| geneid | 27332 |
|---|---|
| ensemblid | ENSG00000075292.19 |
| hgncid | 17894 |
| symbol | ZNF638 |
| name | zinc finger protein 638 |
| refseq_nuc | NM_014497.5 |
| refseq_prot | NP_055312.2 |
| ensembl_nuc | ENST00000264447.9 |
| ensembl_prot | ENSP00000264447.4 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 71331782 |
| end | 71435061 |
| strand | + |
| ver | v1.2 |
| region | chr2:71331782-71435061 |
| region5000 | chr2:71326782-71440061 |
| regionname0 | ZNF638_chr2_71331782_71435061 |
| regionname5000 | ZNF638_chr2_71326782_71440061 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1978 | 188 | 65 | 44 | 46 | 7 | 24 | 36 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0002 | 0/0 | 1978 | 78 | 1 | 17 | 46 | 3 | 11 | 32 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0003 | 0/0 | 1978 | 52 | 13 | 2 | 31 | 2 | 4 | 28 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0004 | 0/0 | 1978 | 7 | 0 | 0 | 6 | 0 | 1 | 6 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0005 | 0/0 | 1978 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0006 | 0/0 | 1978 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0007 | 0/0 | 1978 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0008 | 0/0 | 1978 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0009 | 0/0 | 1978 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0010 | 0/0 | 1978 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0011 | 0/0 | 1978 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0012 | 0/0 | 1978 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0013 | 0/0 | 1978 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0014 | 0/0 | 1978 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0015 | 0/0 | 1978 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0016 | 0/0 | 1978 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0017 | 0/0 | 1978 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0018 | 0/0 | 1978 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0019 | 0/0 | 1978 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0020 | 0/0 | 1978 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0021 | 0/0 | 1978 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 5937 | 106 | 10 | 27 | 46 | 4 | 18 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| c0002 | 0/0 | 5937 | 77 | 1 | 17 | 45 | 3 | 11 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| c0003 | 1/0 | 5937 | 59 | 35 | 14 | 0 | 3 | 6 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| c0004 | 0/0 | 5937 | 48 | 12 | 2 | 28 | 2 | 4 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| c0005 | 0/0 | 5937 | 13 | 12 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| c0006 | 0/0 | 5937 | 7 | 0 | 0 | 6 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| c0007 | 0/0 | 5937 | 6 | 6 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| c0008 | 0/0 | 5937 | 3 | 0 | 0 | 3 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| c0009 | 0/0 | 5937 | 2 | 0 | 2 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| c0010 | 0/0 | 5937 | 2 | 2 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| c0011 | 0/0 | 5937 | 2 | 0 | 0 | 2 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| c0012 | 0/0 | 5937 | 2 | 0 | 0 | 2 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| c0013 | 0/0 | 5937 | 2 | 2 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| c0014 | 0/0 | 5937 | 2 | 0 | 0 | 2 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| c0015 | 0/0 | 5937 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| c0016 | 0/0 | 5937 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| c0017 | 0/0 | 5937 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| c0018 | 0/0 | 5937 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| c0019 | 0/0 | 5937 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| c0020 | 0/0 | 5937 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| c0021 | 0/0 | 5937 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| c0022 | 0/0 | 5937 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| c0023 | 0/0 | 5937 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| c0024 | 0/0 | 5937 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| c0025 | 0/0 | 5937 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| c0026 | 0/0 | 5937 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| c0027 | 0/0 | 5937 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| c0028 | 0/0 | 5937 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| c0029 | 0/0 | 5937 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| c0030 | 0/0 | 5937 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| c0031 | 0/0 | 5937 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 551 | 290 | 71 | 62 | 110 | 10 | 36 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| t0002 | 1/0 | 551 | 54 | 15 | 2 | 30 | 2 | 4 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| t0003 | 0/0 | 551 | 2 | 2 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| t0004 | 0/0 | 551 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| t0005 | 0/0 | 551 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0004 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0054 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0220 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0316 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0324 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 5937 | 106 | 10 | 27 | 46 | 4 | 18 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0001c0003 | 1/0 | 5937 | 59 | 35 | 14 | 0 | 3 | 6 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0001c0005 | 0/0 | 5937 | 13 | 12 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0001c0007 | 0/0 | 5937 | 6 | 6 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0001c0009 | 0/0 | 5937 | 2 | 0 | 2 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0001c0020 | 0/0 | 5937 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0001c0024 | 0/0 | 5937 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0002c0002 | 0/0 | 5937 | 77 | 1 | 17 | 45 | 3 | 11 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0002c0019 | 0/0 | 5937 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0003c0004 | 0/0 | 5937 | 48 | 12 | 2 | 28 | 2 | 4 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0003c0012 | 0/0 | 5937 | 2 | 0 | 0 | 2 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0003c0015 | 0/0 | 5937 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0003c0029 | 0/0 | 5937 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0004c0006 | 0/0 | 5937 | 7 | 0 | 0 | 6 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0005c0008 | 0/0 | 5937 | 3 | 0 | 0 | 3 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0006c0014 | 0/0 | 5937 | 2 | 0 | 0 | 2 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0007c0011 | 0/0 | 5937 | 2 | 0 | 0 | 2 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0008c0010 | 0/0 | 5937 | 2 | 2 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0009c0013 | 0/0 | 5937 | 2 | 2 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0010c0016 | 0/0 | 5937 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0011c0026 | 0/0 | 5937 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0012c0025 | 0/0 | 5937 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0013c0018 | 0/0 | 5937 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0014c0021 | 0/0 | 5937 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0015c0022 | 0/0 | 5937 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0016c0023 | 0/0 | 5937 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0017c0017 | 0/0 | 5937 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0018c0027 | 0/0 | 5937 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0019c0028 | 0/0 | 5937 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0020c0030 | 0/0 | 5937 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0021c0031 | 0/0 | 5937 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 6487 | 106 | 10 | 27 | 46 | 4 | 18 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0001c0003t0001 | 0/0 | 6487 | 55 | 32 | 14 | 0 | 3 | 6 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0001c0003t0002 | 1/0 | 6487 | 2 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0001c0003t0003 | 0/0 | 6487 | 2 | 2 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0001c0005t0001 | 0/0 | 6487 | 13 | 12 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0001c0007t0001 | 0/0 | 6487 | 5 | 5 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0001c0007t0005 | 0/0 | 6487 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0001c0009t0001 | 0/0 | 6487 | 2 | 0 | 2 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0001c0020t0001 | 0/0 | 6487 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0001c0024t0001 | 0/0 | 6487 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0002c0002t0001 | 0/0 | 6487 | 77 | 1 | 17 | 45 | 3 | 11 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0002c0019t0001 | 0/0 | 6487 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0003c0004t0001 | 0/0 | 6487 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0003c0004t0002 | 0/0 | 6487 | 47 | 12 | 2 | 27 | 2 | 4 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0003c0012t0002 | 0/0 | 6487 | 2 | 0 | 0 | 2 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0003c0015t0002 | 0/0 | 6487 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0003c0029t0002 | 0/0 | 6487 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0004c0006t0001 | 0/0 | 6487 | 7 | 0 | 0 | 6 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0005c0008t0001 | 0/0 | 6487 | 3 | 0 | 0 | 3 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0006c0014t0001 | 0/0 | 6487 | 2 | 0 | 0 | 2 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0007c0011t0001 | 0/0 | 6487 | 2 | 0 | 0 | 2 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0008c0010t0002 | 0/0 | 6487 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0008c0010t0004 | 0/0 | 6487 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0009c0013t0001 | 0/0 | 6487 | 2 | 2 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0010c0016t0001 | 0/0 | 6487 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0011c0026t0001 | 0/0 | 6487 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0012c0025t0001 | 0/0 | 6487 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0013c0018t0001 | 0/0 | 6487 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0014c0021t0001 | 0/0 | 6487 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0015c0022t0001 | 0/0 | 6487 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0016c0023t0001 | 0/0 | 6487 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0017c0017t0001 | 0/0 | 6487 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0018c0027t0001 | 0/0 | 6487 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0019c0028t0001 | 0/0 | 6487 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0020c0030t0001 | 0/0 | 6487 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| a0021c0031t0001 | 0/0 | 6487 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | copy fasta | chr2 | 71326782 | 71440061 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0054 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0001t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0003t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0003t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0003t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0003t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0003t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0003t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0003t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0003t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0003t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0003t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0003t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0003t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0003t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0003t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0003t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0003t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0003t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0003t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0003t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0003t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0003t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0003t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0003t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0003t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0003t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0003t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0003t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0003t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0003t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0003t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0003t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0003t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0003t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0003t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0003t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0003t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0003t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0003t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0003t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0003t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0003t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0003t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0003t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0003t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0003t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0003t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0003t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0003t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0003t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0003t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0003t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0003t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0003t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0003t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0003t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0003t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0003t0002g0220 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0003t0003g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0003t0003g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0005t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0005t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0005t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0005t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0005t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0005t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0005t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0005t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0005t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0005t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0005t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0005t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0005t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0007t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0007t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0007t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0007t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0007t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0007t0005g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0009t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0009t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0020t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0001c0024t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0002c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0002c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0002c0002t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0002c0002t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0002c0002t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0002c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0002c0002t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0002c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0002c0002t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0002c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0002c0002t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0002c0002t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0002c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0002c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0002c0002t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0002c0002t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0002c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0002c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0002c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0002c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0002c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0002c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0002c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0002c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0002c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0002c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0002c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0002c0002t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0002c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0002c0002t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0002c0002t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0002c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0002c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0002c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0002c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0002c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0002c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0002c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0002c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0002c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0002c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0002c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0002c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0002c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0002c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0002c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0002c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0002c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0002c0002t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0002c0002t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0002c0002t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0002c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0002c0002t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0002c0002t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0002c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0002c0002t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0002c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0002c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0002c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0002c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0002c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0002c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0002c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0002c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0002c0002t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0002c0002t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0002c0002t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0002c0002t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0002c0002t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0002c0002t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0002c0002t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0002c0002t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0002c0002t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0002c0002t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0002c0002t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0002c0019t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0003c0004t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0003c0004t0002g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0003c0004t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0003c0004t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0003c0004t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0003c0004t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0003c0004t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0003c0004t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0003c0004t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0003c0004t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0003c0004t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0003c0004t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0003c0004t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0003c0004t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0003c0004t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0003c0004t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0003c0004t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0003c0004t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0003c0004t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0003c0004t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0003c0004t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0003c0004t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0003c0004t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0003c0004t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0003c0004t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0003c0004t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0003c0004t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0003c0004t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0003c0004t0002g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0003c0004t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0003c0004t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0003c0004t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0003c0004t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0003c0004t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0003c0004t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0003c0004t0002g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0003c0004t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0003c0004t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0003c0004t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0003c0004t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0003c0004t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0003c0004t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0003c0004t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0003c0004t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0003c0004t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0003c0004t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0003c0004t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0003c0004t0002g0324 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0003c0012t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0003c0012t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0003c0015t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0003c0029t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0004c0006t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0004c0006t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0004c0006t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0004c0006t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0004c0006t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0004c0006t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0004c0006t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0005c0008t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0005c0008t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0005c0008t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0006c0014t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0006c0014t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0007c0011t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0007c0011t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0008c0010t0002g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0008c0010t0004g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0009c0013t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0009c0013t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0010c0016t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0011c0026t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0012c0025t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0013c0018t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0014c0021t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0015c0022t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0016c0023t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0017c0017t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0018c0027t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0019c0028t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0020c0030t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| a0021c0031t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0003 | t0001 | g0111 | EUR | FIN | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | FIN | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG00323 | hp1 | a0003 | c0004 | t0002 | g0244 | EUR | FIN | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0022 | EUR | FIN | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | CHS | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG00423 | hp2 | a0003 | c0004 | t0002 | g0226 | EAS | CHS | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG00438 | hp1 | a0002 | c0002 | t0001 | g0192 | EAS | CHS | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG00438 | hp2 | a0010 | c0016 | t0001 | g0265 | EAS | CHS | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG00544 | hp1 | a0002 | c0002 | t0001 | g0286 | EAS | CHS | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | CHS | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | CHS | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG00597 | hp2 | a0002 | c0002 | t0001 | g0288 | EAS | CHS | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG00609 | hp1 | a0002 | c0002 | t0001 | g0306 | EAS | CHS | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG00609 | hp2 | a0002 | c0002 | t0001 | g0311 | EAS | CHS | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG00673 | hp1 | a0002 | c0002 | t0001 | g0312 | EAS | CHS | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | CHS | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG00733 | hp1 | a0001 | c0003 | t0001 | g0144 | AMR | PUR | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG00733 | hp2 | a0003 | c0004 | t0002 | g0247 | AMR | PUR | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG00735 | hp1 | a0001 | c0003 | t0001 | g0133 | AMR | PUR | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG00738 | hp1 | a0001 | c0003 | t0001 | g0170 | AMR | PUR | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG00741 | hp1 | a0002 | c0002 | t0001 | g0271 | AMR | PUR | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG01069 | hp2 | a0002 | c0002 | t0001 | g0193 | AMR | PUR | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG01070 | hp1 | a0001 | c0003 | t0001 | g0166 | AMR | PUR | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG01071 | hp1 | a0001 | c0003 | t0001 | g0167 | AMR | PUR | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG01074 | hp1 | a0002 | c0002 | t0001 | g0190 | AMR | PUR | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG01074 | hp2 | a0002 | c0002 | t0001 | g0268 | AMR | PUR | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG01081 | hp2 | a0001 | c0003 | t0001 | g0139 | AMR | PUR | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG01099 | hp2 | a0001 | c0003 | t0001 | g0120 | AMR | PUR | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG01109 | hp1 | a0002 | c0002 | t0001 | g0183 | AMR | PUR | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG01167 | hp1 | a0001 | c0003 | t0001 | g0115 | AMR | PUR | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG01167 | hp2 | a0001 | c0003 | t0001 | g0130 | AMR | PUR | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG01169 | hp1 | a0001 | c0003 | t0001 | g0116 | AMR | PUR | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG01175 | hp1 | a0002 | c0002 | t0001 | g0300 | AMR | PUR | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG01192 | hp1 | a0001 | c0003 | t0001 | g0169 | AMR | PUR | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG01243 | hp1 | a0001 | c0003 | t0001 | g0135 | AMR | PUR | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG01243 | hp2 | a0001 | c0005 | t0001 | g0174 | AMR | PUR | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | CLM | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG01255 | hp2 | a0002 | c0002 | t0001 | g0189 | AMR | CLM | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG01256 | hp1 | a0001 | c0003 | t0001 | g0114 | AMR | CLM | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | CLM | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | CLM | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG01358 | hp2 | a0002 | c0002 | t0001 | g0194 | AMR | CLM | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG01361 | hp1 | a0002 | c0002 | t0001 | g0185 | AMR | CLM | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG01361 | hp2 | a0001 | c0009 | t0001 | g0136 | AMR | CLM | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG01496 | hp1 | a0002 | c0002 | t0001 | g0180 | AMR | CLM | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG01496 | hp2 | a0001 | c0003 | t0001 | g0164 | AMR | CLM | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG01516 | hp1 | a0003 | c0004 | t0002 | g0324 | EUR | IBS | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG01516 | hp2 | a0001 | c0003 | t0001 | g0175 | EUR | IBS | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG01517 | hp1 | a0002 | c0002 | t0001 | g0186 | EUR | IBS | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG01517 | hp2 | a0001 | c0003 | t0001 | g0176 | EUR | IBS | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG01884 | hp1 | a0021 | c0031 | t0001 | g0341 | AFR | ACB | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG01884 | hp2 | a0001 | c0007 | t0001 | g0328 | AFR | ACB | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG01891 | hp1 | a0001 | c0005 | t0001 | g0152 | AFR | ACB | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG01891 | hp2 | a0001 | c0003 | t0001 | g0171 | AFR | ACB | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG01928 | hp2 | a0002 | c0002 | t0001 | g0298 | AMR | PEL | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG01943 | hp1 | a0001 | c0009 | t0001 | g0110 | AMR | PEL | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PEL | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG01952 | hp2 | a0017 | c0017 | t0001 | g0267 | AMR | PEL | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG01975 | hp2 | a0002 | c0002 | t0001 | g0293 | AMR | PEL | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG01981 | hp1 | a0002 | c0002 | t0001 | g0179 | AMR | PEL | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG01993 | hp1 | a0002 | c0002 | t0001 | g0297 | AMR | PEL | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PEL | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG02004 | hp2 | a0002 | c0002 | t0001 | g0294 | AMR | PEL | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG02015 | hp1 | a0002 | c0002 | t0001 | g0289 | EAS | KHV | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG02040 | hp2 | a0002 | c0002 | t0001 | g0182 | EAS | KHV | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG02055 | hp1 | a0001 | c0003 | t0001 | g0150 | AFR | ACB | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG02055 | hp2 | a0003 | c0004 | t0002 | g0211 | AFR | ACB | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG02080 | hp1 | a0003 | c0004 | t0002 | g0207 | EAS | KHV | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG02080 | hp2 | a0002 | c0002 | t0001 | g0256 | EAS | KHV | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG02083 | hp1 | a0003 | c0004 | t0002 | g0219 | EAS | KHV | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG02083 | hp2 | a0002 | c0002 | t0001 | g0275 | EAS | KHV | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | KHV | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG02129 | hp2 | a0002 | c0002 | t0001 | g0255 | EAS | KHV | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | ACB | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG02145 | hp2 | a0001 | c0003 | t0001 | g0106 | AFR | ACB | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | CDX | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG02155 | hp2 | a0002 | c0002 | t0001 | g0276 | EAS | CDX | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | CDX | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG02165 | hp2 | a0002 | c0002 | t0001 | g0269 | EAS | CDX | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG02258 | hp1 | a0001 | c0003 | t0001 | g0138 | AFR | ACB | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG02258 | hp2 | a0001 | c0003 | t0001 | g0121 | AFR | ACB | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG02280 | hp1 | a0001 | c0003 | t0001 | g0131 | AFR | ACB | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG02280 | hp2 | a0001 | c0003 | t0002 | g0218 | AFR | ACB | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PEL | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG02293 | hp2 | a0002 | c0002 | t0001 | g0295 | AMR | PEL | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG02300 | hp2 | a0003 | c0004 | t0002 | g0202 | AMR | PEL | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG02451 | hp1 | a0001 | c0005 | t0001 | g0156 | AFR | ACB | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG02451 | hp2 | a0001 | c0007 | t0001 | g0327 | AFR | ACB | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0326 | AFR | GWD | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG02572 | hp2 | a0001 | c0003 | t0001 | g0112 | AFR | GWD | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG02615 | hp1 | a0001 | c0003 | t0001 | g0107 | AFR | GWD | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG02615 | hp2 | a0013 | c0018 | t0001 | g0331 | AFR | GWD | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG02622 | hp2 | a0001 | c0003 | t0001 | g0173 | AFR | GWD | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0334 | AFR | GWD | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG02630 | hp2 | a0019 | c0028 | t0001 | g0195 | AFR | GWD | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG02647 | hp1 | a0001 | c0003 | t0001 | g0119 | AFR | GWD | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG02647 | hp2 | a0001 | c0024 | t0001 | g0145 | AFR | GWD | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG02683 | hp2 | a0002 | c0002 | t0001 | g0188 | SAS | PJL | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG02717 | hp1 | a0001 | c0003 | t0001 | g0151 | AFR | GWD | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG02717 | hp2 | a0001 | c0003 | t0001 | g0140 | AFR | GWD | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG02723 | hp1 | a0001 | c0003 | t0001 | g0141 | AFR | GWD | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0338 | AFR | GWD | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG02735 | hp2 | a0001 | c0003 | t0001 | g0124 | SAS | PJL | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG02738 | hp2 | a0001 | c0003 | t0001 | g0108 | SAS | PJL | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG02809 | hp1 | a0001 | c0003 | t0001 | g0137 | AFR | GWD | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG02809 | hp2 | a0001 | c0005 | t0001 | g0122 | AFR | GWD | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG02818 | hp1 | a0003 | c0004 | t0002 | g0250 | AFR | GWD | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG02818 | hp2 | a0001 | c0003 | t0001 | g0128 | AFR | GWD | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG02895 | hp1 | a0001 | c0003 | t0001 | g0134 | AFR | GWD | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG02895 | hp2 | a0001 | c0007 | t0001 | g0333 | AFR | GWD | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG02896 | hp1 | a0001 | c0007 | t0001 | g0330 | AFR | GWD | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG02896 | hp2 | a0001 | c0003 | t0001 | g0129 | AFR | GWD | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG02922 | hp1 | a0001 | c0005 | t0001 | g0160 | AFR | ESN | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG02922 | hp2 | a0003 | c0004 | t0002 | g0243 | AFR | ESN | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0340 | AFR | ESN | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG02965 | hp2 | a0003 | c0004 | t0002 | g0246 | AFR | ESN | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG02970 | hp1 | a0001 | c0005 | t0001 | g0161 | AFR | ESN | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG02970 | hp2 | a0003 | c0004 | t0002 | g0221 | AFR | ESN | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG02976 | hp1 | a0001 | c0003 | t0001 | g0127 | AFR | ESN | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG02976 | hp2 | a0014 | c0021 | t0001 | g0181 | AFR | ESN | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG03017 | hp1 | a0003 | c0004 | t0002 | g0239 | SAS | PJL | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG03017 | hp2 | a0001 | c0003 | t0001 | g0148 | SAS | PJL | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG03041 | hp1 | a0001 | c0003 | t0001 | g0325 | AFR | GWD | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG03041 | hp2 | a0001 | c0005 | t0001 | g0153 | AFR | GWD | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG03098 | hp1 | a0001 | c0005 | t0001 | g0158 | AFR | MSL | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG03098 | hp2 | a0001 | c0003 | t0003 | g0162 | AFR | MSL | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG03139 | hp1 | a0003 | c0015 | t0002 | g0245 | AFR | ESN | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG03139 | hp2 | a0001 | c0003 | t0001 | g0142 | AFR | ESN | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG03195 | hp1 | a0001 | c0003 | t0001 | g0146 | AFR | ESN | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0339 | AFR | ESN | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG03209 | hp1 | a0003 | c0004 | t0002 | g0248 | AFR | MSL | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG03209 | hp2 | a0001 | c0003 | t0001 | g0147 | AFR | MSL | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG03225 | hp1 | a0003 | c0004 | t0002 | g0252 | AFR | MSL | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG03225 | hp2 | a0001 | c0003 | t0001 | g0113 | AFR | MSL | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG03239 | hp1 | a0002 | c0002 | t0001 | g0200 | SAS | PJL | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG03453 | hp1 | a0009 | c0013 | t0001 | g0103 | AFR | MSL | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG03453 | hp2 | a0001 | c0003 | t0001 | g0172 | AFR | MSL | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG03486 | hp1 | a0001 | c0005 | t0001 | g0157 | AFR | MSL | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG03486 | hp2 | a0008 | c0010 | t0004 | g0253 | AFR | MSL | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG03491 | hp2 | a0003 | c0004 | t0002 | g0209 | SAS | PJL | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG03492 | hp1 | a0003 | c0004 | t0002 | g0236 | SAS | PJL | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0196 | SAS | PJL | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG03516 | hp1 | a0001 | c0007 | t0001 | g0329 | AFR | ESN | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG03516 | hp2 | a0001 | c0003 | t0001 | g0118 | AFR | ESN | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG03540 | hp1 | a0001 | c0003 | t0001 | g0105 | AFR | GWD | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG03540 | hp2 | a0001 | c0003 | t0001 | g0109 | AFR | GWD | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG03579 | hp1 | a0003 | c0004 | t0002 | g0249 | AFR | MSL | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG03579 | hp2 | a0009 | c0013 | t0001 | g0102 | AFR | MSL | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG03654 | hp1 | a0002 | c0002 | t0001 | g0277 | SAS | PJL | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG03669 | hp1 | a0004 | c0006 | t0001 | g0257 | SAS | PJL | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | STU | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG03688 | hp2 | a0003 | c0004 | t0002 | g0231 | SAS | STU | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG03704 | hp2 | a0002 | c0002 | t0001 | g0299 | SAS | PJL | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG03710 | hp2 | a0002 | c0002 | t0001 | g0308 | SAS | PJL | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | BEB | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0198 | SAS | BEB | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG03927 | hp1 | a0001 | c0003 | t0001 | g0125 | SAS | BEB | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | BEB | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG03942 | hp1 | a0001 | c0003 | t0001 | g0123 | SAS | BEB | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | BEB | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG04115 | hp1 | a0002 | c0002 | t0001 | g0199 | SAS | STU | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG04115 | hp2 | a0002 | c0002 | t0001 | g0184 | SAS | STU | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | STU | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG04199 | hp2 | a0001 | c0003 | t0001 | g0143 | SAS | STU | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG04228 | hp1 | a0002 | c0002 | t0001 | g0262 | SAS | STU | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | STU | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0337 | AFR | YRI | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA18522 | hp2 | a0001 | c0005 | t0001 | g0165 | AFR | YRI | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA18747 | hp1 | a0002 | c0002 | t0001 | g0302 | EAS | CHB | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA18939 | hp1 | a0003 | c0004 | t0002 | g0222 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA18939 | hp2 | a0007 | c0011 | t0001 | g0303 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA18941 | hp1 | a0003 | c0029 | t0002 | g0230 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA18942 | hp1 | a0002 | c0002 | t0001 | g0301 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA18943 | hp2 | a0003 | c0004 | t0002 | g0241 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA18944 | hp2 | a0016 | c0023 | t0001 | g0264 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA18945 | hp1 | a0007 | c0011 | t0001 | g0304 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA18945 | hp2 | a0002 | c0019 | t0001 | g0084 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA18947 | hp2 | a0003 | c0004 | t0002 | g0213 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA18948 | hp1 | a0003 | c0012 | t0002 | g0240 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA18948 | hp2 | a0004 | c0006 | t0001 | g0284 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA18951 | hp1 | a0012 | c0025 | t0001 | g0073 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA18951 | hp2 | a0003 | c0004 | t0002 | g0223 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA18952 | hp2 | a0003 | c0012 | t0002 | g0232 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA18953 | hp2 | a0002 | c0002 | t0001 | g0287 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA18954 | hp1 | a0003 | c0004 | t0002 | g0235 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA18954 | hp2 | a0004 | c0006 | t0001 | g0283 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA18956 | hp1 | a0003 | c0004 | t0002 | g0225 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA18956 | hp2 | a0002 | c0002 | t0001 | g0273 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA18963 | hp2 | a0003 | c0004 | t0002 | g0217 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA18964 | hp2 | a0002 | c0002 | t0001 | g0317 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA18965 | hp1 | a0002 | c0002 | t0001 | g0314 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA18965 | hp2 | a0003 | c0004 | t0002 | g0229 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA18967 | hp2 | a0003 | c0004 | t0001 | g0259 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA18971 | hp1 | a0002 | c0002 | t0001 | g0274 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA18971 | hp2 | a0005 | c0008 | t0001 | g0043 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA18972 | hp1 | a0002 | c0002 | t0001 | g0343 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA18972 | hp2 | a0003 | c0004 | t0002 | g0210 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA18978 | hp2 | a0002 | c0002 | t0001 | g0263 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA18980 | hp1 | a0004 | c0006 | t0001 | g0281 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA18980 | hp2 | a0003 | c0004 | t0002 | g0228 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA18981 | hp1 | a0002 | c0002 | t0001 | g0272 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA18982 | hp2 | a0002 | c0002 | t0001 | g0291 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA18983 | hp2 | a0003 | c0004 | t0002 | g0216 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA18985 | hp2 | a0002 | c0002 | t0001 | g0254 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA18986 | hp1 | a0005 | c0008 | t0001 | g0042 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA18986 | hp2 | a0003 | c0004 | t0002 | g0206 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA18992 | hp1 | a0002 | c0002 | t0001 | g0178 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA18992 | hp2 | a0004 | c0006 | t0001 | g0260 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA18993 | hp1 | a0003 | c0004 | t0002 | g0237 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA18994 | hp2 | a0004 | c0006 | t0001 | g0261 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA18998 | hp1 | a0003 | c0004 | t0002 | g0234 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA18999 | hp2 | a0002 | c0002 | t0001 | g0285 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA19004 | hp1 | a0002 | c0002 | t0001 | g0310 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA19004 | hp2 | a0003 | c0004 | t0002 | g0204 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA19007 | hp2 | a0003 | c0004 | t0002 | g0227 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA19010 | hp1 | a0002 | c0002 | t0001 | g0278 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA19010 | hp2 | a0002 | c0002 | t0001 | g0177 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA19012 | hp1 | a0003 | c0004 | t0002 | g0205 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA19012 | hp2 | a0004 | c0006 | t0001 | g0282 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA19030 | hp1 | a0001 | c0003 | t0003 | g0163 | AFR | LWK | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA19030 | hp2 | a0003 | c0004 | t0002 | g0251 | AFR | LWK | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA19043 | hp1 | a0001 | c0003 | t0001 | g0132 | AFR | LWK | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | LWK | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA19055 | hp1 | a0002 | c0002 | t0001 | g0307 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA19055 | hp2 | a0003 | c0004 | t0002 | g0214 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA19056 | hp1 | a0003 | c0004 | t0002 | g0215 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA19056 | hp2 | a0020 | c0030 | t0001 | g0315 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA19057 | hp2 | a0002 | c0002 | t0001 | g0258 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA19058 | hp2 | a0002 | c0002 | t0001 | g0319 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA19062 | hp2 | a0002 | c0002 | t0001 | g0320 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA19063 | hp1 | a0003 | c0004 | t0002 | g0208 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA19064 | hp2 | a0002 | c0002 | t0001 | g0321 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA19065 | hp1 | a0003 | c0004 | t0002 | g0224 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA19068 | hp1 | a0002 | c0002 | t0001 | g0296 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA19070 | hp1 | a0002 | c0002 | t0001 | g0280 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA19075 | hp1 | a0002 | c0002 | t0001 | g0279 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA19075 | hp2 | a0003 | c0004 | t0002 | g0242 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA19078 | hp2 | a0002 | c0002 | t0001 | g0344 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA19079 | hp1 | a0002 | c0002 | t0001 | g0322 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA19080 | hp1 | a0006 | c0014 | t0001 | g0309 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA19080 | hp2 | a0003 | c0004 | t0002 | g0003 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA19083 | hp1 | a0005 | c0008 | t0001 | g0008 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA19083 | hp2 | a0002 | c0002 | t0001 | g0313 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA19084 | hp2 | a0006 | c0014 | t0001 | g0318 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA19085 | hp1 | a0002 | c0002 | t0001 | g0290 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA19085 | hp2 | a0003 | c0004 | t0002 | g0212 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA19088 | hp2 | a0002 | c0002 | t0001 | g0305 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA19091 | hp2 | a0002 | c0002 | t0001 | g0266 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA19240 | hp1 | a0001 | c0003 | t0001 | g0104 | AFR | YRI | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA19240 | hp2 | a0001 | c0003 | t0001 | g0117 | AFR | YRI | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA20129 | hp1 | a0002 | c0002 | t0001 | g0187 | AFR | ASW | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA20129 | hp2 | a0008 | c0010 | t0002 | g0342 | AFR | ASW | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA20752 | hp2 | a0002 | c0002 | t0001 | g0191 | EUR | TSI | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0028 | EUR | TSI | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA20805 | hp2 | a0002 | c0002 | t0001 | g0316 | EUR | TSI | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | GIH | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA20905 | hp2 | a0002 | c0002 | t0001 | g0197 | SAS | GIH | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG01123 | hp1 | a0002 | c0002 | t0001 | g0270 | AMR | CLM | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG02109 | hp1 | a0003 | c0004 | t0002 | g0238 | AFR | ACB | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG02109 | hp2 | a0001 | c0020 | t0001 | g0323 | AFR | ACB | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG02486 | hp1 | a0001 | c0005 | t0001 | g0159 | AFR | ACB | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG02486 | hp2 | a0001 | c0003 | t0001 | g0168 | AFR | ACB | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG02559 | hp1 | a0001 | c0005 | t0001 | g0155 | AFR | ACB | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG02559 | hp2 | a0011 | c0026 | t0001 | g0336 | AFR | ACB | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG03471 | hp1 | a0001 | c0007 | t0005 | g0332 | AFR | MSL | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0335 | AFR | MSL | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG06807 | hp1 | a0015 | c0022 | t0001 | g0126 | AFR | USA | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| HG06807 | hp2 | a0001 | c0005 | t0001 | g0154 | AFR | USA | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA18955 | hp1 | a0002 | c0002 | t0001 | g0292 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA20300 | hp1 | a0003 | c0004 | t0002 | g0233 | AFR | USA | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA20300 | hp2 | a0001 | c0003 | t0001 | g0149 | AFR | USA | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA21309 | hp1 | a0018 | c0027 | t0001 | g0201 | AFR | LWK | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| NA21309 | hp2 | a0003 | c0004 | t0002 | g0203 | AFR | LWK | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0054 | REF | REF | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| homoSapiens_grch38 | hp1 | a0001 | c0003 | t0002 | g0220 | REF | REF | ZNF638_chr2_71326782_71440061 | ZNF638 | chr2 | 71326782 | 71440061 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:71349033
|
C | T | 1 | a0021 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.79C>T | p.Pro27Ser | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 2/28 | 375/6487 | 79/5937 | 27/1978 | chr2 | 71349033 | ||
| chr2:71349282
|
A | G | 1 | a0020 | 1 | NA19056.hp2 | missense_variant | MODERATE | c.328A>G | p.Ile110Val | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 2/28 | 624/6487 | 328/5937 | 110/1978 | chr2 | 71349282 | ||
| chr2:71349676
|
A | C | 1 | a0006 | 2 | NA19080.hp1 NA19084.hp2 |
missense_variant | MODERATE | c.722A>C | p.Glu241Ala | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 2/28 | 1018/6487 | 722/5937 | 241/1978 | chr2 | 71349676 | ||
| chr2:71349723
|
G | A | 1 | a0010 | 1 | HG00438.hp2 | missense_variant | MODERATE | c.769G>A | p.Val257Met | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 2/28 | 1065/6487 | 769/5937 | 257/1978 | chr2 | 71349723 | ||
| chr2:71349897
|
A | G | 1 | a0009 | 2 | HG03453.hp1 HG03579.hp2 |
missense_variant | MODERATE | c.943A>G | p.Ile315Val | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 2/28 | 1239/6487 | 943/5937 | 315/1978 | chr2 | 71349897 | ||
| chr2:71350042
|
A | C | 1 | a0019 | 1 | HG02630.hp2 | missense_variant | MODERATE | c.1088A>C | p.His363Pro | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 2/28 | 1384/6487 | 1088/5937 | 363/1978 | chr2 | 71350042 | ||
| chr2:71364168
|
A | G | 1 | a0018 | 1 | NA21309.hp1 | missense_variant | MODERATE | c.1633A>G | p.Ile545Val | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 5/28 | 1929/6487 | 1633/5937 | 545/1978 | chr2 | 71364168 | ||
| chr2:71365465
|
C | T | 1 | a0007 | 2 | NA18939.hp2 NA18945.hp1 |
missense_variant | MODERATE | c.1754C>T | p.Ser585Phe | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 6/28 | 2050/6487 | 1754/5937 | 585/1978 | chr2 | 71365465 | ||
| chr2:71365593
|
A | G | 1 | a0011 | 1 | HG02559.hp2 | missense_variant | MODERATE | c.1882A>G | p.Ser628Gly | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 6/28 | 2178/6487 | 1882/5937 | 628/1978 | chr2 | 71365593 | ||
| chr2:71368403
|
C | A | 1 | a0017 | 1 | HG01952.hp2 | missense_variant | MODERATE | c.2017C>A | p.His673Asn | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 7/28 | 2313/6487 | 2017/5937 | 673/1978 | chr2 | 71368403 | ||
| chr2:71400132
|
A | G | 1 | a0012 | 1 | NA18951.hp1 | missense_variant | MODERATE | c.2608A>G | p.Ser870Gly | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 14/28 | 2904/6487 | 2608/5937 | 870/1978 | chr2 | 71400132 | ||
| chr2:71403979
|
A | G | 2 | a0003a0008 | 54 | HG00323.hp1 HG00423.hp2 HG00733.hp2 others(51): Show |
missense_variant | MODERATE | c.2939A>G | p.Asn980Ser | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 17/28 | 3235/6487 | 2939/5937 | 980/1978 | chr2 | 71403979 | ||
| chr2:71422836
|
A | G | 1 | a0004 | 7 | HG03669.hp1 NA18948.hp2 NA18954.hp2 others(4): Show |
missense_variant | MODERATE | c.3322A>G | p.Ile1108Val | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 22/28 | 3618/6487 | 3322/5937 | 1108/1978 | chr2 | 71422836 | ||
| chr2:71423296
|
C | G | 1 | a0016 | 1 | NA18944.hp2 | missense_variant | MODERATE | c.3782C>G | p.Ala1261Gly | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 22/28 | 4078/6487 | 3782/5937 | 1261/1978 | chr2 | 71423296 | ||
| chr2:71423517
|
G | A | 1 | a0005 | 3 | NA18971.hp2 NA18986.hp1 NA19083.hp1 |
missense_variant | MODERATE | c.4003G>A | p.Glu1335Lys | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 22/28 | 4299/6487 | 4003/5937 | 1335/1978 | chr2 | 71423517 | ||
| chr2:71423899
|
G | A | 1 | a0008 | 2 | HG03486.hp2 NA20129.hp2 |
missense_variant | MODERATE | c.4385G>A | p.Ser1462Asn | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 22/28 | 4681/6487 | 4385/5937 | 1462/1978 | chr2 | 71423899 | ||
| chr2:71426562
|
A | G | 1 | a0013 | 1 | HG02615.hp2 | missense_variant | MODERATE | c.4693A>G | p.Arg1565Gly | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 24/28 | 4989/6487 | 4693/5937 | 1565/1978 | chr2 | 71426562 | ||
| chr2:71427045
|
G | A | 13 | a0002a0003a0004others(10): Show | 151 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(148): Show |
missense_variant | MODERATE | c.5176G>A | p.Val1726Met | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 24/28 | 5472/6487 | 5176/5937 | 1726/1978 | chr2 | 71427045 | ||
| chr2:71428549
|
A | G | 1 | a0015 | 1 | HG06807.hp1 | missense_variant&splice_region_variant | MODERATE | c.5548A>G | p.Lys1850Glu | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 25/28 | 5844/6487 | 5548/5937 | 1850/1978 | chr2 | 71428549 | ||
| chr2:71431411
|
C | T | 2 | a0003a0008 | 54 | HG00323.hp1 HG00423.hp2 HG00733.hp2 others(51): Show |
missense_variant | MODERATE | c.5735C>T | p.Ala1912Val | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 26/28 | 6031/6487 | 5735/5937 | 1912/1978 | chr2 | 71431411 | ||
| chr2:71433234
|
A | G | 1 | a0014 | 1 | HG02976.hp2 | missense_variant | MODERATE | c.5822A>G | p.Lys1941Arg | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 27/28 | 6118/6487 | 5822/5937 | 1941/1978 | chr2 | 71433234 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:71349416
|
A | G | 1 | a0003c0029 | 1 | NA18941.hp1 | synonymous_variant | LOW | c.462A>G | p.Leu154Leu | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 2/28 | 758/6487 | 462/5937 | 154/1978 | chr2 | 71349416 | ||
| chr2:71349492
|
C | A | 1 | a0003c0015 | 1 | HG03139.hp1 | synonymous_variant | LOW | c.538C>A | p.Arg180Arg | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 2/28 | 834/6487 | 538/5937 | 180/1978 | chr2 | 71349492 | ||
| chr2:71350037
|
C | T | 1 | a0003c0012 | 2 | NA18948.hp1 NA18952.hp2 |
synonymous_variant | LOW | c.1083C>T | p.Asn361Asn | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 2/28 | 1379/6487 | 1083/5937 | 361/1978 | chr2 | 71350037 | ||
| chr2:71400500
|
G | A | 4 | a0001c0007a0009c0013a0013c0018others(1): Show | 10 | HG01884.hp2 HG02451.hp2 HG02615.hp2 others(7): Show |
synonymous_variant | LOW | c.2679G>A | p.Glu893Glu | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 15/28 | 2975/6487 | 2679/5937 | 893/1978 | chr2 | 71400500 | ||
| chr2:71403959
|
A | C | 1 | a0001c0024 | 1 | HG02647.hp2 | synonymous_variant | LOW | c.2919A>C | p.Ser973Ser | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 17/28 | 3215/6487 | 2919/5937 | 973/1978 | chr2 | 71403959 | ||
| chr2:71406145
|
T | C | 7 | a0001c0001a0001c0009a0002c0019others(4): Show | 115 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(112): Show |
synonymous_variant | LOW | c.3018T>C | p.Ile1006Ile | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 19/28 | 3314/6487 | 3018/5937 | 1006/1978 | chr2 | 71406145 | ||
| chr2:71406259
|
C | T | 8 | a0001c0001a0001c0007a0002c0019others(5): Show | 120 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(117): Show |
synonymous_variant | LOW | c.3132C>T | p.Asn1044Asn | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 19/28 | 3428/6487 | 3132/5937 | 1044/1978 | chr2 | 71406259 | ||
| chr2:71423240
|
A | G | 1 | a0012c0025 | 1 | NA18951.hp1 | synonymous_variant | LOW | c.3726A>G | p.Glu1242Glu | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 22/28 | 4022/6487 | 3726/5937 | 1242/1978 | chr2 | 71423240 | ||
| chr2:71426555
|
G | A | 1 | a0001c0020 | 1 | HG02109.hp2 | synonymous_variant | LOW | c.4686G>A | p.Lys1562Lys | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 24/28 | 4982/6487 | 4686/5937 | 1562/1978 | chr2 | 71426555 | ||
| chr2:71426990
|
T | C | 1 | a0001c0005 | 13 | HG01243.hp2 HG01891.hp1 HG02451.hp1 others(10): Show |
synonymous_variant | LOW | c.5121T>C | p.Thr1707Thr | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 24/28 | 5417/6487 | 5121/5937 | 1707/1978 | chr2 | 71426990 | ||
| chr2:71427320
|
A | G | 6 | a0003c0004a0003c0012a0003c0015others(3): Show | 56 | HG00323.hp1 HG00423.hp2 HG00733.hp2 others(53): Show |
synonymous_variant | LOW | c.5451A>G | p.Lys1817Lys | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 24/28 | 5747/6487 | 5451/5937 | 1817/1978 | chr2 | 71427320 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:71331794
|
G | T | 29 | a0001c0001t0001a0001c0003t0001a0001c0003t0003others(26): Show | 293 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(290): Show |
5_prime_UTR_variant | MODIFIER | c.-284G>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/28 | 17161 | chr2 | 71331794 | |||||
| chr2:71348767
|
T | G | 1 | a0001c0003t0003 | 2 | HG03098.hp2 NA19030.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-188T>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 2/28 | chr2 | 71348767 | ||||||
| chr2:71434894
|
G | A | 1 | a0001c0007t0005 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*87G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 28/28 | 87 | chr2 | 71434894 | |||||
| chr2:71434967
|
T | C | 1 | a0008c0010t0004 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*160T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 28/28 | 160 | chr2 | 71434967 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:71331962
|
G | A | 1 | a0003c0004t0002g0003 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.-203+87G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71331962 | ||||||
| chr2:71331977
|
T | G | 100 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(97): Show | 104 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.-203+102T>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71331977 | ||||||
| chr2:71332147
|
C | G | 2 | a0002c0002t0001g0343a0002c0002t0001g0344 | 2 | NA18972.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.-203+272C>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71332147 | ||||||
| chr2:71332240
|
C | T | 1 | a0001c0001t0001g0101 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-203+365C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71332240 | ||||||
| chr2:71332245
|
C | G | 1 | a0008c0010t0002g0342 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-203+370C>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71332245 | ||||||
| chr2:71332315
|
C | G | 115 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(112): Show | 119 | HG00323.hp2 HG00423.hp1 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.-203+440C>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71332315 | ||||||
| chr2:71332359
|
C | G | 1 | a0001c0003t0001g0325 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-203+484C>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71332359 | ||||||
| chr2:71332708
|
A | T | 2 | a0001c0001t0001g0099a0001c0001t0001g0100 | 2 | HG01169.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.-203+833A>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71332708 | ||||||
| chr2:71332713
|
T | C | 2 | a0009c0013t0001g0102a0009c0013t0001g0103 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-203+838T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71332713 | ||||||
| chr2:71332878
|
C | G | 1 | a0003c0004t0002g0324 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-203+1003C>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71332878 | ||||||
| chr2:71332962
|
T | C | 1 | a0001c0001t0001g0005 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-203+1087T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71332962 | ||||||
| chr2:71333273
|
C | T | 1 | a0001c0020t0001g0323 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-203+1398C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71333273 | ||||||
| chr2:71333478
|
T | C | 1 | a0001c0001t0001g0326 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-203+1603T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71333478 | ||||||
| chr2:71333535
|
A | T | 71 | a0002c0002t0001g0254a0002c0002t0001g0255a0002c0002t0001g0256others(68): Show | 71 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.-203+1660A>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71333535 | ||||||
| chr2:71333695
|
A | G | 2 | a0009c0013t0001g0102a0009c0013t0001g0103 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-203+1820A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71333695 | ||||||
| chr2:71333747
|
CT | C | 218 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(215): Show | 222 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(219): Show |
intron_variant | MODIFIER | c.-203+1874delT | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 71333747 | |||||
| chr2:71333923
|
G | A | 287 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(284): Show | 291 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(288): Show |
intron_variant | MODIFIER | c.-203+2048G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71333923 | ||||||
| chr2:71334025
|
C | T | 1 | a0018c0027t0001g0201 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-203+2150C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71334025 | ||||||
| chr2:71334049
|
C | T | 2 | a0008c0010t0002g0342a0008c0010t0004g0253 | 2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-203+2174C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71334049 | ||||||
| chr2:71334126
|
C | G | 24 | a0002c0002t0001g0177a0002c0002t0001g0178a0002c0002t0001g0179others(21): Show | 24 | HG00438.hp1 HG01069.hp2 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.-203+2251C>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71334126 | ||||||
| chr2:71334243
|
T | A | 2 | a0009c0013t0001g0102a0009c0013t0001g0103 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-203+2368T>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71334243 | ||||||
| chr2:71334359
|
A | C | 1 | a0018c0027t0001g0201 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-203+2484A>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71334359 | ||||||
| chr2:71334365
|
A | T | 2 | a0008c0010t0002g0342a0008c0010t0004g0253 | 2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-203+2490A>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71334365 | ||||||
| chr2:71334477
|
C | T | 6 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(3): Show | 6 | NA18953.hp1 NA18964.hp1 NA18982.hp1 others(3): Show |
intron_variant | MODIFIER | c.-203+2602C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71334477 | ||||||
| chr2:71334605
|
T | C | 5 | a0001c0003t0001g0104a0001c0003t0001g0105a0001c0003t0001g0106others(2): Show | 5 | HG02145.hp2 HG02615.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.-203+2730T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71334605 | ||||||
| chr2:71334623
|
C | T | 3 | a0002c0002t0001g0320a0002c0002t0001g0321a0002c0002t0001g0322 | 3 | NA19062.hp2 NA19064.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.-203+2748C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71334623 | ||||||
| chr2:71334673
|
C | T | 2 | a0009c0013t0001g0102a0009c0013t0001g0103 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-203+2798C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71334673 | ||||||
| chr2:71334761
|
T | C | 1 | a0001c0003t0001g0108 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-203+2886T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71334761 | ||||||
| chr2:71334814
|
G | C | 75 | a0001c0003t0001g0104a0001c0003t0001g0105a0001c0003t0001g0106others(72): Show | 75 | HG00280.hp1 HG00733.hp1 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.-203+2939G>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71334814 | ||||||
| chr2:71334879
|
C | T | 1 | a0001c0001t0001g0092 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-203+3004C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71334879 | ||||||
| chr2:71334921
|
C | CA | 7 | a0001c0001t0001g0006a0001c0001t0001g0099a0002c0002t0001g0254others(4): Show | 7 | HG01123.hp2 HG01169.hp2 HG02080.hp2 others(4): Show |
intron_variant | MODIFIER | c.-203+3057dupA | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 71334921 | |||||
| chr2:71334934
|
A | C | 1 | a0002c0002t0001g0319 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-203+3059A>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71334934 | ||||||
| chr2:71334965
|
AAGGGTTT others(19): Show |
A | 1 | a0001c0001t0001g0007 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-203+3120_-203+314 others(30): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 71334965 | |||||
| chr2:71335007
|
A | G | 1 | a0001c0001t0001g0091 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-203+3132A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71335007 | ||||||
| chr2:71335298
|
G | A | 75 | a0001c0003t0001g0104a0001c0003t0001g0105a0001c0003t0001g0106others(72): Show | 75 | HG00280.hp1 HG00733.hp1 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.-203+3423G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71335298 | ||||||
| chr2:71335373
|
T | C | 77 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(74): Show | 81 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.-203+3498T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71335373 | ||||||
| chr2:71335434
|
A | T | 6 | a0003c0004t0002g0248a0003c0004t0002g0249a0003c0004t0002g0250others(3): Show | 6 | HG02818.hp1 HG03209.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.-203+3559A>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71335434 | ||||||
| chr2:71335523
|
G | A | 1 | a0001c0020t0001g0323 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-203+3648G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71335523 | ||||||
| chr2:71335540
|
CAAAA | C | 5 | a0003c0004t0002g0248a0003c0004t0002g0249a0003c0004t0002g0250others(2): Show | 5 | HG02818.hp1 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-203+3671_-203+367 others(8): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 71335540 | |||||
| chr2:71335640
|
A | G | 2 | a0001c0003t0001g0175a0001c0003t0001g0176 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.-203+3765A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71335640 | ||||||
| chr2:71335742
|
T | G | 1 | a0009c0013t0001g0102 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-203+3867T>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71335742 | ||||||
| chr2:71335832
|
C | T | 4 | a0002c0002t0001g0198a0002c0002t0001g0199a0002c0002t0001g0200others(1): Show | 4 | HG03239.hp1 HG03831.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.-203+3957C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71335832 | ||||||
| chr2:71335833
|
C | G | 1 | a0018c0027t0001g0201 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-203+3958C>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71335833 | ||||||
| chr2:71335888
|
G | A | 2 | a0002c0002t0001g0177a0002c0002t0001g0178 | 2 | NA18992.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.-203+4013G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71335888 | ||||||
| chr2:71336094
|
G | C | 2 | a0009c0013t0001g0102a0009c0013t0001g0103 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-203+4219G>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71336094 | ||||||
| chr2:71336099
|
C | T | 1 | a0001c0005t0001g0174 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-203+4224C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71336099 | ||||||
| chr2:71336199
|
C | G | 1 | a0002c0002t0001g0197 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-203+4324C>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71336199 | ||||||
| chr2:71336332
|
T | A | 1 | a0001c0003t0001g0109 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-203+4457T>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71336332 | ||||||
| chr2:71336372
|
C | CA | 17 | a0003c0004t0002g0003a0003c0004t0002g0202a0003c0004t0002g0203others(14): Show | 17 | HG02055.hp2 HG02080.hp1 HG02300.hp2 others(14): Show |
intron_variant | MODIFIER | c.-203+4525dupA | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 71336372 | |||||
| chr2:71336372
|
CA | C | 36 | a0002c0002t0001g0179a0002c0002t0001g0180a0002c0002t0001g0182others(33): Show | 36 | HG00438.hp2 HG00741.hp1 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.-203+4525delA | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 71336372 | |||||
| chr2:71336372
|
CAA | C | 55 | a0002c0002t0001g0177a0002c0002t0001g0178a0002c0002t0001g0183others(52): Show | 55 | HG00438.hp1 HG00544.hp1 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.-203+4524_-203+452 others(6): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 71336372 | |||||
| chr2:71336372
|
CAAAAAAA others(3): Show |
C | 15 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(12): Show | 15 | HG00741.hp2 HG01109.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.-203+4516_-203+452 others(14): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 71336372 | |||||
| chr2:71336372
|
CAAAAAAA others(4): Show |
C | 109 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(106): Show | 113 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.-203+4515_-203+452 others(15): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 71336372 | |||||
| chr2:71336372
|
CAAAAAAA others(5): Show |
C | 69 | a0001c0001t0001g0098a0001c0003t0001g0108a0001c0003t0001g0109others(66): Show | 69 | HG00733.hp1 HG00735.hp1 HG00738.hp1 others(66): Show |
intron_variant | MODIFIER | c.-203+4514_-203+452 others(16): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 71336372 | |||||
| chr2:71336419
|
T | G | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(113): Show | 120 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.-203+4544T>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71336419 | ||||||
| chr2:71336423
|
TAAAC | T | 3 | a0001c0003t0001g0171a0001c0003t0001g0172a0001c0003t0001g0173 | 3 | HG01891.hp2 HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-203+4552_-203+455 others(8): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 71336423 | |||||
| chr2:71336491
|
T | C | 1 | a0002c0002t0001g0262 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-203+4616T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71336491 | ||||||
| chr2:71336525
|
C | T | 75 | a0001c0003t0001g0104a0001c0003t0001g0105a0001c0003t0001g0106others(72): Show | 75 | HG00280.hp1 HG00733.hp1 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.-203+4650C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71336525 | ||||||
| chr2:71336544
|
A | G | 6 | a0001c0001t0001g0011a0001c0001t0001g0063a0001c0001t0001g0064others(3): Show | 6 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.-203+4669A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71336544 | ||||||
| chr2:71336565
|
T | G | 2 | a0001c0003t0001g0112a0001c0003t0001g0113 | 2 | HG02572.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-203+4690T>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71336565 | ||||||
| chr2:71336636
|
A | G | 5 | a0003c0004t0002g0248a0003c0004t0002g0249a0003c0004t0002g0250others(2): Show | 5 | HG02818.hp1 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-203+4761A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71336636 | ||||||
| chr2:71336827
|
C | CT | 5 | a0001c0003t0001g0166a0001c0003t0001g0167a0001c0003t0001g0168others(2): Show | 5 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.-203+4953dupT | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 71336827 | |||||
| chr2:71336834
|
C | T | 2 | a0001c0003t0001g0172a0001c0003t0001g0173 | 2 | HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-203+4959C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71336834 | ||||||
| chr2:71337011
|
T | A | 1 | a0003c0004t0002g0217 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-203+5136T>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71337011 | ||||||
| chr2:71337013
|
A | G | 1 | a0003c0004t0002g0217 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-203+5138A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71337013 | ||||||
| chr2:71337016
|
A | G | 1 | a0003c0004t0002g0217 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-203+5141A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71337016 | ||||||
| chr2:71337016
|
A | T | 15 | a0001c0003t0001g0164a0001c0003t0003g0162a0001c0003t0003g0163others(12): Show | 15 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.-203+5141A>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71337016 | ||||||
| chr2:71337137
|
G | GT | 39 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(36): Show | 39 | HG00438.hp1 HG01069.hp2 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.-203+5278dupT | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 71337137 | |||||
| chr2:71337137
|
GT | G | 7 | a0001c0001t0001g0012a0001c0001t0001g0013a0002c0002t0001g0254others(4): Show | 7 | HG00544.hp1 HG00597.hp2 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.-203+5278delT | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 71337137 | |||||
| chr2:71337392
|
C | T | 7 | a0001c0003t0001g0146a0001c0003t0001g0147a0001c0003t0001g0148others(4): Show | 7 | HG02055.hp1 HG02647.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-203+5517C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71337392 | ||||||
| chr2:71337394
|
A | G | 1 | a0018c0027t0001g0201 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-203+5519A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71337394 | ||||||
| chr2:71337501
|
C | T | 2 | a0009c0013t0001g0102a0009c0013t0001g0103 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-203+5626C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71337501 | ||||||
| chr2:71337534
|
G | A | 95 | a0002c0002t0001g0177a0002c0002t0001g0178a0002c0002t0001g0179others(92): Show | 95 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.-203+5659G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71337534 | ||||||
| chr2:71337592
|
G | A | 11 | a0001c0005t0001g0152a0001c0005t0001g0153a0001c0005t0001g0154others(8): Show | 11 | HG01243.hp2 HG01891.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-203+5717G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71337592 | ||||||
| chr2:71337593
|
A | T | 11 | a0001c0005t0001g0152a0001c0005t0001g0153a0001c0005t0001g0154others(8): Show | 11 | HG01243.hp2 HG01891.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-203+5718A>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71337593 | ||||||
| chr2:71337645
|
T | TTCCACCT others(102): Show |
24 | a0002c0002t0001g0177a0002c0002t0001g0178a0002c0002t0001g0179others(21): Show | 24 | HG00438.hp1 HG01069.hp2 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.-203+5771_-203+587 others(113): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 71337645 | |||||
| chr2:71337774
|
GT | G | 102 | a0002c0002t0001g0177a0002c0002t0001g0178a0002c0002t0001g0179others(99): Show | 102 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.-203+5908delT | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 71337774 | |||||
| chr2:71338083
|
A | G | 1 | a0001c0001t0001g0090 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-203+6208A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71338083 | ||||||
| chr2:71338093
|
C | G | 2 | a0001c0001t0001g0088a0001c0001t0001g0089 | 2 | HG02622.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-203+6218C>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71338093 | ||||||
| chr2:71338191
|
G | A | 75 | a0001c0003t0001g0104a0001c0003t0001g0105a0001c0003t0001g0106others(72): Show | 75 | HG00280.hp1 HG00733.hp1 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.-203+6316G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71338191 | ||||||
| chr2:71338284
|
T | G | 9 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0014others(6): Show | 9 | HG00642.hp1 HG02040.hp1 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.-203+6409T>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71338284 | ||||||
| chr2:71338461
|
C | A | 7 | a0001c0007t0001g0327a0001c0007t0001g0328a0001c0007t0001g0329others(4): Show | 7 | HG01884.hp2 HG02451.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.-203+6586C>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71338461 | ||||||
| chr2:71338521
|
A | T | 2 | a0009c0013t0001g0102a0009c0013t0001g0103 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-203+6646A>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71338521 | ||||||
| chr2:71338790
|
A | G | 1 | a0001c0007t0001g0333 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-203+6915A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71338790 | ||||||
| chr2:71338899
|
T | C | 12 | a0001c0003t0001g0104a0001c0003t0001g0105a0001c0003t0001g0106others(9): Show | 12 | HG02055.hp1 HG02145.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.-203+7024T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71338899 | ||||||
| chr2:71339083
|
C | T | 2 | a0003c0004t0002g0215a0003c0004t0002g0216 | 2 | NA18983.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.-203+7208C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71339083 | ||||||
| chr2:71339116
|
G | A | 1 | a0002c0002t0001g0319 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-203+7241G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71339116 | ||||||
| chr2:71339150
|
GT | G | 202 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(199): Show | 206 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(203): Show |
intron_variant | MODIFIER | c.-203+7293delT | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 71339150 | |||||
| chr2:71339168
|
T | A | 1 | a0001c0003t0001g0114 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-203+7293T>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71339168 | ||||||
| chr2:71339168
|
T | G | 1 | a0001c0001t0001g0088 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-203+7293T>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71339168 | ||||||
| chr2:71339168
|
T | TA | 73 | a0001c0003t0001g0104a0001c0003t0001g0105a0001c0003t0001g0106others(70): Show | 73 | HG00280.hp1 HG00733.hp1 HG00735.hp1 others(70): Show |
intron_variant | MODIFIER | c.-203+7294dupA | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 71339168 | |||||
| chr2:71339313
|
C | T | 6 | a0001c0001t0001g0020a0001c0003t0001g0142a0001c0003t0001g0143others(3): Show | 6 | HG00733.hp1 HG02040.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-203+7438C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71339313 | ||||||
| chr2:71339332
|
T | C | 5 | a0001c0003t0001g0115a0001c0003t0001g0116a0001c0003t0001g0171others(2): Show | 5 | HG01167.hp1 HG01169.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.-203+7457T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71339332 | ||||||
| chr2:71339440
|
C | T | 71 | a0002c0002t0001g0254a0002c0002t0001g0255a0002c0002t0001g0256others(68): Show | 71 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.-203+7565C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71339440 | ||||||
| chr2:71339711
|
G | T | 109 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(106): Show | 113 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.-203+7836G>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71339711 | ||||||
| chr2:71339712
|
G | C | 1 | a0003c0004t0002g0249 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-203+7837G>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71339712 | ||||||
| chr2:71339912
|
A | G | 20 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(17): Show | 23 | HG00642.hp2 HG00735.hp2 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.-203+8037A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71339912 | ||||||
| chr2:71339947
|
T | C | 7 | a0001c0007t0001g0327a0001c0007t0001g0328a0001c0007t0001g0329others(4): Show | 7 | HG01884.hp2 HG02451.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.-203+8072T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71339947 | ||||||
| chr2:71339953
|
G | A | 1 | a0003c0004t0002g0219 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-203+8078G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71339953 | ||||||
| chr2:71339975
|
T | C | 1 | a0001c0001t0001g0020 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-203+8100T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71339975 | ||||||
| chr2:71340219
|
T | C | 12 | a0001c0003t0001g0104a0001c0003t0001g0105a0001c0003t0001g0106others(9): Show | 12 | HG02055.hp1 HG02145.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.-203+8344T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71340219 | ||||||
| chr2:71340381
|
G | A | 1 | a0001c0003t0001g0117 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-202-8372G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71340381 | ||||||
| chr2:71340440
|
C | T | 7 | a0001c0003t0001g0146a0001c0003t0001g0147a0001c0003t0001g0148others(4): Show | 7 | HG02055.hp1 HG02647.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-202-8313C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71340440 | ||||||
| chr2:71340441
|
A | G | 1 | a0001c0001t0001g0048 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.-202-8312A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71340441 | ||||||
| chr2:71340834
|
A | G | 37 | a0001c0003t0001g0108a0001c0003t0001g0109a0001c0003t0001g0111others(34): Show | 37 | HG00280.hp1 HG00735.hp1 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.-202-7919A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71340834 | ||||||
| chr2:71340856
|
C | G | 290 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(287): Show | 294 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(291): Show |
intron_variant | MODIFIER | c.-202-7897C>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71340856 | ||||||
| chr2:71340876
|
G | A | 1 | a0004c0006t0001g0261 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-202-7877G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71340876 | ||||||
| chr2:71340918
|
G | A | 1 | a0001c0024t0001g0145 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-202-7835G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71340918 | ||||||
| chr2:71340993
|
A | T | 6 | a0004c0006t0001g0260a0004c0006t0001g0261a0004c0006t0001g0281others(3): Show | 6 | NA18948.hp2 NA18954.hp2 NA18980.hp1 others(3): Show |
intron_variant | MODIFIER | c.-202-7760A>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71340993 | ||||||
| chr2:71341041
|
G | C | 1 | a0002c0002t0001g0183 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-202-7712G>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71341041 | ||||||
| chr2:71341076
|
A | G | 109 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(106): Show | 113 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.-202-7677A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71341076 | ||||||
| chr2:71341085
|
A | G | 1 | a0002c0002t0001g0317 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-202-7668A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71341085 | ||||||
| chr2:71341098
|
G | A | 1 | a0001c0003t0001g0146 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-202-7655G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71341098 | ||||||
| chr2:71341152
|
A | G | 95 | a0002c0002t0001g0177a0002c0002t0001g0178a0002c0002t0001g0179others(92): Show | 95 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.-202-7601A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71341152 | ||||||
| chr2:71341240
|
T | G | 1 | a0001c0003t0001g0146 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-202-7513T>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71341240 | ||||||
| chr2:71341400
|
T | C | 13 | a0001c0005t0001g0122a0001c0005t0001g0152a0001c0005t0001g0153others(10): Show | 13 | HG01243.hp2 HG01891.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.-202-7353T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71341400 | ||||||
| chr2:71341565
|
C | G | 343 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(340): Show | 347 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(344): Show |
intron_variant | MODIFIER | c.-202-7188C>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71341565 | ||||||
| chr2:71341962
|
G | C | 1 | a0018c0027t0001g0201 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-202-6791G>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71341962 | ||||||
| chr2:71342101
|
G | A | 7 | a0001c0007t0001g0327a0001c0007t0001g0328a0001c0007t0001g0329others(4): Show | 7 | HG01884.hp2 HG02451.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.-202-6652G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71342101 | ||||||
| chr2:71342115
|
T | TATTTGGT others(370): Show |
2 | a0009c0013t0001g0102a0009c0013t0001g0103 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-202-6638_-202-663 others(381): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71342115 | ||||||
| chr2:71342174
|
C | T | 113 | a0001c0003t0001g0164a0001c0003t0003g0162a0001c0003t0003g0163others(110): Show | 113 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.-202-6579C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71342174 | ||||||
