Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 57680 |
|---|---|
| ensemblid | ENSG00000100888.15 |
| hgncid | 20153 |
| symbol | CHD8 |
| name | chromodomain helicase DNA binding protein 8 |
| refseq_nuc | NM_001170629.2 |
| refseq_prot | NP_001164100.1 |
| ensembl_nuc | ENST00000646647.2 |
| ensembl_prot | ENSP00000495240.1 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 21385199 |
| end | 21456123 |
| strand | - |
| ver | v1.2 |
| region | chr14:21385199-21456123 |
| region5000 | chr14:21380199-21461123 |
| regionname0 | CHD8_chr14_21385199_21456123 |
| regionname5000 | CHD8_chr14_21380199_21461123 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 2581 | 177 | 67 | 38 | 43 | 6 | 21 | 31 | CHD8_chr14_21380199_21461123 | CHD8 | copy fasta | chr14 | 21380199 | 21461123 |
| a0002 | 0/0 | 2581 | 74 | 22 | 12 | 32 | 4 | 4 | 22 | CHD8_chr14_21380199_21461123 | CHD8 | copy fasta | chr14 | 21380199 | 21461123 |
| a0003 | 0/0 | 2581 | 4 | 0 | 0 | 4 | 0 | 0 | 1 | CHD8_chr14_21380199_21461123 | CHD8 | copy fasta | chr14 | 21380199 | 21461123 |
| a0004 | 0/0 | 2581 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | copy fasta | chr14 | 21380199 | 21461123 |
| a0005 | 0/0 | 2581 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | copy fasta | chr14 | 21380199 | 21461123 |
| a0006 | 0/0 | 2581 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | copy fasta | chr14 | 21380199 | 21461123 |
| a0007 | 0/0 | 2581 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | copy fasta | chr14 | 21380199 | 21461123 |
| a0008 | 0/0 | 2581 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | copy fasta | chr14 | 21380199 | 21461123 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 7746 | 123 | 54 | 23 | 27 | 4 | 14 | CHD8_chr14_21380199_21461123 | CHD8 | copy fasta | chr14 | 21380199 | 21461123 |
| c0002 | 0/0 | 7746 | 71 | 20 | 12 | 32 | 4 | 3 | CHD8_chr14_21380199_21461123 | CHD8 | copy fasta | chr14 | 21380199 | 21461123 |
| c0003 | 1/0 | 7746 | 42 | 3 | 14 | 15 | 2 | 7 | CHD8_chr14_21380199_21461123 | CHD8 | copy fasta | chr14 | 21380199 | 21461123 |
| c0004 | 0/0 | 7746 | 4 | 0 | 0 | 4 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | copy fasta | chr14 | 21380199 | 21461123 |
| c0005 | 0/0 | 7746 | 3 | 3 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | copy fasta | chr14 | 21380199 | 21461123 |
| c0006 | 0/0 | 7746 | 3 | 3 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | copy fasta | chr14 | 21380199 | 21461123 |
| c0007 | 0/0 | 7746 | 2 | 2 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | copy fasta | chr14 | 21380199 | 21461123 |
| c0008 | 0/0 | 7746 | 2 | 2 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | copy fasta | chr14 | 21380199 | 21461123 |
| c0009 | 0/0 | 7746 | 2 | 2 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | copy fasta | chr14 | 21380199 | 21461123 |
| c0010 | 0/0 | 7746 | 1 | 0 | 0 | 0 | 0 | 1 | CHD8_chr14_21380199_21461123 | CHD8 | copy fasta | chr14 | 21380199 | 21461123 |
| c0011 | 0/0 | 7746 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | copy fasta | chr14 | 21380199 | 21461123 |
| c0012 | 0/0 | 7746 | 1 | 0 | 0 | 0 | 0 | 1 | CHD8_chr14_21380199_21461123 | CHD8 | copy fasta | chr14 | 21380199 | 21461123 |
| c0013 | 0/0 | 7746 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | copy fasta | chr14 | 21380199 | 21461123 |
| c0014 | 0/0 | 7746 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | copy fasta | chr14 | 21380199 | 21461123 |
| c0015 | 0/0 | 7746 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | copy fasta | chr14 | 21380199 | 21461123 |
| c0016 | 0/0 | 7746 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | copy fasta | chr14 | 21380199 | 21461123 |
| c0017 | 0/0 | 7746 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | copy fasta | chr14 | 21380199 | 21461123 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 722 | 192 | 45 | 41 | 70 | 10 | 24 | CHD8_chr14_21380199_21461123 | CHD8 | copy fasta | chr14 | 21380199 | 21461123 |
| t0002 | 0/0 | 722 | 40 | 22 | 10 | 6 | 0 | 2 | CHD8_chr14_21380199_21461123 | CHD8 | copy fasta | chr14 | 21380199 | 21461123 |
| t0003 | 0/0 | 721 | 22 | 21 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | copy fasta | chr14 | 21380199 | 21461123 |
| t0004 | 0/0 | 722 | 4 | 0 | 0 | 4 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | copy fasta | chr14 | 21380199 | 21461123 |
| t0005 | 0/0 | 721 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | copy fasta | chr14 | 21380199 | 21461123 |
| t0006 | 0/0 | 722 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | copy fasta | chr14 | 21380199 | 21461123 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0051 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0205 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 7746 | 123 | 54 | 23 | 27 | 4 | 14 | CHD8_chr14_21380199_21461123 | CHD8 | copy fasta | chr14 | 21380199 | 21461123 |
| a0001c0003 | 1/0 | 7746 | 42 | 3 | 14 | 15 | 2 | 7 | CHD8_chr14_21380199_21461123 | CHD8 | copy fasta | chr14 | 21380199 | 21461123 |
| a0001c0005 | 0/0 | 7746 | 3 | 3 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | copy fasta | chr14 | 21380199 | 21461123 |
| a0001c0006 | 0/0 | 7746 | 3 | 3 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | copy fasta | chr14 | 21380199 | 21461123 |
| a0001c0008 | 0/0 | 7746 | 2 | 2 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | copy fasta | chr14 | 21380199 | 21461123 |
| a0001c0009 | 0/0 | 7746 | 2 | 2 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | copy fasta | chr14 | 21380199 | 21461123 |
| a0001c0013 | 0/0 | 7746 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | copy fasta | chr14 | 21380199 | 21461123 |
| a0001c0014 | 0/0 | 7746 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | copy fasta | chr14 | 21380199 | 21461123 |
| a0002c0002 | 0/0 | 7746 | 71 | 20 | 12 | 32 | 4 | 3 | CHD8_chr14_21380199_21461123 | CHD8 | copy fasta | chr14 | 21380199 | 21461123 |
| a0002c0007 | 0/0 | 7746 | 2 | 2 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | copy fasta | chr14 | 21380199 | 21461123 |
| a0002c0010 | 0/0 | 7746 | 1 | 0 | 0 | 0 | 0 | 1 | CHD8_chr14_21380199_21461123 | CHD8 | copy fasta | chr14 | 21380199 | 21461123 |
| a0003c0004 | 0/0 | 7746 | 4 | 0 | 0 | 4 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | copy fasta | chr14 | 21380199 | 21461123 |
| a0004c0011 | 0/0 | 7746 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | copy fasta | chr14 | 21380199 | 21461123 |
| a0005c0016 | 0/0 | 7746 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | copy fasta | chr14 | 21380199 | 21461123 |
| a0006c0012 | 0/0 | 7746 | 1 | 0 | 0 | 0 | 0 | 1 | CHD8_chr14_21380199_21461123 | CHD8 | copy fasta | chr14 | 21380199 | 21461123 |
| a0007c0015 | 0/0 | 7746 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | copy fasta | chr14 | 21380199 | 21461123 |
| a0008c0017 | 0/0 | 7746 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | copy fasta | chr14 | 21380199 | 21461123 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 8467 | 66 | 16 | 13 | 19 | 4 | 13 | CHD8_chr14_21380199_21461123 | CHD8 | copy fasta | chr14 | 21380199 | 21461123 |
| a0001c0001t0002 | 0/0 | 8467 | 31 | 15 | 10 | 5 | 0 | 1 | CHD8_chr14_21380199_21461123 | CHD8 | copy fasta | chr14 | 21380199 | 21461123 |
| a0001c0001t0003 | 0/0 | 8466 | 21 | 21 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | copy fasta | chr14 | 21380199 | 21461123 |
| a0001c0001t0004 | 0/0 | 8467 | 3 | 0 | 0 | 3 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | copy fasta | chr14 | 21380199 | 21461123 |
| a0001c0001t0005 | 0/0 | 8466 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | copy fasta | chr14 | 21380199 | 21461123 |
| a0001c0001t0006 | 0/0 | 8467 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | copy fasta | chr14 | 21380199 | 21461123 |
| a0001c0003t0001 | 1/0 | 8467 | 39 | 0 | 14 | 15 | 2 | 7 | CHD8_chr14_21380199_21461123 | CHD8 | copy fasta | chr14 | 21380199 | 21461123 |
| a0001c0003t0002 | 0/0 | 8467 | 3 | 3 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | copy fasta | chr14 | 21380199 | 21461123 |
| a0001c0005t0002 | 0/0 | 8467 | 3 | 3 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | copy fasta | chr14 | 21380199 | 21461123 |
| a0001c0006t0001 | 0/0 | 8467 | 3 | 3 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | copy fasta | chr14 | 21380199 | 21461123 |
| a0001c0008t0001 | 0/0 | 8467 | 2 | 2 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | copy fasta | chr14 | 21380199 | 21461123 |
| a0001c0009t0001 | 0/0 | 8467 | 2 | 2 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | copy fasta | chr14 | 21380199 | 21461123 |
| a0001c0013t0002 | 0/0 | 8467 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | copy fasta | chr14 | 21380199 | 21461123 |
| a0001c0014t0001 | 0/0 | 8467 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | copy fasta | chr14 | 21380199 | 21461123 |
| a0002c0002t0001 | 0/0 | 8467 | 70 | 20 | 12 | 31 | 4 | 3 | CHD8_chr14_21380199_21461123 | CHD8 | copy fasta | chr14 | 21380199 | 21461123 |
| a0002c0002t0004 | 0/0 | 8467 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | copy fasta | chr14 | 21380199 | 21461123 |
| a0002c0007t0001 | 0/0 | 8467 | 2 | 2 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | copy fasta | chr14 | 21380199 | 21461123 |
| a0002c0010t0001 | 0/0 | 8467 | 1 | 0 | 0 | 0 | 0 | 1 | CHD8_chr14_21380199_21461123 | CHD8 | copy fasta | chr14 | 21380199 | 21461123 |
| a0003c0004t0001 | 0/0 | 8467 | 4 | 0 | 0 | 4 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | copy fasta | chr14 | 21380199 | 21461123 |
| a0004c0011t0001 | 0/0 | 8467 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | copy fasta | chr14 | 21380199 | 21461123 |
| a0005c0016t0003 | 0/0 | 8466 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | copy fasta | chr14 | 21380199 | 21461123 |
| a0006c0012t0002 | 0/0 | 8467 | 1 | 0 | 0 | 0 | 0 | 1 | CHD8_chr14_21380199_21461123 | CHD8 | copy fasta | chr14 | 21380199 | 21461123 |
| a0007c0015t0001 | 0/0 | 8467 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | copy fasta | chr14 | 21380199 | 21461123 |
| a0008c0017t0002 | 0/0 | 8467 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | copy fasta | chr14 | 21380199 | 21461123 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0001g0205 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0002g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0002g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0002g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0002g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0002g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0002g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0002g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0002g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0002g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0003g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0003g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0003g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0003g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0003g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0003g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0003g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0003g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0003g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0003g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0003g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0003g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0003g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0003g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0003g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0003g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0003g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0003g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0004g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0004g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0004g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0005g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0001t0006g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0003t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0003t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0003t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0003t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0003t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0003t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0003t0001g0051 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0003t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0003t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0003t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0003t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0003t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0003t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0003t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0003t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0003t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0003t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0003t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0003t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0003t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0003t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0003t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0003t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0003t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0003t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0003t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0003t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0003t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0003t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0003t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0003t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0003t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0003t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0003t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0003t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0003t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0003t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0003t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0003t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0003t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0003t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0003t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0005t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0005t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0005t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0006t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0006t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0008t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0008t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0009t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0009t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0013t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0001c0014t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0002c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0002c0002t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0002c0002t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0002c0002t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0002c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0002c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0002c0002t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0002c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0002c0002t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0002c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0002c0002t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0002c0002t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0002c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0002c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0002c0002t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0002c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0002c0002t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0002c0002t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0002c0002t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0002c0002t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0002c0002t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0002c0002t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0002c0002t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0002c0002t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0002c0002t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0002c0002t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0002c0002t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0002c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0002c0002t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0002c0002t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0002c0002t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0002c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0002c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0002c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0002c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0002c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0002c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0002c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0002c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0002c0002t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0002c0002t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0002c0002t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0002c0002t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0002c0002t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0002c0002t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0002c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0002c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0002c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0002c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0002c0002t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0002c0002t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0002c0002t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0002c0002t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0002c0002t0004g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0002c0007t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0002c0007t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0002c0010t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0003c0004t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0003c0004t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0003c0004t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0003c0004t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0004c0011t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0005c0016t0003g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0006c0012t0002g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0007c0015t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| a0008c0017t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0149 | EUR | FIN | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG00280 | hp2 | a0001 | c0003 | t0001 | g0161 | EUR | FIN | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG00323 | hp1 | a0002 | c0002 | t0001 | g0092 | EUR | FIN | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG00323 | hp2 | a0001 | c0003 | t0001 | g0056 | EUR | FIN | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG00408 | hp1 | a0003 | c0004 | t0001 | g0156 | EAS | CHS | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | CHS | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG00438 | hp1 | a0002 | c0002 | t0001 | g0215 | EAS | CHS | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG00438 | hp2 | a0002 | c0002 | t0001 | g0110 | EAS | CHS | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG00544 | hp1 | a0002 | c0002 | t0001 | g0246 | EAS | CHS | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | CHS | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG00609 | hp1 | a0001 | c0013 | t0002 | g0026 | EAS | CHS | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | CHS | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | CHS | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG00673 | hp2 | a0002 | c0002 | t0001 | g0191 | EAS | CHS | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG00735 | hp1 | a0002 | c0002 | t0001 | g0120 | AMR | PUR | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG00738 | hp2 | a0001 | c0003 | t0001 | g0067 | AMR | PUR | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0032 | AMR | PUR | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0253 | AMR | PUR | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG01069 | hp2 | a0001 | c0003 | t0001 | g0044 | AMR | PUR | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG01070 | hp1 | a0002 | c0002 | t0001 | g0250 | AMR | PUR | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG01071 | hp1 | a0001 | c0003 | t0001 | g0045 | AMR | PUR | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG01081 | hp2 | a0002 | c0002 | t0001 | g0104 | AMR | PUR | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG01109 | hp1 | a0002 | c0002 | t0001 | g0224 | AMR | PUR | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0247 | AMR | PUR | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG01167 | hp1 | a0001 | c0003 | t0001 | g0059 | AMR | PUR | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG01167 | hp2 | a0002 | c0002 | t0001 | g0108 | AMR | PUR | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG01169 | hp1 | a0001 | c0003 | t0001 | g0062 | AMR | PUR | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG01169 | hp2 | a0002 | c0002 | t0001 | g0251 | AMR | PUR | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG01175 | hp1 | a0002 | c0002 | t0001 | g0252 | AMR | PUR | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG01175 | hp2 | a0001 | c0003 | t0001 | g0068 | AMR | PUR | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG01192 | hp2 | a0001 | c0003 | t0001 | g0061 | AMR | PUR | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG01243 | hp2 | a0005 | c0016 | t0003 | g0145 | AMR | PUR | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG01255 | hp2 | a0001 | c0003 | t0001 | g0073 | AMR | CLM | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0022 | AMR | CLM | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG01258 | hp2 | a0002 | c0002 | t0001 | g0114 | AMR | CLM | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG01261 | hp1 | a0001 | c0003 | t0001 | g0063 | AMR | CLM | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG01261 | hp2 | a0001 | c0014 | t0001 | g0125 | AMR | CLM | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG01346 | hp2 | a0001 | c0003 | t0001 | g0050 | AMR | CLM | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0028 | AMR | CLM | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG01496 | hp1 | a0001 | c0003 | t0001 | g0076 | AMR | CLM | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG01496 | hp2 | a0002 | c0002 | t0001 | g0115 | AMR | CLM | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0186 | EUR | IBS | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG01515 | hp2 | a0002 | c0002 | t0001 | g0101 | EUR | IBS | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG01517 | hp1 | a0002 | c0002 | t0001 | g0241 | EUR | IBS | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0189 | EUR | IBS | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | ACB | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG01891 | hp2 | a0002 | c0002 | t0001 | g0254 | AFR | ACB | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG01975 | hp1 | a0002 | c0002 | t0001 | g0192 | AMR | PEL | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG01975 | hp2 | a0001 | c0003 | t0001 | g0064 | AMR | PEL | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG01978 | hp1 | a0002 | c0002 | t0001 | g0094 | AMR | PEL | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG01978 | hp2 | a0004 | c0011 | t0001 | g0095 | AMR | PEL | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG01993 | hp2 | a0001 | c0003 | t0001 | g0074 | AMR | PEL | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0031 | AMR | PEL | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG02004 | hp2 | a0002 | c0002 | t0001 | g0180 | AMR | PEL | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0198 | AFR | ACB | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | ACB | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG02074 | hp1 | a0007 | c0015 | t0001 | g0137 | EAS | KHV | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG02074 | hp2 | a0002 | c0002 | t0001 | g0107 | EAS | KHV | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG02080 | hp1 | a0002 | c0002 | t0001 | g0057 | EAS | KHV | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG02080 | hp2 | a0001 | c0003 | t0001 | g0055 | EAS | KHV | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | KHV | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG02083 | hp2 | a0002 | c0002 | t0001 | g0212 | EAS | KHV | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG02135 | hp1 | a0003 | c0004 | t0001 | g0133 | EAS | KHV | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG02135 | hp2 | a0002 | c0002 | t0001 | g0121 | EAS | KHV | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0218 | AFR | ACB | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | ACB | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PEL | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG02148 | hp2 | a0001 | c0003 | t0001 | g0069 | AMR | PEL | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG02155 | hp1 | a0002 | c0002 | t0001 | g0211 | EAS | CDX | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | CDX | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0039 | AFR | ACB | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG02257 | hp2 | a0002 | c0002 | t0001 | g0184 | AFR | ACB | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0130 | AFR | ACB | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | ACB | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | ACB | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG02280 | hp2 | a0002 | c0002 | t0001 | g0200 | AFR | ACB | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0027 | AMR | PEL | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0018 | AMR | PEL | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG02451 | hp1 | a0002 | c0002 | t0001 | g0225 | AFR | ACB | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0163 | AFR | ACB | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0017 | AFR | GWD | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0168 | AFR | GWD | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0242 | AFR | GWD | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG02615 | hp2 | a0002 | c0002 | t0001 | g0159 | AFR | GWD | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG02622 | hp1 | a0001 | c0003 | t0002 | g0035 | AFR | GWD | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG02622 | hp2 | a0002 | c0002 | t0001 | g0083 | AFR | GWD | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0040 | AFR | GWD | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | GWD | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG02683 | hp2 | a0001 | c0003 | t0001 | g0077 | SAS | PJL | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0235 | AFR | GWD | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0023 | AFR | GWD | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG02738 | hp1 | a0006 | c0012 | t0002 | g0021 | SAS | PJL | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG02738 | hp2 | a0001 | c0003 | t0001 | g0053 | SAS | PJL | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | GWD | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0143 | AFR | GWD | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG02818 | hp1 | a0001 | c0005 | t0002 | g0042 | AFR | GWD | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0216 | AFR | GWD | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0185 | AFR | GWD | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG02886 | hp2 | a0002 | c0002 | t0001 | g0190 | AFR | GWD | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0144 | AFR | GWD | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG02895 | hp2 | a0002 | c0007 | t0001 | g0232 | AFR | GWD | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0142 | AFR | GWD | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG02897 | hp2 | a0002 | c0002 | t0001 | g0182 | AFR | GWD | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG02922 | hp1 | a0002 | c0002 | t0001 | g0199 | AFR | ESN | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG02922 | hp2 | a0002 | c0002 | t0001 | g0227 | AFR | ESN | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0131 | AFR | ESN | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG02965 | hp2 | a0001 | c0001 | t0006 | g0043 | AFR | ESN | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0217 | AFR | ESN | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0041 | AFR | ESN | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | ESN | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0195 | AFR | ESN | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | GWD | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG03041 | hp2 | a0001 | c0006 | t0001 | g0001 | AFR | GWD | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0128 | AFR | MSL | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | MSL | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG03130 | hp1 | a0001 | c0008 | t0001 | g0087 | AFR | ESN | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG03130 | hp2 | a0001 | c0003 | t0002 | g0033 | AFR | ESN | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG03139 | hp1 | a0001 | c0009 | t0001 | g0240 | AFR | ESN | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0024 | AFR | ESN | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG03195 | hp1 | a0002 | c0002 | t0001 | g0219 | AFR | ESN | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG03195 | hp2 | a0001 | c0006 | t0001 | g0126 | AFR | ESN | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | MSL | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0243 | AFR | MSL | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0234 | AFR | MSL | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG03225 | hp2 | a0001 | c0009 | t0001 | g0239 | AFR | MSL | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | MSL | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG03453 | hp2 | a0001 | c0003 | t0002 | g0034 | AFR | MSL | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG03486 | hp1 | a0002 | c0002 | t0001 | g0188 | AFR | MSL | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | MSL | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0020 | SAS | PJL | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG03540 | hp1 | a0001 | c0005 | t0002 | g0037 | AFR | GWD | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG03540 | hp2 | a0002 | c0002 | t0001 | g0226 | AFR | GWD | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | MSL | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG03579 | hp2 | a0002 | c0002 | t0001 | g0084 | AFR | MSL | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG03654 | hp1 | a0001 | c0003 | t0001 | g0058 | SAS | PJL | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG03654 | hp2 | a0002 | c0002 | t0001 | g0099 | SAS | PJL | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG03704 | hp1 | a0001 | c0003 | t0001 | g0065 | SAS | PJL | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0223 | SAS | PJL | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | BEB | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | BEB | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0206 | SAS | BEB | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG03834 | hp2 | a0002 | c0002 | t0001 | g0124 | SAS | BEB | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG03927 | hp1 | a0001 | c0003 | t0001 | g0049 | SAS | BEB | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | BEB | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | BEB | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | BEB | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | BEB | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG04184 | hp2 | a0001 | c0003 | t0001 | g0078 | SAS | BEB | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG04199 | hp1 | a0002 | c0010 | t0001 | g0093 | SAS | STU | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG04199 | hp2 | a0001 | c0003 | t0001 | g0229 | SAS | STU | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | STU | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | STU | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| NA18522 | hp1 | a0002 | c0002 | t0001 | g0183 | AFR | YRI | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | YRI | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| NA18612 | hp1 | a0003 | c0004 | t0001 | g0151 | EAS | CHB | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| NA18612 | hp2 | a0001 | c0003 | t0001 | g0052 | EAS | CHB | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| NA18747 | hp1 | a0001 | c0001 | t0004 | g0256 | EAS | CHB | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| NA18747 | hp2 | a0002 | c0002 | t0001 | g0113 | EAS | CHB | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| NA18906 | hp1 | a0001 | c0008 | t0001 | g0088 | AFR | YRI | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | YRI | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| NA18942 | hp1 | a0001 | c0001 | t0004 | g0259 | EAS | JPT | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| NA18942 | hp2 | a0002 | c0002 | t0001 | g0112 | EAS | JPT | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| NA18945 | hp2 | a0002 | c0002 | t0001 | g0209 | EAS | JPT | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| NA18947 | hp1 | a0002 | c0002 | t0001 | g0117 | EAS | JPT | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| NA18947 | hp2 | a0001 | c0003 | t0001 | g0046 | EAS | JPT | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| NA18948 | hp1 | a0001 | c0003 | t0001 | g0048 | EAS | JPT | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| NA18948 | hp2 | a0002 | c0002 | t0001 | g0122 | EAS | JPT | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| NA18951 | hp1 | a0002 | c0002 | t0001 | g0106 | EAS | JPT | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| NA18951 | hp2 | a0002 | c0002 | t0001 | g0207 | EAS | JPT | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| NA18957 | hp1 | a0001 | c0003 | t0001 | g0075 | EAS | JPT | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| NA18957 | hp2 | a0002 | c0002 | t0001 | g0201 | EAS | JPT | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| NA18962 | hp2 | a0002 | c0002 | t0001 | g0213 | EAS | JPT | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| NA18964 | hp2 | a0002 | c0002 | t0001 | g0208 | EAS | JPT | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| NA18967 | hp1 | a0002 | c0002 | t0001 | g0119 | EAS | JPT | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| NA18971 | hp1 | a0002 | c0002 | t0001 | g0102 | EAS | JPT | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| NA18978 | hp1 | a0001 | c0003 | t0001 | g0091 | EAS | JPT | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| NA18978 | hp2 | a0003 | c0004 | t0001 | g0170 | EAS | JPT | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| NA18979 | hp2 | a0001 | c0003 | t0001 | g0214 | EAS | JPT | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| NA18982 | hp1 | a0002 | c0002 | t0001 | g0111 | EAS | JPT | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| NA18982 | hp2 | a0002 | c0002 | t0001 | g0098 | EAS | JPT | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| NA18988 | hp1 | a0001 | c0001 | t0004 | g0258 | EAS | JPT | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| NA18988 | hp2 | a0001 | c0003 | t0001 | g0072 | EAS | JPT | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| NA18990 | hp2 | a0002 | c0002 | t0001 | g0210 | EAS | JPT | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| NA19001 | hp1 | a0002 | c0002 | t0001 | g0089 | EAS | JPT | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| NA19001 | hp2 | a0001 | c0003 | t0001 | g0090 | EAS | JPT | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| NA19004 | hp1 | a0001 | c0003 | t0001 | g0255 | EAS | JPT | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| NA19005 | hp1 | a0001 | c0003 | t0001 | g0071 | EAS | JPT | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| NA19005 | hp2 | a0002 | c0002 | t0001 | g0118 | EAS | JPT | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| NA19007 | hp1 | a0001 | c0003 | t0001 | g0066 | EAS | JPT | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| NA19012 | hp1 | a0002 | c0002 | t0001 | g0100 | EAS | JPT | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| NA19012 | hp2 | a0002 | c0002 | t0001 | g0230 | EAS | JPT | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0025 | AFR | LWK | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| NA19030 | hp2 | a0002 | c0002 | t0001 | g0148 | AFR | LWK | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | LWK | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0038 | AFR | LWK | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| NA19057 | hp1 | a0001 | c0003 | t0001 | g0202 | EAS | JPT | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| NA19057 | hp2 | a0002 | c0002 | t0001 | g0105 | EAS | JPT | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| NA19060 | hp2 | a0001 | c0003 | t0001 | g0054 | EAS | JPT | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| NA19074 | hp2 | a0002 | c0002 | t0001 | g0109 | EAS | JPT | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| NA19084 | hp2 | a0001 | c0003 | t0001 | g0060 | EAS | JPT | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| NA19089 | hp1 | a0002 | c0002 | t0004 | g0257 | EAS | JPT | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| NA19091 | hp1 | a0002 | c0002 | t0001 | g0116 | EAS | JPT | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| NA19240 | hp1 | a0001 | c0001 | t0005 | g0030 | AFR | YRI | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| NA19240 | hp2 | a0002 | c0002 | t0001 | g0160 | AFR | YRI | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0196 | AFR | ASW | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | ASW | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0141 | EUR | TSI | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| NA20752 | hp2 | a0002 | c0002 | t0001 | g0249 | EUR | TSI | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0103 | SAS | GIH | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0221 | SAS | GIH | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG02109 | hp1 | a0002 | c0002 | t0001 | g0220 | AFR | ACB | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0248 | AFR | ACB | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG02559 | hp1 | a0008 | c0017 | t0002 | g0029 | AFR | ACB | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG02559 | hp2 | a0001 | c0006 | t0001 | g0001 | AFR | ACB | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG03471 | hp1 | a0002 | c0007 | t0001 | g0231 | AFR | MSL | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG03471 | hp2 | a0002 | c0002 | t0001 | g0136 | AFR | MSL | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG06807 | hp1 | a0001 | c0005 | t0002 | g0036 | AFR | USA | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | USA | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | USA | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0197 | AFR | USA | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | LWK | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| NA21309 | hp2 | a0002 | c0002 | t0001 | g0179 | AFR | LWK | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0205 | REF | REF | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| homoSapiens_grch38 | hp1 | a0001 | c0003 | t0001 | g0051 | REF | REF | CHD8_chr14_21380199_21461123 | CHD8 | chr14 | 21380199 | 21461123 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:21392628
|
C | T | 1 | a0004 | 1 | HG01978.hp2 | missense_variant | MODERATE | c.6650G>A | p.Arg2217Gln | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 34/38 | 6957/8467 | 6650/7746 | 2217/2581 | chr14 | 21392628 | ||
| chr14:21393676
|
T | C | 1 | a0003 | 4 | HG00408.hp1 HG02135.hp1 NA18612.hp1 others(1): Show |
missense_variant | MODERATE | c.6119A>G | p.Asp2040Gly | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 32/38 | 6426/8467 | 6119/7746 | 2040/2581 | chr14 | 21393676 | ||
| chr14:21428155
|
G | A | 1 | a0007 | 1 | HG02074.hp1 | missense_variant | MODERATE | c.1315C>T | p.His439Tyr | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 4/38 | 1622/8467 | 1315/7746 | 439/2581 | chr14 | 21428155 | ||
| chr14:21429271
|
C | T | 1 | a0006 | 1 | HG02738.hp1 | missense_variant | MODERATE | c.908G>A | p.Arg303Gln | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 3/38 | 1215/8467 | 908/7746 | 303/2581 | chr14 | 21429271 | ||
| chr14:21431306
|
G | A | 1 | a0005 | 1 | HG01243.hp2 | missense_variant | MODERATE | c.338C>T | p.Ser113Leu | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 2/38 | 645/8467 | 338/7746 | 113/2581 | chr14 | 21431306 | ||
| chr14:21431472
|
C | T | 2 | a0002a0004 | 75 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(72): Show |
missense_variant | MODERATE | c.172G>A | p.Val58Met | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 2/38 | 479/8467 | 172/7746 | 58/2581 | chr14 | 21431472 | ||
| chr14:21431499
|
T | C | 1 | a0008 | 1 | HG02559.hp1 | missense_variant | MODERATE | c.145A>G | p.Met49Val | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 2/38 | 452/8467 | 145/7746 | 49/2581 | chr14 | 21431499 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:21392741
|
G | A | 1 | a0001c0006 | 3 | HG02559.hp2 HG03041.hp2 HG03195.hp2 |
synonymous_variant | LOW | c.6537C>T | p.Ser2179Ser | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 34/38 | 6844/8467 | 6537/7746 | 2179/2581 | chr14 | 21392741 | ||
| chr14:21393229
|
A | G | 1 | a0002c0010 | 1 | HG04199.hp1 | synonymous_variant | LOW | c.6345T>C | p.Tyr2115Tyr | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 33/38 | 6652/8467 | 6345/7746 | 2115/2581 | chr14 | 21393229 | ||
| chr14:21393483
|
C | T | 1 | a0001c0013 | 1 | HG00609.hp1 | synonymous_variant | LOW | c.6312G>A | p.Glu2104Glu | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 32/38 | 6619/8467 | 6312/7746 | 2104/2581 | chr14 | 21393483 | ||
| chr14:21395823
|
A | G | 1 | a0002c0007 | 2 | HG02895.hp2 HG03471.hp1 |
synonymous_variant | LOW | c.5121T>C | p.Asp1707Asp | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 28/38 | 5428/8467 | 5121/7746 | 1707/2581 | chr14 | 21395823 | ||
| chr14:21397867
|
T | C | 1 | a0001c0009 | 2 | HG03139.hp1 HG03225.hp2 |
synonymous_variant | LOW | c.5007A>G | p.Ala1669Ala | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 27/38 | 5314/8467 | 5007/7746 | 1669/2581 | chr14 | 21397867 | ||
| chr14:21399989
|
C | T | 1 | a0001c0005 | 3 | HG02818.hp1 HG03540.hp1 HG06807.hp1 |
synonymous_variant | LOW | c.4809G>A | p.Ala1603Ala | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 25/38 | 5116/8467 | 4809/7746 | 1603/2581 | chr14 | 21399989 | ||
| chr14:21403494
|
C | T | 14 | a0001c0001a0001c0005a0001c0006others(11): Show | 216 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(213): Show |
synonymous_variant | LOW | c.3477G>A | p.Val1159Val | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 17/38 | 3784/8467 | 3477/7746 | 1159/2581 | chr14 | 21403494 | ||
| chr14:21408817
|
C | T | 1 | a0001c0008 | 2 | HG03130.hp1 NA18906.hp1 |
synonymous_variant | LOW | c.2373G>A | p.Pro791Pro | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 12/38 | 2680/8467 | 2373/7746 | 791/2581 | chr14 | 21408817 | ||
| chr14:21414952
|
G | C | 1 | a0001c0014 | 1 | HG01261.hp2 | synonymous_variant | LOW | c.2010C>G | p.Val670Val | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 8/38 | 2317/8467 | 2010/7746 | 670/2581 | chr14 | 21414952 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:21385470
|
AT | A | 3 | a0001c0001t0003a0001c0001t0005a0005c0016t0003 | 23 | HG01243.hp2 HG02055.hp1 HG02109.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*142delA | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 38/38 | 142 | chr14 | 21385470 | |||||
| chr14:21456038
|
A | G | 1 | a0001c0001t0006 | 1 | HG02965.hp2 | 5_prime_UTR_variant | MODIFIER | c.-222T>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/38 | 24395 | chr14 | 21456038 | |||||
| chr14:21456048
|
A | G | 7 | a0001c0001t0002a0001c0001t0005a0001c0003t0002others(4): Show | 41 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(38): Show |
5_prime_UTR_variant | MODIFIER | c.-232T>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/38 | 24405 | chr14 | 21456048 | |||||
| chr14:21456066
|
G | A | 2 | a0001c0001t0004a0002c0002t0004 | 4 | NA18747.hp1 NA18942.hp1 NA18988.hp1 others(1): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-250C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/38 | chr14 | 21456066 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:21386240
|
C | T | 1 | a0001c0003t0002g0034 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.7183-64G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 37/37 | chr14 | 21386240 | ||||||
| chr14:21386331
|
A | T | 2 | a0002c0002t0001g0136a0002c0002t0001g0159 | 2 | HG02615.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.7183-155T>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 37/37 | chr14 | 21386331 | ||||||
| chr14:21386552
|
T | C | 4 | a0001c0001t0001g0147a0001c0001t0001g0164a0001c0001t0001g0165others(1): Show | 4 | HG00733.hp2 HG00735.hp2 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.7183-376A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 37/37 | chr14 | 21386552 | ||||||
| chr14:21386559
|
C | T | 1 | a0001c0001t0001g0080 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.7183-383G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 37/37 | chr14 | 21386559 | ||||||
| chr14:21386705
|
C | T | 6 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0017others(3): Show | 6 | HG02258.hp2 HG02280.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.7183-529G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 37/37 | chr14 | 21386705 | ||||||
| chr14:21386796
|
G | A | 1 | a0001c0001t0003g0235 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.7183-620C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 37/37 | chr14 | 21386796 | ||||||
| chr14:21386821
|
A | G | 1 | a0001c0001t0001g0244 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.7183-645T>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 37/37 | chr14 | 21386821 | ||||||
| chr14:21386833
|
T | G | 6 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(3): Show | 6 | HG01109.hp2 HG02976.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.7183-657A>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 37/37 | chr14 | 21386833 | ||||||
| chr14:21386836
|
CA | C | 110 | a0001c0001t0001g0070a0001c0001t0001g0082a0001c0001t0001g0132others(107): Show | 111 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.7183-661delT | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 37/37 | chr14 | 21386836 | ||||||
| chr14:21386859
|
G | A | 1 | a0001c0003t0001g0069 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.7183-683C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 37/37 | chr14 | 21386859 | ||||||
| chr14:21386984
|
C | G | 1 | a0002c0002t0001g0220 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.7183-808G>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 37/37 | chr14 | 21386984 | ||||||
| chr14:21386997
|
A | C | 1 | a0001c0001t0003g0243 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.7183-821T>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 37/37 | chr14 | 21386997 | ||||||
| chr14:21387040
|
G | C | 1 | a0001c0001t0004g0259 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.7183-864C>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 37/37 | chr14 | 21387040 | ||||||
| chr14:21387163
|
G | A | 2 | a0002c0002t0001g0107a0002c0002t0001g0113 | 2 | HG02074.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.7183-987C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 37/37 | chr14 | 21387163 | ||||||
| chr14:21387172
|
G | C | 1 | a0001c0014t0001g0125 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.7183-996C>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 37/37 | chr14 | 21387172 | ||||||
| chr14:21387223
|
TGCCTGTA others(139): Show |
T | 1 | a0001c0014t0001g0125 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.7183-1193_7183-104 others(4): Show |
CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 37/37 | chr14 | 21387223 | ||||||
| chr14:21387228
|
G | A | 1 | a0002c0002t0001g0124 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.7183-1052C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 37/37 | chr14 | 21387228 | ||||||
| chr14:21387280
|
G | C | 6 | a0001c0001t0003g0218a0001c0001t0003g0242a0001c0006t0001g0001others(3): Show | 7 | HG02145.hp1 HG02559.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.7183-1104C>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 37/37 | chr14 | 21387280 | ||||||
| chr14:21387405
|
G | A | 1 | a0006c0012t0002g0021 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.7183-1229C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 37/37 | chr14 | 21387405 | ||||||
| chr14:21387408
|
G | A | 2 | a0001c0001t0003g0218a0001c0001t0003g0242 | 2 | HG02145.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.7183-1232C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 37/37 | chr14 | 21387408 | ||||||
| chr14:21387439
|
C | G | 3 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0018 | 3 | HG01070.hp2 HG01071.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.7183-1263G>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 37/37 | chr14 | 21387439 | ||||||
| chr14:21387503
|
G | A | 5 | a0001c0001t0001g0167a0001c0001t0001g0237a0001c0001t0002g0039others(2): Show | 5 | HG01884.hp1 HG02257.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.7183-1327C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 37/37 | chr14 | 21387503 | ||||||
| chr14:21387550
|
C | A | 1 | a0001c0001t0001g0187 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.7183-1374G>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 37/37 | chr14 | 21387550 | ||||||
| chr14:21387577
|
T | C | 1 | a0001c0001t0003g0163 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.7183-1401A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 37/37 | chr14 | 21387577 | ||||||
| chr14:21387581
|
C | T | 1 | a0001c0001t0002g0015 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.7183-1405G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 37/37 | chr14 | 21387581 | ||||||
| chr14:21387638
|
C | CA | 104 | a0001c0001t0001g0047a0001c0001t0001g0079a0001c0001t0001g0096others(101): Show | 105 | HG00280.hp1 HG00408.hp1 HG00609.hp2 others(102): Show |
intron_variant | MODIFIER | c.7183-1463dupT | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 37/37 | chr14 | 21387638 | ||||||
| chr14:21387638
|
C | CAA | 5 | a0001c0001t0001g0157a0001c0001t0002g0002a0001c0001t0002g0039others(2): Show | 5 | HG02257.hp1 HG02809.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.7183-1464_7183-146 others(6): Show |
CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 37/37 | chr14 | 21387638 | ||||||
| chr14:21387638
|
CA | C | 6 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0017others(3): Show | 6 | HG02258.hp2 HG02280.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.7183-1463delT | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 37/37 | chr14 | 21387638 | ||||||
| chr14:21387721
|
A | G | 191 | a0001c0001t0001g0047a0001c0001t0001g0070a0001c0001t0001g0079others(188): Show | 192 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.7183-1545T>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 37/37 | chr14 | 21387721 | ||||||
| chr14:21387767
|
C | T | 1 | a0002c0002t0001g0106 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.7183-1591G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 37/37 | chr14 | 21387767 | ||||||
| chr14:21387796
|
