| geneid | 1106 |
|---|---|
| ensemblid | ENSG00000173575.24 |
| hgncid | 1917 |
| symbol | CHD2 |
| name | chromodomain helicase DNA binding protein 2 |
| refseq_nuc | NM_001271.4 |
| refseq_prot | NP_001262.3 |
| ensembl_nuc | ENST00000394196.9 |
| ensembl_prot | ENSP00000377747.4 |
| mane_status | MANE Select |
| chr | chr15 |
| start | 92900324 |
| end | 93027996 |
| strand | + |
| ver | v1.2 |
| region | chr15:92900324-93027996 |
| region5000 | chr15:92895324-93032996 |
| regionname0 | CHD2_chr15_92900324_93027996 |
| regionname5000 | CHD2_chr15_92895324_93032996 |
| 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 | 1/1 | 1828 | 306 | 72 | 74 | 106 | 16 | 36 | 76 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| 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 | 0/0 | 5487 | 163 | 16 | 45 | 72 | 7 | 23 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| c0002 | 0/0 | 5487 | 47 | 14 | 7 | 24 | 1 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| c0003 | 1/0 | 5487 | 38 | 23 | 9 | 0 | 0 | 5 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| c0004 | 0/0 | 5487 | 18 | 2 | 5 | 7 | 1 | 3 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| c0005 | 0/0 | 5487 | 12 | 1 | 3 | 0 | 6 | 2 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| c0006 | 0/0 | 5487 | 5 | 3 | 0 | 0 | 0 | 2 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| c0007 | 0/0 | 5487 | 4 | 3 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| c0008 | 0/1 | 5487 | 3 | 1 | 0 | 0 | 1 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| c0009 | 0/0 | 5487 | 3 | 2 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| c0010 | 0/0 | 5487 | 2 | 2 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| c0011 | 0/0 | 5487 | 2 | 0 | 2 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| c0012 | 0/0 | 5487 | 2 | 2 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| c0013 | 0/0 | 5487 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| c0014 | 0/0 | 5487 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| c0015 | 0/0 | 5487 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| c0016 | 0/0 | 5487 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| c0017 | 0/0 | 5487 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| c0018 | 0/0 | 5487 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| c0019 | 0/0 | 5487 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| 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 | 0/1 | 3867 | 154 | 10 | 33 | 83 | 6 | 21 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| t0002 | 0/0 | 3864 | 26 | 20 | 3 | 2 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| t0003 | 1/0 | 3864 | 25 | 17 | 4 | 0 | 2 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| t0004 | 0/0 | 3861 | 17 | 3 | 2 | 1 | 4 | 7 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| t0005 | 0/0 | 3867 | 15 | 13 | 2 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| t0006 | 0/0 | 3864 | 14 | 1 | 12 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| t0007 | 0/0 | 3864 | 10 | 3 | 4 | 0 | 3 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| t0008 | 0/0 | 3867 | 8 | 0 | 3 | 0 | 0 | 5 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| t0009 | 0/0 | 3867 | 8 | 0 | 3 | 5 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| t0010 | 0/0 | 3864 | 6 | 0 | 0 | 6 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| t0011 | 0/0 | 3867 | 5 | 0 | 2 | 3 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| t0012 | 0/0 | 3864 | 4 | 1 | 2 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| t0013 | 0/0 | 3864 | 2 | 1 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| t0014 | 0/0 | 3864 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| t0015 | 0/0 | 3861 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| t0016 | 0/0 | 3864 | 1 | 0 | 0 | 0 | 1 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| t0017 | 0/0 | 3864 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| t0018 | 0/0 | 3864 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| t0019 | 0/0 | 3867 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| t0020 | 0/0 | 3867 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| t0021 | 0/0 | 3867 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| t0022 | 0/0 | 3867 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| t0023 | 0/0 | 3867 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| t0024 | 0/0 | 3867 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| t0025 | 0/0 | 3867 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| 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 | 2 | 0 | 0 | 0 | 2 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0003 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0131 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0146 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| 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 | 0/0 | 5487 | 163 | 16 | 45 | 72 | 7 | 23 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| a0001c0002 | 0/0 | 5487 | 47 | 14 | 7 | 24 | 1 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| a0001c0003 | 1/0 | 5487 | 38 | 23 | 9 | 0 | 0 | 5 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| a0001c0004 | 0/0 | 5487 | 18 | 2 | 5 | 7 | 1 | 3 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| a0001c0005 | 0/0 | 5487 | 12 | 1 | 3 | 0 | 6 | 2 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| a0001c0006 | 0/0 | 5487 | 5 | 3 | 0 | 0 | 0 | 2 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| a0001c0007 | 0/0 | 5487 | 4 | 3 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| a0001c0008 | 0/1 | 5487 | 3 | 1 | 0 | 0 | 1 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| a0001c0009 | 0/0 | 5487 | 3 | 2 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| a0001c0010 | 0/0 | 5487 | 2 | 2 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| a0001c0011 | 0/0 | 5487 | 2 | 0 | 2 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| a0001c0012 | 0/0 | 5487 | 2 | 2 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| a0001c0013 | 0/0 | 5487 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| a0001c0014 | 0/0 | 5487 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| a0001c0015 | 0/0 | 5487 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| a0001c0016 | 0/0 | 5487 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| a0001c0017 | 0/0 | 5487 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| a0001c0018 | 0/0 | 5487 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| a0001c0019 | 0/0 | 5487 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 9353 | 121 | 8 | 29 | 61 | 5 | 18 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| a0001c0001t0002 | 0/0 | 9350 | 6 | 4 | 0 | 1 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| a0001c0001t0003 | 0/0 | 9350 | 3 | 1 | 0 | 0 | 2 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| a0001c0001t0005 | 0/0 | 9353 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| a0001c0001t0006 | 0/0 | 9350 | 14 | 1 | 12 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| a0001c0001t0007 | 0/0 | 9350 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| a0001c0001t0008 | 0/0 | 9353 | 4 | 0 | 0 | 0 | 0 | 4 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| a0001c0001t0009 | 0/0 | 9353 | 4 | 0 | 1 | 3 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| a0001c0001t0011 | 0/0 | 9353 | 3 | 0 | 2 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| a0001c0001t0020 | 0/0 | 9353 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| a0001c0001t0021 | 0/0 | 9353 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| a0001c0001t0022 | 0/0 | 9353 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| a0001c0001t0023 | 0/0 | 9353 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| a0001c0001t0024 | 0/0 | 9353 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| a0001c0001t0025 | 0/0 | 9353 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| a0001c0002t0001 | 0/0 | 9353 | 23 | 0 | 1 | 21 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| a0001c0002t0002 | 0/0 | 9350 | 8 | 7 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| a0001c0002t0003 | 0/0 | 9350 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| a0001c0002t0005 | 0/0 | 9353 | 8 | 6 | 2 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| a0001c0002t0008 | 0/0 | 9353 | 2 | 0 | 2 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| a0001c0002t0009 | 0/0 | 9353 | 2 | 0 | 1 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| a0001c0002t0011 | 0/0 | 9353 | 2 | 0 | 0 | 2 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| a0001c0002t0016 | 0/0 | 9350 | 1 | 0 | 0 | 0 | 1 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| a0001c0003t0001 | 0/0 | 9353 | 4 | 1 | 1 | 0 | 0 | 2 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| a0001c0003t0002 | 0/0 | 9350 | 5 | 4 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| a0001c0003t0003 | 1/0 | 9350 | 20 | 14 | 4 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| a0001c0003t0005 | 0/0 | 9353 | 3 | 3 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| a0001c0003t0008 | 0/0 | 9353 | 2 | 0 | 1 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| a0001c0003t0012 | 0/0 | 9350 | 3 | 0 | 2 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| a0001c0003t0014 | 0/0 | 9350 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| a0001c0004t0004 | 0/0 | 9347 | 4 | 0 | 0 | 1 | 0 | 3 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| a0001c0004t0007 | 0/0 | 9350 | 6 | 1 | 4 | 0 | 1 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| a0001c0004t0010 | 0/0 | 9350 | 6 | 0 | 0 | 6 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| a0001c0004t0017 | 0/0 | 9350 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| a0001c0004t0018 | 0/0 | 9350 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| a0001c0005t0004 | 0/0 | 9347 | 9 | 1 | 2 | 0 | 4 | 2 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| a0001c0005t0007 | 0/0 | 9350 | 2 | 0 | 0 | 0 | 2 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| a0001c0005t0015 | 0/0 | 9347 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| a0001c0006t0004 | 0/0 | 9347 | 4 | 2 | 0 | 0 | 0 | 2 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| a0001c0006t0005 | 0/0 | 9353 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| a0001c0007t0003 | 0/0 | 9350 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| a0001c0007t0007 | 0/0 | 9350 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| a0001c0007t0013 | 0/0 | 9350 | 2 | 1 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| a0001c0008t0001 | 0/1 | 9353 | 3 | 1 | 0 | 0 | 1 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| a0001c0009t0002 | 0/0 | 9350 | 2 | 1 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| a0001c0009t0012 | 0/0 | 9350 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| a0001c0010t0002 | 0/0 | 9350 | 2 | 2 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| a0001c0011t0001 | 0/0 | 9353 | 2 | 0 | 2 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| a0001c0012t0002 | 0/0 | 9350 | 2 | 2 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| a0001c0013t0019 | 0/0 | 9353 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| a0001c0014t0005 | 0/0 | 9353 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| a0001c0015t0005 | 0/0 | 9353 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| a0001c0016t0002 | 0/0 | 9350 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| a0001c0017t0009 | 0/0 | 9353 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| a0001c0018t0009 | 0/0 | 9353 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| a0001c0019t0001 | 0/0 | 9353 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | copy fasta | chr15 | 92895324 | 93032996 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0002g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0003g0001 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0003g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0005g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0006g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0006g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0006g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0006g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0006g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0006g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0006g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0006g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0006g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0006g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0006g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0006g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0006g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0006g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0007g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0008g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0008g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0008g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0008g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0009g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0009g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0009g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0009g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0011g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0011g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0011g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0020g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0021g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0022g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0023g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0024g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0025g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0003g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0005g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0005g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0005g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0005g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0005g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0005g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0005g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0005g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0008g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0008g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0009g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0009g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0011g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0011g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0016g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0003t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0003t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0003t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0003t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0003t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0003t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0003t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0003t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0003t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0003t0003g0003 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0003t0003g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0003t0003g0131 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0003t0003g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0003t0003g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0003t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0003t0003g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0003t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0003t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0003t0003g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0003t0003g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0003t0003g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0003t0003g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0003t0003g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0003t0003g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0003t0003g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0003t0003g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0003t0003g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0003t0003g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0003t0005g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0003t0005g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0003t0005g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0003t0008g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0003t0008g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0003t0012g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0003t0012g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0003t0012g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0003t0014g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0004t0004g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0004t0004g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0004t0004g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0004t0004g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0004t0007g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0004t0007g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0004t0007g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0004t0007g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0004t0007g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0004t0007g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0004t0010g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0004t0010g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0004t0010g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0004t0010g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0004t0010g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0004t0010g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0004t0017g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0004t0018g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0005t0004g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0005t0004g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0005t0004g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0005t0004g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0005t0004g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0005t0004g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0005t0004g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0005t0004g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0005t0004g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0005t0007g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0005t0007g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0005t0015g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0006t0004g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0006t0004g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0006t0004g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0006t0005g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0007t0003g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0007t0007g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0007t0013g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0007t0013g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0008t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0008t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0008t0001g0146 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0009t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0009t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0009t0012g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0010t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0010t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0011t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0011t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0012t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0012t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0013t0019g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0014t0005g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0015t0005g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0016t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0017t0009g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0018t0009g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0019t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0005 | t0007 | g0050 | EUR | GBR | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG00099 | hp2 | a0001 | c0002 | t0016 | g0280 | EUR | GBR | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG00140 | hp1 | a0001 | c0005 | t0007 | g0090 | EUR | GBR | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG00140 | hp2 | a0001 | c0005 | t0004 | g0180 | EUR | GBR | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0086 | EUR | FIN | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG00323 | hp2 | a0001 | c0008 | t0001 | g0127 | EUR | FIN | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | CHS | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG00423 | hp2 | a0001 | c0002 | t0001 | g0236 | EAS | CHS | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | CHS | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | CHS | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0293 | EAS | CHS | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | CHS | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0246 | EAS | CHS | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | CHS | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG00621 | hp1 | a0001 | c0001 | t0020 | g0113 | EAS | CHS | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG00621 | hp2 | a0001 | c0001 | t0025 | g0104 | EAS | CHS | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG00639 | hp1 | a0001 | c0004 | t0007 | g0014 | AMR | PUR | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG00639 | hp2 | a0001 | c0011 | t0001 | g0023 | AMR | PUR | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG00642 | hp1 | a0001 | c0016 | t0002 | g0047 | AMR | PUR | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0234 | AMR | PUR | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | CHS | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG00673 | hp2 | a0001 | c0009 | t0002 | g0048 | EAS | CHS | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG00735 | hp1 | a0001 | c0001 | t0009 | g0296 | AMR | PUR | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG00735 | hp2 | a0001 | c0001 | t0006 | g0263 | AMR | PUR | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG00738 | hp1 | a0001 | c0011 | t0001 | g0024 | AMR | PUR | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG00738 | hp2 | a0001 | c0005 | t0004 | g0287 | AMR | PUR | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG00741 | hp1 | a0001 | c0002 | t0008 | g0012 | AMR | PUR | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG00741 | hp2 | a0001 | c0003 | t0001 | g0135 | AMR | PUR | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01069 | hp1 | a0001 | c0005 | t0004 | g0159 | AMR | PUR | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01069 | hp2 | a0001 | c0003 | t0002 | g0125 | AMR | PUR | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01070 | hp1 | a0001 | c0003 | t0003 | g0175 | AMR | PUR | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01070 | hp2 | a0001 | c0002 | t0008 | g0015 | AMR | PUR | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01074 | hp1 | a0001 | c0001 | t0011 | g0282 | AMR | PUR | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01081 | hp1 | a0001 | c0005 | t0015 | g0073 | AMR | PUR | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01099 | hp2 | a0001 | c0001 | t0006 | g0262 | AMR | PUR | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01106 | hp1 | a0001 | c0001 | t0006 | g0261 | AMR | PUR | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01109 | hp2 | a0001 | c0003 | t0003 | g0171 | AMR | PUR | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01167 | hp2 | a0001 | c0002 | t0005 | g0279 | AMR | PUR | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01168 | hp2 | a0001 | c0004 | t0007 | g0020 | AMR | PUR | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01169 | hp2 | a0001 | c0002 | t0005 | g0277 | AMR | PUR | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01175 | hp1 | a0001 | c0001 | t0011 | g0292 | AMR | PUR | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01192 | hp1 | a0001 | c0017 | t0009 | g0037 | AMR | PUR | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01243 | hp1 | a0001 | c0003 | t0003 | g0003 | AMR | PUR | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01243 | hp2 | a0001 | c0007 | t0013 | g0151 | AMR | PUR | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01255 | hp1 | a0001 | c0001 | t0006 | g0266 | AMR | CLM | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | CLM | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01257 | hp1 | a0001 | c0003 | t0012 | g0126 | AMR | CLM | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01257 | hp2 | a0001 | c0001 | t0024 | g0077 | AMR | CLM | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01258 | hp1 | a0001 | c0003 | t0012 | g0134 | AMR | CLM | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | CLM | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | CLM | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01346 | hp2 | a0001 | c0003 | t0003 | g0128 | AMR | CLM | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01361 | hp1 | a0001 | c0002 | t0009 | g0022 | AMR | CLM | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01433 | hp2 | a0001 | c0004 | t0007 | g0021 | AMR | CLM | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | CLM | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01496 | hp2 | a0001 | c0001 | t0006 | g0265 | AMR | CLM | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01515 | hp1 | a0001 | c0005 | t0004 | g0289 | EUR | IBS | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0026 | EUR | IBS | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0078 | EUR | IBS | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0001 | EUR | IBS | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0001 | EUR | IBS | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01517 | hp2 | a0001 | c0005 | t0004 | g0276 | EUR | IBS | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01884 | hp1 | a0001 | c0003 | t0005 | g0160 | AFR | ACB | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01884 | hp2 | a0001 | c0002 | t0005 | g0229 | AFR | ACB | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | PEL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01943 | hp2 | a0001 | c0001 | t0006 | g0248 | AMR | PEL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PEL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01952 | hp2 | a0001 | c0003 | t0008 | g0140 | AMR | PEL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01975 | hp1 | a0001 | c0002 | t0002 | g0275 | AMR | PEL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PEL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PEL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PEL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02004 | hp1 | a0001 | c0004 | t0007 | g0018 | AMR | PEL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02004 | hp2 | a0001 | c0001 | t0006 | g0084 | AMR | PEL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | KHV | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02027 | hp2 | a0001 | c0001 | t0021 | g0074 | EAS | KHV | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02040 | hp1 | a0001 | c0002 | t0009 | g0243 | EAS | KHV | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02055 | hp1 | a0001 | c0001 | t0007 | g0174 | AFR | ACB | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02055 | hp2 | a0001 | c0003 | t0003 | g0161 | AFR | ACB | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | KHV | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02074 | hp2 | a0001 | c0002 | t0001 | g0254 | EAS | KHV | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | KHV | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | KHV | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02148 | hp1 | a0001 | c0001 | t0006 | g0080 | AMR | PEL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02148 | hp2 | a0001 | c0001 | t0006 | g0269 | AMR | PEL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | CDX | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | CDX | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0085 | AFR | ACB | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02257 | hp2 | a0001 | c0002 | t0005 | g0230 | AFR | ACB | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02258 | hp1 | a0001 | c0009 | t0012 | g0044 | AFR | ACB | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0299 | AFR | ACB | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02273 | hp1 | a0001 | c0001 | t0006 | g0267 | AMR | PEL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02280 | hp1 | a0001 | c0012 | t0002 | g0055 | AFR | ACB | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02280 | hp2 | a0001 | c0015 | t0005 | g0288 | AFR | ACB | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02293 | hp2 | a0001 | c0001 | t0006 | g0260 | AMR | PEL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PEL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02300 | hp2 | a0001 | c0001 | t0006 | g0264 | AMR | PEL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02451 | hp1 | a0001 | c0004 | t0007 | g0013 | AFR | ACB | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02451 | hp2 | a0001 | c0002 | t0003 | g0228 | AFR | ACB | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | KHV | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02572 | hp1 | a0001 | c0002 | t0005 | g0227 | AFR | GWD | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02572 | hp2 | a0001 | c0002 | t0002 | g0223 | AFR | GWD | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0294 | SAS | PJL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02630 | hp1 | a0001 | c0007 | t0007 | g0030 | AFR | GWD | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02630 | hp2 | a0001 | c0006 | t0004 | g0163 | AFR | GWD | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02683 | hp1 | a0001 | c0003 | t0003 | g0143 | SAS | PJL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02698 | hp2 | a0001 | c0003 | t0001 | g0144 | SAS | PJL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02717 | hp1 | a0001 | c0009 | t0002 | g0043 | AFR | GWD | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | GWD | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02735 | hp2 | a0001 | c0003 | t0012 | g0133 | SAS | PJL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02809 | hp1 | a0001 | c0014 | t0005 | g0226 | AFR | GWD | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02809 | hp2 | a0001 | c0003 | t0005 | g0166 | AFR | GWD | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02886 | hp1 | a0001 | c0003 | t0003 | g0149 | AFR | GWD | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02886 | hp2 | a0001 | c0004 | t0018 | g0025 | AFR | GWD | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02922 | hp1 | a0001 | c0003 | t0005 | g0124 | AFR | ESN | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02922 | hp2 | a0001 | c0012 | t0002 | g0031 | AFR | ESN | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0278 | AFR | ESN | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0300 | AFR | ESN | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02970 | hp1 | a0001 | c0003 | t0003 | g0136 | AFR | ESN | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02970 | hp2 | a0001 | c0010 | t0002 | g0222 | AFR | ESN | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02976 | hp1 | a0001 | c0003 | t0003 | g0138 | AFR | ESN | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02976 | hp2 | a0001 | c0002 | t0002 | g0156 | AFR | ESN | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03041 | hp1 | a0001 | c0003 | t0002 | g0137 | AFR | GWD | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03041 | hp2 | a0001 | c0003 | t0003 | g0170 | AFR | GWD | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03098 | hp1 | a0001 | c0003 | t0002 | g0221 | AFR | MSL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03098 | hp2 | a0001 | c0003 | t0003 | g0173 | AFR | MSL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03130 | hp1 | a0001 | c0006 | t0004 | g0158 | AFR | ESN | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03130 | hp2 | a0001 | c0003 | t0003 | g0167 | AFR | ESN | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | ESN | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03139 | hp2 | a0001 | c0003 | t0003 | g0152 | AFR | ESN | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0298 | AFR | ESN | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03195 | hp2 | a0001 | c0006 | t0005 | g0130 | AFR | ESN | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03209 | hp1 | a0001 | c0002 | t0005 | g0224 | AFR | MSL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03209 | hp2 | a0001 | c0003 | t0003 | g0164 | AFR | MSL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03225 | hp1 | a0001 | c0003 | t0003 | g0003 | AFR | MSL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03225 | hp2 | a0001 | c0007 | t0003 | g0157 | AFR | MSL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03239 | hp2 | a0001 | c0001 | t0008 | g0219 | SAS | PJL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03453 | hp1 | a0001 | c0002 | t0002 | g0181 | AFR | MSL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03453 | hp2 | a0001 | c0002 | t0002 | g0232 | AFR | MSL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03486 | hp1 | a0001 | c0007 | t0013 | g0150 | AFR | MSL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03486 | hp2 | a0001 | c0002 | t0005 | g0220 | AFR | MSL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03490 | hp1 | a0001 | c0006 | t0004 | g0004 | SAS | PJL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03490 | hp2 | a0001 | c0005 | t0004 | g0291 | SAS | PJL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03492 | hp1 | a0001 | c0006 | t0004 | g0004 | SAS | PJL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | PJL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03516 | hp1 | a0001 | c0003 | t0003 | g0139 | AFR | ESN | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03516 | hp2 | a0001 | c0002 | t0002 | g0231 | AFR | ESN | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | GWD | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03540 | hp2 | a0001 | c0003 | t0002 | g0162 | AFR | GWD | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03579 | hp1 | a0001 | c0003 | t0001 | g0129 | AFR | MSL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03579 | hp2 | a0001 | c0003 | t0003 | g0290 | AFR | MSL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0272 | SAS | PJL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03669 | hp2 | a0001 | c0004 | t0004 | g0284 | SAS | PJL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03688 | hp1 | a0001 | c0004 | t0004 | g0297 | SAS | STU | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03688 | hp2 | a0001 | c0001 | t0008 | g0218 | SAS | STU | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03710 | hp1 | a0001 | c0004 | t0004 | g0285 | SAS | PJL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | BEB | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03831 | hp2 | a0001 | c0005 | t0004 | g0283 | SAS | BEB | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0091 | SAS | BEB | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0271 | SAS | BEB | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | BEB | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03942 | hp2 | a0001 | c0003 | t0001 | g0142 | SAS | BEB | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG04115 | hp1 | a0001 | c0001 | t0008 | g0040 | SAS | STU | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0200 | SAS | STU | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | STU | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG04204 | hp2 | a0001 | c0001 | t0008 | g0217 | SAS | STU | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG04228 | hp1 | a0001 | c0003 | t0008 | g0147 | SAS | STU | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0209 | SAS | STU | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18522 | hp1 | a0001 | c0002 | t0002 | g0046 | AFR | YRI | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | YRI | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18612 | hp1 | a0001 | c0001 | t0023 | g0052 | EAS | CHB | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18612 | hp2 | a0001 | c0004 | t0010 | g0107 | EAS | CHB | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | CHB | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | CHB | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18906 | hp1 | a0001 | c0002 | t0002 | g0045 | AFR | YRI | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18906 | hp2 | a0001 | c0003 | t0014 | g0165 | AFR | YRI | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18939 | hp2 | a0001 | c0002 | t0001 | g0251 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18944 | hp1 | a0001 | c0002 | t0001 | g0241 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18948 | hp2 | a0001 | c0002 | t0001 | g0244 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18950 | hp1 | a0001 | c0002 | t0001 | g0237 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18952 | hp1 | a0001 | c0004 | t0010 | g0108 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18953 | hp2 | a0001 | c0002 | t0001 | g0286 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18956 | hp1 | a0001 | c0004 | t0010 | g0245 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18956 | hp2 | a0001 | c0001 | t0006 | g0268 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18959 | hp2 | a0001 | c0002 | t0001 | g0242 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18963 | hp2 | a0001 | c0018 | t0009 | g0039 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18966 | hp1 | a0001 | c0002 | t0001 | g0253 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18967 | hp1 | a0001 | c0002 | t0001 | g0250 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18967 | hp2 | a0001 | c0001 | t0009 | g0011 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18968 | hp1 | a0001 | c0002 | t0001 | g0258 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0247 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18973 | hp2 | a0001 | c0002 | t0001 | g0238 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18978 | hp2 | a0001 | c0002 | t0001 | g0249 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18979 | hp2 | a0001 | c0004 | t0004 | g0092 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18983 | hp1 | a0001 | c0002 | t0001 | g0240 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18993 | hp1 | a0001 | c0001 | t0011 | g0176 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18994 | hp2 | a0001 | c0001 | t0009 | g0009 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA19000 | hp1 | a0001 | c0019 | t0001 | g0119 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA19000 | hp2 | a0001 | c0002 | t0011 | g0257 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA19002 | hp2 | a0001 | c0002 | t0001 | g0252 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA19007 | hp1 | a0001 | c0002 | t0011 | g0256 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | LWK | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA19043 | hp2 | a0001 | c0013 | t0019 | g0168 | AFR | LWK | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA19065 | hp1 | a0001 | c0002 | t0001 | g0233 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA19065 | hp2 | a0001 | c0001 | t0009 | g0010 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA19068 | hp1 | a0001 | c0001 | t0022 | g0097 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA19081 | hp2 | a0001 | c0002 | t0001 | g0255 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA19083 | hp1 | a0001 | c0004 | t0010 | g0105 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA19084 | hp2 | a0001 | c0002 | t0001 | g0239 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA19085 | hp2 | a0001 | c0004 | t0010 | g0109 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA19086 | hp1 | a0001 | c0002 | t0001 | g0235 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA19088 | hp2 | a0001 | c0004 | t0010 | g0106 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0274 | AFR | YRI | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA19240 | hp2 | a0001 | c0003 | t0002 | g0169 | AFR | YRI | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA20129 | hp1 | a0001 | c0003 | t0003 | g0172 | AFR | ASW | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA20129 | hp2 | a0001 | c0002 | t0005 | g0225 | AFR | ASW | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0036 | EUR | TSI | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA20752 | hp2 | a0001 | c0005 | t0004 | g0153 | EUR | TSI | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0121 | EUR | TSI | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA20805 | hp2 | a0001 | c0004 | t0007 | g0017 | EUR | TSI | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01123 | hp1 | a0001 | c0004 | t0017 | g0019 | AMR | CLM | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | CLM | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02486 | hp1 | a0001 | c0008 | t0001 | g0145 | AFR | ACB | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02486 | hp2 | a0001 | c0010 | t0002 | g0182 | AFR | ACB | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | MSL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0295 | AFR | MSL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA20300 | hp1 | a0001 | c0003 | t0003 | g0148 | AFR | USA | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA20300 | hp2 | a0001 | c0001 | t0006 | g0270 | AFR | USA | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA21309 | hp1 | a0001 | c0001 | t0005 | g0179 | AFR | LWK | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA21309 | hp2 | a0001 | c0005 | t0004 | g0154 | AFR | LWK | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0008 | t0001 | g0146 | REF | REF | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| homoSapiens_grch38 | hp1 | a0001 | c0003 | t0003 | g0131 | REF | REF | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:92924411
|
C | T | 1 | a0001c0019 | 1 | NA19000.hp1 | synonymous_variant | LOW | c.153C>T | p.Ser51Ser | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 3/39 | 725/9350 | 153/5487 | 51/1828 | chr15 | 92924411 | ||
| chr15:92927279
|
G | A | 1 | a0001c0010 | 2 | HG02486.hp2 HG02970.hp2 |
synonymous_variant | LOW | c.330G>A | p.Arg110Arg | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 4/39 | 902/9350 | 330/5487 | 110/1828 | chr15 | 92927279 | ||
| chr15:92955491
|
T | C | 1 | a0001c0011 | 2 | HG00639.hp2 HG00738.hp1 |
synonymous_variant | LOW | c.1788T>C | p.Tyr596Tyr | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 15/39 | 2360/9350 | 1788/5487 | 596/1828 | chr15 | 92955491 | ||
| chr15:92967373
|
A | G | 13 | a0001c0001a0001c0002a0001c0004others(10): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
synonymous_variant | LOW | c.2049A>G | p.Glu683Glu | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/39 | 2621/9350 | 2049/5487 | 683/1828 | chr15 | 92967373 | ||
| chr15:92971912
|
A | G | 1 | a0001c0018 | 1 | NA18963.hp2 | synonymous_variant | LOW | c.2337A>G | p.Gly779Gly | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 18/39 | 2909/9350 | 2337/5487 | 779/1828 | chr15 | 92971912 | ||
| chr15:92978374
|
A | G | 12 | a0001c0001a0001c0002a0001c0004others(9): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
synonymous_variant | LOW | c.2718A>G | p.Gln906Gln | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 21/39 | 3290/9350 | 2718/5487 | 906/1828 | chr15 | 92978374 | ||
| chr15:92984389
|
C | T | 1 | a0001c0017 | 1 | HG01192.hp1 | synonymous_variant | LOW | c.3126C>T | p.Asp1042Asp | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 25/39 | 3698/9350 | 3126/5487 | 1042/1828 | chr15 | 92984389 | ||
| chr15:92985575
|
G | A | 1 | a0001c0015 | 1 | HG02280.hp2 | synonymous_variant | LOW | c.3315G>A | p.Thr1105Thr | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/39 | 3887/9350 | 3315/5487 | 1105/1828 | chr15 | 92985575 | ||
| chr15:92985581
|
C | T | 1 | a0001c0012 | 2 | HG02280.hp1 HG02922.hp2 |
synonymous_variant | LOW | c.3321C>T | p.Asp1107Asp | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/39 | 3893/9350 | 3321/5487 | 1107/1828 | chr15 | 92985581 | ||
| chr15:92992943
|
C | T | 2 | a0001c0009a0001c0016 | 4 | HG00642.hp1 HG00673.hp2 HG02258.hp1 others(1): Show |
synonymous_variant | LOW | c.3540C>T | p.Ser1180Ser | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/39 | 4112/9350 | 3540/5487 | 1180/1828 | chr15 | 92992943 | ||
| chr15:92992967
|
C | T | 4 | a0001c0002a0001c0004a0001c0013others(1): Show | 67 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(64): Show |
synonymous_variant | LOW | c.3564C>T | p.Tyr1188Tyr | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/39 | 4136/9350 | 3564/5487 | 1188/1828 | chr15 | 92992967 | ||
| chr15:93009258
|
C | T | 1 | a0001c0008 | 3 | HG00323.hp2 HG02486.hp1 homoSapiens_chm13v2.hp1 |
synonymous_variant | LOW | c.4527C>T | p.Ile1509Ile | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 35/39 | 5099/9350 | 4527/5487 | 1509/1828 | chr15 | 93009258 | ||
