| geneid | 26038 |
|---|---|
| ensemblid | ENSG00000116254.18 |
| hgncid | 16816 |
| symbol | CHD5 |
| name | chromodomain helicase DNA binding protein 5 |
| refseq_nuc | NM_015557.3 |
| refseq_prot | NP_056372.1 |
| ensembl_nuc | ENST00000262450.8 |
| ensembl_prot | ENSP00000262450.3 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 6101787 |
| end | 6180321 |
| strand | - |
| ver | v1.2 |
| region | chr1:6101787-6180321 |
| region5000 | chr1:6096787-6185321 |
| regionname0 | CHD5_chr1_6101787_6180321 |
| regionname5000 | CHD5_chr1_6096787_6185321 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 1954 | 244 | 58 | 31 | 118 | 6 | 31 | 82 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0002 | 1/1 | 1954 | 69 | 36 | 21 | 0 | 4 | 6 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0003 | 0/0 | 1954 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0004 | 0/0 | 1954 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0005 | 0/0 | 1954 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0006 | 0/0 | 1954 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| 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 | 5865 | 52 | 8 | 2 | 33 | 1 | 8 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| c0002 | 1/1 | 5865 | 38 | 11 | 17 | 0 | 3 | 5 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| c0003 | 0/0 | 5865 | 37 | 0 | 4 | 29 | 2 | 2 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| c0004 | 0/0 | 5865 | 30 | 4 | 2 | 17 | 1 | 6 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| c0005 | 0/0 | 5865 | 19 | 4 | 5 | 9 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| c0006 | 0/0 | 5865 | 14 | 12 | 2 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| c0007 | 0/0 | 5865 | 12 | 0 | 7 | 3 | 0 | 2 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| c0008 | 0/0 | 5865 | 12 | 6 | 0 | 5 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| c0009 | 0/0 | 5865 | 10 | 7 | 1 | 1 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| c0010 | 0/0 | 5865 | 10 | 4 | 3 | 0 | 0 | 3 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| c0011 | 0/0 | 5865 | 10 | 0 | 0 | 9 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| c0012 | 0/0 | 5865 | 6 | 6 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| c0013 | 0/0 | 5865 | 6 | 5 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| c0014 | 0/0 | 5865 | 5 | 5 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| c0015 | 0/0 | 5865 | 5 | 0 | 0 | 5 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| c0016 | 0/0 | 5865 | 4 | 0 | 2 | 0 | 1 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| c0017 | 0/0 | 5865 | 4 | 4 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| c0018 | 0/0 | 5865 | 4 | 0 | 0 | 4 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| c0019 | 0/0 | 5865 | 3 | 3 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| c0020 | 0/0 | 5865 | 3 | 0 | 1 | 2 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| c0021 | 0/0 | 5865 | 2 | 2 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| c0022 | 0/0 | 5865 | 2 | 0 | 2 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| c0023 | 0/0 | 5865 | 2 | 0 | 0 | 0 | 0 | 2 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| c0024 | 0/0 | 5865 | 2 | 0 | 2 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| c0025 | 0/0 | 5865 | 2 | 1 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| c0026 | 0/0 | 5865 | 2 | 2 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| c0027 | 0/0 | 5865 | 2 | 0 | 0 | 0 | 1 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| c0028 | 0/0 | 5865 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| c0029 | 0/0 | 5865 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| c0030 | 0/0 | 5865 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| c0031 | 0/0 | 5865 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| c0032 | 0/0 | 5865 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| c0033 | 0/0 | 5865 | 1 | 0 | 0 | 0 | 1 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| c0034 | 0/0 | 5865 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| c0035 | 0/0 | 5865 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| c0036 | 0/0 | 5865 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| c0037 | 0/0 | 5865 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| c0038 | 0/0 | 5865 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| c0039 | 0/0 | 5865 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| c0040 | 0/0 | 5865 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| c0041 | 0/0 | 5865 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| c0042 | 0/0 | 5865 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| c0043 | 0/0 | 5865 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| c0044 | 0/0 | 5865 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| c0045 | 0/0 | 5865 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| c0046 | 0/0 | 5865 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| c0047 | 0/0 | 5865 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| c0048 | 0/0 | 5865 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| c0049 | 0/0 | 5865 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| 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 | 0/0 | 3988 | 31 | 20 | 6 | 0 | 1 | 4 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0002 | 0/0 | 3984 | 25 | 0 | 6 | 16 | 2 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0003 | 0/0 | 3986 | 24 | 3 | 0 | 14 | 0 | 7 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0004 | 0/0 | 3986 | 24 | 2 | 4 | 14 | 2 | 2 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0005 | 0/0 | 3986 | 20 | 9 | 7 | 0 | 0 | 4 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0006 | 0/0 | 3988 | 18 | 1 | 1 | 16 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0007 | 0/0 | 3986 | 15 | 0 | 0 | 13 | 1 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0008 | 0/0 | 3985 | 13 | 0 | 0 | 13 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0009 | 0/1 | 3988 | 11 | 0 | 9 | 0 | 1 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0010 | 0/0 | 3985 | 9 | 0 | 0 | 8 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0011 | 0/0 | 3988 | 9 | 9 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0012 | 0/0 | 3986 | 6 | 4 | 2 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0013 | 1/0 | 3986 | 5 | 0 | 4 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0014 | 0/0 | 3986 | 5 | 5 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0015 | 0/0 | 3984 | 4 | 0 | 0 | 2 | 0 | 2 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0016 | 0/0 | 3988 | 4 | 0 | 2 | 0 | 1 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0017 | 0/0 | 3988 | 4 | 2 | 1 | 0 | 1 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0018 | 0/0 | 3986 | 4 | 0 | 0 | 4 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0019 | 0/0 | 3988 | 3 | 2 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0020 | 0/0 | 3988 | 3 | 3 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0021 | 0/0 | 3988 | 3 | 0 | 0 | 3 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0022 | 0/0 | 3985 | 3 | 0 | 0 | 3 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0023 | 0/0 | 3988 | 3 | 0 | 0 | 0 | 0 | 3 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0024 | 0/0 | 3986 | 3 | 0 | 0 | 3 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0025 | 0/0 | 3989 | 3 | 3 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0026 | 0/0 | 3988 | 2 | 2 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0027 | 0/0 | 3986 | 2 | 0 | 0 | 0 | 0 | 2 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0028 | 0/0 | 3988 | 2 | 1 | 0 | 0 | 1 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0029 | 0/0 | 3987 | 2 | 0 | 1 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0030 | 0/0 | 3986 | 2 | 0 | 0 | 2 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0031 | 0/0 | 3987 | 2 | 0 | 0 | 0 | 0 | 2 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0032 | 0/0 | 3986 | 2 | 2 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0033 | 0/0 | 3987 | 2 | 2 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0034 | 0/0 | 3988 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0035 | 0/0 | 3986 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0036 | 0/0 | 3985 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0037 | 0/0 | 3988 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0038 | 0/0 | 3986 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0039 | 0/0 | 3986 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0040 | 0/0 | 3988 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0041 | 0/0 | 3986 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0042 | 0/0 | 4029 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0043 | 0/0 | 3986 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0044 | 0/0 | 3988 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0045 | 0/0 | 3988 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0046 | 0/0 | 3984 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0047 | 0/0 | 3984 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0048 | 0/0 | 3989 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0049 | 0/0 | 3984 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0050 | 0/0 | 3986 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0051 | 0/0 | 3986 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0052 | 0/0 | 3987 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0053 | 0/0 | 3988 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0054 | 0/0 | 3988 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0055 | 0/0 | 3988 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0056 | 0/0 | 3985 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0057 | 0/0 | 3986 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0058 | 0/0 | 3988 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0059 | 0/0 | 3988 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0060 | 0/0 | 3986 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0061 | 0/0 | 3988 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0062 | 0/0 | 3987 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0063 | 0/0 | 3986 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0064 | 0/0 | 3989 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0065 | 0/0 | 3987 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0066 | 0/0 | 3988 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0067 | 0/0 | 3986 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0068 | 0/0 | 3986 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0069 | 0/0 | 3986 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0070 | 0/0 | 3986 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0071 | 0/0 | 3986 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0072 | 0/0 | 3986 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0073 | 0/0 | 3986 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0074 | 0/0 | 3986 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0075 | 0/0 | 3987 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0076 | 0/0 | 3987 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0077 | 0/0 | 3987 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0078 | 0/0 | 3989 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0079 | 0/0 | 3989 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0080 | 0/0 | 3987 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0081 | 0/0 | 3987 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0082 | 0/0 | 3987 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0083 | 0/0 | 3987 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0084 | 0/0 | 3988 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| t0085 | 0/0 | 3986 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| 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 | 0/1 | 3 | 0 | 2 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0299 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| 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 | 5865 | 52 | 8 | 2 | 33 | 1 | 8 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0003 | 0/0 | 5865 | 37 | 0 | 4 | 29 | 2 | 2 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0004 | 0/0 | 5865 | 30 | 4 | 2 | 17 | 1 | 6 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0005 | 0/0 | 5865 | 19 | 4 | 5 | 9 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0007 | 0/0 | 5865 | 12 | 0 | 7 | 3 | 0 | 2 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0008 | 0/0 | 5865 | 12 | 6 | 0 | 5 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0009 | 0/0 | 5865 | 10 | 7 | 1 | 1 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0010 | 0/0 | 5865 | 10 | 4 | 3 | 0 | 0 | 3 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0011 | 0/0 | 5865 | 10 | 0 | 0 | 9 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0013 | 0/0 | 5865 | 6 | 5 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0014 | 0/0 | 5865 | 5 | 5 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0015 | 0/0 | 5865 | 5 | 0 | 0 | 5 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0016 | 0/0 | 5865 | 4 | 0 | 2 | 0 | 1 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0019 | 0/0 | 5865 | 3 | 3 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0020 | 0/0 | 5865 | 3 | 0 | 1 | 2 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0021 | 0/0 | 5865 | 2 | 2 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0023 | 0/0 | 5865 | 2 | 0 | 0 | 0 | 0 | 2 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0024 | 0/0 | 5865 | 2 | 0 | 2 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0026 | 0/0 | 5865 | 2 | 2 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0027 | 0/0 | 5865 | 2 | 0 | 0 | 0 | 1 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0028 | 0/0 | 5865 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0029 | 0/0 | 5865 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0030 | 0/0 | 5865 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0031 | 0/0 | 5865 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0032 | 0/0 | 5865 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0035 | 0/0 | 5865 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0036 | 0/0 | 5865 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0038 | 0/0 | 5865 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0039 | 0/0 | 5865 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0041 | 0/0 | 5865 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0042 | 0/0 | 5865 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0043 | 0/0 | 5865 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0044 | 0/0 | 5865 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0045 | 0/0 | 5865 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0048 | 0/0 | 5865 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0049 | 0/0 | 5865 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0002c0002 | 1/1 | 5865 | 38 | 11 | 17 | 0 | 3 | 5 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0002c0006 | 0/0 | 5865 | 14 | 12 | 2 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0002c0012 | 0/0 | 5865 | 6 | 6 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0002c0017 | 0/0 | 5865 | 4 | 4 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0002c0022 | 0/0 | 5865 | 2 | 0 | 2 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0002c0025 | 0/0 | 5865 | 2 | 1 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0002c0033 | 0/0 | 5865 | 1 | 0 | 0 | 0 | 1 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0002c0040 | 0/0 | 5865 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0002c0047 | 0/0 | 5865 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0003c0018 | 0/0 | 5865 | 4 | 0 | 0 | 4 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0004c0037 | 0/0 | 5865 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0005c0034 | 0/0 | 5865 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0006c0046 | 0/0 | 5865 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0003 | 0/0 | 9850 | 15 | 1 | 0 | 10 | 0 | 4 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0001t0004 | 0/0 | 9850 | 4 | 1 | 0 | 3 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0001t0005 | 0/0 | 9850 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0001t0006 | 0/0 | 9852 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0001t0007 | 0/0 | 9850 | 15 | 0 | 0 | 13 | 1 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0001t0008 | 0/0 | 9849 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0001t0011 | 0/0 | 9852 | 3 | 3 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0001t0027 | 0/0 | 9850 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0001t0029 | 0/0 | 9851 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0001t0038 | 0/0 | 9850 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0001t0050 | 0/0 | 9850 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0001t0054 | 0/0 | 9852 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0001t0064 | 0/0 | 9853 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0001t0068 | 0/0 | 9850 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0001t0069 | 0/0 | 9850 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0001t0070 | 0/0 | 9850 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0001t0071 | 0/0 | 9850 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0001t0077 | 0/0 | 9851 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0001t0084 | 0/0 | 9852 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0003t0002 | 0/0 | 9848 | 15 | 0 | 4 | 9 | 2 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0003t0008 | 0/0 | 9849 | 9 | 0 | 0 | 9 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0003t0010 | 0/0 | 9849 | 3 | 0 | 0 | 3 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0003t0015 | 0/0 | 9848 | 2 | 0 | 0 | 0 | 0 | 2 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0003t0021 | 0/0 | 9852 | 2 | 0 | 0 | 2 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0003t0022 | 0/0 | 9849 | 3 | 0 | 0 | 3 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0003t0036 | 0/0 | 9849 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0003t0046 | 0/0 | 9848 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0003t0047 | 0/0 | 9848 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0004t0003 | 0/0 | 9850 | 2 | 0 | 0 | 0 | 0 | 2 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0004t0004 | 0/0 | 9850 | 11 | 0 | 2 | 7 | 1 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0004t0006 | 0/0 | 9852 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0004t0011 | 0/0 | 9852 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0004t0018 | 0/0 | 9850 | 4 | 0 | 0 | 4 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0004t0024 | 0/0 | 9850 | 3 | 0 | 0 | 3 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0004t0027 | 0/0 | 9850 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0004t0030 | 0/0 | 9850 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0004t0031 | 0/0 | 9851 | 2 | 0 | 0 | 0 | 0 | 2 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0004t0066 | 0/0 | 9852 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0004t0072 | 0/0 | 9850 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0004t0075 | 0/0 | 9851 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0004t0083 | 0/0 | 9851 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0005t0001 | 0/0 | 9852 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0005t0002 | 0/0 | 9848 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0005t0004 | 0/0 | 9850 | 2 | 0 | 2 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0005t0005 | 0/0 | 9850 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0005t0006 | 0/0 | 9852 | 9 | 1 | 0 | 8 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0005t0013 | 0/0 | 9850 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0005t0030 | 0/0 | 9850 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0005t0043 | 0/0 | 9850 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0005t0055 | 0/0 | 9852 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0005t0057 | 0/0 | 9850 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0007t0003 | 0/0 | 9850 | 4 | 0 | 0 | 3 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0007t0005 | 0/0 | 9850 | 5 | 0 | 4 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0007t0044 | 0/0 | 9852 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0007t0058 | 0/0 | 9852 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0007t0059 | 0/0 | 9852 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0008t0001 | 0/0 | 9852 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0008t0002 | 0/0 | 9848 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0008t0003 | 0/0 | 9850 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0008t0005 | 0/0 | 9850 | 2 | 2 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0008t0006 | 0/0 | 9852 | 3 | 0 | 0 | 3 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0008t0012 | 0/0 | 9850 | 3 | 3 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0008t0037 | 0/0 | 9852 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0009t0003 | 0/0 | 9850 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0009t0004 | 0/0 | 9850 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0009t0011 | 0/0 | 9852 | 2 | 2 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0009t0014 | 0/0 | 9850 | 2 | 2 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0009t0039 | 0/0 | 9850 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0009t0041 | 0/0 | 9850 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0009t0073 | 0/0 | 9850 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0009t0079 | 0/0 | 9853 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0010t0003 | 0/0 | 9850 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0010t0004 | 0/0 | 9850 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0010t0005 | 0/0 | 9850 | 3 | 0 | 2 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0010t0012 | 0/0 | 9850 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0010t0014 | 0/0 | 9850 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0010t0051 | 0/0 | 9850 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0010t0056 | 0/0 | 9849 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0010t0080 | 0/0 | 9851 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0011t0008 | 0/0 | 9849 | 2 | 0 | 0 | 2 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0011t0010 | 0/0 | 9849 | 6 | 0 | 0 | 5 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0011t0021 | 0/0 | 9852 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0011t0048 | 0/0 | 9853 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0013t0005 | 0/0 | 9850 | 2 | 1 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0013t0032 | 0/0 | 9850 | 2 | 2 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0013t0042 | 0/0 | 9893 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0013t0060 | 0/0 | 9850 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0014t0001 | 0/0 | 9852 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0014t0011 | 0/0 | 9852 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0014t0033 | 0/0 | 9851 | 2 | 2 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0014t0081 | 0/0 | 9851 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0015t0002 | 0/0 | 9848 | 3 | 0 | 0 | 3 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0015t0006 | 0/0 | 9852 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0015t0008 | 0/0 | 9849 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0016t0016 | 0/0 | 9852 | 4 | 0 | 2 | 0 | 1 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0019t0011 | 0/0 | 9852 | 2 | 2 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0019t0085 | 0/0 | 9850 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0020t0002 | 0/0 | 9848 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0020t0004 | 0/0 | 9850 | 2 | 0 | 0 | 2 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0021t0005 | 0/0 | 9850 | 2 | 2 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0023t0002 | 0/0 | 9848 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0023t0074 | 0/0 | 9850 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0024t0012 | 0/0 | 9850 | 2 | 0 | 2 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0026t0005 | 0/0 | 9850 | 2 | 2 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0027t0004 | 0/0 | 9850 | 1 | 0 | 0 | 0 | 1 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0027t0067 | 0/0 | 9850 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0028t0014 | 0/0 | 9850 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0029t0076 | 0/0 | 9851 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0030t0029 | 0/0 | 9851 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0031t0034 | 0/0 | 9852 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0032t0004 | 0/0 | 9850 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0035t0002 | 0/0 | 9848 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0036t0006 | 0/0 | 9852 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0038t0035 | 0/0 | 9850 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0039t0063 | 0/0 | 9850 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0041t0014 | 0/0 | 9850 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0042t0005 | 0/0 | 9850 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0043t0053 | 0/0 | 9852 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0044t0082 | 0/0 | 9851 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0045t0004 | 0/0 | 9850 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0048t0005 | 0/0 | 9850 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0001c0049t0049 | 0/0 | 9848 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0002c0002t0001 | 0/0 | 9852 | 10 | 3 | 4 | 0 | 1 | 2 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0002c0002t0009 | 0/1 | 9852 | 9 | 0 | 8 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0002c0002t0013 | 1/0 | 9850 | 4 | 0 | 3 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0002c0002t0017 | 0/0 | 9852 | 4 | 2 | 1 | 0 | 1 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0002c0002t0020 | 0/0 | 9852 | 3 | 3 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0002c0002t0023 | 0/0 | 9852 | 3 | 0 | 0 | 0 | 0 | 3 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0002c0002t0026 | 0/0 | 9852 | 2 | 2 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0002c0002t0028 | 0/0 | 9852 | 1 | 0 | 0 | 0 | 1 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0002c0002t0045 | 0/0 | 9852 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0002c0002t0062 | 0/0 | 9851 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0002c0006t0001 | 0/0 | 9852 | 9 | 8 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0002c0006t0019 | 0/0 | 9852 | 3 | 2 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0002c0006t0040 | 0/0 | 9852 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0002c0006t0061 | 0/0 | 9852 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0002c0012t0001 | 0/0 | 9852 | 2 | 2 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0002c0012t0025 | 0/0 | 9853 | 3 | 3 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0002c0012t0052 | 0/0 | 9851 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0002c0017t0001 | 0/0 | 9852 | 3 | 3 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0002c0017t0028 | 0/0 | 9852 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0002c0022t0001 | 0/0 | 9852 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0002c0022t0009 | 0/0 | 9852 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0002c0025t0001 | 0/0 | 9852 | 2 | 1 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0002c0033t0009 | 0/0 | 9852 | 1 | 0 | 0 | 0 | 1 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0002c0040t0001 | 0/0 | 9852 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0002c0047t0078 | 0/0 | 9853 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0003c0018t0002 | 0/0 | 9848 | 2 | 0 | 0 | 2 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0003c0018t0015 | 0/0 | 9848 | 2 | 0 | 0 | 2 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0004c0037t0065 | 0/0 | 9851 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0005c0034t0006 | 0/0 | 9852 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| a0006c0046t0006 | 0/0 | 9852 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | copy fasta | chr1 | 6096787 | 6185321 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0001t0003g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0001t0004g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0001t0004g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0001t0004g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0001t0004g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0001t0005g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0001t0006g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0001t0007g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0001t0007g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0001t0007g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0001t0007g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0001t0007g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0001t0007g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0001t0007g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0001t0007g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0001t0007g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0001t0007g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0001t0007g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0001t0007g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0001t0007g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0001t0007g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0001t0007g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0001t0008g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0001t0011g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0001t0011g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0001t0011g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0001t0027g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0001t0029g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0001t0038g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0001t0050g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0001t0054g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0001t0064g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0001t0068g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0001t0069g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0001t0070g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0001t0071g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0001t0077g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0001t0084g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0003t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0003t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0003t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0003t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0003t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0003t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0003t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0003t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0003t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0003t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0003t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0003t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0003t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0003t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0003t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0003t0008g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0003t0008g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0003t0008g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0003t0008g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0003t0008g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0003t0008g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0003t0008g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0003t0008g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0003t0008g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0003t0010g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0003t0010g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0003t0010g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0003t0015g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0003t0015g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0003t0021g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0003t0021g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0003t0022g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0003t0022g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0003t0022g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0003t0036g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0003t0046g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0003t0047g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0004t0003g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0004t0003g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0004t0004g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0004t0004g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0004t0004g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0004t0004g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0004t0004g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0004t0004g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0004t0004g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0004t0004g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0004t0004g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0004t0004g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0004t0004g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0004t0006g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0004t0011g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0004t0018g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0004t0018g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0004t0018g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0004t0018g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0004t0024g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0004t0024g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0004t0024g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0004t0027g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0004t0030g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0004t0031g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0004t0031g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0004t0066g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0004t0072g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0004t0075g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0004t0083g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0005t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0005t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0005t0004g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0005t0004g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0005t0005g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0005t0006g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0005t0006g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0005t0006g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0005t0006g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0005t0006g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0005t0006g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0005t0006g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0005t0006g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0005t0006g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0005t0013g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0005t0030g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0005t0043g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0005t0055g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0005t0057g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0007t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0007t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0007t0003g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0007t0003g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0007t0005g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0007t0005g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0007t0005g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0007t0005g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0007t0005g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0007t0044g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0007t0058g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0007t0059g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0008t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0008t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0008t0003g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0008t0005g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0008t0005g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0008t0006g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0008t0006g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0008t0006g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0008t0012g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0008t0012g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0008t0012g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0008t0037g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0009t0003g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0009t0004g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0009t0011g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0009t0011g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0009t0014g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0009t0014g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0009t0039g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0009t0041g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0009t0073g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0009t0079g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0010t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0010t0004g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0010t0005g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0010t0005g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0010t0005g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0010t0012g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0010t0014g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0010t0051g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0010t0056g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0010t0080g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0011t0008g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0011t0008g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0011t0010g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0011t0010g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0011t0010g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0011t0010g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0011t0010g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0011t0010g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0011t0021g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0011t0048g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0013t0005g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0013t0005g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0013t0032g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0013t0032g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0013t0042g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0013t0060g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0014t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0014t0011g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0014t0033g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0014t0033g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0014t0081g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0015t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0015t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0015t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0015t0006g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0015t0008g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0016t0016g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0016t0016g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0016t0016g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0016t0016g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0019t0011g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0019t0011g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0019t0085g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0020t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0020t0004g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0020t0004g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0021t0005g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0021t0005g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0023t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0023t0074g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0024t0012g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0026t0005g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0026t0005g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0027t0004g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0027t0067g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0028t0014g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0029t0076g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0030t0029g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0031t0034g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0032t0004g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0035t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0036t0006g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0038t0035g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0039t0063g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0041t0014g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0042t0005g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0043t0053g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0044t0082g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0045t0004g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0048t0005g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0001c0049t0049g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0002c0002t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0002c0002t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0002c0002t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0002c0002t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0002c0002t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0002c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0002c0002t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0002c0002t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0002c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0002c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0002c0002t0009g0001 | 0/1 | 3 | 0 | 2 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0002c0002t0009g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0002c0002t0009g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0002c0002t0009g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0002c0002t0009g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0002c0002t0009g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0002c0002t0009g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0002c0002t0013g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0002c0002t0013g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0002c0002t0013g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0002c0002t0013g0299 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0002c0002t0017g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0002c0002t0017g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0002c0002t0017g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0002c0002t0017g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0002c0002t0020g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0002c0002t0020g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0002c0002t0020g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0002c0002t0023g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0002c0002t0023g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0002c0002t0023g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0002c0002t0026g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0002c0002t0026g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0002c0002t0028g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0002c0002t0045g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0002c0002t0062g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0002c0006t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0002c0006t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0002c0006t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0002c0006t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0002c0006t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0002c0006t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0002c0006t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0002c0006t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0002c0006t0019g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0002c0006t0019g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0002c0006t0019g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0002c0006t0040g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0002c0006t0061g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0002c0012t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0002c0012t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0002c0012t0025g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0002c0012t0025g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0002c0012t0025g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0002c0012t0052g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0002c0017t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0002c0017t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0002c0017t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0002c0017t0028g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0002c0022t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0002c0022t0009g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0002c0025t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0002c0025t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0002c0033t0009g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0002c0040t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0002c0047t0078g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0003c0018t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0003c0018t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0003c0018t0015g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0003c0018t0015g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0004c0037t0065g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0005c0034t0006g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| a0006c0046t0006g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0033 | t0009 | g0243 | EUR | GBR | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG00099 | hp2 | a0002 | c0002 | t0017 | g0247 | EUR | GBR | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG00140 | hp1 | a0002 | c0002 | t0001 | g0244 | EUR | GBR | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG00140 | hp2 | a0001 | c0016 | t0016 | g0074 | EUR | GBR | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG00323 | hp1 | a0001 | c0003 | t0002 | g0120 | EUR | FIN | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG00323 | hp2 | a0001 | c0001 | t0007 | g0221 | EUR | FIN | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG00408 | hp1 | a0001 | c0003 | t0002 | g0158 | EAS | CHS | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG00408 | hp2 | a0001 | c0011 | t0010 | g0168 | EAS | CHS | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG00423 | hp1 | a0001 | c0004 | t0024 | g0171 | EAS | CHS | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG00423 | hp2 | a0001 | c0001 | t0071 | g0194 | EAS | CHS | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG00438 | hp1 | a0001 | c0003 | t0046 | g0204 | EAS | CHS | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG00438 | hp2 | a0001 | c0001 | t0007 | g0113 | EAS | CHS | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG00544 | hp1 | a0001 | c0001 | t0050 | g0035 | EAS | CHS | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG00544 | hp2 | a0001 | c0020 | t0004 | g0277 | EAS | CHS | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG00609 | hp1 | a0001 | c0011 | t0008 | g0265 | EAS | CHS | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG00609 | hp2 | a0001 | c0003 | t0010 | g0117 | EAS | CHS | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0159 | EAS | CHS | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG00673 | hp2 | a0001 | c0004 | t0004 | g0118 | EAS | CHS | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG00738 | hp1 | a0001 | c0004 | t0004 | g0094 | AMR | PUR | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG00738 | hp2 | a0001 | c0020 | t0002 | g0051 | AMR | PUR | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG00741 | hp1 | a0002 | c0002 | t0001 | g0108 | AMR | PUR | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG00741 | hp2 | a0002 | c0002 | t0013 | g0088 | AMR | PUR | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG01069 | hp1 | a0001 | c0005 | t0055 | g0052 | AMR | PUR | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG01069 | hp2 | a0002 | c0002 | t0001 | g0107 | AMR | PUR | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG01070 | hp1 | a0001 | c0003 | t0002 | g0122 | AMR | PUR | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG01070 | hp2 | a0001 | c0007 | t0059 | g0029 | AMR | PUR | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG01081 | hp1 | a0002 | c0002 | t0009 | g0086 | AMR | PUR | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG01081 | hp2 | a0002 | c0002 | t0017 | g0073 | AMR | PUR | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG01099 | hp1 | a0001 | c0009 | t0073 | g0142 | AMR | PUR | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG01099 | hp2 | a0002 | c0002 | t0001 | g0105 | AMR | PUR | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG01106 | hp1 | a0001 | c0001 | t0029 | g0055 | AMR | PUR | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG01106 | hp2 | a0001 | c0003 | t0002 | g0089 | AMR | PUR | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG01109 | hp1 | a0002 | c0006 | t0019 | g0011 | AMR | PUR | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG01109 | hp2 | a0001 | c0005 | t0002 | g0112 | AMR | PUR | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG01167 | hp1 | a0001 | c0010 | t0080 | g0303 | AMR | PUR | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG01167 | hp2 | a0001 | c0024 | t0012 | g0003 | AMR | PUR | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG01168 | hp1 | a0002 | c0002 | t0009 | g0077 | AMR | PUR | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG01168 | hp2 | a0001 | c0005 | t0004 | g0144 | AMR | PUR | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG01169 | hp1 | a0001 | c0024 | t0012 | g0003 | AMR | PUR | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG01169 | hp2 | a0001 | c0005 | t0004 | g0076 | AMR | PUR | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG01243 | hp1 | a0001 | c0013 | t0005 | g0156 | AMR | PUR | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG01243 | hp2 | a0001 | c0001 | t0054 | g0292 | AMR | PUR | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG01255 | hp1 | a0001 | c0007 | t0005 | g0041 | AMR | CLM | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG01255 | hp2 | a0002 | c0022 | t0009 | g0036 | AMR | CLM | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG01256 | hp1 | a0001 | c0007 | t0058 | g0028 | AMR | CLM | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG01256 | hp2 | a0002 | c0002 | t0013 | g0082 | AMR | CLM | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG01257 | hp1 | a0001 | c0003 | t0002 | g0128 | AMR | CLM | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG01257 | hp2 | a0002 | c0002 | t0062 | g0268 | AMR | CLM | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0200 | AMR | CLM | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG01261 | hp2 | a0001 | c0010 | t0005 | g0143 | AMR | CLM | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG01346 | hp1 | a0002 | c0002 | t0009 | g0109 | AMR | CLM | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG01346 | hp2 | a0001 | c0016 | t0016 | g0137 | AMR | CLM | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG01358 | hp1 | a0001 | c0016 | t0016 | g0136 | AMR | CLM | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG01358 | hp2 | a0002 | c0006 | t0001 | g0145 | AMR | CLM | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG01361 | hp1 | a0002 | c0002 | t0009 | g0001 | AMR | CLM | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG01361 | hp2 | a0001 | c0010 | t0005 | g0123 | AMR | CLM | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG01496 | hp1 | a0002 | c0002 | t0009 | g0091 | AMR | CLM | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG01496 | hp2 | a0001 | c0036 | t0006 | g0210 | AMR | CLM | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG01884 | hp1 | a0002 | c0047 | t0078 | g0314 | AFR | ACB | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG01884 | hp2 | a0001 | c0008 | t0003 | g0249 | AFR | ACB | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG01891 | hp1 | a0001 | c0010 | t0012 | g0043 | AFR | ACB | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG01891 | hp2 | a0001 | c0038 | t0035 | g0005 | AFR | ACB | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG01928 | hp1 | a0002 | c0002 | t0009 | g0110 | AMR | PEL | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG01928 | hp2 | a0001 | c0007 | t0005 | g0141 | AMR | PEL | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG01934 | hp1 | a0002 | c0002 | t0009 | g0034 | AMR | PEL | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG01934 | hp2 | a0001 | c0003 | t0002 | g0090 | AMR | PEL | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG01975 | hp1 | a0001 | c0007 | t0005 | g0197 | AMR | PEL | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG01975 | hp2 | a0002 | c0022 | t0001 | g0023 | AMR | PEL | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG02015 | hp1 | a0001 | c0005 | t0006 | g0025 | EAS | KHV | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG02015 | hp2 | a0001 | c0003 | t0010 | g0212 | EAS | KHV | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG02027 | hp1 | a0001 | c0001 | t0004 | g0138 | EAS | KHV | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG02027 | hp2 | a0001 | c0003 | t0047 | g0175 | EAS | KHV | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG02055 | hp1 | a0001 | c0014 | t0033 | g0305 | AFR | ACB | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG02055 | hp2 | a0002 | c0017 | t0001 | g0295 | AFR | ACB | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG02071 | hp1 | a0001 | c0001 | t0007 | g0237 | EAS | KHV | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG02071 | hp2 | a0001 | c0007 | t0003 | g0068 | EAS | KHV | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG02074 | hp1 | a0001 | c0005 | t0006 | g0147 | EAS | KHV | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG02074 | hp2 | a0001 | c0003 | t0021 | g0039 | EAS | KHV | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG02080 | hp1 | a0001 | c0004 | t0004 | g0290 | EAS | KHV | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG02080 | hp2 | a0001 | c0001 | t0007 | g0100 | EAS | KHV | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG02083 | hp1 | a0001 | c0008 | t0006 | g0264 | EAS | KHV | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG02083 | hp2 | a0001 | c0003 | t0002 | g0130 | EAS | KHV | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG02129 | hp1 | a0001 | c0003 | t0010 | g0040 | EAS | KHV | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG02129 | hp2 | a0001 | c0004 | t0066 | g0111 | EAS | KHV | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0079 | EAS | KHV | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG02135 | hp2 | a0001 | c0015 | t0008 | g0209 | EAS | KHV | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG02145 | hp1 | a0001 | c0004 | t0011 | g0226 | AFR | ACB | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG02145 | hp2 | a0002 | c0012 | t0052 | g0045 | AFR | ACB | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG02155 | hp1 | a0001 | c0005 | t0006 | g0215 | EAS | CDX | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG02155 | hp2 | a0001 | c0003 | t0002 | g0022 | EAS | CDX | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG02165 | hp1 | a0001 | c0007 | t0003 | g0067 | EAS | CDX | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG02165 | hp2 | a0001 | c0043 | t0053 | g0271 | EAS | CDX | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG02257 | hp1 | a0001 | c0004 | t0075 | g0300 | AFR | ACB | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG02257 | hp2 | a0001 | c0001 | t0084 | g0310 | AFR | ACB | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG02258 | hp1 | a0001 | c0008 | t0012 | g0222 | AFR | ACB | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG02258 | hp2 | a0002 | c0002 | t0017 | g0092 | AFR | ACB | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG02273 | hp1 | a0001 | c0007 | t0005 | g0140 | AMR | PEL | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG02273 | hp2 | a0002 | c0002 | t0009 | g0001 | AMR | PEL | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG02280 | hp1 | a0002 | c0002 | t0020 | g0021 | AFR | ACB | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG02280 | hp2 | a0001 | c0013 | t0032 | g0228 | AFR | ACB | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG02293 | hp1 | a0001 | c0007 | t0044 | g0016 | AMR | PEL | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG02293 | hp2 | a0002 | c0002 | t0013 | g0127 | AMR | PEL | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG02451 | hp1 | a0001 | c0001 | t0068 | g0085 | AFR | ACB | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG02451 | hp2 | a0002 | c0017 | t0028 | g0293 | AFR | ACB | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG02572 | hp1 | a0002 | c0012 | t0001 | g0048 | AFR | GWD | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG02572 | hp2 | a0001 | c0039 | t0063 | g0241 | AFR | GWD | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG02602 | hp1 | a0001 | c0027 | t0067 | g0205 | SAS | PJL | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0176 | SAS | PJL | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG02615 | hp1 | a0002 | c0002 | t0001 | g0225 | AFR | GWD | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG02615 | hp2 | a0001 | c0009 | t0011 | g0240 | AFR | GWD | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG02622 | hp1 | a0001 | c0005 | t0043 | g0017 | AFR | GWD | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG02622 | hp2 | a0002 | c0006 | t0001 | g0216 | AFR | GWD | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG02630 | hp1 | a0001 | c0041 | t0014 | g0250 | AFR | GWD | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG02630 | hp2 | a0002 | c0012 | t0025 | g0306 | AFR | GWD | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG02647 | hp1 | a0001 | c0009 | t0041 | g0014 | AFR | GWD | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG02647 | hp2 | a0001 | c0014 | t0001 | g0049 | AFR | GWD | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0182 | SAS | PJL | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG02698 | hp2 | a0001 | c0001 | t0069 | g0190 | SAS | PJL | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG02717 | hp1 | a0002 | c0002 | t0001 | g0126 | AFR | GWD | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG02717 | hp2 | a0001 | c0013 | t0032 | g0224 | AFR | GWD | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG02723 | hp1 | a0002 | c0006 | t0040 | g0009 | AFR | GWD | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG02723 | hp2 | a0001 | c0013 | t0060 | g0227 | AFR | GWD | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG02735 | hp1 | a0002 | c0002 | t0001 | g0245 | SAS | PJL | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG02735 | hp2 | a0001 | c0007 | t0003 | g0284 | SAS | PJL | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG02738 | hp1 | a0001 | c0023 | t0074 | g0315 | SAS | PJL | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG02738 | hp2 | a0001 | c0004 | t0031 | g0084 | SAS | PJL | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG02809 | hp1 | a0001 | c0026 | t0005 | g0235 | AFR | GWD | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG02809 | hp2 | a0002 | c0006 | t0001 | g0064 | AFR | GWD | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG02818 | hp1 | a0001 | c0005 | t0006 | g0202 | AFR | GWD | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG02818 | hp2 | a0001 | c0019 | t0085 | g0316 | AFR | GWD | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0282 | AFR | GWD | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG02886 | hp2 | a0001 | c0010 | t0014 | g0242 | AFR | GWD | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG02895 | hp1 | a0001 | c0010 | t0004 | g0030 | AFR | GWD | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG02895 | hp2 | a0001 | c0004 | t0072 | g0065 | AFR | GWD | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG02896 | hp1 | a0002 | c0002 | t0026 | g0285 | AFR | GWD | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG02896 | hp2 | a0001 | c0019 | t0011 | g0231 | AFR | GWD | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG02922 | hp1 | a0001 | c0013 | t0005 | g0236 | AFR | ESN | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG02922 | hp2 | a0001 | c0001 | t0011 | g0297 | AFR | ESN | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG02965 | hp1 | a0001 | c0008 | t0012 | g0296 | AFR | ESN | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG02965 | hp2 | a0002 | c0002 | t0017 | g0286 | AFR | ESN | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG02970 | hp1 | a0002 | c0012 | t0001 | g0037 | AFR | ESN | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG02970 | hp2 | a0002 | c0002 | t0045 | g0020 | AFR | ESN | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG02976 | hp1 | a0002 | c0012 | t0025 | g0312 | AFR | ESN | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG02976 | hp2 | a0002 | c0002 | t0020 | g0019 | AFR | ESN | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG03017 | hp1 | a0002 | c0002 | t0001 | g0154 | SAS | PJL | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0239 | SAS | PJL | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG03041 | hp1 | a0001 | c0028 | t0014 | g0058 | AFR | GWD | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG03041 | hp2 | a0001 | c0009 | t0039 | g0013 | AFR | GWD | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG03098 | hp1 | a0001 | c0001 | t0011 | g0232 | AFR | MSL | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG03098 | hp2 | a0001 | c0008 | t0012 | g0223 | AFR | MSL | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG03130 | hp1 | a0002 | c0017 | t0001 | g0294 | AFR | ESN | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG03130 | hp2 | a0002 | c0006 | t0001 | g0060 | AFR | ESN | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG03139 | hp1 | a0001 | c0008 | t0005 | g0056 | AFR | ESN | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG03139 | hp2 | a0002 | c0002 | t0020 | g0018 | AFR | ESN | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG03195 | hp1 | a0002 | c0002 | t0026 | g0042 | AFR | ESN | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG03195 | hp2 | a0001 | c0029 | t0076 | g0309 | AFR | ESN | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG03209 | hp1 | a0001 | c0013 | t0042 | g0015 | AFR | MSL | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG03209 | hp2 | a0002 | c0006 | t0019 | g0010 | AFR | MSL | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG03225 | hp1 | a0001 | c0014 | t0033 | g0304 | AFR | MSL | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG03225 | hp2 | a0001 | c0044 | t0082 | g0313 | AFR | MSL | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG03453 | hp1 | a0002 | c0006 | t0061 | g0061 | AFR | MSL | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG03453 | hp2 | a0001 | c0009 | t0014 | g0229 | AFR | MSL | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG03486 | hp1 | a0001 | c0021 | t0005 | g0027 | AFR | MSL | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG03486 | hp2 | a0001 | c0009 | t0014 | g0059 | AFR | MSL | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG03491 | hp1 | a0002 | c0002 | t0023 | g0213 | SAS | PJL | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG03491 | hp2 | a0001 | c0009 | t0004 | g0139 | SAS | PJL | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG03492 | hp1 | a0001 | c0004 | t0004 | g0081 | SAS | PJL | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG03492 | hp2 | a0002 | c0002 | t0023 | g0214 | SAS | PJL | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG03516 | hp1 | a0001 | c0021 | t0005 | g0026 | AFR | ESN | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG03516 | hp2 | a0002 | c0040 | t0001 | g0031 | AFR | ESN | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG03540 | hp1 | a0001 | c0009 | t0011 | g0252 | AFR | GWD | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG03540 | hp2 | a0002 | c0017 | t0001 | g0248 | AFR | GWD | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG03579 | hp1 | a0002 | c0006 | t0001 | g0002 | AFR | MSL | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG03579 | hp2 | a0002 | c0006 | t0019 | g0012 | AFR | MSL | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG03654 | hp1 | a0001 | c0004 | t0027 | g0104 | SAS | PJL | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG03654 | hp2 | a0001 | c0016 | t0016 | g0069 | SAS | PJL | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG03669 | hp1 | a0001 | c0023 | t0002 | g0260 | SAS | PJL | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG03669 | hp2 | a0001 | c0030 | t0029 | g0211 | SAS | PJL | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG03688 | hp1 | a0001 | c0003 | t0015 | g0157 | SAS | STU | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG03688 | hp2 | a0001 | c0010 | t0005 | g0098 | SAS | STU | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG03834 | hp1 | a0001 | c0004 | t0003 | g0024 | SAS | BEB | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG03834 | hp2 | a0001 | c0011 | t0010 | g0148 | SAS | BEB | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG03927 | hp1 | a0001 | c0001 | t0077 | g0301 | SAS | BEB | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG03927 | hp2 | a0001 | c0010 | t0051 | g0238 | SAS | BEB | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG03942 | hp1 | a0002 | c0002 | t0023 | g0199 | SAS | BEB | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG03942 | hp2 | a0001 | c0003 | t0015 | g0181 | SAS | BEB | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG04115 | hp1 | a0004 | c0037 | t0065 | g0125 | SAS | STU | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG04115 | hp2 | a0001 | c0001 | t0027 | g0132 | SAS | STU | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG04184 | hp1 | a0001 | c0048 | t0005 | g0133 | SAS | BEB | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG04184 | hp2 | a0001 | c0007 | t0005 | g0246 | SAS | BEB | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG04199 | hp1 | a0001 | c0004 | t0031 | g0283 | SAS | STU | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG04199 | hp2 | a0001 | c0008 | t0001 | g0106 | SAS | STU | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0135 | SAS | STU | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG04204 | hp2 | a0002 | c0025 | t0001 | g0189 | SAS | STU | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG04228 | hp1 | a0001 | c0004 | t0003 | g0267 | SAS | STU | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG04228 | hp2 | a0001 | c0005 | t0005 | g0099 | SAS | STU | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA18522 | hp1 | a0002 | c0006 | t0001 | g0002 | AFR | YRI | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA18522 | hp2 | a0001 | c0010 | t0003 | g0044 | AFR | YRI | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA18612 | hp1 | a0001 | c0005 | t0006 | g0151 | EAS | CHB | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA18612 | hp2 | a0001 | c0001 | t0007 | g0080 | EAS | CHB | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA18747 | hp1 | a0001 | c0011 | t0010 | g0103 | EAS | CHB | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA18747 | hp2 | a0001 | c0001 | t0007 | g0203 | EAS | CHB | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA18906 | hp1 | a0001 | c0014 | t0081 | g0307 | AFR | YRI | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA18906 | hp2 | a0001 | c0008 | t0005 | g0230 | AFR | YRI | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA18939 | hp1 | a0001 | c0003 | t0022 | g0207 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA18939 | hp2 | a0001 | c0001 | t0003 | g0206 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA18942 | hp1 | a0005 | c0034 | t0006 | g0218 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA18942 | hp2 | a0001 | c0001 | t0004 | g0054 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA18943 | hp1 | a0001 | c0007 | t0003 | g0287 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA18943 | hp2 | a0001 | c0008 | t0006 | g0179 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA18944 | hp1 | a0001 | c0045 | t0004 | g0272 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA18944 | hp2 | a0001 | c0003 | t0002 | g0256 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA18945 | hp1 | a0001 | c0005 | t0006 | g0288 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA18945 | hp2 | a0001 | c0015 | t0006 | g0102 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA18947 | hp1 | a0001 | c0004 | t0004 | g0270 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA18947 | hp2 | a0001 | c0011 | t0010 | g0160 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA18948 | hp1 | a0001 | c0003 | t0002 | g0253 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA18948 | hp2 | a0001 | c0001 | t0003 | g0146 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA18950 | hp1 | a0001 | c0003 | t0022 | g0192 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA18950 | hp2 | a0001 | c0005 | t0006 | g0289 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA18951 | hp1 | a0001 | c0032 | t0004 | g0172 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA18951 | hp2 | a0001 | c0003 | t0022 | g0220 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA18952 | hp1 | a0001 | c0001 | t0003 | g0150 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA18952 | hp2 | a0001 | c0003 | t0008 | g0119 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA18953 | hp1 | a0001 | c0003 | t0008 | g0155 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA18953 | hp2 | a0001 | c0004 | t0004 | g0177 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA18959 | hp1 | a0001 | c0005 | t0030 | g0259 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA18959 | hp2 | a0001 | c0003 | t0021 | g0298 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA18962 | hp1 | a0001 | c0011 | t0010 | g0183 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA18962 | hp2 | a0001 | c0001 | t0007 | g0078 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA18963 | hp1 | a0001 | c0001 | t0007 | g0219 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA18963 | hp2 | a0001 | c0015 | t0002 | g0170 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA18967 | hp1 | a0001 | c0001 | t0008 | g0095 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA18967 | hp2 | a0001 | c0009 | t0003 | g0281 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA18968 | hp1 | a0001 | c0011 | t0010 | g0184 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA18968 | hp2 | a0001 | c0005 | t0006 | g0124 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA18969 | hp1 | a0001 | c0015 | t0002 | g0169 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA18969 | hp2 | a0001 | c0020 | t0004 | g0278 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA18970 | hp1 | a0001 | c0011 | t0021 | g0161 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA18970 | hp2 | a0001 | c0001 | t0007 | g0258 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA18971 | hp1 | a0001 | c0001 | t0007 | g0263 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA18971 | hp2 | a0003 | c0018 | t0015 | g0188 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA18973 | hp1 | a0001 | c0001 | t0007 | g0191 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA18973 | hp2 | a0001 | c0003 | t0008 | g0166 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA18979 | hp1 | a0001 | c0005 | t0006 | g0087 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA18979 | hp2 | a0001 | c0003 | t0008 | g0280 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA18980 | hp1 | a0001 | c0004 | t0004 | g0198 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA18980 | hp2 | a0003 | c0018 | t0002 | g0167 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA18982 | hp1 | a0001 | c0035 | t0002 | g0033 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA18982 | hp2 | a0001 | c0008 | t0006 | g0266 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA18983 | hp1 | a0001 | c0003 | t0002 | g0070 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA18983 | hp2 | a0001 | c0001 | t0004 | g0180 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA18992 | hp1 | a0001 | c0004 | t0024 | g0255 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA18992 | hp2 | a0001 | c0003 | t0008 | g0174 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA18993 | hp1 | a0001 | c0001 | t0007 | g0196 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA18993 | hp2 | a0001 | c0011 | t0008 | g0208 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA18998 | hp1 | a0001 | c0003 | t0008 | g0116 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0164 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0097 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA19000 | hp2 | a0001 | c0003 | t0008 | g0053 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA19002 | hp1 | a0001 | c0004 | t0018 | g0083 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA19002 | hp2 | a0001 | c0003 | t0008 | g0273 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA19007 | hp1 | a0001 | c0004 | t0018 | g0134 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA19007 | hp2 | a0001 | c0001 | t0003 | g0162 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA19009 | hp1 | a0001 | c0004 | t0018 | g0071 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA19009 | hp2 | a0001 | c0003 | t0036 | g0008 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0114 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA19010 | hp2 | a0001 | c0003 | t0008 | g0153 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA19011 | hp1 | a0001 | c0001 | t0006 | g0165 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA19011 | hp2 | a0001 | c0003 | t0002 | g0152 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA19012 | hp1 | a0003 | c0018 | t0015 | g0186 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA19012 | hp2 | a0006 | c0046 | t0006 | g0131 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA19030 | hp1 | a0001 | c0005 | t0001 | g0075 | AFR | LWK | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA19030 | hp2 | a0002 | c0006 | t0001 | g0057 | AFR | LWK | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA19043 | hp1 | a0001 | c0031 | t0034 | g0004 | AFR | LWK | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA19043 | hp2 | a0001 | c0009 | t0079 | g0308 | AFR | LWK | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA19060 | hp1 | a0001 | c0001 | t0007 | g0195 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA19060 | hp2 | a0001 | c0004 | t0006 | g0101 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA19066 | hp1 | a0001 | c0011 | t0048 | g0185 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA19066 | hp2 | a0001 | c0049 | t0049 | g0096 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA19068 | hp1 | a0003 | c0018 | t0002 | g0291 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA19068 | hp2 | a0001 | c0004 | t0004 | g0032 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA19074 | hp1 | a0001 | c0004 | t0004 | g0257 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA19074 | hp2 | a0001 | c0004 | t0030 | g0269 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA19081 | hp1 | a0001 | c0015 | t0002 | g0129 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA19081 | hp2 | a0001 | c0001 | t0038 | g0006 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA19083 | hp1 | a0001 | c0008 | t0037 | g0007 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA19083 | hp2 | a0001 | c0001 | t0007 | g0274 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0163 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA19088 | hp2 | a0001 | c0003 | t0002 | g0187 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA19090 | hp1 | a0001 | c0004 | t0024 | g0254 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA19090 | hp2 | a0001 | c0001 | t0064 | g0173 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA19091 | hp1 | a0001 | c0008 | t0002 | g0178 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA19091 | hp2 | a0001 | c0003 | t0002 | g0279 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA19240 | hp1 | a0002 | c0012 | t0025 | g0302 | AFR | YRI | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA19240 | hp2 | a0001 | c0005 | t0057 | g0093 | AFR | YRI | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA20129 | hp1 | a0001 | c0001 | t0004 | g0115 | AFR | ASW | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA20129 | hp2 | a0002 | c0006 | t0001 | g0047 | AFR | ASW | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA20752 | hp1 | a0001 | c0003 | t0002 | g0121 | EUR | TSI | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA20752 | hp2 | a0001 | c0004 | t0004 | g0261 | EUR | TSI | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA20805 | hp1 | a0001 | c0027 | t0004 | g0066 | EUR | TSI | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA20805 | hp2 | a0002 | c0002 | t0028 | g0217 | EUR | TSI | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA20905 | hp1 | a0001 | c0010 | t0056 | g0072 | SAS | GIH | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA20905 | hp2 | a0001 | c0001 | t0007 | g0275 | SAS | GIH | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG01123 | hp1 | a0001 | c0005 | t0013 | g0193 | AMR | CLM | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG01123 | hp2 | a0001 | c0004 | t0004 | g0262 | AMR | CLM | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG02109 | hp1 | a0002 | c0025 | t0001 | g0050 | AFR | ACB | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG02109 | hp2 | a0001 | c0019 | t0011 | g0201 | AFR | ACB | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG02559 | hp1 | a0001 | c0026 | t0005 | g0063 | AFR | ACB | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG02559 | hp2 | a0001 | c0001 | t0011 | g0234 | AFR | ACB | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG03471 | hp1 | a0002 | c0002 | t0001 | g0046 | AFR | MSL | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG03471 | hp2 | a0001 | c0014 | t0011 | g0038 | AFR | MSL | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG06807 | hp1 | a0001 | c0042 | t0005 | g0233 | AFR | USA | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| HG06807 | hp2 | a0001 | c0004 | t0083 | g0311 | AFR | USA | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA18955 | hp1 | a0001 | c0001 | t0070 | g0276 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA18955 | hp2 | a0001 | c0004 | t0018 | g0149 | EAS | JPT | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA21309 | hp1 | a0001 | c0001 | t0005 | g0251 | AFR | LWK | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| NA21309 | hp2 | a0002 | c0006 | t0001 | g0062 | AFR | LWK | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0009 | g0001 | REF | REF | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| homoSapiens_grch38 | hp1 | a0002 | c0002 | t0013 | g0299 | REF | REF | CHD5_chr1_6096787_6185321 | CHD5 | chr1 | 6096787 | 6185321 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:6112200
|
T | C | 1 | a0005 | 1 | NA18942.hp1 | missense_variant | MODERATE | c.5080A>G | p.Lys1694Glu | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 35/42 | 5378/9850 | 5080/5865 | 1694/1954 | chr1 | 6112200 | ||
| chr1:6123963
|
G | A | 1 | a0006 | 1 | NA19012.hp2 | missense_variant | MODERATE | c.4684C>T | p.Pro1562Ser | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 31/42 | 4982/9850 | 4684/5865 | 1562/1954 | chr1 | 6123963 | ||
| chr1:6124032
|
A | G | 5 | a0001a0003a0004others(2): Show | 251 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(248): Show |
missense_variant | MODERATE | c.4615T>C | p.Ser1539Pro | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 31/42 | 4913/9850 | 4615/5865 | 1539/1954 | chr1 | 6124032 | ||
| chr1:6143828
|
C | A | 1 | a0004 | 1 | HG04115.hp1 | missense_variant | MODERATE | c.2038G>T | p.Val680Leu | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 13/42 | 2336/9850 | 2038/5865 | 680/1954 | chr1 | 6143828 | ||
| chr1:6155635
|
G | A | 1 | a0003 | 4 | NA18971.hp2 NA18980.hp2 NA19012.hp1 others(1): Show |
missense_variant | MODERATE | c.470C>T | p.Thr157Met | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 4/42 | 768/9850 | 470/5865 | 157/1954 | chr1 | 6155635 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:6106751
|
G | A | 1 | a0001c0043 | 1 | HG02165.hp2 | synonymous_variant | LOW | c.5607C>T | p.Ser1869Ser | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 39/42 | 5905/9850 | 5607/5865 | 1869/1954 | chr1 | 6106751 | ||
| chr1:6109928
|
C | T | 5 | a0001c0013a0001c0021a0001c0026others(2): Show | 12 | HG01243.hp1 HG02280.hp2 HG02559.hp1 others(9): Show |
synonymous_variant | LOW | c.5445G>A | p.Thr1815Thr | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 38/42 | 5743/9850 | 5445/5865 | 1815/1954 | chr1 | 6109928 | ||
| chr1:6124559
|
G | A | 1 | a0001c0049 | 1 | NA19066.hp2 | synonymous_variant | LOW | c.4497C>T | p.His1499His | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 30/42 | 4795/9850 | 4497/5865 | 1499/1954 | chr1 | 6124559 | ||
| chr1:6125548
|
G | A | 1 | a0001c0016 | 4 | HG00140.hp2 HG01346.hp2 HG01358.hp1 others(1): Show |
synonymous_variant | LOW | c.4236C>T | p.Leu1412Leu | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 28/42 | 4534/9850 | 4236/5865 | 1412/1954 | chr1 | 6125548 | ||
| chr1:6128914
|
C | T | 1 | a0002c0033 | 1 | HG00099.hp1 | synonymous_variant | LOW | c.3543G>A | p.Ser1181Ser | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 23/42 | 3841/9850 | 3543/5865 | 1181/1954 | chr1 | 6128914 | ||
| chr1:6128932
|
G | A | 1 | a0001c0044 | 1 | HG03225.hp2 | synonymous_variant | LOW | c.3525C>T | p.Pro1175Pro | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 23/42 | 3823/9850 | 3525/5865 | 1175/1954 | chr1 | 6128932 | ||
| chr1:6130255
|
C | T | 5 | a0001c0003a0001c0011a0001c0015others(2): Show | 57 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(54): Show |
synonymous_variant | LOW | c.3336G>A | p.Ala1112Ala | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 22/42 | 3634/9850 | 3336/5865 | 1112/1954 | chr1 | 6130255 | ||
| chr1:6134786
|
G | A | 1 | a0001c0045 | 1 | NA18944.hp1 | synonymous_variant | LOW | c.2944C>T | p.Leu982Leu | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 19/42 | 3242/9850 | 2944/5865 | 982/1954 | chr1 | 6134786 | ||
| chr1:6136809
|
A | G | 26 | a0001c0001a0001c0003a0001c0004others(23): Show | 188 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(185): Show |
synonymous_variant | LOW | c.2493T>C | p.Ile831Ile | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 16/42 | 2791/9850 | 2493/5865 | 831/1954 | chr1 | 6136809 | ||
| chr1:6142164
|
G | A | 1 | a0001c0049 | 1 | NA19066.hp2 | synonymous_variant | LOW | c.2400C>T | p.Asn800Asn | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/42 | 2698/9850 | 2400/5865 | 800/1954 | chr1 | 6142164 | ||
| chr1:6142185
|
G | A | 11 | a0001c0003a0001c0015a0001c0020others(8): Show | 57 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(54): Show |
synonymous_variant | LOW | c.2379C>T | p.Asn793Asn | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/42 | 2677/9850 | 2379/5865 | 793/1954 | chr1 | 6142185 | ||
| chr1:6143841
|
C | T | 1 | a0001c0042 | 1 | HG06807.hp1 | synonymous_variant | LOW | c.2025G>A | p.Pro675Pro | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 13/42 | 2323/9850 | 2025/5865 | 675/1954 | chr1 | 6143841 | ||
| chr1:6144101
|
G | A | 6 | a0001c0007a0001c0027a0001c0030others(3): Show | 18 | HG01070.hp2 HG01255.hp1 HG01256.hp1 others(15): Show |
synonymous_variant | LOW | c.1857C>T | p.Tyr619Tyr | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 12/42 | 2155/9850 | 1857/5865 | 619/1954 | chr1 | 6144101 | ||
| chr1:6146689
|
A | G | 5 | a0001c0014a0001c0019a0001c0029others(2): Show | 16 | HG01891.hp2 HG02055.hp1 HG02109.hp2 others(13): Show |
synonymous_variant | LOW | c.1566T>C | p.His522His | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 10/42 | 1864/9850 | 1566/5865 | 522/1954 | chr1 | 6146689 | ||
| chr1:6149019
|
G | A | 1 | a0002c0022 | 2 | HG01255.hp2 HG01975.hp2 |
synonymous_variant | LOW | c.1218C>T | p.Gly406Gly | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 9/42 | 1516/9850 | 1218/5865 | 406/1954 | chr1 | 6149019 | ||
| chr1:6149303
|
T | C | 35 | a0001c0001a0001c0003a0001c0008others(32): Show | 202 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(199): Show |
synonymous_variant | LOW | c.1104A>G | p.Val368Val | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 8/42 | 1402/9850 | 1104/5865 | 368/1954 | chr1 | 6149303 | ||
| chr1:6151087
|
G | C | 1 | a0001c0024 | 2 | HG01167.hp2 HG01169.hp1 |
synonymous_variant | LOW | c.939C>G | p.Ser313Ser | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 7/42 | 1237/9850 | 939/5865 | 313/1954 | chr1 | 6151087 | ||
| chr1:6151123
|
G | A | 29 | a0001c0001a0001c0003a0001c0008others(26): Show | 194 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(191): Show |
synonymous_variant | LOW | c.903C>T | p.Phe301Phe | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 7/42 | 1201/9850 | 903/5865 | 301/1954 | chr1 | 6151123 | ||
| chr1:6152418
|
G | A | 1 | a0001c0031 | 1 | NA19043.hp1 | synonymous_variant | LOW | c.864C>T | p.Gly288Gly | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 6/42 | 1162/9850 | 864/5865 | 288/1954 | chr1 | 6152418 | ||
| chr1:6154730
|
C | T | 1 | a0001c0032 | 1 | NA18951.hp1 | synonymous_variant | LOW | c.675G>A | p.Pro225Pro | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 5/42 | 973/9850 | 675/5865 | 225/1954 | chr1 | 6154730 | ||
| chr1:6155676
|
C | G | 9 | a0001c0009a0001c0010a0001c0014others(6): Show | 49 | HG01099.hp1 HG01109.hp1 HG01167.hp1 others(46): Show |
synonymous_variant | LOW | c.429G>C | p.Leu143Leu | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 4/42 | 727/9850 | 429/5865 | 143/1954 | chr1 | 6155676 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:6101899
|
G | A | 25 | a0001c0001t0008a0001c0003t0002a0001c0003t0008others(22): Show | 62 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*3575C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 42/42 | 4381 | chr1 | 6101899 | |||||
| chr1:6101952
|
C | T | 1 | a0001c0007t0058 | 1 | HG01256.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3522G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 42/42 | 4328 | chr1 | 6101952 | |||||
| chr1:6101991
|
G | A | 2 | a0001c0001t0070a0001c0004t0024 | 4 | HG00423.hp1 NA18955.hp1 NA18992.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3483C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 42/42 | 4289 | chr1 | 6101991 | |||||
| chr1:6101994
|
T | C | 106 | a0001c0001t0004a0001c0001t0006a0001c0001t0007others(103): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
3_prime_UTR_variant | MODIFIER | c.*3480A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 42/42 | 4286 | chr1 | 6101994 | |||||
| chr1:6102050
|
G | A | 1 | a0001c0001t0068 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3424C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 42/42 | 4230 | chr1 | 6102050 | |||||
| chr1:6102169
|
A | G | 1 | a0002c0002t0023 | 3 | HG03491.hp1 HG03492.hp2 HG03942.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3305T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 42/42 | 4111 | chr1 | 6102169 | |||||
| chr1:6102190
|
G | GAC | 3 | a0001c0007t0044a0001c0007t0058a0001c0007t0059 | 3 | HG01070.hp2 HG01256.hp1 HG02293.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3282_*3283dupGT | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 42/42 | 4089 | chr1 | 6102190 | |||||
| chr1:6102295
|
A | T | 24 | a0001c0001t0008a0001c0003t0002a0001c0003t0008others(21): Show | 61 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*3179T>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 42/42 | 3985 | chr1 | 6102295 | |||||
| chr1:6102347
|
A | G | 68 | a0001c0001t0003a0001c0001t0004a0001c0001t0007others(65): Show | 159 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(156): Show |
3_prime_UTR_variant | MODIFIER | c.*3127T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 42/42 | 3933 | chr1 | 6102347 | |||||
| chr1:6102372
|
G | A | 1 | a0001c0039t0063 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3102C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 42/42 | 3908 | chr1 | 6102372 | |||||
| chr1:6102405
|
G | C | 1 | a0001c0001t0069 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3069C>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 42/42 | 3875 | chr1 | 6102405 | |||||
| chr1:6102495
|
T | C | 2 | a0001c0001t0068a0001c0039t0063 | 2 | HG02451.hp1 HG02572.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2979A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 42/42 | 3785 | chr1 | 6102495 | |||||
| chr1:6102523
|
G | A | 101 | a0001c0001t0003a0001c0001t0004a0001c0001t0006others(98): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
3_prime_UTR_variant | MODIFIER | c.*2951C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 42/42 | 3757 | chr1 | 6102523 | |||||
| chr1:6102541
|
T | C | 25 | a0001c0001t0003a0001c0001t0007a0001c0001t0029others(22): Show | 58 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*2933A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 42/42 | 3739 | chr1 | 6102541 | |||||
| chr1:6102573
|
C | T | 24 | a0001c0001t0008a0001c0003t0002a0001c0003t0008others(21): Show | 61 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*2901G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 42/42 | 3707 | chr1 | 6102573 | |||||
| chr1:6102585
|
C | T | 24 | a0001c0001t0008a0001c0003t0002a0001c0003t0008others(21): Show | 61 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*2889G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 42/42 | 3695 | chr1 | 6102585 | |||||
| chr1:6102608
|
G | A | 2 | a0001c0001t0068a0001c0039t0063 | 2 | HG02451.hp1 HG02572.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2866C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 42/42 | 3672 | chr1 | 6102608 | |||||
| chr1:6102737
|
G | T | 6 | a0001c0001t0011a0001c0004t0011a0001c0009t0011others(3): Show | 10 | HG02109.hp2 HG02145.hp1 HG02559.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2737C>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 42/42 | 3543 | chr1 | 6102737 | |||||
| chr1:6102760
|
CT | C | 24 | a0001c0001t0008a0001c0003t0002a0001c0003t0008others(21): Show | 61 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*2713delA | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 42/42 | 3519 | chr1 | 6102760 | |||||
| chr1:6102787
|
G | A | 1 | a0001c0001t0054 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2687C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 42/42 | 3493 | chr1 | 6102787 | |||||
| chr1:6102821
|
G | A | 24 | a0001c0001t0008a0001c0003t0002a0001c0003t0008others(21): Show | 61 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*2653C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 42/42 | 3459 | chr1 | 6102821 | |||||
| chr1:6102874
|
C | T | 1 | a0001c0005t0057 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2600G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 42/42 | 3406 | chr1 | 6102874 | |||||
| chr1:6102879
|
A | C | 2 | a0001c0004t0030a0001c0005t0030 | 2 | NA18959.hp1 NA19074.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2595T>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 42/42 | 3401 | chr1 | 6102879 | |||||
| chr1:6103005
|
G | A | 26 | a0001c0001t0008a0001c0001t0068a0001c0003t0002others(23): Show | 63 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*2469C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 42/42 | 3275 | chr1 | 6103005 | |||||
| chr1:6103065
|
G | A | 1 | a0001c0009t0073 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2409C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 42/42 | 3215 | chr1 | 6103065 | |||||
| chr1:6103075
|
C | T | 27 | a0001c0005t0001a0001c0008t0001a0001c0014t0001others(24): Show | 68 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*2399G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 42/42 | 3205 | chr1 | 6103075 | |||||
| chr1:6103081
|
C | T | 27 | a0001c0005t0001a0001c0008t0001a0001c0014t0001others(24): Show | 68 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*2393G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 42/42 | 3199 | chr1 | 6103081 | |||||
| chr1:6103174
|
G | T | 1 | a0002c0002t0020 | 3 | HG02280.hp1 HG02976.hp2 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2300C>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 42/42 | 3106 | chr1 | 6103174 | |||||
| chr1:6103187
|
T | C | 1 | a0002c0006t0061 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2287A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 42/42 | 3093 | chr1 | 6103187 | |||||
| chr1:6103201
|
C | T | 2 | a0001c0005t0055a0001c0016t0016 | 5 | HG00140.hp2 HG01069.hp1 HG01346.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2273G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 42/42 | 3079 | chr1 | 6103201 | |||||
| chr1:6103391
|
G | A | 1 | a0001c0005t0055 | 1 | HG01069.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2083C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 42/42 | 2889 | chr1 | 6103391 | |||||
| chr1:6103397
|
G | A | 3 | a0001c0004t0072a0001c0004t0083a0001c0009t0073 | 3 | HG01099.hp1 HG02895.hp2 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2077C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 42/42 | 2883 | chr1 | 6103397 | |||||