ACT | A | 9 | a0001c0001t0001g0236a0001c0001t0001g0238a0001c0001t0001g0244others(6): Show | 9 | HG01243.hp2 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.7183-1622_7183-162 others(6): Show |
CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 37/37 | chr14 | 21387796 | ||||||
| chr14:21387809
|
C | CA | 29 | a0001c0001t0001g0167a0001c0001t0001g0236a0001c0001t0001g0237others(26): Show | 29 | HG01243.hp2 HG01261.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.7183-1634dupT | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 37/37 | chr14 | 21387809 | ||||||
| chr14:21387809
|
CA | C | 161 | a0001c0001t0001g0070a0001c0001t0001g0079a0001c0001t0001g0080others(158): Show | 161 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.7183-1634delT | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 37/37 | chr14 | 21387809 | ||||||
| chr14:21387812
|
A | G | 1 | a0001c0001t0002g0019 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.7183-1636T>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 37/37 | chr14 | 21387812 | ||||||
| chr14:21387921
|
T | C | 178 | a0001c0001t0001g0047a0001c0001t0001g0070a0001c0001t0001g0079others(175): Show | 178 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.7183-1745A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 37/37 | chr14 | 21387921 | ||||||
| chr14:21387979
|
GTTAAA | G | 2 | a0001c0009t0001g0239a0001c0009t0001g0240 | 2 | HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.7183-1808_7183-180 others(9): Show |
CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 37/37 | chr14 | 21387979 | ||||||
| chr14:21388113
|
C | T | 1 | a0002c0002t0001g0220 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.7183-1937G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 37/37 | chr14 | 21388113 | ||||||
| chr14:21388186
|
T | C | 1 | a0002c0002t0001g0188 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.7183-2010A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 37/37 | chr14 | 21388186 | ||||||
| chr14:21388193
|
C | T | 1 | a0001c0001t0002g0008 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.7183-2017G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 37/37 | chr14 | 21388193 | ||||||
| chr14:21388197
|
A | G | 6 | a0001c0001t0003g0218a0001c0001t0003g0242a0001c0006t0001g0001others(3): Show | 7 | HG02145.hp1 HG02559.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.7183-2021T>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 37/37 | chr14 | 21388197 | ||||||
| chr14:21388246
|
A | G | 2 | a0001c0001t0003g0218a0001c0001t0003g0242 | 2 | HG02145.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.7183-2070T>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 37/37 | chr14 | 21388246 | ||||||
| chr14:21388294
|
A | G | 3 | a0001c0001t0001g0157a0001c0001t0001g0169a0001c0001t0001g0176 | 3 | HG02083.hp1 HG02155.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.7183-2118T>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 37/37 | chr14 | 21388294 | ||||||
| chr14:21388483
|
TTTTA | T | 6 | a0001c0001t0003g0218a0001c0001t0003g0242a0001c0006t0001g0001others(3): Show | 7 | HG02145.hp1 HG02559.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.7183-2311_7183-230 others(8): Show |
CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 37/37 | chr14 | 21388483 | ||||||
| chr14:21388642
|
C | G | 1 | a0001c0001t0001g0181 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.7182+2305G>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 37/37 | chr14 | 21388642 | ||||||
| chr14:21388727
|
T | G | 2 | a0001c0006t0001g0001a0001c0006t0001g0126 | 3 | HG02559.hp2 HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.7182+2220A>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 37/37 | chr14 | 21388727 | ||||||
| chr14:21388798
|
A | G | 1 | a0001c0001t0002g0009 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.7182+2149T>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 37/37 | chr14 | 21388798 | ||||||
| chr14:21388821
|
G | A | 2 | a0001c0001t0001g0186a0001c0001t0001g0189 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.7182+2126C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 37/37 | chr14 | 21388821 | ||||||
| chr14:21388890
|
A | G | 1 | a0001c0001t0001g0174 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.7182+2057T>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 37/37 | chr14 | 21388890 | ||||||
| chr14:21388976
|
C | T | 1 | a0001c0001t0001g0238 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.7182+1971G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 37/37 | chr14 | 21388976 | ||||||
| chr14:21389129
|
G | C | 171 | a0001c0001t0001g0047a0001c0001t0001g0070a0001c0001t0001g0079others(168): Show | 171 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.7182+1818C>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 37/37 | chr14 | 21389129 | ||||||
| chr14:21389170
|
C | T | 1 | a0001c0001t0001g0194 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.7182+1777G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 37/37 | chr14 | 21389170 | ||||||
| chr14:21389171
|
A | G | 185 | a0001c0001t0001g0047a0001c0001t0001g0070a0001c0001t0001g0079others(182): Show | 186 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.7182+1776T>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 37/37 | chr14 | 21389171 | ||||||
| chr14:21389173
|
AC | A | 5 | a0001c0001t0001g0167a0001c0001t0001g0237a0001c0001t0002g0039others(2): Show | 5 | HG01884.hp1 HG02257.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.7182+1773delG | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 37/37 | chr14 | 21389173 | ||||||
| chr14:21389272
|
C | T | 4 | a0001c0001t0001g0147a0001c0001t0001g0164a0001c0001t0001g0165others(1): Show | 4 | HG00733.hp2 HG00735.hp2 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.7182+1675G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 37/37 | chr14 | 21389272 | ||||||
| chr14:21389295
|
G | A | 2 | a0001c0008t0001g0087a0001c0008t0001g0088 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.7182+1652C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 37/37 | chr14 | 21389295 | ||||||
| chr14:21389302
|
G | GA | 10 | a0001c0001t0001g0245a0001c0001t0002g0002a0001c0001t0002g0003others(7): Show | 10 | HG01261.hp2 HG01884.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.7182+1644dupT | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 37/37 | chr14 | 21389302 | ||||||
| chr14:21389302
|
GA | G | 68 | a0001c0001t0001g0146a0001c0001t0006g0043a0001c0003t0001g0062others(65): Show | 68 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.7182+1644delT | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 37/37 | chr14 | 21389302 | ||||||
| chr14:21389362
|
G | T | 1 | a0001c0001t0002g0020 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.7182+1585C>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 37/37 | chr14 | 21389362 | ||||||
| chr14:21389424
|
A | C | 6 | a0001c0001t0001g0167a0001c0001t0001g0237a0001c0001t0002g0039others(3): Show | 6 | HG01884.hp1 HG02257.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.7182+1523T>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 37/37 | chr14 | 21389424 | ||||||
| chr14:21389467
|
T | C | 191 | a0001c0001t0001g0047a0001c0001t0001g0070a0001c0001t0001g0079others(188): Show | 192 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.7182+1480A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 37/37 | chr14 | 21389467 | ||||||
| chr14:21389483
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.7182+1464G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 37/37 | chr14 | 21389483 | ||||||
| chr14:21389579
|
C | G | 1 | a0002c0002t0001g0148 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.7182+1368G>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 37/37 | chr14 | 21389579 | ||||||
| chr14:21389621
|
A | G | 1 | a0005c0016t0003g0145 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.7182+1326T>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 37/37 | chr14 | 21389621 | ||||||
| chr14:21389682
|
T | C | 1 | a0001c0001t0001g0245 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.7182+1265A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 37/37 | chr14 | 21389682 | ||||||
| chr14:21389757
|
G | A | 6 | a0001c0001t0003g0218a0001c0001t0003g0242a0001c0006t0001g0001others(3): Show | 7 | HG02145.hp1 HG02559.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.7182+1190C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 37/37 | chr14 | 21389757 | ||||||
| chr14:21389963
|
G | A | 1 | a0001c0001t0003g0130 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.7182+984C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 37/37 | chr14 | 21389963 | ||||||
| chr14:21390064
|
G | A | 5 | a0002c0002t0001g0083a0002c0002t0001g0084a0002c0002t0001g0219others(2): Show | 5 | HG02109.hp1 HG02622.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.7182+883C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 37/37 | chr14 | 21390064 | ||||||
| chr14:21390160
|
GGGGA | G | 3 | a0002c0002t0001g0179a0002c0002t0001g0183a0002c0002t0001g0184 | 3 | HG02257.hp2 NA18522.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.7182+783_7182+786d others(6): Show |
CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 37/37 | chr14 | 21390160 | ||||||
| chr14:21390189
|
T | C | 9 | a0001c0001t0001g0236a0001c0001t0001g0238a0001c0001t0001g0244others(6): Show | 9 | HG01243.hp2 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.7182+758A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 37/37 | chr14 | 21390189 | ||||||
| chr14:21390452
|
T | C | 1 | a0001c0001t0001g0138 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.7182+495A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 37/37 | chr14 | 21390452 | ||||||
| chr14:21390581
|
C | T | 1 | a0001c0001t0001g0222 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.7182+366G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 37/37 | chr14 | 21390581 | ||||||
| chr14:21390582
|
G | A | 1 | a0001c0001t0001g0141 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.7182+365C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 37/37 | chr14 | 21390582 | ||||||
| chr14:21390663
|
A | C | 1 | a0001c0001t0001g0204 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.7182+284T>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 37/37 | chr14 | 21390663 | ||||||
| chr14:21390710
|
G | A | 1 | a0001c0014t0001g0125 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.7182+237C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 37/37 | chr14 | 21390710 | ||||||
| chr14:21390734
|
C | T | 1 | a0001c0001t0001g0140 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.7182+213G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 37/37 | chr14 | 21390734 | ||||||
| chr14:21390764
|
G | A | 1 | a0002c0002t0001g0191 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.7182+183C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 37/37 | chr14 | 21390764 | ||||||
| chr14:21390768
|
C | CA | 11 | a0001c0001t0001g0167a0001c0001t0001g0238a0001c0001t0003g0163others(8): Show | 12 | HG01884.hp1 HG02055.hp2 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.7182+178dupT | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 37/37 | chr14 | 21390768 | ||||||
| chr14:21390768
|
CA | C | 7 | a0001c0001t0001g0245a0001c0001t0002g0002a0001c0001t0002g0003others(4): Show | 7 | HG01884.hp2 HG01891.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.7182+178delT | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 37/37 | chr14 | 21390768 | ||||||
| chr14:21390768
|
CAA | C | 167 | a0001c0001t0001g0047a0001c0001t0001g0070a0001c0001t0001g0079others(164): Show | 167 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.7182+177_7182+178d others(4): Show |
CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 37/37 | chr14 | 21390768 | ||||||
| chr14:21390785
|
C | A | 6 | a0001c0001t0003g0218a0001c0001t0003g0242a0001c0006t0001g0001others(3): Show | 7 | HG02145.hp1 HG02559.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.7182+162G>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 37/37 | chr14 | 21390785 | ||||||
| chr14:21390846
|
T | C | 1 | a0001c0003t0001g0058 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.7182+101A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 37/37 | chr14 | 21390846 | ||||||
| chr14:21390920
|
GA | G | 70 | a0001c0001t0001g0146a0002c0002t0001g0057a0002c0002t0001g0083others(67): Show | 70 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.7182+26delT | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 37/37 | chr14 | 21390920 | ||||||
| chr14:21391332
|
G | C | 1 | a0002c0002t0001g0213 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.7065+131C>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 36/37 | chr14 | 21391332 | ||||||
| chr14:21391377
|
T | C | 178 | a0001c0001t0001g0047a0001c0001t0001g0070a0001c0001t0001g0079others(175): Show | 178 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.7065+86A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 36/37 | chr14 | 21391377 | ||||||
| chr14:21391687
|
G | A | 1 | a0001c0014t0001g0125 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.6886-45C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 35/37 | chr14 | 21391687 | ||||||
| chr14:21392004
|
G | T | 1 | a0001c0003t0001g0061 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.6772-58C>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 34/37 | chr14 | 21392004 | ||||||
| chr14:21392049
|
A | C | 2 | a0001c0003t0002g0033a0001c0003t0002g0034 | 2 | HG03130.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.6772-103T>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 34/37 | chr14 | 21392049 | ||||||
| chr14:21392114
|
C | G | 1 | a0001c0014t0001g0125 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.6772-168G>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 34/37 | chr14 | 21392114 | ||||||
| chr14:21392201
|
G | A | 178 | a0001c0001t0001g0047a0001c0001t0001g0070a0001c0001t0001g0079others(175): Show | 178 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.6772-255C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 34/37 | chr14 | 21392201 | ||||||
| chr14:21392862
|
T | C | 2 | a0001c0003t0001g0075a0001c0003t0001g0255 | 2 | NA18957.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.6469-53A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 33/37 | chr14 | 21392862 | ||||||
| chr14:21392974
|
G | GA | 202 | a0001c0001t0001g0047a0001c0001t0001g0070a0001c0001t0001g0079others(199): Show | 203 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.6468+131dupT | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 33/37 | chr14 | 21392974 | ||||||
| chr14:21392974
|
G | GAA | 5 | a0001c0001t0002g0010a0001c0001t0003g0218a0001c0001t0003g0242others(2): Show | 5 | HG01243.hp2 HG02145.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.6468+130_6468+131d others(4): Show |
CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 33/37 | chr14 | 21392974 | ||||||
| chr14:21393052
|
C | A | 185 | a0001c0001t0001g0047a0001c0001t0001g0070a0001c0001t0001g0079others(182): Show | 186 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.6468+54G>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 33/37 | chr14 | 21393052 | ||||||
| chr14:21394507
|
A | G | 5 | a0001c0001t0001g0150a0001c0001t0002g0005a0001c0001t0002g0006others(2): Show | 5 | HG00408.hp2 HG00544.hp2 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.5391-22T>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 30/37 | chr14 | 21394507 | ||||||
| chr14:21394525
|
A | G | 3 | a0001c0001t0003g0131a0001c0001t0003g0248a0005c0016t0003g0145 | 3 | HG01243.hp2 HG02109.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.5391-40T>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 30/37 | chr14 | 21394525 | ||||||
| chr14:21394526
|
C | A | 1 | a0001c0001t0003g0163 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.5391-41G>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 30/37 | chr14 | 21394526 | ||||||
| chr14:21394601
|
G | A | 4 | a0001c0001t0003g0218a0001c0001t0003g0242a0001c0009t0001g0239others(1): Show | 4 | HG02145.hp1 HG02615.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.5391-116C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 30/37 | chr14 | 21394601 | ||||||
| chr14:21394605
|
C | CA | 111 | a0001c0001t0001g0047a0001c0001t0001g0070a0001c0001t0001g0079others(108): Show | 111 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.5391-121dupT | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 30/37 | chr14 | 21394605 | ||||||
| chr14:21394605
|
C | CAA | 88 | a0001c0001t0001g0081a0001c0001t0001g0135a0001c0001t0001g0158others(85): Show | 88 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.5391-122_5391-121d others(4): Show |
CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 30/37 | chr14 | 21394605 | ||||||
| chr14:21394605
|
C | CAAA | 6 | a0001c0006t0001g0001a0001c0006t0001g0126a0001c0009t0001g0240others(3): Show | 7 | HG01175.hp1 HG01496.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.5391-123_5391-121d others(5): Show |
CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 30/37 | chr14 | 21394605 | ||||||
| chr14:21394605
|
CA | C | 5 | a0001c0001t0003g0234a0001c0003t0001g0048a0001c0003t0001g0060others(2): Show | 5 | HG01261.hp2 HG03225.hp1 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.5391-121delT | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 30/37 | chr14 | 21394605 | ||||||
| chr14:21395548
|
T | C | 1 | a0001c0001t0001g0245 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.5128-196A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 28/37 | chr14 | 21395548 | ||||||
| chr14:21395557
|
C | T | 171 | a0001c0001t0001g0047a0001c0001t0001g0070a0001c0001t0001g0079others(168): Show | 171 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.5128-205G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 28/37 | chr14 | 21395557 | ||||||
| chr14:21395571
|
T | C | 1 | a0001c0001t0001g0138 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.5128-219A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 28/37 | chr14 | 21395571 | ||||||
| chr14:21395965
|
C | A | 177 | a0001c0001t0001g0047a0001c0001t0001g0070a0001c0001t0001g0079others(174): Show | 177 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.5052-73G>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 27/37 | chr14 | 21395965 | ||||||
| chr14:21396056
|
G | A | 1 | a0002c0002t0001g0124 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.5052-164C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 27/37 | chr14 | 21396056 | ||||||
| chr14:21396151
|
C | T | 1 | a0001c0001t0003g0163 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.5052-259G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 27/37 | chr14 | 21396151 | ||||||
| chr14:21396204
|
C | T | 1 | a0001c0014t0001g0125 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.5052-312G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 27/37 | chr14 | 21396204 | ||||||
| chr14:21396242
|
C | T | 2 | a0001c0009t0001g0239a0001c0009t0001g0240 | 2 | HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.5052-350G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 27/37 | chr14 | 21396242 | ||||||
| chr14:21396400
|
G | A | 2 | a0001c0009t0001g0239a0001c0009t0001g0240 | 2 | HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.5052-508C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 27/37 | chr14 | 21396400 | ||||||
| chr14:21396566
|
T | TTTTATTT others(9): Show |
4 | a0001c0001t0001g0237a0001c0001t0002g0039a0001c0001t0002g0040others(1): Show | 4 | HG02257.hp1 HG02630.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.5052-690_5052-675d others(18): Show |
CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 27/37 | chr14 | 21396566 | ||||||
| chr14:21396566
|
T | TTTTATTT others(13): Show |
1 | a0001c0001t0001g0167 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.5052-694_5052-675d others(22): Show |
CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 27/37 | chr14 | 21396566 | ||||||
| chr14:21396566
|
TTTTATTT others(1): Show |
T | 3 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004 | 3 | HG01884.hp2 HG01891.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.5052-682_5052-675d others(10): Show |
CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 27/37 | chr14 | 21396566 | ||||||
| chr14:21396607
|
C | A | 1 | a0001c0001t0003g0163 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.5052-715G>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 27/37 | chr14 | 21396607 | ||||||
| chr14:21396733
|
C | G | 171 | a0001c0001t0001g0047a0001c0001t0001g0070a0001c0001t0001g0079others(168): Show | 171 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.5052-841G>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 27/37 | chr14 | 21396733 | ||||||
| chr14:21396743
|
T | C | 1 | a0001c0005t0002g0042 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.5052-851A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 27/37 | chr14 | 21396743 | ||||||
| chr14:21396765
|
C | T | 1 | a0001c0001t0002g0039 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.5052-873G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 27/37 | chr14 | 21396765 | ||||||
| chr14:21396787
|
T | C | 1 | a0002c0002t0001g0109 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.5052-895A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 27/37 | chr14 | 21396787 | ||||||
| chr14:21396830
|
C | A | 1 | a0001c0014t0001g0125 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.5052-938G>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 27/37 | chr14 | 21396830 | ||||||
| chr14:21397094
|
T | C | 1 | a0001c0001t0001g0166 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.5051+729A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 27/37 | chr14 | 21397094 | ||||||
| chr14:21397100
|
T | G | 179 | a0001c0001t0001g0047a0001c0001t0001g0070a0001c0001t0001g0079others(176): Show | 180 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.5051+723A>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 27/37 | chr14 | 21397100 | ||||||
| chr14:21397396
|
T | C | 11 | a0002c0002t0001g0098a0002c0002t0001g0188a0002c0002t0001g0199others(8): Show | 11 | HG00438.hp1 HG02280.hp2 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.5051+427A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 27/37 | chr14 | 21397396 | ||||||
| chr14:21397737
|
A | G | 1 | a0002c0002t0001g0211 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.5051+86T>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 27/37 | chr14 | 21397737 | ||||||
| chr14:21397750
|
T | C | 16 | a0001c0001t0001g0167a0001c0001t0001g0237a0001c0001t0002g0002others(13): Show | 16 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.5051+73A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 27/37 | chr14 | 21397750 | ||||||
| chr14:21398602
|
T | C | 2 | a0001c0001t0001g0221a0001c0001t0001g0223 | 2 | HG03704.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.4922-650A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 26/37 | chr14 | 21398602 | ||||||
| chr14:21398636
|
T | G | 7 | a0001c0001t0001g0167a0001c0001t0001g0237a0001c0001t0002g0039others(4): Show | 8 | HG01884.hp1 HG02257.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.4922-684A>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 26/37 | chr14 | 21398636 | ||||||
| chr14:21398699
|
C | T | 1 | a0001c0001t0001g0245 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.4922-747G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 26/37 | chr14 | 21398699 | ||||||
| chr14:21398987
|
C | T | 2 | a0002c0002t0001g0114a0002c0002t0001g0115 | 2 | HG01258.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.4921+615G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 26/37 | chr14 | 21398987 | ||||||
| chr14:21399039
|
G | A | 3 | a0001c0001t0001g0236a0001c0001t0001g0238a0001c0001t0002g0038 | 3 | HG02055.hp2 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.4921+563C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 26/37 | chr14 | 21399039 | ||||||
| chr14:21399068
|
A | C | 3 | a0001c0001t0001g0135a0001c0001t0001g0153a0001c0001t0001g0158 | 3 | HG02071.hp1 HG02071.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.4921+534T>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 26/37 | chr14 | 21399068 | ||||||
| chr14:21399100
|
G | A | 15 | a0001c0001t0003g0128a0001c0001t0003g0130a0001c0001t0003g0142others(12): Show | 15 | HG02055.hp1 HG02258.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.4921+502C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 26/37 | chr14 | 21399100 | ||||||
| chr14:21399870
|
T | C | 14 | a0001c0001t0003g0128a0001c0001t0003g0130a0001c0001t0003g0142others(11): Show | 14 | HG02055.hp1 HG02258.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.4817+111A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 25/37 | chr14 | 21399870 | ||||||
| chr14:21400089
|
G | A | 1 | a0002c0002t0001g0104 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.4728-19C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 24/37 | chr14 | 21400089 | ||||||
| chr14:21400639
|
T | A | 1 | a0001c0001t0001g0166 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.4371-27A>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 22/37 | chr14 | 21400639 | ||||||
| chr14:21400857
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.4370+18C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 22/37 | chr14 | 21400857 | ||||||
| chr14:21401117
|
C | T | 2 | a0002c0007t0001g0231a0002c0007t0001g0232 | 2 | HG02895.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.4174-46G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 21/37 | chr14 | 21401117 | ||||||
| chr14:21401199
|
T | C | 2 | a0001c0001t0003g0218a0001c0001t0003g0242 | 2 | HG02145.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.4174-128A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 21/37 | chr14 | 21401199 | ||||||
| chr14:21401546
|
C | CT | 184 | a0001c0001t0001g0047a0001c0001t0001g0070a0001c0001t0001g0079others(181): Show | 185 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.4063-34dupA | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 20/37 | chr14 | 21401546 | ||||||
| chr14:21401549
|
T | C | 4 | a0001c0001t0003g0218a0001c0001t0003g0242a0001c0009t0001g0239others(1): Show | 4 | HG02145.hp1 HG02615.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.4063-36A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 20/37 | chr14 | 21401549 | ||||||
