| geneid | 79776 |
|---|---|
| ensemblid | ENSG00000091656.19 |
| hgncid | 30939 |
| symbol | ZFHX4 |
| name | zinc finger homeobox 4 |
| refseq_nuc | NM_024721.5 |
| refseq_prot | NP_078997.4 |
| ensembl_nuc | ENST00000651372.2 |
| ensembl_prot | ENSP00000498627.1 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 76681247 |
| end | 76867281 |
| strand | + |
| ver | v1.2 |
| region | chr8:76681247-76867281 |
| region5000 | chr8:76676247-76872281 |
| regionname0 | ZFHX4_chr8_76681247_76867281 |
| regionname5000 | ZFHX4_chr8_76676247_76872281 |
| 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 | 1/0 | 3616 | 58 | 8 | 12 | 30 | 2 | 5 | 21 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0002 | 0/0 | 3616 | 43 | 7 | 1 | 33 | 1 | 1 | 23 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0003 | 0/0 | 3615 | 42 | 35 | 1 | 3 | 1 | 2 | 3 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0004 | 0/0 | 2138 | 19 | 3 | 2 | 10 | 0 | 4 | 4 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0005 | 0/0 | 3615 | 14 | 1 | 3 | 10 | 0 | 0 | 9 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0006 | 0/0 | 2137 | 14 | 8 | 2 | 1 | 0 | 3 | 1 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0007 | 0/0 | 2138 | 7 | 0 | 0 | 7 | 0 | 0 | 6 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0008 | 0/0 | 3616 | 6 | 1 | 0 | 5 | 0 | 0 | 3 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0009 | 0/0 | 3616 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0010 | 0/0 | 2137 | 5 | 0 | 2 | 3 | 0 | 0 | 2 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0011 | 0/0 | 3615 | 3 | 0 | 0 | 3 | 0 | 0 | 1 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0012 | 0/0 | 3616 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0013 | 0/0 | 3615 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0014 | 0/0 | 3615 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0015 | 0/1 | 3616 | 2 | 0 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0016 | 0/0 | 3616 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0017 | 0/0 | 3615 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0018 | 0/0 | 3615 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0019 | 0/0 | 3615 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0020 | 0/0 | 3616 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0021 | 0/0 | 3616 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0022 | 0/0 | 3616 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0023 | 0/0 | 3616 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0024 | 0/0 | 3616 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0025 | 0/0 | 3616 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0026 | 0/0 | 3615 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0027 | 0/0 | 3615 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0028 | 0/0 | 3615 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0029 | 0/0 | 3616 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0030 | 0/0 | 2138 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0031 | 0/0 | 3615 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0032 | 0/0 | 2138 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0033 | 0/0 | 2137 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0034 | 0/0 | 3616 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 10851 | 25 | 2 | 1 | 21 | 1 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| c0002 | 0/0 | 10848 | 23 | 20 | 1 | 0 | 0 | 2 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| c0003 | 1/0 | 10851 | 17 | 0 | 3 | 9 | 2 | 2 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| c0004 | 0/0 | 10851 | 13 | 2 | 1 | 7 | 0 | 3 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| c0005 | 0/0 | 10848 | 12 | 1 | 3 | 8 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| c0006 | 0/0 | 10851 | 11 | 3 | 0 | 8 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| c0007 | 0/0 | 10848 | 8 | 7 | 0 | 0 | 1 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| c0008 | 0/0 | 10851 | 8 | 1 | 4 | 3 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| c0009 | 0/0 | 10849 | 5 | 3 | 1 | 0 | 0 | 1 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| c0010 | 0/0 | 10851 | 5 | 0 | 0 | 5 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| c0011 | 0/0 | 10851 | 5 | 5 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| c0012 | 0/0 | 10852 | 5 | 3 | 1 | 0 | 0 | 1 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| c0013 | 0/0 | 10849 | 5 | 0 | 2 | 3 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| c0014 | 0/0 | 10852 | 4 | 0 | 0 | 4 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| c0015 | 0/0 | 10851 | 4 | 2 | 1 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| c0016 | 0/0 | 10849 | 4 | 4 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| c0017 | 0/0 | 10851 | 3 | 0 | 0 | 3 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| c0018 | 0/0 | 10852 | 3 | 0 | 0 | 3 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| c0019 | 0/0 | 10852 | 3 | 0 | 0 | 1 | 0 | 2 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| c0020 | 0/0 | 10848 | 3 | 0 | 0 | 3 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| c0021 | 0/0 | 10851 | 3 | 0 | 0 | 3 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| c0022 | 0/0 | 10852 | 3 | 0 | 1 | 1 | 0 | 1 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| c0023 | 0/0 | 10848 | 2 | 1 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| c0024 | 0/0 | 10851 | 2 | 0 | 0 | 0 | 0 | 2 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| c0025 | 0/0 | 10851 | 2 | 0 | 0 | 2 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| c0026 | 0/0 | 10852 | 2 | 0 | 0 | 2 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| c0027 | 0/0 | 10848 | 2 | 2 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| c0028 | 0/0 | 10851 | 2 | 1 | 0 | 0 | 0 | 1 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| c0029 | 0/0 | 10849 | 2 | 1 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| c0030 | 0/0 | 10852 | 2 | 0 | 0 | 2 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| c0031 | 0/0 | 10851 | 2 | 0 | 0 | 2 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| c0032 | 0/0 | 10848 | 2 | 0 | 0 | 2 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| c0033 | 0/0 | 10851 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| c0034 | 0/0 | 10848 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| c0035 | 0/0 | 10848 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| c0036 | 0/0 | 10851 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| c0037 | 0/0 | 10848 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| c0038 | 0/0 | 10851 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| c0039 | 0/0 | 10848 | 1 | 0 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| c0040 | 0/0 | 10848 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| c0041 | 0/0 | 10848 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| c0042 | 0/0 | 10851 | 1 | 0 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| c0043 | 0/0 | 10848 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| c0044 | 0/0 | 10852 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| c0045 | 0/0 | 10848 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| c0046 | 0/0 | 10852 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| c0047 | 0/0 | 10851 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| c0048 | 0/0 | 10849 | 1 | 0 | 0 | 0 | 0 | 1 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| c0049 | 0/0 | 10848 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| c0050 | 0/0 | 10848 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| c0051 | 0/0 | 10851 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| c0052 | 0/0 | 10851 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| c0053 | 0/0 | 10851 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| c0054 | 0/0 | 10851 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| c0055 | 0/0 | 10851 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| c0056 | 0/1 | 10851 | 1 | 0 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| c0057 | 0/0 | 10848 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| c0058 | 0/0 | 10848 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| c0059 | 0/0 | 10848 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| c0060 | 0/0 | 10848 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| c0061 | 0/0 | 10848 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| c0062 | 0/0 | 10849 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| c0063 | 0/0 | 10851 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| c0064 | 0/0 | 10848 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| c0065 | 0/0 | 10851 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| c0066 | 0/0 | 10848 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| c0067 | 0/0 | 10851 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| c0068 | 0/0 | 10852 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| c0069 | 0/0 | 10851 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| c0070 | 0/0 | 10852 | 1 | 0 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| c0071 | 0/0 | 10851 | 1 | 0 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| c0072 | 0/0 | 10852 | 1 | 0 | 0 | 0 | 0 | 1 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| c0073 | 0/0 | 10849 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| c0074 | 0/0 | 10849 | 1 | 0 | 0 | 0 | 0 | 1 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| c0075 | 0/0 | 10851 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| c0076 | 0/0 | 10851 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| c0077 | 0/0 | 10851 | 1 | 0 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| c0078 | 0/0 | 10851 | 1 | 0 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| c0079 | 0/0 | 10851 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| c0080 | 0/0 | 10851 | 1 | 0 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| c0081 | 0/0 | 10852 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| c0082 | 0/0 | 10848 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| c0083 | 0/0 | 10851 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| c0084 | 0/0 | 10851 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 3138 | 55 | 42 | 4 | 3 | 0 | 6 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| t0002 | 0/1 | 3137 | 51 | 8 | 8 | 26 | 1 | 7 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| t0003 | 0/0 | 3135 | 47 | 2 | 0 | 44 | 1 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| t0004 | 0/0 | 3137 | 25 | 2 | 4 | 19 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| t0005 | 1/0 | 3137 | 24 | 9 | 5 | 5 | 0 | 4 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| t0006 | 0/0 | 3137 | 13 | 4 | 1 | 8 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| t0007 | 0/0 | 3136 | 6 | 5 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| t0008 | 0/0 | 3139 | 4 | 3 | 0 | 0 | 0 | 1 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| t0009 | 0/0 | 3139 | 3 | 0 | 2 | 0 | 1 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| t0010 | 0/0 | 3137 | 3 | 3 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| t0011 | 0/0 | 3138 | 2 | 0 | 2 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| t0012 | 0/0 | 3137 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| t0013 | 0/0 | 3138 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| t0014 | 0/0 | 3138 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| t0015 | 0/0 | 3138 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| t0016 | 0/0 | 3138 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| t0017 | 0/0 | 3134 | 1 | 0 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| t0018 | 0/0 | 3135 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| t0019 | 0/0 | 3137 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| t0020 | 0/0 | 3137 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| t0021 | 0/0 | 3135 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| t0022 | 0/0 | 3138 | 1 | 0 | 0 | 0 | 1 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0042 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0237 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0003 | 1/0 | 10851 | 17 | 0 | 3 | 9 | 2 | 2 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0001c0004 | 0/0 | 10851 | 13 | 2 | 1 | 7 | 0 | 3 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0001c0008 | 0/0 | 10851 | 8 | 1 | 4 | 3 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0001c0015 | 0/0 | 10851 | 4 | 2 | 1 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0001c0017 | 0/0 | 10851 | 3 | 0 | 0 | 3 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0001c0025 | 0/0 | 10851 | 2 | 0 | 0 | 2 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0001c0031 | 0/0 | 10851 | 2 | 0 | 0 | 2 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0001c0033 | 0/0 | 10851 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0001c0042 | 0/0 | 10851 | 1 | 0 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0001c0047 | 0/0 | 10851 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0001c0051 | 0/0 | 10851 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0001c0052 | 0/0 | 10851 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0001c0055 | 0/0 | 10851 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0001c0063 | 0/0 | 10851 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0001c0078 | 0/0 | 10851 | 1 | 0 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0001c0080 | 0/0 | 10851 | 1 | 0 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0002c0001 | 0/0 | 10851 | 25 | 2 | 1 | 21 | 1 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0002c0006 | 0/0 | 10851 | 11 | 3 | 0 | 8 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0002c0021 | 0/0 | 10851 | 3 | 0 | 0 | 3 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0002c0028 | 0/0 | 10851 | 2 | 1 | 0 | 0 | 0 | 1 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0002c0036 | 0/0 | 10851 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0002c0038 | 0/0 | 10851 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0003c0002 | 0/0 | 10848 | 23 | 20 | 1 | 0 | 0 | 2 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0003c0007 | 0/0 | 10848 | 8 | 7 | 0 | 0 | 1 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0003c0027 | 0/0 | 10848 | 2 | 2 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0003c0034 | 0/0 | 10848 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0003c0035 | 0/0 | 10848 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0003c0037 | 0/0 | 10848 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0003c0040 | 0/0 | 10848 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0003c0045 | 0/0 | 10848 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0003c0058 | 0/0 | 10848 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0003c0059 | 0/0 | 10848 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0003c0060 | 0/0 | 10848 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0003c0061 | 0/0 | 10848 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0004c0012 | 0/0 | 10852 | 5 | 3 | 1 | 0 | 0 | 1 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0004c0018 | 0/0 | 10852 | 3 | 0 | 0 | 3 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0004c0019 | 0/0 | 10852 | 3 | 0 | 0 | 1 | 0 | 2 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0004c0022 | 0/0 | 10852 | 3 | 0 | 1 | 1 | 0 | 1 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0004c0026 | 0/0 | 10852 | 2 | 0 | 0 | 2 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0004c0046 | 0/0 | 10852 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0004c0068 | 0/0 | 10852 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0004c0081 | 0/0 | 10852 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0005c0005 | 0/0 | 10848 | 12 | 1 | 3 | 8 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0005c0032 | 0/0 | 10848 | 2 | 0 | 0 | 2 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0006c0009 | 0/0 | 10849 | 5 | 3 | 1 | 0 | 0 | 1 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0006c0016 | 0/0 | 10849 | 4 | 4 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0006c0029 | 0/0 | 10849 | 2 | 1 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0006c0048 | 0/0 | 10849 | 1 | 0 | 0 | 0 | 0 | 1 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0006c0062 | 0/0 | 10849 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0006c0074 | 0/0 | 10849 | 1 | 0 | 0 | 0 | 0 | 1 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0007c0014 | 0/0 | 10852 | 4 | 0 | 0 | 4 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0007c0030 | 0/0 | 10852 | 2 | 0 | 0 | 2 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0007c0044 | 0/0 | 10852 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0008c0010 | 0/0 | 10851 | 5 | 0 | 0 | 5 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0008c0067 | 0/0 | 10851 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0009c0011 | 0/0 | 10851 | 5 | 5 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0009c0069 | 0/0 | 10851 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0010c0013 | 0/0 | 10849 | 5 | 0 | 2 | 3 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0011c0020 | 0/0 | 10848 | 3 | 0 | 0 | 3 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0012c0024 | 0/0 | 10851 | 2 | 0 | 0 | 0 | 0 | 2 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0013c0023 | 0/0 | 10848 | 2 | 1 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0014c0039 | 0/0 | 10848 | 1 | 0 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0014c0050 | 0/0 | 10848 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0015c0056 | 0/1 | 10851 | 1 | 0 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0015c0071 | 0/0 | 10851 | 1 | 0 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0016c0083 | 0/0 | 10851 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0017c0057 | 0/0 | 10848 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0018c0064 | 0/0 | 10848 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0019c0082 | 0/0 | 10848 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0020c0053 | 0/0 | 10851 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0021c0054 | 0/0 | 10851 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0022c0075 | 0/0 | 10851 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0023c0077 | 0/0 | 10851 | 1 | 0 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0024c0079 | 0/0 | 10851 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0025c0076 | 0/0 | 10851 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0026c0041 | 0/0 | 10848 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0027c0066 | 0/0 | 10848 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0028c0043 | 0/0 | 10848 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0029c0065 | 0/0 | 10851 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0030c0070 | 0/0 | 10852 | 1 | 0 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0031c0049 | 0/0 | 10848 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0032c0072 | 0/0 | 10852 | 1 | 0 | 0 | 0 | 0 | 1 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0033c0073 | 0/0 | 10849 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0034c0084 | 0/0 | 10851 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0003t0002 | 0/0 | 13987 | 11 | 0 | 3 | 5 | 1 | 2 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0001c0003t0003 | 0/0 | 13985 | 3 | 0 | 0 | 3 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0001c0003t0005 | 1/0 | 13987 | 1 | 0 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0001c0003t0012 | 0/0 | 13987 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0001c0003t0022 | 0/0 | 13988 | 1 | 0 | 0 | 0 | 1 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0001c0004t0001 | 0/0 | 13988 | 2 | 0 | 0 | 0 | 0 | 2 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0001c0004t0002 | 0/0 | 13987 | 8 | 0 | 1 | 6 | 0 | 1 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0001c0004t0005 | 0/0 | 13987 | 2 | 2 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0001c0004t0019 | 0/0 | 13987 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0001c0008t0005 | 0/0 | 13987 | 8 | 1 | 4 | 3 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0001c0015t0001 | 0/0 | 13988 | 1 | 0 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0001c0015t0005 | 0/0 | 13987 | 3 | 2 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0001c0017t0003 | 0/0 | 13985 | 2 | 0 | 0 | 2 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0001c0017t0021 | 0/0 | 13985 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0001c0025t0002 | 0/0 | 13987 | 2 | 0 | 0 | 2 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0001c0031t0002 | 0/0 | 13987 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0001c0031t0020 | 0/0 | 13987 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0001c0033t0002 | 0/0 | 13987 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0001c0042t0002 | 0/0 | 13987 | 1 | 0 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0001c0047t0016 | 0/0 | 13988 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0001c0051t0002 | 0/0 | 13987 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0001c0052t0001 | 0/0 | 13988 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0001c0055t0002 | 0/0 | 13987 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0001c0063t0001 | 0/0 | 13988 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0001c0078t0006 | 0/0 | 13987 | 1 | 0 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0001c0080t0005 | 0/0 | 13987 | 1 | 0 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0002c0001t0001 | 0/0 | 13988 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0002c0001t0002 | 0/0 | 13987 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0002c0001t0003 | 0/0 | 13985 | 20 | 0 | 0 | 19 | 1 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0002c0001t0004 | 0/0 | 13987 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0002c0001t0010 | 0/0 | 13987 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0002c0001t0017 | 0/0 | 13984 | 1 | 0 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0002c0006t0002 | 0/0 | 13987 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0002c0006t0003 | 0/0 | 13985 | 7 | 0 | 0 | 7 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0002c0006t0004 | 0/0 | 13987 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0002c0006t0010 | 0/0 | 13987 | 2 | 2 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0002c0021t0003 | 0/0 | 13985 | 2 | 0 | 0 | 2 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0002c0021t0018 | 0/0 | 13985 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0002c0028t0002 | 0/0 | 13987 | 1 | 0 | 0 | 0 | 0 | 1 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0002c0028t0003 | 0/0 | 13985 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0002c0036t0003 | 0/0 | 13985 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0002c0038t0002 | 0/0 | 13987 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0003c0002t0001 | 0/0 | 13985 | 18 | 16 | 0 | 0 | 0 | 2 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0003c0002t0005 | 0/0 | 13984 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0003c0002t0006 | 0/0 | 13984 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0003c0002t0008 | 0/0 | 13986 | 2 | 2 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0003c0002t0009 | 0/0 | 13986 | 1 | 0 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0003c0007t0001 | 0/0 | 13985 | 5 | 5 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0003c0007t0005 | 0/0 | 13984 | 2 | 2 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0003c0007t0009 | 0/0 | 13986 | 1 | 0 | 0 | 0 | 1 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0003c0027t0001 | 0/0 | 13985 | 2 | 2 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0003c0034t0001 | 0/0 | 13985 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0003c0035t0013 | 0/0 | 13985 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0003c0037t0002 | 0/0 | 13984 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0003c0040t0001 | 0/0 | 13985 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0003c0045t0004 | 0/0 | 13984 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0003c0058t0001 | 0/0 | 13985 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0003c0059t0006 | 0/0 | 13984 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0003c0060t0001 | 0/0 | 13985 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0003c0061t0001 | 0/0 | 13985 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0004c0012t0002 | 0/0 | 13988 | 5 | 3 | 1 | 0 | 0 | 1 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0004c0018t0002 | 0/0 | 13988 | 3 | 0 | 0 | 3 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0004c0019t0005 | 0/0 | 13988 | 3 | 0 | 0 | 1 | 0 | 2 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0004c0022t0002 | 0/0 | 13988 | 2 | 0 | 0 | 1 | 0 | 1 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0004c0022t0004 | 0/0 | 13988 | 1 | 0 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0004c0026t0006 | 0/0 | 13988 | 2 | 0 | 0 | 2 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0004c0046t0002 | 0/0 | 13988 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0004c0068t0006 | 0/0 | 13988 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0004c0081t0002 | 0/0 | 13988 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0005c0005t0004 | 0/0 | 13984 | 10 | 1 | 1 | 8 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0005c0005t0011 | 0/0 | 13985 | 2 | 0 | 2 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0005c0032t0004 | 0/0 | 13984 | 2 | 0 | 0 | 2 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0006c0009t0001 | 0/0 | 13986 | 4 | 2 | 1 | 0 | 0 | 1 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0006c0009t0006 | 0/0 | 13985 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0006c0016t0001 | 0/0 | 13986 | 3 | 3 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0006c0016t0008 | 0/0 | 13987 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0006c0029t0001 | 0/0 | 13986 | 2 | 1 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0006c0048t0001 | 0/0 | 13986 | 1 | 0 | 0 | 0 | 0 | 1 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0006c0062t0001 | 0/0 | 13986 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0006c0074t0008 | 0/0 | 13987 | 1 | 0 | 0 | 0 | 0 | 1 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0007c0014t0003 | 0/0 | 13986 | 4 | 0 | 0 | 4 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0007c0030t0003 | 0/0 | 13986 | 2 | 0 | 0 | 2 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0007c0044t0003 | 0/0 | 13986 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0008c0010t0006 | 0/0 | 13987 | 5 | 0 | 0 | 5 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0008c0067t0003 | 0/0 | 13985 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0009c0011t0006 | 0/0 | 13987 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0009c0011t0007 | 0/0 | 13986 | 4 | 4 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0009c0069t0007 | 0/0 | 13986 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0010c0013t0004 | 0/0 | 13985 | 5 | 0 | 2 | 3 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0011c0020t0004 | 0/0 | 13984 | 3 | 0 | 0 | 3 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0012c0024t0005 | 0/0 | 13987 | 2 | 0 | 0 | 0 | 0 | 2 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0013c0023t0001 | 0/0 | 13985 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0013c0023t0009 | 0/0 | 13986 | 1 | 0 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0014c0039t0001 | 0/0 | 13985 | 1 | 0 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0014c0050t0015 | 0/0 | 13985 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0015c0056t0002 | 0/1 | 13987 | 1 | 0 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0015c0071t0002 | 0/0 | 13987 | 1 | 0 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0016c0083t0001 | 0/0 | 13988 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0017c0057t0001 | 0/0 | 13985 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0018c0064t0001 | 0/0 | 13985 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0019c0082t0014 | 0/0 | 13985 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0020c0053t0002 | 0/0 | 13987 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0021c0054t0003 | 0/0 | 13985 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0022c0075t0001 | 0/0 | 13988 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0023c0077t0002 | 0/0 | 13987 | 1 | 0 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0024c0079t0002 | 0/0 | 13987 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0025c0076t0002 | 0/0 | 13987 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0026c0041t0005 | 0/0 | 13984 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0027c0066t0003 | 0/0 | 13982 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0028c0043t0001 | 0/0 | 13985 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0029c0065t0003 | 0/0 | 13985 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0030c0070t0007 | 0/0 | 13987 | 1 | 0 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0031c0049t0001 | 0/0 | 13985 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0032c0072t0002 | 0/0 | 13988 | 1 | 0 | 0 | 0 | 0 | 1 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0033c0073t0004 | 0/0 | 13985 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| a0034c0084t0002 | 0/0 | 13987 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | copy fasta | chr8 | 76676247 | 76872281 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0003t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0001c0003t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0001c0003t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0001c0003t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0001c0003t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0001c0003t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0001c0003t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0001c0003t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0001c0003t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0001c0003t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0001c0003t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0001c0003t0003g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0001c0003t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0001c0003t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0001c0003t0005g0237 