| chr15:93020154
|
C | T | 1 | a0001c0016 | 1 | HG00642.hp1 | synonymous_variant | LOW | c.5049C>T | p.Ala1683Ala | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/39 | 5621/9350 | 5049/5487 | 1683/1828 | chr15 | 93020154 | ||
| chr15:93024634
|
A | C | 3 | a0001c0004a0001c0005a0001c0006 | 35 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(32): Show |
synonymous_variant | LOW | c.5416A>C | p.Arg1806Arg | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 39/39 | 5988/9350 | 5416/5487 | 1806/1828 | chr15 | 93024634 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:93024778
|
G | A | 2 | a0001c0001t0011a0001c0002t0011 | 5 | HG01074.hp1 HG01175.hp1 NA18993.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*73G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 39/39 | 73 | chr15 | 93024778 | |||||
| chr15:93024787
|
G | A | 1 | a0001c0003t0014 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*82G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 39/39 | 82 | chr15 | 93024787 | |||||
| chr15:93024852
|
G | T | 1 | a0001c0001t0025 | 1 | HG00621.hp2 | 3_prime_UTR_variant | MODIFIER | c.*147G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 39/39 | 147 | chr15 | 93024852 | |||||
| chr15:93025065
|
G | A | 6 | a0001c0001t0005a0001c0002t0005a0001c0003t0005others(3): Show | 15 | HG01167.hp2 HG01169.hp2 HG01884.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*360G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 39/39 | 360 | chr15 | 93025065 | |||||
| chr15:93025197
|
G | A | 1 | a0001c0001t0006 | 14 | HG00735.hp2 HG01099.hp2 HG01106.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*492G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 39/39 | 492 | chr15 | 93025197 | |||||
| chr15:93025236
|
A | AGGG | 28 | a0001c0001t0001a0001c0001t0005a0001c0001t0008others(25): Show | 197 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(194): Show |
3_prime_UTR_variant | MODIFIER | c.*533_*535dupGGG | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 39/39 | 536 | INFO_REALIGN_3_PRIME | chr15 | 93025236 | ||||
| chr15:93025595
|
C | T | 1 | a0001c0004t0018 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*890C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 39/39 | 890 | chr15 | 93025595 | |||||
| chr15:93025654
|
A | C | 20 | a0001c0001t0001a0001c0001t0005a0001c0001t0020others(17): Show | 179 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(176): Show |
3_prime_UTR_variant | MODIFIER | c.*949A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 39/39 | 949 | chr15 | 93025654 | |||||
| chr15:93025709
|
G | A | 1 | a0001c0005t0015 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1004G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 39/39 | 1004 | chr15 | 93025709 | |||||
| chr15:93025852
|
ACAT | A | 4 | a0001c0004t0004a0001c0005t0004a0001c0005t0015others(1): Show | 18 | HG00140.hp2 HG00738.hp2 HG01069.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1151_*1153delCAT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 39/39 | 1151 | INFO_REALIGN_3_PRIME | chr15 | 93025852 | ||||
| chr15:93026295
|
C | T | 1 | a0001c0001t0024 | 1 | HG01257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1590C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 39/39 | 1590 | chr15 | 93026295 | |||||
| chr15:93026317
|
C | T | 1 | a0001c0001t0023 | 1 | NA18612.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1612C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 39/39 | 1612 | chr15 | 93026317 | |||||
| chr15:93026509
|
G | A | 1 | a0001c0004t0010 | 6 | NA18612.hp2 NA18952.hp1 NA18956.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1804G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 39/39 | 1804 | chr15 | 93026509 | |||||
| chr15:93026608
|
C | T | 1 | a0001c0013t0019 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1903C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 39/39 | 1903 | chr15 | 93026608 | |||||
| chr15:93026613
|
C | G | 1 | a0001c0004t0017 | 1 | HG01123.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1908C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 39/39 | 1908 | chr15 | 93026613 | |||||
| chr15:93026624
|
G | A | 4 | a0001c0001t0008a0001c0002t0008a0001c0003t0008others(1): Show | 9 | HG00741.hp1 HG01070.hp2 HG01952.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1919G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 39/39 | 1919 | chr15 | 93026624 | |||||
| chr15:93026665
|
T | C | 8 | a0001c0001t0005a0001c0002t0005a0001c0003t0005others(5): Show | 19 | HG01167.hp2 HG01169.hp2 HG01257.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1960T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 39/39 | 1960 | chr15 | 93026665 | |||||
| chr15:93026669
|
C | T | 1 | a0001c0007t0013 | 2 | HG01243.hp2 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1964C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 39/39 | 1964 | chr15 | 93026669 | |||||
| chr15:93026822
|
C | T | 1 | a0001c0001t0022 | 1 | NA19068.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2117C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 39/39 | 2117 | chr15 | 93026822 | |||||
| chr15:93027011
|
T | C | 51 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(48): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
3_prime_UTR_variant | MODIFIER | c.*2306T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 39/39 | 2306 | chr15 | 93027011 | |||||
| chr15:93027051
|
C | T | 1 | a0001c0004t0018 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2346C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 39/39 | 2346 | chr15 | 93027051 | |||||
| chr15:93027309
|
T | A | 1 | a0001c0002t0016 | 1 | HG00099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2604T>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 39/39 | 2604 | chr15 | 93027309 | |||||
| chr15:93027362
|
G | C | 1 | a0001c0001t0020 | 1 | HG00621.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2657G>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 39/39 | 2657 | chr15 | 93027362 | |||||
| chr15:93027493
|
T | C | 11 | a0001c0001t0001a0001c0001t0020a0001c0001t0022others(8): Show | 159 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(156): Show |
3_prime_UTR_variant | MODIFIER | c.*2788T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 39/39 | 2788 | chr15 | 93027493 | |||||
| chr15:93027556
|
G | C | 11 | a0001c0001t0007a0001c0001t0011a0001c0001t0021others(8): Show | 26 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*2851G>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 39/39 | 2851 | chr15 | 93027556 | |||||
| chr15:93027767
|
T | C | 3 | a0001c0001t0011a0001c0001t0021a0001c0002t0011 | 6 | HG01074.hp1 HG01175.hp1 HG02027.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3062T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 39/39 | 3062 | chr15 | 93027767 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:92901339
|
T | G | 2 | a0001c0001t0001g0007a0001c0001t0002g0008 | 2 | HG02717.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.62+40T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92901339 | ||||||
| chr15:92901795
|
A | G | 3 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0300 | 3 | HG02258.hp2 HG02965.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.62+496A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92901795 | ||||||
| chr15:92901973
|
CAG | C | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0011 | 3 | NA18967.hp2 NA18994.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.62+676_62+677delGA | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 92901973 | |||||
| chr15:92902553
|
G | A | 16 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0003g0001others(13): Show | 17 | HG00639.hp1 HG00639.hp2 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.62+1254G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92902553 | ||||||
| chr15:92902628
|
G | T | 26 | a0001c0001t0001g0281a0001c0001t0001g0298a0001c0001t0001g0299others(23): Show | 26 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.62+1329G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92902628 | ||||||
| chr15:92903085
|
T | C | 3 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029 | 3 | NA18942.hp1 NA18951.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.62+1786T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92903085 | ||||||
| chr15:92903239
|
C | G | 1 | a0001c0001t0003g0274 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.62+1940C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92903239 | ||||||
| chr15:92903242
|
C | G | 138 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0016others(135): Show | 141 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.62+1943C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92903242 | ||||||
| chr15:92903569
|
CTT | C | 26 | a0001c0001t0001g0281a0001c0001t0001g0298a0001c0001t0001g0299others(23): Show | 26 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.62+2272_62+2273del others(2): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 92903569 | |||||
| chr15:92903639
|
C | T | 138 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0016others(135): Show | 141 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.62+2340C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92903639 | ||||||
| chr15:92903747
|
A | G | 4 | a0001c0001t0001g0006a0001c0001t0001g0271a0001c0001t0001g0272others(1): Show | 5 | HG01123.hp2 HG02683.hp2 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.62+2448A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92903747 | ||||||
| chr15:92903815
|
A | G | 12 | a0001c0001t0001g0259a0001c0001t0006g0260a0001c0001t0006g0261others(9): Show | 12 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.62+2516A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92903815 | ||||||
| chr15:92903836
|
C | A | 1 | a0001c0002t0008g0012 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.62+2537C>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92903836 | ||||||
| chr15:92904063
|
T | C | 26 | a0001c0001t0001g0281a0001c0001t0001g0298a0001c0001t0001g0299others(23): Show | 26 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.62+2764T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92904063 | ||||||
| chr15:92904085
|
C | A | 101 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0016others(98): Show | 104 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.62+2786C>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92904085 | ||||||
| chr15:92904325
|
T | C | 3 | a0001c0002t0002g0156a0001c0007t0003g0157a0001c0007t0007g0030 | 3 | HG02630.hp1 HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.62+3026T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92904325 | ||||||
| chr15:92904401
|
T | G | 139 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0016others(136): Show | 142 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.62+3102T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92904401 | ||||||
| chr15:92904403
|
G | T | 1 | a0001c0002t0002g0232 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.62+3104G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92904403 | ||||||
| chr15:92904444
|
A | G | 11 | a0001c0002t0002g0223a0001c0002t0002g0231a0001c0002t0002g0232others(8): Show | 11 | HG01884.hp2 HG02257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.62+3145A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92904444 | ||||||
| chr15:92904508
|
T | C | 1 | a0001c0012t0002g0031 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.62+3209T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92904508 | ||||||
| chr15:92904512
|
G | C | 3 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034 | 3 | HG02083.hp1 NA18965.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.62+3213G>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92904512 | ||||||
| chr15:92904536
|
T | G | 9 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0038others(6): Show | 9 | HG01192.hp1 HG01433.hp1 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.62+3237T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92904536 | ||||||
| chr15:92904547
|
C | A | 1 | a0001c0001t0001g0035 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.62+3248C>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92904547 | ||||||
| chr15:92904563
|
A | G | 1 | a0001c0004t0004g0297 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.62+3264A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92904563 | ||||||
| chr15:92904618
|
C | T | 1 | a0001c0002t0002g0232 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.62+3319C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92904618 | ||||||
| chr15:92904766
|
G | A | 25 | a0001c0001t0001g0006a0001c0001t0001g0271a0001c0001t0001g0272others(22): Show | 26 | HG01069.hp1 HG01070.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.62+3467G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92904766 | ||||||
| chr15:92904833
|
A | G | 2 | a0001c0005t0004g0153a0001c0005t0004g0154 | 2 | NA20752.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.62+3534A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92904833 | ||||||
| chr15:92904992
|
G | A | 26 | a0001c0001t0001g0281a0001c0001t0001g0298a0001c0001t0001g0299others(23): Show | 26 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.62+3693G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92904992 | ||||||
| chr15:92905575
|
T | C | 93 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0027others(90): Show | 94 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.62+4276T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92905575 | ||||||
| chr15:92905597
|
T | G | 1 | a0001c0006t0004g0158 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.62+4298T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92905597 | ||||||
| chr15:92905653
|
C | G | 93 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0027others(90): Show | 94 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.62+4354C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92905653 | ||||||
| chr15:92905780
|
A | G | 2 | a0001c0002t0005g0220a0001c0003t0002g0221 | 2 | HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.62+4481A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92905780 | ||||||
| chr15:92905834
|
G | A | 62 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0026others(59): Show | 64 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.62+4535G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92905834 | ||||||
| chr15:92905988
|
A | G | 1 | a0001c0003t0003g0152 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.62+4689A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92905988 | ||||||
| chr15:92906030
|
A | G | 6 | a0001c0002t0002g0231a0001c0002t0003g0228a0001c0002t0005g0227others(3): Show | 6 | HG01884.hp2 HG02257.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.62+4731A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92906030 | ||||||
| chr15:92906095
|
C | T | 3 | a0001c0001t0008g0217a0001c0001t0008g0218a0001c0001t0008g0219 | 3 | HG03239.hp2 HG03688.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.62+4796C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92906095 | ||||||
| chr15:92906144
|
T | A | 121 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0016others(118): Show | 124 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.62+4845T>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92906144 | ||||||
| chr15:92906183
|
C | CT | 9 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0038others(6): Show | 9 | HG01192.hp1 HG01433.hp1 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.62+4891dupT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 92906183 | |||||
| chr15:92906238
|
T | C | 2 | a0001c0002t0002g0156a0001c0007t0003g0157 | 2 | HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.62+4939T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92906238 | ||||||
| chr15:92906267
|
C | T | 1 | a0001c0003t0002g0221 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.62+4968C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92906267 | ||||||
| chr15:92906359
|
G | A | 12 | a0001c0001t0001g0259a0001c0001t0006g0260a0001c0001t0006g0261others(9): Show | 12 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.62+5060G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92906359 | ||||||
| chr15:92906411
|
A | G | 9 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0038others(6): Show | 9 | HG01192.hp1 HG01433.hp1 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.62+5112A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92906411 | ||||||
| chr15:92906413
|
T | C | 1 | a0001c0001t0011g0176 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.62+5114T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92906413 | ||||||
| chr15:92906466
|
C | A | 1 | a0001c0001t0001g0041 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.62+5167C>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92906466 | ||||||
| chr15:92906521
|
A | C | 3 | a0001c0002t0002g0223a0001c0002t0005g0224a0001c0002t0005g0225 | 3 | HG02572.hp2 HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.62+5222A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92906521 | ||||||
| chr15:92906539
|
C | T | 1 | a0001c0001t0001g0216 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.62+5240C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92906539 | ||||||
| chr15:92906559
|
C | G | 1 | a0001c0002t0001g0258 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.62+5260C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92906559 | ||||||
| chr15:92906629
|
T | C | 1 | a0001c0005t0004g0159 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.62+5330T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92906629 | ||||||
| chr15:92906662
|
A | AT | 8 | a0001c0002t0001g0236a0001c0002t0001g0237a0001c0002t0001g0238others(5): Show | 8 | HG00423.hp2 HG02040.hp1 NA18944.hp1 others(5): Show |
intron_variant | MODIFIER | c.62+5364dupT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 92906662 | |||||
| chr15:92906662
|
A | ATT | 15 | a0001c0001t0006g0248a0001c0002t0001g0244a0001c0002t0001g0246others(12): Show | 15 | HG00558.hp1 HG01943.hp2 HG02074.hp2 others(12): Show |
intron_variant | MODIFIER | c.62+5364_62+5365ins others(2): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 92906662 | |||||
| chr15:92906664
|
C | T | 26 | a0001c0001t0006g0248a0001c0002t0001g0233a0001c0002t0001g0234others(23): Show | 26 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.62+5365C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92906664 | ||||||
| chr15:92906664
|
CT | C | 8 | a0001c0001t0001g0026a0001c0001t0001g0259a0001c0001t0002g0278others(5): Show | 9 | HG01074.hp2 HG01169.hp2 HG01515.hp2 others(6): Show |
intron_variant | MODIFIER | c.62+5385delT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 92906664 | |||||
| chr15:92906664
|
CTT | C | 95 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0016others(92): Show | 97 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.62+5384_62+5385del others(2): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 92906664 | |||||
| chr15:92906664
|
CTTT | C | 91 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0027others(88): Show | 92 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.62+5383_62+5385del others(3): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 92906664 | |||||
| chr15:92906720
|
T | C | 12 | a0001c0001t0001g0259a0001c0001t0006g0260a0001c0001t0006g0261others(9): Show | 12 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.62+5421T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92906720 | ||||||
| chr15:92906733
|
T | G | 2 | a0001c0005t0004g0153a0001c0005t0004g0154 | 2 | NA20752.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.62+5434T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92906733 | ||||||
| chr15:92906739
|
A | G | 121 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0016others(118): Show | 124 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.62+5440A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92906739 | ||||||
| chr15:92906775
|
A | C | 1 | a0001c0001t0008g0219 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.62+5476A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92906775 | ||||||
| chr15:92906814
|
G | A | 1 | a0001c0004t0007g0014 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.62+5515G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92906814 | ||||||
| chr15:92906927
|
A | G | 19 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(16): Show | 19 | HG00438.hp1 HG00621.hp1 HG02083.hp1 others(16): Show |
intron_variant | MODIFIER | c.62+5628A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92906927 | ||||||
| chr15:92907002
|
A | G | 4 | a0001c0001t0001g0212a0001c0001t0001g0213a0001c0001t0001g0214others(1): Show | 4 | HG00438.hp2 HG02040.hp2 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.62+5703A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92907002 | ||||||
| chr15:92907038
|
G | C | 2 | a0001c0002t0005g0220a0001c0003t0002g0221 | 2 | HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.62+5739G>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92907038 | ||||||
| chr15:92907136
|
A | T | 62 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0026others(59): Show | 64 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.62+5837A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92907136 | ||||||
| chr15:92907142
|
A | C | 113 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0016others(110): Show | 116 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.62+5843A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92907142 | ||||||
| chr15:92907236
|
A | G | 1 | a0001c0003t0002g0221 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.62+5937A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92907236 | ||||||
| chr15:92907754
|
A | G | 3 | a0001c0007t0007g0030a0001c0007t0013g0150a0001c0007t0013g0151 | 3 | HG01243.hp2 HG02630.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.62+6455A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92907754 | ||||||
| chr15:92907807
|
A | T | 1 | a0001c0003t0003g0149 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.62+6508A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92907807 | ||||||
| chr15:92908003
|
A | AT | 119 | a0001c0001t0001g0002a0001c0001t0001g0027a0001c0001t0001g0028others(116): Show | 121 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.62+6728dupT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 92908003 | |||||
| chr15:92908003
|
A | ATT | 12 | a0001c0001t0001g0007a0001c0001t0001g0029a0001c0001t0001g0041others(9): Show | 12 | HG00621.hp2 HG01258.hp2 HG02040.hp1 others(9): Show |
intron_variant | MODIFIER | c.62+6727_62+6728dup others(2): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 92908003 | |||||
| chr15:92908003
|
AT | A | 46 | a0001c0001t0001g0006a0001c0001t0001g0035a0001c0001t0001g0178others(43): Show | 47 | HG00323.hp2 HG00735.hp2 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.62+6728delT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 92908003 | |||||
| chr15:92908102
|
G | C | 1 | a0001c0003t0003g0128 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.62+6803G>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92908102 | ||||||
| chr15:92908380
|
A | G | 1 | a0001c0001t0001g0007 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.62+7081A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92908380 | ||||||
| chr15:92908396
|
T | A | 12 | a0001c0001t0001g0259a0001c0001t0006g0260a0001c0001t0006g0261others(9): Show | 12 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.62+7097T>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92908396 | ||||||
| chr15:92908486
|
G | A | 12 | a0001c0001t0001g0259a0001c0001t0006g0260a0001c0001t0006g0261others(9): Show | 12 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.62+7187G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92908486 | ||||||
| chr15:92908556
|
G | C | 6 | a0001c0002t0002g0045a0001c0002t0002g0046a0001c0009t0002g0043others(3): Show | 6 | HG00642.hp1 HG00673.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.62+7257G>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92908556 | ||||||
| chr15:92908559
|
T | C | 1 | a0001c0002t0002g0232 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.62+7260T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92908559 | ||||||
| chr15:92908668
|
C | T | 17 | a0001c0001t0007g0174a0001c0003t0002g0162a0001c0003t0002g0169others(14): Show | 17 | HG01070.hp1 HG01109.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.62+7369C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92908668 | ||||||
| chr15:92908865
|
T | G | 1 | a0001c0005t0004g0180 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.62+7566T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92908865 | ||||||
| chr15:92908896
|
A | T | 2 | a0001c0007t0013g0150a0001c0007t0013g0151 | 2 | HG01243.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.62+7597A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92908896 | ||||||
| chr15:92908980
|
A | G | 1 | a0001c0002t0002g0232 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.62+7681A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92908980 | ||||||
| chr15:92909035
|
C | T | 1 | a0001c0001t0001g0210 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.62+7736C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92909035 | ||||||
| chr15:92909067
|
T | C | 123 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0016others(120): Show | 126 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.62+7768T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92909067 | ||||||
| chr15:92909073
|
G | GACACACC | 93 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0027others(90): Show | 94 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.62+7777_62+7783dup others(7): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 92909073 | |||||
| chr15:92909211
|
C | G | 9 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0038others(6): Show | 9 | HG01192.hp1 HG01433.hp1 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.62+7912C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92909211 | ||||||
| chr15:92909410
|
C | T | 2 | a0001c0001t0003g0274a0001c0001t0005g0179 | 2 | NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.62+8111C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92909410 | ||||||
| chr15:92909616
|
G | A | 269 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(266): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.62+8317G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92909616 | ||||||
| chr15:92909630
|
A | G | 1 | a0001c0013t0019g0168 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.62+8331A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92909630 | ||||||
| chr15:92909803
|
C | T | 4 | a0001c0002t0002g0223a0001c0002t0002g0232a0001c0002t0005g0224others(1): Show | 4 | HG02572.hp2 HG03209.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.62+8504C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92909803 | ||||||
| chr15:92909813
|
G | A | 12 | a0001c0001t0001g0259a0001c0001t0006g0260a0001c0001t0006g0261others(9): Show | 12 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.62+8514G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92909813 | ||||||
| chr15:92909850
|
A | G | 1 | a0001c0002t0002g0232 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.62+8551A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92909850 | ||||||
| chr15:92909939
|
C | CGT | 11 | a0001c0001t0001g0259a0001c0001t0002g0278a0001c0001t0002g0295others(8): Show | 11 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.62+8669_62+8670dup others(2): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 92909939 | |||||
| chr15:92909939
|
C | CGTGT | 7 | a0001c0001t0006g0268a0001c0001t0006g0269a0001c0002t0002g0045others(4): Show | 7 | HG00642.hp1 HG02148.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.62+8667_62+8670dup others(4): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 92909939 | |||||
| chr15:92909939
|
C | CGTGTGT | 24 | a0001c0001t0006g0248a0001c0002t0001g0233a0001c0002t0001g0234others(21): Show | 24 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.62+8665_62+8670dup others(6): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 92909939 | |||||
| chr15:92909939
|
C | CGTGTGTG others(1): Show |
3 | a0001c0002t0001g0242a0001c0002t0001g0255a0001c0005t0004g0153 | 3 | NA18959.hp2 NA19081.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.62+8663_62+8670dup others(8): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 92909939 | |||||
| chr15:92909939
|
C | CGTGTGTG others(3): Show |
1 | a0001c0005t0004g0154 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.62+8661_62+8670dup others(10): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 92909939 | |||||
| chr15:92909939
|
CGT | C | 3 | a0001c0002t0002g0275a0001c0002t0016g0280a0001c0003t0005g0124 | 3 | HG00099.hp2 HG01975.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.62+8669_62+8670del others(2): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 92909939 | |||||
| chr15:92909939
|
CGTGTGTG others(3): Show |
C | 10 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0098others(7): Show | 10 | HG01346.hp1 HG01361.hp2 HG01928.hp1 others(7): Show |
intron_variant | MODIFIER | c.62+8661_62+8670del others(10): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 92909939 | |||||
| chr15:92909939
|
CGTGTGTG others(5): Show |
C | 178 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(175): Show | 182 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.62+8659_62+8670del others(12): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 92909939 | |||||
| chr15:92910044
|
T | C | 36 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0038others(33): Show | 36 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.62+8745T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92910044 | ||||||
| chr15:92910116
|
C | T | 25 | a0001c0001t0001g0281a0001c0001t0001g0298a0001c0001t0001g0299others(22): Show | 25 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.62+8817C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92910116 | ||||||
| chr15:92910648
|
C | T | 1 | a0001c0003t0003g0167 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.62+9349C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92910648 | ||||||
| chr15:92911020
|
G | A | 85 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0016others(82): Show | 88 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.62+9721G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92911020 | ||||||
| chr15:92911093
|
C | A | 1 | a0001c0013t0019g0168 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.62+9794C>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92911093 | ||||||
| chr15:92911152
|
C | T | 108 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0016others(105): Show | 111 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.62+9853C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92911152 | ||||||
| chr15:92911491
|
A | C | 1 | a0001c0010t0002g0222 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.62+10192A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92911491 | ||||||
| chr15:92911519
|
C | T | 1 | a0001c0004t0018g0025 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.62+10220C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92911519 | ||||||
| chr15:92911562
|
A | G | 94 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0027others(91): Show | 95 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.62+10263A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92911562 | ||||||
| chr15:92911583
|
C | G | 2 | a0001c0001t0001g0026a0001c0001t0003g0001 | 3 | HG01515.hp2 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.62+10284C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92911583 | ||||||
| chr15:92911654
|
G | A | 1 | a0001c0003t0005g0160 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.62+10355G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92911654 | ||||||
| chr15:92911689
|
C | T | 2 | a0001c0001t0002g0293a0001c0001t0002g0294 | 2 | HG00544.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.62+10390C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92911689 | ||||||
| chr15:92911692
|
A | G | 1 | a0001c0016t0002g0047 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.62+10393A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92911692 | ||||||
| chr15:92911801
|
C | G | 106 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0016others(103): Show | 109 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.62+10502C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92911801 | ||||||
| chr15:92911960
|
T | C | 12 | a0001c0001t0001g0259a0001c0001t0006g0260a0001c0001t0006g0261others(9): Show | 12 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.62+10661T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92911960 | ||||||
| chr15:92912012
|
A | C | 1 | a0001c0002t0001g0254 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.62+10713A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92912012 | ||||||
| chr15:92912147
|
G | GT | 12 | a0001c0001t0001g0259a0001c0001t0006g0260a0001c0001t0006g0261others(9): Show | 12 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.62+10857dupT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 92912147 | |||||
| chr15:92912241
|
G | A | 102 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0026others(99): Show | 104 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.62+10942G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92912241 | ||||||
| chr15:92912336
|
G | A | 1 | a0001c0001t0006g0261 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.62+11037G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92912336 | ||||||
| chr15:92912387
|
C | T | 1 | a0001c0001t0001g0041 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.62+11088C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92912387 | ||||||
| chr15:92912550
|
T | C | 3 | a0001c0001t0001g0281a0001c0001t0002g0278a0001c0001t0002g0295 | 3 | HG02965.hp1 HG03471.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.62+11251T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92912550 | ||||||
| chr15:92912582
|
A | G | 2 | a0001c0001t0001g0096a0001c0001t0001g0122 | 2 | HG02602.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.62+11283A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92912582 | ||||||
| chr15:92912602
|
T | C | 1 | a0001c0004t0018g0025 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.62+11303T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92912602 | ||||||
| chr15:92912690
|
C | T | 9 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0038others(6): Show | 9 | HG01192.hp1 HG01433.hp1 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.62+11391C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92912690 | ||||||
| chr15:92912723
|
CA | C | 37 | a0001c0001t0001g0095a0001c0001t0011g0292a0001c0001t0025g0104others(34): Show | 37 | HG00621.hp2 HG00673.hp2 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.62+11425delA | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92912723 | ||||||
| chr15:92912748
|
C | A | 3 | a0001c0002t0001g0233a0001c0002t0001g0237a0001c0002t0001g0238 | 3 | NA18950.hp1 NA18973.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.62+11449C>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92912748 | ||||||
| chr15:92912752
|
T | C | 29 | a0001c0001t0001g0016a0001c0001t0001g0049a0001c0001t0001g0183others(26): Show | 29 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.62+11453T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92912752 | ||||||
| chr15:92912764
|
GACCTCGT others(9): Show |
G | 3 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0209 | 3 | HG03492.hp2 HG03710.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.62+11470_62+11485d others(18): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 92912764 | |||||
| chr15:92912769
|
CGTGATCC others(9): Show |
C | 1 | a0001c0002t0002g0156 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.62+11481_62+11496d others(18): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 92912769 | |||||
| chr15:92912770
|
G | A | 1 | a0001c0006t0004g0004 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.62+11471G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92912770 | ||||||
| chr15:92912780
|
A | C | 268 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(265): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.62+11481A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92912780 | ||||||
| chr15:92912781
|
A | G | 2 | a0001c0001t0002g0293a0001c0001t0002g0294 | 2 | HG00544.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.62+11482A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92912781 | ||||||
| chr15:92912797
|
G | A | 1 | a0001c0002t0002g0156 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.62+11498G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92912797 | ||||||
| chr15:92912802
|
G | A | 1 | a0001c0002t0002g0156 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.62+11503G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92912802 | ||||||
| chr15:92912839
|
T | C | 133 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0016others(130): Show | 135 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.63-11482T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92912839 | ||||||
| chr15:92912912
|
C | T | 1 | a0001c0001t0003g0274 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.63-11409C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92912912 | ||||||
| chr15:92913166
|
A | G | 1 | a0001c0002t0001g0244 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.63-11155A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92913166 | ||||||
| chr15:92913228
|
G | A | 3 | a0001c0003t0012g0126a0001c0003t0012g0133a0001c0003t0012g0134 | 3 | HG01257.hp1 HG01258.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.63-11093G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92913228 | ||||||
| chr15:92913425
|
C | T | 2 | a0001c0001t0001g0095a0001c0001t0025g0104 | 2 | HG00621.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.63-10896C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92913425 | ||||||
| chr15:92913689
|
A | C | 18 | a0001c0001t0001g0281a0001c0001t0001g0298a0001c0001t0001g0299others(15): Show | 18 | HG00544.hp1 HG00735.hp1 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.63-10632A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92913689 | ||||||
| chr15:92913786
|
C | T | 6 | a0001c0002t0002g0231a0001c0002t0003g0228a0001c0002t0005g0227others(3): Show | 6 | HG01884.hp2 HG02257.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.63-10535C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92913786 | ||||||
| chr15:92913813
|
C | T | 1 | a0001c0002t0002g0156 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.63-10508C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92913813 | ||||||
| chr15:92913818
|
A | T | 52 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0177others(49): Show | 54 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.63-10503A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92913818 | ||||||
| chr15:92913844
|
C | T | 2 | a0001c0002t0005g0220a0001c0003t0002g0221 | 2 | HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.63-10477C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92913844 | ||||||
| chr15:92913910
|
T | G | 2 | a0001c0001t0003g0274a0001c0001t0005g0179 | 2 | NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.63-10411T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92913910 | ||||||
| chr15:92914278
|
T | G | 1 | a0001c0006t0005g0130 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.63-10043T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92914278 | ||||||
| chr15:92914287
|
A | G | 2 | a0001c0001t0001g0093a0001c0001t0001g0094 | 2 | HG00673.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.63-10034A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92914287 | ||||||
| chr15:92914420
|
T | C | 67 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0016others(64): Show | 70 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.63-9901T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92914420 | ||||||
| chr15:92914561
|
A | C | 2 | a0001c0002t0009g0022a0001c0004t0018g0025 | 2 | HG01361.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.63-9760A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92914561 | ||||||
| chr15:92914731
|
A | T | 88 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0027others(85): Show | 89 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.63-9590A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92914731 | ||||||
| chr15:92914923
|
T | C | 1 | a0001c0002t0002g0232 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.63-9398T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92914923 | ||||||
| chr15:92915020
|
A | C | 1 | a0001c0003t0003g0148 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.63-9301A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92915020 | ||||||
| chr15:92915071
|
C | T | 2 | a0001c0001t0003g0274a0001c0001t0005g0179 | 2 | NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.63-9250C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92915071 | ||||||
| chr15:92915124
|
T | G | 61 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0026others(58): Show | 63 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.63-9197T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92915124 | ||||||
| chr15:92915279
|
G | GT | 16 | a0001c0001t0001g0118a0001c0001t0001g0259a0001c0001t0006g0248others(13): Show | 16 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.63-9029dupT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 92915279 | |||||
| chr15:92915306
|
G | A | 1 | a0001c0005t0007g0050 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63-9015G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92915306 | ||||||
| chr15:92915401
|
A | T | 2 | a0001c0002t0002g0045a0001c0002t0002g0046 | 2 | NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.63-8920A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92915401 | ||||||
| chr15:92915451
|
T | C | 1 | a0001c0003t0001g0135 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.63-8870T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92915451 | ||||||
| chr15:92915475
|
C | T | 83 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0026others(80): Show | 86 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.63-8846C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92915475 | ||||||
| chr15:92915575
|
A | G | 1 | a0001c0001t0001g0117 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.63-8746A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92915575 | ||||||
| chr15:92915614
|
C | G | 4 | a0001c0002t0002g0181a0001c0002t0002g0223a0001c0002t0005g0224others(1): Show | 4 | HG02572.hp2 HG03209.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.63-8707C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92915614 | ||||||
| chr15:92915695
|
T | C | 6 | a0001c0002t0002g0231a0001c0002t0003g0228a0001c0002t0005g0227others(3): Show | 6 | HG01884.hp2 HG02257.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.63-8626T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92915695 | ||||||
| chr15:92915882
|
G | A | 239 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(236): Show | 243 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.63-8439G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92915882 | ||||||
| chr15:92915927
|
C | T | 1 | a0001c0001t0001g0116 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.63-8394C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92915927 | ||||||
| chr15:92916011
|
ACTCTCTT | A | 108 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0016others(105): Show | 111 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.63-8306_63-8300del others(7): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 92916011 | |||||
| chr15:92916102
|
C | T | 65 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0016others(62): Show | 68 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.63-8219C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92916102 | ||||||
| chr15:92916223
|
C | T | 13 | a0001c0001t0001g0132a0001c0001t0001g0141a0001c0003t0001g0135others(10): Show | 14 | HG00323.hp2 HG00741.hp2 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.63-8098C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92916223 | ||||||
| chr15:92916236
|
T | TA | 110 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0016others(107): Show | 113 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.63-8084dupA | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 92916236 | |||||
| chr15:92916490
|
C | T | 2 | a0001c0002t0002g0275a0001c0002t0016g0280 | 2 | HG00099.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.63-7831C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92916490 | ||||||
| chr15:92916519
|
C | T | 1 | a0001c0004t0004g0092 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.63-7802C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92916519 | ||||||
| chr15:92916565
|
T | G | 3 | a0001c0003t0003g0161a0001c0003t0005g0160a0001c0007t0003g0157 | 3 | HG01884.hp1 HG02055.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.63-7756T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92916565 | ||||||
| chr15:92917025
|