| chr1:6103424
|
G | A | 3 | a0001c0008t0012a0001c0010t0012a0001c0024t0012 | 6 | HG01167.hp2 HG01169.hp1 HG01891.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2050C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 42/42 | 2856 | chr1 | 6103424 | |||||
| chr1:6103524
|
C | T | 44 | a0001c0001t0006a0001c0001t0054a0001c0001t0064others(41): Show | 99 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*1950G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 42/42 | 2756 | chr1 | 6103524 | |||||
| chr1:6103562
|
G | A | 1 | a0001c0004t0018 | 4 | NA18955.hp2 NA19002.hp1 NA19007.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1912C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 42/42 | 2718 | chr1 | 6103562 | |||||
| chr1:6103592
|
G | A | 1 | a0002c0012t0052 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1882C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 42/42 | 2688 | chr1 | 6103592 | |||||
| chr1:6103666
|
G | A | 1 | a0001c0031t0034 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1808C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 42/42 | 2614 | chr1 | 6103666 | |||||
| chr1:6103865
|
C | T | 110 | a0001c0001t0004a0001c0001t0006a0001c0001t0008others(107): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
3_prime_UTR_variant | MODIFIER | c.*1609G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 42/42 | 2415 | chr1 | 6103865 | |||||
| chr1:6103969
|
C | T | 15 | a0001c0001t0003a0001c0001t0007a0001c0001t0029others(12): Show | 47 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*1505G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 42/42 | 2311 | chr1 | 6103969 | |||||
| chr1:6104078
|
C | T | 1 | a0001c0001t0068 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1396G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 42/42 | 2202 | chr1 | 6104078 | |||||
| chr1:6104094
|
C | G | 3 | a0002c0002t0020a0002c0006t0019a0002c0047t0078 | 7 | HG01109.hp1 HG01884.hp1 HG02280.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1380G>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 42/42 | 2186 | chr1 | 6104094 | |||||
| chr1:6104136
|
G | A | 1 | a0001c0003t0022 | 3 | NA18939.hp1 NA18950.hp1 NA18951.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1338C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 42/42 | 2144 | chr1 | 6104136 | |||||
| chr1:6104220
|
G | A | 6 | a0001c0001t0011a0001c0004t0011a0001c0009t0011others(3): Show | 10 | HG02109.hp2 HG02145.hp1 HG02559.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1254C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 42/42 | 2060 | chr1 | 6104220 | |||||
| chr1:6104286
|
G | A | 1 | a0001c0004t0083 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1188C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 42/42 | 1994 | chr1 | 6104286 | |||||
| chr1:6104348
|
G | A | 27 | a0001c0001t0004a0001c0001t0027a0001c0001t0069others(24): Show | 49 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*1126C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 42/42 | 1932 | chr1 | 6104348 | |||||
| chr1:6104490
|
A | AGG | 52 | a0001c0001t0006a0001c0001t0011a0001c0001t0054others(49): Show | 111 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*982_*983dupCC | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 42/42 | 1789 | chr1 | 6104490 | |||||
| chr1:6104542
|
C | A | 1 | a0001c0013t0060 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*932G>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 42/42 | 1738 | chr1 | 6104542 | |||||
| chr1:6104542
|
C | T | 1 | a0001c0003t0046 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*932G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 42/42 | 1738 | chr1 | 6104542 | |||||
| chr1:6104611
|
A | G | 37 | a0001c0001t0003a0001c0001t0006a0001c0001t0007others(34): Show | 92 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*863T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 42/42 | 1669 | chr1 | 6104611 | |||||
| chr1:6104617
|
T | TG | 7 | a0001c0001t0029a0001c0001t0064a0001c0001t0084others(4): Show | 8 | HG01106.hp1 HG02257.hp2 HG02738.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*856dupC | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 42/42 | 1662 | chr1 | 6104617 | |||||
| chr1:6104618
|
GC | G | 14 | a0001c0003t0002a0001c0003t0015a0001c0003t0046others(11): Show | 33 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*855delG | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 42/42 | 1661 | chr1 | 6104618 | |||||
| chr1:6104619
|
C | G | 95 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(92): Show | 195 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(192): Show |
3_prime_UTR_variant | MODIFIER | c.*855G>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 42/42 | 1661 | chr1 | 6104619 | |||||
| chr1:6104620
|
C | A | 2 | a0002c0002t0017a0002c0002t0026 | 6 | HG00099.hp2 HG01081.hp2 HG02258.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*854G>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 42/42 | 1660 | chr1 | 6104620 | |||||
| chr1:6104620
|
C | G | 13 | a0001c0003t0002a0001c0003t0015a0001c0003t0046others(10): Show | 32 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*854G>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 42/42 | 1660 | chr1 | 6104620 | |||||
| chr1:6104622
|
C | A | 2 | a0001c0009t0041a0001c0010t0080 | 2 | HG01167.hp1 HG02647.hp1 |
3_prime_UTR_variant | MODIFIER | c.*852G>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 42/42 | 1658 | chr1 | 6104622 | |||||
| chr1:6104622
|
C | G | 2 | a0001c0001t0050a0001c0010t0051 | 2 | HG00544.hp1 HG03927.hp2 |
3_prime_UTR_variant | MODIFIER | c.*852G>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 42/42 | 1658 | chr1 | 6104622 | |||||
| chr1:6104626
|
C | A | 3 | a0002c0002t0009a0002c0022t0009a0002c0033t0009 | 11 | HG00099.hp1 HG01081.hp1 HG01168.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*848G>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 42/42 | 1654 | chr1 | 6104626 | |||||
| chr1:6104626
|
C | T | 3 | a0001c0008t0012a0001c0010t0012a0001c0024t0012 | 6 | HG01167.hp2 HG01169.hp1 HG01891.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*848G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 42/42 | 1654 | chr1 | 6104626 | |||||
| chr1:6104628
|
C | A | 5 | a0001c0001t0084a0001c0004t0072a0001c0004t0083others(2): Show | 5 | HG01099.hp1 HG02257.hp2 HG02895.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*846G>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 42/42 | 1652 | chr1 | 6104628 | |||||
| chr1:6104642
|
T | C | 1 | a0001c0003t0036 | 1 | NA19009.hp2 | 3_prime_UTR_variant | MODIFIER | c.*832A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 42/42 | 1638 | chr1 | 6104642 | |||||
| chr1:6104643
|
G | T | 1 | a0001c0003t0036 | 1 | NA19009.hp2 | 3_prime_UTR_variant | MODIFIER | c.*831C>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 42/42 | 1637 | chr1 | 6104643 | |||||
| chr1:6104852
|
G | C | 33 | a0001c0001t0004a0001c0001t0068a0001c0001t0069others(30): Show | 56 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*622C>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 42/42 | 1428 | chr1 | 6104852 | |||||
| chr1:6105219
|
G | A | 1 | a0001c0049t0049 | 1 | NA19066.hp2 | 3_prime_UTR_variant | MODIFIER | c.*255C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 42/42 | 1061 | chr1 | 6105219 | |||||
| chr1:6105359
|
C | T | 25 | a0001c0001t0008a0001c0003t0002a0001c0003t0008others(22): Show | 63 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*115G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 42/42 | 921 | chr1 | 6105359 | |||||
| chr1:6106251
|
G | A | 1 | a0001c0013t0032 | 2 | HG02280.hp2 HG02717.hp2 |
3_prime_UTR_variant | MODIFIER | c.*29C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 41/42 | 29 | chr1 | 6106251 | |||||
| chr1:6106277
|
C | T | 1 | a0002c0002t0026 | 2 | HG02896.hp1 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 41/42 | 3 | chr1 | 6106277 | |||||
| chr1:6180053
|
G | GC | 13 | a0001c0001t0077a0001c0001t0084a0001c0004t0075others(10): Show | 16 | HG01167.hp1 HG01884.hp1 HG02055.hp1 others(13): Show |
5_prime_UTR_variant | MODIFIER | c.-31dupG | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/42 | 31 | chr1 | 6180053 | |||||
| chr1:6180115
|
G | T | 4 | a0001c0005t0043a0001c0007t0044a0002c0002t0020others(1): Show | 6 | HG02280.hp1 HG02293.hp1 HG02622.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-92C>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/42 | 92 | chr1 | 6180115 | |||||
| chr1:6180138
|
G | A | 1 | a0001c0013t0042 | 1 | HG03209.hp1 | 5_prime_UTR_variant | MODIFIER | c.-115C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/42 | 115 | chr1 | 6180138 | |||||
| chr1:6180139
|
A | ACAAGAGA others(36): Show |
1 | a0001c0013t0042 | 1 | HG03209.hp1 | 5_prime_UTR_variant | MODIFIER | c.-117_-116insGTGTCT others(37): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/42 | 117 | chr1 | 6180139 | |||||
| chr1:6180142
|
A | G | 1 | a0001c0013t0042 | 1 | HG03209.hp1 | 5_prime_UTR_variant | MODIFIER | c.-119T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/42 | 119 | chr1 | 6180142 | |||||
| chr1:6180210
|
C | T | 4 | a0001c0009t0039a0001c0009t0041a0002c0006t0019others(1): Show | 6 | HG01109.hp1 HG02647.hp1 HG02723.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-187G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/42 | 187 | chr1 | 6180210 | |||||
| chr1:6180236
|
C | G | 3 | a0001c0001t0038a0001c0003t0036a0001c0008t0037 | 3 | NA19009.hp2 NA19081.hp2 NA19083.hp1 |
5_prime_UTR_variant | MODIFIER | c.-213G>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/42 | 213 | chr1 | 6180236 | |||||
| chr1:6180268
|
G | C | 1 | a0001c0019t0085 | 1 | HG02818.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-245C>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/42 | chr1 | 6180268 | ||||||
| chr1:6180305
|
C | T | 2 | a0001c0031t0034a0001c0038t0035 | 2 | HG01891.hp2 NA19043.hp1 |
5_prime_UTR_variant | MODIFIER | c.-282G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/42 | 282 | chr1 | 6180305 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:6105539
|
G | C | 1 | a0001c0011t0021g0161 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.*47-112C>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 41/41 | chr1 | 6105539 | ||||||
| chr1:6105608
|
G | A | 6 | a0001c0001t0084g0310a0001c0009t0014g0059a0001c0010t0014g0242others(3): Show | 6 | HG02257.hp2 HG02630.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.*47-181C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 41/41 | chr1 | 6105608 | ||||||
| chr1:6105684
|
G | A | 1 | a0001c0009t0039g0013 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.*47-257C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 41/41 | chr1 | 6105684 | ||||||
| chr1:6106376
|
G | A | 1 | a0001c0019t0011g0201 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.5857+19C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 40/41 | chr1 | 6106376 | ||||||
| chr1:6106845
|
A | AGGATGGA others(1): Show |
3 | a0001c0007t0044g0016a0001c0007t0058g0028a0001c0007t0059g0029 | 3 | HG01070.hp2 HG01256.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.5579-74_5579-67dup others(8): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 38/41 | chr1 | 6106845 | ||||||
| chr1:6106859
|
G | A | 1 | a0001c0001t0070g0276 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.5579-80C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 38/41 | chr1 | 6106859 | ||||||
| chr1:6106888
|
G | GTGGAAGG others(9): Show |
2 | a0001c0003t0002g0253a0001c0003t0002g0256 | 2 | NA18944.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.5579-125_5579-110d others(18): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 38/41 | chr1 | 6106888 | ||||||
| chr1:6106920
|
ATGGAGGG others(1): Show |
A | 112 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(109): Show | 112 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.5579-149_5579-142d others(10): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 38/41 | chr1 | 6106920 | ||||||
| chr1:6106928
|
G | GTGGAGGG others(89): Show |
4 | a0001c0001t0084g0310a0001c0009t0014g0059a0001c0010t0014g0242others(1): Show | 4 | HG02257.hp2 HG02886.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.5579-150_5579-149i others(98): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 38/41 | chr1 | 6106928 | ||||||
| chr1:6106990
|
GGATGGAG others(4): Show |
G | 1 | a0001c0039t0063g0241 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.5579-222_5579-212d others(13): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 38/41 | chr1 | 6106990 | ||||||
| chr1:6107004
|
T | G | 1 | a0001c0001t0027g0132 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.5579-225A>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 38/41 | chr1 | 6107004 | ||||||
| chr1:6107061
|
C | A | 116 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(113): Show | 116 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.5579-282G>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 38/41 | chr1 | 6107061 | ||||||
| chr1:6107072
|
T | TGATGGAG others(1): Show |
116 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(113): Show | 116 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.5579-301_5579-294d others(10): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 38/41 | chr1 | 6107072 | ||||||
| chr1:6107134
|
T | C | 116 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(113): Show | 116 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.5579-355A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 38/41 | chr1 | 6107134 | ||||||
| chr1:6107174
|
G | A | 116 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(113): Show | 116 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.5579-395C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 38/41 | chr1 | 6107174 | ||||||
| chr1:6107190
|
A | G | 1 | a0001c0004t0004g0032 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.5579-411T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 38/41 | chr1 | 6107190 | ||||||
| chr1:6107274
|
G | A | 1 | a0002c0002t0020g0019 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.5579-495C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 38/41 | chr1 | 6107274 | ||||||
| chr1:6107330
|
T | A | 1 | a0001c0024t0012g0003 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.5579-551A>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 38/41 | chr1 | 6107330 | ||||||
| chr1:6107360
|
G | C | 1 | a0001c0001t0007g0258 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.5579-581C>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 38/41 | chr1 | 6107360 | ||||||
| chr1:6107372
|
AGATGGAG others(36): Show |
A | 116 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(113): Show | 116 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.5579-636_5579-594d others(45): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 38/41 | chr1 | 6107372 | ||||||
| chr1:6107521
|
C | G | 116 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(113): Show | 116 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.5579-742G>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 38/41 | chr1 | 6107521 | ||||||
| chr1:6107522
|
G | A | 1 | a0001c0026t0005g0235 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.5579-743C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 38/41 | chr1 | 6107522 | ||||||
| chr1:6107530
|
G | C | 63 | a0001c0001t0008g0095a0001c0003t0002g0022a0001c0003t0002g0070others(60): Show | 63 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.5579-751C>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 38/41 | chr1 | 6107530 | ||||||
| chr1:6107542
|
G | GAGGGATG others(30): Show |
155 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(152): Show | 156 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.5579-764_5579-763i others(39): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 38/41 | chr1 | 6107542 | ||||||
| chr1:6107549
|
A | G | 245 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(242): Show | 246 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(243): Show |
intron_variant | MODIFIER | c.5579-770T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 38/41 | chr1 | 6107549 | ||||||
| chr1:6107555
|
G | GGGATGAT others(29): Show |
1 | a0001c0003t0002g0128 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.5579-777_5579-776i others(38): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 38/41 | chr1 | 6107555 | ||||||
| chr1:6107573
|
AG | A | 62 | a0001c0001t0008g0095a0001c0003t0002g0022a0001c0003t0002g0070others(59): Show | 62 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.5579-795delC | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 38/41 | chr1 | 6107573 | ||||||
| chr1:6107580
|
T | G | 53 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(50): Show | 53 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.5579-801A>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 38/41 | chr1 | 6107580 | ||||||
| chr1:6107601
|
G | GGAGAGAT others(27): Show |
62 | a0001c0001t0008g0095a0001c0003t0002g0022a0001c0003t0002g0070others(59): Show | 62 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.5579-823_5579-822i others(36): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 38/41 | chr1 | 6107601 | ||||||
| chr1:6107604
|
T | G | 116 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(113): Show | 116 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.5579-825A>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 38/41 | chr1 | 6107604 | ||||||
| chr1:6107605
|
A | G | 62 | a0001c0001t0008g0095a0001c0003t0002g0022a0001c0003t0002g0070others(59): Show | 62 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.5579-826T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 38/41 | chr1 | 6107605 | ||||||
| chr1:6107629
|
C | T | 2 | a0001c0009t0039g0013a0001c0010t0003g0044 | 2 | HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.5579-850G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 38/41 | chr1 | 6107629 | ||||||
| chr1:6107675
|
G | A | 1 | a0002c0012t0025g0302 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.5579-896C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 38/41 | chr1 | 6107675 | ||||||
| chr1:6107696
|
G | GGGATGAT others(30): Show |
52 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(49): Show | 52 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.5579-918_5579-917i others(39): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 38/41 | chr1 | 6107696 | ||||||
| chr1:6107696
|
G | GGGATGAT others(74): Show |
63 | a0001c0001t0004g0054a0001c0001t0004g0115a0001c0001t0004g0138others(60): Show | 63 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.5579-918_5579-917i others(83): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 38/41 | chr1 | 6107696 | ||||||
| chr1:6107715
|
G | GGAATAAT others(29): Show |
1 | a0001c0001t0007g0195 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.5579-937_5579-936i others(38): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 38/41 | chr1 | 6107715 | ||||||
| chr1:6107815
|
T | C | 116 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(113): Show | 116 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.5579-1036A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 38/41 | chr1 | 6107815 | ||||||
| chr1:6108052
|
G | T | 1 | a0001c0001t0003g0206 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.5579-1273C>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 38/41 | chr1 | 6108052 | ||||||
| chr1:6108116
|
A | T | 1 | a0001c0001t0007g0195 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.5579-1337T>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 38/41 | chr1 | 6108116 | ||||||
| chr1:6108145
|
G | A | 1 | a0001c0001t0029g0055 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.5579-1366C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 38/41 | chr1 | 6108145 | ||||||
| chr1:6108257
|
G | A | 1 | a0001c0039t0063g0241 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.5579-1478C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 38/41 | chr1 | 6108257 | ||||||
| chr1:6108307
|
A | T | 1 | a0001c0001t0007g0195 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.5578+1488T>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 38/41 | chr1 | 6108307 | ||||||
| chr1:6108367
|
G | A | 1 | a0001c0005t0057g0093 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.5578+1428C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 38/41 | chr1 | 6108367 | ||||||
| chr1:6108400
|
A | G | 1 | a0001c0008t0005g0056 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.5578+1395T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 38/41 | chr1 | 6108400 | ||||||
| chr1:6108448
|
T | C | 1 | a0001c0021t0005g0027 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.5578+1347A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 38/41 | chr1 | 6108448 | ||||||
| chr1:6108579
|
A | T | 1 | a0001c0001t0007g0195 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.5578+1216T>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 38/41 | chr1 | 6108579 | ||||||
| chr1:6108618
|
CAG | C | 44 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(41): Show | 44 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.5578+1175_5578+117 others(6): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 38/41 | chr1 | 6108618 | ||||||
| chr1:6108661
|
A | G | 1 | a0001c0001t0007g0195 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.5578+1134T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 38/41 | chr1 | 6108661 | ||||||
| chr1:6108662
|
T | A | 1 | a0001c0001t0007g0195 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.5578+1133A>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 38/41 | chr1 | 6108662 | ||||||
| chr1:6108663
|
A | T | 1 | a0001c0001t0007g0195 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.5578+1132T>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 38/41 | chr1 | 6108663 | ||||||
| chr1:6108753
|
G | C | 12 | a0001c0001t0011g0232a0001c0001t0011g0234a0001c0001t0011g0297others(9): Show | 12 | HG01167.hp1 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.5578+1042C>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 38/41 | chr1 | 6108753 | ||||||
| chr1:6108778
|
T | C | 1 | a0001c0005t0005g0099 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.5578+1017A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 38/41 | chr1 | 6108778 | ||||||
| chr1:6108797
|
A | T | 1 | a0001c0001t0007g0195 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.5578+998T>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 38/41 | chr1 | 6108797 | ||||||
| chr1:6109008
|
C | T | 1 | a0001c0001t0068g0085 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.5578+787G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 38/41 | chr1 | 6109008 | ||||||
| chr1:6109225
|
G | A | 1 | a0001c0003t0008g0174 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.5578+570C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 38/41 | chr1 | 6109225 | ||||||
| chr1:6109303
|
C | T | 6 | a0002c0002t0001g0126a0002c0006t0001g0047a0002c0006t0040g0009others(3): Show | 6 | HG02109.hp1 HG02717.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.5578+492G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 38/41 | chr1 | 6109303 | ||||||
| chr1:6109315
|
C | CG | 5 | a0001c0008t0012g0222a0001c0008t0012g0223a0001c0008t0012g0296others(2): Show | 6 | HG01167.hp2 HG01169.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.5578+479dupC | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 38/41 | chr1 | 6109315 | ||||||
| chr1:6109351
|
C | T | 53 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(50): Show | 53 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.5578+444G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 38/41 | chr1 | 6109351 | ||||||
| chr1:6109669
|
A | C | 1 | a0001c0013t0042g0015 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.5578+126T>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 38/41 | chr1 | 6109669 | ||||||
| chr1:6109770
|
A | G | 2 | a0001c0008t0002g0178a0001c0035t0002g0033 | 2 | NA18982.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.5578+25T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 38/41 | chr1 | 6109770 | ||||||
| chr1:6110003
|
C | T | 5 | a0001c0008t0012g0222a0001c0008t0012g0223a0001c0008t0012g0296others(2): Show | 6 | HG01167.hp2 HG01169.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.5383-13G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 37/41 | chr1 | 6110003 | ||||||
| chr1:6110004
|
G | A | 1 | a0001c0004t0004g0198 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.5383-14C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 37/41 | chr1 | 6110004 | ||||||
| chr1:6110012
|
G | A | 1 | a0001c0001t0007g0203 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.5383-22C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 37/41 | chr1 | 6110012 | ||||||
| chr1:6110240
|
CACT | C | 24 | a0001c0001t0006g0165a0001c0001t0064g0173a0001c0004t0006g0101others(21): Show | 24 | HG00140.hp2 HG01069.hp1 HG01346.hp2 others(21): Show |
intron_variant | MODIFIER | c.5382+151_5382+153d others(5): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 37/41 | chr1 | 6110240 | ||||||
| chr1:6110293
|
C | T | 61 | a0001c0001t0004g0054a0001c0001t0004g0115a0001c0001t0004g0138others(58): Show | 61 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.5382+101G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 37/41 | chr1 | 6110293 | ||||||
| chr1:6110364
|
CG | C | 181 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(178): Show | 182 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(179): Show |
intron_variant | MODIFIER | c.5382+29delC | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 37/41 | chr1 | 6110364 | ||||||
| chr1:6110608
|
G | A | 1 | a0001c0001t0068g0085 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.5250-82C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 36/41 | chr1 | 6110608 | ||||||
| chr1:6110639
|
C | G | 59 | a0001c0001t0004g0054a0001c0001t0004g0115a0001c0001t0004g0138others(56): Show | 59 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.5250-113G>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 36/41 | chr1 | 6110639 | ||||||
| chr1:6110841
|
G | A | 1 | a0001c0004t0004g0261 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.5250-315C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 36/41 | chr1 | 6110841 | ||||||
| chr1:6110846
|
T | C | 1 | a0001c0049t0049g0096 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.5250-320A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 36/41 | chr1 | 6110846 | ||||||
| chr1:6110885
|
T | A | 41 | a0001c0001t0004g0054a0001c0001t0004g0115a0001c0001t0004g0138others(38): Show | 41 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(38): Show |
intron_variant | MODIFIER | c.5250-359A>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 36/41 | chr1 | 6110885 | ||||||
| chr1:6110928
|
G | A | 132 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(129): Show | 133 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(130): Show |
intron_variant | MODIFIER | c.5250-402C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 36/41 | chr1 | 6110928 | ||||||
| chr1:6111236
|
AAAAG | A | 67 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(64): Show | 67 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.5249+535_5249+538d others(6): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 36/41 | chr1 | 6111236 | ||||||
| chr1:6111239
|
AG | A | 6 | a0001c0005t0004g0144a0001c0007t0005g0197a0001c0007t0058g0028others(3): Show | 6 | HG01168.hp2 HG01256.hp1 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.5249+535delC | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 36/41 | chr1 | 6111239 | ||||||
| chr1:6111240
|
G | A | 167 | a0001c0001t0004g0054a0001c0001t0004g0115a0001c0001t0004g0138others(164): Show | 168 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(165): Show |
intron_variant | MODIFIER | c.5249+535C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 36/41 | chr1 | 6111240 | ||||||
| chr1:6111345
|
C | A | 1 | a0001c0009t0041g0014 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.5249+430G>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 36/41 | chr1 | 6111345 | ||||||
| chr1:6111346
|
C | A | 1 | a0001c0009t0041g0014 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.5249+429G>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 36/41 | chr1 | 6111346 | ||||||
| chr1:6111362
|
C | T | 1 | a0001c0001t0011g0297 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.5249+413G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 36/41 | chr1 | 6111362 | ||||||
| chr1:6111474
|
C | T | 10 | a0001c0001t0005g0251a0001c0001t0068g0085a0001c0001t0084g0310others(7): Show | 10 | HG02257.hp2 HG02451.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.5249+301G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 36/41 | chr1 | 6111474 | ||||||
| chr1:6111532
|
T | A | 4 | a0001c0004t0024g0171a0001c0004t0024g0254a0001c0004t0024g0255others(1): Show | 4 | HG00423.hp1 HG02129.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.5249+243A>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 36/41 | chr1 | 6111532 | ||||||
| chr1:6111533
|
C | CA | 8 | a0001c0003t0008g0153a0001c0003t0008g0174a0001c0011t0010g0160others(5): Show | 8 | HG03195.hp1 HG03942.hp1 HG04204.hp2 others(5): Show |
intron_variant | MODIFIER | c.5249+241dupT | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 36/41 | chr1 | 6111533 | ||||||
| chr1:6111533
|
CA | C | 10 | a0001c0001t0004g0054a0001c0001t0007g0191a0001c0004t0018g0149others(7): Show | 10 | HG01243.hp1 HG01975.hp2 NA18942.hp2 others(7): Show |
intron_variant | MODIFIER | c.5249+241delT | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 36/41 | chr1 | 6111533 | ||||||
| chr1:6111549
|
A | G | 1 | a0001c0004t0031g0084 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.5249+226T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 36/41 | chr1 | 6111549 | ||||||
| chr1:6111590
|
G | A | 2 | a0001c0001t0007g0263a0001c0001t0038g0006 | 2 | NA18971.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.5249+185C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 36/41 | chr1 | 6111590 | ||||||
| chr1:6111729
|
G | A | 1 | a0001c0004t0004g0290 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.5249+46C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 36/41 | chr1 | 6111729 | ||||||
| chr1:6111932
|
C | A | 39 | a0001c0004t0075g0300a0001c0005t0005g0099a0001c0005t0043g0017others(36): Show | 40 | HG01070.hp2 HG01167.hp1 HG01167.hp2 others(37): Show |
intron_variant | MODIFIER | c.5141-49G>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 35/41 | chr1 | 6111932 | ||||||
| chr1:6111938
|
G | A | 2 | a0001c0001t0007g0191a0001c0001t0007g0258 | 2 | NA18970.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.5141-55C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 35/41 | chr1 | 6111938 | ||||||
| chr1:6112780
|
C | T | 39 | a0001c0004t0075g0300a0001c0005t0005g0099a0001c0005t0043g0017others(36): Show | 40 | HG01070.hp2 HG01167.hp1 HG01167.hp2 others(37): Show |
intron_variant | MODIFIER | c.5002+129G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 34/41 | chr1 | 6112780 | ||||||
| chr1:6112815
|
G | A | 252 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(249): Show | 253 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(250): Show |
intron_variant | MODIFIER | c.5002+94C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 34/41 | chr1 | 6112815 | ||||||
| chr1:6113105
|
G | A | 1 | a0001c0028t0014g0058 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.4913-107C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6113105 | ||||||
| chr1:6113189
|
C | T | 1 | a0001c0001t0003g0135 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.4913-191G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6113189 | ||||||
| chr1:6113224
|
G | C | 1 | a0002c0002t0001g0225 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.4913-226C>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6113224 | ||||||
| chr1:6113240
|
T | G | 1 | a0001c0028t0014g0058 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.4913-242A>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6113240 | ||||||
| chr1:6113268
|
C | T | 1 | a0002c0002t0028g0217 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.4913-270G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6113268 | ||||||
| chr1:6113296
|
C | T | 1 | a0001c0009t0041g0014 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.4913-298G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6113296 | ||||||
| chr1:6113297
|
G | A | 1 | a0001c0048t0005g0133 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.4913-299C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6113297 | ||||||
| chr1:6113335
|
G | A | 1 | a0001c0005t0005g0099 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.4913-337C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6113335 | ||||||
| chr1:6113411
|
A | G | 1 | a0002c0006t0019g0012 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.4913-413T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6113411 | ||||||
| chr1:6113416
|
G | A | 14 | a0001c0005t0043g0017a0001c0008t0005g0230a0001c0013t0005g0156others(11): Show | 14 | HG01243.hp1 HG02280.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.4913-418C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6113416 | ||||||
| chr1:6113589
|
A | G | 246 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(243): Show | 247 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(244): Show |
intron_variant | MODIFIER | c.4913-591T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6113589 | ||||||
| chr1:6113741
|
G | A | 1 | a0001c0009t0041g0014 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.4913-743C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6113741 | ||||||
| chr1:6113759
|
T | A | 73 | a0001c0001t0005g0251a0001c0001t0008g0095a0001c0001t0068g0085others(70): Show | 73 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.4913-761A>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6113759 | ||||||
| chr1:6113882
|
C | T | 1 | a0001c0010t0005g0098 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.4913-884G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6113882 | ||||||
| chr1:6113937
|
C | A | 1 | a0001c0009t0004g0139 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.4913-939G>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6113937 | ||||||
| chr1:6113989
|
C | T | 2 | a0001c0005t0004g0076a0001c0005t0004g0144 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.4913-991G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6113989 | ||||||
| chr1:6114016
|
G | A | 63 | a0001c0001t0008g0095a0001c0003t0002g0022a0001c0003t0002g0070others(60): Show | 63 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.4913-1018C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6114016 | ||||||
| chr1:6114150
|
G | A | 1 | a0002c0002t0001g0200 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.4913-1152C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6114150 | ||||||
| chr1:6114171
|
T | G | 2 | a0001c0009t0039g0013a0001c0010t0003g0044 | 2 | HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.4913-1173A>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6114171 | ||||||
| chr1:6114177
|
C | T | 4 | a0001c0001t0006g0165a0001c0008t0006g0266a0001c0008t0037g0007others(1): Show | 4 | NA18982.hp2 NA19011.hp1 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.4913-1179G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6114177 | ||||||
| chr1:6114252
|
C | CA | 189 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(186): Show | 190 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.4913-1255dupT | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6114252 | ||||||
| chr1:6114507
|
A | AAC | 121 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(118): Show | 122 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.4913-1511_4913-151 others(6): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6114507 | ||||||
| chr1:6114647
|
T | C | 1 | a0002c0017t0028g0293 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.4913-1649A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6114647 | ||||||
| chr1:6114652
|
A | T | 1 | a0001c0001t0068g0085 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.4913-1654T>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6114652 | ||||||
| chr1:6114729
|
G | A | 3 | a0001c0007t0003g0067a0001c0007t0003g0068a0001c0007t0003g0287 | 3 | HG02071.hp2 HG02165.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.4913-1731C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6114729 | ||||||
| chr1:6114737
|
T | A | 1 | a0001c0004t0004g0081 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.4913-1739A>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6114737 | ||||||
| chr1:6114904
|
C | A | 3 | a0002c0002t0001g0107a0002c0002t0001g0108a0002c0002t0001g0154 | 3 | HG00741.hp1 HG01069.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.4913-1906G>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6114904 | ||||||
| chr1:6115013
|
C | CA | 59 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(56): Show | 59 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.4913-2016dupT | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6115013 | ||||||
| chr1:6115013
|
CA | C | 40 | a0001c0004t0075g0300a0001c0005t0004g0144a0001c0005t0005g0099others(37): Show | 41 | HG01070.hp2 HG01167.hp1 HG01167.hp2 others(38): Show |
intron_variant | MODIFIER | c.4913-2016delT | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6115013 | ||||||
| chr1:6115024
|
A | G | 4 | a0001c0001t0005g0251a0001c0011t0010g0160a0001c0011t0010g0183others(1): Show | 4 | NA18947.hp2 NA18962.hp1 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.4913-2026T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6115024 | ||||||
| chr1:6115025
|
A | C | 1 | a0001c0001t0005g0251 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.4913-2027T>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6115025 | ||||||
| chr1:6115025
|
A | G | 94 | a0001c0001t0006g0165a0001c0001t0008g0095a0001c0001t0068g0085others(91): Show | 94 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.4913-2027T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6115025 | ||||||
| chr1:6115027
|
G | C | 98 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(95): Show | 99 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.4913-2029C>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6115027 | ||||||
| chr1:6115057
|
A | C | 64 | a0001c0001t0008g0095a0001c0003t0002g0022a0001c0003t0002g0070others(61): Show | 64 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.4913-2059T>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6115057 | ||||||
| chr1:6115064
|
G | A | 1 | a0001c0001t0068g0085 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.4913-2066C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6115064 | ||||||
| chr1:6115084
|
G | A | 1 | a0002c0002t0009g0034 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.4913-2086C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6115084 | ||||||
| chr1:6115094
|
C | G | 1 | a0001c0001t0054g0292 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.4913-2096G>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6115094 | ||||||
| chr1:6115094
|
C | T | 58 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(55): Show | 58 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.4913-2096G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6115094 | ||||||
| chr1:6115095
|
G | A | 1 | a0001c0010t0056g0072 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.4913-2097C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6115095 | ||||||
| chr1:6115234
|
G | A | 1 | a0001c0028t0014g0058 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.4913-2236C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6115234 | ||||||
| chr1:6115250
|
C | CA | 90 | a0001c0001t0005g0251a0001c0001t0006g0165a0001c0001t0008g0095others(87): Show | 90 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.4913-2253dupT | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6115250 | ||||||
| chr1:6115299
|
C | A | 1 | a0001c0009t0041g0014 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.4913-2301G>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6115299 | ||||||
| chr1:6115357
|
C | T | 2 | a0002c0002t0001g0105a0002c0002t0028g0217 | 2 | HG01099.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.4913-2359G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6115357 | ||||||
| chr1:6115423
|
C | A | 1 | a0001c0008t0003g0249 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.4913-2425G>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6115423 | ||||||
| chr1:6115429
|
G | A | 95 | a0001c0001t0005g0251a0001c0001t0006g0165a0001c0001t0008g0095others(92): Show | 95 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.4913-2431C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6115429 | ||||||
| chr1:6115447
|
G | C | 100 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(97): Show | 101 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.4913-2449C>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6115447 | ||||||
| chr1:6115571
|
C | T | 6 | a0002c0002t0001g0126a0002c0006t0001g0047a0002c0006t0040g0009others(3): Show | 6 | HG02109.hp1 HG02717.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.4913-2573G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6115571 | ||||||
| chr1:6115580
|
A | G | 1 | a0001c0004t0004g0032 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.4913-2582T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6115580 | ||||||
| chr1:6115770
|
C | A | 1 | a0001c0001t0068g0085 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.4913-2772G>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6115770 | ||||||
| chr1:6115775
|
T | C | 1 | a0001c0010t0080g0303 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.4913-2777A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6115775 | ||||||
| chr1:6116124
|
G | A | 63 | a0001c0001t0008g0095a0001c0003t0002g0022a0001c0003t0002g0070others(60): Show | 63 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.4913-3126C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6116124 | ||||||
| chr1:6116124
|
G | C | 1 | a0001c0030t0029g0211 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.4913-3126C>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6116124 | ||||||
| chr1:6116296
|
C | A | 1 | a0001c0005t0006g0202 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.4913-3298G>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6116296 | ||||||
| chr1:6116397
|
G | T | 1 | a0001c0001t0007g0100 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.4913-3399C>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6116397 | ||||||
| chr1:6116748
|
G | T | 1 | a0001c0013t0060g0227 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.4913-3750C>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6116748 | ||||||
| chr1:6116786
|
C | T | 1 | a0001c0005t0006g0202 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.4913-3788G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6116786 | ||||||
| chr1:6117008
|
G | A | 1 | a0001c0005t0005g0099 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.4913-4010C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6117008 | ||||||
| chr1:6117032
|
C | T | 1 | a0001c0001t0007g0275 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.4913-4034G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6117032 | ||||||
| chr1:6117142
|
G | T | 17 | a0001c0005t0043g0017a0001c0005t0057g0093a0001c0008t0005g0056others(14): Show | 17 | HG01167.hp1 HG01243.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.4912+3963C>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6117142 | ||||||
| chr1:6117450
|
G | A | 63 | a0001c0001t0008g0095a0001c0003t0002g0022a0001c0003t0002g0070others(60): Show | 63 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.4912+3655C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6117450 | ||||||
| chr1:6117503
|
G | A | 2 | a0001c0001t0064g0173a0001c0001t0070g0276 | 2 | NA18955.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.4912+3602C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6117503 | ||||||
| chr1:6117732
|
A | G | 22 | a0001c0005t0043g0017a0001c0005t0057g0093a0001c0008t0005g0056others(19): Show | 23 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(20): Show |
intron_variant | MODIFIER | c.4912+3373T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6117732 | ||||||
| chr1:6117770
|
C | A | 5 | a0001c0008t0012g0222a0001c0008t0012g0223a0001c0008t0012g0296others(2): Show | 6 | HG01167.hp2 HG01169.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.4912+3335G>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6117770 | ||||||
| chr1:6117785
|
T | C | 1 | a0002c0002t0017g0286 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.4912+3320A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6117785 | ||||||
| chr1:6117798
|
C | T | 1 | a0001c0005t0006g0202 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.4912+3307G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6117798 | ||||||
| chr1:6117802
|
T | C | 1 | a0001c0001t0068g0085 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.4912+3303A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6117802 | ||||||
| chr1:6117838
|
A | G | 246 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(243): Show | 247 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(244): Show |
intron_variant | MODIFIER | c.4912+3267T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6117838 | ||||||
| chr1:6117842
|
T | C | 1 | a0001c0030t0029g0211 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.4912+3263A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6117842 | ||||||
| chr1:6118210
|
T | C | 1 | a0001c0005t0006g0202 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.4912+2895A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6118210 | ||||||
| chr1:6118232
|
C | T | 90 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(87): Show | 90 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.4912+2873G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6118232 | ||||||
| chr1:6118292
|
C | T | 1 | a0001c0003t0010g0212 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.4912+2813G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6118292 | ||||||
| chr1:6118337
|
C | A | 1 | a0002c0002t0017g0286 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.4912+2768G>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6118337 | ||||||
| chr1:6118378
|
C | CA | 7 | a0001c0003t0010g0212a0001c0003t0047g0175a0001c0010t0014g0242others(4): Show | 7 | HG02015.hp2 HG02027.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.4912+2726dupT | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6118378 | ||||||
| chr1:6118378
|
CA | C | 137 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(134): Show | 138 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.4912+2726delT | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6118378 | ||||||
| chr1:6118378
|
CAA | C | 8 | a0001c0001t0011g0297a0001c0001t0068g0085a0001c0004t0072g0065others(5): Show | 8 | HG01099.hp1 HG01975.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.4912+2725_4912+272 others(6): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6118378 | ||||||
| chr1:6118558
|
G | A | 91 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(88): Show | 91 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.4912+2547C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6118558 | ||||||