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0001c0003t0012g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0001c0003t0022g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0001c0004t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0001c0004t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0001c0004t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0001c0004t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0001c0004t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0001c0004t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0001c0004t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0001c0004t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0001c0004t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0001c0004t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0001c0004t0005g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0001c0004t0005g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0001c0004t0019g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0001c0008t0005g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0001c0008t0005g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0001c0008t0005g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0001c0008t0005g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0001c0008t0005g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0001c0008t0005g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0001c0008t0005g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0001c0008t0005g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0001c0015t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0001c0015t0005g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0001c0015t0005g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0001c0015t0005g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0001c0017t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0001c0017t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0001c0017t0021g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0001c0025t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0001c0025t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0001c0031t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0001c0031t0020g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0001c0033t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0001c0042t0002g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0001c0047t0016g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0001c0051t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0001c0052t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0001c0055t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0001c0063t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0001c0078t0006g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0001c0080t0005g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0002c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0002c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0002c0001t0003g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0002c0001t0003g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0002c0001t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0002c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0002c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0002c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0002c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0002c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0002c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0002c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0002c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0002c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0002c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0002c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0002c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0002c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0002c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0002c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0002c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0002c0001t0004g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0002c0001t0010g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0002c0001t0017g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0002c0006t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0002c0006t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0002c0006t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0002c0006t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0002c0006t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0002c0006t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0002c0006t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0002c0006t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0002c0006t0004g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0002c0006t0010g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0002c0006t0010g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0002c0021t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0002c0021t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0002c0021t0018g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0002c0028t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0002c0028t0003g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0002c0036t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0002c0038t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0003c0002t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0003c0002t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0003c0002t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0003c0002t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0003c0002t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0003c0002t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0003c0002t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0003c0002t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0003c0002t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0003c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0003c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0003c0002t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0003c0002t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0003c0002t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0003c0002t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0003c0002t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0003c0002t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0003c0002t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0003c0002t0005g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0003c0002t0006g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0003c0002t0008g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0003c0002t0008g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0003c0002t0009g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0003c0007t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0003c0007t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0003c0007t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0003c0007t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0003c0007t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0003c0007t0005g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0003c0007t0005g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0003c0007t0009g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0003c0027t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0003c0027t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0003c0034t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0003c0035t0013g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0003c0037t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0003c0040t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0003c0045t0004g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0003c0058t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0003c0059t0006g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0003c0060t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0003c0061t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0004c0012t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0004c0012t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0004c0012t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0004c0012t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0004c0012t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0004c0018t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0004c0018t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0004c0018t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0004c0019t0005g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0004c0019t0005g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0004c0019t0005g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0004c0022t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0004c0022t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0004c0022t0004g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0004c0026t0006g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0004c0026t0006g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0004c0046t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0004c0068t0006g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0004c0081t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0005c0005t0004g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0005c0005t0004g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0005c0005t0004g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0005c0005t0004g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0005c0005t0004g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0005c0005t0004g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0005c0005t0004g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0005c0005t0004g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0005c0005t0004g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0005c0005t0004g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0005c0005t0011g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0005c0005t0011g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0005c0032t0004g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0005c0032t0004g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0006c0009t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0006c0009t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0006c0009t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0006c0009t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0006c0009t0006g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0006c0016t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0006c0016t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0006c0016t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0006c0016t0008g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0006c0029t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0006c0029t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0006c0048t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0006c0062t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0006c0074t0008g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0007c0014t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0007c0014t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0007c0014t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0007c0014t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0007c0030t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0007c0030t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0007c0044t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0008c0010t0006g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0008c0010t0006g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0008c0010t0006g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0008c0010t0006g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0008c0010t0006g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0008c0067t0003g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0009c0011t0006g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0009c0011t0007g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0009c0011t0007g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0009c0011t0007g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0009c0011t0007g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0009c0069t0007g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0010c0013t0004g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0010c0013t0004g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0010c0013t0004g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0010c0013t0004g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0010c0013t0004g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0011c0020t0004g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0011c0020t0004g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0011c0020t0004g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0012c0024t0005g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0013c0023t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0013c0023t0009g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0014c0039t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0014c0050t0015g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0015c0056t0002g0042 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0015c0071t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0016c0083t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0017c0057t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0018c0064t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0019c0082t0014g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0020c0053t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0021c0054t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0022c0075t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0023c0077t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0024c0079t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0025c0076t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0026c0041t0005g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0027c0066t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0028c0043t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0029c0065t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0030c0070t0007g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0031c0049t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0032c0072t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0033c0073t0004g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| a0034c0084t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0003 | c0007 | t0009 | g0082 | EUR | GBR | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG00099 | hp2 | a0001 | c0003 | t0022 | g0135 | EUR | GBR | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG00280 | hp1 | a0001 | c0003 | t0002 | g0097 | EUR | FIN | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG00280 | hp2 | a0002 | c0001 | t0003 | g0193 | EUR | FIN | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG00408 | hp1 | a0004 | c0018 | t0002 | g0105 | EAS | CHS | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG00408 | hp2 | a0002 | c0001 | t0003 | g0034 | EAS | CHS | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG00423 | hp1 | a0002 | c0001 | t0003 | g0077 | EAS | CHS | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG00423 | hp2 | a0004 | c0068 | t0006 | g0109 | EAS | CHS | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG00438 | hp1 | a0008 | c0010 | t0006 | g0021 | EAS | CHS | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG00438 | hp2 | a0005 | c0032 | t0004 | g0046 | EAS | CHS | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG00544 | hp1 | a0001 | c0004 | t0019 | g0050 | EAS | CHS | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG00544 | hp2 | a0002 | c0006 | t0003 | g0177 | EAS | CHS | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG00597 | hp1 | a0004 | c0081 | t0002 | g0045 | EAS | CHS | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG00597 | hp2 | a0004 | c0046 | t0002 | g0075 | EAS | CHS | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG00609 | hp1 | a0004 | c0019 | t0005 | g0234 | EAS | CHS | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG00609 | hp2 | a0002 | c0001 | t0003 | g0191 | EAS | CHS | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG00621 | hp1 | a0002 | c0036 | t0003 | g0225 | EAS | CHS | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG00621 | hp2 | a0010 | c0013 | t0004 | g0227 | EAS | CHS | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG00639 | hp1 | a0003 | c0002 | t0009 | g0038 | AMR | PUR | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG00639 | hp2 | a0015 | c0071 | t0002 | g0088 | AMR | PUR | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG00735 | hp1 | a0001 | c0080 | t0005 | g0006 | AMR | PUR | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG00735 | hp2 | a0001 | c0008 | t0005 | g0236 | AMR | PUR | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG01069 | hp1 | a0014 | c0039 | t0001 | g0072 | AMR | PUR | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG01069 | hp2 | a0001 | c0008 | t0005 | g0093 | AMR | PUR | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG01070 | hp1 | a0001 | c0042 | t0002 | g0010 | AMR | PUR | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG01070 | hp2 | a0001 | c0003 | t0002 | g0134 | AMR | PUR | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG01074 | hp1 | a0002 | c0001 | t0017 | g0194 | AMR | PUR | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG01074 | hp2 | a0001 | c0003 | t0002 | g0083 | AMR | PUR | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG01081 | hp1 | a0006 | c0029 | t0001 | g0154 | AMR | PUR | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG01081 | hp2 | a0023 | c0077 | t0002 | g0094 | AMR | PUR | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG01109 | hp1 | a0001 | c0015 | t0001 | g0003 | AMR | PUR | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG01109 | hp2 | a0004 | c0012 | t0002 | g0190 | AMR | PUR | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG01167 | hp1 | a0001 | c0008 | t0005 | g0157 | AMR | PUR | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG01167 | hp2 | a0030 | c0070 | t0007 | g0100 | AMR | PUR | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG01168 | hp1 | a0005 | c0005 | t0011 | g0095 | AMR | PUR | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG01168 | hp2 | a0013 | c0023 | t0009 | g0144 | AMR | PUR | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG01169 | hp1 | a0005 | c0005 | t0011 | g0099 | AMR | PUR | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG01169 | hp2 | a0001 | c0008 | t0005 | g0096 | AMR | PUR | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG01175 | hp1 | a0010 | c0013 | t0004 | g0130 | AMR | PUR | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG01175 | hp2 | a0006 | c0009 | t0001 | g0146 | AMR | PUR | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG01261 | hp1 | a0004 | c0022 | t0004 | g0161 | AMR | CLM | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG01261 | hp2 | a0010 | c0013 | t0004 | g0104 | AMR | CLM | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG01884 | hp1 | a0001 | c0004 | t0005 | g0064 | AFR | ACB | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG01884 | hp2 | a0016 | c0083 | t0001 | g0152 | AFR | ACB | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG01891 | hp1 | a0003 | c0007 | t0001 | g0090 | AFR | ACB | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG01891 | hp2 | a0002 | c0028 | t0003 | g0138 | AFR | ACB | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG01952 | hp1 | a0001 | c0004 | t0002 | g0212 | AMR | PEL | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG01952 | hp2 | a0001 | c0078 | t0006 | g0159 | AMR | PEL | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG01975 | hp1 | a0001 | c0003 | t0002 | g0174 | AMR | PEL | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG01975 | hp2 | a0005 | c0005 | t0004 | g0126 | AMR | PEL | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG02027 | hp1 | a0007 | c0030 | t0003 | g0175 | EAS | KHV | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG02027 | hp2 | a0001 | c0004 | t0002 | g0069 | EAS | KHV | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG02040 | hp1 | a0008 | c0010 | t0006 | g0017 | EAS | KHV | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG02040 | hp2 | a0002 | c0001 | t0003 | g0181 | EAS | KHV | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG02055 | hp1 | a0006 | c0009 | t0001 | g0028 | AFR | ACB | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG02055 | hp2 | a0006 | c0009 | t0006 | g0151 | AFR | ACB | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG02056 | hp1 | a0001 | c0003 | t0002 | g0164 | EAS | KHV | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG02056 | hp2 | a0002 | c0001 | t0003 | g0044 | EAS | KHV | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG02071 | hp1 | a0002 | c0001 | t0003 | g0195 | EAS | KHV | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG02071 | hp2 | a0004 | c0018 | t0002 | g0125 | EAS | KHV | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG02074 | hp1 | a0011 | c0020 | t0004 | g0167 | EAS | KHV | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG02074 | hp2 | a0001 | c0003 | t0003 | g0120 | EAS | KHV | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG02080 | hp1 | a0001 | c0008 | t0005 | g0231 | EAS | KHV | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG02080 | hp2 | a0001 | c0004 | t0002 | g0067 | EAS | KHV | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG02132 | hp1 | a0001 | c0047 | t0016 | g0066 | EAS | KHV | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG02132 | hp2 | a0001 | c0031 | t0020 | g0163 | EAS | KHV | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG02165 | hp1 | a0011 | c0020 | t0004 | g0113 | EAS | CDX | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG02165 | hp2 | a0001 | c0003 | t0012 | g0043 | EAS | CDX | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG02258 | hp1 | a0013 | c0023 | t0001 | g0143 | AFR | ACB | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG02258 | hp2 | a0003 | c0059 | t0006 | g0085 | AFR | ACB | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG02451 | hp1 | a0001 | c0008 | t0005 | g0230 | AFR | ACB | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG02451 | hp2 | a0003 | c0002 | t0001 | g0076 | AFR | ACB | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG02572 | hp1 | a0003 | c0045 | t0004 | g0136 | AFR | GWD | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG02572 | hp2 | a0003 | c0002 | t0001 | g0026 | AFR | GWD | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG02615 | hp1 | a0006 | c0029 | t0001 | g0158 | AFR | GWD | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG02615 | hp2 | a0031 | c0049 | t0001 | g0060 | AFR | GWD | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG02622 | hp1 | a0003 | c0037 | t0002 | g0024 | AFR | GWD | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG02622 | hp2 | a0026 | c0041 | t0005 | g0073 | AFR | GWD | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG02717 | hp1 | a0003 | c0002 | t0001 | g0150 | AFR | GWD | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG02717 | hp2 | a0009 | c0011 | t0007 | g0221 | AFR | GWD | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG02723 | hp1 | a0003 | c0007 | t0001 | g0102 | AFR | GWD | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG02723 | hp2 | a0003 | c0002 | t0008 | g0012 | AFR | GWD | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG02735 | hp1 | a0001 | c0004 | t0002 | g0197 | SAS | PJL | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG02735 | hp2 | a0032 | c0072 | t0002 | g0080 | SAS | PJL | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG02809 | hp1 | a0001 | c0051 | t0002 | g0141 | AFR | GWD | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG02809 | hp2 | a0009 | c0011 | t0007 | g0025 | AFR | GWD | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG02818 | hp1 | a0002 | c0006 | t0010 | g0031 | AFR | GWD | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG02818 | hp2 | a0003 | c0002 | t0001 | g0081 | AFR | GWD | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG02886 | hp1 | a0003 | c0002 | t0006 | g0058 | AFR | GWD | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG02886 | hp2 | a0022 | c0075 | t0001 | g0089 | AFR | GWD | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG02896 | hp1 | a0003 | c0002 | t0001 | g0145 | AFR | GWD | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG02896 | hp2 | a0003 | c0007 | t0005 | g0086 | AFR | GWD | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG02897 | hp1 | a0002 | c0001 | t0010 | g0014 | AFR | GWD | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG02897 | hp2 | a0003 | c0002 | t0001 | g0147 | AFR | GWD | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG02922 | hp1 | a0009 | c0069 | t0007 | g0057 | AFR | ESN | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG02922 | hp2 | a0003 | c0061 | t0001 | g0156 | AFR | ESN | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG02965 | hp1 | a0002 | c0001 | t0001 | g0149 | AFR | ESN | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG02965 | hp2 | a0001 | c0063 | t0001 | g0053 | AFR | ESN | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG02970 | hp1 | a0003 | c0002 | t0001 | g0054 | AFR | ESN | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG02970 | hp2 | a0003 | c0002 | t0005 | g0023 | AFR | ESN | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG02976 | hp1 | a0003 | c0007 | t0001 | g0241 | AFR | ESN | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG02976 | hp2 | a0019 | c0082 | t0014 | g0139 | AFR | ESN | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG03041 | hp1 | a0006 | c0016 | t0001 | g0084 | AFR | GWD | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG03041 | hp2 | a0002 | c0038 | t0002 | g0153 | AFR | GWD | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG03098 | hp1 | a0001 | c0052 | t0001 | g0063 | AFR | MSL | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG03098 | hp2 | a0006 | c0016 | t0008 | g0101 | AFR | MSL | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG03130 | hp1 | a0003 | c0007 | t0001 | g0240 | AFR | ESN | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG03130 | hp2 | a0014 | c0050 | t0015 | g0220 | AFR | ESN | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG03139 | hp1 | a0024 | c0079 | t0002 | g0169 | AFR | ESN | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG03139 | hp2 | a0003 | c0002 | t0001 | g0004 | AFR | ESN | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG03195 | hp1 | a0003 | c0058 | t0001 | g0238 | AFR | ESN | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG03195 | hp2 | a0009 | c0011 | t0007 | g0223 | AFR | ESN | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG03209 | hp1 | a0004 | c0012 | t0002 | g0061 | AFR | MSL | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG03209 | hp2 | a0006 | c0009 | t0001 | g0008 | AFR | MSL | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG03239 | hp1 | a0006 | c0009 | t0001 | g0059 | SAS | PJL | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG03239 | hp2 | a0004 | c0019 | t0005 | g0091 | SAS | PJL | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG03453 | hp1 | a0003 | c0002 | t0001 | g0032 | AFR | MSL | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG03453 | hp2 | a0003 | c0002 | t0001 | g0068 | AFR | MSL | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG03486 | hp1 | a0017 | c0057 | t0001 | g0033 | AFR | MSL | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG03486 | hp2 | a0003 | c0027 | t0001 | g0056 | AFR | MSL | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG03490 | hp1 | a0001 | c0003 | t0002 | g0110 | SAS | PJL | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG03490 | hp2 | a0012 | c0024 | t0005 | g0001 | SAS | PJL | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG03491 | hp1 | a0003 | c0002 | t0001 | g0071 | SAS | PJL | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG03491 | hp2 | a0001 | c0004 | t0001 | g0204 | SAS | PJL | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG03492 | hp1 | a0012 | c0024 | t0005 | g0001 | SAS | PJL | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG03492 | hp2 | a0001 | c0004 | t0001 | g0203 | SAS | PJL | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG03516 | hp1 | a0002 | c0006 | t0002 | g0098 | AFR | ESN | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG03516 | hp2 | a0001 | c0015 | t0005 | g0005 | AFR | ESN | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG03540 | hp1 | a0002 | c0006 | t0010 | g0155 | AFR | GWD | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG03540 | hp2 | a0003 | c0002 | t0001 | g0074 | AFR | GWD | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG03579 | hp1 | a0003 | c0002 | t0001 | g0009 | AFR | MSL | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG03579 | hp2 | a0001 | c0004 | t0005 | g0219 | AFR | MSL | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG03669 | hp1 | a0004 | c0012 | t0002 | g0196 | SAS | PJL | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG03669 | hp2 | a0006 | c0048 | t0001 | g0022 | SAS | PJL | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG04115 | hp1 | a0003 | c0002 | t0001 | g0070 | SAS | STU | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG04115 | hp2 | a0006 | c0074 | t0008 | g0166 | SAS | STU | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG04199 | hp1 | a0002 | c0028 | t0002 | g0202 | SAS | STU | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG04199 | hp2 | a0001 | c0003 | t0002 | g0087 | SAS | STU | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG04228 | hp1 | a0004 | c0019 | t0005 | g0235 | SAS | STU | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG04228 | hp2 | a0004 | c0022 | t0002 | g0242 | SAS | STU | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA18747 | hp1 | a0002 | c0001 | t0003 | g0205 | EAS | CHB | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA18747 | hp2 | a0002 | c0021 | t0018 | g0133 | EAS | CHB | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA18939 | hp1 | a0001 | c0033 | t0002 | g0224 | EAS | JPT | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA18939 | hp2 | a0002 | c0001 | t0003 | g0185 | EAS | JPT | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA18940 | hp1 | a0007 | c0014 | t0003 | g0209 | EAS | JPT | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA18940 | hp2 | a0034 | c0084 | t0002 | g0131 | EAS | JPT | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA18945 | hp1 | a0005 | c0005 | t0004 | g0111 | EAS | JPT | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA18945 | hp2 | a0002 | c0001 | t0003 | g0002 | EAS | JPT | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA18946 | hp1 | a0003 | c0035 | t0013 | g0228 | EAS | JPT | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA18946 | hp2 | a0001 | c0003 | t0002 | g0176 | EAS | JPT | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA18953 | hp1 | a0004 | c0026 | t0006 | g0048 | EAS | JPT | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA18953 | hp2 | a0002 | c0001 | t0003 | g0182 | EAS | JPT | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA18957 | hp1 | a0002 | c0021 | t0003 | g0128 | EAS | JPT | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA18957 | hp2 | a0003 | c0060 | t0001 | g0173 | EAS | JPT | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA18960 | hp1 | a0005 | c0005 | t0004 | g0226 | EAS | JPT | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA18960 | hp2 | a0001 | c0004 | t0002 | g0040 | EAS | JPT | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA18962 | hp1 | a0021 | c0054 | t0003 | g0030 | EAS | JPT | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA18962 | hp2 | a0002 | c0006 | t0003 | g0170 | EAS | JPT | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA18964 | hp1 | a0007 | c0014 | t0003 | g0188 | EAS | JPT | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA18964 | hp2 | a0006 | c0062 | t0001 | g0124 | EAS | JPT | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA18967 | hp1 | a0025 | c0076 | t0002 | g0178 | EAS | JPT | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA18967 | hp2 | a0011 | c0020 | t0004 | g0041 | EAS | JPT | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA18968 | hp1 | a0010 | c0013 | t0004 | g0112 | EAS | JPT | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA18968 | hp2 | a0002 | c0001 | t0002 | g0198 | EAS | JPT | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA18971 | hp1 | a0005 | c0005 | t0004 | g0123 | EAS | JPT | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA18971 | hp2 | a0003 | c0040 | t0001 | g0049 | EAS | JPT | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA18975 | hp1 | a0002 | c0006 | t0003 | g0160 | EAS | JPT | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA18975 | hp2 | a0005 | c0005 | t0004 | g0119 | EAS | JPT | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA18980 | hp1 | a0005 | c0005 | t0004 | g0117 | EAS | JPT | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA18980 | hp2 | a0007 | c0014 | t0003 | g0186 | EAS | JPT | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA18981 | hp1 | a0001 | c0003 | t0002 | g0216 | EAS | JPT | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA18981 | hp2 | a0007 | c0044 | t0003 | g0192 | EAS | JPT | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA18982 | hp1 | a0001 | c0031 | t0002 | g0127 | EAS | JPT | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA18982 | hp2 | a0002 | c0001 | t0003 | g0215 | EAS | JPT | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA18983 | hp1 | a0002 | c0001 | t0004 | g0199 | EAS | JPT | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA18983 | hp2 | a0001 | c0017 | t0003 | g0107 | EAS | JPT | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA18986 | hp1 | a0002 | c0001 | t0003 | g0187 | EAS | JPT | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA18986 | hp2 | a0001 | c0003 | t0002 | g0168 | EAS | JPT | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA18988 | hp1 | a0002 | c0021 | t0003 | g0171 | EAS | JPT | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA18988 | hp2 | a0005 | c0005 | t0004 | g0047 | EAS | JPT | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA18989 | hp1 | a0002 | c0001 | t0003 | g0051 | EAS | JPT | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA18989 | hp2 | a0001 | c0003 | t0002 | g0179 | EAS | JPT | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA18990 | hp1 | a0008 | c0010 | t0006 | g0015 | EAS | JPT | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA18990 | hp2 | a0005 | c0005 | t0004 | g0118 | EAS | JPT | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA18991 | hp1 | a0004 | c0026 | t0006 | g0019 | EAS | JPT | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA18991 | hp2 | a0007 | c0014 | t0003 | g0079 | EAS | JPT | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA18992 | hp1 | a0002 | c0001 | t0003 | g0037 | EAS | JPT | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA18992 | hp2 | a0010 | c0013 | t0004 | g0172 | EAS | JPT | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA18994 | hp1 | a0002 | c0001 | t0003 | g0214 | EAS | JPT | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA18994 | hp2 | a0005 | c0005 | t0004 | g0121 | EAS | JPT | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA18999 | hp1 | a0029 | c0065 | t0003 | g0114 | EAS | JPT | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA18999 | hp2 | a0001 | c0003 | t0003 | g0036 | EAS | JPT | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA19005 | hp1 | a0002 | c0001 | t0003 | g0020 | EAS | JPT | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA19005 | hp2 | a0004 | c0022 | t0002 | g0180 | EAS | JPT | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA19007 | hp1 | a0001 | c0025 | t0002 | g0200 | EAS | JPT | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA19007 | hp2 | a0002 | c0001 | t0003 | g0039 | EAS | JPT | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA19010 | hp1 | a0001 | c0055 | t0002 | g0201 | EAS | JPT | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA19010 | hp2 | a0002 | c0006 | t0003 | g0211 | EAS | JPT | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA19011 | hp1 | a0001 | c0025 | t0002 | g0210 | EAS | JPT | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA19011 | hp2 | a0033 | c0073 | t0004 | g0132 | EAS | JPT | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA19030 | hp1 | a0003 | c0002 | t0001 | g0027 | AFR | LWK | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA19030 | hp2 | a0004 | c0012 | t0002 | g0218 | AFR | LWK | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA19043 | hp1 | a0003 | c0007 | t0001 | g0092 | AFR | LWK | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA19043 | hp2 | a0001 | c0015 | t0005 | g0011 | AFR | LWK | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA19056 | hp1 | a0005 | c0032 | t0004 | g0184 | EAS | JPT | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA19056 | hp2 | a0002 | c0006 | t0003 | g0122 | EAS | JPT | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA19062 | hp1 | a0001 | c0015 | t0005 | g0213 | EAS | JPT | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA19062 | hp2 | a0007 | c0030 | t0003 | g0229 | EAS | JPT | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA19064 | hp1 | a0008 | c0010 | t0006 | g0016 | EAS | JPT | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA19064 | hp2 | a0001 | c0017 | t0021 | g0129 | EAS | JPT | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA19072 | hp1 | a0002 | c0006 | t0003 | g0165 | EAS | JPT | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA19072 | hp2 | a0001 | c0004 | t0002 | g0189 | EAS | JPT | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA19074 | hp1 | a0001 | c0004 | t0002 | g0183 | EAS | JPT | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA19074 | hp2 | a0001 | c0017 | t0003 | g0108 | EAS | JPT | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA19076 | hp1 | a0027 | c0066 | t0003 | g0115 | EAS | JPT | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA19076 | hp2 | a0001 | c0003 | t0003 | g0035 | EAS | JPT | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA19077 | hp1 | a0001 | c0008 | t0005 | g0232 | EAS | JPT | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA19077 | hp2 | a0002 | c0001 | t0003 | g0002 | EAS | JPT | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA19079 | hp1 | a0002 | c0006 | t0004 | g0217 | EAS | JPT | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA19079 | hp2 | a0020 | c0053 | t0002 | g0208 | EAS | JPT | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA19082 | hp1 | a0001 | c0004 | t0002 | g0206 | EAS | JPT | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA19082 | hp2 | a0002 | c0006 | t0003 | g0162 | EAS | JPT | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA19088 | hp1 | a0001 | c0008 | t0005 | g0233 | EAS | JPT | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA19088 | hp2 | a0008 | c0010 | t0006 | g0018 | EAS | JPT | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA19091 | hp1 | a0002 | c0001 | t0003 | g0207 | EAS | JPT | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA19091 | hp2 | a0004 | c0018 | t0002 | g0116 | EAS | JPT | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA19240 | hp1 | a0028 | c0043 | t0001 | g0140 | AFR | YRI | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA19240 | hp2 | a0006 | c0016 | t0001 | g0103 | AFR | YRI | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA20129 | hp1 | a0003 | c0002 | t0001 | g0007 | AFR | ASW | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA20129 | hp2 | a0003 | c0007 | t0005 | g0052 | AFR | ASW | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG02109 | hp1 | a0003 | c0034 | t0001 | g0142 | AFR | ACB | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG02109 | hp2 | a0006 | c0016 | t0001 | g0239 | AFR | ACB | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG02486 | hp1 | a0003 | c0002 | t0001 | g0029 | AFR | ACB | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG02486 | hp2 | a0009 | c0011 | t0007 | g0222 | AFR | ACB | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG03471 | hp1 | a0004 | c0012 | t0002 | g0062 | AFR | MSL | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG03471 | hp2 | a0018 | c0064 | t0001 | g0137 | AFR | MSL | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG06807 | hp1 | a0003 | c0002 | t0008 | g0013 | AFR | USA | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| HG06807 | hp2 | a0003 | c0027 | t0001 | g0055 | AFR | USA | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA20300 | hp1 | a0009 | c0011 | t0006 | g0065 | AFR | USA | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA20300 | hp2 | a0003 | c0002 | t0001 | g0148 | AFR | USA | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA21309 | hp1 | a0005 | c0005 | t0004 | g0078 | AFR | LWK | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| NA21309 | hp2 | a0008 | c0067 | t0003 | g0106 | AFR | LWK | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| homoSapiens_chm13v2 | hp1 | a0015 | c0056 | t0002 | g0042 | REF | REF | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| homoSapiens_grch38 | hp1 | a0001 | c0003 | t0005 | g0237 | REF | REF | ZFHX4_chr8_76676247_76872281 | ZFHX4 | chr8 | 76676247 | 76872281 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:76704284
|
G | C | 2 | a0012a0013 | 4 | HG01168.hp2 HG02258.hp1 HG03490.hp2 others(1): Show |
missense_variant | MODERATE | c.196G>C | p.Val66Leu | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 2/11 | 616/13987 | 196/10851 | 66/3616 | chr8 | 76704284 | ||
| chr8:76704387
|
G | T | 1 | a0034 | 1 | NA18940.hp2 | missense_variant | MODERATE | c.299G>T | p.Cys100Phe | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 2/11 | 719/13987 | 299/10851 | 100/3616 | chr8 | 76704387 | ||
| chr8:76704388
|
C | A | 1 | a0034 | 1 | NA18940.hp2 | stop_gained | HIGH | c.300C>A | p.Cys100* | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 2/11 | 720/13987 | 300/10851 | 100/3616 | chr8 | 76704388 | ||
| chr8:76704390
|
C | A | 1 | a0034 | 1 | NA18940.hp2 | missense_variant | MODERATE | c.302C>A | p.Pro101His | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 2/11 | 722/13987 | 302/10851 | 101/3616 | chr8 | 76704390 | ||
| chr8:76704393
|
A | G | 1 | a0034 | 1 | NA18940.hp2 | missense_variant | MODERATE | c.305A>G | p.Asn102Ser | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 2/11 | 725/13987 | 305/10851 | 102/3616 | chr8 | 76704393 | ||
| chr8:76704398
|
C | T | 1 | a0034 | 1 | NA18940.hp2 | missense_variant | MODERATE | c.310C>T | p.Arg104Cys | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 2/11 | 730/13987 | 310/10851 | 104/3616 | chr8 | 76704398 | ||
| chr8:76704401
|
C | T | 1 | a0034 | 1 | NA18940.hp2 | missense_variant | MODERATE | c.313C>T | p.Leu105Phe | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 2/11 | 733/13987 | 313/10851 | 105/3616 | chr8 | 76704401 | ||
| chr8:76705563
|
C | T | 1 | a0016 | 1 | HG01884.hp2 | missense_variant | MODERATE | c.1475C>T | p.Thr492Ile | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 2/11 | 1895/13987 | 1475/10851 | 492/3616 | chr8 | 76705563 | ||
| chr8:76778394
|
C | T | 1 | a0017 | 1 | HG03486.hp1 | missense_variant | MODERATE | c.3280C>T | p.Leu1094Phe | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/11 | 3700/13987 | 3280/10851 | 1094/3616 | chr8 | 76778394 | ||
| chr8:76842721
|
A | T | 2 | a0011a0033 | 4 | HG02074.hp1 HG02165.hp1 NA18967.hp2 others(1): Show |
missense_variant | MODERATE | c.3461A>T | p.Asp1154Val | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 6/11 | 3881/13987 | 3461/10851 | 1154/3616 | chr8 | 76842721 | ||
| chr8:76849126
|
C | G | 1 | a0018 | 1 | HG03471.hp2 | missense_variant&splice_region_variant | MODERATE | c.3643C>G | p.Gln1215Glu | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 7/11 | 4063/13987 | 3643/10851 | 1215/3616 | chr8 | 76849126 | ||
| chr8:76849683
|
C | T | 2 | a0015a0032 | 3 | HG00639.hp2 HG02735.hp2 homoSapiens_chm13v2.hp1 |
missense_variant | MODERATE | c.3817C>T | p.Pro1273Ser | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 8/11 | 4237/13987 | 3817/10851 | 1273/3616 | chr8 | 76849683 | ||
| chr8:76849695
|
G | A | 1 | a0031 | 1 | HG02615.hp2 | missense_variant | MODERATE | c.3829G>A | p.Glu1277Lys | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 8/11 | 4249/13987 | 3829/10851 | 1277/3616 | chr8 | 76849695 | ||
| chr8:76850948
|
G | A | 1 | a0019 | 1 | HG02976.hp2 | missense_variant | MODERATE | c.4027G>A | p.Val1343Ile | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 10/11 | 4447/13987 | 4027/10851 | 1343/3616 | chr8 | 76850948 | ||
| chr8:76851837
|
C | T | 2 | a0009a0030 | 7 | HG01167.hp2 HG02486.hp2 HG02717.hp2 others(4): Show |
missense_variant | MODERATE | c.4916C>T | p.Ala1639Val | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 10/11 | 5336/13987 | 4916/10851 | 1639/3616 | chr8 | 76851837 | ||
| chr8:76851971
|
G | A | 5 | a0002a0007a0009others(2): Show | 58 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(55): Show |
missense_variant | MODERATE | c.5050G>A | p.Ala1684Thr | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 10/11 | 5470/13987 | 5050/10851 | 1684/3616 | chr8 | 76851971 | ||
| chr8:76852776
|
G | A | 1 | a0020 | 1 | NA19079.hp2 | missense_variant | MODERATE | c.5855G>A | p.Gly1952Asp | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 10/11 | 6275/13987 | 5855/10851 | 1952/3616 | chr8 | 76852776 | ||
| chr8:76852850
|
G | T | 1 | a0028 | 1 | NA19240.hp1 | missense_variant | MODERATE | c.5929G>T | p.Ala1977Ser | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 10/11 | 6349/13987 | 5929/10851 | 1977/3616 | chr8 | 76852850 | ||
| chr8:76852919
|
C | T | 1 | a0029 | 1 | NA18999.hp1 | missense_variant | MODERATE | c.5998C>T | p.Pro2000Ser | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 10/11 | 6418/13987 | 5998/10851 | 2000/3616 | chr8 | 76852919 | ||
| chr8:76853062
|
ACCT | A | 12 | a0003a0005a0011others(9): Show | 70 | HG00099.hp1 HG00438.hp2 HG00639.hp1 others(67): Show |
disruptive_inframe_deletion | MODERATE | c.6162_6164delTCC | p.Pro2055del | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 10/11 | 6582/13987 | 6162/10851 | 2054/3616 | INFO_REALIGN_3_PRIME | chr8 | 76853062 | |
| chr8:76853081
|
CCT | C | 3 | a0006a0010a0033 | 20 | HG00621.hp2 HG01081.hp1 HG01175.hp1 others(17): Show |
frameshift_variant | HIGH | c.6162_6163delTC | p.Pro2057fs | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 10/11 | 6582/13987 | 6162/10851 | 2054/3616 | INFO_REALIGN_3_PRIME | chr8 | 76853081 | |
| chr8:76853083
|
T | TC | 4 | a0004a0007a0030others(1): Show | 28 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(25): Show |
frameshift_variant | HIGH | c.6170dupC | p.Pro2058fs | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 10/11 | 6591/13987 | 6171/10851 | 2057/3616 | INFO_REALIGN_3_PRIME | chr8 | 76853083 | |
| chr8:76853162
|
A | G | 5 | a0005a0010a0011others(2): Show | 24 | HG00438.hp2 HG00621.hp2 HG01168.hp1 others(21): Show |
missense_variant | MODERATE | c.6241A>G | p.Ile2081Val | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 10/11 | 6661/13987 | 6241/10851 | 2081/3616 | chr8 | 76853162 | ||
| chr8:76854327
|
C | T | 1 | a0006 | 1 | HG03669.hp2 | missense_variant | MODERATE | c.7406C>T | p.Pro2469Leu | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 10/11 | 7826/13987 | 7406/10851 | 2469/3616 | chr8 | 76854327 | ||
| chr8:76854358
|
G | A | 1 | a0014 | 2 | HG01069.hp1 HG03130.hp2 |
missense_variant | MODERATE | c.7437G>A | p.Met2479Ile | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 10/11 | 7857/13987 | 7437/10851 | 2479/3616 | chr8 | 76854358 | ||
| chr8:76854866
|
G | A | 1 | a0021 | 1 | NA18962.hp1 | missense_variant | MODERATE | c.7945G>A | p.Val2649Met | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 10/11 | 8365/13987 | 7945/10851 | 2649/3616 | chr8 | 76854866 | ||
| chr8:76855425
|
C | T | 1 | a0022 | 1 | HG02886.hp2 | missense_variant | MODERATE | c.8504C>T | p.Pro2835Leu | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 10/11 | 8924/13987 | 8504/10851 | 2835/3616 | chr8 | 76855425 | ||
| chr8:76855925
|
A | G | 1 | a0007 | 1 | NA18981.hp2 | missense_variant | MODERATE | c.9004A>G | p.Thr3002Ala | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 10/11 | 9424/13987 | 9004/10851 | 3002/3616 | chr8 | 76855925 | ||
| chr8:76856154
|
T | G | 4 | a0005a0010a0011others(1): Show | 23 | HG00438.hp2 HG00621.hp2 HG01168.hp1 others(20): Show |
missense_variant | MODERATE | c.9233T>G | p.Val3078Gly | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 10/11 | 9653/13987 | 9233/10851 | 3078/3616 | chr8 | 76856154 | ||
| chr8:76856228
|
G | A | 1 | a0025 | 1 | NA18967.hp1 | missense_variant | MODERATE | c.9307G>A | p.Gly3103Ser | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 10/11 | 9727/13987 | 9307/10851 | 3103/3616 | chr8 | 76856228 | ||
| chr8:76856262
|
G | A | 1 | a0023 | 1 | HG01081.hp2 | missense_variant | MODERATE | c.9341G>A | p.Gly3114Asp | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 10/11 | 9761/13987 | 9341/10851 | 3114/3616 | chr8 | 76856262 | ||
| chr8:76856276
|
C | A | 2 | a0004a0008 | 9 | HG00423.hp2 HG00438.hp1 HG02040.hp1 others(6): Show |
missense_variant | MODERATE | c.9355C>A | p.Pro3119Thr | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 10/11 | 9775/13987 | 9355/10851 | 3119/3616 | chr8 | 76856276 | ||
| chr8:76863231
|
C | T | 1 | a0026 | 1 | HG02622.hp2 | missense_variant | MODERATE | c.9517C>T | p.Pro3173Ser | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 11/11 | 9937/13987 | 9517/10851 | 3173/3616 | chr8 | 76863231 | ||
| chr8:76863346
|
A | G | 1 | a0024 | 1 | HG03139.hp1 | missense_variant | MODERATE | c.9632A>G | p.Lys3211Arg | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 11/11 | 10052/13987 | 9632/10851 | 3211/3616 | chr8 | 76863346 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:76704307
|
G | A | 1 | a0001c0033 | 1 | NA18939.hp1 | synonymous_variant | LOW | c.219G>A | p.Gln73Gln | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 2/11 | 639/13987 | 219/10851 | 73/3616 | chr8 | 76704307 | ||
| chr8:76704397
|
C | A | 1 | a0034c0084 | 1 | NA18940.hp2 | synonymous_variant | LOW | c.309C>A | p.Ala103Ala | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 2/11 | 729/13987 | 309/10851 | 103/3616 | chr8 | 76704397 | ||
| chr8:76704400
|
C | T | 1 | a0034c0084 | 1 | NA18940.hp2 | synonymous_variant | LOW | c.312C>T | p.Arg104Arg | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 2/11 | 732/13987 | 312/10851 | 104/3616 | chr8 | 76704400 | ||
| chr8:76705585
|
T | C | 1 | a0003c0034 | 1 | HG02109.hp1 | synonymous_variant | LOW | c.1497T>C | p.Asp499Asp | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 2/11 | 1917/13987 | 1497/10851 | 499/3616 | chr8 | 76705585 | ||
| chr8:76705825
|
G | C | 2 | a0002c0036a0003c0035 | 2 | HG00621.hp1 NA18946.hp1 |
synonymous_variant | LOW | c.1737G>C | p.Arg579Arg | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 2/11 | 2157/13987 | 1737/10851 | 579/3616 | chr8 | 76705825 | ||
| chr8:76706326
|
C | T | 1 | a0019c0082 | 1 | HG02976.hp2 | synonymous_variant | LOW | c.2238C>T | p.Pro746Pro | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 2/11 | 2658/13987 | 2238/10851 | 746/3616 | chr8 | 76706326 | ||
| chr8:76706626
|
C | A | 1 | a0003c0037 | 1 | HG02622.hp1 | synonymous_variant | LOW | c.2538C>A | p.Ile846Ile | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 2/11 | 2958/13987 | 2538/10851 | 846/3616 | chr8 | 76706626 | ||
| chr8:76778327
|
T | C | 38 | a0001c0004a0001c0015a0001c0025others(35): Show | 124 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(121): Show |
synonymous_variant | LOW | c.3213T>C | p.His1071His | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/11 | 3633/13987 | 3213/10851 | 1071/3616 | chr8 | 76778327 | ||
| chr8:76833399
|
G | A | 58 | a0001c0008a0001c0015a0001c0017others(55): Show | 179 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(176): Show |
synonymous_variant | LOW | c.3387G>A | p.Ser1129Ser | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/11 | 3807/13987 | 3387/10851 | 1129/3616 | chr8 | 76833399 | ||
| chr8:76842668
|
G | A | 32 | a0001c0017a0001c0042a0001c0051others(29): Show | 73 | HG00099.hp1 HG00639.hp1 HG01069.hp1 others(70): Show |
synonymous_variant | LOW | c.3408G>A | p.Glu1136Glu | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 6/11 | 3828/13987 | 3408/10851 | 1136/3616 | chr8 | 76842668 | ||
| chr8:76849598
|
G | A | 1 | a0003c0058 | 1 | HG03195.hp1 | synonymous_variant | LOW | c.3732G>A | p.Pro1244Pro | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 8/11 | 4152/13987 | 3732/10851 | 1244/3616 | chr8 | 76849598 | ||
| chr8:76849604
|
C | T | 1 | a0006c0048 | 1 | HG03669.hp2 | synonymous_variant | LOW | c.3738C>T | p.Ile1246Ile | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 8/11 | 4158/13987 | 3738/10851 | 1246/3616 | chr8 | 76849604 | ||
| chr8:76850355
|
A | G | 2 | a0001c0055a0004c0081 | 2 | HG00597.hp1 NA19010.hp1 |
synonymous_variant | LOW | c.3957A>G | p.Lys1319Lys | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 9/11 | 4377/13987 | 3957/10851 | 1319/3616 | chr8 | 76850355 | ||
| chr8:76852141
|
A | G | 1 | a0001c0047 | 1 | HG02132.hp1 | synonymous_variant | LOW | c.5220A>G | p.Pro1740Pro | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 10/11 | 5640/13987 | 5220/10851 | 1740/3616 | chr8 | 76852141 | ||
| chr8:76853068
|
T | A | 1 | a0003c0059 | 1 | HG02258.hp2 | synonymous_variant | LOW | c.6147T>A | p.Pro2049Pro | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 10/11 | 6567/13987 | 6147/10851 | 2049/3616 | chr8 | 76853068 | ||
| chr8:76853629
|
C | T | 6 | a0001c0008a0001c0015a0001c0080others(3): Show | 19 | HG00609.hp1 HG00735.hp1 HG00735.hp2 others(16): Show |
synonymous_variant | LOW | c.6708C>T | p.Tyr2236Tyr | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 10/11 | 7128/13987 | 6708/10851 | 2236/3616 | chr8 | 76853629 | ||
| chr8:76853714
|
C | T | 4 | a0004c0026a0004c0068a0008c0010others(1): Show | 9 | HG00423.hp2 HG00438.hp1 HG02040.hp1 others(6): Show |
synonymous_variant | LOW | c.6793C>T | p.Leu2265Leu | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 10/11 | 7213/13987 | 6793/10851 | 2265/3616 | chr8 | 76853714 | ||
| chr8:76854100
|
A | G | 2 | a0015c0071a0032c0072 | 2 | HG00639.hp2 HG02735.hp2 |
synonymous_variant | LOW | c.7179A>G | p.Pro2393Pro | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 10/11 | 7599/13987 | 7179/10851 | 2393/3616 | chr8 | 76854100 | ||
| chr8:76854568
|
A | G | 2 | a0003c0061a0006c0029 | 3 | HG01081.hp1 HG02615.hp1 HG02922.hp2 |
synonymous_variant | LOW | c.7647A>G | p.Gly2549Gly | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 10/11 | 8067/13987 | 7647/10851 | 2549/3616 | chr8 | 76854568 | ||
| chr8:76855561
|
C | T | 29 | a0001c0042a0001c0052a0001c0063others(26): Show | 68 | HG00099.hp1 HG00639.hp1 HG01069.hp1 others(65): Show |
synonymous_variant | LOW | c.8640C>T | p.Gly2880Gly | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 10/11 | 9060/13987 | 8640/10851 | 2880/3616 | chr8 | 76855561 | ||
| chr8:76855693
|
T | C | 4 | a0004c0026a0004c0068a0008c0010others(1): Show | 9 | HG00423.hp2 HG00438.hp1 HG02040.hp1 others(6): Show |
synonymous_variant | LOW | c.8772T>C | p.Asn2924Asn | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 10/11 | 9192/13987 | 8772/10851 | 2924/3616 | chr8 | 76855693 | ||
| chr8:76856054
|
C | A | 4 | a0003c0035a0003c0040a0003c0060others(1): Show | 4 | NA18946.hp1 NA18957.hp2 NA18964.hp2 others(1): Show |
synonymous_variant | LOW | c.9133C>A | p.Arg3045Arg | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 10/11 | 9553/13987 | 9133/10851 | 3045/3616 | chr8 | 76856054 | ||
| chr8:76863470
|
T | C | 1 | a0001c0078 | 1 | HG01952.hp2 | synonymous_variant | LOW | c.9756T>C | p.Gly3252Gly | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 11/11 | 10176/13987 | 9756/10851 | 3252/3616 | chr8 | 76863470 | ||
| chr8:76863506
|
A | G | 1 | a0002c0038 | 1 | HG03041.hp2 | synonymous_variant | LOW | c.9792A>G | p.Pro3264Pro | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 11/11 | 10212/13987 | 9792/10851 | 3264/3616 | chr8 | 76863506 | ||
| chr8:76863797
|
C | T | 1 | a0015c0056 | 1 | homoSapiens_chm13v2.hp1 | synonymous_variant | LOW | c.10083C>T | p.Asn3361Asn | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 11/11 | 10503/13987 | 10083/10851 | 3361/3616 | chr8 | 76863797 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:76681286
|
T | C | 1 | a0001c0003t0012 | 1 | HG02165.hp2 | 5_prime_UTR_variant | MODIFIER | c.-381T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/11 | 22803 | chr8 | 76681286 | |||||
| chr8:76681502
|
T | A | 1 | a0003c0035t0013 | 1 | NA18946.hp1 | 5_prime_UTR_variant | MODIFIER | c.-165T>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/11 | 22587 | chr8 | 76681502 | |||||
| chr8:76681527
|
T | C | 1 | a0019c0082t0014 | 1 | HG02976.hp2 | 5_prime_UTR_variant | MODIFIER | c.-140T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/11 | 22562 | chr8 | 76681527 | |||||
| chr8:76864612
|
TA | T | 69 | a0001c0003t0002a0001c0003t0003a0001c0003t0012others(66): Show | 153 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(150): Show |
3_prime_UTR_variant | MODIFIER | c.*57delA | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 11/11 | 57 | INFO_REALIGN_3_PRIME | chr8 | 76864612 | ||||
| chr8:76864621
|
A | G | 1 | a0001c0003t0022 | 1 | HG00099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*56A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 11/11 | 56 | chr8 | 76864621 | |||||
| chr8:76864767
|
C | T | 1 | a0001c0017t0021 | 1 | NA19064.hp2 | 3_prime_UTR_variant | MODIFIER | c.*202C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 11/11 | 202 | chr8 | 76864767 | |||||
| chr8:76865499
|
C | G | 36 | a0001c0003t0002a0001c0003t0012a0001c0003t0022others(33): Show | 65 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*934C>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 11/11 | 934 | chr8 | 76865499 | |||||
| chr8:76865770
|
A | G | 1 | a0002c0021t0018 | 1 | NA18747.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1205A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 11/11 | 1205 | chr8 | 76865770 | |||||
| chr8:76865883
|
G | T | 10 | a0002c0001t0004a0002c0006t0004a0003c0045t0004others(7): Show | 27 | HG00438.hp2 HG00621.hp2 HG01168.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*1318G>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 11/11 | 1318 | chr8 | 76865883 | |||||
| chr8:76865969
|
T | C | 2 | a0002c0001t0010a0002c0006t0010 | 3 | HG02818.hp1 HG02897.hp1 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1404T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 11/11 | 1404 | chr8 | 76865969 | |||||
| chr8:76866460
|
A | AT | 7 | a0003c0002t0008a0003c0002t0009a0003c0007t0009others(4): Show | 9 | HG00099.hp1 HG00639.hp1 HG01168.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1909dupT | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 11/11 | 1910 | INFO_REALIGN_3_PRIME | chr8 | 76866460 | ||||
| chr8:76866460
|
AT | A | 3 | a0009c0011t0007a0009c0069t0007a0030c0070t0007 | 6 | HG01167.hp2 HG02486.hp2 HG02717.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1909delT | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 11/11 | 1909 | INFO_REALIGN_3_PRIME | chr8 | 76866460 | ||||
| chr8:76866526
|
G | A | 3 | a0003c0002t0009a0003c0007t0009a0013c0023t0009 | 3 | HG00099.hp1 HG00639.hp1 HG01168.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1961G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 11/11 | 1961 | chr8 | 76866526 | |||||
| chr8:76866749
|
C | T | 1 | a0001c0031t0020 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2184C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 11/11 | 2184 | chr8 | 76866749 | |||||
| chr8:76866763
|
CAT | C | 17 | a0001c0003t0003a0001c0017t0003a0001c0017t0021others(14): Show | 50 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*2200_*2201delTA | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 11/11 | 2200 | INFO_REALIGN_3_PRIME | chr8 | 76866763 | ||||
| chr8:76866809
|
G | GA | 105 | a0001c0003t0002a0001c0003t0003a0001c0003t0012others(102): Show | 219 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(216): Show |
3_prime_UTR_variant | MODIFIER | c.*2252dupA | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 11/11 | 2253 | INFO_REALIGN_3_PRIME | chr8 | 76866809 | ||||
| chr8:76866953
|
C | T | 1 | a0014c0050t0015 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2388C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 11/11 | 2388 | chr8 | 76866953 | |||||
| chr8:76867270
|
T | C | 1 | a0001c0004t0019 | 1 | HG00544.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2705T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 11/11 | 2705 | chr8 | 76867270 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:76681897
|
T | C | 3 | a0001c0015t0001g0003a0001c0015t0005g0005a0003c0002t0001g0004 | 3 | HG01109.hp1 HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-47+277T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76681897 | ||||||
| chr8:76681989
|
T | C | 228 | a0001c0003t0002g0083a0001c0003t0002g0087a0001c0003t0002g0097others(225): Show | 230 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.-47+369T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76681989 | ||||||
| chr8:76682032
|
T | C | 1 | a0001c0080t0005g0006 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-47+412T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76682032 | ||||||
| chr8:76682051
|
A | G | 5 | a0001c0033t0002g0224a0002c0036t0003g0225a0003c0035t0013g0228others(2): Show | 5 | HG00621.hp1 HG00621.hp2 NA18939.hp1 others(2): Show |
intron_variant | MODIFIER | c.-47+431A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76682051 | ||||||
| chr8:76682267
|
T | G | 27 | a0001c0015t0005g0011a0001c0042t0002g0010a0002c0001t0003g0020others(24): Show | 27 | HG00438.hp1 HG01070.hp1 HG02040.hp1 others(24): Show |
intron_variant | MODIFIER | c.-47+647T>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76682267 | ||||||
| chr8:76682281
|
T | G | 1 | a0002c0001t0003g0034 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-47+661T>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76682281 | ||||||
| chr8:76682291
|
G | T | 1 | a0002c0001t0003g0034 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-47+671G>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76682291 | ||||||
| chr8:76682292
|
C | A | 1 | a0002c0001t0003g0034 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-47+672C>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76682292 | ||||||
| chr8:76682599
|
C | G | 6 | a0001c0004t0005g0219a0004c0012t0002g0218a0009c0011t0007g0221others(3): Show | 6 | HG02486.hp2 HG02717.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.-47+979C>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76682599 | ||||||
| chr8:76683022
|
C | T | 1 | a0017c0057t0001g0033 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-47+1402C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76683022 | ||||||
| chr8:76683023
|
G | A | 12 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0012g0043others(9): Show | 12 | HG00408.hp2 HG00597.hp1 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.-47+1403G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76683023 | ||||||
| chr8:76683033
|
T | G | 2 | a0005c0005t0004g0047a0005c0032t0004g0046 | 2 | HG00438.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.-47+1413T>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76683033 | ||||||
| chr8:76683091
|
T | G | 1 | a0007c0030t0003g0229 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-47+1471T>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76683091 | ||||||
