22 | a0001c0005t0001g0215a0001c0005t0004g0078a0001c0005t0004g0104others(19): Show | 22 | HG01167.hp2 HG01884.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.-164-6336dupT | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53149576 | |||||
| chr16:53149576
|
AT | A | 46 | a0001c0001t0002g0171a0001c0001t0002g0175a0001c0001t0003g0226others(43): Show | 46 | HG00140.hp2 HG00558.hp2 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.-164-6336delT | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53149576 | |||||
| chr16:53149653
|
A | G | 2 | a0001c0005t0004g0169a0001c0005t0018g0001 | 2 | HG03139.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-164-6273A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53149653 | ||||||
| chr16:53149693
|
T | A | 65 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.-164-6233T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53149693 | ||||||
| chr16:53149721
|
A | AAT | 3 | a0001c0001t0001g0091a0001c0001t0001g0124a0001c0001t0001g0225 | 3 | HG03098.hp2 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-164-6190_-164-618 others(6): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53149721 | |||||
| chr16:53149742
|
T | TAGAAATG others(310): Show |
40 | a0001c0001t0001g0159a0001c0001t0015g0166a0001c0003t0002g0002others(37): Show | 40 | HG00140.hp2 HG00558.hp2 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.-164-6168_-164-616 others(321): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53149742 | |||||
| chr16:53149742
|
T | TAGAAATG others(311): Show |
2 | a0001c0003t0001g0158a0001c0003t0002g0033 | 2 | HG01109.hp1 HG02027.hp2 |
intron_variant | MODIFIER | c.-164-6168_-164-616 others(322): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53149742 | |||||
| chr16:53149742
|
T | TAGAAATG others(315): Show |
1 | a0006c0009t0004g0107 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-164-6168_-164-616 others(326): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53149742 | |||||
| chr16:53149742
|
T | TAGAAATG others(319): Show |
1 | a0001c0001t0002g0171 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-164-6168_-164-616 others(330): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53149742 | |||||
| chr16:53149742
|
T | TAGAAATG others(320): Show |
1 | a0008c0011t0003g0062 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-164-6168_-164-616 others(331): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53149742 | |||||
| chr16:53149742
|
T | TAGAAATG others(351): Show |
1 | a0001c0001t0002g0175 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-164-6168_-164-616 others(362): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53149742 | |||||
| chr16:53149760
|
G | A | 1 | a0001c0001t0002g0171 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-164-6166G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53149760 | ||||||
| chr16:53149835
|
T | C | 76 | a0001c0005t0001g0215a0001c0005t0004g0078a0001c0005t0004g0097others(73): Show | 76 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.-164-6091T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53149835 | ||||||
| chr16:53149924
|
G | A | 65 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.-164-6002G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53149924 | ||||||
| chr16:53149939
|
G | A | 4 | a0003c0004t0001g0134a0003c0004t0001g0141a0003c0004t0001g0143others(1): Show | 4 | HG02559.hp2 HG02895.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-164-5987G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53149939 | ||||||
| chr16:53149968
|
A | T | 53 | a0002c0002t0001g0009a0002c0002t0001g0010a0002c0002t0001g0012others(50): Show | 53 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.-164-5958A>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53149968 | ||||||
| chr16:53149984
|
G | A | 3 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0182 | 3 | HG02615.hp1 HG02970.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-164-5942G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53149984 | ||||||
| chr16:53150035
|
A | G | 74 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(71): Show | 74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.-164-5891A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53150035 | ||||||
| chr16:53150215
|
A | AT | 66 | a0001c0001t0003g0172a0001c0001t0003g0183a0001c0003t0002g0023others(63): Show | 66 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(63): Show |
intron_variant | MODIFIER | c.-164-5698dupT | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53150215 | |||||
| chr16:53150215
|
A | ATT | 5 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(2): Show | 5 | HG01167.hp2 HG01884.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-164-5699_-164-569 others(6): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53150215 | |||||
| chr16:53150432
|
T | A | 2 | a0001c0003t0002g0083a0001c0003t0017g0181 | 2 | HG03017.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.-164-5494T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53150432 | ||||||
| chr16:53150473
|
C | T | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.-164-5453C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53150473 | ||||||
| chr16:53150569
|
A | G | 1 | a0003c0004t0001g0134 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-164-5357A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53150569 | ||||||
| chr16:53150833
|
A | G | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.-164-5093A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53150833 | ||||||
| chr16:53150861
|
T | G | 2 | a0003c0004t0001g0187a0003c0004t0001g0194 | 2 | HG02165.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.-164-5065T>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53150861 | ||||||
| chr16:53150880
|
T | G | 1 | a0001c0001t0001g0091 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-164-5046T>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53150880 | ||||||
| chr16:53150927
|
A | G | 44 | a0001c0001t0002g0171a0001c0001t0002g0175a0001c0001t0015g0166others(41): Show | 44 | HG00140.hp2 HG00558.hp2 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.-164-4999A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53150927 | ||||||
| chr16:53150965
|
C | T | 1 | a0003c0004t0001g0143 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-164-4961C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53150965 | ||||||
| chr16:53150966
|
G | A | 1 | a0002c0002t0001g0042 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-164-4960G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53150966 | ||||||
| chr16:53151061
|
C | G | 1 | a0001c0005t0001g0215 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-164-4865C>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53151061 | ||||||
| chr16:53151130
|
T | A | 1 | a0001c0001t0001g0052 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.-164-4796T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53151130 | ||||||
| chr16:53151131
|
T | G | 1 | a0003c0004t0001g0194 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-164-4795T>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53151131 | ||||||
| chr16:53151193
|
TCCCTC | T | 11 | a0001c0001t0003g0022a0001c0001t0003g0096a0001c0001t0003g0105others(8): Show | 11 | HG01891.hp1 HG02257.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.-164-4714_-164-471 others(9): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53151193 | |||||
| chr16:53151208
|
CCCCT | C | 8 | a0001c0001t0003g0079a0001c0001t0003g0112a0001c0001t0003g0133others(5): Show | 8 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-164-4714_-164-471 others(8): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53151208 | |||||
| chr16:53151212
|
T | C | 2 | a0003c0004t0001g0100a0003c0004t0001g0213 | 2 | HG01515.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.-164-4714T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53151212 | ||||||
| chr16:53151212
|
T | TC | 106 | a0001c0001t0001g0008a0001c0001t0001g0021a0001c0001t0001g0025others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(103): Show |
intron_variant | MODIFIER | c.-164-4707dupC | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53151212 | |||||
| chr16:53151244
|
C | A | 9 | a0001c0001t0003g0022a0001c0001t0003g0079a0001c0001t0003g0105others(6): Show | 9 | HG01891.hp1 HG02257.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.-164-4682C>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53151244 | ||||||
| chr16:53151345
|
G | A | 1 | a0001c0003t0002g0070 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-164-4581G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53151345 | ||||||
| chr16:53151351
|
A | G | 53 | a0002c0002t0001g0009a0002c0002t0001g0010a0002c0002t0001g0012others(50): Show | 53 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.-164-4575A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53151351 | ||||||
| chr16:53151399
|
G | A | 1 | a0002c0002t0001g0063 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-164-4527G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53151399 | ||||||
| chr16:53151420
|
G | C | 2 | a0001c0001t0001g0021a0001c0001t0001g0058 | 2 | NA18939.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.-164-4506G>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53151420 | ||||||
| chr16:53151521
|
G | A | 1 | a0001c0001t0015g0166 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-164-4405G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53151521 | ||||||
| chr16:53151578
|
A | T | 1 | a0001c0001t0001g0052 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.-164-4348A>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53151578 | ||||||
| chr16:53151659
|
C | T | 2 | a0001c0003t0002g0040a0001c0003t0002g0070 | 2 | HG02080.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.-164-4267C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53151659 | ||||||
| chr16:53151896
|
C | G | 1 | a0009c0018t0005g0155 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.-164-4030C>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53151896 | ||||||
| chr16:53151968
|
ATG | A | 72 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(69): Show | 72 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.-164-3933_-164-393 others(6): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53151968 | |||||
| chr16:53151968
|
ATGTG | A | 3 | a0001c0003t0002g0170a0002c0002t0001g0120a0002c0002t0001g0163 | 3 | HG02895.hp1 HG02897.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-164-3935_-164-393 others(8): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53151968 | |||||
| chr16:53152088
|
AAG | A | 5 | a0001c0003t0002g0028a0001c0003t0002g0029a0001c0003t0002g0125others(2): Show | 5 | HG02129.hp1 NA18955.hp1 NA18961.hp1 others(2): Show |
intron_variant | MODIFIER | c.-164-3836_-164-383 others(6): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr16 | 53152088 | |||||
| chr16:53152118
|
G | T | 141 | a0001c0001t0002g0171a0001c0001t0002g0175a0001c0001t0003g0016others(138): Show | 141 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.-164-3808G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53152118 | ||||||
| chr16:53152633
|
G | A | 1 | a0006c0009t0004g0107 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-164-3293G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53152633 | ||||||
| chr16:53152714
|
A | G | 1 | a0001c0005t0001g0215 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-164-3212A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53152714 | ||||||
| chr16:53152791
|
T | A | 1 | a0001c0005t0005g0032 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-164-3135T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53152791 | ||||||
| chr16:53152796
|
G | T | 1 | a0001c0005t0005g0032 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-164-3130G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53152796 | ||||||
| chr16:53152880
|
A | G | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.-164-3046A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53152880 | ||||||
| chr16:53153080
|
C | T | 1 | a0001c0005t0004g0097 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-164-2846C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53153080 | ||||||
| chr16:53153775
|
A | C | 1 | a0001c0005t0001g0215 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-164-2151A>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53153775 | ||||||
| chr16:53154102
|
C | T | 65 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.-164-1824C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53154102 | ||||||
| chr16:53154202
|
T | A | 1 | a0001c0005t0001g0215 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-164-1724T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53154202 | ||||||
| chr16:53154251
|
A | T | 1 | a0002c0002t0001g0147 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-164-1675A>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53154251 | ||||||
| chr16:53154280
|
T | C | 1 | a0001c0001t0003g0105 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-164-1646T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53154280 | ||||||
| chr16:53154345
|
A | G | 19 | a0001c0001t0003g0022a0001c0001t0003g0079a0001c0001t0003g0096others(16): Show | 19 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.-164-1581A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53154345 | ||||||
| chr16:53154481
|
A | G | 52 | a0002c0002t0001g0009a0002c0002t0001g0010a0002c0002t0001g0012others(49): Show | 52 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(49): Show |
intron_variant | MODIFIER | c.-164-1445A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53154481 | ||||||
| chr16:53154487
|
C | A | 1 | a0001c0013t0001g0055 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-164-1439C>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53154487 | ||||||
| chr16:53154530
|
G | A | 1 | a0001c0005t0001g0215 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-164-1396G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53154530 | ||||||
| chr16:53154609
|
A | G | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.-164-1317A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53154609 | ||||||
| chr16:53154757
|
T | C | 142 | a0001c0001t0001g0159a0001c0001t0002g0171a0001c0001t0002g0175others(139): Show | 142 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.-164-1169T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53154757 | ||||||
| chr16:53154789
|
C | G | 2 | a0003c0004t0001g0123a0003c0004t0001g0207 | 2 | HG01255.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.-164-1137C>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53154789 | ||||||
| chr16:53154792
|
G | A | 1 | a0003c0004t0001g0207 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-164-1134G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53154792 | ||||||
| chr16:53154943
|
A | T | 1 | a0001c0001t0001g0056 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-164-983A>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53154943 | ||||||
| chr16:53155011
|
G | A | 7 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0168others(4): Show | 7 | HG01891.hp2 HG02451.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-164-915G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53155011 | ||||||
| chr16:53155126
|
A | G | 1 | a0002c0002t0001g0063 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-164-800A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53155126 | ||||||
| chr16:53155214
|
G | C | 2 | a0001c0001t0001g0045a0001c0001t0001g0051 | 2 | HG00558.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-164-712G>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53155214 | ||||||
| chr16:53155263
|
C | T | 1 | a0001c0005t0005g0032 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-164-663C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53155263 | ||||||
| chr16:53155432
|
G | T | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.-164-494G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53155432 | ||||||
| chr16:53155760
|
A | C | 61 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(58): Show | 61 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.-164-166A>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 1/38 | chr16 | 53155760 | ||||||
| chr16:53157558
|
T | C | 65 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.1452+17T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53157558 | ||||||
| chr16:53157741
|
G | C | 2 | a0003c0004t0001g0007a0003c0004t0001g0030 | 2 | HG00597.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.1452+200G>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53157741 | ||||||
| chr16:53158135
|
T | C | 1 | a0001c0005t0004g0097 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1452+594T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53158135 | ||||||
| chr16:53158252
|
C | G | 1 | a0001c0001t0001g0230 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1452+711C>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53158252 | ||||||
| chr16:53158419
|
T | C | 74 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(71): Show | 74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.1452+878T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53158419 | ||||||
| chr16:53158442
|
A | G | 141 | a0001c0001t0002g0171a0001c0001t0002g0175a0001c0001t0003g0016others(138): Show | 141 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.1452+901A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53158442 | ||||||
| chr16:53158516
|
G | A | 7 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0168others(4): Show | 7 | HG01891.hp2 HG02451.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1452+975G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53158516 | ||||||
| chr16:53158519
|
C | T | 53 | a0002c0002t0001g0009a0002c0002t0001g0010a0002c0002t0001g0012others(50): Show | 53 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.1452+978C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53158519 | ||||||
| chr16:53158642
|
T | A | 1 | a0001c0005t0004g0097 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1452+1101T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53158642 | ||||||
| chr16:53158732
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1452+1191G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53158732 | ||||||
| chr16:53159096
|
G | A | 1 | a0001c0001t0001g0119 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1452+1555G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53159096 | ||||||
| chr16:53159174
|
C | T | 45 | a0001c0001t0002g0171a0001c0001t0002g0175a0001c0001t0003g0016others(42): Show | 45 | HG00140.hp2 HG00558.hp2 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.1452+1633C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53159174 | ||||||
| chr16:53159215
|
C | T | 1 | a0001c0005t0001g0215 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1452+1674C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53159215 | ||||||
| chr16:53159365
|
C | T | 1 | a0003c0004t0001g0007 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1452+1824C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53159365 | ||||||
| chr16:53159714
|
A | G | 2 | a0002c0002t0001g0012a0002c0002t0014g0011 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1452+2173A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53159714 | ||||||
| chr16:53159840
|
C | A | 1 | a0001c0005t0011g0228 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1452+2299C>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53159840 | ||||||
| chr16:53159877
|
A | G | 2 | a0003c0004t0001g0213a0003c0004t0001g0217 | 2 | NA18974.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.1452+2336A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53159877 | ||||||
| chr16:53159900
|
A | C | 3 | a0003c0004t0001g0203a0003c0004t0001g0204a0003c0004t0001g0216 | 3 | HG01168.hp1 HG01169.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1452+2359A>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53159900 | ||||||
| chr16:53160041
|
A | G | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1452+2500A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53160041 | ||||||
| chr16:53160236
|
C | T | 74 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(71): Show | 74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.1452+2695C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53160236 | ||||||
| chr16:53160711
|
C | A | 76 | a0001c0005t0001g0215a0001c0005t0004g0078a0001c0005t0004g0097others(73): Show | 76 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.1452+3170C>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53160711 | ||||||
| chr16:53161035
|
T | A | 53 | a0002c0002t0001g0009a0002c0002t0001g0010a0002c0002t0001g0012others(50): Show | 53 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.1452+3494T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53161035 | ||||||
| chr16:53161282
|
A | G | 1 | a0001c0001t0001g0160 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1452+3741A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53161282 | ||||||
| chr16:53161283
|
T | C | 1 | a0001c0001t0003g0112 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1452+3742T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53161283 | ||||||
| chr16:53161352
|
A | T | 53 | a0002c0002t0001g0009a0002c0002t0001g0010a0002c0002t0001g0012others(50): Show | 53 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.1452+3811A>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53161352 | ||||||
| chr16:53161620
|
T | C | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1452+4079T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53161620 | ||||||
| chr16:53161661
|
T | C | 1 | a0003c0004t0001g0187 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1452+4120T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53161661 | ||||||
| chr16:53161883
|
C | G | 12 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(9): Show | 12 | HG01167.hp2 HG01884.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.1452+4342C>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53161883 | ||||||
| chr16:53162030
|
G | A | 2 | a0002c0002t0001g0120a0002c0002t0001g0163 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1452+4489G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53162030 | ||||||
| chr16:53162130
|
A | G | 42 | a0001c0001t0003g0016a0001c0001t0015g0166a0001c0003t0001g0158others(39): Show | 42 | HG00140.hp2 HG00558.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.1452+4589A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53162130 | ||||||
| chr16:53162364
|
T | A | 53 | a0002c0002t0001g0009a0002c0002t0001g0010a0002c0002t0001g0012others(50): Show | 53 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.1452+4823T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53162364 | ||||||
| chr16:53162480
|
T | C | 1 | a0002c0002t0001g0208 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1452+4939T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53162480 | ||||||
| chr16:53162494
|
CAT | C | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1452+4954_1452+495 others(6): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53162494 | ||||||
| chr16:53162585
|
A | C | 1 | a0001c0005t0004g0169 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1452+5044A>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53162585 | ||||||
| chr16:53162603
|
G | A | 1 | a0001c0005t0001g0215 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1452+5062G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53162603 | ||||||
| chr16:53162620
|
TATACTC | T | 52 | a0002c0002t0001g0009a0002c0002t0001g0010a0002c0002t0001g0012others(49): Show | 52 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(49): Show |
intron_variant | MODIFIER | c.1452+5084_1452+508 others(10): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53162620 | |||||
| chr16:53162783
|
C | CA | 12 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(9): Show | 12 | HG01167.hp2 HG01884.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.1452+5242_1452+524 others(5): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53162783 | ||||||
| chr16:53162783
|
C | CT | 7 | a0001c0001t0003g0167a0001c0003t0002g0029a0001c0003t0002g0153others(4): Show | 7 | HG01243.hp1 HG02559.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1452+5258dupT | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53162783 | |||||
| chr16:53162833
|
A | G | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1452+5292A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53162833 | ||||||
| chr16:53163073
|
G | C | 1 | a0001c0005t0004g0234 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1452+5532G>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53163073 | ||||||
| chr16:53163171
|
CTT | C | 65 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.1452+5631_1452+563 others(6): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53163171 | ||||||
| chr16:53163196
|
A | G | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1452+5655A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53163196 | ||||||
| chr16:53163267
|
A | G | 2 | a0001c0005t0004g0104a0001c0005t0012g0229 | 2 | HG01167.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1452+5726A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53163267 | ||||||
| chr16:53163313
|
C | T | 2 | a0002c0002t0001g0019a0002c0002t0001g0020 | 2 | NA18939.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.1452+5772C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53163313 | ||||||
| chr16:53163358
|
G | A | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1452+5817G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53163358 | ||||||
| chr16:53163381
|
T | C | 1 | a0001c0001t0003g0112 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1452+5840T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53163381 | ||||||
| chr16:53163443
|
C | G | 1 | a0001c0005t0004g0097 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1452+5902C>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53163443 | ||||||
| chr16:53163454
|
C | T | 3 | a0002c0002t0001g0145a0002c0002t0001g0146a0002c0002t0001g0149 | 3 | NA19009.hp1 NA19010.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.1452+5913C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53163454 | ||||||
| chr16:53163478
|
G | A | 2 | a0001c0001t0002g0171a0001c0001t0002g0175 | 2 | HG02451.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1452+5937G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53163478 | ||||||
| chr16:53163547
|
T | C | 65 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.1452+6006T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53163547 | ||||||
| chr16:53163654
|
A | G | 1 | a0002c0019t0001g0180 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1452+6113A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53163654 | ||||||
| chr16:53163717
|
T | C | 1 | a0001c0001t0001g0038 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1452+6176T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53163717 | ||||||
| chr16:53163774
|
C | T | 1 | a0001c0001t0001g0225 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1452+6233C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53163774 | ||||||
| chr16:53163951
|
C | T | 141 | a0001c0001t0002g0171a0001c0001t0002g0175a0001c0001t0003g0016others(138): Show | 141 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.1452+6410C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53163951 | ||||||
| chr16:53164019
|
G | C | 1 | a0001c0001t0001g0072 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1452+6478G>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53164019 | ||||||
| chr16:53164022
|
A | G | 141 | a0001c0001t0002g0171a0001c0001t0002g0175a0001c0001t0003g0016others(138): Show | 141 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.1452+6481A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53164022 | ||||||
| chr16:53164205
|
C | T | 1 | a0001c0005t0004g0097 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1452+6664C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53164205 | ||||||
| chr16:53164288
|
A | G | 1 | a0002c0002t0001g0024 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1452+6747A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53164288 | ||||||
| chr16:53164571
|
C | T | 9 | a0001c0001t0003g0022a0001c0001t0003g0079a0001c0001t0003g0105others(6): Show | 9 | HG01891.hp1 HG02257.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1452+7030C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53164571 | ||||||
| chr16:53164632
|
G | GT | 59 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0165others(56): Show | 59 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(56): Show |
intron_variant | MODIFIER | c.1452+7101dupT | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53164632 | |||||
| chr16:53164632
|
GT | G | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1452+7101delT | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53164632 | |||||
| chr16:53164660
|
G | A | 5 | a0001c0001t0001g0117a0001c0001t0001g0168a0001c0001t0001g0173others(2): Show | 5 | HG01891.hp2 HG02451.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1452+7119G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53164660 | ||||||
| chr16:53164695
|
C | A | 1 | a0002c0002t0001g0126 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1452+7154C>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53164695 | ||||||
| chr16:53164770
|
C | T | 12 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(9): Show | 12 | HG01167.hp2 HG01884.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.1452+7229C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53164770 | ||||||
| chr16:53164843
|
C | T | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1452+7302C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53164843 | ||||||
| chr16:53164930
|
T | C | 74 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(71): Show | 74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.1452+7389T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53164930 | ||||||
| chr16:53165001
|
G | T | 1 | a0002c0002t0001g0193 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1452+7460G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53165001 | ||||||
| chr16:53165330
|
A | G | 1 | a0001c0001t0002g0171 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1452+7789A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53165330 | ||||||
| chr16:53165397
|
A | G | 1 | a0001c0001t0001g0085 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1452+7856A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53165397 | ||||||
| chr16:53165415
|
G | A | 2 | a0001c0001t0001g0052a0001c0001t0001g0060 | 2 | NA18946.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.1452+7874G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53165415 | ||||||
| chr16:53165716
|
A | AAGAATTT others(9): Show |
74 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(71): Show | 74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.1452+8175_1452+817 others(20): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53165716 | ||||||
| chr16:53166370
|
A | G | 74 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(71): Show | 74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.1452+8829A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53166370 | ||||||
| chr16:53166591
|
C | T | 19 | a0001c0001t0003g0022a0001c0001t0003g0079a0001c0001t0003g0096others(16): Show | 19 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.1452+9050C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53166591 | ||||||
| chr16:53166666
|
G | T | 1 | a0001c0001t0001g0081 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1452+9125G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53166666 | ||||||
| chr16:53166990
|
C | T | 1 | a0001c0014t0001g0115 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1452+9449C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53166990 | ||||||
| chr16:53167011
|
T | TA | 53 | a0002c0002t0001g0009a0002c0002t0001g0010a0002c0002t0001g0012others(50): Show | 53 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.1452+9472dupA | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53167011 | |||||
| chr16:53167166
|
C | A | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1452+9625C>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53167166 | ||||||
| chr16:53167266
|
T | C | 1 | a0001c0005t0004g0097 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1452+9725T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53167266 | ||||||
| chr16:53167620
|
CTT | C | 10 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0231others(7): Show | 10 | HG01167.hp2 HG01884.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1452+10081_1452+10 others(8): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53167620 | |||||
| chr16:53167670
|
A | G | 3 | a0001c0001t0001g0027a0001c0001t0001g0064a0001c0001t0001g0218 | 3 | HG02027.hp1 HG02040.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1452+10129A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53167670 | ||||||
| chr16:53167674
|
T | TATATACA others(29): Show |
2 | a0002c0002t0001g0048a0002c0002t0001g0049 | 2 | HG01099.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.1452+10139_1452+10 others(42): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53167674 | |||||
| chr16:53167879
|
G | A | 74 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(71): Show | 74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.1452+10338G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53167879 | ||||||
| chr16:53167913
|
T | C | 1 | a0001c0001t0003g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1452+10372T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53167913 | ||||||
| chr16:53167967
|
A | T | 1 | a0003c0004t0001g0200 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1452+10426A>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53167967 | ||||||
| chr16:53167994
|
A | G | 1 | a0003c0004t0001g0200 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1452+10453A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53167994 | ||||||
| chr16:53167996
|
T | A | 1 | a0003c0004t0001g0200 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1452+10455T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53167996 | ||||||
| chr16:53168038
|
A | G | 65 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.1452+10497A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53168038 | ||||||
| chr16:53168072
|
A | T | 1 | a0001c0005t0005g0089 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1452+10531A>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53168072 | ||||||
| chr16:53168092
|
T | C | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1452+10551T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53168092 | ||||||
| chr16:53168098
|
G | A | 65 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.1452+10557G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53168098 | ||||||
| chr16:53168280
|
C | T | 1 | a0001c0001t0001g0008 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1452+10739C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53168280 | ||||||
| chr16:53168306
|
A | C | 1 | a0001c0001t0015g0166 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1452+10765A>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53168306 | ||||||
| chr16:53168353
|
A | G | 142 | a0001c0001t0001g0159a0001c0001t0002g0171a0001c0001t0002g0175others(139): Show | 142 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.1452+10812A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53168353 | ||||||
| chr16:53168545
|
G | A | 1 | a0001c0005t0004g0097 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1452+11004G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53168545 | ||||||
| chr16:53168609
|
A | G | 2 | a0001c0001t0001g0045a0001c0001t0001g0051 | 2 | HG00558.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1452+11068A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53168609 | ||||||
| chr16:53168612
|
G | C | 53 | a0002c0002t0001g0009a0002c0002t0001g0010a0002c0002t0001g0012others(50): Show | 53 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.1452+11071G>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53168612 | ||||||
| chr16:53168900
|
C | A | 1 | a0001c0001t0003g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1452+11359C>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53168900 | ||||||
| chr16:53169043
|
C | G | 1 | a0009c0018t0005g0155 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1452+11502C>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53169043 | ||||||
| chr16:53169072
|
G | T | 1 | a0009c0018t0005g0155 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1452+11531G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53169072 | ||||||
| chr16:53169427
|
A | C | 1 | a0003c0004t0001g0148 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1452+11886A>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53169427 | ||||||
| chr16:53169434
|
T | C | 65 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.1452+11893T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53169434 | ||||||
| chr16:53169722
|
A | G | 52 | a0002c0002t0001g0009a0002c0002t0001g0010a0002c0002t0001g0012others(49): Show | 52 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(49): Show |
intron_variant | MODIFIER | c.1452+12181A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53169722 | ||||||
| chr16:53169793
|
T | C | 1 | a0003c0004t0001g0143 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1452+12252T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53169793 | ||||||
| chr16:53169812
|
T | G | 1 | a0003c0004t0001g0143 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1452+12271T>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53169812 | ||||||
| chr16:53169929
|
A | T | 1 | a0001c0001t0003g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1452+12388A>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53169929 | ||||||
| chr16:53170039
|
G | GT | 53 | a0001c0003t0002g0046a0002c0002t0001g0009a0002c0002t0001g0010others(50): Show | 53 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.1452+12507dupT | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53170039 | |||||
| chr16:53170040
|
T | G | 1 | a0001c0005t0001g0215 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1452+12499T>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53170040 | ||||||
| chr16:53170048
|
T | TTG | 13 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(10): Show | 13 | HG01167.hp2 HG01884.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.1452+12507_1452+12 others(8): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53170048 | ||||||
| chr16:53170049
|
G | T | 13 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(10): Show | 13 | HG01167.hp2 HG01884.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.1452+12508G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53170049 | ||||||
| chr16:53170058
|
TG | T | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1452+12518delG | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53170058 | ||||||
| chr16:53170059
|
G | T | 67 | a0001c0005t0001g0215a0001c0005t0004g0078a0001c0005t0004g0097others(64): Show | 67 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.1452+12518G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53170059 | ||||||
| chr16:53170063
|
G | T | 1 | a0001c0005t0001g0215 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1452+12522G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53170063 | ||||||
| chr16:53170063
|
GT | G | 10 | a0001c0005t0004g0097a0001c0005t0005g0017a0001c0005t0005g0018others(7): Show | 10 | HG01884.hp1 HG02257.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1452+12531delT | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53170063 | |||||
| chr16:53170064
|
T | G | 1 | a0001c0005t0001g0215 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1452+12523T>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53170064 | ||||||
| chr16:53170065
|
T | G | 53 | a0002c0002t0001g0009a0002c0002t0001g0010a0002c0002t0001g0012others(50): Show | 53 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.1452+12524T>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53170065 | ||||||
| chr16:53170244
|
T | C | 19 | a0001c0001t0003g0022a0001c0001t0003g0079a0001c0001t0003g0096others(16): Show | 19 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.1452+12703T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53170244 | ||||||