G | A | 15 | a0001c0001t0001g0006a0001c0001t0001g0035a0001c0001t0001g0036others(12): Show | 16 | HG01069.hp1 HG01123.hp2 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.63-7296G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92917025 | ||||||
| chr15:92917033
|
G | C | 2 | a0001c0007t0013g0150a0001c0007t0013g0151 | 2 | HG01243.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.63-7288G>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92917033 | ||||||
| chr15:92917160
|
A | G | 1 | a0001c0001t0001g0016 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.63-7161A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92917160 | ||||||
| chr15:92917219
|
C | T | 1 | a0001c0003t0005g0166 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.63-7102C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92917219 | ||||||
| chr15:92917375
|
A | G | 6 | a0001c0002t0002g0181a0001c0002t0002g0223a0001c0002t0002g0232others(3): Show | 6 | HG02572.hp2 HG02970.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.63-6946A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92917375 | ||||||
| chr15:92917403
|
A | G | 6 | a0001c0002t0002g0231a0001c0002t0003g0228a0001c0002t0005g0227others(3): Show | 6 | HG01884.hp2 HG02257.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.63-6918A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92917403 | ||||||
| chr15:92917461
|
T | C | 3 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0300 | 3 | HG02258.hp2 HG02965.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.63-6860T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92917461 | ||||||
| chr15:92917475
|
C | T | 2 | a0001c0001t0003g0274a0001c0001t0005g0179 | 2 | NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.63-6846C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92917475 | ||||||
| chr15:92917510
|
G | A | 1 | a0001c0001t0001g0051 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.63-6811G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92917510 | ||||||
| chr15:92917547
|
C | T | 1 | a0001c0001t0001g0115 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.63-6774C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92917547 | ||||||
| chr15:92917605
|
T | C | 2 | a0001c0002t0002g0275a0001c0002t0016g0280 | 2 | HG00099.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.63-6716T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92917605 | ||||||
| chr15:92917614
|
C | T | 4 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(1): Show | 4 | HG02080.hp2 NA18953.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.63-6707C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92917614 | ||||||
| chr15:92917761
|
A | G | 82 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0027others(79): Show | 83 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.63-6560A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92917761 | ||||||
| chr15:92918015
|
G | C | 1 | a0001c0001t0001g0049 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.63-6306G>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92918015 | ||||||
| chr15:92918033
|
C | G | 239 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(236): Show | 243 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.63-6288C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92918033 | ||||||
| chr15:92918141
|
C | G | 192 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(189): Show | 196 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.63-6180C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92918141 | ||||||
| chr15:92918266
|
T | C | 1 | a0001c0001t0001g0185 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.63-6055T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92918266 | ||||||
| chr15:92918301
|
A | G | 24 | a0001c0001t0001g0281a0001c0001t0001g0298a0001c0001t0001g0299others(21): Show | 24 | HG00544.hp1 HG00735.hp1 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.63-6020A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92918301 | ||||||
| chr15:92918347
|
G | GT | 6 | a0001c0002t0002g0181a0001c0002t0002g0223a0001c0002t0002g0232others(3): Show | 6 | HG02572.hp2 HG02970.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.63-5967dupT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 92918347 | |||||
| chr15:92918562
|
T | G | 1 | a0001c0001t0001g0027 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.63-5759T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92918562 | ||||||
| chr15:92918582
|
C | G | 8 | a0001c0003t0003g0161a0001c0003t0003g0164a0001c0003t0003g0167others(5): Show | 8 | HG01109.hp2 HG01884.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.63-5739C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92918582 | ||||||
| chr15:92918737
|
TGTC | T | 5 | a0001c0001t0001g0042a0001c0001t0001g0098a0001c0001t0001g0099others(2): Show | 5 | HG01346.hp1 HG01361.hp2 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.63-5581_63-5579del others(3): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 92918737 | |||||
| chr15:92918806
|
C | T | 1 | a0001c0013t0019g0168 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.63-5515C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92918806 | ||||||
| chr15:92918820
|
T | C | 148 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(145): Show | 152 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.63-5501T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92918820 | ||||||
| chr15:92918856
|
CATATAT | C | 6 | a0001c0002t0002g0231a0001c0002t0003g0228a0001c0002t0005g0227others(3): Show | 6 | HG01884.hp2 HG02257.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.63-5456_63-5451del others(6): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 92918856 | |||||
| chr15:92919029
|
T | C | 3 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0023g0052 | 3 | HG00544.hp2 NA18612.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.63-5292T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92919029 | ||||||
| chr15:92919056
|
G | A | 2 | a0001c0002t0005g0220a0001c0003t0002g0221 | 2 | HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.63-5265G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92919056 | ||||||
| chr15:92919112
|
T | C | 1 | a0001c0003t0005g0166 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.63-5209T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92919112 | ||||||
| chr15:92919136
|
T | G | 13 | a0001c0001t0001g0259a0001c0001t0006g0248a0001c0001t0006g0260others(10): Show | 13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.63-5185T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92919136 | ||||||
| chr15:92919307
|
CT | C | 41 | a0001c0002t0001g0233a0001c0002t0001g0234a0001c0002t0001g0235others(38): Show | 41 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.63-5004delT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 92919307 | |||||
| chr15:92919374
|
G | C | 1 | a0001c0003t0003g0290 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.63-4947G>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92919374 | ||||||
| chr15:92919579
|
A | G | 3 | a0001c0001t0001g0095a0001c0001t0025g0104a0001c0002t0001g0091 | 3 | HG00621.hp2 HG03834.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.63-4742A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92919579 | ||||||
| chr15:92919705
|
A | T | 172 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(169): Show | 176 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.63-4616A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92919705 | ||||||
| chr15:92919730
|
G | T | 172 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(169): Show | 176 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.63-4591G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92919730 | ||||||
| chr15:92919778
|
C | G | 1 | a0001c0001t0001g0095 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.63-4543C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92919778 | ||||||
| chr15:92919843
|
A | G | 2 | a0001c0002t0005g0220a0001c0003t0002g0221 | 2 | HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.63-4478A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92919843 | ||||||
| chr15:92920042
|
C | A | 15 | a0001c0001t0001g0006a0001c0001t0001g0035a0001c0001t0001g0036others(12): Show | 16 | HG01069.hp1 HG01123.hp2 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.63-4279C>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92920042 | ||||||
| chr15:92920050
|
C | A | 1 | a0001c0004t0010g0105 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.63-4271C>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92920050 | ||||||
| chr15:92920129
|
T | C | 3 | a0001c0002t0002g0156a0001c0007t0003g0157a0001c0007t0007g0030 | 3 | HG02630.hp1 HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.63-4192T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92920129 | ||||||
| chr15:92920145
|
G | A | 8 | a0001c0002t0002g0045a0001c0002t0002g0046a0001c0002t0005g0220others(5): Show | 8 | HG00642.hp1 HG00673.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.63-4176G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92920145 | ||||||
| chr15:92920146
|
CT | C | 42 | a0001c0001t0001g0016a0001c0002t0001g0233a0001c0002t0001g0234others(39): Show | 42 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.63-4165delT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 92920146 | |||||
| chr15:92920247
|
G | A | 11 | a0001c0002t0001g0286a0001c0002t0002g0156a0001c0002t0002g0275others(8): Show | 11 | HG00099.hp2 HG01167.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.63-4074G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92920247 | ||||||
| chr15:92920278
|
A | G | 8 | a0001c0002t0001g0286a0001c0002t0002g0275a0001c0002t0005g0277others(5): Show | 8 | HG00099.hp2 HG01167.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.63-4043A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92920278 | ||||||
| chr15:92920344
|
T | C | 13 | a0001c0001t0001g0016a0001c0002t0001g0234a0001c0002t0008g0012others(10): Show | 13 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.63-3977T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92920344 | ||||||
| chr15:92920350
|
A | C | 3 | a0001c0002t0002g0223a0001c0002t0005g0224a0001c0002t0005g0225 | 3 | HG02572.hp2 HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.63-3971A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92920350 | ||||||
| chr15:92920383
|
G | A | 13 | a0001c0001t0001g0259a0001c0001t0006g0248a0001c0001t0006g0260others(10): Show | 13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.63-3938G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92920383 | ||||||
| chr15:92920401
|
T | C | 147 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(144): Show | 151 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.63-3920T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92920401 | ||||||
| chr15:92920472
|
C | T | 46 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0177others(43): Show | 48 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.63-3849C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92920472 | ||||||
| chr15:92920592
|
C | CT | 3 | a0001c0007t0007g0030a0001c0007t0013g0150a0001c0007t0013g0151 | 3 | HG01243.hp2 HG02630.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.63-3725dupT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 92920592 | |||||
| chr15:92920625
|
G | C | 5 | a0001c0001t0001g0042a0001c0001t0001g0098a0001c0001t0001g0099others(2): Show | 5 | HG01346.hp1 HG01361.hp2 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.63-3696G>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92920625 | ||||||
| chr15:92920644
|
A | C | 1 | a0001c0016t0002g0047 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.63-3677A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92920644 | ||||||
| chr15:92920677
|
T | C | 3 | a0001c0002t0002g0156a0001c0007t0003g0157a0001c0007t0007g0030 | 3 | HG02630.hp1 HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.63-3644T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92920677 | ||||||
| chr15:92920930
|
A | T | 2 | a0001c0005t0004g0153a0001c0005t0004g0154 | 2 | NA20752.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.63-3391A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92920930 | ||||||
| chr15:92921146
|
A | G | 42 | a0001c0001t0001g0016a0001c0002t0001g0233a0001c0002t0001g0234others(39): Show | 42 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.63-3175A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92921146 | ||||||
| chr15:92921155
|
A | C | 1 | a0001c0001t0001g0049 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.63-3166A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92921155 | ||||||
| chr15:92921236
|
T | C | 6 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0058others(3): Show | 6 | HG01109.hp1 HG02280.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.63-3085T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92921236 | ||||||
| chr15:92921239
|
G | A | 1 | a0001c0005t0004g0287 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.63-3082G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92921239 | ||||||
| chr15:92921279
|
A | G | 190 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(187): Show | 194 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.63-3042A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92921279 | ||||||
| chr15:92921384
|
G | C | 1 | a0001c0003t0005g0124 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.63-2937G>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92921384 | ||||||
| chr15:92921398
|
C | T | 1 | a0001c0010t0002g0222 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.63-2923C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92921398 | ||||||
| chr15:92921632
|
A | G | 1 | a0001c0001t0001g0094 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.63-2689A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92921632 | ||||||
| chr15:92921695
|
T | C | 1 | a0001c0002t0002g0181 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.63-2626T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92921695 | ||||||
| chr15:92921701
|
G | A | 1 | a0001c0001t0006g0270 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.63-2620G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92921701 | ||||||
| chr15:92921776
|
C | T | 1 | a0001c0001t0001g0059 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.63-2545C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92921776 | ||||||
| chr15:92921821
|
C | T | 1 | a0001c0003t0003g0173 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.63-2500C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92921821 | ||||||
| chr15:92921954
|
A | G | 1 | a0001c0002t0005g0220 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.63-2367A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92921954 | ||||||
| chr15:92921957
|
G | A | 251 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(248): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.63-2364G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92921957 | ||||||
| chr15:92922162
|
G | T | 2 | a0001c0002t0001g0233a0001c0002t0001g0238 | 2 | NA18973.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.63-2159G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92922162 | ||||||
| chr15:92922199
|
G | A | 1 | a0001c0003t0003g0003 | 2 | HG01243.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.63-2122G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92922199 | ||||||
| chr15:92922314
|
G | A | 6 | a0001c0002t0002g0231a0001c0002t0003g0228a0001c0002t0005g0227others(3): Show | 6 | HG01884.hp2 HG02257.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.63-2007G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92922314 | ||||||
| chr15:92922466
|
T | C | 2 | a0001c0001t0001g0095a0001c0001t0025g0104 | 2 | HG00621.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.63-1855T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92922466 | ||||||
| chr15:92922475
|
G | A | 1 | a0001c0003t0005g0160 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.63-1846G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92922475 | ||||||
| chr15:92922697
|
C | T | 171 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(168): Show | 175 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.63-1624C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92922697 | ||||||
| chr15:92922772
|
C | T | 2 | a0001c0001t0001g0202a0001c0001t0001g0203 | 2 | HG02523.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.63-1549C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92922772 | ||||||
| chr15:92923039
|
C | T | 1 | a0001c0001t0001g0201 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.63-1282C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92923039 | ||||||
| chr15:92923078
|
T | C | 1 | a0001c0001t0011g0176 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.63-1243T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92923078 | ||||||
| chr15:92923143
|
T | C | 2 | a0001c0002t0011g0256a0001c0002t0011g0257 | 2 | NA19000.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.63-1178T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92923143 | ||||||
| chr15:92923167
|
C | T | 131 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(128): Show | 134 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.63-1154C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92923167 | ||||||
| chr15:92923304
|
A | C | 2 | a0001c0001t0002g0278a0001c0001t0002g0295 | 2 | HG02965.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.63-1017A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92923304 | ||||||
| chr15:92923385
|
C | T | 131 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(128): Show | 134 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.63-936C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92923385 | ||||||
| chr15:92923392
|
C | CTG | 13 | a0001c0001t0001g0259a0001c0001t0006g0248a0001c0001t0006g0260others(10): Show | 13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.63-928_63-927dupTG | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 92923392 | |||||
| chr15:92923413
|
A | G | 1 | a0001c0003t0014g0165 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.63-908A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92923413 | ||||||
| chr15:92923561
|
G | GT | 26 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0117others(23): Show | 26 | HG00140.hp1 HG00438.hp1 HG00673.hp2 others(23): Show |
intron_variant | MODIFIER | c.63-740dupT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 92923561 | |||||
| chr15:92923561
|
GT | G | 26 | a0001c0001t0001g0006a0001c0001t0001g0035a0001c0001t0001g0036others(23): Show | 27 | HG00735.hp2 HG01069.hp1 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.63-740delT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 92923561 | |||||
| chr15:92923569
|
T | TG | 5 | a0001c0002t0002g0181a0001c0002t0002g0223a0001c0002t0005g0224others(2): Show | 5 | HG02572.hp2 HG02970.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.63-752_63-751insG | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92923569 | ||||||
| chr15:92923668
|
C | T | 1 | a0001c0003t0014g0165 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.63-653C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92923668 | ||||||
| chr15:92923800
|
G | A | 1 | a0001c0003t0008g0140 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.63-521G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92923800 | ||||||
| chr15:92923927
|
A | G | 6 | a0001c0002t0002g0181a0001c0002t0002g0223a0001c0002t0002g0232others(3): Show | 6 | HG02572.hp2 HG02970.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.63-394A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92923927 | ||||||
| chr15:92924124
|
G | T | 189 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(186): Show | 193 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.63-197G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92924124 | ||||||
| chr15:92924161
|
C | T | 147 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(144): Show | 151 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.63-160C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92924161 | ||||||
| chr15:92924212
|
T | C | 1 | a0001c0003t0002g0221 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.63-109T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92924212 | ||||||
| chr15:92924664
|
T | A | 23 | a0001c0001t0007g0174a0001c0002t0002g0231a0001c0002t0003g0228others(20): Show | 23 | HG01070.hp1 HG01109.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.294+112T>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 3/38 | chr15 | 92924664 | ||||||
| chr15:92924846
|
T | A | 3 | a0001c0002t0002g0156a0001c0007t0003g0157a0001c0007t0007g0030 | 3 | HG02630.hp1 HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.294+294T>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 3/38 | chr15 | 92924846 | ||||||
| chr15:92924854
|
G | A | 2 | a0001c0002t0011g0256a0001c0002t0011g0257 | 2 | NA19000.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.294+302G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 3/38 | chr15 | 92924854 | ||||||
| chr15:92924863
|
C | T | 1 | a0001c0001t0001g0087 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.294+311C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 3/38 | chr15 | 92924863 | ||||||
| chr15:92924913
|
G | T | 2 | a0001c0001t0001g0213a0001c0001t0001g0214 | 2 | HG00438.hp2 HG02040.hp2 |
intron_variant | MODIFIER | c.294+361G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 3/38 | chr15 | 92924913 | ||||||
| chr15:92925045
|
C | G | 1 | a0001c0002t0001g0241 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.294+493C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 3/38 | chr15 | 92925045 | ||||||
| chr15:92925046
|
C | G | 199 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(196): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.294+494C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 3/38 | chr15 | 92925046 | ||||||
| chr15:92925297
|
C | T | 2 | a0001c0002t0005g0220a0001c0003t0002g0221 | 2 | HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.294+745C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 3/38 | chr15 | 92925297 | ||||||
| chr15:92925320
|
A | G | 42 | a0001c0001t0001g0016a0001c0002t0001g0233a0001c0002t0001g0234others(39): Show | 42 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.294+768A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 3/38 | chr15 | 92925320 | ||||||
| chr15:92925491
|
T | C | 1 | a0001c0001t0001g0035 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.294+939T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 3/38 | chr15 | 92925491 | ||||||
| chr15:92925539
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.294+987C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 3/38 | chr15 | 92925539 | ||||||
| chr15:92925645
|
G | A | 1 | a0001c0013t0019g0168 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.294+1093G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 3/38 | chr15 | 92925645 | ||||||
| chr15:92925838
|
T | C | 13 | a0001c0001t0001g0259a0001c0001t0006g0248a0001c0001t0006g0260others(10): Show | 13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.294+1286T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 3/38 | chr15 | 92925838 | ||||||
| chr15:92925965
|
T | C | 1 | a0001c0001t0001g0098 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.295-1279T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 3/38 | chr15 | 92925965 | ||||||
| chr15:92926119
|
G | A | 4 | a0001c0001t0001g0141a0001c0003t0001g0142a0001c0003t0003g0128others(1): Show | 4 | HG01346.hp2 HG02683.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.295-1125G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 3/38 | chr15 | 92926119 | ||||||
| chr15:92926209
|
G | A | 1 | a0001c0001t0001g0060 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.295-1035G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 3/38 | chr15 | 92926209 | ||||||
| chr15:92926212
|
A | T | 1 | a0001c0001t0001g0200 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.295-1032A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 3/38 | chr15 | 92926212 | ||||||
| chr15:92926258
|
C | T | 1 | a0001c0002t0001g0091 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.295-986C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 3/38 | chr15 | 92926258 | ||||||
| chr15:92926304
|
T | G | 2 | a0001c0001t0001g0049a0001c0001t0001g0184 | 2 | HG01167.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.295-940T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 3/38 | chr15 | 92926304 | ||||||
| chr15:92926366
|
T | C | 1 | a0001c0002t0002g0232 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.295-878T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 3/38 | chr15 | 92926366 | ||||||
| chr15:92926630
|
A | G | 13 | a0001c0001t0001g0259a0001c0001t0006g0248a0001c0001t0006g0260others(10): Show | 13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.295-614A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 3/38 | chr15 | 92926630 | ||||||
| chr15:92926702
|
G | T | 41 | a0001c0002t0001g0233a0001c0002t0001g0234a0001c0002t0001g0235others(38): Show | 41 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.295-542G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 3/38 | chr15 | 92926702 | ||||||
| chr15:92926766
|
G | A | 13 | a0001c0001t0001g0259a0001c0001t0006g0248a0001c0001t0006g0260others(10): Show | 13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.295-478G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 3/38 | chr15 | 92926766 | ||||||
| chr15:92926871
|
G | A | 2 | a0001c0001t0003g0274a0001c0001t0005g0179 | 2 | NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.295-373G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 3/38 | chr15 | 92926871 | ||||||
| chr15:92926987
|
G | GTATGTT | 267 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(264): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.295-254_295-253ins others(6): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr15 | 92926987 | |||||
| chr15:92927090
|
A | T | 15 | a0001c0001t0001g0259a0001c0001t0006g0248a0001c0001t0006g0260others(12): Show | 15 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.295-154A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 3/38 | chr15 | 92927090 | ||||||
| chr15:92927149
|
T | C | 1 | a0001c0001t0001g0061 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.295-95T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 3/38 | chr15 | 92927149 | ||||||
| chr15:92927762
|
T | C | 1 | a0001c0001t0022g0097 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.381+432T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 4/38 | chr15 | 92927762 | ||||||
| chr15:92927830
|
A | T | 1 | a0001c0001t0001g0114 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.381+500A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 4/38 | chr15 | 92927830 | ||||||
| chr15:92927841
|
C | T | 4 | a0001c0001t0001g0200a0001c0001t0008g0217a0001c0001t0008g0218others(1): Show | 4 | HG03239.hp2 HG03688.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.381+511C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 4/38 | chr15 | 92927841 | ||||||
| chr15:92927905
|
A | G | 1 | a0001c0001t0001g0201 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.381+575A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 4/38 | chr15 | 92927905 | ||||||
| chr15:92927986
|
G | A | 2 | a0001c0001t0001g0102a0001c0001t0001g0103 | 2 | HG01258.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.381+656G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 4/38 | chr15 | 92927986 | ||||||
| chr15:92928200
|
T | C | 13 | a0001c0001t0001g0259a0001c0001t0006g0248a0001c0001t0006g0260others(10): Show | 13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.382-830T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 4/38 | chr15 | 92928200 | ||||||
| chr15:92928233
|
C | G | 14 | a0001c0001t0001g0006a0001c0001t0001g0035a0001c0001t0001g0036others(11): Show | 15 | HG01069.hp1 HG01123.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.382-797C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 4/38 | chr15 | 92928233 | ||||||
| chr15:92928496
|
C | CATTT | 152 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(149): Show | 156 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.382-534_382-533ins others(4): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 4/38 | chr15 | 92928496 | ||||||
| chr15:92928691
|
C | T | 15 | a0001c0001t0001g0006a0001c0001t0001g0035a0001c0001t0001g0036others(12): Show | 16 | HG01069.hp1 HG01123.hp2 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.382-339C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 4/38 | chr15 | 92928691 | ||||||
| chr15:92928726
|
T | C | 18 | a0001c0001t0001g0281a0001c0001t0001g0298a0001c0001t0001g0299others(15): Show | 18 | HG00544.hp1 HG00735.hp1 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.382-304T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 4/38 | chr15 | 92928726 | ||||||
| chr15:92929219
|
T | G | 1 | a0001c0001t0001g0062 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.443+128T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92929219 | ||||||
| chr15:92929260
|
A | G | 1 | a0001c0010t0002g0222 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.443+169A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92929260 | ||||||
| chr15:92929308
|
G | A | 5 | a0001c0002t0002g0156a0001c0002t0002g0181a0001c0002t0002g0223others(2): Show | 5 | HG02572.hp2 HG02976.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.443+217G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92929308 | ||||||
| chr15:92929332
|
T | G | 1 | a0001c0001t0001g0016 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.443+241T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92929332 | ||||||
| chr15:92929352
|
C | T | 12 | a0001c0002t0001g0234a0001c0002t0008g0012a0001c0002t0008g0015others(9): Show | 12 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.443+261C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92929352 | ||||||
| chr15:92929398
|
T | A | 1 | a0001c0001t0001g0063 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.443+307T>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92929398 | ||||||
| chr15:92929416
|
G | C | 3 | a0001c0002t0002g0045a0001c0002t0002g0046a0001c0002t0002g0232 | 3 | HG03453.hp2 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.443+325G>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92929416 | ||||||
| chr15:92929459
|
A | G | 13 | a0001c0001t0001g0259a0001c0001t0006g0248a0001c0001t0006g0260others(10): Show | 13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.443+368A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92929459 | ||||||
| chr15:92929656
|
A | AT | 13 | a0001c0001t0001g0259a0001c0001t0006g0248a0001c0001t0006g0260others(10): Show | 13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.443+568dupT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | INFO_REALIGN_3_PRIME | chr15 | 92929656 | |||||
| chr15:92929733
|
A | G | 5 | a0001c0004t0010g0105a0001c0004t0010g0106a0001c0004t0010g0107others(2): Show | 5 | NA18612.hp2 NA18952.hp1 NA19083.hp1 others(2): Show |
intron_variant | MODIFIER | c.443+642A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92929733 | ||||||
| chr15:92929750
|
T | C | 14 | a0001c0001t0001g0006a0001c0001t0001g0035a0001c0001t0001g0036others(11): Show | 15 | HG01069.hp1 HG01123.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.443+659T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92929750 | ||||||
| chr15:92929866
|
T | C | 1 | a0001c0010t0002g0222 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.443+775T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92929866 | ||||||
| chr15:92930004
|
T | A | 3 | a0001c0002t0002g0045a0001c0002t0002g0046a0001c0002t0002g0232 | 3 | HG03453.hp2 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.443+913T>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92930004 | ||||||
| chr15:92930006
|
A | T | 3 | a0001c0002t0002g0045a0001c0002t0002g0046a0001c0002t0002g0232 | 3 | HG03453.hp2 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.443+915A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92930006 | ||||||
| chr15:92930021
|
A | AAAGTC | 208 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(205): Show | 212 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.443+934_443+935ins others(5): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | INFO_REALIGN_3_PRIME | chr15 | 92930021 | |||||
| chr15:92930023
|
A | AGTCAG | 3 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0300 | 3 | HG02258.hp2 HG02965.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.443+934_443+935ins others(5): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | INFO_REALIGN_3_PRIME | chr15 | 92930023 | |||||
| chr15:92930220
|
T | G | 1 | a0001c0001t0001g0061 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.443+1129T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92930220 | ||||||
| chr15:92930264
|
G | A | 2 | a0001c0005t0004g0153a0001c0005t0004g0154 | 2 | NA20752.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.443+1173G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92930264 | ||||||
| chr15:92930364
|
C | T | 18 | a0001c0001t0007g0174a0001c0003t0002g0162a0001c0003t0002g0169others(15): Show | 18 | HG01070.hp1 HG01109.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.443+1273C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92930364 | ||||||
| chr15:92930394
|
C | T | 209 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(206): Show | 213 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.443+1303C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92930394 | ||||||
| chr15:92930417
|
T | C | 3 | a0001c0003t0003g0167a0001c0003t0003g0171a0001c0003t0003g0290 | 3 | HG01109.hp2 HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.443+1326T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92930417 | ||||||
| chr15:92930513
|
G | A | 1 | a0001c0016t0002g0047 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.443+1422G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92930513 | ||||||
| chr15:92930522
|
T | C | 212 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(209): Show | 216 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.443+1431T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92930522 | ||||||
| chr15:92930655
|
C | G | 4 | a0001c0009t0002g0043a0001c0009t0002g0048a0001c0009t0012g0044others(1): Show | 4 | HG00642.hp1 HG00673.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.443+1564C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92930655 | ||||||
| chr15:92930947
|
C | A | 41 | a0001c0002t0001g0233a0001c0002t0001g0234a0001c0002t0001g0235others(38): Show | 41 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.443+1856C>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92930947 | ||||||
| chr15:92931268
|
A | C | 1 | a0001c0001t0001g0086 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.443+2177A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92931268 | ||||||
| chr15:92931421
|
C | G | 1 | a0001c0002t0001g0237 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.443+2330C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92931421 | ||||||
| chr15:92931650
|
G | A | 1 | a0001c0001t0001g0064 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.443+2559G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92931650 | ||||||
| chr15:92931863
|
C | CT | 76 | a0001c0001t0001g0016a0001c0001t0007g0174a0001c0002t0001g0233others(73): Show | 76 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.443+2790dupT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | INFO_REALIGN_3_PRIME | chr15 | 92931863 | |||||
| chr15:92931887
|
G | A | 2 | a0001c0002t0001g0242a0001c0002t0001g0255 | 2 | NA18959.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.443+2796G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92931887 | ||||||
| chr15:92931903
|
G | A | 1 | a0001c0003t0001g0129 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.443+2812G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92931903 | ||||||
| chr15:92931927
|
A | G | 14 | a0001c0001t0001g0006a0001c0001t0001g0035a0001c0001t0001g0036others(11): Show | 15 | HG01069.hp1 HG01123.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.443+2836A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92931927 | ||||||
| chr15:92931939
|
T | C | 1 | a0001c0010t0002g0222 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.443+2848T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92931939 | ||||||
| chr15:92932008
|
G | A | 6 | a0001c0002t0003g0228a0001c0002t0005g0220a0001c0002t0005g0227others(3): Show | 6 | HG01884.hp2 HG02257.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.443+2917G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92932008 | ||||||
| chr15:92932011
|
C | T | 1 | a0001c0005t0004g0159 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.443+2920C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92932011 | ||||||
| chr15:92932289
|
C | CT | 50 | a0001c0001t0001g0016a0001c0002t0001g0233a0001c0002t0001g0234others(47): Show | 50 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.443+3213dupT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | INFO_REALIGN_3_PRIME | chr15 | 92932289 | |||||
| chr15:92932324
|
G | A | 1 | a0001c0003t0014g0165 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.443+3233G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92932324 | ||||||
| chr15:92932328
|
G | A | 247 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(244): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.443+3237G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92932328 | ||||||
| chr15:92932400
|
G | A | 12 | a0001c0001t0001g0281a0001c0001t0002g0278a0001c0001t0002g0293others(9): Show | 12 | HG00544.hp1 HG00735.hp1 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.443+3309G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92932400 | ||||||
| chr15:92932418
|
A | G | 1 | a0001c0003t0003g0149 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.443+3327A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92932418 | ||||||
| chr15:92932443
|
TC | T | 298 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(295): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.443+3359delC | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | INFO_REALIGN_3_PRIME | chr15 | 92932443 | |||||
| chr15:92932728
|
G | A | 1 | a0001c0002t0002g0156 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.443+3637G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92932728 | ||||||
| chr15:92932760
|
T | G | 18 | a0001c0001t0001g0281a0001c0001t0001g0298a0001c0001t0001g0299others(15): Show | 18 | HG00544.hp1 HG00735.hp1 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.443+3669T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92932760 | ||||||
| chr15:92932835
|
G | GCAACCTC others(8): Show |
249 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(246): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.443+3744_443+3745i others(17): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92932835 | ||||||
| chr15:92932836
|
T | C | 1 | a0001c0001t0001g0117 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.443+3745T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92932836 | ||||||
| chr15:92932836
|
T | G | 249 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(246): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.443+3745T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92932836 | ||||||
| chr15:92932837
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.443+3746G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92932837 | ||||||
| chr15:92932838
|
A | ACCTCCGC others(3): Show |
1 | a0001c0001t0001g0117 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.443+3748_443+3749i others(12): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | INFO_REALIGN_3_PRIME | chr15 | 92932838 | |||||
| chr15:92932841
|
C | G | 1 | a0001c0001t0001g0117 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.443+3750C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92932841 | ||||||
| chr15:92932842
|
A | G | 1 | a0001c0001t0001g0117 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.443+3751A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92932842 | ||||||
| chr15:92932971
|
G | T | 1 | a0001c0002t0001g0286 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.443+3880G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92932971 | ||||||
| chr15:92932996
|
G | A | 1 | a0001c0002t0001g0247 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.443+3905G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92932996 | ||||||
| chr15:92933039
|
GC | G | 282 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(279): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.443+3952delC | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | INFO_REALIGN_3_PRIME | chr15 | 92933039 | |||||
| chr15:92933042
|
CCT | C | 3 | a0001c0001t0001g0026a0001c0001t0001g0099a0001c0001t0001g0186 | 3 | HG00423.hp1 HG01515.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.443+3952_443+3953d others(4): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92933042 | ||||||
| chr15:92933043
|
C | T | 13 | a0001c0001t0001g0062a0001c0001t0001g0281a0001c0002t0001g0286others(10): Show | 13 | HG00642.hp1 HG00673.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.443+3952C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92933043 | ||||||
| chr15:92933070
|
A | G | 13 | a0001c0001t0001g0259a0001c0001t0006g0248a0001c0001t0006g0260others(10): Show | 13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.443+3979A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92933070 | ||||||
| chr15:92933120
|
A | C | 174 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(171): Show | 178 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.443+4029A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92933120 | ||||||
| chr15:92933548
|
A | T | 1 | a0001c0002t0005g0230 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.444-3970A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92933548 | ||||||
| chr15:92933751
|
G | A | 3 | a0001c0002t0002g0223a0001c0002t0005g0224a0001c0002t0005g0225 | 3 | HG02572.hp2 HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.444-3767G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92933751 | ||||||
| chr15:92934017
|
G | A | 13 | a0001c0001t0001g0281a0001c0001t0002g0278a0001c0001t0002g0293others(10): Show | 13 | HG00544.hp1 HG00735.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.444-3501G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92934017 | ||||||
| chr15:92934073
|
TC | T | 13 | a0001c0001t0001g0259a0001c0001t0006g0248a0001c0001t0006g0260others(10): Show | 13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.444-3443delC | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | INFO_REALIGN_3_PRIME | chr15 | 92934073 | |||||
| chr15:92934184
|
T | C | 1 | a0001c0003t0002g0162 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.444-3334T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92934184 | ||||||
| chr15:92934424
|
AGG | A | 172 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(169): Show | 176 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.444-3089_444-3088d others(4): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | INFO_REALIGN_3_PRIME | chr15 | 92934424 | |||||
| chr15:92934505
|
C | G | 1 | a0001c0001t0001g0210 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.444-3013C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92934505 | ||||||
| chr15:92934595
|
T | C | 13 | a0001c0001t0001g0259a0001c0001t0006g0248a0001c0001t0006g0260others(10): Show | 13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.444-2923T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92934595 | ||||||
| chr15:92934745
|
C | T | 3 | a0001c0003t0012g0126a0001c0003t0012g0133a0001c0003t0012g0134 | 3 | HG01257.hp1 HG01258.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.444-2773C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92934745 | ||||||
| chr15:92935015
|
G | GT | 5 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0300others(2): Show | 6 | HG01243.hp1 HG02258.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.444-2493dupT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | INFO_REALIGN_3_PRIME | chr15 | 92935015 | |||||
| chr15:92935038
|
C | CT | 63 | a0001c0001t0001g0016a0001c0001t0001g0033a0001c0001t0001g0199others(60): Show | 63 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.444-2466dupT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | INFO_REALIGN_3_PRIME | chr15 | 92935038 | |||||
| chr15:92935176
|
C | T | 14 | a0001c0001t0001g0259a0001c0001t0006g0248a0001c0001t0006g0260others(11): Show | 14 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.444-2342C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92935176 | ||||||
| chr15:92935196
|
T | C | 24 | a0001c0001t0001g0259a0001c0001t0006g0248a0001c0001t0006g0260others(21): Show | 24 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.444-2322T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92935196 | ||||||
| chr15:92935224
|
T | G | 1 | a0001c0003t0001g0135 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.444-2294T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92935224 | ||||||
| chr15:92935257
|
C | G | 7 | a0001c0002t0002g0231a0001c0002t0003g0228a0001c0002t0005g0220others(4): Show | 7 | HG01884.hp2 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.444-2261C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92935257 | ||||||
| chr15:92935282
|
C | T | 1 | a0001c0010t0002g0182 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.444-2236C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92935282 | ||||||