| chr8:76683232
|
A | AC | 40 | a0001c0003t0002g0216a0001c0004t0001g0203a0001c0004t0001g0204others(37): Show | 41 | HG00280.hp2 HG00597.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.-47+1620dupC | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 76683232 | |||||
| chr8:76683336
|
T | C | 4 | a0001c0004t0019g0050a0002c0001t0003g0051a0003c0040t0001g0049others(1): Show | 4 | HG00544.hp1 NA18953.hp1 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47+1716T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76683336 | ||||||
| chr8:76683407
|
C | A | 73 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0067others(70): Show | 74 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.-47+1787C>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76683407 | ||||||
| chr8:76683554
|
C | A | 2 | a0001c0063t0001g0053a0003c0007t0005g0052 | 2 | HG02965.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-47+1934C>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76683554 | ||||||
| chr8:76683639
|
A | AG | 5 | a0001c0003t0002g0179a0001c0080t0005g0006a0003c0035t0013g0228others(2): Show | 5 | HG00735.hp1 NA18946.hp1 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.-47+2020dupG | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 76683639 | |||||
| chr8:76683640
|
GA | G | 5 | a0001c0033t0002g0224a0001c0078t0006g0159a0002c0006t0003g0160others(2): Show | 5 | HG01261.hp1 HG01952.hp2 NA18939.hp1 others(2): Show |
intron_variant | MODIFIER | c.-47+2021delA | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76683640 | ||||||
| chr8:76683641
|
A | G | 25 | a0001c0003t0002g0164a0001c0003t0002g0168a0001c0003t0002g0174others(22): Show | 25 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(22): Show |
intron_variant | MODIFIER | c.-47+2021A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76683641 | ||||||
| chr8:76683655
|
GGA | G | 140 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0012g0043others(137): Show | 142 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.-47+2053_-47+2054d others(4): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 76683655 | |||||
| chr8:76683703
|
G | GT | 7 | a0001c0003t0002g0179a0002c0001t0003g0214a0002c0006t0003g0177others(4): Show | 7 | HG00544.hp2 NA18946.hp1 NA18989.hp2 others(4): Show |
intron_variant | MODIFIER | c.-47+2096dupT | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 76683703 | |||||
| chr8:76683999
|
A | T | 5 | a0001c0003t0002g0174a0001c0003t0002g0176a0001c0080t0005g0006others(2): Show | 5 | HG00735.hp1 HG01975.hp1 HG02027.hp1 others(2): Show |
intron_variant | MODIFIER | c.-47+2379A>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76683999 | ||||||
| chr8:76684048
|
G | GT | 9 | a0001c0004t0002g0212a0001c0008t0005g0157a0001c0015t0005g0005others(6): Show | 9 | HG01081.hp1 HG01167.hp1 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.-47+2439dupT | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 76684048 | |||||
| chr8:76684051
|
T | G | 1 | a0002c0001t0003g0181 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-47+2431T>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76684051 | ||||||
| chr8:76684116
|
G | A | 36 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0183others(33): Show | 37 | HG00280.hp2 HG00609.hp2 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.-47+2496G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76684116 | ||||||
| chr8:76684246
|
C | T | 1 | a0004c0022t0002g0242 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-47+2626C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76684246 | ||||||
| chr8:76684759
|
A | C | 2 | a0001c0003t0002g0134a0001c0003t0022g0135 | 2 | HG00099.hp2 HG01070.hp2 |
intron_variant | MODIFIER | c.-47+3139A>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76684759 | ||||||
| chr8:76684800
|
G | A | 41 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0183others(38): Show | 42 | HG00280.hp2 HG00609.hp2 HG01074.hp1 others(39): Show |
intron_variant | MODIFIER | c.-47+3180G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76684800 | ||||||
| chr8:76684871
|
T | G | 3 | a0001c0015t0001g0003a0001c0015t0005g0005a0003c0002t0001g0004 | 3 | HG01109.hp1 HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-47+3251T>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76684871 | ||||||
| chr8:76685386
|
T | C | 1 | a0002c0028t0003g0138 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-47+3766T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76685386 | ||||||
| chr8:76685421
|
C | T | 32 | a0001c0003t0002g0110a0001c0003t0003g0120a0001c0017t0003g0107others(29): Show | 32 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.-47+3801C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76685421 | ||||||
| chr8:76685423
|
T | G | 1 | a0010c0013t0004g0104 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-47+3803T>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76685423 | ||||||
| chr8:76685528
|
G | A | 1 | a0019c0082t0014g0139 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-47+3908G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76685528 | ||||||
| chr8:76685529
|
A | G | 1 | a0002c0001t0003g0044 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-47+3909A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76685529 | ||||||
| chr8:76685584
|
T | G | 2 | a0001c0003t0003g0035a0001c0003t0003g0036 | 2 | NA18999.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.-47+3964T>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76685584 | ||||||
| chr8:76685630
|
G | A | 3 | a0003c0002t0001g0054a0003c0027t0001g0055a0003c0027t0001g0056 | 3 | HG02970.hp1 HG03486.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-47+4010G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76685630 | ||||||
| chr8:76685724
|
T | C | 1 | a0028c0043t0001g0140 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-47+4104T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76685724 | ||||||
| chr8:76686175
|
G | A | 27 | a0001c0015t0005g0011a0001c0042t0002g0010a0001c0051t0002g0141others(24): Show | 27 | HG00438.hp1 HG01070.hp1 HG02040.hp1 others(24): Show |
intron_variant | MODIFIER | c.-47+4555G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76686175 | ||||||
| chr8:76686249
|
A | G | 1 | a0002c0038t0002g0153 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-47+4629A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76686249 | ||||||
| chr8:76686629
|
CTTGCTAT others(2): Show |
C | 6 | a0001c0063t0001g0053a0003c0002t0001g0054a0003c0007t0005g0052others(3): Show | 6 | HG02965.hp2 HG02970.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-47+5015_-47+5023d others(11): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 76686629 | |||||
| chr8:76686748
|
T | C | 38 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0183others(35): Show | 39 | HG00280.hp2 HG00609.hp2 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.-47+5128T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76686748 | ||||||
| chr8:76686758
|
G | A | 3 | a0001c0063t0001g0053a0003c0007t0005g0052a0005c0005t0004g0078 | 3 | HG02965.hp2 NA20129.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-47+5138G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76686758 | ||||||
| chr8:76687134
|
T | C | 41 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0183others(38): Show | 42 | HG00280.hp2 HG00609.hp2 HG01074.hp1 others(39): Show |
intron_variant | MODIFIER | c.-47+5514T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76687134 | ||||||
| chr8:76688074
|
A | G | 1 | a0016c0083t0001g0152 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-47+6454A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76688074 | ||||||
| chr8:76688455
|
G | C | 1 | a0032c0072t0002g0080 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-47+6835G>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76688455 | ||||||
| chr8:76688550
|
T | A | 1 | a0001c0008t0005g0230 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-47+6930T>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76688550 | ||||||
| chr8:76688680
|
T | A | 1 | a0003c0034t0001g0142 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-47+7060T>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76688680 | ||||||
| chr8:76688800
|
G | A | 1 | a0001c0051t0002g0141 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-47+7180G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76688800 | ||||||
| chr8:76689117
|
A | C | 1 | a0006c0009t0006g0151 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-47+7497A>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76689117 | ||||||
| chr8:76689181
|
T | C | 2 | a0003c0002t0006g0058a0009c0069t0007g0057 | 2 | HG02886.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-47+7561T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76689181 | ||||||
| chr8:76689276
|
C | G | 41 | a0001c0004t0002g0067a0001c0004t0002g0069a0001c0004t0005g0064others(38): Show | 41 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.-47+7656C>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76689276 | ||||||
| chr8:76689483
|
C | A | 1 | a0028c0043t0001g0140 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-47+7863C>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76689483 | ||||||
| chr8:76690153
|
C | A | 1 | a0001c0031t0020g0163 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-47+8533C>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76690153 | ||||||
| chr8:76690197
|
T | C | 1 | a0006c0009t0001g0059 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-47+8577T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76690197 | ||||||
| chr8:76690302
|
T | A | 25 | a0001c0015t0005g0011a0001c0042t0002g0010a0002c0001t0003g0020others(22): Show | 25 | HG00438.hp1 HG01070.hp1 HG02040.hp1 others(22): Show |
intron_variant | MODIFIER | c.-47+8682T>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76690302 | ||||||
| chr8:76690307
|
A | G | 1 | a0003c0034t0001g0142 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-47+8687A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76690307 | ||||||
| chr8:76690495
|
T | A | 1 | a0004c0018t0002g0105 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-47+8875T>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76690495 | ||||||
| chr8:76690569
|
T | C | 4 | a0001c0008t0005g0231a0001c0008t0005g0232a0001c0008t0005g0233others(1): Show | 4 | HG02080.hp1 NA19062.hp2 NA19077.hp1 others(1): Show |
intron_variant | MODIFIER | c.-47+8949T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76690569 | ||||||
| chr8:76690569
|
T | G | 27 | a0001c0015t0005g0011a0001c0042t0002g0010a0001c0051t0002g0141others(24): Show | 27 | HG00438.hp1 HG01070.hp1 HG02040.hp1 others(24): Show |
intron_variant | MODIFIER | c.-47+8949T>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76690569 | ||||||
| chr8:76690572
|
C | A | 1 | a0001c0003t0002g0164 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-47+8952C>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76690572 | ||||||
| chr8:76690852
|
C | G | 1 | a0009c0011t0007g0223 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-47+9232C>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76690852 | ||||||
| chr8:76691065
|
T | C | 1 | a0008c0067t0003g0106 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-47+9445T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76691065 | ||||||
| chr8:76691190
|
T | C | 1 | a0006c0009t0001g0059 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-47+9570T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76691190 | ||||||
| chr8:76691289
|
T | C | 1 | a0003c0002t0001g0081 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-47+9669T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76691289 | ||||||
| chr8:76691404
|
A | G | 113 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0067others(110): Show | 114 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.-47+9784A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76691404 | ||||||
| chr8:76691431
|
T | A | 1 | a0002c0001t0003g0181 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-47+9811T>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76691431 | ||||||
| chr8:76691484
|
A | T | 46 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0183others(43): Show | 47 | HG00280.hp2 HG00609.hp2 HG01074.hp1 others(44): Show |
intron_variant | MODIFIER | c.-47+9864A>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76691484 | ||||||
| chr8:76691572
|
A | G | 18 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0012g0043others(15): Show | 18 | HG00408.hp2 HG00597.hp1 HG00639.hp1 others(15): Show |
intron_variant | MODIFIER | c.-47+9952A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76691572 | ||||||
| chr8:76691619
|
A | C | 1 | a0003c0034t0001g0142 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-47+9999A>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76691619 | ||||||
| chr8:76691754
|
C | T | 30 | a0001c0003t0002g0164a0001c0003t0002g0168a0001c0003t0002g0174others(27): Show | 30 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.-47+10134C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76691754 | ||||||
| chr8:76691788
|
G | T | 1 | a0010c0013t0004g0227 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-47+10168G>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76691788 | ||||||
| chr8:76691886
|
A | G | 39 | a0001c0004t0002g0067a0001c0004t0002g0069a0001c0004t0005g0064others(36): Show | 39 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.-47+10266A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76691886 | ||||||
| chr8:76691909
|
A | T | 3 | a0001c0015t0001g0003a0001c0015t0005g0005a0003c0002t0001g0004 | 3 | HG01109.hp1 HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-47+10289A>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76691909 | ||||||
| chr8:76691954
|
C | T | 37 | a0001c0003t0002g0110a0001c0003t0003g0120a0001c0017t0003g0107others(34): Show | 37 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.-47+10334C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76691954 | ||||||
| chr8:76692012
|
T | C | 46 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0183others(43): Show | 47 | HG00280.hp2 HG00609.hp2 HG01074.hp1 others(44): Show |
intron_variant | MODIFIER | c.-47+10392T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76692012 | ||||||
| chr8:76692127
|
T | C | 2 | a0005c0005t0011g0099a0030c0070t0007g0100 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-47+10507T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76692127 | ||||||
| chr8:76692177
|
A | C | 1 | a0002c0006t0010g0031 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-47+10557A>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76692177 | ||||||
| chr8:76692420
|
G | A | 2 | a0001c0017t0003g0107a0001c0017t0003g0108 | 2 | NA18983.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.-47+10800G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76692420 | ||||||
| chr8:76692440
|
A | G | 2 | a0003c0002t0006g0058a0009c0069t0007g0057 | 2 | HG02886.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-47+10820A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76692440 | ||||||
| chr8:76692469
|
T | C | 114 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0067others(111): Show | 115 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.-47+10849T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76692469 | ||||||
| chr8:76692717
|
T | G | 1 | a0017c0057t0001g0033 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-47+11097T>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76692717 | ||||||
| chr8:76693099
|
C | T | 1 | a0001c0015t0005g0005 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-46-10944C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76693099 | ||||||
| chr8:76693204
|
A | G | 3 | a0012c0024t0005g0001a0013c0023t0001g0143a0013c0023t0009g0144 | 4 | HG01168.hp2 HG02258.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.-46-10839A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76693204 | ||||||
| chr8:76693227
|
A | G | 1 | a0017c0057t0001g0033 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-46-10816A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76693227 | ||||||
| chr8:76693237
|
A | G | 1 | a0001c0025t0002g0210 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-46-10806A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76693237 | ||||||
| chr8:76693516
|
C | CGT | 20 | a0001c0004t0002g0067a0001c0004t0002g0069a0001c0004t0005g0064others(17): Show | 20 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(17): Show |
intron_variant | MODIFIER | c.-46-10518_-46-1051 others(6): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 76693516 | |||||
| chr8:76693527
|
A | G | 82 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0067others(79): Show | 83 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.-46-10516A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76693527 | ||||||
| chr8:76693853
|
G | A | 3 | a0012c0024t0005g0001a0013c0023t0001g0143a0013c0023t0009g0144 | 4 | HG01168.hp2 HG02258.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.-46-10190G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76693853 | ||||||
| chr8:76693861
|
T | C | 4 | a0002c0006t0010g0031a0003c0002t0001g0007a0003c0002t0001g0009others(1): Show | 4 | HG02818.hp1 HG03209.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-46-10182T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76693861 | ||||||
| chr8:76693989
|
A | G | 1 | a0002c0001t0003g0077 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-46-10054A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76693989 | ||||||
| chr8:76694064
|
A | G | 1 | a0017c0057t0001g0033 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-46-9979A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76694064 | ||||||
| chr8:76694352
|
G | A | 1 | a0031c0049t0001g0060 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-46-9691G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76694352 | ||||||
| chr8:76694361
|
G | T | 3 | a0012c0024t0005g0001a0013c0023t0001g0143a0013c0023t0009g0144 | 4 | HG01168.hp2 HG02258.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.-46-9682G>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76694361 | ||||||
| chr8:76694374
|
T | A | 3 | a0012c0024t0005g0001a0013c0023t0001g0143a0013c0023t0009g0144 | 4 | HG01168.hp2 HG02258.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.-46-9669T>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76694374 | ||||||
| chr8:76694494
|
C | G | 1 | a0010c0013t0004g0172 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.-46-9549C>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76694494 | ||||||
| chr8:76694513
|
C | T | 3 | a0012c0024t0005g0001a0013c0023t0001g0143a0013c0023t0009g0144 | 4 | HG01168.hp2 HG02258.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.-46-9530C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76694513 | ||||||
| chr8:76694638
|
CT | C | 35 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0183others(32): Show | 36 | HG00280.hp2 HG00609.hp2 HG01074.hp1 others(33): Show |
intron_variant | MODIFIER | c.-46-9395delT | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 76694638 | |||||
| chr8:76694649
|
C | G | 1 | a0021c0054t0003g0030 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-46-9394C>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76694649 | ||||||
| chr8:76694695
|
C | T | 25 | a0001c0004t0002g0067a0001c0004t0002g0069a0001c0004t0005g0064others(22): Show | 25 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(22): Show |
intron_variant | MODIFIER | c.-46-9348C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76694695 | ||||||
| chr8:76694703
|
T | TGCCCCC | 5 | a0002c0001t0003g0207a0002c0001t0003g0215a0007c0014t0003g0079others(2): Show | 5 | NA18940.hp1 NA18982.hp2 NA18991.hp2 others(2): Show |
intron_variant | MODIFIER | c.-46-9328_-46-9323d others(8): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 76694703 | |||||
| chr8:76694861
|
T | C | 10 | a0001c0004t0005g0219a0001c0052t0001g0063a0004c0012t0002g0061others(7): Show | 10 | HG02486.hp2 HG02615.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.-46-9182T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76694861 | ||||||
| chr8:76695000
|
G | A | 1 | a0003c0034t0001g0142 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-46-9043G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76695000 | ||||||
| chr8:76695075
|
G | A | 25 | a0001c0015t0005g0011a0001c0042t0002g0010a0002c0001t0003g0020others(22): Show | 25 | HG00438.hp1 HG01070.hp1 HG02040.hp1 others(22): Show |
intron_variant | MODIFIER | c.-46-8968G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76695075 | ||||||
| chr8:76695179
|
A | C | 36 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0183others(33): Show | 37 | HG00280.hp2 HG00609.hp2 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.-46-8864A>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76695179 | ||||||
| chr8:76695246
|
G | A | 20 | a0001c0004t0002g0067a0001c0004t0002g0069a0001c0004t0005g0064others(17): Show | 20 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(17): Show |
intron_variant | MODIFIER | c.-46-8797G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76695246 | ||||||
| chr8:76695568
|
A | T | 1 | a0003c0034t0001g0142 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-46-8475A>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76695568 | ||||||
| chr8:76695871
|
C | T | 1 | a0003c0002t0001g0150 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-46-8172C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76695871 | ||||||
| chr8:76695889
|
T | G | 5 | a0001c0008t0005g0157a0002c0006t0010g0155a0003c0061t0001g0156others(2): Show | 5 | HG01081.hp1 HG01167.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-46-8154T>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76695889 | ||||||
| chr8:76696004
|
T | C | 1 | a0002c0001t0003g0037 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-46-8039T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76696004 | ||||||
| chr8:76696547
|
A | G | 1 | a0001c0025t0002g0210 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-46-7496A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76696547 | ||||||
| chr8:76696595
|
C | G | 1 | a0031c0049t0001g0060 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-46-7448C>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76696595 | ||||||
| chr8:76696634
|
CA | C | 97 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0012g0043others(94): Show | 98 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.-46-7392delA | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 76696634 | |||||
| chr8:76696634
|
CAA | C | 43 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0183others(40): Show | 44 | HG00280.hp2 HG00609.hp2 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.-46-7393_-46-7392d others(4): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 76696634 | |||||
| chr8:76696744
|
A | G | 41 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0183others(38): Show | 42 | HG00280.hp2 HG00609.hp2 HG01074.hp1 others(39): Show |
intron_variant | MODIFIER | c.-46-7299A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76696744 | ||||||
| chr8:76696796
|
A | C | 1 | a0005c0005t0004g0047 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-46-7247A>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76696796 | ||||||
| chr8:76697046
|
T | A | 3 | a0012c0024t0005g0001a0013c0023t0001g0143a0013c0023t0009g0144 | 4 | HG01168.hp2 HG02258.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.-46-6997T>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76697046 | ||||||
| chr8:76697328
|
C | T | 27 | a0001c0015t0005g0011a0001c0042t0002g0010a0001c0051t0002g0141others(24): Show | 27 | HG00438.hp1 HG01070.hp1 HG02040.hp1 others(24): Show |
intron_variant | MODIFIER | c.-46-6715C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76697328 | ||||||
| chr8:76697335
|
T | C | 1 | a0031c0049t0001g0060 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-46-6708T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76697335 | ||||||
| chr8:76697405
|
A | G | 32 | a0001c0008t0005g0157a0001c0015t0005g0011a0001c0042t0002g0010others(29): Show | 32 | HG00438.hp1 HG01070.hp1 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.-46-6638A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76697405 | ||||||
| chr8:76697607
|
T | C | 1 | a0001c0004t0005g0064 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-46-6436T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76697607 | ||||||
| chr8:76697807
|
A | G | 139 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0012g0043others(136): Show | 141 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.-46-6236A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76697807 | ||||||
| chr8:76697810
|
A | G | 1 | a0003c0002t0001g0076 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-46-6233A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76697810 | ||||||
| chr8:76697825
|
G | A | 5 | a0001c0015t0005g0011a0001c0042t0002g0010a0002c0001t0010g0014others(2): Show | 5 | HG01070.hp1 HG02723.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-46-6218G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76697825 | ||||||
| chr8:76697861
|
T | G | 36 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0183others(33): Show | 37 | HG00280.hp2 HG00609.hp2 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.-46-6182T>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76697861 | ||||||
| chr8:76697955
|
A | G | 1 | a0017c0057t0001g0033 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-46-6088A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76697955 | ||||||
| chr8:76698061
|
C | T | 1 | a0002c0038t0002g0153 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-46-5982C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76698061 | ||||||
| chr8:76698302
|
A | G | 10 | a0002c0006t0010g0031a0003c0002t0001g0007a0003c0002t0001g0009others(7): Show | 10 | HG02055.hp1 HG02486.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.-46-5741A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76698302 | ||||||
| chr8:76698593
|
T | TGA | 139 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0012g0043others(136): Show | 141 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.-46-5446_-46-5445d others(4): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 76698593 | |||||
| chr8:76698769
|
G | A | 5 | a0001c0008t0005g0157a0002c0006t0010g0155a0003c0061t0001g0156others(2): Show | 5 | HG01081.hp1 HG01167.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-46-5274G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76698769 | ||||||
| chr8:76698777
|
A | T | 141 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0012g0043others(138): Show | 143 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.-46-5266A>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76698777 | ||||||
| chr8:76699059
|
C | T | 1 | a0006c0029t0001g0158 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-46-4984C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76699059 | ||||||
| chr8:76699223
|
C | T | 27 | a0001c0015t0005g0011a0001c0042t0002g0010a0001c0051t0002g0141others(24): Show | 27 | HG00438.hp1 HG01070.hp1 HG02040.hp1 others(24): Show |
intron_variant | MODIFIER | c.-46-4820C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76699223 | ||||||
| chr8:76699358
|
CCTT | C | 5 | a0001c0008t0005g0157a0002c0006t0010g0155a0003c0061t0001g0156others(2): Show | 5 | HG01081.hp1 HG01167.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-46-4681_-46-4679d others(5): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 76699358 | |||||
| chr8:76699390
|
A | G | 139 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0012g0043others(136): Show | 141 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.-46-4653A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76699390 | ||||||
| chr8:76699499
|
C | A | 1 | a0009c0011t0006g0065 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-46-4544C>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76699499 | ||||||
| chr8:76699517
|
A | G | 2 | a0001c0003t0012g0043a0004c0081t0002g0045 | 2 | HG00597.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.-46-4526A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76699517 | ||||||
| chr8:76699569
|
G | C | 3 | a0002c0001t0001g0149a0003c0002t0001g0150a0006c0009t0006g0151 | 3 | HG02055.hp2 HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-46-4474G>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76699569 | ||||||
| chr8:76699744
|
C | CA | 55 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0012g0043others(52): Show | 55 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.-46-4283dupA | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 76699744 | |||||
| chr8:76699744
|
CA | C | 5 | a0001c0008t0005g0157a0002c0006t0010g0155a0003c0061t0001g0156others(2): Show | 5 | HG01081.hp1 HG01167.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-46-4283delA | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 76699744 | |||||
| chr8:76699775
|
CT | C | 66 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0012g0043others(63): Show | 67 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.-46-4258delT | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 76699775 | |||||
| chr8:76699977
|
T | C | 1 | a0013c0023t0001g0143 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-46-4066T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76699977 | ||||||
| chr8:76700025
|
C | G | 1 | a0004c0046t0002g0075 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-46-4018C>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76700025 | ||||||
| chr8:76700145
|
G | A | 3 | a0003c0007t0001g0102a0006c0016t0001g0103a0006c0016t0008g0101 | 3 | HG02723.hp1 HG03098.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-46-3898G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76700145 | ||||||
| chr8:76700238
|
G | A | 1 | a0004c0012t0002g0061 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-46-3805G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76700238 | ||||||
| chr8:76700256
|
A | G | 1 | a0003c0002t0001g0150 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-46-3787A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76700256 | ||||||
| chr8:76700556
|
G | A | 1 | a0003c0002t0001g0054 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-46-3487G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76700556 | ||||||
| chr8:76700584
|
G | T | 1 | a0015c0056t0002g0042 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-46-3459G>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76700584 | ||||||
| chr8:76701266
|
T | C | 1 | a0001c0004t0002g0183 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-46-2777T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76701266 | ||||||
| chr8:76701312
|
G | A | 41 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0183others(38): Show | 42 | HG00280.hp2 HG00609.hp2 HG01074.hp1 others(39): Show |
intron_variant | MODIFIER | c.-46-2731G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76701312 | ||||||
| chr8:76701350
|
C | T | 2 | a0001c0003t0003g0035a0001c0003t0003g0036 | 2 | NA18999.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.-46-2693C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76701350 | ||||||
| chr8:76701745
|
T | C | 8 | a0002c0001t0003g0020a0004c0026t0006g0019a0008c0010t0006g0015others(5): Show | 8 | HG00438.hp1 HG02040.hp1 NA18962.hp1 others(5): Show |