| chr1:6118563
|
G | T | 1 | a0001c0028t0014g0058 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.4912+2542C>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6118563 | ||||||
| chr1:6118694
|
CT | C | 6 | a0001c0001t0084g0310a0001c0009t0014g0059a0001c0010t0014g0242others(3): Show | 6 | HG02257.hp2 HG02630.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.4912+2410delA | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6118694 | ||||||
| chr1:6118702
|
CTT | C | 114 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(111): Show | 115 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.4912+2401_4912+240 others(6): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6118702 | ||||||
| chr1:6118731
|
C | T | 1 | a0001c0001t0007g0195 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.4912+2374G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6118731 | ||||||
| chr1:6118766
|
C | T | 1 | a0001c0028t0014g0058 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.4912+2339G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6118766 | ||||||
| chr1:6118767
|
G | A | 1 | a0001c0008t0002g0178 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.4912+2338C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6118767 | ||||||
| chr1:6118917
|
C | T | 2 | a0001c0001t0054g0292a0001c0005t0006g0202 | 2 | HG01243.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.4912+2188G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6118917 | ||||||
| chr1:6118946
|
C | T | 1 | a0001c0020t0002g0051 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.4912+2159G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6118946 | ||||||
| chr1:6119065
|
TA | T | 257 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(254): Show | 258 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(255): Show |
intron_variant | MODIFIER | c.4912+2039delT | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6119065 | ||||||
| chr1:6119148
|
CT | C | 13 | a0001c0001t0011g0232a0001c0001t0011g0234a0001c0001t0011g0297others(10): Show | 13 | HG02109.hp2 HG02145.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.4912+1956delA | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6119148 | ||||||
| chr1:6119232
|
G | T | 1 | a0001c0003t0010g0212 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.4912+1873C>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6119232 | ||||||
| chr1:6119388
|
G | A | 1 | a0001c0001t0003g0164 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.4912+1717C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6119388 | ||||||
| chr1:6119741
|
A | C | 1 | a0001c0007t0005g0246 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.4912+1364T>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6119741 | ||||||
| chr1:6119746
|
T | C | 6 | a0002c0002t0001g0126a0002c0006t0001g0047a0002c0006t0040g0009others(3): Show | 6 | HG02109.hp1 HG02717.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.4912+1359A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6119746 | ||||||
| chr1:6119751
|
G | A | 1 | a0001c0001t0004g0138 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.4912+1354C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6119751 | ||||||
| chr1:6119761
|
G | A | 47 | a0001c0001t0004g0054a0001c0001t0004g0115a0001c0001t0004g0138others(44): Show | 47 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.4912+1344C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6119761 | ||||||
| chr1:6119762
|
C | T | 4 | a0001c0003t0002g0070a0001c0003t0010g0040a0001c0015t0002g0169others(1): Show | 4 | HG02129.hp1 NA18963.hp2 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.4912+1343G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6119762 | ||||||
| chr1:6119783
|
G | A | 44 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(41): Show | 44 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.4912+1322C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6119783 | ||||||
| chr1:6119783
|
G | T | 6 | a0001c0001t0084g0310a0001c0009t0014g0059a0001c0010t0014g0242others(3): Show | 6 | HG02257.hp2 HG02630.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.4912+1322C>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6119783 | ||||||
| chr1:6119803
|
G | A | 1 | a0001c0005t0057g0093 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.4912+1302C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6119803 | ||||||
| chr1:6119815
|
G | GTATA | 41 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(38): Show | 41 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.4912+1286_4912+128 others(8): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6119815 | ||||||
| chr1:6119827
|
G | A | 2 | a0001c0011t0010g0103a0001c0011t0010g0148 | 2 | HG03834.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.4912+1278C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6119827 | ||||||
| chr1:6119850
|
T | TTA | 18 | a0001c0004t0004g0032a0001c0004t0004g0118a0001c0004t0075g0300others(15): Show | 18 | HG00673.hp2 HG01070.hp2 HG01255.hp1 others(15): Show |
intron_variant | MODIFIER | c.4912+1253_4912+125 others(6): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6119850 | ||||||
| chr1:6119850
|
T | TTATA | 3 | a0001c0004t0072g0065a0001c0004t0083g0311a0001c0009t0073g0142 | 3 | HG01099.hp1 HG02895.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.4912+1251_4912+125 others(8): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6119850 | ||||||
| chr1:6119862
|
A | T | 1 | a0002c0002t0009g0110 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.4912+1243T>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6119862 | ||||||
| chr1:6119862
|
ATATT | A | 15 | a0001c0001t0011g0232a0001c0001t0011g0234a0001c0001t0011g0297others(12): Show | 15 | HG02109.hp2 HG02145.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.4912+1239_4912+124 others(8): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6119862 | ||||||
| chr1:6119863
|
TA | T | 14 | a0001c0005t0043g0017a0001c0008t0005g0230a0001c0013t0005g0156others(11): Show | 14 | HG01243.hp1 HG02280.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.4912+1241delT | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6119863 | ||||||
| chr1:6119864
|
A | ATT | 38 | a0001c0001t0004g0054a0001c0001t0004g0115a0001c0001t0004g0138others(35): Show | 38 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.4912+1239_4912+124 others(6): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6119864 | ||||||
| chr1:6119864
|
A | T | 33 | a0001c0004t0031g0084a0001c0005t0013g0193a0002c0002t0001g0107others(30): Show | 35 | HG00099.hp1 HG00140.hp1 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.4912+1241T>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6119864 | ||||||
| chr1:6119864
|
AT | A | 9 | a0001c0008t0005g0056a0001c0008t0012g0222a0001c0008t0012g0223others(6): Show | 10 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.4912+1240delA | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6119864 | ||||||
| chr1:6119864
|
ATTT | A | 43 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(40): Show | 43 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.4912+1238_4912+124 others(7): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6119864 | ||||||
| chr1:6119864
|
ATTTT | A | 34 | a0001c0001t0005g0251a0001c0001t0006g0165a0001c0001t0068g0085others(31): Show | 34 | HG00140.hp2 HG01069.hp1 HG01168.hp2 others(31): Show |
intron_variant | MODIFIER | c.4912+1237_4912+124 others(8): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6119864 | ||||||
| chr1:6119866
|
T | A | 63 | a0001c0001t0008g0095a0001c0003t0002g0022a0001c0003t0002g0070others(60): Show | 63 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.4912+1239A>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6119866 | ||||||
| chr1:6119867
|
T | A | 1 | a0001c0010t0080g0303 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.4912+1238A>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6119867 | ||||||
| chr1:6119899
|
T | C | 179 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(176): Show | 180 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(177): Show |
intron_variant | MODIFIER | c.4912+1206A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6119899 | ||||||
| chr1:6120033
|
G | T | 2 | a0001c0005t0006g0288a0001c0005t0006g0289 | 2 | NA18945.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.4912+1072C>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6120033 | ||||||
| chr1:6120110
|
C | T | 1 | a0001c0013t0060g0227 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.4912+995G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6120110 | ||||||
| chr1:6120116
|
C | T | 1 | a0001c0001t0077g0301 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.4912+989G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6120116 | ||||||
| chr1:6120122
|
A | C | 2 | a0001c0019t0085g0316a0001c0041t0014g0250 | 2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.4912+983T>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6120122 | ||||||
| chr1:6120249
|
G | A | 13 | a0001c0001t0011g0232a0001c0001t0011g0234a0001c0001t0011g0297others(10): Show | 13 | HG02109.hp2 HG02145.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.4912+856C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6120249 | ||||||
| chr1:6120384
|
G | A | 116 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(113): Show | 117 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.4912+721C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6120384 | ||||||
| chr1:6120435
|
G | A | 179 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(176): Show | 180 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(177): Show |
intron_variant | MODIFIER | c.4912+670C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6120435 | ||||||
| chr1:6120499
|
A | AT | 3 | a0001c0001t0003g0182a0003c0018t0015g0186a0003c0018t0015g0188 | 3 | HG02698.hp1 NA18971.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.4912+605dupA | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6120499 | ||||||
| chr1:6120501
|
T | A | 1 | a0001c0001t0068g0085 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.4912+604A>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6120501 | ||||||
| chr1:6120501
|
T | TA | 60 | a0001c0001t0008g0095a0001c0003t0002g0022a0001c0003t0002g0070others(57): Show | 60 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(57): Show |
intron_variant | MODIFIER | c.4912+603dupT | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6120501 | ||||||
| chr1:6120501
|
TA | T | 8 | a0001c0001t0003g0146a0001c0005t0030g0259a0001c0007t0058g0028others(5): Show | 8 | HG01167.hp1 HG01256.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.4912+603delT | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6120501 | ||||||
| chr1:6120502
|
A | T | 63 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(60): Show | 64 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.4912+603T>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6120502 | ||||||
| chr1:6120503
|
A | T | 2 | a0001c0001t0003g0146a0001c0010t0080g0303 | 2 | HG01167.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.4912+602T>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6120503 | ||||||
| chr1:6120508
|
A | T | 1 | a0001c0001t0068g0085 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.4912+597T>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6120508 | ||||||
| chr1:6120530
|
G | A | 2 | a0001c0001t0027g0132a0001c0001t0077g0301 | 2 | HG03927.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.4912+575C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6120530 | ||||||
| chr1:6120579
|
G | A | 116 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(113): Show | 117 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.4912+526C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6120579 | ||||||
| chr1:6120600
|
G | A | 1 | a0001c0028t0014g0058 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.4912+505C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6120600 | ||||||
| chr1:6120684
|
C | T | 2 | a0001c0005t0006g0087a0001c0005t0006g0151 | 2 | NA18612.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.4912+421G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6120684 | ||||||
| chr1:6120703
|
G | A | 1 | a0001c0007t0003g0287 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.4912+402C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6120703 | ||||||
| chr1:6120705
|
C | T | 6 | a0002c0002t0001g0126a0002c0006t0001g0047a0002c0006t0040g0009others(3): Show | 6 | HG02109.hp1 HG02717.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.4912+400G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6120705 | ||||||
| chr1:6120903
|
C | CA | 43 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(40): Show | 43 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.4912+201dupT | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6120903 | ||||||
| chr1:6120926
|
G | A | 93 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(90): Show | 93 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.4912+179C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6120926 | ||||||
| chr1:6120970
|
G | C | 1 | a0001c0001t0068g0085 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.4912+135C>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6120970 | ||||||
| chr1:6121071
|
G | T | 1 | a0002c0006t0001g0060 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.4912+34C>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 33/41 | chr1 | 6121071 | ||||||
| chr1:6121240
|
G | A | 5 | a0001c0008t0012g0222a0001c0008t0012g0223a0001c0008t0012g0296others(2): Show | 6 | HG01167.hp2 HG01169.hp1 HG01891.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.4780-3C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 32/41 | chr1 | 6121240 | ||||||
| chr1:6121341
|
G | A | 6 | a0001c0001t0084g0310a0001c0009t0014g0059a0001c0010t0014g0242others(3): Show | 6 | HG02257.hp2 HG02630.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.4780-104C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 32/41 | chr1 | 6121341 | ||||||
| chr1:6121750
|
G | A | 1 | a0001c0001t0004g0115 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.4700-177C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 31/41 | chr1 | 6121750 | ||||||
| chr1:6121820
|
G | A | 63 | a0001c0001t0008g0095a0001c0003t0002g0022a0001c0003t0002g0070others(60): Show | 63 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.4700-247C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 31/41 | chr1 | 6121820 | ||||||
| chr1:6121875
|
C | T | 2 | a0001c0001t0064g0173a0001c0001t0070g0276 | 2 | NA18955.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.4700-302G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 31/41 | chr1 | 6121875 | ||||||
| chr1:6122068
|
T | G | 1 | a0001c0009t0041g0014 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.4700-495A>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 31/41 | chr1 | 6122068 | ||||||
| chr1:6122071
|
G | T | 63 | a0001c0001t0008g0095a0001c0003t0002g0022a0001c0003t0002g0070others(60): Show | 63 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.4700-498C>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 31/41 | chr1 | 6122071 | ||||||
| chr1:6122241
|
G | A | 3 | a0001c0004t0072g0065a0001c0004t0083g0311a0001c0009t0073g0142 | 3 | HG01099.hp1 HG02895.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.4700-668C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 31/41 | chr1 | 6122241 | ||||||
| chr1:6122261
|
A | G | 69 | a0001c0001t0003g0163a0001c0001t0003g0164a0001c0001t0004g0054others(66): Show | 69 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.4700-688T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 31/41 | chr1 | 6122261 | ||||||
| chr1:6122303
|
C | T | 1 | a0001c0004t0004g0198 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.4700-730G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 31/41 | chr1 | 6122303 | ||||||
| chr1:6122304
|
G | A | 1 | a0001c0027t0067g0205 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.4700-731C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 31/41 | chr1 | 6122304 | ||||||
| chr1:6122384
|
G | A | 2 | a0002c0002t0017g0073a0002c0002t0017g0247 | 2 | HG00099.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.4700-811C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 31/41 | chr1 | 6122384 | ||||||
| chr1:6122571
|
G | A | 1 | a0001c0031t0034g0004 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4700-998C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 31/41 | chr1 | 6122571 | ||||||
| chr1:6122640
|
C | G | 1 | a0001c0009t0039g0013 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.4700-1067G>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 31/41 | chr1 | 6122640 | ||||||
| chr1:6122782
|
G | A | 3 | a0001c0004t0072g0065a0001c0004t0083g0311a0001c0009t0073g0142 | 3 | HG01099.hp1 HG02895.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.4699+1166C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 31/41 | chr1 | 6122782 | ||||||
| chr1:6122826
|
T | C | 1 | a0001c0001t0068g0085 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.4699+1122A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 31/41 | chr1 | 6122826 | ||||||
| chr1:6123067
|
C | CA | 11 | a0001c0001t0011g0232a0001c0001t0011g0234a0001c0001t0011g0297others(8): Show | 11 | HG02109.hp2 HG02145.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.4699+880dupT | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 31/41 | chr1 | 6123067 | ||||||
| chr1:6123222
|
T | C | 2 | a0001c0001t0084g0310a0001c0014t0081g0307 | 2 | HG02257.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.4699+726A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 31/41 | chr1 | 6123222 | ||||||
| chr1:6123240
|
C | T | 1 | a0002c0002t0001g0244 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.4699+708G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 31/41 | chr1 | 6123240 | ||||||
| chr1:6123298
|
C | T | 1 | a0001c0001t0007g0263 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.4699+650G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 31/41 | chr1 | 6123298 | ||||||
| chr1:6123305
|
G | A | 1 | a0001c0044t0082g0313 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.4699+643C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 31/41 | chr1 | 6123305 | ||||||
| chr1:6123318
|
G | A | 1 | a0001c0010t0056g0072 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.4699+630C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 31/41 | chr1 | 6123318 | ||||||
| chr1:6123370
|
G | A | 18 | a0001c0001t0011g0232a0001c0001t0011g0234a0001c0001t0011g0297others(15): Show | 18 | HG02109.hp2 HG02145.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.4699+578C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 31/41 | chr1 | 6123370 | ||||||
| chr1:6123388
|
T | C | 93 | a0001c0001t0008g0095a0001c0003t0002g0022a0001c0003t0002g0070others(90): Show | 94 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.4699+560A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 31/41 | chr1 | 6123388 | ||||||
| chr1:6123431
|
C | A | 1 | a0001c0013t0005g0236 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.4699+517G>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 31/41 | chr1 | 6123431 | ||||||
| chr1:6123431
|
C | CT | 52 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(49): Show | 52 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.4699+516dupA | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 31/41 | chr1 | 6123431 | ||||||
| chr1:6123468
|
C | T | 97 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(94): Show | 98 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.4699+480G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 31/41 | chr1 | 6123468 | ||||||
| chr1:6123688
|
A | G | 59 | a0001c0001t0004g0054a0001c0001t0006g0165a0001c0001t0027g0132others(56): Show | 59 | HG00423.hp1 HG00673.hp2 HG00738.hp1 others(56): Show |
intron_variant | MODIFIER | c.4699+260T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 31/41 | chr1 | 6123688 | ||||||
| chr1:6123701
|
TA | T | 223 | a0001c0001t0003g0239a0001c0001t0004g0054a0001c0001t0005g0251others(220): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.4699+246delT | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 31/41 | chr1 | 6123701 | ||||||
| chr1:6123777
|
G | A | 1 | a0001c0009t0014g0229 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.4699+171C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 31/41 | chr1 | 6123777 | ||||||
| chr1:6123787
|
T | C | 57 | a0001c0001t0004g0054a0001c0001t0006g0165a0001c0001t0027g0132others(54): Show | 57 | HG00423.hp1 HG00673.hp2 HG00738.hp1 others(54): Show |
intron_variant | MODIFIER | c.4699+161A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 31/41 | chr1 | 6123787 | ||||||
| chr1:6123866
|
T | C | 56 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(53): Show | 56 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.4699+82A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 31/41 | chr1 | 6123866 | ||||||
| chr1:6124132
|
A | G | 224 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(221): Show | 225 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.4540-25T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 30/41 | chr1 | 6124132 | ||||||
| chr1:6124183
|
C | A | 1 | a0001c0008t0006g0264 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.4540-76G>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 30/41 | chr1 | 6124183 | ||||||
| chr1:6124226
|
A | G | 227 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(224): Show | 228 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.4540-119T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 30/41 | chr1 | 6124226 | ||||||
| chr1:6124333
|
C | A | 1 | a0002c0012t0001g0037 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.4539+184G>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 30/41 | chr1 | 6124333 | ||||||
| chr1:6124479
|
G | A | 4 | a0002c0002t0001g0200a0002c0002t0023g0199a0002c0002t0023g0213others(1): Show | 4 | HG01261.hp1 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.4539+38C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 30/41 | chr1 | 6124479 | ||||||
| chr1:6124668
|
T | TG | 141 | a0001c0001t0003g0146a0001c0001t0003g0150a0001c0001t0003g0159others(138): Show | 142 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(139): Show |
splice_region_variant&intron_variant | LOW | c.4395-8dupC | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 29/41 | chr1 | 6124668 | ||||||
| chr1:6124668
|
T | TGG | 61 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(58): Show | 61 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(58): Show |
splice_region_variant&intron_variant | LOW | c.4395-9_4395-8dupCC | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 29/41 | chr1 | 6124668 | ||||||
| chr1:6124800
|
C | T | 7 | a0002c0002t0001g0225a0002c0002t0017g0073a0002c0002t0017g0092others(4): Show | 7 | HG00099.hp2 HG01081.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.4395-139G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 29/41 | chr1 | 6124800 | ||||||
| chr1:6124829
|
G | A | 63 | a0001c0001t0008g0095a0001c0003t0002g0022a0001c0003t0002g0070others(60): Show | 63 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.4395-168C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 29/41 | chr1 | 6124829 | ||||||
| chr1:6124860
|
C | G | 57 | a0001c0001t0004g0054a0001c0001t0006g0165a0001c0001t0027g0132others(54): Show | 57 | HG00423.hp1 HG00673.hp2 HG00738.hp1 others(54): Show |
intron_variant | MODIFIER | c.4395-199G>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 29/41 | chr1 | 6124860 | ||||||
| chr1:6124873
|
G | A | 14 | a0001c0001t0011g0232a0001c0001t0011g0234a0001c0001t0011g0297others(11): Show | 14 | HG02109.hp2 HG02145.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.4395-212C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 29/41 | chr1 | 6124873 | ||||||
| chr1:6125004
|
G | A | 57 | a0001c0001t0004g0054a0001c0001t0006g0165a0001c0001t0027g0132others(54): Show | 57 | HG00423.hp1 HG00673.hp2 HG00738.hp1 others(54): Show |
intron_variant | MODIFIER | c.4394+96C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 29/41 | chr1 | 6125004 | ||||||
| chr1:6125075
|
C | T | 1 | a0002c0006t0001g0064 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4394+25G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 29/41 | chr1 | 6125075 | ||||||
| chr1:6125369
|
G | A | 13 | a0001c0001t0011g0232a0001c0001t0011g0234a0001c0001t0011g0297others(10): Show | 13 | HG02109.hp2 HG02145.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.4261-136C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 28/41 | chr1 | 6125369 | ||||||
| chr1:6125472
|
G | A | 58 | a0001c0001t0004g0054a0001c0001t0006g0165a0001c0001t0027g0132others(55): Show | 58 | HG00423.hp1 HG00673.hp2 HG00738.hp1 others(55): Show |
intron_variant | MODIFIER | c.4260+52C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 28/41 | chr1 | 6125472 | ||||||
| chr1:6125678
|
G | A | 1 | a0001c0004t0004g0262 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.4172-66C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 27/41 | chr1 | 6125678 | ||||||
| chr1:6125872
|
G | T | 1 | a0001c0005t0006g0215 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.4079-14C>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 26/41 | chr1 | 6125872 | ||||||
| chr1:6125890
|
G | A | 1 | a0001c0010t0080g0303 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.4079-32C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 26/41 | chr1 | 6125890 | ||||||
| chr1:6126088
|
C | T | 1 | a0002c0002t0013g0088 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.4079-230G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 26/41 | chr1 | 6126088 | ||||||
| chr1:6126089
|
G | T | 1 | a0001c0004t0003g0024 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.4079-231C>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 26/41 | chr1 | 6126089 | ||||||
| chr1:6126223
|
C | T | 1 | a0001c0005t0057g0093 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.4078+349G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 26/41 | chr1 | 6126223 | ||||||
| chr1:6126254
|
G | A | 6 | a0001c0001t0084g0310a0001c0009t0014g0059a0001c0010t0014g0242others(3): Show | 6 | HG02257.hp2 HG02630.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.4078+318C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 26/41 | chr1 | 6126254 | ||||||
| chr1:6126334
|
G | A | 1 | a0001c0031t0034g0004 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4078+238C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 26/41 | chr1 | 6126334 | ||||||
| chr1:6126504
|
C | T | 23 | a0001c0003t0002g0070a0001c0003t0002g0158a0001c0003t0002g0253others(20): Show | 23 | HG00408.hp1 HG00609.hp2 HG02027.hp2 others(20): Show |
intron_variant | MODIFIER | c.4078+68G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 26/41 | chr1 | 6126504 | ||||||
| chr1:6126755
|
G | A | 2 | a0001c0005t0057g0093a0001c0039t0063g0241 | 2 | HG02572.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3904-9C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 25/41 | chr1 | 6126755 | ||||||
| chr1:6126778
|
G | A | 11 | a0001c0001t0011g0232a0001c0001t0011g0234a0001c0001t0011g0297others(8): Show | 11 | HG02109.hp2 HG02145.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.3904-32C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 25/41 | chr1 | 6126778 | ||||||
| chr1:6126846
|
C | A | 1 | a0001c0039t0063g0241 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3904-100G>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 25/41 | chr1 | 6126846 | ||||||
| chr1:6126884
|
C | T | 2 | a0001c0005t0057g0093a0001c0039t0063g0241 | 2 | HG02572.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3904-138G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 25/41 | chr1 | 6126884 | ||||||
| chr1:6127026
|
C | T | 59 | a0001c0001t0008g0095a0001c0003t0002g0022a0001c0003t0002g0070others(56): Show | 59 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.3904-280G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 25/41 | chr1 | 6127026 | ||||||
| chr1:6127078
|
C | T | 89 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(86): Show | 90 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.3904-332G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 25/41 | chr1 | 6127078 | ||||||
| chr1:6127104
|
G | A | 1 | a0001c0038t0035g0005 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3904-358C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 25/41 | chr1 | 6127104 | ||||||
| chr1:6127167
|
G | A | 23 | a0001c0005t0043g0017a0001c0008t0005g0056a0001c0008t0005g0230others(20): Show | 24 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.3904-421C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 25/41 | chr1 | 6127167 | ||||||
| chr1:6127195
|
A | C | 3 | a0001c0004t0072g0065a0001c0004t0083g0311a0001c0031t0034g0004 | 3 | HG02895.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.3904-449T>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 25/41 | chr1 | 6127195 | ||||||
| chr1:6127214
|
G | A | 3 | a0002c0002t0020g0018a0002c0002t0020g0019a0002c0002t0020g0021 | 3 | HG02280.hp1 HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.3904-468C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 25/41 | chr1 | 6127214 | ||||||
| chr1:6127276
|
C | G | 6 | a0001c0001t0084g0310a0001c0009t0014g0059a0001c0010t0014g0242others(3): Show | 6 | HG02257.hp2 HG02630.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.3904-530G>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 25/41 | chr1 | 6127276 | ||||||
| chr1:6127339
|
T | C | 65 | a0001c0001t0008g0095a0001c0001t0084g0310a0001c0003t0002g0022others(62): Show | 65 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(62): Show |
intron_variant | MODIFIER | c.3904-593A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 25/41 | chr1 | 6127339 | ||||||
| chr1:6127488
|
G | GAA | 68 | a0001c0001t0005g0251a0001c0001t0008g0095a0001c0001t0084g0310others(65): Show | 68 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.3903+556_3903+557d others(4): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 25/41 | chr1 | 6127488 | ||||||
| chr1:6127514
|
C | G | 70 | a0001c0001t0005g0251a0001c0001t0008g0095a0001c0001t0084g0310others(67): Show | 70 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.3903+532G>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 25/41 | chr1 | 6127514 | ||||||
| chr1:6127553
|
T | C | 6 | a0001c0001t0084g0310a0001c0009t0014g0059a0001c0010t0014g0242others(3): Show | 6 | HG02257.hp2 HG02630.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.3903+493A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 25/41 | chr1 | 6127553 | ||||||
| chr1:6127573
|
C | T | 3 | a0001c0001t0011g0297a0001c0009t0011g0240a0001c0009t0011g0252 | 3 | HG02615.hp2 HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3903+473G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 25/41 | chr1 | 6127573 | ||||||
| chr1:6127760
|
G | A | 2 | a0001c0005t0057g0093a0001c0039t0063g0241 | 2 | HG02572.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3903+286C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 25/41 | chr1 | 6127760 | ||||||
| chr1:6127818
|
G | A | 1 | a0001c0004t0075g0300 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3903+228C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 25/41 | chr1 | 6127818 | ||||||
| chr1:6127891
|
G | A | 1 | a0001c0005t0005g0099 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3903+155C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 25/41 | chr1 | 6127891 | ||||||
| chr1:6127923
|
C | T | 2 | a0001c0005t0057g0093a0001c0039t0063g0241 | 2 | HG02572.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3903+123G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 25/41 | chr1 | 6127923 | ||||||
| chr1:6127977
|
G | C | 1 | a0001c0028t0014g0058 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3903+69C>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 25/41 | chr1 | 6127977 | ||||||
| chr1:6127984
|
TG | T | 62 | a0001c0001t0004g0054a0001c0001t0005g0251a0001c0001t0006g0165others(59): Show | 62 | HG00423.hp1 HG00673.hp2 HG00738.hp1 others(59): Show |
intron_variant | MODIFIER | c.3903+61delC | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 25/41 | chr1 | 6127984 | ||||||
| chr1:6128002
|
A | G | 23 | a0001c0005t0043g0017a0001c0008t0005g0056a0001c0008t0005g0230others(20): Show | 24 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.3903+44T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 25/41 | chr1 | 6128002 | ||||||
| chr1:6128015
|
C | T | 1 | a0001c0003t0008g0153 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.3903+31G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 25/41 | chr1 | 6128015 | ||||||
| chr1:6128030
|
G | A | 2 | a0001c0005t0057g0093a0001c0039t0063g0241 | 2 | HG02572.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3903+16C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 25/41 | chr1 | 6128030 | ||||||
| chr1:6128040
|
C | T | 11 | a0001c0001t0011g0232a0001c0001t0011g0234a0001c0001t0011g0297others(8): Show | 11 | HG02109.hp2 HG02145.hp1 HG02559.hp2 others(8): Show |
splice_region_variant&intron_variant | LOW | c.3903+6G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 25/41 | chr1 | 6128040 | ||||||
| chr1:6128295
|
A | G | 1 | a0001c0028t0014g0058 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3731-77T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 24/41 | chr1 | 6128295 | ||||||
| chr1:6128297
|
A | G | 1 | a0001c0005t0030g0259 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.3731-79T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 24/41 | chr1 | 6128297 | ||||||
| chr1:6128317
|
G | A | 59 | a0001c0001t0004g0054a0001c0001t0006g0165a0001c0001t0027g0132others(56): Show | 59 | HG00423.hp1 HG00673.hp2 HG00738.hp1 others(56): Show |
intron_variant | MODIFIER | c.3731-99C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 24/41 | chr1 | 6128317 | ||||||
| chr1:6128407
|
G | T | 1 | a0001c0005t0057g0093 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3730+92C>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 24/41 | chr1 | 6128407 | ||||||
| chr1:6128486
|
G | A | 59 | a0001c0001t0004g0054a0001c0001t0006g0165a0001c0001t0027g0132others(56): Show | 59 | HG00423.hp1 HG00673.hp2 HG00738.hp1 others(56): Show |
intron_variant | MODIFIER | c.3730+13C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 24/41 | chr1 | 6128486 | ||||||
| chr1:6128719
|
G | C | 59 | a0001c0001t0004g0054a0001c0001t0006g0165a0001c0001t0027g0132others(56): Show | 59 | HG00423.hp1 HG00673.hp2 HG00738.hp1 others(56): Show |
intron_variant | MODIFIER | c.3620-110C>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 23/41 | chr1 | 6128719 | ||||||
| chr1:6128743
|
T | A | 59 | a0001c0001t0008g0095a0001c0003t0002g0022a0001c0003t0002g0070others(56): Show | 59 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.3619+95A>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 23/41 | chr1 | 6128743 | ||||||
| chr1:6128776
|
G | T | 1 | a0001c0003t0021g0039 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.3619+62C>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 23/41 | chr1 | 6128776 | ||||||
| chr1:6129334
|
AGT | A | 5 | a0001c0008t0012g0222a0001c0008t0012g0223a0001c0008t0012g0296others(2): Show | 6 | HG01167.hp2 HG01169.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.3388-267_3388-266d others(4): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 22/41 | chr1 | 6129334 | ||||||
| chr1:6129393
|
G | A | 62 | a0001c0001t0008g0095a0001c0001t0084g0310a0001c0003t0002g0022others(59): Show | 62 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.3388-324C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 22/41 | chr1 | 6129393 | ||||||
| chr1:6129448
|
G | A | 1 | a0001c0015t0002g0129 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.3388-379C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 22/41 | chr1 | 6129448 | ||||||
| chr1:6129456
|
A | G | 1 | a0001c0009t0041g0014 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3388-387T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 22/41 | chr1 | 6129456 | ||||||
| chr1:6129691
|
G | A | 2 | a0001c0001t0068g0085a0001c0005t0057g0093 | 2 | HG02451.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3387+513C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 22/41 | chr1 | 6129691 | ||||||
| chr1:6129891
|
C | T | 1 | a0001c0028t0014g0058 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3387+313G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 22/41 | chr1 | 6129891 | ||||||
| chr1:6129943
|
C | G | 1 | a0001c0004t0004g0261 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.3387+261G>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 22/41 | chr1 | 6129943 | ||||||
| chr1:6129957
|
G | A | 1 | a0001c0031t0034g0004 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3387+247C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 22/41 | chr1 | 6129957 | ||||||
| chr1:6129986
|
G | A | 1 | a0001c0004t0075g0300 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3387+218C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 22/41 | chr1 | 6129986 | ||||||
| chr1:6130155
|
C | T | 123 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(120): Show | 123 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.3387+49G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 22/41 | chr1 | 6130155 | ||||||
| chr1:6130368
|
G | T | 7 | a0001c0001t0011g0232a0001c0001t0011g0234a0001c0004t0011g0226others(4): Show | 7 | HG02145.hp1 HG02559.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.3263-40C>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 21/41 | chr1 | 6130368 | ||||||
| chr1:6130551
|
A | G | 218 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(215): Show | 219 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.3263-223T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 21/41 | chr1 | 6130551 | ||||||
| chr1:6130765
|
C | T | 2 | a0001c0001t0004g0054a0001c0004t0004g0290 | 2 | HG02080.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.3263-437G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 21/41 | chr1 | 6130765 | ||||||
| chr1:6130957
|
C | T | 1 | a0002c0002t0001g0154 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3263-629G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 21/41 | chr1 | 6130957 | ||||||
| chr1:6130988
|
G | A | 1 | a0001c0005t0057g0093 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3262+643C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 21/41 | chr1 | 6130988 | ||||||
| chr1:6131071
|
G | C | 38 | a0001c0001t0005g0251a0001c0001t0011g0297a0001c0001t0054g0292others(35): Show | 39 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(36): Show |
intron_variant | MODIFIER | c.3262+560C>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 21/41 | chr1 | 6131071 | ||||||
| chr1:6131100
|
C | T | 1 | a0001c0001t0054g0292 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3262+531G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 21/41 | chr1 | 6131100 | ||||||
| chr1:6131145
|
C | G | 1 | a0001c0001t0005g0251 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3262+486G>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 21/41 | chr1 | 6131145 | ||||||
| chr1:6131294
|
G | A | 7 | a0001c0001t0011g0232a0001c0001t0011g0234a0001c0004t0011g0226others(4): Show | 7 | HG02145.hp1 HG02559.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.3262+337C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 21/41 | chr1 | 6131294 | ||||||
| chr1:6131572
|
C | T | 53 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(50): Show | 53 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.3262+59G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 21/41 | chr1 | 6131572 | ||||||
| chr1:6131970
|
C | T | 1 | a0001c0008t0003g0249 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3145-222G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 20/41 | chr1 | 6131970 | ||||||
| chr1:6132077
|
GC | G | 4 | a0001c0005t0013g0193a0002c0002t0013g0082a0002c0002t0013g0088others(1): Show | 4 | HG00741.hp2 HG01123.hp1 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.3145-330delG | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 20/41 | chr1 | 6132077 | ||||||
| chr1:6132251
|
G | A | 16 | a0001c0008t0005g0056a0001c0008t0005g0230a0001c0010t0003g0044others(13): Show | 16 | HG01243.hp1 HG02280.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.3145-503C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 20/41 | chr1 | 6132251 | ||||||
| chr1:6132630
|
A | G | 1 | a0001c0001t0007g0275 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.3145-882T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 20/41 | chr1 | 6132630 | ||||||
| chr1:6132655
|
C | T | 121 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(118): Show | 121 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.3145-907G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 20/41 | chr1 | 6132655 | ||||||
| chr1:6132805
|
G | A | 119 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(116): Show | 119 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.3145-1057C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 20/41 | chr1 | 6132805 | ||||||
| chr1:6132880
|
T | TCTCTCTC others(12): Show |
1 | a0001c0009t0014g0059 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3145-1133_3145-113 others(23): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 20/41 | chr1 | 6132880 | ||||||
| chr1:6132880
|
T | TTC | 25 | a0001c0001t0011g0297a0001c0005t0006g0202a0001c0008t0005g0056others(22): Show | 26 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.3145-1134_3145-113 others(6): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 20/41 | chr1 | 6132880 | ||||||
| chr1:6132880
|
T | TTCTC | 4 | a0001c0001t0003g0163a0001c0001t0003g0164a0001c0005t0057g0093others(1): Show | 4 | HG02647.hp2 NA18998.hp2 NA19088.hp1 others(1): Show |
intron_variant | MODIFIER | c.3145-1136_3145-113 others(8): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 20/41 | chr1 | 6132880 | ||||||
| chr1:6132880
|
T | TTCTCTCT others(1): Show |
35 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(32): Show | 35 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(32): Show |
intron_variant | MODIFIER | c.3145-1140_3145-113 others(12): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 20/41 | chr1 | 6132880 | ||||||
| chr1:6132880
|
T | TTCTCTCT others(3): Show |
54 | a0001c0001t0003g0135a0001c0001t0003g0176a0001c0001t0003g0239others(51): Show | 54 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.3145-1142_3145-113 others(14): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 20/41 | chr1 | 6132880 | ||||||
| chr1:6132880
|
T | TTCTCTCT others(5): Show |
19 | a0001c0001t0007g0196a0001c0001t0068g0085a0001c0001t0084g0310others(16): Show | 19 | HG00408.hp2 HG00609.hp1 HG00609.hp2 others(16): Show |
intron_variant | MODIFIER | c.3145-1144_3145-113 others(16): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 20/41 | chr1 | 6132880 | ||||||
| chr1:6132880
|
T | TTCTCTCT others(9): Show |
1 | a0002c0047t0078g0314 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3145-1148_3145-113 others(20): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 20/41 | chr1 | 6132880 | ||||||
| chr1:6132880
|
T | TTCTCTCT others(13): Show |
1 | a0001c0019t0085g0316 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3145-1152_3145-113 others(24): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 20/41 | chr1 | 6132880 | ||||||
| chr1:6132880
|
T | TTCTCTCT others(15): Show |
1 | a0001c0010t0014g0242 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3145-1154_3145-113 others(26): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 20/41 | chr1 | 6132880 | ||||||
| chr1:6132880
|
T | TTCTCTCT others(17): Show |
1 | a0001c0041t0014g0250 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3145-1156_3145-113 others(28): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 20/41 | chr1 | 6132880 | ||||||
| chr1:6132880
|
TTC | T | 7 | a0001c0001t0007g0274a0001c0004t0006g0101a0001c0009t0011g0240others(4): Show | 7 | HG02109.hp2 HG02615.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.3145-1134_3145-113 others(6): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 20/41 | chr1 | 6132880 | ||||||
| chr1:6132880
|
TTCTC | T | 4 | a0001c0001t0054g0292a0001c0009t0041g0014a0001c0039t0063g0241others(1): Show | 4 | HG01243.hp2 HG02572.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.3145-1136_3145-113 others(8): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 20/41 | chr1 | 6132880 | ||||||
| chr1:6133024
|
C | T | 53 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(50): Show | 53 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.3144+1104G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 20/41 | chr1 | 6133024 | ||||||
| chr1:6133025
|
G | A | 7 | a0001c0005t0043g0017a0002c0002t0020g0018a0002c0002t0020g0019others(4): Show | 7 | HG01109.hp1 HG02280.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.3144+1103C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 20/41 | chr1 | 6133025 | ||||||
| chr1:6133155
|
G | A | 1 | a0002c0002t0001g0225 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3144+973C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 20/41 | chr1 | 6133155 | ||||||
| chr1:6133177
|
C | T | 119 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(116): Show | 119 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.3144+951G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 20/41 | chr1 | 6133177 | ||||||
| chr1:6133178
|
G | A | 22 | a0001c0008t0005g0056a0001c0008t0005g0230a0001c0008t0012g0222others(19): Show | 23 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(20): Show |
intron_variant | MODIFIER | c.3144+950C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 20/41 | chr1 | 6133178 | ||||||
| chr1:6133244
|
A | G | 119 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(116): Show | 119 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.3144+884T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 20/41 | chr1 | 6133244 | ||||||
| chr1:6133263
|
T | C | 27 | a0001c0001t0068g0085a0001c0005t0006g0202a0001c0005t0057g0093others(24): Show | 28 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(25): Show |
intron_variant | MODIFIER | c.3144+865A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 20/41 | chr1 | 6133263 | ||||||
| chr1:6133287
|
G | A | 9 | a0001c0001t0005g0251a0001c0001t0011g0232a0001c0001t0011g0234others(6): Show | 9 | HG02145.hp1 HG02559.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.3144+841C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 20/41 | chr1 | 6133287 | ||||||
| chr1:6133318
|
G | C | 6 | a0001c0001t0011g0297a0001c0009t0011g0240a0001c0009t0011g0252others(3): Show | 6 | HG02109.hp2 HG02615.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.3144+810C>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 20/41 | chr1 | 6133318 | ||||||
| chr1:6133331
|
G | A | 5 | a0001c0008t0012g0222a0001c0008t0012g0223a0001c0008t0012g0296others(2): Show | 6 | HG01167.hp2 HG01169.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.3144+797C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 20/41 | chr1 | 6133331 | ||||||
| chr1:6133349
|
T | A | 1 | a0003c0018t0002g0167 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.3144+779A>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 20/41 | chr1 | 6133349 | ||||||
| chr1:6133404
|