| chr15:92935287
|
C | T | 1 | a0001c0001t0001g0116 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.444-2231C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92935287 | ||||||
| chr15:92935331
|
C | T | 1 | a0001c0002t0001g0233 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.444-2187C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92935331 | ||||||
| chr15:92935333
|
A | G | 240 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(237): Show | 245 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.444-2185A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92935333 | ||||||
| chr15:92935386
|
A | C | 1 | a0001c0001t0002g0085 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.444-2132A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92935386 | ||||||
| chr15:92935932
|
A | AT | 6 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(3): Show | 6 | HG01175.hp1 HG02083.hp1 HG02083.hp2 others(3): Show |
intron_variant | MODIFIER | c.444-1573dupT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | INFO_REALIGN_3_PRIME | chr15 | 92935932 | |||||
| chr15:92935982
|
G | A | 1 | a0001c0004t0010g0106 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.444-1536G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92935982 | ||||||
| chr15:92936061
|
C | T | 173 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(170): Show | 177 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.444-1457C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92936061 | ||||||
| chr15:92936110
|
C | A | 1 | a0001c0001t0007g0174 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.444-1408C>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92936110 | ||||||
| chr15:92936115
|
G | A | 1 | a0001c0002t0001g0246 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.444-1403G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92936115 | ||||||
| chr15:92936147
|
A | G | 7 | a0001c0002t0002g0231a0001c0002t0003g0228a0001c0002t0005g0220others(4): Show | 7 | HG01884.hp2 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.444-1371A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92936147 | ||||||
| chr15:92936211
|
C | G | 174 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(171): Show | 178 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.444-1307C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92936211 | ||||||
| chr15:92936230
|
A | G | 1 | a0001c0007t0003g0157 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.444-1288A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92936230 | ||||||
| chr15:92936282
|
C | T | 3 | a0001c0002t0008g0015a0001c0004t0007g0020a0001c0004t0017g0019 | 3 | HG01070.hp2 HG01123.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.444-1236C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92936282 | ||||||
| chr15:92936406
|
A | G | 161 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(158): Show | 165 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.444-1112A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92936406 | ||||||
| chr15:92936432
|
C | T | 1 | a0001c0002t0001g0234 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.444-1086C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92936432 | ||||||
| chr15:92936568
|
T | C | 175 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(172): Show | 179 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.444-950T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92936568 | ||||||
| chr15:92936702
|
G | T | 1 | a0001c0001t0006g0267 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.444-816G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92936702 | ||||||
| chr15:92936725
|
G | A | 1 | a0001c0009t0002g0048 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.444-793G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92936725 | ||||||
| chr15:92936824
|
A | C | 1 | a0001c0001t0008g0040 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.444-694A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92936824 | ||||||
| chr15:92936890
|
C | T | 1 | a0001c0002t0001g0233 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.444-628C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92936890 | ||||||
| chr15:92936975
|
C | T | 1 | a0001c0001t0001g0210 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.444-543C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92936975 | ||||||
| chr15:92937139
|
A | G | 1 | a0001c0002t0002g0156 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.444-379A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92937139 | ||||||
| chr15:92937168
|
A | G | 1 | a0001c0003t0003g0003 | 2 | HG01243.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.444-350A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92937168 | ||||||
| chr15:92937233
|
G | A | 5 | a0001c0001t0001g0006a0001c0001t0001g0271a0001c0001t0001g0272others(2): Show | 6 | HG01069.hp1 HG01123.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.444-285G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92937233 | ||||||
| chr15:92937275
|
G | GA | 175 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(172): Show | 179 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.444-237dupA | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | INFO_REALIGN_3_PRIME | chr15 | 92937275 | |||||
| chr15:92937365
|
T | C | 1 | a0001c0004t0007g0014 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.444-153T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92937365 | ||||||
| chr15:92937638
|
C | T | 1 | a0001c0001t0001g0054 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.551+13C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 6/38 | chr15 | 92937638 | ||||||
| chr15:92937777
|
A | G | 18 | a0001c0001t0001g0281a0001c0001t0001g0298a0001c0001t0001g0299others(15): Show | 18 | HG00544.hp1 HG00735.hp1 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.551+152A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 6/38 | chr15 | 92937777 | ||||||
| chr15:92937806
|
G | A | 4 | a0001c0001t0001g0026a0001c0001t0003g0001a0001c0011t0001g0023others(1): Show | 5 | HG00639.hp2 HG00738.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.551+181G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 6/38 | chr15 | 92937806 | ||||||
| chr15:92937817
|
A | G | 1 | a0001c0001t0001g0114 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.551+192A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 6/38 | chr15 | 92937817 | ||||||
| chr15:92938116
|
A | T | 132 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(129): Show | 135 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.551+491A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 6/38 | chr15 | 92938116 | ||||||
| chr15:92938226
|
A | G | 1 | a0001c0010t0002g0182 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.551+601A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 6/38 | chr15 | 92938226 | ||||||
| chr15:92938310
|
A | G | 6 | a0001c0002t0002g0045a0001c0002t0002g0046a0001c0002t0002g0223others(3): Show | 6 | HG02572.hp2 HG03209.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.551+685A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 6/38 | chr15 | 92938310 | ||||||
| chr15:92938441
|
C | T | 42 | a0001c0001t0001g0016a0001c0002t0001g0233a0001c0002t0001g0234others(39): Show | 42 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.551+816C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 6/38 | chr15 | 92938441 | ||||||
| chr15:92938666
|
G | T | 1 | a0001c0004t0010g0245 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.552-912G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 6/38 | chr15 | 92938666 | ||||||
| chr15:92938770
|
T | G | 25 | a0001c0001t0001g0281a0001c0001t0001g0298a0001c0001t0001g0299others(22): Show | 26 | HG00544.hp1 HG00735.hp1 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.552-808T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 6/38 | chr15 | 92938770 | ||||||
| chr15:92938996
|
C | G | 14 | a0001c0001t0001g0259a0001c0001t0006g0248a0001c0001t0006g0260others(11): Show | 14 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.552-582C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 6/38 | chr15 | 92938996 | ||||||
| chr15:92939047
|
C | CT | 153 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(150): Show | 156 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.552-520dupT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr15 | 92939047 | |||||
| chr15:92939047
|
C | CTT | 6 | a0001c0001t0001g0042a0001c0001t0001g0098a0001c0001t0001g0099others(3): Show | 6 | HG01346.hp1 HG01361.hp2 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.552-521_552-520dup others(2): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr15 | 92939047 | |||||
| chr15:92939047
|
CT | C | 14 | a0001c0001t0001g0006a0001c0001t0001g0035a0001c0001t0001g0036others(11): Show | 15 | HG01069.hp1 HG01123.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.552-520delT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr15 | 92939047 | |||||
| chr15:92939337
|
C | T | 1 | a0001c0015t0005g0288 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.552-241C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 6/38 | chr15 | 92939337 | ||||||
| chr15:92939386
|
C | T | 5 | a0001c0003t0002g0221a0001c0009t0002g0043a0001c0009t0002g0048others(2): Show | 5 | HG00642.hp1 HG00673.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.552-192C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 6/38 | chr15 | 92939386 | ||||||
| chr15:92939426
|
G | A | 161 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(158): Show | 165 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.552-152G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 6/38 | chr15 | 92939426 | ||||||
| chr15:92939554
|
C | T | 3 | a0001c0002t0002g0045a0001c0002t0002g0046a0001c0002t0002g0232 | 3 | HG03453.hp2 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.552-24C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 6/38 | chr15 | 92939554 | ||||||
| chr15:92939834
|
C | G | 13 | a0001c0001t0001g0259a0001c0001t0006g0248a0001c0001t0006g0260others(10): Show | 13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.692+116C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92939834 | ||||||
| chr15:92939844
|
T | A | 13 | a0001c0001t0001g0259a0001c0001t0006g0248a0001c0001t0006g0260others(10): Show | 13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.692+126T>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92939844 | ||||||
| chr15:92939872
|
A | G | 13 | a0001c0001t0001g0259a0001c0001t0006g0248a0001c0001t0006g0260others(10): Show | 13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.692+154A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92939872 | ||||||
| chr15:92939879
|
G | A | 14 | a0001c0001t0001g0259a0001c0001t0006g0248a0001c0001t0006g0260others(11): Show | 14 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.692+161G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92939879 | ||||||
| chr15:92939946
|
A | T | 7 | a0001c0002t0002g0045a0001c0002t0002g0046a0001c0002t0002g0156others(4): Show | 7 | HG02572.hp2 HG02976.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.692+228A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92939946 | ||||||
| chr15:92940024
|
A | G | 1 | a0001c0009t0002g0048 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.692+306A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92940024 | ||||||
| chr15:92940082
|
G | A | 2 | a0001c0001t0001g0032a0001c0001t0001g0034 | 2 | NA18965.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.692+364G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92940082 | ||||||
| chr15:92940172
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.692+454G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92940172 | ||||||
| chr15:92940311
|
G | C | 1 | a0001c0002t0002g0046 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.692+593G>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92940311 | ||||||
| chr15:92940340
|
A | G | 4 | a0001c0003t0002g0162a0001c0003t0002g0169a0001c0003t0003g0170others(1): Show | 4 | HG02630.hp2 HG03041.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.692+622A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92940340 | ||||||
| chr15:92940407
|
A | G | 1 | a0001c0003t0005g0166 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.692+689A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92940407 | ||||||
| chr15:92940595
|
T | A | 1 | a0001c0002t0001g0250 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.692+877T>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92940595 | ||||||
| chr15:92940596
|
A | G | 1 | a0001c0002t0001g0250 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.692+878A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92940596 | ||||||
| chr15:92940597
|
T | A | 1 | a0001c0002t0001g0250 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.692+879T>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92940597 | ||||||
| chr15:92940601
|
A | G | 1 | a0001c0002t0001g0250 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.692+883A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92940601 | ||||||
| chr15:92940602
|
T | C | 1 | a0001c0002t0001g0250 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.692+884T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92940602 | ||||||
| chr15:92940605
|
A | G | 1 | a0001c0002t0001g0250 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.692+887A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92940605 | ||||||
| chr15:92940607
|
C | T | 1 | a0001c0002t0001g0250 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.692+889C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92940607 | ||||||
| chr15:92940772
|
TA | T | 6 | a0001c0003t0002g0221a0001c0009t0002g0043a0001c0009t0002g0048others(3): Show | 6 | HG00642.hp1 HG00673.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.693-1044delA | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr15 | 92940772 | |||||
| chr15:92940775
|
AAAATATA others(10): Show |
A | 4 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0011others(1): Show | 4 | NA18963.hp2 NA18967.hp2 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.693-1039_693-1023d others(19): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr15 | 92940775 | |||||
| chr15:92940784
|
AAAATATA others(1): Show |
A | 10 | a0001c0001t0001g0006a0001c0001t0001g0035a0001c0001t0001g0036others(7): Show | 11 | HG01069.hp1 HG01123.hp2 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.693-1024_693-1017d others(10): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr15 | 92940784 | |||||
| chr15:92940823
|
ATAT | A | 13 | a0001c0001t0001g0259a0001c0001t0006g0248a0001c0001t0006g0260others(10): Show | 13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.693-995_693-993del others(3): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr15 | 92940823 | |||||
| chr15:92940839
|
A | T | 2 | a0001c0002t0003g0228a0001c0002t0005g0229 | 2 | HG01884.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.693-983A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92940839 | ||||||
| chr15:92940843
|
TATATATA others(1): Show |
T | 45 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0054others(42): Show | 47 | HG00140.hp2 HG00423.hp1 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.693-961_693-954del others(8): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr15 | 92940843 | |||||
| chr15:92940846
|
A | G | 2 | a0001c0003t0012g0126a0001c0003t0012g0134 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.693-976A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92940846 | ||||||
| chr15:92940851
|
A | T | 1 | a0001c0001t0001g0214 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.693-971A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92940851 | ||||||
| chr15:92940876
|
A | G | 52 | a0001c0001t0001g0016a0001c0002t0001g0233a0001c0002t0001g0234others(49): Show | 52 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.693-946A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92940876 | ||||||
| chr15:92940889
|
TA | T | 147 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(144): Show | 151 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.693-928delA | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr15 | 92940889 | |||||
| chr15:92940895
|
T | A | 13 | a0001c0001t0001g0259a0001c0001t0006g0248a0001c0001t0006g0260others(10): Show | 13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.693-927T>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92940895 | ||||||
| chr15:92940903
|
AAT | A | 8 | a0001c0001t0001g0141a0001c0003t0001g0142a0001c0003t0001g0144others(5): Show | 8 | HG01346.hp2 HG01952.hp2 HG02683.hp1 others(5): Show |
intron_variant | MODIFIER | c.693-909_693-908del others(2): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr15 | 92940903 | |||||
| chr15:92940913
|
T | TAA | 191 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(188): Show | 196 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.693-907_693-906dup others(2): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr15 | 92940913 | |||||
| chr15:92940913
|
T | TATAA | 3 | a0001c0002t0002g0045a0001c0002t0002g0046a0001c0002t0002g0232 | 3 | HG03453.hp2 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.693-908_693-907ins others(4): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr15 | 92940913 | |||||
| chr15:92940921
|
CATATAAA others(20): Show |
C | 1 | a0001c0002t0002g0181 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.693-883_693-857del others(27): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr15 | 92940921 | |||||
| chr15:92940938
|
A | T | 13 | a0001c0001t0001g0259a0001c0001t0006g0248a0001c0001t0006g0260others(10): Show | 13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.693-884A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92940938 | ||||||
| chr15:92940940
|
T | A | 9 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0038others(6): Show | 9 | HG01192.hp1 HG01433.hp1 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.693-882T>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92940940 | ||||||
| chr15:92940940
|
TATATATA others(7): Show |
T | 1 | a0001c0010t0002g0182 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.693-874_693-861del others(14): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr15 | 92940940 | |||||
| chr15:92940946
|
TAA | T | 3 | a0001c0002t0002g0045a0001c0002t0002g0046a0001c0002t0002g0232 | 3 | HG03453.hp2 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.693-874_693-873del others(2): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr15 | 92940946 | |||||
| chr15:92940954
|
AATATATA others(23): Show |
A | 1 | a0001c0001t0002g0085 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.693-852_693-823del others(30): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr15 | 92940954 | |||||
| chr15:92940958
|
TATATAAA others(5): Show |
T | 181 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(178): Show | 186 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.693-846_693-835del others(12): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr15 | 92940958 | |||||
| chr15:92940960
|
T | A | 1 | a0001c0002t0002g0181 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.693-862T>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92940960 | ||||||
| chr15:92940964
|
A | T | 1 | a0001c0002t0002g0181 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.693-858A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92940964 | ||||||
| chr15:92940966
|
T | TATTTA | 3 | a0001c0002t0002g0045a0001c0002t0002g0046a0001c0002t0002g0232 | 3 | HG03453.hp2 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.693-854_693-853ins others(5): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr15 | 92940966 | |||||
| chr15:92940970
|
A | T | 3 | a0001c0002t0002g0045a0001c0002t0002g0046a0001c0002t0002g0232 | 3 | HG03453.hp2 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.693-852A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92940970 | ||||||
| chr15:92940976
|
A | T | 8 | a0001c0001t0001g0100a0001c0002t0002g0231a0001c0002t0003g0228others(5): Show | 8 | HG01884.hp2 HG01928.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.693-846A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92940976 | ||||||
| chr15:92940986
|
TATATATA others(1): Show |
T | 7 | a0001c0002t0002g0231a0001c0002t0003g0228a0001c0002t0005g0220others(4): Show | 7 | HG01884.hp2 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.693-828_693-821del others(8): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr15 | 92940986 | |||||
| chr15:92940992
|
T | A | 2 | a0001c0002t0001g0250a0001c0002t0002g0156 | 2 | HG02976.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.693-830T>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92940992 | ||||||
| chr15:92940994
|
A | T | 1 | a0001c0001t0001g0100 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.693-828A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92940994 | ||||||
| chr15:92940995
|
A | T | 1 | a0001c0002t0001g0250 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.693-827A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92940995 | ||||||
| chr15:92941006
|
T | A | 8 | a0001c0002t0001g0250a0001c0002t0002g0231a0001c0002t0003g0228others(5): Show | 8 | HG01884.hp2 HG02257.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.693-816T>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92941006 | ||||||
| chr15:92941007
|
A | T | 8 | a0001c0002t0001g0250a0001c0002t0002g0231a0001c0002t0003g0228others(5): Show | 8 | HG01884.hp2 HG02257.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.693-815A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92941007 | ||||||
| chr15:92941008
|
A | AT | 185 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(182): Show | 190 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.693-803dupT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr15 | 92941008 | |||||
| chr15:92941008
|
A | T | 8 | a0001c0001t0001g0100a0001c0002t0002g0231a0001c0002t0003g0228others(5): Show | 8 | HG01884.hp2 HG01928.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.693-814A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92941008 | ||||||
| chr15:92941181
|
C | A | 194 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(191): Show | 199 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.693-641C>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92941181 | ||||||
| chr15:92941186
|
C | T | 1 | a0001c0002t0002g0156 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.693-636C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92941186 | ||||||
| chr15:92941281
|
C | T | 44 | a0001c0001t0001g0016a0001c0002t0001g0233a0001c0002t0001g0234others(41): Show | 44 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.693-541C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92941281 | ||||||
| chr15:92941460
|
T | C | 52 | a0001c0001t0001g0016a0001c0002t0001g0233a0001c0002t0001g0234others(49): Show | 52 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.693-362T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92941460 | ||||||
| chr15:92941609
|
A | T | 1 | a0001c0001t0001g0058 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.693-213A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92941609 | ||||||
| chr15:92941655
|
T | G | 1 | a0001c0007t0003g0157 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.693-167T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92941655 | ||||||
| chr15:92941697
|
G | T | 1 | a0001c0001t0001g0086 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.693-125G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92941697 | ||||||
| chr15:92941802
|
C | T | 13 | a0001c0001t0001g0259a0001c0001t0006g0248a0001c0001t0006g0260others(10): Show | 13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.693-20C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92941802 | ||||||
| chr15:92942070
|
T | C | 2 | a0001c0001t0001g0093a0001c0001t0001g0094 | 2 | HG00673.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.826+115T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 8/38 | chr15 | 92942070 | ||||||
| chr15:92942111
|
A | G | 1 | a0001c0001t0020g0113 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.826+156A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 8/38 | chr15 | 92942111 | ||||||
| chr15:92942226
|
C | G | 44 | a0001c0001t0001g0016a0001c0002t0001g0233a0001c0002t0001g0234others(41): Show | 44 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.826+271C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 8/38 | chr15 | 92942226 | ||||||
| chr15:92942405
|
CT | C | 15 | a0001c0001t0001g0006a0001c0001t0001g0035a0001c0001t0001g0036others(12): Show | 16 | HG01069.hp1 HG01123.hp2 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.827-424delT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 8/38 | INFO_REALIGN_3_PRIME | chr15 | 92942405 | |||||
| chr15:92942411
|
T | C | 1 | a0001c0001t0007g0174 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.827-432T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 8/38 | chr15 | 92942411 | ||||||
| chr15:92942471
|
C | T | 1 | a0001c0003t0003g0139 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.827-372C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 8/38 | chr15 | 92942471 | ||||||
| chr15:92942648
|
T | TG | 194 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(191): Show | 199 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.827-193dupG | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 8/38 | INFO_REALIGN_3_PRIME | chr15 | 92942648 | |||||
| chr15:92942697
|
G | C | 7 | a0001c0002t0002g0045a0001c0002t0002g0046a0001c0002t0002g0156others(4): Show | 7 | HG02572.hp2 HG02976.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.827-146G>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 8/38 | chr15 | 92942697 | ||||||
| chr15:92943159
|
G | A | 1 | a0001c0006t0004g0004 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1052+91G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 9/38 | chr15 | 92943159 | ||||||
| chr15:92943173
|
G | A | 1 | a0001c0004t0010g0107 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1052+105G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 9/38 | chr15 | 92943173 | ||||||
| chr15:92943323
|
T | C | 1 | a0001c0001t0001g0063 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1052+255T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 9/38 | chr15 | 92943323 | ||||||
| chr15:92943343
|
A | G | 1 | a0001c0001t0006g0084 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1052+275A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 9/38 | chr15 | 92943343 | ||||||
| chr15:92943391
|
A | G | 47 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0054others(44): Show | 49 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.1052+323A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 9/38 | chr15 | 92943391 | ||||||
| chr15:92943477
|
G | A | 13 | a0001c0001t0001g0259a0001c0001t0006g0248a0001c0001t0006g0260others(10): Show | 13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.1052+409G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 9/38 | chr15 | 92943477 | ||||||
| chr15:92943596
|
T | C | 1 | a0001c0002t0002g0181 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1052+528T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 9/38 | chr15 | 92943596 | ||||||
| chr15:92943673
|
G | A | 14 | a0001c0001t0001g0006a0001c0001t0001g0035a0001c0001t0001g0036others(11): Show | 15 | HG01069.hp1 HG01123.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.1052+605G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 9/38 | chr15 | 92943673 | ||||||
| chr15:92943905
|
G | A | 1 | a0001c0001t0001g0201 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1053-510G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 9/38 | chr15 | 92943905 | ||||||
| chr15:92944001
|
G | A | 1 | a0001c0001t0001g0187 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1053-414G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 9/38 | chr15 | 92944001 | ||||||
| chr15:92944115
|
C | T | 1 | a0001c0001t0007g0174 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1053-300C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 9/38 | chr15 | 92944115 | ||||||
| chr15:92944156
|
T | C | 1 | a0001c0001t0001g0067 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1053-259T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 9/38 | chr15 | 92944156 | ||||||
| chr15:92944231
|
AGT | A | 4 | a0001c0009t0002g0043a0001c0009t0002g0048a0001c0009t0012g0044others(1): Show | 4 | HG00642.hp1 HG00673.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.1053-181_1053-180d others(4): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 9/38 | INFO_REALIGN_3_PRIME | chr15 | 92944231 | |||||
| chr15:92944268
|
C | T | 2 | a0001c0001t0001g0051a0001c0001t0001g0087 | 2 | NA18973.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.1053-147C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 9/38 | chr15 | 92944268 | ||||||
| chr15:92944270
|
C | G | 1 | a0001c0015t0005g0288 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1053-145C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 9/38 | chr15 | 92944270 | ||||||
| chr15:92944624
|
G | C | 174 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(171): Show | 178 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.1153+109G>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 10/38 | chr15 | 92944624 | ||||||
| chr15:92944678
|
G | A | 13 | a0001c0001t0001g0259a0001c0001t0006g0248a0001c0001t0006g0260others(10): Show | 13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.1153+163G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 10/38 | chr15 | 92944678 | ||||||
| chr15:92944864
|
T | TAGTGAAG others(1): Show |
52 | a0001c0001t0001g0016a0001c0002t0001g0233a0001c0002t0001g0234others(49): Show | 52 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.1153+350_1153+357d others(10): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 10/38 | INFO_REALIGN_3_PRIME | chr15 | 92944864 | |||||
| chr15:92944884
|
G | A | 1 | a0001c0006t0004g0158 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1153+369G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 10/38 | chr15 | 92944884 | ||||||
| chr15:92944965
|
A | G | 8 | a0001c0001t0007g0174a0001c0002t0002g0045a0001c0002t0002g0046others(5): Show | 8 | HG02055.hp1 HG02572.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.1153+450A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 10/38 | chr15 | 92944965 | ||||||
| chr15:92945085
|
T | A | 160 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(157): Show | 164 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.1153+570T>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 10/38 | chr15 | 92945085 | ||||||
| chr15:92945174
|
C | T | 9 | a0001c0001t0001g0026a0001c0001t0001g0298a0001c0001t0001g0299others(6): Show | 10 | HG00639.hp2 HG00738.hp1 HG01515.hp2 others(7): Show |
intron_variant | MODIFIER | c.1154-647C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 10/38 | chr15 | 92945174 | ||||||
| chr15:92945302
|
T | C | 6 | a0001c0001t0001g0007a0001c0003t0002g0221a0001c0009t0002g0043others(3): Show | 6 | HG00642.hp1 HG00673.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1154-519T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 10/38 | chr15 | 92945302 | ||||||
| chr15:92945389
|
C | CT | 48 | a0001c0001t0001g0016a0001c0001t0001g0038a0001c0001t0001g0100others(45): Show | 48 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.1154-430dupT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 10/38 | INFO_REALIGN_3_PRIME | chr15 | 92945389 | |||||
| chr15:92945392
|
C | CTT | 11 | a0001c0001t0006g0248a0001c0001t0006g0260a0001c0001t0006g0261others(8): Show | 11 | HG00735.hp2 HG01099.hp2 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.1154-428_1154-427d others(4): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 10/38 | INFO_REALIGN_3_PRIME | chr15 | 92945392 | |||||
| chr15:92945392
|
C | T | 223 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(220): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.1154-429C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 10/38 | chr15 | 92945392 | ||||||
| chr15:92945395
|
C | T | 296 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(293): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.1154-426C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 10/38 | chr15 | 92945395 | ||||||
| chr15:92945696
|
AT | A | 10 | a0001c0001t0003g0274a0001c0001t0005g0179a0001c0002t0001g0242others(7): Show | 10 | HG01884.hp2 HG02257.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1154-113delT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 10/38 | INFO_REALIGN_3_PRIME | chr15 | 92945696 | |||||
| chr15:92945946
|
A | G | 2 | a0001c0001t0001g0112a0001c0001t0001g0118 | 2 | NA18939.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.1198+81A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 11/38 | chr15 | 92945946 | ||||||
| chr15:92946472
|
C | CTTTTA | 3 | a0001c0002t0002g0231a0001c0002t0005g0220a0001c0002t0005g0227 | 3 | HG02572.hp1 HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1377+274_1377+278d others(7): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 12/38 | INFO_REALIGN_3_PRIME | chr15 | 92946472 | |||||
| chr15:92946517
|
C | T | 13 | a0001c0001t0001g0016a0001c0002t0001g0234a0001c0002t0008g0012others(10): Show | 13 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.1377+301C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 12/38 | chr15 | 92946517 | ||||||
| chr15:92946805
|
A | G | 1 | a0001c0003t0003g0138 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1377+589A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 12/38 | chr15 | 92946805 | ||||||
| chr15:92946862
|
C | T | 3 | a0001c0002t0002g0045a0001c0002t0002g0046a0001c0002t0002g0232 | 3 | HG03453.hp2 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1377+646C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 12/38 | chr15 | 92946862 | ||||||
| chr15:92946926
|
G | A | 5 | a0001c0002t0002g0231a0001c0002t0005g0220a0001c0002t0005g0227others(2): Show | 5 | HG02257.hp2 HG02572.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1377+710G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 12/38 | chr15 | 92946926 | ||||||
| chr15:92946931
|
C | CT | 9 | a0001c0003t0003g0161a0001c0003t0003g0167a0001c0003t0003g0171others(6): Show | 9 | HG01109.hp2 HG01884.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.1377+716dupT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 12/38 | INFO_REALIGN_3_PRIME | chr15 | 92946931 | |||||
| chr15:92946932
|
T | TA | 91 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0027others(88): Show | 92 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.1377+731dupA | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 12/38 | INFO_REALIGN_3_PRIME | chr15 | 92946932 | |||||
| chr15:92946959
|
A | C | 146 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(143): Show | 150 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.1377+743A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 12/38 | chr15 | 92946959 | ||||||
| chr15:92947014
|
G | T | 1 | a0001c0002t0002g0156 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1377+798G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 12/38 | chr15 | 92947014 | ||||||
| chr15:92947403
|
A | G | 3 | a0001c0001t0001g0082a0001c0001t0001g0093a0001c0001t0001g0094 | 3 | HG00673.hp1 HG02155.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.1377+1187A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 12/38 | chr15 | 92947403 | ||||||
| chr15:92947426
|
G | C | 131 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0026others(128): Show | 134 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.1377+1210G>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 12/38 | chr15 | 92947426 | ||||||
| chr15:92947526
|
C | T | 5 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0038others(2): Show | 5 | HG01192.hp1 HG01433.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.1377+1310C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 12/38 | chr15 | 92947526 | ||||||
| chr15:92947588
|
G | A | 1 | a0001c0002t0002g0156 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1378-1364G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 12/38 | chr15 | 92947588 | ||||||
| chr15:92947661
|
C | T | 1 | a0001c0001t0001g0184 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1378-1291C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 12/38 | chr15 | 92947661 | ||||||
| chr15:92947787
|
A | G | 175 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(172): Show | 179 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.1378-1165A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 12/38 | chr15 | 92947787 | ||||||
| chr15:92947812
|
G | A | 1 | a0001c0002t0002g0181 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1378-1140G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 12/38 | chr15 | 92947812 | ||||||
| chr15:92948081
|
A | G | 1 | a0001c0003t0002g0162 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1378-871A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 12/38 | chr15 | 92948081 | ||||||
| chr15:92948270
|
C | T | 129 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0026others(126): Show | 132 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.1378-682C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 12/38 | chr15 | 92948270 | ||||||
| chr15:92948320
|
C | A | 172 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(169): Show | 176 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.1378-632C>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 12/38 | chr15 | 92948320 | ||||||
| chr15:92948506
|
G | A | 1 | a0001c0010t0002g0182 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1378-446G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 12/38 | chr15 | 92948506 | ||||||
| chr15:92948523
|
T | C | 1 | a0001c0001t0007g0174 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1378-429T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 12/38 | chr15 | 92948523 | ||||||
| chr15:92948629
|
C | G | 1 | a0001c0002t0002g0156 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1378-323C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 12/38 | chr15 | 92948629 | ||||||
| chr15:92948829
|
A | G | 3 | a0001c0002t0002g0045a0001c0002t0002g0046a0001c0002t0002g0232 | 3 | HG03453.hp2 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1378-123A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 12/38 | chr15 | 92948829 | ||||||
| chr15:92948856
|
T | G | 1 | a0001c0001t0007g0174 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1378-96T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 12/38 | chr15 | 92948856 | ||||||
| chr15:92949221
|
A | G | 1 | a0001c0002t0002g0275 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1502+145A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 13/38 | chr15 | 92949221 | ||||||
| chr15:92949222
|
T | A | 1 | a0001c0001t0001g0201 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1502+146T>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 13/38 | chr15 | 92949222 | ||||||
| chr15:92949581
|
G | C | 173 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(170): Show | 177 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.1502+505G>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 13/38 | chr15 | 92949581 | ||||||
| chr15:92949607
|
C | T | 1 | a0001c0002t0002g0156 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1502+531C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 13/38 | chr15 | 92949607 | ||||||
| chr15:92949862
|
G | A | 2 | a0001c0002t0008g0015a0001c0004t0007g0020 | 2 | HG01070.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.1502+786G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 13/38 | chr15 | 92949862 | ||||||
| chr15:92949989
|
C | T | 4 | a0001c0002t0002g0156a0001c0002t0002g0223a0001c0002t0005g0224others(1): Show | 4 | HG02572.hp2 HG02976.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1502+913C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 13/38 | chr15 | 92949989 | ||||||
| chr15:92950120
|
A | G | 8 | a0001c0001t0007g0174a0001c0002t0002g0045a0001c0002t0002g0046others(5): Show | 8 | HG02055.hp1 HG02572.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.1502+1044A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 13/38 | chr15 | 92950120 | ||||||
| chr15:92950121
|
T | C | 20 | a0001c0001t0001g0281a0001c0001t0001g0298a0001c0001t0001g0299others(17): Show | 20 | HG00544.hp1 HG00735.hp1 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.1502+1045T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 13/38 | chr15 | 92950121 | ||||||
| chr15:92950209
|
C | T | 1 | a0001c0001t0007g0174 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1502+1133C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 13/38 | chr15 | 92950209 | ||||||
| chr15:92950210
|
A | C | 1 | a0001c0003t0002g0221 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1502+1134A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 13/38 | chr15 | 92950210 | ||||||
| chr15:92950401
|
T | A | 7 | a0001c0002t0002g0231a0001c0002t0003g0228a0001c0002t0005g0220others(4): Show | 7 | HG01884.hp2 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1502+1325T>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 13/38 | chr15 | 92950401 | ||||||
| chr15:92950494
|
A | T | 3 | a0001c0002t0002g0223a0001c0002t0005g0224a0001c0002t0005g0225 | 3 | HG02572.hp2 HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1502+1418A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 13/38 | chr15 | 92950494 | ||||||
| chr15:92950646
|
T | C | 1 | a0001c0001t0001g0042 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1502+1570T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 13/38 | chr15 | 92950646 | ||||||
| chr15:92950707
|
C | T | 1 | a0001c0004t0007g0014 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1502+1631C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 13/38 | chr15 | 92950707 | ||||||
| chr15:92950752
|
T | TA | 91 | a0001c0001t0001g0007a0001c0001t0001g0016a0001c0001t0001g0207others(88): Show | 91 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.1502+1690dupA | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 13/38 | INFO_REALIGN_3_PRIME | chr15 | 92950752 | |||||
| chr15:92950796
|
T | A | 173 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(170): Show | 177 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.1502+1720T>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 13/38 | chr15 | 92950796 | ||||||
| chr15:92950841
|
C | T | 9 | a0001c0002t0001g0286a0001c0002t0005g0277a0001c0002t0005g0279others(6): Show | 9 | HG00099.hp2 HG01167.hp2 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.1502+1765C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 13/38 | chr15 | 92950841 | ||||||
| chr15:92950967
|
A | G | 20 | a0001c0001t0001g0281a0001c0001t0001g0298a0001c0001t0001g0299others(17): Show | 20 | HG00544.hp1 HG00735.hp1 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.1502+1891A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 13/38 | chr15 | 92950967 | ||||||
| chr15:92950975
|
A | G | 1 | a0001c0002t0002g0181 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1502+1899A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 13/38 | chr15 | 92950975 | ||||||
| chr15:92951181
|
G | A | 1 | a0001c0002t0002g0181 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1502+2105G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 13/38 | chr15 | 92951181 | ||||||
| chr15:92951458
|
A | G | 13 | a0001c0001t0001g0259a0001c0001t0006g0248a0001c0001t0006g0260others(10): Show | 13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.1503-1899A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 13/38 | chr15 | 92951458 | ||||||
| chr15:92951461
|
G | A | 1 | a0001c0001t0001g0068 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1503-1896G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 13/38 | chr15 | 92951461 | ||||||
| chr15:92951524
|
G | A | 1 | a0001c0003t0005g0166 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1503-1833G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 13/38 | chr15 | 92951524 | ||||||
| chr15:92951616
|
C | T | 1 | a0001c0010t0002g0222 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1503-1741C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 13/38 | chr15 | 92951616 | ||||||
| chr15:92951748
|
A | G | 126 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(123): Show | 129 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.1503-1609A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 13/38 | chr15 | 92951748 | ||||||
| chr15:92951751
|
A | G | 9 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0038others(6): Show | 9 | HG01192.hp1 HG01433.hp1 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.1503-1606A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 13/38 | chr15 | 92951751 | ||||||
| chr15:92951771
|
A | G | 10 | a0001c0002t0001g0286a0001c0002t0002g0275a0001c0002t0005g0277others(7): Show | 10 | HG00099.hp2 HG01167.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.1503-1586A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 13/38 | chr15 | 92951771 | ||||||
| chr15:92951856
|
A | G | 1 | a0001c0002t0002g0156 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1503-1501A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 13/38 | chr15 | 92951856 | ||||||
| chr15:92951886
|
A | C | 1 | a0001c0001t0011g0292 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1503-1471A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 13/38 | chr15 | 92951886 | ||||||