intron_variant | MODIFIER | c.-46-2298T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76701745 | ||||||
| chr8:76701809
|
T | TA | 6 | a0001c0004t0002g0189a0002c0001t0003g0185a0002c0001t0003g0187others(3): Show | 6 | NA18939.hp2 NA18964.hp1 NA18980.hp2 others(3): Show |
intron_variant | MODIFIER | c.-46-2233dupA | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 76701809 | |||||
| chr8:76702054
|
G | T | 38 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0183others(35): Show | 39 | HG00280.hp2 HG00609.hp2 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.-46-1989G>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76702054 | ||||||
| chr8:76702203
|
T | A | 2 | a0003c0002t0006g0058a0009c0069t0007g0057 | 2 | HG02886.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-46-1840T>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76702203 | ||||||
| chr8:76702204
|
T | A | 2 | a0003c0002t0006g0058a0009c0069t0007g0057 | 2 | HG02886.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-46-1839T>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76702204 | ||||||
| chr8:76702209
|
A | G | 1 | a0012c0024t0005g0001 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-46-1834A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76702209 | ||||||
| chr8:76702440
|
C | T | 1 | a0002c0021t0018g0133 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-46-1603C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76702440 | ||||||
| chr8:76702524
|
A | G | 1 | a0003c0002t0001g0150 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-46-1519A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76702524 | ||||||
| chr8:76702766
|
A | G | 1 | a0003c0002t0001g0150 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-46-1277A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76702766 | ||||||
| chr8:76702819
|
A | G | 1 | a0001c0003t0002g0097 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-46-1224A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76702819 | ||||||
| chr8:76702876
|
A | G | 2 | a0001c0008t0005g0096a0005c0005t0011g0095 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-46-1167A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76702876 | ||||||
| chr8:76702963
|
G | GAC | 25 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0012g0043others(22): Show | 25 | HG00408.hp2 HG00597.hp1 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.-46-1054_-46-1053d others(4): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 76702963 | |||||
| chr8:76702963
|
G | GACAC | 31 | a0001c0015t0001g0003a0001c0015t0005g0005a0001c0015t0005g0011others(28): Show | 31 | HG00438.hp1 HG01070.hp1 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.-46-1056_-46-1053d others(6): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 76702963 | |||||
| chr8:76702963
|
G | GACACAC | 38 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0183others(35): Show | 39 | HG00280.hp2 HG00609.hp2 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.-46-1058_-46-1053d others(8): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 76702963 | |||||
| chr8:76702963
|
GAC | G | 10 | a0001c0003t0002g0179a0001c0003t0002g0216a0001c0008t0005g0157others(7): Show | 10 | HG01081.hp1 HG01167.hp1 HG02132.hp1 others(7): Show |
intron_variant | MODIFIER | c.-46-1054_-46-1053d others(4): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 76702963 | |||||
| chr8:76703120
|
C | T | 3 | a0001c0015t0001g0003a0001c0015t0005g0005a0003c0002t0001g0004 | 3 | HG01109.hp1 HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-46-923C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76703120 | ||||||
| chr8:76703245
|
T | C | 1 | a0026c0041t0005g0073 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-46-798T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76703245 | ||||||
| chr8:76703261
|
G | T | 1 | a0019c0082t0014g0139 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-46-782G>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76703261 | ||||||
| chr8:76703285
|
G | A | 1 | a0003c0007t0009g0082 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-46-758G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76703285 | ||||||
| chr8:76703412
|
G | T | 2 | a0009c0011t0007g0222a0009c0011t0007g0223 | 2 | HG02486.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-46-631G>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76703412 | ||||||
| chr8:76703577
|
C | A | 3 | a0002c0001t0001g0149a0003c0002t0001g0150a0006c0009t0006g0151 | 3 | HG02055.hp2 HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-46-466C>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76703577 | ||||||
| chr8:76703594
|
C | G | 1 | a0003c0002t0001g0032 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-46-449C>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76703594 | ||||||
| chr8:76703668
|
G | T | 3 | a0002c0001t0001g0149a0003c0002t0001g0150a0006c0009t0006g0151 | 3 | HG02055.hp2 HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-46-375G>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76703668 | ||||||
| chr8:76703678
|
A | G | 3 | a0002c0001t0001g0149a0003c0002t0001g0150a0006c0009t0006g0151 | 3 | HG02055.hp2 HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-46-365A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76703678 | ||||||
| chr8:76703811
|
A | G | 1 | a0002c0001t0003g0051 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-46-232A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76703811 | ||||||
| chr8:76703937
|
T | G | 1 | a0001c0003t0003g0035 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.-46-106T>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 1/10 | chr8 | 76703937 | ||||||
| chr8:76706705
|
G | A | 2 | a0001c0003t0002g0083a0001c0003t0002g0097 | 2 | HG00280.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.2590+27G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 2/10 | chr8 | 76706705 | ||||||
| chr8:76706737
|
G | A | 2 | a0001c0051t0002g0141a0017c0057t0001g0033 | 2 | HG02809.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2590+59G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 2/10 | chr8 | 76706737 | ||||||
| chr8:76706894
|
A | G | 1 | a0003c0002t0001g0150 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2590+216A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 2/10 | chr8 | 76706894 | ||||||
| chr8:76706915
|
C | T | 1 | a0001c0004t0002g0183 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.2590+237C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 2/10 | chr8 | 76706915 | ||||||
| chr8:76706988
|
G | A | 38 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0183others(35): Show | 39 | HG00280.hp2 HG00609.hp2 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.2590+310G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 2/10 | chr8 | 76706988 | ||||||
| chr8:76707034
|
G | A | 36 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0183others(33): Show | 37 | HG00280.hp2 HG00609.hp2 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.2590+356G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 2/10 | chr8 | 76707034 | ||||||
| chr8:76707066
|
A | G | 1 | a0005c0005t0004g0078 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2590+388A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 2/10 | chr8 | 76707066 | ||||||
| chr8:76707087
|
A | G | 3 | a0002c0038t0002g0153a0016c0083t0001g0152a0019c0082t0014g0139 | 3 | HG01884.hp2 HG02976.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.2590+409A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 2/10 | chr8 | 76707087 | ||||||
| chr8:76707334
|
T | C | 2 | a0003c0045t0004g0136a0018c0064t0001g0137 | 2 | HG02572.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2591-212T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 2/10 | chr8 | 76707334 | ||||||
| chr8:76707425
|
C | T | 1 | a0018c0064t0001g0137 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2591-121C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 2/10 | chr8 | 76707425 | ||||||
| chr8:76707529
|
AT | A | 5 | a0001c0003t0002g0134a0001c0015t0005g0011a0001c0042t0002g0010others(2): Show | 5 | HG01070.hp1 HG01070.hp2 HG02723.hp2 others(2): Show |
splice_region_variant&intron_variant | LOW | c.2591-8delT | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr8 | 76707529 | |||||
| chr8:76708306
|
A | G | 1 | a0011c0020t0004g0041 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.3093+258A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76708306 | ||||||
| chr8:76708345
|
T | G | 1 | a0006c0009t0006g0151 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3093+297T>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76708345 | ||||||
| chr8:76708359
|
A | AT | 76 | a0001c0003t0002g0134a0001c0003t0002g0164a0001c0003t0003g0035others(73): Show | 76 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.3093+325dupT | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76708359 | |||||
| chr8:76708359
|
A | ATT | 20 | a0002c0001t0003g0020a0002c0028t0003g0138a0003c0002t0001g0007others(17): Show | 21 | HG00438.hp1 HG01168.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.3093+324_3093+325d others(4): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76708359 | |||||
| chr8:76708400
|
G | A | 1 | a0001c0033t0002g0224 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.3093+352G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76708400 | ||||||
| chr8:76708503
|
T | G | 1 | a0002c0028t0003g0138 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3093+455T>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76708503 | ||||||
| chr8:76708816
|
C | T | 38 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0183others(35): Show | 39 | HG00280.hp2 HG00609.hp2 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.3093+768C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76708816 | ||||||
| chr8:76708818
|
GT | G | 41 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0183others(38): Show | 42 | HG00280.hp2 HG00609.hp2 HG01074.hp1 others(39): Show |
intron_variant | MODIFIER | c.3093+773delT | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76708818 | |||||
| chr8:76709237
|
A | G | 1 | a0003c0002t0001g0148 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3093+1189A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76709237 | ||||||
| chr8:76709332
|
C | T | 1 | a0001c0052t0001g0063 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3093+1284C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76709332 | ||||||
| chr8:76709434
|
C | G | 3 | a0001c0015t0001g0003a0001c0015t0005g0005a0003c0002t0001g0004 | 3 | HG01109.hp1 HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.3093+1386C>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76709434 | ||||||
| chr8:76709537
|
C | T | 4 | a0001c0003t0002g0179a0001c0003t0002g0216a0002c0006t0003g0165others(1): Show | 4 | NA18981.hp1 NA18989.hp2 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.3093+1489C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76709537 | ||||||
| chr8:76709674
|
C | A | 1 | a0002c0038t0002g0153 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3093+1626C>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76709674 | ||||||
| chr8:76709792
|
CGTGTGTG others(9): Show |
C | 3 | a0002c0006t0010g0155a0003c0061t0001g0156a0006c0029t0001g0158 | 3 | HG02615.hp1 HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3093+1754_3093+176 others(20): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76709792 | |||||
| chr8:76709802
|
C | CGT | 34 | a0001c0004t0002g0067a0001c0004t0002g0069a0001c0004t0005g0064others(31): Show | 34 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.3093+1783_3093+178 others(6): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76709802 | |||||
| chr8:76709802
|
C | CGTGT | 3 | a0003c0045t0004g0136a0006c0009t0001g0059a0018c0064t0001g0137 | 3 | HG02572.hp1 HG03239.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.3093+1781_3093+178 others(8): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76709802 | |||||
| chr8:76709802
|
CGT | C | 48 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0183others(45): Show | 49 | HG00280.hp2 HG00609.hp2 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.3093+1783_3093+178 others(6): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76709802 | |||||
| chr8:76709802
|
CGTGT | C | 20 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0012g0043others(17): Show | 20 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(17): Show |
intron_variant | MODIFIER | c.3093+1781_3093+178 others(8): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76709802 | |||||
| chr8:76709802
|
CGTGTGTG others(3): Show |
C | 3 | a0012c0024t0005g0001a0013c0023t0001g0143a0013c0023t0009g0144 | 4 | HG01168.hp2 HG02258.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.3093+1775_3093+178 others(14): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76709802 | |||||
| chr8:76709830
|
TGTAA | T | 3 | a0002c0001t0001g0149a0003c0002t0001g0150a0006c0009t0006g0151 | 3 | HG02055.hp2 HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.3093+1785_3093+178 others(8): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76709830 | |||||
| chr8:76709939
|
G | A | 3 | a0002c0001t0001g0149a0003c0002t0001g0150a0006c0009t0006g0151 | 3 | HG02055.hp2 HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.3093+1891G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76709939 | ||||||
| chr8:76709979
|
G | T | 36 | a0001c0004t0002g0067a0001c0004t0002g0069a0001c0004t0005g0064others(33): Show | 36 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(33): Show |
intron_variant | MODIFIER | c.3093+1931G>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76709979 | ||||||
| chr8:76710174
|
C | A | 36 | a0001c0004t0002g0067a0001c0004t0002g0069a0001c0004t0005g0064others(33): Show | 36 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(33): Show |
intron_variant | MODIFIER | c.3093+2126C>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76710174 | ||||||
| chr8:76710470
|
A | T | 9 | a0001c0004t0019g0050a0001c0047t0016g0066a0002c0001t0003g0051others(6): Show | 9 | HG00544.hp1 HG00597.hp2 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.3093+2422A>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76710470 | ||||||
| chr8:76710499
|
A | G | 3 | a0001c0015t0001g0003a0001c0015t0005g0005a0003c0002t0001g0004 | 3 | HG01109.hp1 HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.3093+2451A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76710499 | ||||||
| chr8:76710654
|
C | T | 2 | a0003c0002t0006g0058a0009c0069t0007g0057 | 2 | HG02886.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.3093+2606C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76710654 | ||||||
| chr8:76710704
|
G | A | 1 | a0031c0049t0001g0060 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.3093+2656G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76710704 | ||||||
| chr8:76711016
|
A | T | 1 | a0009c0011t0007g0221 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3093+2968A>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76711016 | ||||||
| chr8:76711063
|
T | C | 2 | a0002c0001t0001g0149a0006c0009t0006g0151 | 2 | HG02055.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3093+3015T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76711063 | ||||||
| chr8:76711180
|
C | G | 1 | a0004c0022t0002g0242 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3093+3132C>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76711180 | ||||||
| chr8:76711206
|
G | C | 44 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0183others(41): Show | 45 | HG00280.hp2 HG00609.hp2 HG01074.hp1 others(42): Show |
intron_variant | MODIFIER | c.3093+3158G>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76711206 | ||||||
| chr8:76711209
|
T | C | 1 | a0001c0078t0006g0159 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.3093+3161T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76711209 | ||||||
| chr8:76711322
|
T | G | 44 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0183others(41): Show | 45 | HG00280.hp2 HG00609.hp2 HG01074.hp1 others(42): Show |
intron_variant | MODIFIER | c.3093+3274T>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76711322 | ||||||
| chr8:76711362
|
T | C | 1 | a0001c0004t0002g0206 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.3093+3314T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76711362 | ||||||
| chr8:76711764
|
A | T | 41 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0183others(38): Show | 42 | HG00280.hp2 HG00609.hp2 HG01074.hp1 others(39): Show |
intron_variant | MODIFIER | c.3093+3716A>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76711764 | ||||||
| chr8:76711765
|
T | A | 1 | a0003c0002t0001g0150 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3093+3717T>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76711765 | ||||||
| chr8:76711789
|
C | T | 1 | a0003c0002t0001g0068 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3093+3741C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76711789 | ||||||
| chr8:76711790
|
G | A | 3 | a0002c0038t0002g0153a0016c0083t0001g0152a0019c0082t0014g0139 | 3 | HG01884.hp2 HG02976.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.3093+3742G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76711790 | ||||||
| chr8:76711949
|
C | G | 1 | a0018c0064t0001g0137 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3093+3901C>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76711949 | ||||||
| chr8:76712031
|
C | T | 1 | a0017c0057t0001g0033 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3093+3983C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76712031 | ||||||
| chr8:76712040
|
T | C | 3 | a0001c0015t0001g0003a0001c0015t0005g0005a0003c0002t0001g0004 | 3 | HG01109.hp1 HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.3093+3992T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76712040 | ||||||
| chr8:76712277
|
A | C | 1 | a0001c0051t0002g0141 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3093+4229A>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76712277 | ||||||
| chr8:76712426
|
C | T | 1 | a0003c0002t0001g0004 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3093+4378C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76712426 | ||||||
| chr8:76712427
|
G | A | 1 | a0032c0072t0002g0080 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.3093+4379G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76712427 | ||||||
| chr8:76712568
|
C | T | 18 | a0001c0004t0002g0067a0001c0004t0002g0069a0001c0004t0005g0064others(15): Show | 18 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(15): Show |
intron_variant | MODIFIER | c.3093+4520C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76712568 | ||||||
| chr8:76712638
|
C | T | 1 | a0006c0029t0001g0158 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3093+4590C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76712638 | ||||||
| chr8:76712863
|
T | C | 1 | a0006c0029t0001g0158 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3093+4815T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76712863 | ||||||
| chr8:76713074
|
C | T | 6 | a0001c0004t0005g0219a0004c0012t0002g0218a0009c0011t0007g0221others(3): Show | 6 | HG02486.hp2 HG02717.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.3093+5026C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76713074 | ||||||
| chr8:76713270
|
GAGATAGA others(5): Show |
G | 1 | a0004c0012t0002g0190 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3093+5234_3093+524 others(16): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76713270 | |||||
| chr8:76713282
|
A | AAGAT | 56 | a0001c0003t0002g0110a0001c0004t0002g0040a0001c0004t0002g0067others(53): Show | 56 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.3093+5267_3093+527 others(8): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76713282 | |||||
| chr8:76713282
|
A | AAGATAGA others(1): Show |
26 | a0001c0003t0003g0036a0001c0003t0012g0043a0001c0004t0002g0069others(23): Show | 27 | HG00408.hp2 HG01167.hp1 HG01167.hp2 others(24): Show |
intron_variant | MODIFIER | c.3093+5263_3093+527 others(12): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76713282 | |||||
| chr8:76713282
|
A | AAGATAGA others(5): Show |
20 | a0001c0003t0003g0035a0001c0052t0001g0063a0001c0063t0001g0053others(17): Show | 20 | HG00639.hp1 HG01168.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.3093+5259_3093+527 others(16): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76713282 | |||||
| chr8:76713282
|
A | T | 2 | a0001c0008t0005g0096a0003c0035t0013g0228 | 2 | HG01169.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.3093+5234A>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76713282 | ||||||
| chr8:76713282
|
AAGATAGA others(1): Show |
A | 42 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0183others(39): Show | 43 | HG00280.hp2 HG01074.hp1 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.3093+5263_3093+527 others(12): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76713282 | |||||
| chr8:76713290
|
T | A | 1 | a0004c0012t0002g0190 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3093+5242T>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76713290 | ||||||
| chr8:76713311
|
A | G | 44 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0183others(41): Show | 45 | HG00280.hp2 HG00609.hp2 HG01074.hp1 others(42): Show |
intron_variant | MODIFIER | c.3093+5263A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76713311 | ||||||
| chr8:76713370
|
C | T | 1 | a0015c0056t0002g0042 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.3093+5322C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76713370 | ||||||
| chr8:76713525
|
G | A | 3 | a0002c0038t0002g0153a0016c0083t0001g0152a0019c0082t0014g0139 | 3 | HG01884.hp2 HG02976.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.3093+5477G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76713525 | ||||||
| chr8:76713658
|
G | C | 19 | a0001c0004t0002g0067a0001c0004t0002g0069a0001c0004t0005g0064others(16): Show | 19 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(16): Show |
intron_variant | MODIFIER | c.3093+5610G>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76713658 | ||||||
| chr8:76713754
|
C | T | 1 | a0003c0034t0001g0142 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3093+5706C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76713754 | ||||||
| chr8:76713946
|
A | C | 3 | a0012c0024t0005g0001a0013c0023t0001g0143a0013c0023t0009g0144 | 4 | HG01168.hp2 HG02258.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.3093+5898A>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76713946 | ||||||
| chr8:76714035
|
T | G | 3 | a0012c0024t0005g0001a0013c0023t0001g0143a0013c0023t0009g0144 | 4 | HG01168.hp2 HG02258.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.3093+5987T>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76714035 | ||||||
| chr8:76714088
|
A | G | 2 | a0003c0002t0006g0058a0009c0069t0007g0057 | 2 | HG02886.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.3093+6040A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76714088 | ||||||
| chr8:76714278
|
G | C | 1 | a0001c0003t0002g0083 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.3093+6230G>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76714278 | ||||||
| chr8:76714300
|
G | C | 1 | a0017c0057t0001g0033 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3093+6252G>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76714300 | ||||||
| chr8:76714408
|
C | T | 3 | a0012c0024t0005g0001a0013c0023t0001g0143a0013c0023t0009g0144 | 4 | HG01168.hp2 HG02258.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.3093+6360C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76714408 | ||||||
| chr8:76714591
|
A | G | 1 | a0013c0023t0009g0144 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.3093+6543A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76714591 | ||||||
| chr8:76714776
|
A | C | 1 | a0006c0009t0001g0146 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3093+6728A>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76714776 | ||||||
| chr8:76714912
|
A | T | 1 | a0002c0001t0003g0037 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.3093+6864A>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76714912 | ||||||
| chr8:76714930
|
T | A | 2 | a0002c0038t0002g0153a0016c0083t0001g0152 | 2 | HG01884.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.3093+6882T>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76714930 | ||||||
| chr8:76714980
|
T | A | 5 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0012g0043others(2): Show | 5 | HG00597.hp1 HG02165.hp2 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.3093+6932T>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76714980 | ||||||
| chr8:76715019
|
G | A | 12 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0012g0043others(9): Show | 12 | HG00408.hp2 HG00597.hp1 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.3093+6971G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76715019 | ||||||
| chr8:76715385
|
G | T | 1 | a0013c0023t0001g0143 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3093+7337G>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76715385 | ||||||
| chr8:76715438
|
C | T | 1 | a0001c0052t0001g0063 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3093+7390C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76715438 | ||||||
| chr8:76715481
|
T | TA | 29 | a0001c0003t0002g0110a0001c0003t0003g0120a0001c0017t0003g0107others(26): Show | 29 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(26): Show |
intron_variant | MODIFIER | c.3093+7460dupA | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76715481 | |||||
| chr8:76715481
|
TA | T | 39 | a0001c0003t0002g0134a0001c0004t0002g0067a0001c0004t0002g0069others(36): Show | 39 | HG00423.hp1 HG00544.hp1 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.3093+7460delA | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76715481 | |||||
| chr8:76715481
|
TAA | T | 92 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0012g0043others(89): Show | 94 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.3093+7459_3093+746 others(6): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76715481 | |||||
| chr8:76715481
|
TAAA | T | 8 | a0001c0004t0002g0040a0002c0001t0001g0149a0002c0001t0003g0205others(5): Show | 8 | HG02897.hp1 HG02897.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.3093+7458_3093+746 others(7): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76715481 | |||||
| chr8:76715832
|
T | C | 3 | a0002c0001t0001g0149a0003c0002t0001g0150a0006c0009t0006g0151 | 3 | HG02055.hp2 HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.3093+7784T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76715832 | ||||||
| chr8:76715845
|
T | C | 3 | a0001c0003t0002g0168a0010c0013t0004g0172a0011c0020t0004g0167 | 3 | HG02074.hp1 NA18986.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.3093+7797T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76715845 | ||||||
| chr8:76716007
|
C | T | 1 | a0001c0051t0002g0141 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3093+7959C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76716007 | ||||||
| chr8:76716029
|
T | G | 3 | a0002c0038t0002g0153a0016c0083t0001g0152a0019c0082t0014g0139 | 3 | HG01884.hp2 HG02976.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.3093+7981T>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76716029 | ||||||
| chr8:76716192
|
C | T | 5 | a0002c0006t0003g0122a0004c0018t0002g0125a0005c0005t0004g0111others(2): Show | 5 | HG02071.hp2 NA18945.hp1 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.3093+8144C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76716192 | ||||||
| chr8:76716291
|
G | T | 1 | a0003c0034t0001g0142 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3093+8243G>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76716291 | ||||||
| chr8:76716327
|
G | A | 1 | a0001c0003t0002g0216 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.3093+8279G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76716327 | ||||||
| chr8:76716484
|
T | C | 44 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0183others(41): Show | 45 | HG00280.hp2 HG00609.hp2 HG01074.hp1 others(42): Show |
intron_variant | MODIFIER | c.3093+8436T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76716484 | ||||||
| chr8:76717049
|
C | A | 1 | a0004c0019t0005g0234 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.3093+9001C>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76717049 | ||||||
| chr8:76717293
|
C | T | 12 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0012g0043others(9): Show | 12 | HG00408.hp2 HG00597.hp1 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.3093+9245C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76717293 | ||||||
| chr8:76717334
|
G | A | 1 | a0003c0034t0001g0142 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3093+9286G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76717334 | ||||||
| chr8:76717376
|
C | T | 1 | a0006c0009t0006g0151 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3093+9328C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76717376 | ||||||
| chr8:76717529
|
A | G | 1 | a0002c0028t0003g0138 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3093+9481A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76717529 | ||||||
| chr8:76717551
|
G | C | 130 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0012g0043others(127): Show | 132 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.3093+9503G>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76717551 | ||||||
| chr8:76717727
|
G | A | 5 | a0001c0015t0005g0011a0001c0042t0002g0010a0002c0001t0010g0014others(2): Show | 5 | HG01070.hp1 HG02723.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.3093+9679G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76717727 | ||||||
| chr8:76717817
|
G | C | 59 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0012g0043others(56): Show | 60 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.3093+9769G>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76717817 | ||||||
| chr8:76717845
|
C | G | 27 | a0001c0015t0005g0011a0001c0042t0002g0010a0001c0051t0002g0141others(24): Show | 27 | HG00438.hp1 HG01070.hp1 HG02040.hp1 others(24): Show |
intron_variant | MODIFIER | c.3093+9797C>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76717845 | ||||||
| chr8:76717974
|
C | A | 1 | a0002c0006t0010g0031 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3093+9926C>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76717974 | ||||||
| chr8:76717996
|
G | A | 103 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0012g0043others(100): Show | 105 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.3093+9948G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76717996 | ||||||
| chr8:76718038
|
T | C | 3 | a0002c0001t0003g0002a0002c0001t0003g0182a0002c0001t0003g0193 | 4 | HG00280.hp2 NA18945.hp2 NA18953.hp2 others(1): Show |
intron_variant | MODIFIER | c.3093+9990T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76718038 | ||||||
| chr8:76718222
|
A | G | 2 | a0001c0004t0001g0203a0001c0004t0001g0204 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.3093+10174A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76718222 | ||||||
| chr8:76718458
|
A | T | 1 | a0005c0005t0004g0078 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3093+10410A>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76718458 | ||||||