| chr2:71342177
|
C | T | 2 | a0001c0003t0001g0140a0001c0003t0001g0141 | 2 | HG02717.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.-202-6576C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71342177 | ||||||
| chr2:71342218
|
C | CA | 52 | a0001c0003t0001g0104a0001c0003t0001g0105a0001c0003t0001g0106others(49): Show | 52 | HG00280.hp1 HG00733.hp1 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.-202-6516dupA | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 71342218 | |||||
| chr2:71342218
|
C | CAA | 87 | a0001c0001t0001g0047a0001c0001t0001g0067a0001c0003t0001g0147others(84): Show | 87 | HG00438.hp2 HG00609.hp1 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.-202-6517_-202-651 others(6): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 71342218 | |||||
| chr2:71342218
|
C | CAAA | 129 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(126): Show | 133 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.-202-6518_-202-651 others(7): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 71342218 | |||||
| chr2:71342218
|
C | CAAAA | 13 | a0001c0001t0001g0012a0001c0001t0001g0021a0001c0001t0001g0049others(10): Show | 13 | HG01081.hp1 HG01169.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.-202-6519_-202-651 others(8): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 71342218 | |||||
| chr2:71342248
|
T | C | 100 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(97): Show | 104 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.-202-6505T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71342248 | ||||||
| chr2:71342385
|
C | T | 2 | a0001c0003t0001g0143a0001c0003t0001g0144 | 2 | HG00733.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.-202-6368C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71342385 | ||||||
| chr2:71342482
|
C | T | 1 | a0001c0003t0001g0137 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-202-6271C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71342482 | ||||||
| chr2:71342538
|
G | A | 290 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(287): Show | 294 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(291): Show |
intron_variant | MODIFIER | c.-202-6215G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71342538 | ||||||
| chr2:71342683
|
CGT | C | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(113): Show | 120 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.-202-6057_-202-605 others(6): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 71342683 | |||||
| chr2:71342773
|
A | G | 1 | a0002c0002t0001g0182 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-202-5980A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71342773 | ||||||
| chr2:71342990
|
T | C | 3 | a0001c0003t0001g0171a0001c0003t0001g0172a0001c0003t0001g0173 | 3 | HG01891.hp2 HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-202-5763T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71342990 | ||||||
| chr2:71343097
|
A | G | 1 | a0001c0003t0001g0146 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-202-5656A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71343097 | ||||||
| chr2:71343398
|
C | G | 5 | a0001c0003t0001g0104a0001c0003t0001g0105a0001c0003t0001g0106others(2): Show | 5 | HG02145.hp2 HG02615.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.-202-5355C>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71343398 | ||||||
| chr2:71343461
|
A | T | 10 | a0001c0003t0001g0114a0001c0003t0001g0138a0001c0003t0001g0139others(7): Show | 10 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.-202-5292A>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71343461 | ||||||
| chr2:71343612
|
T | G | 24 | a0002c0002t0001g0177a0002c0002t0001g0178a0002c0002t0001g0179others(21): Show | 24 | HG00438.hp1 HG01069.hp2 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.-202-5141T>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71343612 | ||||||
| chr2:71343675
|
C | T | 1 | a0001c0005t0001g0161 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-202-5078C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71343675 | ||||||
| chr2:71343700
|
T | A | 1 | a0001c0001t0001g0022 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-202-5053T>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71343700 | ||||||
| chr2:71343858
|
CGGTGGCT others(37): Show |
C | 109 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(106): Show | 113 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.-202-4889_-202-484 others(48): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 71343858 | |||||
| chr2:71343880
|
T | C | 181 | a0001c0003t0001g0104a0001c0003t0001g0105a0001c0003t0001g0106others(178): Show | 181 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(178): Show |
intron_variant | MODIFIER | c.-202-4873T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71343880 | ||||||
| chr2:71343881
|
G | A | 2 | a0009c0013t0001g0102a0009c0013t0001g0103 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-202-4872G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71343881 | ||||||
| chr2:71343954
|
C | T | 2 | a0001c0007t0001g0330a0013c0018t0001g0331 | 2 | HG02615.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.-202-4799C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71343954 | ||||||
| chr2:71343992
|
T | C | 7 | a0001c0007t0001g0327a0001c0007t0001g0328a0001c0007t0001g0329others(4): Show | 7 | HG01884.hp2 HG02451.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.-202-4761T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71343992 | ||||||
| chr2:71343997
|
G | A | 1 | a0001c0001t0001g0100 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-202-4756G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71343997 | ||||||
| chr2:71344001
|
G | A | 1 | a0008c0010t0002g0342 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-202-4752G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71344001 | ||||||
| chr2:71344061
|
C | T | 2 | a0001c0001t0001g0045a0001c0001t0001g0046 | 2 | NA18942.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.-202-4692C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71344061 | ||||||
| chr2:71344098
|
C | T | 1 | a0002c0002t0001g0196 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.-202-4655C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71344098 | ||||||
| chr2:71344108
|
C | T | 10 | a0002c0002t0001g0280a0002c0002t0001g0310a0002c0002t0001g0311others(7): Show | 10 | HG00609.hp2 HG00673.hp1 NA18965.hp1 others(7): Show |
intron_variant | MODIFIER | c.-202-4645C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71344108 | ||||||
| chr2:71344224
|
T | C | 3 | a0001c0003t0001g0164a0001c0003t0003g0162a0001c0003t0003g0163 | 3 | HG01496.hp2 HG03098.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-202-4529T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71344224 | ||||||
| chr2:71344313
|
A | G | 1 | a0019c0028t0001g0195 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-202-4440A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71344313 | ||||||
| chr2:71344430
|
G | T | 2 | a0008c0010t0002g0342a0008c0010t0004g0253 | 2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-202-4323G>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71344430 | ||||||
| chr2:71344532
|
G | GGTCCTTC others(18): Show |
73 | a0002c0002t0001g0254a0002c0002t0001g0255a0002c0002t0001g0256others(70): Show | 73 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.-202-4218_-202-421 others(29): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 71344532 | |||||
| chr2:71344532
|
G | GGTCCTTC others(18): Show |
24 | a0002c0002t0001g0177a0002c0002t0001g0178a0002c0002t0001g0179others(21): Show | 24 | HG00438.hp1 HG01069.hp2 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.-202-4218_-202-421 others(29): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 71344532 | |||||
| chr2:71344535
|
C | T | 1 | a0001c0001t0001g0019 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-202-4218C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71344535 | ||||||
| chr2:71344641
|
C | T | 1 | a0002c0002t0001g0322 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-202-4112C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71344641 | ||||||
| chr2:71344807
|
A | G | 1 | a0001c0003t0001g0107 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-202-3946A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71344807 | ||||||
| chr2:71345004
|
A | T | 2 | a0009c0013t0001g0102a0009c0013t0001g0103 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-202-3749A>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71345004 | ||||||
| chr2:71345072
|
A | G | 1 | a0001c0020t0001g0323 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-202-3681A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71345072 | ||||||
| chr2:71345325
|
C | T | 192 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(189): Show | 196 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.-202-3428C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71345325 | ||||||
| chr2:71345389
|
A | T | 1 | a0009c0013t0001g0102 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-202-3364A>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71345389 | ||||||
| chr2:71345390
|
T | C | 1 | a0009c0013t0001g0102 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-202-3363T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71345390 | ||||||
| chr2:71345459
|
A | G | 1 | a0001c0001t0001g0044 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-202-3294A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71345459 | ||||||
| chr2:71345787
|
T | G | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(113): Show | 120 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.-202-2966T>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71345787 | ||||||
| chr2:71345831
|
A | C | 1 | a0001c0007t0001g0329 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-202-2922A>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71345831 | ||||||
| chr2:71346034
|
C | T | 1 | a0003c0015t0002g0245 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-202-2719C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71346034 | ||||||
| chr2:71346132
|
T | C | 2 | a0009c0013t0001g0102a0009c0013t0001g0103 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-202-2621T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71346132 | ||||||
| chr2:71346210
|
A | G | 75 | a0001c0003t0001g0104a0001c0003t0001g0105a0001c0003t0001g0106others(72): Show | 75 | HG00280.hp1 HG00733.hp1 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.-202-2543A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71346210 | ||||||
| chr2:71346288
|
T | C | 2 | a0009c0013t0001g0102a0009c0013t0001g0103 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-202-2465T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71346288 | ||||||
| chr2:71346450
|
A | G | 7 | a0001c0007t0001g0327a0001c0007t0001g0328a0001c0007t0001g0329others(4): Show | 7 | HG01884.hp2 HG02451.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.-202-2303A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71346450 | ||||||
| chr2:71346522
|
A | G | 7 | a0001c0003t0001g0146a0001c0003t0001g0147a0001c0003t0001g0148others(4): Show | 7 | HG02055.hp1 HG02647.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-202-2231A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71346522 | ||||||
| chr2:71346606
|
C | T | 342 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(339): Show | 346 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(343): Show |
intron_variant | MODIFIER | c.-202-2147C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71346606 | ||||||
| chr2:71346678
|
G | A | 289 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(286): Show | 293 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(290): Show |
intron_variant | MODIFIER | c.-202-2075G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71346678 | ||||||
| chr2:71346894
|
C | A | 1 | a0001c0001t0001g0049 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-202-1859C>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71346894 | ||||||
| chr2:71347039
|
AAAAG | A | 71 | a0002c0002t0001g0254a0002c0002t0001g0255a0002c0002t0001g0256others(68): Show | 71 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.-202-1708_-202-170 others(8): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 71347039 | |||||
| chr2:71347472
|
C | T | 1 | a0001c0003t0001g0164 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-202-1281C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71347472 | ||||||
| chr2:71347493
|
C | T | 2 | a0002c0002t0001g0193a0002c0002t0001g0194 | 2 | HG01069.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.-202-1260C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71347493 | ||||||
| chr2:71347585
|
T | C | 1 | a0018c0027t0001g0201 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-202-1168T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71347585 | ||||||
| chr2:71348125
|
T | C | 1 | a0019c0028t0001g0195 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-202-628T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71348125 | ||||||
| chr2:71348129
|
A | G | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(113): Show | 120 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.-202-624A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71348129 | ||||||
| chr2:71348134
|
A | T | 1 | a0001c0001t0001g0056 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-202-619A>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71348134 | ||||||
| chr2:71348283
|
C | G | 71 | a0002c0002t0001g0254a0002c0002t0001g0255a0002c0002t0001g0256others(68): Show | 71 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.-202-470C>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71348283 | ||||||
| chr2:71348340
|
A | T | 77 | a0001c0003t0001g0104a0001c0003t0001g0105a0001c0003t0001g0106others(74): Show | 77 | HG00280.hp1 HG00733.hp1 HG00735.hp1 others(74): Show |
intron_variant | MODIFIER | c.-202-413A>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71348340 | ||||||
| chr2:71348513
|
A | T | 24 | a0002c0002t0001g0177a0002c0002t0001g0178a0002c0002t0001g0179others(21): Show | 24 | HG00438.hp1 HG01069.hp2 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.-202-240A>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 1/27 | chr2 | 71348513 | ||||||
| chr2:71350482
|
C | T | 1 | a0002c0002t0001g0289 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1317+211C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 2/27 | chr2 | 71350482 | ||||||
| chr2:71350488
|
A | G | 1 | a0001c0001t0001g0087 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1317+217A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 2/27 | chr2 | 71350488 | ||||||
| chr2:71350499
|
G | A | 96 | a0002c0002t0001g0177a0002c0002t0001g0178a0002c0002t0001g0179others(93): Show | 96 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.1317+228G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 2/27 | chr2 | 71350499 | ||||||
| chr2:71350521
|
T | C | 1 | a0002c0002t0001g0184 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1317+250T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 2/27 | chr2 | 71350521 | ||||||
| chr2:71350641
|
G | A | 1 | a0004c0006t0001g0257 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1317+370G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 2/27 | chr2 | 71350641 | ||||||
| chr2:71351068
|
G | A | 1 | a0002c0002t0001g0193 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1317+797G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 2/27 | chr2 | 71351068 | ||||||
| chr2:71351211
|
G | T | 75 | a0001c0003t0001g0104a0001c0003t0001g0105a0001c0003t0001g0106others(72): Show | 75 | HG00280.hp1 HG00733.hp1 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.1317+940G>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 2/27 | chr2 | 71351211 | ||||||
| chr2:71351379
|
G | A | 1 | a0001c0001t0001g0044 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1317+1108G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 2/27 | chr2 | 71351379 | ||||||
| chr2:71351421
|
G | A | 2 | a0009c0013t0001g0102a0009c0013t0001g0103 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1317+1150G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 2/27 | chr2 | 71351421 | ||||||
| chr2:71351554
|
T | G | 77 | a0001c0003t0001g0104a0001c0003t0001g0105a0001c0003t0001g0106others(74): Show | 77 | HG00280.hp1 HG00733.hp1 HG00735.hp1 others(74): Show |
intron_variant | MODIFIER | c.1317+1283T>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 2/27 | chr2 | 71351554 | ||||||
| chr2:71351571
|
G | A | 24 | a0002c0002t0001g0177a0002c0002t0001g0178a0002c0002t0001g0179others(21): Show | 24 | HG00438.hp1 HG01069.hp2 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.1317+1300G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 2/27 | chr2 | 71351571 | ||||||
| chr2:71351815
|
A | T | 1 | a0019c0028t0001g0195 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1317+1544A>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 2/27 | chr2 | 71351815 | ||||||
| chr2:71351857
|
T | C | 1 | a0001c0005t0001g0152 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1317+1586T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 2/27 | chr2 | 71351857 | ||||||
| chr2:71351890
|
G | A | 2 | a0001c0001t0001g0075a0001c0001t0001g0076 | 2 | NA18941.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.1317+1619G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 2/27 | chr2 | 71351890 | ||||||
| chr2:71352140
|
T | C | 1 | a0002c0002t0001g0184 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1317+1869T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 2/27 | chr2 | 71352140 | ||||||
| chr2:71352165
|
T | C | 22 | a0002c0002t0001g0263a0002c0002t0001g0266a0002c0002t0001g0268others(19): Show | 22 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.1317+1894T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 2/27 | chr2 | 71352165 | ||||||
| chr2:71352172
|
T | C | 17 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0071others(14): Show | 17 | HG02015.hp2 HG02155.hp1 NA18941.hp2 others(14): Show |
intron_variant | MODIFIER | c.1317+1901T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 2/27 | chr2 | 71352172 | ||||||
| chr2:71352297
|
G | T | 2 | a0009c0013t0001g0102a0009c0013t0001g0103 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1317+2026G>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 2/27 | chr2 | 71352297 | ||||||
| chr2:71352372
|
G | A | 70 | a0002c0002t0001g0254a0002c0002t0001g0255a0002c0002t0001g0256others(67): Show | 70 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.1317+2101G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 2/27 | chr2 | 71352372 | ||||||
| chr2:71352494
|
AT | A | 23 | a0002c0002t0001g0177a0002c0002t0001g0178a0002c0002t0001g0179others(20): Show | 23 | HG00438.hp1 HG01069.hp2 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.1317+2224delT | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 2/27 | chr2 | 71352494 | ||||||
| chr2:71352495
|
TA | T | 189 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(186): Show | 193 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.1317+2239delA | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr2 | 71352495 | |||||
| chr2:71352495
|
TAA | T | 73 | a0001c0001t0001g0013a0001c0001t0001g0022a0001c0001t0001g0067others(70): Show | 73 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.1317+2238_1317+223 others(6): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr2 | 71352495 | |||||
| chr2:71352495
|
TAAAAA | T | 6 | a0003c0004t0002g0248a0003c0004t0002g0249a0003c0004t0002g0250others(3): Show | 6 | HG02818.hp1 HG03139.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.1317+2235_1317+223 others(9): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr2 | 71352495 | |||||
| chr2:71352497
|
A | T | 1 | a0019c0028t0001g0195 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1317+2226A>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 2/27 | chr2 | 71352497 | ||||||
| chr2:71352528
|
G | A | 1 | a0001c0003t0001g0123 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1317+2257G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 2/27 | chr2 | 71352528 | ||||||
| chr2:71352567
|
T | C | 70 | a0002c0002t0001g0254a0002c0002t0001g0255a0002c0002t0001g0256others(67): Show | 70 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.1317+2296T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 2/27 | chr2 | 71352567 | ||||||
| chr2:71352999
|
G | A | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(113): Show | 120 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.1318-2720G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 2/27 | chr2 | 71352999 | ||||||
| chr2:71353072
|
AGC | A | 94 | a0002c0002t0001g0177a0002c0002t0001g0178a0002c0002t0001g0179others(91): Show | 94 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.1318-2646_1318-264 others(6): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 2/27 | chr2 | 71353072 | ||||||
| chr2:71353292
|
G | T | 1 | a0001c0003t0001g0141 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1318-2427G>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 2/27 | chr2 | 71353292 | ||||||
| chr2:71353805
|
T | C | 1 | a0001c0003t0001g0112 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1318-1914T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 2/27 | chr2 | 71353805 | ||||||
| chr2:71353981
|
A | G | 3 | a0005c0008t0001g0008a0005c0008t0001g0042a0005c0008t0001g0043 | 3 | NA18971.hp2 NA18986.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.1318-1738A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 2/27 | chr2 | 71353981 | ||||||
| chr2:71354164
|
T | C | 1 | a0003c0004t0002g0324 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1318-1555T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 2/27 | chr2 | 71354164 | ||||||
| chr2:71354343
|
C | CT | 279 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(276): Show | 283 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(280): Show |
intron_variant | MODIFIER | c.1318-1362dupT | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr2 | 71354343 | |||||
| chr2:71354433
|
A | G | 1 | a0001c0003t0001g0151 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1318-1286A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 2/27 | chr2 | 71354433 | ||||||
| chr2:71354444
|
A | G | 70 | a0002c0002t0001g0254a0002c0002t0001g0255a0002c0002t0001g0256others(67): Show | 70 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.1318-1275A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 2/27 | chr2 | 71354444 | ||||||
| chr2:71354472
|
C | T | 1 | a0001c0003t0001g0146 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1318-1247C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 2/27 | chr2 | 71354472 | ||||||
| chr2:71354537
|
A | G | 1 | a0021c0031t0001g0341 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1318-1182A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 2/27 | chr2 | 71354537 | ||||||
| chr2:71354553
|
T | G | 1 | a0001c0001t0001g0098 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1318-1166T>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 2/27 | chr2 | 71354553 | ||||||
| chr2:71354673
|
A | G | 1 | a0002c0002t0001g0262 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1318-1046A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 2/27 | chr2 | 71354673 | ||||||
| chr2:71354691
|
C | G | 2 | a0009c0013t0001g0102a0009c0013t0001g0103 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1318-1028C>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 2/27 | chr2 | 71354691 | ||||||
| chr2:71354701
|
C | T | 7 | a0001c0007t0001g0327a0001c0007t0001g0328a0001c0007t0001g0329others(4): Show | 7 | HG01884.hp2 HG02451.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1318-1018C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 2/27 | chr2 | 71354701 | ||||||
| chr2:71354735
|
CA | C | 286 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(283): Show | 290 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(287): Show |
intron_variant | MODIFIER | c.1318-974delA | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr2 | 71354735 | |||||
| chr2:71355039
|
G | T | 1 | a0004c0006t0001g0261 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1318-680G>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 2/27 | chr2 | 71355039 | ||||||
| chr2:71355123
|
A | C | 219 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(216): Show | 223 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(220): Show |
intron_variant | MODIFIER | c.1318-596A>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 2/27 | chr2 | 71355123 | ||||||
| chr2:71355125
|
C | T | 70 | a0002c0002t0001g0254a0002c0002t0001g0255a0002c0002t0001g0256others(67): Show | 70 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.1318-594C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 2/27 | chr2 | 71355125 | ||||||
| chr2:71355154
|
G | C | 193 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(190): Show | 197 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.1318-565G>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 2/27 | chr2 | 71355154 | ||||||
| chr2:71355178
|
G | C | 193 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(190): Show | 197 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.1318-541G>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 2/27 | chr2 | 71355178 | ||||||
| chr2:71355199
|
G | A | 2 | a0003c0004t0002g0003a0003c0004t0002g0223 | 2 | NA18951.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.1318-520G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 2/27 | chr2 | 71355199 | ||||||
| chr2:71355235
|
C | T | 12 | a0001c0001t0001g0086a0001c0001t0001g0088a0001c0001t0001g0089others(9): Show | 12 | HG01192.hp2 HG01884.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1318-484C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 2/27 | chr2 | 71355235 | ||||||
| chr2:71355251
|
C | T | 1 | a0002c0002t0001g0262 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1318-468C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 2/27 | chr2 | 71355251 | ||||||
| chr2:71355404
|
G | GT | 4 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(1): Show | 4 | HG01256.hp2 HG02129.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.1318-309dupT | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr2 | 71355404 | |||||
| chr2:71355468
|
C | T | 1 | a0001c0003t0001g0111 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1318-251C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 2/27 | chr2 | 71355468 | ||||||
| chr2:71355575
|
A | G | 2 | a0001c0007t0001g0330a0013c0018t0001g0331 | 2 | HG02615.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1318-144A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 2/27 | chr2 | 71355575 | ||||||
| chr2:71355608
|
G | A | 1 | a0001c0001t0001g0024 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1318-111G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 2/27 | chr2 | 71355608 | ||||||
| chr2:71355899
|
T | C | 1 | a0002c0002t0001g0313 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1379+119T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 3/27 | chr2 | 71355899 | ||||||
| chr2:71356012
|
T | C | 1 | a0001c0003t0001g0118 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1379+232T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 3/27 | chr2 | 71356012 | ||||||
| chr2:71356032
|
T | C | 1 | a0001c0001t0001g0007 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1379+252T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 3/27 | chr2 | 71356032 | ||||||
| chr2:71356044
|
C | G | 24 | a0002c0002t0001g0177a0002c0002t0001g0178a0002c0002t0001g0179others(21): Show | 24 | HG00438.hp1 HG01069.hp2 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.1379+264C>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 3/27 | chr2 | 71356044 | ||||||
| chr2:71356061
|
A | G | 24 | a0002c0002t0001g0177a0002c0002t0001g0178a0002c0002t0001g0179others(21): Show | 24 | HG00438.hp1 HG01069.hp2 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.1379+281A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 3/27 | chr2 | 71356061 | ||||||
| chr2:71356303
|
A | G | 1 | a0004c0006t0001g0284 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1379+523A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 3/27 | chr2 | 71356303 | ||||||
| chr2:71356504
|
G | T | 15 | a0001c0003t0001g0164a0001c0003t0003g0162a0001c0003t0003g0163others(12): Show | 15 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.1379+724G>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 3/27 | chr2 | 71356504 | ||||||
| chr2:71356780
|
CA | C | 7 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0016others(4): Show | 7 | HG02735.hp1 HG03669.hp2 HG03831.hp1 others(4): Show |
intron_variant | MODIFIER | c.1379+1014delA | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | 71356780 | |||||
| chr2:71356793
|
AAT | A | 16 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0071others(13): Show | 16 | HG02015.hp2 HG02155.hp1 NA18941.hp2 others(13): Show |
intron_variant | MODIFIER | c.1379+1014_1379+101 others(6): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 3/27 | chr2 | 71356793 | ||||||
| chr2:71356794
|
A | T | 88 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(85): Show | 92 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.1379+1014A>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 3/27 | chr2 | 71356794 | ||||||
| chr2:71356917
|
G | A | 1 | a0003c0004t0002g0247 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1379+1137G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 3/27 | chr2 | 71356917 | ||||||
| chr2:71357071
|
C | T | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(113): Show | 120 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.1379+1291C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 3/27 | chr2 | 71357071 | ||||||
| chr2:71357092
|
A | G | 71 | a0002c0002t0001g0254a0002c0002t0001g0255a0002c0002t0001g0256others(68): Show | 71 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.1379+1312A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 3/27 | chr2 | 71357092 | ||||||
| chr2:71357142
|
T | G | 37 | a0001c0003t0001g0108a0001c0003t0001g0109a0001c0003t0001g0111others(34): Show | 37 | HG00280.hp1 HG00735.hp1 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.1379+1362T>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 3/27 | chr2 | 71357142 | ||||||
| chr2:71357207
|
T | C | 2 | a0003c0004t0002g0221a0003c0004t0002g0243 | 2 | HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1379+1427T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 3/27 | chr2 | 71357207 | ||||||
| chr2:71357209
|
A | C | 1 | a0002c0002t0001g0298 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1379+1429A>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 3/27 | chr2 | 71357209 | ||||||
| chr2:71357277
|
T | C | 24 | a0002c0002t0001g0177a0002c0002t0001g0178a0002c0002t0001g0179others(21): Show | 24 | HG00438.hp1 HG01069.hp2 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.1379+1497T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 3/27 | chr2 | 71357277 | ||||||
| chr2:71357336
|
C | T | 2 | a0001c0003t0001g0118a0001c0003t0001g0121 | 2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1379+1556C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 3/27 | chr2 | 71357336 | ||||||
| chr2:71357355
|
G | A | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(113): Show | 120 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.1379+1575G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 3/27 | chr2 | 71357355 | ||||||
| chr2:71357378
|
G | C | 12 | a0001c0005t0001g0152a0001c0005t0001g0153a0001c0005t0001g0154others(9): Show | 12 | HG01243.hp2 HG01891.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.1379+1598G>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 3/27 | chr2 | 71357378 | ||||||
| chr2:71357461
|
C | T | 1 | a0001c0003t0001g0117 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1379+1681C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 3/27 | chr2 | 71357461 | ||||||
| chr2:71357468
|
C | G | 5 | a0001c0003t0001g0104a0001c0003t0001g0105a0001c0003t0001g0106others(2): Show | 5 | HG02145.hp2 HG02615.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1379+1688C>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 3/27 | chr2 | 71357468 | ||||||
| chr2:71357543
|
A | T | 1 | a0002c0002t0001g0280 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1379+1763A>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 3/27 | chr2 | 71357543 | ||||||
| chr2:71357608
|
G | A | 1 | a0008c0010t0002g0342 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1379+1828G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 3/27 | chr2 | 71357608 | ||||||
| chr2:71357863
|
T | C | 2 | a0008c0010t0002g0342a0008c0010t0004g0253 | 2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1379+2083T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 3/27 | chr2 | 71357863 | ||||||
| chr2:71357902
|
T | TCAAG | 292 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(289): Show | 296 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(293): Show |
intron_variant | MODIFIER | c.1379+2123_1379+212 others(8): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | 71357902 | |||||
| chr2:71357940
|
T | G | 1 | a0002c0002t0001g0270 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1379+2160T>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 3/27 | chr2 | 71357940 | ||||||
| chr2:71357961
|
GA | G | 15 | a0001c0003t0001g0164a0001c0003t0003g0162a0001c0003t0003g0163others(12): Show | 15 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.1379+2183delA | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | 71357961 | |||||
| chr2:71358052
|
C | G | 1 | a0018c0027t0001g0201 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1379+2272C>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 3/27 | chr2 | 71358052 | ||||||
| chr2:71358082
|
G | A | 2 | a0001c0003t0003g0162a0001c0003t0003g0163 | 2 | HG03098.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1379+2302G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 3/27 | chr2 | 71358082 | ||||||
| chr2:71358382
|
T | G | 24 | a0002c0002t0001g0177a0002c0002t0001g0178a0002c0002t0001g0179others(21): Show | 24 | HG00438.hp1 HG01069.hp2 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.1379+2602T>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 3/27 | chr2 | 71358382 | ||||||
| chr2:71358511
|
A | G | 1 | a0003c0004t0002g0219 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1379+2731A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 3/27 | chr2 | 71358511 | ||||||
| chr2:71358769
|
G | A | 2 | a0001c0003t0001g0124a0001c0003t0001g0125 | 2 | HG02735.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1379+2989G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 3/27 | chr2 | 71358769 | ||||||
| chr2:71358793
|
G | A | 2 | a0009c0013t0001g0102a0009c0013t0001g0103 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1379+3013G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 3/27 | chr2 | 71358793 | ||||||
| chr2:71358798
|
C | T | 24 | a0002c0002t0001g0177a0002c0002t0001g0178a0002c0002t0001g0179others(21): Show | 24 | HG00438.hp1 HG01069.hp2 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.1379+3018C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 3/27 | chr2 | 71358798 | ||||||
| chr2:71358865
|
A | G | 1 | a0001c0001t0001g0340 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1379+3085A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 3/27 | chr2 | 71358865 | ||||||
| chr2:71358947
|
T | C | 2 | a0009c0013t0001g0102a0009c0013t0001g0103 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1379+3167T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 3/27 | chr2 | 71358947 | ||||||
| chr2:71359115
|
G | A | 2 | a0009c0013t0001g0102a0009c0013t0001g0103 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1379+3335G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 3/27 | chr2 | 71359115 | ||||||
| chr2:71359247
|
A | C | 2 | a0001c0001t0001g0088a0001c0001t0001g0089 | 2 | HG02622.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1379+3467A>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 3/27 | chr2 | 71359247 | ||||||
| chr2:71359405
|
G | A | 5 | a0001c0003t0001g0104a0001c0003t0001g0105a0001c0003t0001g0106others(2): Show | 5 | HG02145.hp2 HG02615.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1379+3625G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 3/27 | chr2 | 71359405 | ||||||
| chr2:71359753
|
T | C | 1 | a0002c0002t0001g0258 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1380-3400T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 3/27 | chr2 | 71359753 | ||||||
| chr2:71359814
|
T | G | 1 | a0003c0004t0002g0203 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1380-3339T>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 3/27 | chr2 | 71359814 | ||||||
| chr2:71360204
|
G | A | 287 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(284): Show | 291 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(288): Show |
intron_variant | MODIFIER | c.1380-2949G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 3/27 | chr2 | 71360204 | ||||||
| chr2:71360283
|
A | G | 3 | a0002c0002t0001g0310a0002c0002t0001g0311a0002c0002t0001g0312 | 3 | HG00609.hp2 HG00673.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1380-2870A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 3/27 | chr2 | 71360283 | ||||||
| chr2:71360334
|
G | A | 1 | a0015c0022t0001g0126 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1380-2819G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 3/27 | chr2 | 71360334 | ||||||
| chr2:71360468
|
CTT | C | 71 | a0002c0002t0001g0254a0002c0002t0001g0255a0002c0002t0001g0256others(68): Show | 71 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.1380-2684_1380-268 others(6): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 3/27 | chr2 | 71360468 | ||||||
| chr2:71360609
|
T | C | 95 | a0002c0002t0001g0177a0002c0002t0001g0178a0002c0002t0001g0179others(92): Show | 95 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.1380-2544T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 3/27 | chr2 | 71360609 | ||||||
| chr2:71360667
|
C | T | 287 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(284): Show | 291 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(288): Show |
intron_variant | MODIFIER | c.1380-2486C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 3/27 | chr2 | 71360667 | ||||||
| chr2:71360835
|
G | A | 4 | a0001c0007t0001g0327a0001c0007t0001g0329a0001c0007t0001g0333others(1): Show | 4 | HG02451.hp2 HG02895.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1380-2318G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 3/27 | chr2 | 71360835 | ||||||
| chr2:71361190
|
C | G | 1 | a0018c0027t0001g0201 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1380-1963C>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 3/27 | chr2 | 71361190 | ||||||
| chr2:71361206
|
G | A | 289 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(286): Show | 293 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(290): Show |
intron_variant | MODIFIER | c.1380-1947G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 3/27 | chr2 | 71361206 | ||||||
| chr2:71361233
|
A | G | 24 | a0002c0002t0001g0177a0002c0002t0001g0178a0002c0002t0001g0179others(21): Show | 24 | HG00438.hp1 HG01069.hp2 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.1380-1920A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 3/27 | chr2 | 71361233 | ||||||
| chr2:71361243
|
A | G | 71 | a0002c0002t0001g0254a0002c0002t0001g0255a0002c0002t0001g0256others(68): Show | 71 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.1380-1910A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 3/27 | chr2 | 71361243 | ||||||
| chr2:71361312
|
C | T | 291 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(288): Show | 295 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(292): Show |
intron_variant | MODIFIER | c.1380-1841C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 3/27 | chr2 | 71361312 | ||||||
| chr2:71361397
|
T | C | 36 | a0001c0003t0001g0108a0001c0003t0001g0109a0001c0003t0001g0111others(33): Show | 36 | HG00280.hp1 HG00735.hp1 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.1380-1756T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 3/27 | chr2 | 71361397 | ||||||
| chr2:71361651
|
C | G | 2 | a0009c0013t0001g0102a0009c0013t0001g0103 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1380-1502C>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 3/27 | chr2 | 71361651 | ||||||
| chr2:71361715
|
C | T | 2 | a0009c0013t0001g0102a0009c0013t0001g0103 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1380-1438C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 3/27 | chr2 | 71361715 | ||||||
| chr2:71361815
|
CT | C | 286 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(283): Show | 290 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(287): Show |
intron_variant | MODIFIER | c.1380-1329delT | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | 71361815 | |||||
| chr2:71362142
|
A | G | 16 | a0001c0003t0001g0164a0001c0003t0003g0162a0001c0003t0003g0163others(13): Show | 16 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.1380-1011A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 3/27 | chr2 | 71362142 | ||||||
| chr2:71362146
|
T | A | 2 | a0001c0001t0001g0340a0021c0031t0001g0341 | 2 | HG01884.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1380-1007T>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 3/27 | chr2 | 71362146 | ||||||
| chr2:71362207
|
C | T | 1 | a0002c0002t0001g0285 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1380-946C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 3/27 | chr2 | 71362207 | ||||||
| chr2:71362266
|
C | T | 71 | a0002c0002t0001g0254a0002c0002t0001g0255a0002c0002t0001g0256others(68): Show | 71 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.1380-887C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 3/27 | chr2 | 71362266 | ||||||
| chr2:71362342
|
C | A | 1 | a0003c0004t0002g0250 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1380-811C>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 3/27 | chr2 | 71362342 | ||||||
| chr2:71362360
|
C | T | 5 | a0001c0003t0001g0112a0001c0003t0001g0113a0001c0003t0001g0118others(2): Show | 5 | HG01099.hp2 HG02258.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1380-793C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 3/27 | chr2 | 71362360 | ||||||
| chr2:71362421
|
A | C | 2 | a0001c0001t0001g0071a0001c0001t0001g0090 | 2 | NA19057.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.1380-732A>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 3/27 | chr2 | 71362421 | ||||||
| chr2:71362421
|
A | G | 71 | a0002c0002t0001g0254a0002c0002t0001g0255a0002c0002t0001g0256others(68): Show | 71 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.1380-732A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 3/27 | chr2 | 71362421 | ||||||
| chr2:71362487
|
C | T | 4 | a0001c0007t0001g0327a0001c0007t0001g0329a0001c0007t0001g0333others(1): Show | 4 | HG02451.hp2 HG02895.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1380-666C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 3/27 | chr2 | 71362487 | ||||||
| chr2:71362488
|
G | A | 95 | a0002c0002t0001g0177a0002c0002t0001g0178a0002c0002t0001g0179others(92): Show | 95 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.1380-665G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 3/27 | chr2 | 71362488 | ||||||
| chr2:71362613
|
A | G | 100 | a0001c0003t0001g0104a0001c0003t0001g0105a0001c0003t0001g0106others(97): Show | 100 | HG00280.hp1 HG00438.hp1 HG00733.hp1 others(97): Show |
intron_variant | MODIFIER | c.1380-540A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 3/27 | chr2 | 71362613 | ||||||
| chr2:71362732
|
G | C | 342 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(339): Show | 346 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(343): Show |
intron_variant | MODIFIER | c.1380-421G>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 3/27 | chr2 | 71362732 | ||||||
| chr2:71362783
|
A | G | 109 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(106): Show | 113 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.1380-370A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 3/27 | chr2 | 71362783 | ||||||
| chr2:71362919
|
C | A | 1 | a0001c0005t0001g0153 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1380-234C>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 3/27 | chr2 | 71362919 | ||||||
| chr2:71362949
|
T | C | 3 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028 | 3 | HG00738.hp2 HG04199.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1380-204T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 3/27 | chr2 | 71362949 | ||||||