| chr14:21401602
|
T | A | 1 | a0002c0002t0001g0083 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.4063-89A>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 20/37 | chr14 | 21401602 | ||||||
| chr14:21401654
|
C | T | 1 | a0002c0002t0001g0190 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.4063-141G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 20/37 | chr14 | 21401654 | ||||||
| chr14:21401661
|
C | T | 1 | a0002c0002t0001g0092 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.4063-148G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 20/37 | chr14 | 21401661 | ||||||
| chr14:21401719
|
G | A | 1 | a0001c0001t0001g0123 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.4063-206C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 20/37 | chr14 | 21401719 | ||||||
| chr14:21401852
|
C | T | 4 | a0002c0002t0001g0102a0002c0002t0001g0111a0002c0002t0001g0112others(1): Show | 4 | NA18942.hp2 NA18967.hp1 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.4062+105G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 20/37 | chr14 | 21401852 | ||||||
| chr14:21402234
|
A | G | 1 | a0001c0003t0001g0058 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.3883-98T>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 19/37 | chr14 | 21402234 | ||||||
| chr14:21402239
|
C | T | 1 | a0001c0003t0001g0058 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.3882+97G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 19/37 | chr14 | 21402239 | ||||||
| chr14:21402261
|
T | G | 1 | a0001c0001t0001g0247 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3882+75A>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 19/37 | chr14 | 21402261 | ||||||
| chr14:21402295
|
A | C | 1 | a0002c0002t0001g0211 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.3882+41T>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 19/37 | chr14 | 21402295 | ||||||
| chr14:21402330
|
A | G | 1 | a0002c0002t0001g0254 | 1 | HG01891.hp2 | splice_region_variant&intron_variant | LOW | c.3882+6T>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 19/37 | chr14 | 21402330 | ||||||
| chr14:21402554
|
C | G | 1 | a0001c0003t0001g0229 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.3715-51G>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 18/37 | chr14 | 21402554 | ||||||
| chr14:21402588
|
C | A | 5 | a0001c0001t0001g0167a0001c0001t0001g0237a0001c0001t0002g0039others(2): Show | 5 | HG01884.hp1 HG02257.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.3715-85G>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 18/37 | chr14 | 21402588 | ||||||
| chr14:21402702
|
C | T | 1 | a0001c0014t0001g0125 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.3715-199G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 18/37 | chr14 | 21402702 | ||||||
| chr14:21402738
|
G | T | 2 | a0002c0002t0001g0114a0002c0002t0001g0115 | 2 | HG01258.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.3715-235C>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 18/37 | chr14 | 21402738 | ||||||
| chr14:21403415
|
GACAGAGT others(4): Show |
G | 1 | a0001c0001t0003g0163 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3518+27_3518+37del others(11): Show |
CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 17/37 | chr14 | 21403415 | ||||||
| chr14:21403826
|
C | A | 2 | a0001c0001t0003g0218a0001c0001t0003g0242 | 2 | HG02145.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.3308-163G>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 16/37 | chr14 | 21403826 | ||||||
| chr14:21403827
|
G | A | 1 | a0001c0001t0003g0235 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3308-164C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 16/37 | chr14 | 21403827 | ||||||
| chr14:21403840
|
T | G | 171 | a0001c0001t0001g0047a0001c0001t0001g0070a0001c0001t0001g0079others(168): Show | 171 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.3308-177A>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 16/37 | chr14 | 21403840 | ||||||
| chr14:21403861
|
G | A | 2 | a0001c0001t0001g0221a0001c0001t0001g0223 | 2 | HG03704.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.3308-198C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 16/37 | chr14 | 21403861 | ||||||
| chr14:21403906
|
C | T | 1 | a0001c0001t0001g0247 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3308-243G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 16/37 | chr14 | 21403906 | ||||||
| chr14:21403920
|
G | A | 1 | a0002c0002t0001g0160 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3308-257C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 16/37 | chr14 | 21403920 | ||||||
| chr14:21403928
|
G | A | 1 | a0001c0001t0003g0234 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3308-265C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 16/37 | chr14 | 21403928 | ||||||
| chr14:21403968
|
G | A | 1 | a0001c0003t0001g0078 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.3308-305C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 16/37 | chr14 | 21403968 | ||||||
| chr14:21403969
|
G | A | 1 | a0001c0001t0001g0244 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3308-306C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 16/37 | chr14 | 21403969 | ||||||
| chr14:21404085
|
C | T | 2 | a0001c0006t0001g0001a0001c0006t0001g0126 | 3 | HG02559.hp2 HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.3308-422G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 16/37 | chr14 | 21404085 | ||||||
| chr14:21404098
|
T | TA | 7 | a0001c0001t0001g0167a0001c0001t0003g0163a0001c0001t0003g0218others(4): Show | 7 | HG01261.hp2 HG01884.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.3308-436dupT | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 16/37 | chr14 | 21404098 | ||||||
| chr14:21404098
|
TA | T | 5 | a0001c0001t0001g0082a0001c0001t0002g0012a0001c0006t0001g0001others(2): Show | 6 | HG02451.hp1 HG02559.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.3308-436delT | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 16/37 | chr14 | 21404098 | ||||||
| chr14:21404140
|
G | A | 1 | a0002c0002t0001g0124 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.3308-477C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 16/37 | chr14 | 21404140 | ||||||
| chr14:21404217
|
G | T | 1 | a0001c0001t0002g0010 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3308-554C>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 16/37 | chr14 | 21404217 | ||||||
| chr14:21404346
|
C | T | 2 | a0001c0001t0003g0218a0001c0001t0003g0242 | 2 | HG02145.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.3308-683G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 16/37 | chr14 | 21404346 | ||||||
| chr14:21404361
|
G | C | 1 | a0001c0001t0001g0079 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3308-698C>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 16/37 | chr14 | 21404361 | ||||||
| chr14:21404382
|
T | C | 1 | a0002c0007t0001g0232 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.3308-719A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 16/37 | chr14 | 21404382 | ||||||
| chr14:21404398
|
T | TA | 16 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0174others(13): Show | 16 | HG00323.hp1 HG01175.hp1 HG01517.hp1 others(13): Show |
intron_variant | MODIFIER | c.3308-736dupT | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 16/37 | chr14 | 21404398 | ||||||
| chr14:21404398
|
TA | T | 26 | a0001c0001t0001g0236a0001c0001t0001g0244a0001c0001t0001g0245others(23): Show | 26 | HG01069.hp2 HG01243.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.3308-736delT | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 16/37 | chr14 | 21404398 | ||||||
| chr14:21404416
|
A | C | 3 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004 | 3 | HG01884.hp2 HG01891.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3308-753T>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 16/37 | chr14 | 21404416 | ||||||
| chr14:21404418
|
A | C | 1 | a0002c0002t0001g0201 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.3308-755T>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 16/37 | chr14 | 21404418 | ||||||
| chr14:21404506
|
T | C | 2 | a0001c0009t0001g0239a0001c0009t0001g0240 | 2 | HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.3307+703A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 16/37 | chr14 | 21404506 | ||||||
| chr14:21404567
|
G | A | 5 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0085others(2): Show | 5 | HG01109.hp2 HG02976.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.3307+642C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 16/37 | chr14 | 21404567 | ||||||
| chr14:21404647
|
T | C | 2 | a0001c0008t0001g0087a0001c0008t0001g0088 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3307+562A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 16/37 | chr14 | 21404647 | ||||||
| chr14:21404715
|
G | A | 1 | a0001c0001t0002g0009 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.3307+494C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 16/37 | chr14 | 21404715 | ||||||
| chr14:21405065
|
G | A | 2 | a0001c0009t0001g0239a0001c0009t0001g0240 | 2 | HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.3307+144C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 16/37 | chr14 | 21405065 | ||||||
| chr14:21405152
|
C | A | 1 | a0002c0002t0001g0190 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3307+57G>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 16/37 | chr14 | 21405152 | ||||||
| chr14:21405526
|
T | C | 1 | a0001c0003t0001g0071 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.3052-62A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 15/37 | chr14 | 21405526 | ||||||
| chr14:21405909
|
G | C | 178 | a0001c0001t0001g0047a0001c0001t0001g0070a0001c0001t0001g0079others(175): Show | 178 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.2908-45C>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 14/37 | chr14 | 21405909 | ||||||
| chr14:21405935
|
A | G | 15 | a0001c0001t0003g0128a0001c0001t0003g0130a0001c0001t0003g0142others(12): Show | 15 | HG02055.hp1 HG02258.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.2908-71T>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 14/37 | chr14 | 21405935 | ||||||
| chr14:21406030
|
CCT | C | 5 | a0001c0001t0001g0167a0001c0001t0001g0237a0001c0001t0002g0039others(2): Show | 5 | HG01884.hp1 HG02257.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2908-168_2908-167d others(4): Show |
CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 14/37 | chr14 | 21406030 | ||||||
| chr14:21406098
|
T | C | 5 | a0001c0001t0003g0163a0001c0001t0003g0218a0001c0001t0003g0242others(2): Show | 5 | HG02145.hp1 HG02451.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.2908-234A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 14/37 | chr14 | 21406098 | ||||||
| chr14:21406156
|
C | T | 2 | a0002c0002t0001g0116a0002c0002t0001g0117 | 2 | NA18947.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.2908-292G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 14/37 | chr14 | 21406156 | ||||||
| chr14:21406312
|
A | G | 8 | a0001c0001t0001g0167a0001c0001t0001g0237a0001c0001t0002g0039others(5): Show | 9 | HG01261.hp2 HG01884.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.2908-448T>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 14/37 | chr14 | 21406312 | ||||||
| chr14:21406425
|
G | A | 1 | a0002c0002t0001g0191 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2907+431C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 14/37 | chr14 | 21406425 | ||||||
| chr14:21406591
|
A | G | 3 | a0001c0001t0001g0082a0001c0001t0002g0010a0001c0001t0002g0012 | 3 | HG02145.hp2 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2907+265T>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 14/37 | chr14 | 21406591 | ||||||
| chr14:21406735
|
C | A | 1 | a0001c0001t0003g0163 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2907+121G>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 14/37 | chr14 | 21406735 | ||||||
| chr14:21406781
|
T | C | 1 | a0001c0001t0003g0234 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2907+75A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 14/37 | chr14 | 21406781 | ||||||
| chr14:21406811
|
G | A | 1 | a0002c0002t0001g0098 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.2907+45C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 14/37 | chr14 | 21406811 | ||||||
| chr14:21406853
|
C | A | 1 | a0001c0003t0001g0077 | 1 | HG02683.hp2 | splice_region_variant&intron_variant | LOW | c.2907+3G>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 14/37 | chr14 | 21406853 | ||||||
| chr14:21407317
|
C | T | 12 | a0001c0001t0001g0167a0001c0001t0002g0039a0001c0001t0002g0040others(9): Show | 13 | HG01261.hp2 HG01884.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.2731-285G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 13/37 | chr14 | 21407317 | ||||||
| chr14:21407328
|
T | C | 177 | a0001c0001t0001g0047a0001c0001t0001g0070a0001c0001t0001g0079others(174): Show | 177 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.2731-296A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 13/37 | chr14 | 21407328 | ||||||
| chr14:21407338
|
A | G | 1 | a0001c0001t0001g0222 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.2731-306T>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 13/37 | chr14 | 21407338 | ||||||
| chr14:21407403
|
C | T | 1 | a0001c0001t0001g0140 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2731-371G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 13/37 | chr14 | 21407403 | ||||||
| chr14:21407556
|
C | T | 1 | a0001c0001t0001g0253 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2731-524G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 13/37 | chr14 | 21407556 | ||||||
| chr14:21407583
|
A | G | 3 | a0001c0001t0001g0236a0001c0001t0001g0238a0001c0001t0002g0038 | 3 | HG02055.hp2 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2731-551T>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 13/37 | chr14 | 21407583 | ||||||
| chr14:21407985
|
T | C | 13 | a0001c0001t0001g0167a0001c0001t0001g0237a0001c0001t0002g0039others(10): Show | 14 | HG01261.hp2 HG01884.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.2730+327A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 13/37 | chr14 | 21407985 | ||||||
| chr14:21408045
|
G | A | 3 | a0002c0002t0001g0100a0002c0002t0001g0105a0002c0002t0001g0212 | 3 | HG02083.hp2 NA19012.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.2730+267C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 13/37 | chr14 | 21408045 | ||||||
| chr14:21408206
|
T | C | 2 | a0001c0001t0003g0218a0001c0001t0003g0242 | 2 | HG02145.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.2730+106A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 13/37 | chr14 | 21408206 | ||||||
| chr14:21408270
|
G | A | 1 | a0001c0014t0001g0125 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2730+42C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 13/37 | chr14 | 21408270 | ||||||
| chr14:21408573
|
G | GA | 9 | a0001c0001t0001g0167a0001c0001t0001g0237a0001c0001t0002g0039others(6): Show | 10 | HG01261.hp2 HG01884.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.2487-19dupT | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 12/37 | chr14 | 21408573 | ||||||
| chr14:21408574
|
A | G | 1 | a0001c0001t0001g0193 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2487-19T>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 12/37 | chr14 | 21408574 | ||||||
| chr14:21408592
|
G | A | 1 | a0001c0001t0001g0129 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2487-37C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 12/37 | chr14 | 21408592 | ||||||
| chr14:21408603
|
T | TA | 16 | a0001c0001t0001g0167a0001c0001t0001g0237a0001c0001t0002g0002others(13): Show | 16 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.2487-49dupT | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 12/37 | chr14 | 21408603 | ||||||
| chr14:21408893
|
T | A | 25 | a0001c0001t0001g0236a0001c0001t0001g0238a0001c0001t0001g0244others(22): Show | 25 | HG01243.hp2 HG02055.hp1 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.2365-68A>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 11/37 | chr14 | 21408893 | ||||||
| chr14:21409149
|
A | C | 1 | a0001c0014t0001g0125 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2365-324T>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 11/37 | chr14 | 21409149 | ||||||
| chr14:21409163
|
G | A | 1 | a0001c0001t0001g0181 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2365-338C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 11/37 | chr14 | 21409163 | ||||||
| chr14:21409171
|
G | C | 76 | a0001c0001t0001g0081a0002c0002t0001g0057a0002c0002t0001g0083others(73): Show | 76 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.2365-346C>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 11/37 | chr14 | 21409171 | ||||||
| chr14:21409347
|
A | C | 25 | a0001c0001t0001g0236a0001c0001t0001g0238a0001c0001t0001g0244others(22): Show | 25 | HG01243.hp2 HG02055.hp1 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.2364+504T>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 11/37 | chr14 | 21409347 | ||||||
| chr14:21409380
|
G | C | 1 | a0001c0001t0001g0175 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2364+471C>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 11/37 | chr14 | 21409380 | ||||||
| chr14:21409498
|
T | C | 2 | a0001c0001t0001g0129a0001c0001t0001g0154 | 2 | HG01346.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.2364+353A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 11/37 | chr14 | 21409498 | ||||||
| chr14:21409508
|
T | C | 1 | a0001c0001t0002g0023 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2364+343A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 11/37 | chr14 | 21409508 | ||||||
| chr14:21409529
|
T | C | 5 | a0001c0001t0003g0218a0001c0001t0003g0242a0001c0009t0001g0239others(2): Show | 5 | HG01261.hp2 HG02145.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.2364+322A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 11/37 | chr14 | 21409529 | ||||||
| chr14:21409586
|
A | T | 2 | a0001c0009t0001g0239a0001c0009t0001g0240 | 2 | HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2364+265T>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 11/37 | chr14 | 21409586 | ||||||
| chr14:21409615
|
G | A | 10 | a0001c0001t0001g0236a0001c0001t0001g0238a0001c0001t0001g0244others(7): Show | 10 | HG01243.hp2 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.2364+236C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 11/37 | chr14 | 21409615 | ||||||
| chr14:21409721
|
T | C | 2 | a0001c0001t0003g0218a0001c0001t0003g0242 | 2 | HG02145.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.2364+130A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 11/37 | chr14 | 21409721 | ||||||
| chr14:21410170
|
T | C | 4 | a0001c0001t0001g0167a0001c0001t0002g0039a0001c0001t0002g0040others(1): Show | 4 | HG01884.hp1 HG02257.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.2227-182A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 10/37 | chr14 | 21410170 | ||||||
| chr14:21410668
|
A | G | 1 | a0001c0001t0002g0027 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2227-680T>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 10/37 | chr14 | 21410668 | ||||||
| chr14:21410805
|
C | T | 1 | a0002c0002t0004g0257 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.2227-817G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 10/37 | chr14 | 21410805 | ||||||
| chr14:21410998
|
T | G | 13 | a0001c0001t0001g0167a0001c0001t0001g0237a0001c0001t0002g0039others(10): Show | 14 | HG01261.hp2 HG01884.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.2227-1010A>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 10/37 | chr14 | 21410998 | ||||||
| chr14:21411452
|
A | G | 1 | a0001c0001t0003g0163 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2226+1461T>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 10/37 | chr14 | 21411452 | ||||||
| chr14:21411508
|
T | A | 1 | a0001c0001t0003g0163 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2226+1405A>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 10/37 | chr14 | 21411508 | ||||||
| chr14:21411788
|
G | A | 5 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0085others(2): Show | 5 | HG01109.hp2 HG02976.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.2226+1125C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 10/37 | chr14 | 21411788 | ||||||
| chr14:21411948
|
C | T | 1 | a0001c0001t0003g0128 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2226+965G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 10/37 | chr14 | 21411948 | ||||||
| chr14:21412049
|
G | A | 2 | a0001c0009t0001g0239a0001c0009t0001g0240 | 2 | HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2226+864C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 10/37 | chr14 | 21412049 | ||||||
| chr14:21412159
|
T | G | 1 | a0001c0014t0001g0125 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2226+754A>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 10/37 | chr14 | 21412159 | ||||||
| chr14:21412198
|
T | G | 2 | a0001c0009t0001g0239a0001c0009t0001g0240 | 2 | HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2226+715A>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 10/37 | chr14 | 21412198 | ||||||
| chr14:21412233
|
C | T | 15 | a0001c0001t0003g0128a0001c0001t0003g0130a0001c0001t0003g0142others(12): Show | 15 | HG02055.hp1 HG02258.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.2226+680G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 10/37 | chr14 | 21412233 | ||||||
| chr14:21412543
|
G | A | 3 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004 | 3 | HG01884.hp2 HG01891.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2226+370C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 10/37 | chr14 | 21412543 | ||||||
| chr14:21412550
|
T | C | 7 | a0001c0001t0001g0167a0001c0001t0001g0237a0001c0001t0002g0039others(4): Show | 8 | HG01884.hp1 HG02257.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.2226+363A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 10/37 | chr14 | 21412550 | ||||||
| chr14:21412605
|
T | G | 5 | a0001c0001t0003g0218a0001c0001t0003g0242a0001c0009t0001g0239others(2): Show | 5 | HG01261.hp2 HG02145.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.2226+308A>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 10/37 | chr14 | 21412605 | ||||||
| chr14:21412808
|
C | T | 4 | a0001c0001t0003g0218a0001c0001t0003g0242a0001c0009t0001g0239others(1): Show | 4 | HG02145.hp1 HG02615.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2226+105G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 10/37 | chr14 | 21412808 | ||||||
| chr14:21412842
|
T | A | 1 | a0002c0002t0001g0188 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2226+71A>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 10/37 | chr14 | 21412842 | ||||||
| chr14:21413122
|
G | A | 2 | a0002c0002t0001g0201a0002c0002t0001g0207 | 2 | NA18951.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.2143-126C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 9/37 | chr14 | 21413122 | ||||||
| chr14:21413192
|
T | G | 1 | a0002c0002t0001g0089 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.2143-196A>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 9/37 | chr14 | 21413192 | ||||||
| chr14:21413346
|
T | C | 2 | a0001c0008t0001g0087a0001c0008t0001g0088 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2143-350A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 9/37 | chr14 | 21413346 | ||||||
| chr14:21413395
|
C | CT | 7 | a0001c0001t0001g0123a0001c0001t0001g0245a0001c0001t0003g0243others(4): Show | 7 | HG01243.hp2 HG02630.hp2 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.2143-400dupA | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 9/37 | chr14 | 21413395 | ||||||
| chr14:21413411
|
T | C | 6 | a0001c0001t0001g0167a0001c0001t0002g0039a0001c0001t0002g0040others(3): Show | 7 | HG01884.hp1 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.2143-415A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 9/37 | chr14 | 21413411 | ||||||
| chr14:21413446
|
G | T | 15 | a0001c0001t0003g0128a0001c0001t0003g0130a0001c0001t0003g0142others(12): Show | 15 | HG02055.hp1 HG02258.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.2143-450C>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 9/37 | chr14 | 21413446 | ||||||
| chr14:21413486
|
C | T | 5 | a0002c0002t0001g0136a0002c0002t0001g0148a0002c0002t0001g0159others(2): Show | 5 | HG02615.hp2 HG02897.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.2143-490G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 9/37 | chr14 | 21413486 | ||||||
| chr14:21413489
|
C | T | 2 | a0001c0009t0001g0239a0001c0009t0001g0240 | 2 | HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2143-493G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 9/37 | chr14 | 21413489 | ||||||
| chr14:21413654
|
T | A | 1 | a0001c0003t0001g0091 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2142+647A>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 9/37 | chr14 | 21413654 | ||||||
| chr14:21413762
|
C | G | 2 | a0001c0006t0001g0001a0001c0006t0001g0126 | 3 | HG02559.hp2 HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2142+539G>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 9/37 | chr14 | 21413762 | ||||||
| chr14:21413825
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2142+476G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 9/37 | chr14 | 21413825 | ||||||
| chr14:21413855
|
C | A | 4 | a0001c0001t0001g0167a0001c0001t0002g0039a0001c0001t0002g0040others(1): Show | 4 | HG01884.hp1 HG02257.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.2142+446G>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 9/37 | chr14 | 21413855 | ||||||
| chr14:21414146
|
G | A | 1 | a0001c0001t0001g0247 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2142+155C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 9/37 | chr14 | 21414146 | ||||||
| chr14:21414266
|
G | A | 1 | a0001c0003t0001g0050 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2142+35C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 9/37 | chr14 | 21414266 | ||||||
| chr14:21414424
|