G | A | 119 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(116): Show | 119 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.3144+724C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 20/41 | chr1 | 6133404 | ||||||
| chr1:6133488
|
G | A | 5 | a0001c0001t0007g0078a0001c0001t0007g0100a0001c0001t0007g0263others(2): Show | 5 | HG02080.hp2 NA18962.hp2 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.3144+640C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 20/41 | chr1 | 6133488 | ||||||
| chr1:6133722
|
G | A | 7 | a0001c0001t0011g0232a0001c0001t0011g0234a0001c0004t0011g0226others(4): Show | 7 | HG02145.hp1 HG02559.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.3144+406C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 20/41 | chr1 | 6133722 | ||||||
| chr1:6133775
|
A | G | 1 | a0001c0020t0002g0051 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.3144+353T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 20/41 | chr1 | 6133775 | ||||||
| chr1:6133789
|
C | G | 5 | a0001c0003t0002g0070a0001c0003t0002g0158a0001c0003t0010g0040others(2): Show | 5 | HG00408.hp1 HG02129.hp1 NA18963.hp2 others(2): Show |
intron_variant | MODIFIER | c.3144+339G>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 20/41 | chr1 | 6133789 | ||||||
| chr1:6133837
|
G | T | 119 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(116): Show | 119 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.3144+291C>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 20/41 | chr1 | 6133837 | ||||||
| chr1:6133894
|
G | C | 1 | a0001c0001t0064g0173 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.3144+234C>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 20/41 | chr1 | 6133894 | ||||||
| chr1:6133931
|
T | C | 2 | a0001c0005t0006g0202a0001c0008t0006g0264 | 2 | HG02083.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.3144+197A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 20/41 | chr1 | 6133931 | ||||||
| chr1:6133958
|
C | T | 155 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(152): Show | 156 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.3144+170G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 20/41 | chr1 | 6133958 | ||||||
| chr1:6134055
|
G | A | 3 | a0001c0001t0054g0292a0001c0009t0041g0014a0001c0039t0063g0241 | 3 | HG01243.hp2 HG02572.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.3144+73C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 20/41 | chr1 | 6134055 | ||||||
| chr1:6134104
|
C | T | 1 | a0001c0001t0005g0251 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3144+24G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 20/41 | chr1 | 6134104 | ||||||
| chr1:6134105
|
G | A | 1 | a0001c0029t0076g0309 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3144+23C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 20/41 | chr1 | 6134105 | ||||||
| chr1:6134287
|
T | G | 146 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(143): Show | 147 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.3013-28A>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 19/41 | chr1 | 6134287 | ||||||
| chr1:6134346
|
T | C | 10 | a0001c0001t0011g0297a0001c0001t0068g0085a0001c0005t0057g0093others(7): Show | 10 | HG02083.hp1 HG02109.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.3013-87A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 19/41 | chr1 | 6134346 | ||||||
| chr1:6134434
|
G | T | 18 | a0001c0005t0006g0202a0001c0008t0005g0056a0001c0008t0005g0230others(15): Show | 18 | HG01167.hp1 HG01243.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.3013-175C>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 19/41 | chr1 | 6134434 | ||||||
| chr1:6134462
|
C | T | 1 | a0001c0010t0005g0143 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.3013-203G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 19/41 | chr1 | 6134462 | ||||||
| chr1:6134485
|
A | C | 1 | a0002c0012t0052g0045 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3013-226T>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 19/41 | chr1 | 6134485 | ||||||
| chr1:6134492
|
C | A | 1 | a0001c0039t0063g0241 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3012+226G>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 19/41 | chr1 | 6134492 | ||||||
| chr1:6134520
|
G | A | 112 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(109): Show | 112 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.3012+198C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 19/41 | chr1 | 6134520 | ||||||
| chr1:6134586
|
C | G | 7 | a0001c0001t0011g0232a0001c0001t0011g0234a0001c0004t0011g0226others(4): Show | 7 | HG02145.hp1 HG02559.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.3012+132G>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 19/41 | chr1 | 6134586 | ||||||
| chr1:6134618
|
G | A | 5 | a0001c0001t0011g0232a0001c0001t0011g0234a0001c0004t0011g0226others(2): Show | 5 | HG02145.hp1 HG02559.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.3012+100C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 19/41 | chr1 | 6134618 | ||||||
| chr1:6134644
|
GACCTACC others(15): Show |
G | 25 | a0001c0001t0011g0297a0001c0001t0068g0085a0001c0001t0084g0310others(22): Show | 25 | HG01884.hp1 HG02055.hp2 HG02083.hp1 others(22): Show |
intron_variant | MODIFIER | c.3012+52_3012+73del others(22): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 19/41 | chr1 | 6134644 | ||||||
| chr1:6134659
|
CCACAGGC others(15): Show |
C | 1 | a0002c0002t0026g0042 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3012+37_3012+58del others(22): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 19/41 | chr1 | 6134659 | ||||||
| chr1:6134678
|
C | T | 2 | a0001c0001t0068g0085a0001c0039t0063g0241 | 2 | HG02451.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.3012+40G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 19/41 | chr1 | 6134678 | ||||||
| chr1:6134900
|
G | A | 22 | a0001c0008t0005g0056a0001c0008t0005g0230a0001c0008t0012g0222others(19): Show | 23 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(20): Show |
intron_variant | MODIFIER | c.2871-41C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 18/41 | chr1 | 6134900 | ||||||
| chr1:6134948
|
G | A | 1 | a0001c0007t0003g0287 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.2871-89C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 18/41 | chr1 | 6134948 | ||||||
| chr1:6134964
|
C | T | 203 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(200): Show | 204 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.2871-105G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 18/41 | chr1 | 6134964 | ||||||
| chr1:6135001
|
C | T | 5 | a0001c0001t0084g0310a0001c0009t0014g0059a0001c0019t0085g0316others(2): Show | 5 | HG01884.hp1 HG02257.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2871-142G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 18/41 | chr1 | 6135001 | ||||||
| chr1:6135120
|
G | A | 12 | a0001c0001t0011g0232a0001c0001t0011g0234a0001c0001t0011g0297others(9): Show | 12 | HG02109.hp2 HG02145.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.2870+110C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 18/41 | chr1 | 6135120 | ||||||
| chr1:6135149
|
G | A | 35 | a0001c0001t0011g0297a0001c0005t0006g0202a0001c0005t0057g0093others(32): Show | 36 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(33): Show |
intron_variant | MODIFIER | c.2870+81C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 18/41 | chr1 | 6135149 | ||||||
| chr1:6135212
|
G | C | 2 | a0002c0006t0019g0011a0002c0006t0019g0012 | 2 | HG01109.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2870+18C>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 18/41 | chr1 | 6135212 | ||||||
| chr1:6135433
|
G | A | 184 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(181): Show | 184 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.2697-30C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 17/41 | chr1 | 6135433 | ||||||
| chr1:6135461
|
G | A | 7 | a0001c0001t0011g0232a0001c0001t0011g0234a0001c0004t0011g0226others(4): Show | 7 | HG02145.hp1 HG02559.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.2697-58C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 17/41 | chr1 | 6135461 | ||||||
| chr1:6135488
|
C | T | 17 | a0001c0004t0075g0300a0001c0007t0005g0041a0001c0007t0005g0140others(14): Show | 17 | HG01070.hp2 HG01099.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.2697-85G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 17/41 | chr1 | 6135488 | ||||||
| chr1:6135489
|
G | A | 7 | a0001c0001t0011g0232a0001c0001t0011g0234a0001c0004t0011g0226others(4): Show | 7 | HG02145.hp1 HG02559.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.2697-86C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 17/41 | chr1 | 6135489 | ||||||
| chr1:6135530
|
A | G | 1 | a0001c0005t0006g0202 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2697-127T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 17/41 | chr1 | 6135530 | ||||||
| chr1:6135538
|
A | C | 186 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(183): Show | 186 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.2697-135T>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 17/41 | chr1 | 6135538 | ||||||
| chr1:6135582
|
T | A | 2 | a0001c0001t0068g0085a0001c0039t0063g0241 | 2 | HG02451.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.2697-179A>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 17/41 | chr1 | 6135582 | ||||||
| chr1:6135622
|
C | T | 184 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(181): Show | 184 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.2697-219G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 17/41 | chr1 | 6135622 | ||||||
| chr1:6135672
|
C | G | 184 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(181): Show | 184 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.2697-269G>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 17/41 | chr1 | 6135672 | ||||||
| chr1:6135716
|
C | T | 16 | a0001c0008t0005g0056a0001c0008t0005g0230a0001c0010t0003g0044others(13): Show | 16 | HG01243.hp1 HG02280.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.2697-313G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 17/41 | chr1 | 6135716 | ||||||
| chr1:6135818
|
G | T | 2 | a0001c0001t0068g0085a0001c0039t0063g0241 | 2 | HG02451.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.2697-415C>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 17/41 | chr1 | 6135818 | ||||||
| chr1:6135952
|
G | A | 2 | a0001c0001t0068g0085a0001c0039t0063g0241 | 2 | HG02451.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.2697-549C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 17/41 | chr1 | 6135952 | ||||||
| chr1:6135966
|
A | G | 5 | a0001c0001t0084g0310a0001c0009t0014g0059a0001c0019t0085g0316others(2): Show | 5 | HG01884.hp1 HG02257.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2696+551T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 17/41 | chr1 | 6135966 | ||||||
| chr1:6135999
|
G | A | 1 | a0001c0043t0053g0271 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2696+518C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 17/41 | chr1 | 6135999 | ||||||
| chr1:6136014
|
T | TA | 10 | a0001c0005t0004g0144a0002c0002t0009g0001a0002c0002t0009g0034others(7): Show | 12 | HG00099.hp1 HG01081.hp1 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.2696+502dupT | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 17/41 | chr1 | 6136014 | ||||||
| chr1:6136021
|
A | C | 203 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(200): Show | 203 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.2696+496T>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 17/41 | chr1 | 6136021 | ||||||
| chr1:6136030
|
A | C | 188 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(185): Show | 188 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.2696+487T>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 17/41 | chr1 | 6136030 | ||||||
| chr1:6136033
|
A | C | 186 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(183): Show | 186 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.2696+484T>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 17/41 | chr1 | 6136033 | ||||||
| chr1:6136038
|
AAC | A | 186 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(183): Show | 186 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.2696+477_2696+478d others(4): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 17/41 | chr1 | 6136038 | ||||||
| chr1:6136082
|
AC | A | 7 | a0001c0001t0011g0232a0001c0001t0011g0234a0001c0004t0011g0226others(4): Show | 7 | HG02145.hp1 HG02559.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.2696+434delG | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 17/41 | chr1 | 6136082 | ||||||
| chr1:6136122
|
G | A | 2 | a0001c0009t0014g0229a0001c0009t0041g0014 | 2 | HG02647.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2696+395C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 17/41 | chr1 | 6136122 | ||||||
| chr1:6136127
|
G | A | 146 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(143): Show | 146 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.2696+390C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 17/41 | chr1 | 6136127 | ||||||
| chr1:6136153
|
G | T | 188 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(185): Show | 188 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.2696+364C>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 17/41 | chr1 | 6136153 | ||||||
| chr1:6136186
|
T | C | 188 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(185): Show | 188 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.2696+331A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 17/41 | chr1 | 6136186 | ||||||
| chr1:6136255
|
G | A | 7 | a0001c0001t0011g0232a0001c0001t0011g0234a0001c0004t0011g0226others(4): Show | 7 | HG02145.hp1 HG02559.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.2696+262C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 17/41 | chr1 | 6136255 | ||||||
| chr1:6136334
|
G | A | 33 | a0001c0001t0004g0054a0001c0001t0006g0165a0001c0001t0027g0132others(30): Show | 33 | HG00423.hp1 HG00673.hp2 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.2696+183C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 17/41 | chr1 | 6136334 | ||||||
| chr1:6136375
|
G | A | 5 | a0001c0001t0084g0310a0001c0009t0014g0059a0001c0019t0085g0316others(2): Show | 5 | HG01884.hp1 HG02257.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2696+142C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 17/41 | chr1 | 6136375 | ||||||
| chr1:6136433
|
A | G | 189 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(186): Show | 189 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.2696+84T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 17/41 | chr1 | 6136433 | ||||||
| chr1:6136457
|
G | A | 188 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(185): Show | 188 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.2696+60C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 17/41 | chr1 | 6136457 | ||||||
| chr1:6136473
|
C | T | 2 | a0001c0009t0014g0229a0001c0009t0041g0014 | 2 | HG02647.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2696+44G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 17/41 | chr1 | 6136473 | ||||||
| chr1:6136679
|
G | A | 1 | a0002c0012t0052g0045 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2575-41C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 16/41 | chr1 | 6136679 | ||||||
| chr1:6136712
|
G | A | 2 | a0001c0001t0068g0085a0001c0039t0063g0241 | 2 | HG02451.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.2574+16C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 16/41 | chr1 | 6136712 | ||||||
| chr1:6136883
|
A | G | 188 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(185): Show | 188 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.2437-18T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6136883 | ||||||
| chr1:6136891
|
T | A | 189 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(186): Show | 189 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.2437-26A>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6136891 | ||||||
| chr1:6137032
|
A | G | 186 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(183): Show | 186 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.2437-167T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6137032 | ||||||
| chr1:6137047
|
G | A | 186 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(183): Show | 186 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.2437-182C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6137047 | ||||||
| chr1:6137081
|
TGGA | T | 184 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(181): Show | 184 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.2437-219_2437-217d others(5): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6137081 | ||||||
| chr1:6137086
|
G | A | 1 | a0001c0001t0068g0085 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2437-221C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6137086 | ||||||
| chr1:6137099
|
G | A | 35 | a0001c0001t0004g0054a0001c0001t0006g0165a0001c0001t0027g0132others(32): Show | 35 | HG00423.hp1 HG00673.hp2 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.2437-234C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6137099 | ||||||
| chr1:6137101
|
C | T | 183 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(180): Show | 183 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.2437-236G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6137101 | ||||||
| chr1:6137105
|
G | C | 183 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(180): Show | 183 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.2437-240C>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6137105 | ||||||
| chr1:6137154
|
T | C | 5 | a0002c0002t0001g0126a0002c0006t0001g0047a0002c0006t0040g0009others(2): Show | 5 | HG02717.hp1 HG02723.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.2437-289A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6137154 | ||||||
| chr1:6137177
|
A | G | 189 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(186): Show | 189 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.2437-312T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6137177 | ||||||
| chr1:6137349
|
C | T | 5 | a0001c0001t0011g0297a0001c0009t0011g0240a0001c0009t0011g0252others(2): Show | 5 | HG02109.hp2 HG02615.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2437-484G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6137349 | ||||||
| chr1:6137354
|
A | G | 195 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(192): Show | 195 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.2437-489T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6137354 | ||||||
| chr1:6137387
|
G | A | 7 | a0001c0001t0011g0232a0001c0001t0011g0234a0001c0004t0011g0226others(4): Show | 7 | HG02145.hp1 HG02559.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.2437-522C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6137387 | ||||||
| chr1:6137387
|
G | C | 1 | a0001c0028t0014g0058 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2437-522C>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6137387 | ||||||
| chr1:6137399
|
G | A | 21 | a0001c0001t0005g0251a0001c0001t0011g0297a0001c0004t0075g0300others(18): Show | 21 | HG01070.hp2 HG01255.hp1 HG01256.hp1 others(18): Show |
intron_variant | MODIFIER | c.2437-534C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6137399 | ||||||
| chr1:6137613
|
G | A | 1 | a0001c0003t0008g0116 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.2437-748C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6137613 | ||||||
| chr1:6137774
|
A | G | 3 | a0001c0001t0068g0085a0001c0009t0014g0229a0001c0039t0063g0241 | 3 | HG02451.hp1 HG02572.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2437-909T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6137774 | ||||||
| chr1:6137835
|
G | C | 57 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(54): Show | 57 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.2437-970C>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6137835 | ||||||
| chr1:6137921
|
T | C | 1 | a0001c0028t0014g0058 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2437-1056A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6137921 | ||||||
| chr1:6137949
|
G | A | 73 | a0001c0001t0005g0251a0001c0001t0006g0165a0001c0001t0011g0297others(70): Show | 73 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.2437-1084C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6137949 | ||||||
| chr1:6137962
|
GT | G | 141 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(138): Show | 141 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.2437-1098delA | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6137962 | ||||||
| chr1:6137971
|
G | A | 1 | a0001c0003t0002g0121 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2437-1106C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6137971 | ||||||
| chr1:6138021
|
G | C | 1 | a0002c0047t0078g0314 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2437-1156C>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6138021 | ||||||
| chr1:6138045
|
G | A | 2 | a0001c0003t0021g0298a0001c0038t0035g0005 | 2 | HG01891.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.2437-1180C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6138045 | ||||||
| chr1:6138197
|
C | G | 57 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(54): Show | 57 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.2437-1332G>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6138197 | ||||||
| chr1:6138247
|
G | T | 4 | a0001c0001t0084g0310a0001c0009t0014g0059a0001c0019t0085g0316others(1): Show | 4 | HG02257.hp2 HG02630.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.2437-1382C>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6138247 | ||||||
| chr1:6138306
|
G | A | 3 | a0001c0004t0004g0261a0001c0004t0004g0262a0001c0004t0027g0104 | 3 | HG01123.hp2 HG03654.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.2437-1441C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6138306 | ||||||
| chr1:6138321
|
G | A | 1 | a0001c0049t0049g0096 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.2437-1456C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6138321 | ||||||
| chr1:6138409
|
C | T | 66 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(63): Show | 66 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.2437-1544G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6138409 | ||||||
| chr1:6138492
|
C | T | 57 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(54): Show | 57 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.2437-1627G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6138492 | ||||||
| chr1:6138554
|
T | C | 116 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(113): Show | 117 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.2437-1689A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6138554 | ||||||
| chr1:6138680
|
T | C | 1 | a0001c0005t0006g0025 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2437-1815A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6138680 | ||||||
| chr1:6138685
|
T | A | 132 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(129): Show | 132 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.2437-1820A>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6138685 | ||||||
| chr1:6139028
|
G | C | 1 | a0001c0003t0010g0117 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2437-2163C>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6139028 | ||||||
| chr1:6139117
|
T | C | 1 | a0001c0009t0004g0139 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2437-2252A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6139117 | ||||||
| chr1:6139193
|
A | T | 43 | a0001c0001t0011g0232a0001c0001t0011g0234a0001c0004t0011g0226others(40): Show | 44 | HG01070.hp2 HG01167.hp1 HG01167.hp2 others(41): Show |
intron_variant | MODIFIER | c.2437-2328T>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6139193 | ||||||
| chr1:6139213
|
CTGTTCTG others(4): Show |
C | 68 | a0001c0001t0005g0251a0001c0001t0006g0165a0001c0001t0054g0292others(65): Show | 68 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.2437-2359_2437-234 others(15): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6139213 | ||||||
| chr1:6139217
|
TCTGTTGT others(7): Show |
T | 1 | a0001c0031t0034g0004 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2437-2366_2437-235 others(18): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6139217 | ||||||
| chr1:6139218
|
C | T | 6 | a0001c0001t0011g0297a0001c0009t0011g0240a0001c0009t0011g0252others(3): Show | 6 | HG02109.hp2 HG02615.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.2437-2353G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6139218 | ||||||
| chr1:6139228
|
T | TTTG | 13 | a0001c0001t0011g0232a0001c0001t0011g0234a0001c0004t0011g0226others(10): Show | 13 | HG01099.hp1 HG01891.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.2437-2366_2437-236 others(7): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6139228 | ||||||
| chr1:6139395
|
C | T | 56 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(53): Show | 56 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.2437-2530G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6139395 | ||||||
| chr1:6139538
|
A | AT | 38 | a0001c0004t0075g0300a0001c0007t0005g0041a0001c0007t0005g0140others(35): Show | 39 | HG01070.hp2 HG01167.hp1 HG01167.hp2 others(36): Show |
intron_variant | MODIFIER | c.2436+2589dupA | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6139538 | ||||||
| chr1:6139555
|
A | T | 1 | a0001c0003t0002g0187 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.2436+2573T>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6139555 | ||||||
| chr1:6139617
|
C | G | 168 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(165): Show | 169 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.2436+2511G>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6139617 | ||||||
| chr1:6139825
|
C | T | 12 | a0001c0001t0011g0232a0001c0001t0011g0234a0001c0001t0011g0297others(9): Show | 12 | HG02109.hp2 HG02145.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.2436+2303G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6139825 | ||||||
| chr1:6139840
|
G | A | 51 | a0001c0001t0011g0232a0001c0001t0011g0234a0001c0001t0068g0085others(48): Show | 52 | HG01070.hp2 HG01167.hp1 HG01167.hp2 others(49): Show |
intron_variant | MODIFIER | c.2436+2288C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6139840 | ||||||
| chr1:6139864
|
G | A | 75 | a0001c0001t0005g0251a0001c0001t0006g0165a0001c0001t0011g0297others(72): Show | 75 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.2436+2264C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6139864 | ||||||
| chr1:6139987
|
C | T | 30 | a0001c0001t0004g0054a0001c0001t0027g0132a0001c0001t0029g0055others(27): Show | 30 | HG00423.hp1 HG00673.hp2 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.2436+2141G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6139987 | ||||||
| chr1:6140133
|
T | C | 1 | a0001c0001t0003g0239 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2436+1995A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6140133 | ||||||
| chr1:6140166
|
G | A | 38 | a0001c0004t0075g0300a0001c0005t0057g0093a0001c0007t0005g0041others(35): Show | 39 | HG01070.hp2 HG01167.hp1 HG01167.hp2 others(36): Show |
intron_variant | MODIFIER | c.2436+1962C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6140166 | ||||||
| chr1:6140178
|
G | A | 3 | a0001c0016t0016g0069a0001c0016t0016g0136a0001c0016t0016g0137 | 3 | HG01346.hp2 HG01358.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.2436+1950C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6140178 | ||||||
| chr1:6140179
|
G | A | 1 | a0001c0001t0077g0301 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2436+1949C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6140179 | ||||||
| chr1:6140209
|
T | C | 1 | a0001c0019t0011g0231 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2436+1919A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6140209 | ||||||
| chr1:6140398
|
C | CA | 56 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(53): Show | 56 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.2436+1729dupT | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6140398 | ||||||
| chr1:6140438
|
G | A | 7 | a0001c0001t0011g0232a0001c0001t0011g0234a0001c0004t0011g0226others(4): Show | 7 | HG02145.hp1 HG02559.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.2436+1690C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6140438 | ||||||
| chr1:6140563
|
C | T | 4 | a0001c0001t0084g0310a0001c0009t0014g0059a0001c0019t0085g0316others(1): Show | 4 | HG02257.hp2 HG02630.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.2436+1565G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6140563 | ||||||
| chr1:6140825
|
A | C | 258 | a0001c0001t0004g0054a0001c0001t0005g0251a0001c0001t0006g0165others(255): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.2436+1303T>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6140825 | ||||||
| chr1:6140849
|
A | T | 1 | a0001c0001t0007g0100 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2436+1279T>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6140849 | ||||||
| chr1:6140948
|
A | G | 1 | a0001c0030t0029g0211 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2436+1180T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6140948 | ||||||
| chr1:6140967
|
A | AAAT | 78 | a0001c0001t0005g0251a0001c0001t0011g0232a0001c0001t0011g0234others(75): Show | 78 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.2436+1158_2436+116 others(7): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6140967 | ||||||
| chr1:6140967
|
A | AAATAAT | 11 | a0001c0003t0010g0212a0001c0008t0006g0264a0001c0009t0014g0059others(8): Show | 11 | HG01099.hp1 HG01891.hp2 HG02015.hp2 others(8): Show |
intron_variant | MODIFIER | c.2436+1155_2436+116 others(10): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6140967 | ||||||
| chr1:6140967
|
A | AAATAATA others(2): Show |
8 | a0001c0001t0006g0165a0001c0009t0041g0014a0001c0011t0010g0160others(5): Show | 8 | HG02630.hp1 HG02647.hp1 NA18947.hp2 others(5): Show |
intron_variant | MODIFIER | c.2436+1152_2436+116 others(13): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6140967 | ||||||
| chr1:6140967
|
A | AAATAATA others(5): Show |
28 | a0001c0001t0004g0054a0001c0001t0027g0132a0001c0001t0029g0055others(25): Show | 29 | HG00423.hp1 HG00673.hp2 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.2436+1149_2436+116 others(16): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6140967 | ||||||
| chr1:6140967
|
A | AAATAATA others(8): Show |
18 | a0001c0005t0057g0093a0001c0007t0005g0041a0001c0007t0005g0140others(15): Show | 18 | HG01255.hp1 HG01256.hp1 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.2436+1146_2436+116 others(19): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6140967 | ||||||
| chr1:6140967
|
A | AAATAATA others(11): Show |
13 | a0001c0004t0075g0300a0001c0007t0059g0029a0001c0008t0005g0056others(10): Show | 13 | HG01070.hp2 HG01167.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.2436+1143_2436+116 others(22): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6140967 | ||||||
| chr1:6140967
|
A | AAATAATA others(14): Show |
3 | a0001c0004t0004g0081a0001c0008t0005g0230a0001c0010t0004g0030 | 3 | HG02895.hp1 HG03492.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2436+1140_2436+116 others(25): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6140967 | ||||||
| chr1:6140967
|
A | AAATAATA others(17): Show |
3 | a0001c0013t0005g0156a0001c0026t0005g0063a0001c0029t0076g0309 | 3 | HG01243.hp1 HG02559.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2436+1137_2436+116 others(28): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6140967 | ||||||
| chr1:6140967
|
A | T | 1 | a0001c0004t0030g0269 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.2436+1161T>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6140967 | ||||||
| chr1:6140967
|
AAAT | A | 93 | a0001c0004t0004g0094a0001c0005t0001g0075a0001c0005t0002g0112others(90): Show | 96 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(93): Show |
intron_variant | MODIFIER | c.2436+1158_2436+116 others(7): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6140967 | ||||||
| chr1:6140994
|
T | TAAA | 54 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(51): Show | 54 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.2436+1133_2436+113 others(7): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6140994 | ||||||
| chr1:6140994
|
T | TAATAAA | 3 | a0001c0043t0053g0271a0001c0048t0005g0133a0002c0006t0019g0011 | 3 | HG01109.hp1 HG02165.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.2436+1133_2436+113 others(10): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6140994 | ||||||
| chr1:6141146
|
T | C | 1 | a0001c0003t0002g0122 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2436+982A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6141146 | ||||||
| chr1:6141192
|
G | A | 45 | a0001c0005t0001g0075a0001c0005t0005g0099a0001c0005t0006g0025others(42): Show | 46 | HG00099.hp2 HG00140.hp2 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.2436+936C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6141192 | ||||||
| chr1:6141238
|
G | A | 1 | a0002c0002t0017g0286 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2436+890C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6141238 | ||||||
| chr1:6141311
|
T | C | 3 | a0002c0017t0001g0294a0002c0017t0001g0295a0002c0017t0028g0293 | 3 | HG02055.hp2 HG02451.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2436+817A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6141311 | ||||||
| chr1:6141342
|
A | G | 1 | a0001c0015t0008g0209 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2436+786T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6141342 | ||||||
| chr1:6141442
|
C | A | 4 | a0001c0001t0084g0310a0001c0009t0014g0059a0001c0019t0085g0316others(1): Show | 4 | HG02257.hp2 HG02630.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.2436+686G>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6141442 | ||||||
| chr1:6141472
|
G | A | 7 | a0001c0001t0011g0232a0001c0001t0011g0234a0001c0004t0011g0226others(4): Show | 7 | HG02145.hp1 HG02559.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.2436+656C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6141472 | ||||||
| chr1:6141536
|
G | T | 56 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(53): Show | 56 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.2436+592C>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6141536 | ||||||
| chr1:6141567
|
A | G | 1 | a0001c0001t0084g0310 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2436+561T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6141567 | ||||||
| chr1:6141614
|
T | A | 1 | a0001c0003t0002g0070 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2436+514A>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6141614 | ||||||
| chr1:6141658
|
C | T | 39 | a0001c0001t0011g0232a0001c0001t0011g0234a0001c0001t0011g0297others(36): Show | 40 | HG01070.hp2 HG01167.hp1 HG01167.hp2 others(37): Show |
intron_variant | MODIFIER | c.2436+470G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6141658 | ||||||
| chr1:6141726
|
G | A | 7 | a0001c0008t0012g0222a0001c0008t0012g0223a0001c0008t0012g0296others(4): Show | 8 | HG01167.hp2 HG01169.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.2436+402C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6141726 | ||||||
| chr1:6141761
|
C | T | 11 | a0001c0001t0011g0297a0001c0008t0012g0222a0001c0008t0012g0223others(8): Show | 12 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.2436+367G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6141761 | ||||||
| chr1:6141808
|
A | G | 1 | a0001c0004t0018g0083 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.2436+320T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6141808 | ||||||
| chr1:6141952
|
G | A | 5 | a0001c0001t0011g0232a0001c0001t0011g0234a0001c0004t0011g0226others(2): Show | 5 | HG02145.hp1 HG02559.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.2436+176C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 15/41 | chr1 | 6141952 | ||||||
| chr1:6142363
|
C | A | 6 | a0001c0016t0016g0074a0002c0002t0017g0073a0002c0002t0017g0247others(3): Show | 6 | HG00099.hp2 HG00140.hp2 HG01081.hp2 others(3): Show |
intron_variant | MODIFIER | c.2236-35G>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 14/41 | chr1 | 6142363 | ||||||
| chr1:6142860
|
G | A | 7 | a0001c0001t0011g0297a0001c0009t0011g0240a0001c0009t0011g0252others(4): Show | 7 | HG02109.hp2 HG02615.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.2044-255C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 13/41 | chr1 | 6142860 | ||||||
| chr1:6143061
|
CT | C | 131 | a0001c0001t0004g0054a0001c0001t0007g0221a0001c0001t0011g0297others(128): Show | 134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.2044-457delA | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 13/41 | chr1 | 6143061 | ||||||
| chr1:6143219
|
T | G | 5 | a0001c0004t0004g0094a0002c0002t0001g0107a0002c0002t0001g0108others(2): Show | 5 | HG00738.hp1 HG00741.hp1 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.2043+604A>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 13/41 | chr1 | 6143219 | ||||||
| chr1:6143229
|
G | A | 108 | a0001c0001t0003g0163a0001c0001t0003g0164a0001c0001t0006g0165others(105): Show | 108 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.2043+594C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 13/41 | chr1 | 6143229 | ||||||
| chr1:6143386
|
G | C | 1 | a0001c0010t0014g0242 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2043+437C>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 13/41 | chr1 | 6143386 | ||||||
| chr1:6143489
|
AGTGT | A | 7 | a0001c0001t0011g0297a0001c0009t0011g0240a0001c0009t0011g0252others(4): Show | 7 | HG02109.hp2 HG02615.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.2043+330_2043+333d others(6): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 13/41 | chr1 | 6143489 | ||||||
| chr1:6143508
|
C | G | 1 | a0001c0001t0077g0301 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2043+315G>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 13/41 | chr1 | 6143508 | ||||||
| chr1:6143531
|
G | C | 1 | a0001c0008t0012g0223 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2043+292C>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 13/41 | chr1 | 6143531 | ||||||
| chr1:6143626
|
G | A | 2 | a0001c0004t0072g0065a0001c0004t0083g0311 | 2 | HG02895.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2043+197C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 13/41 | chr1 | 6143626 | ||||||
| chr1:6143934
|
G | A | 1 | a0001c0009t0041g0014 | 1 | HG02647.hp1 | splice_region_variant&intron_variant | LOW | c.1935-3C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 12/41 | chr1 | 6143934 | ||||||
| chr1:6143941
|
G | A | 1 | a0001c0004t0031g0283 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1935-10C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 12/41 | chr1 | 6143941 | ||||||
| chr1:6144162
|
C | G | 49 | a0001c0001t0054g0292a0001c0001t0068g0085a0001c0004t0003g0267others(46): Show | 49 | HG00423.hp1 HG00673.hp2 HG01099.hp1 others(46): Show |
splice_region_variant&intron_variant | LOW | c.1803-7G>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 11/41 | chr1 | 6144162 | ||||||
| chr1:6144206
|
A | G | 251 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(248): Show | 253 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(250): Show |
intron_variant | MODIFIER | c.1803-51T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 11/41 | chr1 | 6144206 | ||||||
| chr1:6144240
|
C | A | 3 | a0001c0010t0012g0043a0001c0024t0012g0003a0002c0006t0061g0061 | 4 | HG01167.hp2 HG01169.hp1 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.1803-85G>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 11/41 | chr1 | 6144240 | ||||||
| chr1:6144321
|
G | A | 2 | a0001c0001t0054g0292a0001c0005t0006g0202 | 2 | HG01243.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1803-166C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 11/41 | chr1 | 6144321 | ||||||
| chr1:6144339
|
C | G | 1 | a0001c0026t0005g0063 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1803-184G>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 11/41 | chr1 | 6144339 | ||||||
| chr1:6144343
|
G | A | 7 | a0001c0009t0014g0059a0001c0010t0004g0030a0001c0014t0001g0049others(4): Show | 7 | HG02572.hp1 HG02630.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1803-188C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 11/41 | chr1 | 6144343 | ||||||
| chr1:6144351
|
G | A | 21 | a0001c0005t0002g0112a0001c0007t0003g0067a0001c0007t0003g0068others(18): Show | 21 | HG01070.hp2 HG01109.hp2 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.1803-196C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 11/41 | chr1 | 6144351 | ||||||
| chr1:6144398
|
G | A | 1 | a0001c0004t0018g0083 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1803-243C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 11/41 | chr1 | 6144398 | ||||||
| chr1:6144773
|
T | C | 133 | a0001c0001t0003g0163a0001c0001t0003g0164a0001c0001t0004g0054others(130): Show | 133 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.1803-618A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 11/41 | chr1 | 6144773 | ||||||
| chr1:6144782
|
A | G | 213 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(210): Show | 214 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(211): Show |
intron_variant | MODIFIER | c.1803-627T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 11/41 | chr1 | 6144782 | ||||||
| chr1:6144812
|
C | G | 1 | a0001c0011t0010g0148 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1803-657G>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 11/41 | chr1 | 6144812 | ||||||
| chr1:6144821
|
G | A | 1 | a0001c0044t0082g0313 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1803-666C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 11/41 | chr1 | 6144821 | ||||||
| chr1:6144872
|
C | T | 15 | a0001c0001t0011g0232a0001c0001t0011g0234a0001c0001t0084g0310others(12): Show | 15 | HG02109.hp1 HG02257.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.1803-717G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 11/41 | chr1 | 6144872 | ||||||
| chr1:6144893
|
T | C | 1 | a0001c0001t0003g0135 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1803-738A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 11/41 | chr1 | 6144893 | ||||||
| chr1:6144919
|
T | C | 1 | a0001c0001t0007g0080 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1803-764A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 11/41 | chr1 | 6144919 | ||||||
| chr1:6144990
|
A | G | 1 | a0002c0025t0001g0050 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1803-835T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 11/41 | chr1 | 6144990 | ||||||
| chr1:6145014
|
T | TTTAGTAA others(9): Show |
1 | a0001c0001t0003g0164 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1803-860_1803-859i others(18): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 11/41 | chr1 | 6145014 | ||||||
| chr1:6145127
|
C | T | 1 | a0001c0004t0011g0226 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1803-972G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 11/41 | chr1 | 6145127 | ||||||
| chr1:6145133
|
T | G | 2 | a0001c0001t0050g0035a0001c0011t0008g0208 | 2 | HG00544.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.1803-978A>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 11/41 | chr1 | 6145133 | ||||||
| chr1:6145159
|
G | A | 4 | a0001c0003t0002g0070a0001c0003t0010g0040a0001c0015t0002g0169others(1): Show | 4 | HG02129.hp1 NA18963.hp2 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.1803-1004C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 11/41 | chr1 | 6145159 | ||||||
| chr1:6145289
|
C | T | 94 | a0001c0001t0003g0163a0001c0001t0003g0164a0001c0001t0004g0054others(91): Show | 94 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.1802+923G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 11/41 | chr1 | 6145289 | ||||||
| chr1:6145291
|
C | T | 1 | a0001c0020t0004g0277 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1802+921G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 11/41 | chr1 | 6145291 | ||||||
| chr1:6145321
|
C | T | 1 | a0001c0001t0027g0132 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1802+891G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 11/41 | chr1 | 6145321 | ||||||
| chr1:6145421
|
G | A | 5 | a0001c0001t0084g0310a0001c0008t0012g0222a0001c0008t0012g0223others(2): Show | 5 | HG02109.hp1 HG02257.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1802+791C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 11/41 | chr1 | 6145421 | ||||||
| chr1:6145730
|
C | G | 78 | a0001c0001t0004g0054a0001c0001t0006g0165a0001c0001t0011g0297others(75): Show | 78 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.1802+482G>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 11/41 | chr1 | 6145730 | ||||||
| chr1:6145753
|
G | A | 1 | a0001c0028t0014g0058 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1802+459C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 11/41 | chr1 | 6145753 | ||||||
| chr1:6145895
|
G | A | 1 | a0001c0007t0005g0041 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1802+317C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 11/41 | chr1 | 6145895 | ||||||
| chr1:6145927
|
A | G | 94 | a0001c0001t0003g0163a0001c0001t0003g0164a0001c0001t0004g0054others(91): Show | 94 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.1802+285T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 11/41 | chr1 | 6145927 | ||||||
| chr1:6145942
|
A | G | 1 | a0001c0008t0005g0056 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1802+270T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 11/41 | chr1 | 6145942 | ||||||
| chr1:6146093
|
T | C | 101 | a0001c0001t0003g0163a0001c0001t0003g0164a0001c0001t0004g0054others(98): Show | 101 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.1802+119A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 11/41 | chr1 | 6146093 | ||||||
| chr1:6146104
|
C | G | 6 | a0001c0009t0014g0229a0001c0009t0073g0142a0001c0010t0012g0043others(3): Show | 6 | HG01099.hp1 HG01891.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.1802+108G>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 11/41 | chr1 | 6146104 | ||||||
| chr1:6146147
|
A | T | 4 | a0001c0009t0014g0229a0001c0010t0012g0043a0002c0006t0001g0047others(1): Show | 4 | HG01891.hp1 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1802+65T>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 11/41 | chr1 | 6146147 | ||||||
| chr1:6146179
|
C | T | 3 | a0001c0039t0063g0241a0001c0041t0014g0250a0002c0040t0001g0031 | 3 | HG02572.hp2 HG02630.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1802+33G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 11/41 | chr1 | 6146179 | ||||||
| chr1:6146530
|
C | T | 16 | a0001c0001t0011g0232a0001c0014t0001g0049a0001c0014t0011g0038others(13): Show | 16 | HG01891.hp2 HG02055.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.1591-107G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 10/41 | chr1 | 6146530 | ||||||
| chr1:6146588
|
C | A | 8 | a0001c0007t0005g0041a0001c0007t0005g0246a0001c0007t0044g0016others(5): Show | 8 | HG00140.hp1 HG01070.hp2 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.1590+77G>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 10/41 | chr1 | 6146588 | ||||||
| chr1:6146598
|