| chr16:53170578
|
C | CGT | 18 | a0001c0001t0001g0178a0001c0001t0001g0218a0001c0001t0002g0175others(15): Show | 18 | HG01168.hp1 HG01169.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.1452+13078_1452+13 others(8): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53170578 | |||||
| chr16:53170578
|
CGT | C | 154 | a0001c0001t0001g0014a0001c0001t0001g0021a0001c0001t0001g0025others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.1452+13078_1452+13 others(8): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53170578 | |||||
| chr16:53170578
|
CGTGT | C | 14 | a0001c0001t0001g0027a0001c0001t0001g0064a0001c0001t0001g0110others(11): Show | 14 | HG01255.hp2 HG01884.hp1 HG02027.hp1 others(11): Show |
intron_variant | MODIFIER | c.1452+13076_1452+13 others(10): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53170578 | |||||
| chr16:53170578
|
CGTGTGT | C | 2 | a0002c0002t0001g0138a0002c0002t0001g0140 | 2 | HG03017.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1452+13074_1452+13 others(12): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53170578 | |||||
| chr16:53170578
|
CGTGTGTG others(1): Show |
C | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1452+13072_1452+13 others(14): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53170578 | |||||
| chr16:53170583
|
G | T | 3 | a0004c0006t0001g0121a0004c0006t0001g0127a0004c0006t0001g0128 | 3 | NA18952.hp1 NA18989.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.1452+13042G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53170583 | ||||||
| chr16:53170647
|
T | A | 2 | a0002c0002t0008g0065a0002c0002t0008g0137 | 2 | HG00408.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.1452+13106T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53170647 | ||||||
| chr16:53171096
|
C | T | 3 | a0003c0004t0001g0203a0003c0004t0001g0204a0003c0004t0001g0216 | 3 | HG01168.hp1 HG01169.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1452+13555C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53171096 | ||||||
| chr16:53171159
|
T | C | 1 | a0002c0002t0001g0054 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1452+13618T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53171159 | ||||||
| chr16:53171245
|
G | A | 1 | a0008c0011t0003g0062 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1452+13704G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53171245 | ||||||
| chr16:53171278
|
G | A | 1 | a0006c0009t0004g0107 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1452+13737G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53171278 | ||||||
| chr16:53171589
|
T | C | 74 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(71): Show | 74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.1452+14048T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53171589 | ||||||
| chr16:53171792
|
A | C | 9 | a0001c0001t0003g0022a0001c0001t0003g0079a0001c0001t0003g0105others(6): Show | 9 | HG01891.hp1 HG02257.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1452+14251A>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53171792 | ||||||
| chr16:53171829
|
A | G | 3 | a0001c0001t0001g0043a0001c0001t0001g0185a0001c0001t0001g0188 | 3 | HG02683.hp2 HG03492.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1452+14288A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53171829 | ||||||
| chr16:53171830
|
CCA | C | 53 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0025others(50): Show | 53 | HG00099.hp1 HG00323.hp2 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.1452+14318_1452+14 others(8): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53171830 | |||||
| chr16:53171833
|
CACACACA others(21): Show |
C | 1 | a0001c0001t0003g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1452+14320_1452+14 others(34): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53171833 | |||||
| chr16:53171839
|
CACACACA others(15): Show |
C | 3 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0012g0229 | 3 | HG01167.hp2 HG01884.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1452+14320_1452+14 others(28): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53171839 | |||||
| chr16:53171841
|
CACACACA others(13): Show |
C | 49 | a0002c0002t0001g0009a0002c0002t0001g0010a0002c0002t0001g0012others(46): Show | 49 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(46): Show |
intron_variant | MODIFIER | c.1452+14320_1452+14 others(26): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53171841 | |||||
| chr16:53171847
|
CACACACA others(7): Show |
C | 2 | a0001c0001t0002g0175a0001c0005t0004g0097 | 2 | HG01884.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1452+14320_1452+14 others(20): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53171847 | |||||
| chr16:53171849
|
CACACACA others(5): Show |
C | 2 | a0001c0001t0003g0096a0001c0001t0003g0131 | 2 | HG01891.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1452+14320_1452+14 others(18): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53171849 | |||||
| chr16:53171851
|
CACACACA others(3): Show |
C | 8 | a0001c0001t0002g0171a0001c0001t0003g0133a0001c0001t0015g0166others(5): Show | 8 | HG00558.hp2 HG02257.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1452+14320_1452+14 others(16): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53171851 | |||||
| chr16:53171853
|
C | CACACAG | 2 | a0001c0001t0001g0124a0001c0001t0001g0225 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1452+14317_1452+14 others(12): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53171853 | |||||
| chr16:53171853
|
CACACACA others(1): Show |
C | 13 | a0001c0001t0001g0211a0001c0001t0003g0022a0001c0001t0003g0079others(10): Show | 13 | HG02257.hp1 HG02280.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.1452+14320_1452+14 others(14): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53171853 | |||||
| chr16:53171855
|
C | CACAG | 2 | a0003c0004t0001g0187a0003c0004t0001g0194 | 2 | HG02165.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.1452+14317_1452+14 others(10): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53171855 | |||||
| chr16:53171855
|
CACACAG | C | 19 | a0001c0001t0001g0084a0001c0001t0001g0230a0001c0001t0003g0112others(16): Show | 19 | HG02055.hp1 HG02109.hp2 HG02155.hp1 others(16): Show |
intron_variant | MODIFIER | c.1452+14320_1452+14 others(12): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53171855 | |||||
| chr16:53171857
|
C | G | 1 | a0001c0008t0001g0077 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1452+14316C>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53171857 | ||||||
| chr16:53171857
|
CACAG | C | 10 | a0001c0001t0001g0021a0001c0001t0001g0058a0001c0001t0001g0068others(7): Show | 10 | HG00621.hp1 HG01255.hp1 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.1452+14320_1452+14 others(10): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53171857 | |||||
| chr16:53171859
|
C | G | 4 | a0001c0001t0001g0067a0001c0001t0001g0081a0001c0001t0001g0098others(1): Show | 4 | HG02129.hp2 HG02135.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.1452+14318C>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53171859 | ||||||
| chr16:53171859
|
CAG | C | 5 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0182others(2): Show | 5 | HG00621.hp2 HG02615.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1452+14320_1452+14 others(8): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53171859 | |||||
| chr16:53171861
|
G | C | 9 | a0001c0001t0001g0067a0001c0001t0001g0081a0001c0001t0001g0098others(6): Show | 9 | HG02129.hp2 HG02135.hp1 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.1452+14320G>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53171861 | ||||||
| chr16:53171861
|
GAC | G | 2 | a0001c0001t0007g0122a0001c0003t0002g0086 | 2 | HG02280.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.1452+14360_1452+14 others(8): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53171861 | |||||
| chr16:53171861
|
GACAC | G | 8 | a0001c0003t0001g0158a0001c0003t0002g0153a0001c0003t0002g0161others(5): Show | 8 | HG00735.hp1 HG01109.hp1 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.1452+14358_1452+14 others(10): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53171861 | |||||
| chr16:53171861
|
GACACAC | G | 30 | a0001c0001t0001g0159a0001c0003t0002g0002a0001c0003t0002g0005others(27): Show | 30 | HG00140.hp2 HG01074.hp1 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.1452+14356_1452+14 others(12): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53171861 | |||||
| chr16:53171861
|
GACACACA others(1): Show |
G | 3 | a0001c0003t0002g0070a0001c0005t0001g0215a0001c0017t0002g0237 | 3 | HG02055.hp2 HG02080.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.1452+14354_1452+14 others(14): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53171861 | |||||
| chr16:53171861
|
GACACACA others(3): Show |
G | 1 | a0001c0003t0002g0152 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1452+14352_1452+14 others(16): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53171861 | |||||
| chr16:53171861
|
GACACACA others(11): Show |
G | 4 | a0002c0002t0001g0034a0002c0002t0001g0035a0002c0002t0001g0205others(1): Show | 4 | HG01257.hp1 HG03831.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.1452+14344_1452+14 others(24): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53171861 | |||||
| chr16:53171861
|
GACACACA others(13): Show |
G | 9 | a0001c0005t0004g0169a0001c0005t0004g0231a0001c0005t0004g0232others(6): Show | 9 | HG02615.hp2 HG02897.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.1452+14342_1452+14 others(26): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53171861 | |||||
| chr16:53171863
|
C | G | 11 | a0001c0001t0001g0021a0001c0001t0001g0058a0001c0001t0001g0068others(8): Show | 11 | HG00621.hp1 HG01255.hp1 HG02965.hp2 others(8): Show |
intron_variant | MODIFIER | c.1452+14322C>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53171863 | ||||||
| chr16:53171865
|
C | G | 24 | a0001c0001t0001g0084a0001c0001t0001g0110a0001c0001t0001g0111others(21): Show | 24 | HG02055.hp1 HG02109.hp2 HG02155.hp1 others(21): Show |
intron_variant | MODIFIER | c.1452+14324C>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53171865 | ||||||
| chr16:53171867
|
C | G | 20 | a0001c0001t0001g0211a0001c0001t0003g0022a0001c0001t0003g0079others(17): Show | 20 | HG00558.hp2 HG00621.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.1452+14326C>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53171867 | ||||||
| chr16:53171869
|
C | G | 1 | a0001c0001t0002g0175 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1452+14328C>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53171869 | ||||||
| chr16:53171871
|
C | G | 2 | a0001c0001t0003g0096a0001c0001t0003g0131 | 2 | HG01891.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1452+14330C>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53171871 | ||||||
| chr16:53171879
|
C | G | 50 | a0001c0001t0003g0016a0002c0002t0001g0009a0002c0002t0001g0010others(47): Show | 50 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(47): Show |
intron_variant | MODIFIER | c.1452+14338C>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53171879 | ||||||
| chr16:53171881
|
C | G | 3 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0012g0229 | 3 | HG01167.hp2 HG01884.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1452+14340C>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53171881 | ||||||
| chr16:53171917
|
C | T | 65 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.1452+14376C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53171917 | ||||||
| chr16:53172056
|
A | G | 74 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(71): Show | 74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.1452+14515A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53172056 | ||||||
| chr16:53172171
|
G | A | 1 | a0001c0001t0001g0111 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1452+14630G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53172171 | ||||||
| chr16:53172378
|
TTAAAA | T | 2 | a0002c0002t0001g0048a0002c0002t0001g0049 | 2 | HG01099.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.1452+14841_1452+14 others(11): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53172378 | |||||
| chr16:53172420
|
G | A | 1 | a0001c0001t0007g0103 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1452+14879G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53172420 | ||||||
| chr16:53172472
|
C | T | 74 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(71): Show | 74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.1452+14931C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53172472 | ||||||
| chr16:53172621
|
A | G | 46 | a0001c0001t0001g0159a0001c0001t0002g0171a0001c0001t0002g0175others(43): Show | 46 | HG00140.hp2 HG00558.hp2 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.1452+15080A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53172621 | ||||||
| chr16:53172651
|
G | A | 76 | a0001c0005t0001g0215a0001c0005t0004g0078a0001c0005t0004g0097others(73): Show | 76 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.1452+15110G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53172651 | ||||||
| chr16:53172923
|
T | G | 1 | a0002c0002t0001g0024 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1452+15382T>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53172923 | ||||||
| chr16:53172985
|
A | G | 12 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(9): Show | 12 | HG01167.hp2 HG01884.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.1452+15444A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53172985 | ||||||
| chr16:53173281
|
G | A | 65 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.1452+15740G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53173281 | ||||||
| chr16:53173530
|
T | C | 142 | a0001c0001t0001g0159a0001c0001t0002g0171a0001c0001t0002g0175others(139): Show | 142 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.1452+15989T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53173530 | ||||||
| chr16:53173553
|
T | A | 42 | a0001c0001t0001g0159a0001c0001t0015g0166a0001c0003t0001g0158others(39): Show | 42 | HG00140.hp2 HG00558.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.1452+16012T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53173553 | ||||||
| chr16:53173555
|
T | A | 1 | a0006c0009t0004g0107 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1452+16014T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53173555 | ||||||
| chr16:53173556
|
T | A | 42 | a0001c0001t0001g0159a0001c0001t0015g0166a0001c0003t0001g0158others(39): Show | 42 | HG00140.hp2 HG00558.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.1452+16015T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53173556 | ||||||
| chr16:53173575
|
C | T | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1452+16034C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53173575 | ||||||
| chr16:53173576
|
G | A | 1 | a0006c0009t0004g0107 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1452+16035G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53173576 | ||||||
| chr16:53173724
|
T | G | 1 | a0001c0001t0001g0026 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1452+16183T>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53173724 | ||||||
| chr16:53173733
|
A | T | 2 | a0001c0005t0005g0017a0001c0005t0005g0018 | 2 | HG02257.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1452+16192A>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53173733 | ||||||
| chr16:53173802
|
C | A | 1 | a0002c0002t0001g0082 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1452+16261C>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53173802 | ||||||
| chr16:53173834
|
G | A | 6 | a0002c0002t0001g0106a0002c0002t0001g0109a0002c0002t0001g0113others(3): Show | 6 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1452+16293G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53173834 | ||||||
| chr16:53173844
|
A | G | 1 | a0001c0003t0002g0202 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1452+16303A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53173844 | ||||||
| chr16:53173975
|
T | C | 65 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.1452+16434T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53173975 | ||||||
| chr16:53174169
|
A | G | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1452+16628A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53174169 | ||||||
| chr16:53174701
|
T | C | 1 | a0002c0002t0001g0149 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1452+17160T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53174701 | ||||||
| chr16:53174887
|
C | T | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1452+17346C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53174887 | ||||||
| chr16:53174994
|
C | T | 1 | a0001c0001t0001g0025 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1452+17453C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53174994 | ||||||
| chr16:53175186
|
C | G | 1 | a0001c0001t0001g0064 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1452+17645C>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53175186 | ||||||
| chr16:53175813
|
T | C | 9 | a0003c0004t0001g0187a0003c0004t0001g0194a0003c0004t0001g0195others(6): Show | 9 | HG02015.hp2 HG02155.hp1 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.1452+18272T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53175813 | ||||||
| chr16:53175874
|
T | C | 10 | a0001c0001t0003g0096a0001c0001t0003g0112a0001c0001t0003g0133others(7): Show | 10 | HG02055.hp1 HG02109.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.1452+18333T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53175874 | ||||||
| chr16:53175965
|
T | C | 74 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(71): Show | 74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.1452+18424T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53175965 | ||||||
| chr16:53176175
|
A | C | 1 | a0001c0003t0002g0036 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1452+18634A>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53176175 | ||||||
| chr16:53176198
|
C | A | 53 | a0002c0002t0001g0009a0002c0002t0001g0010a0002c0002t0001g0012others(50): Show | 53 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.1452+18657C>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53176198 | ||||||
| chr16:53176513
|
A | C | 42 | a0001c0001t0001g0159a0001c0001t0015g0166a0001c0003t0001g0158others(39): Show | 42 | HG00140.hp2 HG00558.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.1452+18972A>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53176513 | ||||||
| chr16:53176641
|
G | C | 65 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.1452+19100G>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53176641 | ||||||
| chr16:53176876
|
A | G | 77 | a0001c0005t0001g0215a0001c0005t0004g0078a0001c0005t0004g0097others(74): Show | 77 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.1452+19335A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53176876 | ||||||
| chr16:53176953
|
A | C | 2 | a0002c0002t0001g0019a0002c0002t0001g0020 | 2 | NA18939.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.1452+19412A>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53176953 | ||||||
| chr16:53176994
|
C | T | 1 | a0002c0019t0001g0180 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1452+19453C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53176994 | ||||||
| chr16:53177102
|
C | T | 2 | a0001c0001t0001g0027a0001c0001t0001g0064 | 2 | HG02027.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.1452+19561C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53177102 | ||||||
| chr16:53177146
|
G | A | 1 | a0006c0009t0004g0107 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1452+19605G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53177146 | ||||||
| chr16:53177251
|
T | C | 77 | a0001c0005t0001g0215a0001c0005t0004g0078a0001c0005t0004g0097others(74): Show | 77 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.1452+19710T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53177251 | ||||||
| chr16:53177305
|
C | A | 1 | a0001c0005t0011g0228 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1452+19764C>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53177305 | ||||||
| chr16:53177311
|
C | A | 1 | a0001c0001t0001g0052 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1452+19770C>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53177311 | ||||||
| chr16:53177414
|
C | G | 1 | a0003c0004t0001g0177 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1452+19873C>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53177414 | ||||||
| chr16:53177473
|
C | T | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1452+19932C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53177473 | ||||||
| chr16:53177720
|
C | T | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1452+20179C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53177720 | ||||||
| chr16:53177753
|
G | A | 65 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.1452+20212G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53177753 | ||||||
| chr16:53177875
|
T | A | 1 | a0001c0005t0001g0215 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1452+20334T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53177875 | ||||||
| chr16:53177940
|
C | T | 65 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.1452+20399C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53177940 | ||||||
| chr16:53178427
|
C | CT | 14 | a0001c0001t0001g0038a0001c0001t0001g0081a0001c0001t0001g0124others(11): Show | 14 | HG00609.hp2 HG02109.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.1452+20909dupT | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53178427 | |||||
| chr16:53178427
|
CT | C | 44 | a0001c0003t0002g0170a0001c0003t0013g0186a0001c0005t0001g0215others(41): Show | 44 | HG00099.hp2 HG00323.hp1 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.1452+20909delT | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53178427 | |||||
| chr16:53178427
|
CTT | C | 19 | a0001c0005t0004g0104a0001c0005t0004g0169a0001c0005t0004g0231others(16): Show | 19 | HG00408.hp1 HG00609.hp1 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.1452+20908_1452+20 others(8): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53178427 | |||||
| chr16:53178427
|
CTTTTTTT | C | 19 | a0001c0001t0003g0022a0001c0001t0003g0079a0001c0001t0003g0096others(16): Show | 19 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.1452+20903_1452+20 others(13): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53178427 | |||||
| chr16:53178543
|
C | T | 1 | a0001c0005t0001g0215 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1452+21002C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53178543 | ||||||
| chr16:53178644
|
T | C | 1 | a0001c0003t0002g0202 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1452+21103T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53178644 | ||||||
| chr16:53178832
|
T | C | 43 | a0001c0001t0001g0159a0001c0001t0003g0016a0001c0001t0015g0166others(40): Show | 43 | HG00140.hp2 HG00558.hp2 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.1452+21291T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53178832 | ||||||
| chr16:53178835
|
A | T | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1452+21294A>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53178835 | ||||||
| chr16:53178869
|
C | T | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1452+21328C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53178869 | ||||||
| chr16:53179014
|
C | T | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1452+21473C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53179014 | ||||||
| chr16:53179023
|
T | TA | 13 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(10): Show | 13 | HG01167.hp2 HG01884.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.1452+21492dupA | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53179023 | |||||
| chr16:53179165
|
T | C | 77 | a0001c0005t0001g0215a0001c0005t0004g0078a0001c0005t0004g0097others(74): Show | 77 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.1452+21624T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53179165 | ||||||
| chr16:53179321
|
A | AT | 67 | a0001c0003t0002g0003a0001c0003t0002g0036a0001c0005t0004g0078others(64): Show | 67 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.1452+21789dupT | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53179321 | |||||
| chr16:53179484
|
G | A | 1 | a0001c0005t0004g0169 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1452+21943G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53179484 | ||||||
| chr16:53179507
|
A | G | 142 | a0001c0001t0001g0159a0001c0001t0002g0171a0001c0001t0002g0175others(139): Show | 142 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.1452+21966A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53179507 | ||||||
| chr16:53179576
|
G | A | 1 | a0006c0009t0004g0107 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1452+22035G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53179576 | ||||||
| chr16:53179789
|
C | T | 8 | a0003c0004t0001g0007a0003c0004t0001g0030a0003c0004t0001g0093others(5): Show | 8 | HG00597.hp2 NA18950.hp2 NA18955.hp2 others(5): Show |
intron_variant | MODIFIER | c.1452+22248C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53179789 | ||||||
| chr16:53179896
|
CA | C | 25 | a0001c0005t0001g0215a0001c0005t0004g0078a0001c0005t0004g0097others(22): Show | 25 | HG01167.hp2 HG01884.hp1 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.1452+22369delA | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53179896 | |||||
| chr16:53179899
|
A | G | 3 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0012g0229 | 3 | HG01167.hp2 HG01884.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1452+22358A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53179899 | ||||||
| chr16:53180028
|
C | CTT | 61 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(58): Show | 61 | HG00099.hp2 HG00408.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.1452+22502_1452+22 others(8): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53180028 | |||||
| chr16:53180083
|
A | G | 12 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(9): Show | 12 | HG01167.hp2 HG01884.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.1452+22542A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53180083 | ||||||
| chr16:53180142
|
G | A | 2 | a0001c0003t0002g0083a0001c0003t0017g0181 | 2 | HG03017.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1452+22601G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53180142 | ||||||
| chr16:53180179
|
G | A | 77 | a0001c0005t0001g0215a0001c0005t0004g0078a0001c0005t0004g0097others(74): Show | 77 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.1452+22638G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53180179 | ||||||
| chr16:53180227
|
G | A | 1 | a0001c0001t0003g0131 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1452+22686G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53180227 | ||||||
| chr16:53180462
|
A | G | 2 | a0001c0001t0001g0090a0001c0001t0001g0179 | 2 | HG01109.hp2 HG01257.hp2 |
intron_variant | MODIFIER | c.1452+22921A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53180462 | ||||||
| chr16:53180494
|
T | C | 1 | a0001c0005t0001g0215 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1452+22953T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53180494 | ||||||
| chr16:53180539
|
A | G | 74 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(71): Show | 74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.1452+22998A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53180539 | ||||||
| chr16:53180652
|
A | G | 65 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.1452+23111A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53180652 | ||||||
| chr16:53180683
|
A | AT | 10 | a0001c0001t0003g0096a0001c0001t0003g0133a0001c0001t0003g0184others(7): Show | 10 | HG02055.hp1 HG02109.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.1452+23151dupT | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53180683 | |||||
| chr16:53180774
|
G | A | 2 | a0001c0003t0002g0003a0001c0003t0002g0036 | 2 | HG00621.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.1452+23233G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53180774 | ||||||
| chr16:53180824
|
C | T | 1 | a0002c0002t0001g0113 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1452+23283C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53180824 | ||||||
| chr16:53180866
|
G | A | 1 | a0001c0001t0003g0022 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1452+23325G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53180866 | ||||||
| chr16:53180877
|
G | A | 2 | a0001c0005t0004g0097a0006c0009t0004g0107 | 2 | HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1452+23336G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53180877 | ||||||
| chr16:53180955
|
G | A | 65 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.1452+23414G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53180955 | ||||||
| chr16:53180991
|
A | G | 1 | a0003c0004t0001g0177 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1452+23450A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53180991 | ||||||
| chr16:53181036
|
G | C | 1 | a0001c0001t0001g0027 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1452+23495G>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53181036 | ||||||
| chr16:53181041
|
G | A | 1 | a0008c0011t0003g0062 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1452+23500G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53181041 | ||||||
| chr16:53181366
|
G | C | 65 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.1452+23825G>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53181366 | ||||||
| chr16:53181409
|
A | G | 10 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0231others(7): Show | 10 | HG01167.hp2 HG01884.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1452+23868A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53181409 | ||||||
| chr16:53181704
|
C | T | 1 | a0003c0004t0001g0209 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1452+24163C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53181704 | ||||||
| chr16:53181788
|
G | A | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1452+24247G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53181788 | ||||||
| chr16:53181940
|
C | T | 4 | a0003c0004t0001g0134a0003c0004t0001g0141a0003c0004t0001g0143others(1): Show | 4 | HG02559.hp2 HG02895.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1452+24399C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53181940 | ||||||
| chr16:53181982
|
G | A | 1 | a0003c0004t0006g0074 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1452+24441G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53181982 | ||||||
| chr16:53182003
|
T | C | 1 | a0001c0003t0002g0094 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1452+24462T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53182003 | ||||||
| chr16:53182059
|
A | G | 52 | a0002c0002t0001g0009a0002c0002t0001g0010a0002c0002t0001g0012others(49): Show | 52 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(49): Show |
intron_variant | MODIFIER | c.1452+24518A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53182059 | ||||||
| chr16:53182567
|
A | T | 77 | a0001c0005t0001g0215a0001c0005t0004g0078a0001c0005t0004g0097others(74): Show | 77 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.1452+25026A>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53182567 | ||||||
| chr16:53183200
|
T | C | 74 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(71): Show | 74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.1452+25659T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53183200 | ||||||
| chr16:53183223
|
C | A | 2 | a0001c0001t0001g0119a0001c0013t0001g0055 | 2 | HG00733.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1452+25682C>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53183223 | ||||||
| chr16:53183511
|
C | T | 1 | a0003c0004t0001g0177 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1452+25970C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53183511 | ||||||
| chr16:53183754
|
A | AAATAC | 53 | a0002c0002t0001g0009a0002c0002t0001g0010a0002c0002t0001g0012others(50): Show | 53 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.1453-25704_1453-25 others(11): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53183754 | |||||
| chr16:53183754
|
A | AAATACAA others(3): Show |
1 | a0001c0005t0004g0097 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1453-25709_1453-25 others(16): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53183754 | |||||
| chr16:53183940
|
T | C | 53 | a0002c0002t0001g0009a0002c0002t0001g0010a0002c0002t0001g0012others(50): Show | 53 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.1453-25542T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53183940 | ||||||
| chr16:53183966
|
A | C | 1 | a0003c0004t0001g0204 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1453-25516A>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53183966 | ||||||
| chr16:53183983
|
C | T | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1453-25499C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53183983 | ||||||
| chr16:53184089
|
C | T | 2 | a0001c0001t0003g0016a0002c0002t0001g0095 | 2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1453-25393C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53184089 | ||||||
| chr16:53184094
|
G | A | 2 | a0001c0005t0004g0097a0006c0009t0004g0107 | 2 | HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1453-25388G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53184094 | ||||||
| chr16:53184106
|
G | A | 1 | a0001c0005t0001g0215 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1453-25376G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53184106 | ||||||
| chr16:53184169
|
C | T | 2 | a0001c0001t0002g0171a0001c0001t0002g0175 | 2 | HG02451.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1453-25313C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53184169 | ||||||
| chr16:53184251
|
C | CTCTA | 144 | a0001c0001t0001g0124a0001c0001t0001g0159a0001c0001t0001g0225others(141): Show | 144 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.1453-25229_1453-25 others(10): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53184251 | |||||
| chr16:53184441
|
A | C | 2 | a0001c0005t0004g0104a0001c0005t0012g0229 | 2 | HG01167.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1453-25041A>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53184441 | ||||||
| chr16:53184455
|
A | G | 12 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(9): Show | 12 | HG01167.hp2 HG01884.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.1453-25027A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53184455 | ||||||
| chr16:53184494
|
G | A | 74 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(71): Show | 74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.1453-24988G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53184494 | ||||||
| chr16:53184579
|
A | G | 1 | a0001c0013t0001g0055 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1453-24903A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53184579 | ||||||
| chr16:53184597
|
A | G | 1 | a0001c0001t0001g0060 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1453-24885A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53184597 | ||||||
| chr16:53184931
|
A | T | 77 | a0001c0005t0001g0215a0001c0005t0004g0078a0001c0005t0004g0097others(74): Show | 77 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.1453-24551A>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53184931 | ||||||
| chr16:53185049
|
A | C | 1 | a0002c0019t0001g0180 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1453-24433A>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53185049 | ||||||
| chr16:53185055
|
G | A | 8 | a0002c0002t0001g0037a0002c0002t0001g0118a0002c0002t0001g0144others(5): Show | 8 | HG02135.hp2 HG02165.hp2 NA18962.hp2 others(5): Show |
intron_variant | MODIFIER | c.1453-24427G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53185055 | ||||||
| chr16:53185214
|
G | A | 74 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(71): Show | 74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.1453-24268G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53185214 | ||||||
| chr16:53185507
|
T | C | 184 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0021others(181): Show | 184 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.1453-23975T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53185507 | ||||||
| chr16:53185583
|
C | T | 2 | a0001c0001t0001g0210a0001c0005t0005g0032 | 2 | HG00140.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1453-23899C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53185583 | ||||||
| chr16:53185916
|
A | T | 1 | a0001c0001t0002g0175 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1453-23566A>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53185916 | ||||||
| chr16:53186040
|
G | A | 1 | a0001c0001t0001g0099 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1453-23442G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53186040 | ||||||
| chr16:53186083
|
C | T | 2 | a0001c0005t0004g0097a0006c0009t0004g0107 | 2 | HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1453-23399C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53186083 | ||||||
| chr16:53186105
|
C | G | 1 | a0001c0001t0003g0227 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1453-23377C>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53186105 | ||||||
| chr16:53186603
|
G | A | 6 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0168others(3): Show | 6 | HG01891.hp2 HG02451.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1453-22879G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53186603 | ||||||
| chr16:53186663
|
G | A | 65 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.1453-22819G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53186663 | ||||||
| chr16:53186730
|
C | G | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1453-22752C>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53186730 | ||||||
| chr16:53186993
|
C | A | 2 | a0001c0005t0004g0097a0006c0009t0004g0107 | 2 | HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1453-22489C>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53186993 | ||||||
| chr16:53187087
|
G | A | 2 | a0001c0005t0004g0097a0006c0009t0004g0107 | 2 | HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1453-22395G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53187087 | ||||||
| chr16:53187739
|
A | G | 1 | a0002c0002t0001g0102 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1453-21743A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53187739 | ||||||
| chr16:53187799
|
C | T | 1 | a0001c0001t0003g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1453-21683C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53187799 | ||||||
| chr16:53187830
|
G | C | 2 | a0003c0004t0001g0203a0003c0004t0001g0216 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1453-21652G>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53187830 | ||||||
| chr16:53188058
|
T | G | 65 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.1453-21424T>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53188058 | ||||||
| chr16:53188126
|
A | C | 1 | a0001c0005t0004g0169 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1453-21356A>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53188126 | ||||||
| chr16:53188270
|
A | G | 2 | a0003c0004t0001g0100a0003c0004t0001g0209 | 2 | HG01515.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1453-21212A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53188270 | ||||||
| chr16:53188288
|
A | G | 22 | a0001c0001t0001g0008a0001c0001t0001g0025a0001c0001t0001g0043others(19): Show | 22 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(19): Show |
intron_variant | MODIFIER | c.1453-21194A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53188288 | ||||||
| chr16:53188474
|
C | T | 41 | a0001c0001t0015g0166a0001c0003t0001g0158a0001c0003t0002g0002others(38): Show | 41 | HG00140.hp2 HG00558.hp2 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.1453-21008C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53188474 | ||||||