| chr2:71363077
|
A | G | 1 | a0002c0002t0001g0184 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1380-76A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 3/27 | chr2 | 71363077 | ||||||
| chr2:71363078
|
T | C | 1 | a0008c0010t0002g0342 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1380-75T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 3/27 | chr2 | 71363078 | ||||||
| chr2:71363296
|
A | G | 1 | a0003c0015t0002g0245 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1418+105A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 4/27 | chr2 | 71363296 | ||||||
| chr2:71363388
|
G | T | 96 | a0002c0002t0001g0177a0002c0002t0001g0178a0002c0002t0001g0179others(93): Show | 96 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.1418+197G>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 4/27 | chr2 | 71363388 | ||||||
| chr2:71363403
|
T | C | 1 | a0001c0001t0001g0334 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1418+212T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 4/27 | chr2 | 71363403 | ||||||
| chr2:71363447
|
AAT | A | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(113): Show | 120 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.1418+257_1418+258d others(4): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 4/27 | chr2 | 71363447 | ||||||
| chr2:71363481
|
T | C | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(113): Show | 120 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.1418+290T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 4/27 | chr2 | 71363481 | ||||||
| chr2:71363509
|
G | A | 3 | a0003c0004t0002g0249a0003c0004t0002g0251a0003c0004t0002g0252 | 3 | HG03225.hp1 HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1418+318G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 4/27 | chr2 | 71363509 | ||||||
| chr2:71363609
|
C | T | 2 | a0009c0013t0001g0102a0009c0013t0001g0103 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1419-345C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 4/27 | chr2 | 71363609 | ||||||
| chr2:71363742
|
T | C | 2 | a0003c0004t0002g0204a0003c0004t0002g0224 | 2 | NA19004.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.1419-212T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 4/27 | chr2 | 71363742 | ||||||
| chr2:71363834
|
C | G | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(113): Show | 120 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.1419-120C>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 4/27 | chr2 | 71363834 | ||||||
| chr2:71363897
|
T | C | 1 | a0008c0010t0002g0342 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1419-57T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 4/27 | chr2 | 71363897 | ||||||
| chr2:71364275
|
G | A | 2 | a0009c0013t0001g0102a0009c0013t0001g0103 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1717+23G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 5/27 | chr2 | 71364275 | ||||||
| chr2:71364344
|
A | G | 2 | a0009c0013t0001g0102a0009c0013t0001g0103 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1717+92A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 5/27 | chr2 | 71364344 | ||||||
| chr2:71364540
|
G | A | 96 | a0002c0002t0001g0177a0002c0002t0001g0178a0002c0002t0001g0179others(93): Show | 96 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.1717+288G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 5/27 | chr2 | 71364540 | ||||||
| chr2:71364725
|
G | A | 2 | a0009c0013t0001g0102a0009c0013t0001g0103 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1717+473G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 5/27 | chr2 | 71364725 | ||||||
| chr2:71364866
|
A | G | 3 | a0001c0003t0001g0142a0001c0003t0001g0143a0001c0003t0001g0144 | 3 | HG00733.hp1 HG03139.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1718-563A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 5/27 | chr2 | 71364866 | ||||||
| chr2:71364896
|
A | G | 75 | a0001c0003t0001g0104a0001c0003t0001g0105a0001c0003t0001g0106others(72): Show | 75 | HG00280.hp1 HG00733.hp1 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.1718-533A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 5/27 | chr2 | 71364896 | ||||||
| chr2:71365030
|
G | T | 1 | a0003c0004t0002g0249 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1718-399G>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 5/27 | chr2 | 71365030 | ||||||
| chr2:71365140
|
A | G | 31 | a0001c0003t0001g0108a0001c0003t0001g0109a0001c0003t0001g0111others(28): Show | 31 | HG00280.hp1 HG00735.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.1718-289A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 5/27 | chr2 | 71365140 | ||||||
| chr2:71365297
|
A | C | 3 | a0001c0001t0001g0086a0001c0001t0001g0088a0001c0001t0001g0089 | 3 | HG01192.hp2 HG02622.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1718-132A>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 5/27 | chr2 | 71365297 | ||||||
| chr2:71365308
|
A | AT | 75 | a0001c0003t0001g0104a0001c0003t0001g0105a0001c0003t0001g0106others(72): Show | 75 | HG00280.hp1 HG00733.hp1 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.1718-116dupT | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr2 | 71365308 | |||||
| chr2:71365314
|
G | T | 289 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(286): Show | 293 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(290): Show |
intron_variant | MODIFIER | c.1718-115G>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 5/27 | chr2 | 71365314 | ||||||
| chr2:71365909
|
G | C | 3 | a0001c0007t0001g0328a0001c0007t0001g0330a0013c0018t0001g0331 | 3 | HG01884.hp2 HG02615.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1995+203G>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 6/27 | chr2 | 71365909 | ||||||
| chr2:71365952
|
C | G | 5 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0041others(2): Show | 5 | HG00544.hp2 HG02165.hp1 NA18988.hp1 others(2): Show |
intron_variant | MODIFIER | c.1995+246C>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 6/27 | chr2 | 71365952 | ||||||
| chr2:71365964
|
C | T | 14 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0034others(11): Show | 15 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(12): Show |
intron_variant | MODIFIER | c.1995+258C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 6/27 | chr2 | 71365964 | ||||||
| chr2:71366034
|
G | A | 1 | a0001c0003t0001g0143 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1995+328G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 6/27 | chr2 | 71366034 | ||||||
| chr2:71366084
|
C | T | 6 | a0003c0004t0002g0248a0003c0004t0002g0249a0003c0004t0002g0250others(3): Show | 6 | HG02818.hp1 HG03139.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.1995+378C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 6/27 | chr2 | 71366084 | ||||||
| chr2:71366134
|
G | T | 2 | a0009c0013t0001g0102a0009c0013t0001g0103 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1995+428G>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 6/27 | chr2 | 71366134 | ||||||
| chr2:71366135
|
A | C | 1 | a0001c0003t0001g0150 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1995+429A>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 6/27 | chr2 | 71366135 | ||||||
| chr2:71366136
|
G | C | 1 | a0001c0003t0001g0150 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1995+430G>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 6/27 | chr2 | 71366136 | ||||||
| chr2:71366141
|
A | G | 2 | a0008c0010t0002g0342a0008c0010t0004g0253 | 2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1995+435A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 6/27 | chr2 | 71366141 | ||||||
| chr2:71366144
|
A | G | 71 | a0002c0002t0001g0254a0002c0002t0001g0255a0002c0002t0001g0256others(68): Show | 71 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.1995+438A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 6/27 | chr2 | 71366144 | ||||||
| chr2:71366177
|
C | T | 2 | a0009c0013t0001g0102a0009c0013t0001g0103 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1995+471C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 6/27 | chr2 | 71366177 | ||||||
| chr2:71366250
|
C | T | 7 | a0001c0001t0001g0326a0001c0001t0001g0334a0001c0001t0001g0335others(4): Show | 7 | HG02559.hp2 HG02572.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1995+544C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 6/27 | chr2 | 71366250 | ||||||
| chr2:71366343
|
G | C | 2 | a0009c0013t0001g0102a0009c0013t0001g0103 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1995+637G>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 6/27 | chr2 | 71366343 | ||||||
| chr2:71366363
|
GA | G | 78 | a0001c0001t0001g0013a0001c0003t0001g0104a0001c0003t0001g0105others(75): Show | 78 | HG00280.hp1 HG00733.hp1 HG00735.hp1 others(75): Show |
intron_variant | MODIFIER | c.1995+670delA | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr2 | 71366363 | |||||
| chr2:71366403
|
G | A | 2 | a0009c0013t0001g0102a0009c0013t0001g0103 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1995+697G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 6/27 | chr2 | 71366403 | ||||||
| chr2:71366405
|
G | A | 194 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(191): Show | 198 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.1995+699G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 6/27 | chr2 | 71366405 | ||||||
| chr2:71366488
|
A | G | 9 | a0001c0003t0001g0146a0001c0003t0001g0147a0001c0003t0001g0148others(6): Show | 9 | HG01361.hp2 HG01943.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1995+782A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 6/27 | chr2 | 71366488 | ||||||
| chr2:71366515
|
T | C | 1 | a0001c0001t0001g0326 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1995+809T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 6/27 | chr2 | 71366515 | ||||||
| chr2:71366591
|
A | C | 1 | a0001c0001t0001g0334 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1995+885A>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 6/27 | chr2 | 71366591 | ||||||
| chr2:71366766
|
C | T | 24 | a0002c0002t0001g0177a0002c0002t0001g0178a0002c0002t0001g0179others(21): Show | 24 | HG00438.hp1 HG01069.hp2 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.1995+1060C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 6/27 | chr2 | 71366766 | ||||||
| chr2:71366987
|
G | A | 1 | a0002c0002t0001g0185 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1995+1281G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 6/27 | chr2 | 71366987 | ||||||
| chr2:71367089
|
G | A | 194 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(191): Show | 198 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.1996-1293G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 6/27 | chr2 | 71367089 | ||||||
| chr2:71367362
|
ATCC | A | 8 | a0002c0002t0001g0268a0002c0002t0001g0293a0002c0002t0001g0294others(5): Show | 8 | HG01074.hp2 HG01928.hp2 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.1996-1015_1996-101 others(7): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr2 | 71367362 | |||||
| chr2:71367374
|
C | G | 1 | a0018c0027t0001g0201 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1996-1008C>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 6/27 | chr2 | 71367374 | ||||||
| chr2:71367404
|
C | T | 109 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(106): Show | 113 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.1996-978C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 6/27 | chr2 | 71367404 | ||||||
| chr2:71367431
|
A | AT | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(218): Show | 225 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(222): Show |
intron_variant | MODIFIER | c.1996-931dupT | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr2 | 71367431 | |||||
| chr2:71367431
|
A | ATT | 12 | a0001c0003t0001g0118a0001c0003t0001g0130a0001c0003t0001g0131others(9): Show | 12 | HG01167.hp2 HG02109.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1996-932_1996-931d others(4): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr2 | 71367431 | |||||
| chr2:71367524
|
C | G | 1 | a0001c0003t0001g0146 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1996-858C>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 6/27 | chr2 | 71367524 | ||||||
| chr2:71367585
|
G | A | 7 | a0001c0007t0001g0327a0001c0007t0001g0328a0001c0007t0001g0329others(4): Show | 7 | HG01884.hp2 HG02451.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1996-797G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 6/27 | chr2 | 71367585 | ||||||
| chr2:71367597
|
G | A | 1 | a0002c0002t0001g0293 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1996-785G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 6/27 | chr2 | 71367597 | ||||||
| chr2:71367641
|
G | A | 1 | a0001c0001t0001g0047 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1996-741G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 6/27 | chr2 | 71367641 | ||||||
| chr2:71367660
|
C | G | 1 | a0003c0015t0002g0245 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1996-722C>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 6/27 | chr2 | 71367660 | ||||||
| chr2:71367738
|
C | CT | 11 | a0001c0001t0001g0061a0001c0007t0001g0327a0001c0007t0001g0328others(8): Show | 11 | HG01256.hp2 HG01884.hp2 HG02083.hp1 others(8): Show |
intron_variant | MODIFIER | c.1996-631dupT | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr2 | 71367738 | |||||
| chr2:71367738
|
C | CTT | 110 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(107): Show | 114 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.1996-632_1996-631d others(4): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr2 | 71367738 | |||||
| chr2:71367738
|
CT | C | 76 | a0001c0003t0001g0104a0001c0003t0001g0105a0001c0003t0001g0106others(73): Show | 76 | HG00280.hp1 HG00733.hp1 HG00735.hp1 others(73): Show |
intron_variant | MODIFIER | c.1996-631delT | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr2 | 71367738 | |||||
| chr2:71367750
|
T | A | 15 | a0001c0003t0001g0142a0001c0003t0001g0143a0001c0003t0001g0144others(12): Show | 15 | HG00733.hp1 HG01243.hp2 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.1996-632T>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 6/27 | chr2 | 71367750 | ||||||
| chr2:71367751
|
T | A | 75 | a0001c0003t0001g0104a0001c0003t0001g0105a0001c0003t0001g0106others(72): Show | 75 | HG00280.hp1 HG00733.hp1 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.1996-631T>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 6/27 | chr2 | 71367751 | ||||||
| chr2:71367751
|
TA | T | 28 | a0002c0002t0001g0177a0002c0002t0001g0178a0002c0002t0001g0179others(25): Show | 28 | HG00438.hp1 HG01069.hp2 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.1996-626delA | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr2 | 71367751 | |||||
| chr2:71367752
|
A | T | 71 | a0002c0002t0001g0254a0002c0002t0001g0256a0002c0002t0001g0258others(68): Show | 71 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.1996-630A>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 6/27 | chr2 | 71367752 | ||||||
| chr2:71367759
|
T | C | 11 | a0001c0003t0001g0114a0001c0003t0001g0123a0001c0003t0001g0138others(8): Show | 11 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.1996-623T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 6/27 | chr2 | 71367759 | ||||||
| chr2:71367776
|
G | A | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(113): Show | 120 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.1996-606G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 6/27 | chr2 | 71367776 | ||||||
| chr2:71367845
|
C | T | 5 | a0003c0004t0002g0248a0003c0004t0002g0249a0003c0004t0002g0250others(2): Show | 5 | HG02818.hp1 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1996-537C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 6/27 | chr2 | 71367845 | ||||||
| chr2:71367957
|
G | C | 10 | a0003c0004t0002g0205a0003c0004t0002g0206a0003c0004t0002g0207others(7): Show | 10 | HG00423.hp2 HG02080.hp1 NA18947.hp2 others(7): Show |
intron_variant | MODIFIER | c.1996-425G>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 6/27 | chr2 | 71367957 | ||||||
| chr2:71368108
|
C | A | 289 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(286): Show | 293 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(290): Show |
intron_variant | MODIFIER | c.1996-274C>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 6/27 | chr2 | 71368108 | ||||||
| chr2:71368151
|
A | G | 1 | a0001c0001t0001g0015 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1996-231A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 6/27 | chr2 | 71368151 | ||||||
| chr2:71368152
|
T | C | 6 | a0001c0003t0001g0104a0001c0003t0001g0105a0001c0003t0001g0106others(3): Show | 6 | HG02145.hp2 HG02615.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1996-230T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 6/27 | chr2 | 71368152 | ||||||
| chr2:71368194
|
A | C | 1 | a0001c0001t0001g0083 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1996-188A>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 6/27 | chr2 | 71368194 | ||||||
| chr2:71368236
|
G | A | 3 | a0001c0001t0001g0086a0001c0001t0001g0088a0001c0001t0001g0089 | 3 | HG01192.hp2 HG02622.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1996-146G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 6/27 | chr2 | 71368236 | ||||||
| chr2:71368288
|
A | G | 3 | a0001c0003t0001g0147a0001c0003t0001g0149a0001c0003t0001g0151 | 3 | HG02717.hp1 HG03209.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1996-94A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 6/27 | chr2 | 71368288 | ||||||
| chr2:71368728
|
G | A | 2 | a0009c0013t0001g0102a0009c0013t0001g0103 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2142+200G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 7/27 | chr2 | 71368728 | ||||||
| chr2:71368834
|
C | T | 1 | a0003c0004t0002g0203 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2142+306C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 7/27 | chr2 | 71368834 | ||||||
| chr2:71368911
|
C | T | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(113): Show | 120 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.2142+383C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 7/27 | chr2 | 71368911 | ||||||
| chr2:71368955
|
T | G | 76 | a0001c0003t0001g0104a0001c0003t0001g0105a0001c0003t0001g0106others(73): Show | 76 | HG00280.hp1 HG00733.hp1 HG00735.hp1 others(73): Show |
intron_variant | MODIFIER | c.2142+427T>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 7/27 | chr2 | 71368955 | ||||||
| chr2:71369041
|
A | G | 2 | a0001c0003t0003g0162a0001c0003t0003g0163 | 2 | HG03098.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2142+513A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 7/27 | chr2 | 71369041 | ||||||
| chr2:71369041
|
ATAGT | A | 28 | a0001c0003t0001g0108a0001c0003t0001g0109a0001c0003t0001g0111others(25): Show | 28 | HG00280.hp1 HG00735.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.2142+520_2142+523d others(6): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr2 | 71369041 | |||||
| chr2:71369075
|
C | T | 9 | a0001c0003t0001g0146a0001c0003t0001g0147a0001c0003t0001g0148others(6): Show | 9 | HG01361.hp2 HG01943.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.2142+547C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 7/27 | chr2 | 71369075 | ||||||
| chr2:71369115
|
G | A | 15 | a0001c0003t0001g0164a0001c0003t0003g0162a0001c0003t0003g0163others(12): Show | 15 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.2142+587G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 7/27 | chr2 | 71369115 | ||||||
| chr2:71369164
|
G | GTGT | 76 | a0001c0003t0001g0104a0001c0003t0001g0105a0001c0003t0001g0106others(73): Show | 76 | HG00280.hp1 HG00733.hp1 HG00735.hp1 others(73): Show |
intron_variant | MODIFIER | c.2142+637_2142+639d others(5): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr2 | 71369164 | |||||
| chr2:71369277
|
G | C | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(192): Show | 199 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.2143-606G>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 7/27 | chr2 | 71369277 | ||||||
| chr2:71369282
|
C | T | 1 | a0015c0022t0001g0126 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2143-601C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 7/27 | chr2 | 71369282 | ||||||
| chr2:71369322
|
C | CA | 69 | a0002c0002t0001g0177a0002c0002t0001g0178a0002c0002t0001g0254others(66): Show | 69 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.2143-541dupA | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr2 | 71369322 | |||||
| chr2:71369322
|
C | CAA | 7 | a0002c0002t0001g0258a0002c0002t0001g0269a0002c0002t0001g0271others(4): Show | 7 | HG00741.hp1 HG01175.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.2143-542_2143-541d others(4): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr2 | 71369322 | |||||
| chr2:71369322
|
CA | C | 169 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(166): Show | 173 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.2143-541delA | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr2 | 71369322 | |||||
| chr2:71369322
|
CAA | C | 9 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0024others(6): Show | 9 | HG00642.hp1 HG00642.hp2 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.2143-542_2143-541d others(4): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr2 | 71369322 | |||||
| chr2:71369340
|
A | G | 2 | a0001c0003t0001g0150a0001c0024t0001g0145 | 2 | HG02055.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.2143-543A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 7/27 | chr2 | 71369340 | ||||||
| chr2:71369363
|
G | A | 1 | a0001c0005t0001g0161 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2143-520G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 7/27 | chr2 | 71369363 | ||||||
| chr2:71369597
|
T | A | 24 | a0002c0002t0001g0177a0002c0002t0001g0178a0002c0002t0001g0179others(21): Show | 24 | HG00438.hp1 HG01069.hp2 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.2143-286T>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 7/27 | chr2 | 71369597 | ||||||
| chr2:71370225
|
A | G | 7 | a0001c0007t0001g0327a0001c0007t0001g0328a0001c0007t0001g0329others(4): Show | 7 | HG01884.hp2 HG02451.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.2265+220A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71370225 | ||||||
| chr2:71370257
|
A | G | 77 | a0001c0003t0001g0104a0001c0003t0001g0105a0001c0003t0001g0106others(74): Show | 77 | HG00280.hp1 HG00733.hp1 HG00735.hp1 others(74): Show |
intron_variant | MODIFIER | c.2265+252A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71370257 | ||||||
| chr2:71370404
|
A | G | 6 | a0003c0004t0002g0248a0003c0004t0002g0249a0003c0004t0002g0250others(3): Show | 6 | HG02818.hp1 HG03139.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.2265+399A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71370404 | ||||||
| chr2:71370411
|
A | G | 2 | a0001c0003t0001g0171a0002c0002t0001g0297 | 2 | HG01891.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.2265+406A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71370411 | ||||||
| chr2:71370500
|
T | C | 1 | a0018c0027t0001g0201 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2265+495T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71370500 | ||||||
| chr2:71370548
|
A | G | 5 | a0003c0004t0002g0248a0003c0004t0002g0249a0003c0004t0002g0250others(2): Show | 5 | HG02818.hp1 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.2265+543A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71370548 | ||||||
| chr2:71370833
|
A | G | 2 | a0009c0013t0001g0102a0009c0013t0001g0103 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2265+828A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71370833 | ||||||
| chr2:71370894
|
C | T | 1 | a0002c0002t0001g0198 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2265+889C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71370894 | ||||||
| chr2:71370954
|
A | C | 1 | a0003c0004t0002g0250 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2265+949A>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71370954 | ||||||
| chr2:71370974
|
C | T | 2 | a0009c0013t0001g0102a0009c0013t0001g0103 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2265+969C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71370974 | ||||||
| chr2:71370977
|
G | A | 296 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(293): Show | 300 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(297): Show |
intron_variant | MODIFIER | c.2265+972G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71370977 | ||||||
| chr2:71371020
|
C | T | 5 | a0001c0001t0001g0326a0001c0001t0001g0337a0001c0001t0001g0338others(2): Show | 5 | HG02559.hp2 HG02572.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.2265+1015C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71371020 | ||||||
| chr2:71371180
|
C | G | 1 | a0001c0001t0001g0046 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2265+1175C>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71371180 | ||||||
| chr2:71371337
|
T | C | 1 | a0018c0027t0001g0201 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2265+1332T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71371337 | ||||||
| chr2:71371679
|
AT | A | 24 | a0002c0002t0001g0177a0002c0002t0001g0178a0002c0002t0001g0179others(21): Show | 24 | HG00438.hp1 HG01069.hp2 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.2265+1684delT | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr2 | 71371679 | |||||
| chr2:71371702
|
GT | G | 292 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(289): Show | 296 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(293): Show |
intron_variant | MODIFIER | c.2265+1708delT | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr2 | 71371702 | |||||
| chr2:71371707
|
T | C | 75 | a0001c0003t0001g0104a0001c0003t0001g0105a0001c0003t0001g0106others(72): Show | 75 | HG00280.hp1 HG00733.hp1 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.2265+1702T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71371707 | ||||||
| chr2:71371757
|
C | A | 4 | a0002c0002t0001g0272a0002c0002t0001g0301a0002c0002t0001g0307others(1): Show | 4 | NA18942.hp1 NA18964.hp2 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.2265+1752C>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71371757 | ||||||
| chr2:71371894
|
G | A | 70 | a0002c0002t0001g0254a0002c0002t0001g0255a0002c0002t0001g0256others(67): Show | 70 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.2265+1889G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71371894 | ||||||
| chr2:71371929
|
T | G | 1 | a0001c0003t0001g0148 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2265+1924T>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71371929 | ||||||
| chr2:71372023
|
T | G | 71 | a0002c0002t0001g0254a0002c0002t0001g0255a0002c0002t0001g0256others(68): Show | 71 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.2265+2018T>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71372023 | ||||||
| chr2:71372089
|
T | A | 5 | a0001c0003t0001g0104a0001c0003t0001g0105a0001c0003t0001g0106others(2): Show | 5 | HG02145.hp2 HG02615.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.2265+2084T>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71372089 | ||||||
| chr2:71372781
|
C | T | 1 | a0001c0003t0001g0120 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2265+2776C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71372781 | ||||||
| chr2:71372791
|
G | A | 1 | a0002c0002t0001g0262 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2265+2786G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71372791 | ||||||
| chr2:71372851
|
C | T | 1 | a0001c0003t0001g0151 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2265+2846C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71372851 | ||||||
| chr2:71372913
|
A | G | 8 | a0001c0001t0001g0326a0001c0001t0001g0334a0001c0001t0001g0335others(5): Show | 8 | HG01884.hp1 HG02559.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2265+2908A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71372913 | ||||||
| chr2:71373011
|
G | A | 2 | a0003c0004t0002g0003a0003c0004t0002g0223 | 2 | NA18951.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.2265+3006G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71373011 | ||||||
| chr2:71373097
|
G | A | 2 | a0001c0003t0003g0162a0001c0003t0003g0163 | 2 | HG03098.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2265+3092G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71373097 | ||||||
| chr2:71373224
|
A | G | 192 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(189): Show | 196 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.2265+3219A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71373224 | ||||||
| chr2:71373280
|
C | G | 1 | a0001c0003t0001g0119 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2265+3275C>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71373280 | ||||||
| chr2:71373296
|
TTTA | T | 145 | a0001c0003t0001g0104a0001c0003t0001g0105a0001c0003t0001g0106others(142): Show | 145 | HG00280.hp1 HG00438.hp2 HG00544.hp1 others(142): Show |
intron_variant | MODIFIER | c.2265+3297_2265+329 others(7): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr2 | 71373296 | |||||
| chr2:71373324
|
T | G | 4 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(1): Show | 4 | HG02735.hp1 HG03669.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.2265+3319T>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71373324 | ||||||
| chr2:71373327
|
T | G | 3 | a0001c0001t0001g0013a0001c0001t0001g0050a0001c0001t0001g0051 | 3 | HG01069.hp1 HG01071.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.2265+3322T>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71373327 | ||||||
| chr2:71373415
|
T | G | 1 | a0001c0003t0001g0148 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2265+3410T>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71373415 | ||||||
| chr2:71373437
|
A | AT | 49 | a0001c0001t0001g0326a0001c0003t0001g0106a0001c0003t0001g0111others(46): Show | 49 | HG00280.hp1 HG00733.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.2265+3459dupT | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr2 | 71373437 | |||||
| chr2:71373437
|
A | ATT | 36 | a0001c0003t0001g0108a0001c0003t0001g0109a0001c0003t0001g0112others(33): Show | 36 | HG00733.hp1 HG00738.hp1 HG01069.hp2 others(33): Show |
intron_variant | MODIFIER | c.2265+3458_2265+345 others(6): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr2 | 71373437 | |||||
| chr2:71373437
|
A | ATTT | 8 | a0001c0003t0001g0129a0001c0003t0001g0150a0002c0002t0001g0179others(5): Show | 8 | HG00438.hp1 HG01981.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.2265+3457_2265+345 others(7): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr2 | 71373437 | |||||
| chr2:71373437
|
AT | A | 105 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(102): Show | 109 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.2265+3459delT | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr2 | 71373437 | |||||
| chr2:71373437
|
ATT | A | 71 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0094others(68): Show | 71 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.2265+3458_2265+345 others(6): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr2 | 71373437 | |||||
| chr2:71373437
|
ATTTTTTT others(6): Show |
A | 3 | a0001c0003t0001g0147a0001c0003t0001g0149a0001c0003t0001g0151 | 3 | HG02717.hp1 HG03209.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2265+3447_2265+345 others(17): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr2 | 71373437 | |||||
| chr2:71373484
|
G | A | 75 | a0001c0003t0001g0104a0001c0003t0001g0105a0001c0003t0001g0106others(72): Show | 75 | HG00280.hp1 HG00733.hp1 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.2265+3479G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71373484 | ||||||
| chr2:71373485
|
C | T | 192 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(189): Show | 196 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.2265+3480C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71373485 | ||||||
| chr2:71373661
|
G | A | 1 | a0001c0005t0001g0174 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2265+3656G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71373661 | ||||||
| chr2:71373664
|
C | T | 1 | a0001c0001t0001g0097 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.2265+3659C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71373664 | ||||||
| chr2:71373794
|
C | T | 192 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(189): Show | 196 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.2265+3789C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71373794 | ||||||
| chr2:71373835
|
C | G | 1 | a0001c0001t0001g0064 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2265+3830C>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71373835 | ||||||
| chr2:71373891
|
C | T | 24 | a0002c0002t0001g0177a0002c0002t0001g0178a0002c0002t0001g0179others(21): Show | 24 | HG00438.hp1 HG01069.hp2 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.2265+3886C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71373891 | ||||||
| chr2:71373980
|
G | A | 2 | a0002c0002t0001g0302a0002c0002t0001g0308 | 2 | HG03710.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.2265+3975G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71373980 | ||||||
| chr2:71374014
|
T | C | 1 | a0003c0004t0002g0247 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2265+4009T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71374014 | ||||||
| chr2:71374014
|
T | G | 24 | a0002c0002t0001g0177a0002c0002t0001g0178a0002c0002t0001g0179others(21): Show | 24 | HG00438.hp1 HG01069.hp2 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.2265+4009T>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71374014 | ||||||
| chr2:71374084
|
C | T | 1 | a0018c0027t0001g0201 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2265+4079C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71374084 | ||||||
| chr2:71374191
|
A | T | 1 | a0002c0002t0001g0307 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.2265+4186A>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71374191 | ||||||
| chr2:71374304
|
T | G | 109 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(106): Show | 113 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.2265+4299T>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71374304 | ||||||
| chr2:71374392
|
C | T | 287 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(284): Show | 291 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(288): Show |
intron_variant | MODIFIER | c.2265+4387C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71374392 | ||||||
| chr2:71374488
|
T | C | 1 | a0001c0001t0001g0334 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2265+4483T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71374488 | ||||||
| chr2:71374689
|
G | A | 341 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(338): Show | 345 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(342): Show |
intron_variant | MODIFIER | c.2265+4684G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71374689 | ||||||
| chr2:71374912
|
A | G | 31 | a0001c0003t0001g0108a0001c0003t0001g0109a0001c0003t0001g0111others(28): Show | 31 | HG00280.hp1 HG00735.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.2265+4907A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71374912 | ||||||
| chr2:71374985
|
AT | A | 14 | a0001c0003t0001g0111a0001c0003t0001g0114a0001c0003t0001g0123others(11): Show | 14 | HG00280.hp1 HG00738.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.2265+4989delT | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr2 | 71374985 | |||||
| chr2:71375115
|
A | G | 2 | a0001c0009t0001g0110a0001c0009t0001g0136 | 2 | HG01361.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.2266-5107A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71375115 | ||||||
| chr2:71375198
|
G | A | 1 | a0002c0002t0001g0196 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.2266-5024G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71375198 | ||||||
| chr2:71375344
|
C | G | 1 | a0003c0012t0002g0240 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2266-4878C>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71375344 | ||||||
| chr2:71375405
|
A | G | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(113): Show | 120 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.2266-4817A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71375405 | ||||||
| chr2:71375667
|
G | A | 1 | a0001c0001t0001g0022 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2266-4555G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71375667 | ||||||
| chr2:71375701
|
A | T | 1 | a0001c0001t0001g0059 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2266-4521A>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71375701 | ||||||
| chr2:71376087
|
A | G | 1 | a0001c0009t0001g0110 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.2266-4135A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71376087 | ||||||
| chr2:71376185
|
G | A | 1 | a0021c0031t0001g0341 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2266-4037G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71376185 | ||||||
| chr2:71376299
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2266-3923G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71376299 | ||||||
| chr2:71376335
|
C | T | 2 | a0009c0013t0001g0102a0009c0013t0001g0103 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2266-3887C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71376335 | ||||||
| chr2:71376378
|
T | C | 1 | a0001c0003t0001g0164 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2266-3844T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71376378 | ||||||
| chr2:71376398
|
G | GTTGT | 177 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(174): Show | 181 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(178): Show |
intron_variant | MODIFIER | c.2266-3809_2266-380 others(8): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr2 | 71376398 | |||||
| chr2:71376652
|
G | A | 2 | a0009c0013t0001g0102a0009c0013t0001g0103 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2266-3570G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71376652 | ||||||
| chr2:71376717
|
TA | T | 288 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(285): Show | 292 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(289): Show |
intron_variant | MODIFIER | c.2266-3497delA | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr2 | 71376717 | |||||
| chr2:71376730
|
A | G | 1 | a0001c0003t0001g0138 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2266-3492A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71376730 | ||||||
| chr2:71376843
|
G | A | 1 | a0001c0001t0001g0340 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2266-3379G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71376843 | ||||||
| chr2:71376870
|
A | G | 7 | a0001c0007t0001g0327a0001c0007t0001g0328a0001c0007t0001g0329others(4): Show | 7 | HG01884.hp2 HG02451.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.2266-3352A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71376870 | ||||||
| chr2:71377052
|
T | G | 2 | a0001c0003t0001g0124a0001c0003t0001g0125 | 2 | HG02735.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.2266-3170T>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71377052 | ||||||
| chr2:71377059
|
G | A | 3 | a0001c0003t0001g0118a0001c0003t0001g0120a0001c0003t0001g0121 | 3 | HG01099.hp2 HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2266-3163G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71377059 | ||||||
| chr2:71377108
|
T | A | 291 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(288): Show | 295 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(292): Show |
intron_variant | MODIFIER | c.2266-3114T>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71377108 | ||||||
| chr2:71377111
|
A | G | 1 | a0001c0009t0001g0110 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.2266-3111A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71377111 | ||||||
| chr2:71377167
|
C | T | 2 | a0009c0013t0001g0102a0009c0013t0001g0103 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2266-3055C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71377167 | ||||||
| chr2:71377228
|
A | C | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(113): Show | 120 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.2266-2994A>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71377228 | ||||||
| chr2:71377336
|
A | C | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(113): Show | 120 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.2266-2886A>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71377336 | ||||||
| chr2:71377344
|
C | CA | 9 | a0001c0001t0001g0068a0001c0003t0001g0121a0002c0002t0001g0307others(6): Show | 9 | HG02258.hp2 HG02976.hp2 HG03453.hp1 others(6): Show |
intron_variant | MODIFIER | c.2266-2870dupA | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr2 | 71377344 | |||||
| chr2:71377355
|
A | G | 24 | a0002c0002t0001g0177a0002c0002t0001g0178a0002c0002t0001g0179others(21): Show | 24 | HG00438.hp1 HG01069.hp2 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.2266-2867A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71377355 | ||||||
| chr2:71377451
|
A | C | 2 | a0009c0013t0001g0102a0009c0013t0001g0103 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2266-2771A>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71377451 | ||||||
| chr2:71377463
|
G | A | 2 | a0009c0013t0001g0102a0009c0013t0001g0103 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2266-2759G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71377463 | ||||||
| chr2:71377474
|
A | G | 70 | a0002c0002t0001g0254a0002c0002t0001g0255a0002c0002t0001g0256others(67): Show | 70 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.2266-2748A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71377474 | ||||||
| chr2:71377729
|
A | G | 24 | a0002c0002t0001g0177a0002c0002t0001g0178a0002c0002t0001g0179others(21): Show | 24 | HG00438.hp1 HG01069.hp2 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.2266-2493A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71377729 | ||||||
| chr2:71377751
|
A | G | 1 | a0001c0003t0001g0148 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2266-2471A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71377751 | ||||||
| chr2:71377760
|
G | C | 1 | a0018c0027t0001g0201 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2266-2462G>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71377760 | ||||||
| chr2:71377904
|
T | G | 1 | a0003c0004t0002g0231 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2266-2318T>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71377904 | ||||||
| chr2:71378001
|
A | C | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(113): Show | 120 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.2266-2221A>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71378001 | ||||||
| chr2:71378015
|
T | G | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(113): Show | 120 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.2266-2207T>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71378015 | ||||||
| chr2:71378047
|
A | G | 1 | a0002c0002t0001g0307 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.2266-2175A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71378047 | ||||||
| chr2:71378103
|
G | A | 70 | a0002c0002t0001g0254a0002c0002t0001g0255a0002c0002t0001g0256others(67): Show | 70 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.2266-2119G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71378103 | ||||||
| chr2:71378164
|
A | G | 14 | a0001c0003t0001g0118a0001c0003t0001g0119a0001c0003t0001g0120others(11): Show | 14 | HG01099.hp2 HG01884.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.2266-2058A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71378164 | ||||||
| chr2:71378209
|
G | A | 2 | a0001c0003t0001g0172a0001c0003t0001g0173 | 2 | HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2266-2013G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71378209 | ||||||
| chr2:71378246
|
G | A | 2 | a0009c0013t0001g0102a0009c0013t0001g0103 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2266-1976G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71378246 | ||||||
| chr2:71378283
|
C | T | 1 | a0001c0003t0001g0150 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2266-1939C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71378283 | ||||||
| chr2:71378339
|
A | G | 1 | a0001c0003t0001g0117 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2266-1883A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71378339 | ||||||
| chr2:71378639