C | G | 1 | a0001c0005t0006g0202 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1590+67G>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 10/41 | chr1 | 6146598 | ||||||
| chr1:6146642
|
C | T | 1 | a0001c0014t0033g0304 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1590+23G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 10/41 | chr1 | 6146642 | ||||||
| chr1:6146923
|
C | G | 5 | a0001c0001t0003g0163a0001c0001t0003g0164a0001c0001t0005g0251others(2): Show | 5 | HG04199.hp2 NA18998.hp2 NA19088.hp1 others(2): Show |
intron_variant | MODIFIER | c.1384-52G>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 9/41 | chr1 | 6146923 | ||||||
| chr1:6146953
|
C | T | 1 | a0001c0028t0014g0058 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1384-82G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 9/41 | chr1 | 6146953 | ||||||
| chr1:6147038
|
G | C | 22 | a0001c0001t0011g0232a0001c0001t0011g0234a0001c0001t0084g0310others(19): Show | 22 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.1384-167C>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 9/41 | chr1 | 6147038 | ||||||
| chr1:6147061
|
T | C | 4 | a0001c0038t0035g0005a0001c0039t0063g0241a0001c0041t0014g0250others(1): Show | 4 | HG01891.hp2 HG02572.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1384-190A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 9/41 | chr1 | 6147061 | ||||||
| chr1:6147157
|
T | C | 197 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(194): Show | 199 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.1384-286A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 9/41 | chr1 | 6147157 | ||||||
| chr1:6147193
|
G | A | 10 | a0001c0004t0075g0300a0001c0005t0004g0144a0002c0002t0009g0001others(7): Show | 12 | HG00099.hp1 HG01081.hp1 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.1384-322C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 9/41 | chr1 | 6147193 | ||||||
| chr1:6147223
|
A | G | 1 | a0001c0011t0010g0103 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1384-352T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 9/41 | chr1 | 6147223 | ||||||
| chr1:6147429
|
G | A | 1 | a0001c0003t0046g0204 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1384-558C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 9/41 | chr1 | 6147429 | ||||||
| chr1:6147465
|
T | C | 1 | a0001c0023t0002g0260 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1384-594A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 9/41 | chr1 | 6147465 | ||||||
| chr1:6147553
|
G | A | 16 | a0001c0001t0011g0232a0001c0001t0011g0234a0001c0014t0001g0049others(13): Show | 16 | HG02055.hp1 HG02145.hp2 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.1384-682C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 9/41 | chr1 | 6147553 | ||||||
| chr1:6147563
|
C | T | 1 | a0001c0031t0034g0004 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1384-692G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 9/41 | chr1 | 6147563 | ||||||
| chr1:6147708
|
C | T | 1 | a0001c0028t0014g0058 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1384-837G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 9/41 | chr1 | 6147708 | ||||||
| chr1:6147716
|
T | C | 1 | a0001c0024t0012g0003 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1384-845A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 9/41 | chr1 | 6147716 | ||||||
| chr1:6147738
|
A | G | 165 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(162): Show | 165 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.1384-867T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 9/41 | chr1 | 6147738 | ||||||
| chr1:6147835
|
C | T | 192 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(189): Show | 193 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.1384-964G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 9/41 | chr1 | 6147835 | ||||||
| chr1:6147947
|
C | T | 22 | a0001c0001t0011g0232a0001c0001t0011g0234a0001c0001t0084g0310others(19): Show | 22 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.1383+907G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 9/41 | chr1 | 6147947 | ||||||
| chr1:6148063
|
T | C | 2 | a0001c0031t0034g0004a0001c0044t0082g0313 | 2 | HG03225.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1383+791A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 9/41 | chr1 | 6148063 | ||||||
| chr1:6148146
|
C | T | 17 | a0001c0008t0006g0264a0001c0009t0003g0281a0001c0009t0004g0139others(14): Show | 18 | HG01261.hp2 HG01358.hp2 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.1383+708G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 9/41 | chr1 | 6148146 | ||||||
| chr1:6148190
|
A | G | 31 | a0001c0008t0006g0264a0001c0009t0003g0281a0001c0009t0004g0139others(28): Show | 32 | HG01099.hp1 HG01109.hp1 HG01261.hp2 others(29): Show |
intron_variant | MODIFIER | c.1383+664T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 9/41 | chr1 | 6148190 | ||||||
| chr1:6148263
|
G | A | 22 | a0001c0001t0011g0232a0001c0001t0011g0234a0001c0001t0084g0310others(19): Show | 22 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.1383+591C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 9/41 | chr1 | 6148263 | ||||||
| chr1:6148424
|
C | A | 1 | a0001c0009t0041g0014 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1383+430G>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 9/41 | chr1 | 6148424 | ||||||
| chr1:6148641
|
C | G | 1 | a0001c0024t0012g0003 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1383+213G>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 9/41 | chr1 | 6148641 | ||||||
| chr1:6148694
|
T | C | 171 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(168): Show | 173 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.1383+160A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 9/41 | chr1 | 6148694 | ||||||
| chr1:6148755
|
G | A | 1 | a0002c0047t0078g0314 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1383+99C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 9/41 | chr1 | 6148755 | ||||||
| chr1:6148795
|
G | A | 1 | a0001c0024t0012g0003 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1383+59C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 9/41 | chr1 | 6148795 | ||||||
| chr1:6149150
|
A | G | 1 | a0001c0001t0068g0085 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1162-75T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 8/41 | chr1 | 6149150 | ||||||
| chr1:6149163
|
G | A | 1 | a0001c0024t0012g0003 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1161+83C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 8/41 | chr1 | 6149163 | ||||||
| chr1:6149205
|
G | T | 47 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(44): Show | 47 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.1161+41C>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 8/41 | chr1 | 6149205 | ||||||
| chr1:6149215
|
G | A | 1 | a0001c0026t0005g0063 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1161+31C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 8/41 | chr1 | 6149215 | ||||||
| chr1:6149418
|
G | A | 2 | a0001c0004t0004g0270a0001c0004t0030g0269 | 2 | NA18947.hp1 NA19074.hp2 |
splice_region_variant&intron_variant | LOW | c.995-6C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 7/41 | chr1 | 6149418 | ||||||
| chr1:6149485
|
G | C | 1 | a0001c0003t0002g0022 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.995-73C>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 7/41 | chr1 | 6149485 | ||||||
| chr1:6149691
|
T | C | 27 | a0001c0008t0006g0264a0001c0009t0003g0281a0001c0009t0004g0139others(24): Show | 28 | HG01099.hp1 HG01109.hp1 HG01261.hp2 others(25): Show |
intron_variant | MODIFIER | c.995-279A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 7/41 | chr1 | 6149691 | ||||||
| chr1:6149707
|
C | T | 1 | a0001c0004t0004g0198 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.995-295G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 7/41 | chr1 | 6149707 | ||||||
| chr1:6149709
|
A | AATGG | 173 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(170): Show | 175 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.995-301_995-298dup others(4): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 7/41 | chr1 | 6149709 | ||||||
| chr1:6149709
|
A | AATGGATG others(1): Show |
3 | a0001c0003t0008g0280a0001c0003t0036g0008a0001c0011t0048g0185 | 3 | NA18979.hp2 NA19009.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.995-305_995-298dup others(8): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 7/41 | chr1 | 6149709 | ||||||
| chr1:6149709
|
AATGG | A | 19 | a0001c0005t0005g0099a0001c0005t0006g0087a0001c0005t0006g0124others(16): Show | 19 | HG01069.hp1 HG01346.hp2 HG01358.hp1 others(16): Show |
intron_variant | MODIFIER | c.995-301_995-298del others(4): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 7/41 | chr1 | 6149709 | ||||||
| chr1:6149813
|
G | A | 1 | a0001c0024t0012g0003 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.995-401C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 7/41 | chr1 | 6149813 | ||||||
| chr1:6149855
|
T | TGATG | 17 | a0001c0008t0006g0264a0001c0009t0003g0281a0001c0009t0004g0139others(14): Show | 18 | HG01261.hp2 HG01358.hp2 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.995-447_995-444dup others(4): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 7/41 | chr1 | 6149855 | ||||||
| chr1:6149902
|
T | C | 1 | a0001c0001t0004g0180 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.995-490A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 7/41 | chr1 | 6149902 | ||||||
| chr1:6149960
|
GAATGGAT others(79): Show |
G | 2 | a0001c0001t0003g0135a0001c0001t0003g0176 | 2 | HG02602.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.995-634_995-549del others(86): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 7/41 | chr1 | 6149960 | ||||||
| chr1:6150000
|
AATGG | A | 24 | a0001c0008t0006g0264a0001c0009t0003g0281a0001c0009t0004g0139others(21): Show | 25 | HG01109.hp1 HG01261.hp2 HG01358.hp2 others(22): Show |
intron_variant | MODIFIER | c.995-592_995-589del others(4): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 7/41 | chr1 | 6150000 | ||||||
| chr1:6150000
|
AATGGATG others(1): Show |
A | 173 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(170): Show | 173 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.995-596_995-589del others(8): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 7/41 | chr1 | 6150000 | ||||||
| chr1:6150083
|
G | C | 1 | a0001c0024t0012g0003 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.995-671C>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 7/41 | chr1 | 6150083 | ||||||
| chr1:6150117
|
T | C | 1 | a0001c0008t0003g0249 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.995-705A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 7/41 | chr1 | 6150117 | ||||||
| chr1:6150196
|
A | AGATG | 197 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(194): Show | 199 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.995-788_995-785dup others(4): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 7/41 | chr1 | 6150196 | ||||||
| chr1:6150212
|
C | A | 2 | a0002c0002t0023g0213a0002c0002t0023g0214 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.995-800G>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 7/41 | chr1 | 6150212 | ||||||
| chr1:6150367
|
A | AGGAT | 35 | a0001c0001t0003g0206a0001c0001t0007g0237a0001c0001t0011g0232others(32): Show | 35 | HG00408.hp1 HG00544.hp2 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.994+661_994+664dup others(4): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 7/41 | chr1 | 6150367 | ||||||
| chr1:6150367
|
AGGAT | A | 41 | a0001c0001t0003g0163a0001c0001t0003g0164a0001c0001t0004g0180others(38): Show | 42 | HG00099.hp2 HG00140.hp2 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.994+661_994+664del others(4): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 7/41 | chr1 | 6150367 | ||||||
| chr1:6150367
|
AGGATGGA others(1): Show |
A | 8 | a0001c0009t0011g0240a0001c0009t0011g0252a0001c0009t0079g0308others(5): Show | 8 | HG01167.hp1 HG02109.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.994+657_994+664del others(8): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 7/41 | chr1 | 6150367 | ||||||
| chr1:6150367
|
AGGATGGA others(9): Show |
A | 6 | a0001c0005t0006g0202a0001c0005t0057g0093a0001c0021t0005g0026others(3): Show | 6 | HG02258.hp2 HG02818.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.994+649_994+664del others(16): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 7/41 | chr1 | 6150367 | ||||||
| chr1:6150431
|
A | AGGAT | 50 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(47): Show | 50 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.994+597_994+600dup others(4): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 7/41 | chr1 | 6150431 | ||||||
| chr1:6150431
|
A | AGGATGGA others(1): Show |
3 | a0001c0009t0041g0014a0001c0010t0012g0043a0002c0006t0061g0061 | 3 | HG01891.hp1 HG02647.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.994+593_994+600dup others(8): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 7/41 | chr1 | 6150431 | ||||||
| chr1:6150431
|
AGGAT | A | 4 | a0001c0001t0054g0292a0001c0013t0032g0224a0001c0013t0032g0228others(1): Show | 5 | HG01167.hp2 HG01169.hp1 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.994+597_994+600del others(4): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 7/41 | chr1 | 6150431 | ||||||
| chr1:6150463
|
TGGAC | T | 109 | a0001c0001t0003g0163a0001c0001t0003g0164a0001c0001t0003g0206others(106): Show | 109 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.994+565_994+568del others(4): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 7/41 | chr1 | 6150463 | ||||||
| chr1:6150467
|
C | T | 84 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(81): Show | 85 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.994+565G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 7/41 | chr1 | 6150467 | ||||||
| chr1:6150471
|
C | T | 30 | a0001c0008t0006g0264a0001c0009t0003g0281a0001c0009t0004g0139others(27): Show | 31 | HG01099.hp1 HG01109.hp1 HG01261.hp2 others(28): Show |
intron_variant | MODIFIER | c.994+561G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 7/41 | chr1 | 6150471 | ||||||
| chr1:6150475
|
CGGACGGA others(5): Show |
C | 1 | a0001c0009t0041g0014 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.994+545_994+556del others(12): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 7/41 | chr1 | 6150475 | ||||||
| chr1:6150483
|
C | T | 1 | a0001c0024t0012g0003 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.994+549G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 7/41 | chr1 | 6150483 | ||||||
| chr1:6150541
|
C | T | 197 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(194): Show | 198 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.994+491G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 7/41 | chr1 | 6150541 | ||||||
| chr1:6150645
|
G | A | 1 | a0001c0005t0006g0025 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.994+387C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 7/41 | chr1 | 6150645 | ||||||
| chr1:6150659
|
G | A | 3 | a0001c0007t0044g0016a0001c0007t0058g0028a0001c0007t0059g0029 | 3 | HG01070.hp2 HG01256.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.994+373C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 7/41 | chr1 | 6150659 | ||||||
| chr1:6150712
|
C | T | 197 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(194): Show | 198 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.994+320G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 7/41 | chr1 | 6150712 | ||||||
| chr1:6150714
|
A | G | 27 | a0001c0008t0006g0264a0001c0009t0003g0281a0001c0009t0004g0139others(24): Show | 28 | HG01099.hp1 HG01109.hp1 HG01261.hp2 others(25): Show |
intron_variant | MODIFIER | c.994+318T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 7/41 | chr1 | 6150714 | ||||||
| chr1:6150886
|
G | C | 4 | a0001c0038t0035g0005a0001c0039t0063g0241a0001c0041t0014g0250others(1): Show | 4 | HG01891.hp2 HG02572.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.994+146C>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 7/41 | chr1 | 6150886 | ||||||
| chr1:6150910
|
G | A | 197 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(194): Show | 198 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.994+122C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 7/41 | chr1 | 6150910 | ||||||
| chr1:6150948
|
G | A | 17 | a0001c0001t0011g0297a0001c0001t0054g0292a0001c0008t0005g0056others(14): Show | 18 | HG01167.hp2 HG01169.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.994+84C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 7/41 | chr1 | 6150948 | ||||||
| chr1:6151190
|
C | A | 2 | a0001c0004t0072g0065a0001c0004t0083g0311 | 2 | HG02895.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.871-35G>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 6/41 | chr1 | 6151190 | ||||||
| chr1:6151197
|
C | A | 7 | a0001c0005t0001g0075a0001c0016t0016g0074a0002c0002t0001g0225others(4): Show | 7 | HG00099.hp2 HG00140.hp2 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.871-42G>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 6/41 | chr1 | 6151197 | ||||||
| chr1:6151280
|
T | C | 218 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(215): Show | 220 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(217): Show |
intron_variant | MODIFIER | c.871-125A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 6/41 | chr1 | 6151280 | ||||||
| chr1:6151527
|
G | C | 218 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(215): Show | 220 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(217): Show |
intron_variant | MODIFIER | c.871-372C>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 6/41 | chr1 | 6151527 | ||||||
| chr1:6151703
|
C | A | 1 | a0002c0006t0001g0064 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.871-548G>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 6/41 | chr1 | 6151703 | ||||||
| chr1:6151762
|
A | G | 26 | a0001c0009t0003g0281a0001c0009t0004g0139a0001c0009t0014g0059others(23): Show | 27 | HG01099.hp1 HG01109.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.871-607T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 6/41 | chr1 | 6151762 | ||||||
| chr1:6151790
|
A | AC | 197 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(194): Show | 198 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.870+621dupG | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 6/41 | chr1 | 6151790 | ||||||
| chr1:6151831
|
T | G | 7 | a0001c0003t0002g0022a0001c0003t0002g0130a0001c0003t0002g0152others(4): Show | 7 | HG02083.hp2 HG02155.hp2 NA18982.hp2 others(4): Show |
intron_variant | MODIFIER | c.870+581A>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 6/41 | chr1 | 6151831 | ||||||
| chr1:6151904
|
G | A | 197 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(194): Show | 198 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.870+508C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 6/41 | chr1 | 6151904 | ||||||
| chr1:6151965
|
C | T | 1 | a0001c0009t0041g0014 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.870+447G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 6/41 | chr1 | 6151965 | ||||||
| chr1:6151982
|
A | G | 199 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(196): Show | 201 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.870+430T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 6/41 | chr1 | 6151982 | ||||||
| chr1:6152026
|
C | T | 6 | a0001c0004t0011g0226a0001c0005t0006g0025a0001c0005t0057g0093others(3): Show | 6 | HG02015.hp1 HG02145.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.870+386G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 6/41 | chr1 | 6152026 | ||||||
| chr1:6152055
|
G | A | 1 | a0001c0004t0004g0032 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.870+357C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 6/41 | chr1 | 6152055 | ||||||
| chr1:6152103
|
T | C | 1 | a0001c0007t0005g0041 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.870+309A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 6/41 | chr1 | 6152103 | ||||||
| chr1:6152250
|
C | G | 1 | a0001c0027t0004g0066 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.870+162G>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 6/41 | chr1 | 6152250 | ||||||
| chr1:6152295
|
C | T | 1 | a0001c0001t0007g0237 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.870+117G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 6/41 | chr1 | 6152295 | ||||||
| chr1:6152296
|
G | A | 21 | a0001c0009t0003g0281a0001c0009t0004g0139a0001c0009t0014g0059others(18): Show | 22 | HG01109.hp1 HG01261.hp2 HG01358.hp2 others(19): Show |
intron_variant | MODIFIER | c.870+116C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 6/41 | chr1 | 6152296 | ||||||
| chr1:6152348
|
G | A | 26 | a0001c0009t0003g0281a0001c0009t0004g0139a0001c0009t0014g0059others(23): Show | 27 | HG01099.hp1 HG01109.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.870+64C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 6/41 | chr1 | 6152348 | ||||||
| chr1:6152388
|
A | G | 4 | a0001c0001t0084g0310a0001c0008t0012g0222a0001c0008t0012g0223others(1): Show | 4 | HG02257.hp2 HG02258.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.870+24T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 6/41 | chr1 | 6152388 | ||||||
| chr1:6152389
|
C | A | 2 | a0001c0005t0006g0288a0001c0005t0006g0289 | 2 | NA18945.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.870+23G>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 6/41 | chr1 | 6152389 | ||||||
| chr1:6152561
|
C | G | 2 | a0002c0012t0025g0302a0002c0012t0025g0312 | 2 | HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.746-25G>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 5/41 | chr1 | 6152561 | ||||||
| chr1:6152615
|
G | A | 2 | a0001c0004t0072g0065a0001c0004t0083g0311 | 2 | HG02895.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.746-79C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 5/41 | chr1 | 6152615 | ||||||
| chr1:6152669
|
G | A | 2 | a0001c0023t0002g0260a0001c0023t0074g0315 | 2 | HG02738.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.746-133C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 5/41 | chr1 | 6152669 | ||||||
| chr1:6152780
|
C | T | 5 | a0001c0009t0014g0229a0001c0009t0073g0142a0001c0010t0012g0043others(2): Show | 5 | HG01099.hp1 HG01891.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.746-244G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 5/41 | chr1 | 6152780 | ||||||
| chr1:6152783
|
T | C | 201 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(198): Show | 203 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.746-247A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 5/41 | chr1 | 6152783 | ||||||
| chr1:6152810
|
G | A | 48 | a0001c0001t0011g0232a0001c0001t0011g0234a0001c0001t0084g0310others(45): Show | 50 | HG01099.hp1 HG01109.hp1 HG01167.hp2 others(47): Show |
intron_variant | MODIFIER | c.746-274C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 5/41 | chr1 | 6152810 | ||||||
| chr1:6152881
|
G | A | 26 | a0001c0009t0003g0281a0001c0009t0004g0139a0001c0009t0014g0059others(23): Show | 27 | HG01099.hp1 HG01109.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.746-345C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 5/41 | chr1 | 6152881 | ||||||
| chr1:6152893
|
G | A | 1 | a0001c0003t0008g0273 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.746-357C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 5/41 | chr1 | 6152893 | ||||||
| chr1:6152936
|
A | T | 1 | a0001c0001t0008g0095 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.746-400T>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 5/41 | chr1 | 6152936 | ||||||
| chr1:6152946
|
C | T | 4 | a0001c0038t0035g0005a0001c0039t0063g0241a0001c0041t0014g0250others(1): Show | 4 | HG01891.hp2 HG02572.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.746-410G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 5/41 | chr1 | 6152946 | ||||||
| chr1:6153103
|
G | T | 144 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(141): Show | 144 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.746-567C>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 5/41 | chr1 | 6153103 | ||||||
| chr1:6153104
|
G | T | 1 | a0001c0003t0015g0181 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.746-568C>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 5/41 | chr1 | 6153104 | ||||||
| chr1:6153163
|
G | A | 2 | a0001c0004t0072g0065a0001c0004t0083g0311 | 2 | HG02895.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.746-627C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 5/41 | chr1 | 6153163 | ||||||
| chr1:6153218
|
G | A | 21 | a0001c0009t0003g0281a0001c0009t0004g0139a0001c0009t0014g0059others(18): Show | 22 | HG01109.hp1 HG01261.hp2 HG01358.hp2 others(19): Show |
intron_variant | MODIFIER | c.746-682C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 5/41 | chr1 | 6153218 | ||||||
| chr1:6153293
|
G | A | 1 | a0001c0001t0005g0251 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.746-757C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 5/41 | chr1 | 6153293 | ||||||
| chr1:6153295
|
G | A | 7 | a0001c0009t0011g0240a0001c0009t0011g0252a0001c0009t0079g0308others(4): Show | 7 | HG01167.hp1 HG02109.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.746-759C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 5/41 | chr1 | 6153295 | ||||||
| chr1:6153296
|
A | C | 1 | a0001c0024t0012g0003 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.746-760T>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 5/41 | chr1 | 6153296 | ||||||
| chr1:6153331
|
A | G | 1 | a0002c0002t0028g0217 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.746-795T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 5/41 | chr1 | 6153331 | ||||||
| chr1:6153355
|
G | A | 1 | a0001c0001t0005g0251 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.746-819C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 5/41 | chr1 | 6153355 | ||||||
| chr1:6153411
|
T | A | 1 | a0001c0003t0002g0279 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.746-875A>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 5/41 | chr1 | 6153411 | ||||||
| chr1:6153478
|
T | C | 1 | a0001c0013t0042g0015 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.746-942A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 5/41 | chr1 | 6153478 | ||||||
| chr1:6153659
|
G | A | 1 | a0001c0001t0007g0274 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.745+1001C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 5/41 | chr1 | 6153659 | ||||||
| chr1:6153785
|
C | T | 5 | a0001c0009t0014g0229a0001c0009t0073g0142a0001c0010t0012g0043others(2): Show | 5 | HG01099.hp1 HG01891.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.745+875G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 5/41 | chr1 | 6153785 | ||||||
| chr1:6153827
|
T | TCAAAACA others(18): Show |
1 | a0001c0024t0012g0003 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.745+808_745+832dup others(25): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 5/41 | chr1 | 6153827 | ||||||
| chr1:6153827
|
TCAAAACA others(3): Show |
T | 4 | a0001c0005t0006g0202a0001c0019t0085g0316a0001c0021t0005g0026others(1): Show | 4 | HG02818.hp1 HG02818.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.745+823_745+832del others(10): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 5/41 | chr1 | 6153827 | ||||||
| chr1:6153900
|
T | G | 3 | a0001c0013t0005g0236a0001c0026t0005g0235a0001c0042t0005g0233 | 3 | HG02809.hp1 HG02922.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.745+760A>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 5/41 | chr1 | 6153900 | ||||||
| chr1:6153910
|
A | G | 1 | a0001c0001t0054g0292 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.745+750T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 5/41 | chr1 | 6153910 | ||||||
| chr1:6153942
|
G | C | 145 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(142): Show | 145 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.745+718C>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 5/41 | chr1 | 6153942 | ||||||
| chr1:6153987
|
C | G | 82 | a0001c0001t0003g0206a0001c0001t0004g0054a0001c0001t0006g0165others(79): Show | 82 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.745+673G>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 5/41 | chr1 | 6153987 | ||||||
| chr1:6154016
|
C | T | 5 | a0001c0001t0084g0310a0001c0008t0012g0222a0001c0008t0012g0223others(2): Show | 5 | HG02109.hp1 HG02257.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.745+644G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 5/41 | chr1 | 6154016 | ||||||
| chr1:6154027
|
T | C | 20 | a0001c0001t0011g0232a0001c0001t0011g0234a0001c0014t0001g0049others(17): Show | 21 | HG01167.hp2 HG01169.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.745+633A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 5/41 | chr1 | 6154027 | ||||||
| chr1:6154336
|
C | A | 48 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(45): Show | 48 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.745+324G>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 5/41 | chr1 | 6154336 | ||||||
| chr1:6154407
|
C | T | 5 | a0001c0024t0012g0003a0001c0038t0035g0005a0001c0039t0063g0241others(2): Show | 6 | HG01167.hp2 HG01169.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.745+253G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 5/41 | chr1 | 6154407 | ||||||
| chr1:6154478
|
G | A | 21 | a0001c0001t0011g0232a0001c0001t0011g0234a0001c0001t0084g0310others(18): Show | 21 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.745+182C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 5/41 | chr1 | 6154478 | ||||||
| chr1:6154628
|
G | A | 2 | a0001c0003t0008g0280a0001c0003t0036g0008 | 2 | NA18979.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.745+32C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 5/41 | chr1 | 6154628 | ||||||
| chr1:6154905
|
G | T | 1 | a0001c0008t0001g0106 | 1 | HG04199.hp2 | splice_region_variant&intron_variant | LOW | c.507-7C>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 4/41 | chr1 | 6154905 | ||||||
| chr1:6154963
|
C | T | 1 | a0002c0002t0001g0225 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.507-65G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 4/41 | chr1 | 6154963 | ||||||
| chr1:6154987
|
A | G | 61 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(58): Show | 62 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.507-89T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 4/41 | chr1 | 6154987 | ||||||
| chr1:6154988
|
T | C | 61 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(58): Show | 62 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.507-90A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 4/41 | chr1 | 6154988 | ||||||
| chr1:6155072
|
CCCCAGCT others(33): Show |
C | 107 | a0001c0001t0003g0097a0001c0001t0007g0275a0001c0001t0008g0095others(104): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.507-214_507-175del others(40): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 4/41 | chr1 | 6155072 | ||||||
| chr1:6155107
|
AAAACACC others(32): Show |
A | 1 | a0001c0004t0006g0101 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.507-248_507-210del others(39): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 4/41 | chr1 | 6155107 | ||||||
| chr1:6155112
|
A | ACCCAGCT others(34): Show |
1 | a0001c0004t0011g0226 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.507-255_507-215dup others(41): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 4/41 | chr1 | 6155112 | ||||||
| chr1:6155112
|
A | ACCCAGCT others(74): Show |
6 | a0001c0005t0043g0017a0002c0002t0001g0046a0002c0002t0020g0018others(3): Show | 6 | HG02280.hp1 HG02622.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.507-295_507-215dup others(81): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 4/41 | chr1 | 6155112 | ||||||
| chr1:6155112
|
A | C | 1 | a0001c0004t0024g0171 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.507-214T>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 4/41 | chr1 | 6155112 | ||||||
| chr1:6155113
|
CCCAGCTT others(32): Show |
C | 1 | a0001c0028t0014g0058 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.507-254_507-216del others(39): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 4/41 | chr1 | 6155113 | ||||||
| chr1:6155152
|
A | AC | 188 | a0001c0001t0003g0079a0001c0001t0003g0114a0001c0001t0003g0135others(185): Show | 190 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(187): Show |
intron_variant | MODIFIER | c.507-255dupG | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 4/41 | chr1 | 6155152 | ||||||
| chr1:6155152
|
A | ACCCAGCT others(34): Show |
5 | a0001c0001t0084g0310a0001c0008t0012g0222a0001c0008t0012g0223others(2): Show | 5 | HG02109.hp1 HG02257.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.507-295_507-255dup others(41): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 4/41 | chr1 | 6155152 | ||||||
| chr1:6155152
|
A | ACCCCAGC others(35): Show |
1 | a0002c0002t0009g0091 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.507-255_507-254ins others(42): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 4/41 | chr1 | 6155152 | ||||||
| chr1:6155286
|
T | C | 62 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(59): Show | 63 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.506+313A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 4/41 | chr1 | 6155286 | ||||||
| chr1:6155338
|
C | A | 1 | a0001c0001t0003g0135 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.506+261G>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 4/41 | chr1 | 6155338 | ||||||
| chr1:6155445
|
T | C | 1 | a0001c0004t0011g0226 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.506+154A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 4/41 | chr1 | 6155445 | ||||||
| chr1:6155467
|
C | T | 1 | a0002c0002t0001g0046 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.506+132G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 4/41 | chr1 | 6155467 | ||||||
| chr1:6155480
|
C | A | 55 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(52): Show | 56 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.506+119G>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 4/41 | chr1 | 6155480 | ||||||
| chr1:6155565
|
C | T | 2 | a0001c0004t0004g0270a0001c0004t0030g0269 | 2 | NA18947.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.506+34G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 4/41 | chr1 | 6155565 | ||||||
| chr1:6155891
|
G | A | 1 | a0001c0008t0006g0264 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.388-174C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 3/41 | chr1 | 6155891 | ||||||
| chr1:6155939
|
G | A | 16 | a0001c0009t0011g0240a0001c0009t0011g0252a0001c0009t0014g0229others(13): Show | 17 | HG01099.hp1 HG01167.hp1 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.388-222C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 3/41 | chr1 | 6155939 | ||||||
| chr1:6155987
|
G | A | 1 | a0001c0001t0027g0132 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.388-270C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 3/41 | chr1 | 6155987 | ||||||
| chr1:6156063
|
T | A | 22 | a0001c0009t0003g0281a0001c0009t0004g0139a0001c0009t0014g0059others(19): Show | 23 | HG01109.hp1 HG01261.hp2 HG01358.hp2 others(20): Show |
intron_variant | MODIFIER | c.388-346A>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 3/41 | chr1 | 6156063 | ||||||
| chr1:6156087
|
G | A | 2 | a0001c0010t0012g0043a0002c0006t0061g0061 | 2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.388-370C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 3/41 | chr1 | 6156087 | ||||||
| chr1:6156331
|
G | T | 1 | a0001c0028t0014g0058 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.388-614C>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 3/41 | chr1 | 6156331 | ||||||
| chr1:6156429
|
G | T | 1 | a0001c0031t0034g0004 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.388-712C>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 3/41 | chr1 | 6156429 | ||||||
| chr1:6156467
|
C | T | 1 | a0001c0004t0004g0081 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.388-750G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 3/41 | chr1 | 6156467 | ||||||
| chr1:6156468
|
G | A | 2 | a0001c0019t0011g0201a0001c0024t0012g0003 | 3 | HG01167.hp2 HG01169.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.388-751C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 3/41 | chr1 | 6156468 | ||||||
| chr1:6156496
|
A | G | 1 | a0001c0001t0003g0079 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.388-779T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 3/41 | chr1 | 6156496 | ||||||
| chr1:6156535
|
CA | C | 44 | a0001c0001t0003g0146a0001c0003t0008g0119a0001c0003t0008g0153others(41): Show | 45 | HG01081.hp2 HG01109.hp1 HG01358.hp2 others(42): Show |
intron_variant | MODIFIER | c.388-819delT | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 3/41 | chr1 | 6156535 | ||||||
| chr1:6156643
|
T | A | 34 | a0001c0009t0003g0281a0001c0009t0004g0139a0001c0009t0014g0059others(31): Show | 35 | HG01109.hp1 HG01261.hp2 HG01358.hp2 others(32): Show |
intron_variant | MODIFIER | c.388-926A>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 3/41 | chr1 | 6156643 | ||||||
| chr1:6156684
|
G | A | 86 | a0001c0001t0003g0206a0001c0001t0004g0054a0001c0001t0006g0165others(83): Show | 86 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.388-967C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 3/41 | chr1 | 6156684 | ||||||
| chr1:6156720
|
G | A | 15 | a0001c0007t0003g0067a0001c0007t0003g0068a0001c0007t0003g0284others(12): Show | 15 | HG00140.hp1 HG01070.hp2 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.388-1003C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 3/41 | chr1 | 6156720 | ||||||
| chr1:6156835
|
A | G | 15 | a0001c0007t0003g0067a0001c0007t0003g0068a0001c0007t0003g0284others(12): Show | 15 | HG00140.hp1 HG01070.hp2 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.388-1118T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 3/41 | chr1 | 6156835 | ||||||
| chr1:6156938
|
C | T | 1 | a0001c0001t0007g0203 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.388-1221G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 3/41 | chr1 | 6156938 | ||||||
| chr1:6156979
|
G | A | 5 | a0001c0009t0039g0013a0002c0006t0019g0010a0002c0006t0019g0011others(2): Show | 5 | HG01109.hp1 HG02723.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.388-1262C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 3/41 | chr1 | 6156979 | ||||||
| chr1:6157200
|
G | A | 1 | a0001c0004t0003g0024 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.388-1483C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 3/41 | chr1 | 6157200 | ||||||
| chr1:6157274
|
C | G | 1 | a0001c0005t0005g0099 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.388-1557G>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 3/41 | chr1 | 6157274 | ||||||
| chr1:6157385
|
G | A | 1 | a0001c0003t0015g0181 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.388-1668C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 3/41 | chr1 | 6157385 | ||||||
| chr1:6157460
|
C | T | 1 | a0001c0008t0001g0106 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.388-1743G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 3/41 | chr1 | 6157460 | ||||||
| chr1:6157495
|
C | A | 1 | a0001c0014t0033g0304 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.388-1778G>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 3/41 | chr1 | 6157495 | ||||||
| chr1:6157530
|
C | T | 1 | a0001c0023t0002g0260 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.387+1806G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 3/41 | chr1 | 6157530 | ||||||
| chr1:6157619
|
C | G | 1 | a0001c0004t0018g0134 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.387+1717G>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 3/41 | chr1 | 6157619 | ||||||
| chr1:6157713
|
C | T | 1 | a0001c0010t0005g0143 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.387+1623G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 3/41 | chr1 | 6157713 | ||||||
| chr1:6157720
|
A | G | 61 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(58): Show | 61 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.387+1616T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 3/41 | chr1 | 6157720 | ||||||
| chr1:6157799
|
A | G | 114 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(111): Show | 116 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.387+1537T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 3/41 | chr1 | 6157799 | ||||||
| chr1:6157808
|
C | G | 2 | a0001c0003t0008g0053a0001c0003t0008g0155 | 2 | NA18953.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.387+1528G>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 3/41 | chr1 | 6157808 | ||||||
| chr1:6158024
|
C | T | 4 | a0001c0038t0035g0005a0001c0039t0063g0241a0001c0041t0014g0250others(1): Show | 4 | HG01891.hp2 HG02572.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.387+1312G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 3/41 | chr1 | 6158024 | ||||||
| chr1:6158201
|
G | T | 1 | a0001c0001t0003g0150 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.387+1135C>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 3/41 | chr1 | 6158201 | ||||||
| chr1:6158477
|
G | A | 1 | a0001c0004t0066g0111 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.387+859C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 3/41 | chr1 | 6158477 | ||||||
| chr1:6158485
|
T | C | 1 | a0001c0001t0003g0206 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.387+851A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 3/41 | chr1 | 6158485 | ||||||
| chr1:6158602
|
T | C | 10 | a0001c0009t0011g0240a0001c0009t0011g0252a0001c0009t0079g0308others(7): Show | 10 | HG01167.hp1 HG02615.hp2 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.387+734A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 3/41 | chr1 | 6158602 | ||||||
| chr1:6158665
|
C | T | 1 | a0001c0004t0004g0032 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.387+671G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 3/41 | chr1 | 6158665 | ||||||
| chr1:6158666
|
G | A | 2 | a0001c0007t0003g0067a0001c0007t0003g0068 | 2 | HG02071.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.387+670C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 3/41 | chr1 | 6158666 | ||||||
| chr1:6158773
|
C | T | 3 | a0001c0011t0010g0160a0001c0011t0010g0183a0001c0011t0010g0184 | 3 | NA18947.hp2 NA18962.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.387+563G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 3/41 | chr1 | 6158773 | ||||||
| chr1:6158774
|
G | A | 1 | a0001c0011t0010g0168 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.387+562C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 3/41 | chr1 | 6158774 | ||||||
| chr1:6158832
|
C | T | 56 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(53): Show | 56 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.387+504G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 3/41 | chr1 | 6158832 | ||||||
| chr1:6158835
|
A | G | 306 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(303): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.387+501T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 3/41 | chr1 | 6158835 | ||||||
| chr1:6158868
|
G | A | 1 | a0001c0001t0077g0301 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.387+468C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 3/41 | chr1 | 6158868 | ||||||
| chr1:6158915
|
G | A | 1 | a0001c0007t0003g0284 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.387+421C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 3/41 | chr1 | 6158915 | ||||||
| chr1:6158932
|
G | A | 1 | a0001c0008t0012g0296 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.387+404C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 3/41 | chr1 | 6158932 | ||||||
| chr1:6158940
|
A | G | 108 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(105): Show | 109 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.387+396T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 3/41 | chr1 | 6158940 | ||||||
| chr1:6158986
|
G | A | 1 | a0001c0014t0033g0304 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.387+350C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 3/41 | chr1 | 6158986 | ||||||
| chr1:6158994
|
G | C | 1 | a0001c0001t0068g0085 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.387+342C>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 3/41 | chr1 | 6158994 | ||||||
| chr1:6159001
|
C | A | 1 | a0001c0001t0068g0085 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.387+335G>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 3/41 | chr1 | 6159001 | ||||||
| chr1:6159003
|
T | C | 86 | a0001c0001t0003g0206a0001c0001t0004g0054a0001c0001t0006g0165others(83): Show | 86 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.387+333A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 3/41 | chr1 | 6159003 | ||||||
| chr1:6159006
|
C | CA | 71 | a0001c0001t0003g0206a0001c0001t0004g0054a0001c0001t0006g0165others(68): Show | 72 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.387+329dupT | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 3/41 | chr1 | 6159006 | ||||||
| chr1:6159006
|
C | CAA | 63 | a0001c0001t0003g0079a0001c0001t0003g0114a0001c0001t0003g0135others(60): Show | 63 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.387+328_387+329dup others(2): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 3/41 | chr1 | 6159006 | ||||||
| chr1:6159006
|
C | CAAA | 43 | a0001c0001t0003g0097a0001c0001t0007g0219a0001c0001t0070g0276others(40): Show | 44 | HG01109.hp1 HG01167.hp1 HG01261.hp2 others(41): Show |
intron_variant | MODIFIER | c.387+327_387+329dup others(3): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 3/41 | chr1 | 6159006 | ||||||
| chr1:6159006
|
CA | C | 19 | a0001c0004t0072g0065a0001c0007t0003g0067a0001c0007t0003g0068others(16): Show | 19 | HG00140.hp1 HG01070.hp2 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.387+329delT | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 3/41 | chr1 | 6159006 | ||||||
| chr1:6159096
|
G | A | 2 | a0001c0009t0014g0229a0001c0009t0041g0014 | 2 | HG02647.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.387+240C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 3/41 | chr1 | 6159096 | ||||||
| chr1:6159106
|
G | A | 1 | a0001c0041t0014g0250 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.387+230C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 3/41 | chr1 | 6159106 | ||||||
| chr1:6159227
|
T | TCA | 11 | a0001c0004t0024g0254a0001c0005t0006g0025a0001c0009t0011g0240others(8): Show | 11 | HG01167.hp1 HG02015.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.387+107_387+108dup others(2): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 3/41 | chr1 | 6159227 | ||||||
| chr1:6159227
|
TCA | T | 103 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(100): Show | 104 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.387+107_387+108del others(2): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 3/41 | chr1 | 6159227 | ||||||
| chr1:6159227
|
TCACA | T | 117 | a0001c0001t0003g0206a0001c0001t0004g0054a0001c0001t0006g0165others(114): Show | 117 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.387+105_387+108del others(4): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 3/41 | chr1 | 6159227 | ||||||
| chr1:6159227
|