| chr16:53188507
|
C | T | 3 | a0004c0006t0001g0121a0004c0006t0001g0127a0004c0006t0001g0128 | 3 | NA18952.hp1 NA18989.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.1453-20975C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53188507 | ||||||
| chr16:53188602
|
C | CT | 29 | a0001c0001t0001g0026a0001c0001t0001g0031a0001c0001t0001g0045others(26): Show | 29 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.1453-20852dupT | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53188602 | |||||
| chr16:53188602
|
C | CTT | 49 | a0001c0001t0001g0225a0001c0003t0017g0181a0002c0002t0001g0010others(46): Show | 49 | HG00099.hp2 HG00323.hp1 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.1453-20853_1453-20 others(8): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53188602 | |||||
| chr16:53188602
|
C | CTTT | 12 | a0001c0005t0001g0215a0001c0005t0004g0078a0001c0005t0004g0104others(9): Show | 12 | HG01167.hp2 HG01884.hp2 HG02897.hp1 others(9): Show |
intron_variant | MODIFIER | c.1453-20854_1453-20 others(9): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53188602 | |||||
| chr16:53188602
|
C | CTTTT | 7 | a0001c0005t0004g0169a0001c0005t0004g0231a0001c0005t0004g0232others(4): Show | 7 | HG00408.hp1 HG02080.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1453-20855_1453-20 others(10): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53188602 | |||||
| chr16:53188602
|
CT | C | 8 | a0001c0001t0001g0051a0001c0001t0001g0092a0001c0001t0003g0220others(5): Show | 8 | HG00558.hp1 HG01884.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.1453-20852delT | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53188602 | |||||
| chr16:53188602
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0005t0005g0089 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1453-20861_1453-20 others(16): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53188602 | |||||
| chr16:53188602
|
CTTTTTTT others(4): Show |
C | 8 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(5): Show | 8 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.1453-20862_1453-20 others(17): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53188602 | |||||
| chr16:53188646
|
G | A | 6 | a0001c0005t0004g0232a0001c0005t0004g0233a0001c0005t0004g0234others(3): Show | 6 | HG02615.hp2 HG02897.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1453-20836G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53188646 | ||||||
| chr16:53188663
|
C | T | 1 | a0006c0009t0004g0107 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1453-20819C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53188663 | ||||||
| chr16:53188751
|
C | T | 3 | a0002c0002t0001g0087a0002c0002t0001g0088a0002c0002t0001g0136 | 3 | HG01255.hp2 HG01433.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.1453-20731C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53188751 | ||||||
| chr16:53188912
|
A | G | 1 | a0002c0002t0001g0205 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1453-20570A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53188912 | ||||||
| chr16:53188919
|
T | C | 1 | a0001c0003t0016g0039 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1453-20563T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53188919 | ||||||
| chr16:53189044
|
G | C | 2 | a0002c0002t0001g0138a0002c0002t0001g0140 | 2 | HG03017.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1453-20438G>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53189044 | ||||||
| chr16:53189085
|
C | T | 1 | a0001c0003t0002g0094 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1453-20397C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53189085 | ||||||
| chr16:53189124
|
C | A | 11 | a0001c0001t0001g0008a0001c0001t0001g0025a0001c0001t0001g0045others(8): Show | 11 | HG00558.hp1 HG00597.hp1 HG02300.hp2 others(8): Show |
intron_variant | MODIFIER | c.1453-20358C>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53189124 | ||||||
| chr16:53189223
|
A | C | 1 | a0001c0001t0001g0160 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1453-20259A>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53189223 | ||||||
| chr16:53189256
|
A | G | 1 | a0001c0003t0002g0094 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1453-20226A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53189256 | ||||||
| chr16:53189399
|
C | A | 9 | a0001c0001t0003g0022a0001c0001t0003g0079a0001c0001t0003g0105others(6): Show | 9 | HG01891.hp1 HG02257.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1453-20083C>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53189399 | ||||||
| chr16:53189522
|
G | A | 10 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0231others(7): Show | 10 | HG01167.hp2 HG01884.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1453-19960G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53189522 | ||||||
| chr16:53189534
|
C | A | 64 | a0001c0001t0001g0091a0001c0001t0002g0171a0001c0001t0002g0175others(61): Show | 64 | HG00140.hp2 HG00621.hp2 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.1453-19948C>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53189534 | ||||||
| chr16:53189538
|
A | C | 65 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.1453-19944A>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53189538 | ||||||
| chr16:53189559
|
T | A | 10 | a0001c0001t0020g0101a0001c0005t0005g0017a0001c0005t0005g0018others(7): Show | 10 | HG02257.hp2 HG02622.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1453-19923T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53189559 | ||||||
| chr16:53190030
|
A | C | 2 | a0001c0001t0001g0124a0001c0001t0001g0225 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1453-19452A>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53190030 | ||||||
| chr16:53190109
|
T | C | 2 | a0002c0002t0001g0019a0002c0002t0001g0020 | 2 | NA18939.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.1453-19373T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53190109 | ||||||
| chr16:53190199
|
A | G | 1 | a0002c0002t0001g0108 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1453-19283A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53190199 | ||||||
| chr16:53190209
|
G | T | 1 | a0001c0001t0001g0060 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1453-19273G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53190209 | ||||||
| chr16:53190275
|
G | T | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1453-19207G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53190275 | ||||||
| chr16:53190425
|
C | T | 1 | a0002c0002t0001g0063 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1453-19057C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53190425 | ||||||
| chr16:53190516
|
C | G | 1 | a0001c0001t0001g0124 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1453-18966C>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53190516 | ||||||
| chr16:53191431
|
C | G | 2 | a0001c0005t0004g0097a0006c0009t0004g0107 | 2 | HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1453-18051C>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53191431 | ||||||
| chr16:53191448
|
C | G | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1453-18034C>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53191448 | ||||||
| chr16:53191469
|
T | G | 7 | a0001c0005t0004g0231a0001c0005t0004g0232a0001c0005t0004g0233others(4): Show | 7 | HG02615.hp2 HG02897.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1453-18013T>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53191469 | ||||||
| chr16:53192066
|
C | CA | 19 | a0001c0001t0002g0171a0001c0001t0003g0022a0001c0003t0002g0152others(16): Show | 19 | HG00099.hp2 HG01167.hp2 HG01515.hp1 others(16): Show |
intron_variant | MODIFIER | c.1453-17399dupA | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53192066 | |||||
| chr16:53192080
|
A | AAG | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1453-17401_1453-17 others(8): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53192080 | |||||
| chr16:53192144
|
C | T | 1 | a0001c0001t0002g0175 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1453-17338C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53192144 | ||||||
| chr16:53192186
|
A | G | 74 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(71): Show | 74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.1453-17296A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53192186 | ||||||
| chr16:53192256
|
C | A | 1 | a0001c0005t0004g0097 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1453-17226C>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53192256 | ||||||
| chr16:53192307
|
A | T | 2 | a0001c0001t0001g0092a0001c0008t0001g0077 | 2 | HG02976.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1453-17175A>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53192307 | ||||||
| chr16:53192729
|
G | A | 1 | a0001c0001t0001g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1453-16753G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53192729 | ||||||
| chr16:53192741
|
T | C | 20 | a0001c0001t0003g0016a0001c0001t0003g0022a0001c0001t0003g0079others(17): Show | 20 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.1453-16741T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53192741 | ||||||
| chr16:53193033
|
C | CT | 65 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.1453-16447dupT | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53193033 | |||||
| chr16:53193176
|
A | G | 237 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0021others(234): Show | 237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.1453-16306A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53193176 | ||||||
| chr16:53193303
|
G | T | 53 | a0002c0002t0001g0009a0002c0002t0001g0010a0002c0002t0001g0012others(50): Show | 53 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.1453-16179G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53193303 | ||||||
| chr16:53193305
|
C | T | 2 | a0001c0003t0002g0059a0001c0003t0002g0224 | 2 | HG02717.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1453-16177C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53193305 | ||||||
| chr16:53193306
|
G | A | 53 | a0002c0002t0001g0009a0002c0002t0001g0010a0002c0002t0001g0012others(50): Show | 53 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.1453-16176G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53193306 | ||||||
| chr16:53193315
|
G | A | 9 | a0001c0001t0003g0096a0001c0001t0003g0133a0001c0001t0003g0184others(6): Show | 9 | HG02055.hp1 HG02109.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1453-16167G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53193315 | ||||||
| chr16:53193422
|
G | A | 65 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.1453-16060G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53193422 | ||||||
| chr16:53193456
|
GA | G | 65 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.1453-16015delA | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53193456 | |||||
| chr16:53193469
|
C | A | 65 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.1453-16013C>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53193469 | ||||||
| chr16:53193761
|
T | A | 1 | a0001c0001t0001g0025 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1453-15721T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53193761 | ||||||
| chr16:53193880
|
T | C | 19 | a0001c0001t0003g0022a0001c0001t0003g0079a0001c0001t0003g0096others(16): Show | 19 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.1453-15602T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53193880 | ||||||
| chr16:53193900
|
A | T | 2 | a0001c0003t0002g0059a0001c0003t0002g0224 | 2 | HG02717.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1453-15582A>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53193900 | ||||||
| chr16:53193961
|
G | A | 2 | a0001c0005t0004g0097a0006c0009t0004g0107 | 2 | HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1453-15521G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53193961 | ||||||
| chr16:53194227
|
TA | T | 6 | a0001c0003t0013g0186a0002c0002t0001g0035a0002c0002t0001g0049others(3): Show | 6 | HG01099.hp1 HG01168.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.1453-15241delA | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53194227 | |||||
| chr16:53194250
|
A | C | 2 | a0001c0005t0004g0097a0006c0009t0004g0107 | 2 | HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1453-15232A>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53194250 | ||||||
| chr16:53194361
|
G | C | 1 | a0001c0001t0001g0066 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1453-15121G>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53194361 | ||||||
| chr16:53194486
|
A | G | 1 | a0001c0003t0002g0170 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1453-14996A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53194486 | ||||||
| chr16:53194521
|
G | A | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1453-14961G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53194521 | ||||||
| chr16:53194899
|
TAATAA | T | 2 | a0001c0005t0004g0097a0006c0009t0004g0107 | 2 | HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1453-14579_1453-14 others(11): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53194899 | |||||
| chr16:53194945
|
G | T | 1 | a0001c0001t0003g0079 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1453-14537G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53194945 | ||||||
| chr16:53195288
|
G | C | 2 | a0001c0005t0004g0097a0006c0009t0004g0107 | 2 | HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1453-14194G>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53195288 | ||||||
| chr16:53195329
|
A | C | 66 | a0001c0001t0001g0188a0001c0005t0004g0078a0001c0005t0004g0104others(63): Show | 66 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(63): Show |
intron_variant | MODIFIER | c.1453-14153A>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53195329 | ||||||
| chr16:53195389
|
A | G | 6 | a0002c0002t0001g0106a0002c0002t0001g0109a0002c0002t0001g0113others(3): Show | 6 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1453-14093A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53195389 | ||||||
| chr16:53195637
|
C | G | 53 | a0002c0002t0001g0009a0002c0002t0001g0010a0002c0002t0001g0012others(50): Show | 53 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.1453-13845C>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53195637 | ||||||
| chr16:53195763
|
C | CT | 22 | a0001c0001t0001g0160a0001c0001t0003g0016a0001c0001t0003g0096others(19): Show | 22 | HG00099.hp1 HG02055.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.1453-13702dupT | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53195763 | |||||
| chr16:53195763
|
C | CTT | 11 | a0001c0001t0003g0022a0001c0001t0003g0079a0001c0001t0003g0105others(8): Show | 11 | HG01891.hp1 HG02257.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1453-13703_1453-13 others(8): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53195763 | |||||
| chr16:53195872
|
C | G | 2 | a0001c0001t0002g0171a0001c0001t0002g0175 | 2 | HG02451.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1453-13610C>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53195872 | ||||||
| chr16:53196006
|
C | T | 1 | a0001c0003t0002g0152 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1453-13476C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53196006 | ||||||
| chr16:53196112
|
T | C | 1 | a0001c0005t0004g0169 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1453-13370T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53196112 | ||||||
| chr16:53196194
|
G | C | 44 | a0001c0001t0001g0068a0001c0001t0002g0171a0001c0001t0002g0175others(41): Show | 44 | HG00140.hp2 HG00558.hp2 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.1453-13288G>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53196194 | ||||||
| chr16:53196430
|
T | C | 74 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(71): Show | 74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.1453-13052T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53196430 | ||||||
| chr16:53196746
|
A | G | 65 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.1453-12736A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53196746 | ||||||
| chr16:53196918
|
A | C | 2 | a0001c0005t0004g0097a0006c0009t0004g0107 | 2 | HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1453-12564A>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53196918 | ||||||
| chr16:53196939
|
G | A | 7 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0168others(4): Show | 7 | HG01891.hp2 HG02451.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1453-12543G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53196939 | ||||||
| chr16:53197107
|
T | A | 5 | a0001c0003t0002g0028a0001c0003t0002g0029a0001c0003t0002g0125others(2): Show | 5 | HG02129.hp1 NA18955.hp1 NA18961.hp1 others(2): Show |
intron_variant | MODIFIER | c.1453-12375T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53197107 | ||||||
| chr16:53197172
|
C | G | 1 | a0001c0003t0017g0181 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1453-12310C>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53197172 | ||||||
| chr16:53197185
|
A | T | 1 | a0001c0003t0019g0004 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1453-12297A>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53197185 | ||||||
| chr16:53197300
|
A | C | 12 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(9): Show | 12 | HG01167.hp2 HG01884.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.1453-12182A>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53197300 | ||||||
| chr16:53197303
|
A | G | 1 | a0001c0001t0003g0112 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1453-12179A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53197303 | ||||||
| chr16:53197400
|
T | C | 1 | a0003c0004t0001g0162 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1453-12082T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53197400 | ||||||
| chr16:53197475
|
A | G | 2 | a0001c0005t0004g0097a0006c0009t0004g0107 | 2 | HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1453-12007A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53197475 | ||||||
| chr16:53197558
|
TTTTAAAT others(1): Show |
T | 19 | a0001c0001t0003g0022a0001c0001t0003g0079a0001c0001t0003g0096others(16): Show | 19 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.1453-11921_1453-11 others(14): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53197558 | |||||
| chr16:53197606
|
A | G | 1 | a0001c0005t0004g0097 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1453-11876A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53197606 | ||||||
| chr16:53197660
|
C | CT | 65 | a0001c0001t0001g0218a0001c0003t0002g0086a0001c0005t0004g0078others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.1453-11808dupT | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53197660 | |||||
| chr16:53197720
|
G | C | 2 | a0001c0001t0002g0171a0001c0001t0002g0175 | 2 | HG02451.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1453-11762G>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53197720 | ||||||
| chr16:53197869
|
G | A | 1 | a0003c0004t0001g0192 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1453-11613G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53197869 | ||||||
| chr16:53197877
|
C | T | 1 | a0008c0011t0003g0062 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1453-11605C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53197877 | ||||||
| chr16:53197953
|
C | T | 1 | a0001c0005t0018g0001 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1453-11529C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53197953 | ||||||
| chr16:53197961
|
C | T | 2 | a0002c0002t0001g0019a0002c0002t0001g0020 | 2 | NA18939.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.1453-11521C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53197961 | ||||||
| chr16:53198047
|
G | A | 65 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.1453-11435G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53198047 | ||||||
| chr16:53198101
|
C | T | 143 | a0001c0001t0001g0068a0001c0001t0001g0159a0001c0001t0002g0171others(140): Show | 143 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.1453-11381C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53198101 | ||||||
| chr16:53198190
|
A | G | 2 | a0001c0001t0001g0092a0001c0008t0001g0077 | 2 | HG02976.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1453-11292A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53198190 | ||||||
| chr16:53198229
|
C | T | 68 | a0001c0005t0001g0215a0001c0005t0004g0078a0001c0005t0004g0097others(65): Show | 68 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.1453-11253C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53198229 | ||||||
| chr16:53198315
|
A | AT | 24 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0056others(21): Show | 24 | HG00099.hp1 HG00621.hp1 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1453-11145dupT | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53198315 | |||||
| chr16:53198315
|
A | ATT | 51 | a0001c0001t0001g0068a0001c0001t0001g0159a0001c0001t0015g0166others(48): Show | 51 | HG00140.hp2 HG00558.hp2 HG01074.hp1 others(48): Show |
intron_variant | MODIFIER | c.1453-11146_1453-11 others(8): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53198315 | |||||
| chr16:53198315
|
AT | A | 6 | a0001c0001t0001g0072a0001c0014t0001g0115a0002c0002t0001g0129others(3): Show | 6 | HG00323.hp1 HG01074.hp2 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.1453-11145delT | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53198315 | |||||
| chr16:53198390
|
G | T | 1 | a0002c0002t0001g0144 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1453-11092G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53198390 | ||||||
| chr16:53198421
|
G | A | 65 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.1453-11061G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53198421 | ||||||
| chr16:53198439
|
G | C | 2 | a0001c0005t0004g0097a0006c0009t0004g0107 | 2 | HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1453-11043G>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53198439 | ||||||
| chr16:53198574
|
C | G | 1 | a0008c0011t0003g0062 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1453-10908C>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53198574 | ||||||
| chr16:53198575
|
C | T | 1 | a0008c0011t0003g0062 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1453-10907C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53198575 | ||||||
| chr16:53198763
|
A | T | 237 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0021others(234): Show | 237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.1453-10719A>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53198763 | ||||||
| chr16:53198906
|
G | A | 1 | a0001c0005t0004g0236 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1453-10576G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53198906 | ||||||
| chr16:53199308
|
T | A | 75 | a0001c0001t0003g0112a0001c0005t0004g0078a0001c0005t0004g0104others(72): Show | 75 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.1453-10174T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53199308 | ||||||
| chr16:53199363
|
T | C | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1453-10119T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53199363 | ||||||
| chr16:53199376
|
T | G | 1 | a0001c0005t0001g0215 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1453-10106T>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53199376 | ||||||
| chr16:53199428
|
C | T | 1 | a0001c0005t0001g0215 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1453-10054C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53199428 | ||||||
| chr16:53199751
|
T | C | 77 | a0001c0005t0001g0215a0001c0005t0004g0078a0001c0005t0004g0097others(74): Show | 77 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.1453-9731T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53199751 | ||||||
| chr16:53199988
|
C | T | 1 | a0001c0001t0007g0103 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1453-9494C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53199988 | ||||||
| chr16:53200007
|
G | A | 3 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0012g0229 | 3 | HG01167.hp2 HG01884.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1453-9475G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53200007 | ||||||
| chr16:53200179
|
T | G | 1 | a0001c0003t0001g0158 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1453-9303T>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53200179 | ||||||
| chr16:53200263
|
T | C | 143 | a0001c0001t0001g0068a0001c0001t0001g0159a0001c0001t0002g0171others(140): Show | 143 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.1453-9219T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53200263 | ||||||
| chr16:53200268
|
G | A | 2 | a0001c0005t0004g0097a0006c0009t0004g0107 | 2 | HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1453-9214G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53200268 | ||||||
| chr16:53200318
|
C | A | 7 | a0001c0001t0003g0133a0001c0001t0003g0184a0001c0001t0003g0220others(4): Show | 7 | HG02055.hp1 HG02109.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1453-9164C>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53200318 | ||||||
| chr16:53200370
|
C | CA | 53 | a0001c0001t0001g0043a0001c0001t0001g0064a0001c0001t0001g0068others(50): Show | 53 | HG00558.hp2 HG00597.hp1 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.1453-9092dupA | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53200370 | |||||
| chr16:53200370
|
C | CAA | 11 | a0001c0001t0001g0159a0001c0001t0001g0188a0001c0003t0002g0003others(8): Show | 11 | HG00140.hp2 HG00621.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.1453-9093_1453-909 others(6): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53200370 | |||||
| chr16:53200370
|
CA | C | 62 | a0001c0001t0001g0014a0001c0001t0001g0026a0001c0001t0001g0081others(59): Show | 62 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(59): Show |
intron_variant | MODIFIER | c.1453-9092delA | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53200370 | |||||
| chr16:53200370
|
CAA | C | 5 | a0001c0005t0005g0018a0001c0005t0005g0135a0001c0005t0005g0151others(2): Show | 5 | HG02622.hp2 NA18981.hp2 NA19068.hp1 others(2): Show |
intron_variant | MODIFIER | c.1453-9093_1453-909 others(6): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53200370 | |||||
| chr16:53200390
|
A | AAC | 5 | a0001c0001t0003g0105a0001c0001t0003g0167a0001c0001t0003g0172others(2): Show | 5 | HG02055.hp1 HG02257.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1453-9092_1453-909 others(6): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53200390 | ||||||
| chr16:53200390
|
A | AC | 13 | a0001c0001t0003g0022a0001c0001t0003g0079a0001c0001t0003g0112others(10): Show | 13 | HG01891.hp1 HG02109.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.1453-9090dupC | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53200390 | |||||
| chr16:53200390
|
A | C | 1 | a0001c0001t0003g0096 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1453-9092A>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53200390 | ||||||
| chr16:53200582
|
T | A | 2 | a0001c0003t0002g0083a0001c0003t0017g0181 | 2 | HG03017.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1453-8900T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53200582 | ||||||
| chr16:53200776
|
G | A | 10 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0231others(7): Show | 10 | HG01167.hp2 HG01884.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1453-8706G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53200776 | ||||||
| chr16:53200924
|
C | T | 2 | a0001c0005t0004g0097a0006c0009t0004g0107 | 2 | HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1453-8558C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53200924 | ||||||
| chr16:53201119
|
A | G | 1 | a0001c0005t0004g0097 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1453-8363A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53201119 | ||||||
| chr16:53201169
|
A | G | 123 | a0001c0001t0001g0068a0001c0001t0001g0159a0001c0001t0002g0171others(120): Show | 123 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.1453-8313A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53201169 | ||||||
| chr16:53201509
|
G | A | 65 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.1453-7973G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53201509 | ||||||
| chr16:53201556
|
C | T | 1 | a0001c0001t0001g0092 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1453-7926C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53201556 | ||||||
| chr16:53201617
|
A | T | 2 | a0001c0003t0002g0083a0001c0003t0017g0181 | 2 | HG03017.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1453-7865A>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53201617 | ||||||
| chr16:53201633
|
A | G | 9 | a0001c0001t0001g0159a0003c0004t0001g0007a0003c0004t0001g0030others(6): Show | 9 | HG00597.hp2 HG04199.hp2 NA18950.hp2 others(6): Show |
intron_variant | MODIFIER | c.1453-7849A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53201633 | ||||||
| chr16:53201707
|
T | G | 1 | a0001c0005t0001g0215 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1453-7775T>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53201707 | ||||||
| chr16:53201854
|
T | G | 17 | a0001c0001t0003g0022a0001c0001t0003g0079a0001c0001t0003g0105others(14): Show | 17 | HG01891.hp1 HG02257.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.1453-7628T>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53201854 | ||||||
| chr16:53201854
|
T | TG | 8 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0061others(5): Show | 8 | HG02257.hp2 HG02622.hp2 HG03688.hp2 others(5): Show |
intron_variant | MODIFIER | c.1453-7628_1453-762 others(5): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53201854 | ||||||
| chr16:53201931
|
T | C | 3 | a0001c0005t0001g0215a0001c0005t0004g0097a0006c0009t0004g0107 | 3 | HG01884.hp1 HG03516.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.1453-7551T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53201931 | ||||||
| chr16:53201992
|
C | A | 65 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.1453-7490C>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53201992 | ||||||
| chr16:53202032
|
AT | A | 66 | a0001c0001t0003g0079a0001c0005t0001g0215a0001c0005t0004g0078others(63): Show | 66 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(63): Show |
intron_variant | MODIFIER | c.1453-7439delT | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53202032 | |||||
| chr16:53202044
|
A | G | 1 | a0008c0011t0003g0062 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1453-7438A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53202044 | ||||||
| chr16:53202243
|
T | C | 65 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.1453-7239T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53202243 | ||||||
| chr16:53202253
|
G | T | 1 | a0001c0001t0001g0178 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1453-7229G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53202253 | ||||||
| chr16:53202274
|
A | G | 1 | a0003c0004t0001g0197 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1453-7208A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53202274 | ||||||
| chr16:53202502
|
G | A | 1 | a0001c0001t0001g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1453-6980G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53202502 | ||||||
| chr16:53202516
|
A | G | 2 | a0001c0001t0007g0103a0001c0001t0007g0122 | 2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1453-6966A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53202516 | ||||||
| chr16:53202561
|
TG | T | 2 | a0001c0005t0004g0233a0001c0005t0004g0234 | 2 | HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1453-6920delG | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53202561 | ||||||
| chr16:53202749
|
G | A | 1 | a0003c0004t0001g0030 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1453-6733G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53202749 | ||||||
| chr16:53202766
|
C | T | 6 | a0001c0001t0001g0056a0001c0001t0001g0071a0001c0001t0001g0072others(3): Show | 6 | HG00140.hp1 HG00323.hp2 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.1453-6716C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53202766 | ||||||
| chr16:53202847
|
C | A | 1 | a0001c0005t0001g0215 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1453-6635C>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53202847 | ||||||
| chr16:53203139
|
T | C | 1 | a0001c0003t0002g0028 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1453-6343T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53203139 | ||||||
| chr16:53203478
|
G | T | 1 | a0001c0001t0003g0176 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1453-6004G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53203478 | ||||||
| chr16:53203893
|
G | A | 1 | a0002c0002t0001g0164 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1453-5589G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53203893 | ||||||
| chr16:53203941
|
G | A | 1 | a0001c0001t0003g0220 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1453-5541G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53203941 | ||||||
| chr16:53204019
|
A | G | 2 | a0003c0004t0001g0134a0003c0004t0001g0141 | 2 | HG02895.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1453-5463A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53204019 | ||||||
| chr16:53204023
|
C | CA | 9 | a0001c0001t0001g0038a0001c0001t0001g0099a0001c0001t0001g0124others(6): Show | 9 | HG00099.hp1 HG00609.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.1453-5433dupA | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53204023 | |||||
| chr16:53204023
|
CA | C | 7 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0002g0171others(4): Show | 7 | HG01074.hp2 HG02280.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1453-5433delA | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53204023 | |||||
| chr16:53204023
|
CAAAAA | C | 10 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0231others(7): Show | 10 | HG01167.hp2 HG01884.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1453-5437_1453-543 others(9): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53204023 | |||||
| chr16:53204044
|
A | ATATATAT | 2 | a0001c0005t0005g0032a0001c0005t0005g0061 | 2 | HG02970.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.1453-5438_1453-543 others(11): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53204044 | ||||||
| chr16:53204045
|
AAAAAT | A | 41 | a0002c0002t0001g0009a0002c0002t0001g0010a0002c0002t0001g0012others(38): Show | 41 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(38): Show |
intron_variant | MODIFIER | c.1453-5435_1453-543 others(9): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53204045 | |||||
| chr16:53204046
|
A | AT | 3 | a0001c0001t0003g0172a0001c0001t0003g0183a0001c0001t0003g0220 | 3 | HG02055.hp1 HG02257.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1453-5436_1453-543 others(5): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53204046 | ||||||
| chr16:53204046
|
A | ATATATAT | 4 | a0001c0005t0005g0089a0001c0005t0005g0135a0001c0005t0005g0151others(1): Show | 4 | HG04184.hp2 NA18981.hp2 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.1453-5436_1453-543 others(11): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53204046 | ||||||
| chr16:53204046
|
A | T | 7 | a0001c0001t0003g0221a0001c0005t0001g0215a0001c0005t0005g0017others(4): Show | 7 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1453-5436A>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53204046 | ||||||
| chr16:53204046
|
AAAAT | A | 6 | a0001c0003t0002g0023a0001c0003t0002g0046a0001c0003t0002g0047others(3): Show | 6 | NA18961.hp1 NA18972.hp2 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.1453-5434_1453-543 others(8): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53204046 | |||||
| chr16:53204046
|
AAAATAT | A | 22 | a0001c0001t0001g0068a0001c0001t0015g0166a0001c0003t0001g0158others(19): Show | 22 | HG00558.hp2 HG00621.hp2 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.1453-5434_1453-542 others(10): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53204046 | |||||
| chr16:53204047
|
AAATAT | A | 8 | a0001c0003t0002g0015a0001c0003t0002g0028a0001c0003t0002g0033others(5): Show | 8 | HG00140.hp2 HG02027.hp2 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.1453-5433_1453-542 others(9): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53204047 | |||||
| chr16:53204048
|
A | T | 39 | a0001c0001t0001g0179a0001c0001t0003g0022a0001c0001t0003g0079others(36): Show | 39 | HG00735.hp2 HG01257.hp2 HG01891.hp1 others(36): Show |
intron_variant | MODIFIER | c.1453-5434A>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53204048 | ||||||
| chr16:53204049
|
AT | A | 2 | a0002c0002t0001g0048a0002c0002t0001g0049 | 2 | HG01099.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.1453-5432delT | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53204049 | ||||||
| chr16:53204050
|
T | A | 3 | a0001c0001t0001g0014a0001c0001t0009g0050a0001c0005t0018g0001 | 3 | HG03195.hp1 HG03579.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.1453-5432T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53204050 | ||||||
| chr16:53204052
|
T | A | 1 | a0001c0005t0018g0001 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1453-5430T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53204052 | ||||||
| chr16:53204054
|
TATATACA others(5): Show |
T | 8 | a0002c0002t0001g0054a0002c0002t0001g0144a0002c0002t0001g0145others(5): Show | 8 | HG00735.hp2 HG02135.hp2 HG02165.hp2 others(5): Show |
intron_variant | MODIFIER | c.1453-5426_1453-541 others(16): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53204054 | |||||
| chr16:53204056
|
T | C | 1 | a0001c0005t0001g0215 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1453-5426T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53204056 | ||||||
| chr16:53204056
|
TATAC | T | 2 | a0001c0003t0002g0073a0001c0003t0002g0202 | 2 | HG01074.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.1453-5424_1453-542 others(8): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53204056 | |||||
| chr16:53204058
|
T | C | 8 | a0001c0001t0001g0182a0001c0005t0001g0215a0001c0005t0005g0032others(5): Show | 8 | HG02615.hp1 HG02970.hp1 HG03688.hp2 others(5): Show |
intron_variant | MODIFIER | c.1453-5424T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53204058 | ||||||
| chr16:53204058
|
T | TAC | 6 | a0001c0001t0001g0090a0001c0001t0001g0111a0001c0001t0001g0159others(3): Show | 6 | HG00597.hp2 HG00733.hp1 HG01109.hp2 others(3): Show |
intron_variant | MODIFIER | c.1453-5396_1453-539 others(6): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53204058 | |||||
| chr16:53204058
|
T | TATATATA others(1): Show |
3 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0011g0228 | 3 | HG02257.hp2 HG02622.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1453-5423_1453-542 others(12): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53204058 | |||||
| chr16:53204058
|
TAC | T | 2 | a0001c0001t0003g0016a0003c0004t0001g0100 | 2 | HG01515.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1453-5396_1453-539 others(6): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53204058 | |||||
| chr16:53204058
|
TACAC | T | 11 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0231others(8): Show | 11 | HG01167.hp2 HG01884.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.1453-5398_1453-539 others(8): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53204058 | |||||
| chr16:53204058
|
TACACACA others(1): Show |
T | 45 | a0002c0002t0001g0009a0002c0002t0001g0010a0002c0002t0001g0012others(42): Show | 45 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(42): Show |
intron_variant | MODIFIER | c.1453-5402_1453-539 others(12): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53204058 | |||||
| chr16:53204060
|
C | T | 38 | a0001c0001t0001g0068a0001c0001t0002g0171a0001c0001t0002g0175others(35): Show | 38 | HG00140.hp2 HG00558.hp2 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.1453-5422C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53204060 | ||||||
| chr16:53204062
|
C | T | 2 | a0001c0005t0004g0169a0001c0005t0018g0001 | 2 | HG03139.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1453-5420C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53204062 | ||||||