| chr8:76718584
|
A | T | 59 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0012g0043others(56): Show | 60 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.3093+10536A>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76718584 | ||||||
| chr8:76718610
|
T | C | 1 | a0010c0013t0004g0172 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3093+10562T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76718610 | ||||||
| chr8:76718715
|
T | C | 27 | a0001c0015t0005g0011a0001c0042t0002g0010a0001c0051t0002g0141others(24): Show | 27 | HG00438.hp1 HG01070.hp1 HG02040.hp1 others(24): Show |
intron_variant | MODIFIER | c.3093+10667T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76718715 | ||||||
| chr8:76718759
|
C | G | 3 | a0001c0003t0012g0043a0004c0081t0002g0045a0011c0020t0004g0041 | 3 | HG00597.hp1 HG02165.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.3093+10711C>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76718759 | ||||||
| chr8:76718935
|
T | TCA | 26 | a0001c0003t0002g0087a0001c0003t0012g0043a0001c0008t0005g0093others(23): Show | 26 | HG00597.hp2 HG00609.hp1 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.3093+10920_3093+10 others(8): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76718935 | |||||
| chr8:76718935
|
T | TCACA | 18 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0004t0002g0040others(15): Show | 18 | HG00408.hp2 HG00597.hp1 HG00639.hp1 others(15): Show |
intron_variant | MODIFIER | c.3093+10918_3093+10 others(10): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76718935 | |||||
| chr8:76718935
|
T | TCACACA | 18 | a0001c0042t0002g0010a0002c0001t0003g0020a0002c0001t0003g0044others(15): Show | 19 | HG00438.hp1 HG01070.hp1 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.3093+10916_3093+10 others(12): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76718935 | |||||
| chr8:76718935
|
T | TCACACAC others(3): Show |
2 | a0002c0028t0003g0138a0028c0043t0001g0140 | 2 | HG01891.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.3093+10912_3093+10 others(16): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76718935 | |||||
| chr8:76718935
|
T | TCACACAC others(5): Show |
1 | a0013c0023t0009g0144 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.3093+10910_3093+10 others(18): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76718935 | |||||
| chr8:76718935
|
TCA | T | 64 | a0001c0003t0002g0164a0001c0003t0002g0168a0001c0003t0002g0174others(61): Show | 65 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.3093+10920_3093+10 others(8): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76718935 | |||||
| chr8:76718935
|
TCACA | T | 8 | a0001c0003t0002g0176a0001c0063t0001g0053a0002c0021t0003g0128others(5): Show | 8 | HG01167.hp2 HG02027.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.3093+10918_3093+10 others(10): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76718935 | |||||
| chr8:76719060
|
G | A | 54 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0012g0043others(51): Show | 54 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.3093+11012G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76719060 | ||||||
| chr8:76719150
|
A | ATG | 10 | a0001c0003t0002g0164a0004c0018t0002g0125a0004c0019t0005g0234others(7): Show | 10 | HG00609.hp1 HG02056.hp1 HG02071.hp2 others(7): Show |
intron_variant | MODIFIER | c.3093+11138_3093+11 others(8): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76719150 | |||||
| chr8:76719150
|
A | ATGTG | 9 | a0001c0003t0002g0168a0001c0003t0003g0120a0001c0008t0005g0232others(6): Show | 9 | HG02055.hp2 HG02074.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.3093+11136_3093+11 others(10): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76719150 | |||||
| chr8:76719150
|
ATG | A | 9 | a0001c0003t0002g0174a0001c0051t0002g0141a0002c0006t0003g0122others(6): Show | 9 | HG01167.hp2 HG01975.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.3093+11138_3093+11 others(8): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76719150 | |||||
| chr8:76719150
|
ATGTG | A | 30 | a0001c0015t0005g0011a0001c0042t0002g0010a0002c0001t0003g0020others(27): Show | 30 | HG00438.hp1 HG00609.hp2 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.3093+11136_3093+11 others(10): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76719150 | |||||
| chr8:76719150
|
ATGTGTG | A | 33 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0183others(30): Show | 34 | HG00280.hp2 HG01074.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.3093+11134_3093+11 others(12): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76719150 | |||||
| chr8:76719150
|
ATGTGTGT others(1): Show |
A | 15 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0015t0001g0003others(12): Show | 15 | HG00597.hp2 HG00639.hp1 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.3093+11132_3093+11 others(14): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76719150 | |||||
| chr8:76719150
|
ATGTGTGT others(3): Show |
A | 49 | a0001c0003t0012g0043a0001c0004t0002g0040a0001c0004t0002g0067others(46): Show | 50 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.3093+11130_3093+11 others(16): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76719150 | |||||
| chr8:76719150
|
ATGTGTGT others(9): Show |
A | 2 | a0001c0008t0005g0236a0004c0019t0005g0235 | 2 | HG00735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.3093+11124_3093+11 others(22): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76719150 | |||||
| chr8:76719380
|
G | A | 11 | a0003c0002t0001g0007a0003c0002t0001g0009a0003c0002t0001g0026others(8): Show | 11 | HG02055.hp1 HG02486.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.3093+11332G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76719380 | ||||||
| chr8:76719399
|
A | G | 3 | a0001c0015t0001g0003a0001c0015t0005g0005a0003c0002t0001g0004 | 3 | HG01109.hp1 HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.3093+11351A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76719399 | ||||||
| chr8:76719519
|
C | T | 238 | a0001c0003t0002g0083a0001c0003t0002g0087a0001c0003t0002g0097others(235): Show | 240 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.3093+11471C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76719519 | ||||||
| chr8:76719526
|
T | A | 5 | a0001c0015t0005g0011a0001c0042t0002g0010a0002c0001t0010g0014others(2): Show | 5 | HG01070.hp1 HG02723.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.3093+11478T>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76719526 | ||||||
| chr8:76719534
|
G | A | 59 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0012g0043others(56): Show | 60 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.3093+11486G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76719534 | ||||||
| chr8:76719599
|
A | T | 44 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0183others(41): Show | 45 | HG00280.hp2 HG00609.hp2 HG01074.hp1 others(42): Show |
intron_variant | MODIFIER | c.3093+11551A>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76719599 | ||||||
| chr8:76719732
|
G | C | 1 | a0002c0028t0003g0138 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3093+11684G>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76719732 | ||||||
| chr8:76719770
|
C | T | 5 | a0003c0002t0001g0032a0003c0002t0001g0145a0003c0002t0001g0147others(2): Show | 5 | HG01175.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.3093+11722C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76719770 | ||||||
| chr8:76719782
|
A | G | 130 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0012g0043others(127): Show | 132 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.3093+11734A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76719782 | ||||||
| chr8:76720349
|
T | A | 1 | a0003c0045t0004g0136 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3093+12301T>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76720349 | ||||||
| chr8:76720384
|
G | A | 1 | a0004c0022t0002g0242 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3093+12336G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76720384 | ||||||
| chr8:76720432
|
G | A | 3 | a0001c0015t0001g0003a0001c0015t0005g0005a0003c0002t0001g0004 | 3 | HG01109.hp1 HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.3093+12384G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76720432 | ||||||
| chr8:76720466
|
T | C | 1 | a0002c0021t0003g0128 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.3093+12418T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76720466 | ||||||
| chr8:76720571
|
G | A | 1 | a0018c0064t0001g0137 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3093+12523G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76720571 | ||||||
| chr8:76721001
|
G | A | 58 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0012g0043others(55): Show | 59 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.3093+12953G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76721001 | ||||||
| chr8:76721030
|
T | TG | 5 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0012g0043others(2): Show | 5 | HG00597.hp1 HG02165.hp2 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.3093+12983dupG | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76721030 | |||||
| chr8:76721065
|
A | G | 39 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0183others(36): Show | 40 | HG00280.hp2 HG00609.hp2 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.3093+13017A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76721065 | ||||||
| chr8:76721108
|
T | C | 133 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0012g0043others(130): Show | 135 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.3093+13060T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76721108 | ||||||
| chr8:76721179
|
A | G | 45 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0183others(42): Show | 46 | HG00280.hp2 HG00609.hp2 HG01074.hp1 others(43): Show |
intron_variant | MODIFIER | c.3093+13131A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76721179 | ||||||
| chr8:76721274
|
A | C | 1 | a0002c0001t0003g0191 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.3093+13226A>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76721274 | ||||||
| chr8:76721370
|
G | A | 27 | a0001c0015t0005g0011a0001c0042t0002g0010a0001c0051t0002g0141others(24): Show | 27 | HG00438.hp1 HG01070.hp1 HG02040.hp1 others(24): Show |
intron_variant | MODIFIER | c.3093+13322G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76721370 | ||||||
| chr8:76721859
|
G | A | 1 | a0001c0031t0020g0163 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.3093+13811G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76721859 | ||||||
| chr8:76721894
|
G | A | 228 | a0001c0003t0002g0110a0001c0003t0002g0164a0001c0003t0002g0168others(225): Show | 230 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(227): Show |
intron_variant | MODIFIER | c.3093+13846G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76721894 | ||||||
| chr8:76721992
|
C | G | 1 | a0005c0005t0004g0119 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.3093+13944C>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76721992 | ||||||
| chr8:76722291
|
T | C | 45 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0183others(42): Show | 46 | HG00280.hp2 HG00609.hp2 HG01074.hp1 others(43): Show |
intron_variant | MODIFIER | c.3093+14243T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76722291 | ||||||
| chr8:76722381
|
G | A | 1 | a0001c0051t0002g0141 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3093+14333G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76722381 | ||||||
| chr8:76722525
|
T | C | 45 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0183others(42): Show | 46 | HG00280.hp2 HG00609.hp2 HG01074.hp1 others(43): Show |
intron_variant | MODIFIER | c.3093+14477T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76722525 | ||||||
| chr8:76722558
|
G | A | 239 | a0001c0003t0002g0083a0001c0003t0002g0087a0001c0003t0002g0097others(236): Show | 241 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.3093+14510G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76722558 | ||||||
| chr8:76722607
|
G | GTT | 5 | a0002c0001t0001g0149a0003c0002t0001g0150a0003c0045t0004g0136others(2): Show | 5 | HG02055.hp2 HG02572.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.3093+14568_3093+14 others(8): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76722607 | |||||
| chr8:76722607
|
G | GTTT | 40 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0183others(37): Show | 41 | HG00280.hp2 HG00609.hp2 HG01074.hp1 others(38): Show |
intron_variant | MODIFIER | c.3093+14567_3093+14 others(9): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76722607 | |||||
| chr8:76722810
|
T | G | 12 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0012g0043others(9): Show | 12 | HG00408.hp2 HG00597.hp1 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.3093+14762T>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76722810 | ||||||
| chr8:76722945
|
T | C | 29 | a0001c0015t0005g0011a0001c0042t0002g0010a0002c0001t0003g0020others(26): Show | 30 | HG00438.hp1 HG01070.hp1 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.3093+14897T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76722945 | ||||||
| chr8:76723053
|
T | C | 45 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0183others(42): Show | 46 | HG00280.hp2 HG00609.hp2 HG01074.hp1 others(43): Show |
intron_variant | MODIFIER | c.3093+15005T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76723053 | ||||||
| chr8:76723116
|
C | G | 1 | a0002c0028t0003g0138 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3093+15068C>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76723116 | ||||||
| chr8:76723201
|
T | C | 45 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0183others(42): Show | 46 | HG00280.hp2 HG00609.hp2 HG01074.hp1 others(43): Show |
intron_variant | MODIFIER | c.3093+15153T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76723201 | ||||||
| chr8:76723284
|
G | T | 1 | a0018c0064t0001g0137 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3093+15236G>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76723284 | ||||||
| chr8:76723556
|
C | CT | 40 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0183others(37): Show | 41 | HG00280.hp2 HG00609.hp2 HG01074.hp1 others(38): Show |
intron_variant | MODIFIER | c.3093+15519dupT | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76723556 | |||||
| chr8:76723882
|
A | C | 45 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0183others(42): Show | 46 | HG00280.hp2 HG00609.hp2 HG01074.hp1 others(43): Show |
intron_variant | MODIFIER | c.3093+15834A>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76723882 | ||||||
| chr8:76723885
|
T | C | 39 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0183others(36): Show | 40 | HG00280.hp2 HG00609.hp2 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.3093+15837T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76723885 | ||||||
| chr8:76723973
|
CAAAAACC others(3): Show |
C | 83 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0012g0043others(80): Show | 84 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.3093+15932_3093+15 others(16): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76723973 | |||||
| chr8:76724093
|
T | C | 1 | a0003c0058t0001g0238 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3093+16045T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76724093 | ||||||
| chr8:76724342
|
G | A | 3 | a0002c0038t0002g0153a0016c0083t0001g0152a0019c0082t0014g0139 | 3 | HG01884.hp2 HG02976.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.3093+16294G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76724342 | ||||||
| chr8:76724407
|
G | A | 1 | a0003c0002t0001g0068 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3093+16359G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76724407 | ||||||
| chr8:76724451
|
T | G | 1 | a0002c0028t0003g0138 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3093+16403T>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76724451 | ||||||
| chr8:76724483
|
G | A | 29 | a0001c0004t0002g0183a0001c0004t0002g0189a0001c0004t0002g0206others(26): Show | 30 | HG00280.hp2 HG00609.hp2 HG02040.hp2 others(27): Show |
intron_variant | MODIFIER | c.3093+16435G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76724483 | ||||||
| chr8:76724822
|
A | G | 2 | a0001c0003t0002g0174a0001c0080t0005g0006 | 2 | HG00735.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.3093+16774A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76724822 | ||||||
| chr8:76724870
|
T | C | 1 | a0003c0002t0009g0038 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.3093+16822T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76724870 | ||||||
| chr8:76724952
|
A | C | 1 | a0002c0028t0002g0202 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.3093+16904A>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76724952 | ||||||
| chr8:76724978
|
T | C | 3 | a0003c0007t0005g0086a0003c0059t0006g0085a0006c0016t0001g0084 | 3 | HG02258.hp2 HG02896.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.3093+16930T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76724978 | ||||||
| chr8:76725045
|
A | G | 1 | a0003c0034t0001g0142 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3093+16997A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76725045 | ||||||
| chr8:76725283
|
G | A | 1 | a0002c0028t0003g0138 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3093+17235G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76725283 | ||||||
| chr8:76725394
|
C | A | 4 | a0002c0036t0003g0225a0003c0035t0013g0228a0005c0005t0004g0226others(1): Show | 4 | HG00621.hp1 HG00621.hp2 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.3093+17346C>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76725394 | ||||||
| chr8:76725673
|
C | G | 130 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0012g0043others(127): Show | 132 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.3093+17625C>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76725673 | ||||||
| chr8:76725699
|
C | T | 1 | a0001c0051t0002g0141 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3093+17651C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76725699 | ||||||
| chr8:76725752
|
A | C | 6 | a0002c0001t0003g0020a0004c0026t0006g0019a0008c0010t0006g0015others(3): Show | 6 | HG00438.hp1 HG02040.hp1 NA18990.hp1 others(3): Show |
intron_variant | MODIFIER | c.3093+17704A>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76725752 | ||||||
| chr8:76725821
|
G | T | 1 | a0001c0015t0005g0213 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.3093+17773G>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76725821 | ||||||
| chr8:76725826
|
A | T | 1 | a0006c0016t0001g0103 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3093+17778A>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76725826 | ||||||
| chr8:76725839
|
G | T | 3 | a0001c0015t0001g0003a0001c0015t0005g0005a0003c0002t0001g0004 | 3 | HG01109.hp1 HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.3093+17791G>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76725839 | ||||||
| chr8:76725896
|
A | G | 1 | a0001c0017t0021g0129 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.3093+17848A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76725896 | ||||||
| chr8:76725985
|
G | A | 3 | a0001c0015t0001g0003a0001c0015t0005g0005a0003c0002t0001g0004 | 3 | HG01109.hp1 HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.3093+17937G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76725985 | ||||||
| chr8:76726029
|
C | T | 3 | a0003c0007t0005g0086a0003c0059t0006g0085a0006c0016t0001g0084 | 3 | HG02258.hp2 HG02896.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.3093+17981C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76726029 | ||||||
| chr8:76726049
|
C | G | 45 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0183others(42): Show | 46 | HG00280.hp2 HG00609.hp2 HG01074.hp1 others(43): Show |
intron_variant | MODIFIER | c.3093+18001C>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76726049 | ||||||
| chr8:76726157
|
T | G | 1 | a0004c0022t0004g0161 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.3093+18109T>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76726157 | ||||||
| chr8:76726166
|
G | A | 1 | a0002c0001t0017g0194 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.3093+18118G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76726166 | ||||||
| chr8:76726232
|
T | C | 3 | a0004c0068t0006g0109a0005c0005t0004g0126a0010c0013t0004g0130 | 3 | HG00423.hp2 HG01175.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.3093+18184T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76726232 | ||||||
| chr8:76726337
|
T | C | 1 | a0009c0069t0007g0057 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3093+18289T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76726337 | ||||||
| chr8:76726463
|
A | G | 10 | a0001c0004t0005g0219a0001c0052t0001g0063a0004c0012t0002g0061others(7): Show | 10 | HG02486.hp2 HG02615.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.3093+18415A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76726463 | ||||||
| chr8:76726514
|
G | T | 1 | a0030c0070t0007g0100 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.3093+18466G>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76726514 | ||||||
| chr8:76726568
|
T | C | 1 | a0003c0034t0001g0142 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3093+18520T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76726568 | ||||||
| chr8:76726903
|
A | C | 1 | a0006c0062t0001g0124 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.3093+18855A>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76726903 | ||||||
| chr8:76726980
|
C | T | 1 | a0003c0002t0001g0150 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3093+18932C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76726980 | ||||||
| chr8:76727011
|
C | T | 10 | a0001c0004t0005g0219a0001c0052t0001g0063a0004c0012t0002g0061others(7): Show | 10 | HG02486.hp2 HG02615.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.3093+18963C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76727011 | ||||||
| chr8:76727315
|
A | T | 2 | a0002c0006t0002g0098a0002c0006t0010g0031 | 2 | HG02818.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3093+19267A>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76727315 | ||||||
| chr8:76727419
|
A | C | 2 | a0001c0051t0002g0141a0017c0057t0001g0033 | 2 | HG02809.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.3093+19371A>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76727419 | ||||||
| chr8:76727629
|
A | G | 1 | a0001c0004t0002g0206 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.3093+19581A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76727629 | ||||||
| chr8:76727640
|
G | T | 45 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0183others(42): Show | 46 | HG00280.hp2 HG00609.hp2 HG01074.hp1 others(43): Show |
intron_variant | MODIFIER | c.3093+19592G>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76727640 | ||||||
| chr8:76727856
|
C | T | 1 | a0015c0056t0002g0042 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.3093+19808C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76727856 | ||||||
| chr8:76728262
|
G | A | 1 | a0022c0075t0001g0089 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3093+20214G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76728262 | ||||||
| chr8:76728337
|
A | T | 3 | a0001c0015t0001g0003a0001c0015t0005g0005a0003c0002t0001g0004 | 3 | HG01109.hp1 HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.3093+20289A>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76728337 | ||||||
| chr8:76728359
|
T | C | 139 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0012g0043others(136): Show | 141 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.3093+20311T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76728359 | ||||||
| chr8:76728367
|
T | C | 4 | a0002c0006t0010g0155a0003c0061t0001g0156a0006c0029t0001g0154others(1): Show | 4 | HG01081.hp1 HG01167.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.3093+20319T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76728367 | ||||||
| chr8:76728376
|
C | T | 3 | a0003c0007t0001g0102a0006c0016t0001g0103a0006c0016t0008g0101 | 3 | HG02723.hp1 HG03098.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3093+20328C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76728376 | ||||||
| chr8:76728619
|
C | T | 1 | a0006c0009t0006g0151 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3093+20571C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76728619 | ||||||
| chr8:76728894
|
C | T | 2 | a0002c0006t0003g0160a0002c0006t0003g0162 | 2 | NA18975.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.3093+20846C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76728894 | ||||||
| chr8:76728900
|
T | C | 84 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0012g0043others(81): Show | 85 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.3093+20852T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76728900 | ||||||
| chr8:76729111
|
A | G | 3 | a0002c0001t0001g0149a0003c0002t0001g0150a0006c0009t0006g0151 | 3 | HG02055.hp2 HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.3093+21063A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76729111 | ||||||
| chr8:76729119
|
A | T | 3 | a0001c0015t0001g0003a0001c0015t0005g0005a0003c0002t0001g0004 | 3 | HG01109.hp1 HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.3093+21071A>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76729119 | ||||||
| chr8:76729177
|
G | C | 42 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0183others(39): Show | 43 | HG00280.hp2 HG00609.hp2 HG01074.hp1 others(40): Show |
intron_variant | MODIFIER | c.3093+21129G>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76729177 | ||||||
| chr8:76729322
|
T | G | 1 | a0007c0044t0003g0192 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.3093+21274T>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76729322 | ||||||
| chr8:76729503
|
A | T | 2 | a0003c0045t0004g0136a0018c0064t0001g0137 | 2 | HG02572.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.3093+21455A>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76729503 | ||||||
| chr8:76729509
|
C | A | 1 | a0005c0005t0004g0078 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3093+21461C>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76729509 | ||||||
| chr8:76729926
|
C | T | 19 | a0001c0004t0002g0067a0001c0004t0002g0069a0001c0004t0005g0064others(16): Show | 19 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(16): Show |
intron_variant | MODIFIER | c.3093+21878C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76729926 | ||||||
| chr8:76729993
|
T | C | 3 | a0012c0024t0005g0001a0013c0023t0001g0143a0013c0023t0009g0144 | 4 | HG01168.hp2 HG02258.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.3093+21945T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76729993 | ||||||
| chr8:76730171
|
A | G | 42 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0183others(39): Show | 43 | HG00280.hp2 HG00609.hp2 HG01074.hp1 others(40): Show |
intron_variant | MODIFIER | c.3093+22123A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76730171 | ||||||
| chr8:76730173
|
A | G | 1 | a0017c0057t0001g0033 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3093+22125A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76730173 | ||||||
| chr8:76730388
|
C | T | 36 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0183others(33): Show | 37 | HG00280.hp2 HG00609.hp2 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.3093+22340C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76730388 | ||||||
| chr8:76730412
|
A | G | 1 | a0009c0069t0007g0057 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3093+22364A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76730412 | ||||||
| chr8:76730452
|
G | A | 42 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0183others(39): Show | 43 | HG00280.hp2 HG00609.hp2 HG01074.hp1 others(40): Show |
intron_variant | MODIFIER | c.3093+22404G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76730452 | ||||||
| chr8:76730508
|
C | T | 1 | a0003c0002t0001g0054 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3093+22460C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76730508 | ||||||
| chr8:76730509
|
T | C | 2 | a0002c0006t0002g0098a0002c0006t0010g0031 | 2 | HG02818.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3093+22461T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76730509 | ||||||
| chr8:76730592
|
G | A | 1 | a0003c0002t0001g0150 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3093+22544G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76730592 | ||||||
| chr8:76730624
|
G | A | 39 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0183others(36): Show | 40 | HG00280.hp2 HG00609.hp2 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.3093+22576G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76730624 | ||||||
| chr8:76730705
|
T | A | 2 | a0001c0051t0002g0141a0017c0057t0001g0033 | 2 | HG02809.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.3093+22657T>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76730705 | ||||||
| chr8:76730709
|
T | A | 1 | a0017c0057t0001g0033 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3093+22661T>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76730709 | ||||||
| chr8:76730729
|
T | C | 3 | a0001c0051t0002g0141a0010c0013t0004g0227a0017c0057t0001g0033 | 3 | HG00621.hp2 HG02809.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.3093+22681T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76730729 | ||||||
| chr8:76730765
|
C | T | 83 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0012g0043others(80): Show | 84 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.3093+22717C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76730765 | ||||||
| chr8:76730767
|
C | G | 1 | a0013c0023t0001g0143 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3093+22719C>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76730767 | ||||||
| chr8:76731112
|
A | G | 133 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0012g0043others(130): Show | 135 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.3093+23064A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76731112 | ||||||
| chr8:76731174
|
C | G | 2 | a0001c0051t0002g0141a0017c0057t0001g0033 | 2 | HG02809.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.3093+23126C>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76731174 | ||||||
| chr8:76731232
|
T | C | 84 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0012g0043others(81): Show | 85 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.3093+23184T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76731232 | ||||||
| chr8:76731255
|
T | C | 1 | a0002c0028t0003g0138 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3093+23207T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76731255 | ||||||
| chr8:76731324
|
C | T | 1 | a0003c0045t0004g0136 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3093+23276C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76731324 | ||||||
| chr8:76731522
|
G | A | 1 | a0001c0004t0005g0064 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3093+23474G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76731522 | ||||||
| chr8:76731730
|