TCACACA | T | 14 | a0001c0009t0003g0281a0001c0009t0004g0139a0001c0009t0014g0059others(11): Show | 15 | HG01358.hp2 HG01361.hp2 HG02809.hp2 others(12): Show |
intron_variant | MODIFIER | c.387+103_387+108del others(6): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 3/41 | chr1 | 6159227 | ||||||
| chr1:6159228
|
C | T | 1 | a0001c0004t0003g0024 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.387+108G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 3/41 | chr1 | 6159228 | ||||||
| chr1:6159303
|
G | T | 69 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(66): Show | 69 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.387+33C>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 3/41 | chr1 | 6159303 | ||||||
| chr1:6159557
|
G | T | 1 | a0001c0007t0005g0197 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.208-42C>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6159557 | ||||||
| chr1:6159611
|
C | T | 1 | a0002c0006t0001g0047 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.208-96G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6159611 | ||||||
| chr1:6159617
|
G | A | 2 | a0001c0010t0014g0242a0001c0031t0034g0004 | 2 | HG02886.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.208-102C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6159617 | ||||||
| chr1:6159625
|
C | T | 4 | a0001c0005t0006g0202a0001c0019t0085g0316a0001c0021t0005g0026others(1): Show | 4 | HG02818.hp1 HG02818.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.208-110G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6159625 | ||||||
| chr1:6159626
|
G | A | 1 | a0001c0001t0007g0258 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.208-111C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6159626 | ||||||
| chr1:6159849
|
A | G | 9 | a0001c0009t0014g0229a0001c0009t0073g0142a0001c0010t0012g0043others(6): Show | 9 | HG01099.hp1 HG01891.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.208-334T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6159849 | ||||||
| chr1:6159859
|
C | T | 2 | a0001c0021t0005g0026a0001c0021t0005g0027 | 2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.208-344G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6159859 | ||||||
| chr1:6159894
|
G | C | 4 | a0001c0005t0006g0202a0001c0019t0085g0316a0001c0021t0005g0026others(1): Show | 4 | HG02818.hp1 HG02818.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.208-379C>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6159894 | ||||||
| chr1:6159904
|
A | G | 1 | a0001c0010t0056g0072 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.208-389T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6159904 | ||||||
| chr1:6159934
|
G | C | 1 | a0001c0001t0007g0191 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.208-419C>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6159934 | ||||||
| chr1:6159992
|
A | T | 1 | a0002c0022t0009g0036 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.208-477T>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6159992 | ||||||
| chr1:6160019
|
G | T | 2 | a0001c0010t0014g0242a0001c0031t0034g0004 | 2 | HG02886.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.208-504C>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6160019 | ||||||
| chr1:6160038
|
A | T | 18 | a0001c0001t0011g0232a0001c0001t0011g0234a0001c0001t0011g0297others(15): Show | 18 | HG01243.hp1 HG01243.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.208-523T>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6160038 | ||||||
| chr1:6160044
|
TCAGCCAG others(226): Show |
T | 8 | a0001c0009t0039g0013a0001c0009t0041g0014a0001c0031t0034g0004others(5): Show | 8 | HG01109.hp1 HG01358.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.208-762_208-530del | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6160044 | ||||||
| chr1:6160060
|
AGCCACAG others(47): Show |
A | 11 | a0001c0010t0014g0242a0001c0014t0001g0049a0001c0014t0011g0038others(8): Show | 11 | HG02055.hp1 HG02572.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.208-599_208-546del others(54): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6160060 | ||||||
| chr1:6160061
|
G | A | 1 | a0002c0012t0052g0045 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.208-546C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6160061 | ||||||
| chr1:6160064
|
A | C | 1 | a0002c0012t0052g0045 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.208-549T>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6160064 | ||||||
| chr1:6160064
|
ACAGCCAG others(189): Show |
A | 56 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(53): Show | 56 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.208-745_208-550del | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6160064 | ||||||
| chr1:6160089
|
A | G | 1 | a0002c0012t0052g0045 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.208-574T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6160089 | ||||||
| chr1:6160092
|
A | AGGGCCCC others(7): Show |
1 | a0002c0012t0052g0045 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.208-578_208-577ins others(14): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6160092 | ||||||
| chr1:6160098
|
A | G | 1 | a0002c0012t0052g0045 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.208-583T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6160098 | ||||||
| chr1:6160098
|
ACCCCAGC others(10): Show |
A | 89 | a0001c0001t0003g0206a0001c0001t0004g0054a0001c0001t0006g0165others(86): Show | 89 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.208-600_208-584del others(17): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6160098 | ||||||
| chr1:6160115
|
G | A | 11 | a0001c0010t0014g0242a0001c0014t0001g0049a0001c0014t0011g0038others(8): Show | 11 | HG02055.hp1 HG02572.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.208-600C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6160115 | ||||||
| chr1:6160115
|
G | GCCCCAGC others(252): Show |
1 | a0002c0012t0052g0045 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.208-601_208-600ins others(259): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6160115 | ||||||
| chr1:6160115
|
GCCCCAGC others(172): Show |
G | 11 | a0001c0005t0006g0202a0001c0009t0014g0059a0001c0019t0085g0316others(8): Show | 12 | HG02622.hp2 HG02809.hp2 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.208-779_208-601del | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6160115 | ||||||
| chr1:6160126
|
G | GGAAGGGC others(135): Show |
2 | a0001c0004t0004g0270a0001c0004t0030g0269 | 2 | NA18947.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.208-612_208-611ins others(142): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6160126 | ||||||
| chr1:6160131
|
G | A | 86 | a0001c0001t0003g0206a0001c0001t0004g0054a0001c0001t0006g0165others(83): Show | 86 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.208-616C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6160131 | ||||||
| chr1:6160131
|
G | GGCCCCAG others(229): Show |
1 | a0001c0001t0007g0195 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.208-617_208-616ins others(236): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6160131 | ||||||
| chr1:6160136
|
CAGCCAGG others(243): Show |
C | 1 | a0001c0001t0003g0146 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.208-871_208-622del | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6160136 | ||||||
| chr1:6160207
|
T | TAGCCAGG others(47): Show |
1 | a0001c0005t0002g0112 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.208-746_208-693dup others(54): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6160207 | ||||||
| chr1:6160207
|
TAGCCAGG others(135): Show |
T | 2 | a0001c0019t0011g0201a0001c0024t0012g0003 | 3 | HG01167.hp2 HG01169.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.208-834_208-693del | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6160207 | ||||||
| chr1:6160231
|
A | G | 5 | a0001c0009t0014g0229a0001c0009t0073g0142a0001c0010t0012g0043others(2): Show | 5 | HG01099.hp1 HG01891.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.208-716T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6160231 | ||||||
| chr1:6160231
|
AGAAGGGC others(209): Show |
A | 2 | a0001c0016t0016g0137a0002c0006t0001g0062 | 2 | HG01346.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.208-932_208-717del | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6160231 | ||||||
| chr1:6160234
|
AGGGCCCC others(98): Show |
A | 10 | a0001c0014t0001g0049a0001c0014t0011g0038a0001c0014t0033g0304others(7): Show | 10 | HG02055.hp1 HG02572.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.208-824_208-720del | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6160234 | ||||||
| chr1:6160236
|
GGCCCCAG others(192): Show |
G | 1 | a0001c0008t0006g0264 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.208-920_208-722del | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6160236 | ||||||
| chr1:6160242
|
A | G | 1 | a0001c0010t0004g0030 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.208-727T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6160242 | ||||||
| chr1:6160256
|
AGCCCCAG others(135): Show |
A | 1 | a0001c0007t0005g0197 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.208-883_208-742del | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6160256 | ||||||
| chr1:6160260
|
C | CCAGCCAG others(67): Show |
1 | a0001c0001t0007g0195 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.208-746_208-745ins others(74): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6160260 | ||||||
| chr1:6160260
|
C | CCAGCCAG others(30): Show |
26 | a0001c0004t0004g0081a0001c0004t0004g0198a0001c0005t0005g0099others(23): Show | 26 | HG01069.hp1 HG01358.hp1 HG02074.hp1 others(23): Show |
intron_variant | MODIFIER | c.208-746_208-745ins others(37): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6160260 | ||||||
| chr1:6160261
|
CAGCCAGG others(118): Show |
C | 4 | a0001c0009t0014g0229a0001c0010t0012g0043a0002c0006t0001g0047others(1): Show | 4 | HG01891.hp1 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.208-871_208-747del | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6160261 | ||||||
| chr1:6160268
|
GGAAGGGC others(135): Show |
G | 26 | a0001c0001t0007g0078a0001c0001t0068g0085a0001c0007t0003g0067others(23): Show | 26 | HG00140.hp1 HG01070.hp2 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.208-895_208-754del | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6160268 | ||||||
| chr1:6160277
|
C | T | 2 | a0001c0001t0007g0258a0001c0005t0006g0124 | 2 | NA18968.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.208-762G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6160277 | ||||||
| chr1:6160290
|
A | G | 1 | a0001c0009t0073g0142 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.208-775T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6160290 | ||||||
| chr1:6160291
|
A | AAAGCCCC others(81): Show |
62 | a0001c0001t0004g0054a0001c0001t0006g0165a0001c0001t0007g0100others(59): Show | 62 | HG00323.hp1 HG00408.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.208-777_208-776ins others(88): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6160291 | ||||||
| chr1:6160292
|
G | A | 24 | a0001c0001t0003g0206a0001c0003t0002g0070a0001c0003t0002g0158others(21): Show | 24 | HG00408.hp1 HG00544.hp2 HG00609.hp2 others(21): Show |
intron_variant | MODIFIER | c.208-777C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6160292 | ||||||
| chr1:6160294
|
A | AGGG | 62 | a0001c0001t0004g0054a0001c0001t0006g0165a0001c0001t0007g0100others(59): Show | 62 | HG00323.hp1 HG00408.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.208-780_208-779ins others(3): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6160294 | ||||||
| chr1:6160294
|
A | G | 27 | a0001c0001t0003g0206a0001c0001t0007g0258a0001c0003t0002g0070others(24): Show | 27 | HG00408.hp1 HG00544.hp2 HG00609.hp2 others(24): Show |
intron_variant | MODIFIER | c.208-779T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6160294 | ||||||
| chr1:6160297
|
C | A | 2 | a0001c0001t0007g0258a0001c0005t0006g0124 | 2 | NA18968.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.208-782G>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6160297 | ||||||
| chr1:6160298
|
CAGCCAGG others(81): Show |
C | 6 | a0001c0009t0003g0281a0001c0009t0004g0139a0001c0010t0005g0098others(3): Show | 6 | HG01261.hp2 HG01361.hp2 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.208-871_208-784del others(88): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6160298 | ||||||
| chr1:6160300
|
G | GCCAGGGA others(10): Show |
1 | a0001c0001t0007g0195 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.208-786_208-785ins others(17): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6160300 | ||||||
| chr1:6160300
|
G | GCCAGGGA others(84): Show |
24 | a0001c0001t0003g0206a0001c0003t0002g0070a0001c0003t0002g0158others(21): Show | 24 | HG00408.hp1 HG00544.hp2 HG00609.hp2 others(21): Show |
intron_variant | MODIFIER | c.208-786_208-785ins others(91): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6160300 | ||||||
| chr1:6160305
|
G | A | 1 | a0001c0009t0073g0142 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.208-790C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6160305 | ||||||
| chr1:6160313
|
C | T | 1 | a0001c0011t0008g0208 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.208-798G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6160313 | ||||||
| chr1:6160321
|
G | GAGA | 26 | a0001c0004t0004g0081a0001c0004t0004g0198a0001c0005t0005g0099others(23): Show | 26 | HG01069.hp1 HG01358.hp1 HG02074.hp1 others(23): Show |
intron_variant | MODIFIER | c.208-807_208-806ins others(3): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6160321 | ||||||
| chr1:6160322
|
G | A | 28 | a0001c0001t0007g0258a0001c0004t0004g0081a0001c0004t0004g0198others(25): Show | 28 | HG01069.hp1 HG01358.hp1 HG02074.hp1 others(25): Show |
intron_variant | MODIFIER | c.208-807C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6160322 | ||||||
| chr1:6160323
|
G | A | 1 | a0001c0001t0004g0054 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.208-808C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6160323 | ||||||
| chr1:6160325
|
A | G | 1 | a0001c0001t0004g0054 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.208-810T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6160325 | ||||||
| chr1:6160325
|
AGGGCCCC others(7): Show |
A | 2 | a0001c0001t0007g0258a0001c0005t0006g0124 | 2 | NA18968.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.208-824_208-811del others(14): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6160325 | ||||||
| chr1:6160327
|
G | A | 26 | a0001c0004t0004g0081a0001c0004t0004g0198a0001c0005t0005g0099others(23): Show | 26 | HG01069.hp1 HG01358.hp1 HG02074.hp1 others(23): Show |
intron_variant | MODIFIER | c.208-812C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6160327 | ||||||
| chr1:6160328
|
G | A | 26 | a0001c0004t0004g0081a0001c0004t0004g0198a0001c0005t0005g0099others(23): Show | 26 | HG01069.hp1 HG01358.hp1 HG02074.hp1 others(23): Show |
intron_variant | MODIFIER | c.208-813C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6160328 | ||||||
| chr1:6160336
|
A | C | 27 | a0001c0004t0004g0081a0001c0004t0004g0198a0001c0005t0005g0099others(24): Show | 27 | HG01069.hp1 HG01099.hp1 HG01358.hp1 others(24): Show |
intron_variant | MODIFIER | c.208-821T>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6160336 | ||||||
| chr1:6160339
|
G | A | 1 | a0001c0009t0073g0142 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.208-824C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6160339 | ||||||
| chr1:6160344
|
A | G | 26 | a0001c0004t0004g0081a0001c0004t0004g0198a0001c0005t0005g0099others(23): Show | 26 | HG01069.hp1 HG01358.hp1 HG02074.hp1 others(23): Show |
intron_variant | MODIFIER | c.208-829T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6160344 | ||||||
| chr1:6160345
|
G | A | 2 | a0001c0001t0007g0258a0001c0005t0006g0124 | 2 | NA18968.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.208-830C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6160345 | ||||||
| chr1:6160345
|
G | GCCCCAGC others(121): Show |
1 | a0001c0004t0031g0283 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.208-831_208-830ins others(128): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6160345 | ||||||
| chr1:6160349
|
C | T | 10 | a0001c0014t0001g0049a0001c0014t0011g0038a0001c0014t0033g0304others(7): Show | 10 | HG02055.hp1 HG02572.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.208-834G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6160349 | ||||||
| chr1:6160356
|
GGAAGGGC others(47): Show |
G | 1 | a0001c0009t0041g0014 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.208-895_208-842del others(54): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6160356 | ||||||
| chr1:6160378
|
A | G | 2 | a0001c0004t0011g0226a0001c0009t0073g0142 | 2 | HG01099.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.208-863T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6160378 | ||||||
| chr1:6160378
|
AAGAGCCC others(47): Show |
A | 1 | a0001c0009t0039g0013 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.208-917_208-864del others(54): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6160378 | ||||||
| chr1:6160381
|
AGCCCTAG others(10): Show |
A | 1 | a0001c0009t0073g0142 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.208-883_208-867del others(17): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6160381 | ||||||
| chr1:6160382
|
G | A | 2 | a0001c0001t0007g0258a0001c0005t0006g0124 | 2 | NA18968.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.208-867C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6160382 | ||||||
| chr1:6160386
|
T | C | 3 | a0001c0001t0007g0258a0001c0004t0011g0226a0001c0005t0006g0124 | 3 | HG02145.hp1 NA18968.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.208-871A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6160386 | ||||||
| chr1:6160386
|
T | TAGCCAGG others(84): Show |
6 | a0001c0003t0002g0089a0001c0003t0002g0090a0001c0003t0002g0120others(3): Show | 6 | HG00323.hp1 HG01070.hp1 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.208-872_208-871ins others(91): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6160386 | ||||||
| chr1:6160390
|
C | A | 1 | a0001c0001t0003g0146 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.208-875G>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6160390 | ||||||
| chr1:6160398
|
G | A | 1 | a0001c0001t0003g0146 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.208-883C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6160398 | ||||||
| chr1:6160398
|
GGCCCCAG others(30): Show |
G | 1 | a0001c0004t0075g0300 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.208-920_208-884del others(37): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6160398 | ||||||
| chr1:6160410
|
A | AGAAGGGC others(30): Show |
22 | a0001c0001t0007g0100a0001c0001t0011g0232a0001c0001t0011g0234others(19): Show | 22 | HG01243.hp1 HG01243.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.208-932_208-896dup others(37): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6160410 | ||||||
| chr1:6160410
|
A | G | 4 | a0001c0001t0003g0146a0001c0001t0007g0258a0001c0005t0006g0124others(1): Show | 4 | HG01099.hp1 NA18948.hp2 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.208-895T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6160410 | ||||||
| chr1:6160410
|
AGAAGGGC others(30): Show |
A | 19 | a0001c0004t0031g0084a0001c0014t0001g0049a0001c0014t0011g0038others(16): Show | 20 | HG01109.hp1 HG01167.hp2 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.208-932_208-896del others(37): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6160410 | ||||||
| chr1:6160415
|
G | GAGA | 4 | a0001c0009t0014g0229a0001c0010t0012g0043a0002c0006t0001g0047others(1): Show | 4 | HG01891.hp1 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.208-901_208-900ins others(3): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6160415 | ||||||
| chr1:6160432
|
G | A | 2 | a0001c0001t0007g0258a0001c0005t0006g0124 | 2 | NA18968.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.208-917C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6160432 | ||||||
| chr1:6160435
|
A | AGCCCTAG others(10): Show |
2 | a0001c0001t0007g0258a0001c0005t0006g0124 | 2 | NA18968.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.208-921_208-920ins others(17): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6160435 | ||||||
| chr1:6160447
|
G | A | 3 | a0001c0001t0007g0258a0001c0005t0006g0124a0001c0009t0039g0013 | 3 | HG03041.hp2 NA18968.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.208-932C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6160447 | ||||||
| chr1:6160572
|
C | T | 1 | a0001c0009t0073g0142 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.208-1057G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6160572 | ||||||
| chr1:6160589
|
C | T | 9 | a0001c0014t0001g0049a0001c0014t0033g0304a0001c0014t0033g0305others(6): Show | 9 | HG02055.hp1 HG02572.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.208-1074G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6160589 | ||||||
| chr1:6160827
|
C | T | 1 | a0001c0010t0005g0098 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.208-1312G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6160827 | ||||||
| chr1:6160868
|
C | T | 1 | a0002c0002t0001g0046 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.208-1353G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6160868 | ||||||
| chr1:6160901
|
CA | C | 3 | a0001c0008t0005g0230a0001c0013t0032g0224a0001c0013t0032g0228 | 3 | HG02280.hp2 HG02717.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.208-1387delT | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6160901 | ||||||
| chr1:6160902
|
A | G | 248 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(245): Show | 251 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(248): Show |
intron_variant | MODIFIER | c.208-1387T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6160902 | ||||||
| chr1:6160922
|
C | T | 1 | a0001c0003t0002g0152 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.208-1407G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6160922 | ||||||
| chr1:6160933
|
C | T | 2 | a0001c0001t0003g0163a0001c0001t0003g0164 | 2 | NA18998.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.208-1418G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6160933 | ||||||
| chr1:6160959
|
T | C | 7 | a0001c0009t0011g0252a0001c0009t0014g0229a0001c0010t0003g0044others(4): Show | 7 | HG01243.hp1 HG02572.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.208-1444A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6160959 | ||||||
| chr1:6160974
|
G | C | 3 | a0001c0001t0069g0190a0002c0002t0001g0154a0002c0025t0001g0189 | 3 | HG02698.hp2 HG03017.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.208-1459C>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6160974 | ||||||
| chr1:6160974
|
G | T | 50 | a0001c0001t0003g0097a0001c0001t0003g0162a0001c0001t0008g0095others(47): Show | 53 | HG00140.hp1 HG00738.hp1 HG01081.hp1 others(50): Show |
intron_variant | MODIFIER | c.208-1459C>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6160974 | ||||||
| chr1:6161061
|
C | T | 3 | a0001c0004t0018g0071a0001c0013t0032g0224a0001c0013t0032g0228 | 3 | HG02280.hp2 HG02717.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.208-1546G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6161061 | ||||||
| chr1:6161095
|
T | A | 3 | a0001c0009t0073g0142a0001c0010t0014g0242a0001c0039t0063g0241 | 3 | HG01099.hp1 HG02572.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.208-1580A>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6161095 | ||||||
| chr1:6161132
|
GAGAAGGA others(14): Show |
G | 1 | a0001c0031t0034g0004 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.208-1638_208-1618d others(23): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6161132 | ||||||
| chr1:6161148
|
G | A | 1 | a0001c0001t0068g0085 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.208-1633C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6161148 | ||||||
| chr1:6161191
|
G | A | 2 | a0001c0009t0039g0013a0001c0010t0004g0030 | 2 | HG02895.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.208-1676C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6161191 | ||||||
| chr1:6161192
|
C | T | 4 | a0001c0001t0003g0282a0001c0009t0011g0252a0002c0002t0017g0286others(1): Show | 4 | HG02886.hp1 HG02896.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.208-1677G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6161192 | ||||||
| chr1:6161205
|
T | C | 19 | a0001c0001t0003g0282a0001c0001t0011g0297a0001c0005t0001g0075others(16): Show | 20 | HG00140.hp2 HG01081.hp2 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.208-1690A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6161205 | ||||||
| chr1:6161424
|
C | T | 1 | a0001c0009t0073g0142 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.208-1909G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6161424 | ||||||
| chr1:6161425
|
G | A | 1 | a0001c0036t0006g0210 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.208-1910C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6161425 | ||||||
| chr1:6161551
|
G | A | 1 | a0001c0003t0010g0040 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.208-2036C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6161551 | ||||||
| chr1:6161732
|
C | T | 2 | a0001c0001t0003g0206a0001c0003t0002g0070 | 2 | NA18939.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.208-2217G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6161732 | ||||||
| chr1:6161765
|
C | T | 6 | a0001c0009t0039g0013a0002c0006t0019g0010a0002c0006t0019g0011others(3): Show | 6 | HG01109.hp1 HG02723.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.208-2250G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6161765 | ||||||
| chr1:6161766
|
T | C | 183 | a0001c0001t0003g0135a0001c0001t0003g0159a0001c0001t0003g0162others(180): Show | 184 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(181): Show |
intron_variant | MODIFIER | c.208-2251A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6161766 | ||||||
| chr1:6161767
|
G | A | 3 | a0001c0004t0004g0261a0001c0004t0004g0262a0002c0022t0009g0036 | 3 | HG01123.hp2 HG01255.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.208-2252C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6161767 | ||||||
| chr1:6161860
|
T | G | 1 | a0001c0005t0006g0151 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.208-2345A>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6161860 | ||||||
| chr1:6161915
|
T | C | 177 | a0001c0001t0003g0135a0001c0001t0003g0159a0001c0001t0003g0162others(174): Show | 178 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(175): Show |
intron_variant | MODIFIER | c.208-2400A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6161915 | ||||||
| chr1:6162015
|
A | G | 175 | a0001c0001t0003g0135a0001c0001t0003g0159a0001c0001t0003g0162others(172): Show | 176 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(173): Show |
intron_variant | MODIFIER | c.208-2500T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6162015 | ||||||
| chr1:6162076
|
G | A | 1 | a0001c0004t0004g0198 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.208-2561C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6162076 | ||||||
| chr1:6162124
|
G | C | 2 | a0001c0026t0005g0063a0002c0006t0001g0064 | 2 | HG02559.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.208-2609C>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6162124 | ||||||
| chr1:6162187
|
G | C | 1 | a0001c0001t0007g0221 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.208-2672C>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6162187 | ||||||
| chr1:6162301
|
G | A | 37 | a0001c0001t0003g0282a0001c0001t0007g0258a0001c0001t0007g0274others(34): Show | 37 | HG00544.hp2 HG00609.hp1 HG01257.hp2 others(34): Show |
intron_variant | MODIFIER | c.208-2786C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6162301 | ||||||
| chr1:6162441
|
C | A | 218 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(215): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.208-2926G>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6162441 | ||||||
| chr1:6162559
|
G | A | 2 | a0001c0001t0007g0191a0001c0003t0022g0192 | 2 | NA18950.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.208-3044C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6162559 | ||||||
| chr1:6162613
|
C | T | 1 | a0001c0001t0003g0159 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.208-3098G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6162613 | ||||||
| chr1:6162823
|
C | T | 86 | a0001c0001t0003g0135a0001c0001t0003g0159a0001c0001t0003g0162others(83): Show | 86 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.208-3308G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6162823 | ||||||
| chr1:6163010
|
T | C | 4 | a0001c0008t0003g0249a0001c0021t0005g0026a0001c0021t0005g0027others(1): Show | 4 | HG01884.hp2 HG03486.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.208-3495A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6163010 | ||||||
| chr1:6163091
|
G | T | 6 | a0001c0001t0011g0232a0001c0001t0011g0234a0001c0013t0005g0236others(3): Show | 6 | HG02559.hp2 HG02809.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.208-3576C>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6163091 | ||||||
| chr1:6163118
|
C | T | 2 | a0001c0001t0005g0251a0001c0041t0014g0250 | 2 | HG02630.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.208-3603G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6163118 | ||||||
| chr1:6163139
|
C | T | 7 | a0001c0001t0011g0297a0001c0001t0054g0292a0001c0008t0012g0296others(4): Show | 7 | HG01243.hp1 HG01243.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.208-3624G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6163139 | ||||||
| chr1:6163171
|
C | T | 1 | a0001c0007t0003g0284 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.208-3656G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6163171 | ||||||
| chr1:6163317
|
G | T | 1 | a0002c0002t0001g0225 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.208-3802C>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6163317 | ||||||
| chr1:6163388
|
G | A | 1 | a0001c0009t0014g0229 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.208-3873C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6163388 | ||||||
| chr1:6163466
|
G | A | 1 | a0001c0004t0083g0311 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.208-3951C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6163466 | ||||||
| chr1:6163524
|
T | C | 1 | a0002c0006t0001g0216 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.208-4009A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6163524 | ||||||
| chr1:6163547
|
T | C | 6 | a0001c0009t0039g0013a0001c0009t0041g0014a0002c0006t0019g0010others(3): Show | 6 | HG01109.hp1 HG02647.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.208-4032A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6163547 | ||||||
| chr1:6163653
|
G | A | 2 | a0001c0021t0005g0026a0001c0021t0005g0027 | 2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.208-4138C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6163653 | ||||||
| chr1:6163745
|
C | T | 1 | a0001c0003t0010g0212 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.208-4230G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6163745 | ||||||
| chr1:6163807
|
T | C | 2 | a0001c0041t0014g0250a0002c0047t0078g0314 | 2 | HG01884.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.208-4292A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6163807 | ||||||
| chr1:6163838
|
T | A | 1 | a0001c0003t0022g0192 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.207+4312A>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6163838 | ||||||
| chr1:6163872
|
C | T | 8 | a0001c0001t0004g0138a0001c0001t0011g0232a0001c0001t0011g0234others(5): Show | 8 | HG02027.hp1 HG02559.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.207+4278G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6163872 | ||||||
| chr1:6164049
|
A | C | 1 | a0001c0003t0002g0158 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.207+4101T>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6164049 | ||||||
| chr1:6164071
|
T | C | 176 | a0001c0001t0003g0135a0001c0001t0003g0159a0001c0001t0003g0162others(173): Show | 177 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(174): Show |
intron_variant | MODIFIER | c.207+4079A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6164071 | ||||||
| chr1:6164184
|
C | T | 1 | a0001c0042t0005g0233 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.207+3966G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6164184 | ||||||
| chr1:6164193
|
G | A | 6 | a0001c0001t0011g0232a0001c0001t0011g0234a0001c0013t0005g0236others(3): Show | 6 | HG02559.hp2 HG02809.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.207+3957C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6164193 | ||||||
| chr1:6164198
|
C | T | 2 | a0001c0001t0029g0055a0001c0027t0067g0205 | 2 | HG01106.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.207+3952G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6164198 | ||||||
| chr1:6164248
|
C | T | 8 | a0001c0001t0003g0239a0001c0009t0011g0240a0001c0010t0014g0242others(5): Show | 8 | HG02572.hp2 HG02615.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.207+3902G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6164248 | ||||||
| chr1:6164468
|
C | T | 1 | a0001c0003t0015g0157 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.207+3682G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6164468 | ||||||
| chr1:6164506
|
C | T | 2 | a0001c0021t0005g0026a0001c0021t0005g0027 | 2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.207+3644G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6164506 | ||||||
| chr1:6164517
|
C | T | 2 | a0001c0005t0004g0144a0002c0002t0009g0086 | 2 | HG01081.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.207+3633G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6164517 | ||||||
| chr1:6164683
|
C | G | 4 | a0001c0008t0003g0249a0001c0021t0005g0026a0001c0021t0005g0027others(1): Show | 4 | HG01884.hp2 HG03486.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.207+3467G>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6164683 | ||||||
| chr1:6164767
|
G | A | 1 | a0001c0001t0005g0251 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.207+3383C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6164767 | ||||||
| chr1:6165073
|
G | A | 1 | a0001c0008t0006g0179 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.207+3077C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6165073 | ||||||
| chr1:6165124
|
G | C | 1 | a0001c0001t0027g0132 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.207+3026C>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6165124 | ||||||
| chr1:6165148
|
G | C | 1 | a0001c0010t0004g0030 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.207+3002C>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6165148 | ||||||
| chr1:6165315
|
T | C | 1 | a0001c0007t0003g0284 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.207+2835A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6165315 | ||||||
| chr1:6165392
|
A | G | 1 | a0001c0014t0033g0305 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.207+2758T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6165392 | ||||||
| chr1:6165397
|
G | C | 104 | a0001c0001t0003g0135a0001c0001t0003g0159a0001c0001t0003g0162others(101): Show | 105 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.207+2753C>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6165397 | ||||||
| chr1:6165508
|
G | T | 1 | a0001c0010t0004g0030 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.207+2642C>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6165508 | ||||||
| chr1:6165634
|
G | T | 3 | a0001c0005t0001g0075a0001c0016t0016g0074a0002c0002t0017g0073 | 3 | HG00140.hp2 HG01081.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.207+2516C>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6165634 | ||||||
| chr1:6165678
|
C | G | 1 | a0002c0012t0052g0045 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.207+2472G>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6165678 | ||||||
| chr1:6165678
|
CA | C | 8 | a0001c0001t0068g0085a0001c0009t0011g0240a0001c0010t0004g0030others(5): Show | 8 | HG02451.hp1 HG02572.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.207+2471delT | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6165678 | ||||||
| chr1:6165679
|
A | C | 165 | a0001c0001t0003g0135a0001c0001t0003g0159a0001c0001t0003g0162others(162): Show | 166 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.207+2471T>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6165679 | ||||||
| chr1:6165697
|
G | A | 6 | a0001c0005t0043g0017a0002c0002t0020g0018a0002c0002t0020g0019others(3): Show | 6 | HG02280.hp1 HG02622.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.207+2453C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6165697 | ||||||
| chr1:6165907
|
C | T | 1 | a0001c0001t0054g0292 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.207+2243G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6165907 | ||||||
| chr1:6165997
|
C | T | 1 | a0001c0036t0006g0210 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.207+2153G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6165997 | ||||||
| chr1:6166002
|
G | C | 8 | a0001c0001t0011g0232a0001c0001t0011g0234a0001c0013t0005g0236others(5): Show | 8 | HG02559.hp2 HG02809.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.207+2148C>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6166002 | ||||||
| chr1:6166138
|
A | G | 8 | a0001c0001t0011g0232a0001c0001t0011g0234a0001c0013t0005g0236others(5): Show | 8 | HG02559.hp2 HG02809.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.207+2012T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6166138 | ||||||
| chr1:6166158
|
G | A | 106 | a0001c0001t0003g0282a0001c0001t0004g0054a0001c0001t0004g0180others(103): Show | 106 | HG00544.hp2 HG00609.hp1 HG01070.hp2 others(103): Show |
intron_variant | MODIFIER | c.207+1992C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6166158 | ||||||
| chr1:6166174
|
T | A | 1 | a0001c0044t0082g0313 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.207+1976A>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6166174 | ||||||
| chr1:6166276
|
T | TG | 152 | a0001c0001t0003g0135a0001c0001t0003g0159a0001c0001t0003g0162others(149): Show | 152 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.207+1873_207+1874i others(3): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6166276 | ||||||
| chr1:6166277
|
C | G | 174 | a0001c0001t0003g0135a0001c0001t0003g0159a0001c0001t0003g0162others(171): Show | 174 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(171): Show |
intron_variant | MODIFIER | c.207+1873G>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6166277 | ||||||
| chr1:6166403
|
A | G | 93 | a0001c0001t0003g0282a0001c0001t0004g0054a0001c0001t0005g0251others(90): Show | 93 | HG00544.hp2 HG00609.hp1 HG01070.hp2 others(90): Show |
intron_variant | MODIFIER | c.207+1747T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6166403 | ||||||
| chr1:6166416
|
T | C | 168 | a0001c0001t0003g0135a0001c0001t0003g0159a0001c0001t0003g0162others(165): Show | 168 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(165): Show |
intron_variant | MODIFIER | c.207+1734A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6166416 | ||||||
| chr1:6166480
|
C | A | 178 | a0001c0001t0003g0135a0001c0001t0003g0159a0001c0001t0003g0162others(175): Show | 178 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(175): Show |
intron_variant | MODIFIER | c.207+1670G>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6166480 | ||||||
| chr1:6166559
|
C | T | 1 | a0001c0014t0033g0304 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.207+1591G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6166559 | ||||||
| chr1:6166596
|
C | T | 99 | a0001c0001t0003g0282a0001c0001t0004g0054a0001c0001t0005g0251others(96): Show | 99 | HG00544.hp2 HG00609.hp1 HG00738.hp2 others(96): Show |
intron_variant | MODIFIER | c.207+1554G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6166596 | ||||||
| chr1:6166708
|
GGGGAAGT | G | 97 | a0001c0001t0003g0282a0001c0001t0005g0251a0001c0001t0007g0258others(94): Show | 97 | HG00544.hp2 HG00609.hp1 HG01070.hp2 others(94): Show |
intron_variant | MODIFIER | c.207+1435_207+1441d others(9): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6166708 | ||||||
| chr1:6166789
|
A | T | 102 | a0001c0001t0003g0239a0001c0001t0003g0282a0001c0001t0004g0054others(99): Show | 102 | HG00544.hp2 HG00609.hp1 HG01070.hp2 others(99): Show |
intron_variant | MODIFIER | c.207+1361T>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6166789 | ||||||
| chr1:6166850
|
G | A | 97 | a0001c0001t0003g0282a0001c0001t0004g0054a0001c0001t0005g0251others(94): Show | 97 | HG00544.hp2 HG00609.hp1 HG01070.hp2 others(94): Show |
intron_variant | MODIFIER | c.207+1300C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6166850 | ||||||
| chr1:6166880
|
G | A | 3 | a0001c0016t0016g0069a0001c0016t0016g0136a0001c0016t0016g0137 | 3 | HG01346.hp2 HG01358.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.207+1270C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6166880 | ||||||
| chr1:6166904
|
A | C | 97 | a0001c0001t0003g0282a0001c0001t0004g0054a0001c0001t0005g0251others(94): Show | 97 | HG00544.hp2 HG00609.hp1 HG01070.hp2 others(94): Show |
intron_variant | MODIFIER | c.207+1246T>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6166904 | ||||||
| chr1:6166912
|
C | A | 8 | a0001c0005t0043g0017a0001c0009t0011g0240a0001c0010t0014g0242others(5): Show | 8 | HG02280.hp1 HG02572.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.207+1238G>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6166912 | ||||||
| chr1:6166943
|
T | C | 122 | a0001c0001t0003g0239a0001c0001t0003g0282a0001c0001t0004g0054others(119): Show | 122 | HG00544.hp2 HG00609.hp1 HG01070.hp2 others(119): Show |
intron_variant | MODIFIER | c.207+1207A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6166943 | ||||||
| chr1:6167157
|
C | CGGGGGAA others(16): Show |
1 | a0001c0010t0004g0030 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.207+970_207+992dup others(23): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6167157 | ||||||
| chr1:6167157
|
C | T | 1 | a0002c0006t0040g0009 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.207+993G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6167157 | ||||||
| chr1:6167162
|
G | A | 1 | a0001c0001t0004g0138 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.207+988C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6167162 | ||||||
| chr1:6167356
|
G | A | 1 | a0001c0010t0004g0030 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.207+794C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6167356 | ||||||
| chr1:6167366
|
T | C | 1 | a0001c0009t0004g0139 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.207+784A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6167366 | ||||||
| chr1:6167432
|
C | T | 1 | a0001c0001t0054g0292 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.207+718G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6167432 | ||||||
| chr1:6167482
|
A | G | 102 | a0001c0001t0003g0239a0001c0001t0003g0282a0001c0001t0004g0054others(99): Show | 102 | HG00544.hp2 HG00609.hp1 HG01070.hp2 others(99): Show |
intron_variant | MODIFIER | c.207+668T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6167482 | ||||||
| chr1:6167520
|
C | T | 2 | a0001c0007t0003g0067a0001c0007t0003g0068 | 2 | HG02071.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.207+630G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6167520 | ||||||
| chr1:6167625
|
G | A | 2 | a0001c0001t0003g0239a0001c0010t0051g0238 | 2 | HG03017.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.207+525C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6167625 | ||||||
| chr1:6167668
|
T | C | 3 | a0001c0007t0005g0140a0001c0007t0005g0141a0001c0009t0073g0142 | 3 | HG01099.hp1 HG01928.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.207+482A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6167668 | ||||||
| chr1:6167670
|
C | T | 1 | a0001c0010t0056g0072 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.207+480G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6167670 | ||||||
| chr1:6167706
|
G | C | 1 | a0001c0010t0004g0030 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.207+444C>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6167706 | ||||||
| chr1:6167852
|
G | C | 7 | a0001c0004t0011g0226a0001c0008t0012g0222a0001c0008t0012g0223others(4): Show | 7 | HG02145.hp1 HG02258.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.207+298C>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6167852 | ||||||
| chr1:6167928
|
C | T | 2 | a0001c0008t0003g0249a0002c0017t0001g0248 | 2 | HG01884.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.207+222G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6167928 | ||||||
| chr1:6167931
|
C | T | 1 | a0001c0001t0003g0146 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.207+219G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6167931 | ||||||
| chr1:6167978
|
T | C | 1 | a0001c0010t0005g0143 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.207+172A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6167978 | ||||||
| chr1:6168100
|
G | A | 1 | a0001c0010t0004g0030 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.207+50C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6168100 | ||||||
| chr1:6168120
|
A | C | 51 | a0001c0001t0003g0282a0001c0001t0007g0258a0001c0001t0007g0263others(48): Show | 51 | HG00544.hp2 HG00609.hp1 HG01109.hp1 others(48): Show |
intron_variant | MODIFIER | c.207+30T>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 2/41 | chr1 | 6168120 | ||||||
| chr1:6168330
|
C | T | 1 | a0001c0010t0004g0030 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.80-53G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6168330 | ||||||
| chr1:6168544
|
G | A | 1 | a0001c0010t0004g0030 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.80-267C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6168544 | ||||||
| chr1:6168567
|
T | A | 1 | a0001c0001t0005g0251 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.80-290A>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6168567 | ||||||
| chr1:6168607
|
A | G | 1 | a0001c0004t0018g0083 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.80-330T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6168607 | ||||||
| chr1:6168619
|
T | A | 2 | a0001c0021t0005g0026a0001c0021t0005g0027 | 2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.80-342A>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6168619 | ||||||
| chr1:6168623
|
TACCAGGA others(3): Show |
T | 1 | a0001c0005t0030g0259 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.80-356_80-347delCC others(8): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6168623 | ||||||
| chr1:6168723
|
G | A | 44 | a0001c0001t0003g0282a0001c0001t0007g0258a0001c0001t0007g0263others(41): Show | 44 | HG00544.hp2 HG00609.hp1 HG01123.hp2 others(41): Show |
intron_variant | MODIFIER | c.80-446C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6168723 | ||||||
| chr1:6168805
|
G | A | 2 | a0001c0011t0010g0183a0001c0011t0010g0184 | 2 | NA18962.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.80-528C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6168805 | ||||||
| chr1:6168838
|
A | G | 102 | a0001c0001t0003g0239a0001c0001t0003g0282a0001c0001t0004g0054others(99): Show | 102 | HG00544.hp2 HG00609.hp1 HG01070.hp2 others(99): Show |