G | A | 1 | a0001c0014t0001g0125 | 1 | HG01261.hp2 | splice_region_variant&intron_variant | LOW | c.2025-6C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 8/37 | chr14 | 21414424 | ||||||
| chr14:21414490
|
G | C | 3 | a0001c0005t0002g0036a0001c0005t0002g0037a0001c0005t0002g0042 | 3 | HG02818.hp1 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2025-72C>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 8/37 | chr14 | 21414490 | ||||||
| chr14:21414490
|
G | T | 6 | a0001c0001t0001g0132a0001c0001t0001g0146a0001c0001t0001g0147others(3): Show | 6 | HG00733.hp2 HG00735.hp2 HG01069.hp1 others(3): Show |
intron_variant | MODIFIER | c.2025-72C>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 8/37 | chr14 | 21414490 | ||||||
| chr14:21414671
|
T | C | 2 | a0002c0002t0001g0083a0002c0002t0001g0084 | 2 | HG02622.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2025-253A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 8/37 | chr14 | 21414671 | ||||||
| chr14:21415132
|
G | T | 6 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(3): Show | 6 | HG01884.hp2 HG01891.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1969-139C>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 7/37 | chr14 | 21415132 | ||||||
| chr14:21415321
|
T | C | 4 | a0001c0001t0003g0218a0001c0001t0003g0242a0001c0009t0001g0239others(1): Show | 4 | HG02145.hp1 HG02615.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1968+253A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 7/37 | chr14 | 21415321 | ||||||
| chr14:21415325
|
A | G | 1 | a0001c0001t0003g0163 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1968+249T>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 7/37 | chr14 | 21415325 | ||||||
| chr14:21415506
|
A | AAAAT | 66 | a0001c0001t0001g0070a0001c0001t0001g0135a0001c0001t0001g0152others(63): Show | 66 | HG00323.hp1 HG00438.hp2 HG00673.hp1 others(63): Show |
intron_variant | MODIFIER | c.1968+64_1968+67dup others(4): Show |
CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 7/37 | chr14 | 21415506 | ||||||
| chr14:21415506
|
A | AAAATAAA others(1): Show |
5 | a0001c0001t0003g0142a0001c0001t0003g0144a0001c0003t0001g0075others(2): Show | 5 | HG02895.hp1 HG02897.hp1 NA18947.hp1 others(2): Show |
intron_variant | MODIFIER | c.1968+60_1968+67dup others(8): Show |
CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 7/37 | chr14 | 21415506 | ||||||
| chr14:21415506
|
AAAATAAA others(1): Show |
A | 4 | a0001c0001t0001g0167a0001c0001t0002g0039a0001c0001t0002g0040others(1): Show | 4 | HG01884.hp1 HG02257.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1968+60_1968+67del others(8): Show |
CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 7/37 | chr14 | 21415506 | ||||||
| chr14:21415506
|
AAAATAAA others(5): Show |
A | 1 | a0001c0003t0001g0255 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1968+56_1968+67del others(12): Show |
CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 7/37 | chr14 | 21415506 | ||||||
| chr14:21415510
|
T | A | 1 | a0001c0014t0001g0125 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1968+64A>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 7/37 | chr14 | 21415510 | ||||||
| chr14:21415514
|
T | A | 1 | a0001c0014t0001g0125 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1968+60A>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 7/37 | chr14 | 21415514 | ||||||
| chr14:21415518
|
T | A | 1 | a0001c0014t0001g0125 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1968+56A>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 7/37 | chr14 | 21415518 | ||||||
| chr14:21415522
|
T | A | 1 | a0001c0014t0001g0125 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1968+52A>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 7/37 | chr14 | 21415522 | ||||||
| chr14:21415536
|
AATAAATA others(5): Show |
A | 2 | a0001c0006t0001g0001a0001c0006t0001g0126 | 3 | HG02559.hp2 HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1968+26_1968+37del others(12): Show |
CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 7/37 | chr14 | 21415536 | ||||||
| chr14:21415542
|
T | A | 1 | a0001c0001t0001g0138 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1968+32A>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 7/37 | chr14 | 21415542 | ||||||
| chr14:21415936
|
T | G | 2 | a0001c0006t0001g0001a0001c0006t0001g0126 | 3 | HG02559.hp2 HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1717-29A>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21415936 | ||||||
| chr14:21415965
|
A | T | 1 | a0001c0003t0002g0035 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1717-58T>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21415965 | ||||||
| chr14:21416247
|
G | T | 12 | a0001c0001t0001g0167a0001c0001t0002g0039a0001c0001t0002g0040others(9): Show | 13 | HG01261.hp2 HG01884.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1717-340C>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21416247 | ||||||
| chr14:21416260
|
T | G | 4 | a0001c0001t0003g0218a0001c0001t0003g0242a0001c0009t0001g0239others(1): Show | 4 | HG02145.hp1 HG02615.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1717-353A>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21416260 | ||||||
| chr14:21416311
|
A | C | 1 | a0001c0003t0001g0091 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1717-404T>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21416311 | ||||||
| chr14:21416340
|
A | C | 2 | a0001c0006t0001g0001a0001c0006t0001g0126 | 3 | HG02559.hp2 HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1717-433T>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21416340 | ||||||
| chr14:21416377
|
C | T | 1 | a0001c0001t0003g0163 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1717-470G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21416377 | ||||||
| chr14:21416484
|
G | A | 3 | a0001c0005t0002g0036a0001c0005t0002g0037a0001c0005t0002g0042 | 3 | HG02818.hp1 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1717-577C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21416484 | ||||||
| chr14:21416494
|
A | C | 1 | a0002c0002t0001g0201 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1717-587T>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21416494 | ||||||
| chr14:21416583
|
T | C | 1 | a0001c0001t0003g0163 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1717-676A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21416583 | ||||||
| chr14:21416614
|
A | C | 1 | a0001c0001t0003g0243 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1717-707T>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21416614 | ||||||
| chr14:21416728
|
A | G | 5 | a0001c0001t0003g0163a0001c0001t0003g0218a0001c0001t0003g0242others(2): Show | 5 | HG02145.hp1 HG02451.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1717-821T>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21416728 | ||||||
| chr14:21416957
|
G | A | 1 | a0002c0002t0001g0230 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1717-1050C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21416957 | ||||||
| chr14:21417041
|
A | C | 1 | a0001c0014t0001g0125 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1717-1134T>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21417041 | ||||||
| chr14:21417059
|
G | A | 1 | a0001c0001t0003g0163 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1717-1152C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21417059 | ||||||
| chr14:21417290
|
G | A | 1 | a0002c0002t0001g0188 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1717-1383C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21417290 | ||||||
| chr14:21417372
|
G | A | 1 | a0001c0014t0001g0125 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1717-1465C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21417372 | ||||||
| chr14:21417448
|
G | C | 1 | a0001c0001t0002g0040 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1717-1541C>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21417448 | ||||||
| chr14:21417559
|
C | A | 12 | a0001c0001t0001g0167a0001c0001t0002g0039a0001c0001t0002g0040others(9): Show | 13 | HG01261.hp2 HG01884.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1717-1652G>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21417559 | ||||||
| chr14:21417621
|
G | A | 2 | a0001c0001t0003g0131a0001c0001t0003g0248 | 2 | HG02109.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1717-1714C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21417621 | ||||||
| chr14:21417631
|
C | G | 12 | a0001c0001t0001g0167a0001c0001t0002g0039a0001c0001t0002g0040others(9): Show | 13 | HG01261.hp2 HG01884.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1717-1724G>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21417631 | ||||||
| chr14:21417638
|
A | G | 36 | a0002c0002t0001g0089a0002c0002t0001g0092a0002c0002t0001g0094others(33): Show | 36 | HG00323.hp1 HG00438.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.1717-1731T>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21417638 | ||||||
| chr14:21417727
|
G | A | 3 | a0002c0002t0001g0179a0002c0002t0001g0183a0002c0002t0001g0184 | 3 | HG02257.hp2 NA18522.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1717-1820C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21417727 | ||||||
| chr14:21417787
|
G | A | 3 | a0001c0005t0002g0036a0001c0005t0002g0037a0001c0005t0002g0042 | 3 | HG02818.hp1 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1717-1880C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21417787 | ||||||
| chr14:21417803
|
G | A | 36 | a0002c0002t0001g0089a0002c0002t0001g0092a0002c0002t0001g0094others(33): Show | 36 | HG00323.hp1 HG00438.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.1717-1896C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21417803 | ||||||
| chr14:21417809
|
G | A | 1 | a0001c0001t0001g0245 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1717-1902C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21417809 | ||||||
| chr14:21417851
|
CA | C | 11 | a0001c0001t0001g0132a0001c0001t0001g0146a0001c0001t0001g0147others(8): Show | 11 | HG00733.hp1 HG00733.hp2 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.1717-1945delT | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21417851 | ||||||
| chr14:21417851
|
CAA | C | 134 | a0001c0001t0001g0047a0001c0001t0001g0070a0001c0001t0001g0079others(131): Show | 134 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.1717-1946_1717-194 others(6): Show |
CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21417851 | ||||||
| chr14:21417852
|
A | T | 1 | a0002c0002t0001g0089 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1717-1945T>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21417852 | ||||||
| chr14:21417853
|
A | C | 1 | a0002c0002t0001g0089 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1717-1946T>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21417853 | ||||||
| chr14:21417865
|
A | T | 14 | a0001c0001t0001g0132a0001c0001t0001g0146a0001c0001t0001g0147others(11): Show | 14 | HG00733.hp1 HG00733.hp2 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.1717-1958T>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21417865 | ||||||
| chr14:21417865
|
AAT | A | 22 | a0001c0001t0001g0080a0001c0001t0001g0085a0001c0001t0001g0086others(19): Show | 22 | HG00280.hp1 HG00438.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1717-1960_1717-195 others(6): Show |
CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21417865 | ||||||
| chr14:21417866
|
AT | A | 17 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0238others(14): Show | 17 | HG01243.hp2 HG01884.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.1717-1960delA | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21417866 | ||||||
| chr14:21417867
|
T | A | 18 | a0001c0001t0001g0167a0001c0001t0002g0002a0001c0001t0003g0128others(15): Show | 18 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.1717-1960A>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21417867 | ||||||
| chr14:21417869
|
T | A | 19 | a0001c0001t0001g0085a0001c0001t0002g0003a0001c0001t0002g0004others(16): Show | 19 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1717-1962A>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21417869 | ||||||
| chr14:21417871
|
T | A | 1 | a0001c0001t0003g0235 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1717-1964A>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21417871 | ||||||
| chr14:21417881
|
T | A | 1 | a0001c0001t0001g0169 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1717-1974A>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21417881 | ||||||
| chr14:21417882
|
A | AAT | 5 | a0001c0001t0002g0039a0001c0001t0002g0040a0001c0001t0002g0041others(2): Show | 5 | HG02257.hp1 HG02630.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1717-1977_1717-197 others(6): Show |
CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21417882 | ||||||
| chr14:21417882
|
A | T | 1 | a0001c0001t0001g0169 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1717-1975T>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21417882 | ||||||
| chr14:21417896
|
T | C | 2 | a0001c0001t0001g0169a0008c0017t0002g0029 | 2 | HG02155.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1717-1989A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21417896 | ||||||
| chr14:21418153
|
C | T | 26 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0238others(23): Show | 26 | HG01243.hp2 HG02055.hp1 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.1717-2246G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21418153 | ||||||
| chr14:21418191
|
G | A | 2 | a0002c0002t0001g0199a0002c0002t0001g0200 | 2 | HG02280.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1717-2284C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21418191 | ||||||
| chr14:21418452
|
G | A | 3 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004 | 3 | HG01884.hp2 HG01891.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1717-2545C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21418452 | ||||||
| chr14:21418554
|
G | C | 5 | a0001c0001t0001g0150a0001c0001t0002g0005a0001c0001t0002g0006others(2): Show | 5 | HG00408.hp2 HG00544.hp2 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.1717-2647C>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21418554 | ||||||
| chr14:21418643
|
G | A | 1 | a0002c0002t0001g0160 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1717-2736C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21418643 | ||||||
| chr14:21418685
|
A | G | 40 | a0001c0001t0001g0140a0001c0001t0001g0152a0001c0003t0001g0066others(37): Show | 40 | HG00323.hp1 HG00438.hp2 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.1717-2778T>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21418685 | ||||||
| chr14:21418771
|
G | A | 6 | a0001c0001t0001g0132a0001c0001t0001g0146a0001c0001t0001g0147others(3): Show | 6 | HG00733.hp2 HG00735.hp2 HG01069.hp1 others(3): Show |
intron_variant | MODIFIER | c.1717-2864C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21418771 | ||||||
| chr14:21418990
|
G | A | 1 | a0002c0002t0001g0226 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1717-3083C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21418990 | ||||||
| chr14:21419067
|
T | A | 1 | a0001c0001t0002g0011 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1717-3160A>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21419067 | ||||||
| chr14:21419212
|
TA | T | 16 | a0001c0001t0001g0146a0001c0001t0003g0128a0001c0001t0003g0130others(13): Show | 16 | HG01069.hp1 HG01261.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.1717-3306delT | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21419212 | ||||||
| chr14:21419286
|
C | T | 4 | a0001c0001t0003g0218a0001c0001t0003g0242a0001c0009t0001g0239others(1): Show | 4 | HG02145.hp1 HG02615.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1717-3379G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21419286 | ||||||
| chr14:21419312
|
G | A | 215 | a0001c0001t0001g0047a0001c0001t0001g0070a0001c0001t0001g0079others(212): Show | 216 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.1717-3405C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21419312 | ||||||
| chr14:21419316
|
C | T | 16 | a0001c0001t0003g0128a0001c0001t0003g0130a0001c0001t0003g0142others(13): Show | 16 | HG01261.hp2 HG02055.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1717-3409G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21419316 | ||||||
| chr14:21419494
|
A | AAAC | 15 | a0001c0001t0003g0128a0001c0001t0003g0130a0001c0001t0003g0142others(12): Show | 15 | HG02055.hp1 HG02258.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.1717-3588_1717-358 others(7): Show |
CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21419494 | ||||||
| chr14:21419514
|
C | T | 1 | a0002c0002t0001g0105 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1717-3607G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21419514 | ||||||
| chr14:21419516
|
T | C | 215 | a0001c0001t0001g0047a0001c0001t0001g0070a0001c0001t0001g0079others(212): Show | 216 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.1717-3609A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21419516 | ||||||
| chr14:21419583
|
C | CA | 7 | a0001c0001t0001g0167a0001c0001t0002g0039a0001c0001t0002g0040others(4): Show | 8 | HG01884.hp1 HG02257.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1717-3677dupT | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21419583 | ||||||
| chr14:21419835
|
A | G | 16 | a0001c0001t0003g0128a0001c0001t0003g0130a0001c0001t0003g0142others(13): Show | 16 | HG01261.hp2 HG02055.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1717-3928T>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21419835 | ||||||
| chr14:21419928
|
C | G | 1 | a0002c0002t0001g0136 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1717-4021G>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21419928 | ||||||
| chr14:21420110
|
C | A | 20 | a0001c0001t0003g0128a0001c0001t0003g0130a0001c0001t0003g0142others(17): Show | 20 | HG01261.hp2 HG02055.hp1 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1717-4203G>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21420110 | ||||||
| chr14:21420520
|
A | G | 1 | a0001c0001t0001g0139 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1717-4613T>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21420520 | ||||||
| chr14:21420524
|
C | A | 1 | a0001c0001t0001g0139 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1717-4617G>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21420524 | ||||||
| chr14:21420571
|
T | G | 28 | a0001c0001t0001g0167a0001c0001t0001g0237a0001c0001t0002g0039others(25): Show | 29 | HG01261.hp2 HG01884.hp1 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.1717-4664A>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21420571 | ||||||
| chr14:21420644
|
T | C | 1 | a0001c0001t0002g0028 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1717-4737A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21420644 | ||||||
| chr14:21420688
|
G | C | 4 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0238others(1): Show | 4 | HG02055.hp2 HG02809.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1717-4781C>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21420688 | ||||||
| chr14:21420707
|
A | C | 4 | a0002c0002t0001g0102a0002c0002t0001g0111a0002c0002t0001g0112others(1): Show | 4 | NA18942.hp2 NA18967.hp1 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.1717-4800T>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21420707 | ||||||
| chr14:21420765
|
A | AT | 5 | a0001c0001t0001g0174a0001c0003t0001g0091a0001c0003t0001g0229others(2): Show | 5 | HG02074.hp2 HG02622.hp1 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.1717-4859dupA | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21420765 | ||||||
| chr14:21420793
|
G | A | 2 | a0001c0006t0001g0001a0001c0006t0001g0126 | 3 | HG02559.hp2 HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1717-4886C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21420793 | ||||||
| chr14:21420974
|
C | G | 6 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(3): Show | 6 | HG01884.hp2 HG01891.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1717-5067G>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21420974 | ||||||
| chr14:21421037
|
C | T | 1 | a0004c0011t0001g0095 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1716+5091G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21421037 | ||||||
| chr14:21421038
|
G | A | 2 | a0001c0001t0003g0218a0001c0001t0003g0242 | 2 | HG02145.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1716+5090C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21421038 | ||||||
| chr14:21421404
|
C | T | 8 | a0001c0001t0001g0149a0001c0001t0001g0162a0001c0001t0001g0175others(5): Show | 8 | HG00280.hp1 HG01192.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.1716+4724G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21421404 | ||||||
| chr14:21421589
|
T | G | 2 | a0001c0009t0001g0239a0001c0009t0001g0240 | 2 | HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1716+4539A>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21421589 | ||||||
| chr14:21421738
|
A | G | 1 | a0001c0001t0001g0206 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1716+4390T>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21421738 | ||||||
| chr14:21421756
|
C | A | 1 | a0002c0002t0001g0200 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1716+4372G>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21421756 | ||||||
| chr14:21421768
|
C | T | 1 | a0001c0001t0003g0163 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1716+4360G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21421768 | ||||||
| chr14:21421806
|
C | G | 27 | a0001c0001t0001g0167a0001c0001t0002g0039a0001c0001t0002g0040others(24): Show | 28 | HG01261.hp2 HG01884.hp1 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.1716+4322G>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21421806 | ||||||
| chr14:21422186
|
C | T | 1 | a0002c0002t0001g0102 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1716+3942G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21422186 | ||||||
| chr14:21422265
|
C | T | 6 | a0001c0001t0001g0134a0001c0001t0001g0155a0001c0001t0001g0171others(3): Show | 6 | HG01070.hp2 HG01071.hp2 HG02293.hp2 others(3): Show |
intron_variant | MODIFIER | c.1716+3863G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21422265 | ||||||
| chr14:21422479
|
CA | C | 15 | a0001c0001t0003g0128a0001c0001t0003g0130a0001c0001t0003g0142others(12): Show | 15 | HG02055.hp1 HG02258.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.1716+3648delT | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21422479 | ||||||
| chr14:21422524
|
C | G | 6 | a0001c0001t0001g0132a0001c0001t0001g0146a0001c0001t0001g0147others(3): Show | 6 | HG00733.hp2 HG00735.hp2 HG01069.hp1 others(3): Show |
intron_variant | MODIFIER | c.1716+3604G>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21422524 | ||||||
| chr14:21422660
|
G | A | 2 | a0001c0003t0002g0035a0008c0017t0002g0029 | 2 | HG02559.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1716+3468C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21422660 | ||||||
| chr14:21422797
|
C | T | 4 | a0001c0001t0001g0167a0001c0001t0002g0039a0001c0001t0002g0040others(1): Show | 4 | HG01884.hp1 HG02257.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1716+3331G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21422797 | ||||||
| chr14:21422892
|
G | A | 1 | a0001c0001t0001g0047 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1716+3236C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21422892 | ||||||
| chr14:21422960
|
G | C | 11 | a0002c0002t0001g0098a0002c0002t0001g0188a0002c0002t0001g0199others(8): Show | 11 | HG00438.hp1 HG02280.hp2 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.1716+3168C>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21422960 | ||||||
| chr14:21423088
|
C | T | 1 | a0001c0005t0002g0037 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1716+3040G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21423088 | ||||||
| chr14:21423174
|
C | T | 1 | a0001c0003t0001g0065 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1716+2954G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21423174 | ||||||
| chr14:21423406
|
C | T | 2 | a0001c0006t0001g0001a0001c0006t0001g0126 | 3 | HG02559.hp2 HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1716+2722G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21423406 | ||||||
| chr14:21423442
|
G | A | 2 | a0001c0008t0001g0087a0001c0008t0001g0088 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1716+2686C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21423442 | ||||||
| chr14:21423478
|
T | C | 1 | a0001c0005t0002g0037 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1716+2650A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21423478 | ||||||
| chr14:21423535
|
G | A | 2 | a0001c0001t0003g0218a0001c0001t0003g0242 | 2 | HG02145.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1716+2593C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21423535 | ||||||
| chr14:21423616
|
A | G | 3 | a0001c0005t0002g0036a0001c0005t0002g0037a0001c0005t0002g0042 | 3 | HG02818.hp1 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1716+2512T>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21423616 | ||||||
| chr14:21423937
|
A | G | 2 | a0001c0009t0001g0239a0001c0009t0001g0240 | 2 | HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1716+2191T>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21423937 | ||||||
| chr14:21424006
|
G | A | 164 | a0001c0001t0001g0047a0001c0001t0001g0070a0001c0001t0001g0079others(161): Show | 164 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.1716+2122C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21424006 | ||||||
| chr14:21424102
|
A | G | 1 | a0001c0008t0001g0087 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1716+2026T>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21424102 | ||||||
| chr14:21424105
|
G | A | 1 | a0002c0002t0001g0160 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1716+2023C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21424105 | ||||||
| chr14:21424320
|
T | C | 1 | a0008c0017t0002g0029 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1716+1808A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21424320 | ||||||