|
T | A | 1 | a0002c0002t0001g0186 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.2266-1583T>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71378639 | ||||||
| chr2:71378671
|
A | G | 24 | a0002c0002t0001g0177a0002c0002t0001g0178a0002c0002t0001g0179others(21): Show | 24 | HG00438.hp1 HG01069.hp2 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.2266-1551A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71378671 | ||||||
| chr2:71378760
|
T | C | 3 | a0002c0002t0001g0286a0002c0002t0001g0287a0002c0002t0001g0289 | 3 | HG00544.hp1 HG02015.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.2266-1462T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71378760 | ||||||
| chr2:71378803
|
T | G | 1 | a0001c0003t0001g0140 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2266-1419T>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71378803 | ||||||
| chr2:71378880
|
G | A | 70 | a0002c0002t0001g0254a0002c0002t0001g0255a0002c0002t0001g0256others(67): Show | 70 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.2266-1342G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71378880 | ||||||
| chr2:71379238
|
C | T | 2 | a0002c0002t0001g0305a0002c0002t0001g0306 | 2 | HG00609.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.2266-984C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71379238 | ||||||
| chr2:71379332
|
CTG | C | 7 | a0001c0007t0001g0327a0001c0007t0001g0328a0001c0007t0001g0329others(4): Show | 7 | HG01884.hp2 HG02451.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.2266-887_2266-886d others(4): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr2 | 71379332 | |||||
| chr2:71379447
|
C | G | 2 | a0009c0013t0001g0102a0009c0013t0001g0103 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2266-775C>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71379447 | ||||||
| chr2:71379525
|
T | A | 1 | a0004c0006t0001g0281 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.2266-697T>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71379525 | ||||||
| chr2:71379556
|
A | G | 76 | a0001c0003t0001g0104a0001c0003t0001g0105a0001c0003t0001g0106others(73): Show | 76 | HG00280.hp1 HG00733.hp1 HG00735.hp1 others(73): Show |
intron_variant | MODIFIER | c.2266-666A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71379556 | ||||||
| chr2:71379703
|
G | A | 97 | a0002c0002t0001g0177a0002c0002t0001g0178a0002c0002t0001g0179others(94): Show | 97 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.2266-519G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71379703 | ||||||
| chr2:71379705
|
A | C | 1 | a0003c0004t0002g0219 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2266-517A>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71379705 | ||||||
| chr2:71379706
|
T | G | 1 | a0003c0004t0002g0219 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2266-516T>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71379706 | ||||||
| chr2:71379713
|
A | G | 13 | a0001c0005t0001g0122a0001c0005t0001g0152a0001c0005t0001g0153others(10): Show | 13 | HG01243.hp2 HG01891.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.2266-509A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71379713 | ||||||
| chr2:71379736
|
A | G | 8 | a0001c0003t0001g0109a0001c0003t0001g0132a0001c0003t0001g0133others(5): Show | 8 | HG00735.hp1 HG01243.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.2266-486A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71379736 | ||||||
| chr2:71379758
|
A | G | 3 | a0001c0001t0001g0072a0001c0001t0001g0074a0012c0025t0001g0073 | 3 | NA18951.hp1 NA18985.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.2266-464A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71379758 | ||||||
| chr2:71379774
|
C | T | 46 | a0001c0003t0001g0108a0001c0003t0001g0109a0001c0003t0001g0111others(43): Show | 46 | HG00280.hp1 HG00733.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.2266-448C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71379774 | ||||||
| chr2:71379775
|
G | A | 7 | a0001c0007t0001g0327a0001c0007t0001g0328a0001c0007t0001g0329others(4): Show | 7 | HG01884.hp2 HG02451.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.2266-447G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71379775 | ||||||
| chr2:71379957
|
G | C | 94 | a0002c0002t0001g0177a0002c0002t0001g0178a0002c0002t0001g0179others(91): Show | 94 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.2266-265G>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71379957 | ||||||
| chr2:71379960
|
C | T | 94 | a0002c0002t0001g0177a0002c0002t0001g0178a0002c0002t0001g0179others(91): Show | 94 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.2266-262C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71379960 | ||||||
| chr2:71379961
|
G | A | 1 | a0001c0001t0001g0029 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2266-261G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | chr2 | 71379961 | ||||||
| chr2:71380066
|
G | GGCT | 4 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0041others(1): Show | 4 | HG02165.hp1 NA18988.hp1 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.2266-154_2266-152d others(5): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr2 | 71380066 | |||||
| chr2:71380291
|
T | C | 1 | a0001c0001t0001g0015 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2324+11T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 9/27 | chr2 | 71380291 | ||||||
| chr2:71380409
|
G | A | 77 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(74): Show | 81 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.2325-104G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 9/27 | chr2 | 71380409 | ||||||
| chr2:71380425
|
C | T | 1 | a0001c0001t0001g0040 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.2325-88C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 9/27 | chr2 | 71380425 | ||||||
| chr2:71380646
|
A | G | 1 | a0002c0002t0001g0200 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2377+81A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71380646 | ||||||
| chr2:71380753
|
G | A | 1 | a0001c0001t0001g0049 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2377+188G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71380753 | ||||||
| chr2:71380945
|
GTTAA | G | 109 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(106): Show | 113 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.2377+383_2377+386d others(6): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr2 | 71380945 | |||||
| chr2:71380996
|
T | C | 1 | a0018c0027t0001g0201 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2377+431T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71380996 | ||||||
| chr2:71381007
|
T | G | 1 | a0001c0001t0001g0334 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2377+442T>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71381007 | ||||||
| chr2:71381065
|
C | T | 288 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(285): Show | 292 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(289): Show |
intron_variant | MODIFIER | c.2377+500C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71381065 | ||||||
| chr2:71381243
|
C | T | 1 | a0001c0003t0001g0119 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2377+678C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71381243 | ||||||
| chr2:71381252
|
T | C | 2 | a0001c0001t0001g0045a0001c0001t0001g0046 | 2 | NA18942.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.2377+687T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71381252 | ||||||
| chr2:71381481
|
A | G | 2 | a0009c0013t0001g0102a0009c0013t0001g0103 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2377+916A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71381481 | ||||||
| chr2:71381501
|
G | A | 1 | a0002c0002t0001g0286 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2377+936G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71381501 | ||||||
| chr2:71381560
|
A | T | 94 | a0002c0002t0001g0177a0002c0002t0001g0178a0002c0002t0001g0179others(91): Show | 94 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.2377+995A>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71381560 | ||||||
| chr2:71381572
|
A | C | 1 | a0018c0027t0001g0201 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2377+1007A>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71381572 | ||||||
| chr2:71381577
|
C | T | 1 | a0018c0027t0001g0201 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2377+1012C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71381577 | ||||||
| chr2:71381741
|
T | C | 1 | a0001c0001t0001g0335 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2377+1176T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71381741 | ||||||
| chr2:71381821
|
A | G | 6 | a0001c0003t0001g0127a0001c0003t0001g0128a0001c0003t0001g0129others(3): Show | 6 | HG01167.hp2 HG02280.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.2377+1256A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71381821 | ||||||
| chr2:71381831
|
G | T | 2 | a0009c0013t0001g0102a0009c0013t0001g0103 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2377+1266G>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71381831 | ||||||
| chr2:71381877
|
G | C | 1 | a0001c0003t0001g0108 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2377+1312G>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71381877 | ||||||
| chr2:71381943
|
A | G | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(113): Show | 120 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.2377+1378A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71381943 | ||||||
| chr2:71381967
|
C | T | 289 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(286): Show | 293 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(290): Show |
intron_variant | MODIFIER | c.2377+1402C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71381967 | ||||||
| chr2:71382060
|
T | G | 3 | a0002c0002t0001g0198a0002c0002t0001g0199a0002c0002t0001g0200 | 3 | HG03239.hp1 HG03831.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.2377+1495T>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71382060 | ||||||
| chr2:71382083
|
A | T | 2 | a0002c0002t0001g0287a0002c0002t0001g0289 | 2 | HG02015.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.2377+1518A>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71382083 | ||||||
| chr2:71382160
|
C | T | 1 | a0001c0005t0001g0156 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2377+1595C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71382160 | ||||||
| chr2:71382303
|
G | T | 24 | a0002c0002t0001g0177a0002c0002t0001g0178a0002c0002t0001g0179others(21): Show | 24 | HG00438.hp1 HG01069.hp2 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.2377+1738G>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71382303 | ||||||
| chr2:71382454
|
A | G | 2 | a0009c0013t0001g0102a0009c0013t0001g0103 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2377+1889A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71382454 | ||||||
| chr2:71382483
|
A | G | 297 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(294): Show | 301 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(298): Show |
intron_variant | MODIFIER | c.2377+1918A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71382483 | ||||||
| chr2:71382655
|
G | A | 14 | a0002c0002t0001g0179a0002c0002t0001g0180a0002c0002t0001g0183others(11): Show | 14 | HG01069.hp2 HG01074.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.2377+2090G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71382655 | ||||||
| chr2:71382886
|
A | G | 289 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(286): Show | 293 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(290): Show |
intron_variant | MODIFIER | c.2377+2321A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71382886 | ||||||
| chr2:71382924
|
A | G | 291 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(288): Show | 295 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(292): Show |
intron_variant | MODIFIER | c.2377+2359A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71382924 | ||||||
| chr2:71383006
|
C | T | 1 | a0002c0002t0001g0200 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2377+2441C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71383006 | ||||||
| chr2:71383083
|
G | T | 1 | a0003c0004t0002g0221 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2377+2518G>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71383083 | ||||||
| chr2:71383151
|
C | T | 1 | a0018c0027t0001g0201 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2377+2586C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71383151 | ||||||
| chr2:71383215
|
C | T | 7 | a0001c0007t0001g0327a0001c0007t0001g0328a0001c0007t0001g0329others(4): Show | 7 | HG01884.hp2 HG02451.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.2377+2650C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71383215 | ||||||
| chr2:71383370
|
G | C | 2 | a0001c0003t0001g0150a0001c0024t0001g0145 | 2 | HG02055.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.2377+2805G>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71383370 | ||||||
| chr2:71383434
|
T | C | 2 | a0001c0003t0001g0143a0001c0003t0001g0144 | 2 | HG00733.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.2377+2869T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71383434 | ||||||
| chr2:71383560
|
G | GT | 12 | a0001c0003t0001g0106a0001c0003t0001g0121a0001c0003t0001g0143others(9): Show | 12 | HG02145.hp2 HG02258.hp2 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.2377+3016dupT | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr2 | 71383560 | |||||
| chr2:71383560
|
GT | G | 61 | a0001c0001t0001g0014a0001c0001t0001g0339a0001c0001t0001g0340others(58): Show | 61 | HG00438.hp1 HG01069.hp2 HG01074.hp1 others(58): Show |
intron_variant | MODIFIER | c.2377+3016delT | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr2 | 71383560 | |||||
| chr2:71383560
|
GTT | G | 177 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(174): Show | 181 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.2377+3015_2377+301 others(6): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr2 | 71383560 | |||||
| chr2:71383564
|
T | G | 2 | a0009c0013t0001g0102a0009c0013t0001g0103 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2377+2999T>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71383564 | ||||||
| chr2:71383565
|
T | G | 34 | a0001c0001t0001g0014a0001c0001t0001g0339a0001c0001t0001g0340others(31): Show | 34 | HG00438.hp1 HG01069.hp2 HG01074.hp1 others(31): Show |
intron_variant | MODIFIER | c.2377+3000T>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71383565 | ||||||
| chr2:71383566
|
T | G | 172 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(169): Show | 176 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.2377+3001T>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71383566 | ||||||
| chr2:71383567
|
T | G | 3 | a0001c0001t0001g0029a0001c0001t0001g0061a0012c0025t0001g0073 | 3 | HG01256.hp2 HG02698.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.2377+3002T>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71383567 | ||||||
| chr2:71383762
|
C | CT | 10 | a0001c0001t0001g0055a0001c0007t0001g0327a0001c0007t0001g0328others(7): Show | 10 | HG00642.hp2 HG01884.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.2377+3216dupT | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr2 | 71383762 | |||||
| chr2:71383762
|
C | CTT | 6 | a0001c0003t0001g0164a0001c0003t0003g0162a0001c0005t0001g0157others(3): Show | 6 | HG01496.hp2 HG02970.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.2377+3215_2377+321 others(6): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr2 | 71383762 | |||||
| chr2:71383762
|
C | CTTT | 11 | a0001c0003t0003g0163a0001c0005t0001g0152a0001c0005t0001g0153others(8): Show | 11 | HG01243.hp2 HG01891.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.2377+3214_2377+321 others(7): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr2 | 71383762 | |||||
| chr2:71383762
|
C | CTTTT | 31 | a0001c0003t0001g0115a0001c0003t0001g0116a0001c0003t0001g0127others(28): Show | 31 | HG00438.hp1 HG01069.hp2 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.2377+3213_2377+321 others(8): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr2 | 71383762 | |||||
| chr2:71383762
|
C | CTTTTT | 37 | a0001c0003t0001g0104a0001c0003t0001g0105a0001c0003t0001g0106others(34): Show | 37 | HG00733.hp1 HG01099.hp2 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.2377+3212_2377+321 others(9): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr2 | 71383762 | |||||
| chr2:71383762
|
C | CTTTTTT | 18 | a0001c0003t0001g0108a0001c0003t0001g0111a0001c0003t0001g0123others(15): Show | 18 | HG00280.hp1 HG00735.hp1 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.2377+3211_2377+321 others(10): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr2 | 71383762 | |||||
| chr2:71383762
|
CT | C | 158 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(155): Show | 162 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.2377+3216delT | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr2 | 71383762 | |||||
| chr2:71383762
|
CTT | C | 11 | a0001c0001t0001g0015a0001c0001t0001g0052a0001c0001t0001g0326others(8): Show | 11 | HG01099.hp1 HG01884.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.2377+3215_2377+321 others(6): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr2 | 71383762 | |||||
| chr2:71383783
|
G | T | 3 | a0001c0007t0001g0328a0001c0007t0001g0330a0013c0018t0001g0331 | 3 | HG01884.hp2 HG02615.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.2377+3218G>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71383783 | ||||||
| chr2:71383832
|
A | C | 289 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(286): Show | 293 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(290): Show |
intron_variant | MODIFIER | c.2377+3267A>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71383832 | ||||||
| chr2:71383926
|
G | C | 97 | a0002c0002t0001g0177a0002c0002t0001g0178a0002c0002t0001g0179others(94): Show | 97 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.2377+3361G>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71383926 | ||||||
| chr2:71384001
|
T | C | 70 | a0002c0002t0001g0254a0002c0002t0001g0255a0002c0002t0001g0256others(67): Show | 70 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.2377+3436T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71384001 | ||||||
| chr2:71384097
|
C | T | 1 | a0001c0001t0001g0051 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2377+3532C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71384097 | ||||||
| chr2:71384115
|
A | G | 4 | a0001c0003t0001g0118a0001c0003t0001g0119a0001c0003t0001g0120others(1): Show | 4 | HG01099.hp2 HG02258.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.2377+3550A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71384115 | ||||||
| chr2:71384219
|
C | T | 1 | a0002c0002t0001g0192 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2377+3654C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71384219 | ||||||
| chr2:71384238
|
G | A | 1 | a0001c0003t0001g0112 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2377+3673G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71384238 | ||||||
| chr2:71384590
|
A | G | 2 | a0001c0003t0001g0112a0001c0003t0001g0113 | 2 | HG02572.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2377+4025A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71384590 | ||||||
| chr2:71384596
|
A | G | 70 | a0002c0002t0001g0254a0002c0002t0001g0255a0002c0002t0001g0256others(67): Show | 70 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.2377+4031A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71384596 | ||||||
| chr2:71384604
|
A | G | 1 | a0002c0002t0001g0198 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2377+4039A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71384604 | ||||||
| chr2:71384675
|
C | T | 2 | a0009c0013t0001g0102a0009c0013t0001g0103 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2377+4110C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71384675 | ||||||
| chr2:71384681
|
TC | T | 24 | a0002c0002t0001g0177a0002c0002t0001g0178a0002c0002t0001g0179others(21): Show | 24 | HG00438.hp1 HG01069.hp2 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.2377+4117delC | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71384681 | ||||||
| chr2:71384699
|
T | C | 24 | a0002c0002t0001g0177a0002c0002t0001g0178a0002c0002t0001g0179others(21): Show | 24 | HG00438.hp1 HG01069.hp2 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.2377+4134T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71384699 | ||||||
| chr2:71384793
|
G | T | 289 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(286): Show | 293 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(290): Show |
intron_variant | MODIFIER | c.2377+4228G>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71384793 | ||||||
| chr2:71384925
|
C | CT | 76 | a0001c0003t0001g0104a0001c0003t0001g0105a0001c0003t0001g0106others(73): Show | 76 | HG00280.hp1 HG00733.hp1 HG00735.hp1 others(73): Show |
intron_variant | MODIFIER | c.2377+4363dupT | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr2 | 71384925 | |||||
| chr2:71385024
|
G | A | 6 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(3): Show | 6 | NA18953.hp1 NA18964.hp1 NA18982.hp1 others(3): Show |
intron_variant | MODIFIER | c.2377+4459G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71385024 | ||||||
| chr2:71385163
|
A | G | 76 | a0001c0003t0001g0104a0001c0003t0001g0105a0001c0003t0001g0106others(73): Show | 76 | HG00280.hp1 HG00733.hp1 HG00735.hp1 others(73): Show |
intron_variant | MODIFIER | c.2377+4598A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71385163 | ||||||
| chr2:71385333
|
C | T | 94 | a0002c0002t0001g0177a0002c0002t0001g0178a0002c0002t0001g0179others(91): Show | 94 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.2377+4768C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71385333 | ||||||
| chr2:71385352
|
T | G | 2 | a0001c0001t0001g0025a0001c0001t0001g0041 | 2 | NA18988.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.2377+4787T>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71385352 | ||||||
| chr2:71385426
|
T | C | 1 | a0003c0004t0002g0248 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2377+4861T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71385426 | ||||||
| chr2:71385488
|
TAGTC | T | 77 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(74): Show | 81 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.2377+4926_2377+492 others(8): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr2 | 71385488 | |||||
| chr2:71385538
|
A | G | 1 | a0002c0002t0001g0262 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2377+4973A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71385538 | ||||||
| chr2:71385540
|
G | A | 1 | a0001c0003t0001g0146 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2377+4975G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71385540 | ||||||
| chr2:71385551
|
G | A | 76 | a0001c0003t0001g0104a0001c0003t0001g0105a0001c0003t0001g0106others(73): Show | 76 | HG00280.hp1 HG00733.hp1 HG00735.hp1 others(73): Show |
intron_variant | MODIFIER | c.2377+4986G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71385551 | ||||||
| chr2:71385569
|
C | T | 1 | a0018c0027t0001g0201 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2377+5004C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71385569 | ||||||
| chr2:71385595
|
T | C | 1 | a0003c0004t0002g0212 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.2377+5030T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71385595 | ||||||
| chr2:71385716
|
G | A | 96 | a0002c0002t0001g0177a0002c0002t0001g0178a0002c0002t0001g0179others(93): Show | 96 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.2377+5151G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71385716 | ||||||
| chr2:71385761
|
G | T | 1 | a0001c0003t0001g0142 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2377+5196G>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71385761 | ||||||
| chr2:71386008
|
A | G | 6 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(3): Show | 6 | NA18953.hp1 NA18964.hp1 NA18982.hp1 others(3): Show |
intron_variant | MODIFIER | c.2377+5443A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71386008 | ||||||
| chr2:71386126
|
G | GAC | 13 | a0001c0005t0001g0122a0001c0005t0001g0152a0001c0005t0001g0153others(10): Show | 13 | HG01243.hp2 HG01891.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.2377+5562_2377+556 others(6): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr2 | 71386126 | |||||
| chr2:71386293
|
CA | C | 111 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(108): Show | 115 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.2377+5752delA | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr2 | 71386293 | |||||
| chr2:71386293
|
CAA | C | 19 | a0001c0001t0001g0013a0001c0001t0001g0018a0001c0001t0001g0061others(16): Show | 19 | HG01069.hp1 HG01070.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.2377+5751_2377+575 others(6): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr2 | 71386293 | |||||
| chr2:71386293
|
CAAA | C | 132 | a0001c0003t0001g0108a0001c0003t0001g0109a0001c0003t0001g0111others(129): Show | 132 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.2377+5750_2377+575 others(7): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr2 | 71386293 | |||||
| chr2:71386293
|
CAAAA | C | 22 | a0001c0003t0001g0112a0001c0003t0001g0117a0001c0003t0001g0129others(19): Show | 22 | HG01123.hp1 HG01243.hp2 HG01496.hp2 others(19): Show |
intron_variant | MODIFIER | c.2377+5749_2377+575 others(8): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr2 | 71386293 | |||||
| chr2:71386325
|
A | T | 1 | a0018c0027t0001g0201 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2377+5760A>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71386325 | ||||||
| chr2:71386334
|
A | ATATGTAT others(5): Show |
2 | a0009c0013t0001g0102a0009c0013t0001g0103 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2377+5773_2377+578 others(16): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr2 | 71386334 | |||||
| chr2:71386348
|
A | G | 97 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(94): Show | 101 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.2377+5783A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71386348 | ||||||
| chr2:71386364
|
A | G | 2 | a0009c0013t0001g0102a0009c0013t0001g0103 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2377+5799A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71386364 | ||||||
| chr2:71386410
|
T | C | 5 | a0001c0003t0001g0104a0001c0003t0001g0105a0001c0003t0001g0106others(2): Show | 5 | HG02145.hp2 HG02615.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.2377+5845T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71386410 | ||||||
| chr2:71386550
|
G | A | 2 | a0009c0013t0001g0102a0009c0013t0001g0103 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2377+5985G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71386550 | ||||||
| chr2:71386640
|
A | G | 3 | a0001c0001t0001g0086a0001c0001t0001g0088a0001c0001t0001g0089 | 3 | HG01192.hp2 HG02622.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2377+6075A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71386640 | ||||||
| chr2:71386652
|
C | T | 11 | a0002c0002t0001g0179a0002c0002t0001g0180a0002c0002t0001g0184others(8): Show | 11 | HG01069.hp2 HG01074.hp1 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.2377+6087C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71386652 | ||||||
| chr2:71386699
|
C | T | 3 | a0001c0001t0001g0053a0001c0001t0001g0055a0001c0001t0001g0101 | 3 | HG00642.hp2 HG03654.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.2377+6134C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71386699 | ||||||
| chr2:71386784
|
A | G | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(113): Show | 120 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.2377+6219A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71386784 | ||||||
| chr2:71386979
|
C | T | 2 | a0001c0003t0003g0162a0001c0003t0003g0163 | 2 | HG03098.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2377+6414C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71386979 | ||||||
| chr2:71387313
|
G | A | 174 | a0001c0003t0001g0104a0001c0003t0001g0105a0001c0003t0001g0106others(171): Show | 174 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(171): Show |
intron_variant | MODIFIER | c.2377+6748G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71387313 | ||||||
| chr2:71387324
|
A | G | 292 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(289): Show | 296 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(293): Show |
intron_variant | MODIFIER | c.2377+6759A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71387324 | ||||||
| chr2:71387348
|
T | C | 24 | a0002c0002t0001g0177a0002c0002t0001g0178a0002c0002t0001g0179others(21): Show | 24 | HG00438.hp1 HG01069.hp2 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.2377+6783T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71387348 | ||||||
| chr2:71387425
|
C | CT | 5 | a0001c0001t0001g0086a0001c0001t0001g0088a0001c0001t0001g0089others(2): Show | 5 | HG01192.hp2 HG02622.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.2377+6863dupT | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr2 | 71387425 | |||||
| chr2:71387629
|
C | T | 2 | a0001c0001t0001g0334a0001c0001t0001g0335 | 2 | HG02630.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2377+7064C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71387629 | ||||||
| chr2:71387660
|
CT | C | 71 | a0002c0002t0001g0254a0002c0002t0001g0255a0002c0002t0001g0256others(68): Show | 71 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.2377+7096delT | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71387660 | ||||||
| chr2:71387660
|
CTCA | C | 193 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(190): Show | 197 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.2377+7096_2377+709 others(7): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71387660 | ||||||
| chr2:71387661
|
T | A | 24 | a0002c0002t0001g0177a0002c0002t0001g0178a0002c0002t0001g0179others(21): Show | 24 | HG00438.hp1 HG01069.hp2 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.2377+7096T>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71387661 | ||||||
| chr2:71387662
|
C | A | 95 | a0002c0002t0001g0177a0002c0002t0001g0178a0002c0002t0001g0179others(92): Show | 95 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.2377+7097C>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71387662 | ||||||
| chr2:71387726
|
A | G | 2 | a0003c0004t0002g0221a0003c0004t0002g0243 | 2 | HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.2377+7161A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71387726 | ||||||
| chr2:71387814
|
A | G | 2 | a0008c0010t0002g0342a0008c0010t0004g0253 | 2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2377+7249A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71387814 | ||||||
| chr2:71387817
|
A | G | 61 | a0001c0003t0001g0104a0001c0003t0001g0105a0001c0003t0001g0106others(58): Show | 61 | HG00280.hp1 HG00733.hp1 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.2377+7252A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71387817 | ||||||
| chr2:71387858
|
G | A | 248 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(245): Show | 252 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(249): Show |
intron_variant | MODIFIER | c.2377+7293G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71387858 | ||||||
| chr2:71388088
|
T | C | 7 | a0001c0003t0001g0114a0001c0003t0001g0138a0001c0003t0001g0166others(4): Show | 7 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.2377+7523T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71388088 | ||||||
| chr2:71388260
|
T | G | 15 | a0001c0003t0001g0164a0001c0003t0003g0162a0001c0003t0003g0163others(12): Show | 15 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.2377+7695T>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71388260 | ||||||
| chr2:71388329
|
CGACCTTT others(8): Show |
C | 6 | a0001c0020t0001g0323a0003c0004t0002g0248a0003c0004t0002g0249others(3): Show | 6 | HG02109.hp2 HG02818.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.2378-7782_2378-776 others(19): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr2 | 71388329 | |||||
| chr2:71388374
|
CGACCTTT others(8): Show |
C | 2 | a0007c0011t0001g0303a0007c0011t0001g0304 | 2 | NA18939.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.2378-7752_2378-773 others(19): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr2 | 71388374 | |||||
| chr2:71388404
|
C | T | 53 | a0001c0003t0001g0130a0001c0003t0001g0131a0003c0004t0002g0003others(50): Show | 53 | HG00323.hp1 HG00423.hp2 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.2378-7737C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71388404 | ||||||
| chr2:71388441
|
C | T | 319 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(316): Show | 323 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(320): Show |
intron_variant | MODIFIER | c.2378-7700C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71388441 | ||||||
| chr2:71388720
|
G | A | 1 | a0001c0005t0001g0161 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2378-7421G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71388720 | ||||||
| chr2:71388721
|
T | C | 1 | a0001c0001t0001g0056 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2378-7420T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71388721 | ||||||
| chr2:71388722
|
C | T | 1 | a0001c0001t0001g0326 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2378-7419C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71388722 | ||||||
| chr2:71388825
|
T | C | 1 | a0002c0002t0001g0255 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2378-7316T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71388825 | ||||||
| chr2:71388901
|
T | G | 1 | a0001c0001t0001g0006 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2378-7240T>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71388901 | ||||||
| chr2:71389122
|
C | G | 1 | a0001c0001t0001g0041 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.2378-7019C>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71389122 | ||||||
| chr2:71389123
|
T | G | 1 | a0001c0003t0001g0149 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2378-7018T>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71389123 | ||||||
| chr2:71389161
|
C | T | 1 | a0001c0003t0001g0109 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2378-6980C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71389161 | ||||||
| chr2:71389298
|
C | T | 5 | a0003c0004t0002g0248a0003c0004t0002g0249a0003c0004t0002g0250others(2): Show | 5 | HG02818.hp1 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.2378-6843C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71389298 | ||||||
| chr2:71389422
|
G | A | 2 | a0001c0003t0001g0112a0001c0003t0001g0113 | 2 | HG02572.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2378-6719G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71389422 | ||||||
| chr2:71389474
|
T | C | 1 | a0001c0003t0001g0150 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2378-6667T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71389474 | ||||||
| chr2:71389692
|
C | T | 1 | a0003c0015t0002g0245 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2378-6449C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71389692 | ||||||
| chr2:71389693
|
G | A | 7 | a0001c0007t0001g0327a0001c0007t0001g0328a0001c0007t0001g0329others(4): Show | 7 | HG01884.hp2 HG02451.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.2378-6448G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71389693 | ||||||
| chr2:71389857
|
T | A | 2 | a0008c0010t0002g0342a0008c0010t0004g0253 | 2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2378-6284T>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71389857 | ||||||
| chr2:71389902
|
C | T | 2 | a0001c0001t0001g0024a0018c0027t0001g0201 | 2 | HG02165.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2378-6239C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71389902 | ||||||
| chr2:71390052
|
A | G | 2 | a0001c0003t0001g0134a0015c0022t0001g0126 | 2 | HG02895.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2378-6089A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71390052 | ||||||
| chr2:71390089
|
A | G | 4 | a0001c0003t0001g0142a0001c0003t0001g0143a0001c0003t0001g0144others(1): Show | 4 | HG00733.hp1 HG02280.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.2378-6052A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71390089 | ||||||
| chr2:71390224
|
G | A | 2 | a0009c0013t0001g0102a0009c0013t0001g0103 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2378-5917G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71390224 | ||||||
| chr2:71390289
|
C | G | 1 | a0001c0001t0001g0010 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2378-5852C>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71390289 | ||||||
| chr2:71390337
|
C | T | 1 | a0001c0001t0001g0058 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2378-5804C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71390337 | ||||||
| chr2:71390514
|
G | A | 319 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(316): Show | 323 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(320): Show |
intron_variant | MODIFIER | c.2378-5627G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71390514 | ||||||
| chr2:71390573
|
C | T | 2 | a0009c0013t0001g0102a0009c0013t0001g0103 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2378-5568C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71390573 | ||||||
| chr2:71390634
|
A | G | 76 | a0001c0003t0001g0104a0001c0003t0001g0105a0001c0003t0001g0106others(73): Show | 76 | HG00280.hp1 HG00733.hp1 HG00735.hp1 others(73): Show |
intron_variant | MODIFIER | c.2378-5507A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71390634 | ||||||
| chr2:71390691
|
C | T | 2 | a0002c0002t0001g0193a0002c0002t0001g0194 | 2 | HG01069.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.2378-5450C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71390691 | ||||||
| chr2:71390725
|
G | A | 2 | a0009c0013t0001g0102a0009c0013t0001g0103 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2378-5416G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71390725 | ||||||
| chr2:71390740
|
A | G | 1 | a0002c0002t0001g0255 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2378-5401A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71390740 | ||||||
| chr2:71390743
|
A | G | 70 | a0002c0002t0001g0254a0002c0002t0001g0255a0002c0002t0001g0256others(67): Show | 70 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.2378-5398A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71390743 | ||||||
| chr2:71390776
|
T | C | 54 | a0003c0004t0001g0259a0003c0004t0002g0003a0003c0004t0002g0202others(51): Show | 54 | HG00323.hp1 HG00423.hp2 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.2378-5365T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71390776 | ||||||
| chr2:71390870
|
AAC | A | 7 | a0001c0007t0001g0327a0001c0007t0001g0328a0001c0007t0001g0329others(4): Show | 7 | HG01884.hp2 HG02451.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.2378-5269_2378-526 others(6): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr2 | 71390870 | |||||
| chr2:71390872
|
CAGTT | C | 70 | a0002c0002t0001g0254a0002c0002t0001g0255a0002c0002t0001g0256others(67): Show | 70 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.2378-5266_2378-526 others(8): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr2 | 71390872 | |||||
| chr2:71390896
|
G | A | 76 | a0001c0003t0001g0104a0001c0003t0001g0105a0001c0003t0001g0106others(73): Show | 76 | HG00280.hp1 HG00733.hp1 HG00735.hp1 others(73): Show |
intron_variant | MODIFIER | c.2378-5245G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71390896 | ||||||
| chr2:71391064
|
A | T | 1 | a0001c0001t0001g0032 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2378-5077A>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71391064 | ||||||
| chr2:71391193
|
A | G | 54 | a0003c0004t0001g0259a0003c0004t0002g0003a0003c0004t0002g0202others(51): Show | 54 | HG00323.hp1 HG00423.hp2 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.2378-4948A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71391193 | ||||||
| chr2:71391300
|
C | A | 70 | a0002c0002t0001g0254a0002c0002t0001g0255a0002c0002t0001g0256others(67): Show | 70 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.2378-4841C>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71391300 | ||||||
| chr2:71391373
|
A | C | 2 | a0009c0013t0001g0102a0009c0013t0001g0103 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2378-4768A>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71391373 | ||||||
| chr2:71391410
|
C | T | 1 | a0001c0001t0001g0081 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.2378-4731C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71391410 | ||||||
| chr2:71391458
|
T | C | 2 | a0002c0002t0001g0193a0002c0002t0001g0194 | 2 | HG01069.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.2378-4683T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71391458 | ||||||
| chr2:71391469
|
T | C | 171 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(168): Show | 175 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.2378-4672T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71391469 | ||||||
| chr2:71391547
|
A | T | 1 | a0001c0003t0001g0150 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2378-4594A>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71391547 | ||||||
| chr2:71391570
|
A | G | 1 | a0001c0003t0001g0109 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2378-4571A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71391570 | ||||||
| chr2:71391575
|
A | T | 2 | a0002c0002t0001g0305a0002c0002t0001g0306 | 2 | HG00609.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.2378-4566A>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71391575 | ||||||
| chr2:71392062
|
T | C | 319 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(316): Show | 323 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(320): Show |
intron_variant | MODIFIER | c.2378-4079T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71392062 | ||||||
| chr2:71392130
|
C | T | 4 | a0006c0014t0001g0309a0006c0014t0001g0318a0009c0013t0001g0102others(1): Show | 4 | HG03453.hp1 HG03579.hp2 NA19080.hp1 others(1): Show |
intron_variant | MODIFIER | c.2378-4011C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71392130 | ||||||
| chr2:71392266
|
T | C | 1 | a0003c0004t0002g0202 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2378-3875T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71392266 | ||||||
| chr2:71392390
|
A | G | 1 | a0003c0004t0002g0203 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2378-3751A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71392390 | ||||||
| chr2:71392654
|
C | T | 1 | a0001c0007t0001g0327 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2378-3487C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71392654 | ||||||
| chr2:71392772
|
G | T | 3 | a0001c0007t0001g0328a0001c0007t0001g0330a0013c0018t0001g0331 | 3 | HG01884.hp2 HG02615.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.2378-3369G>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71392772 | ||||||
| chr2:71392886
|
T | C | 1 | a0003c0012t0002g0240 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2378-3255T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71392886 | ||||||
| chr2:71392889
|
A | G | 2 | a0001c0001t0001g0075a0001c0001t0001g0076 | 2 | NA18941.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.2378-3252A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71392889 | ||||||
| chr2:71392926
|
G | A | 2 | a0001c0003t0001g0130a0001c0003t0001g0131 | 2 | HG01167.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.2378-3215G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71392926 | ||||||
| chr2:71392974
|
T | C | 1 | a0004c0006t0001g0282 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.2378-3167T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71392974 | ||||||
| chr2:71392981
|
T | C | 180 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(177): Show | 184 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(181): Show |
intron_variant | MODIFIER | c.2378-3160T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71392981 | ||||||
| chr2:71393121
|
C | T | 5 | a0001c0003t0001g0104a0001c0003t0001g0105a0001c0003t0001g0106others(2): Show | 5 | HG02145.hp2 HG02615.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.2378-3020C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71393121 | ||||||
| chr2:71393161
|