intron_variant | MODIFIER | c.80-561T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6168838 | ||||||
| chr1:6168961
|
G | A | 1 | a0001c0009t0041g0014 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.80-684C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6168961 | ||||||
| chr1:6169016
|
CA | C | 23 | a0001c0001t0003g0079a0001c0001t0003g0239a0001c0001t0007g0078others(20): Show | 23 | HG00140.hp1 HG01167.hp1 HG01256.hp1 others(20): Show |
intron_variant | MODIFIER | c.80-740delT | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6169016 | ||||||
| chr1:6169033
|
A | G | 92 | a0001c0001t0003g0239a0001c0001t0003g0282a0001c0001t0004g0054others(89): Show | 92 | HG00544.hp2 HG00609.hp1 HG01070.hp2 others(89): Show |
intron_variant | MODIFIER | c.80-756T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6169033 | ||||||
| chr1:6169034
|
A | G | 1 | a0001c0005t0030g0259 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.80-757T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6169034 | ||||||
| chr1:6169194
|
G | C | 121 | a0001c0001t0003g0239a0001c0001t0003g0282a0001c0001t0004g0054others(118): Show | 121 | HG00544.hp2 HG00609.hp1 HG01070.hp2 others(118): Show |
intron_variant | MODIFIER | c.80-917C>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6169194 | ||||||
| chr1:6169202
|
C | T | 1 | a0001c0019t0085g0316 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.80-925G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6169202 | ||||||
| chr1:6169217
|
A | G | 51 | a0001c0001t0003g0282a0001c0001t0007g0258a0001c0001t0007g0263others(48): Show | 51 | HG00544.hp2 HG00609.hp1 HG01109.hp1 others(48): Show |
intron_variant | MODIFIER | c.80-940T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6169217 | ||||||
| chr1:6169405
|
C | T | 1 | a0001c0019t0085g0316 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.80-1128G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6169405 | ||||||
| chr1:6169507
|
G | A | 1 | a0001c0009t0041g0014 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.80-1230C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6169507 | ||||||
| chr1:6169547
|
G | A | 8 | a0001c0005t0043g0017a0001c0009t0011g0240a0001c0010t0014g0242others(5): Show | 8 | HG02280.hp1 HG02572.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.80-1270C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6169547 | ||||||
| chr1:6169583
|
C | G | 2 | a0001c0021t0005g0026a0001c0021t0005g0027 | 2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.80-1306G>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6169583 | ||||||
| chr1:6169586
|
C | A | 1 | a0001c0005t0004g0144 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.80-1309G>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6169586 | ||||||
| chr1:6169799
|
C | T | 2 | a0001c0008t0003g0249a0002c0017t0001g0248 | 2 | HG01884.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.80-1522G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6169799 | ||||||
| chr1:6169805
|
G | A | 13 | a0001c0001t0003g0239a0001c0005t0043g0017a0001c0009t0011g0240others(10): Show | 13 | HG02280.hp1 HG02572.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.80-1528C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6169805 | ||||||
| chr1:6169836
|
A | G | 99 | a0001c0001t0003g0239a0001c0001t0003g0282a0001c0001t0004g0054others(96): Show | 99 | HG00544.hp2 HG00609.hp1 HG01070.hp2 others(96): Show |
intron_variant | MODIFIER | c.80-1559T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6169836 | ||||||
| chr1:6169953
|
C | G | 2 | a0001c0021t0005g0026a0001c0021t0005g0027 | 2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.80-1676G>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6169953 | ||||||
| chr1:6169980
|
C | A | 101 | a0001c0001t0003g0239a0001c0001t0003g0282a0001c0001t0004g0054others(98): Show | 101 | HG00544.hp2 HG00609.hp1 HG01070.hp2 others(98): Show |
intron_variant | MODIFIER | c.80-1703G>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6169980 | ||||||
| chr1:6170076
|
C | T | 1 | a0001c0001t0003g0206 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.80-1799G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6170076 | ||||||
| chr1:6170089
|
T | C | 80 | a0001c0001t0003g0282a0001c0001t0004g0054a0001c0001t0005g0251others(77): Show | 80 | HG00544.hp2 HG00609.hp1 HG01070.hp2 others(77): Show |
intron_variant | MODIFIER | c.80-1812A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6170089 | ||||||
| chr1:6170134
|
G | A | 1 | a0002c0006t0001g0145 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.80-1857C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6170134 | ||||||
| chr1:6170239
|
C | T | 100 | a0001c0001t0003g0239a0001c0001t0003g0282a0001c0001t0004g0054others(97): Show | 100 | HG00544.hp2 HG00609.hp1 HG01070.hp2 others(97): Show |
intron_variant | MODIFIER | c.80-1962G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6170239 | ||||||
| chr1:6170298
|
G | A | 6 | a0001c0001t0011g0232a0001c0001t0011g0234a0001c0013t0005g0236others(3): Show | 6 | HG02559.hp2 HG02809.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.80-2021C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6170298 | ||||||
| chr1:6170321
|
G | A | 1 | a0001c0010t0004g0030 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.80-2044C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6170321 | ||||||
| chr1:6170372
|
G | A | 126 | a0001c0001t0003g0146a0001c0001t0003g0150a0001c0001t0003g0239others(123): Show | 126 | HG00544.hp2 HG00609.hp1 HG01070.hp2 others(123): Show |
intron_variant | MODIFIER | c.80-2095C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6170372 | ||||||
| chr1:6170393
|
G | A | 1 | a0001c0007t0003g0284 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.80-2116C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6170393 | ||||||
| chr1:6170425
|
C | T | 104 | a0001c0001t0003g0239a0001c0001t0003g0282a0001c0001t0004g0054others(101): Show | 104 | HG00544.hp2 HG00609.hp1 HG01070.hp2 others(101): Show |
intron_variant | MODIFIER | c.80-2148G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6170425 | ||||||
| chr1:6170426
|
G | T | 1 | a0001c0019t0011g0231 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.80-2149C>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6170426 | ||||||
| chr1:6170471
|
T | C | 120 | a0001c0001t0003g0239a0001c0001t0003g0282a0001c0001t0004g0054others(117): Show | 120 | HG00544.hp2 HG00609.hp1 HG01070.hp2 others(117): Show |
intron_variant | MODIFIER | c.80-2194A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6170471 | ||||||
| chr1:6170476
|
T | C | 1 | a0001c0001t0005g0251 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.80-2199A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6170476 | ||||||
| chr1:6170507
|
T | C | 4 | a0001c0003t0002g0187a0001c0011t0048g0185a0003c0018t0015g0186others(1): Show | 4 | NA18971.hp2 NA19012.hp1 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.80-2230A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6170507 | ||||||
| chr1:6170566
|
G | A | 3 | a0001c0001t0069g0190a0002c0002t0001g0154a0002c0025t0001g0189 | 3 | HG02698.hp2 HG03017.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.80-2289C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6170566 | ||||||
| chr1:6170660
|
C | T | 1 | a0001c0004t0072g0065 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.80-2383G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6170660 | ||||||
| chr1:6170686
|
G | A | 1 | a0001c0027t0004g0066 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.80-2409C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6170686 | ||||||
| chr1:6170723
|
G | A | 2 | a0001c0001t0007g0191a0001c0003t0022g0192 | 2 | NA18950.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.80-2446C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6170723 | ||||||
| chr1:6170752
|
T | C | 1 | a0001c0010t0003g0044 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.80-2475A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6170752 | ||||||
| chr1:6170792
|
G | A | 56 | a0001c0001t0003g0159a0001c0001t0003g0162a0001c0001t0003g0163others(53): Show | 56 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.80-2515C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6170792 | ||||||
| chr1:6170820
|
T | C | 1 | a0001c0013t0032g0228 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.80-2543A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6170820 | ||||||
| chr1:6170910
|
G | A | 2 | a0002c0012t0025g0302a0002c0012t0025g0312 | 2 | HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.80-2633C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6170910 | ||||||
| chr1:6170914
|
T | C | 114 | a0001c0001t0003g0239a0001c0001t0003g0282a0001c0001t0004g0054others(111): Show | 115 | HG00423.hp2 HG00544.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.80-2637A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6170914 | ||||||
| chr1:6171038
|
G | A | 3 | a0001c0001t0005g0251a0001c0041t0014g0250a0002c0047t0078g0314 | 3 | HG01884.hp1 HG02630.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.80-2761C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6171038 | ||||||
| chr1:6171075
|
G | A | 1 | a0001c0013t0005g0236 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.80-2798C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6171075 | ||||||
| chr1:6171146
|
C | T | 1 | a0001c0001t0038g0006 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.80-2869G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6171146 | ||||||
| chr1:6171244
|
C | A | 2 | a0001c0007t0003g0067a0001c0007t0003g0068 | 2 | HG02071.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.80-2967G>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6171244 | ||||||
| chr1:6171267
|
C | T | 2 | a0001c0005t0004g0076a0002c0002t0009g0077 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.80-2990G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6171267 | ||||||
| chr1:6171394
|
G | A | 6 | a0001c0001t0011g0232a0001c0001t0011g0234a0001c0013t0005g0236others(3): Show | 6 | HG02559.hp2 HG02809.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.80-3117C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6171394 | ||||||
| chr1:6171487
|
G | A | 6 | a0001c0001t0003g0239a0001c0008t0003g0249a0001c0010t0051g0238others(3): Show | 6 | HG01884.hp2 HG02970.hp1 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.80-3210C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6171487 | ||||||
| chr1:6171507
|
G | GC | 96 | a0001c0001t0003g0239a0001c0001t0003g0282a0001c0001t0005g0251others(93): Show | 96 | HG00544.hp2 HG00609.hp1 HG01109.hp1 others(93): Show |
intron_variant | MODIFIER | c.80-3231dupG | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6171507 | ||||||
| chr1:6171749
|
C | T | 6 | a0001c0001t0007g0258a0001c0003t0002g0253a0001c0003t0002g0256others(3): Show | 6 | NA18944.hp2 NA18948.hp1 NA18970.hp2 others(3): Show |
intron_variant | MODIFIER | c.80-3472G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6171749 | ||||||
| chr1:6171787
|
C | T | 2 | a0001c0021t0005g0026a0001c0021t0005g0027 | 2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.80-3510G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6171787 | ||||||
| chr1:6171813
|
G | C | 8 | a0001c0001t0011g0297a0001c0001t0054g0292a0001c0008t0012g0296others(5): Show | 8 | HG01243.hp2 HG02055.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.80-3536C>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6171813 | ||||||
| chr1:6171875
|
A | C | 3 | a0001c0001t0005g0251a0001c0041t0014g0250a0002c0047t0078g0314 | 3 | HG01884.hp1 HG02630.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.80-3598T>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6171875 | ||||||
| chr1:6172097
|
C | T | 3 | a0001c0005t0001g0075a0001c0016t0016g0074a0002c0002t0017g0073 | 3 | HG00140.hp2 HG01081.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.80-3820G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6172097 | ||||||
| chr1:6172098
|
G | A | 1 | a0001c0007t0005g0197 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.80-3821C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6172098 | ||||||
| chr1:6172154
|
C | T | 2 | a0001c0008t0003g0249a0002c0017t0001g0248 | 2 | HG01884.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.80-3877G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6172154 | ||||||
| chr1:6172200
|
T | C | 2 | a0001c0008t0012g0222a0001c0008t0012g0223 | 2 | HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.80-3923A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6172200 | ||||||
| chr1:6172329
|
CTTTA | C | 16 | a0001c0001t0084g0310a0001c0004t0011g0226a0001c0004t0083g0311others(13): Show | 16 | HG01167.hp1 HG02055.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.80-4056_80-4053del others(4): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6172329 | ||||||
| chr1:6172509
|
C | T | 99 | a0001c0001t0003g0239a0001c0001t0003g0282a0001c0001t0005g0251others(96): Show | 99 | HG00544.hp2 HG00609.hp1 HG01109.hp1 others(96): Show |
intron_variant | MODIFIER | c.80-4232G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6172509 | ||||||
| chr1:6172588
|
AGCT | A | 104 | a0001c0001t0003g0239a0001c0001t0003g0282a0001c0001t0004g0054others(101): Show | 104 | HG00544.hp2 HG00609.hp1 HG01070.hp2 others(101): Show |
intron_variant | MODIFIER | c.80-4314_80-4312del others(3): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6172588 | ||||||
| chr1:6172595
|
AC | A | 104 | a0001c0001t0003g0239a0001c0001t0003g0282a0001c0001t0004g0054others(101): Show | 104 | HG00544.hp2 HG00609.hp1 HG01070.hp2 others(101): Show |
intron_variant | MODIFIER | c.80-4319delG | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6172595 | ||||||
| chr1:6172597
|
T | G | 104 | a0001c0001t0003g0239a0001c0001t0003g0282a0001c0001t0004g0054others(101): Show | 104 | HG00544.hp2 HG00609.hp1 HG01070.hp2 others(101): Show |
intron_variant | MODIFIER | c.80-4320A>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6172597 | ||||||
| chr1:6172600
|
T | C | 1 | a0001c0004t0004g0198 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.80-4323A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6172600 | ||||||
| chr1:6172632
|
C | T | 1 | a0001c0003t0010g0212 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.80-4355G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6172632 | ||||||
| chr1:6172644
|
C | G | 104 | a0001c0001t0003g0239a0001c0001t0003g0282a0001c0001t0004g0054others(101): Show | 104 | HG00544.hp2 HG00609.hp1 HG01070.hp2 others(101): Show |
intron_variant | MODIFIER | c.80-4367G>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6172644 | ||||||
| chr1:6172681
|
A | G | 1 | a0001c0010t0056g0072 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.80-4404T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6172681 | ||||||
| chr1:6172685
|
G | A | 3 | a0001c0013t0032g0224a0001c0013t0032g0228a0001c0013t0060g0227 | 3 | HG02280.hp2 HG02717.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.80-4408C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6172685 | ||||||
| chr1:6172851
|
G | A | 104 | a0001c0001t0003g0239a0001c0001t0003g0282a0001c0001t0004g0054others(101): Show | 104 | HG00544.hp2 HG00609.hp1 HG01070.hp2 others(101): Show |
intron_variant | MODIFIER | c.80-4574C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6172851 | ||||||
| chr1:6172916
|
G | C | 3 | a0001c0001t0077g0301a0002c0002t0001g0200a0002c0002t0023g0199 | 3 | HG01261.hp1 HG03927.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.80-4639C>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6172916 | ||||||
| chr1:6172926
|
C | T | 1 | a0002c0012t0025g0302 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.80-4649G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6172926 | ||||||
| chr1:6172942
|
A | C | 2 | a0001c0021t0005g0026a0001c0021t0005g0027 | 2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.80-4665T>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6172942 | ||||||
| chr1:6172946
|
T | G | 56 | a0001c0001t0003g0239a0001c0001t0004g0054a0001c0001t0011g0232others(53): Show | 57 | HG01070.hp2 HG01106.hp1 HG01167.hp1 others(54): Show |
intron_variant | MODIFIER | c.80-4669A>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6172946 | ||||||
| chr1:6173005
|
G | A | 2 | a0001c0001t0003g0239a0001c0010t0051g0238 | 2 | HG03017.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.80-4728C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6173005 | ||||||
| chr1:6173019
|
C | A | 2 | a0001c0001t0007g0203a0001c0003t0046g0204 | 2 | HG00438.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.80-4742G>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6173019 | ||||||
| chr1:6173101
|
G | A | 1 | a0005c0034t0006g0218 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.80-4824C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6173101 | ||||||
| chr1:6173108
|
CT | C | 110 | a0001c0001t0003g0206a0001c0001t0003g0239a0001c0001t0003g0282others(107): Show | 110 | HG00544.hp2 HG00609.hp1 HG01070.hp2 others(107): Show |
intron_variant | MODIFIER | c.80-4832delA | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6173108 | ||||||
| chr1:6173206
|
G | A | 51 | a0001c0001t0003g0282a0001c0001t0005g0251a0001c0001t0007g0258others(48): Show | 51 | HG00544.hp2 HG00609.hp1 HG01109.hp1 others(48): Show |
intron_variant | MODIFIER | c.80-4929C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6173206 | ||||||
| chr1:6173211
|
T | G | 2 | a0001c0021t0005g0026a0001c0021t0005g0027 | 2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.80-4934A>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6173211 | ||||||
| chr1:6173230
|
A | G | 106 | a0001c0001t0003g0239a0001c0001t0003g0282a0001c0001t0004g0054others(103): Show | 106 | HG00544.hp2 HG00609.hp1 HG01070.hp2 others(103): Show |
intron_variant | MODIFIER | c.80-4953T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6173230 | ||||||
| chr1:6173253
|
C | T | 7 | a0001c0009t0014g0229a0001c0009t0039g0013a0001c0009t0041g0014others(4): Show | 7 | HG01109.hp1 HG02647.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.80-4976G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6173253 | ||||||
| chr1:6173258
|
C | T | 1 | a0001c0004t0018g0071 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.80-4981G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6173258 | ||||||
| chr1:6173295
|
A | G | 106 | a0001c0001t0003g0239a0001c0001t0003g0282a0001c0001t0004g0054others(103): Show | 106 | HG00544.hp2 HG00609.hp1 HG01070.hp2 others(103): Show |
intron_variant | MODIFIER | c.80-5018T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6173295 | ||||||
| chr1:6173306
|
A | G | 109 | a0001c0001t0003g0239a0001c0001t0003g0282a0001c0001t0004g0054others(106): Show | 109 | HG00544.hp2 HG00609.hp1 HG01070.hp2 others(106): Show |
intron_variant | MODIFIER | c.80-5029T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6173306 | ||||||
| chr1:6173415
|
T | C | 1 | a0001c0003t0022g0207 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.80-5138A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6173415 | ||||||
| chr1:6173454
|
A | G | 48 | a0001c0001t0003g0282a0001c0001t0007g0258a0001c0001t0007g0263others(45): Show | 48 | HG00544.hp2 HG00609.hp1 HG01109.hp1 others(45): Show |
intron_variant | MODIFIER | c.80-5177T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6173454 | ||||||
| chr1:6173513
|
A | C | 104 | a0001c0001t0003g0239a0001c0001t0003g0282a0001c0001t0004g0054others(101): Show | 104 | HG00544.hp2 HG00609.hp1 HG01070.hp2 others(101): Show |
intron_variant | MODIFIER | c.80-5236T>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6173513 | ||||||
| chr1:6173513
|
A | T | 2 | a0001c0021t0005g0026a0001c0021t0005g0027 | 2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.80-5236T>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6173513 | ||||||
| chr1:6173525
|
T | C | 2 | a0001c0008t0012g0222a0001c0008t0012g0223 | 2 | HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.80-5248A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6173525 | ||||||
| chr1:6173693
|
C | A | 3 | a0001c0001t0005g0251a0001c0041t0014g0250a0002c0047t0078g0314 | 3 | HG01884.hp1 HG02630.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.80-5416G>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6173693 | ||||||
| chr1:6173761
|
C | T | 3 | a0001c0010t0003g0044a0001c0010t0012g0043a0002c0002t0026g0042 | 3 | HG01891.hp1 HG03195.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.80-5484G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6173761 | ||||||
| chr1:6173862
|
C | T | 105 | a0001c0001t0003g0239a0001c0001t0003g0282a0001c0001t0004g0054others(102): Show | 105 | HG00544.hp2 HG00609.hp1 HG01070.hp2 others(102): Show |
intron_variant | MODIFIER | c.80-5585G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6173862 | ||||||
| chr1:6173881
|
G | A | 2 | a0001c0021t0005g0026a0001c0021t0005g0027 | 2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.80-5604C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6173881 | ||||||
| chr1:6173897
|
A | G | 2 | a0001c0021t0005g0026a0001c0021t0005g0027 | 2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.80-5620T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6173897 | ||||||
| chr1:6173914
|
T | C | 4 | a0001c0001t0003g0239a0001c0008t0003g0249a0001c0010t0051g0238others(1): Show | 4 | HG01884.hp2 HG03017.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.80-5637A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6173914 | ||||||
| chr1:6173972
|
G | C | 1 | a0001c0011t0008g0208 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.80-5695C>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6173972 | ||||||
| chr1:6173995
|
C | T | 7 | a0001c0009t0014g0229a0001c0009t0039g0013a0001c0009t0041g0014others(4): Show | 7 | HG01109.hp1 HG02647.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.80-5718G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6173995 | ||||||
| chr1:6174070
|
G | T | 1 | a0001c0003t0002g0070 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.80-5793C>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6174070 | ||||||
| chr1:6174140
|
G | A | 2 | a0001c0031t0034g0004a0001c0038t0035g0005 | 2 | HG01891.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.79+5805C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6174140 | ||||||
| chr1:6174204
|
G | T | 1 | a0001c0016t0016g0069 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.79+5741C>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6174204 | ||||||
| chr1:6174208
|
C | T | 1 | a0002c0033t0009g0243 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.79+5737G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6174208 | ||||||
| chr1:6174373
|
C | T | 47 | a0001c0001t0004g0054a0001c0001t0011g0297a0001c0001t0029g0055others(44): Show | 47 | HG01070.hp2 HG01106.hp1 HG01167.hp1 others(44): Show |
intron_variant | MODIFIER | c.79+5572G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6174373 | ||||||
| chr1:6174392
|
T | C | 1 | a0001c0015t0008g0209 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.79+5553A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6174392 | ||||||
| chr1:6174408
|
A | G | 119 | a0001c0001t0003g0239a0001c0001t0003g0282a0001c0001t0004g0054others(116): Show | 119 | HG00544.hp2 HG00609.hp1 HG01070.hp2 others(116): Show |
intron_variant | MODIFIER | c.79+5537T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6174408 | ||||||
| chr1:6174513
|
G | GTGGA | 3 | a0001c0021t0005g0026a0001c0021t0005g0027a0001c0036t0006g0210 | 3 | HG01496.hp2 HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.79+5428_79+5431dup others(4): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6174513 | ||||||
| chr1:6174513
|
GTGGA | G | 104 | a0001c0001t0003g0239a0001c0001t0003g0282a0001c0001t0004g0054others(101): Show | 104 | HG00544.hp2 HG00609.hp1 HG01070.hp2 others(101): Show |
intron_variant | MODIFIER | c.79+5428_79+5431del others(4): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6174513 | ||||||
| chr1:6174517
|
A | G | 2 | a0001c0007t0003g0067a0001c0007t0003g0068 | 2 | HG02071.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.79+5428T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6174517 | ||||||
| chr1:6174545
|
T | C | 1 | a0002c0006t0001g0216 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.79+5400A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6174545 | ||||||
| chr1:6174567
|
T | C | 1 | a0001c0005t0055g0052 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.79+5378A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6174567 | ||||||
| chr1:6174582
|
T | A | 2 | a0002c0002t0017g0286a0002c0002t0026g0285 | 2 | HG02896.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.79+5363A>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6174582 | ||||||
| chr1:6174667
|
G | A | 41 | a0001c0001t0004g0054a0001c0001t0029g0055a0001c0001t0084g0310others(38): Show | 41 | HG01070.hp2 HG01106.hp1 HG01167.hp1 others(38): Show |
intron_variant | MODIFIER | c.79+5278C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6174667 | ||||||
| chr1:6174689
|
G | A | 11 | a0001c0001t0011g0297a0001c0001t0054g0292a0001c0008t0012g0296others(8): Show | 11 | HG01243.hp2 HG01891.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.79+5256C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6174689 | ||||||
| chr1:6174861
|
G | A | 4 | a0001c0004t0004g0290a0001c0005t0006g0288a0001c0005t0006g0289others(1): Show | 4 | HG02080.hp1 NA18943.hp1 NA18945.hp1 others(1): Show |
intron_variant | MODIFIER | c.79+5084C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6174861 | ||||||
| chr1:6174895
|
A | AGATGGTG others(34): Show |
11 | a0001c0004t0072g0065a0001c0008t0005g0056a0001c0009t0014g0059others(8): Show | 12 | HG02559.hp1 HG02809.hp2 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.79+5009_79+5049dup others(41): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6174895 | ||||||
| chr1:6174895
|
AGATGGTG others(34): Show |
A | 2 | a0001c0008t0012g0222a0001c0008t0012g0223 | 2 | HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.79+5009_79+5049del others(41): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6174895 | ||||||
| chr1:6174950
|
TGGATGGA others(15): Show |
T | 2 | a0001c0005t0055g0052a0001c0020t0002g0051 | 2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.79+4973_79+4994del others(22): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6174950 | ||||||
| chr1:6174972
|
AGGAT | A | 102 | a0001c0001t0003g0239a0001c0001t0003g0282a0001c0001t0004g0054others(99): Show | 102 | HG00544.hp2 HG00609.hp1 HG01070.hp2 others(99): Show |
intron_variant | MODIFIER | c.79+4969_79+4972del others(4): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6174972 | ||||||
| chr1:6174975
|
A | ATGGATGG others(12): Show |
2 | a0001c0021t0005g0026a0001c0021t0005g0027 | 2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.79+4951_79+4969dup others(19): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6174975 | ||||||
| chr1:6174999
|
C | T | 102 | a0001c0001t0003g0239a0001c0001t0003g0282a0001c0001t0004g0054others(99): Show | 102 | HG00544.hp2 HG00609.hp1 HG01070.hp2 others(99): Show |
intron_variant | MODIFIER | c.79+4946G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6174999 | ||||||
| chr1:6175010
|
C | A | 2 | a0001c0021t0005g0026a0001c0021t0005g0027 | 2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.79+4935G>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6175010 | ||||||
| chr1:6175044
|
T | C | 2 | a0001c0021t0005g0026a0001c0021t0005g0027 | 2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.79+4901A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6175044 | ||||||
| chr1:6175159
|
T | C | 1 | a0001c0001t0007g0237 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.79+4786A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6175159 | ||||||
| chr1:6175260
|
G | GTGGA | 100 | a0001c0001t0003g0239a0001c0001t0003g0282a0001c0001t0005g0251others(97): Show | 100 | HG00544.hp2 HG00609.hp1 HG01109.hp1 others(97): Show |
intron_variant | MODIFIER | c.79+4681_79+4684dup others(4): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6175260 | ||||||
| chr1:6175306
|
A | C | 1 | a0001c0003t0008g0053 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.79+4639T>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6175306 | ||||||
| chr1:6175334
|
T | A | 1 | a0001c0003t0008g0053 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.79+4611A>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6175334 | ||||||
| chr1:6175349
|
GTGGATGG others(16): Show |
G | 63 | a0001c0001t0003g0239a0001c0001t0003g0282a0001c0001t0005g0251others(60): Show | 63 | HG00544.hp2 HG00609.hp1 HG01109.hp1 others(60): Show |
intron_variant | MODIFIER | c.79+4573_79+4595del others(23): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6175349 | ||||||
| chr1:6175368
|
A | C | 1 | a0001c0003t0008g0053 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.79+4577T>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6175368 | ||||||
| chr1:6175385
|
G | A | 35 | a0001c0001t0084g0310a0001c0004t0011g0226a0001c0004t0083g0311others(32): Show | 35 | HG01167.hp1 HG01891.hp1 HG02055.hp1 others(32): Show |
intron_variant | MODIFIER | c.79+4560C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6175385 | ||||||
| chr1:6175390
|
C | A | 35 | a0001c0001t0084g0310a0001c0004t0011g0226a0001c0004t0083g0311others(32): Show | 35 | HG01167.hp1 HG01891.hp1 HG02055.hp1 others(32): Show |
intron_variant | MODIFIER | c.79+4555G>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6175390 | ||||||
| chr1:6175391
|
A | C | 1 | a0001c0003t0008g0053 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.79+4554T>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6175391 | ||||||
| chr1:6175392
|
T | A | 1 | a0001c0003t0008g0053 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.79+4553A>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6175392 | ||||||
| chr1:6175400
|
T | TGACG | 35 | a0001c0001t0084g0310a0001c0004t0011g0226a0001c0004t0083g0311others(32): Show | 35 | HG01167.hp1 HG01891.hp1 HG02055.hp1 others(32): Show |
intron_variant | MODIFIER | c.79+4544_79+4545ins others(4): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6175400 | ||||||
| chr1:6175408
|
A | C | 1 | a0001c0003t0008g0053 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.79+4537T>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6175408 | ||||||
| chr1:6175413
|
A | C | 1 | a0001c0003t0008g0053 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.79+4532T>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6175413 | ||||||
| chr1:6175414
|
A | C | 1 | a0001c0003t0008g0053 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.79+4531T>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6175414 | ||||||
| chr1:6175425
|
A | C | 1 | a0001c0003t0008g0053 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.79+4520T>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6175425 | ||||||
| chr1:6175440
|
G | T | 1 | a0001c0003t0008g0053 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.79+4505C>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6175440 | ||||||
| chr1:6175441
|
A | G | 1 | a0001c0003t0008g0053 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.79+4504T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6175441 | ||||||
| chr1:6175442
|
T | A | 1 | a0001c0003t0008g0053 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.79+4503A>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6175442 | ||||||
| chr1:6175445
|
A | C | 1 | a0001c0003t0008g0053 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.79+4500T>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6175445 | ||||||
| chr1:6175464
|
A | C | 1 | a0001c0003t0008g0053 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.79+4481T>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6175464 | ||||||
| chr1:6175501
|
AATGGTGG others(16): Show |
A | 3 | a0001c0001t0005g0251a0001c0041t0014g0250a0002c0047t0078g0314 | 3 | HG01884.hp1 HG02630.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.79+4421_79+4443del others(23): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6175501 | ||||||
| chr1:6175591
|
G | A | 1 | a0001c0010t0004g0030 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.79+4354C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6175591 | ||||||
| chr1:6175681
|
A | AATGG | 41 | a0001c0001t0003g0282a0001c0001t0005g0251a0001c0001t0007g0258others(38): Show | 41 | HG00544.hp2 HG00609.hp1 HG01123.hp2 others(38): Show |
intron_variant | MODIFIER | c.79+4260_79+4263dup others(4): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6175681 | ||||||
| chr1:6175681
|
A | AATGGATG others(1): Show |
3 | a0001c0009t0011g0252a0001c0021t0005g0026a0001c0021t0005g0027 | 3 | HG03486.hp1 HG03516.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.79+4256_79+4263dup others(8): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6175681 | ||||||
| chr1:6175681
|
A | AATGGATG others(9): Show |
3 | a0001c0008t0012g0222a0001c0008t0012g0223a0001c0010t0004g0030 | 3 | HG02258.hp1 HG02895.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.79+4248_79+4263dup others(16): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6175681 | ||||||
| chr1:6175683
|
T | C | 1 | a0001c0003t0010g0212 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.79+4262A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6175683 | ||||||
| chr1:6175707
|
TGGAC | T | 6 | a0001c0001t0011g0232a0001c0001t0011g0234a0001c0013t0005g0236others(3): Show | 6 | HG02559.hp2 HG02809.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.79+4234_79+4237del others(4): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6175707 | ||||||
| chr1:6175711
|
C | T | 91 | a0001c0001t0003g0239a0001c0001t0003g0282a0001c0001t0005g0251others(88): Show | 91 | HG00544.hp2 HG00609.hp1 HG01109.hp1 others(88): Show |
intron_variant | MODIFIER | c.79+4234G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6175711 | ||||||
| chr1:6175712
|
G | A | 2 | a0001c0014t0011g0038a0002c0012t0001g0037 | 2 | HG02970.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.79+4233C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6175712 | ||||||
| chr1:6175735
|
T | C | 6 | a0001c0001t0011g0232a0001c0001t0011g0234a0001c0013t0005g0236others(3): Show | 6 | HG02559.hp2 HG02809.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.79+4210A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6175735 | ||||||
| chr1:6175736
|
GGATA | G | 48 | a0001c0001t0003g0282a0001c0001t0007g0258a0001c0001t0007g0263others(45): Show | 48 | HG00544.hp2 HG00609.hp1 HG01109.hp1 others(45): Show |
intron_variant | MODIFIER | c.79+4205_79+4208del others(4): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6175736 | ||||||
| chr1:6175743
|
T | C | 2 | a0002c0002t0023g0213a0002c0002t0023g0214 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.79+4202A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6175743 | ||||||
| chr1:6175940
|
C | T | 2 | a0001c0005t0055g0052a0001c0020t0002g0051 | 2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.79+4005G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6175940 | ||||||
| chr1:6175970
|
G | C | 1 | a0001c0001t0005g0251 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.79+3975C>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6175970 | ||||||
| chr1:6176052
|
T | C | 2 | a0001c0021t0005g0026a0001c0021t0005g0027 | 2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.79+3893A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6176052 | ||||||
| chr1:6176346
|
A | T | 93 | a0001c0001t0003g0239a0001c0001t0003g0282a0001c0001t0005g0251others(90): Show | 93 | HG00544.hp2 HG00609.hp1 HG01123.hp2 others(90): Show |
intron_variant | MODIFIER | c.79+3599T>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6176346 | ||||||
| chr1:6176353
|
G | A | 44 | a0001c0001t0003g0282a0001c0001t0005g0251a0001c0001t0007g0258others(41): Show | 44 | HG00544.hp2 HG00609.hp1 HG01123.hp2 others(41): Show |
intron_variant | MODIFIER | c.79+3592C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6176353 | ||||||
| chr1:6176406
|
G | A | 2 | a0001c0021t0005g0026a0001c0021t0005g0027 | 2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.79+3539C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6176406 | ||||||
| chr1:6176424
|
T | C | 1 | a0001c0005t0006g0215 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.79+3521A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6176424 | ||||||
| chr1:6176433
|
G | A | 5 | a0001c0005t0043g0017a0002c0002t0020g0018a0002c0002t0020g0019others(2): Show | 5 | HG02280.hp1 HG02622.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.79+3512C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6176433 | ||||||
| chr1:6176466
|
C | T | 1 | a0001c0013t0032g0224 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.79+3479G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6176466 | ||||||
| chr1:6176839
|
G | T | 5 | a0001c0008t0012g0222a0001c0008t0012g0223a0001c0010t0004g0030others(2): Show | 5 | HG02258.hp1 HG02895.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.79+3106C>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6176839 | ||||||
| chr1:6176869
|
C | T | 1 | a0001c0013t0032g0224 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.79+3076G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6176869 | ||||||
| chr1:6177013
|
C | T | 3 | a0001c0008t0012g0222a0001c0008t0012g0223a0001c0010t0004g0030 | 3 | HG02258.hp1 HG02895.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.79+2932G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6177013 | ||||||
| chr1:6177023
|
C | T | 1 | a0001c0007t0005g0041 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.79+2922G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6177023 | ||||||
| chr1:6177030
|
G | A | 41 | a0001c0001t0003g0282a0001c0001t0007g0258a0001c0001t0007g0263others(38): Show | 41 | HG00544.hp2 HG00609.hp1 HG01123.hp2 others(38): Show |
intron_variant | MODIFIER | c.79+2915C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6177030 | ||||||
| chr1:6177045
|
A | C | 15 | a0001c0001t0003g0239a0001c0005t0043g0017a0001c0007t0044g0016others(12): Show | 15 | HG01884.hp2 HG02280.hp1 HG02293.hp1 others(12): Show |
intron_variant | MODIFIER | c.79+2900T>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6177045 | ||||||
| chr1:6177072
|
A | G | 2 | a0001c0003t0010g0040a0001c0003t0021g0039 | 2 | HG02074.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.79+2873T>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6177072 | ||||||
| chr1:6177073
|
G | C | 2 | a0001c0021t0005g0026a0001c0021t0005g0027 | 2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.79+2872C>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6177073 | ||||||
| chr1:6177142
|
C | T | 75 | a0001c0001t0003g0239a0001c0001t0003g0282a0001c0001t0005g0251others(72): Show | 75 | HG00544.hp2 HG00609.hp1 HG01123.hp2 others(72): Show |
intron_variant | MODIFIER | c.79+2803G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6177142 | ||||||
| chr1:6177337
|
C | T | 5 | a0001c0001t0050g0035a0001c0004t0004g0032a0001c0035t0002g0033others(2): Show | 5 | HG00544.hp1 HG01255.hp2 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.79+2608G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6177337 | ||||||
| chr1:6177588
|
G | A | 1 | a0002c0006t0001g0216 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.79+2357C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6177588 | ||||||
| chr1:6177708
|
C | A | 2 | a0001c0008t0003g0249a0002c0017t0001g0248 | 2 | HG01884.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.79+2237G>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6177708 | ||||||
| chr1:6177739
|
G | A | 1 | a0002c0002t0028g0217 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.79+2206C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6177739 | ||||||
| chr1:6177810
|
G | A | 1 | a0005c0034t0006g0218 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.79+2135C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6177810 | ||||||
| chr1:6177845
|
G | A | 2 | a0001c0001t0007g0219a0001c0003t0022g0220 | 2 | NA18951.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.79+2100C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6177845 | ||||||
| chr1:6177908
|
C | A | 1 | a0001c0001t0007g0221 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.79+2037G>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6177908 | ||||||
| chr1:6177973
|
G | T | 16 | a0001c0001t0011g0297a0001c0001t0054g0292a0001c0008t0012g0222others(13): Show | 16 | HG01243.hp2 HG01891.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.79+1972C>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6177973 | ||||||
| chr1:6177975
|
A | C | 3 | a0001c0001t0005g0251a0001c0041t0014g0250a0002c0047t0078g0314 | 3 | HG01884.hp1 HG02630.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.79+1970T>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6177975 | ||||||
| chr1:6177976
|
G | A | 2 | a0001c0001t0003g0239a0001c0010t0051g0238 | 2 | HG03017.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.79+1969C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6177976 | ||||||
| chr1:6178003
|
C | A | 2 | a0001c0008t0012g0222a0001c0008t0012g0223 | 2 | HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.79+1942G>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6178003 | ||||||
| chr1:6178005
|
G | A | 2 | a0001c0021t0005g0026a0001c0021t0005g0027 | 2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.79+1940C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6178005 | ||||||
| chr1:6178280
|
ACCT | A | 17 | a0001c0001t0084g0310a0001c0004t0011g0226a0001c0004t0083g0311others(14): Show | 17 | HG01167.hp1 HG02055.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.79+1662_79+1664del others(3): Show |
CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6178280 | ||||||
| chr1:6178284
|
T | G | 17 | a0001c0001t0084g0310a0001c0004t0011g0226a0001c0004t0083g0311others(14): Show | 17 | HG01167.hp1 HG02055.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.79+1661A>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6178284 | ||||||
| chr1:6178285
|
C | A | 17 | a0001c0001t0084g0310a0001c0004t0011g0226a0001c0004t0083g0311others(14): Show | 17 | HG01167.hp1 HG02055.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.79+1660G>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6178285 | ||||||
| chr1:6178286
|
C | A | 17 | a0001c0001t0084g0310a0001c0004t0011g0226a0001c0004t0083g0311others(14): Show | 17 | HG01167.hp1 HG02055.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.79+1659G>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6178286 | ||||||
| chr1:6178440
|
T | C | 7 | a0001c0009t0014g0229a0001c0009t0039g0013a0001c0009t0041g0014others(4): Show | 7 | HG01109.hp1 HG02647.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.79+1505A>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6178440 | ||||||
| chr1:6178582
|
C | A | 1 | a0001c0008t0005g0230 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.79+1363G>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6178582 | ||||||
| chr1:6178841
|
G | A | 6 | a0001c0001t0011g0232a0001c0001t0011g0234a0001c0013t0005g0236others(3): Show | 6 | HG02559.hp2 HG02809.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.79+1104C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6178841 | ||||||
| chr1:6178907
|
C | G | 2 | a0001c0007t0058g0028a0001c0007t0059g0029 | 2 | HG01070.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.79+1038G>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6178907 | ||||||
| chr1:6178940
|
G | A | 1 | a0001c0001t0007g0237 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.79+1005C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6178940 | ||||||
| chr1:6178966
|
C | A | 2 | a0001c0021t0005g0026a0001c0021t0005g0027 | 2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.79+979G>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6178966 | ||||||
| chr1:6178971
|
G | C | 1 | a0003c0018t0002g0291 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.79+974C>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6178971 | ||||||
| chr1:6179071
|
G | A | 3 | a0001c0009t0011g0240a0001c0010t0014g0242a0001c0039t0063g0241 | 3 | HG02572.hp2 HG02615.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.79+874C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6179071 | ||||||
| chr1:6179192
|
C | T | 2 | a0001c0021t0005g0026a0001c0021t0005g0027 | 2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.79+753G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6179192 | ||||||
| chr1:6179322
|
G | A | 57 | a0001c0001t0003g0239a0001c0001t0003g0282a0001c0001t0005g0251others(54): Show | 57 | HG00544.hp2 HG00609.hp1 HG01123.hp2 others(54): Show |
intron_variant | MODIFIER | c.79+623C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6179322 | ||||||
| chr1:6179462
|
G | C | 4 | a0001c0007t0005g0246a0002c0002t0001g0244a0002c0002t0001g0245others(1): Show | 4 | HG00099.hp1 HG00140.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.79+483C>G | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6179462 | ||||||
| chr1:6179562
|
C | A | 1 | a0002c0002t0017g0247 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.79+383G>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6179562 | ||||||
| chr1:6179670
|
G | A | 2 | a0001c0008t0003g0249a0002c0017t0001g0248 | 2 | HG01884.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.79+275C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6179670 | ||||||
| chr1:6179748
|
G | GC | 315 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(312): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.79+196_79+197insG | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6179748 | ||||||
| chr1:6179791
|
C | G | 1 | a0001c0005t0006g0025 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.79+154G>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6179791 | ||||||
| chr1:6179801
|
G | A | 44 | a0001c0001t0003g0282a0001c0001t0005g0251a0001c0001t0007g0258others(41): Show | 44 | HG00544.hp2 HG00609.hp1 HG01123.hp2 others(41): Show |
intron_variant | MODIFIER | c.79+144C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6179801 | ||||||
| chr1:6179818
|
C | A | 6 | a0001c0001t0011g0297a0001c0001t0054g0292a0001c0008t0012g0296others(3): Show | 6 | HG01243.hp2 HG02055.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.79+127G>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6179818 | ||||||
| chr1:6179819
|
C | A | 6 | a0001c0001t0011g0297a0001c0001t0054g0292a0001c0008t0012g0296others(3): Show | 6 | HG01243.hp2 HG02055.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.79+126G>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6179819 | ||||||
| chr1:6179840
|
C | T | 1 | a0001c0004t0003g0024 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.79+105G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6179840 | ||||||
| chr1:6179855
|
G | A | 1 | a0001c0003t0021g0298 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.79+90C>T | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6179855 | ||||||
| chr1:6179877
|
C | CG | 315 | a0001c0001t0003g0079a0001c0001t0003g0097a0001c0001t0003g0114others(312): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.79+67dupC | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6179877 | ||||||
| chr1:6179898
|
C | G | 1 | a0002c0022t0001g0023 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.79+47G>C | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6179898 | ||||||
| chr1:6179936
|
C | T | 1 | a0001c0003t0002g0022 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.79+9G>A | CHD5 | ENSG00000116254.18 | transcript | ENST00000262450.8 | protein_coding | 1/41 | chr1 | 6179936 |