| chr14:21424405
|
A | G | 1 | a0001c0001t0003g0234 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1716+1723T>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21424405 | ||||||
| chr14:21424466
|
CTTTT | C | 15 | a0001c0001t0003g0128a0001c0001t0003g0130a0001c0001t0003g0142others(12): Show | 15 | HG02055.hp1 HG02258.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.1716+1658_1716+166 others(8): Show |
CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21424466 | ||||||
| chr14:21424531
|
C | T | 4 | a0001c0001t0001g0167a0001c0001t0002g0039a0001c0001t0002g0040others(1): Show | 4 | HG01884.hp1 HG02257.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1716+1597G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21424531 | ||||||
| chr14:21424661
|
C | T | 1 | a0001c0001t0004g0256 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1716+1467G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21424661 | ||||||
| chr14:21424781
|
T | C | 16 | a0001c0001t0003g0128a0001c0001t0003g0130a0001c0001t0003g0142others(13): Show | 16 | HG01261.hp2 HG02055.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1716+1347A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21424781 | ||||||
| chr14:21424899
|
G | A | 1 | a0001c0003t0001g0072 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1716+1229C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21424899 | ||||||
| chr14:21424900
|
T | A | 1 | a0001c0003t0001g0072 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1716+1228A>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21424900 | ||||||
| chr14:21424901
|
C | A | 1 | a0001c0003t0001g0072 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1716+1227G>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21424901 | ||||||
| chr14:21424902
|
C | A | 1 | a0001c0003t0001g0072 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1716+1226G>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21424902 | ||||||
| chr14:21424906
|
T | A | 1 | a0001c0003t0001g0072 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1716+1222A>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21424906 | ||||||
| chr14:21424907
|
C | T | 1 | a0001c0003t0001g0072 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1716+1221G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21424907 | ||||||
| chr14:21424908
|
T | G | 1 | a0001c0003t0001g0072 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1716+1220A>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21424908 | ||||||
| chr14:21424911
|
A | T | 1 | a0001c0003t0001g0072 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1716+1217T>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21424911 | ||||||
| chr14:21424953
|
C | G | 1 | a0001c0001t0003g0131 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1716+1175G>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21424953 | ||||||
| chr14:21425122
|
T | C | 2 | a0001c0001t0003g0218a0001c0001t0003g0242 | 2 | HG02145.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1716+1006A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21425122 | ||||||
| chr14:21425206
|
G | A | 15 | a0001c0001t0003g0128a0001c0001t0003g0130a0001c0001t0003g0142others(12): Show | 15 | HG02055.hp1 HG02258.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.1716+922C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21425206 | ||||||
| chr14:21425235
|
G | A | 25 | a0001c0001t0001g0167a0001c0001t0002g0039a0001c0001t0002g0040others(22): Show | 26 | HG01261.hp2 HG01884.hp1 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1716+893C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21425235 | ||||||
| chr14:21425283
|
T | C | 2 | a0001c0001t0003g0218a0001c0001t0003g0242 | 2 | HG02145.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1716+845A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21425283 | ||||||
| chr14:21425312
|
C | T | 2 | a0002c0002t0001g0199a0002c0002t0001g0200 | 2 | HG02280.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1716+816G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21425312 | ||||||
| chr14:21425323
|
A | AT | 25 | a0001c0001t0001g0070a0001c0001t0001g0175a0001c0001t0001g0193others(22): Show | 25 | HG01192.hp1 HG01243.hp2 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.1716+804dupA | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21425323 | ||||||
| chr14:21425323
|
AT | A | 7 | a0001c0001t0003g0143a0001c0001t0003g0163a0001c0003t0001g0059others(4): Show | 7 | HG01167.hp1 HG02451.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1716+804delA | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21425323 | ||||||
| chr14:21425617
|
G | A | 2 | a0001c0003t0001g0044a0001c0003t0001g0045 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1716+511C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21425617 | ||||||
| chr14:21425851
|
G | A | 1 | a0001c0001t0001g0194 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1716+277C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21425851 | ||||||
| chr14:21426048
|
G | A | 6 | a0001c0001t0001g0096a0001c0001t0001g0173a0001c0001t0001g0193others(3): Show | 6 | NA18747.hp1 NA18942.hp1 NA18962.hp1 others(3): Show |
intron_variant | MODIFIER | c.1716+80C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 5/37 | chr14 | 21426048 | ||||||
| chr14:21426296
|
T | C | 1 | a0001c0001t0003g0163 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1602-54A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 4/37 | chr14 | 21426296 | ||||||
| chr14:21426367
|
T | C | 19 | a0001c0001t0001g0081a0001c0001t0001g0147a0001c0001t0001g0164others(16): Show | 19 | HG00544.hp1 HG00673.hp2 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.1602-125A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 4/37 | chr14 | 21426367 | ||||||
| chr14:21426393
|
G | C | 15 | a0001c0001t0003g0128a0001c0001t0003g0130a0001c0001t0003g0142others(12): Show | 15 | HG02055.hp1 HG02258.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.1602-151C>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 4/37 | chr14 | 21426393 | ||||||
| chr14:21426407
|
AG | A | 3 | a0002c0002t0001g0179a0002c0002t0001g0183a0002c0002t0001g0184 | 3 | HG02257.hp2 NA18522.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1602-166delC | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 4/37 | chr14 | 21426407 | ||||||
| chr14:21426447
|
A | G | 6 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(3): Show | 6 | HG01884.hp2 HG01891.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1602-205T>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 4/37 | chr14 | 21426447 | ||||||
| chr14:21426471
|
C | T | 6 | a0002c0002t0001g0057a0002c0002t0001g0191a0002c0002t0001g0211others(3): Show | 6 | HG00544.hp1 HG00673.hp2 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.1602-229G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 4/37 | chr14 | 21426471 | ||||||
| chr14:21426576
|
A | G | 1 | a0001c0001t0002g0031 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1602-334T>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 4/37 | chr14 | 21426576 | ||||||
| chr14:21426792
|
C | T | 1 | a0002c0002t0001g0190 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1602-550G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 4/37 | chr14 | 21426792 | ||||||
| chr14:21426800
|
T | C | 2 | a0002c0002t0001g0094a0002c0002t0001g0241 | 2 | HG01517.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.1602-558A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 4/37 | chr14 | 21426800 | ||||||
| chr14:21427264
|
G | C | 1 | a0001c0001t0003g0243 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1601+605C>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 4/37 | chr14 | 21427264 | ||||||
| chr14:21427352
|
GTAGCAAG others(87): Show |
G | 171 | a0001c0001t0001g0047a0001c0001t0001g0070a0001c0001t0001g0079others(168): Show | 171 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.1601+423_1601+516d others(96): Show |
CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 4/37 | chr14 | 21427352 | ||||||
| chr14:21427446
|
AT | A | 2 | a0001c0006t0001g0001a0001c0006t0001g0126 | 3 | HG02559.hp2 HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1601+422delA | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 4/37 | chr14 | 21427446 | ||||||
| chr14:21427626
|
T | A | 4 | a0001c0001t0001g0167a0001c0001t0002g0039a0001c0001t0002g0040others(1): Show | 4 | HG01884.hp1 HG02257.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1601+243A>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 4/37 | chr14 | 21427626 | ||||||
| chr14:21427639
|
T | C | 1 | a0001c0003t0001g0067 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1601+230A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 4/37 | chr14 | 21427639 | ||||||
| chr14:21427795
|
A | C | 28 | a0001c0001t0001g0167a0001c0001t0002g0039a0001c0001t0002g0040others(25): Show | 29 | HG01261.hp2 HG01884.hp1 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.1601+74T>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 4/37 | chr14 | 21427795 | ||||||
| chr14:21428876
|
C | T | 1 | a0001c0001t0003g0243 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1215+88G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 3/37 | chr14 | 21428876 | ||||||
| chr14:21429457
|
C | T | 27 | a0001c0001t0001g0167a0001c0001t0002g0039a0001c0001t0002g0040others(24): Show | 28 | HG01261.hp2 HG01884.hp1 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.844-122G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 2/37 | chr14 | 21429457 | ||||||
| chr14:21429483
|
C | A | 1 | a0001c0001t0002g0023 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.844-148G>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 2/37 | chr14 | 21429483 | ||||||
| chr14:21429936
|
T | G | 1 | a0001c0001t0002g0039 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.844-601A>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 2/37 | chr14 | 21429936 | ||||||
| chr14:21430106
|
T | G | 2 | a0001c0003t0002g0033a0001c0003t0002g0034 | 2 | HG03130.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.843+695A>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 2/37 | chr14 | 21430106 | ||||||
| chr14:21430356
|
A | G | 2 | a0001c0009t0001g0239a0001c0009t0001g0240 | 2 | HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.843+445T>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 2/37 | chr14 | 21430356 | ||||||
| chr14:21430499
|
T | G | 3 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004 | 3 | HG01884.hp2 HG01891.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.843+302A>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 2/37 | chr14 | 21430499 | ||||||
| chr14:21430547
|
C | T | 2 | a0002c0002t0001g0114a0002c0002t0001g0115 | 2 | HG01258.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.843+254G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 2/37 | chr14 | 21430547 | ||||||
| chr14:21430620
|
T | A | 2 | a0002c0002t0001g0208a0002c0002t0001g0215 | 2 | HG00438.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.843+181A>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 2/37 | chr14 | 21430620 | ||||||
| chr14:21432149
|
A | G | 2 | a0001c0006t0001g0001a0001c0006t0001g0126 | 3 | HG02559.hp2 HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-215-291T>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21432149 | ||||||
| chr14:21432302
|
T | A | 4 | a0001c0001t0001g0167a0001c0001t0002g0039a0001c0001t0002g0040others(1): Show | 4 | HG01884.hp1 HG02257.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.-215-444A>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21432302 | ||||||
| chr14:21432520
|
T | C | 1 | a0001c0003t0001g0064 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-215-662A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21432520 | ||||||
| chr14:21432575
|
C | G | 2 | a0001c0003t0002g0033a0001c0003t0002g0034 | 2 | HG03130.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-215-717G>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21432575 | ||||||
| chr14:21432623
|
T | A | 11 | a0002c0002t0001g0098a0002c0002t0001g0188a0002c0002t0001g0199others(8): Show | 11 | HG00438.hp1 HG02280.hp2 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.-215-765A>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21432623 | ||||||
| chr14:21432713
|
C | A | 1 | a0001c0001t0003g0131 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-215-855G>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21432713 | ||||||
| chr14:21432823
|
G | C | 1 | a0001c0001t0003g0131 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-215-965C>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21432823 | ||||||
| chr14:21432914
|
CAA | C | 2 | a0001c0006t0001g0001a0001c0006t0001g0126 | 3 | HG02559.hp2 HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-215-1058_-215-105 others(6): Show |
CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21432914 | ||||||
| chr14:21433003
|
C | T | 1 | a0002c0002t0001g0101 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-215-1145G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21433003 | ||||||
| chr14:21433109
|
C | T | 2 | a0001c0001t0003g0218a0001c0001t0003g0242 | 2 | HG02145.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.-215-1251G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21433109 | ||||||
| chr14:21433116
|
T | C | 1 | a0001c0014t0001g0125 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-215-1258A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21433116 | ||||||
| chr14:21433434
|
T | C | 1 | a0001c0001t0001g0138 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-215-1576A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21433434 | ||||||
| chr14:21433561
|
C | T | 2 | a0001c0006t0001g0001a0001c0006t0001g0126 | 3 | HG02559.hp2 HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-215-1703G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21433561 | ||||||
| chr14:21433720
|
A | G | 1 | a0001c0001t0002g0008 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-215-1862T>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21433720 | ||||||
| chr14:21433928
|
G | A | 258 | a0001c0001t0001g0047a0001c0001t0001g0070a0001c0001t0001g0079others(255): Show | 259 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.-215-2070C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21433928 | ||||||
| chr14:21434039
|
C | CT | 13 | a0001c0001t0001g0096a0001c0001t0001g0141a0001c0001t0001g0194others(10): Show | 13 | HG02109.hp2 HG02257.hp2 HG02738.hp1 others(10): Show |
intron_variant | MODIFIER | c.-215-2182dupA | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21434039 | ||||||
| chr14:21434039
|
CT | C | 8 | a0001c0001t0001g0171a0001c0001t0004g0259a0001c0003t0001g0059others(5): Show | 8 | HG01167.hp1 NA18942.hp1 NA18951.hp1 others(5): Show |
intron_variant | MODIFIER | c.-215-2182delA | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21434039 | ||||||
| chr14:21434039
|
CTTTTTT | C | 15 | a0001c0001t0003g0128a0001c0001t0003g0130a0001c0001t0003g0142others(12): Show | 15 | HG01261.hp2 HG02055.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.-215-2187_-215-218 others(10): Show |
CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21434039 | ||||||
| chr14:21434039
|
CTTTTTTT | C | 8 | a0001c0001t0001g0149a0001c0001t0001g0162a0001c0001t0003g0144others(5): Show | 8 | HG00280.hp1 HG02818.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.-215-2188_-215-218 others(11): Show |
CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21434039 | ||||||
| chr14:21434115
|
G | A | 1 | a0001c0001t0002g0008 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-215-2257C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21434115 | ||||||
| chr14:21434170
|
C | T | 9 | a0001c0003t0001g0050a0001c0003t0001g0059a0001c0003t0001g0061others(6): Show | 9 | HG00738.hp2 HG01167.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.-215-2312G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21434170 | ||||||
| chr14:21434242
|
G | C | 2 | a0001c0006t0001g0001a0001c0006t0001g0126 | 3 | HG02559.hp2 HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-215-2384C>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21434242 | ||||||
| chr14:21434249
|
T | C | 1 | a0001c0001t0003g0163 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-215-2391A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21434249 | ||||||
| chr14:21434285
|
GAGCCGTC others(5): Show |
G | 1 | a0002c0002t0001g0219 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-215-2439_-215-242 others(16): Show |
CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21434285 | ||||||
| chr14:21434800
|
C | T | 1 | a0001c0005t0002g0042 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-215-2942G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21434800 | ||||||
| chr14:21434842
|
C | A | 12 | a0001c0001t0001g0167a0001c0001t0001g0236a0001c0001t0001g0237others(9): Show | 12 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.-215-2984G>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21434842 | ||||||
| chr14:21435027
|
T | C | 1 | a0001c0003t0001g0046 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-215-3169A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21435027 | ||||||
| chr14:21435110
|
T | C | 2 | a0002c0002t0001g0199a0002c0002t0001g0200 | 2 | HG02280.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-215-3252A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21435110 | ||||||
| chr14:21435159
|
C | T | 3 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004 | 3 | HG01884.hp2 HG01891.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-215-3301G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21435159 | ||||||
| chr14:21435766
|
C | T | 4 | a0001c0001t0001g0167a0001c0001t0002g0039a0001c0001t0002g0040others(1): Show | 4 | HG01884.hp1 HG02257.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.-215-3908G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21435766 | ||||||
| chr14:21435812
|
G | T | 1 | a0001c0001t0001g0162 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-215-3954C>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21435812 | ||||||
| chr14:21435887
|
T | C | 1 | a0001c0001t0003g0163 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-215-4029A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21435887 | ||||||
| chr14:21435983
|
C | T | 1 | a0001c0001t0006g0043 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-215-4125G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21435983 | ||||||
| chr14:21436412
|
T | C | 1 | a0001c0001t0002g0006 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-215-4554A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21436412 | ||||||
| chr14:21436582
|
T | A | 1 | a0001c0001t0001g0194 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-215-4724A>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21436582 | ||||||
| chr14:21436817
|
G | C | 1 | a0001c0005t0002g0037 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-215-4959C>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21436817 | ||||||
| chr14:21436850
|
G | C | 1 | a0001c0001t0001g0205 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-215-4992C>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21436850 | ||||||
| chr14:21436919
|
T | A | 1 | a0001c0001t0001g0238 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-215-5061A>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21436919 | ||||||
| chr14:21436982
|
G | A | 1 | a0001c0001t0005g0030 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-215-5124C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21436982 | ||||||
| chr14:21437018
|
C | T | 1 | a0002c0002t0004g0257 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-215-5160G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21437018 | ||||||
| chr14:21437294
|
G | A | 1 | a0001c0003t0001g0202 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-215-5436C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21437294 | ||||||
| chr14:21437328
|
C | T | 4 | a0001c0001t0001g0167a0001c0001t0002g0039a0001c0001t0002g0040others(1): Show | 4 | HG01884.hp1 HG02257.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.-215-5470G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21437328 | ||||||
| chr14:21437349
|
C | G | 1 | a0001c0005t0002g0037 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-215-5491G>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21437349 | ||||||
| chr14:21437361
|
T | C | 2 | a0001c0001t0003g0218a0001c0001t0003g0242 | 2 | HG02145.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.-215-5503A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21437361 | ||||||
| chr14:21437397
|
G | T | 1 | a0001c0001t0001g0187 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-215-5539C>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21437397 | ||||||
| chr14:21437544
|
T | A | 215 | a0001c0001t0001g0047a0001c0001t0001g0070a0001c0001t0001g0079others(212): Show | 216 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.-215-5686A>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21437544 | ||||||
| chr14:21437584
|
G | C | 1 | a0001c0001t0003g0243 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-215-5726C>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21437584 | ||||||
| chr14:21437589
|
C | A | 15 | a0001c0001t0003g0128a0001c0001t0003g0130a0001c0001t0003g0142others(12): Show | 15 | HG02055.hp1 HG02258.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.-215-5731G>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21437589 | ||||||
| chr14:21437678
|
A | G | 2 | a0001c0003t0002g0033a0001c0003t0002g0034 | 2 | HG03130.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-215-5820T>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21437678 | ||||||
| chr14:21437700
|
A | C | 1 | a0002c0002t0001g0201 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-215-5842T>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21437700 | ||||||
| chr14:21437904
|
T | C | 24 | a0001c0001t0003g0128a0001c0001t0003g0130a0001c0001t0003g0142others(21): Show | 25 | HG01261.hp2 HG02055.hp1 HG02145.hp1 others(22): Show |
intron_variant | MODIFIER | c.-215-6046A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21437904 | ||||||
| chr14:21438006
|
T | C | 4 | a0001c0001t0003g0218a0001c0001t0003g0242a0001c0006t0001g0001others(1): Show | 5 | HG02145.hp1 HG02559.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-215-6148A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21438006 | ||||||
| chr14:21438091
|
G | C | 31 | a0001c0001t0001g0167a0001c0001t0002g0039a0001c0001t0002g0040others(28): Show | 32 | HG01261.hp2 HG01884.hp1 HG02055.hp1 others(29): Show |
intron_variant | MODIFIER | c.-215-6233C>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21438091 | ||||||
| chr14:21438193
|
TG | T | 4 | a0001c0001t0001g0167a0001c0001t0002g0039a0001c0001t0002g0040others(1): Show | 4 | HG01884.hp1 HG02257.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.-215-6336delC | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21438193 | ||||||
| chr14:21438296
|
A | G | 6 | a0001c0001t0001g0132a0001c0001t0001g0146a0001c0001t0001g0147others(3): Show | 6 | HG00733.hp2 HG00735.hp2 HG01069.hp1 others(3): Show |
intron_variant | MODIFIER | c.-215-6438T>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21438296 | ||||||
| chr14:21438343
|
G | A | 6 | a0001c0001t0001g0134a0001c0001t0001g0155a0001c0001t0001g0171others(3): Show | 6 | HG01070.hp2 HG01071.hp2 HG02293.hp2 others(3): Show |
intron_variant | MODIFIER | c.-215-6485C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21438343 | ||||||
| chr14:21438488
|
A | G | 3 | a0003c0004t0001g0133a0003c0004t0001g0151a0003c0004t0001g0170 | 3 | HG02135.hp1 NA18612.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.-215-6630T>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21438488 | ||||||
| chr14:21438507
|
T | C | 24 | a0001c0001t0003g0128a0001c0001t0003g0130a0001c0001t0003g0142others(21): Show | 25 | HG01261.hp2 HG02055.hp1 HG02145.hp1 others(22): Show |
intron_variant | MODIFIER | c.-215-6649A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21438507 | ||||||
| chr14:21438512
|
T | TA | 23 | a0001c0001t0001g0167a0001c0001t0001g0228a0001c0001t0001g0236others(20): Show | 23 | HG00323.hp1 HG00408.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.-215-6655dupT | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21438512 | ||||||
| chr14:21438512
|
T | TAA | 172 | a0001c0001t0001g0047a0001c0001t0001g0070a0001c0001t0001g0079others(169): Show | 172 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(169): Show |
intron_variant | MODIFIER | c.-215-6656_-215-665 others(6): Show |
CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21438512 | ||||||
| chr14:21438512
|
T | TAAA | 13 | a0001c0001t0001g0123a0001c0001t0001g0147a0001c0001t0001g0193others(10): Show | 13 | HG00438.hp2 HG01358.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.-215-6657_-215-665 others(7): Show |
CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21438512 | ||||||
| chr14:21438512
|
TA | T | 6 | a0001c0003t0001g0044a0001c0003t0001g0060a0001c0003t0001g0065others(3): Show | 6 | HG00280.hp2 HG01069.hp2 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.-215-6655delT | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21438512 | ||||||
| chr14:21438557
|
G | A | 2 | a0001c0001t0001g0127a0001c0001t0001g0204 | 2 | NA18971.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.-215-6699C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21438557 | ||||||
| chr14:21438628
|
A | T | 1 | a0001c0001t0001g0175 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-215-6770T>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21438628 | ||||||
| chr14:21438743
|
C | A | 1 | a0001c0001t0001g0174 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-215-6885G>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21438743 | ||||||
| chr14:21438915
|
C | T | 1 | a0001c0001t0002g0005 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-215-7057G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21438915 | ||||||
| chr14:21439035
|
G | A | 2 | a0001c0009t0001g0239a0001c0009t0001g0240 | 2 | HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-215-7177C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21439035 | ||||||
| chr14:21439252
|