| chr16:53204064
|
C | T | 12 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(9): Show | 12 | HG01167.hp2 HG01884.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.1453-5418C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53204064 | ||||||
| chr16:53204066
|
C | T | 2 | a0001c0005t0004g0169a0001c0005t0018g0001 | 2 | HG03139.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1453-5416C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53204066 | ||||||
| chr16:53204107
|
TTCTTTA | T | 20 | a0001c0001t0003g0016a0001c0001t0003g0022a0001c0001t0003g0079others(17): Show | 20 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.1453-5371_1453-536 others(10): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53204107 | |||||
| chr16:53204123
|
C | CGT | 33 | a0001c0001t0001g0068a0001c0001t0001g0092a0001c0001t0001g0173others(30): Show | 33 | HG00140.hp2 HG00597.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.1453-5334_1453-533 others(6): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53204123 | |||||
| chr16:53204123
|
C | CGTGT | 8 | a0001c0003t0002g0023a0001c0003t0002g0046a0001c0005t0005g0018others(5): Show | 8 | HG03688.hp2 HG04184.hp2 NA18974.hp1 others(5): Show |
intron_variant | MODIFIER | c.1453-5336_1453-533 others(8): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53204123 | |||||
| chr16:53204123
|
C | CGTGTGT | 2 | a0001c0005t0001g0215a0001c0005t0005g0017 | 2 | HG02257.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.1453-5338_1453-533 others(10): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53204123 | |||||
| chr16:53204123
|
CGT | C | 19 | a0001c0001t0003g0022a0001c0001t0003g0079a0001c0001t0003g0096others(16): Show | 19 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.1453-5334_1453-533 others(6): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53204123 | |||||
| chr16:53204123
|
CGTGTGT | C | 65 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.1453-5338_1453-533 others(10): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53204123 | |||||
| chr16:53204341
|
T | G | 77 | a0001c0005t0001g0215a0001c0005t0004g0078a0001c0005t0004g0097others(74): Show | 77 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.1453-5141T>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53204341 | ||||||
| chr16:53204428
|
C | T | 74 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(71): Show | 74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.1453-5054C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53204428 | ||||||
| chr16:53204714
|
C | T | 9 | a0001c0001t0003g0096a0001c0001t0003g0133a0001c0001t0003g0184others(6): Show | 9 | HG02055.hp1 HG02109.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1453-4768C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53204714 | ||||||
| chr16:53204836
|
T | C | 10 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0231others(7): Show | 10 | HG01167.hp2 HG01884.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1453-4646T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53204836 | ||||||
| chr16:53204891
|
T | A | 1 | a0001c0001t0003g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1453-4591T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53204891 | ||||||
| chr16:53204892
|
A | T | 1 | a0001c0001t0003g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1453-4590A>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53204892 | ||||||
| chr16:53204901
|
T | C | 1 | a0001c0001t0003g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1453-4581T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53204901 | ||||||
| chr16:53204902
|
G | A | 1 | a0001c0001t0003g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1453-4580G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53204902 | ||||||
| chr16:53205093
|
T | G | 12 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(9): Show | 12 | HG01167.hp2 HG01884.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.1453-4389T>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53205093 | ||||||
| chr16:53205165
|
T | C | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1453-4317T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53205165 | ||||||
| chr16:53205249
|
C | G | 53 | a0002c0002t0001g0009a0002c0002t0001g0010a0002c0002t0001g0012others(50): Show | 53 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.1453-4233C>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53205249 | ||||||
| chr16:53205504
|
A | G | 1 | a0001c0003t0002g0023 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1453-3978A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53205504 | ||||||
| chr16:53206014
|
A | G | 1 | a0006c0009t0004g0107 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1453-3468A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53206014 | ||||||
| chr16:53206244
|
C | T | 1 | a0002c0002t0001g0063 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1453-3238C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53206244 | ||||||
| chr16:53206353
|
C | T | 1 | a0008c0011t0003g0062 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1453-3129C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53206353 | ||||||
| chr16:53206359
|
G | GA | 25 | a0001c0001t0001g0031a0001c0001t0001g0091a0001c0001t0003g0079others(22): Show | 25 | HG00733.hp1 HG01891.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.1453-3108dupA | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53206359 | |||||
| chr16:53206359
|
GA | G | 11 | a0001c0001t0001g0045a0001c0005t0001g0215a0001c0005t0005g0017others(8): Show | 11 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(8): Show |
intron_variant | MODIFIER | c.1453-3108delA | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53206359 | |||||
| chr16:53206373
|
AAC | A | 65 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.1453-3108_1453-310 others(6): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53206373 | ||||||
| chr16:53206497
|
A | G | 65 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.1453-2985A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53206497 | ||||||
| chr16:53206547
|
A | G | 2 | a0001c0005t0004g0097a0006c0009t0004g0107 | 2 | HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1453-2935A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53206547 | ||||||
| chr16:53206697
|
A | G | 74 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(71): Show | 74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.1453-2785A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53206697 | ||||||
| chr16:53206721
|
T | C | 1 | a0001c0005t0001g0215 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1453-2761T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53206721 | ||||||
| chr16:53206869
|
G | A | 1 | a0001c0005t0004g0235 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1453-2613G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53206869 | ||||||
| chr16:53206934
|
A | G | 12 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(9): Show | 12 | HG01167.hp2 HG01884.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.1453-2548A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53206934 | ||||||
| chr16:53207123
|
G | T | 1 | a0008c0011t0003g0062 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1453-2359G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53207123 | ||||||
| chr16:53207487
|
T | G | 1 | a0001c0005t0004g0169 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1453-1995T>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53207487 | ||||||
| chr16:53207647
|
T | TCAGCTAT others(330): Show |
1 | a0001c0005t0004g0169 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1453-1825_1453-182 others(341): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53207647 | |||||
| chr16:53207647
|
T | TCAGCTAT others(337): Show |
1 | a0001c0005t0018g0001 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1453-1825_1453-182 others(348): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53207647 | |||||
| chr16:53207786
|
A | AT | 8 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0061others(5): Show | 8 | HG02257.hp2 HG02622.hp2 HG03688.hp2 others(5): Show |
intron_variant | MODIFIER | c.1453-1685dupT | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr16 | 53207786 | |||||
| chr16:53207851
|
G | A | 65 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.1453-1631G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53207851 | ||||||
| chr16:53207990
|
T | C | 1 | a0001c0001t0001g0188 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1453-1492T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53207990 | ||||||
| chr16:53209028
|
G | A | 1 | a0001c0005t0001g0215 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1453-454G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53209028 | ||||||
| chr16:53209040
|
T | C | 74 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(71): Show | 74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.1453-442T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53209040 | ||||||
| chr16:53209046
|
T | G | 2 | a0001c0003t0002g0059a0001c0003t0002g0224 | 2 | HG02717.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1453-436T>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53209046 | ||||||
| chr16:53209248
|
T | C | 1 | a0001c0005t0001g0215 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1453-234T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53209248 | ||||||
| chr16:53209267
|
C | A | 1 | a0001c0001t0001g0056 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1453-215C>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53209267 | ||||||
| chr16:53209305
|
G | T | 1 | a0002c0002t0001g0102 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1453-177G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53209305 | ||||||
| chr16:53209351
|
G | T | 65 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.1453-131G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 2/38 | chr16 | 53209351 | ||||||
| chr16:53210290
|
C | CA | 14 | a0001c0001t0001g0056a0001c0001t0001g0099a0001c0001t0001g0117others(11): Show | 14 | HG01099.hp1 HG02055.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.1784+493dupA | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr16 | 53210290 | |||||
| chr16:53210290
|
CA | C | 76 | a0001c0001t0001g0008a0001c0001t0001g0052a0001c0001t0001g0060others(73): Show | 76 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.1784+493delA | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr16 | 53210290 | |||||
| chr16:53210354
|
A | C | 1 | a0001c0001t0001g0075 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1784+541A>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53210354 | ||||||
| chr16:53210650
|
G | A | 19 | a0001c0001t0003g0022a0001c0001t0003g0079a0001c0001t0003g0096others(16): Show | 19 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.1784+837G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53210650 | ||||||
| chr16:53210889
|
A | G | 2 | a0001c0001t0001g0038a0001c0001t0001g0098 | 2 | HG00609.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.1784+1076A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53210889 | ||||||
| chr16:53210899
|
T | C | 2 | a0001c0005t0004g0169a0001c0005t0018g0001 | 2 | HG03139.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1784+1086T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53210899 | ||||||
| chr16:53210980
|
A | G | 1 | a0001c0001t0001g0210 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1784+1167A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53210980 | ||||||
| chr16:53211138
|
A | G | 1 | a0002c0002t0001g0063 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1784+1325A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53211138 | ||||||
| chr16:53211194
|
T | G | 3 | a0001c0001t0001g0052a0001c0001t0001g0060a0001c0001t0001g0075 | 3 | NA18946.hp1 NA18972.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.1784+1381T>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53211194 | ||||||
| chr16:53211227
|
A | G | 2 | a0001c0001t0002g0171a0001c0001t0002g0175 | 2 | HG02451.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1784+1414A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53211227 | ||||||
| chr16:53211731
|
C | CTT | 74 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(71): Show | 74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.1784+1918_1784+191 others(6): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53211731 | ||||||
| chr16:53212092
|
A | C | 65 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.1784+2279A>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53212092 | ||||||
| chr16:53212252
|
A | G | 1 | a0001c0001t0002g0175 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1784+2439A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53212252 | ||||||
| chr16:53212262
|
A | G | 77 | a0001c0005t0001g0215a0001c0005t0004g0078a0001c0005t0004g0097others(74): Show | 77 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.1784+2449A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53212262 | ||||||
| chr16:53212273
|
T | C | 74 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(71): Show | 74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.1784+2460T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53212273 | ||||||
| chr16:53212345
|
C | T | 2 | a0001c0005t0004g0097a0006c0009t0004g0107 | 2 | HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1784+2532C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53212345 | ||||||
| chr16:53212404
|
CA | C | 106 | a0001c0001t0001g0043a0001c0001t0015g0166a0001c0003t0001g0158others(103): Show | 106 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.1784+2607delA | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr16 | 53212404 | |||||
| chr16:53212419
|
A | T | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1784+2606A>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53212419 | ||||||
| chr16:53212420
|
A | T | 77 | a0001c0005t0001g0215a0001c0005t0004g0078a0001c0005t0004g0097others(74): Show | 77 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.1784+2607A>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53212420 | ||||||
| chr16:53212641
|
G | A | 65 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.1784+2828G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53212641 | ||||||
| chr16:53212808
|
A | G | 19 | a0001c0001t0003g0022a0001c0001t0003g0079a0001c0001t0003g0096others(16): Show | 19 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.1784+2995A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53212808 | ||||||
| chr16:53213028
|
T | C | 12 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(9): Show | 12 | HG01167.hp2 HG01884.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.1784+3215T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53213028 | ||||||
| chr16:53213077
|
T | C | 2 | a0003c0004t0001g0213a0003c0004t0001g0217 | 2 | NA18974.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.1784+3264T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53213077 | ||||||
| chr16:53213471
|
A | T | 1 | a0001c0001t0003g0105 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1784+3658A>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53213471 | ||||||
| chr16:53213486
|
G | A | 1 | a0003c0004t0001g0198 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1784+3673G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53213486 | ||||||
| chr16:53213514
|
G | T | 10 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0231others(7): Show | 10 | HG01167.hp2 HG01884.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1784+3701G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53213514 | ||||||
| chr16:53213644
|
C | T | 1 | a0002c0002t0001g0063 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1784+3831C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53213644 | ||||||
| chr16:53213846
|
T | C | 74 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(71): Show | 74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.1784+4033T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53213846 | ||||||
| chr16:53213899
|
T | A | 2 | a0001c0005t0005g0017a0001c0005t0005g0018 | 2 | HG02257.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1784+4086T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53213899 | ||||||
| chr16:53213947
|
G | A | 2 | a0001c0005t0005g0061a0001c0005t0005g0089 | 2 | HG03688.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.1784+4134G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53213947 | ||||||
| chr16:53214144
|
G | A | 2 | a0001c0001t0002g0171a0001c0001t0002g0175 | 2 | HG02451.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1784+4331G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53214144 | ||||||
| chr16:53214249
|
T | A | 1 | a0001c0001t0001g0111 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1784+4436T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53214249 | ||||||
| chr16:53214416
|
G | A | 1 | a0001c0001t0001g0124 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1784+4603G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53214416 | ||||||
| chr16:53214517
|
G | GTAAGT | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1784+4705_1784+470 others(9): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr16 | 53214517 | |||||
| chr16:53214602
|
C | T | 65 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.1784+4789C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53214602 | ||||||
| chr16:53214662
|
G | A | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1784+4849G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53214662 | ||||||
| chr16:53214664
|
G | A | 1 | a0001c0003t0002g0029 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1784+4851G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53214664 | ||||||
| chr16:53214850
|
A | G | 2 | a0001c0005t0004g0097a0006c0009t0004g0107 | 2 | HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1784+5037A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53214850 | ||||||
| chr16:53214915
|
CT | C | 205 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0021others(202): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.1784+5118delT | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr16 | 53214915 | |||||
| chr16:53214945
|
A | G | 68 | a0001c0005t0001g0215a0001c0005t0004g0078a0001c0005t0004g0097others(65): Show | 68 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.1784+5132A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53214945 | ||||||
| chr16:53214999
|
G | A | 7 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0168others(4): Show | 7 | HG01891.hp2 HG02451.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1784+5186G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53214999 | ||||||
| chr16:53215152
|
G | A | 1 | a0001c0001t0003g0183 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1784+5339G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53215152 | ||||||
| chr16:53215158
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1784+5345C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53215158 | ||||||
| chr16:53215211
|
C | T | 1 | a0001c0003t0002g0033 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1784+5398C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53215211 | ||||||
| chr16:53215720
|
G | C | 143 | a0001c0001t0001g0068a0001c0001t0001g0159a0001c0001t0002g0171others(140): Show | 143 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.1784+5907G>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53215720 | ||||||
| chr16:53215788
|
G | A | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1784+5975G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53215788 | ||||||
| chr16:53215820
|
G | A | 1 | a0001c0001t0001g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1784+6007G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53215820 | ||||||
| chr16:53215951
|
C | T | 43 | a0001c0001t0002g0171a0001c0001t0002g0175a0001c0001t0015g0166others(40): Show | 43 | HG00140.hp2 HG00558.hp2 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.1784+6138C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53215951 | ||||||
| chr16:53215956
|
A | G | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1784+6143A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53215956 | ||||||
| chr16:53216007
|
T | C | 1 | a0001c0001t0015g0166 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1784+6194T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53216007 | ||||||
| chr16:53216010
|
A | C | 1 | a0006c0009t0004g0107 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1784+6197A>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53216010 | ||||||
| chr16:53216135
|
A | G | 1 | a0001c0001t0003g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1784+6322A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53216135 | ||||||
| chr16:53216210
|
T | C | 1 | a0001c0001t0015g0166 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1784+6397T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53216210 | ||||||
| chr16:53216280
|
G | A | 1 | a0002c0002t0001g0118 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1785-6364G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53216280 | ||||||
| chr16:53216837
|
T | C | 2 | a0001c0003t0002g0059a0001c0003t0002g0224 | 2 | HG02717.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1785-5807T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53216837 | ||||||
| chr16:53216855
|
A | T | 2 | a0003c0004t0001g0007a0003c0004t0001g0030 | 2 | HG00597.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.1785-5789A>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53216855 | ||||||
| chr16:53216859
|
G | A | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1785-5785G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53216859 | ||||||
| chr16:53216859
|
G | T | 2 | a0003c0004t0001g0007a0003c0004t0001g0030 | 2 | HG00597.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.1785-5785G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53216859 | ||||||
| chr16:53217014
|
G | A | 121 | a0001c0001t0002g0171a0001c0001t0002g0175a0001c0001t0015g0166others(118): Show | 121 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.1785-5630G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53217014 | ||||||
| chr16:53217049
|
G | A | 1 | a0002c0019t0001g0180 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1785-5595G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53217049 | ||||||
| chr16:53217167
|
G | A | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1785-5477G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53217167 | ||||||
| chr16:53217267
|
T | C | 1 | a0002c0002t0001g0106 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1785-5377T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53217267 | ||||||
| chr16:53217411
|
G | A | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1785-5233G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53217411 | ||||||
| chr16:53217536
|
G | T | 2 | a0001c0005t0004g0169a0001c0005t0018g0001 | 2 | HG03139.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1785-5108G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53217536 | ||||||
| chr16:53217540
|
C | T | 3 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0178 | 3 | HG01891.hp2 HG02630.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1785-5104C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53217540 | ||||||
| chr16:53217555
|
G | C | 1 | a0003c0004t0001g0198 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1785-5089G>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53217555 | ||||||
| chr16:53217618
|
C | T | 77 | a0001c0005t0001g0215a0001c0005t0004g0078a0001c0005t0004g0097others(74): Show | 77 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.1785-5026C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53217618 | ||||||
| chr16:53217912
|
T | TTTTC | 14 | a0001c0001t0001g0052a0001c0001t0001g0069a0001c0001t0001g0075others(11): Show | 14 | HG00099.hp1 HG01168.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.1785-4688_1785-468 others(8): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr16 | 53217912 | |||||
| chr16:53217912
|
T | TTTTCTTT others(1): Show |
6 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0188others(3): Show | 6 | HG01109.hp2 HG03098.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.1785-4692_1785-468 others(12): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr16 | 53217912 | |||||
| chr16:53217912
|
T | TTTTCTTT others(5): Show |
1 | a0001c0001t0001g0056 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1785-4696_1785-468 others(16): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr16 | 53217912 | |||||
| chr16:53217912
|
TTTTC | T | 9 | a0001c0001t0001g0026a0001c0001t0001g0092a0001c0001t0001g0098others(6): Show | 9 | HG02055.hp1 HG02129.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.1785-4688_1785-468 others(8): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr16 | 53217912 | |||||
| chr16:53217912
|
TTTTCTTT others(1): Show |
T | 18 | a0001c0001t0002g0171a0001c0001t0002g0175a0001c0001t0003g0022others(15): Show | 18 | HG01891.hp1 HG02109.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.1785-4692_1785-468 others(12): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr16 | 53217912 | |||||
| chr16:53217912
|
TTTTCTTT others(5): Show |
T | 4 | a0001c0001t0003g0222a0001c0003t0002g0152a0001c0005t0001g0215others(1): Show | 4 | HG03516.hp2 HG03579.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.1785-4696_1785-468 others(16): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr16 | 53217912 | |||||
| chr16:53217912
|
TTTTCTTT others(9): Show |
T | 43 | a0001c0001t0001g0068a0001c0001t0001g0159a0001c0001t0003g0016others(40): Show | 43 | HG00140.hp2 HG00558.hp2 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.1785-4700_1785-468 others(20): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr16 | 53217912 | |||||
| chr16:53217912
|
TTTTCTTT others(13): Show |
T | 64 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(61): Show | 64 | HG00099.hp2 HG00408.hp1 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.1785-4704_1785-468 others(24): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr16 | 53217912 | |||||
| chr16:53217912
|
TTTTCTTT others(17): Show |
T | 1 | a0002c0002t0001g0129 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1785-4708_1785-468 others(28): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr16 | 53217912 | |||||
| chr16:53217912
|
TTTTCTTT others(21): Show |
T | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1785-4712_1785-468 others(32): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr16 | 53217912 | |||||
| chr16:53218013
|
A | T | 1 | a0001c0014t0001g0115 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1785-4631A>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53218013 | ||||||
| chr16:53218014
|
C | T | 3 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0178 | 3 | HG01891.hp2 HG02630.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1785-4630C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53218014 | ||||||
| chr16:53218024
|
C | A | 2 | a0001c0003t0002g0059a0001c0003t0002g0224 | 2 | HG02717.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1785-4620C>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53218024 | ||||||
| chr16:53218083
|
G | A | 2 | a0001c0005t0004g0097a0006c0009t0004g0107 | 2 | HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1785-4561G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53218083 | ||||||
| chr16:53218108
|
C | T | 77 | a0001c0005t0001g0215a0001c0005t0004g0078a0001c0005t0004g0097others(74): Show | 77 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.1785-4536C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53218108 | ||||||
| chr16:53218165
|
C | T | 6 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0168others(3): Show | 6 | HG01891.hp2 HG02451.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1785-4479C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53218165 | ||||||
| chr16:53218358
|
C | CT | 12 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(9): Show | 12 | HG01167.hp2 HG01884.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.1785-4284dupT | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr16 | 53218358 | |||||
| chr16:53218491
|
A | C | 1 | a0006c0009t0004g0107 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1785-4153A>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53218491 | ||||||
| chr16:53218586
|
C | T | 1 | a0001c0003t0002g0154 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1785-4058C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53218586 | ||||||
| chr16:53218625
|
C | T | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1785-4019C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53218625 | ||||||
| chr16:53218834
|
CTACAAAC others(4): Show |
C | 1 | a0001c0001t0001g0230 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1785-3808_1785-379 others(15): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr16 | 53218834 | |||||
| chr16:53218960
|
CT | C | 2 | a0001c0005t0004g0097a0006c0009t0004g0107 | 2 | HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1785-3683delT | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53218960 | ||||||
| chr16:53219024
|
G | A | 2 | a0001c0005t0004g0097a0006c0009t0004g0107 | 2 | HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1785-3620G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53219024 | ||||||
| chr16:53219203
|
C | T | 1 | a0002c0002t0001g0205 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1785-3441C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53219203 | ||||||
| chr16:53219220
|
G | T | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1785-3424G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53219220 | ||||||
| chr16:53219246
|
A | G | 1 | a0001c0001t0001g0091 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1785-3398A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53219246 | ||||||
| chr16:53219332
|
A | G | 1 | a0001c0001t0001g0230 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1785-3312A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53219332 | ||||||
| chr16:53219357
|
A | G | 1 | a0001c0001t0003g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1785-3287A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53219357 | ||||||
| chr16:53219487
|
G | A | 3 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0012g0229 | 3 | HG01167.hp2 HG01884.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1785-3157G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53219487 | ||||||
| chr16:53219506
|
C | T | 2 | a0001c0003t0010g0006a0001c0003t0010g0013 | 2 | NA18950.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.1785-3138C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53219506 | ||||||
| chr16:53219547
|
T | C | 1 | a0001c0017t0002g0237 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1785-3097T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53219547 | ||||||
| chr16:53219614
|
G | A | 3 | a0001c0001t0001g0092a0001c0001t0020g0101a0001c0008t0001g0077 | 3 | HG02630.hp1 HG02976.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1785-3030G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53219614 | ||||||
| chr16:53219614
|
G | C | 1 | a0003c0004t0001g0162 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1785-3030G>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53219614 | ||||||
| chr16:53219665
|
A | G | 2 | a0001c0001t0007g0103a0001c0001t0007g0122 | 2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1785-2979A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53219665 | ||||||
| chr16:53219798
|
T | C | 77 | a0001c0005t0001g0215a0001c0005t0004g0078a0001c0005t0004g0097others(74): Show | 77 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.1785-2846T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53219798 | ||||||
| chr16:53219807
|
A | G | 53 | a0002c0002t0001g0009a0002c0002t0001g0010a0002c0002t0001g0012others(50): Show | 53 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.1785-2837A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53219807 | ||||||
| chr16:53219814
|
G | T | 2 | a0003c0004t0001g0213a0003c0004t0001g0217 | 2 | NA18974.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.1785-2830G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53219814 | ||||||
| chr16:53219967
|
C | T | 1 | a0008c0011t0003g0062 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1785-2677C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53219967 | ||||||
| chr16:53220263
|
C | T | 1 | a0001c0003t0002g0033 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1785-2381C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53220263 | ||||||
| chr16:53220264
|
G | A | 52 | a0002c0002t0001g0009a0002c0002t0001g0010a0002c0002t0001g0012others(49): Show | 52 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(49): Show |
intron_variant | MODIFIER | c.1785-2380G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53220264 | ||||||
| chr16:53220332
|
T | A | 2 | a0001c0005t0004g0169a0001c0005t0018g0001 | 2 | HG03139.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1785-2312T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53220332 | ||||||
| chr16:53220567
|
T | C | 1 | a0001c0001t0001g0165 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1785-2077T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53220567 | ||||||
| chr16:53220758
|
A | G | 41 | a0001c0001t0015g0166a0001c0003t0001g0158a0001c0003t0002g0002others(38): Show | 41 | HG00140.hp2 HG00558.hp2 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.1785-1886A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53220758 | ||||||
| chr16:53220813
|
C | A | 1 | a0001c0005t0004g0097 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1785-1831C>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53220813 | ||||||
| chr16:53220960
|
T | G | 1 | a0001c0003t0002g0036 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1785-1684T>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53220960 | ||||||
| chr16:53220969
|
G | A | 1 | a0001c0017t0002g0237 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1785-1675G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53220969 | ||||||
| chr16:53221148
|
T | G | 1 | a0002c0002t0001g0102 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1785-1496T>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53221148 | ||||||
| chr16:53221357
|
G | A | 19 | a0001c0001t0003g0022a0001c0001t0003g0079a0001c0001t0003g0096others(16): Show | 19 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.1785-1287G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53221357 | ||||||
| chr16:53221493
|
C | T | 1 | a0001c0001t0001g0069 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1785-1151C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53221493 | ||||||
| chr16:53221800
|
T | C | 1 | a0001c0005t0001g0215 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1785-844T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53221800 | ||||||
| chr16:53221892
|
A | T | 77 | a0001c0005t0001g0215a0001c0005t0004g0078a0001c0005t0004g0097others(74): Show | 77 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.1785-752A>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53221892 | ||||||
| chr16:53222023
|
CT | C | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1785-610delT | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr16 | 53222023 | |||||
| chr16:53222137
|
T | C | 74 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(71): Show | 74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.1785-507T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53222137 | ||||||
| chr16:53222341
|
G | T | 1 | a0001c0005t0001g0215 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1785-303G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53222341 | ||||||
| chr16:53222364
|
G | A | 1 | a0001c0001t0001g0084 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1785-280G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53222364 | ||||||
| chr16:53222524
|
C | T | 3 | a0001c0003t0002g0033a0001c0003t0002g0046a0001c0003t0002g0073 | 3 | HG02027.hp2 NA18946.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.1785-120C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53222524 | ||||||
| chr16:53222582
|
T | A | 65 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.1785-62T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 3/38 | chr16 | 53222582 | ||||||
| chr16:53223251
|
C | CT | 6 | a0001c0001t0001g0084a0001c0001t0001g0211a0001c0001t0020g0101others(3): Show | 6 | HG01168.hp1 HG01169.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1896+512dupT | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 4/38 | INFO_REALIGN_3_PRIME | chr16 | 53223251 | |||||
| chr16:53223251
|
CT | C | 71 | a0001c0001t0001g0069a0001c0001t0002g0171a0001c0001t0003g0016others(68): Show | 71 | HG00140.hp2 HG00323.hp1 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.1896+512delT | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 4/38 | INFO_REALIGN_3_PRIME | chr16 | 53223251 | |||||
| chr16:53223251
|
CTT | C | 53 | a0001c0001t0002g0175a0001c0005t0001g0215a0002c0002t0001g0009others(50): Show | 53 | HG00099.hp2 HG00408.hp1 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.1896+511_1896+512d others(4): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 4/38 | INFO_REALIGN_3_PRIME | chr16 | 53223251 | |||||
| chr16:53223251
|
CTTT | C | 10 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(7): Show | 10 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.1896+510_1896+512d others(5): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 4/38 | INFO_REALIGN_3_PRIME | chr16 | 53223251 | |||||
| chr16:53223316
|
G | C | 1 | a0003c0004t0001g0148 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1896+561G>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 4/38 | chr16 | 53223316 | ||||||
| chr16:53223371
|
T | C | 12 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(9): Show | 12 | HG01167.hp2 HG01884.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.1896+616T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 4/38 | chr16 | 53223371 | ||||||
| chr16:53223379
|
G | T | 1 | a0001c0001t0001g0027 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1896+624G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 4/38 | chr16 | 53223379 | ||||||
| chr16:53223729
|
A | G | 2 | a0001c0005t0004g0097a0006c0009t0004g0107 | 2 | HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1896+974A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 4/38 | chr16 | 53223729 | ||||||
| chr16:53224362
|
G | A | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1896+1607G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 4/38 | chr16 | 53224362 | ||||||
| chr16:53224740
|
A | G | 1 | a0002c0002t0001g0113 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1897-1626A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 4/38 | chr16 | 53224740 | ||||||
| chr16:53224787
|
T | C | 1 | a0007c0010t0001g0212 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1897-1579T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 4/38 | chr16 | 53224787 | ||||||
| chr16:53224792
|
A | G | 1 | a0003c0004t0001g0200 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1897-1574A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 4/38 | chr16 | 53224792 | ||||||
| chr16:53224856
|
A | G | 1 | a0002c0002t0001g0208 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1897-1510A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 4/38 | chr16 | 53224856 | ||||||
| chr16:53225012
|
A | G | 3 | a0004c0006t0001g0121a0004c0006t0001g0127a0004c0006t0001g0128 | 3 | NA18952.hp1 NA18989.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.1897-1354A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 4/38 | chr16 | 53225012 | ||||||
| chr16:53225293
|
T | C | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1897-1073T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 4/38 | chr16 | 53225293 | ||||||
| chr16:53225776
|
A | G | 1 | a0001c0003t0002g0036 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1897-590A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 4/38 | chr16 | 53225776 | ||||||
| chr16:53225781
|
G | C | 6 | a0002c0002t0001g0106a0002c0002t0001g0109a0002c0002t0001g0113others(3): Show | 6 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1897-585G>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 4/38 | chr16 | 53225781 | ||||||