T | C | 1 | a0010c0013t0004g0130 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.3093+23682T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76731730 | ||||||
| chr8:76731856
|
C | CATT | 33 | a0001c0004t0002g0067a0001c0004t0002g0069a0001c0004t0005g0064others(30): Show | 33 | HG00423.hp1 HG00597.hp2 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.3093+23842_3093+23 others(9): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76731856 | |||||
| chr8:76731856
|
C | CATTATT | 65 | a0001c0003t0002g0174a0001c0003t0003g0035a0001c0003t0003g0036others(62): Show | 66 | HG00280.hp2 HG00597.hp1 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.3093+23839_3093+23 others(12): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76731856 | |||||
| chr8:76731856
|
C | CATTATTA others(2): Show |
23 | a0001c0003t0002g0110a0001c0003t0002g0164a0001c0003t0002g0168others(20): Show | 23 | HG00408.hp2 HG01109.hp1 HG01952.hp1 others(20): Show |
intron_variant | MODIFIER | c.3093+23836_3093+23 others(15): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76731856 | |||||
| chr8:76731856
|
C | CATTATTA others(5): Show |
12 | a0002c0001t0003g0181a0002c0006t0003g0162a0002c0006t0003g0177others(9): Show | 12 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(9): Show |
intron_variant | MODIFIER | c.3093+23833_3093+23 others(18): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76731856 | |||||
| chr8:76731856
|
C | CATTATTA others(8): Show |
1 | a0001c0078t0006g0159 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.3093+23830_3093+23 others(21): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76731856 | |||||
| chr8:76731856
|
C | CATTATTA others(11): Show |
2 | a0002c0006t0003g0160a0004c0022t0004g0161 | 2 | HG01261.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.3093+23827_3093+23 others(24): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76731856 | |||||
| chr8:76731856
|
CATT | C | 39 | a0001c0004t0019g0050a0001c0015t0005g0011a0001c0042t0002g0010others(36): Show | 40 | HG00438.hp1 HG00544.hp1 HG01070.hp1 others(37): Show |
intron_variant | MODIFIER | c.3093+23842_3093+23 others(9): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76731856 | |||||
| chr8:76731892
|
T | A | 1 | a0001c0015t0005g0011 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3093+23844T>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76731892 | ||||||
| chr8:76731894
|
T | A | 2 | a0001c0003t0003g0120a0003c0027t0001g0055 | 2 | HG02074.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.3093+23846T>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76731894 | ||||||
| chr8:76732000
|
C | T | 41 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0183others(38): Show | 42 | HG00280.hp2 HG00609.hp2 HG01074.hp1 others(39): Show |
intron_variant | MODIFIER | c.3093+23952C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76732000 | ||||||
| chr8:76732043
|
T | C | 9 | a0001c0004t0019g0050a0001c0047t0016g0066a0002c0001t0003g0051others(6): Show | 9 | HG00544.hp1 HG00597.hp2 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.3093+23995T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76732043 | ||||||
| chr8:76732088
|
T | C | 44 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0183others(41): Show | 45 | HG00280.hp2 HG00609.hp2 HG01074.hp1 others(42): Show |
intron_variant | MODIFIER | c.3093+24040T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76732088 | ||||||
| chr8:76732170
|
A | G | 3 | a0012c0024t0005g0001a0013c0023t0001g0143a0013c0023t0009g0144 | 4 | HG01168.hp2 HG02258.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.3093+24122A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76732170 | ||||||
| chr8:76732250
|
G | T | 3 | a0002c0001t0001g0149a0003c0002t0001g0150a0006c0009t0006g0151 | 3 | HG02055.hp2 HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.3093+24202G>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76732250 | ||||||
| chr8:76732254
|
A | G | 1 | a0002c0001t0001g0149 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3093+24206A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76732254 | ||||||
| chr8:76732382
|
T | C | 1 | a0002c0001t0003g0044 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.3093+24334T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76732382 | ||||||
| chr8:76732462
|
C | A | 1 | a0001c0051t0002g0141 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3093+24414C>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76732462 | ||||||
| chr8:76732732
|
T | A | 44 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0183others(41): Show | 45 | HG00280.hp2 HG00609.hp2 HG01074.hp1 others(42): Show |
intron_variant | MODIFIER | c.3093+24684T>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76732732 | ||||||
| chr8:76732833
|
T | C | 44 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0183others(41): Show | 45 | HG00280.hp2 HG00609.hp2 HG01074.hp1 others(42): Show |
intron_variant | MODIFIER | c.3093+24785T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76732833 | ||||||
| chr8:76732986
|
AC | A | 38 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0183others(35): Show | 39 | HG00280.hp2 HG00609.hp2 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.3093+24939delC | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76732986 | ||||||
| chr8:76733130
|
G | A | 1 | a0015c0056t0002g0042 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.3093+25082G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76733130 | ||||||
| chr8:76733137
|
C | G | 44 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0183others(41): Show | 45 | HG00280.hp2 HG00609.hp2 HG01074.hp1 others(42): Show |
intron_variant | MODIFIER | c.3093+25089C>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76733137 | ||||||
| chr8:76733138
|
G | A | 1 | a0002c0001t0003g0037 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.3093+25090G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76733138 | ||||||
| chr8:76733143
|
G | T | 2 | a0001c0051t0002g0141a0017c0057t0001g0033 | 2 | HG02809.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.3093+25095G>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76733143 | ||||||
| chr8:76733278
|
T | C | 1 | a0004c0018t0002g0125 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.3093+25230T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76733278 | ||||||
| chr8:76733368
|
C | A | 12 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0012g0043others(9): Show | 12 | HG00408.hp2 HG00597.hp1 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.3093+25320C>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76733368 | ||||||
| chr8:76733453
|
A | C | 44 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0183others(41): Show | 45 | HG00280.hp2 HG00609.hp2 HG01074.hp1 others(42): Show |
intron_variant | MODIFIER | c.3093+25405A>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76733453 | ||||||
| chr8:76733529
|
G | T | 1 | a0010c0013t0004g0172 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3093+25481G>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76733529 | ||||||
| chr8:76733641
|
G | T | 44 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0183others(41): Show | 45 | HG00280.hp2 HG00609.hp2 HG01074.hp1 others(42): Show |
intron_variant | MODIFIER | c.3093+25593G>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76733641 | ||||||
| chr8:76733857
|
T | C | 1 | a0003c0034t0001g0142 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3093+25809T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76733857 | ||||||
| chr8:76733961
|
T | C | 2 | a0003c0002t0009g0038a0015c0056t0002g0042 | 2 | HG00639.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.3093+25913T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76733961 | ||||||
| chr8:76734016
|
C | G | 1 | a0002c0028t0003g0138 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3093+25968C>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76734016 | ||||||
| chr8:76734420
|
C | T | 3 | a0002c0006t0010g0155a0003c0061t0001g0156a0006c0029t0001g0154 | 3 | HG01081.hp1 HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3093+26372C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76734420 | ||||||
| chr8:76734491
|
G | A | 2 | a0003c0002t0001g0070a0003c0002t0001g0071 | 2 | HG03491.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.3093+26443G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76734491 | ||||||
| chr8:76734669
|
T | C | 1 | a0005c0005t0004g0119 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.3093+26621T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76734669 | ||||||
| chr8:76734693
|
A | G | 1 | a0001c0004t0005g0219 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3093+26645A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76734693 | ||||||
| chr8:76734791
|
C | G | 1 | a0002c0006t0003g0122 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.3093+26743C>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76734791 | ||||||
| chr8:76735029
|
G | A | 1 | a0006c0009t0006g0151 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3093+26981G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76735029 | ||||||
| chr8:76735063
|
T | C | 1 | a0031c0049t0001g0060 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.3093+27015T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76735063 | ||||||
| chr8:76735153
|
T | C | 1 | a0003c0045t0004g0136 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3093+27105T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76735153 | ||||||
| chr8:76735193
|
A | C | 2 | a0001c0008t0005g0236a0004c0019t0005g0235 | 2 | HG00735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.3093+27145A>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76735193 | ||||||
| chr8:76735224
|
A | G | 5 | a0003c0002t0001g0032a0003c0002t0001g0145a0003c0002t0001g0147others(2): Show | 5 | HG01175.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.3093+27176A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76735224 | ||||||
| chr8:76735639
|
T | C | 3 | a0001c0003t0002g0176a0002c0021t0003g0128a0007c0030t0003g0175 | 3 | HG02027.hp1 NA18946.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.3093+27591T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76735639 | ||||||
| chr8:76735715
|
A | G | 6 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0197others(3): Show | 6 | HG02572.hp1 HG02735.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.3093+27667A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76735715 | ||||||
| chr8:76735960
|
G | A | 4 | a0001c0078t0006g0159a0002c0006t0003g0160a0002c0006t0003g0162others(1): Show | 4 | HG01261.hp1 HG01952.hp2 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.3093+27912G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76735960 | ||||||
| chr8:76736151
|
A | T | 1 | a0034c0084t0002g0131 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3093+28103A>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76736151 | ||||||
| chr8:76736601
|
CT | C | 132 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0012g0043others(129): Show | 134 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.3093+28555delT | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76736601 | |||||
| chr8:76736815
|
A | G | 3 | a0002c0001t0003g0191a0002c0001t0003g0214a0007c0044t0003g0192 | 3 | HG00609.hp2 NA18981.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.3093+28767A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76736815 | ||||||
| chr8:76736886
|
T | A | 1 | a0005c0032t0004g0184 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.3093+28838T>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76736886 | ||||||
| chr8:76737284
|
G | T | 1 | a0001c0003t0002g0174 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.3093+29236G>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76737284 | ||||||
| chr8:76737359
|
A | T | 3 | a0002c0001t0001g0149a0003c0002t0001g0150a0006c0009t0006g0151 | 3 | HG02055.hp2 HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.3093+29311A>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76737359 | ||||||
| chr8:76737413
|
C | A | 9 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0197others(6): Show | 9 | HG02055.hp2 HG02572.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.3093+29365C>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76737413 | ||||||
| chr8:76737532
|
T | A | 5 | a0001c0004t0005g0064a0003c0002t0001g0074a0003c0002t0001g0076others(2): Show | 5 | HG01069.hp1 HG01884.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.3093+29484T>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76737532 | ||||||
| chr8:76737582
|
T | C | 3 | a0002c0038t0002g0153a0016c0083t0001g0152a0019c0082t0014g0139 | 3 | HG01884.hp2 HG02976.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.3093+29534T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76737582 | ||||||
| chr8:76737632
|
T | C | 1 | a0006c0009t0006g0151 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3093+29584T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76737632 | ||||||
| chr8:76738145
|
G | A | 1 | a0001c0025t0002g0210 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.3093+30097G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76738145 | ||||||
| chr8:76738224
|
C | T | 10 | a0001c0004t0005g0219a0001c0052t0001g0063a0004c0012t0002g0061others(7): Show | 10 | HG02486.hp2 HG02615.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.3093+30176C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76738224 | ||||||
| chr8:76738316
|
A | T | 3 | a0002c0038t0002g0153a0016c0083t0001g0152a0019c0082t0014g0139 | 3 | HG01884.hp2 HG02976.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.3093+30268A>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76738316 | ||||||
| chr8:76738339
|
G | A | 9 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0197others(6): Show | 9 | HG02055.hp2 HG02572.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.3093+30291G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76738339 | ||||||
| chr8:76738599
|
T | TTTCC | 42 | a0001c0003t0002g0179a0001c0004t0002g0069a0001c0004t0019g0050others(39): Show | 43 | HG00544.hp1 HG00544.hp2 HG01168.hp1 others(40): Show |
intron_variant | MODIFIER | c.3093+30575_3093+30 others(10): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76738599 | |||||
| chr8:76738599
|
T | TTTCCTTC others(1): Show |
21 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0012g0043others(18): Show | 21 | HG00597.hp1 HG00597.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.3093+30571_3093+30 others(14): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76738599 | |||||
| chr8:76738599
|
T | TTTCCTTC others(5): Show |
5 | a0001c0004t0002g0040a0001c0004t0002g0206a0002c0001t0003g0044others(2): Show | 5 | HG02056.hp2 HG03239.hp1 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.3093+30567_3093+30 others(18): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76738599 | |||||
| chr8:76738604
|
T | C | 1 | a0023c0077t0002g0094 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.3093+30556T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76738604 | ||||||
| chr8:76738607
|
CTTCCTTC others(13): Show |
C | 1 | a0028c0043t0001g0140 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3093+30579_3093+30 others(26): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76738607 | |||||
| chr8:76738611
|
CTTCCTTC others(9): Show |
C | 5 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0197others(2): Show | 5 | HG00609.hp1 HG02735.hp1 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.3093+30579_3093+30 others(22): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76738611 | |||||
| chr8:76738615
|
CTTCCTTC others(5): Show |
C | 4 | a0003c0002t0001g0054a0003c0002t0005g0023a0003c0034t0001g0142others(1): Show | 4 | HG02109.hp1 HG02258.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.3093+30579_3093+30 others(18): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76738615 | |||||
| chr8:76738619
|
CTTCCTTC others(1): Show |
C | 40 | a0001c0003t0002g0110a0001c0003t0002g0168a0001c0008t0005g0096others(37): Show | 41 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(38): Show |
intron_variant | MODIFIER | c.3093+30579_3093+30 others(14): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76738619 | |||||
| chr8:76738623
|
CTTCT | C | 33 | a0001c0003t0002g0087a0001c0003t0003g0120a0001c0004t0005g0219others(30): Show | 33 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(30): Show |
intron_variant | MODIFIER | c.3093+30579_3093+30 others(10): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76738623 | |||||
| chr8:76738627
|
T | C | 157 | a0001c0003t0002g0083a0001c0003t0002g0097a0001c0003t0002g0134others(154): Show | 158 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.3093+30579T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76738627 | ||||||
| chr8:76738651
|
T | C | 2 | a0001c0008t0005g0231a0002c0001t0003g0185 | 2 | HG02080.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.3093+30603T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76738651 | ||||||
| chr8:76738652
|
T | C | 1 | a0003c0007t0005g0052 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3093+30604T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76738652 | ||||||
| chr8:76738655
|
C | T | 1 | a0001c0008t0005g0231 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.3093+30607C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76738655 | ||||||
| chr8:76738661
|
C | T | 1 | a0001c0008t0005g0231 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.3093+30613C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76738661 | ||||||
| chr8:76738665
|
C | T | 1 | a0002c0001t0003g0185 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.3093+30617C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76738665 | ||||||
| chr8:76738677
|
T | C | 1 | a0002c0001t0003g0185 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.3093+30629T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76738677 | ||||||
| chr8:76738688
|
T | G | 3 | a0002c0001t0001g0149a0003c0002t0001g0150a0006c0009t0006g0151 | 3 | HG02055.hp2 HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.3093+30640T>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76738688 | ||||||
| chr8:76738712
|
T | TTCTC | 7 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0197others(4): Show | 7 | HG02717.hp1 HG02735.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.3093+30685_3093+30 others(10): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76738712 | |||||
| chr8:76738739
|
T | C | 1 | a0018c0064t0001g0137 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3093+30691T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76738739 | ||||||
| chr8:76738791
|
T | C | 2 | a0002c0001t0001g0149a0006c0009t0006g0151 | 2 | HG02055.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3093+30743T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76738791 | ||||||
| chr8:76738862
|
G | C | 3 | a0001c0017t0003g0107a0001c0017t0003g0108a0001c0017t0021g0129 | 3 | NA18983.hp2 NA19064.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.3093+30814G>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76738862 | ||||||
| chr8:76739003
|
C | G | 3 | a0001c0003t0002g0134a0001c0003t0022g0135a0023c0077t0002g0094 | 3 | HG00099.hp2 HG01070.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.3093+30955C>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76739003 | ||||||
| chr8:76739401
|
C | T | 132 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0012g0043others(129): Show | 134 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.3093+31353C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76739401 | ||||||
| chr8:76739837
|
C | A | 1 | a0001c0080t0005g0006 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.3093+31789C>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76739837 | ||||||
| chr8:76739938
|
T | C | 132 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0012g0043others(129): Show | 134 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.3093+31890T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76739938 | ||||||
| chr8:76739953
|
T | C | 1 | a0019c0082t0014g0139 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3093+31905T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76739953 | ||||||
| chr8:76740002
|
G | A | 118 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0012g0043others(115): Show | 120 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.3093+31954G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76740002 | ||||||
| chr8:76740049
|
C | A | 6 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0197others(3): Show | 6 | HG02572.hp1 HG02735.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.3093+32001C>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76740049 | ||||||
| chr8:76740168
|
T | G | 3 | a0004c0018t0002g0116a0005c0005t0004g0121a0034c0084t0002g0131 | 3 | NA18940.hp2 NA18994.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.3093+32120T>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76740168 | ||||||
| chr8:76740287
|
A | G | 2 | a0001c0051t0002g0141a0017c0057t0001g0033 | 2 | HG02809.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.3093+32239A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76740287 | ||||||
| chr8:76740495
|
GA | G | 9 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0197others(6): Show | 9 | HG02055.hp2 HG02572.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.3093+32457delA | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76740495 | |||||
| chr8:76740520
|
G | A | 3 | a0002c0038t0002g0153a0016c0083t0001g0152a0019c0082t0014g0139 | 3 | HG01884.hp2 HG02976.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.3093+32472G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76740520 | ||||||
| chr8:76740543
|
A | C | 9 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0197others(6): Show | 9 | HG02055.hp2 HG02572.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.3093+32495A>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76740543 | ||||||
| chr8:76740701
|
G | A | 1 | a0003c0034t0001g0142 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3093+32653G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76740701 | ||||||
| chr8:76740784
|
G | A | 4 | a0002c0006t0010g0155a0003c0061t0001g0156a0006c0029t0001g0154others(1): Show | 4 | HG01081.hp1 HG01167.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.3093+32736G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76740784 | ||||||
| chr8:76740841
|
G | A | 1 | a0002c0028t0003g0138 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3093+32793G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76740841 | ||||||
| chr8:76740955
|
A | G | 1 | a0002c0001t0003g0181 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.3093+32907A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76740955 | ||||||
| chr8:76740969
|
T | C | 1 | a0001c0004t0002g0183 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.3093+32921T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76740969 | ||||||
| chr8:76741336
|
C | T | 1 | a0001c0051t0002g0141 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3093+33288C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76741336 | ||||||
| chr8:76741434
|
G | T | 1 | a0002c0001t0003g0185 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.3093+33386G>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76741434 | ||||||
| chr8:76741609
|
G | A | 5 | a0001c0004t0002g0189a0002c0001t0003g0185a0002c0001t0003g0187others(2): Show | 5 | NA18939.hp2 NA18964.hp1 NA18980.hp2 others(2): Show |
intron_variant | MODIFIER | c.3093+33561G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76741609 | ||||||
| chr8:76741709
|
C | G | 139 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0012g0043others(136): Show | 141 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.3093+33661C>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76741709 | ||||||
| chr8:76741721
|
A | G | 2 | a0012c0024t0005g0001a0013c0023t0009g0144 | 3 | HG01168.hp2 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.3093+33673A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76741721 | ||||||
| chr8:76741916
|
C | A | 2 | a0002c0001t0001g0149a0006c0009t0006g0151 | 2 | HG02055.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3093+33868C>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76741916 | ||||||
| chr8:76742080
|
G | A | 5 | a0001c0004t0005g0064a0003c0002t0001g0074a0003c0002t0001g0076others(2): Show | 5 | HG01069.hp1 HG01884.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.3093+34032G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76742080 | ||||||
| chr8:76742114
|
G | A | 3 | a0002c0001t0001g0149a0003c0002t0001g0150a0006c0009t0006g0151 | 3 | HG02055.hp2 HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.3093+34066G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76742114 | ||||||
| chr8:76742416
|
G | A | 1 | a0002c0001t0001g0149 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3093+34368G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76742416 | ||||||
| chr8:76742753
|
T | C | 1 | a0026c0041t0005g0073 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3093+34705T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76742753 | ||||||
| chr8:76742813
|
C | T | 3 | a0001c0004t0002g0067a0001c0004t0002g0069a0002c0001t0003g0077 | 3 | HG00423.hp1 HG02027.hp2 HG02080.hp2 |
intron_variant | MODIFIER | c.3093+34765C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76742813 | ||||||
| chr8:76742879
|
G | A | 5 | a0002c0006t0003g0122a0004c0018t0002g0125a0005c0005t0004g0111others(2): Show | 5 | HG02071.hp2 NA18945.hp1 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.3093+34831G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76742879 | ||||||
| chr8:76742920
|
G | A | 4 | a0002c0036t0003g0225a0003c0035t0013g0228a0005c0005t0004g0226others(1): Show | 4 | HG00621.hp1 HG00621.hp2 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.3093+34872G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76742920 | ||||||
| chr8:76742965
|
A | AAC | 132 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0012g0043others(129): Show | 134 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.3093+34925_3093+34 others(8): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76742965 | |||||
| chr8:76743186
|
T | G | 122 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0012g0043others(119): Show | 124 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.3094-35022T>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76743186 | ||||||
| chr8:76743199
|
T | C | 3 | a0002c0001t0001g0149a0003c0002t0001g0150a0006c0009t0006g0151 | 3 | HG02055.hp2 HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.3094-35009T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76743199 | ||||||
| chr8:76743211
|
G | C | 1 | a0015c0056t0002g0042 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.3094-34997G>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76743211 | ||||||
| chr8:76743393
|
T | A | 2 | a0003c0007t0001g0090a0022c0075t0001g0089 | 2 | HG01891.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.3094-34815T>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76743393 | ||||||
| chr8:76743453
|
A | T | 1 | a0002c0001t0003g0185 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.3094-34755A>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76743453 | ||||||
| chr8:76743484
|
A | G | 9 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0197others(6): Show | 9 | HG02055.hp2 HG02572.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.3094-34724A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76743484 | ||||||
| chr8:76743580
|
T | A | 1 | a0001c0042t0002g0010 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.3094-34628T>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76743580 | ||||||
| chr8:76743625
|
A | G | 1 | a0002c0028t0003g0138 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3094-34583A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76743625 | ||||||
| chr8:76744049
|
A | G | 3 | a0002c0038t0002g0153a0016c0083t0001g0152a0019c0082t0014g0139 | 3 | HG01884.hp2 HG02976.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.3094-34159A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76744049 | ||||||
| chr8:76744074
|
A | G | 132 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0012g0043others(129): Show | 134 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.3094-34134A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76744074 | ||||||
| chr8:76744133
|
G | A | 3 | a0002c0038t0002g0153a0016c0083t0001g0152a0019c0082t0014g0139 | 3 | HG01884.hp2 HG02976.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.3094-34075G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76744133 | ||||||
| chr8:76744143
|
C | T | 1 | a0008c0010t0006g0021 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.3094-34065C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76744143 | ||||||
| chr8:76744206
|
T | C | 9 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0197others(6): Show | 9 | HG02055.hp2 HG02572.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.3094-34002T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76744206 | ||||||
| chr8:76744207
|
G | A | 9 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0197others(6): Show | 9 | HG02055.hp2 HG02572.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.3094-34001G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76744207 | ||||||
| chr8:76744294
|
C | T | 8 | a0001c0003t0002g0168a0001c0003t0002g0174a0001c0003t0002g0176others(5): Show | 8 | HG00735.hp1 HG01975.hp1 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.3094-33914C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76744294 | ||||||
| chr8:76744324
|
C | T | 1 | a0014c0039t0001g0072 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.3094-33884C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76744324 | ||||||
| chr8:76744332
|
C | T | 1 | a0002c0001t0003g0037 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.3094-33876C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76744332 | ||||||
| chr8:76744337
|
C | G | 1 | a0001c0003t0002g0164 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.3094-33871C>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76744337 | ||||||
| chr8:76744494
|
C | A | 1 | a0002c0028t0003g0138 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3094-33714C>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76744494 | ||||||
| chr8:76744612
|
C | T | 2 | a0001c0003t0002g0134a0001c0003t0022g0135 | 2 | HG00099.hp2 HG01070.hp2 |
intron_variant | MODIFIER | c.3094-33596C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76744612 | ||||||
| chr8:76744635
|
A | G | 6 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0197others(3): Show | 6 | HG02572.hp1 HG02735.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.3094-33573A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76744635 | ||||||
| chr8:76744716
|
A | G | 2 | a0002c0001t0001g0149a0006c0009t0006g0151 | 2 | HG02055.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3094-33492A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76744716 | ||||||
| chr8:76744900
|
G | T | 1 | a0002c0006t0003g0165 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.3094-33308G>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76744900 | ||||||
| chr8:76744928
|
A | G | 1 | a0003c0045t0004g0136 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3094-33280A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76744928 | ||||||