AAG | A | 46 | a0003c0004t0001g0259a0003c0004t0002g0003a0003c0004t0002g0202others(43): Show | 46 | HG00323.hp1 HG00423.hp2 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.2378-2979_2378-297 others(6): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71393161 | ||||||
| chr2:71393366
|
G | T | 2 | a0001c0003t0001g0175a0001c0003t0001g0176 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.2378-2775G>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71393366 | ||||||
| chr2:71393433
|
A | G | 54 | a0003c0004t0001g0259a0003c0004t0002g0003a0003c0004t0002g0202others(51): Show | 54 | HG00323.hp1 HG00423.hp2 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.2378-2708A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71393433 | ||||||
| chr2:71393580
|
C | A | 2 | a0002c0002t0001g0287a0002c0002t0001g0289 | 2 | HG02015.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.2378-2561C>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71393580 | ||||||
| chr2:71393688
|
C | T | 319 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(316): Show | 323 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(320): Show |
intron_variant | MODIFIER | c.2378-2453C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71393688 | ||||||
| chr2:71393708
|
T | A | 1 | a0001c0001t0001g0047 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.2378-2433T>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71393708 | ||||||
| chr2:71393716
|
A | G | 1 | a0001c0001t0001g0007 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2378-2425A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71393716 | ||||||
| chr2:71393748
|
C | G | 1 | a0002c0002t0001g0190 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2378-2393C>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71393748 | ||||||
| chr2:71393833
|
G | C | 1 | a0002c0002t0001g0273 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2378-2308G>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71393833 | ||||||
| chr2:71393852
|
A | G | 54 | a0003c0004t0001g0259a0003c0004t0002g0003a0003c0004t0002g0202others(51): Show | 54 | HG00323.hp1 HG00423.hp2 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.2378-2289A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71393852 | ||||||
| chr2:71393875
|
A | G | 2 | a0009c0013t0001g0102a0009c0013t0001g0103 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2378-2266A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71393875 | ||||||
| chr2:71393903
|
A | G | 4 | a0001c0003t0001g0166a0001c0003t0001g0167a0001c0003t0001g0169others(1): Show | 4 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.2378-2238A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71393903 | ||||||
| chr2:71393965
|
T | A | 319 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(316): Show | 323 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(320): Show |
intron_variant | MODIFIER | c.2378-2176T>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71393965 | ||||||
| chr2:71393978
|
C | A | 1 | a0003c0012t0002g0232 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.2378-2163C>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71393978 | ||||||
| chr2:71394100
|
G | A | 108 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(105): Show | 112 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.2378-2041G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71394100 | ||||||
| chr2:71394158
|
C | T | 233 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(230): Show | 237 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(234): Show |
intron_variant | MODIFIER | c.2378-1983C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71394158 | ||||||
| chr2:71394186
|
G | A | 7 | a0001c0003t0001g0146a0001c0003t0001g0147a0001c0003t0001g0148others(4): Show | 7 | HG02055.hp1 HG02647.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.2378-1955G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71394186 | ||||||
| chr2:71394251
|
A | G | 319 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(316): Show | 323 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(320): Show |
intron_variant | MODIFIER | c.2378-1890A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71394251 | ||||||
| chr2:71394276
|
C | T | 2 | a0001c0005t0001g0157a0001c0005t0001g0158 | 2 | HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2378-1865C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71394276 | ||||||
| chr2:71394384
|
C | T | 1 | a0001c0003t0001g0117 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2378-1757C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71394384 | ||||||
| chr2:71394533
|
A | G | 4 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(1): Show | 4 | HG01256.hp2 HG02129.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.2378-1608A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71394533 | ||||||
| chr2:71394569
|
A | G | 71 | a0001c0001t0001g0044a0002c0002t0001g0254a0002c0002t0001g0255others(68): Show | 71 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.2378-1572A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71394569 | ||||||
| chr2:71394820
|
G | A | 1 | a0003c0004t0002g0207 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2378-1321G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71394820 | ||||||
| chr2:71394849
|
C | CA | 49 | a0001c0003t0001g0108a0001c0003t0001g0109a0001c0003t0001g0111others(46): Show | 49 | HG00280.hp1 HG00733.hp1 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.2378-1289dupA | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr2 | 71394849 | |||||
| chr2:71394883
|
C | G | 1 | a0003c0015t0002g0245 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2378-1258C>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71394883 | ||||||
| chr2:71394883
|
C | T | 15 | a0001c0003t0001g0164a0001c0003t0003g0162a0001c0003t0003g0163others(12): Show | 15 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.2378-1258C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71394883 | ||||||
| chr2:71394921
|
C | T | 1 | a0018c0027t0001g0201 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2378-1220C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71394921 | ||||||
| chr2:71394988
|
A | C | 1 | a0019c0028t0001g0195 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2378-1153A>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71394988 | ||||||
| chr2:71394996
|
A | G | 1 | a0001c0003t0001g0148 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2378-1145A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71394996 | ||||||
| chr2:71395025
|
C | T | 7 | a0001c0003t0001g0146a0001c0003t0001g0147a0001c0003t0001g0148others(4): Show | 7 | HG02055.hp1 HG02647.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.2378-1116C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71395025 | ||||||
| chr2:71395188
|
T | C | 7 | a0001c0003t0001g0146a0001c0003t0001g0147a0001c0003t0001g0148others(4): Show | 7 | HG02055.hp1 HG02647.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.2378-953T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71395188 | ||||||
| chr2:71395402
|
G | A | 1 | a0001c0003t0001g0172 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2378-739G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71395402 | ||||||
| chr2:71395441
|
C | T | 3 | a0001c0007t0001g0328a0001c0007t0001g0330a0013c0018t0001g0331 | 3 | HG01884.hp2 HG02615.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.2378-700C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71395441 | ||||||
| chr2:71395442
|
G | A | 1 | a0001c0003t0001g0123 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2378-699G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71395442 | ||||||
| chr2:71395480
|
C | T | 3 | a0001c0003t0001g0164a0001c0003t0003g0162a0001c0003t0003g0163 | 3 | HG01496.hp2 HG03098.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2378-661C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71395480 | ||||||
| chr2:71395483
|
T | C | 1 | a0001c0001t0001g0024 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2378-658T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71395483 | ||||||
| chr2:71395486
|
C | T | 7 | a0001c0007t0001g0327a0001c0007t0001g0328a0001c0007t0001g0329others(4): Show | 7 | HG01884.hp2 HG02451.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.2378-655C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71395486 | ||||||
| chr2:71395578
|
C | T | 2 | a0003c0004t0002g0221a0003c0004t0002g0243 | 2 | HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.2378-563C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71395578 | ||||||
| chr2:71395580
|
C | T | 5 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0074others(2): Show | 5 | NA18951.hp1 NA18985.hp1 NA19057.hp1 others(2): Show |
intron_variant | MODIFIER | c.2378-561C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71395580 | ||||||
| chr2:71395879
|
C | T | 1 | a0001c0001t0001g0019 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2378-262C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 10/27 | chr2 | 71395879 | ||||||
| chr2:71396295
|
T | C | 1 | a0001c0003t0001g0139 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2428+104T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 11/27 | chr2 | 71396295 | ||||||
| chr2:71396318
|
A | T | 3 | a0005c0008t0001g0008a0005c0008t0001g0042a0005c0008t0001g0043 | 3 | NA18971.hp2 NA18986.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.2428+127A>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 11/27 | chr2 | 71396318 | ||||||
| chr2:71396459
|
C | T | 1 | a0003c0004t0002g0228 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.2428+268C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 11/27 | chr2 | 71396459 | ||||||
| chr2:71396616
|
G | T | 2 | a0009c0013t0001g0102a0009c0013t0001g0103 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2428+425G>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 11/27 | chr2 | 71396616 | ||||||
| chr2:71396734
|
C | T | 75 | a0001c0003t0001g0104a0001c0003t0001g0105a0001c0003t0001g0106others(72): Show | 75 | HG00280.hp1 HG00733.hp1 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.2428+543C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 11/27 | chr2 | 71396734 | ||||||
| chr2:71396758
|
A | G | 1 | a0001c0001t0001g0340 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2428+567A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 11/27 | chr2 | 71396758 | ||||||
| chr2:71397107
|
TCTTGAAG | T | 6 | a0001c0003t0001g0127a0001c0003t0001g0128a0001c0003t0001g0129others(3): Show | 6 | HG01167.hp2 HG02280.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.2428+919_2428+925d others(9): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 11/27 | INFO_REALIGN_3_PRIME | chr2 | 71397107 | |||||
| chr2:71397172
|
T | C | 7 | a0001c0007t0001g0327a0001c0007t0001g0328a0001c0007t0001g0329others(4): Show | 7 | HG01884.hp2 HG02451.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.2428+981T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 11/27 | chr2 | 71397172 | ||||||
| chr2:71397199
|
C | A | 8 | a0001c0007t0001g0327a0001c0007t0001g0328a0001c0007t0001g0329others(5): Show | 8 | HG01884.hp2 HG02451.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.2428+1008C>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 11/27 | chr2 | 71397199 | ||||||
| chr2:71397235
|
C | T | 2 | a0009c0013t0001g0102a0009c0013t0001g0103 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2428+1044C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 11/27 | chr2 | 71397235 | ||||||
| chr2:71397236
|
A | G | 319 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(316): Show | 323 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(320): Show |
intron_variant | MODIFIER | c.2428+1045A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 11/27 | chr2 | 71397236 | ||||||
| chr2:71397367
|
T | C | 3 | a0001c0001t0001g0086a0001c0001t0001g0088a0001c0001t0001g0089 | 3 | HG01192.hp2 HG02622.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2428+1176T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 11/27 | chr2 | 71397367 | ||||||
| chr2:71397489
|
A | G | 2 | a0009c0013t0001g0102a0009c0013t0001g0103 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2429-1212A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 11/27 | chr2 | 71397489 | ||||||
| chr2:71397563
|
C | G | 3 | a0001c0003t0001g0164a0001c0003t0003g0162a0001c0003t0003g0163 | 3 | HG01496.hp2 HG03098.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2429-1138C>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 11/27 | chr2 | 71397563 | ||||||
| chr2:71397640
|
A | G | 1 | a0001c0001t0001g0100 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2429-1061A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 11/27 | chr2 | 71397640 | ||||||
| chr2:71397787
|
C | G | 4 | a0001c0003t0001g0127a0001c0003t0001g0128a0001c0003t0001g0129others(1): Show | 4 | HG02809.hp1 HG02818.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.2429-914C>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 11/27 | chr2 | 71397787 | ||||||
| chr2:71397879
|
A | T | 1 | a0002c0002t0001g0262 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2429-822A>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 11/27 | chr2 | 71397879 | ||||||
| chr2:71397943
|
T | A | 1 | a0002c0002t0001g0316 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2429-758T>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 11/27 | chr2 | 71397943 | ||||||
| chr2:71398024
|
G | T | 71 | a0002c0002t0001g0254a0002c0002t0001g0255a0002c0002t0001g0256others(68): Show | 71 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.2429-677G>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 11/27 | chr2 | 71398024 | ||||||
| chr2:71398052
|
G | A | 319 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(316): Show | 323 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(320): Show |
intron_variant | MODIFIER | c.2429-649G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 11/27 | chr2 | 71398052 | ||||||
| chr2:71398118
|
T | C | 44 | a0001c0003t0001g0108a0001c0003t0001g0109a0001c0003t0001g0111others(41): Show | 44 | HG00280.hp1 HG00733.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.2429-583T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 11/27 | chr2 | 71398118 | ||||||
| chr2:71398226
|
A | G | 1 | a0001c0003t0001g0146 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2429-475A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 11/27 | chr2 | 71398226 | ||||||
| chr2:71398335
|
T | C | 2 | a0001c0003t0003g0162a0001c0003t0003g0163 | 2 | HG03098.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2429-366T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 11/27 | chr2 | 71398335 | ||||||
| chr2:71398412
|
C | T | 1 | a0001c0001t0001g0340 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2429-289C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 11/27 | chr2 | 71398412 | ||||||
| chr2:71398473
|
A | G | 12 | a0001c0005t0001g0152a0001c0005t0001g0153a0001c0005t0001g0154others(9): Show | 12 | HG01243.hp2 HG01891.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.2429-228A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 11/27 | chr2 | 71398473 | ||||||
| chr2:71398497
|
C | T | 1 | a0002c0002t0001g0256 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2429-204C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 11/27 | chr2 | 71398497 | ||||||
| chr2:71398579
|
G | A | 1 | a0001c0003t0001g0111 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2429-122G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 11/27 | chr2 | 71398579 | ||||||
| chr2:71398637
|
G | A | 59 | a0001c0003t0001g0112a0001c0003t0001g0113a0001c0003t0001g0118others(56): Show | 59 | HG00323.hp1 HG00423.hp2 HG00733.hp2 others(56): Show |
intron_variant | MODIFIER | c.2429-64G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 11/27 | chr2 | 71398637 | ||||||
| chr2:71398831
|
G | A | 1 | a0018c0027t0001g0201 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2500+59G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 12/27 | chr2 | 71398831 | ||||||
| chr2:71398846
|
G | A | 5 | a0001c0003t0001g0104a0001c0003t0001g0105a0001c0003t0001g0106others(2): Show | 5 | HG02145.hp2 HG02615.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.2500+74G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 12/27 | chr2 | 71398846 | ||||||
| chr2:71398925
|
G | A | 3 | a0001c0001t0001g0013a0001c0001t0001g0050a0001c0001t0001g0051 | 3 | HG01069.hp1 HG01071.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.2500+153G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 12/27 | chr2 | 71398925 | ||||||
| chr2:71399033
|
C | T | 8 | a0001c0007t0001g0327a0001c0007t0001g0328a0001c0007t0001g0329others(5): Show | 8 | HG01884.hp2 HG02451.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.2500+261C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 12/27 | chr2 | 71399033 | ||||||
| chr2:71399109
|
C | T | 1 | a0002c0002t0001g0279 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2500+337C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 12/27 | chr2 | 71399109 | ||||||
| chr2:71399251
|
A | G | 1 | a0008c0010t0002g0342 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2501-308A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 12/27 | chr2 | 71399251 | ||||||
| chr2:71399439
|
CTA | C | 66 | a0001c0003t0001g0104a0001c0003t0001g0105a0001c0003t0001g0106others(63): Show | 66 | HG00323.hp1 HG00423.hp2 HG00733.hp2 others(63): Show |
intron_variant | MODIFIER | c.2501-118_2501-117d others(4): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr2 | 71399439 | |||||
| chr2:71399549
|
CT | C | 53 | a0001c0003t0001g0104a0001c0003t0001g0105a0001c0003t0001g0106others(50): Show | 53 | HG00280.hp1 HG00733.hp1 HG00735.hp1 others(50): Show |
splice_region_variant&intron_variant | LOW | c.2501-6delT | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr2 | 71399549 | |||||
| chr2:71399551
|
T | C | 2 | a0002c0002t0001g0305a0002c0002t0001g0306 | 2 | HG00609.hp1 NA19088.hp2 |
splice_region_variant&intron_variant | LOW | c.2501-8T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 12/27 | chr2 | 71399551 | ||||||
| chr2:71399655
|
A | T | 1 | a0001c0001t0001g0039 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.2587+10A>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 13/27 | chr2 | 71399655 | ||||||
| chr2:71399816
|
T | A | 5 | a0001c0003t0001g0104a0001c0003t0001g0105a0001c0003t0001g0106others(2): Show | 5 | HG02145.hp2 HG02615.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.2587+171T>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 13/27 | chr2 | 71399816 | ||||||
| chr2:71400087
|
T | C | 1 | a0001c0001t0001g0053 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2588-25T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 13/27 | chr2 | 71400087 | ||||||
| chr2:71400349
|
C | T | 10 | a0001c0007t0001g0327a0001c0007t0001g0328a0001c0007t0001g0329others(7): Show | 10 | HG01884.hp2 HG02451.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.2657-129C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 14/27 | chr2 | 71400349 | ||||||
| chr2:71400409
|
C | T | 97 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(94): Show | 101 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.2657-69C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 14/27 | chr2 | 71400409 | ||||||
| chr2:71400630
|
C | T | 2 | a0009c0013t0001g0102a0009c0013t0001g0103 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2697+112C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 15/27 | chr2 | 71400630 | ||||||
| chr2:71400730
|
G | T | 336 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(333): Show | 340 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(337): Show |
intron_variant | MODIFIER | c.2697+212G>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 15/27 | chr2 | 71400730 | ||||||
| chr2:71400987
|
A | G | 2 | a0001c0001t0001g0023a0001c0001t0001g0031 | 2 | HG03239.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.2697+469A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 15/27 | chr2 | 71400987 | ||||||
| chr2:71401072
|
T | C | 8 | a0001c0007t0001g0327a0001c0007t0001g0328a0001c0007t0001g0329others(5): Show | 8 | HG01884.hp2 HG02451.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.2697+554T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 15/27 | chr2 | 71401072 | ||||||
| chr2:71401117
|
T | C | 1 | a0003c0004t0002g0207 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2697+599T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 15/27 | chr2 | 71401117 | ||||||
| chr2:71401199
|
T | C | 2 | a0009c0013t0001g0102a0009c0013t0001g0103 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2697+681T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 15/27 | chr2 | 71401199 | ||||||
| chr2:71401248
|
T | C | 3 | a0001c0001t0001g0086a0001c0001t0001g0088a0001c0001t0001g0089 | 3 | HG01192.hp2 HG02622.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2698-708T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 15/27 | chr2 | 71401248 | ||||||
| chr2:71401281
|
A | G | 1 | a0002c0002t0001g0316 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2698-675A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 15/27 | chr2 | 71401281 | ||||||
| chr2:71401347
|
CA | C | 319 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(316): Show | 323 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(320): Show |
intron_variant | MODIFIER | c.2698-605delA | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr2 | 71401347 | |||||
| chr2:71401453
|
A | G | 6 | a0003c0004t0002g0248a0003c0004t0002g0249a0003c0004t0002g0250others(3): Show | 6 | HG02818.hp1 HG03139.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.2698-503A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 15/27 | chr2 | 71401453 | ||||||
| chr2:71401637
|
A | G | 1 | a0021c0031t0001g0341 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2698-319A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 15/27 | chr2 | 71401637 | ||||||
| chr2:71401862
|
A | G | 2 | a0009c0013t0001g0102a0009c0013t0001g0103 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2698-94A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 15/27 | chr2 | 71401862 | ||||||
| chr2:71401865
|
A | G | 1 | a0001c0007t0001g0329 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2698-91A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 15/27 | chr2 | 71401865 | ||||||
| chr2:71402162
|
AAAAAG | A | 3 | a0001c0003t0001g0147a0001c0003t0001g0149a0001c0003t0001g0151 | 3 | HG02717.hp1 HG03209.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2829+81_2829+85del others(5): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr2 | 71402162 | |||||
| chr2:71402225
|
TA | T | 5 | a0001c0003t0001g0104a0001c0003t0001g0105a0001c0003t0001g0106others(2): Show | 5 | HG02145.hp2 HG02615.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.2829+142delA | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr2 | 71402225 | |||||
| chr2:71402314
|
C | T | 319 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(316): Show | 323 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(320): Show |
intron_variant | MODIFIER | c.2829+227C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 16/27 | chr2 | 71402314 | ||||||
| chr2:71402343
|
G | A | 70 | a0002c0002t0001g0254a0002c0002t0001g0255a0002c0002t0001g0256others(67): Show | 70 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.2829+256G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 16/27 | chr2 | 71402343 | ||||||
| chr2:71402616
|
A | T | 5 | a0001c0003t0001g0115a0001c0003t0001g0116a0001c0003t0001g0171others(2): Show | 5 | HG01167.hp1 HG01169.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.2829+529A>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 16/27 | chr2 | 71402616 | ||||||
| chr2:71402901
|
T | G | 319 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(316): Show | 323 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(320): Show |
intron_variant | MODIFIER | c.2829+814T>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 16/27 | chr2 | 71402901 | ||||||
| chr2:71402911
|
A | C | 193 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(190): Show | 197 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(194): Show |
intron_variant | MODIFIER | c.2829+824A>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 16/27 | chr2 | 71402911 | ||||||
| chr2:71402915
|
G | A | 3 | a0003c0004t0002g0003a0003c0004t0002g0223a0003c0004t0002g0233 | 3 | NA18951.hp2 NA19080.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2829+828G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 16/27 | chr2 | 71402915 | ||||||
| chr2:71402972
|
G | A | 6 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0033others(3): Show | 6 | HG02300.hp1 NA18942.hp2 NA18944.hp1 others(3): Show |
intron_variant | MODIFIER | c.2829+885G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 16/27 | chr2 | 71402972 | ||||||
| chr2:71403115
|
A | T | 3 | a0002c0002t0001g0263a0002c0002t0001g0343a0002c0002t0001g0344 | 3 | NA18972.hp1 NA18978.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.2830-755A>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 16/27 | chr2 | 71403115 | ||||||
| chr2:71403341
|
G | A | 1 | a0002c0002t0001g0262 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2830-529G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 16/27 | chr2 | 71403341 | ||||||
| chr2:71403699
|
C | T | 70 | a0002c0002t0001g0254a0002c0002t0001g0255a0002c0002t0001g0256others(67): Show | 70 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.2830-171C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 16/27 | chr2 | 71403699 | ||||||
| chr2:71404063
|
TTA | T | 3 | a0001c0003t0001g0104a0001c0003t0001g0105a0001c0003t0001g0106 | 3 | HG02145.hp2 HG03540.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2958+67_2958+68del others(2): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr2 | 71404063 | |||||
| chr2:71404125
|
C | T | 3 | a0001c0005t0001g0152a0001c0005t0001g0154a0001c0005t0001g0156 | 3 | HG01891.hp1 HG02451.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2958+127C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 17/27 | chr2 | 71404125 | ||||||
| chr2:71404166
|
T | C | 52 | a0003c0004t0001g0259a0003c0004t0002g0003a0003c0004t0002g0202others(49): Show | 52 | HG00323.hp1 HG00423.hp2 HG00733.hp2 others(49): Show |
intron_variant | MODIFIER | c.2958+168T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 17/27 | chr2 | 71404166 | ||||||
| chr2:71404215
|
A | T | 117 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(114): Show | 121 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.2958+217A>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 17/27 | chr2 | 71404215 | ||||||
| chr2:71404552
|
A | G | 1 | a0001c0001t0001g0338 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2958+554A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 17/27 | chr2 | 71404552 | ||||||
| chr2:71404555
|
A | G | 22 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0014others(19): Show | 22 | HG00544.hp2 HG00642.hp1 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.2958+557A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 17/27 | chr2 | 71404555 | ||||||
| chr2:71404593
|
C | T | 2 | a0009c0013t0001g0102a0009c0013t0001g0103 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2958+595C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 17/27 | chr2 | 71404593 | ||||||
| chr2:71404633
|
C | T | 1 | a0001c0001t0001g0066 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.2958+635C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 17/27 | chr2 | 71404633 | ||||||
| chr2:71404667
|
T | C | 2 | a0002c0002t0001g0271a0002c0002t0001g0300 | 2 | HG00741.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.2958+669T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 17/27 | chr2 | 71404667 | ||||||
| chr2:71404752
|
A | G | 2 | a0001c0003t0001g0130a0001c0003t0001g0131 | 2 | HG01167.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.2958+754A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 17/27 | chr2 | 71404752 | ||||||
| chr2:71404849
|
G | T | 1 | a0003c0004t0002g0207 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2959-752G>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 17/27 | chr2 | 71404849 | ||||||
| chr2:71404886
|
T | C | 1 | a0002c0002t0001g0199 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2959-715T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 17/27 | chr2 | 71404886 | ||||||
| chr2:71404910
|
G | A | 83 | a0001c0003t0001g0104a0001c0003t0001g0105a0001c0003t0001g0106others(80): Show | 83 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.2959-691G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 17/27 | chr2 | 71404910 | ||||||
| chr2:71404938
|
T | C | 256 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(253): Show | 260 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(257): Show |
intron_variant | MODIFIER | c.2959-663T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 17/27 | chr2 | 71404938 | ||||||
| chr2:71405051
|
C | T | 83 | a0001c0003t0001g0104a0001c0003t0001g0105a0001c0003t0001g0106others(80): Show | 83 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.2959-550C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 17/27 | chr2 | 71405051 | ||||||
| chr2:71405084
|
T | C | 13 | a0001c0005t0001g0122a0001c0005t0001g0152a0001c0005t0001g0153others(10): Show | 13 | HG01243.hp2 HG01891.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.2959-517T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 17/27 | chr2 | 71405084 | ||||||
| chr2:71405094
|
G | GT | 9 | a0001c0001t0001g0326a0001c0001t0001g0334a0001c0001t0001g0335others(6): Show | 9 | HG01884.hp1 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.2959-505dupT | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr2 | 71405094 | |||||
| chr2:71405105
|
G | A | 1 | a0001c0003t0001g0112 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2959-496G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 17/27 | chr2 | 71405105 | ||||||
| chr2:71405107
|
A | G | 1 | a0008c0010t0004g0253 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2959-494A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 17/27 | chr2 | 71405107 | ||||||
| chr2:71405162
|
T | G | 2 | a0009c0013t0001g0102a0009c0013t0001g0103 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2959-439T>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 17/27 | chr2 | 71405162 | ||||||
| chr2:71405407
|
T | C | 1 | a0021c0031t0001g0341 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2959-194T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 17/27 | chr2 | 71405407 | ||||||
| chr2:71405500
|
T | C | 1 | a0001c0001t0001g0036 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2959-101T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 17/27 | chr2 | 71405500 | ||||||
| chr2:71405846
|
AGTGCATA others(16): Show |
A | 15 | a0001c0003t0001g0108a0001c0003t0001g0111a0001c0003t0001g0114others(12): Show | 15 | HG00280.hp1 HG00738.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.3000+207_3000+229d others(25): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 18/27 | INFO_REALIGN_3_PRIME | chr2 | 71405846 | |||||
| chr2:71405919
|
G | A | 1 | a0001c0003t0001g0119 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3001-209G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 18/27 | chr2 | 71405919 | ||||||
| chr2:71405964
|
C | T | 10 | a0001c0005t0001g0122a0001c0005t0001g0152a0001c0005t0001g0153others(7): Show | 10 | HG01243.hp2 HG01891.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.3001-164C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 18/27 | chr2 | 71405964 | ||||||
| chr2:71406082
|
T | C | 1 | a0018c0027t0001g0201 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3001-46T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 18/27 | chr2 | 71406082 | ||||||
| chr2:71406095
|
G | GT | 7 | a0001c0007t0001g0327a0001c0007t0001g0328a0001c0007t0001g0329others(4): Show | 7 | HG01884.hp2 HG02451.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.3001-27dupT | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 18/27 | INFO_REALIGN_3_PRIME | chr2 | 71406095 | |||||
| chr2:71406287
|
C | T | 3 | a0001c0001t0001g0013a0001c0001t0001g0050a0001c0001t0001g0051 | 3 | HG01069.hp1 HG01071.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.3135+25C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 19/27 | chr2 | 71406287 | ||||||
| chr2:71406429
|
G | A | 70 | a0002c0002t0001g0254a0002c0002t0001g0255a0002c0002t0001g0256others(67): Show | 70 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.3135+167G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 19/27 | chr2 | 71406429 | ||||||
| chr2:71406493
|
G | C | 3 | a0001c0005t0001g0152a0001c0005t0001g0154a0001c0005t0001g0156 | 3 | HG01891.hp1 HG02451.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.3135+231G>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 19/27 | chr2 | 71406493 | ||||||
| chr2:71406507
|
AGT | A | 3 | a0001c0003t0001g0164a0001c0003t0003g0162a0001c0003t0003g0163 | 3 | HG01496.hp2 HG03098.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3135+248_3135+249d others(4): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 19/27 | INFO_REALIGN_3_PRIME | chr2 | 71406507 | |||||
| chr2:71406829
|
G | A | 1 | a0003c0029t0002g0230 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.3135+567G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 19/27 | chr2 | 71406829 | ||||||
| chr2:71407072
|
G | A | 3 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0048 | 3 | NA18947.hp1 NA18952.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.3135+810G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 19/27 | chr2 | 71407072 | ||||||
| chr2:71407107
|
C | T | 2 | a0009c0013t0001g0102a0009c0013t0001g0103 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.3135+845C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 19/27 | chr2 | 71407107 | ||||||
| chr2:71407108
|
A | G | 2 | a0002c0002t0001g0305a0002c0002t0001g0306 | 2 | HG00609.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.3135+846A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 19/27 | chr2 | 71407108 | ||||||
| chr2:71407209
|
C | A | 1 | a0001c0003t0001g0135 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3136-913C>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 19/27 | chr2 | 71407209 | ||||||
| chr2:71407458
|
G | A | 319 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(316): Show | 323 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(320): Show |
intron_variant | MODIFIER | c.3136-664G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 19/27 | chr2 | 71407458 | ||||||
| chr2:71407500
|
T | C | 53 | a0003c0004t0001g0259a0003c0004t0002g0003a0003c0004t0002g0202others(50): Show | 53 | HG00323.hp1 HG00423.hp2 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.3136-622T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 19/27 | chr2 | 71407500 | ||||||
| chr2:71407554
|
G | A | 1 | a0002c0002t0001g0278 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.3136-568G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 19/27 | chr2 | 71407554 | ||||||
| chr2:71407712
|
G | C | 1 | a0001c0020t0001g0323 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3136-410G>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 19/27 | chr2 | 71407712 | ||||||
| chr2:71407773
|
A | G | 2 | a0003c0004t0002g0251a0003c0004t0002g0252 | 2 | HG03225.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.3136-349A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 19/27 | chr2 | 71407773 | ||||||
| chr2:71408029
|
T | C | 1 | a0003c0004t0002g0244 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.3136-93T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 19/27 | chr2 | 71408029 | ||||||
| chr2:71408262
|
T | C | 3 | a0001c0001t0001g0013a0001c0001t0001g0050a0001c0001t0001g0051 | 3 | HG01069.hp1 HG01071.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.3261+15T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71408262 | ||||||
| chr2:71408301
|
A | G | 1 | a0001c0003t0001g0148 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.3261+54A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71408301 | ||||||
| chr2:71408332
|
T | G | 55 | a0003c0004t0001g0259a0003c0004t0002g0003a0003c0004t0002g0202others(52): Show | 55 | HG00323.hp1 HG00423.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.3261+85T>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71408332 | ||||||
| chr2:71408801
|
G | T | 319 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(316): Show | 323 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(320): Show |
intron_variant | MODIFIER | c.3261+554G>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71408801 | ||||||
| chr2:71408906
|
A | G | 118 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(115): Show | 122 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.3261+659A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71408906 | ||||||
| chr2:71409110
|
T | C | 118 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(115): Show | 122 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.3261+863T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71409110 | ||||||
| chr2:71409597
|
G | A | 5 | a0001c0003t0001g0104a0001c0003t0001g0105a0001c0003t0001g0106others(2): Show | 5 | HG02145.hp2 HG02615.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.3261+1350G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71409597 | ||||||
| chr2:71409985
|
C | T | 7 | a0001c0007t0001g0327a0001c0007t0001g0328a0001c0007t0001g0329others(4): Show | 7 | HG01884.hp2 HG02451.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.3261+1738C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71409985 | ||||||
| chr2:71410004
|
A | G | 1 | a0008c0010t0004g0253 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3261+1757A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71410004 | ||||||
| chr2:71410145
|
G | C | 55 | a0003c0004t0001g0259a0003c0004t0002g0003a0003c0004t0002g0202others(52): Show | 55 | HG00323.hp1 HG00423.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.3261+1898G>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71410145 | ||||||
| chr2:71410374
|
T | G | 2 | a0009c0013t0001g0102a0009c0013t0001g0103 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.3261+2127T>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71410374 | ||||||
| chr2:71410374
|
T | TTG | 10 | a0003c0004t0002g0234a0003c0004t0002g0235a0003c0004t0002g0241others(7): Show | 10 | HG02818.hp1 HG03209.hp1 HG03225.hp1 others(7): Show |
intron_variant | MODIFIER | c.3261+2128_3261+212 others(6): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr2 | 71410374 | |||||
| chr2:71410376
|
T | G | 21 | a0001c0001t0001g0039a0001c0007t0001g0327a0001c0007t0001g0328others(18): Show | 21 | HG01517.hp1 HG01884.hp2 HG02451.hp2 others(18): Show |
intron_variant | MODIFIER | c.3261+2129T>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71410376 | ||||||
| chr2:71410376
|
T | TTG | 38 | a0002c0002t0001g0177a0002c0002t0001g0178a0003c0004t0001g0259others(35): Show | 38 | HG00323.hp1 HG00423.hp2 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.3261+2130_3261+213 others(6): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr2 | 71410376 | |||||
| chr2:71410376
|
T | TTGTG | 15 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(12): Show | 18 | HG00642.hp2 HG00735.hp2 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.3261+2130_3261+213 others(8): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr2 | 71410376 | |||||
| chr2:71410378
|
T | G | 192 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(189): Show | 196 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.3261+2131T>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71410378 | ||||||
| chr2:71410378
|
T | TTG | 7 | a0002c0002t0001g0316a0003c0004t0002g0211a0003c0004t0002g0221others(4): Show | 7 | HG02055.hp2 HG02109.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.3261+2147_3261+214 others(6): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr2 | 71410378 | |||||
| chr2:71410380
|
G | T | 58 | a0001c0003t0001g0125a0002c0002t0001g0255a0002c0002t0001g0258others(55): Show | 58 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.3261+2133G>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71410380 | ||||||
| chr2:71410567
|
G | A | 51 | a0003c0004t0001g0259a0003c0004t0002g0003a0003c0004t0002g0202others(48): Show | 51 | HG00323.hp1 HG00423.hp2 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.3261+2320G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71410567 | ||||||
| chr2:71410648
|
T | C | 7 | a0001c0007t0001g0327a0001c0007t0001g0328a0001c0007t0001g0329others(4): Show | 7 | HG01884.hp2 HG02451.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.3261+2401T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71410648 | ||||||
| chr2:71410692
|
G | C | 1 | a0001c0003t0001g0146 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3261+2445G>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71410692 | ||||||
| chr2:71410772
|
A | C | 7 | a0001c0007t0001g0327a0001c0007t0001g0328a0001c0007t0001g0329others(4): Show | 7 | HG01884.hp2 HG02451.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.3261+2525A>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71410772 | ||||||
| chr2:71410925
|
G | A | 1 | a0001c0001t0001g0054 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.3261+2678G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71410925 | ||||||
| chr2:71410970
|
C | T | 5 | a0001c0001t0001g0068a0001c0001t0001g0075a0001c0001t0001g0076others(2): Show | 5 | HG02155.hp1 NA18941.hp2 NA18993.hp2 others(2): Show |
intron_variant | MODIFIER | c.3261+2723C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71410970 | ||||||
| chr2:71410978
|
C | A | 1 | a0003c0004t0002g0231 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.3261+2731C>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71410978 | ||||||
| chr2:71410981
|
CCT | C | 39 | a0002c0002t0001g0255a0002c0002t0001g0258a0002c0002t0001g0268others(36): Show | 39 | HG00597.hp2 HG00609.hp1 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.3261+2736_3261+273 others(6): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr2 | 71410981 | |||||
| chr2:71410982
|
CT | C | 21 | a0002c0002t0001g0254a0002c0002t0001g0256a0002c0002t0001g0263others(18): Show | 21 | HG00544.hp1 HG00673.hp1 HG01928.hp2 others(18): Show |
intron_variant | MODIFIER | c.3261+2736delT | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71410982 | ||||||
| chr2:71410983
|
T | A | 1 | a0007c0011t0001g0303 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.3261+2736T>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71410983 | ||||||
| chr2:71410983
|
T | C | 180 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(177): Show | 184 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.3261+2736T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71410983 | ||||||
| chr2:71410983
|
T | G | 1 | a0001c0001t0001g0006 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.3261+2736T>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71410983 | ||||||
| chr2:71410983
|
T | TC | 41 | a0001c0003t0001g0104a0001c0003t0001g0105a0001c0003t0001g0107others(38): Show | 41 | HG00280.hp1 HG00733.hp1 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.3261+2745dupC | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr2 | 71410983 | |||||
| chr2:71410983
|
T | TCC | 16 | a0001c0003t0001g0106a0001c0003t0001g0108a0001c0003t0001g0109others(13): Show | 16 | HG01243.hp1 HG01496.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.3261+2744_3261+274 others(6): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr2 | 71410983 | |||||
| chr2:71410985
|
C | A | 1 | a0007c0011t0001g0304 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.3261+2738C>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71410985 | ||||||
| chr2:71410990
|
C | CTT | 27 | a0003c0004t0002g0003a0003c0004t0002g0203a0003c0004t0002g0204others(24): Show | 27 | HG00323.hp1 HG01516.hp1 HG02083.hp1 others(24): Show |
intron_variant | MODIFIER | c.3261+2743_3261+274 others(6): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71410990 | ||||||
| chr2:71410990
|
C | CTTT | 6 | a0003c0004t0002g0205a0003c0004t0002g0229a0003c0004t0002g0231others(3): Show | 6 | HG03688.hp2 NA18943.hp2 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.3261+2743_3261+274 others(7): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71410990 | ||||||
| chr2:71410990
|
C | G | 1 | a0002c0002t0001g0184 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.3261+2743C>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71410990 | ||||||
| chr2:71410990
|
C | T | 8 | a0001c0007t0001g0327a0001c0007t0001g0328a0001c0007t0001g0329others(5): Show | 8 | HG01884.hp2 HG02451.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.3261+2743C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71410990 | ||||||
| chr2:71410991
|