| chr15:92952256
|
A | G | 3 | a0001c0002t0002g0223a0001c0002t0005g0224a0001c0002t0005g0225 | 3 | HG02572.hp2 HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1503-1101A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 13/38 | chr15 | 92952256 | ||||||
| chr15:92952389
|
C | T | 5 | a0001c0002t0002g0231a0001c0002t0005g0220a0001c0002t0005g0227others(2): Show | 5 | HG02257.hp2 HG02572.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1503-968C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 13/38 | chr15 | 92952389 | ||||||
| chr15:92952461
|
G | A | 1 | a0001c0001t0001g0034 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1503-896G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 13/38 | chr15 | 92952461 | ||||||
| chr15:92952743
|
A | C | 132 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(129): Show | 135 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.1503-614A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 13/38 | chr15 | 92952743 | ||||||
| chr15:92952778
|
G | T | 1 | a0001c0001t0007g0174 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1503-579G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 13/38 | chr15 | 92952778 | ||||||
| chr15:92952836
|
G | A | 1 | a0001c0001t0003g0274 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1503-521G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 13/38 | chr15 | 92952836 | ||||||
| chr15:92952918
|
G | A | 14 | a0001c0001t0001g0006a0001c0001t0001g0035a0001c0001t0001g0036others(11): Show | 15 | HG01069.hp1 HG01123.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.1503-439G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 13/38 | chr15 | 92952918 | ||||||
| chr15:92953176
|
A | G | 1 | a0001c0001t0006g0084 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1503-181A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 13/38 | chr15 | 92953176 | ||||||
| chr15:92953644
|
C | T | 237 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(234): Show | 241 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(238): Show |
intron_variant | MODIFIER | c.1719+71C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 14/38 | chr15 | 92953644 | ||||||
| chr15:92953717
|
T | C | 3 | a0001c0002t0002g0045a0001c0002t0002g0046a0001c0002t0002g0232 | 3 | HG03453.hp2 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1719+144T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 14/38 | chr15 | 92953717 | ||||||
| chr15:92953808
|
G | A | 42 | a0001c0001t0001g0016a0001c0002t0001g0233a0001c0002t0001g0234others(39): Show | 42 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.1719+235G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 14/38 | chr15 | 92953808 | ||||||
| chr15:92953875
|
T | C | 5 | a0001c0001t0001g0007a0001c0009t0002g0043a0001c0009t0002g0048others(2): Show | 5 | HG00642.hp1 HG00673.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1719+302T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 14/38 | chr15 | 92953875 | ||||||
| chr15:92953880
|
A | G | 2 | a0001c0010t0002g0182a0001c0010t0002g0222 | 2 | HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1719+307A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 14/38 | chr15 | 92953880 | ||||||
| chr15:92953948
|
T | C | 54 | a0001c0001t0001g0016a0001c0001t0002g0293a0001c0001t0002g0294others(51): Show | 54 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.1719+375T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 14/38 | chr15 | 92953948 | ||||||
| chr15:92954208
|
C | G | 13 | a0001c0001t0001g0281a0001c0001t0002g0278a0001c0001t0002g0295others(10): Show | 13 | HG00735.hp1 HG00738.hp2 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.1719+635C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 14/38 | chr15 | 92954208 | ||||||
| chr15:92954250
|
C | T | 133 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0026others(130): Show | 136 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.1719+677C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 14/38 | chr15 | 92954250 | ||||||
| chr15:92954332
|
C | T | 49 | a0001c0002t0001g0233a0001c0002t0001g0234a0001c0002t0001g0235others(46): Show | 49 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.1719+759C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 14/38 | chr15 | 92954332 | ||||||
| chr15:92954395
|
G | A | 2 | a0001c0001t0003g0274a0001c0001t0005g0179 | 2 | NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1719+822G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 14/38 | chr15 | 92954395 | ||||||
| chr15:92954635
|
C | T | 2 | a0001c0002t0002g0275a0001c0002t0016g0280 | 2 | HG00099.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.1720-788C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 14/38 | chr15 | 92954635 | ||||||
| chr15:92954875
|
T | C | 64 | a0001c0001t0001g0016a0001c0001t0002g0293a0001c0001t0002g0294others(61): Show | 64 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.1720-548T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 14/38 | chr15 | 92954875 | ||||||
| chr15:92954892
|
A | G | 235 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(232): Show | 239 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.1720-531A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 14/38 | chr15 | 92954892 | ||||||
| chr15:92955025
|
G | T | 1 | a0001c0002t0002g0156 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1720-398G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 14/38 | chr15 | 92955025 | ||||||
| chr15:92955067
|
A | G | 20 | a0001c0001t0001g0281a0001c0001t0002g0278a0001c0001t0002g0295others(17): Show | 20 | HG00735.hp1 HG00738.hp2 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1720-356A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 14/38 | chr15 | 92955067 | ||||||
| chr15:92955143
|
G | C | 2 | a0001c0003t0012g0126a0001c0003t0012g0134 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1720-280G>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 14/38 | chr15 | 92955143 | ||||||
| chr15:92955207
|
A | G | 1 | a0001c0003t0005g0160 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1720-216A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 14/38 | chr15 | 92955207 | ||||||
| chr15:92955312
|
A | G | 1 | a0001c0001t0001g0062 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1720-111A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 14/38 | chr15 | 92955312 | ||||||
| chr15:92955353
|
A | G | 9 | a0001c0002t0002g0045a0001c0002t0002g0046a0001c0002t0002g0181others(6): Show | 9 | HG02572.hp2 HG02630.hp1 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.1720-70A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 14/38 | chr15 | 92955353 | ||||||
| chr15:92955764
|
A | G | 1 | a0001c0001t0025g0104 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1809+252A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 15/38 | chr15 | 92955764 | ||||||
| chr15:92956155
|
A | G | 251 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(248): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.1810-304A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 15/38 | chr15 | 92956155 | ||||||
| chr15:92956301
|
A | G | 1 | a0001c0003t0003g0128 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1810-158A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 15/38 | chr15 | 92956301 | ||||||
| chr15:92956405
|
A | C | 1 | a0001c0006t0004g0163 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1810-54A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 15/38 | chr15 | 92956405 | ||||||
| chr15:92956677
|
G | A | 1 | a0001c0002t0002g0156 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2000+28G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92956677 | ||||||
| chr15:92956850
|
G | A | 1 | a0001c0002t0001g0286 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.2000+201G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92956850 | ||||||
| chr15:92956950
|
A | G | 3 | a0001c0002t0002g0045a0001c0002t0002g0046a0001c0002t0002g0232 | 3 | HG03453.hp2 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2000+301A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92956950 | ||||||
| chr15:92956958
|
A | T | 14 | a0001c0001t0001g0006a0001c0001t0001g0035a0001c0001t0001g0036others(11): Show | 15 | HG01069.hp1 HG01123.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.2000+309A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92956958 | ||||||
| chr15:92956993
|
G | T | 5 | a0001c0001t0001g0006a0001c0001t0001g0271a0001c0001t0001g0272others(2): Show | 6 | HG01069.hp1 HG01123.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.2000+344G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92956993 | ||||||
| chr15:92957360
|
C | T | 2 | a0001c0010t0002g0182a0001c0010t0002g0222 | 2 | HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.2000+711C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92957360 | ||||||
| chr15:92957632
|
A | G | 13 | a0001c0001t0001g0281a0001c0001t0002g0278a0001c0001t0002g0293others(10): Show | 13 | HG00544.hp1 HG00738.hp2 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.2000+983A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92957632 | ||||||
| chr15:92957738
|
T | A | 2 | a0001c0003t0005g0124a0001c0006t0005g0130 | 2 | HG02922.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2000+1089T>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92957738 | ||||||
| chr15:92957805
|
G | T | 212 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(209): Show | 216 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.2000+1156G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92957805 | ||||||
| chr15:92957900
|
A | G | 1 | a0001c0001t0001g0281 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2000+1251A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92957900 | ||||||
| chr15:92957902
|
A | G | 2 | a0001c0010t0002g0182a0001c0010t0002g0222 | 2 | HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.2000+1253A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92957902 | ||||||
| chr15:92957935
|
G | A | 73 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0027others(70): Show | 74 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.2000+1286G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92957935 | ||||||
| chr15:92958031
|
G | T | 1 | a0001c0001t0001g0273 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2000+1382G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92958031 | ||||||
| chr15:92958041
|
G | A | 5 | a0001c0001t0007g0174a0001c0009t0002g0043a0001c0009t0002g0048others(2): Show | 5 | HG00642.hp1 HG00673.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.2000+1392G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92958041 | ||||||
| chr15:92958168
|
T | A | 225 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(222): Show | 229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.2000+1519T>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92958168 | ||||||
| chr15:92958178
|
C | G | 1 | a0001c0002t0002g0181 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2000+1529C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92958178 | ||||||
| chr15:92958360
|
C | T | 1 | a0001c0002t0001g0241 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2000+1711C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92958360 | ||||||
| chr15:92958755
|
C | T | 133 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0026others(130): Show | 136 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.2000+2106C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92958755 | ||||||
| chr15:92958782
|
G | A | 134 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(131): Show | 137 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.2000+2133G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92958782 | ||||||
| chr15:92958829
|
C | T | 1 | a0001c0001t0001g0206 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.2000+2180C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92958829 | ||||||
| chr15:92958865
|
G | A | 7 | a0001c0002t0002g0231a0001c0002t0003g0228a0001c0002t0005g0220others(4): Show | 7 | HG01884.hp2 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.2000+2216G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92958865 | ||||||
| chr15:92958872
|
G | A | 3 | a0001c0002t0002g0223a0001c0002t0005g0224a0001c0002t0005g0225 | 3 | HG02572.hp2 HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2000+2223G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92958872 | ||||||
| chr15:92958889
|
T | G | 2 | a0001c0002t0005g0230a0001c0014t0005g0226 | 2 | HG02257.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.2000+2240T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92958889 | ||||||
| chr15:92959017
|
C | G | 15 | a0001c0001t0001g0281a0001c0001t0002g0278a0001c0001t0002g0293others(12): Show | 15 | HG00544.hp1 HG00735.hp1 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.2000+2368C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92959017 | ||||||
| chr15:92959082
|
T | G | 1 | a0001c0001t0001g0082 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.2000+2433T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92959082 | ||||||
| chr15:92959414
|
T | C | 1 | a0001c0006t0004g0158 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2000+2765T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92959414 | ||||||
| chr15:92959711
|
C | T | 1 | a0001c0002t0001g0249 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.2000+3062C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92959711 | ||||||
| chr15:92959832
|
T | C | 63 | a0001c0001t0001g0016a0001c0001t0002g0293a0001c0001t0002g0294others(60): Show | 63 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.2000+3183T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92959832 | ||||||
| chr15:92959960
|
C | T | 1 | a0001c0015t0005g0288 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2000+3311C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92959960 | ||||||
| chr15:92960160
|
A | G | 15 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0001g0259others(12): Show | 15 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.2000+3511A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92960160 | ||||||
| chr15:92960163
|
G | A | 5 | a0001c0001t0007g0174a0001c0009t0002g0043a0001c0009t0002g0048others(2): Show | 5 | HG00642.hp1 HG00673.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.2000+3514G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92960163 | ||||||
| chr15:92960356
|
G | A | 2 | a0001c0001t0001g0202a0001c0001t0001g0203 | 2 | HG02523.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.2000+3707G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92960356 | ||||||
| chr15:92960544
|
C | T | 7 | a0001c0002t0002g0231a0001c0002t0003g0228a0001c0002t0005g0220others(4): Show | 7 | HG01884.hp2 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.2000+3895C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92960544 | ||||||
| chr15:92960580
|
T | C | 1 | a0001c0003t0003g0161 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2000+3931T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92960580 | ||||||
| chr15:92960597
|
T | G | 135 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(132): Show | 138 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.2000+3948T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92960597 | ||||||
| chr15:92960686
|
A | AT | 3 | a0001c0002t0002g0045a0001c0002t0002g0046a0001c0002t0002g0232 | 3 | HG03453.hp2 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2000+4042dupT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr15 | 92960686 | |||||
| chr15:92960686
|
A | G | 13 | a0001c0001t0001g0259a0001c0001t0006g0248a0001c0001t0006g0260others(10): Show | 13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.2000+4037A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92960686 | ||||||
| chr15:92960705
|
G | GT | 47 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0067others(44): Show | 49 | HG00438.hp1 HG00621.hp1 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.2000+4083dupT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr15 | 92960705 | |||||
| chr15:92960705
|
G | GTT | 16 | a0001c0001t0001g0200a0001c0001t0002g0293a0001c0001t0011g0292others(13): Show | 16 | HG00544.hp1 HG01175.hp1 HG01515.hp1 others(13): Show |
intron_variant | MODIFIER | c.2000+4082_2000+408 others(6): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr15 | 92960705 | |||||
| chr15:92960705
|
G | GTTT | 34 | a0001c0001t0001g0006a0001c0001t0001g0035a0001c0001t0001g0036others(31): Show | 35 | HG00099.hp2 HG00558.hp1 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.2000+4081_2000+408 others(7): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr15 | 92960705 | |||||
| chr15:92960705
|
G | GTTTT | 20 | a0001c0001t0001g0016a0001c0001t0009g0010a0001c0002t0001g0236others(17): Show | 20 | HG00423.hp2 HG00639.hp1 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.2000+4080_2000+408 others(8): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr15 | 92960705 | |||||
| chr15:92960950
|
G | A | 1 | a0001c0003t0003g0138 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2000+4301G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92960950 | ||||||
| chr15:92961271
|
G | A | 134 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0026others(131): Show | 137 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.2000+4622G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92961271 | ||||||
| chr15:92961289
|
A | AT | 250 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(247): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.2000+4642dupT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr15 | 92961289 | |||||
| chr15:92961441
|
C | A | 7 | a0001c0002t0002g0231a0001c0002t0003g0228a0001c0002t0005g0220others(4): Show | 7 | HG01884.hp2 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.2000+4792C>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92961441 | ||||||
| chr15:92961456
|
G | A | 8 | a0001c0002t0002g0045a0001c0002t0002g0046a0001c0002t0002g0181others(5): Show | 8 | HG02572.hp2 HG02630.hp1 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.2000+4807G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92961456 | ||||||
| chr15:92961824
|
C | G | 1 | a0001c0001t0001g0281 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2000+5175C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92961824 | ||||||
| chr15:92961876
|
C | CTT | 17 | a0001c0001t0001g0259a0001c0001t0006g0248a0001c0001t0006g0260others(14): Show | 17 | HG00735.hp2 HG01074.hp2 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.2000+5249_2000+525 others(6): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr15 | 92961876 | |||||
| chr15:92961876
|
C | CTTTT | 15 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0069others(12): Show | 15 | HG00099.hp1 HG00544.hp1 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.2000+5247_2000+525 others(8): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr15 | 92961876 | |||||
| chr15:92961876
|
C | CTTTTT | 124 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0027others(121): Show | 127 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.2000+5246_2000+525 others(9): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr15 | 92961876 | |||||
| chr15:92961876
|
C | CTTTTTT | 21 | a0001c0001t0001g0006a0001c0001t0001g0035a0001c0001t0001g0036others(18): Show | 22 | HG00738.hp2 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.2000+5245_2000+525 others(10): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr15 | 92961876 | |||||
| chr15:92961876
|
CTTTTTTT others(2): Show |
C | 60 | a0001c0001t0001g0016a0001c0002t0001g0091a0001c0002t0001g0233others(57): Show | 60 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.2000+5242_2000+525 others(13): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr15 | 92961876 | |||||
| chr15:92961947
|
T | C | 14 | a0001c0001t0001g0006a0001c0001t0001g0035a0001c0001t0001g0036others(11): Show | 15 | HG01069.hp1 HG01123.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.2000+5298T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92961947 | ||||||
| chr15:92961950
|
C | T | 13 | a0001c0001t0001g0259a0001c0001t0006g0248a0001c0001t0006g0260others(10): Show | 13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.2000+5301C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92961950 | ||||||
| chr15:92962160
|
G | A | 41 | a0001c0001t0001g0016a0001c0002t0001g0233a0001c0002t0001g0234others(38): Show | 41 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.2001-5165G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92962160 | ||||||
| chr15:92962354
|
A | G | 1 | a0001c0010t0002g0222 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2001-4971A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92962354 | ||||||
| chr15:92962419
|
T | G | 25 | a0001c0001t0001g0281a0001c0001t0002g0278a0001c0001t0002g0293others(22): Show | 25 | HG00544.hp1 HG00735.hp1 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.2001-4906T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92962419 | ||||||
| chr15:92962545
|
T | C | 1 | a0001c0002t0002g0181 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2001-4780T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92962545 | ||||||
| chr15:92962567
|
T | C | 14 | a0001c0001t0001g0006a0001c0001t0001g0035a0001c0001t0001g0036others(11): Show | 15 | HG01069.hp1 HG01123.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.2001-4758T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92962567 | ||||||
| chr15:92962651
|
G | A | 1 | a0001c0006t0004g0158 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2001-4674G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92962651 | ||||||
| chr15:92962677
|
T | TC | 22 | a0001c0001t0001g0281a0001c0001t0002g0278a0001c0001t0002g0293others(19): Show | 22 | HG00544.hp1 HG00735.hp1 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.2001-4647dupC | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr15 | 92962677 | |||||
| chr15:92962854
|
G | A | 130 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0026others(127): Show | 133 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.2001-4471G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92962854 | ||||||
| chr15:92962878
|
T | C | 251 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(248): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.2001-4447T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92962878 | ||||||
| chr15:92963002
|
C | T | 1 | a0001c0002t0001g0286 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.2001-4323C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92963002 | ||||||
| chr15:92963085
|
T | G | 1 | a0001c0001t0001g0086 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2001-4240T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92963085 | ||||||
| chr15:92963125
|
G | T | 15 | a0001c0001t0001g0281a0001c0001t0002g0278a0001c0001t0002g0293others(12): Show | 15 | HG00544.hp1 HG00735.hp1 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.2001-4200G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92963125 | ||||||
| chr15:92963443
|
T | C | 22 | a0001c0001t0001g0281a0001c0001t0002g0278a0001c0001t0002g0293others(19): Show | 22 | HG00544.hp1 HG00735.hp1 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.2001-3882T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92963443 | ||||||
| chr15:92963475
|
C | T | 5 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112others(2): Show | 5 | NA18939.hp1 NA18944.hp2 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.2001-3850C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92963475 | ||||||
| chr15:92963562
|
T | C | 251 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(248): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.2001-3763T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92963562 | ||||||
| chr15:92963612
|
G | C | 1 | a0001c0001t0001g0281 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2001-3713G>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92963612 | ||||||
| chr15:92963713
|
A | G | 6 | a0001c0001t0001g0007a0001c0001t0007g0174a0001c0009t0002g0043others(3): Show | 6 | HG00642.hp1 HG00673.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.2001-3612A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92963713 | ||||||
| chr15:92963809
|
T | C | 15 | a0001c0001t0001g0281a0001c0001t0002g0278a0001c0001t0002g0293others(12): Show | 15 | HG00544.hp1 HG00735.hp1 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.2001-3516T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92963809 | ||||||
| chr15:92963831
|
A | G | 1 | a0001c0001t0001g0081 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2001-3494A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92963831 | ||||||
| chr15:92964093
|
T | G | 1 | a0001c0001t0020g0113 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2001-3232T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92964093 | ||||||
| chr15:92964231
|
CT | C | 248 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(245): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.2001-3087delT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr15 | 92964231 | |||||
| chr15:92964286
|
C | A | 2 | a0001c0001t0001g0070a0001c0001t0001g0071 | 2 | NA18993.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.2001-3039C>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92964286 | ||||||
| chr15:92964312
|
A | G | 1 | a0001c0001t0002g0278 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2001-3013A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92964312 | ||||||
| chr15:92964801
|
G | A | 17 | a0001c0001t0001g0281a0001c0001t0002g0278a0001c0001t0002g0293others(14): Show | 17 | HG00544.hp1 HG00735.hp1 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.2001-2524G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92964801 | ||||||
| chr15:92964958
|
A | G | 14 | a0001c0001t0001g0259a0001c0001t0006g0248a0001c0001t0006g0260others(11): Show | 14 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.2001-2367A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92964958 | ||||||
| chr15:92965051
|
C | T | 7 | a0001c0002t0002g0231a0001c0002t0003g0228a0001c0002t0005g0220others(4): Show | 7 | HG01884.hp2 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.2001-2274C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92965051 | ||||||
| chr15:92965107
|
A | G | 1 | a0001c0004t0010g0107 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2001-2218A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92965107 | ||||||
| chr15:92965448
|
CAGGAGGC others(5): Show |
C | 14 | a0001c0001t0001g0006a0001c0001t0001g0035a0001c0001t0001g0036others(11): Show | 15 | HG01069.hp1 HG01123.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.2001-1876_2001-186 others(16): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92965448 | ||||||
| chr15:92965512
|
C | T | 1 | a0001c0001t0001g0141 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2001-1813C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92965512 | ||||||
| chr15:92965565
|
C | CA | 19 | a0001c0003t0001g0129a0001c0003t0001g0144a0001c0003t0002g0169others(16): Show | 19 | HG00323.hp2 HG01109.hp2 HG01346.hp2 others(16): Show |
intron_variant | MODIFIER | c.2001-1730dupA | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr15 | 92965565 | |||||
| chr15:92965565
|
C | CAA | 8 | a0001c0003t0001g0135a0001c0003t0001g0142a0001c0003t0003g0136others(5): Show | 8 | HG00741.hp2 HG01243.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.2001-1731_2001-173 others(6): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr15 | 92965565 | |||||
| chr15:92965565
|
C | CAAAAAAA | 6 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0271others(3): Show | 6 | HG01123.hp2 HG01192.hp1 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.2001-1736_2001-173 others(11): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr15 | 92965565 | |||||
| chr15:92965565
|
C | CAAAAAAA others(3): Show |
1 | a0001c0001t0009g0010 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.2001-1739_2001-173 others(14): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr15 | 92965565 | |||||
| chr15:92965565
|
C | CAAAAAAA others(4): Show |
2 | a0001c0001t0009g0009a0001c0001t0009g0011 | 2 | NA18967.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.2001-1740_2001-173 others(15): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr15 | 92965565 | |||||
| chr15:92965565
|
CA | C | 6 | a0001c0001t0002g0294a0001c0001t0002g0295a0001c0001t0011g0292others(3): Show | 6 | HG00738.hp2 HG01175.hp1 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.2001-1730delA | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr15 | 92965565 | |||||
| chr15:92965565
|
CAA | C | 18 | a0001c0001t0001g0281a0001c0001t0002g0278a0001c0001t0002g0293others(15): Show | 18 | HG00544.hp1 HG00735.hp1 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.2001-1731_2001-173 others(6): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr15 | 92965565 | |||||
| chr15:92965565
|
CAAA | C | 7 | a0001c0001t0007g0174a0001c0002t0001g0091a0001c0002t0002g0232others(4): Show | 7 | HG00099.hp2 HG01975.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.2001-1732_2001-173 others(7): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr15 | 92965565 | |||||
| chr15:92965565
|
CAAAAA | C | 9 | a0001c0001t0001g0007a0001c0001t0003g0274a0001c0001t0005g0179others(6): Show | 9 | HG00642.hp1 HG00673.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.2001-1734_2001-173 others(9): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr15 | 92965565 | |||||
| chr15:92965565
|
CAAAAAA | C | 7 | a0001c0002t0002g0231a0001c0002t0003g0228a0001c0002t0005g0220others(4): Show | 7 | HG01884.hp2 HG02451.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.2001-1735_2001-173 others(10): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr15 | 92965565 | |||||
| chr15:92965565
|
CAAAAAAA others(1): Show |
C | 11 | a0001c0001t0001g0259a0001c0001t0006g0260a0001c0001t0006g0261others(8): Show | 11 | HG00735.hp2 HG01074.hp2 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.2001-1737_2001-173 others(12): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr15 | 92965565 | |||||
| chr15:92965565
|
CAAAAAAA others(7): Show |
C | 3 | a0001c0001t0001g0070a0001c0001t0008g0217a0001c0019t0001g0119 | 3 | HG04204.hp2 NA18993.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.2001-1743_2001-173 others(18): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr15 | 92965565 | |||||
| chr15:92965565
|
CAAAAAAA others(8): Show |
C | 128 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0016others(125): Show | 131 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.2001-1744_2001-173 others(19): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr15 | 92965565 | |||||
| chr15:92965565
|
CAAAAAAA others(10): Show |
C | 39 | a0001c0002t0001g0233a0001c0002t0001g0234a0001c0002t0001g0235others(36): Show | 39 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.2001-1746_2001-173 others(21): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr15 | 92965565 | |||||
| chr15:92965591
|
A | G | 6 | a0001c0001t0001g0007a0001c0001t0007g0174a0001c0009t0002g0043others(3): Show | 6 | HG00642.hp1 HG00673.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.2001-1734A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92965591 | ||||||
| chr15:92965593
|
A | AC | 3 | a0001c0003t0012g0126a0001c0003t0012g0133a0001c0003t0012g0134 | 3 | HG01257.hp1 HG01258.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.2001-1732_2001-173 others(5): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92965593 | ||||||
| chr15:92965617
|
A | C | 1 | a0001c0002t0002g0156 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2001-1708A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92965617 | ||||||
| chr15:92965641
|
C | T | 1 | a0001c0002t0001g0234 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2001-1684C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92965641 | ||||||
| chr15:92965692
|
A | G | 1 | a0001c0001t0001g0194 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.2001-1633A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92965692 | ||||||
| chr15:92965720
|
A | G | 4 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(1): Show | 4 | HG02080.hp2 NA18953.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.2001-1605A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92965720 | ||||||
| chr15:92965875
|
A | C | 14 | a0001c0001t0001g0259a0001c0001t0006g0248a0001c0001t0006g0260others(11): Show | 14 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.2001-1450A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92965875 | ||||||
| chr15:92965913
|
G | C | 9 | a0001c0002t0001g0235a0001c0002t0001g0244a0001c0002t0001g0247others(6): Show | 9 | NA18939.hp2 NA18948.hp2 NA18966.hp1 others(6): Show |
intron_variant | MODIFIER | c.2001-1412G>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92965913 | ||||||
| chr15:92965930
|
C | T | 1 | a0001c0002t0001g0091 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2001-1395C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92965930 | ||||||
| chr15:92965952
|
T | G | 1 | a0001c0001t0001g0212 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2001-1373T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92965952 | ||||||
| chr15:92966034
|
T | C | 5 | a0001c0001t0001g0066a0001c0001t0001g0070a0001c0001t0001g0071others(2): Show | 5 | NA18963.hp1 NA18968.hp2 NA18993.hp2 others(2): Show |
intron_variant | MODIFIER | c.2001-1291T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92966034 | ||||||
| chr15:92966066
|
C | CT | 7 | a0001c0001t0001g0081a0001c0001t0009g0296a0001c0002t0002g0046others(4): Show | 7 | HG00639.hp1 HG00735.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.2001-1242dupT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr15 | 92966066 | |||||
| chr15:92966066
|
CT | C | 16 | a0001c0001t0001g0078a0001c0001t0001g0259a0001c0001t0006g0248others(13): Show | 16 | HG00735.hp2 HG01069.hp2 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.2001-1242delT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr15 | 92966066 | |||||
| chr15:92966144
|
A | G | 4 | a0001c0001t0008g0217a0001c0001t0008g0218a0001c0001t0008g0219others(1): Show | 4 | HG01361.hp1 HG03239.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.2001-1181A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92966144 | ||||||
| chr15:92966238
|
A | G | 1 | a0001c0002t0002g0156 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2001-1087A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92966238 | ||||||
| chr15:92966378
|
T | A | 15 | a0001c0001t0001g0281a0001c0001t0002g0278a0001c0001t0002g0293others(12): Show | 15 | HG00544.hp1 HG00735.hp1 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.2001-947T>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92966378 | ||||||
| chr15:92966433
|
G | C | 1 | a0001c0003t0003g0167 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2001-892G>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92966433 | ||||||
| chr15:92966576
|
G | A | 6 | a0001c0002t0002g0231a0001c0002t0003g0228a0001c0002t0005g0220others(3): Show | 6 | HG01884.hp2 HG02257.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.2001-749G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92966576 | ||||||
| chr15:92966676
|
C | T | 16 | a0001c0001t0001g0095a0001c0001t0001g0259a0001c0001t0006g0248others(13): Show | 16 | HG00621.hp2 HG00735.hp2 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.2001-649C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92966676 | ||||||
| chr15:92966737
|
C | T | 154 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(151): Show | 158 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.2001-588C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92966737 | ||||||
| chr15:92966866
|
T | C | 249 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(246): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.2001-459T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92966866 | ||||||
| chr15:92966889
|
G | A | 1 | a0001c0001t0001g0141 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2001-436G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92966889 | ||||||
| chr15:92966909
|
C | CA | 243 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(240): Show | 247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.2001-401dupA | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr15 | 92966909 | |||||
| chr15:92966909
|
C | T | 2 | a0001c0003t0002g0125a0001c0003t0003g0138 | 2 | HG01069.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2001-416C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92966909 | ||||||
| chr15:92967013
|
G | C | 215 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(212): Show | 219 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.2001-312G>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92967013 | ||||||
| chr15:92967161
|
T | A | 1 | a0001c0002t0002g0181 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2001-164T>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92967161 | ||||||
| chr15:92967581
|
T | C | 14 | a0001c0001t0001g0259a0001c0001t0006g0248a0001c0001t0006g0260others(11): Show | 14 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.2189+68T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | chr15 | 92967581 | ||||||
| chr15:92967598
|
GT | G | 151 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(148): Show | 155 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.2189+99delT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | INFO_REALIGN_3_PRIME | chr15 | 92967598 | |||||
| chr15:92967764
|
G | T | 40 | a0001c0001t0001g0016a0001c0002t0001g0233a0001c0002t0001g0234others(37): Show | 40 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.2189+251G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | chr15 | 92967764 | ||||||
| chr15:92967992
|
G | T | 2 | a0001c0001t0002g0278a0001c0001t0002g0295 | 2 | HG02965.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2189+479G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | chr15 | 92967992 | ||||||
| chr15:92968014
|
C | G | 15 | a0001c0001t0001g0281a0001c0001t0002g0278a0001c0001t0002g0293others(12): Show | 15 | HG00544.hp1 HG00735.hp1 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.2189+501C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | chr15 | 92968014 | ||||||
| chr15:92968041
|
T | C | 1 | a0001c0009t0002g0048 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2189+528T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | chr15 | 92968041 | ||||||
| chr15:92968063
|
C | T | 3 | a0001c0002t0002g0223a0001c0002t0005g0224a0001c0002t0005g0225 | 3 | HG02572.hp2 HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2189+550C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | chr15 | 92968063 | ||||||
| chr15:92968112
|
T | A | 14 | a0001c0001t0001g0006a0001c0001t0001g0035a0001c0001t0001g0036others(11): Show | 15 | HG01069.hp1 HG01123.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.2189+599T>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | chr15 | 92968112 | ||||||
| chr15:92968119
|
CA | C | 134 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0026others(131): Show | 137 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.2189+608delA | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | INFO_REALIGN_3_PRIME | chr15 | 92968119 | |||||
| chr15:92968453
|
A | C | 1 | a0001c0017t0009g0037 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2189+940A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | chr15 | 92968453 | ||||||
| chr15:92968524
|
C | T | 1 | a0001c0001t0001g0078 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.2189+1011C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | chr15 | 92968524 | ||||||
| chr15:92968618
|
T | C | 250 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(247): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.2189+1105T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | chr15 | 92968618 | ||||||
| chr15:92968953
|
A | G | 1 | a0001c0002t0005g0230 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2189+1440A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | chr15 | 92968953 | ||||||
| chr15:92969384
|
G | A | 1 | a0001c0018t0009g0039 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.2189+1871G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | chr15 | 92969384 | ||||||
| chr15:92969448
|
G | A | 232 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(229): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.2189+1935G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | chr15 | 92969448 | ||||||
| chr15:92969453
|
C | T | 1 | a0001c0003t0001g0129 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2189+1940C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | chr15 | 92969453 | ||||||
| chr15:92969726
|
A | G | 1 | a0001c0002t0001g0286 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.2190-2039A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | chr15 | 92969726 | ||||||
| chr15:92969749
|
A | T | 14 | a0001c0001t0001g0259a0001c0001t0006g0248a0001c0001t0006g0260others(11): Show | 14 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.2190-2016A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | chr15 | 92969749 | ||||||
| chr15:92969756
|
C | A | 14 | a0001c0001t0001g0259a0001c0001t0006g0248a0001c0001t0006g0260others(11): Show | 14 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.2190-2009C>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | chr15 | 92969756 | ||||||
| chr15:92969812
|
C | CT | 14 | a0001c0001t0001g0006a0001c0001t0001g0035a0001c0001t0001g0036others(11): Show | 15 | HG01069.hp1 HG01123.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.2190-1936dupT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | INFO_REALIGN_3_PRIME | chr15 | 92969812 | |||||
| chr15:92969812
|
CT | C | 64 | a0001c0002t0001g0091a0001c0002t0001g0233a0001c0002t0001g0234others(61): Show | 64 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.2190-1936delT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | INFO_REALIGN_3_PRIME | chr15 | 92969812 | |||||
| chr15:92969825
|
T | C | 1 | a0001c0002t0002g0156 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2190-1940T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | chr15 | 92969825 | ||||||
| chr15:92969881
|
A | C | 5 | a0001c0001t0001g0007a0001c0009t0002g0043a0001c0009t0002g0048others(2): Show | 5 | HG00642.hp1 HG00673.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.2190-1884A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | chr15 | 92969881 | ||||||
| chr15:92969948
|
A | G | 1 | a0001c0003t0008g0140 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2190-1817A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | chr15 | 92969948 | ||||||
| chr15:92970029
|
T | A | 1 | a0001c0002t0002g0181 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2190-1736T>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | chr15 | 92970029 | ||||||
| chr15:92970283
|
C | G | 2 | a0001c0003t0005g0124a0001c0006t0005g0130 | 2 | HG02922.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2190-1482C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | chr15 | 92970283 | ||||||
| chr15:92970351
|
A | G | 1 | a0001c0001t0001g0061 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2190-1414A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | chr15 | 92970351 | ||||||
| chr15:92970629
|
A | G | 14 | a0001c0001t0001g0259a0001c0001t0006g0248a0001c0001t0006g0260others(11): Show | 14 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.2190-1136A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | chr15 | 92970629 | ||||||
| chr15:92970835
|
A | G | 1 | a0001c0001t0008g0217 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2190-930A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | chr15 | 92970835 | ||||||
| chr15:92970928
|
A | G | 1 | a0001c0002t0002g0181 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2190-837A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | chr15 | 92970928 | ||||||
| chr15:92971018
|
T | C | 2 | a0001c0003t0003g0172a0001c0003t0003g0173 | 2 | HG03098.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2190-747T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | chr15 | 92971018 | ||||||
| chr15:92971143
|
T | C | 1 | a0001c0010t0002g0222 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2190-622T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | chr15 | 92971143 | ||||||
| chr15:92971192
|
T | C | 133 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(130): Show | 136 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.2190-573T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | chr15 | 92971192 | ||||||
| chr15:92971234
|
T | A | 1 | a0001c0001t0008g0219 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2190-531T>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | chr15 | 92971234 | ||||||
| chr15:92971240
|
C | A | 14 | a0001c0001t0001g0259a0001c0001t0006g0248a0001c0001t0006g0260others(11): Show | 14 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.2190-525C>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | chr15 | 92971240 | ||||||
| chr15:92971322
|
G | C | 5 | a0001c0002t0002g0223a0001c0002t0005g0224a0001c0002t0005g0225others(2): Show | 5 | HG02572.hp2 HG02630.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.2190-443G>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | chr15 | 92971322 | ||||||
| chr15:92971445
|
A | G | 14 | a0001c0001t0001g0259a0001c0001t0006g0248a0001c0001t0006g0260others(11): Show | 14 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.2190-320A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | chr15 | 92971445 | ||||||