| chr16:53225866
|
A | G | 65 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.1897-500A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 4/38 | chr16 | 53225866 | ||||||
| chr16:53226247
|
T | A | 77 | a0001c0005t0001g0215a0001c0005t0004g0078a0001c0005t0004g0097others(74): Show | 77 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.1897-119T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 4/38 | chr16 | 53226247 | ||||||
| chr16:53226760
|
A | G | 1 | a0001c0003t0002g0094 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2043+248A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 5/38 | chr16 | 53226760 | ||||||
| chr16:53226859
|
A | G | 1 | a0001c0001t0003g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2043+347A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 5/38 | chr16 | 53226859 | ||||||
| chr16:53226976
|
G | A | 121 | a0001c0001t0002g0171a0001c0001t0002g0175a0001c0001t0015g0166others(118): Show | 121 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.2044-420G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 5/38 | chr16 | 53226976 | ||||||
| chr16:53227039
|
C | A | 1 | a0002c0002t0001g0102 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2044-357C>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 5/38 | chr16 | 53227039 | ||||||
| chr16:53227864
|
T | C | 1 | a0001c0001t0003g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2168+261T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 7/38 | chr16 | 53227864 | ||||||
| chr16:53227947
|
G | A | 1 | a0001c0003t0002g0028 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2168+344G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 7/38 | chr16 | 53227947 | ||||||
| chr16:53228035
|
G | A | 2 | a0001c0005t0004g0097a0006c0009t0004g0107 | 2 | HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2168+432G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 7/38 | chr16 | 53228035 | ||||||
| chr16:53228343
|
T | TA | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.2169-630dupA | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr16 | 53228343 | |||||
| chr16:53228537
|
G | GT | 34 | a0001c0001t0001g0064a0001c0001t0001g0084a0001c0001t0001g0091others(31): Show | 34 | HG00099.hp2 HG01167.hp2 HG01243.hp1 others(31): Show |
intron_variant | MODIFIER | c.2169-425dupT | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr16 | 53228537 | |||||
| chr16:53228537
|
G | GTT | 49 | a0001c0005t0004g0231a0001c0005t0005g0018a0001c0005t0005g0089others(46): Show | 49 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.2169-426_2169-425d others(4): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr16 | 53228537 | |||||
| chr16:53228537
|
G | GTTT | 10 | a0001c0005t0005g0017a0002c0002t0001g0009a0002c0002t0001g0054others(7): Show | 10 | HG00735.hp2 HG02135.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.2169-427_2169-425d others(5): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr16 | 53228537 | |||||
| chr16:53228567
|
G | A | 1 | a0001c0005t0001g0215 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.2169-416G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 7/38 | chr16 | 53228567 | ||||||
| chr16:53228616
|
C | T | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.2169-367C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 7/38 | chr16 | 53228616 | ||||||
| chr16:53229305
|
A | T | 4 | a0002c0002t0001g0095a0002c0002t0001g0126a0002c0002t0001g0130others(1): Show | 4 | HG00099.hp2 HG01515.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.2286+205A>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 8/38 | chr16 | 53229305 | ||||||
| chr16:53229442
|
A | G | 53 | a0002c0002t0001g0009a0002c0002t0001g0010a0002c0002t0001g0012others(50): Show | 53 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.2286+342A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 8/38 | chr16 | 53229442 | ||||||
| chr16:53229489
|
T | C | 1 | a0001c0005t0018g0001 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2286+389T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 8/38 | chr16 | 53229489 | ||||||
| chr16:53229700
|
A | C | 2 | a0001c0001t0002g0171a0001c0001t0002g0175 | 2 | HG02451.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.2286+600A>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 8/38 | chr16 | 53229700 | ||||||
| chr16:53229753
|
C | G | 1 | a0002c0002t0001g0205 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2286+653C>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 8/38 | chr16 | 53229753 | ||||||
| chr16:53229761
|
T | C | 1 | a0004c0006t0001g0128 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.2286+661T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 8/38 | chr16 | 53229761 | ||||||
| chr16:53229810
|
A | G | 19 | a0001c0001t0003g0022a0001c0001t0003g0079a0001c0001t0003g0096others(16): Show | 19 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.2286+710A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 8/38 | chr16 | 53229810 | ||||||
| chr16:53229863
|
A | T | 1 | a0001c0005t0001g0215 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.2286+763A>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 8/38 | chr16 | 53229863 | ||||||
| chr16:53230023
|
G | A | 1 | a0001c0003t0002g0041 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2286+923G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 8/38 | chr16 | 53230023 | ||||||
| chr16:53230026
|
G | T | 64 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(61): Show | 64 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(61): Show |
intron_variant | MODIFIER | c.2286+926G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 8/38 | chr16 | 53230026 | ||||||
| chr16:53230203
|
A | G | 1 | a0001c0012t0001g0132 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2286+1103A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 8/38 | chr16 | 53230203 | ||||||
| chr16:53230287
|
C | A | 1 | a0001c0001t0001g0230 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2287-1132C>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 8/38 | chr16 | 53230287 | ||||||
| chr16:53230464
|
A | T | 1 | a0002c0002t0001g0138 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2287-955A>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 8/38 | chr16 | 53230464 | ||||||
| chr16:53230615
|
G | C | 1 | a0001c0005t0004g0104 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2287-804G>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 8/38 | chr16 | 53230615 | ||||||
| chr16:53230773
|
TGAA | T | 65 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.2287-641_2287-639d others(5): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 8/38 | INFO_REALIGN_3_PRIME | chr16 | 53230773 | |||||
| chr16:53230938
|
A | AG | 74 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(71): Show | 74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.2287-481_2287-480i others(3): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 8/38 | chr16 | 53230938 | ||||||
| chr16:53231254
|
T | A | 141 | a0001c0001t0001g0159a0001c0001t0002g0171a0001c0001t0002g0175others(138): Show | 141 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.2287-165T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 8/38 | chr16 | 53231254 | ||||||
| chr16:53231319
|
C | T | 1 | a0001c0001t0003g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2287-100C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 8/38 | chr16 | 53231319 | ||||||
| chr16:53231512
|
A | G | 1 | a0001c0005t0005g0032 | 1 | HG02970.hp1 | splice_region_variant&intron_variant | LOW | c.2373+7A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 9/38 | chr16 | 53231512 | ||||||
| chr16:53232119
|
T | C | 10 | a0001c0001t0003g0096a0001c0001t0003g0112a0001c0001t0003g0133others(7): Show | 10 | HG02055.hp1 HG02109.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.2511+335T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 10/38 | chr16 | 53232119 | ||||||
| chr16:53232277
|
G | C | 65 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.2511+493G>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 10/38 | chr16 | 53232277 | ||||||
| chr16:53232338
|
A | G | 1 | a0001c0005t0001g0215 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.2511+554A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 10/38 | chr16 | 53232338 | ||||||
| chr16:53232366
|
A | G | 3 | a0003c0004t0006g0074a0003c0004t0006g0190a0003c0004t0006g0199 | 3 | NA18950.hp2 NA18999.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.2511+582A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 10/38 | chr16 | 53232366 | ||||||
| chr16:53232375
|
A | G | 1 | a0001c0001t0001g0111 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2511+591A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 10/38 | chr16 | 53232375 | ||||||
| chr16:53232404
|
A | T | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.2511+620A>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 10/38 | chr16 | 53232404 | ||||||
| chr16:53232805
|
C | CACTT | 74 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(71): Show | 74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.2511+1023_2511+102 others(8): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 10/38 | INFO_REALIGN_3_PRIME | chr16 | 53232805 | |||||
| chr16:53232859
|
T | A | 2 | a0001c0001t0001g0021a0001c0001t0001g0058 | 2 | NA18939.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.2511+1075T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 10/38 | chr16 | 53232859 | ||||||
| chr16:53233324
|
A | G | 1 | a0001c0005t0004g0238 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.2511+1540A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 10/38 | chr16 | 53233324 | ||||||
| chr16:53233467
|
C | T | 65 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.2511+1683C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 10/38 | chr16 | 53233467 | ||||||
| chr16:53233586
|
T | C | 3 | a0001c0005t0004g0097a0006c0009t0004g0107a0008c0011t0003g0062 | 3 | HG01884.hp1 HG02109.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2512-1599T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 10/38 | chr16 | 53233586 | ||||||
| chr16:53233588
|
A | ACCTTCTC others(18): Show |
1 | a0001c0001t0002g0175 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2512-1593_2512-156 others(29): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 10/38 | INFO_REALIGN_3_PRIME | chr16 | 53233588 | |||||
| chr16:53233629
|
C | T | 12 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(9): Show | 12 | HG01167.hp2 HG01884.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.2512-1556C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 10/38 | chr16 | 53233629 | ||||||
| chr16:53233637
|
C | T | 1 | a0001c0014t0001g0115 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2512-1548C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 10/38 | chr16 | 53233637 | ||||||
| chr16:53233797
|
C | T | 6 | a0001c0003t0002g0086a0001c0003t0002g0153a0001c0003t0002g0161others(3): Show | 6 | HG00735.hp1 HG01074.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.2512-1388C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 10/38 | chr16 | 53233797 | ||||||
| chr16:53233807
|
A | G | 1 | a0001c0001t0001g0069 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.2512-1378A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 10/38 | chr16 | 53233807 | ||||||
| chr16:53233829
|
A | T | 1 | a0001c0005t0001g0215 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.2512-1356A>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 10/38 | chr16 | 53233829 | ||||||
| chr16:53234150
|
T | C | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.2512-1035T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 10/38 | chr16 | 53234150 | ||||||
| chr16:53234202
|
T | C | 3 | a0003c0004t0006g0074a0003c0004t0006g0190a0003c0004t0006g0199 | 3 | NA18950.hp2 NA18999.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.2512-983T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 10/38 | chr16 | 53234202 | ||||||
| chr16:53234213
|
G | A | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.2512-972G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 10/38 | chr16 | 53234213 | ||||||
| chr16:53234287
|
A | G | 1 | a0001c0001t0001g0091 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2512-898A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 10/38 | chr16 | 53234287 | ||||||
| chr16:53234418
|
G | A | 1 | a0001c0001t0001g0119 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2512-767G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 10/38 | chr16 | 53234418 | ||||||
| chr16:53234511
|
A | G | 53 | a0002c0002t0001g0009a0002c0002t0001g0010a0002c0002t0001g0012others(50): Show | 53 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.2512-674A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 10/38 | chr16 | 53234511 | ||||||
| chr16:53234558
|
CT | C | 65 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.2512-622delT | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 10/38 | INFO_REALIGN_3_PRIME | chr16 | 53234558 | |||||
| chr16:53234583
|
C | G | 1 | a0001c0005t0004g0097 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2512-602C>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 10/38 | chr16 | 53234583 | ||||||
| chr16:53234596
|
G | T | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.2512-589G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 10/38 | chr16 | 53234596 | ||||||
| chr16:53234813
|
TA | T | 74 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(71): Show | 74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.2512-361delA | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 10/38 | INFO_REALIGN_3_PRIME | chr16 | 53234813 | |||||
| chr16:53234850
|
T | C | 1 | a0001c0001t0003g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2512-335T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 10/38 | chr16 | 53234850 | ||||||
| chr16:53235119
|
GC | G | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.2512-65delC | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 10/38 | chr16 | 53235119 | ||||||
| chr16:53235334
|
T | A | 2 | a0001c0001t0003g0016a0001c0005t0001g0215 | 2 | HG02965.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.2633+28T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 11/38 | chr16 | 53235334 | ||||||
| chr16:53235404
|
T | A | 141 | a0001c0001t0001g0068a0001c0001t0002g0171a0001c0001t0002g0175others(138): Show | 141 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.2633+98T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 11/38 | chr16 | 53235404 | ||||||
| chr16:53235610
|
G | A | 6 | a0002c0002t0001g0106a0002c0002t0001g0109a0002c0002t0001g0113others(3): Show | 6 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.2633+304G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 11/38 | chr16 | 53235610 | ||||||
| chr16:53236210
|
C | T | 2 | a0001c0001t0002g0171a0001c0001t0002g0175 | 2 | HG02451.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.2633+904C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 11/38 | chr16 | 53236210 | ||||||
| chr16:53236420
|
C | T | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.2633+1114C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 11/38 | chr16 | 53236420 | ||||||
| chr16:53236614
|
T | TC | 19 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0231others(16): Show | 19 | HG01167.hp2 HG01884.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.2633+1315dupC | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 11/38 | INFO_REALIGN_3_PRIME | chr16 | 53236614 | |||||
| chr16:53236619
|
C | A | 1 | a0001c0016t0002g0156 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2633+1313C>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 11/38 | chr16 | 53236619 | ||||||
| chr16:53236718
|
C | T | 1 | a0008c0011t0003g0062 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2633+1412C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 11/38 | chr16 | 53236718 | ||||||
| chr16:53236840
|
T | A | 53 | a0002c0002t0001g0009a0002c0002t0001g0010a0002c0002t0001g0012others(50): Show | 53 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.2634-1503T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 11/38 | chr16 | 53236840 | ||||||
| chr16:53236932
|
A | G | 211 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0021others(208): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.2634-1411A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 11/38 | chr16 | 53236932 | ||||||
| chr16:53237045
|
C | T | 2 | a0001c0005t0004g0097a0006c0009t0004g0107 | 2 | HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2634-1298C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 11/38 | chr16 | 53237045 | ||||||
| chr16:53237145
|
A | G | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.2634-1198A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 11/38 | chr16 | 53237145 | ||||||
| chr16:53237229
|
T | A | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.2634-1114T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 11/38 | chr16 | 53237229 | ||||||
| chr16:53237337
|
T | C | 74 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(71): Show | 74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.2634-1006T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 11/38 | chr16 | 53237337 | ||||||
| chr16:53237596
|
C | CA | 3 | a0001c0003t0001g0158a0001c0003t0002g0086a0001c0003t0002g0153 | 3 | HG01109.hp1 HG01243.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.2634-746dupA | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 11/38 | INFO_REALIGN_3_PRIME | chr16 | 53237596 | |||||
| chr16:53237801
|
A | G | 12 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(9): Show | 12 | HG01167.hp2 HG01884.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.2634-542A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 11/38 | chr16 | 53237801 | ||||||
| chr16:53237837
|
C | CTG | 71 | a0001c0005t0001g0215a0001c0005t0004g0078a0001c0005t0004g0097others(68): Show | 71 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(68): Show |
intron_variant | MODIFIER | c.2634-505_2634-504i others(4): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 11/38 | INFO_REALIGN_3_PRIME | chr16 | 53237837 | |||||
| chr16:53237837
|
C | CTGT | 7 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0061others(4): Show | 7 | HG02257.hp2 HG03688.hp2 HG04184.hp2 others(4): Show |
intron_variant | MODIFIER | c.2634-505_2634-504i others(5): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 11/38 | INFO_REALIGN_3_PRIME | chr16 | 53237837 | |||||
| chr16:53237868
|
T | C | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.2634-475T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 11/38 | chr16 | 53237868 | ||||||
| chr16:53238059
|
T | C | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.2634-284T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 11/38 | chr16 | 53238059 | ||||||
| chr16:53238304
|
A | C | 75 | a0001c0001t0003g0184a0001c0005t0004g0078a0001c0005t0004g0104others(72): Show | 75 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.2634-39A>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 11/38 | chr16 | 53238304 | ||||||
| chr16:53238653
|
C | T | 7 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0061others(4): Show | 7 | HG02257.hp2 HG03688.hp2 HG04184.hp2 others(4): Show |
intron_variant | MODIFIER | c.2877+67C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 12/38 | chr16 | 53238653 | ||||||
| chr16:53239510
|
T | C | 1 | a0001c0001t0001g0031 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2877+924T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 12/38 | chr16 | 53239510 | ||||||
| chr16:53239528
|
A | G | 1 | a0002c0002t0001g0208 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2877+942A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 12/38 | chr16 | 53239528 | ||||||
| chr16:53239696
|
T | G | 1 | a0001c0005t0001g0215 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.2877+1110T>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 12/38 | chr16 | 53239696 | ||||||
| chr16:53239741
|
G | A | 1 | a0001c0001t0001g0051 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2877+1155G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 12/38 | chr16 | 53239741 | ||||||
| chr16:53239981
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.2877+1395C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 12/38 | chr16 | 53239981 | ||||||
| chr16:53240100
|
A | C | 1 | a0003c0004t0001g0209 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2877+1514A>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 12/38 | chr16 | 53240100 | ||||||
| chr16:53240198
|
C | T | 2 | a0001c0005t0004g0097a0006c0009t0004g0107 | 2 | HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2877+1612C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 12/38 | chr16 | 53240198 | ||||||
| chr16:53240313
|
A | G | 1 | a0001c0001t0003g0112 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2877+1727A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 12/38 | chr16 | 53240313 | ||||||
| chr16:53240393
|
G | A | 9 | a0001c0001t0003g0022a0001c0001t0003g0079a0001c0001t0003g0105others(6): Show | 9 | HG01891.hp1 HG02257.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.2877+1807G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 12/38 | chr16 | 53240393 | ||||||
| chr16:53240566
|
A | T | 40 | a0001c0001t0015g0166a0001c0003t0002g0002a0001c0003t0002g0003others(37): Show | 40 | HG00140.hp2 HG00558.hp2 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.2877+1980A>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 12/38 | chr16 | 53240566 | ||||||
| chr16:53241238
|
T | C | 66 | a0001c0001t0007g0103a0001c0005t0004g0078a0001c0005t0004g0104others(63): Show | 66 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(63): Show |
intron_variant | MODIFIER | c.2878-1602T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 12/38 | chr16 | 53241238 | ||||||
| chr16:53241448
|
C | G | 1 | a0002c0002t0001g0126 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.2878-1392C>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 12/38 | chr16 | 53241448 | ||||||
| chr16:53241684
|
T | G | 1 | a0002c0002t0001g0042 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2878-1156T>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 12/38 | chr16 | 53241684 | ||||||
| chr16:53241788
|
C | G | 1 | a0002c0002t0008g0065 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2878-1052C>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 12/38 | chr16 | 53241788 | ||||||
| chr16:53241825
|
G | C | 52 | a0002c0002t0001g0009a0002c0002t0001g0010a0002c0002t0001g0012others(49): Show | 52 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(49): Show |
intron_variant | MODIFIER | c.2878-1015G>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 12/38 | chr16 | 53241825 | ||||||
| chr16:53242155
|
A | G | 1 | a0001c0005t0004g0097 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2878-685A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 12/38 | chr16 | 53242155 | ||||||
| chr16:53243151
|
G | C | 2 | a0001c0005t0004g0097a0006c0009t0004g0107 | 2 | HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3054+135G>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 13/38 | chr16 | 53243151 | ||||||
| chr16:53243165
|
C | T | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.3054+149C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 13/38 | chr16 | 53243165 | ||||||
| chr16:53243166
|
C | A | 1 | a0006c0009t0004g0107 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3054+150C>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 13/38 | chr16 | 53243166 | ||||||
| chr16:53243200
|
G | A | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.3054+184G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 13/38 | chr16 | 53243200 | ||||||
| chr16:53243266
|
A | G | 52 | a0002c0002t0001g0009a0002c0002t0001g0010a0002c0002t0001g0012others(49): Show | 52 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(49): Show |
intron_variant | MODIFIER | c.3054+250A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 13/38 | chr16 | 53243266 | ||||||
| chr16:53243328
|
T | C | 1 | a0001c0005t0005g0151 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.3054+312T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 13/38 | chr16 | 53243328 | ||||||
| chr16:53243417
|
G | A | 1 | a0001c0005t0011g0228 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3054+401G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 13/38 | chr16 | 53243417 | ||||||
| chr16:53243442
|
C | T | 74 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(71): Show | 74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.3054+426C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 13/38 | chr16 | 53243442 | ||||||
| chr16:53243613
|
A | G | 1 | a0001c0003t0013g0186 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.3054+597A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 13/38 | chr16 | 53243613 | ||||||
| chr16:53244192
|
CT | C | 8 | a0001c0001t0001g0058a0001c0003t0002g0029a0001c0005t0004g0232others(5): Show | 8 | HG01167.hp2 HG01169.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.3055-1126delT | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 13/38 | INFO_REALIGN_3_PRIME | chr16 | 53244192 | |||||
| chr16:53244519
|
G | C | 12 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(9): Show | 12 | HG01167.hp2 HG01884.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.3055-817G>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 13/38 | chr16 | 53244519 | ||||||
| chr16:53244565
|
A | G | 1 | a0002c0002t0001g0102 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3055-771A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 13/38 | chr16 | 53244565 | ||||||
| chr16:53244773
|
C | T | 120 | a0001c0001t0001g0159a0001c0001t0002g0171a0001c0001t0002g0175others(117): Show | 120 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.3055-563C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 13/38 | chr16 | 53244773 | ||||||
| chr16:53244848
|
T | A | 1 | a0001c0001t0002g0171 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3055-488T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 13/38 | chr16 | 53244848 | ||||||
| chr16:53245050
|
A | G | 1 | a0001c0005t0018g0001 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3055-286A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 13/38 | chr16 | 53245050 | ||||||
| chr16:53245099
|
G | A | 65 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.3055-237G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 13/38 | chr16 | 53245099 | ||||||
| chr16:53245185
|
T | C | 1 | a0001c0001t0001g0090 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3055-151T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 13/38 | chr16 | 53245185 | ||||||
| chr16:53245191
|
T | C | 1 | a0006c0009t0004g0107 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3055-145T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 13/38 | chr16 | 53245191 | ||||||
| chr16:53245195
|
T | C | 3 | a0004c0006t0001g0121a0004c0006t0001g0127a0004c0006t0001g0128 | 3 | NA18952.hp1 NA18989.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.3055-141T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 13/38 | chr16 | 53245195 | ||||||
| chr16:53245211
|
T | C | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.3055-125T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 13/38 | chr16 | 53245211 | ||||||
| chr16:53245211
|
TA | T | 68 | a0001c0005t0001g0215a0001c0005t0004g0078a0001c0005t0004g0097others(65): Show | 68 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.3055-123delA | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 13/38 | INFO_REALIGN_3_PRIME | chr16 | 53245211 | |||||
| chr16:53245212
|
A | AT | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.3055-124_3055-123i others(3): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 13/38 | chr16 | 53245212 | ||||||
| chr16:53245863
|
G | A | 1 | a0003c0004t0001g0198 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.3454+13G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 15/38 | chr16 | 53245863 | ||||||
| chr16:53246027
|
G | A | 1 | a0006c0009t0004g0107 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3454+177G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 15/38 | chr16 | 53246027 | ||||||
| chr16:53246085
|
GTCCTCTT others(6): Show |
G | 1 | a0001c0005t0004g0236 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3454+241_3454+253d others(15): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 15/38 | INFO_REALIGN_3_PRIME | chr16 | 53246085 | |||||
| chr16:53246212
|
G | A | 1 | a0001c0001t0001g0225 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3454+362G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 15/38 | chr16 | 53246212 | ||||||
| chr16:53246239
|
T | C | 2 | a0001c0005t0004g0097a0006c0009t0004g0107 | 2 | HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3454+389T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 15/38 | chr16 | 53246239 | ||||||
| chr16:53246304
|
C | T | 3 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0182 | 3 | HG02615.hp1 HG02970.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.3454+454C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 15/38 | chr16 | 53246304 | ||||||
| chr16:53246318
|
CTTTA | C | 6 | a0002c0002t0001g0009a0002c0002t0001g0010a0002c0002t0001g0024others(3): Show | 6 | HG00609.hp1 HG02040.hp2 NA18992.hp2 others(3): Show |
intron_variant | MODIFIER | c.3454+471_3454+474d others(6): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 15/38 | INFO_REALIGN_3_PRIME | chr16 | 53246318 | |||||
| chr16:53246324
|
T | A | 6 | a0002c0002t0001g0009a0002c0002t0001g0010a0002c0002t0001g0024others(3): Show | 6 | HG00609.hp1 HG02040.hp2 NA18992.hp2 others(3): Show |
intron_variant | MODIFIER | c.3454+474T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 15/38 | chr16 | 53246324 | ||||||
| chr16:53246435
|
A | G | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.3454+585A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 15/38 | chr16 | 53246435 | ||||||
| chr16:53246505
|
T | TTTG | 53 | a0002c0002t0001g0009a0002c0002t0001g0010a0002c0002t0001g0012others(50): Show | 53 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.3454+667_3454+669d others(5): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 15/38 | INFO_REALIGN_3_PRIME | chr16 | 53246505 | |||||
| chr16:53246646
|
A | G | 1 | a0001c0001t0001g0210 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.3455-647A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 15/38 | chr16 | 53246646 | ||||||
| chr16:53247005
|
A | G | 123 | a0001c0001t0001g0159a0001c0001t0002g0171a0001c0001t0002g0175others(120): Show | 123 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.3455-288A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 15/38 | chr16 | 53247005 | ||||||
| chr16:53247103
|
A | G | 1 | a0001c0001t0001g0230 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3455-190A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 15/38 | chr16 | 53247103 | ||||||
| chr16:53247248
|
C | CCTGCACA others(3): Show |
2 | a0002c0002t0001g0087a0002c0002t0001g0088 | 2 | HG01255.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.3455-40_3455-39ins others(10): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 15/38 | INFO_REALIGN_3_PRIME | chr16 | 53247248 | |||||
| chr16:53248163
|
TA | T | 77 | a0001c0005t0001g0215a0001c0005t0004g0078a0001c0005t0004g0097others(74): Show | 77 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.3665+674delA | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr16 | 53248163 | |||||
| chr16:53248193
|
G | A | 1 | a0001c0005t0001g0215 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.3665+690G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 16/38 | chr16 | 53248193 | ||||||
| chr16:53248291
|
G | A | 65 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.3665+788G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 16/38 | chr16 | 53248291 | ||||||
| chr16:53248335
|
CA | C | 127 | a0001c0001t0002g0171a0001c0001t0002g0175a0001c0001t0003g0016others(124): Show | 127 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.3665+848delA | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr16 | 53248335 | |||||
| chr16:53248491
|
T | G | 1 | a0001c0001t0003g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3665+988T>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 16/38 | chr16 | 53248491 | ||||||
| chr16:53248514
|
GT | G | 5 | a0001c0001t0001g0027a0001c0001t0001g0064a0001c0005t0018g0001others(2): Show | 5 | HG02027.hp1 HG02040.hp1 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.3665+1022delT | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr16 | 53248514 | |||||
| chr16:53248524
|
TTG | T | 63 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0231others(60): Show | 63 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.3665+1023_3665+102 others(6): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr16 | 53248524 | |||||
| chr16:53248526
|
G | GT | 6 | a0001c0001t0001g0031a0003c0004t0001g0134a0003c0004t0001g0162others(3): Show | 6 | HG03453.hp1 HG03831.hp1 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.3665+1039dupT | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr16 | 53248526 | |||||
| chr16:53248526
|
G | T | 1 | a0001c0001t0001g0211 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.3665+1023G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 16/38 | chr16 | 53248526 | ||||||
| chr16:53248526
|
GT | G | 67 | a0001c0001t0002g0171a0001c0001t0002g0175a0001c0001t0003g0016others(64): Show | 67 | HG00140.hp2 HG00558.hp2 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.3665+1039delT | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr16 | 53248526 | |||||
| chr16:53248527
|
T | G | 63 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0231others(60): Show | 63 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.3665+1024T>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 16/38 | chr16 | 53248527 | ||||||
| chr16:53248532
|
T | G | 1 | a0001c0003t0002g0073 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.3665+1029T>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 16/38 | chr16 | 53248532 | ||||||
| chr16:53249097
|
T | C | 74 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(71): Show | 74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.3666-774T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 16/38 | chr16 | 53249097 | ||||||
| chr16:53249499
|
A | G | 1 | a0002c0002t0001g0106 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3666-372A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 16/38 | chr16 | 53249499 | ||||||
| chr16:53249554
|
T | C | 44 | a0001c0001t0001g0159a0001c0001t0002g0171a0001c0001t0002g0175others(41): Show | 44 | HG00140.hp2 HG00558.hp2 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.3666-317T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 16/38 | chr16 | 53249554 | ||||||
| chr16:53249634
|
T | A | 42 | a0001c0001t0001g0159a0001c0001t0003g0016a0001c0001t0015g0166others(39): Show | 42 | HG00140.hp2 HG00558.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.3666-237T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 16/38 | chr16 | 53249634 | ||||||
| chr16:53249756
|
T | C | 12 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(9): Show | 12 | HG01167.hp2 HG01884.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.3666-115T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 16/38 | chr16 | 53249756 | ||||||
| chr16:53250172
|
A | G | 1 | a0008c0011t0003g0062 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3861+106A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 17/38 | chr16 | 53250172 | ||||||
| chr16:53250395
|
G | A | 1 | a0002c0002t0001g0054 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.3861+329G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 17/38 | chr16 | 53250395 | ||||||
| chr16:53250465
|
C | T | 1 | a0001c0005t0005g0061 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.3861+399C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 17/38 | chr16 | 53250465 | ||||||
| chr16:53250491
|
T | A | 2 | a0001c0003t0010g0006a0001c0003t0010g0013 | 2 | NA18950.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.3861+425T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 17/38 | chr16 | 53250491 | ||||||
| chr16:53250525
|
A | C | 65 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.3861+459A>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 17/38 | chr16 | 53250525 | ||||||
| chr16:53251010
|
T | C | 74 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(71): Show | 74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.3861+944T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 17/38 | chr16 | 53251010 | ||||||
| chr16:53251044
|
A | G | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.3861+978A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 17/38 | chr16 | 53251044 | ||||||
| chr16:53251125
|
T | C | 2 | a0003c0004t0001g0100a0003c0004t0001g0209 | 2 | HG01515.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.3861+1059T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 17/38 | chr16 | 53251125 | ||||||
| chr16:53251249
|
C | T | 1 | a0002c0002t0001g0145 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.3861+1183C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 17/38 | chr16 | 53251249 | ||||||
| chr16:53251391
|
A | C | 54 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0021others(51): Show | 54 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.3861+1325A>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 17/38 | chr16 | 53251391 | ||||||
| chr16:53251472
|
C | T | 1 | a0003c0004t0001g0148 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3861+1406C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 17/38 | chr16 | 53251472 | ||||||
| chr16:53251890
|
A | G | 1 | a0006c0009t0004g0107 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3861+1824A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 17/38 | chr16 | 53251890 | ||||||
| chr16:53251917
|
G | T | 1 | a0001c0003t0002g0028 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.3861+1851G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 17/38 | chr16 | 53251917 | ||||||
| chr16:53251966
|
C | A | 77 | a0001c0005t0001g0215a0001c0005t0004g0078a0001c0005t0004g0097others(74): Show | 77 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.3861+1900C>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 17/38 | chr16 | 53251966 | ||||||
| chr16:53252278
|
A | G | 237 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0021others(234): Show | 237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.3862-2160A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 17/38 | chr16 | 53252278 | ||||||
| chr16:53252316
|
C | T | 1 | a0001c0005t0001g0215 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.3862-2122C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 17/38 | chr16 | 53252316 | ||||||
| chr16:53252388
|
T | C | 1 | a0002c0019t0001g0180 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.3862-2050T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 17/38 | chr16 | 53252388 | ||||||
| chr16:53252427
|
A | G | 4 | a0002c0002t0001g0087a0002c0002t0001g0088a0002c0002t0001g0108others(1): Show | 4 | HG01255.hp2 HG01433.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.3862-2011A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 17/38 | chr16 | 53252427 | ||||||
| chr16:53252444
|
A | G | 1 | a0002c0002t0001g0149 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.3862-1994A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 17/38 | chr16 | 53252444 | ||||||
| chr16:53252521
|
G | A | 2 | a0003c0004t0001g0203a0003c0004t0001g0216 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.3862-1917G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 17/38 | chr16 | 53252521 | ||||||
| chr16:53252640
|
A | G | 6 | a0001c0001t0001g0027a0001c0001t0001g0031a0001c0001t0001g0064others(3): Show | 6 | HG01109.hp2 HG01257.hp2 HG02027.hp1 others(3): Show |
intron_variant | MODIFIER | c.3862-1798A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 17/38 | chr16 | 53252640 | ||||||
| chr16:53252645
|
G | T | 1 | a0001c0001t0001g0038 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.3862-1793G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 17/38 | chr16 | 53252645 | ||||||
| chr16:53253027
|