T | C | 8 | a0001c0003t0001g0052a0001c0003t0001g0054a0001c0003t0001g0055others(5): Show | 8 | HG02080.hp2 HG04184.hp2 NA18612.hp2 others(5): Show |
intron_variant | MODIFIER | c.-215-7394A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21439252 | ||||||
| chr14:21439255
|
C | G | 1 | a0002c0002t0001g0226 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-215-7397G>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21439255 | ||||||
| chr14:21439412
|
G | C | 1 | a0001c0003t0001g0058 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-215-7554C>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21439412 | ||||||
| chr14:21439416
|
T | C | 1 | a0001c0001t0001g0253 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-215-7558A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21439416 | ||||||
| chr14:21439685
|
G | A | 212 | a0001c0001t0001g0047a0001c0001t0001g0070a0001c0001t0001g0079others(209): Show | 213 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(210): Show |
intron_variant | MODIFIER | c.-215-7827C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21439685 | ||||||
| chr14:21439804
|
A | G | 1 | a0001c0001t0006g0043 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-215-7946T>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21439804 | ||||||
| chr14:21439825
|
G | A | 1 | a0001c0001t0001g0139 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-215-7967C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21439825 | ||||||
| chr14:21440070
|
T | C | 1 | a0005c0016t0003g0145 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-215-8212A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21440070 | ||||||
| chr14:21440299
|
C | T | 7 | a0001c0001t0001g0132a0001c0001t0001g0146a0001c0001t0001g0147others(4): Show | 7 | HG00733.hp2 HG00735.hp2 HG00741.hp2 others(4): Show |
intron_variant | MODIFIER | c.-215-8441G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21440299 | ||||||
| chr14:21440352
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-215-8494C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21440352 | ||||||
| chr14:21440548
|
G | A | 2 | a0001c0001t0003g0163a0001c0001t0003g0234 | 2 | HG02451.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-215-8690C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21440548 | ||||||
| chr14:21440604
|
G | A | 1 | a0002c0002t0001g0210 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-215-8746C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21440604 | ||||||
| chr14:21440608
|
G | A | 1 | a0001c0001t0003g0131 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-215-8750C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21440608 | ||||||
| chr14:21440683
|
T | A | 2 | a0001c0009t0001g0239a0001c0009t0001g0240 | 2 | HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-215-8825A>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21440683 | ||||||
| chr14:21440743
|
C | T | 3 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004 | 3 | HG01884.hp2 HG01891.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-215-8885G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21440743 | ||||||
| chr14:21440755
|
G | C | 1 | a0002c0002t0001g0084 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-215-8897C>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21440755 | ||||||
| chr14:21440790
|
G | A | 16 | a0001c0001t0003g0128a0001c0001t0003g0130a0001c0001t0003g0142others(13): Show | 16 | HG01261.hp2 HG02055.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-215-8932C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21440790 | ||||||
| chr14:21440854
|
G | C | 1 | a0007c0015t0001g0137 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-215-8996C>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21440854 | ||||||
| chr14:21440897
|
G | C | 10 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0238others(7): Show | 10 | HG01243.hp2 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.-215-9039C>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21440897 | ||||||
| chr14:21441374
|
CTGT | C | 4 | a0001c0001t0001g0167a0001c0001t0002g0039a0001c0001t0002g0040others(1): Show | 4 | HG01884.hp1 HG02257.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.-215-9519_-215-951 others(7): Show |
CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21441374 | ||||||
| chr14:21441616
|
T | C | 20 | a0001c0001t0001g0097a0001c0001t0001g0164a0001c0001t0003g0128others(17): Show | 20 | HG01255.hp1 HG02055.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.-215-9758A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21441616 | ||||||
| chr14:21441626
|
T | C | 39 | a0001c0001t0001g0140a0001c0001t0001g0164a0001c0001t0001g0166others(36): Show | 39 | HG00733.hp2 HG01243.hp2 HG01255.hp1 others(36): Show |
intron_variant | MODIFIER | c.-215-9768A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21441626 | ||||||
| chr14:21441655
|
A | G | 3 | a0001c0009t0001g0239a0001c0009t0001g0240a0002c0002t0001g0180 | 3 | HG02004.hp2 HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-215-9797T>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21441655 | ||||||
| chr14:21441659
|
C | T | 163 | a0001c0001t0001g0047a0001c0001t0001g0070a0001c0001t0001g0079others(160): Show | 163 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.-215-9801G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21441659 | ||||||
| chr14:21441664
|
A | G | 2 | a0002c0002t0001g0121a0002c0002t0001g0180 | 2 | HG02004.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.-215-9806T>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21441664 | ||||||
| chr14:21441665
|
T | G | 3 | a0001c0003t0001g0073a0002c0002t0001g0121a0002c0002t0001g0180 | 3 | HG01255.hp2 HG02004.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.-215-9807A>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21441665 | ||||||
| chr14:21441681
|
G | A | 1 | a0002c0002t0001g0180 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-215-9823C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21441681 | ||||||
| chr14:21441684
|
G | C | 8 | a0001c0001t0001g0204a0001c0003t0001g0090a0001c0003t0001g0214others(5): Show | 8 | HG00408.hp1 HG01978.hp2 NA18947.hp1 others(5): Show |
intron_variant | MODIFIER | c.-215-9826C>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21441684 | ||||||
| chr14:21441684
|
G | T | 1 | a0002c0002t0001g0180 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-215-9826C>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21441684 | ||||||
| chr14:21441686
|
A | T | 8 | a0001c0001t0003g0128a0001c0001t0003g0130a0001c0001t0003g0142others(5): Show | 8 | HG02258.hp1 HG02572.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.-215-9828T>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21441686 | ||||||
| chr14:21441687
|
G | A | 8 | a0001c0001t0003g0128a0001c0001t0003g0130a0001c0001t0003g0142others(5): Show | 8 | HG02258.hp1 HG02572.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.-215-9829C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21441687 | ||||||
| chr14:21441692
|
T | C | 4 | a0002c0002t0001g0249a0002c0002t0001g0250a0002c0002t0001g0251others(1): Show | 4 | HG01070.hp1 HG01169.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.-215-9834A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21441692 | ||||||
| chr14:21441700
|
A | C | 1 | a0006c0012t0002g0021 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-215-9842T>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21441700 | ||||||
| chr14:21441704
|
C | T | 1 | a0001c0001t0002g0020 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-215-9846G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21441704 | ||||||
| chr14:21441713
|
C | A | 1 | a0001c0014t0001g0125 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-215-9855G>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21441713 | ||||||
| chr14:21441715
|
C | T | 2 | a0001c0001t0001g0244a0001c0001t0003g0243 | 2 | HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-215-9857G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21441715 | ||||||
| chr14:21441732
|
CA | C | 3 | a0001c0001t0001g0194a0001c0003t0001g0044a0001c0003t0001g0045 | 3 | HG01069.hp2 HG01071.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.-215-9875delT | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21441732 | ||||||
| chr14:21441745
|
T | C | 219 | a0001c0001t0001g0047a0001c0001t0001g0070a0001c0001t0001g0079others(216): Show | 220 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.-215-9887A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21441745 | ||||||
| chr14:21441757
|
T | C | 10 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0238others(7): Show | 10 | HG01243.hp2 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.-215-9899A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21441757 | ||||||
| chr14:21441802
|
T | C | 1 | a0001c0013t0002g0026 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-215-9944A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21441802 | ||||||
| chr14:21441806
|
A | G | 2 | a0002c0002t0001g0109a0002c0002t0001g0230 | 2 | NA19012.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.-215-9948T>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21441806 | ||||||
| chr14:21441827
|
T | A | 2 | a0001c0001t0003g0163a0001c0001t0003g0234 | 2 | HG02451.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-215-9969A>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21441827 | ||||||
| chr14:21441838
|
A | G | 2 | a0001c0001t0001g0172a0008c0017t0002g0029 | 2 | HG02559.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.-215-9980T>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21441838 | ||||||
| chr14:21441843
|
T | C | 1 | a0008c0017t0002g0029 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-215-9985A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21441843 | ||||||
| chr14:21441846
|
G | A | 1 | a0008c0017t0002g0029 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-215-9988C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21441846 | ||||||
| chr14:21441855
|
C | G | 6 | a0001c0001t0001g0132a0001c0001t0001g0146a0001c0001t0001g0147others(3): Show | 6 | HG00733.hp2 HG00735.hp2 HG01069.hp1 others(3): Show |
intron_variant | MODIFIER | c.-215-9997G>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21441855 | ||||||
| chr14:21441876
|
G | A | 1 | a0001c0001t0001g0172 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-215-10018C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21441876 | ||||||
| chr14:21441890
|
A | AAAAC | 166 | a0001c0001t0001g0047a0001c0001t0001g0070a0001c0001t0001g0079others(163): Show | 166 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.-215-10036_-215-10 others(10): Show |
CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21441890 | ||||||
| chr14:21441890
|
A | AAAACAAA others(1): Show |
4 | a0001c0001t0001g0082a0001c0001t0002g0010a0001c0001t0002g0012others(1): Show | 4 | HG02145.hp2 HG03453.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.-215-10040_-215-10 others(14): Show |
CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21441890 | ||||||
| chr14:21441916
|
C | A | 1 | a0001c0001t0002g0020 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-215-10058G>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21441916 | ||||||
| chr14:21441918
|
A | C | 1 | a0001c0001t0002g0020 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-215-10060T>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21441918 | ||||||
| chr14:21442005
|
T | C | 2 | a0001c0003t0001g0076a0001c0003t0001g0077 | 2 | HG01496.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.-215-10147A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21442005 | ||||||
| chr14:21442013
|
G | T | 1 | a0001c0001t0001g0169 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-215-10155C>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21442013 | ||||||
| chr14:21442103
|
C | T | 1 | a0001c0001t0003g0248 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-215-10245G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21442103 | ||||||
| chr14:21442546
|
G | GGAGGATC others(3): Show |
1 | a0001c0001t0002g0017 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-215-10698_-215-10 others(16): Show |
CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21442546 | ||||||
| chr14:21442636
|
A | AAGGGGAG others(8): Show |
4 | a0001c0001t0001g0162a0001c0001t0001g0203a0001c0001t0003g0248others(1): Show | 4 | HG02109.hp2 HG03490.hp2 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.-215-10793_-215-10 others(21): Show |
CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21442636 | ||||||
| chr14:21442636
|
AAGGGGAG others(8): Show |
A | 3 | a0001c0001t0003g0218a0001c0001t0003g0242a0002c0002t0001g0254 | 3 | HG01891.hp2 HG02145.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.-215-10793_-215-10 others(21): Show |
CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21442636 | ||||||
| chr14:21442665
|
AGAGGGGA others(13): Show |
A | 4 | a0001c0001t0001g0167a0001c0001t0002g0039a0001c0001t0002g0040others(1): Show | 4 | HG01884.hp1 HG02257.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.-215-10827_-215-10 others(26): Show |
CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21442665 | ||||||
| chr14:21442680
|
A | AGAGGG | 3 | a0001c0001t0003g0163a0001c0001t0003g0234a0001c0003t0001g0090 | 3 | HG02451.hp2 HG03225.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.-215-10827_-215-10 others(11): Show |
CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21442680 | ||||||
| chr14:21442680
|
A | AGAGGGGA others(13): Show |
2 | a0001c0009t0001g0239a0001c0009t0001g0240 | 2 | HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-215-10823_-215-10 others(26): Show |
CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21442680 | ||||||
| chr14:21442680
|
AGAGGG | A | 16 | a0001c0001t0003g0128a0001c0001t0003g0130a0001c0001t0003g0142others(13): Show | 16 | HG01261.hp2 HG02055.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-215-10827_-215-10 others(11): Show |
CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21442680 | ||||||
| chr14:21442689
|
G | A | 1 | a0002c0002t0001g0110 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-215-10831C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21442689 | ||||||
| chr14:21442707
|
A | G | 1 | a0001c0001t0002g0017 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-215-10849T>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21442707 | ||||||
| chr14:21442718
|
A | G | 1 | a0001c0001t0002g0017 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-215-10860T>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21442718 | ||||||
| chr14:21442718
|
AGGGAGGA others(33): Show |
A | 2 | a0001c0001t0003g0218a0001c0001t0003g0242 | 2 | HG02145.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.-215-10900_-215-10 others(46): Show |
CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21442718 | ||||||
| chr14:21442718
|
AGGGAGGA others(43): Show |
A | 1 | a0001c0006t0001g0001 | 2 | HG02559.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-215-10910_-215-10 others(56): Show |
CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21442718 | ||||||
| chr14:21442718
|
AGGGAGGA others(53): Show |
A | 1 | a0001c0006t0001g0126 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-215-10920_-215-10 others(66): Show |
CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21442718 | ||||||
| chr14:21442733
|
A | G | 1 | a0001c0001t0002g0017 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-215-10875T>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21442733 | ||||||
| chr14:21442738
|
C | CGGGAGGA others(3): Show |
29 | a0001c0001t0001g0070a0001c0001t0001g0079a0001c0001t0001g0081others(26): Show | 29 | HG00544.hp2 HG00609.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.-215-10890_-215-10 others(16): Show |
CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21442738 | ||||||
| chr14:21442738
|
C | CGGGAGGA others(13): Show |
15 | a0001c0001t0001g0085a0001c0001t0001g0150a0001c0001t0002g0005others(12): Show | 15 | HG00408.hp2 HG01070.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.-215-10900_-215-10 others(26): Show |
CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21442738 | ||||||
| chr14:21442738
|
C | CGGGAGGA others(23): Show |
1 | a0001c0001t0001g0247 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-215-10910_-215-10 others(36): Show |
CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21442738 | ||||||
| chr14:21442738
|
C | CGGGAGGA others(33): Show |
1 | a0001c0001t0001g0080 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-215-10920_-215-10 others(46): Show |
CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21442738 | ||||||
| chr14:21442738
|
CGGGAGGA others(3): Show |
C | 48 | a0001c0001t0001g0166a0001c0001t0001g0173a0001c0001t0001g0174others(45): Show | 48 | HG00323.hp1 HG00733.hp2 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.-215-10890_-215-10 others(16): Show |
CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21442738 | ||||||
| chr14:21442738
|
CGGGAGGA others(13): Show |
C | 12 | a0001c0001t0003g0163a0001c0001t0003g0234a0001c0003t0002g0035others(9): Show | 12 | HG00438.hp2 HG01891.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.-215-10900_-215-10 others(26): Show |
CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21442738 | ||||||
| chr14:21442738
|
CGGGAGGA others(23): Show |
C | 1 | a0001c0001t0001g0181 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-215-10910_-215-10 others(36): Show |
CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21442738 | ||||||
| chr14:21442738
|
CGGGAGGA others(33): Show |
C | 2 | a0001c0003t0002g0033a0001c0003t0002g0034 | 2 | HG03130.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-215-10920_-215-10 others(46): Show |
CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21442738 | ||||||
| chr14:21442815
|
A | G | 1 | a0002c0002t0004g0257 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-215-10957T>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21442815 | ||||||
| chr14:21442818
|
GGGGAGGA others(12): Show |
G | 1 | a0002c0002t0004g0257 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-215-10979_-215-10 others(25): Show |
CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21442818 | ||||||
| chr14:21442886
|
T | C | 2 | a0002c0002t0001g0111a0002c0002t0001g0112 | 2 | NA18942.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.-215-11028A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21442886 | ||||||
| chr14:21443207
|
C | T | 2 | a0001c0006t0001g0001a0001c0006t0001g0126 | 3 | HG02559.hp2 HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-215-11349G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21443207 | ||||||
| chr14:21443219
|
G | A | 1 | a0002c0002t0001g0213 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-215-11361C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21443219 | ||||||
| chr14:21443315
|
C | T | 2 | a0001c0001t0002g0020a0006c0012t0002g0021 | 2 | HG02738.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.-215-11457G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21443315 | ||||||
| chr14:21443336
|
A | G | 1 | a0001c0003t0002g0033 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-215-11478T>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21443336 | ||||||
| chr14:21443348
|
G | A | 2 | a0001c0006t0001g0001a0001c0006t0001g0126 | 3 | HG02559.hp2 HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-215-11490C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21443348 | ||||||
| chr14:21443432
|
C | T | 1 | a0001c0001t0001g0193 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-215-11574G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21443432 | ||||||
| chr14:21443497
|
G | A | 1 | a0001c0001t0006g0043 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-215-11639C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21443497 | ||||||
| chr14:21443671
|
G | A | 1 | a0002c0002t0001g0089 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-215-11813C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21443671 | ||||||
| chr14:21443814
|
C | T | 1 | a0001c0001t0003g0234 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-215-11956G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21443814 | ||||||
| chr14:21443855
|
C | CA | 57 | a0001c0001t0001g0070a0001c0001t0001g0086a0001c0001t0001g0096others(54): Show | 57 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.-215-11998dupT | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21443855 | ||||||
| chr14:21443855
|
C | CAA | 6 | a0001c0001t0001g0167a0001c0001t0002g0039a0001c0001t0002g0040others(3): Show | 6 | HG01884.hp1 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-215-11999_-215-11 others(8): Show |
CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21443855 | ||||||
| chr14:21443855
|
CA | C | 8 | a0001c0001t0001g0221a0001c0001t0002g0020a0001c0001t0003g0144others(5): Show | 8 | HG02895.hp1 HG03130.hp2 HG03453.hp2 others(5): Show |
intron_variant | MODIFIER | c.-215-11998delT | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21443855 | ||||||
| chr14:21443869
|
A | AC | 2 | a0001c0006t0001g0001a0001c0006t0001g0126 | 3 | HG02559.hp2 HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-215-12012_-215-12 others(7): Show |
CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21443869 | ||||||
| chr14:21443869
|
A | C | 2 | a0001c0001t0003g0218a0001c0001t0003g0242 | 2 | HG02145.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.-215-12011T>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21443869 | ||||||
| chr14:21443873
|
A | C | 1 | a0001c0001t0002g0011 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-215-12015T>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21443873 | ||||||
| chr14:21443880
|
C | A | 2 | a0001c0009t0001g0239a0001c0009t0001g0240 | 2 | HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-215-12022G>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21443880 | ||||||
| chr14:21443910
|
A | T | 2 | a0002c0002t0001g0136a0002c0002t0001g0159 | 2 | HG02615.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-215-12052T>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21443910 | ||||||
| chr14:21443994
|
G | A | 20 | a0001c0001t0003g0128a0001c0001t0003g0130a0001c0001t0003g0142others(17): Show | 21 | HG01261.hp2 HG02055.hp1 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.-216+12038C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21443994 | ||||||
| chr14:21444019
|
T | C | 4 | a0001c0001t0003g0163a0001c0001t0003g0234a0001c0009t0001g0239others(1): Show | 4 | HG02451.hp2 HG03139.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-216+12013A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21444019 | ||||||
| chr14:21444201
|
G | A | 1 | a0001c0001t0001g0206 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-216+11831C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21444201 | ||||||
| chr14:21444704
|
T | A | 35 | a0001c0001t0001g0132a0001c0001t0001g0146a0001c0001t0001g0147others(32): Show | 36 | HG00438.hp1 HG00733.hp2 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.-216+11328A>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21444704 | ||||||
| chr14:21444705
|
A | T | 9 | a0001c0001t0001g0150a0001c0001t0002g0005a0001c0001t0002g0006others(6): Show | 9 | HG00408.hp2 HG00544.hp2 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.-216+11327T>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21444705 | ||||||
| chr14:21444886
|
C | T | 6 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0017others(3): Show | 6 | HG02258.hp2 HG02280.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-216+11146G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21444886 | ||||||
| chr14:21445080
|
C | T | 2 | a0001c0001t0003g0142a0001c0001t0003g0144 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-216+10952G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21445080 | ||||||
| chr14:21445328
|
T | C | 1 | a0007c0015t0001g0137 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-216+10704A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21445328 | ||||||
| chr14:21445373
|
C | A | 2 | a0001c0009t0001g0239a0001c0009t0001g0240 | 2 | HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-216+10659G>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21445373 | ||||||
| chr14:21445405
|
G | T | 1 | a0001c0001t0001g0177 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-216+10627C>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21445405 | ||||||
| chr14:21445446
|
C | T | 2 | a0001c0009t0001g0239a0001c0009t0001g0240 | 2 | HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-216+10586G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21445446 | ||||||
| chr14:21445562
|
A | G | 28 | a0001c0001t0001g0167a0001c0001t0002g0039a0001c0001t0002g0040others(25): Show | 29 | HG01261.hp2 HG01884.hp1 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.-216+10470T>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21445562 | ||||||
| chr14:21445664
|
G | A | 1 | a0002c0002t0001g0098 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-216+10368C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21445664 | ||||||
| chr14:21445688
|
C | CA | 45 | a0001c0001t0001g0047a0001c0001t0001g0070a0001c0001t0001g0097others(42): Show | 45 | HG00738.hp1 HG00741.hp1 HG00741.hp2 others(42): Show |
intron_variant | MODIFIER | c.-216+10343dupT | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21445688 | ||||||
| chr14:21445688
|
C | CAA | 7 | a0001c0001t0003g0197a0001c0001t0003g0198a0001c0001t0003g0216others(4): Show | 7 | HG01109.hp1 HG01243.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.-216+10342_-216+10 others(8): Show |
CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21445688 | ||||||
| chr14:21445688
|
CA | C | 12 | a0001c0001t0001g0186a0001c0001t0001g0247a0001c0003t0001g0056others(9): Show | 12 | HG00323.hp1 HG00323.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.-216+10343delT | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21445688 | ||||||
| chr14:21445932
|
G | T | 1 | a0001c0001t0002g0040 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-216+10100C>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21445932 | ||||||
| chr14:21445985
|
C | T | 3 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004 | 3 | HG01884.hp2 HG01891.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-216+10047G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21445985 | ||||||