| chr15:92971449
|
ATG | A | 14 | a0001c0001t0001g0259a0001c0001t0006g0248a0001c0001t0006g0260others(11): Show | 14 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.2190-304_2190-303d others(4): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | INFO_REALIGN_3_PRIME | chr15 | 92971449 | |||||
| chr15:92971503
|
A | G | 1 | a0001c0001t0001g0081 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2190-262A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | chr15 | 92971503 | ||||||
| chr15:92971568
|
T | A | 1 | a0001c0003t0003g0128 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2190-197T>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | chr15 | 92971568 | ||||||
| chr15:92971621
|
C | G | 6 | a0001c0002t0002g0231a0001c0002t0003g0228a0001c0002t0005g0220others(3): Show | 6 | HG01884.hp2 HG02257.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.2190-144C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | chr15 | 92971621 | ||||||
| chr15:92971642
|
T | A | 3 | a0001c0002t0002g0223a0001c0002t0005g0224a0001c0002t0005g0225 | 3 | HG02572.hp2 HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2190-123T>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | chr15 | 92971642 | ||||||
| chr15:92971674
|
A | G | 9 | a0001c0002t0002g0045a0001c0002t0002g0046a0001c0002t0002g0181others(6): Show | 9 | HG02572.hp2 HG02630.hp1 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.2190-91A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | chr15 | 92971674 | ||||||
| chr15:92971706
|
G | T | 14 | a0001c0001t0001g0259a0001c0001t0006g0248a0001c0001t0006g0260others(11): Show | 14 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.2190-59G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | chr15 | 92971706 | ||||||
| chr15:92972002
|
A | C | 6 | a0001c0003t0002g0137a0001c0003t0002g0162a0001c0003t0002g0169others(3): Show | 6 | HG02280.hp1 HG02630.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.2352+75A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 18/38 | chr15 | 92972002 | ||||||
| chr15:92972209
|
G | A | 14 | a0001c0003t0001g0135a0001c0003t0001g0142a0001c0003t0001g0144others(11): Show | 15 | HG00323.hp2 HG00741.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.2353-56G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 18/38 | chr15 | 92972209 | ||||||
| chr15:92972456
|
C | G | 14 | a0001c0001t0001g0259a0001c0001t0006g0248a0001c0001t0006g0260others(11): Show | 14 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.2505+39C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 19/38 | chr15 | 92972456 | ||||||
| chr15:92972480
|
A | C | 1 | a0001c0007t0007g0030 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2505+63A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 19/38 | chr15 | 92972480 | ||||||
| chr15:92972557
|
TAAGATTC others(306): Show |
T | 249 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(246): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.2505+152_2505+464d others(2): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 19/38 | INFO_REALIGN_3_PRIME | chr15 | 92972557 | |||||
| chr15:92972783
|
G | A | 1 | a0001c0003t0003g0173 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2505+366G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 19/38 | chr15 | 92972783 | ||||||
| chr15:92972963
|
G | T | 1 | a0001c0001t0001g0201 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2505+546G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 19/38 | chr15 | 92972963 | ||||||
| chr15:92972986
|
A | G | 2 | a0001c0005t0004g0153a0001c0005t0004g0154 | 2 | NA20752.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2505+569A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 19/38 | chr15 | 92972986 | ||||||
| chr15:92973019
|
C | T | 1 | a0001c0003t0003g0175 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2505+602C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 19/38 | chr15 | 92973019 | ||||||
| chr15:92973121
|
C | G | 2 | a0001c0005t0004g0153a0001c0005t0004g0154 | 2 | NA20752.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2505+704C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 19/38 | chr15 | 92973121 | ||||||
| chr15:92973190
|
C | T | 7 | a0001c0002t0002g0231a0001c0002t0003g0228a0001c0002t0005g0220others(4): Show | 7 | HG01884.hp2 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.2505+773C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 19/38 | chr15 | 92973190 | ||||||
| chr15:92973197
|
A | G | 154 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(151): Show | 158 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.2505+780A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 19/38 | chr15 | 92973197 | ||||||
| chr15:92973266
|
T | C | 1 | a0001c0001t0001g0281 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2505+849T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 19/38 | chr15 | 92973266 | ||||||
| chr15:92973367
|
C | T | 7 | a0001c0001t0001g0100a0001c0001t0001g0178a0001c0001t0001g0187others(4): Show | 7 | HG01081.hp2 HG01261.hp2 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.2505+950C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 19/38 | chr15 | 92973367 | ||||||
| chr15:92973544
|
T | C | 1 | a0001c0001t0001g0007 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.2505+1127T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 19/38 | chr15 | 92973544 | ||||||
| chr15:92973564
|
C | T | 2 | a0001c0001t0002g0008a0001c0001t0002g0085 | 2 | HG02257.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.2505+1147C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 19/38 | chr15 | 92973564 | ||||||
| chr15:92973681
|
C | G | 40 | a0001c0002t0001g0233a0001c0002t0001g0234a0001c0002t0001g0235others(37): Show | 40 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.2506-1198C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 19/38 | chr15 | 92973681 | ||||||
| chr15:92973790
|
G | A | 1 | a0001c0002t0001g0236 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.2506-1089G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 19/38 | chr15 | 92973790 | ||||||
| chr15:92973876
|
T | C | 11 | a0001c0003t0001g0135a0001c0003t0001g0142a0001c0003t0001g0144others(8): Show | 12 | HG00323.hp2 HG00741.hp2 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.2506-1003T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 19/38 | chr15 | 92973876 | ||||||
| chr15:92973984
|
G | A | 248 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(245): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.2506-895G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 19/38 | chr15 | 92973984 | ||||||
| chr15:92974011
|
A | G | 14 | a0001c0001t0001g0006a0001c0001t0001g0035a0001c0001t0001g0036others(11): Show | 15 | HG01069.hp1 HG01123.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.2506-868A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 19/38 | chr15 | 92974011 | ||||||
| chr15:92974084
|
A | C | 2 | a0001c0001t0001g0051a0001c0001t0001g0087 | 2 | NA18973.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.2506-795A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 19/38 | chr15 | 92974084 | ||||||
| chr15:92974188
|
G | A | 1 | a0001c0001t0001g0177 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2506-691G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 19/38 | chr15 | 92974188 | ||||||
| chr15:92974192
|
A | G | 15 | a0001c0001t0001g0259a0001c0001t0006g0248a0001c0001t0006g0260others(12): Show | 15 | HG00642.hp2 HG00735.hp2 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.2506-687A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 19/38 | chr15 | 92974192 | ||||||
| chr15:92974439
|
G | A | 1 | a0001c0002t0002g0181 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2506-440G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 19/38 | chr15 | 92974439 | ||||||
| chr15:92974463
|
T | C | 16 | a0001c0001t0001g0281a0001c0001t0002g0278a0001c0001t0002g0293others(13): Show | 16 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.2506-416T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 19/38 | chr15 | 92974463 | ||||||
| chr15:92974718
|
G | T | 1 | a0001c0002t0009g0243 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2506-161G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 19/38 | chr15 | 92974718 | ||||||
| chr15:92975209
|
G | A | 2 | a0001c0001t0001g0183a0001c0001t0023g0052 | 2 | NA18612.hp1 NA18941.hp2 |
intron_variant | MODIFIER | c.2577+259G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 20/38 | chr15 | 92975209 | ||||||
| chr15:92975376
|
C | T | 2 | a0001c0002t0011g0256a0001c0002t0011g0257 | 2 | NA19000.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.2577+426C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 20/38 | chr15 | 92975376 | ||||||
| chr15:92975426
|
G | C | 2 | a0001c0002t0005g0230a0001c0014t0005g0226 | 2 | HG02257.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.2577+476G>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 20/38 | chr15 | 92975426 | ||||||
| chr15:92975788
|
A | G | 1 | a0001c0003t0002g0221 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2577+838A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 20/38 | chr15 | 92975788 | ||||||
| chr15:92975853
|
TAATC | T | 248 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(245): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.2577+904_2577+907d others(6): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 20/38 | chr15 | 92975853 | ||||||
| chr15:92975877
|
C | G | 248 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(245): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.2577+927C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 20/38 | chr15 | 92975877 | ||||||
| chr15:92976153
|
A | T | 51 | a0001c0001t0001g0016a0001c0002t0001g0091a0001c0002t0001g0233others(48): Show | 51 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.2577+1203A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 20/38 | chr15 | 92976153 | ||||||
| chr15:92976186
|
C | G | 1 | a0001c0001t0002g0085 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2577+1236C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 20/38 | chr15 | 92976186 | ||||||
| chr15:92976191
|
GA | G | 14 | a0001c0001t0001g0259a0001c0001t0006g0248a0001c0001t0006g0260others(11): Show | 14 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.2577+1251delA | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 20/38 | INFO_REALIGN_3_PRIME | chr15 | 92976191 | |||||
| chr15:92976248
|
T | G | 1 | a0001c0001t0001g0068 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2577+1298T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 20/38 | chr15 | 92976248 | ||||||
| chr15:92976581
|
A | G | 1 | a0001c0003t0003g0164 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2577+1631A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 20/38 | chr15 | 92976581 | ||||||
| chr15:92976653
|
CA | C | 227 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(224): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.2578-1565delA | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 20/38 | INFO_REALIGN_3_PRIME | chr15 | 92976653 | |||||
| chr15:92976878
|
G | A | 59 | a0001c0001t0001g0016a0001c0002t0001g0091a0001c0002t0001g0233others(56): Show | 59 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.2578-1356G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 20/38 | chr15 | 92976878 | ||||||
| chr15:92976898
|
CA | C | 6 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0038others(3): Show | 6 | HG01167.hp2 HG01169.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.2578-1321delA | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 20/38 | INFO_REALIGN_3_PRIME | chr15 | 92976898 | |||||
| chr15:92977026
|
A | C | 1 | a0001c0004t0004g0285 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2578-1208A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 20/38 | chr15 | 92977026 | ||||||
| chr15:92977077
|
A | G | 15 | a0001c0001t0001g0281a0001c0001t0002g0278a0001c0001t0002g0293others(12): Show | 15 | HG00544.hp1 HG00735.hp1 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.2578-1157A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 20/38 | chr15 | 92977077 | ||||||
| chr15:92977183
|
G | T | 3 | a0001c0003t0012g0126a0001c0003t0012g0133a0001c0003t0012g0134 | 3 | HG01257.hp1 HG01258.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.2578-1051G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 20/38 | chr15 | 92977183 | ||||||
| chr15:92977494
|
A | G | 2 | a0001c0010t0002g0182a0001c0010t0002g0222 | 2 | HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.2578-740A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 20/38 | chr15 | 92977494 | ||||||
| chr15:92977609
|
T | C | 62 | a0001c0001t0001g0016a0001c0001t0002g0293a0001c0001t0002g0294others(59): Show | 62 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.2578-625T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 20/38 | chr15 | 92977609 | ||||||
| chr15:92977646
|
C | A | 101 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(98): Show | 103 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.2578-588C>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 20/38 | chr15 | 92977646 | ||||||
| chr15:92977652
|
A | G | 2 | a0001c0003t0003g0175a0001c0003t0003g0290 | 2 | HG01070.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2578-582A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 20/38 | chr15 | 92977652 | ||||||
| chr15:92978421
|
T | G | 249 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(246): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.2727+38T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 21/38 | chr15 | 92978421 | ||||||
| chr15:92978428
|
CA | C | 14 | a0001c0001t0001g0259a0001c0001t0006g0248a0001c0001t0006g0260others(11): Show | 14 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.2727+46delA | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 21/38 | chr15 | 92978428 | ||||||
| chr15:92978750
|
A | G | 14 | a0001c0001t0001g0006a0001c0001t0001g0035a0001c0001t0001g0036others(11): Show | 15 | HG01069.hp1 HG01123.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.2727+367A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 21/38 | chr15 | 92978750 | ||||||
| chr15:92979082
|
G | A | 197 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(194): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.2728-53G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 21/38 | chr15 | 92979082 | ||||||
| chr15:92979132
|
C | T | 1 | a0001c0001t0001g0201 | 1 | NA19060.hp2 | splice_region_variant&intron_variant | LOW | c.2728-3C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 21/38 | chr15 | 92979132 | ||||||
| chr15:92979322
|
T | C | 7 | a0001c0002t0002g0231a0001c0002t0003g0228a0001c0002t0005g0220others(4): Show | 7 | HG01884.hp2 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.2876+39T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 22/38 | chr15 | 92979322 | ||||||
| chr15:92979418
|
A | G | 1 | a0001c0001t0008g0040 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2876+135A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 22/38 | chr15 | 92979418 | ||||||
| chr15:92979469
|
C | A | 1 | a0001c0015t0005g0288 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2876+186C>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 22/38 | chr15 | 92979469 | ||||||
| chr15:92979529
|
T | C | 15 | a0001c0001t0001g0281a0001c0001t0002g0278a0001c0001t0002g0293others(12): Show | 15 | HG00544.hp1 HG00735.hp1 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.2876+246T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 22/38 | chr15 | 92979529 | ||||||
| chr15:92979619
|
C | T | 14 | a0001c0001t0001g0259a0001c0001t0006g0248a0001c0001t0006g0260others(11): Show | 14 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.2876+336C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 22/38 | chr15 | 92979619 | ||||||
| chr15:92979637
|
G | GT | 15 | a0001c0001t0001g0006a0001c0001t0001g0035a0001c0001t0001g0036others(12): Show | 16 | HG01069.hp1 HG01123.hp2 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.2876+366dupT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 22/38 | INFO_REALIGN_3_PRIME | chr15 | 92979637 | |||||
| chr15:92979896
|
C | T | 6 | a0001c0001t0001g0007a0001c0003t0008g0147a0001c0009t0002g0043others(3): Show | 6 | HG00642.hp1 HG00673.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.2876+613C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 22/38 | chr15 | 92979896 | ||||||
| chr15:92979901
|
G | GATA | 7 | a0001c0002t0002g0231a0001c0002t0003g0228a0001c0002t0005g0220others(4): Show | 7 | HG01884.hp2 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.2876+634_2876+636d others(5): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 22/38 | INFO_REALIGN_3_PRIME | chr15 | 92979901 | |||||
| chr15:92979977
|
A | C | 1 | a0001c0015t0005g0288 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2876+694A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 22/38 | chr15 | 92979977 | ||||||
| chr15:92980037
|
T | TTTTG | 5 | a0001c0001t0001g0121a0001c0002t0003g0228a0001c0002t0005g0229others(2): Show | 5 | HG01884.hp2 HG02451.hp2 NA19000.hp2 others(2): Show |
intron_variant | MODIFIER | c.2877-758_2877-755d others(6): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 22/38 | INFO_REALIGN_3_PRIME | chr15 | 92980037 | |||||
| chr15:92980037
|
T | TTTTGTTT others(1): Show |
236 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(233): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.2877-762_2877-755d others(10): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 22/38 | INFO_REALIGN_3_PRIME | chr15 | 92980037 | |||||
| chr15:92980037
|
T | TTTTGTTT others(5): Show |
8 | a0001c0001t0001g0006a0001c0001t0001g0271a0001c0001t0001g0272others(5): Show | 9 | HG01069.hp1 HG01123.hp2 HG02683.hp2 others(6): Show |
intron_variant | MODIFIER | c.2876+766_2877-755d others(14): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 22/38 | INFO_REALIGN_3_PRIME | chr15 | 92980037 | |||||
| chr15:92980084
|
G | A | 1 | a0001c0001t0001g0036 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2877-731G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 22/38 | chr15 | 92980084 | ||||||
| chr15:92980222
|
CT | C | 24 | a0001c0001t0001g0007a0001c0001t0001g0029a0001c0001t0001g0041others(21): Show | 24 | HG00642.hp1 HG00673.hp2 HG01255.hp2 others(21): Show |
intron_variant | MODIFIER | c.2877-575delT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 22/38 | INFO_REALIGN_3_PRIME | chr15 | 92980222 | |||||
| chr15:92980222
|
CTT | C | 219 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(216): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.2877-576_2877-575d others(4): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 22/38 | INFO_REALIGN_3_PRIME | chr15 | 92980222 | |||||
| chr15:92980224
|
T | C | 3 | a0001c0001t0002g0278a0001c0002t0005g0277a0001c0002t0005g0279 | 3 | HG01167.hp2 HG01169.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2877-591T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 22/38 | chr15 | 92980224 | ||||||
| chr15:92980271
|
G | T | 14 | a0001c0001t0001g0006a0001c0001t0001g0035a0001c0001t0001g0036others(11): Show | 15 | HG01069.hp1 HG01123.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.2877-544G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 22/38 | chr15 | 92980271 | ||||||
| chr15:92980402
|
A | G | 61 | a0001c0001t0001g0016a0001c0001t0002g0293a0001c0001t0002g0294others(58): Show | 61 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.2877-413A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 22/38 | chr15 | 92980402 | ||||||
| chr15:92980433
|
G | A | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0011 | 3 | NA18967.hp2 NA18994.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.2877-382G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 22/38 | chr15 | 92980433 | ||||||
| chr15:92980477
|
G | A | 9 | a0001c0002t0001g0235a0001c0002t0001g0244a0001c0002t0001g0247others(6): Show | 9 | NA18939.hp2 NA18948.hp2 NA18966.hp1 others(6): Show |
intron_variant | MODIFIER | c.2877-338G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 22/38 | chr15 | 92980477 | ||||||
| chr15:92980751
|
A | G | 1 | a0001c0003t0014g0165 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2877-64A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 22/38 | chr15 | 92980751 | ||||||
| chr15:92980768
|
T | G | 5 | a0001c0001t0001g0067a0001c0001t0001g0082a0001c0001t0001g0093others(2): Show | 5 | HG00673.hp1 HG02155.hp1 HG02523.hp2 others(2): Show |
intron_variant | MODIFIER | c.2877-47T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 22/38 | chr15 | 92980768 | ||||||
| chr15:92980962
|
G | A | 1 | a0001c0001t0001g0072 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2973+51G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 23/38 | chr15 | 92980962 | ||||||
| chr15:92980968
|
A | G | 13 | a0001c0001t0001g0281a0001c0001t0002g0278a0001c0001t0002g0295others(10): Show | 13 | HG00735.hp1 HG00738.hp2 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.2973+57A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 23/38 | chr15 | 92980968 | ||||||
| chr15:92980972
|
T | C | 15 | a0001c0001t0002g0293a0001c0001t0002g0294a0001c0002t0001g0091others(12): Show | 15 | HG00099.hp2 HG00544.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.2973+61T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 23/38 | chr15 | 92980972 | ||||||
| chr15:92981082
|
A | G | 3 | a0001c0002t0002g0045a0001c0002t0002g0046a0001c0002t0002g0232 | 3 | HG03453.hp2 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2973+171A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 23/38 | chr15 | 92981082 | ||||||
| chr15:92981198
|
T | G | 7 | a0001c0002t0002g0231a0001c0002t0003g0228a0001c0002t0005g0220others(4): Show | 7 | HG01884.hp2 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.2974-167T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 23/38 | chr15 | 92981198 | ||||||
| chr15:92981300
|
C | G | 2 | a0001c0001t0001g0111a0001c0001t0001g0123 | 2 | NA18944.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.2974-65C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 23/38 | chr15 | 92981300 | ||||||
| chr15:92981309
|
T | C | 13 | a0001c0001t0001g0259a0001c0001t0006g0248a0001c0001t0006g0260others(10): Show | 13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.2974-56T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 23/38 | chr15 | 92981309 | ||||||
| chr15:92981315
|
A | G | 1 | a0001c0001t0007g0174 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2974-50A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 23/38 | chr15 | 92981315 | ||||||
| chr15:92981501
|
T | G | 1 | a0001c0010t0002g0182 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3066+44T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 24/38 | chr15 | 92981501 | ||||||
| chr15:92981619
|
A | C | 2 | a0001c0003t0003g0175a0001c0003t0003g0290 | 2 | HG01070.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.3066+162A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 24/38 | chr15 | 92981619 | ||||||
| chr15:92981620
|
G | C | 14 | a0001c0001t0001g0006a0001c0001t0001g0035a0001c0001t0001g0036others(11): Show | 15 | HG01069.hp1 HG01123.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.3066+163G>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 24/38 | chr15 | 92981620 | ||||||
| chr15:92981637
|
G | A | 51 | a0001c0002t0001g0091a0001c0002t0001g0233a0001c0002t0001g0234others(48): Show | 51 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.3066+180G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 24/38 | chr15 | 92981637 | ||||||
| chr15:92981779
|
A | G | 1 | a0001c0001t0002g0293 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.3066+322A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 24/38 | chr15 | 92981779 | ||||||
| chr15:92982120
|
T | C | 1 | a0001c0001t0001g0060 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.3066+663T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 24/38 | chr15 | 92982120 | ||||||
| chr15:92982383
|
T | C | 2 | a0001c0001t0001g0098a0001c0001t0001g0101 | 2 | HG01346.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.3066+926T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 24/38 | chr15 | 92982383 | ||||||
| chr15:92982420
|
G | A | 7 | a0001c0002t0002g0231a0001c0002t0003g0228a0001c0002t0005g0220others(4): Show | 7 | HG01884.hp2 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.3066+963G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 24/38 | chr15 | 92982420 | ||||||
| chr15:92982636
|
T | A | 1 | a0001c0007t0007g0030 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3066+1179T>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 24/38 | chr15 | 92982636 | ||||||
| chr15:92982651
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.3066+1194G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 24/38 | chr15 | 92982651 | ||||||
| chr15:92982671
|
T | C | 3 | a0001c0002t0002g0045a0001c0002t0002g0046a0001c0002t0002g0232 | 3 | HG03453.hp2 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3066+1214T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 24/38 | chr15 | 92982671 | ||||||
| chr15:92982773
|
A | G | 70 | a0001c0001t0001g0016a0001c0001t0002g0293a0001c0001t0002g0294others(67): Show | 70 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.3066+1316A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 24/38 | chr15 | 92982773 | ||||||
| chr15:92982869
|
G | A | 5 | a0001c0001t0007g0174a0001c0009t0002g0043a0001c0009t0002g0048others(2): Show | 5 | HG00642.hp1 HG00673.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.3066+1412G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 24/38 | chr15 | 92982869 | ||||||
| chr15:92982878
|
G | T | 1 | a0001c0001t0007g0174 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3066+1421G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 24/38 | chr15 | 92982878 | ||||||
| chr15:92983008
|
T | C | 2 | a0001c0002t0003g0228a0001c0002t0005g0229 | 2 | HG01884.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.3067-1322T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 24/38 | chr15 | 92983008 | ||||||
| chr15:92983135
|
A | G | 6 | a0001c0001t0001g0007a0001c0001t0007g0174a0001c0009t0002g0043others(3): Show | 6 | HG00642.hp1 HG00673.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.3067-1195A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 24/38 | chr15 | 92983135 | ||||||
| chr15:92983219
|
A | G | 1 | a0001c0001t0008g0040 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.3067-1111A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 24/38 | chr15 | 92983219 | ||||||
| chr15:92983300
|
A | C | 1 | a0001c0016t0002g0047 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.3067-1030A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 24/38 | chr15 | 92983300 | ||||||
| chr15:92983651
|
C | T | 3 | a0001c0008t0001g0127a0001c0008t0001g0145a0001c0008t0001g0146 | 3 | HG00323.hp2 HG02486.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.3067-679C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 24/38 | chr15 | 92983651 | ||||||
| chr15:92983663
|
T | G | 62 | a0001c0001t0001g0016a0001c0001t0002g0293a0001c0001t0002g0294others(59): Show | 62 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.3067-667T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 24/38 | chr15 | 92983663 | ||||||
| chr15:92983671
|
G | A | 1 | a0001c0013t0019g0168 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3067-659G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 24/38 | chr15 | 92983671 | ||||||
| chr15:92983738
|
A | G | 236 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(233): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.3067-592A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 24/38 | chr15 | 92983738 | ||||||
| chr15:92983808
|
C | T | 5 | a0001c0001t0001g0007a0001c0009t0002g0043a0001c0009t0002g0048others(2): Show | 5 | HG00642.hp1 HG00673.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.3067-522C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 24/38 | chr15 | 92983808 | ||||||
| chr15:92984166
|
G | T | 1 | a0001c0001t0001g0212 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3067-164G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 24/38 | chr15 | 92984166 | ||||||
| chr15:92984564
|
A | T | 59 | a0001c0001t0001g0016a0001c0002t0001g0091a0001c0002t0001g0233others(56): Show | 59 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.3237+64A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 25/38 | chr15 | 92984564 | ||||||
| chr15:92984613
|
G | A | 234 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(231): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.3237+113G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 25/38 | chr15 | 92984613 | ||||||
| chr15:92984629
|
T | C | 1 | a0001c0001t0001g0072 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.3237+129T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 25/38 | chr15 | 92984629 | ||||||
| chr15:92984650
|
A | G | 13 | a0001c0001t0001g0259a0001c0001t0006g0248a0001c0001t0006g0260others(10): Show | 13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.3237+150A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 25/38 | chr15 | 92984650 | ||||||
| chr15:92984758
|
G | C | 59 | a0001c0001t0001g0016a0001c0002t0001g0091a0001c0002t0001g0233others(56): Show | 59 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.3237+258G>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 25/38 | chr15 | 92984758 | ||||||
| chr15:92984785
|
C | T | 77 | a0001c0001t0001g0002a0001c0001t0001g0027a0001c0001t0001g0028others(74): Show | 78 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.3237+285C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 25/38 | chr15 | 92984785 | ||||||
| chr15:92984823
|
A | G | 8 | a0001c0001t0001g0007a0001c0001t0007g0174a0001c0009t0002g0043others(5): Show | 8 | HG00642.hp1 HG00673.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.3237+323A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 25/38 | chr15 | 92984823 | ||||||
| chr15:92984824
|
G | A | 4 | a0001c0002t0008g0015a0001c0004t0007g0020a0001c0004t0017g0019others(1): Show | 4 | HG01070.hp2 HG01123.hp1 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.3237+324G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 25/38 | chr15 | 92984824 | ||||||
| chr15:92985222
|
A | G | 2 | a0001c0002t0003g0228a0001c0002t0005g0229 | 2 | HG01884.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.3238-276A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 25/38 | chr15 | 92985222 | ||||||
| chr15:92985243
|
T | C | 224 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(221): Show | 228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.3238-255T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 25/38 | chr15 | 92985243 | ||||||
| chr15:92985689
|
G | A | 5 | a0001c0003t0003g0161a0001c0003t0003g0167a0001c0003t0003g0171others(2): Show | 5 | HG01109.hp2 HG01884.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.3413+16G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92985689 | ||||||
| chr15:92985715
|
C | T | 1 | a0001c0002t0002g0156 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3413+42C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92985715 | ||||||
| chr15:92985716
|
G | A | 4 | a0001c0002t0002g0181a0001c0002t0002g0223a0001c0002t0005g0224others(1): Show | 4 | HG02572.hp2 HG03209.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.3413+43G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92985716 | ||||||
| chr15:92986482
|
G | C | 1 | a0001c0001t0008g0040 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.3413+809G>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92986482 | ||||||
| chr15:92986496
|
TACTG | T | 4 | a0001c0002t0002g0181a0001c0002t0002g0223a0001c0002t0005g0224others(1): Show | 4 | HG02572.hp2 HG03209.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.3413+826_3413+829d others(6): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | INFO_REALIGN_3_PRIME | chr15 | 92986496 | |||||
| chr15:92986510
|
C | T | 2 | a0001c0004t0007g0018a0001c0004t0007g0021 | 2 | HG01433.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.3413+837C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92986510 | ||||||
| chr15:92986785
|
A | G | 1 | a0001c0013t0019g0168 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3413+1112A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92986785 | ||||||
| chr15:92986906
|
T | A | 14 | a0001c0001t0001g0006a0001c0001t0001g0035a0001c0001t0001g0036others(11): Show | 15 | HG01069.hp1 HG01123.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.3413+1233T>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92986906 | ||||||
| chr15:92986952
|
G | A | 2 | a0001c0001t0001g0116a0001c0001t0001g0117 | 2 | HG00438.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.3413+1279G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92986952 | ||||||
| chr15:92986989
|
G | C | 1 | a0001c0002t0001g0250 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.3413+1316G>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92986989 | ||||||
| chr15:92987029
|
C | T | 1 | a0001c0003t0003g0290 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3413+1356C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92987029 | ||||||
| chr15:92987030
|
G | C | 234 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(231): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.3413+1357G>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92987030 | ||||||
| chr15:92987137
|
G | A | 1 | a0001c0001t0002g0085 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3413+1464G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92987137 | ||||||
| chr15:92987185
|
G | A | 148 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(145): Show | 152 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.3413+1512G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92987185 | ||||||
| chr15:92987319
|
C | A | 1 | a0001c0002t0016g0280 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.3413+1646C>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92987319 | ||||||
| chr15:92987335
|
C | T | 1 | a0001c0003t0003g0139 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3413+1662C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92987335 | ||||||
| chr15:92987473
|
C | T | 134 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0016others(131): Show | 137 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.3413+1800C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92987473 | ||||||
| chr15:92987616
|
GA | G | 235 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(232): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.3413+1956delA | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | INFO_REALIGN_3_PRIME | chr15 | 92987616 | |||||
| chr15:92987781
|
T | G | 1 | a0001c0002t0002g0156 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3413+2108T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92987781 | ||||||
| chr15:92987800
|
A | G | 1 | a0001c0013t0019g0168 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3413+2127A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92987800 | ||||||
| chr15:92987806
|
C | T | 2 | a0001c0002t0003g0228a0001c0002t0005g0229 | 2 | HG01884.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.3413+2133C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92987806 | ||||||
| chr15:92987857
|
T | A | 253 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(250): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.3413+2184T>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92987857 | ||||||
| chr15:92988011
|
C | T | 13 | a0001c0001t0001g0259a0001c0001t0006g0248a0001c0001t0006g0260others(10): Show | 13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.3413+2338C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92988011 | ||||||
| chr15:92988082
|
CT | C | 51 | a0001c0002t0001g0091a0001c0002t0001g0233a0001c0002t0001g0234others(48): Show | 51 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.3413+2421delT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | INFO_REALIGN_3_PRIME | chr15 | 92988082 | |||||
| chr15:92988105
|
G | A | 1 | a0001c0002t0002g0181 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3413+2432G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92988105 | ||||||
| chr15:92988245
|
C | T | 13 | a0001c0001t0001g0259a0001c0001t0006g0248a0001c0001t0006g0260others(10): Show | 13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.3413+2572C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92988245 | ||||||
| chr15:92988484
|
C | T | 222 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(219): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.3413+2811C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92988484 | ||||||
| chr15:92988568
|
G | A | 4 | a0001c0009t0002g0043a0001c0009t0002g0048a0001c0009t0012g0044others(1): Show | 4 | HG00642.hp1 HG00673.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.3413+2895G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92988568 | ||||||
| chr15:92988594
|
A | G | 14 | a0001c0001t0001g0006a0001c0001t0001g0035a0001c0001t0001g0036others(11): Show | 15 | HG01069.hp1 HG01123.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.3414-2882A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92988594 | ||||||
| chr15:92988640
|
A | G | 1 | a0001c0001t0001g0185 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.3414-2836A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92988640 | ||||||
| chr15:92988677
|
A | T | 1 | a0001c0014t0005g0226 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3414-2799A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92988677 | ||||||
| chr15:92988777
|
A | G | 14 | a0001c0001t0001g0006a0001c0001t0001g0035a0001c0001t0001g0036others(11): Show | 15 | HG01069.hp1 HG01123.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.3414-2699A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92988777 | ||||||
| chr15:92989025
|
CT | C | 88 | a0001c0001t0001g0016a0001c0001t0001g0072a0001c0001t0001g0259others(85): Show | 88 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.3414-2428delT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | INFO_REALIGN_3_PRIME | chr15 | 92989025 | |||||
| chr15:92989025
|
CTT | C | 136 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(133): Show | 139 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.3414-2429_3414-242 others(6): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | INFO_REALIGN_3_PRIME | chr15 | 92989025 | |||||
| chr15:92989025
|
CTTT | C | 16 | a0001c0001t0001g0006a0001c0001t0001g0035a0001c0001t0001g0036others(13): Show | 17 | HG01123.hp2 HG01192.hp1 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.3414-2430_3414-242 others(7): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | INFO_REALIGN_3_PRIME | chr15 | 92989025 | |||||
| chr15:92989141
|
C | A | 4 | a0001c0001t0024g0077a0001c0005t0007g0050a0001c0005t0007g0090others(1): Show | 4 | HG00099.hp1 HG00140.hp1 HG01081.hp1 others(1): Show |
intron_variant | MODIFIER | c.3414-2335C>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92989141 | ||||||
| chr15:92989321
|
C | T | 1 | a0001c0001t0007g0174 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3414-2155C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92989321 | ||||||
| chr15:92989520
|
T | C | 1 | a0001c0003t0003g0175 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.3414-1956T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92989520 | ||||||
| chr15:92989877
|
C | T | 16 | a0001c0001t0001g0281a0001c0001t0002g0278a0001c0001t0002g0295others(13): Show | 16 | HG00099.hp2 HG00735.hp1 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.3414-1599C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92989877 | ||||||
| chr15:92989970
|
C | T | 9 | a0001c0002t0002g0156a0001c0002t0002g0231a0001c0002t0003g0228others(6): Show | 9 | HG01884.hp2 HG02257.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.3414-1506C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92989970 | ||||||
| chr15:92990035
|
G | A | 1 | a0001c0001t0007g0174 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3414-1441G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92990035 | ||||||
| chr15:92990181
|
C | G | 1 | a0001c0001t0006g0264 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.3414-1295C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92990181 | ||||||
| chr15:92990316
|
T | C | 14 | a0001c0001t0001g0006a0001c0001t0001g0035a0001c0001t0001g0036others(11): Show | 15 | HG01069.hp1 HG01123.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.3414-1160T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92990316 | ||||||
| chr15:92990341
|
C | T | 3 | a0001c0002t0002g0045a0001c0002t0002g0046a0001c0002t0002g0232 | 3 | HG03453.hp2 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3414-1135C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92990341 | ||||||
| chr15:92990392
|
C | T | 1 | a0001c0007t0007g0030 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3414-1084C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92990392 | ||||||
| chr15:92990716
|
C | T | 3 | a0001c0002t0002g0045a0001c0002t0002g0046a0001c0002t0002g0232 | 3 | HG03453.hp2 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3414-760C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92990716 | ||||||
| chr15:92990875
|
G | A | 3 | a0001c0002t0002g0223a0001c0002t0005g0224a0001c0002t0005g0225 | 3 | HG02572.hp2 HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3414-601G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92990875 | ||||||
| chr15:92991147
|
GAC | G | 14 | a0001c0001t0001g0006a0001c0001t0001g0035a0001c0001t0001g0036others(11): Show | 15 | HG01069.hp1 HG01123.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.3414-325_3414-324d others(4): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | INFO_REALIGN_3_PRIME | chr15 | 92991147 | |||||
| chr15:92991222
|
C | T | 128 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0026others(125): Show | 131 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.3414-254C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92991222 | ||||||
| chr15:92991703
|
A | G | 144 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(141): Show | 148 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.3455+186A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 27/38 | chr15 | 92991703 | ||||||
| chr15:92991708
|
G | C | 1 | a0001c0002t0002g0156 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3455+191G>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 27/38 | chr15 | 92991708 | ||||||
| chr15:92991709
|
A | C | 1 | a0001c0002t0002g0156 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3455+192A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 27/38 | chr15 | 92991709 | ||||||
| chr15:92991964
|
G | A | 5 | a0001c0001t0007g0174a0001c0009t0002g0043a0001c0009t0002g0048others(2): Show | 5 | HG00642.hp1 HG00673.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.3455+447G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 27/38 | chr15 | 92991964 | ||||||
| chr15:92992150
|
A | C | 1 | a0001c0002t0009g0022 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.3455+633A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 27/38 | chr15 | 92992150 | ||||||
| chr15:92992263
|
A | G | 1 | a0001c0003t0005g0166 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3456-596A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 27/38 | chr15 | 92992263 | ||||||
| chr15:92992323
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.3456-536C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 27/38 | chr15 | 92992323 | ||||||
| chr15:92992467
|
A | T | 1 | a0001c0001t0001g0098 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.3456-392A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 27/38 | chr15 | 92992467 | ||||||
| chr15:92992560
|
C | T | 1 | a0001c0001t0002g0085 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3456-299C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 27/38 | chr15 | 92992560 | ||||||
| chr15:92992725
|
A | G | 1 | a0001c0015t0005g0288 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3456-134A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 27/38 | chr15 | 92992725 | ||||||
| chr15:92992843
|
A | G | 1 | a0001c0001t0001g0100 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.3456-16A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 27/38 | chr15 | 92992843 | ||||||
| chr15:92993049
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.3595+51G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92993049 | ||||||
| chr15:92993174
|
C | T | 1 | a0001c0002t0002g0181 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3595+176C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92993174 | ||||||
| chr15:92993219
|
T | C | 1 | a0001c0001t0006g0269 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.3595+221T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92993219 | ||||||
| chr15:92993394
|
A | C | 3 | a0001c0002t0002g0223a0001c0002t0005g0224a0001c0002t0005g0225 | 3 | HG02572.hp2 HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3595+396A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92993394 | ||||||
| chr15:92993396
|
G | T | 134 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(131): Show | 137 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.3595+398G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92993396 | ||||||
| chr15:92993436
|
G | A | 234 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(231): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.3595+438G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92993436 | ||||||