C | CT | 40 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(37): Show | 41 | HG00280.hp2 HG00544.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.3261+2744_3261+274 others(5): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71410991 | ||||||
| chr2:71410991
|
C | CTT | 9 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0022others(6): Show | 9 | HG00323.hp2 HG00741.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.3261+2744_3261+274 others(6): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71410991 | ||||||
| chr2:71410991
|
C | CTTT | 16 | a0001c0001t0001g0062a0003c0004t0001g0259a0003c0004t0002g0207others(13): Show | 16 | HG00733.hp2 HG02055.hp2 HG02080.hp1 others(13): Show |
intron_variant | MODIFIER | c.3261+2744_3261+274 others(7): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71410991 | ||||||
| chr2:71410991
|
C | T | 46 | a0001c0001t0001g0020a0001c0001t0001g0029a0001c0001t0001g0044others(43): Show | 46 | HG00323.hp1 HG01516.hp1 HG01884.hp2 others(43): Show |
intron_variant | MODIFIER | c.3261+2744C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71410991 | ||||||
| chr2:71410992
|
C | CT | 12 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0047others(9): Show | 12 | HG00738.hp2 HG01884.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.3261+2765dupT | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr2 | 71410992 | |||||
| chr2:71410992
|
C | CTT | 33 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0014others(30): Show | 36 | HG00423.hp1 HG00597.hp1 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.3261+2764_3261+276 others(6): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr2 | 71410992 | |||||
| chr2:71410992
|
C | CTTT | 6 | a0001c0001t0001g0010a0001c0001t0001g0033a0001c0001t0001g0036others(3): Show | 6 | HG00673.hp2 HG01070.hp2 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.3261+2763_3261+276 others(7): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr2 | 71410992 | |||||
| chr2:71410992
|
C | T | 125 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(122): Show | 126 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.3261+2745C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71410992 | ||||||
| chr2:71410993
|
T | C | 8 | a0001c0003t0001g0132a0001c0003t0001g0133a0001c0003t0001g0134others(5): Show | 8 | HG00735.hp1 HG01243.hp1 HG02165.hp2 others(5): Show |
intron_variant | MODIFIER | c.3261+2746T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71410993 | ||||||
| chr2:71411034
|
G | A | 2 | a0003c0004t0002g0208a0003c0004t0002g0225 | 2 | NA18956.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.3261+2787G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71411034 | ||||||
| chr2:71411144
|
C | T | 7 | a0001c0003t0001g0112a0001c0003t0001g0113a0001c0003t0001g0118others(4): Show | 7 | HG01099.hp2 HG02258.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.3261+2897C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71411144 | ||||||
| chr2:71411220
|
G | A | 7 | a0001c0007t0001g0327a0001c0007t0001g0328a0001c0007t0001g0329others(4): Show | 7 | HG01884.hp2 HG02451.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.3261+2973G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71411220 | ||||||
| chr2:71411255
|
T | C | 319 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(316): Show | 323 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(320): Show |
intron_variant | MODIFIER | c.3261+3008T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71411255 | ||||||
| chr2:71411345
|
T | A | 46 | a0003c0004t0001g0259a0003c0004t0002g0003a0003c0004t0002g0202others(43): Show | 46 | HG00323.hp1 HG00423.hp2 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.3261+3098T>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71411345 | ||||||
| chr2:71411378
|
C | A | 2 | a0009c0013t0001g0102a0009c0013t0001g0103 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.3261+3131C>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71411378 | ||||||
| chr2:71411442
|
T | TTTTA | 54 | a0003c0004t0001g0259a0003c0004t0002g0003a0003c0004t0002g0202others(51): Show | 54 | HG00323.hp1 HG00423.hp2 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.3261+3198_3261+319 others(8): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr2 | 71411442 | |||||
| chr2:71411442
|
TTTTTTTA | T | 7 | a0001c0007t0001g0327a0001c0007t0001g0328a0001c0007t0001g0329others(4): Show | 7 | HG01884.hp2 HG02451.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.3261+3199_3261+320 others(11): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr2 | 71411442 | |||||
| chr2:71411446
|
T | A | 2 | a0003c0012t0002g0232a0018c0027t0001g0201 | 2 | NA18952.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3261+3199T>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71411446 | ||||||
| chr2:71411449
|
A | T | 2 | a0003c0012t0002g0232a0018c0027t0001g0201 | 2 | NA18952.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3261+3202A>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71411449 | ||||||
| chr2:71411453
|
A | T | 231 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(228): Show | 235 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(232): Show |
intron_variant | MODIFIER | c.3261+3206A>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71411453 | ||||||
| chr2:71411466
|
T | A | 7 | a0001c0007t0001g0327a0001c0007t0001g0328a0001c0007t0001g0329others(4): Show | 7 | HG01884.hp2 HG02451.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.3261+3219T>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71411466 | ||||||
| chr2:71411468
|
TTTTTAA | T | 7 | a0001c0007t0001g0327a0001c0007t0001g0328a0001c0007t0001g0329others(4): Show | 7 | HG01884.hp2 HG02451.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.3261+3226_3261+323 others(10): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr2 | 71411468 | |||||
| chr2:71411474
|
A | AT | 179 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(176): Show | 183 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.3261+3240dupT | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr2 | 71411474 | |||||
| chr2:71411474
|
A | T | 1 | a0001c0001t0001g0019 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.3261+3227A>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71411474 | ||||||
| chr2:71411474
|
AT | A | 17 | a0001c0003t0001g0164a0001c0003t0003g0162a0001c0003t0003g0163others(14): Show | 17 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.3261+3240delT | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr2 | 71411474 | |||||
| chr2:71411475
|
T | TG | 52 | a0003c0004t0001g0259a0003c0004t0002g0003a0003c0004t0002g0202others(49): Show | 52 | HG00323.hp1 HG00423.hp2 HG00733.hp2 others(49): Show |
intron_variant | MODIFIER | c.3261+3228_3261+322 others(5): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71411475 | ||||||
| chr2:71411476
|
T | G | 1 | a0008c0010t0004g0253 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3261+3229T>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71411476 | ||||||
| chr2:71411529
|
G | C | 1 | a0001c0003t0001g0120 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.3261+3282G>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71411529 | ||||||
| chr2:71411597
|
G | T | 8 | a0001c0003t0001g0109a0001c0003t0001g0132a0001c0003t0001g0133others(5): Show | 8 | HG00735.hp1 HG01243.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.3261+3350G>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71411597 | ||||||
| chr2:71411609
|
A | G | 70 | a0002c0002t0001g0254a0002c0002t0001g0255a0002c0002t0001g0256others(67): Show | 70 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.3261+3362A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71411609 | ||||||
| chr2:71411614
|
A | C | 55 | a0003c0004t0001g0259a0003c0004t0002g0003a0003c0004t0002g0202others(52): Show | 55 | HG00323.hp1 HG00423.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.3261+3367A>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71411614 | ||||||
| chr2:71411628
|
C | T | 1 | a0018c0027t0001g0201 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3261+3381C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71411628 | ||||||
| chr2:71411672
|
G | C | 1 | a0002c0002t0001g0295 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.3261+3425G>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71411672 | ||||||
| chr2:71411696
|
A | G | 1 | a0002c0002t0001g0277 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.3261+3449A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71411696 | ||||||
| chr2:71411721
|
C | T | 1 | a0001c0001t0001g0340 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3261+3474C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71411721 | ||||||
| chr2:71411722
|
G | A | 56 | a0003c0004t0001g0259a0003c0004t0002g0003a0003c0004t0002g0202others(53): Show | 56 | HG00323.hp1 HG00423.hp2 HG00733.hp2 others(53): Show |
intron_variant | MODIFIER | c.3261+3475G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71411722 | ||||||
| chr2:71411810
|
A | C | 11 | a0001c0003t0001g0104a0001c0003t0001g0105a0001c0003t0001g0106others(8): Show | 11 | HG02055.hp1 HG02145.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.3261+3563A>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71411810 | ||||||
| chr2:71411820
|
G | T | 3 | a0001c0001t0001g0086a0001c0001t0001g0088a0001c0001t0001g0089 | 3 | HG01192.hp2 HG02622.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.3261+3573G>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71411820 | ||||||
| chr2:71411874
|
A | G | 1 | a0016c0023t0001g0264 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.3261+3627A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71411874 | ||||||
| chr2:71411925
|
G | T | 10 | a0001c0003t0001g0114a0001c0003t0001g0138a0001c0003t0001g0139others(7): Show | 10 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.3261+3678G>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71411925 | ||||||
| chr2:71412016
|
T | G | 55 | a0003c0004t0001g0259a0003c0004t0002g0003a0003c0004t0002g0202others(52): Show | 55 | HG00323.hp1 HG00423.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.3261+3769T>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71412016 | ||||||
| chr2:71412046
|
A | G | 55 | a0003c0004t0001g0259a0003c0004t0002g0003a0003c0004t0002g0202others(52): Show | 55 | HG00323.hp1 HG00423.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.3261+3799A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71412046 | ||||||
| chr2:71412057
|
T | C | 1 | a0002c0002t0001g0290 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.3261+3810T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71412057 | ||||||
| chr2:71412098
|
TA | T | 4 | a0001c0007t0001g0328a0001c0007t0001g0330a0002c0002t0001g0178others(1): Show | 4 | HG01884.hp2 HG02615.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.3261+3855delA | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr2 | 71412098 | |||||
| chr2:71412135
|
C | T | 1 | a0001c0001t0001g0098 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.3261+3888C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71412135 | ||||||
| chr2:71412136
|
G | T | 58 | a0001c0001t0001g0070a0001c0001t0001g0098a0003c0004t0001g0259others(55): Show | 58 | HG00323.hp1 HG00423.hp2 HG00733.hp2 others(55): Show |
intron_variant | MODIFIER | c.3261+3889G>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71412136 | ||||||
| chr2:71412206
|
T | C | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(113): Show | 120 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.3261+3959T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71412206 | ||||||
| chr2:71412242
|
C | T | 1 | a0001c0003t0001g0135 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3261+3995C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71412242 | ||||||
| chr2:71412252
|
C | T | 319 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(316): Show | 323 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(320): Show |
intron_variant | MODIFIER | c.3261+4005C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71412252 | ||||||
| chr2:71412300
|
T | C | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(113): Show | 120 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.3261+4053T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71412300 | ||||||
| chr2:71412302
|
C | T | 3 | a0002c0002t0001g0180a0002c0002t0001g0190a0002c0002t0001g0191 | 3 | HG01074.hp1 HG01496.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.3261+4055C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71412302 | ||||||
| chr2:71412303
|
G | T | 1 | a0018c0027t0001g0201 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3261+4056G>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71412303 | ||||||
| chr2:71412400
|
C | T | 1 | a0002c0002t0001g0293 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.3261+4153C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71412400 | ||||||
| chr2:71412401
|
G | A | 2 | a0009c0013t0001g0102a0009c0013t0001g0103 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.3261+4154G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71412401 | ||||||
| chr2:71412482
|
T | G | 23 | a0002c0002t0001g0263a0002c0002t0001g0266a0002c0002t0001g0268others(20): Show | 23 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.3261+4235T>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71412482 | ||||||
| chr2:71412617
|
G | A | 3 | a0002c0002t0001g0320a0002c0002t0001g0321a0002c0002t0001g0322 | 3 | NA19062.hp2 NA19064.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.3261+4370G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71412617 | ||||||
| chr2:71412656
|
A | C | 1 | a0001c0003t0001g0148 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.3261+4409A>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71412656 | ||||||
| chr2:71412719
|
T | C | 55 | a0003c0004t0001g0259a0003c0004t0002g0003a0003c0004t0002g0202others(52): Show | 55 | HG00323.hp1 HG00423.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.3261+4472T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71412719 | ||||||
| chr2:71412731
|
G | C | 1 | a0001c0001t0001g0055 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.3261+4484G>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71412731 | ||||||
| chr2:71412747
|
T | C | 1 | a0001c0003t0001g0137 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3261+4500T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71412747 | ||||||
| chr2:71412748
|
G | A | 1 | a0001c0003t0001g0137 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3261+4501G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71412748 | ||||||
| chr2:71412760
|
C | T | 2 | a0009c0013t0001g0102a0009c0013t0001g0103 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.3261+4513C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71412760 | ||||||
| chr2:71412794
|
C | T | 1 | a0018c0027t0001g0201 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3261+4547C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71412794 | ||||||
| chr2:71412795
|
G | A | 15 | a0001c0003t0001g0164a0001c0003t0003g0162a0001c0003t0003g0163others(12): Show | 15 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.3261+4548G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71412795 | ||||||
| chr2:71412798
|
A | G | 1 | a0001c0003t0001g0129 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.3261+4551A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71412798 | ||||||
| chr2:71412983
|
C | A | 1 | a0001c0001t0001g0018 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.3261+4736C>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71412983 | ||||||
| chr2:71413018
|
T | G | 3 | a0001c0003t0001g0142a0001c0003t0002g0218a0008c0010t0004g0253 | 3 | HG02280.hp2 HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.3261+4771T>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71413018 | ||||||
| chr2:71413050
|
C | G | 8 | a0001c0001t0001g0033a0001c0007t0001g0327a0001c0007t0001g0328others(5): Show | 8 | HG01884.hp2 HG02300.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.3261+4803C>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71413050 | ||||||
| chr2:71413069
|
G | T | 2 | a0009c0013t0001g0102a0009c0013t0001g0103 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.3261+4822G>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71413069 | ||||||
| chr2:71413084
|
C | T | 1 | a0001c0001t0001g0018 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.3261+4837C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71413084 | ||||||
| chr2:71413089
|
T | C | 2 | a0001c0001t0001g0098a0001c0001t0001g0339 | 2 | HG03195.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.3261+4842T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71413089 | ||||||
| chr2:71413090
|
T | G | 3 | a0002c0002t0001g0183a0002c0002t0001g0187a0014c0021t0001g0181 | 3 | HG01109.hp1 HG02976.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.3261+4843T>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71413090 | ||||||
| chr2:71413136
|
G | C | 1 | a0001c0001t0001g0011 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.3261+4889G>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71413136 | ||||||
| chr2:71413151
|
C | G | 135 | a0001c0003t0001g0104a0001c0003t0001g0105a0001c0003t0001g0106others(132): Show | 135 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(132): Show |
intron_variant | MODIFIER | c.3261+4904C>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71413151 | ||||||
| chr2:71413229
|
G | C | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(113): Show | 120 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.3261+4982G>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71413229 | ||||||
| chr2:71413273
|
CTGTT | C | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(113): Show | 120 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.3261+5030_3261+503 others(8): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr2 | 71413273 | |||||
| chr2:71413284
|
T | C | 2 | a0001c0003t0001g0112a0001c0003t0001g0113 | 2 | HG02572.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3261+5037T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71413284 | ||||||
| chr2:71413294
|
A | C | 1 | a0001c0001t0001g0016 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.3261+5047A>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71413294 | ||||||
| chr2:71413358
|
C | T | 7 | a0001c0007t0001g0327a0001c0007t0001g0328a0001c0007t0001g0329others(4): Show | 7 | HG01884.hp2 HG02451.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.3261+5111C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71413358 | ||||||
| chr2:71413385
|
G | A | 51 | a0003c0004t0001g0259a0003c0004t0002g0003a0003c0004t0002g0202others(48): Show | 51 | HG00323.hp1 HG00423.hp2 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.3261+5138G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71413385 | ||||||
| chr2:71413387
|
T | C | 51 | a0003c0004t0001g0259a0003c0004t0002g0003a0003c0004t0002g0202others(48): Show | 51 | HG00323.hp1 HG00423.hp2 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.3261+5140T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71413387 | ||||||
| chr2:71413388
|
G | A | 51 | a0003c0004t0001g0259a0003c0004t0002g0003a0003c0004t0002g0202others(48): Show | 51 | HG00323.hp1 HG00423.hp2 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.3261+5141G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71413388 | ||||||
| chr2:71413399
|
G | C | 1 | a0003c0004t0002g0219 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.3261+5152G>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71413399 | ||||||
| chr2:71413404
|
A | G | 5 | a0003c0004t0002g0204a0003c0004t0002g0222a0003c0004t0002g0224others(2): Show | 5 | NA18939.hp1 NA18965.hp2 NA19004.hp2 others(2): Show |
intron_variant | MODIFIER | c.3261+5157A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71413404 | ||||||
| chr2:71413420
|
C | G | 7 | a0001c0003t0001g0112a0001c0003t0001g0113a0001c0003t0001g0118others(4): Show | 7 | HG01099.hp2 HG02258.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.3261+5173C>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71413420 | ||||||
| chr2:71413505
|
C | T | 1 | a0001c0001t0001g0101 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.3262-5097C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71413505 | ||||||
| chr2:71413526
|
C | T | 5 | a0001c0003t0001g0142a0001c0003t0001g0164a0001c0003t0002g0218others(2): Show | 5 | HG01496.hp2 HG02280.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.3262-5076C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71413526 | ||||||
| chr2:71413527
|
G | A | 1 | a0004c0006t0001g0284 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.3262-5075G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71413527 | ||||||
| chr2:71413538
|
G | A | 7 | a0001c0007t0001g0327a0001c0007t0001g0328a0001c0007t0001g0329others(4): Show | 7 | HG01884.hp2 HG02451.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.3262-5064G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71413538 | ||||||
| chr2:71413599
|
A | C | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(113): Show | 120 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.3262-5003A>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71413599 | ||||||
| chr2:71413727
|
T | G | 1 | a0004c0006t0001g0257 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.3262-4875T>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71413727 | ||||||
| chr2:71413783
|
T | C | 1 | a0001c0001t0001g0057 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.3262-4819T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71413783 | ||||||
| chr2:71413791
|
A | C | 318 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(315): Show | 322 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(319): Show |
intron_variant | MODIFIER | c.3262-4811A>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71413791 | ||||||
| chr2:71413929
|
C | G | 3 | a0005c0008t0001g0008a0005c0008t0001g0042a0005c0008t0001g0043 | 3 | NA18971.hp2 NA18986.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.3262-4673C>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71413929 | ||||||
| chr2:71413961
|
C | T | 1 | a0001c0001t0001g0036 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.3262-4641C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71413961 | ||||||
| chr2:71414099
|
A | G | 2 | a0001c0005t0001g0157a0001c0005t0001g0158 | 2 | HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.3262-4503A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71414099 | ||||||
| chr2:71414127
|
A | G | 71 | a0001c0020t0001g0323a0002c0002t0001g0254a0002c0002t0001g0255others(68): Show | 71 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.3262-4475A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71414127 | ||||||
| chr2:71414153
|
A | C | 71 | a0001c0020t0001g0323a0002c0002t0001g0254a0002c0002t0001g0255others(68): Show | 71 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.3262-4449A>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71414153 | ||||||
| chr2:71414154
|
G | T | 71 | a0001c0020t0001g0323a0002c0002t0001g0254a0002c0002t0001g0255others(68): Show | 71 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.3262-4448G>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71414154 | ||||||
| chr2:71414220
|
C | G | 319 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(316): Show | 323 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(320): Show |
intron_variant | MODIFIER | c.3262-4382C>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71414220 | ||||||
| chr2:71414227
|
G | C | 1 | a0001c0003t0001g0146 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3262-4375G>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71414227 | ||||||
| chr2:71414284
|
C | G | 55 | a0003c0004t0001g0259a0003c0004t0002g0003a0003c0004t0002g0202others(52): Show | 55 | HG00323.hp1 HG00423.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.3262-4318C>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71414284 | ||||||
| chr2:71414391
|
C | T | 8 | a0001c0007t0001g0327a0001c0007t0001g0328a0001c0007t0001g0329others(5): Show | 8 | HG01884.hp2 HG02451.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.3262-4211C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71414391 | ||||||
| chr2:71414635
|
C | G | 3 | a0001c0001t0001g0086a0001c0001t0001g0088a0001c0001t0001g0089 | 3 | HG01192.hp2 HG02622.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.3262-3967C>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71414635 | ||||||
| chr2:71414651
|
C | T | 1 | a0001c0003t0001g0173 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3262-3951C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71414651 | ||||||
| chr2:71414796
|
A | T | 2 | a0001c0003t0001g0130a0001c0003t0001g0131 | 2 | HG01167.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.3262-3806A>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71414796 | ||||||
| chr2:71414852
|
T | C | 2 | a0001c0001t0001g0023a0001c0001t0001g0031 | 2 | HG03239.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.3262-3750T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71414852 | ||||||
| chr2:71414856
|
T | C | 2 | a0002c0002t0001g0193a0002c0002t0001g0194 | 2 | HG01069.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.3262-3746T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71414856 | ||||||
| chr2:71414899
|
A | G | 78 | a0001c0001t0001g0010a0001c0003t0001g0104a0001c0003t0001g0105others(75): Show | 78 | HG00280.hp1 HG00733.hp1 HG00735.hp1 others(75): Show |
intron_variant | MODIFIER | c.3262-3703A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71414899 | ||||||
| chr2:71414925
|
C | G | 172 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(169): Show | 176 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.3262-3677C>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71414925 | ||||||
| chr2:71415018
|
T | G | 6 | a0004c0006t0001g0260a0004c0006t0001g0261a0004c0006t0001g0281others(3): Show | 6 | NA18948.hp2 NA18954.hp2 NA18980.hp1 others(3): Show |
intron_variant | MODIFIER | c.3262-3584T>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71415018 | ||||||
| chr2:71415027
|
G | A | 319 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(316): Show | 323 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(320): Show |
intron_variant | MODIFIER | c.3262-3575G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71415027 | ||||||
| chr2:71415048
|
C | T | 1 | a0003c0004t0002g0203 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3262-3554C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71415048 | ||||||
| chr2:71415049
|
G | A | 1 | a0001c0001t0001g0339 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3262-3553G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71415049 | ||||||
| chr2:71415082
|
A | C | 1 | a0018c0027t0001g0201 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3262-3520A>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71415082 | ||||||
| chr2:71415132
|
G | C | 55 | a0003c0004t0001g0259a0003c0004t0002g0003a0003c0004t0002g0202others(52): Show | 55 | HG00323.hp1 HG00423.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.3262-3470G>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71415132 | ||||||
| chr2:71415309
|
T | C | 1 | a0001c0003t0001g0131 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3262-3293T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71415309 | ||||||
| chr2:71415363
|
A | G | 2 | a0009c0013t0001g0102a0009c0013t0001g0103 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.3262-3239A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71415363 | ||||||
| chr2:71415432
|
A | G | 194 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(191): Show | 198 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.3262-3170A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71415432 | ||||||
| chr2:71415630
|
C | T | 2 | a0009c0013t0001g0102a0009c0013t0001g0103 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.3262-2972C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71415630 | ||||||
| chr2:71415639
|
C | T | 3 | a0003c0004t0002g0211a0003c0004t0002g0238a0003c0004t0002g0246 | 3 | HG02055.hp2 HG02109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.3262-2963C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71415639 | ||||||
| chr2:71415700
|
T | C | 55 | a0003c0004t0001g0259a0003c0004t0002g0003a0003c0004t0002g0202others(52): Show | 55 | HG00323.hp1 HG00423.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.3262-2902T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71415700 | ||||||
| chr2:71415706
|
A | G | 1 | a0003c0015t0002g0245 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3262-2896A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71415706 | ||||||
| chr2:71415712
|
T | G | 1 | a0003c0015t0002g0245 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3262-2890T>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71415712 | ||||||
| chr2:71415759
|
A | G | 1 | a0003c0015t0002g0245 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3262-2843A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71415759 | ||||||
| chr2:71415777
|
C | A | 1 | a0003c0015t0002g0245 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3262-2825C>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71415777 | ||||||
| chr2:71415799
|
A | G | 11 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0030others(8): Show | 11 | HG00544.hp2 HG02165.hp1 HG02300.hp1 others(8): Show |
intron_variant | MODIFIER | c.3262-2803A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71415799 | ||||||
| chr2:71415845
|
C | T | 109 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(106): Show | 113 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.3262-2757C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71415845 | ||||||
| chr2:71415846
|
C | G | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(113): Show | 120 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.3262-2756C>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71415846 | ||||||
| chr2:71415946
|
A | G | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(113): Show | 120 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.3262-2656A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71415946 | ||||||
| chr2:71416061
|
C | G | 71 | a0001c0020t0001g0323a0002c0002t0001g0254a0002c0002t0001g0255others(68): Show | 71 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.3262-2541C>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71416061 | ||||||
| chr2:71416096
|
A | C | 77 | a0001c0003t0001g0104a0001c0003t0001g0105a0001c0003t0001g0106others(74): Show | 77 | HG00280.hp1 HG00733.hp1 HG00735.hp1 others(74): Show |
intron_variant | MODIFIER | c.3262-2506A>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71416096 | ||||||
| chr2:71416210
|
T | C | 2 | a0009c0013t0001g0102a0009c0013t0001g0103 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.3262-2392T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71416210 | ||||||
| chr2:71416210
|
T | G | 193 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(190): Show | 197 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.3262-2392T>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71416210 | ||||||
| chr2:71416240
|
G | A | 2 | a0001c0003t0001g0169a0001c0003t0001g0170 | 2 | HG00738.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.3262-2362G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71416240 | ||||||
| chr2:71416271
|
G | A | 46 | a0003c0004t0001g0259a0003c0004t0002g0003a0003c0004t0002g0202others(43): Show | 46 | HG00323.hp1 HG00423.hp2 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.3262-2331G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71416271 | ||||||
| chr2:71416446
|
A | C | 1 | a0003c0004t0002g0252 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3262-2156A>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71416446 | ||||||
| chr2:71416453
|
C | T | 1 | a0001c0005t0001g0153 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3262-2149C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71416453 | ||||||
| chr2:71416463
|
C | G | 1 | a0003c0004t0002g0213 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.3262-2139C>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71416463 | ||||||
| chr2:71416477
|
T | C | 2 | a0007c0011t0001g0303a0007c0011t0001g0304 | 2 | NA18939.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.3262-2125T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71416477 | ||||||
| chr2:71416510
|
G | C | 2 | a0009c0013t0001g0102a0009c0013t0001g0103 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.3262-2092G>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71416510 | ||||||
| chr2:71416558
|
G | A | 6 | a0001c0003t0001g0146a0001c0003t0001g0147a0001c0003t0001g0148others(3): Show | 6 | HG02055.hp1 HG02647.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.3262-2044G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71416558 | ||||||
| chr2:71416564
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.3262-2038G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71416564 | ||||||
| chr2:71416656
|
G | A | 2 | a0009c0013t0001g0102a0009c0013t0001g0103 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.3262-1946G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71416656 | ||||||
| chr2:71416675
|
C | G | 2 | a0009c0013t0001g0102a0009c0013t0001g0103 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.3262-1927C>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71416675 | ||||||
| chr2:71416736
|
C | G | 51 | a0003c0004t0001g0259a0003c0004t0002g0003a0003c0004t0002g0202others(48): Show | 51 | HG00323.hp1 HG00423.hp2 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.3262-1866C>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71416736 | ||||||
| chr2:71416767
|
G | C | 1 | a0001c0001t0001g0091 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3262-1835G>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71416767 | ||||||
| chr2:71416817
|
A | C | 2 | a0009c0013t0001g0102a0009c0013t0001g0103 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.3262-1785A>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71416817 | ||||||
| chr2:71416833
|
G | A | 2 | a0003c0004t0002g0221a0003c0004t0002g0243 | 2 | HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.3262-1769G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71416833 | ||||||
| chr2:71416840
|
G | C | 2 | a0003c0004t0002g0221a0003c0004t0002g0243 | 2 | HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.3262-1762G>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71416840 | ||||||
| chr2:71416885
|
G | C | 1 | a0018c0027t0001g0201 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3262-1717G>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71416885 | ||||||
| chr2:71416962
|
C | T | 1 | a0002c0002t0001g0189 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.3262-1640C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71416962 | ||||||
| chr2:71416967
|
G | GAGGC | 5 | a0001c0003t0001g0115a0001c0003t0001g0116a0001c0003t0001g0171others(2): Show | 5 | HG01167.hp1 HG01169.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.3262-1626_3262-162 others(8): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr2 | 71416967 | |||||
| chr2:71417020
|
C | T | 30 | a0001c0003t0001g0108a0001c0003t0001g0109a0001c0003t0001g0111others(27): Show | 30 | HG00280.hp1 HG00735.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.3262-1582C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71417020 | ||||||
| chr2:71417040
|
G | T | 1 | a0001c0001t0001g0036 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.3262-1562G>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71417040 | ||||||
| chr2:71417060
|
G | A | 1 | a0001c0009t0001g0136 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.3262-1542G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71417060 | ||||||
| chr2:71417069
|
C | T | 1 | a0004c0006t0001g0282 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.3262-1533C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71417069 | ||||||
| chr2:71417084
|
C | T | 2 | a0001c0003t0001g0140a0001c0003t0001g0141 | 2 | HG02717.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.3262-1518C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71417084 | ||||||
| chr2:71417106
|
G | C | 319 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(316): Show | 323 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(320): Show |
intron_variant | MODIFIER | c.3262-1496G>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71417106 | ||||||
| chr2:71417133
|
C | T | 1 | a0003c0015t0002g0245 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3262-1469C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71417133 | ||||||
| chr2:71417178
|
G | C | 1 | a0002c0002t0001g0254 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.3262-1424G>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71417178 | ||||||
| chr2:71417251
|
C | T | 1 | a0018c0027t0001g0201 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3262-1351C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71417251 | ||||||
| chr2:71417323
|
C | T | 2 | a0009c0013t0001g0102a0009c0013t0001g0103 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.3262-1279C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71417323 | ||||||
| chr2:71417332
|
G | A | 1 | a0001c0003t0001g0117 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3262-1270G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71417332 | ||||||
| chr2:71417354
|
A | C | 1 | a0003c0004t0002g0247 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.3262-1248A>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71417354 | ||||||
| chr2:71417360
|
A | G | 319 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(316): Show | 323 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(320): Show |
intron_variant | MODIFIER | c.3262-1242A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71417360 | ||||||
| chr2:71417456
|
A | G | 194 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(191): Show | 198 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.3262-1146A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71417456 | ||||||
| chr2:71417538
|
T | C | 7 | a0001c0007t0001g0327a0001c0007t0001g0328a0001c0007t0001g0329others(4): Show | 7 | HG01884.hp2 HG02451.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.3262-1064T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71417538 | ||||||
| chr2:71417598
|
A | T | 53 | a0003c0004t0001g0259a0003c0004t0002g0003a0003c0004t0002g0202others(50): Show | 53 | HG00323.hp1 HG00423.hp2 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.3262-1004A>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71417598 | ||||||
| chr2:71417660
|
G | GT | 6 | a0001c0003t0003g0162a0002c0002t0001g0198a0002c0002t0001g0344others(3): Show | 6 | HG03098.hp2 HG03486.hp2 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.3262-929dupT | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr2 | 71417660 | |||||
| chr2:71417661
|
T | G | 51 | a0003c0004t0001g0259a0003c0004t0002g0003a0003c0004t0002g0202others(48): Show | 51 | HG00323.hp1 HG00423.hp2 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.3262-941T>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71417661 | ||||||
| chr2:71417768
|
T | G | 5 | a0002c0002t0001g0254a0002c0002t0001g0286a0002c0002t0001g0287others(2): Show | 5 | HG00544.hp1 HG00597.hp2 HG02015.hp1 others(2): Show |
intron_variant | MODIFIER | c.3262-834T>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71417768 | ||||||
| chr2:71417807
|
G | C | 2 | a0001c0001t0001g0004a0001c0001t0001g0100 | 2 | HG00280.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.3262-795G>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71417807 | ||||||
| chr2:71418054
|
A | G | 1 | a0001c0001t0001g0338 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3262-548A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71418054 | ||||||
| chr2:71418103
|
G | C | 2 | a0008c0010t0002g0342a0008c0010t0004g0253 | 2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.3262-499G>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71418103 | ||||||
| chr2:71418124
|
C | G | 1 | a0001c0003t0001g0118 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3262-478C>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71418124 | ||||||
| chr2:71418127
|
A | G | 111 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(108): Show | 115 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.3262-475A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71418127 | ||||||
| chr2:71418451
|
A | G | 2 | a0001c0001t0001g0017a0001c0001t0001g0018 | 2 | HG03704.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.3262-151A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71418451 | ||||||
| chr2:71418498
|
G | GT | 61 | a0001c0001t0001g0065a0001c0003t0001g0147a0001c0003t0001g0149others(58): Show | 61 | HG00323.hp1 HG00423.hp2 HG00733.hp2 others(58): Show |
intron_variant | MODIFIER | c.3262-93dupT | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr2 | 71418498 | |||||
| chr2:71418498
|
G | GTT | 65 | a0001c0003t0001g0108a0001c0003t0001g0109a0001c0003t0001g0111others(62): Show | 65 | HG00280.hp1 HG00733.hp1 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.3262-94_3262-93dup others(2): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr2 | 71418498 | |||||
| chr2:71418510
|
G | T | 1 | a0001c0020t0001g0323 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3262-92G>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 20/27 | chr2 | 71418510 | ||||||
| chr2:71418675
|
G | T | 1 | a0001c0001t0001g0027 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.3299+36G>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | chr2 | 71418675 | ||||||
| chr2:71418698
|
G | A | 111 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(108): Show | 115 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.3299+59G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | chr2 | 71418698 | ||||||
| chr2:71418724
|
TGTA | T | 62 | a0001c0003t0001g0108a0001c0003t0001g0109a0001c0003t0001g0111others(59): Show | 62 | HG00280.hp1 HG00733.hp1 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.3299+88_3299+90del others(3): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr2 | 71418724 | |||||
| chr2:71418760
|
G | C | 180 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(177): Show | 184 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.3299+121G>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | chr2 | 71418760 | ||||||
| chr2:71418766
|
A | G | 1 | a0009c0013t0001g0103 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3299+127A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | chr2 | 71418766 | ||||||
| chr2:71418816
|
G | A | 111 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(108): Show | 115 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.3299+177G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | chr2 | 71418816 | ||||||
| chr2:71418839
|
C | T | 2 | a0007c0011t0001g0303a0007c0011t0001g0304 | 2 | NA18939.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.3299+200C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | chr2 | 71418839 | ||||||
| chr2:71418874
|
G | A | 71 | a0001c0020t0001g0323a0002c0002t0001g0254a0002c0002t0001g0255others(68): Show | 71 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.3299+235G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | chr2 | 71418874 | ||||||
| chr2:71418887
|
T | A | 118 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(115): Show | 122 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.3299+248T>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | chr2 | 71418887 | ||||||
| chr2:71419020
|
A | G | 1 | a0001c0003t0001g0105 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3299+381A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | chr2 | 71419020 | ||||||
| chr2:71419022
|
G | A | 4 | a0001c0003t0001g0118a0001c0003t0001g0119a0001c0003t0001g0120others(1): Show | 4 | HG01099.hp2 HG02258.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.3299+383G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | chr2 | 71419022 | ||||||
| chr2:71419242
|
T | C | 12 | a0001c0005t0001g0122a0001c0005t0001g0152a0001c0005t0001g0153others(9): Show | 12 | HG01243.hp2 HG01891.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.3299+603T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | chr2 | 71419242 | ||||||
| chr2:71419425
|
T | G | 55 | a0003c0004t0001g0259a0003c0004t0002g0003a0003c0004t0002g0202others(52): Show | 55 | HG00323.hp1 HG00423.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.3299+786T>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | chr2 | 71419425 | ||||||
| chr2:71419477
|
C | T | 5 | a0003c0004t0002g0248a0003c0004t0002g0249a0003c0004t0002g0250others(2): Show | 5 | HG02818.hp1 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.3299+838C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | chr2 | 71419477 | ||||||