A | G | 1 | a0001c0005t0004g0097 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3862-1411A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 17/38 | chr16 | 53253027 | ||||||
| chr16:53253208
|
G | A | 12 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(9): Show | 12 | HG01167.hp2 HG01884.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.3862-1230G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 17/38 | chr16 | 53253208 | ||||||
| chr16:53253226
|
G | GTA | 68 | a0001c0001t0003g0221a0001c0003t0002g0033a0001c0003t0002g0046others(65): Show | 68 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.3862-1196_3862-119 others(6): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 17/38 | INFO_REALIGN_3_PRIME | chr16 | 53253226 | |||||
| chr16:53253226
|
GTA | G | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.3862-1196_3862-119 others(6): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 17/38 | INFO_REALIGN_3_PRIME | chr16 | 53253226 | |||||
| chr16:53253228
|
A | G | 1 | a0003c0004t0001g0187 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.3862-1210A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 17/38 | chr16 | 53253228 | ||||||
| chr16:53253631
|
T | C | 77 | a0001c0005t0001g0215a0001c0005t0004g0078a0001c0005t0004g0097others(74): Show | 77 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.3862-807T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 17/38 | chr16 | 53253631 | ||||||
| chr16:53253666
|
G | A | 1 | a0001c0001t0003g0222 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3862-772G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 17/38 | chr16 | 53253666 | ||||||
| chr16:53253879
|
C | T | 1 | a0001c0005t0004g0097 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3862-559C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 17/38 | chr16 | 53253879 | ||||||
| chr16:53254184
|
A | C | 65 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.3862-254A>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 17/38 | chr16 | 53254184 | ||||||
| chr16:53254353
|
G | A | 77 | a0001c0005t0001g0215a0001c0005t0004g0078a0001c0005t0004g0097others(74): Show | 77 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.3862-85G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 17/38 | chr16 | 53254353 | ||||||
| chr16:53255006
|
A | G | 1 | a0001c0005t0018g0001 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.4029+401A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 18/38 | chr16 | 53255006 | ||||||
| chr16:53255195
|
A | T | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.4030-405A>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 18/38 | chr16 | 53255195 | ||||||
| chr16:53255285
|
G | T | 1 | a0001c0005t0004g0236 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.4030-315G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 18/38 | chr16 | 53255285 | ||||||
| chr16:53255300
|
C | A | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.4030-300C>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 18/38 | chr16 | 53255300 | ||||||
| chr16:53255322
|
A | T | 19 | a0001c0001t0003g0022a0001c0001t0003g0079a0001c0001t0003g0096others(16): Show | 19 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.4030-278A>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 18/38 | chr16 | 53255322 | ||||||
| chr16:53256030
|
A | G | 1 | a0001c0001t0001g0064 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.4209+251A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 19/38 | chr16 | 53256030 | ||||||
| chr16:53256186
|
G | A | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.4209+407G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 19/38 | chr16 | 53256186 | ||||||
| chr16:53256316
|
T | C | 1 | a0006c0009t0004g0107 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.4209+537T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 19/38 | chr16 | 53256316 | ||||||
| chr16:53256381
|
C | CT | 25 | a0001c0001t0001g0026a0001c0001t0001g0043a0001c0001t0001g0052others(22): Show | 25 | HG01884.hp1 HG02109.hp1 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.4209+624dupT | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 19/38 | INFO_REALIGN_3_PRIME | chr16 | 53256381 | |||||
| chr16:53256381
|
C | CTT | 10 | a0001c0001t0003g0131a0001c0001t0003g0139a0001c0001t0003g0220others(7): Show | 10 | HG01891.hp1 HG02055.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.4209+623_4209+624d others(4): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 19/38 | INFO_REALIGN_3_PRIME | chr16 | 53256381 | |||||
| chr16:53256381
|
CT | C | 15 | a0001c0001t0001g0185a0001c0001t0002g0171a0001c0005t0004g0078others(12): Show | 15 | HG01167.hp1 HG01167.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.4209+624delT | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 19/38 | INFO_REALIGN_3_PRIME | chr16 | 53256381 | |||||
| chr16:53256497
|
A | G | 1 | a0001c0001t0001g0060 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.4209+718A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 19/38 | chr16 | 53256497 | ||||||
| chr16:53256538
|
G | T | 1 | a0002c0002t0001g0219 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.4209+759G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 19/38 | chr16 | 53256538 | ||||||
| chr16:53256598
|
C | T | 14 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0031others(11): Show | 14 | HG00408.hp2 HG00621.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.4209+819C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 19/38 | chr16 | 53256598 | ||||||
| chr16:53256647
|
CT | C | 68 | a0001c0005t0001g0215a0001c0005t0004g0078a0001c0005t0004g0097others(65): Show | 68 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.4209+882delT | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 19/38 | INFO_REALIGN_3_PRIME | chr16 | 53256647 | |||||
| chr16:53256677
|
A | G | 144 | a0001c0001t0001g0159a0001c0001t0002g0171a0001c0001t0002g0175others(141): Show | 144 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.4209+898A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 19/38 | chr16 | 53256677 | ||||||
| chr16:53256687
|
C | G | 2 | a0001c0005t0004g0097a0006c0009t0004g0107 | 2 | HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.4209+908C>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 19/38 | chr16 | 53256687 | ||||||
| chr16:53256912
|
C | G | 65 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.4209+1133C>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 19/38 | chr16 | 53256912 | ||||||
| chr16:53256929
|
A | G | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.4209+1150A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 19/38 | chr16 | 53256929 | ||||||
| chr16:53257079
|
A | G | 1 | a0008c0011t0003g0062 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.4209+1300A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 19/38 | chr16 | 53257079 | ||||||
| chr16:53257632
|
T | C | 74 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(71): Show | 74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.4209+1853T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 19/38 | chr16 | 53257632 | ||||||
| chr16:53257765
|
T | G | 65 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.4209+1986T>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 19/38 | chr16 | 53257765 | ||||||
| chr16:53257853
|
G | A | 1 | a0001c0005t0001g0215 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.4209+2074G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 19/38 | chr16 | 53257853 | ||||||
| chr16:53257872
|
G | A | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.4209+2093G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 19/38 | chr16 | 53257872 | ||||||
| chr16:53258022
|
G | GTTGTT | 2 | a0001c0001t0002g0171a0001c0001t0002g0175 | 2 | HG02451.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.4209+2256_4209+226 others(9): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 19/38 | INFO_REALIGN_3_PRIME | chr16 | 53258022 | |||||
| chr16:53258082
|
G | A | 1 | a0001c0001t0001g0051 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.4209+2303G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 19/38 | chr16 | 53258082 | ||||||
| chr16:53258601
|
A | G | 2 | a0001c0005t0004g0097a0006c0009t0004g0107 | 2 | HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.4209+2822A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 19/38 | chr16 | 53258601 | ||||||
| chr16:53259299
|
A | G | 65 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.4209+3520A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 19/38 | chr16 | 53259299 | ||||||
| chr16:53259578
|
C | G | 1 | a0008c0011t0003g0062 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.4210-3409C>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 19/38 | chr16 | 53259578 | ||||||
| chr16:53259845
|
C | T | 9 | a0001c0001t0001g0008a0001c0001t0001g0025a0001c0001t0001g0052others(6): Show | 9 | HG00597.hp1 HG02300.hp2 HG04184.hp1 others(6): Show |
intron_variant | MODIFIER | c.4210-3142C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 19/38 | chr16 | 53259845 | ||||||
| chr16:53260361
|
C | T | 1 | a0001c0001t0001g0230 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.4210-2626C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 19/38 | chr16 | 53260361 | ||||||
| chr16:53260465
|
T | A | 1 | a0001c0003t0002g0073 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.4210-2522T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 19/38 | chr16 | 53260465 | ||||||
| chr16:53260510
|
A | T | 1 | a0001c0005t0004g0231 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.4210-2477A>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 19/38 | chr16 | 53260510 | ||||||
| chr16:53260590
|
A | G | 1 | a0008c0011t0003g0062 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.4210-2397A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 19/38 | chr16 | 53260590 | ||||||
| chr16:53260608
|
A | G | 10 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0231others(7): Show | 10 | HG01167.hp2 HG01884.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.4210-2379A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 19/38 | chr16 | 53260608 | ||||||
| chr16:53260621
|
A | T | 8 | a0001c0003t0002g0028a0001c0003t0002g0029a0001c0003t0002g0033others(5): Show | 8 | HG02027.hp2 HG02129.hp1 NA18946.hp2 others(5): Show |
intron_variant | MODIFIER | c.4210-2366A>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 19/38 | chr16 | 53260621 | ||||||
| chr16:53260709
|
G | A | 1 | a0008c0011t0003g0062 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.4210-2278G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 19/38 | chr16 | 53260709 | ||||||
| chr16:53260767
|
G | A | 2 | a0001c0005t0004g0097a0006c0009t0004g0107 | 2 | HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.4210-2220G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 19/38 | chr16 | 53260767 | ||||||
| chr16:53260853
|
G | C | 1 | a0002c0002t0001g0208 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.4210-2134G>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 19/38 | chr16 | 53260853 | ||||||
| chr16:53261095
|
C | CA | 115 | a0001c0001t0001g0026a0001c0001t0001g0031a0001c0001t0001g0159others(112): Show | 115 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.4210-1878dupA | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 19/38 | INFO_REALIGN_3_PRIME | chr16 | 53261095 | |||||
| chr16:53261095
|
C | CAA | 11 | a0001c0005t0004g0104a0001c0005t0004g0169a0001c0005t0004g0231others(8): Show | 11 | HG01167.hp2 HG02615.hp2 HG02897.hp1 others(8): Show |
intron_variant | MODIFIER | c.4210-1879_4210-187 others(6): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 19/38 | INFO_REALIGN_3_PRIME | chr16 | 53261095 | |||||
| chr16:53261109
|
A | G | 1 | a0001c0001t0001g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.4210-1878A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 19/38 | chr16 | 53261109 | ||||||
| chr16:53261220
|
A | G | 3 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0182 | 3 | HG02615.hp1 HG02970.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.4210-1767A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 19/38 | chr16 | 53261220 | ||||||
| chr16:53261357
|
G | T | 1 | a0006c0009t0004g0107 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.4210-1630G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 19/38 | chr16 | 53261357 | ||||||
| chr16:53261359
|
C | CT | 78 | a0001c0001t0001g0008a0001c0001t0001g0067a0001c0001t0001g0069others(75): Show | 78 | HG00140.hp2 HG00558.hp2 HG00735.hp1 others(75): Show |
intron_variant | MODIFIER | c.4210-1602dupT | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 19/38 | INFO_REALIGN_3_PRIME | chr16 | 53261359 | |||||
| chr16:53261359
|
C | CTT | 7 | a0001c0001t0003g0112a0001c0001t0003g0220a0001c0003t0002g0003others(4): Show | 7 | HG00621.hp2 HG02055.hp1 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.4210-1603_4210-160 others(6): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 19/38 | INFO_REALIGN_3_PRIME | chr16 | 53261359 | |||||
| chr16:53261359
|
C | CTTT | 5 | a0002c0002t0001g0044a0002c0002t0001g0102a0002c0002t0001g0120others(2): Show | 5 | HG01167.hp1 HG02897.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.4210-1604_4210-160 others(7): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 19/38 | INFO_REALIGN_3_PRIME | chr16 | 53261359 | |||||
| chr16:53261359
|
C | CTTTT | 42 | a0002c0002t0001g0009a0002c0002t0001g0010a0002c0002t0001g0012others(39): Show | 42 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(39): Show |
intron_variant | MODIFIER | c.4210-1605_4210-160 others(8): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 19/38 | INFO_REALIGN_3_PRIME | chr16 | 53261359 | |||||
| chr16:53261359
|
C | CTTTTT | 7 | a0002c0002t0001g0034a0002c0002t0001g0048a0002c0002t0001g0049others(4): Show | 7 | HG01099.hp2 HG01168.hp2 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.4210-1606_4210-160 others(9): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 19/38 | INFO_REALIGN_3_PRIME | chr16 | 53261359 | |||||
| chr16:53261359
|
C | G | 2 | a0001c0001t0001g0173a0001c0001t0001g0174 | 2 | HG01891.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.4210-1628C>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 19/38 | chr16 | 53261359 | ||||||
| chr16:53261385
|
T | A | 2 | a0001c0001t0001g0092a0001c0008t0001g0077 | 2 | HG02976.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.4210-1602T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 19/38 | chr16 | 53261385 | ||||||
| chr16:53261577
|
A | G | 1 | a0001c0001t0001g0092 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.4210-1410A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 19/38 | chr16 | 53261577 | ||||||
| chr16:53261796
|
G | T | 1 | a0001c0001t0001g0099 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.4210-1191G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 19/38 | chr16 | 53261796 | ||||||
| chr16:53261824
|
A | T | 53 | a0002c0002t0001g0009a0002c0002t0001g0010a0002c0002t0001g0012others(50): Show | 53 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.4210-1163A>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 19/38 | chr16 | 53261824 | ||||||
| chr16:53261906
|
G | C | 1 | a0002c0002t0001g0102 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.4210-1081G>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 19/38 | chr16 | 53261906 | ||||||
| chr16:53262108
|
T | C | 1 | a0001c0003t0002g0023 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.4210-879T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 19/38 | chr16 | 53262108 | ||||||
| chr16:53262237
|
T | A | 7 | a0001c0001t0003g0133a0001c0001t0003g0184a0001c0001t0003g0220others(4): Show | 7 | HG02055.hp1 HG02109.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.4210-750T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 19/38 | chr16 | 53262237 | ||||||
| chr16:53262290
|
A | G | 2 | a0001c0005t0004g0097a0006c0009t0004g0107 | 2 | HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.4210-697A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 19/38 | chr16 | 53262290 | ||||||
| chr16:53262569
|
A | C | 1 | a0006c0009t0004g0107 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.4210-418A>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 19/38 | chr16 | 53262569 | ||||||
| chr16:53262692
|
C | T | 1 | a0003c0004t0001g0195 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.4210-295C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 19/38 | chr16 | 53262692 | ||||||
| chr16:53262744
|
A | G | 1 | a0001c0005t0004g0169 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.4210-243A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 19/38 | chr16 | 53262744 | ||||||
| chr16:53263263
|
A | G | 1 | a0001c0001t0001g0098 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.4320+166A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 20/38 | chr16 | 53263263 | ||||||
| chr16:53263483
|
T | C | 52 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0021others(49): Show | 52 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(49): Show |
intron_variant | MODIFIER | c.4320+386T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 20/38 | chr16 | 53263483 | ||||||
| chr16:53263629
|
G | A | 5 | a0003c0004t0001g0007a0003c0004t0001g0030a0003c0004t0001g0093others(2): Show | 5 | HG00597.hp2 NA18955.hp2 NA18993.hp2 others(2): Show |
intron_variant | MODIFIER | c.4320+532G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 20/38 | chr16 | 53263629 | ||||||
| chr16:53263676
|
G | A | 1 | a0002c0002t0001g0208 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.4320+579G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 20/38 | chr16 | 53263676 | ||||||
| chr16:53263701
|
T | C | 1 | a0001c0003t0002g0033 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.4320+604T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 20/38 | chr16 | 53263701 | ||||||
| chr16:53263773
|
T | G | 65 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.4320+676T>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 20/38 | chr16 | 53263773 | ||||||
| chr16:53263895
|
G | T | 14 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0031others(11): Show | 14 | HG00408.hp2 HG00621.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.4320+798G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 20/38 | chr16 | 53263895 | ||||||
| chr16:53264385
|
C | G | 2 | a0001c0001t0007g0103a0001c0001t0007g0122 | 2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.4320+1288C>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 20/38 | chr16 | 53264385 | ||||||
| chr16:53264471
|
G | C | 74 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(71): Show | 74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.4320+1374G>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 20/38 | chr16 | 53264471 | ||||||
| chr16:53264655
|
C | T | 74 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(71): Show | 74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.4320+1558C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 20/38 | chr16 | 53264655 | ||||||
| chr16:53264732
|
A | G | 1 | a0003c0004t0001g0143 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.4320+1635A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 20/38 | chr16 | 53264732 | ||||||
| chr16:53264953
|
G | A | 1 | a0002c0002t0001g0219 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.4320+1856G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 20/38 | chr16 | 53264953 | ||||||
| chr16:53264955
|
G | A | 1 | a0001c0001t0003g0131 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.4320+1858G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 20/38 | chr16 | 53264955 | ||||||
| chr16:53264967
|
G | T | 3 | a0004c0006t0001g0121a0004c0006t0001g0127a0004c0006t0001g0128 | 3 | NA18952.hp1 NA18989.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.4320+1870G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 20/38 | chr16 | 53264967 | ||||||
| chr16:53265218
|
T | C | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.4321-2076T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 20/38 | chr16 | 53265218 | ||||||
| chr16:53265292
|
C | T | 1 | a0001c0017t0002g0237 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4321-2002C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 20/38 | chr16 | 53265292 | ||||||
| chr16:53265304
|
A | G | 12 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(9): Show | 12 | HG01167.hp2 HG01884.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.4321-1990A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 20/38 | chr16 | 53265304 | ||||||
| chr16:53265335
|
C | T | 1 | a0001c0017t0002g0237 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4321-1959C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 20/38 | chr16 | 53265335 | ||||||
| chr16:53265463
|
A | G | 65 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.4321-1831A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 20/38 | chr16 | 53265463 | ||||||
| chr16:53265768
|
G | T | 1 | a0001c0005t0005g0018 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.4321-1526G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 20/38 | chr16 | 53265768 | ||||||
| chr16:53265768
|
GC | G | 9 | a0001c0001t0003g0096a0001c0001t0003g0133a0001c0001t0003g0184others(6): Show | 9 | HG02055.hp1 HG02109.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.4321-1525delC | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 20/38 | chr16 | 53265768 | ||||||
| chr16:53265848
|
CAT | C | 65 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.4321-1445_4321-144 others(6): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 20/38 | chr16 | 53265848 | ||||||
| chr16:53266102
|
C | T | 74 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(71): Show | 74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.4321-1192C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 20/38 | chr16 | 53266102 | ||||||
| chr16:53266153
|
G | C | 4 | a0002c0002t0001g0087a0002c0002t0001g0088a0002c0002t0001g0108others(1): Show | 4 | HG01255.hp2 HG01433.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.4321-1141G>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 20/38 | chr16 | 53266153 | ||||||
| chr16:53266321
|
T | C | 1 | a0001c0001t0003g0096 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4321-973T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 20/38 | chr16 | 53266321 | ||||||
| chr16:53266376
|
C | A | 1 | a0008c0011t0003g0062 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.4321-918C>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 20/38 | chr16 | 53266376 | ||||||
| chr16:53266575
|
A | T | 65 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.4321-719A>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 20/38 | chr16 | 53266575 | ||||||
| chr16:53266617
|
G | A | 1 | a0001c0005t0004g0097 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.4321-677G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 20/38 | chr16 | 53266617 | ||||||
| chr16:53266632
|
T | C | 1 | a0001c0005t0004g0097 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.4321-662T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 20/38 | chr16 | 53266632 | ||||||
| chr16:53266820
|
C | A | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.4321-474C>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 20/38 | chr16 | 53266820 | ||||||
| chr16:53266920
|
A | G | 1 | a0002c0002t0001g0118 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.4321-374A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 20/38 | chr16 | 53266920 | ||||||
| chr16:53268170
|
A | G | 1 | a0001c0005t0001g0215 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.4717+44A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 22/38 | chr16 | 53268170 | ||||||
| chr16:53268389
|
C | A | 1 | a0002c0002t0001g0042 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.4717+263C>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 22/38 | chr16 | 53268389 | ||||||
| chr16:53268425
|
G | C | 1 | a0001c0001t0002g0171 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.4717+299G>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 22/38 | chr16 | 53268425 | ||||||
| chr16:53268471
|
G | A | 119 | a0001c0001t0002g0171a0001c0001t0002g0175a0001c0001t0015g0166others(116): Show | 119 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.4717+345G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 22/38 | chr16 | 53268471 | ||||||
| chr16:53268854
|
G | A | 1 | a0001c0001t0001g0185 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.4717+728G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 22/38 | chr16 | 53268854 | ||||||
| chr16:53268955
|
A | T | 2 | a0003c0004t0001g0187a0003c0004t0001g0194 | 2 | HG02165.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.4717+829A>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 22/38 | chr16 | 53268955 | ||||||
| chr16:53268985
|
A | G | 1 | a0001c0003t0002g0002 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.4717+859A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 22/38 | chr16 | 53268985 | ||||||
| chr16:53269012
|
G | A | 2 | a0001c0005t0004g0097a0006c0009t0004g0107 | 2 | HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.4717+886G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 22/38 | chr16 | 53269012 | ||||||
| chr16:53269152
|
A | G | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.4717+1026A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 22/38 | chr16 | 53269152 | ||||||
| chr16:53269204
|
C | G | 1 | a0001c0001t0001g0045 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.4717+1078C>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 22/38 | chr16 | 53269204 | ||||||
| chr16:53269310
|
A | G | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.4717+1184A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 22/38 | chr16 | 53269310 | ||||||
| chr16:53269758
|
A | T | 1 | a0001c0001t0001g0056 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.4717+1632A>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 22/38 | chr16 | 53269758 | ||||||
| chr16:53269945
|
A | G | 1 | a0001c0001t0003g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.4717+1819A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 22/38 | chr16 | 53269945 | ||||||
| chr16:53269971
|
T | A | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.4717+1845T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 22/38 | chr16 | 53269971 | ||||||
| chr16:53270036
|
G | T | 2 | a0002c0002t0001g0120a0002c0002t0001g0163 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.4717+1910G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 22/38 | chr16 | 53270036 | ||||||
| chr16:53270065
|
C | T | 1 | a0001c0005t0011g0228 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.4717+1939C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 22/38 | chr16 | 53270065 | ||||||
| chr16:53270161
|
A | AT | 71 | a0001c0001t0001g0064a0001c0001t0001g0090a0001c0001t0001g0173others(68): Show | 71 | HG00099.hp2 HG00408.hp1 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.4717+2058dupT | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 22/38 | INFO_REALIGN_3_PRIME | chr16 | 53270161 | |||||
| chr16:53270161
|
A | ATT | 6 | a0002c0002t0001g0037a0002c0002t0001g0054a0002c0002t0001g0102others(3): Show | 6 | HG00733.hp2 HG00735.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.4717+2057_4717+205 others(6): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 22/38 | INFO_REALIGN_3_PRIME | chr16 | 53270161 | |||||
| chr16:53270202
|
T | G | 1 | a0003c0004t0001g0100 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.4717+2076T>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 22/38 | chr16 | 53270202 | ||||||
| chr16:53270209
|
C | T | 1 | a0003c0004t0001g0197 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.4717+2083C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 22/38 | chr16 | 53270209 | ||||||
| chr16:53270468
|
C | T | 70 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(67): Show | 70 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(67): Show |
intron_variant | MODIFIER | c.4717+2342C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 22/38 | chr16 | 53270468 | ||||||
| chr16:53270558
|
G | A | 1 | a0001c0001t0001g0211 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.4717+2432G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 22/38 | chr16 | 53270558 | ||||||
| chr16:53270600
|
A | T | 1 | a0001c0005t0011g0228 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.4717+2474A>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 22/38 | chr16 | 53270600 | ||||||
| chr16:53270752
|
G | A | 70 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(67): Show | 70 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(67): Show |
intron_variant | MODIFIER | c.4717+2626G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 22/38 | chr16 | 53270752 | ||||||
| chr16:53270826
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.4717+2700G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 22/38 | chr16 | 53270826 | ||||||
| chr16:53270964
|
G | A | 2 | a0001c0005t0004g0097a0006c0009t0004g0107 | 2 | HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.4718-2662G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 22/38 | chr16 | 53270964 | ||||||
| chr16:53270989
|
C | T | 1 | a0001c0001t0003g0133 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.4718-2637C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 22/38 | chr16 | 53270989 | ||||||
| chr16:53271182
|
A | G | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.4718-2444A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 22/38 | chr16 | 53271182 | ||||||
| chr16:53271296
|
C | T | 1 | a0006c0009t0004g0107 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.4718-2330C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 22/38 | chr16 | 53271296 | ||||||
| chr16:53271395
|
C | T | 1 | a0001c0005t0001g0215 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.4718-2231C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 22/38 | chr16 | 53271395 | ||||||
| chr16:53271398
|
G | C | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.4718-2228G>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 22/38 | chr16 | 53271398 | ||||||
| chr16:53271586
|
A | G | 2 | a0001c0001t0003g0220a0001c0001t0003g0223 | 2 | HG02055.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.4718-2040A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 22/38 | chr16 | 53271586 | ||||||
| chr16:53271676
|
A | G | 1 | a0001c0001t0001g0025 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.4718-1950A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 22/38 | chr16 | 53271676 | ||||||
| chr16:53271704
|
G | A | 1 | a0001c0003t0002g0170 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.4718-1922G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 22/38 | chr16 | 53271704 | ||||||
| chr16:53271971
|
AGAAG | A | 2 | a0002c0002t0001g0087a0002c0002t0001g0088 | 2 | HG01255.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.4718-1649_4718-164 others(8): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 22/38 | INFO_REALIGN_3_PRIME | chr16 | 53271971 | |||||
| chr16:53272243
|
T | TA | 70 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(67): Show | 70 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(67): Show |
intron_variant | MODIFIER | c.4718-1374dupA | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 22/38 | INFO_REALIGN_3_PRIME | chr16 | 53272243 | |||||
| chr16:53272307
|
A | G | 1 | a0002c0002t0001g0219 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.4718-1319A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 22/38 | chr16 | 53272307 | ||||||
| chr16:53272316
|
C | T | 2 | a0001c0005t0004g0097a0006c0009t0004g0107 | 2 | HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.4718-1310C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 22/38 | chr16 | 53272316 | ||||||
| chr16:53272530
|
G | A | 10 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0231others(7): Show | 10 | HG01167.hp2 HG01884.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.4718-1096G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 22/38 | chr16 | 53272530 | ||||||
| chr16:53272850
|
C | T | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.4718-776C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 22/38 | chr16 | 53272850 | ||||||
| chr16:53272982
|
A | G | 1 | a0002c0002t0001g0044 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.4718-644A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 22/38 | chr16 | 53272982 | ||||||
| chr16:53273038
|
G | A | 9 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0231others(6): Show | 9 | HG01884.hp2 HG02615.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.4718-588G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 22/38 | chr16 | 53273038 | ||||||
| chr16:53273093
|
AAC | A | 61 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(58): Show | 61 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.4718-531_4718-530d others(4): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 22/38 | INFO_REALIGN_3_PRIME | chr16 | 53273093 | |||||
| chr16:53274403
|
A | T | 70 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(67): Show | 70 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(67): Show |
intron_variant | MODIFIER | c.4967+101A>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 24/38 | chr16 | 53274403 | ||||||
| chr16:53274408
|
C | T | 1 | a0003c0004t0001g0143 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.4967+106C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 24/38 | chr16 | 53274408 | ||||||
| chr16:53274902
|
C | T | 6 | a0001c0003t0002g0086a0001c0003t0002g0153a0001c0003t0002g0161others(3): Show | 6 | HG00735.hp1 HG01074.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.4967+600C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 24/38 | chr16 | 53274902 | ||||||
| chr16:53275039
|
T | G | 49 | a0002c0002t0001g0009a0002c0002t0001g0010a0002c0002t0001g0012others(46): Show | 49 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(46): Show |
intron_variant | MODIFIER | c.4967+737T>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 24/38 | chr16 | 53275039 | ||||||
| chr16:53275155
|
C | T | 1 | a0001c0005t0001g0215 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.4967+853C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 24/38 | chr16 | 53275155 | ||||||
| chr16:53275316
|
C | G | 12 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(9): Show | 12 | HG01167.hp2 HG01884.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.4967+1014C>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 24/38 | chr16 | 53275316 | ||||||
| chr16:53275504
|
T | C | 1 | a0001c0001t0003g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.4967+1202T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 24/38 | chr16 | 53275504 | ||||||
| chr16:53275833
|
T | C | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.4967+1531T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 24/38 | chr16 | 53275833 | ||||||
| chr16:53276089
|
C | T | 1 | a0002c0002t0001g0037 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.4967+1787C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 24/38 | chr16 | 53276089 | ||||||
| chr16:53276464
|
C | T | 61 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(58): Show | 61 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.4967+2162C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 24/38 | chr16 | 53276464 | ||||||
| chr16:53276740
|
A | G | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.4967+2438A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 24/38 | chr16 | 53276740 | ||||||
| chr16:53276904
|
G | T | 70 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(67): Show | 70 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(67): Show |
intron_variant | MODIFIER | c.4967+2602G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 24/38 | chr16 | 53276904 | ||||||
| chr16:53277013
|
G | T | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.4967+2711G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 24/38 | chr16 | 53277013 | ||||||
| chr16:53277502
|
A | G | 47 | a0001c0001t0002g0171a0001c0001t0002g0175a0001c0001t0015g0166others(44): Show | 47 | HG00140.hp2 HG00558.hp2 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.4967+3200A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 24/38 | chr16 | 53277502 | ||||||
| chr16:53277785
|
G | A | 32 | a0001c0001t0001g0008a0001c0001t0001g0025a0001c0001t0001g0043others(29): Show | 32 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.4967+3483G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 24/38 | chr16 | 53277785 | ||||||
| chr16:53277785
|
G | C | 1 | a0001c0001t0003g0079 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.4967+3483G>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 24/38 | chr16 | 53277785 | ||||||
| chr16:53277930
|
T | A | 1 | a0001c0001t0001g0008 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.4967+3628T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 24/38 | chr16 | 53277930 | ||||||
| chr16:53278014
|
GA | G | 11 | a0001c0001t0003g0022a0001c0001t0003g0079a0001c0001t0003g0105others(8): Show | 11 | HG01891.hp1 HG02257.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.4967+3724delA | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 24/38 | INFO_REALIGN_3_PRIME | chr16 | 53278014 | |||||
| chr16:53278034
|
A | G | 1 | a0001c0008t0001g0077 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.4967+3732A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 24/38 | chr16 | 53278034 | ||||||
| chr16:53278161
|
A | G | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.4967+3859A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 24/38 | chr16 | 53278161 | ||||||
| chr16:53278239
|
A | G | 70 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(67): Show | 70 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(67): Show |
intron_variant | MODIFIER | c.4967+3937A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 24/38 | chr16 | 53278239 | ||||||
| chr16:53278364
|
A | G | 2 | a0001c0005t0004g0097a0006c0009t0004g0107 | 2 | HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.4967+4062A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 24/38 | chr16 | 53278364 | ||||||
| chr16:53278472
|
C | A | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.4967+4170C>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 24/38 | chr16 | 53278472 | ||||||
| chr16:53278879
|
G | A | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.4967+4577G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 24/38 | chr16 | 53278879 | ||||||
| chr16:53279111
|
A | G | 48 | a0002c0002t0001g0009a0002c0002t0001g0010a0002c0002t0001g0012others(45): Show | 48 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(45): Show |
intron_variant | MODIFIER | c.4967+4809A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 24/38 | chr16 | 53279111 | ||||||
| chr16:53279201
|
T | C | 118 | a0001c0001t0001g0159a0001c0001t0002g0171a0001c0001t0002g0175others(115): Show | 118 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.4967+4899T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 24/38 | chr16 | 53279201 | ||||||
| chr16:53279333
|
G | T | 61 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(58): Show | 61 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.4967+5031G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 24/38 | chr16 | 53279333 | ||||||
| chr16:53279375
|
G | C | 1 | a0001c0001t0003g0112 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.4967+5073G>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 24/38 | chr16 | 53279375 | ||||||
| chr16:53279600
|
T | G | 1 | a0003c0004t0001g0207 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.4967+5298T>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 24/38 | chr16 | 53279600 | ||||||
| chr16:53279754
|
A | G | 73 | a0001c0005t0001g0215a0001c0005t0004g0078a0001c0005t0004g0097others(70): Show | 73 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.4967+5452A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 24/38 | chr16 | 53279754 | ||||||
| chr16:53279929
|
A | G | 1 | a0001c0001t0003g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.4967+5627A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 24/38 | chr16 | 53279929 | ||||||
| chr16:53280047
|
A | G | 49 | a0002c0002t0001g0009a0002c0002t0001g0010a0002c0002t0001g0012others(46): Show | 49 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(46): Show |