| chr15:92993440
|
C | A | 1 | a0001c0003t0003g0171 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3595+442C>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92993440 | ||||||
| chr15:92993568
|
A | AAGATATA others(7): Show |
79 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0027others(76): Show | 80 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.3595+572_3595+573i others(16): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | INFO_REALIGN_3_PRIME | chr15 | 92993568 | |||||
| chr15:92993571
|
C | G | 79 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0027others(76): Show | 80 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.3595+573C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92993571 | ||||||
| chr15:92993574
|
G | T | 79 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0027others(76): Show | 80 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.3595+576G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92993574 | ||||||
| chr15:92993578
|
T | A | 79 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0027others(76): Show | 80 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.3595+580T>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92993578 | ||||||
| chr15:92993581
|
A | G | 79 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0027others(76): Show | 80 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.3595+583A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92993581 | ||||||
| chr15:92993635
|
T | C | 135 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(132): Show | 138 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.3595+637T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92993635 | ||||||
| chr15:92993680
|
C | G | 71 | a0001c0001t0002g0293a0001c0001t0002g0294a0001c0002t0001g0091others(68): Show | 71 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.3595+682C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92993680 | ||||||
| chr15:92993769
|
G | A | 1 | a0001c0001t0007g0174 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3595+771G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92993769 | ||||||
| chr15:92993806
|
A | C | 1 | a0001c0001t0001g0081 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3595+808A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92993806 | ||||||
| chr15:92993839
|
A | G | 1 | a0001c0001t0001g0068 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3595+841A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92993839 | ||||||
| chr15:92993883
|
GGCTGCAG others(17): Show |
G | 1 | a0001c0002t0001g0239 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.3595+910_3595+933d others(26): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | INFO_REALIGN_3_PRIME | chr15 | 92993883 | |||||
| chr15:92993938
|
C | T | 3 | a0001c0002t0002g0045a0001c0002t0002g0046a0001c0002t0002g0232 | 3 | HG03453.hp2 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3595+940C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92993938 | ||||||
| chr15:92994149
|
G | A | 1 | a0001c0001t0001g0067 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.3595+1151G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92994149 | ||||||
| chr15:92994418
|
A | G | 1 | a0001c0004t0007g0018 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.3595+1420A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92994418 | ||||||
| chr15:92994589
|
T | C | 1 | a0001c0001t0001g0215 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.3595+1591T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92994589 | ||||||
| chr15:92994632
|
A | G | 1 | a0001c0002t0002g0275 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.3595+1634A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92994632 | ||||||
| chr15:92994687
|
G | A | 1 | a0001c0013t0019g0168 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3595+1689G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92994687 | ||||||
| chr15:92994728
|
G | A | 56 | a0001c0001t0002g0293a0001c0001t0002g0294a0001c0002t0001g0091others(53): Show | 56 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.3595+1730G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92994728 | ||||||
| chr15:92994886
|
T | C | 1 | a0001c0001t0001g0281 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3595+1888T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92994886 | ||||||
| chr15:92994900
|
T | C | 1 | a0001c0001t0006g0269 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.3595+1902T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92994900 | ||||||
| chr15:92995200
|
C | G | 131 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(128): Show | 134 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.3596-1757C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92995200 | ||||||
| chr15:92995246
|
C | T | 1 | a0001c0001t0001g0027 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.3596-1711C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92995246 | ||||||
| chr15:92995299
|
C | T | 1 | a0001c0003t0014g0165 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3596-1658C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92995299 | ||||||
| chr15:92995421
|
T | C | 64 | a0001c0001t0002g0293a0001c0001t0002g0294a0001c0002t0001g0091others(61): Show | 64 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.3596-1536T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92995421 | ||||||
| chr15:92995427
|
G | T | 1 | a0001c0002t0002g0156 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3596-1530G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92995427 | ||||||
| chr15:92995452
|
T | C | 1 | a0001c0013t0019g0168 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3596-1505T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92995452 | ||||||
| chr15:92995491
|
CGTGT | C | 148 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(145): Show | 152 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.3596-1463_3596-146 others(8): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | INFO_REALIGN_3_PRIME | chr15 | 92995491 | |||||
| chr15:92995653
|
CT | C | 13 | a0001c0001t0001g0259a0001c0001t0006g0248a0001c0001t0006g0260others(10): Show | 13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.3596-1303delT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92995653 | ||||||
| chr15:92995776
|
G | T | 3 | a0001c0001t0001g0007a0001c0009t0002g0048a0001c0016t0002g0047 | 3 | HG00642.hp1 HG00673.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.3596-1181G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92995776 | ||||||
| chr15:92995814
|
C | T | 1 | a0001c0001t0001g0059 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3596-1143C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92995814 | ||||||
| chr15:92995861
|
A | G | 2 | a0001c0009t0002g0043a0001c0009t0012g0044 | 2 | HG02258.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.3596-1096A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92995861 | ||||||
| chr15:92996160
|
C | CT | 15 | a0001c0001t0001g0006a0001c0001t0001g0028a0001c0001t0001g0035others(12): Show | 16 | HG01069.hp1 HG01123.hp2 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.3596-780dupT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | INFO_REALIGN_3_PRIME | chr15 | 92996160 | |||||
| chr15:92996160
|
CT | C | 149 | a0001c0001t0001g0007a0001c0001t0001g0099a0001c0001t0001g0132others(146): Show | 151 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(148): Show |
intron_variant | MODIFIER | c.3596-780delT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | INFO_REALIGN_3_PRIME | chr15 | 92996160 | |||||
| chr15:92996190
|
C | T | 4 | a0001c0003t0003g0139a0001c0003t0003g0170a0001c0010t0002g0182others(1): Show | 4 | HG02486.hp2 HG02970.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.3596-767C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92996190 | ||||||
| chr15:92996191
|
G | A | 6 | a0001c0001t0001g0007a0001c0001t0007g0174a0001c0009t0002g0043others(3): Show | 6 | HG00642.hp1 HG00673.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.3596-766G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92996191 | ||||||
| chr15:92996251
|
C | A | 1 | a0001c0002t0002g0181 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3596-706C>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92996251 | ||||||
| chr15:92996378
|
T | G | 3 | a0001c0002t0002g0045a0001c0002t0002g0046a0001c0002t0002g0232 | 3 | HG03453.hp2 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3596-579T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92996378 | ||||||
| chr15:92996395
|
C | T | 134 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0016others(131): Show | 137 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.3596-562C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92996395 | ||||||
| chr15:92996436
|
A | T | 134 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0016others(131): Show | 137 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.3596-521A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92996436 | ||||||
| chr15:92996730
|
C | G | 2 | a0001c0003t0001g0129a0001c0006t0004g0163 | 2 | HG02630.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.3596-227C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92996730 | ||||||
| chr15:92996759
|
C | A | 2 | a0001c0005t0004g0153a0001c0005t0004g0154 | 2 | NA20752.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3596-198C>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92996759 | ||||||
| chr15:92996859
|
T | C | 63 | a0001c0001t0001g0016a0001c0001t0002g0293a0001c0001t0002g0294others(60): Show | 63 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.3596-98T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92996859 | ||||||
| chr15:92996937
|
G | A | 6 | a0001c0002t0002g0181a0001c0002t0002g0223a0001c0002t0005g0224others(3): Show | 6 | HG01243.hp2 HG02572.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.3596-20G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92996937 | ||||||
| chr15:92997526
|
G | A | 2 | a0001c0005t0004g0153a0001c0005t0004g0154 | 2 | NA20752.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3885+123G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 30/38 | chr15 | 92997526 | ||||||
| chr15:92997538
|
A | G | 13 | a0001c0001t0001g0259a0001c0001t0006g0248a0001c0001t0006g0260others(10): Show | 13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.3885+135A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 30/38 | chr15 | 92997538 | ||||||
| chr15:92997699
|
T | C | 5 | a0001c0001t0001g0007a0001c0009t0002g0043a0001c0009t0002g0048others(2): Show | 5 | HG00642.hp1 HG00673.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.3885+296T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 30/38 | chr15 | 92997699 | ||||||
| chr15:92997702
|
A | G | 1 | a0001c0001t0001g0210 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.3885+299A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 30/38 | chr15 | 92997702 | ||||||
| chr15:92997767
|
C | T | 209 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(206): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.3885+364C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 30/38 | chr15 | 92997767 | ||||||
| chr15:92997892
|
A | G | 1 | a0001c0006t0004g0158 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3885+489A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 30/38 | chr15 | 92997892 | ||||||
| chr15:92997959
|
A | AC | 237 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(234): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.3886-540_3886-539i others(3): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 30/38 | chr15 | 92997959 | ||||||
| chr15:92998479
|
C | T | 1 | a0001c0001t0001g0111 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.3886-20C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 30/38 | chr15 | 92998479 | ||||||
| chr15:92998719
|
A | G | 1 | a0001c0003t0003g0175 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.4008+98A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 31/38 | chr15 | 92998719 | ||||||
| chr15:92998723
|
T | G | 1 | a0001c0001t0001g0027 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.4008+102T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 31/38 | chr15 | 92998723 | ||||||
| chr15:92998769
|
G | C | 1 | a0001c0002t0002g0156 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4008+148G>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 31/38 | chr15 | 92998769 | ||||||
| chr15:92998770
|
C | G | 250 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(247): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.4008+149C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 31/38 | chr15 | 92998770 | ||||||
| chr15:92998849
|
T | C | 235 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(232): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.4008+228T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 31/38 | chr15 | 92998849 | ||||||
| chr15:92998858
|
C | T | 130 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0026others(127): Show | 133 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.4008+237C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 31/38 | chr15 | 92998858 | ||||||
| chr15:92998879
|
T | C | 1 | a0001c0004t0010g0106 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.4008+258T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 31/38 | chr15 | 92998879 | ||||||
| chr15:92998941
|
G | A | 1 | a0001c0005t0004g0154 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4008+320G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 31/38 | chr15 | 92998941 | ||||||
| chr15:92998961
|
GTAATCCC others(9): Show |
G | 1 | a0001c0010t0002g0182 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.4008+341_4008+356d others(18): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 31/38 | chr15 | 92998961 | ||||||
| chr15:92998987
|
G | A | 1 | a0001c0010t0002g0222 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.4008+366G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 31/38 | chr15 | 92998987 | ||||||
| chr15:92999051
|
T | C | 130 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0026others(127): Show | 133 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.4008+430T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 31/38 | chr15 | 92999051 | ||||||
| chr15:92999083
|
C | CA | 21 | a0001c0003t0001g0129a0001c0003t0002g0125a0001c0003t0002g0137others(18): Show | 22 | HG01069.hp2 HG01243.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.4008+496dupA | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 31/38 | INFO_REALIGN_3_PRIME | chr15 | 92999083 | |||||
| chr15:92999083
|
C | CAA | 6 | a0001c0003t0002g0162a0001c0003t0003g0167a0001c0003t0003g0171others(3): Show | 6 | HG01109.hp2 HG01884.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.4008+495_4008+496d others(4): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 31/38 | INFO_REALIGN_3_PRIME | chr15 | 92999083 | |||||
| chr15:92999083
|
C | CAAAAAAA others(5): Show |
1 | a0001c0001t0001g0281 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.4008+485_4008+496d others(14): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 31/38 | INFO_REALIGN_3_PRIME | chr15 | 92999083 | |||||
| chr15:92999083
|
C | CAAAAAAA others(8): Show |
1 | a0001c0005t0004g0287 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.4008+482_4008+496d others(17): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 31/38 | INFO_REALIGN_3_PRIME | chr15 | 92999083 | |||||
| chr15:92999083
|
C | CAAAAAAA others(13): Show |
1 | a0001c0005t0004g0154 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4008+477_4008+496d others(22): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 31/38 | INFO_REALIGN_3_PRIME | chr15 | 92999083 | |||||
| chr15:92999083
|
CA | C | 10 | a0001c0001t0002g0278a0001c0003t0001g0144a0001c0003t0003g0128others(7): Show | 11 | HG00323.hp2 HG01070.hp1 HG01346.hp2 others(8): Show |
intron_variant | MODIFIER | c.4008+496delA | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 31/38 | INFO_REALIGN_3_PRIME | chr15 | 92999083 | |||||
| chr15:92999083
|
CAAA | C | 6 | a0001c0001t0002g0294a0001c0001t0006g0264a0001c0001t0006g0270others(3): Show | 6 | HG00642.hp1 HG01361.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.4008+494_4008+496d others(5): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 31/38 | INFO_REALIGN_3_PRIME | chr15 | 92999083 | |||||
| chr15:92999083
|
CAAAA | C | 25 | a0001c0001t0001g0259a0001c0001t0002g0293a0001c0001t0006g0248others(22): Show | 25 | HG00544.hp1 HG00639.hp1 HG00673.hp2 others(22): Show |
intron_variant | MODIFIER | c.4008+493_4008+496d others(6): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 31/38 | INFO_REALIGN_3_PRIME | chr15 | 92999083 | |||||
| chr15:92999083
|
CAAAAA | C | 52 | a0001c0001t0001g0007a0001c0001t0001g0016a0001c0001t0006g0266others(49): Show | 52 | HG00099.hp2 HG00558.hp1 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.4008+492_4008+496d others(7): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 31/38 | INFO_REALIGN_3_PRIME | chr15 | 92999083 | |||||
| chr15:92999083
|
CAAAAAA | C | 9 | a0001c0001t0001g0207a0001c0001t0009g0009a0001c0001t0009g0011others(6): Show | 9 | HG00423.hp2 HG03453.hp1 HG03453.hp2 others(6): Show |
intron_variant | MODIFIER | c.4008+491_4008+496d others(8): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 31/38 | INFO_REALIGN_3_PRIME | chr15 | 92999083 | |||||
| chr15:92999083
|
CAAAAAAA | C | 26 | a0001c0001t0001g0006a0001c0001t0001g0034a0001c0001t0001g0035others(23): Show | 27 | HG00423.hp1 HG01069.hp1 HG01123.hp2 others(24): Show |
intron_variant | MODIFIER | c.4008+490_4008+496d others(9): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 31/38 | INFO_REALIGN_3_PRIME | chr15 | 92999083 | |||||
| chr15:92999083
|
CAAAAAAA others(1): Show |
C | 115 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0026others(112): Show | 118 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(115): Show |
intron_variant | MODIFIER | c.4008+489_4008+496d others(10): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 31/38 | INFO_REALIGN_3_PRIME | chr15 | 92999083 | |||||
| chr15:92999083
|
CAAAAAAA others(7): Show |
C | 1 | a0001c0013t0019g0168 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4008+483_4008+496d others(16): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 31/38 | INFO_REALIGN_3_PRIME | chr15 | 92999083 | |||||
| chr15:92999214
|
C | G | 13 | a0001c0001t0001g0259a0001c0001t0006g0248a0001c0001t0006g0260others(10): Show | 13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.4008+593C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 31/38 | chr15 | 92999214 | ||||||
| chr15:92999279
|
C | T | 1 | a0001c0002t0001g0286 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.4008+658C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 31/38 | chr15 | 92999279 | ||||||
| chr15:92999365
|
T | G | 26 | a0001c0001t0001g0007a0001c0001t0001g0259a0001c0001t0006g0248others(23): Show | 26 | HG00642.hp1 HG00673.hp2 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.4008+744T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 31/38 | chr15 | 92999365 | ||||||
| chr15:92999683
|
C | T | 2 | a0001c0002t0003g0228a0001c0002t0005g0229 | 2 | HG01884.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.4009-829C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 31/38 | chr15 | 92999683 | ||||||
| chr15:92999698
|
A | T | 6 | a0001c0001t0001g0007a0001c0001t0007g0174a0001c0009t0002g0043others(3): Show | 6 | HG00642.hp1 HG00673.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.4009-814A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 31/38 | chr15 | 92999698 | ||||||
| chr15:92999705
|
G | T | 41 | a0001c0002t0001g0233a0001c0002t0001g0234a0001c0002t0001g0235others(38): Show | 41 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.4009-807G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 31/38 | chr15 | 92999705 | ||||||
| chr15:92999712
|
A | G | 15 | a0001c0001t0001g0281a0001c0001t0002g0278a0001c0001t0002g0293others(12): Show | 15 | HG00544.hp1 HG00735.hp1 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.4009-800A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 31/38 | chr15 | 92999712 | ||||||
| chr15:92999812
|
A | G | 14 | a0001c0003t0001g0135a0001c0003t0001g0142a0001c0003t0001g0144others(11): Show | 15 | HG00323.hp2 HG00741.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.4009-700A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 31/38 | chr15 | 92999812 | ||||||
| chr15:92999907
|
A | T | 2 | a0001c0001t0003g0274a0001c0001t0005g0179 | 2 | NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.4009-605A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 31/38 | chr15 | 92999907 | ||||||
| chr15:93000057
|
G | A | 1 | a0001c0002t0002g0156 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4009-455G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 31/38 | chr15 | 93000057 | ||||||
| chr15:93000301
|
A | T | 59 | a0001c0001t0001g0016a0001c0002t0001g0091a0001c0002t0001g0233others(56): Show | 59 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.4009-211A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 31/38 | chr15 | 93000301 | ||||||
| chr15:93000677
|
A | G | 1 | a0001c0004t0007g0017 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.4137+37A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 32/38 | chr15 | 93000677 | ||||||
| chr15:93000726
|
G | A | 133 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0026others(130): Show | 136 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.4137+86G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 32/38 | chr15 | 93000726 | ||||||
| chr15:93000782
|
G | A | 1 | a0001c0003t0012g0133 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.4137+142G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 32/38 | chr15 | 93000782 | ||||||
| chr15:93000821
|
A | T | 1 | a0001c0001t0001g0076 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.4137+181A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 32/38 | chr15 | 93000821 | ||||||
| chr15:93000823
|
A | G | 133 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0026others(130): Show | 136 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.4137+183A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 32/38 | chr15 | 93000823 | ||||||
| chr15:93000873
|
T | C | 1 | a0001c0013t0019g0168 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4137+233T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 32/38 | chr15 | 93000873 | ||||||
| chr15:93000893
|
A | G | 2 | a0001c0005t0004g0153a0001c0005t0004g0154 | 2 | NA20752.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.4137+253A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 32/38 | chr15 | 93000893 | ||||||
| chr15:93000909
|
G | A | 1 | a0001c0002t0002g0156 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4137+269G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 32/38 | chr15 | 93000909 | ||||||
| chr15:93001041
|
G | A | 3 | a0001c0002t0002g0045a0001c0002t0002g0046a0001c0002t0002g0232 | 3 | HG03453.hp2 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.4137+401G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 32/38 | chr15 | 93001041 | ||||||
| chr15:93001216
|
C | G | 6 | a0001c0001t0001g0065a0001c0001t0001g0069a0001c0001t0024g0077others(3): Show | 6 | HG00099.hp1 HG00140.hp1 HG01081.hp1 others(3): Show |
intron_variant | MODIFIER | c.4137+576C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 32/38 | chr15 | 93001216 | ||||||
| chr15:93001223
|
C | T | 1 | a0001c0001t0006g0080 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.4137+583C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 32/38 | chr15 | 93001223 | ||||||
| chr15:93001376
|
A | G | 1 | a0001c0003t0008g0147 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.4137+736A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 32/38 | chr15 | 93001376 | ||||||
| chr15:93001466
|
T | C | 237 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(234): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.4138-711T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 32/38 | chr15 | 93001466 | ||||||
| chr15:93001999
|
A | G | 1 | a0001c0005t0007g0050 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.4138-178A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 32/38 | chr15 | 93001999 | ||||||
| chr15:93002018
|
G | A | 3 | a0001c0002t0002g0223a0001c0002t0005g0224a0001c0002t0005g0225 | 3 | HG02572.hp2 HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.4138-159G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 32/38 | chr15 | 93002018 | ||||||
| chr15:93002105
|
T | G | 1 | a0001c0001t0001g0281 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.4138-72T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 32/38 | chr15 | 93002105 | ||||||
| chr15:93002118
|
A | G | 1 | a0001c0001t0024g0077 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.4138-59A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 32/38 | chr15 | 93002118 | ||||||
| chr15:93002145
|
G | A | 1 | a0001c0001t0024g0077 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.4138-32G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 32/38 | chr15 | 93002145 | ||||||
| chr15:93002162
|
T | G | 5 | a0001c0001t0001g0007a0001c0009t0002g0043a0001c0009t0002g0048others(2): Show | 5 | HG00642.hp1 HG00673.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.4138-15T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 32/38 | chr15 | 93002162 | ||||||
| chr15:93002344
|
A | G | 13 | a0001c0001t0001g0259a0001c0001t0006g0248a0001c0001t0006g0260others(10): Show | 13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.4278+27A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 33/38 | chr15 | 93002344 | ||||||
| chr15:93002369
|
A | G | 13 | a0001c0001t0001g0259a0001c0001t0006g0248a0001c0001t0006g0260others(10): Show | 13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.4278+52A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 33/38 | chr15 | 93002369 | ||||||
| chr15:93002523
|
A | G | 1 | a0001c0003t0003g0148 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.4278+206A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 33/38 | chr15 | 93002523 | ||||||
| chr15:93002601
|
G | T | 249 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(246): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.4278+284G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 33/38 | chr15 | 93002601 | ||||||
| chr15:93002619
|
C | T | 1 | a0001c0004t0004g0297 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.4278+302C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 33/38 | chr15 | 93002619 | ||||||
| chr15:93002704
|
T | C | 147 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(144): Show | 151 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.4278+387T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 33/38 | chr15 | 93002704 | ||||||
| chr15:93002717
|
T | C | 7 | a0001c0002t0002g0231a0001c0002t0003g0228a0001c0002t0005g0220others(4): Show | 7 | HG01884.hp2 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.4278+400T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 33/38 | chr15 | 93002717 | ||||||
| chr15:93002843
|
TA | T | 5 | a0001c0002t0002g0231a0001c0002t0005g0220a0001c0002t0005g0227others(2): Show | 5 | HG02257.hp2 HG02572.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.4278+530delA | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 33/38 | INFO_REALIGN_3_PRIME | chr15 | 93002843 | |||||
| chr15:93002862
|
C | A | 1 | a0001c0014t0005g0226 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.4278+545C>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 33/38 | chr15 | 93002862 | ||||||
| chr15:93002866
|
C | T | 5 | a0001c0001t0001g0007a0001c0009t0002g0043a0001c0009t0002g0048others(2): Show | 5 | HG00642.hp1 HG00673.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.4278+549C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 33/38 | chr15 | 93002866 | ||||||
| chr15:93003089
|
G | GCAAC | 14 | a0001c0001t0001g0006a0001c0001t0001g0035a0001c0001t0001g0036others(11): Show | 15 | HG01069.hp1 HG01123.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.4278+773_4278+776d others(6): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 33/38 | INFO_REALIGN_3_PRIME | chr15 | 93003089 | |||||
| chr15:93003163
|
C | T | 1 | a0001c0003t0002g0221 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.4278+846C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 33/38 | chr15 | 93003163 | ||||||
| chr15:93003244
|
C | G | 55 | a0001c0001t0001g0016a0001c0002t0001g0091a0001c0002t0001g0233others(52): Show | 55 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.4278+927C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 33/38 | chr15 | 93003244 | ||||||
| chr15:93003286
|
C | CA | 51 | a0001c0001t0001g0007a0001c0001t0001g0016a0001c0001t0002g0293others(48): Show | 51 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.4278+988dupA | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 33/38 | INFO_REALIGN_3_PRIME | chr15 | 93003286 | |||||
| chr15:93003286
|
CA | C | 24 | a0001c0001t0001g0079a0001c0001t0001g0210a0001c0001t0002g0278others(21): Show | 24 | HG00099.hp2 HG01070.hp1 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.4278+988delA | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 33/38 | INFO_REALIGN_3_PRIME | chr15 | 93003286 | |||||
| chr15:93003286
|
CAA | C | 142 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0026others(139): Show | 145 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.4278+987_4278+988d others(4): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 33/38 | INFO_REALIGN_3_PRIME | chr15 | 93003286 | |||||
| chr15:93003286
|
CAAA | C | 22 | a0001c0001t0001g0006a0001c0001t0001g0035a0001c0001t0001g0036others(19): Show | 23 | HG01069.hp1 HG01123.hp2 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.4278+986_4278+988d others(5): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 33/38 | INFO_REALIGN_3_PRIME | chr15 | 93003286 | |||||
| chr15:93003309
|
T | C | 131 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0026others(128): Show | 134 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.4278+992T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 33/38 | chr15 | 93003309 | ||||||
| chr15:93003412
|
C | G | 13 | a0001c0001t0001g0007a0001c0001t0007g0174a0001c0002t0002g0231others(10): Show | 13 | HG00642.hp1 HG00673.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.4278+1095C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 33/38 | chr15 | 93003412 | ||||||
| chr15:93003445
|
C | T | 3 | a0001c0002t0002g0223a0001c0002t0005g0224a0001c0002t0005g0225 | 3 | HG02572.hp2 HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.4278+1128C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 33/38 | chr15 | 93003445 | ||||||
| chr15:93003577
|
C | CT | 13 | a0001c0001t0001g0081a0001c0002t0001g0091a0001c0002t0001g0249others(10): Show | 13 | HG00099.hp2 HG01167.hp2 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.4279-1025dupT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 33/38 | INFO_REALIGN_3_PRIME | chr15 | 93003577 | |||||
| chr15:93003604
|
G | T | 1 | a0001c0001t0001g0067 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.4279-1013G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 33/38 | chr15 | 93003604 | ||||||
| chr15:93004073
|
G | A | 25 | a0001c0001t0001g0259a0001c0001t0006g0248a0001c0001t0006g0260others(22): Show | 25 | HG00642.hp1 HG00673.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.4279-544G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 33/38 | chr15 | 93004073 | ||||||
| chr15:93004083
|
C | T | 3 | a0001c0002t0002g0045a0001c0002t0002g0046a0001c0002t0002g0232 | 3 | HG03453.hp2 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.4279-534C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 33/38 | chr15 | 93004083 | ||||||
| chr15:93004107
|
G | C | 15 | a0001c0001t0002g0293a0001c0001t0002g0294a0001c0002t0001g0091others(12): Show | 15 | HG00099.hp2 HG00544.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.4279-510G>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 33/38 | chr15 | 93004107 | ||||||
| chr15:93004110
|
C | T | 1 | a0001c0001t0007g0174 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.4279-507C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 33/38 | chr15 | 93004110 | ||||||
| chr15:93004123
|
C | CA | 44 | a0001c0001t0001g0006a0001c0001t0001g0032a0001c0001t0001g0035others(41): Show | 45 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(42): Show |
intron_variant | MODIFIER | c.4279-475dupA | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 33/38 | INFO_REALIGN_3_PRIME | chr15 | 93004123 | |||||
| chr15:93004123
|
C | CAA | 11 | a0001c0001t0007g0174a0001c0002t0002g0231a0001c0002t0005g0220others(8): Show | 11 | HG00642.hp1 HG00673.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.4279-476_4279-475d others(4): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 33/38 | INFO_REALIGN_3_PRIME | chr15 | 93004123 | |||||
| chr15:93004345
|
T | C | 223 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(220): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.4279-272T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 33/38 | chr15 | 93004345 | ||||||
| chr15:93004495
|
T | TC | 7 | a0001c0002t0002g0231a0001c0002t0003g0228a0001c0002t0005g0220others(4): Show | 7 | HG01884.hp2 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.4279-122_4279-121i others(3): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 33/38 | chr15 | 93004495 | ||||||
| chr15:93004496
|
T | A | 7 | a0001c0002t0002g0231a0001c0002t0003g0228a0001c0002t0005g0220others(4): Show | 7 | HG01884.hp2 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.4279-121T>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 33/38 | chr15 | 93004496 | ||||||
| chr15:93004564
|
G | A | 1 | a0001c0002t0001g0251 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.4279-53G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 33/38 | chr15 | 93004564 | ||||||
| chr15:93004766
|
C | T | 2 | a0001c0001t0002g0008a0001c0001t0002g0085 | 2 | HG02257.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.4413+15C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | chr15 | 93004766 | ||||||
| chr15:93004789
|
C | T | 7 | a0001c0002t0002g0231a0001c0002t0003g0228a0001c0002t0005g0220others(4): Show | 7 | HG01884.hp2 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.4413+38C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | chr15 | 93004789 | ||||||
| chr15:93005292
|
G | C | 1 | a0001c0001t0001g0081 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.4413+541G>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | chr15 | 93005292 | ||||||
| chr15:93005373
|
G | T | 1 | a0001c0002t0001g0091 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.4413+622G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | chr15 | 93005373 | ||||||
| chr15:93005417
|
C | A | 1 | a0001c0001t0001g0209 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.4413+666C>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | chr15 | 93005417 | ||||||
| chr15:93005448
|
C | T | 1 | a0001c0013t0019g0168 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4413+697C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | chr15 | 93005448 | ||||||
| chr15:93005477
|
G | C | 1 | a0001c0002t0002g0156 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4413+726G>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | chr15 | 93005477 | ||||||
| chr15:93005534
|
GA | G | 7 | a0001c0002t0002g0231a0001c0002t0003g0228a0001c0002t0005g0220others(4): Show | 7 | HG01884.hp2 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.4413+786delA | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | INFO_REALIGN_3_PRIME | chr15 | 93005534 | |||||
| chr15:93005567
|
A | G | 2 | a0001c0002t0002g0275a0001c0002t0016g0280 | 2 | HG00099.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.4413+816A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | chr15 | 93005567 | ||||||
| chr15:93005632
|
T | G | 3 | a0001c0002t0002g0045a0001c0002t0002g0046a0001c0002t0002g0232 | 3 | HG03453.hp2 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.4413+881T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | chr15 | 93005632 | ||||||
| chr15:93005998
|
A | T | 5 | a0001c0001t0009g0296a0001c0001t0011g0282a0001c0001t0011g0292others(2): Show | 5 | HG00735.hp1 HG01074.hp1 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.4413+1247A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | chr15 | 93005998 | ||||||
| chr15:93006124
|
C | CT | 57 | a0001c0001t0001g0007a0001c0001t0001g0016a0001c0001t0001g0057others(54): Show | 57 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.4413+1393dupT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | INFO_REALIGN_3_PRIME | chr15 | 93006124 | |||||
| chr15:93006125
|
T | TC | 6 | a0001c0003t0002g0137a0001c0003t0002g0162a0001c0003t0002g0169others(3): Show | 6 | HG02280.hp1 HG02922.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.4413+1374_4413+137 others(5): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | chr15 | 93006125 | ||||||
| chr15:93006126
|
T | C | 2 | a0001c0001t0001g0118a0001c0001t0001g0177 | 2 | NA18979.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.4413+1375T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | chr15 | 93006126 | ||||||
| chr15:93006127
|
T | C | 2 | a0001c0001t0001g0054a0001c0001t0001g0112 | 2 | NA18939.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.4413+1376T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | chr15 | 93006127 | ||||||
| chr15:93006157
|
T | G | 1 | a0001c0015t0005g0288 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.4413+1406T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | chr15 | 93006157 | ||||||
| chr15:93006195
|
C | T | 4 | a0001c0001t0001g0007a0001c0009t0002g0043a0001c0009t0002g0048others(1): Show | 4 | HG00673.hp2 HG02258.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.4413+1444C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | chr15 | 93006195 | ||||||
| chr15:93006433
|
C | G | 42 | a0001c0001t0001g0016a0001c0002t0001g0233a0001c0002t0001g0234others(39): Show | 42 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.4413+1682C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | chr15 | 93006433 | ||||||
| chr15:93006603
|
C | G | 235 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(232): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.4413+1852C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | chr15 | 93006603 | ||||||
| chr15:93006736
|
A | G | 173 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(170): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.4413+1985A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | chr15 | 93006736 | ||||||
| chr15:93007120
|
G | A | 1 | a0001c0007t0007g0030 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.4414-2025G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | chr15 | 93007120 | ||||||
| chr15:93007139
|
T | G | 1 | a0001c0002t0002g0156 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4414-2006T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | chr15 | 93007139 | ||||||
| chr15:93007334
|
A | C | 1 | a0001c0001t0001g0115 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.4414-1811A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | chr15 | 93007334 | ||||||
| chr15:93007350
|
T | C | 42 | a0001c0001t0001g0016a0001c0002t0001g0233a0001c0002t0001g0234others(39): Show | 42 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.4414-1795T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | chr15 | 93007350 | ||||||
| chr15:93007720
|
TTACC | T | 170 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(167): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.4414-1423_4414-142 others(8): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | INFO_REALIGN_3_PRIME | chr15 | 93007720 | |||||
| chr15:93007750
|
A | G | 7 | a0001c0002t0002g0231a0001c0002t0003g0228a0001c0002t0005g0220others(4): Show | 7 | HG01884.hp2 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.4414-1395A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | chr15 | 93007750 | ||||||
| chr15:93007878
|
C | T | 170 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(167): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.4414-1267C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | chr15 | 93007878 | ||||||
| chr15:93007911
|
TC | T | 2 | a0001c0001t0001g0026a0001c0001t0003g0001 | 3 | HG01515.hp2 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.4414-1232delC | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | INFO_REALIGN_3_PRIME | chr15 | 93007911 | |||||
| chr15:93008063
|
G | C | 10 | a0001c0002t0001g0091a0001c0002t0001g0286a0001c0002t0002g0275others(7): Show | 10 | HG00099.hp2 HG01167.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.4414-1082G>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | chr15 | 93008063 | ||||||
| chr15:93008116
|
G | C | 134 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(131): Show | 137 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.4414-1029G>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | chr15 | 93008116 | ||||||
| chr15:93008165
|
G | A | 13 | a0001c0001t0001g0259a0001c0001t0006g0248a0001c0001t0006g0260others(10): Show | 13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.4414-980G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | chr15 | 93008165 | ||||||
| chr15:93008289
|
C | T | 3 | a0001c0002t0002g0223a0001c0002t0005g0224a0001c0002t0005g0225 | 3 | HG02572.hp2 HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.4414-856C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | chr15 | 93008289 | ||||||
| chr15:93008317
|
C | T | 170 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(167): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.4414-828C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | chr15 | 93008317 | ||||||
| chr15:93008454
|
C | T | 2 | a0001c0002t0002g0275a0001c0002t0016g0280 | 2 | HG00099.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.4414-691C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | chr15 | 93008454 | ||||||
| chr15:93008470
|
C | T | 1 | a0001c0001t0001g0203 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.4414-675C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | chr15 | 93008470 | ||||||
| chr15:93008521
|
C | G | 1 | a0001c0005t0004g0154 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4414-624C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | chr15 | 93008521 | ||||||
| chr15:93008570
|
G | A | 249 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(246): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.4414-575G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | chr15 | 93008570 | ||||||
| chr15:93008573
|
C | T | 1 | a0001c0015t0005g0288 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.4414-572C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | chr15 | 93008573 | ||||||
| chr15:93008623
|
G | T | 4 | a0001c0002t0002g0181a0001c0002t0002g0223a0001c0002t0005g0224others(1): Show | 4 | HG02572.hp2 HG03209.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.4414-522G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | chr15 | 93008623 | ||||||
| chr15:93008746
|
A | C | 6 | a0001c0002t0002g0181a0001c0002t0002g0223a0001c0002t0005g0224others(3): Show | 6 | HG01243.hp2 HG02572.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.4414-399A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | chr15 | 93008746 | ||||||
| chr15:93008995
|
C | G | 3 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0209 | 3 | HG03492.hp2 HG03710.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.4414-150C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | chr15 | 93008995 | ||||||
| chr15:93008999
|
C | A | 1 | a0001c0002t0002g0156 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4414-146C>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | chr15 | 93008999 | ||||||
| chr15:93009100
|
C | T | 249 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(246): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.4414-45C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | chr15 | 93009100 | ||||||
| chr15:93009119
|
G | A | 4 | a0001c0001t0001g0002a0001c0001t0001g0049a0001c0001t0001g0078others(1): Show | 5 | HG01167.hp1 HG01192.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.4414-26G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | chr15 | 93009119 | ||||||
| chr15:93009426
|
C | T | 250 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(247): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.4592+103C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 35/38 | chr15 | 93009426 | ||||||
| chr15:93009501
|
G | A | 13 | a0001c0001t0001g0259a0001c0001t0006g0248a0001c0001t0006g0260others(10): Show | 13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.4592+178G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 35/38 | chr15 | 93009501 | ||||||
| chr15:93009545
|
T | G | 1 | a0001c0001t0001g0298 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.4592+222T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 35/38 | chr15 | 93009545 | ||||||
| chr15:93009701
|
A | G | 14 | a0001c0001t0001g0259a0001c0001t0006g0084a0001c0001t0006g0248others(11): Show | 14 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.4592+378A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 35/38 | chr15 | 93009701 | ||||||
| chr15:93009735
|
A | T | 13 | a0001c0001t0001g0006a0001c0001t0001g0035a0001c0001t0001g0036others(10): Show | 14 | HG01069.hp1 HG01123.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.4592+412A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 35/38 | chr15 | 93009735 | ||||||