| chr14:21446036
|
G | A | 28 | a0001c0001t0001g0167a0001c0001t0002g0039a0001c0001t0002g0040others(25): Show | 29 | HG01261.hp2 HG01884.hp1 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.-216+9996C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21446036 | ||||||
| chr14:21446047
|
C | T | 1 | a0002c0002t0001g0100 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-216+9985G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21446047 | ||||||
| chr14:21446054
|
C | T | 3 | a0001c0005t0002g0036a0001c0005t0002g0037a0001c0005t0002g0042 | 3 | HG02818.hp1 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-216+9978G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21446054 | ||||||
| chr14:21446082
|
C | T | 3 | a0002c0002t0001g0179a0002c0002t0001g0183a0002c0002t0001g0184 | 3 | HG02257.hp2 NA18522.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-216+9950G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21446082 | ||||||
| chr14:21446305
|
TTTC | T | 9 | a0001c0001t0003g0163a0001c0001t0003g0198a0001c0001t0003g0217others(6): Show | 9 | HG02055.hp1 HG02451.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.-216+9724_-216+972 others(7): Show |
CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21446305 | ||||||
| chr14:21446317
|
C | CT | 193 | a0001c0001t0001g0047a0001c0001t0001g0070a0001c0001t0001g0079others(190): Show | 193 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.-216+9714dupA | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21446317 | ||||||
| chr14:21446317
|
C | CTT | 9 | a0001c0001t0001g0193a0001c0001t0001g0253a0001c0001t0002g0010others(6): Show | 10 | HG00741.hp2 HG02145.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.-216+9713_-216+971 others(6): Show |
CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21446317 | ||||||
| chr14:21446499
|
C | T | 4 | a0001c0001t0003g0218a0001c0001t0003g0242a0001c0006t0001g0001others(1): Show | 5 | HG02145.hp1 HG02559.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-216+9533G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21446499 | ||||||
| chr14:21446508
|
G | A | 1 | a0001c0014t0001g0125 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-216+9524C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21446508 | ||||||
| chr14:21446758
|
A | G | 1 | a0002c0002t0001g0224 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-216+9274T>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21446758 | ||||||
| chr14:21447016
|
A | T | 1 | a0001c0003t0001g0049 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-216+9016T>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21447016 | ||||||
| chr14:21447160
|
G | A | 1 | a0001c0009t0001g0240 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-216+8872C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21447160 | ||||||
| chr14:21447357
|
G | A | 172 | a0001c0001t0001g0047a0001c0001t0001g0070a0001c0001t0001g0079others(169): Show | 172 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.-216+8675C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21447357 | ||||||
| chr14:21447372
|
C | T | 4 | a0001c0001t0003g0163a0001c0001t0003g0234a0001c0009t0001g0239others(1): Show | 4 | HG02451.hp2 HG03139.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-216+8660G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21447372 | ||||||
| chr14:21447561
|
G | A | 5 | a0002c0002t0001g0083a0002c0002t0001g0084a0002c0002t0001g0219others(2): Show | 5 | HG02109.hp1 HG02622.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.-216+8471C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21447561 | ||||||
| chr14:21447702
|
T | C | 2 | a0001c0001t0003g0163a0001c0001t0003g0234 | 2 | HG02451.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-216+8330A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21447702 | ||||||
| chr14:21447720
|
T | C | 4 | a0001c0001t0001g0167a0001c0001t0002g0039a0001c0001t0002g0040others(1): Show | 4 | HG01884.hp1 HG02257.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.-216+8312A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21447720 | ||||||
| chr14:21447726
|
T | C | 1 | a0001c0001t0001g0127 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-216+8306A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21447726 | ||||||
| chr14:21447747
|
A | AT | 6 | a0001c0001t0001g0132a0001c0001t0001g0146a0001c0001t0001g0147others(3): Show | 6 | HG00733.hp2 HG00735.hp2 HG01069.hp1 others(3): Show |
intron_variant | MODIFIER | c.-216+8284dupA | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21447747 | ||||||
| chr14:21447757
|
T | C | 65 | a0001c0001t0001g0081a0001c0003t0001g0090a0002c0002t0001g0057others(62): Show | 65 | HG00323.hp1 HG00438.hp2 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.-216+8275A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21447757 | ||||||
| chr14:21448705
|
C | T | 2 | a0001c0001t0002g0013a0001c0001t0002g0014 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-216+7327G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21448705 | ||||||
| chr14:21448853
|
G | A | 1 | a0001c0001t0001g0140 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-216+7179C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21448853 | ||||||
| chr14:21448880
|
A | G | 1 | a0001c0001t0001g0081 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-216+7152T>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21448880 | ||||||
| chr14:21448916
|
T | A | 2 | a0001c0009t0001g0239a0001c0009t0001g0240 | 2 | HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-216+7116A>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21448916 | ||||||
| chr14:21448950
|
A | G | 4 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0085others(1): Show | 4 | HG02976.hp1 HG03209.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-216+7082T>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21448950 | ||||||
| chr14:21448983
|
G | A | 15 | a0001c0001t0003g0128a0001c0001t0003g0130a0001c0001t0003g0142others(12): Show | 15 | HG02055.hp1 HG02258.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.-216+7049C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21448983 | ||||||
| chr14:21449075
|
G | A | 3 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004 | 3 | HG01884.hp2 HG01891.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-216+6957C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21449075 | ||||||
| chr14:21449123
|
A | G | 2 | a0001c0006t0001g0001a0001c0006t0001g0126 | 3 | HG02559.hp2 HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-216+6909T>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21449123 | ||||||
| chr14:21449161
|
G | A | 1 | a0002c0002t0001g0119 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-216+6871C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21449161 | ||||||
| chr14:21449315
|
G | A | 10 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0238others(7): Show | 10 | HG01243.hp2 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.-216+6717C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21449315 | ||||||
| chr14:21449396
|
T | C | 1 | a0001c0003t0001g0214 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-216+6636A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21449396 | ||||||
| chr14:21449851
|
G | A | 173 | a0001c0001t0001g0047a0001c0001t0001g0070a0001c0001t0001g0079others(170): Show | 173 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.-216+6181C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21449851 | ||||||
| chr14:21450289
|
C | T | 4 | a0001c0003t0001g0048a0001c0003t0001g0060a0001c0003t0001g0071others(1): Show | 4 | NA18948.hp1 NA18988.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.-216+5743G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21450289 | ||||||
| chr14:21450523
|
G | A | 1 | a0001c0014t0001g0125 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-216+5509C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21450523 | ||||||
| chr14:21450574
|
G | C | 1 | a0001c0003t0001g0214 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-216+5458C>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21450574 | ||||||
| chr14:21450611
|
A | G | 5 | a0002c0002t0001g0083a0002c0002t0001g0084a0002c0002t0001g0219others(2): Show | 5 | HG02109.hp1 HG02622.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.-216+5421T>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21450611 | ||||||
| chr14:21450669
|
C | T | 1 | a0001c0001t0003g0243 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-216+5363G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21450669 | ||||||
| chr14:21450685
|
GA | G | 5 | a0002c0002t0001g0092a0002c0002t0001g0094a0002c0002t0001g0241others(2): Show | 5 | HG00323.hp1 HG01517.hp1 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.-216+5346delT | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21450685 | ||||||
| chr14:21450698
|
G | T | 1 | a0001c0001t0003g0163 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-216+5334C>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21450698 | ||||||
| chr14:21450709
|
T | C | 4 | a0001c0001t0003g0163a0001c0001t0003g0234a0001c0009t0001g0239others(1): Show | 4 | HG02451.hp2 HG03139.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-216+5323A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21450709 | ||||||
| chr14:21450717
|
C | T | 172 | a0001c0001t0001g0047a0001c0001t0001g0070a0001c0001t0001g0079others(169): Show | 172 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.-216+5315G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21450717 | ||||||
| chr14:21450817
|
C | CAAAAAGG others(311): Show |
2 | a0001c0006t0001g0001a0001c0006t0001g0126 | 3 | HG02559.hp2 HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-216+5214_-216+521 others(322): Show |
CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21450817 | ||||||
| chr14:21451441
|
C | T | 10 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0238others(7): Show | 10 | HG01243.hp2 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.-216+4591G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21451441 | ||||||
| chr14:21451443
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-216+4589G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21451443 | ||||||
| chr14:21451444
|
G | A | 4 | a0001c0001t0001g0167a0001c0001t0002g0039a0001c0001t0002g0040others(1): Show | 4 | HG01884.hp1 HG02257.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.-216+4588C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21451444 | ||||||
| chr14:21451496
|
C | A | 4 | a0001c0001t0001g0167a0001c0001t0002g0039a0001c0001t0002g0040others(1): Show | 4 | HG01884.hp1 HG02257.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.-216+4536G>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21451496 | ||||||
| chr14:21451571
|
C | CA | 42 | a0001c0001t0001g0070a0001c0001t0001g0082a0001c0001t0001g0138others(39): Show | 43 | HG00438.hp1 HG00544.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.-216+4460dupT | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21451571 | ||||||
| chr14:21451571
|
CA | C | 12 | a0001c0001t0001g0149a0001c0001t0001g0186a0001c0001t0001g0244others(9): Show | 12 | HG00280.hp1 HG01070.hp1 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.-216+4460delT | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21451571 | ||||||
| chr14:21451571
|
CAAAAAAA | C | 6 | a0001c0001t0001g0132a0001c0001t0001g0146a0001c0001t0001g0147others(3): Show | 6 | HG00733.hp2 HG00735.hp2 HG01069.hp1 others(3): Show |
intron_variant | MODIFIER | c.-216+4454_-216+446 others(11): Show |
CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21451571 | ||||||
| chr14:21451571
|
CAAAAAAA others(3): Show |
C | 14 | a0001c0001t0003g0128a0001c0001t0003g0130a0001c0001t0003g0143others(11): Show | 14 | HG02055.hp1 HG02258.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.-216+4451_-216+446 others(14): Show |
CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21451571 | ||||||
| chr14:21451571
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0003g0142 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-216+4450_-216+446 others(15): Show |
CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21451571 | ||||||
| chr14:21451635
|
G | A | 2 | a0001c0001t0001g0228a0001c0001t0001g0233 | 2 | HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-216+4397C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21451635 | ||||||
| chr14:21451790
|
G | A | 6 | a0001c0001t0001g0132a0001c0001t0001g0146a0001c0001t0001g0147others(3): Show | 6 | HG00733.hp2 HG00735.hp2 HG01069.hp1 others(3): Show |
intron_variant | MODIFIER | c.-216+4242C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21451790 | ||||||
| chr14:21451808
|
A | G | 16 | a0001c0001t0003g0128a0001c0001t0003g0130a0001c0001t0003g0142others(13): Show | 16 | HG01261.hp2 HG02055.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-216+4224T>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21451808 | ||||||
| chr14:21451835
|
C | T | 3 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004 | 3 | HG01884.hp2 HG01891.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-216+4197G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21451835 | ||||||
| chr14:21451859
|
C | T | 1 | a0001c0001t0001g0245 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-216+4173G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21451859 | ||||||
| chr14:21451861
|
T | G | 2 | a0001c0003t0001g0044a0001c0003t0001g0045 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-216+4171A>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21451861 | ||||||
| chr14:21451954
|
T | C | 2 | a0001c0009t0001g0239a0001c0009t0001g0240 | 2 | HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-216+4078A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21451954 | ||||||
| chr14:21452004
|
G | A | 1 | a0001c0001t0001g0141 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-216+4028C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21452004 | ||||||
| chr14:21452065
|
A | G | 30 | a0001c0001t0001g0167a0001c0001t0002g0039a0001c0001t0002g0040others(27): Show | 31 | HG01261.hp2 HG01884.hp1 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.-216+3967T>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21452065 | ||||||
| chr14:21452166
|
G | A | 1 | a0001c0003t0002g0035 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-216+3866C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21452166 | ||||||
| chr14:21452169
|
T | C | 1 | a0001c0001t0001g0129 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-216+3863A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21452169 | ||||||
| chr14:21452174
|
G | A | 1 | a0002c0002t0001g0183 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-216+3858C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21452174 | ||||||
| chr14:21452181
|
C | T | 5 | a0001c0001t0001g0167a0001c0001t0002g0039a0001c0001t0002g0040others(2): Show | 5 | HG01884.hp1 HG02257.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-216+3851G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21452181 | ||||||
| chr14:21452489
|
C | T | 2 | a0001c0001t0003g0163a0001c0001t0003g0234 | 2 | HG02451.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-216+3543G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21452489 | ||||||
| chr14:21452647
|
G | GA | 13 | a0001c0001t0003g0128a0001c0001t0003g0130a0001c0001t0003g0142others(10): Show | 13 | HG01261.hp2 HG02055.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.-216+3384dupT | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21452647 | ||||||
| chr14:21452761
|
C | T | 2 | a0001c0003t0002g0035a0008c0017t0002g0029 | 2 | HG02559.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.-216+3271G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21452761 | ||||||
| chr14:21452864
|
GTCCCAGC others(1167): Show |
G | 4 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0238others(1): Show | 4 | HG02055.hp2 HG02809.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.-216+1994_-216+316 others(4): Show |
CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21452864 | ||||||
| chr14:21452970
|
G | A | 3 | a0001c0009t0001g0239a0001c0009t0001g0240a0002c0002t0001g0241 | 3 | HG01517.hp1 HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-216+3062C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21452970 | ||||||
| chr14:21452982
|
C | CA | 8 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(5): Show | 8 | HG01884.hp2 HG01891.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.-216+3049dupT | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21452982 | ||||||
| chr14:21452982
|
CA | C | 20 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0003g0128others(17): Show | 21 | HG01261.hp2 HG02055.hp1 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.-216+3049delT | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21452982 | ||||||
| chr14:21453008
|
C | CAAAGAAA others(311): Show |
1 | a0002c0002t0001g0183 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-216+3023_-216+302 others(322): Show |
CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21453008 | ||||||
| chr14:21453008
|
C | CAAAGAAA others(316): Show |
1 | a0002c0002t0001g0184 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-216+3023_-216+302 others(327): Show |
CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21453008 | ||||||
| chr14:21453036
|
T | C | 2 | a0001c0003t0001g0044a0001c0003t0001g0045 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-216+2996A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21453036 | ||||||
| chr14:21453066
|
C | T | 33 | a0001c0001t0001g0132a0001c0001t0001g0146a0001c0001t0001g0147others(30): Show | 34 | HG00733.hp2 HG00735.hp2 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.-216+2966G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21453066 | ||||||
| chr14:21453170
|
T | G | 1 | a0001c0001t0003g0234 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-216+2862A>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21453170 | ||||||
| chr14:21453221
|
A | G | 185 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(182): Show | 186 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.-216+2811T>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21453221 | ||||||
| chr14:21453271
|
T | C | 1 | a0001c0003t0002g0035 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-216+2761A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21453271 | ||||||
| chr14:21453354
|
C | T | 2 | a0001c0006t0001g0001a0001c0006t0001g0126 | 3 | HG02559.hp2 HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-216+2678G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21453354 | ||||||
| chr14:21453497
|
G | C | 1 | a0001c0001t0001g0247 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-216+2535C>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21453497 | ||||||
| chr14:21453529
|
T | C | 2 | a0001c0001t0003g0163a0001c0001t0003g0234 | 2 | HG02451.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-216+2503A>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21453529 | ||||||
| chr14:21453914
|
G | A | 12 | a0001c0001t0003g0128a0001c0001t0003g0130a0001c0001t0003g0142others(9): Show | 12 | HG02055.hp1 HG02258.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.-216+2118C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21453914 | ||||||
| chr14:21454030
|
C | T | 1 | a0001c0001t0002g0039 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-216+2002G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21454030 | ||||||
| chr14:21454162
|
A | AAAAAG | 27 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082others(24): Show | 27 | HG00408.hp2 HG00609.hp2 HG00673.hp2 others(24): Show |
intron_variant | MODIFIER | c.-216+1865_-216+186 others(9): Show |
CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21454162 | ||||||
| chr14:21454162
|
A | AAAAAGAA others(3): Show |
26 | a0001c0001t0001g0079a0001c0001t0001g0164a0001c0001t0001g0165others(23): Show | 26 | HG00733.hp2 HG00735.hp2 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.-216+1860_-216+186 others(14): Show |
CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21454162 | ||||||
| chr14:21454162
|
A | AAAAAGAA others(8): Show |
20 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0149others(17): Show | 20 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(17): Show |
intron_variant | MODIFIER | c.-216+1855_-216+186 others(19): Show |
CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21454162 | ||||||
| chr14:21454162
|
A | AAAAAGAA others(13): Show |
14 | a0001c0001t0001g0132a0001c0001t0001g0134a0001c0001t0001g0135others(11): Show | 14 | HG01358.hp2 HG02071.hp1 HG02074.hp1 others(11): Show |
intron_variant | MODIFIER | c.-216+1850_-216+186 others(24): Show |
CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21454162 | ||||||
| chr14:21454162
|
A | AAAAAGAA others(18): Show |
2 | a0001c0001t0001g0129a0001c0001t0003g0130 | 2 | HG01346.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.-216+1845_-216+186 others(29): Show |
CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21454162 | ||||||
| chr14:21454162
|
A | AAAAAGAA others(23): Show |
1 | a0001c0001t0003g0248 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-216+1840_-216+186 others(34): Show |
CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21454162 | ||||||
| chr14:21454162
|
A | AAAAAGAA others(28): Show |
1 | a0001c0001t0003g0128 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-216+1835_-216+186 others(39): Show |
CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21454162 | ||||||
| chr14:21454162
|
A | AAAAAGAA others(48): Show |
1 | a0001c0001t0001g0127 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-216+1815_-216+186 others(59): Show |
CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21454162 | ||||||
| chr14:21454162
|
AAAAAG | A | 70 | a0001c0001t0001g0070a0001c0001t0001g0096a0001c0001t0001g0097others(67): Show | 70 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.-216+1865_-216+186 others(9): Show |
CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21454162 | ||||||
| chr14:21454162
|
AAAAAGAA others(3): Show |
A | 19 | a0001c0001t0001g0123a0001c0001t0001g0233a0001c0001t0002g0031others(16): Show | 19 | HG00741.hp1 HG01496.hp1 HG02004.hp1 others(16): Show |
intron_variant | MODIFIER | c.-216+1860_-216+186 others(14): Show |
CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21454162 | ||||||
| chr14:21454162
|
AAAAAGAA others(8): Show |
A | 8 | a0001c0001t0001g0247a0001c0001t0002g0002a0001c0001t0002g0003others(5): Show | 9 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.-216+1855_-216+186 others(19): Show |
CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21454162 | ||||||
| chr14:21454162
|
AAAAAGAA others(13): Show |
A | 12 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0238others(9): Show | 12 | HG01517.hp1 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.-216+1850_-216+186 others(24): Show |
CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21454162 | ||||||
| chr14:21454162
|
AAAAAGAA others(18): Show |
A | 2 | a0001c0001t0001g0244a0001c0001t0003g0243 | 2 | HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-216+1845_-216+186 others(29): Show |
CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21454162 | ||||||
| chr14:21454162
|
AAAAAGAA others(28): Show |
A | 1 | a0001c0001t0001g0245 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-216+1835_-216+186 others(39): Show |
CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21454162 | ||||||
| chr14:21454217
|
G | C | 1 | a0002c0002t0001g0246 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-216+1815C>G | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21454217 | ||||||
| chr14:21454355
|
T | A | 1 | a0001c0001t0001g0247 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-216+1677A>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21454355 | ||||||
| chr14:21454485
|
T | G | 1 | a0001c0001t0003g0248 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-216+1547A>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21454485 | ||||||
| chr14:21454832
|
T | A | 4 | a0002c0002t0001g0249a0002c0002t0001g0250a0002c0002t0001g0251others(1): Show | 4 | HG01070.hp1 HG01169.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.-216+1200A>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21454832 | ||||||
| chr14:21454921
|
C | G | 3 | a0001c0006t0001g0001a0001c0006t0001g0126a0001c0014t0001g0125 | 4 | HG01261.hp2 HG02559.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-216+1111G>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21454921 | ||||||
| chr14:21455200
|
C | A | 1 | a0001c0001t0001g0253 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-216+832G>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21455200 | ||||||
| chr14:21455209
|
A | G | 51 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(48): Show | 51 | HG00323.hp1 HG00438.hp2 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.-216+823T>C | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21455209 | ||||||
| chr14:21455253
|
C | T | 3 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004 | 3 | HG01884.hp2 HG01891.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-216+779G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21455253 | ||||||
| chr14:21455388
|
C | A | 223 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(220): Show | 224 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.-216+644G>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21455388 | ||||||
| chr14:21455472
|
C | A | 1 | a0002c0002t0001g0254 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-216+560G>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21455472 | ||||||
| chr14:21455547
|
C | A | 1 | a0001c0003t0001g0255 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-216+485G>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21455547 | ||||||
| chr14:21455842
|
C | T | 2 | a0001c0003t0001g0044a0001c0003t0001g0045 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-216+190G>A | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21455842 | ||||||
| chr14:21455924
|
G | A | 1 | a0001c0005t0002g0042 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-216+108C>T | CHD8 | ENSG00000100888.15 | transcript | ENST00000646647.2 | protein_coding | 1/37 | chr14 | 21455924 |