intron_variant | MODIFIER | c.4968-5549A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 24/38 | chr16 | 53280047 | ||||||
| chr16:53280109
|
G | A | 1 | a0001c0017t0002g0237 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4968-5487G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 24/38 | chr16 | 53280109 | ||||||
| chr16:53280201
|
ATT | A | 2 | a0001c0001t0001g0230a0003c0004t0001g0134 | 2 | HG03453.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.4968-5394_4968-539 others(6): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 24/38 | chr16 | 53280201 | ||||||
| chr16:53280260
|
G | A | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.4968-5336G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 24/38 | chr16 | 53280260 | ||||||
| chr16:53280306
|
CTG | C | 19 | a0001c0001t0003g0022a0001c0001t0003g0079a0001c0001t0003g0096others(16): Show | 19 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.4968-5287_4968-528 others(6): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 24/38 | INFO_REALIGN_3_PRIME | chr16 | 53280306 | |||||
| chr16:53280535
|
G | C | 1 | a0001c0003t0019g0004 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.4968-5061G>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 24/38 | chr16 | 53280535 | ||||||
| chr16:53280619
|
T | G | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.4968-4977T>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 24/38 | chr16 | 53280619 | ||||||
| chr16:53280623
|
G | T | 1 | a0001c0001t0003g0184 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4968-4973G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 24/38 | chr16 | 53280623 | ||||||
| chr16:53280633
|
A | G | 1 | a0001c0001t0001g0067 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.4968-4963A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 24/38 | chr16 | 53280633 | ||||||
| chr16:53280641
|
A | G | 1 | a0002c0002t0001g0106 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.4968-4955A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 24/38 | chr16 | 53280641 | ||||||
| chr16:53280681
|
T | TA | 10 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(7): Show | 10 | HG02257.hp2 HG02622.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.4968-4902dupA | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 24/38 | INFO_REALIGN_3_PRIME | chr16 | 53280681 | |||||
| chr16:53280713
|
C | T | 2 | a0001c0001t0001g0119a0001c0013t0001g0055 | 2 | HG00733.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.4968-4883C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 24/38 | chr16 | 53280713 | ||||||
| chr16:53280767
|
C | T | 137 | a0001c0001t0001g0159a0001c0001t0002g0171a0001c0001t0002g0175others(134): Show | 137 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.4968-4829C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 24/38 | chr16 | 53280767 | ||||||
| chr16:53280834
|
C | T | 4 | a0001c0003t0002g0005a0001c0003t0002g0047a0001c0003t0002g0191others(1): Show | 4 | NA18972.hp2 NA19012.hp2 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.4968-4762C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 24/38 | chr16 | 53280834 | ||||||
| chr16:53280862
|
C | T | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.4968-4734C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 24/38 | chr16 | 53280862 | ||||||
| chr16:53280962
|
C | T | 1 | a0001c0001t0001g0068 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.4968-4634C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 24/38 | chr16 | 53280962 | ||||||
| chr16:53281268
|
A | C | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.4968-4328A>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 24/38 | chr16 | 53281268 | ||||||
| chr16:53281410
|
A | G | 1 | a0001c0005t0001g0215 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.4968-4186A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 24/38 | chr16 | 53281410 | ||||||
| chr16:53281807
|
A | G | 1 | a0002c0002t0001g0219 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.4968-3789A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 24/38 | chr16 | 53281807 | ||||||
| chr16:53281898
|
A | G | 45 | a0001c0001t0001g0159a0001c0001t0002g0171a0001c0001t0002g0175others(42): Show | 45 | HG00140.hp2 HG00558.hp2 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.4968-3698A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 24/38 | chr16 | 53281898 | ||||||
| chr16:53282145
|
T | C | 19 | a0001c0001t0003g0022a0001c0001t0003g0079a0001c0001t0003g0096others(16): Show | 19 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.4968-3451T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 24/38 | chr16 | 53282145 | ||||||
| chr16:53282449
|
T | C | 1 | a0001c0001t0001g0178 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.4968-3147T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 24/38 | chr16 | 53282449 | ||||||
| chr16:53282655
|
T | C | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.4968-2941T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 24/38 | chr16 | 53282655 | ||||||
| chr16:53282709
|
C | G | 1 | a0001c0003t0013g0186 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.4968-2887C>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 24/38 | chr16 | 53282709 | ||||||
| chr16:53282942
|
A | G | 65 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.4968-2654A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 24/38 | chr16 | 53282942 | ||||||
| chr16:53283406
|
AATGTGCT others(1): Show |
A | 41 | a0001c0001t0001g0159a0001c0001t0015g0166a0001c0003t0002g0002others(38): Show | 41 | HG00140.hp2 HG00558.hp2 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.4968-2186_4968-217 others(12): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 24/38 | INFO_REALIGN_3_PRIME | chr16 | 53283406 | |||||
| chr16:53283549
|
G | A | 3 | a0001c0005t0001g0215a0001c0005t0004g0097a0006c0009t0004g0107 | 3 | HG01884.hp1 HG03516.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.4968-2047G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 24/38 | chr16 | 53283549 | ||||||
| chr16:53283579
|
G | T | 1 | a0003c0004t0001g0162 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.4968-2017G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 24/38 | chr16 | 53283579 | ||||||
| chr16:53283844
|
G | A | 65 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.4968-1752G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 24/38 | chr16 | 53283844 | ||||||
| chr16:53283976
|
C | T | 41 | a0001c0001t0001g0159a0001c0001t0015g0166a0001c0003t0002g0002others(38): Show | 41 | HG00140.hp2 HG00558.hp2 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.4968-1620C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 24/38 | chr16 | 53283976 | ||||||
| chr16:53284048
|
A | C | 1 | a0001c0003t0002g0154 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.4968-1548A>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 24/38 | chr16 | 53284048 | ||||||
| chr16:53284182
|
C | A | 1 | a0002c0002t0001g0106 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.4968-1414C>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 24/38 | chr16 | 53284182 | ||||||
| chr16:53284351
|
G | A | 65 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.4968-1245G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 24/38 | chr16 | 53284351 | ||||||
| chr16:53284380
|
G | A | 1 | a0003c0004t0001g0141 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.4968-1216G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 24/38 | chr16 | 53284380 | ||||||
| chr16:53284521
|
A | G | 7 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0061others(4): Show | 7 | HG02257.hp2 HG03688.hp2 HG04184.hp2 others(4): Show |
intron_variant | MODIFIER | c.4968-1075A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 24/38 | chr16 | 53284521 | ||||||
| chr16:53284662
|
A | G | 3 | a0001c0003t0002g0005a0001c0003t0002g0047a0001c0003t0002g0191 | 3 | NA18972.hp2 NA19012.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.4968-934A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 24/38 | chr16 | 53284662 | ||||||
| chr16:53284817
|
G | A | 3 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0012g0229 | 3 | HG01167.hp2 HG01884.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.4968-779G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 24/38 | chr16 | 53284817 | ||||||
| chr16:53285021
|
C | T | 65 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.4968-575C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 24/38 | chr16 | 53285021 | ||||||
| chr16:53285040
|
T | C | 65 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.4968-556T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 24/38 | chr16 | 53285040 | ||||||
| chr16:53285086
|
C | T | 1 | a0001c0005t0001g0215 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.4968-510C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 24/38 | chr16 | 53285086 | ||||||
| chr16:53285226
|
C | T | 19 | a0001c0001t0003g0022a0001c0001t0003g0079a0001c0001t0003g0096others(16): Show | 19 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.4968-370C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 24/38 | chr16 | 53285226 | ||||||
| chr16:53285307
|
C | G | 1 | a0001c0001t0001g0230 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.4968-289C>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 24/38 | chr16 | 53285307 | ||||||
| chr16:53285396
|
C | T | 2 | a0003c0004t0001g0134a0003c0004t0001g0141 | 2 | HG02895.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.4968-200C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 24/38 | chr16 | 53285396 | ||||||
| chr16:53285438
|
T | C | 1 | a0001c0001t0001g0165 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.4968-158T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 24/38 | chr16 | 53285438 | ||||||
| chr16:53285478
|
T | TAATGA | 237 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0021others(234): Show | 237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.4968-114_4968-110d others(7): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 24/38 | INFO_REALIGN_3_PRIME | chr16 | 53285478 | |||||
| chr16:53285885
|
G | A | 1 | a0001c0001t0001g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.5071+186G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 25/38 | chr16 | 53285885 | ||||||
| chr16:53285933
|
A | G | 65 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.5071+234A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 25/38 | chr16 | 53285933 | ||||||
| chr16:53285963
|
G | A | 1 | a0001c0005t0005g0061 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.5072-263G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 25/38 | chr16 | 53285963 | ||||||
| chr16:53285965
|
G | A | 1 | a0001c0001t0001g0085 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.5072-261G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 25/38 | chr16 | 53285965 | ||||||
| chr16:53285995
|
A | G | 1 | a0001c0005t0004g0169 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.5072-231A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 25/38 | chr16 | 53285995 | ||||||
| chr16:53286113
|
G | A | 65 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.5072-113G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 25/38 | chr16 | 53286113 | ||||||
| chr16:53286439
|
G | A | 5 | a0001c0001t0003g0022a0001c0001t0003g0079a0001c0001t0003g0105others(2): Show | 5 | HG02280.hp1 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.5189+96G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 26/38 | chr16 | 53286439 | ||||||
| chr16:53286770
|
A | G | 1 | a0001c0001t0003g0112 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.5189+427A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 26/38 | chr16 | 53286770 | ||||||
| chr16:53286856
|
T | C | 1 | a0006c0009t0004g0107 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.5189+513T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 26/38 | chr16 | 53286856 | ||||||
| chr16:53287076
|
A | C | 1 | a0001c0001t0003g0221 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.5189+733A>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 26/38 | chr16 | 53287076 | ||||||
| chr16:53287237
|
C | T | 65 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.5190-720C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 26/38 | chr16 | 53287237 | ||||||
| chr16:53287323
|
C | T | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.5190-634C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 26/38 | chr16 | 53287323 | ||||||
| chr16:53287446
|
G | A | 1 | a0001c0003t0013g0186 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.5190-511G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 26/38 | chr16 | 53287446 | ||||||
| chr16:53287557
|
G | A | 1 | a0003c0004t0006g0074 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.5190-400G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 26/38 | chr16 | 53287557 | ||||||
| chr16:53287697
|
G | A | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.5190-260G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 26/38 | chr16 | 53287697 | ||||||
| chr16:53287815
|
TGTGTCTT others(17): Show |
T | 1 | a0001c0001t0001g0091 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.5190-140_5190-117d others(26): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 26/38 | INFO_REALIGN_3_PRIME | chr16 | 53287815 | |||||
| chr16:53287822
|
T | C | 110 | a0001c0001t0001g0159a0001c0001t0002g0171a0001c0001t0002g0175others(107): Show | 110 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.5190-135T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 26/38 | chr16 | 53287822 | ||||||
| chr16:53287841
|
A | G | 1 | a0001c0001t0001g0091 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.5190-116A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 26/38 | chr16 | 53287841 | ||||||
| chr16:53288110
|
T | C | 2 | a0002c0002t0001g0120a0002c0002t0001g0163 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.5247+96T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 27/38 | chr16 | 53288110 | ||||||
| chr16:53288208
|
T | C | 74 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(71): Show | 74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.5247+194T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 27/38 | chr16 | 53288208 | ||||||
| chr16:53288227
|
G | A | 1 | a0001c0001t0001g0092 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.5247+213G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 27/38 | chr16 | 53288227 | ||||||
| chr16:53288240
|
G | C | 1 | a0001c0001t0015g0166 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.5247+226G>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 27/38 | chr16 | 53288240 | ||||||
| chr16:53288281
|
A | G | 65 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.5247+267A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 27/38 | chr16 | 53288281 | ||||||
| chr16:53288709
|
G | T | 1 | a0001c0001t0001g0110 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.5247+695G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 27/38 | chr16 | 53288709 | ||||||
| chr16:53288752
|
T | G | 1 | a0001c0001t0001g0124 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.5247+738T>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 27/38 | chr16 | 53288752 | ||||||
| chr16:53289001
|
G | C | 77 | a0001c0005t0001g0215a0001c0005t0004g0078a0001c0005t0004g0097others(74): Show | 77 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.5247+987G>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 27/38 | chr16 | 53289001 | ||||||
| chr16:53289213
|
G | A | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.5247+1199G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 27/38 | chr16 | 53289213 | ||||||
| chr16:53289293
|
C | T | 2 | a0001c0005t0004g0233a0001c0005t0004g0234 | 2 | HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.5247+1279C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 27/38 | chr16 | 53289293 | ||||||
| chr16:53289342
|
C | T | 6 | a0002c0002t0001g0106a0002c0002t0001g0109a0002c0002t0001g0113others(3): Show | 6 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.5247+1328C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 27/38 | chr16 | 53289342 | ||||||
| chr16:53289367
|
C | A | 1 | a0001c0005t0011g0228 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.5247+1353C>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 27/38 | chr16 | 53289367 | ||||||
| chr16:53289384
|
A | T | 53 | a0002c0002t0001g0009a0002c0002t0001g0010a0002c0002t0001g0012others(50): Show | 53 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.5247+1370A>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 27/38 | chr16 | 53289384 | ||||||
| chr16:53289528
|
G | A | 42 | a0001c0001t0002g0171a0001c0001t0002g0175a0001c0001t0015g0166others(39): Show | 42 | HG00140.hp2 HG00558.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.5247+1514G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 27/38 | chr16 | 53289528 | ||||||
| chr16:53289837
|
C | T | 52 | a0002c0002t0001g0009a0002c0002t0001g0010a0002c0002t0001g0012others(49): Show | 52 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(49): Show |
intron_variant | MODIFIER | c.5247+1823C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 27/38 | chr16 | 53289837 | ||||||
| chr16:53289958
|
G | A | 1 | a0006c0009t0004g0107 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.5248-1767G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 27/38 | chr16 | 53289958 | ||||||
| chr16:53289968
|
A | G | 74 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(71): Show | 74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.5248-1757A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 27/38 | chr16 | 53289968 | ||||||
| chr16:53290011
|
T | C | 1 | a0003c0004t0001g0192 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.5248-1714T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 27/38 | chr16 | 53290011 | ||||||
| chr16:53290066
|
G | T | 2 | a0001c0001t0007g0103a0001c0001t0007g0122 | 2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.5248-1659G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 27/38 | chr16 | 53290066 | ||||||
| chr16:53290120
|
A | G | 1 | a0001c0001t0003g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.5248-1605A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 27/38 | chr16 | 53290120 | ||||||
| chr16:53290146
|
T | C | 140 | a0001c0001t0002g0171a0001c0001t0002g0175a0001c0001t0003g0016others(137): Show | 140 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.5248-1579T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 27/38 | chr16 | 53290146 | ||||||
| chr16:53290206
|
G | A | 1 | a0001c0001t0003g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.5248-1519G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 27/38 | chr16 | 53290206 | ||||||
| chr16:53290311
|
G | A | 3 | a0001c0003t0002g0005a0001c0003t0002g0047a0001c0003t0002g0191 | 3 | NA18972.hp2 NA19012.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.5248-1414G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 27/38 | chr16 | 53290311 | ||||||
| chr16:53290485
|
CA | C | 140 | a0001c0001t0002g0171a0001c0001t0002g0175a0001c0001t0003g0016others(137): Show | 140 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.5248-1228delA | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 27/38 | INFO_REALIGN_3_PRIME | chr16 | 53290485 | |||||
| chr16:53290527
|
T | C | 77 | a0001c0005t0001g0215a0001c0005t0004g0078a0001c0005t0004g0097others(74): Show | 77 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.5248-1198T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 27/38 | chr16 | 53290527 | ||||||
| chr16:53290679
|
G | A | 1 | a0001c0012t0001g0132 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.5248-1046G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 27/38 | chr16 | 53290679 | ||||||
| chr16:53290693
|
G | A | 1 | a0001c0005t0001g0215 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.5248-1032G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 27/38 | chr16 | 53290693 | ||||||
| chr16:53290784
|
C | A | 74 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(71): Show | 74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.5248-941C>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 27/38 | chr16 | 53290784 | ||||||
| chr16:53290940
|
A | G | 1 | a0001c0001t0002g0175 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.5248-785A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 27/38 | chr16 | 53290940 | ||||||
| chr16:53291161
|
C | A | 12 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(9): Show | 12 | HG01167.hp2 HG01884.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.5248-564C>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 27/38 | chr16 | 53291161 | ||||||
| chr16:53291188
|
A | G | 1 | a0006c0009t0004g0107 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.5248-537A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 27/38 | chr16 | 53291188 | ||||||
| chr16:53291270
|
G | T | 4 | a0001c0001t0003g0131a0001c0001t0003g0139a0001c0001t0003g0172others(1): Show | 4 | HG01891.hp1 HG02257.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.5248-455G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 27/38 | chr16 | 53291270 | ||||||
| chr16:53291493
|
G | C | 1 | a0001c0001t0001g0206 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.5248-232G>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 27/38 | chr16 | 53291493 | ||||||
| chr16:53291618
|
T | C | 1 | a0002c0002t0001g0063 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.5248-107T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 27/38 | chr16 | 53291618 | ||||||
| chr16:53291672
|
A | G | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.5248-53A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 27/38 | chr16 | 53291672 | ||||||
| chr16:53291685
|
C | A | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.5248-40C>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 27/38 | chr16 | 53291685 | ||||||
| chr16:53291779
|
G | A | 65 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.5290+12G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 28/38 | chr16 | 53291779 | ||||||
| chr16:53291914
|
G | C | 1 | a0001c0003t0002g0041 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.5290+147G>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 28/38 | chr16 | 53291914 | ||||||
| chr16:53292013
|
C | T | 74 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(71): Show | 74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.5290+246C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 28/38 | chr16 | 53292013 | ||||||
| chr16:53292018
|
A | G | 2 | a0001c0005t0004g0169a0001c0005t0018g0001 | 2 | HG03139.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.5290+251A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 28/38 | chr16 | 53292018 | ||||||
| chr16:53292389
|
C | A | 1 | a0001c0001t0001g0230 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.5291-444C>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 28/38 | chr16 | 53292389 | ||||||
| chr16:53292584
|
C | T | 1 | a0001c0001t0001g0178 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.5291-249C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 28/38 | chr16 | 53292584 | ||||||
| chr16:53292718
|
T | C | 1 | a0002c0002t0001g0106 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.5291-115T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 28/38 | chr16 | 53292718 | ||||||
| chr16:53293061
|
A | G | 1 | a0001c0005t0005g0032 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.5510+9A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 29/38 | chr16 | 53293061 | ||||||
| chr16:53293075
|
T | C | 2 | a0001c0005t0004g0097a0006c0009t0004g0107 | 2 | HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.5510+23T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 29/38 | chr16 | 53293075 | ||||||
| chr16:53293129
|
A | G | 65 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.5510+77A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 29/38 | chr16 | 53293129 | ||||||
| chr16:53293415
|
G | C | 1 | a0001c0001t0001g0031 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.5510+363G>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 29/38 | chr16 | 53293415 | ||||||
| chr16:53293475
|
G | T | 1 | a0006c0009t0004g0107 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.5510+423G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 29/38 | chr16 | 53293475 | ||||||
| chr16:53293506
|
C | G | 49 | a0002c0002t0001g0009a0002c0002t0001g0010a0002c0002t0001g0012others(46): Show | 49 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(46): Show |
intron_variant | MODIFIER | c.5510+454C>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 29/38 | chr16 | 53293506 | ||||||
| chr16:53293509
|
G | A | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.5510+457G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 29/38 | chr16 | 53293509 | ||||||
| chr16:53293549
|
C | T | 1 | a0001c0001t0001g0085 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.5510+497C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 29/38 | chr16 | 53293549 | ||||||
| chr16:53293607
|
C | T | 1 | a0002c0002t0001g0102 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.5510+555C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 29/38 | chr16 | 53293607 | ||||||
| chr16:53293656
|
G | C | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.5510+604G>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 29/38 | chr16 | 53293656 | ||||||
| chr16:53293714
|
G | A | 1 | a0003c0004t0001g0204 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.5510+662G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 29/38 | chr16 | 53293714 | ||||||
| chr16:53293782
|
C | T | 9 | a0001c0001t0003g0022a0001c0001t0003g0079a0001c0001t0003g0105others(6): Show | 9 | HG01891.hp1 HG02257.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.5510+730C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 29/38 | chr16 | 53293782 | ||||||
| chr16:53293863
|
G | A | 1 | a0001c0017t0002g0237 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.5510+811G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 29/38 | chr16 | 53293863 | ||||||
| chr16:53294052
|
C | T | 1 | a0002c0002t0001g0118 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.5510+1000C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 29/38 | chr16 | 53294052 | ||||||
| chr16:53294067
|
T | C | 77 | a0001c0005t0001g0215a0001c0005t0004g0078a0001c0005t0004g0097others(74): Show | 77 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.5510+1015T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 29/38 | chr16 | 53294067 | ||||||
| chr16:53294200
|
A | G | 1 | a0001c0001t0001g0051 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.5510+1148A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 29/38 | chr16 | 53294200 | ||||||
| chr16:53294223
|
G | T | 1 | a0001c0001t0001g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.5510+1171G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 29/38 | chr16 | 53294223 | ||||||
| chr16:53294373
|
C | T | 1 | a0003c0004t0001g0197 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.5510+1321C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 29/38 | chr16 | 53294373 | ||||||
| chr16:53294490
|
G | T | 1 | a0001c0005t0005g0032 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.5510+1438G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 29/38 | chr16 | 53294490 | ||||||
| chr16:53294760
|
C | T | 1 | a0003c0004t0001g0209 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.5510+1708C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 29/38 | chr16 | 53294760 | ||||||
| chr16:53294875
|
T | C | 74 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(71): Show | 74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.5510+1823T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 29/38 | chr16 | 53294875 | ||||||
| chr16:53295149
|
C | T | 1 | a0001c0005t0005g0032 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.5511-1807C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 29/38 | chr16 | 53295149 | ||||||
| chr16:53295350
|
T | C | 6 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0168others(3): Show | 6 | HG01891.hp2 HG02451.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.5511-1606T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 29/38 | chr16 | 53295350 | ||||||
| chr16:53295572
|
G | A | 53 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0021others(50): Show | 53 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(50): Show |
intron_variant | MODIFIER | c.5511-1384G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 29/38 | chr16 | 53295572 | ||||||
| chr16:53295653
|
T | G | 1 | a0008c0011t0003g0062 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.5511-1303T>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 29/38 | chr16 | 53295653 | ||||||
| chr16:53295788
|
T | C | 1 | a0001c0001t0001g0230 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.5511-1168T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 29/38 | chr16 | 53295788 | ||||||
| chr16:53295855
|
T | C | 1 | a0008c0011t0003g0062 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.5511-1101T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 29/38 | chr16 | 53295855 | ||||||
| chr16:53295973
|
A | G | 1 | a0003c0004t0006g0199 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.5511-983A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 29/38 | chr16 | 53295973 | ||||||
| chr16:53296026
|
C | G | 44 | a0001c0001t0002g0171a0001c0001t0002g0175a0001c0001t0003g0016others(41): Show | 44 | HG00140.hp2 HG00558.hp2 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.5511-930C>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 29/38 | chr16 | 53296026 | ||||||
| chr16:53296171
|
C | T | 1 | a0008c0011t0003g0062 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.5511-785C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 29/38 | chr16 | 53296171 | ||||||
| chr16:53296216
|
T | A | 65 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.5511-740T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 29/38 | chr16 | 53296216 | ||||||
| chr16:53296434
|
A | AT | 65 | a0001c0001t0001g0025a0001c0001t0001g0056a0001c0001t0001g0084others(62): Show | 65 | HG00140.hp2 HG00733.hp1 HG01074.hp1 others(62): Show |
intron_variant | MODIFIER | c.5511-498dupT | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr16 | 53296434 | |||||
| chr16:53296434
|
A | ATT | 32 | a0001c0001t0002g0171a0001c0001t0002g0175a0001c0001t0003g0079others(29): Show | 32 | HG00323.hp1 HG00558.hp2 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.5511-499_5511-498d others(4): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr16 | 53296434 | |||||
| chr16:53296434
|
A | ATTT | 53 | a0001c0001t0003g0022a0001c0001t0003g0131a0001c0001t0003g0183others(50): Show | 53 | HG00099.hp2 HG00609.hp1 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.5511-500_5511-498d others(5): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr16 | 53296434 | |||||
| chr16:53296434
|
A | ATTTT | 14 | a0001c0005t0018g0001a0002c0002t0001g0009a0002c0002t0001g0012others(11): Show | 14 | HG00408.hp1 HG00735.hp2 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.5511-501_5511-498d others(6): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr16 | 53296434 | |||||
| chr16:53296434
|
A | T | 1 | a0001c0001t0001g0185 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.5511-522A>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 29/38 | chr16 | 53296434 | ||||||
| chr16:53296489
|
A | G | 77 | a0001c0005t0001g0215a0001c0005t0004g0078a0001c0005t0004g0097others(74): Show | 77 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.5511-467A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 29/38 | chr16 | 53296489 | ||||||
| chr16:53296648
|
T | C | 1 | a0001c0001t0001g0008 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.5511-308T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 29/38 | chr16 | 53296648 | ||||||
| chr16:53296688
|
G | A | 12 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(9): Show | 12 | HG01167.hp2 HG01884.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.5511-268G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 29/38 | chr16 | 53296688 | ||||||
| chr16:53296737
|
G | A | 1 | a0002c0002t0001g0063 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.5511-219G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 29/38 | chr16 | 53296737 | ||||||
| chr16:53296740
|
C | T | 2 | a0003c0004t0001g0007a0003c0004t0001g0030 | 2 | HG00597.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.5511-216C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 29/38 | chr16 | 53296740 | ||||||
| chr16:53297630
|
A | C | 1 | a0001c0005t0004g0097 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.5713+472A>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 30/38 | chr16 | 53297630 | ||||||
| chr16:53297679
|
A | T | 65 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.5713+521A>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 30/38 | chr16 | 53297679 | ||||||
| chr16:53297927
|
G | T | 1 | a0006c0009t0004g0107 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.5713+769G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 30/38 | chr16 | 53297927 | ||||||
| chr16:53298014
|
T | A | 4 | a0001c0001t0002g0171a0001c0001t0002g0175a0001c0005t0004g0097others(1): Show | 4 | HG01884.hp1 HG02451.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.5713+856T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 30/38 | chr16 | 53298014 | ||||||
| chr16:53298028
|
A | C | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.5713+870A>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 30/38 | chr16 | 53298028 | ||||||
| chr16:53298085
|
A | G | 1 | a0001c0001t0001g0211 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.5713+927A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 30/38 | chr16 | 53298085 | ||||||
| chr16:53298166
|
A | G | 74 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(71): Show | 74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.5713+1008A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 30/38 | chr16 | 53298166 | ||||||
| chr16:53298189
|
C | T | 1 | a0001c0003t0002g0154 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.5713+1031C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 30/38 | chr16 | 53298189 | ||||||
| chr16:53298264
|
C | T | 4 | a0001c0005t0004g0232a0001c0005t0004g0235a0001c0005t0004g0236others(1): Show | 4 | HG02615.hp2 HG02897.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.5713+1106C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 30/38 | chr16 | 53298264 | ||||||
| chr16:53298278
|
G | A | 65 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.5713+1120G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 30/38 | chr16 | 53298278 | ||||||
| chr16:53298325
|
A | G | 2 | a0001c0005t0004g0097a0006c0009t0004g0107 | 2 | HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.5713+1167A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 30/38 | chr16 | 53298325 | ||||||
| chr16:53298530
|
T | C | 74 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(71): Show | 74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.5713+1372T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 30/38 | chr16 | 53298530 | ||||||
| chr16:53298710
|
A | G | 1 | a0002c0002t0001g0109 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.5713+1552A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 30/38 | chr16 | 53298710 | ||||||
| chr16:53299097
|
C | T | 9 | a0001c0001t0003g0096a0001c0001t0003g0133a0001c0001t0003g0184others(6): Show | 9 | HG02055.hp1 HG02109.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.5713+1939C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 30/38 | chr16 | 53299097 | ||||||
| chr16:53299104
|
A | G | 2 | a0002c0002t0008g0065a0002c0002t0008g0137 | 2 | HG00408.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.5713+1946A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 30/38 | chr16 | 53299104 | ||||||
| chr16:53299187
|
C | G | 2 | a0001c0001t0003g0131a0001c0001t0003g0139 | 2 | HG01891.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.5713+2029C>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 30/38 | chr16 | 53299187 | ||||||
| chr16:53299386
|
G | C | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.5713+2228G>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 30/38 | chr16 | 53299386 | ||||||
| chr16:53299441
|
G | A | 3 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0182 | 3 | HG02615.hp1 HG02970.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.5713+2283G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 30/38 | chr16 | 53299441 | ||||||
| chr16:53299657
|
G | T | 54 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0021others(51): Show | 54 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.5713+2499G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 30/38 | chr16 | 53299657 | ||||||
| chr16:53299749
|
G | A | 1 | a0001c0001t0015g0166 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.5713+2591G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 30/38 | chr16 | 53299749 | ||||||
| chr16:53299881
|
C | G | 2 | a0001c0005t0004g0097a0006c0009t0004g0107 | 2 | HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.5713+2723C>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 30/38 | chr16 | 53299881 | ||||||
| chr16:53299881
|
C | T | 10 | a0001c0001t0003g0096a0001c0001t0003g0112a0001c0001t0003g0133others(7): Show | 10 | HG02055.hp1 HG02109.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.5713+2723C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 30/38 | chr16 | 53299881 | ||||||
| chr16:53299926
|
C | G | 1 | a0002c0002t0001g0102 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.5713+2768C>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 30/38 | chr16 | 53299926 | ||||||
| chr16:53300113
|
G | C | 1 | a0006c0009t0004g0107 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.5713+2955G>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 30/38 | chr16 | 53300113 | ||||||
| chr16:53300284
|
C | T | 22 | a0001c0001t0003g0022a0001c0001t0003g0079a0001c0001t0003g0096others(19): Show | 22 | HG01884.hp1 HG01891.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.5713+3126C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 30/38 | chr16 | 53300284 | ||||||
| chr16:53300352
|
C | CA | 10 | a0001c0003t0002g0041a0001c0005t0005g0017a0001c0005t0005g0018others(7): Show | 10 | HG00140.hp2 HG02257.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.5713+3207dupA | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 30/38 | INFO_REALIGN_3_PRIME | chr16 | 53300352 | |||||
| chr16:53300362
|
A | G | 1 | a0001c0005t0004g0232 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.5713+3204A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 30/38 | chr16 | 53300362 | ||||||
| chr16:53300404
|
C | T | 74 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(71): Show | 74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.5713+3246C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 30/38 | chr16 | 53300404 | ||||||
| chr16:53300414
|
C | CA | 46 | a0001c0001t0001g0159a0001c0001t0002g0171a0001c0001t0002g0175others(43): Show | 46 | HG00140.hp2 HG00558.hp2 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.5713+3260dupA | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 30/38 | INFO_REALIGN_3_PRIME | chr16 | 53300414 | |||||
| chr16:53300564
|
G | A | 1 | a0002c0002t0001g0205 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.5714-3156G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 30/38 | chr16 | 53300564 | ||||||
| chr16:53300842
|
A | T | 2 | a0001c0005t0004g0097a0006c0009t0004g0107 | 2 | HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.5714-2878A>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 30/38 | chr16 | 53300842 | ||||||
| chr16:53300874
|
G | A | 1 | a0003c0004t0001g0201 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.5714-2846G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 30/38 | chr16 | 53300874 | ||||||
| chr16:53300917
|
A | G | 1 | a0006c0009t0004g0107 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.5714-2803A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 30/38 | chr16 | 53300917 | ||||||
| chr16:53300930
|
A | G | 74 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(71): Show | 74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.5714-2790A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 30/38 | chr16 | 53300930 | ||||||