| chr15:93009738
|
G | T | 1 | a0001c0001t0001g0299 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.4592+415G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 35/38 | chr15 | 93009738 | ||||||
| chr15:93009898
|
A | G | 14 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0002t0001g0091others(11): Show | 15 | HG00099.hp2 HG01069.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.4592+575A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 35/38 | chr15 | 93009898 | ||||||
| chr15:93010317
|
G | T | 1 | a0001c0015t0005g0288 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.4592+994G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 35/38 | chr15 | 93010317 | ||||||
| chr15:93010319
|
CTTCTT | C | 38 | a0001c0001t0001g0016a0001c0001t0020g0113a0001c0002t0001g0234others(35): Show | 38 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.4592+1000_4592+100 others(9): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 35/38 | INFO_REALIGN_3_PRIME | chr15 | 93010319 | |||||
| chr15:93010410
|
A | AT | 13 | a0001c0001t0001g0281a0001c0001t0002g0278a0001c0001t0002g0293others(10): Show | 13 | HG00544.hp1 HG00735.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.4592+1108dupT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 35/38 | INFO_REALIGN_3_PRIME | chr15 | 93010410 | |||||
| chr15:93010410
|
ATTT | A | 174 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(171): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.4592+1106_4592+110 others(7): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 35/38 | INFO_REALIGN_3_PRIME | chr15 | 93010410 | |||||
| chr15:93010410
|
ATTTT | A | 29 | a0001c0001t0001g0007a0001c0001t0001g0056a0001c0001t0001g0093others(26): Show | 29 | HG00639.hp2 HG00735.hp2 HG01074.hp2 others(26): Show |
intron_variant | MODIFIER | c.4592+1105_4592+110 others(8): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 35/38 | INFO_REALIGN_3_PRIME | chr15 | 93010410 | |||||
| chr15:93010462
|
A | G | 142 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(139): Show | 145 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.4592+1139A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 35/38 | chr15 | 93010462 | ||||||
| chr15:93010693
|
G | C | 1 | a0001c0007t0007g0030 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.4592+1370G>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 35/38 | chr15 | 93010693 | ||||||
| chr15:93010715
|
C | T | 17 | a0001c0001t0001g0006a0001c0001t0001g0035a0001c0001t0001g0036others(14): Show | 18 | HG01123.hp2 HG01192.hp1 HG01433.hp1 others(15): Show |
intron_variant | MODIFIER | c.4592+1392C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 35/38 | chr15 | 93010715 | ||||||
| chr15:93010868
|
C | T | 4 | a0001c0002t0002g0231a0001c0002t0005g0227a0001c0002t0005g0230others(1): Show | 4 | HG02257.hp2 HG02572.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.4593-1477C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 35/38 | chr15 | 93010868 | ||||||
| chr15:93010956
|
T | C | 1 | a0001c0001t0001g0102 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.4593-1389T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 35/38 | chr15 | 93010956 | ||||||
| chr15:93010990
|
G | A | 1 | a0001c0004t0004g0285 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.4593-1355G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 35/38 | chr15 | 93010990 | ||||||
| chr15:93011071
|
G | A | 13 | a0001c0001t0001g0259a0001c0001t0006g0248a0001c0001t0006g0260others(10): Show | 13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.4593-1274G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 35/38 | chr15 | 93011071 | ||||||
| chr15:93011073
|
C | CT | 6 | a0001c0001t0001g0007a0001c0001t0006g0268a0001c0009t0002g0043others(3): Show | 6 | HG00642.hp1 HG00673.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.4593-1260dupT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 35/38 | INFO_REALIGN_3_PRIME | chr15 | 93011073 | |||||
| chr15:93011108
|
A | G | 1 | a0001c0001t0001g0081 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.4593-1237A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 35/38 | chr15 | 93011108 | ||||||
| chr15:93011329
|
A | G | 1 | a0001c0013t0019g0168 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4593-1016A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 35/38 | chr15 | 93011329 | ||||||
| chr15:93011473
|
A | G | 16 | a0001c0001t0008g0217a0001c0001t0008g0218a0001c0001t0008g0219others(13): Show | 16 | HG00323.hp2 HG00741.hp2 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.4593-872A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 35/38 | chr15 | 93011473 | ||||||
| chr15:93011585
|
G | C | 2 | a0001c0001t0001g0096a0001c0001t0001g0122 | 2 | HG02602.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.4593-760G>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 35/38 | chr15 | 93011585 | ||||||
| chr15:93011723
|
G | A | 2 | a0001c0001t0001g0204a0001c0001t0001g0211 | 2 | NA19007.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.4593-622G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 35/38 | chr15 | 93011723 | ||||||
| chr15:93011878
|
A | G | 4 | a0001c0002t0002g0231a0001c0002t0005g0227a0001c0002t0005g0230others(1): Show | 4 | HG02257.hp2 HG02572.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.4593-467A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 35/38 | chr15 | 93011878 | ||||||
| chr15:93011969
|
G | A | 225 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(222): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.4593-376G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 35/38 | chr15 | 93011969 | ||||||
| chr15:93012020
|
A | G | 135 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0026others(132): Show | 138 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.4593-325A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 35/38 | chr15 | 93012020 | ||||||
| chr15:93012141
|
C | G | 1 | a0001c0003t0003g0128 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.4593-204C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 35/38 | chr15 | 93012141 | ||||||
| chr15:93012199
|
A | G | 1 | a0001c0003t0001g0135 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.4593-146A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 35/38 | chr15 | 93012199 | ||||||
| chr15:93012233
|
A | G | 2 | a0001c0001t0008g0040a0001c0002t0002g0156 | 2 | HG02976.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.4593-112A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 35/38 | chr15 | 93012233 | ||||||
| chr15:93012311
|
A | G | 2 | a0001c0001t0001g0102a0001c0001t0001g0103 | 2 | HG01258.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.4593-34A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 35/38 | chr15 | 93012311 | ||||||
| chr15:93012487
|
A | G | 43 | a0001c0001t0001g0016a0001c0001t0020g0113a0001c0002t0001g0234others(40): Show | 43 | HG00423.hp2 HG00558.hp1 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.4692+43A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 36/38 | chr15 | 93012487 | ||||||
| chr15:93012504
|
C | G | 1 | a0001c0001t0001g0209 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.4692+60C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 36/38 | chr15 | 93012504 | ||||||
| chr15:93012643
|
T | A | 4 | a0001c0002t0005g0220a0001c0003t0005g0124a0001c0003t0005g0166others(1): Show | 4 | HG02809.hp2 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.4692+199T>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 36/38 | chr15 | 93012643 | ||||||
| chr15:93012695
|
C | A | 4 | a0001c0002t0002g0231a0001c0002t0005g0227a0001c0002t0005g0230others(1): Show | 4 | HG02257.hp2 HG02572.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.4692+251C>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 36/38 | chr15 | 93012695 | ||||||
| chr15:93012800
|
T | A | 1 | a0001c0001t0001g0082 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.4692+356T>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 36/38 | chr15 | 93012800 | ||||||
| chr15:93013088
|
G | A | 1 | a0001c0001t0001g0299 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.4692+644G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 36/38 | chr15 | 93013088 | ||||||
| chr15:93013161
|
C | T | 2 | a0001c0001t0008g0040a0001c0002t0002g0156 | 2 | HG02976.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.4692+717C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 36/38 | chr15 | 93013161 | ||||||
| chr15:93013212
|
G | A | 224 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(221): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.4692+768G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 36/38 | chr15 | 93013212 | ||||||
| chr15:93013302
|
TCCGGAAA others(2): Show |
T | 79 | a0001c0001t0001g0002a0001c0001t0001g0027a0001c0001t0001g0028others(76): Show | 80 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.4692+861_4692+869d others(11): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr15 | 93013302 | |||||
| chr15:93013662
|
C | T | 4 | a0001c0002t0002g0231a0001c0002t0005g0227a0001c0002t0005g0230others(1): Show | 4 | HG02257.hp2 HG02572.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.4693-1034C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 36/38 | chr15 | 93013662 | ||||||
| chr15:93013725
|
G | A | 13 | a0001c0001t0001g0259a0001c0001t0006g0248a0001c0001t0006g0260others(10): Show | 13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.4693-971G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 36/38 | chr15 | 93013725 | ||||||
| chr15:93013736
|
A | G | 3 | a0001c0003t0003g0161a0001c0003t0005g0160a0001c0007t0003g0157 | 3 | HG01884.hp1 HG02055.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.4693-960A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 36/38 | chr15 | 93013736 | ||||||
| chr15:93013746
|
C | G | 39 | a0001c0001t0020g0113a0001c0002t0001g0234a0001c0002t0001g0235others(36): Show | 39 | HG00423.hp2 HG00558.hp1 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.4693-950C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 36/38 | chr15 | 93013746 | ||||||
| chr15:93013832
|
G | A | 1 | a0001c0002t0001g0236 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.4693-864G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 36/38 | chr15 | 93013832 | ||||||
| chr15:93013928
|
C | CA | 17 | a0001c0001t0001g0188a0001c0001t0006g0268a0001c0001t0006g0269others(14): Show | 17 | HG01109.hp2 HG01257.hp1 HG01258.hp1 others(14): Show |
intron_variant | MODIFIER | c.4693-740dupA | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr15 | 93013928 | |||||
| chr15:93013928
|
CA | C | 131 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0027others(128): Show | 133 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.4693-740delA | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr15 | 93013928 | |||||
| chr15:93013928
|
CAA | C | 65 | a0001c0001t0001g0006a0001c0001t0001g0035a0001c0001t0001g0036others(62): Show | 66 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.4693-741_4693-740d others(4): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr15 | 93013928 | |||||
| chr15:93013928
|
CAAA | C | 9 | a0001c0002t0001g0239a0001c0002t0002g0045a0001c0002t0002g0046others(6): Show | 9 | HG02280.hp2 HG02572.hp2 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.4693-742_4693-740d others(5): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr15 | 93013928 | |||||
| chr15:93013928
|
CAAAAAA | C | 12 | a0001c0001t0001g0141a0001c0002t0001g0091a0001c0002t0001g0286others(9): Show | 13 | HG00099.hp2 HG01167.hp2 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.4693-745_4693-740d others(8): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr15 | 93013928 | |||||
| chr15:93013928
|
CAAAAAAA others(9): Show |
C | 5 | a0001c0001t0001g0007a0001c0009t0002g0043a0001c0009t0002g0048others(2): Show | 5 | HG00642.hp1 HG00673.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.4693-755_4693-740d others(18): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr15 | 93013928 | |||||
| chr15:93014098
|
A | G | 1 | a0001c0001t0001g0184 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.4693-598A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 36/38 | chr15 | 93014098 | ||||||
| chr15:93014235
|
A | T | 1 | a0001c0003t0008g0147 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.4693-461A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 36/38 | chr15 | 93014235 | ||||||
| chr15:93014518
|
C | T | 12 | a0001c0001t0008g0217a0001c0001t0008g0218a0001c0001t0008g0219others(9): Show | 12 | HG00323.hp2 HG00741.hp2 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.4693-178C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 36/38 | chr15 | 93014518 | ||||||
| chr15:93014950
|
A | G | 4 | a0001c0002t0002g0231a0001c0002t0005g0227a0001c0002t0005g0230others(1): Show | 4 | HG02257.hp2 HG02572.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.4906+41A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93014950 | ||||||
| chr15:93014970
|
T | C | 1 | a0001c0015t0005g0288 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.4906+61T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93014970 | ||||||
| chr15:93015096
|
T | G | 2 | a0001c0002t0011g0256a0001c0002t0011g0257 | 2 | NA19000.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.4906+187T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93015096 | ||||||
| chr15:93015188
|
C | T | 2 | a0001c0001t0001g0190a0001c0001t0001g0199 | 2 | HG02083.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.4906+279C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93015188 | ||||||
| chr15:93015400
|
T | C | 1 | a0001c0001t0003g0274 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.4906+491T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93015400 | ||||||
| chr15:93015505
|
G | C | 1 | a0001c0001t0001g0049 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.4906+596G>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93015505 | ||||||
| chr15:93015531
|
TAACTG | T | 12 | a0001c0001t0001g0141a0001c0002t0001g0091a0001c0002t0001g0286others(9): Show | 13 | HG00099.hp2 HG01167.hp2 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.4906+625_4906+629d others(7): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | INFO_REALIGN_3_PRIME | chr15 | 93015531 | |||||
| chr15:93015570
|
A | ACAGTTTA others(25): Show |
13 | a0001c0001t0001g0259a0001c0001t0006g0248a0001c0001t0006g0260others(10): Show | 13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.4906+663_4906+694d others(34): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | INFO_REALIGN_3_PRIME | chr15 | 93015570 | |||||
| chr15:93015754
|
A | G | 2 | a0001c0001t0008g0040a0001c0002t0002g0156 | 2 | HG02976.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.4906+845A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93015754 | ||||||
| chr15:93015839
|
A | C | 3 | a0001c0002t0002g0045a0001c0002t0002g0046a0001c0002t0002g0232 | 3 | HG03453.hp2 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.4906+930A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93015839 | ||||||
| chr15:93015849
|
C | T | 1 | a0001c0001t0001g0041 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.4906+940C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93015849 | ||||||
| chr15:93015948
|
A | G | 208 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(205): Show | 212 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.4906+1039A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93015948 | ||||||
| chr15:93016074
|
T | G | 17 | a0001c0001t0001g0141a0001c0001t0003g0274a0001c0002t0001g0091others(14): Show | 18 | HG00099.hp2 HG00642.hp1 HG00673.hp2 others(15): Show |
intron_variant | MODIFIER | c.4906+1165T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93016074 | ||||||
| chr15:93016093
|
T | TA | 13 | a0001c0001t0001g0259a0001c0001t0006g0248a0001c0001t0006g0260others(10): Show | 13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.4906+1185dupA | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | INFO_REALIGN_3_PRIME | chr15 | 93016093 | |||||
| chr15:93016105
|
C | T | 5 | a0001c0004t0007g0013a0001c0004t0007g0014a0001c0004t0007g0017others(2): Show | 5 | HG00639.hp1 HG01433.hp2 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.4906+1196C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93016105 | ||||||
| chr15:93016123
|
G | A | 33 | a0001c0001t0001g0141a0001c0001t0001g0259a0001c0001t0006g0248others(30): Show | 34 | HG00099.hp2 HG00642.hp1 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.4906+1214G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93016123 | ||||||
| chr15:93016156
|
T | C | 1 | a0001c0004t0004g0092 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.4906+1247T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93016156 | ||||||
| chr15:93016157
|
C | T | 50 | a0001c0001t0001g0141a0001c0002t0001g0091a0001c0002t0001g0234others(47): Show | 51 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.4906+1248C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93016157 | ||||||
| chr15:93016265
|
A | G | 1 | a0001c0005t0007g0050 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.4906+1356A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93016265 | ||||||
| chr15:93016285
|
C | G | 13 | a0001c0001t0001g0259a0001c0001t0006g0248a0001c0001t0006g0260others(10): Show | 13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.4906+1376C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93016285 | ||||||
| chr15:93016285
|
C | T | 244 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(241): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.4906+1376C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93016285 | ||||||
| chr15:93016381
|
A | G | 40 | a0001c0001t0001g0016a0001c0002t0001g0234a0001c0002t0001g0235others(37): Show | 40 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.4906+1472A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93016381 | ||||||
| chr15:93016383
|
G | A | 4 | a0001c0002t0002g0231a0001c0002t0005g0227a0001c0002t0005g0230others(1): Show | 4 | HG02257.hp2 HG02572.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.4906+1474G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93016383 | ||||||
| chr15:93016489
|
G | A | 4 | a0001c0001t0001g0006a0001c0001t0001g0271a0001c0001t0001g0272others(1): Show | 5 | HG01123.hp2 HG02683.hp2 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.4906+1580G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93016489 | ||||||
| chr15:93016519
|
T | A | 1 | a0001c0009t0002g0048 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.4906+1610T>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93016519 | ||||||
| chr15:93016539
|
T | C | 13 | a0001c0001t0001g0259a0001c0001t0006g0248a0001c0001t0006g0260others(10): Show | 13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.4906+1630T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93016539 | ||||||
| chr15:93016747
|
G | A | 1 | a0001c0015t0005g0288 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.4906+1838G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93016747 | ||||||
| chr15:93016779
|
C | CAAAAAAA others(2): Show |
27 | a0001c0001t0001g0281a0001c0001t0002g0278a0001c0001t0002g0293others(24): Show | 27 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(24): Show |
intron_variant | MODIFIER | c.4906+1877_4906+188 others(13): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | INFO_REALIGN_3_PRIME | chr15 | 93016779 | |||||
| chr15:93016779
|
C | CAAAAAAA others(3): Show |
62 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0068others(59): Show | 63 | HG00099.hp2 HG00423.hp2 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.4906+1876_4906+188 others(14): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | INFO_REALIGN_3_PRIME | chr15 | 93016779 | |||||
| chr15:93016779
|
C | CAAAAAAA others(4): Show |
137 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0028others(134): Show | 139 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.4906+1875_4906+188 others(15): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | INFO_REALIGN_3_PRIME | chr15 | 93016779 | |||||
| chr15:93016779
|
C | CAAAAAAA others(5): Show |
16 | a0001c0001t0001g0007a0001c0001t0001g0026a0001c0001t0001g0032others(13): Show | 17 | HG00673.hp1 HG00735.hp2 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.4906+1874_4906+188 others(16): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | INFO_REALIGN_3_PRIME | chr15 | 93016779 | |||||
| chr15:93016779
|
C | CAAAAAAA others(6): Show |
4 | a0001c0001t0001g0200a0001c0002t0002g0045a0001c0002t0002g0046others(1): Show | 4 | HG03453.hp2 HG04115.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.4906+1873_4906+188 others(17): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | INFO_REALIGN_3_PRIME | chr15 | 93016779 | |||||
| chr15:93016779
|
CA | C | 13 | a0001c0001t0001g0006a0001c0001t0001g0035a0001c0001t0001g0036others(10): Show | 14 | HG01123.hp2 HG01192.hp1 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.4906+1885delA | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | INFO_REALIGN_3_PRIME | chr15 | 93016779 | |||||
| chr15:93016799
|
A | G | 1 | a0001c0002t0002g0156 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4906+1890A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93016799 | ||||||
| chr15:93016814
|
C | T | 2 | a0001c0010t0002g0182a0001c0010t0002g0222 | 2 | HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.4906+1905C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93016814 | ||||||
| chr15:93016862
|
A | G | 1 | a0001c0002t0001g0251 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.4906+1953A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93016862 | ||||||
| chr15:93016865
|
A | T | 2 | a0001c0001t0001g0190a0001c0001t0001g0199 | 2 | HG02083.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.4906+1956A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93016865 | ||||||
| chr15:93017057
|
G | A | 1 | a0001c0001t0011g0176 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.4906+2148G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93017057 | ||||||
| chr15:93017101
|
G | T | 46 | a0001c0001t0001g0006a0001c0001t0001g0035a0001c0001t0001g0036others(43): Show | 47 | HG00323.hp2 HG00642.hp1 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.4906+2192G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93017101 | ||||||
| chr15:93017327
|
C | CT | 216 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(213): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.4906+2421dupT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | INFO_REALIGN_3_PRIME | chr15 | 93017327 | |||||
| chr15:93017331
|
C | T | 263 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(260): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.4906+2422C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93017331 | ||||||
| chr15:93017492
|
A | AT | 34 | a0001c0001t0001g0033a0001c0001t0001g0056a0001c0001t0001g0057others(31): Show | 34 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.4907-2493dupT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | INFO_REALIGN_3_PRIME | chr15 | 93017492 | |||||
| chr15:93017492
|
A | ATTT | 10 | a0001c0001t0001g0259a0001c0001t0006g0248a0001c0001t0006g0260others(7): Show | 10 | HG01074.hp2 HG01099.hp2 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.4907-2495_4907-249 others(7): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | INFO_REALIGN_3_PRIME | chr15 | 93017492 | |||||
| chr15:93017492
|
AT | A | 33 | a0001c0001t0001g0027a0001c0001t0003g0274a0001c0001t0008g0040others(30): Show | 33 | HG00323.hp2 HG00735.hp1 HG01123.hp1 others(30): Show |
intron_variant | MODIFIER | c.4907-2493delT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | INFO_REALIGN_3_PRIME | chr15 | 93017492 | |||||
| chr15:93017492
|
ATT | A | 57 | a0001c0001t0001g0006a0001c0001t0001g0035a0001c0001t0001g0036others(54): Show | 58 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.4907-2494_4907-249 others(6): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | INFO_REALIGN_3_PRIME | chr15 | 93017492 | |||||
| chr15:93017571
|
T | C | 38 | a0001c0002t0001g0234a0001c0002t0001g0235a0001c0002t0001g0236others(35): Show | 38 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.4907-2441T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93017571 | ||||||
| chr15:93017620
|
A | T | 263 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(260): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.4907-2392A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93017620 | ||||||
| chr15:93017829
|
G | C | 3 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0038 | 3 | HG01433.hp1 HG02735.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.4907-2183G>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93017829 | ||||||
| chr15:93017962
|
A | T | 5 | a0001c0002t0002g0181a0001c0002t0002g0223a0001c0002t0005g0224others(2): Show | 5 | HG02572.hp2 HG02630.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.4907-2050A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93017962 | ||||||
| chr15:93018187
|
T | C | 1 | a0001c0002t0002g0181 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4907-1825T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93018187 | ||||||
| chr15:93018259
|
T | A | 2 | a0001c0001t0001g0065a0001c0001t0001g0069 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.4907-1753T>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93018259 | ||||||
| chr15:93018305
|
G | A | 5 | a0001c0002t0002g0181a0001c0002t0002g0223a0001c0002t0005g0224others(2): Show | 5 | HG02572.hp2 HG02630.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.4907-1707G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93018305 | ||||||
| chr15:93018370
|
T | G | 2 | a0001c0001t0008g0040a0001c0002t0002g0156 | 2 | HG02976.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.4907-1642T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93018370 | ||||||
| chr15:93018412
|
G | T | 55 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0026others(52): Show | 57 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.4907-1600G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93018412 | ||||||
| chr15:93018415
|
A | G | 2 | a0001c0009t0002g0043a0001c0009t0012g0044 | 2 | HG02258.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.4907-1597A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93018415 | ||||||
| chr15:93018667
|
C | T | 1 | a0001c0006t0004g0004 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.4907-1345C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93018667 | ||||||
| chr15:93018683
|
C | G | 13 | a0001c0001t0001g0006a0001c0001t0001g0035a0001c0001t0001g0036others(10): Show | 14 | HG01123.hp2 HG01192.hp1 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.4907-1329C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93018683 | ||||||
| chr15:93018713
|
C | G | 218 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(215): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.4907-1299C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93018713 | ||||||
| chr15:93018736
|
C | G | 22 | a0001c0001t0001g0016a0001c0002t0001g0234a0001c0002t0008g0012others(19): Show | 22 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.4907-1276C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93018736 | ||||||
| chr15:93018767
|
A | G | 13 | a0001c0001t0001g0259a0001c0001t0006g0248a0001c0001t0006g0260others(10): Show | 13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.4907-1245A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93018767 | ||||||
| chr15:93018770
|
C | G | 1 | a0001c0002t0001g0246 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.4907-1242C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93018770 | ||||||
| chr15:93019090
|
A | T | 1 | a0001c0002t0001g0247 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.4907-922A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93019090 | ||||||
| chr15:93019135
|
T | C | 2 | a0001c0002t0003g0228a0001c0002t0005g0229 | 2 | HG01884.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.4907-877T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93019135 | ||||||
| chr15:93019293
|
T | C | 21 | a0001c0001t0001g0281a0001c0001t0002g0278a0001c0001t0002g0293others(18): Show | 21 | HG00544.hp1 HG00639.hp1 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.4907-719T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93019293 | ||||||
| chr15:93019306
|
G | A | 13 | a0001c0001t0001g0259a0001c0001t0006g0248a0001c0001t0006g0260others(10): Show | 13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.4907-706G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93019306 | ||||||
| chr15:93019334
|
T | G | 13 | a0001c0001t0001g0259a0001c0001t0006g0248a0001c0001t0006g0260others(10): Show | 13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.4907-678T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93019334 | ||||||
| chr15:93019390
|
C | T | 1 | a0001c0005t0004g0154 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4907-622C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93019390 | ||||||
| chr15:93019433
|
G | A | 1 | a0001c0001t0009g0011 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.4907-579G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93019433 | ||||||
| chr15:93019435
|
C | A | 1 | a0001c0001t0009g0011 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.4907-577C>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93019435 | ||||||
| chr15:93019436
|
T | C | 1 | a0001c0001t0009g0011 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.4907-576T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93019436 | ||||||
| chr15:93019439
|
A | G | 1 | a0001c0001t0009g0011 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.4907-573A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93019439 | ||||||
| chr15:93019441
|
A | C | 1 | a0001c0001t0009g0011 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.4907-571A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93019441 | ||||||
| chr15:93019442
|
T | G | 1 | a0001c0001t0009g0011 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.4907-570T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93019442 | ||||||
| chr15:93019444
|
T | G | 1 | a0001c0001t0009g0011 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.4907-568T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93019444 | ||||||
| chr15:93019446
|
G | T | 1 | a0001c0001t0009g0011 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.4907-566G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93019446 | ||||||
| chr15:93019527
|
T | C | 2 | a0001c0002t0002g0156a0001c0003t0002g0169 | 2 | HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.4907-485T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93019527 | ||||||
| chr15:93019607
|
A | C | 4 | a0001c0001t0003g0274a0001c0002t0005g0224a0001c0002t0005g0225others(1): Show | 4 | HG03041.hp1 HG03209.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.4907-405A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93019607 | ||||||
| chr15:93019676
|
G | A | 1 | a0001c0001t0005g0179 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.4907-336G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93019676 | ||||||
| chr15:93019683
|
C | T | 1 | a0001c0004t0010g0107 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.4907-329C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93019683 | ||||||
| chr15:93019708
|
C | T | 3 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0209 | 3 | HG03492.hp2 HG03710.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.4907-304C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93019708 | ||||||
| chr15:93019743
|
A | G | 7 | a0001c0001t0001g0053a0001c0001t0009g0009a0001c0001t0009g0010others(4): Show | 7 | HG00544.hp2 HG01192.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.4907-269A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93019743 | ||||||
| chr15:93019825
|
T | C | 1 | a0001c0010t0002g0182 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.4907-187T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93019825 | ||||||
| chr15:93019934
|
C | CA | 34 | a0001c0001t0001g0006a0001c0001t0001g0072a0001c0001t0001g0197others(31): Show | 35 | HG00558.hp2 HG00735.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.4907-65dupA | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | INFO_REALIGN_3_PRIME | chr15 | 93019934 | |||||
| chr15:93019934
|
C | CAA | 27 | a0001c0001t0001g0086a0001c0001t0001g0201a0001c0001t0002g0293others(24): Show | 28 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(25): Show |
intron_variant | MODIFIER | c.4907-66_4907-65dup others(2): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | INFO_REALIGN_3_PRIME | chr15 | 93019934 | |||||
| chr15:93020325
|
A | G | 1 | a0001c0001t0001g0075 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.5153+67A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93020325 | ||||||
| chr15:93020366
|
C | G | 1 | a0001c0001t0001g0061 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.5153+108C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93020366 | ||||||
| chr15:93020382
|
C | G | 1 | a0001c0002t0009g0022 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.5153+124C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93020382 | ||||||
| chr15:93020399
|
A | G | 1 | a0001c0003t0003g0170 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.5153+141A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93020399 | ||||||
| chr15:93020431
|
G | C | 254 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(251): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.5153+173G>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93020431 | ||||||
| chr15:93020556
|
G | A | 1 | a0001c0001t0001g0042 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.5153+298G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93020556 | ||||||
| chr15:93020677
|
A | G | 27 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0086others(24): Show | 27 | HG00323.hp1 HG00639.hp1 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.5153+419A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93020677 | ||||||
| chr15:93020707
|
G | A | 299 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(296): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.5153+449G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93020707 | ||||||
| chr15:93020793
|
A | G | 15 | a0001c0001t0001g0193a0001c0001t0006g0080a0001c0001t0006g0084others(12): Show | 15 | HG00735.hp2 HG01099.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.5153+535A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93020793 | ||||||
| chr15:93020815
|
T | C | 1 | a0001c0001t0001g0206 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.5153+557T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93020815 | ||||||
| chr15:93020987
|
G | A | 1 | a0001c0001t0002g0008 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.5153+729G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93020987 | ||||||
| chr15:93021271
|
CATCCTT | C | 9 | a0001c0001t0002g0008a0001c0001t0002g0278a0001c0001t0002g0295others(6): Show | 9 | HG01069.hp2 HG02280.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.5153+1017_5153+102 others(10): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | INFO_REALIGN_3_PRIME | chr15 | 93021271 | |||||
| chr15:93021538
|
T | C | 85 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0065others(82): Show | 86 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(83): Show |
intron_variant | MODIFIER | c.5153+1280T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93021538 | ||||||
| chr15:93021697
|
A | C | 1 | a0001c0006t0004g0158 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.5153+1439A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93021697 | ||||||
| chr15:93021742
|
T | C | 185 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(182): Show | 188 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.5153+1484T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93021742 | ||||||
| chr15:93021854
|
G | A | 1 | a0001c0007t0007g0030 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.5153+1596G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93021854 | ||||||
| chr15:93021860
|
T | C | 14 | a0001c0001t0006g0080a0001c0001t0006g0084a0001c0001t0006g0248others(11): Show | 14 | HG00735.hp2 HG01099.hp2 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.5153+1602T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93021860 | ||||||
| chr15:93021936
|
A | C | 1 | a0001c0001t0001g0191 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.5153+1678A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93021936 | ||||||
| chr15:93021942
|
C | A | 1 | a0001c0010t0002g0222 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.5153+1684C>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93021942 | ||||||
| chr15:93022149
|
A | G | 3 | a0001c0002t0002g0045a0001c0002t0002g0046a0001c0002t0002g0232 | 3 | HG03453.hp2 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.5153+1891A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93022149 | ||||||
| chr15:93022260
|
C | G | 175 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(172): Show | 178 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(175): Show |
intron_variant | MODIFIER | c.5153+2002C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93022260 | ||||||
| chr15:93022260
|
C | T | 2 | a0001c0003t0003g0149a0001c0003t0003g0290 | 2 | HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.5153+2002C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93022260 | ||||||
| chr15:93022339
|
G | A | 17 | a0001c0001t0001g0016a0001c0004t0007g0013a0001c0004t0007g0014others(14): Show | 17 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(14): Show |
intron_variant | MODIFIER | c.5154-2033G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93022339 | ||||||
| chr15:93022499
|
G | A | 3 | a0001c0001t0002g0278a0001c0001t0002g0295a0001c0003t0002g0125 | 3 | HG01069.hp2 HG02965.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.5154-1873G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93022499 | ||||||
| chr15:93022520
|
G | A | 1 | a0001c0013t0019g0168 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.5154-1852G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93022520 | ||||||
| chr15:93022601
|
C | G | 4 | a0001c0002t0001g0235a0001c0002t0001g0249a0001c0002t0001g0250others(1): Show | 4 | NA18967.hp1 NA18978.hp2 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.5154-1771C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93022601 | ||||||
| chr15:93022830
|
A | C | 9 | a0001c0001t0008g0040a0001c0001t0008g0217a0001c0001t0008g0218others(6): Show | 9 | HG00741.hp1 HG01070.hp2 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.5154-1542A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93022830 | ||||||
| chr15:93022915
|
G | A | 276 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(273): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.5154-1457G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93022915 | ||||||
| chr15:93022924
|
C | T | 12 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0038others(9): Show | 12 | HG00323.hp1 HG00735.hp1 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.5154-1448C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93022924 | ||||||
| chr15:93023009
|
C | T | 1 | a0001c0003t0014g0165 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.5154-1363C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93023009 | ||||||
| chr15:93023034
|
T | C | 9 | a0001c0001t0008g0040a0001c0001t0008g0217a0001c0001t0008g0218others(6): Show | 9 | HG00741.hp1 HG01070.hp2 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.5154-1338T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93023034 | ||||||
| chr15:93023075
|
A | G | 1 | a0001c0001t0001g0049 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.5154-1297A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93023075 | ||||||
| chr15:93023136
|
T | C | 1 | a0001c0007t0007g0030 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.5154-1236T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93023136 | ||||||
| chr15:93023181
|
A | C | 23 | a0001c0001t0001g0029a0001c0002t0001g0091a0001c0003t0012g0126others(20): Show | 24 | HG00140.hp2 HG00738.hp2 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.5154-1191A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93023181 | ||||||
| chr15:93023193
|
C | G | 12 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0038others(9): Show | 12 | HG00323.hp1 HG00735.hp1 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.5154-1179C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93023193 | ||||||
| chr15:93023247
|
C | T | 1 | a0001c0001t0001g0281 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.5154-1125C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93023247 | ||||||
| chr15:93023452
|
G | A | 204 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(201): Show | 207 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(204): Show |
intron_variant | MODIFIER | c.5154-920G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93023452 | ||||||
| chr15:93023573
|
A | G | 1 | a0001c0001t0001g0115 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.5154-799A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93023573 | ||||||
| chr15:93023604
|
A | G | 1 | a0001c0005t0004g0287 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.5154-768A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93023604 | ||||||
| chr15:93023668
|
G | GTT | 8 | a0001c0001t0008g0040a0001c0001t0008g0217a0001c0001t0008g0218others(5): Show | 8 | HG00741.hp1 HG01070.hp2 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.5154-695_5154-694d others(4): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | INFO_REALIGN_3_PRIME | chr15 | 93023668 | |||||
| chr15:93023677
|
T | G | 2 | a0001c0002t0003g0228a0001c0003t0003g0152 | 2 | HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.5154-695T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93023677 | ||||||
| chr15:93023679
|
G | GT | 34 | a0001c0001t0002g0008a0001c0001t0002g0085a0001c0001t0002g0278others(31): Show | 34 | HG00099.hp2 HG00544.hp1 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.5154-692dupT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | INFO_REALIGN_3_PRIME | chr15 | 93023679 | |||||
| chr15:93023679
|
G | GTT | 23 | a0001c0002t0001g0091a0001c0003t0012g0126a0001c0003t0012g0133others(20): Show | 24 | HG00140.hp2 HG00738.hp2 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.5154-692_5154-691i others(4): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | INFO_REALIGN_3_PRIME | chr15 | 93023679 | |||||
| chr15:93023681
|
G | T | 58 | a0001c0001t0002g0008a0001c0001t0002g0085a0001c0001t0002g0278others(55): Show | 59 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.5154-691G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93023681 | ||||||
| chr15:93023822
|
A | G | 1 | a0001c0004t0004g0284 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.5154-550A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93023822 | ||||||
| chr15:93023922
|
T | TCCAAGCT others(312): Show |
7 | a0001c0005t0004g0153a0001c0005t0004g0154a0001c0005t0004g0287others(4): Show | 7 | HG00738.hp2 HG01081.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.5154-434_5154-433i others(321): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | INFO_REALIGN_3_PRIME | chr15 | 93023922 | |||||
| chr15:93023922
|
T | TCCAAGCT others(313): Show |
1 | a0001c0005t0004g0283 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.5154-434_5154-433i others(322): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | INFO_REALIGN_3_PRIME | chr15 | 93023922 | |||||
| chr15:93024122
|
G | A | 92 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0028others(89): Show | 92 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.5154-250G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93024122 | ||||||
| chr15:93024137
|
C | T | 1 | a0001c0001t0001g0177 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.5154-235C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93024137 | ||||||
| chr15:93024150
|
T | C | 1 | a0001c0007t0007g0030 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.5154-222T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93024150 | ||||||
| chr15:93024158
|
T | TGTAC | 166 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(163): Show | 169 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(166): Show |
intron_variant | MODIFIER | c.5154-213_5154-210d others(6): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | INFO_REALIGN_3_PRIME | chr15 | 93024158 | |||||
| chr15:93024296
|
G | A | 167 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(164): Show | 170 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(167): Show |
intron_variant | MODIFIER | c.5154-76G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93024296 | ||||||
| chr15:93024297
|
C | T | 11 | a0001c0004t0007g0013a0001c0004t0007g0014a0001c0004t0007g0017others(8): Show | 11 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(8): Show |
intron_variant | MODIFIER | c.5154-75C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93024297 | ||||||
| chr15:93024298
|
C | T | 11 | a0001c0004t0007g0013a0001c0004t0007g0014a0001c0004t0007g0017others(8): Show | 11 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(8): Show |
intron_variant | MODIFIER | c.5154-74C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93024298 |