| chr2:71419505
|
A | G | 1 | a0001c0001t0001g0009 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3299+866A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | chr2 | 71419505 | ||||||
| chr2:71419526
|
C | T | 55 | a0003c0004t0001g0259a0003c0004t0002g0003a0003c0004t0002g0202others(52): Show | 55 | HG00323.hp1 HG00423.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.3299+887C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | chr2 | 71419526 | ||||||
| chr2:71419636
|
C | T | 55 | a0003c0004t0001g0259a0003c0004t0002g0003a0003c0004t0002g0202others(52): Show | 55 | HG00323.hp1 HG00423.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.3299+997C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | chr2 | 71419636 | ||||||
| chr2:71419692
|
A | G | 2 | a0002c0002t0001g0302a0002c0002t0001g0308 | 2 | HG03710.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.3299+1053A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | chr2 | 71419692 | ||||||
| chr2:71419735
|
T | C | 3 | a0001c0001t0001g0086a0001c0001t0001g0088a0001c0001t0001g0089 | 3 | HG01192.hp2 HG02622.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.3299+1096T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | chr2 | 71419735 | ||||||
| chr2:71419738
|
G | A | 1 | a0002c0002t0001g0177 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.3299+1099G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | chr2 | 71419738 | ||||||
| chr2:71419862
|
A | G | 1 | a0002c0002t0001g0317 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.3299+1223A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | chr2 | 71419862 | ||||||
| chr2:71419866
|
C | T | 1 | a0008c0010t0004g0253 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3299+1227C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | chr2 | 71419866 | ||||||
| chr2:71419932
|
A | G | 46 | a0003c0004t0001g0259a0003c0004t0002g0003a0003c0004t0002g0202others(43): Show | 46 | HG00323.hp1 HG00423.hp2 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.3299+1293A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | chr2 | 71419932 | ||||||
| chr2:71419962
|
A | AC | 153 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(150): Show | 157 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.3299+1332dupC | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr2 | 71419962 | |||||
| chr2:71419962
|
A | ACC | 66 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0016others(63): Show | 66 | HG00544.hp1 HG00597.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.3299+1331_3299+133 others(6): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr2 | 71419962 | |||||
| chr2:71419962
|
A | ACCC | 25 | a0002c0002t0001g0263a0002c0002t0001g0271a0002c0002t0001g0272others(22): Show | 25 | HG00438.hp2 HG00741.hp1 HG01175.hp1 others(22): Show |
intron_variant | MODIFIER | c.3299+1330_3299+133 others(7): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr2 | 71419962 | |||||
| chr2:71419965
|
C | CG | 46 | a0001c0003t0001g0108a0001c0003t0001g0109a0001c0003t0001g0111others(43): Show | 46 | HG00280.hp1 HG00735.hp1 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.3299+1326_3299+132 others(5): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | chr2 | 71419965 | ||||||
| chr2:71419972
|
G | C | 9 | a0001c0001t0001g0005a0001c0001t0001g0037a0001c0001t0001g0083others(6): Show | 9 | HG00423.hp1 HG01243.hp2 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.3299+1333G>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | chr2 | 71419972 | ||||||
| chr2:71419973
|
C | G | 2 | a0001c0005t0001g0154a0001c0005t0001g0161 | 2 | HG02970.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.3299+1334C>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | chr2 | 71419973 | ||||||
| chr2:71419974
|
C | CT | 19 | a0002c0002t0001g0185a0002c0002t0001g0186a0002c0002t0001g0198others(16): Show | 19 | HG00423.hp2 HG01361.hp1 HG01516.hp1 others(16): Show |
intron_variant | MODIFIER | c.3299+1364dupT | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr2 | 71419974 | |||||
| chr2:71419974
|
C | CTTTTT | 6 | a0002c0002t0001g0262a0002c0002t0001g0276a0002c0002t0001g0299others(3): Show | 6 | HG01952.hp2 HG02155.hp2 HG03704.hp2 others(3): Show |
intron_variant | MODIFIER | c.3299+1360_3299+136 others(9): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr2 | 71419974 | |||||
| chr2:71419974
|
C | CTTTTTT | 27 | a0001c0003t0001g0104a0002c0002t0001g0263a0002c0002t0001g0266others(24): Show | 27 | HG00609.hp2 HG00673.hp1 HG01975.hp2 others(24): Show |
intron_variant | MODIFIER | c.3299+1359_3299+136 others(10): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr2 | 71419974 | |||||
| chr2:71419974
|
C | CTTTTTTT | 23 | a0001c0003t0001g0105a0001c0003t0001g0106a0001c0003t0001g0107others(20): Show | 23 | HG00438.hp2 HG00609.hp1 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.3299+1358_3299+136 others(11): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr2 | 71419974 | |||||
| chr2:71419974
|
C | CTTTTTTT others(1): Show |
8 | a0002c0002t0001g0277a0002c0002t0001g0285a0002c0002t0001g0301others(5): Show | 8 | HG03654.hp1 NA18942.hp1 NA18944.hp2 others(5): Show |
intron_variant | MODIFIER | c.3299+1357_3299+136 others(12): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr2 | 71419974 | |||||
| chr2:71419974
|
C | CTTTTTTT others(3): Show |
5 | a0001c0003t0001g0149a0001c0003t0001g0151a0002c0002t0001g0270others(2): Show | 5 | HG00741.hp1 HG01123.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.3299+1355_3299+136 others(14): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr2 | 71419974 | |||||
| chr2:71419974
|
C | CTTTTTTT others(4): Show |
3 | a0001c0003t0001g0147a0001c0003t0001g0150a0001c0024t0001g0145 | 3 | HG02055.hp1 HG02647.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.3299+1354_3299+136 others(15): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr2 | 71419974 | |||||
| chr2:71419974
|
C | G | 2 | a0001c0003t0003g0162a0001c0005t0001g0174 | 2 | HG01243.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.3299+1335C>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | chr2 | 71419974 | ||||||
| chr2:71419974
|
CT | C | 28 | a0001c0003t0001g0108a0001c0003t0001g0109a0001c0003t0001g0115others(25): Show | 28 | HG00733.hp1 HG00735.hp1 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.3299+1364delT | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr2 | 71419974 | |||||
| chr2:71419974
|
CTT | C | 37 | a0001c0001t0001g0037a0001c0003t0001g0111a0001c0003t0001g0112others(34): Show | 37 | HG00280.hp1 HG00423.hp1 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.3299+1363_3299+136 others(6): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr2 | 71419974 | |||||
| chr2:71419974
|
CTTT | C | 13 | a0001c0001t0001g0005a0001c0001t0001g0083a0001c0003t0001g0114others(10): Show | 13 | HG00544.hp1 HG00597.hp2 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.3299+1362_3299+136 others(7): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr2 | 71419974 | |||||
| chr2:71419974
|
CTTTTTT | C | 89 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(86): Show | 93 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.3299+1359_3299+136 others(10): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr2 | 71419974 | |||||
| chr2:71419974
|
CTTTTTTT | C | 23 | a0001c0001t0001g0013a0001c0001t0001g0022a0001c0001t0001g0048others(20): Show | 23 | HG00323.hp2 HG01069.hp1 HG01256.hp2 others(20): Show |
intron_variant | MODIFIER | c.3299+1358_3299+136 others(11): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr2 | 71419974 | |||||
| chr2:71419974
|
CTTTTTTT others(3): Show |
C | 1 | a0002c0002t0001g0273 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3299+1355_3299+136 others(14): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr2 | 71419974 | |||||
| chr2:71419975
|
T | C | 6 | a0001c0003t0001g0164a0001c0003t0003g0162a0001c0003t0003g0163others(3): Show | 6 | HG01243.hp2 HG01496.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.3299+1336T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | chr2 | 71419975 | ||||||
| chr2:71419976
|
T | C | 3 | a0001c0003t0001g0164a0001c0003t0003g0162a0001c0005t0001g0174 | 3 | HG01243.hp2 HG01496.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.3299+1337T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | chr2 | 71419976 | ||||||
| chr2:71419977
|
T | G | 1 | a0001c0001t0001g0037 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.3299+1338T>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | chr2 | 71419977 | ||||||
| chr2:71419978
|
T | C | 1 | a0001c0001t0001g0037 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.3299+1339T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | chr2 | 71419978 | ||||||
| chr2:71419978
|
T | G | 2 | a0001c0001t0001g0005a0001c0001t0001g0083 | 2 | NA18955.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.3299+1339T>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | chr2 | 71419978 | ||||||
| chr2:71419979
|
T | C | 3 | a0001c0001t0001g0005a0001c0001t0001g0037a0001c0001t0001g0083 | 3 | HG00423.hp1 NA18955.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.3299+1340T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | chr2 | 71419979 | ||||||
| chr2:71419980
|
T | C | 2 | a0001c0001t0001g0005a0001c0001t0001g0083 | 2 | NA18955.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.3299+1341T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | chr2 | 71419980 | ||||||
| chr2:71420003
|
T | A | 2 | a0009c0013t0001g0102a0009c0013t0001g0103 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.3299+1364T>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | chr2 | 71420003 | ||||||
| chr2:71420069
|
G | T | 55 | a0003c0004t0001g0259a0003c0004t0002g0003a0003c0004t0002g0202others(52): Show | 55 | HG00323.hp1 HG00423.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.3299+1430G>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | chr2 | 71420069 | ||||||
| chr2:71420167
|
G | C | 11 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0030others(8): Show | 11 | HG00544.hp2 HG02165.hp1 HG02300.hp1 others(8): Show |
intron_variant | MODIFIER | c.3299+1528G>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | chr2 | 71420167 | ||||||
| chr2:71420307
|
A | ACTC | 7 | a0001c0003t0001g0112a0001c0003t0001g0113a0001c0003t0001g0118others(4): Show | 7 | HG01099.hp2 HG02109.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.3299+1669_3299+167 others(7): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr2 | 71420307 | |||||
| chr2:71420333
|
A | T | 70 | a0002c0002t0001g0254a0002c0002t0001g0255a0002c0002t0001g0256others(67): Show | 70 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.3299+1694A>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | chr2 | 71420333 | ||||||
| chr2:71420334
|
A | T | 70 | a0002c0002t0001g0254a0002c0002t0001g0255a0002c0002t0001g0256others(67): Show | 70 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.3299+1695A>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | chr2 | 71420334 | ||||||
| chr2:71420603
|
G | A | 1 | a0003c0015t0002g0245 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3299+1964G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | chr2 | 71420603 | ||||||
| chr2:71420610
|
G | C | 82 | a0001c0003t0001g0104a0001c0003t0001g0105a0001c0003t0001g0106others(79): Show | 82 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.3299+1971G>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | chr2 | 71420610 | ||||||
| chr2:71420640
|
A | G | 1 | a0001c0001t0001g0058 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.3299+2001A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | chr2 | 71420640 | ||||||
| chr2:71420679
|
C | A | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(113): Show | 120 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.3299+2040C>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | chr2 | 71420679 | ||||||
| chr2:71420866
|
A | T | 2 | a0009c0013t0001g0102a0009c0013t0001g0103 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.3300-1948A>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | chr2 | 71420866 | ||||||
| chr2:71420879
|
A | G | 54 | a0003c0004t0001g0259a0003c0004t0002g0003a0003c0004t0002g0202others(51): Show | 54 | HG00323.hp1 HG00423.hp2 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.3300-1935A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | chr2 | 71420879 | ||||||
| chr2:71421024
|
A | G | 1 | a0002c0002t0001g0185 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.3300-1790A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | chr2 | 71421024 | ||||||
| chr2:71421249
|
G | A | 2 | a0009c0013t0001g0102a0009c0013t0001g0103 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.3300-1565G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | chr2 | 71421249 | ||||||
| chr2:71421285
|
A | G | 2 | a0003c0004t0002g0208a0003c0004t0002g0225 | 2 | NA18956.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.3300-1529A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | chr2 | 71421285 | ||||||
| chr2:71421295
|
G | T | 125 | a0001c0003t0001g0108a0001c0003t0001g0109a0001c0003t0001g0111others(122): Show | 125 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.3300-1519G>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | chr2 | 71421295 | ||||||
| chr2:71421308
|
A | G | 2 | a0008c0010t0002g0342a0008c0010t0004g0253 | 2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.3300-1506A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | chr2 | 71421308 | ||||||
| chr2:71421325
|
T | C | 16 | a0001c0003t0001g0164a0001c0003t0003g0162a0001c0003t0003g0163others(13): Show | 16 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.3300-1489T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | chr2 | 71421325 | ||||||
| chr2:71421361
|
AT | A | 66 | a0001c0003t0001g0108a0001c0003t0001g0109a0001c0003t0001g0111others(63): Show | 66 | HG00280.hp1 HG00733.hp1 HG00735.hp1 others(63): Show |
intron_variant | MODIFIER | c.3300-1449delT | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr2 | 71421361 | |||||
| chr2:71421364
|
T | TA | 4 | a0003c0004t0002g0234a0003c0004t0002g0235a0003c0004t0002g0237others(1): Show | 4 | NA18943.hp2 NA18954.hp1 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.3300-1450_3300-144 others(5): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | chr2 | 71421364 | ||||||
| chr2:71421365
|
T | A | 60 | a0001c0001t0001g0015a0001c0003t0001g0118a0001c0003t0001g0171others(57): Show | 60 | HG00323.hp1 HG00423.hp2 HG00733.hp2 others(57): Show |
intron_variant | MODIFIER | c.3300-1449T>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | chr2 | 71421365 | ||||||
| chr2:71421365
|
TA | T | 108 | a0001c0001t0001g0013a0001c0003t0001g0104a0001c0003t0001g0105others(105): Show | 108 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.3300-1439delA | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr2 | 71421365 | |||||
| chr2:71421453
|
T | C | 1 | a0001c0001t0001g0019 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.3300-1361T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | chr2 | 71421453 | ||||||
| chr2:71421517
|
T | C | 6 | a0003c0004t0002g0248a0003c0004t0002g0249a0003c0004t0002g0250others(3): Show | 6 | HG02818.hp1 HG03139.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.3300-1297T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | chr2 | 71421517 | ||||||
| chr2:71421612
|
A | T | 6 | a0002c0002t0001g0179a0002c0002t0001g0180a0002c0002t0001g0188others(3): Show | 6 | HG01074.hp1 HG01255.hp2 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.3300-1202A>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | chr2 | 71421612 | ||||||
| chr2:71421727
|
T | C | 5 | a0002c0002t0001g0310a0002c0002t0001g0311a0002c0002t0001g0312others(2): Show | 5 | HG00609.hp2 HG00673.hp1 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.3300-1087T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | chr2 | 71421727 | ||||||
| chr2:71421732
|
G | C | 11 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0014others(8): Show | 11 | HG00642.hp1 HG01081.hp1 HG02040.hp1 others(8): Show |
intron_variant | MODIFIER | c.3300-1082G>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | chr2 | 71421732 | ||||||
| chr2:71421934
|
T | G | 24 | a0002c0002t0001g0177a0002c0002t0001g0178a0002c0002t0001g0179others(21): Show | 24 | HG00438.hp1 HG01069.hp2 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.3300-880T>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | chr2 | 71421934 | ||||||
| chr2:71421962
|
T | G | 1 | a0003c0004t0001g0259 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.3300-852T>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | chr2 | 71421962 | ||||||
| chr2:71422013
|
A | G | 1 | a0001c0005t0001g0161 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3300-801A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | chr2 | 71422013 | ||||||
| chr2:71422236
|
A | G | 1 | a0002c0002t0001g0262 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.3300-578A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | chr2 | 71422236 | ||||||
| chr2:71422308
|
A | G | 1 | a0003c0004t0002g0203 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3300-506A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | chr2 | 71422308 | ||||||
| chr2:71422444
|
A | G | 1 | a0002c0002t0001g0314 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.3300-370A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | chr2 | 71422444 | ||||||
| chr2:71422595
|
T | C | 83 | a0001c0003t0001g0104a0001c0003t0001g0105a0001c0003t0001g0106others(80): Show | 83 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.3300-219T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 21/27 | chr2 | 71422595 | ||||||
| chr2:71424176
|
T | C | 1 | a0002c0002t0001g0185 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.4524+138T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 22/27 | chr2 | 71424176 | ||||||
| chr2:71424291
|
TA | T | 12 | a0001c0001t0001g0013a0001c0001t0001g0026a0001c0001t0001g0027others(9): Show | 12 | HG00738.hp2 HG01069.hp1 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.4524+270delA | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr2 | 71424291 | |||||
| chr2:71424291
|
TAAAAAAA others(1): Show |
T | 7 | a0001c0007t0001g0327a0001c0007t0001g0328a0001c0007t0001g0329others(4): Show | 7 | HG01884.hp2 HG02451.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.4524+263_4524+270d others(10): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr2 | 71424291 | |||||
| chr2:71424292
|
A | T | 2 | a0001c0003t0001g0115a0001c0003t0001g0116 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.4524+254A>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 22/27 | chr2 | 71424292 | ||||||
| chr2:71424460
|
A | G | 1 | a0002c0002t0001g0312 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.4525-190A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 22/27 | chr2 | 71424460 | ||||||
| chr2:71424467
|
C | G | 224 | a0001c0003t0001g0104a0001c0003t0001g0105a0001c0003t0001g0106others(221): Show | 224 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(221): Show |
intron_variant | MODIFIER | c.4525-183C>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 22/27 | chr2 | 71424467 | ||||||
| chr2:71424561
|
G | GT | 61 | a0001c0003t0001g0112a0001c0003t0001g0113a0002c0002t0001g0183others(58): Show | 61 | HG00323.hp1 HG00423.hp2 HG00733.hp2 others(58): Show |
intron_variant | MODIFIER | c.4525-80dupT | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr2 | 71424561 | |||||
| chr2:71424579
|
T | G | 6 | a0001c0003t0001g0112a0001c0003t0001g0113a0001c0003t0001g0118others(3): Show | 6 | HG01099.hp2 HG02258.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.4525-71T>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 22/27 | chr2 | 71424579 | ||||||
| chr2:71424587
|
T | C | 1 | a0001c0001t0001g0057 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.4525-63T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 22/27 | chr2 | 71424587 | ||||||
| chr2:71424809
|
T | A | 232 | a0001c0003t0001g0104a0001c0003t0001g0105a0001c0003t0001g0106others(229): Show | 232 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(229): Show |
intron_variant | MODIFIER | c.4590+94T>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 23/27 | chr2 | 71424809 | ||||||
| chr2:71424998
|
A | G | 1 | a0001c0003t0001g0171 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.4590+283A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 23/27 | chr2 | 71424998 | ||||||
| chr2:71425020
|
G | A | 61 | a0001c0003t0001g0108a0001c0003t0001g0109a0001c0003t0001g0111others(58): Show | 61 | HG00280.hp1 HG00733.hp1 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.4590+305G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 23/27 | chr2 | 71425020 | ||||||
| chr2:71425084
|
G | A | 11 | a0002c0002t0001g0179a0002c0002t0001g0180a0002c0002t0001g0184others(8): Show | 11 | HG01069.hp2 HG01074.hp1 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.4590+369G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 23/27 | chr2 | 71425084 | ||||||
| chr2:71425087
|
A | G | 1 | a0003c0004t0002g0219 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.4590+372A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 23/27 | chr2 | 71425087 | ||||||
| chr2:71425118
|
C | G | 1 | a0001c0003t0001g0114 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.4590+403C>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 23/27 | chr2 | 71425118 | ||||||
| chr2:71425135
|
C | CT | 6 | a0003c0004t0002g0248a0003c0004t0002g0249a0003c0004t0002g0250others(3): Show | 6 | HG02818.hp1 HG03139.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.4590+421dupT | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr2 | 71425135 | |||||
| chr2:71425149
|
A | G | 1 | a0001c0003t0001g0108 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.4590+434A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 23/27 | chr2 | 71425149 | ||||||
| chr2:71425283
|
G | A | 2 | a0009c0013t0001g0102a0009c0013t0001g0103 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.4590+568G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 23/27 | chr2 | 71425283 | ||||||
| chr2:71425294
|
A | G | 1 | a0018c0027t0001g0201 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.4590+579A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 23/27 | chr2 | 71425294 | ||||||
| chr2:71425307
|
TAAGCAGA others(20): Show |
T | 3 | a0002c0002t0001g0263a0002c0002t0001g0343a0002c0002t0001g0344 | 3 | NA18972.hp1 NA18978.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.4590+628_4590+654d others(29): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr2 | 71425307 | |||||
| chr2:71425316
|
A | ATAAGGAT others(20): Show |
1 | a0003c0004t0002g0205 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.4590+627_4590+628i others(29): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr2 | 71425316 | |||||
| chr2:71425343
|
A | G | 229 | a0001c0003t0001g0104a0001c0003t0001g0105a0001c0003t0001g0106others(226): Show | 229 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(226): Show |
intron_variant | MODIFIER | c.4590+628A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 23/27 | chr2 | 71425343 | ||||||
| chr2:71425540
|
T | C | 1 | a0002c0002t0001g0319 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.4590+825T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 23/27 | chr2 | 71425540 | ||||||
| chr2:71425608
|
T | C | 1 | a0001c0001t0001g0004 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.4591-852T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 23/27 | chr2 | 71425608 | ||||||
| chr2:71425820
|
A | T | 24 | a0002c0002t0001g0177a0002c0002t0001g0178a0002c0002t0001g0179others(21): Show | 24 | HG00438.hp1 HG01069.hp2 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.4591-640A>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 23/27 | chr2 | 71425820 | ||||||
| chr2:71425861
|
C | T | 7 | a0001c0007t0001g0327a0001c0007t0001g0328a0001c0007t0001g0329others(4): Show | 7 | HG01884.hp2 HG02451.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.4591-599C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 23/27 | chr2 | 71425861 | ||||||
| chr2:71425933
|
G | C | 1 | a0001c0001t0001g0070 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.4591-527G>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 23/27 | chr2 | 71425933 | ||||||
| chr2:71425977
|
C | T | 1 | a0002c0002t0001g0187 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.4591-483C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 23/27 | chr2 | 71425977 | ||||||
| chr2:71426130
|
C | G | 46 | a0003c0004t0001g0259a0003c0004t0002g0003a0003c0004t0002g0202others(43): Show | 46 | HG00323.hp1 HG00423.hp2 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.4591-330C>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 23/27 | chr2 | 71426130 | ||||||
| chr2:71426148
|
A | G | 1 | a0002c0002t0001g0263 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.4591-312A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 23/27 | chr2 | 71426148 | ||||||
| chr2:71426246
|
T | G | 46 | a0001c0003t0001g0108a0001c0003t0001g0109a0001c0003t0001g0111others(43): Show | 46 | HG00280.hp1 HG00733.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.4591-214T>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 23/27 | chr2 | 71426246 | ||||||
| chr2:71426406
|
C | G | 1 | a0002c0002t0001g0188 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.4591-54C>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 23/27 | chr2 | 71426406 | ||||||
| chr2:71427482
|
A | G | 3 | a0001c0003t0001g0118a0001c0003t0001g0120a0001c0003t0001g0121 | 3 | HG01099.hp2 HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.5545+68A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 24/27 | chr2 | 71427482 | ||||||
| chr2:71427607
|
C | T | 1 | a0001c0003t0001g0140 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.5545+193C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 24/27 | chr2 | 71427607 | ||||||
| chr2:71427850
|
C | CG | 12 | a0001c0005t0001g0122a0001c0005t0001g0152a0001c0005t0001g0153others(9): Show | 12 | HG01243.hp2 HG01891.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.5545+438dupG | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr2 | 71427850 | |||||
| chr2:71427854
|
A | G | 66 | a0002c0002t0001g0254a0002c0002t0001g0255a0002c0002t0001g0256others(63): Show | 66 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(63): Show |
intron_variant | MODIFIER | c.5545+440A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 24/27 | chr2 | 71427854 | ||||||
| chr2:71427865
|
C | T | 2 | a0002c0002t0001g0183a0014c0021t0001g0181 | 2 | HG01109.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.5545+451C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 24/27 | chr2 | 71427865 | ||||||
| chr2:71427866
|
G | A | 3 | a0004c0006t0001g0260a0004c0006t0001g0261a0004c0006t0001g0283 | 3 | NA18954.hp2 NA18992.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.5545+452G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 24/27 | chr2 | 71427866 | ||||||
| chr2:71427914
|
A | G | 71 | a0002c0002t0001g0254a0002c0002t0001g0255a0002c0002t0001g0256others(68): Show | 71 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.5545+500A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 24/27 | chr2 | 71427914 | ||||||
| chr2:71427957
|
C | T | 5 | a0001c0003t0001g0115a0001c0003t0001g0116a0001c0003t0001g0171others(2): Show | 5 | HG01167.hp1 HG01169.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.5545+543C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 24/27 | chr2 | 71427957 | ||||||
| chr2:71428058
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.5546-489G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 24/27 | chr2 | 71428058 | ||||||
| chr2:71428065
|
G | A | 1 | a0001c0001t0001g0338 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.5546-482G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 24/27 | chr2 | 71428065 | ||||||
| chr2:71428173
|
C | T | 2 | a0009c0013t0001g0102a0009c0013t0001g0103 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.5546-374C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 24/27 | chr2 | 71428173 | ||||||
| chr2:71428317
|
A | G | 1 | a0001c0001t0001g0070 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.5546-230A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 24/27 | chr2 | 71428317 | ||||||
| chr2:71428373
|
A | G | 1 | a0001c0001t0001g0017 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.5546-174A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 24/27 | chr2 | 71428373 | ||||||
| chr2:71428427
|
C | T | 1 | a0018c0027t0001g0201 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.5546-120C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 24/27 | chr2 | 71428427 | ||||||
| chr2:71428456
|
T | A | 52 | a0003c0004t0001g0259a0003c0004t0002g0003a0003c0004t0002g0202others(49): Show | 52 | HG00323.hp1 HG00423.hp2 HG00733.hp2 others(49): Show |
intron_variant | MODIFIER | c.5546-91T>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 24/27 | chr2 | 71428456 | ||||||
| chr2:71428691
|
A | G | 3 | a0001c0001t0001g0065a0001c0001t0001g0067a0001c0003t0001g0146 | 3 | HG01070.hp2 HG01175.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.5650+40A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 25/27 | chr2 | 71428691 | ||||||
| chr2:71428696
|
G | T | 1 | a0003c0004t0002g0226 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.5650+45G>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 25/27 | chr2 | 71428696 | ||||||
| chr2:71428786
|
T | C | 1 | a0001c0001t0001g0092 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.5650+135T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 25/27 | chr2 | 71428786 | ||||||
| chr2:71428839
|
T | C | 2 | a0009c0013t0001g0102a0009c0013t0001g0103 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.5650+188T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 25/27 | chr2 | 71428839 | ||||||
| chr2:71429285
|
A | G | 1 | a0001c0001t0001g0021 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.5650+634A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 25/27 | chr2 | 71429285 | ||||||
| chr2:71429385
|
A | G | 2 | a0002c0002t0001g0276a0002c0002t0001g0299 | 2 | HG02155.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.5650+734A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 25/27 | chr2 | 71429385 | ||||||
| chr2:71429414
|
C | T | 97 | a0001c0003t0001g0108a0001c0003t0001g0109a0001c0003t0001g0111others(94): Show | 97 | HG00280.hp1 HG00438.hp1 HG00733.hp1 others(94): Show |
intron_variant | MODIFIER | c.5650+763C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 25/27 | chr2 | 71429414 | ||||||
| chr2:71429418
|
C | A | 52 | a0003c0004t0001g0259a0003c0004t0002g0003a0003c0004t0002g0202others(49): Show | 52 | HG00323.hp1 HG00423.hp2 HG00733.hp2 others(49): Show |
intron_variant | MODIFIER | c.5650+767C>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 25/27 | chr2 | 71429418 | ||||||
| chr2:71429419
|
C | A | 52 | a0003c0004t0001g0259a0003c0004t0002g0003a0003c0004t0002g0202others(49): Show | 52 | HG00323.hp1 HG00423.hp2 HG00733.hp2 others(49): Show |
intron_variant | MODIFIER | c.5650+768C>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 25/27 | chr2 | 71429419 | ||||||
| chr2:71429617
|
T | G | 1 | a0002c0002t0001g0177 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.5650+966T>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 25/27 | chr2 | 71429617 | ||||||
| chr2:71429786
|
A | C | 1 | a0001c0001t0001g0026 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.5650+1135A>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 25/27 | chr2 | 71429786 | ||||||
| chr2:71429798
|
C | T | 1 | a0002c0002t0001g0277 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.5650+1147C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 25/27 | chr2 | 71429798 | ||||||
| chr2:71430036
|
C | T | 2 | a0008c0010t0002g0342a0008c0010t0004g0253 | 2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.5651-1291C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 25/27 | chr2 | 71430036 | ||||||
| chr2:71430038
|
G | A | 94 | a0001c0003t0001g0108a0001c0003t0001g0109a0001c0003t0001g0111others(91): Show | 94 | HG00280.hp1 HG00438.hp1 HG00733.hp1 others(91): Show |
intron_variant | MODIFIER | c.5651-1289G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 25/27 | chr2 | 71430038 | ||||||
| chr2:71430111
|
A | G | 1 | a0008c0010t0002g0342 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.5651-1216A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 25/27 | chr2 | 71430111 | ||||||
| chr2:71430177
|
A | T | 1 | a0002c0002t0001g0178 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.5651-1150A>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 25/27 | chr2 | 71430177 | ||||||
| chr2:71430178
|
A | G | 1 | a0001c0001t0001g0340 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.5651-1149A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 25/27 | chr2 | 71430178 | ||||||
| chr2:71430245
|
G | C | 1 | a0001c0003t0001g0144 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.5651-1082G>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 25/27 | chr2 | 71430245 | ||||||
| chr2:71430396
|
A | G | 3 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028 | 3 | HG00738.hp2 HG04199.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.5651-931A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 25/27 | chr2 | 71430396 | ||||||
| chr2:71430626
|
A | G | 9 | a0001c0003t0001g0109a0001c0003t0001g0132a0001c0003t0001g0133others(6): Show | 9 | HG00735.hp1 HG01243.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.5651-701A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 25/27 | chr2 | 71430626 | ||||||
| chr2:71430738
|
T | TACTGAGG others(19): Show |
1 | a0001c0001t0001g0085 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.5651-587_5651-562d others(28): Show |
ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr2 | 71430738 | |||||
| chr2:71430740
|
C | T | 4 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(1): Show | 4 | HG02735.hp1 HG03669.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.5651-587C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 25/27 | chr2 | 71430740 | ||||||
| chr2:71430758
|
G | C | 60 | a0001c0003t0001g0108a0001c0003t0001g0109a0001c0003t0001g0111others(57): Show | 60 | HG00280.hp1 HG00733.hp1 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.5651-569G>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 25/27 | chr2 | 71430758 | ||||||
| chr2:71430881
|
C | G | 61 | a0001c0003t0001g0108a0001c0003t0001g0109a0001c0003t0001g0111others(58): Show | 61 | HG00280.hp1 HG00733.hp1 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.5651-446C>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 25/27 | chr2 | 71430881 | ||||||
| chr2:71430887
|
T | A | 263 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(260): Show | 263 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(260): Show |
intron_variant | MODIFIER | c.5651-440T>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 25/27 | chr2 | 71430887 | ||||||
| chr2:71431005
|
G | A | 2 | a0003c0004t0002g0209a0003c0004t0002g0236 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.5651-322G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 25/27 | chr2 | 71431005 | ||||||
| chr2:71431036
|
C | G | 26 | a0002c0002t0001g0177a0002c0002t0001g0178a0002c0002t0001g0179others(23): Show | 26 | HG00438.hp1 HG01069.hp2 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.5651-291C>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 25/27 | chr2 | 71431036 | ||||||
| chr2:71431056
|
A | G | 8 | a0003c0004t0002g0003a0003c0004t0002g0208a0003c0004t0002g0210others(5): Show | 8 | NA18951.hp2 NA18956.hp1 NA18963.hp2 others(5): Show |
intron_variant | MODIFIER | c.5651-271A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 25/27 | chr2 | 71431056 | ||||||
| chr2:71431070
|
G | A | 11 | a0001c0005t0001g0152a0001c0005t0001g0153a0001c0005t0001g0154others(8): Show | 11 | HG01243.hp2 HG01891.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.5651-257G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 25/27 | chr2 | 71431070 | ||||||
| chr2:71431206
|
C | T | 1 | a0001c0003t0001g0117 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.5651-121C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 25/27 | chr2 | 71431206 | ||||||
| chr2:71431234
|
C | T | 46 | a0003c0004t0001g0259a0003c0004t0002g0003a0003c0004t0002g0202others(43): Show | 46 | HG00323.hp1 HG00423.hp2 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.5651-93C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 25/27 | chr2 | 71431234 | ||||||
| chr2:71431303
|
C | G | 1 | a0001c0001t0001g0326 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.5651-24C>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 25/27 | chr2 | 71431303 | ||||||
| chr2:71431477
|
C | T | 1 | a0001c0003t0001g0132 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.5752+49C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 26/27 | chr2 | 71431477 | ||||||
| chr2:71431633
|
G | A | 1 | a0001c0001t0001g0075 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.5752+205G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 26/27 | chr2 | 71431633 | ||||||
| chr2:71431676
|
C | T | 1 | a0001c0001t0001g0055 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.5752+248C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 26/27 | chr2 | 71431676 | ||||||
| chr2:71431684
|
C | T | 46 | a0003c0004t0001g0259a0003c0004t0002g0003a0003c0004t0002g0202others(43): Show | 46 | HG00323.hp1 HG00423.hp2 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.5752+256C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 26/27 | chr2 | 71431684 | ||||||
| chr2:71431741
|
C | T | 1 | a0003c0004t0002g0202 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.5752+313C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 26/27 | chr2 | 71431741 | ||||||
| chr2:71431759
|
C | CA | 34 | a0001c0001t0001g0052a0001c0001t0001g0059a0001c0001t0001g0065others(31): Show | 34 | HG00544.hp1 HG00741.hp2 HG01099.hp1 others(31): Show |
intron_variant | MODIFIER | c.5752+346dupA | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 26/27 | INFO_REALIGN_3_PRIME | chr2 | 71431759 | |||||
| chr2:71431759
|
CA | C | 51 | a0001c0003t0001g0109a0001c0003t0001g0111a0001c0003t0001g0114others(48): Show | 51 | HG00280.hp1 HG00438.hp1 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.5752+346delA | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 26/27 | INFO_REALIGN_3_PRIME | chr2 | 71431759 | |||||
| chr2:71431768
|
A | C | 9 | a0001c0001t0001g0326a0001c0001t0001g0334a0001c0001t0001g0335others(6): Show | 9 | HG01884.hp1 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.5752+340A>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 26/27 | chr2 | 71431768 | ||||||
| chr2:71431980
|
T | G | 1 | a0003c0004t0002g0248 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.5752+552T>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 26/27 | chr2 | 71431980 | ||||||
| chr2:71432209
|
A | G | 1 | a0001c0001t0001g0060 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.5752+781A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 26/27 | chr2 | 71432209 | ||||||
| chr2:71432273
|
T | C | 1 | a0001c0005t0001g0155 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.5752+845T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 26/27 | chr2 | 71432273 | ||||||
| chr2:71432345
|
C | T | 2 | a0001c0001t0001g0334a0001c0001t0001g0335 | 2 | HG02630.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.5753-820C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 26/27 | chr2 | 71432345 | ||||||
| chr2:71432691
|
T | TA | 37 | a0001c0003t0001g0108a0001c0003t0001g0109a0001c0003t0001g0111others(34): Show | 37 | HG00280.hp1 HG00735.hp1 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.5753-473dupA | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 26/27 | INFO_REALIGN_3_PRIME | chr2 | 71432691 | |||||
| chr2:71432717
|
A | G | 2 | a0001c0005t0001g0157a0001c0005t0001g0158 | 2 | HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.5753-448A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 26/27 | chr2 | 71432717 | ||||||
| chr2:71432790
|
T | C | 12 | a0001c0003t0001g0104a0001c0003t0001g0105a0001c0003t0001g0106others(9): Show | 12 | HG02055.hp1 HG02145.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.5753-375T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 26/27 | chr2 | 71432790 | ||||||
| chr2:71433042
|
G | A | 1 | a0002c0002t0001g0344 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.5753-123G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 26/27 | chr2 | 71433042 | ||||||
| chr2:71433358
|
G | A | 1 | a0003c0004t0002g0203 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.5871+75G>A | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 27/27 | chr2 | 71433358 | ||||||
| chr2:71433365
|
T | TC | 56 | a0003c0004t0001g0259a0003c0004t0002g0003a0003c0004t0002g0202others(53): Show | 56 | HG00323.hp1 HG00423.hp2 HG00733.hp2 others(53): Show |
intron_variant | MODIFIER | c.5871+88dupC | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr2 | 71433365 | |||||
| chr2:71433674
|
C | T | 225 | a0001c0003t0001g0104a0001c0003t0001g0105a0001c0003t0001g0106others(222): Show | 225 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(222): Show |
intron_variant | MODIFIER | c.5871+391C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 27/27 | chr2 | 71433674 | ||||||
| chr2:71433684
|
C | T | 2 | a0008c0010t0002g0342a0008c0010t0004g0253 | 2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.5871+401C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 27/27 | chr2 | 71433684 | ||||||
| chr2:71433983
|
C | T | 1 | a0003c0004t0002g0228 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.5871+700C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 27/27 | chr2 | 71433983 | ||||||
| chr2:71434105
|
C | G | 1 | a0003c0004t0002g0211 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.5872-637C>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 27/27 | chr2 | 71434105 | ||||||
| chr2:71434189
|
T | G | 1 | a0008c0010t0004g0253 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.5872-553T>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 27/27 | chr2 | 71434189 | ||||||
| chr2:71434292
|
C | T | 225 | a0001c0003t0001g0104a0001c0003t0001g0105a0001c0003t0001g0106others(222): Show | 225 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(222): Show |
intron_variant | MODIFIER | c.5872-450C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 27/27 | chr2 | 71434292 | ||||||
| chr2:71434343
|
G | C | 4 | a0001c0003t0001g0118a0001c0003t0001g0119a0001c0003t0001g0120others(1): Show | 4 | HG01099.hp2 HG02258.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.5872-399G>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 27/27 | chr2 | 71434343 | ||||||
| chr2:71434388
|
T | C | 2 | a0008c0010t0002g0342a0008c0010t0004g0253 | 2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.5872-354T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 27/27 | chr2 | 71434388 | ||||||
| chr2:71434397
|
A | G | 4 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(1): Show | 4 | HG02735.hp1 HG03669.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.5872-345A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 27/27 | chr2 | 71434397 | ||||||
| chr2:71434433
|
C | T | 1 | a0002c0002t0001g0180 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.5872-309C>T | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 27/27 | chr2 | 71434433 | ||||||
| chr2:71434438
|
C | G | 13 | a0001c0003t0001g0104a0001c0003t0001g0105a0001c0003t0001g0106others(10): Show | 13 | HG02055.hp1 HG02145.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.5872-304C>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 27/27 | chr2 | 71434438 | ||||||
| chr2:71434499
|
T | C | 85 | a0001c0003t0001g0104a0001c0003t0001g0105a0001c0003t0001g0106others(82): Show | 85 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.5872-243T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 27/27 | chr2 | 71434499 | ||||||
| chr2:71434571
|
A | G | 1 | a0002c0002t0001g0263 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.5872-171A>G | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 27/27 | chr2 | 71434571 | ||||||
| chr2:71434668
|
T | C | 2 | a0001c0005t0001g0157a0001c0005t0001g0158 | 2 | HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.5872-74T>C | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 27/27 | chr2 | 71434668 | ||||||
| chr2:71434725
|
C | CA | 86 | a0001c0003t0001g0108a0001c0003t0001g0109a0001c0003t0001g0111others(83): Show | 86 | HG00280.hp1 HG00438.hp1 HG00733.hp1 others(83): Show |
intron_variant | MODIFIER | c.5872-14dupA | ZNF638 | ENSG00000075292.19 | transcript | ENST00000264447.9 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr2 | 71434725 |