| chr16:53300999
|
G | C | 1 | a0001c0001t0001g0075 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.5714-2721G>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 30/38 | chr16 | 53300999 | ||||||
| chr16:53301052
|
A | G | 74 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(71): Show | 74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.5714-2668A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 30/38 | chr16 | 53301052 | ||||||
| chr16:53301058
|
G | A | 9 | a0001c0001t0003g0022a0001c0001t0003g0079a0001c0001t0003g0105others(6): Show | 9 | HG01891.hp1 HG02257.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.5714-2662G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 30/38 | chr16 | 53301058 | ||||||
| chr16:53301200
|
A | G | 1 | a0001c0005t0001g0215 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.5714-2520A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 30/38 | chr16 | 53301200 | ||||||
| chr16:53301576
|
A | G | 1 | a0001c0001t0001g0084 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.5714-2144A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 30/38 | chr16 | 53301576 | ||||||
| chr16:53301665
|
A | G | 1 | a0001c0003t0002g0003 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.5714-2055A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 30/38 | chr16 | 53301665 | ||||||
| chr16:53301767
|
C | CT | 6 | a0001c0001t0001g0218a0001c0012t0001g0132a0001c0013t0001g0055others(3): Show | 6 | HG00597.hp1 HG00733.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.5714-1937dupT | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 30/38 | INFO_REALIGN_3_PRIME | chr16 | 53301767 | |||||
| chr16:53301767
|
CT | C | 73 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(70): Show | 73 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.5714-1937delT | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 30/38 | INFO_REALIGN_3_PRIME | chr16 | 53301767 | |||||
| chr16:53301805
|
G | A | 2 | a0001c0001t0001g0038a0001c0001t0001g0098 | 2 | HG00609.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.5714-1915G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 30/38 | chr16 | 53301805 | ||||||
| chr16:53301827
|
G | A | 1 | a0001c0003t0002g0080 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.5714-1893G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 30/38 | chr16 | 53301827 | ||||||
| chr16:53301905
|
C | T | 1 | a0001c0005t0005g0089 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.5714-1815C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 30/38 | chr16 | 53301905 | ||||||
| chr16:53301953
|
C | T | 2 | a0001c0005t0004g0097a0006c0009t0004g0107 | 2 | HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.5714-1767C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 30/38 | chr16 | 53301953 | ||||||
| chr16:53301985
|
A | G | 74 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(71): Show | 74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.5714-1735A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 30/38 | chr16 | 53301985 | ||||||
| chr16:53302010
|
G | A | 1 | a0003c0004t0001g0093 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.5714-1710G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 30/38 | chr16 | 53302010 | ||||||
| chr16:53302214
|
A | G | 42 | a0001c0001t0001g0159a0001c0001t0015g0166a0001c0003t0001g0158others(39): Show | 42 | HG00140.hp2 HG00558.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.5714-1506A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 30/38 | chr16 | 53302214 | ||||||
| chr16:53302383
|
T | C | 1 | a0008c0011t0003g0062 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.5714-1337T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 30/38 | chr16 | 53302383 | ||||||
| chr16:53302385
|
C | G | 1 | a0002c0002t0001g0042 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.5714-1335C>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 30/38 | chr16 | 53302385 | ||||||
| chr16:53302474
|
T | A | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.5714-1246T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 30/38 | chr16 | 53302474 | ||||||
| chr16:53302476
|
T | C | 1 | a0001c0001t0009g0050 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.5714-1244T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 30/38 | chr16 | 53302476 | ||||||
| chr16:53302506
|
A | G | 1 | a0001c0005t0001g0215 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.5714-1214A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 30/38 | chr16 | 53302506 | ||||||
| chr16:53302509
|
C | T | 4 | a0001c0001t0001g0021a0001c0001t0001g0058a0001c0001t0001g0084others(1): Show | 4 | HG00621.hp1 NA18939.hp1 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.5714-1211C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 30/38 | chr16 | 53302509 | ||||||
| chr16:53302534
|
T | A | 43 | a0001c0001t0001g0159a0001c0001t0002g0171a0001c0001t0002g0175others(40): Show | 43 | HG00140.hp2 HG00558.hp2 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.5714-1186T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 30/38 | chr16 | 53302534 | ||||||
| chr16:53302675
|
T | C | 2 | a0001c0005t0004g0169a0001c0005t0018g0001 | 2 | HG03139.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.5714-1045T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 30/38 | chr16 | 53302675 | ||||||
| chr16:53302731
|
T | C | 122 | a0001c0001t0001g0159a0001c0001t0002g0171a0001c0001t0002g0175others(119): Show | 122 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.5714-989T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 30/38 | chr16 | 53302731 | ||||||
| chr16:53302840
|
A | G | 74 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(71): Show | 74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.5714-880A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 30/38 | chr16 | 53302840 | ||||||
| chr16:53303182
|
G | GT | 68 | a0001c0001t0001g0099a0001c0001t0003g0220a0001c0003t0002g0191others(65): Show | 68 | HG00099.hp2 HG00323.hp1 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.5714-522dupT | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 30/38 | INFO_REALIGN_3_PRIME | chr16 | 53303182 | |||||
| chr16:53303182
|
G | GTT | 11 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0231others(8): Show | 11 | HG00408.hp1 HG01167.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.5714-523_5714-522d others(4): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 30/38 | INFO_REALIGN_3_PRIME | chr16 | 53303182 | |||||
| chr16:53303274
|
A | G | 1 | a0001c0003t0002g0161 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.5714-446A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 30/38 | chr16 | 53303274 | ||||||
| chr16:53303447
|
C | T | 1 | a0001c0003t0002g0152 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.5714-273C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 30/38 | chr16 | 53303447 | ||||||
| chr16:53304631
|
A | G | 1 | a0001c0005t0004g0097 | 1 | HG01884.hp1 | splice_region_variant&intron_variant | LOW | c.6619+6A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 31/38 | chr16 | 53304631 | ||||||
| chr16:53304662
|
ACTTTTCT others(3): Show |
A | 1 | a0002c0002t0001g0140 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.6619+63_6619+72del others(10): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 31/38 | INFO_REALIGN_3_PRIME | chr16 | 53304662 | |||||
| chr16:53304683
|
CTTTTCTT others(4): Show |
C | 42 | a0001c0001t0003g0016a0001c0001t0015g0166a0001c0003t0001g0158others(39): Show | 42 | HG00140.hp2 HG00558.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.6619+63_6619+73del others(11): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 31/38 | INFO_REALIGN_3_PRIME | chr16 | 53304683 | |||||
| chr16:53304683
|
CTTTTCTT others(5): Show |
C | 6 | a0001c0005t0004g0232a0001c0005t0004g0233a0001c0005t0004g0234others(3): Show | 6 | HG02615.hp2 HG02897.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.6619+63_6619+74del others(12): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 31/38 | INFO_REALIGN_3_PRIME | chr16 | 53304683 | |||||
| chr16:53304693
|
CT | C | 29 | a0001c0001t0002g0171a0001c0001t0002g0175a0001c0001t0003g0022others(26): Show | 29 | HG01167.hp1 HG01168.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.6619+86delT | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 31/38 | INFO_REALIGN_3_PRIME | chr16 | 53304693 | |||||
| chr16:53304693
|
CTT | C | 5 | a0001c0005t0004g0104a0001c0005t0004g0169a0001c0005t0004g0231others(2): Show | 5 | HG01167.hp2 HG03139.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.6619+85_6619+86del others(2): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 31/38 | INFO_REALIGN_3_PRIME | chr16 | 53304693 | |||||
| chr16:53304694
|
T | C | 1 | a0001c0005t0001g0215 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.6619+69T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 31/38 | chr16 | 53304694 | ||||||
| chr16:53304802
|
C | G | 1 | a0001c0005t0001g0215 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.6619+177C>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 31/38 | chr16 | 53304802 | ||||||
| chr16:53304825
|
G | T | 1 | a0001c0001t0002g0171 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.6619+200G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 31/38 | chr16 | 53304825 | ||||||
| chr16:53304974
|
A | G | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.6619+349A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 31/38 | chr16 | 53304974 | ||||||
| chr16:53304986
|
G | T | 41 | a0001c0001t0015g0166a0001c0003t0001g0158a0001c0003t0002g0002others(38): Show | 41 | HG00140.hp2 HG00558.hp2 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.6619+361G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 31/38 | chr16 | 53304986 | ||||||
| chr16:53305092
|
C | T | 10 | a0001c0001t0001g0056a0001c0001t0001g0071a0001c0001t0001g0072others(7): Show | 10 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(7): Show |
intron_variant | MODIFIER | c.6619+467C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 31/38 | chr16 | 53305092 | ||||||
| chr16:53305101
|
G | A | 1 | a0001c0005t0001g0215 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.6619+476G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 31/38 | chr16 | 53305101 | ||||||
| chr16:53305358
|
G | A | 1 | a0001c0005t0004g0169 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.6619+733G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 31/38 | chr16 | 53305358 | ||||||
| chr16:53305422
|
G | C | 1 | a0001c0001t0001g0085 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.6619+797G>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 31/38 | chr16 | 53305422 | ||||||
| chr16:53305517
|
G | A | 1 | a0001c0001t0001g0124 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.6620-720G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 31/38 | chr16 | 53305517 | ||||||
| chr16:53305541
|
C | T | 2 | a0001c0003t0002g0040a0001c0003t0002g0070 | 2 | HG02080.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.6620-696C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 31/38 | chr16 | 53305541 | ||||||
| chr16:53305647
|
G | T | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.6620-590G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 31/38 | chr16 | 53305647 | ||||||
| chr16:53305771
|
G | T | 2 | a0001c0005t0004g0169a0001c0005t0018g0001 | 2 | HG03139.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.6620-466G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 31/38 | chr16 | 53305771 | ||||||
| chr16:53305964
|
C | T | 64 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(61): Show | 64 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.6620-273C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 31/38 | chr16 | 53305964 | ||||||
| chr16:53306015
|
A | G | 1 | a0001c0003t0016g0039 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.6620-222A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 31/38 | chr16 | 53306015 | ||||||
| chr16:53306033
|
G | A | 1 | a0001c0001t0001g0027 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.6620-204G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 31/38 | chr16 | 53306033 | ||||||
| chr16:53306168
|
G | A | 119 | a0001c0001t0002g0171a0001c0001t0002g0175a0001c0001t0015g0166others(116): Show | 119 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.6620-69G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 31/38 | chr16 | 53306168 | ||||||
| chr16:53306536
|
A | G | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.6780+139A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 32/38 | chr16 | 53306536 | ||||||
| chr16:53306559
|
T | C | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.6780+162T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 32/38 | chr16 | 53306559 | ||||||
| chr16:53306611
|
T | C | 1 | a0001c0003t0013g0186 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.6780+214T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 32/38 | chr16 | 53306611 | ||||||
| chr16:53306654
|
T | G | 1 | a0001c0005t0001g0215 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.6780+257T>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 32/38 | chr16 | 53306654 | ||||||
| chr16:53306794
|
C | CT | 65 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(62): Show | 65 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.6780+406dupT | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 32/38 | INFO_REALIGN_3_PRIME | chr16 | 53306794 | |||||
| chr16:53306818
|
C | T | 2 | a0001c0003t0002g0002a0001c0003t0002g0015 | 2 | NA18970.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.6780+421C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 32/38 | chr16 | 53306818 | ||||||
| chr16:53306840
|
C | A | 2 | a0002c0002t0008g0065a0002c0002t0008g0137 | 2 | HG00408.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.6780+443C>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 32/38 | chr16 | 53306840 | ||||||
| chr16:53306926
|
C | T | 1 | a0001c0005t0005g0032 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.6780+529C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 32/38 | chr16 | 53306926 | ||||||
| chr16:53307406
|
C | T | 52 | a0002c0002t0001g0009a0002c0002t0001g0010a0002c0002t0001g0012others(49): Show | 52 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.6781-275C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 32/38 | chr16 | 53307406 | ||||||
| chr16:53307444
|
G | C | 2 | a0001c0001t0003g0022a0001c0001t0003g0176 | 2 | HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.6781-237G>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 32/38 | chr16 | 53307444 | ||||||
| chr16:53307655
|
C | T | 1 | a0001c0005t0001g0215 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.6781-26C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 32/38 | chr16 | 53307655 | ||||||
| chr16:53308196
|
A | G | 1 | a0001c0005t0004g0097 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.7053+243A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 33/38 | chr16 | 53308196 | ||||||
| chr16:53308412
|
TA | T | 19 | a0001c0001t0003g0022a0001c0001t0003g0079a0001c0001t0003g0096others(16): Show | 19 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.7054-269delA | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 33/38 | INFO_REALIGN_3_PRIME | chr16 | 53308412 | |||||
| chr16:53308542
|
C | T | 74 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(71): Show | 74 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.7054-144C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 33/38 | chr16 | 53308542 | ||||||
| chr16:53308927
|
T | C | 4 | a0002c0002t0001g0087a0002c0002t0001g0088a0002c0002t0001g0108others(1): Show | 4 | HG01255.hp2 HG01433.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.7222+73T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 34/38 | chr16 | 53308927 | ||||||
| chr16:53308948
|
C | T | 51 | a0002c0002t0001g0009a0002c0002t0001g0010a0002c0002t0001g0012others(48): Show | 51 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.7222+94C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 34/38 | chr16 | 53308948 | ||||||
| chr16:53309159
|
T | G | 64 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(61): Show | 64 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.7222+305T>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 34/38 | chr16 | 53309159 | ||||||
| chr16:53309242
|
C | A | 1 | a0003c0004t0001g0148 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.7222+388C>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 34/38 | chr16 | 53309242 | ||||||
| chr16:53309257
|
A | G | 1 | a0001c0005t0012g0229 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.7222+403A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 34/38 | chr16 | 53309257 | ||||||
| chr16:53309267
|
T | C | 140 | a0001c0001t0001g0159a0001c0001t0002g0171a0001c0001t0002g0175others(137): Show | 140 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.7222+413T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 34/38 | chr16 | 53309267 | ||||||
| chr16:53309442
|
C | T | 1 | a0001c0005t0001g0215 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.7222+588C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 34/38 | chr16 | 53309442 | ||||||
| chr16:53309668
|
A | G | 1 | a0001c0005t0011g0228 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.7222+814A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 34/38 | chr16 | 53309668 | ||||||
| chr16:53309670
|
G | A | 3 | a0001c0003t0002g0033a0001c0003t0002g0046a0001c0003t0002g0073 | 3 | HG02027.hp2 NA18946.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.7222+816G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 34/38 | chr16 | 53309670 | ||||||
| chr16:53309688
|
A | G | 64 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(61): Show | 64 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.7222+834A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 34/38 | chr16 | 53309688 | ||||||
| chr16:53309894
|
G | A | 1 | a0001c0001t0001g0060 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.7222+1040G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 34/38 | chr16 | 53309894 | ||||||
| chr16:53309961
|
T | G | 65 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.7222+1107T>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 34/38 | chr16 | 53309961 | ||||||
| chr16:53310399
|
G | C | 43 | a0001c0001t0001g0159a0001c0001t0003g0016a0001c0001t0015g0166others(40): Show | 43 | HG00140.hp2 HG00558.hp2 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.7222+1545G>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 34/38 | chr16 | 53310399 | ||||||
| chr16:53310477
|
A | G | 43 | a0001c0001t0001g0159a0001c0001t0003g0016a0001c0001t0015g0166others(40): Show | 43 | HG00140.hp2 HG00558.hp2 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.7222+1623A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 34/38 | chr16 | 53310477 | ||||||
| chr16:53310691
|
C | CA | 6 | a0001c0001t0001g0056a0001c0001t0001g0210a0001c0001t0009g0050others(3): Show | 6 | HG00099.hp2 HG00140.hp1 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.7222+1852dupA | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 34/38 | INFO_REALIGN_3_PRIME | chr16 | 53310691 | |||||
| chr16:53310712
|
G | C | 3 | a0001c0001t0003g0220a0001c0001t0003g0222a0001c0001t0003g0223 | 3 | HG02055.hp1 HG03540.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.7222+1858G>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 34/38 | chr16 | 53310712 | ||||||
| chr16:53310722
|
G | A | 5 | a0001c0001t0002g0171a0001c0001t0002g0175a0001c0005t0001g0215others(2): Show | 5 | HG01884.hp1 HG02451.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.7222+1868G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 34/38 | chr16 | 53310722 | ||||||
| chr16:53310806
|
G | A | 1 | a0001c0003t0019g0004 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.7222+1952G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 34/38 | chr16 | 53310806 | ||||||
| chr16:53310857
|
C | CAAT | 60 | a0001c0001t0001g0099a0001c0001t0001g0124a0001c0001t0001g0225others(57): Show | 60 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.7222+2035_7222+203 others(7): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 34/38 | INFO_REALIGN_3_PRIME | chr16 | 53310857 | |||||
| chr16:53310857
|
C | CAATAAT | 55 | a0001c0001t0001g0092a0001c0001t0002g0175a0001c0001t0003g0016others(52): Show | 55 | HG00140.hp2 HG00558.hp2 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.7222+2032_7222+203 others(10): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 34/38 | INFO_REALIGN_3_PRIME | chr16 | 53310857 | |||||
| chr16:53310857
|
C | CAATAATA others(2): Show |
9 | a0001c0001t0002g0171a0001c0001t0003g0139a0001c0001t0003g0183others(6): Show | 9 | HG02155.hp2 HG02451.hp1 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.7222+2029_7222+203 others(13): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 34/38 | INFO_REALIGN_3_PRIME | chr16 | 53310857 | |||||
| chr16:53310857
|
C | CAATAATA others(5): Show |
7 | a0001c0001t0003g0105a0001c0001t0003g0131a0001c0001t0003g0167others(4): Show | 7 | HG01884.hp1 HG01891.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.7222+2026_7222+203 others(16): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 34/38 | INFO_REALIGN_3_PRIME | chr16 | 53310857 | |||||
| chr16:53310857
|
C | CAATAATA others(8): Show |
4 | a0001c0001t0001g0159a0001c0001t0003g0022a0001c0001t0003g0079others(1): Show | 4 | HG02280.hp1 HG03516.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.7222+2023_7222+203 others(19): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 34/38 | INFO_REALIGN_3_PRIME | chr16 | 53310857 | |||||
| chr16:53310857
|
C | T | 10 | a0001c0001t0001g0119a0003c0004t0001g0187a0003c0004t0001g0194others(7): Show | 10 | HG02015.hp2 HG02155.hp1 HG02165.hp1 others(7): Show |
intron_variant | MODIFIER | c.7222+2003C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 34/38 | chr16 | 53310857 | ||||||
| chr16:53310857
|
CAAT | C | 10 | a0001c0001t0001g0178a0001c0005t0005g0017a0001c0005t0005g0018others(7): Show | 10 | HG02109.hp1 HG02257.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.7222+2035_7222+203 others(7): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 34/38 | INFO_REALIGN_3_PRIME | chr16 | 53310857 | |||||
| chr16:53310969
|
C | T | 209 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0021others(206): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.7222+2115C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 34/38 | chr16 | 53310969 | ||||||
| chr16:53311011
|
A | T | 1 | a0001c0001t0007g0103 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.7222+2157A>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 34/38 | chr16 | 53311011 | ||||||
| chr16:53311123
|
T | C | 43 | a0001c0001t0001g0159a0001c0001t0003g0016a0001c0001t0015g0166others(40): Show | 43 | HG00140.hp2 HG00558.hp2 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.7222+2269T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 34/38 | chr16 | 53311123 | ||||||
| chr16:53311174
|
C | CA | 12 | a0001c0003t0002g0015a0001c0003t0017g0181a0001c0005t0005g0017others(9): Show | 12 | HG02109.hp1 HG02257.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.7222+2337dupA | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 34/38 | INFO_REALIGN_3_PRIME | chr16 | 53311174 | |||||
| chr16:53311193
|
T | C | 42 | a0001c0001t0001g0159a0001c0001t0015g0166a0001c0003t0001g0158others(39): Show | 42 | HG00140.hp2 HG00558.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.7222+2339T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 34/38 | chr16 | 53311193 | ||||||
| chr16:53311292
|
A | G | 1 | a0001c0001t0003g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.7222+2438A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 34/38 | chr16 | 53311292 | ||||||
| chr16:53311511
|
T | C | 1 | a0001c0005t0001g0215 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.7222+2657T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 34/38 | chr16 | 53311511 | ||||||
| chr16:53311926
|
CA | C | 77 | a0001c0005t0001g0215a0001c0005t0004g0078a0001c0005t0004g0097others(74): Show | 77 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.7223-2444delA | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 34/38 | INFO_REALIGN_3_PRIME | chr16 | 53311926 | |||||
| chr16:53311949
|
G | T | 1 | a0002c0002t0001g0037 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.7223-2428G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 34/38 | chr16 | 53311949 | ||||||
| chr16:53312137
|
A | C | 1 | a0002c0002t0001g0219 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.7223-2240A>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 34/38 | chr16 | 53312137 | ||||||
| chr16:53312393
|
G | A | 1 | a0001c0003t0013g0186 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.7223-1984G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 34/38 | chr16 | 53312393 | ||||||
| chr16:53312836
|
A | G | 1 | a0001c0003t0002g0070 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.7223-1541A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 34/38 | chr16 | 53312836 | ||||||
| chr16:53312840
|
C | T | 1 | a0003c0004t0001g0189 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.7223-1537C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 34/38 | chr16 | 53312840 | ||||||
| chr16:53312907
|
T | A | 53 | a0002c0002t0001g0009a0002c0002t0001g0010a0002c0002t0001g0012others(50): Show | 53 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.7223-1470T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 34/38 | chr16 | 53312907 | ||||||
| chr16:53313073
|
T | G | 1 | a0001c0005t0018g0001 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.7223-1304T>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 34/38 | chr16 | 53313073 | ||||||
| chr16:53313248
|
G | GA | 234 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0021others(231): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.7223-1120dupA | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 34/38 | INFO_REALIGN_3_PRIME | chr16 | 53313248 | |||||
| chr16:53313306
|
A | T | 3 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0182 | 3 | HG02615.hp1 HG02970.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.7223-1071A>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 34/38 | chr16 | 53313306 | ||||||
| chr16:53313704
|
GGAGGCC | G | 74 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(71): Show | 74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.7223-659_7223-654d others(8): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 34/38 | INFO_REALIGN_3_PRIME | chr16 | 53313704 | |||||
| chr16:53313835
|
C | T | 65 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.7223-542C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 34/38 | chr16 | 53313835 | ||||||
| chr16:53313878
|
A | G | 73 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(70): Show | 73 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.7223-499A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 34/38 | chr16 | 53313878 | ||||||
| chr16:53313953
|
C | CA | 10 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(7): Show | 10 | HG02080.hp1 HG02257.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.7223-412dupA | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 34/38 | INFO_REALIGN_3_PRIME | chr16 | 53313953 | |||||
| chr16:53314034
|
T | A | 1 | a0001c0014t0001g0115 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.7223-343T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 34/38 | chr16 | 53314034 | ||||||
| chr16:53314035
|
A | T | 1 | a0002c0002t0001g0063 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.7223-342A>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 34/38 | chr16 | 53314035 | ||||||
| chr16:53314081
|
A | G | 1 | a0003c0004t0001g0030 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.7223-296A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 34/38 | chr16 | 53314081 | ||||||
| chr16:53314245
|
T | A | 53 | a0002c0002t0001g0009a0002c0002t0001g0010a0002c0002t0001g0012others(50): Show | 53 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.7223-132T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 34/38 | chr16 | 53314245 | ||||||
| chr16:53314295
|
T | A | 74 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(71): Show | 74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.7223-82T>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 34/38 | chr16 | 53314295 | ||||||
| chr16:53314335
|
A | G | 6 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0168others(3): Show | 6 | HG01891.hp2 HG02451.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.7223-42A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 34/38 | chr16 | 53314335 | ||||||
| chr16:53314671
|
T | C | 65 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.7363-152T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 35/38 | chr16 | 53314671 | ||||||
| chr16:53314799
|
A | G | 1 | a0002c0002t0001g0208 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.7363-24A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 35/38 | chr16 | 53314799 | ||||||
| chr16:53315088
|
G | A | 74 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(71): Show | 74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.7584+44G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 36/38 | chr16 | 53315088 | ||||||
| chr16:53315316
|
A | T | 65 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.7584+272A>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 36/38 | chr16 | 53315316 | ||||||
| chr16:53315464
|
C | A | 1 | a0002c0002t0001g0102 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.7584+420C>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 36/38 | chr16 | 53315464 | ||||||
| chr16:53315619
|
C | T | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.7584+575C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 36/38 | chr16 | 53315619 | ||||||
| chr16:53315759
|
A | G | 142 | a0001c0001t0001g0159a0001c0001t0002g0171a0001c0001t0002g0175others(139): Show | 142 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.7584+715A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 36/38 | chr16 | 53315759 | ||||||
| chr16:53315875
|
G | A | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.7584+831G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 36/38 | chr16 | 53315875 | ||||||
| chr16:53316129
|
G | A | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.7584+1085G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 36/38 | chr16 | 53316129 | ||||||
| chr16:53316186
|
T | C | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.7584+1142T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 36/38 | chr16 | 53316186 | ||||||
| chr16:53316240
|
G | C | 1 | a0001c0001t0003g0221 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.7584+1196G>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 36/38 | chr16 | 53316240 | ||||||
| chr16:53316523
|
T | C | 1 | a0002c0019t0001g0180 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.7584+1479T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 36/38 | chr16 | 53316523 | ||||||
| chr16:53316870
|
A | C | 43 | a0001c0001t0001g0159a0001c0001t0003g0016a0001c0001t0015g0166others(40): Show | 43 | HG00140.hp2 HG00558.hp2 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.7585-1342A>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 36/38 | chr16 | 53316870 | ||||||
| chr16:53316906
|
A | G | 1 | a0001c0005t0001g0215 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.7585-1306A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 36/38 | chr16 | 53316906 | ||||||
| chr16:53316927
|
G | A | 65 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.7585-1285G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 36/38 | chr16 | 53316927 | ||||||
| chr16:53317073
|
G | A | 1 | a0001c0001t0003g0226 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.7585-1139G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 36/38 | chr16 | 53317073 | ||||||
| chr16:53317163
|
C | CAA | 53 | a0001c0003t0002g0041a0001c0005t0004g0169a0001c0005t0018g0001others(50): Show | 53 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(50): Show |
intron_variant | MODIFIER | c.7585-1032_7585-103 others(6): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr16 | 53317163 | |||||
| chr16:53317163
|
C | CAAA | 12 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0231others(9): Show | 12 | HG01167.hp2 HG01884.hp2 HG02602.hp1 others(9): Show |
intron_variant | MODIFIER | c.7585-1033_7585-103 others(7): Show |
CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr16 | 53317163 | |||||
| chr16:53317163
|
CA | C | 6 | a0001c0001t0001g0008a0001c0001t0001g0026a0001c0005t0001g0215others(3): Show | 6 | NA18982.hp2 NA18989.hp2 NA18992.hp1 others(3): Show |
intron_variant | MODIFIER | c.7585-1031delA | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr16 | 53317163 | |||||
| chr16:53317194
|
G | T | 120 | a0001c0001t0002g0171a0001c0001t0002g0175a0001c0001t0015g0166others(117): Show | 120 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.7585-1018G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 36/38 | chr16 | 53317194 | ||||||
| chr16:53317245
|
C | T | 4 | a0001c0001t0003g0131a0001c0001t0003g0139a0001c0001t0003g0172others(1): Show | 4 | HG01891.hp1 HG02257.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.7585-967C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 36/38 | chr16 | 53317245 | ||||||
| chr16:53317553
|
C | G | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.7585-659C>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 36/38 | chr16 | 53317553 | ||||||
| chr16:53317572
|
A | G | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.7585-640A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 36/38 | chr16 | 53317572 | ||||||
| chr16:53317871
|
C | T | 74 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(71): Show | 74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.7585-341C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 36/38 | chr16 | 53317871 | ||||||
| chr16:53317872
|
G | A | 1 | a0001c0003t0002g0152 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.7585-340G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 36/38 | chr16 | 53317872 | ||||||
| chr16:53318417
|
T | C | 74 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(71): Show | 74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.7713+77T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 37/38 | chr16 | 53318417 | ||||||
| chr16:53318777
|
A | G | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.7713+437A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 37/38 | chr16 | 53318777 | ||||||
| chr16:53319119
|
A | G | 1 | a0008c0011t0003g0062 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.7713+779A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 37/38 | chr16 | 53319119 | ||||||
| chr16:53319219
|
G | A | 1 | a0002c0002t0001g0010 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.7713+879G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 37/38 | chr16 | 53319219 | ||||||
| chr16:53319247
|
T | C | 53 | a0002c0002t0001g0009a0002c0002t0001g0010a0002c0002t0001g0012others(50): Show | 53 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.7713+907T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 37/38 | chr16 | 53319247 | ||||||
| chr16:53319372
|
G | A | 2 | a0002c0002t0001g0087a0002c0002t0001g0088 | 2 | HG01255.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.7713+1032G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 37/38 | chr16 | 53319372 | ||||||
| chr16:53319423
|
T | C | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.7713+1083T>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 37/38 | chr16 | 53319423 | ||||||
| chr16:53319577
|
C | T | 74 | a0001c0005t0004g0078a0001c0005t0004g0104a0001c0005t0004g0169others(71): Show | 74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.7713+1237C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 37/38 | chr16 | 53319577 | ||||||
| chr16:53320198
|
T | TA | 59 | a0001c0001t0001g0069a0001c0005t0004g0078a0001c0005t0004g0104others(56): Show | 59 | HG00408.hp1 HG00609.hp1 HG00733.hp2 others(56): Show |
intron_variant | MODIFIER | c.7714-1310dupA | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 37/38 | INFO_REALIGN_3_PRIME | chr16 | 53320198 | |||||
| chr16:53320198
|
TA | T | 11 | a0001c0001t0001g0068a0001c0001t0001g0165a0001c0001t0015g0166others(8): Show | 11 | HG00558.hp2 HG01168.hp1 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.7714-1310delA | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 37/38 | INFO_REALIGN_3_PRIME | chr16 | 53320198 | |||||
| chr16:53320208
|
A | G | 1 | a0008c0011t0003g0062 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.7714-1318A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 37/38 | chr16 | 53320208 | ||||||
| chr16:53320485
|
A | G | 9 | a0001c0005t0005g0017a0001c0005t0005g0018a0001c0005t0005g0032others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.7714-1041A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 37/38 | chr16 | 53320485 | ||||||
| chr16:53320614
|
G | T | 1 | a0001c0003t0002g0023 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.7714-912G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 37/38 | chr16 | 53320614 | ||||||
| chr16:53320819
|
C | A | 77 | a0001c0005t0001g0215a0001c0005t0004g0078a0001c0005t0004g0097others(74): Show | 77 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.7714-707C>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 37/38 | chr16 | 53320819 | ||||||
| chr16:53321272
|
A | G | 1 | a0006c0009t0004g0107 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.7714-254A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 37/38 | chr16 | 53321272 | ||||||
| chr16:53321453
|
A | C | 1 | a0001c0001t0001g0069 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.7714-73A>C | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 37/38 | chr16 | 53321453 | ||||||
| chr16:53321918
|
A | G | 204 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0021others(201): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.7818+288A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 38/38 | chr16 | 53321918 | ||||||
| chr16:53322000
|
C | CT | 10 | a0001c0001t0001g0230a0003c0004t0001g0187a0003c0004t0001g0194others(7): Show | 10 | HG02015.hp2 HG02155.hp1 HG02165.hp1 others(7): Show |
intron_variant | MODIFIER | c.7818+386dupT | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 38/38 | INFO_REALIGN_3_PRIME | chr16 | 53322000 | |||||
| chr16:53322000
|
CT | C | 76 | a0001c0005t0001g0215a0001c0005t0004g0078a0001c0005t0004g0097others(73): Show | 76 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.7818+386delT | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 38/38 | INFO_REALIGN_3_PRIME | chr16 | 53322000 | |||||
| chr16:53322078
|
A | G | 17 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0031others(14): Show | 17 | HG00408.hp2 HG00621.hp1 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.7818+448A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 38/38 | chr16 | 53322078 | ||||||
| chr16:53322708
|
G | T | 2 | a0001c0005t0004g0169a0001c0005t0018g0001 | 2 | HG03139.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.7818+1078G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 38/38 | chr16 | 53322708 | ||||||
| chr16:53322879
|
A | G | 1 | a0003c0004t0001g0123 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.7819-1141A>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 38/38 | chr16 | 53322879 | ||||||
| chr16:53322925
|
T | G | 1 | a0003c0004t0001g0209 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.7819-1095T>G | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 38/38 | chr16 | 53322925 | ||||||
| chr16:53322989
|
G | A | 1 | a0001c0005t0004g0097 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.7819-1031G>A | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 38/38 | chr16 | 53322989 | ||||||
| chr16:53323023
|
C | T | 5 | a0001c0001t0001g0008a0001c0001t0001g0052a0001c0001t0001g0060others(2): Show | 5 | NA18946.hp1 NA18972.hp1 NA18992.hp1 others(2): Show |
intron_variant | MODIFIER | c.7819-997C>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 38/38 | chr16 | 53323023 | ||||||
| chr16:53323989
|
G | T | 1 | a0001c0003t0002g0002 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.7819-31G>T | CHD9 | ENSG00000177200.18 | transcript | ENST00000447540.6 | protein_coding | 38/38 | chr16 | 53323989 |