| chr8:76744949
|
T | G | 1 | a0006c0029t0001g0158 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3094-33259T>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76744949 | ||||||
| chr8:76745031
|
T | C | 1 | a0004c0012t0002g0190 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3094-33177T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76745031 | ||||||
| chr8:76745166
|
G | A | 1 | a0003c0002t0001g0148 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3094-33042G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76745166 | ||||||
| chr8:76745384
|
A | G | 8 | a0002c0001t0003g0020a0004c0026t0006g0019a0008c0010t0006g0015others(5): Show | 8 | HG00438.hp1 HG02040.hp1 NA18962.hp1 others(5): Show |
intron_variant | MODIFIER | c.3094-32824A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76745384 | ||||||
| chr8:76745412
|
G | A | 1 | a0002c0028t0003g0138 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3094-32796G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76745412 | ||||||
| chr8:76745505
|
A | G | 1 | a0003c0002t0001g0007 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3094-32703A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76745505 | ||||||
| chr8:76745522
|
T | C | 1 | a0019c0082t0014g0139 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3094-32686T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76745522 | ||||||
| chr8:76745580
|
GAT | G | 123 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0012g0043others(120): Show | 125 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.3094-32616_3094-32 others(8): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76745580 | |||||
| chr8:76745625
|
G | T | 6 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0197others(3): Show | 6 | HG02572.hp1 HG02735.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.3094-32583G>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76745625 | ||||||
| chr8:76745698
|
C | A | 9 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0197others(6): Show | 9 | HG02055.hp2 HG02572.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.3094-32510C>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76745698 | ||||||
| chr8:76745786
|
G | A | 1 | a0001c0055t0002g0201 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.3094-32422G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76745786 | ||||||
| chr8:76745879
|
G | A | 9 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0197others(6): Show | 9 | HG02055.hp2 HG02572.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.3094-32329G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76745879 | ||||||
| chr8:76746038
|
G | T | 6 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0197others(3): Show | 6 | HG02572.hp1 HG02735.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.3094-32170G>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76746038 | ||||||
| chr8:76746164
|
A | G | 2 | a0001c0063t0001g0053a0003c0007t0005g0052 | 2 | HG02965.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.3094-32044A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76746164 | ||||||
| chr8:76746303
|
G | A | 1 | a0018c0064t0001g0137 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3094-31905G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76746303 | ||||||
| chr8:76746409
|
G | A | 137 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0012g0043others(134): Show | 139 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(136): Show |
intron_variant | MODIFIER | c.3094-31799G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76746409 | ||||||
| chr8:76746414
|
C | T | 2 | a0008c0010t0006g0016a0021c0054t0003g0030 | 2 | NA18962.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.3094-31794C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76746414 | ||||||
| chr8:76746495
|
G | C | 1 | a0003c0007t0001g0092 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3094-31713G>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76746495 | ||||||
| chr8:76746685
|
AT | A | 6 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0197others(3): Show | 6 | HG02572.hp1 HG02735.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.3094-31519delT | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76746685 | |||||
| chr8:76746898
|
C | A | 36 | a0001c0004t0002g0067a0001c0004t0002g0069a0001c0004t0005g0064others(33): Show | 36 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(33): Show |
intron_variant | MODIFIER | c.3094-31310C>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76746898 | ||||||
| chr8:76747063
|
G | T | 1 | a0001c0052t0001g0063 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3094-31145G>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76747063 | ||||||
| chr8:76747147
|
T | A | 9 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0197others(6): Show | 9 | HG02055.hp2 HG02572.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.3094-31061T>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76747147 | ||||||
| chr8:76747150
|
T | G | 1 | a0003c0002t0008g0012 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3094-31058T>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76747150 | ||||||
| chr8:76747261
|
C | T | 130 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0012g0043others(127): Show | 132 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.3094-30947C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76747261 | ||||||
| chr8:76747264
|
T | C | 2 | a0002c0001t0001g0149a0006c0009t0006g0151 | 2 | HG02055.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3094-30944T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76747264 | ||||||
| chr8:76747337
|
G | A | 3 | a0002c0001t0001g0149a0003c0002t0001g0150a0006c0009t0006g0151 | 3 | HG02055.hp2 HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.3094-30871G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76747337 | ||||||
| chr8:76747371
|
T | C | 1 | a0003c0034t0001g0142 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3094-30837T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76747371 | ||||||
| chr8:76747604
|
G | A | 1 | a0017c0057t0001g0033 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3094-30604G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76747604 | ||||||
| chr8:76747669
|
C | T | 1 | a0004c0018t0002g0105 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.3094-30539C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76747669 | ||||||
| chr8:76747698
|
G | A | 6 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0197others(3): Show | 6 | HG02572.hp1 HG02735.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.3094-30510G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76747698 | ||||||
| chr8:76747707
|
G | A | 1 | a0032c0072t0002g0080 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.3094-30501G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76747707 | ||||||
| chr8:76747889
|
G | A | 3 | a0001c0033t0002g0224a0002c0036t0003g0225a0003c0035t0013g0228 | 3 | HG00621.hp1 NA18939.hp1 NA18946.hp1 |
intron_variant | MODIFIER | c.3094-30319G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76747889 | ||||||
| chr8:76747897
|
A | G | 1 | a0014c0039t0001g0072 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.3094-30311A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76747897 | ||||||
| chr8:76747933
|
A | AAAAC | 3 | a0001c0003t0002g0087a0005c0005t0004g0078a0008c0067t0003g0106 | 3 | HG04199.hp2 NA21309.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3094-30243_3094-30 others(10): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76747933 | |||||
| chr8:76747933
|
AAAAC | A | 129 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0012g0043others(126): Show | 131 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.3094-30243_3094-30 others(10): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76747933 | |||||
| chr8:76748041
|
C | T | 9 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0197others(6): Show | 9 | HG02055.hp2 HG02572.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.3094-30167C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76748041 | ||||||
| chr8:76748163
|
C | T | 1 | a0002c0028t0002g0202 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.3094-30045C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76748163 | ||||||
| chr8:76748272
|
C | T | 1 | a0012c0024t0005g0001 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.3094-29936C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76748272 | ||||||
| chr8:76748301
|
A | T | 4 | a0001c0004t0019g0050a0002c0001t0003g0051a0003c0040t0001g0049others(1): Show | 4 | HG00544.hp1 NA18953.hp1 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.3094-29907A>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76748301 | ||||||
| chr8:76748312
|
G | A | 64 | a0001c0004t0002g0183a0001c0004t0002g0189a0001c0004t0002g0206others(61): Show | 66 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.3094-29896G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76748312 | ||||||
| chr8:76748376
|
T | C | 5 | a0001c0015t0005g0213a0001c0025t0002g0210a0001c0055t0002g0201others(2): Show | 5 | HG02040.hp2 NA18968.hp2 NA19010.hp1 others(2): Show |
intron_variant | MODIFIER | c.3094-29832T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76748376 | ||||||
| chr8:76748646
|
G | C | 3 | a0012c0024t0005g0001a0013c0023t0001g0143a0013c0023t0009g0144 | 4 | HG01168.hp2 HG02258.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.3094-29562G>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76748646 | ||||||
| chr8:76748738
|
C | T | 2 | a0002c0001t0001g0149a0006c0009t0006g0151 | 2 | HG02055.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3094-29470C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76748738 | ||||||
| chr8:76748752
|
TAACAGCC others(4): Show |
T | 3 | a0002c0038t0002g0153a0016c0083t0001g0152a0019c0082t0014g0139 | 3 | HG01884.hp2 HG02976.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.3094-29452_3094-29 others(17): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76748752 | |||||
| chr8:76748853
|
C | A | 1 | a0003c0045t0004g0136 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3094-29355C>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76748853 | ||||||
| chr8:76748873
|
G | C | 1 | a0001c0003t0022g0135 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.3094-29335G>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76748873 | ||||||
| chr8:76749324
|
C | G | 132 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0012g0043others(129): Show | 134 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.3094-28884C>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76749324 | ||||||
| chr8:76749358
|
AAC | A | 3 | a0002c0038t0002g0153a0016c0083t0001g0152a0019c0082t0014g0139 | 3 | HG01884.hp2 HG02976.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.3094-28847_3094-28 others(8): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76749358 | |||||
| chr8:76749442
|
C | A | 12 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0012g0043others(9): Show | 12 | HG00408.hp2 HG00597.hp1 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.3094-28766C>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76749442 | ||||||
| chr8:76749486
|
G | A | 1 | a0004c0046t0002g0075 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.3094-28722G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76749486 | ||||||
| chr8:76749798
|
C | G | 118 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0012g0043others(115): Show | 120 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.3094-28410C>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76749798 | ||||||
| chr8:76749913
|
T | A | 1 | a0018c0064t0001g0137 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3094-28295T>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76749913 | ||||||
| chr8:76750133
|
C | T | 1 | a0006c0016t0008g0101 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3094-28075C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76750133 | ||||||
| chr8:76750305
|
T | C | 36 | a0001c0004t0002g0067a0001c0004t0002g0069a0001c0004t0005g0064others(33): Show | 36 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(33): Show |
intron_variant | MODIFIER | c.3094-27903T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76750305 | ||||||
| chr8:76750560
|
A | G | 119 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0012g0043others(116): Show | 121 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.3094-27648A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76750560 | ||||||
| chr8:76750769
|
T | A | 2 | a0002c0036t0003g0225a0003c0035t0013g0228 | 2 | HG00621.hp1 NA18946.hp1 |
intron_variant | MODIFIER | c.3094-27439T>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76750769 | ||||||
| chr8:76750776
|
C | T | 3 | a0002c0001t0001g0149a0003c0002t0001g0150a0006c0009t0006g0151 | 3 | HG02055.hp2 HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.3094-27432C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76750776 | ||||||
| chr8:76750802
|
C | T | 118 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0012g0043others(115): Show | 120 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.3094-27406C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76750802 | ||||||
| chr8:76750907
|
C | A | 34 | a0001c0004t0002g0183a0001c0004t0002g0189a0001c0004t0002g0206others(31): Show | 35 | HG00280.hp2 HG00609.hp2 HG01074.hp1 others(32): Show |
intron_variant | MODIFIER | c.3094-27301C>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76750907 | ||||||
| chr8:76750945
|
C | T | 121 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0012g0043others(118): Show | 123 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.3094-27263C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76750945 | ||||||
| chr8:76751010
|
T | C | 121 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0012g0043others(118): Show | 123 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.3094-27198T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76751010 | ||||||
| chr8:76751023
|
T | G | 132 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0012g0043others(129): Show | 134 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.3094-27185T>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76751023 | ||||||
| chr8:76751166
|
C | T | 118 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0012g0043others(115): Show | 120 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.3094-27042C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76751166 | ||||||
| chr8:76751363
|
C | T | 9 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0197others(6): Show | 9 | HG02055.hp2 HG02572.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.3094-26845C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76751363 | ||||||
| chr8:76751455
|
C | G | 1 | a0003c0007t0001g0090 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3094-26753C>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76751455 | ||||||
| chr8:76751717
|
A | G | 1 | a0001c0033t0002g0224 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.3094-26491A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76751717 | ||||||
| chr8:76751792
|
G | T | 2 | a0002c0001t0003g0002a0002c0001t0003g0193 | 3 | HG00280.hp2 NA18945.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.3094-26416G>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76751792 | ||||||
| chr8:76752102
|
G | T | 5 | a0003c0007t0001g0240a0003c0007t0001g0241a0003c0058t0001g0238others(2): Show | 5 | HG02109.hp2 HG02615.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.3094-26106G>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76752102 | ||||||
| chr8:76752305
|
A | T | 15 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0197others(12): Show | 16 | HG00280.hp2 HG02055.hp2 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.3094-25903A>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76752305 | ||||||
| chr8:76752316
|
A | G | 1 | a0002c0001t0003g0037 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.3094-25892A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76752316 | ||||||
| chr8:76752348
|
A | C | 3 | a0002c0038t0002g0153a0016c0083t0001g0152a0019c0082t0014g0139 | 3 | HG01884.hp2 HG02976.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.3094-25860A>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76752348 | ||||||
| chr8:76752485
|
T | TA | 7 | a0001c0003t0002g0087a0001c0003t0002g0164a0002c0006t0004g0217others(4): Show | 7 | HG02056.hp1 HG02735.hp2 HG03239.hp2 others(4): Show |
intron_variant | MODIFIER | c.3094-25723_3094-25 others(7): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76752485 | ||||||
| chr8:76752485
|
TCC | T | 6 | a0001c0004t0002g0197a0001c0004t0005g0064a0002c0038t0002g0153others(3): Show | 6 | HG01884.hp1 HG01884.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.3094-25722_3094-25 others(8): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76752485 | ||||||
| chr8:76752486
|
C | A | 227 | a0001c0003t0002g0083a0001c0003t0002g0097a0001c0003t0002g0110others(224): Show | 229 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.3094-25722C>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76752486 | ||||||
| chr8:76752487
|
C | A | 7 | a0001c0003t0002g0087a0001c0003t0002g0164a0002c0006t0004g0217others(4): Show | 7 | HG02056.hp1 HG02735.hp2 HG03239.hp2 others(4): Show |
intron_variant | MODIFIER | c.3094-25721C>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76752487 | ||||||
| chr8:76752487
|
CA | C | 114 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0012g0043others(111): Show | 115 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.3094-25699delA | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76752487 | |||||
| chr8:76752489
|
A | C | 6 | a0001c0004t0002g0197a0001c0004t0005g0064a0002c0038t0002g0153others(3): Show | 6 | HG01884.hp1 HG01884.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.3094-25719A>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76752489 | ||||||
| chr8:76752490
|
A | C | 1 | a0004c0026t0006g0019 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.3094-25718A>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76752490 | ||||||
| chr8:76752504
|
A | G | 35 | a0001c0004t0002g0067a0001c0004t0002g0069a0001c0004t0002g0183others(32): Show | 36 | HG00280.hp2 HG00423.hp1 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.3094-25704A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76752504 | ||||||
| chr8:76752747
|
G | T | 3 | a0012c0024t0005g0001a0013c0023t0001g0143a0013c0023t0009g0144 | 4 | HG01168.hp2 HG02258.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.3094-25461G>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76752747 | ||||||
| chr8:76752789
|
C | A | 12 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0012g0043others(9): Show | 12 | HG00408.hp2 HG00597.hp1 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.3094-25419C>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76752789 | ||||||
| chr8:76752907
|
T | G | 4 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0197others(1): Show | 4 | HG02735.hp1 HG03491.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.3094-25301T>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76752907 | ||||||
| chr8:76752932
|
T | G | 2 | a0003c0002t0006g0058a0009c0069t0007g0057 | 2 | HG02886.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.3094-25276T>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76752932 | ||||||
| chr8:76753084
|
G | A | 2 | a0001c0051t0002g0141a0017c0057t0001g0033 | 2 | HG02809.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.3094-25124G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76753084 | ||||||
| chr8:76753112
|
A | G | 9 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0197others(6): Show | 9 | HG02055.hp2 HG02572.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.3094-25096A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76753112 | ||||||
| chr8:76753185
|
A | G | 130 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0012g0043others(127): Show | 132 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.3094-25023A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76753185 | ||||||
| chr8:76753196
|
T | G | 3 | a0002c0038t0002g0153a0016c0083t0001g0152a0019c0082t0014g0139 | 3 | HG01884.hp2 HG02976.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.3094-25012T>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76753196 | ||||||
| chr8:76753286
|
C | G | 1 | a0011c0020t0004g0041 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.3094-24922C>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76753286 | ||||||
| chr8:76753357
|
A | G | 3 | a0002c0001t0001g0149a0003c0002t0001g0150a0006c0009t0006g0151 | 3 | HG02055.hp2 HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.3094-24851A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76753357 | ||||||
| chr8:76753629
|
C | CT | 31 | a0001c0003t0002g0174a0001c0003t0002g0179a0001c0003t0003g0120others(28): Show | 32 | HG00597.hp2 HG01168.hp2 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.3094-24557dupT | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76753629 | |||||
| chr8:76753629
|
CT | C | 7 | a0001c0015t0001g0003a0001c0015t0005g0005a0002c0001t0003g0207others(4): Show | 7 | HG01109.hp1 HG03139.hp2 HG03516.hp2 others(4): Show |
intron_variant | MODIFIER | c.3094-24557delT | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76753629 | |||||
| chr8:76753629
|
CTTTTTTT others(4): Show |
C | 2 | a0001c0051t0002g0141a0017c0057t0001g0033 | 2 | HG02809.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.3094-24567_3094-24 others(17): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76753629 | |||||
| chr8:76753745
|
C | T | 121 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0012g0043others(118): Show | 123 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.3094-24463C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76753745 | ||||||
| chr8:76753876
|
C | A | 2 | a0003c0002t0006g0058a0009c0069t0007g0057 | 2 | HG02886.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.3094-24332C>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76753876 | ||||||
| chr8:76753906
|
G | A | 35 | a0001c0003t0002g0110a0001c0008t0005g0096a0001c0008t0005g0157others(32): Show | 35 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(32): Show |
intron_variant | MODIFIER | c.3094-24302G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76753906 | ||||||
| chr8:76753910
|
G | A | 3 | a0001c0025t0002g0200a0002c0001t0003g0195a0002c0001t0004g0199 | 3 | HG02071.hp1 NA18983.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.3094-24298G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76753910 | ||||||
| chr8:76753943
|
C | CA | 240 | a0001c0003t0002g0083a0001c0003t0002g0087a0001c0003t0002g0097others(237): Show | 242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.3094-24258dupA | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76753943 | |||||
| chr8:76754086
|
TA | T | 3 | a0002c0001t0001g0149a0003c0002t0001g0150a0006c0009t0006g0151 | 3 | HG02055.hp2 HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.3094-24121delA | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76754086 | ||||||
| chr8:76754236
|
T | C | 130 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0012g0043others(127): Show | 132 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.3094-23972T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76754236 | ||||||
| chr8:76754379
|
C | T | 118 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0012g0043others(115): Show | 120 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.3094-23829C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76754379 | ||||||
| chr8:76754480
|
C | T | 1 | a0001c0003t0002g0164 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.3094-23728C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76754480 | ||||||
| chr8:76754495
|
AC | A | 129 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0012g0043others(126): Show | 131 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.3094-23712delC | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76754495 | ||||||
| chr8:76754496
|
C | A | 3 | a0001c0004t0002g0040a0003c0002t0001g0070a0007c0014t0003g0186 | 3 | HG04115.hp1 NA18960.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.3094-23712C>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76754496 | ||||||
| chr8:76754556
|
C | T | 1 | a0005c0032t0004g0184 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.3094-23652C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76754556 | ||||||
| chr8:76754849
|
C | A | 3 | a0012c0024t0005g0001a0013c0023t0001g0143a0013c0023t0009g0144 | 4 | HG01168.hp2 HG02258.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.3094-23359C>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76754849 | ||||||
| chr8:76754932
|
A | G | 1 | a0002c0006t0003g0170 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.3094-23276A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76754932 | ||||||
| chr8:76755113
|
T | A | 1 | a0001c0004t0005g0064 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3094-23095T>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76755113 | ||||||
| chr8:76755238
|
C | T | 5 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0197others(2): Show | 5 | HG02735.hp1 HG03491.hp2 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.3094-22970C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76755238 | ||||||
| chr8:76755396
|
C | A | 1 | a0001c0003t0002g0097 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.3094-22812C>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76755396 | ||||||
| chr8:76755519
|
G | A | 2 | a0002c0006t0003g0211a0002c0021t0018g0133 | 2 | NA18747.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.3094-22689G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76755519 | ||||||
| chr8:76755778
|
T | C | 1 | a0005c0005t0004g0078 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3094-22430T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76755778 | ||||||
| chr8:76756041
|
AG | A | 9 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0197others(6): Show | 9 | HG02055.hp2 HG02572.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.3094-22166delG | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76756041 | ||||||
| chr8:76756089
|
G | A | 1 | a0001c0015t0005g0213 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.3094-22119G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76756089 | ||||||
| chr8:76756210
|
C | A | 9 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0197others(6): Show | 9 | HG02055.hp2 HG02572.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.3094-21998C>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76756210 | ||||||
| chr8:76756327
|
T | C | 120 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0012g0043others(117): Show | 122 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.3094-21881T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76756327 | ||||||
| chr8:76756401
|
A | T | 5 | a0001c0015t0005g0213a0001c0025t0002g0210a0001c0055t0002g0201others(2): Show | 5 | HG02040.hp2 NA18968.hp2 NA19010.hp1 others(2): Show |
intron_variant | MODIFIER | c.3094-21807A>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76756401 | ||||||
| chr8:76756454
|
G | T | 2 | a0002c0001t0001g0149a0006c0009t0006g0151 | 2 | HG02055.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3094-21754G>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76756454 | ||||||
| chr8:76756468
|
C | T | 9 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0197others(6): Show | 9 | HG02055.hp2 HG02572.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.3094-21740C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76756468 | ||||||
| chr8:76756583
|
C | A | 1 | a0001c0004t0005g0219 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3094-21625C>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76756583 | ||||||
| chr8:76756630
|
C | CA | 2 | a0012c0024t0005g0001a0013c0023t0009g0144 | 3 | HG01168.hp2 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.3094-21576dupA | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76756630 | |||||
| chr8:76756831
|
C | CATG | 9 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0197others(6): Show | 9 | HG02055.hp2 HG02572.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.3094-21373_3094-21 others(9): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76756831 | |||||
| chr8:76756901
|
A | G | 1 | a0001c0003t0002g0216 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.3094-21307A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76756901 | ||||||
| chr8:76757084
|
T | C | 1 | a0002c0028t0003g0138 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3094-21124T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76757084 | ||||||
| chr8:76757257
|
A | T | 6 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0197others(3): Show | 6 | HG02572.hp1 HG02735.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.3094-20951A>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76757257 | ||||||
| chr8:76757276
|
A | C | 132 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0012g0043others(129): Show | 134 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.3094-20932A>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76757276 | ||||||
| chr8:76757311
|
G | C | 14 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0012g0043others(11): Show | 14 | HG00408.hp2 HG00597.hp1 HG00639.hp1 others(11): Show |
intron_variant | MODIFIER | c.3094-20897G>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76757311 | ||||||
| chr8:76757449
|
C | T | 3 | a0002c0038t0002g0153a0016c0083t0001g0152a0019c0082t0014g0139 | 3 | HG01884.hp2 HG02976.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.3094-20759C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76757449 | ||||||
| chr8:76757529
|
C | T | 1 | a0016c0083t0001g0152 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3094-20679C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76757529 | ||||||
| chr8:76757551
|
T | G | 5 | a0003c0002t0001g0032a0003c0002t0001g0145a0003c0002t0001g0147others(2): Show | 5 | HG01175.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.3094-20657T>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76757551 | ||||||
| chr8:76757840
|
G | C | 1 | a0018c0064t0001g0137 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3094-20368G>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76757840 | ||||||
| chr8:76757872
|
A | G | 9 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0197others(6): Show | 9 | HG02055.hp2 HG02572.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.3094-20336A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76757872 | ||||||
| chr8:76757980
|
T | A | 6 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0197others(3): Show | 6 | HG02572.hp1 HG02735.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.3094-20228T>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76757980 | ||||||
| chr8:76758007
|
T | C | 1 | a0003c0002t0001g0148 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3094-20201T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76758007 | ||||||
| chr8:76758112
|
T | G | 1 | a0001c0047t0016g0066 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.3094-20096T>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76758112 | ||||||
| chr8:76758474
|
A | G | 1 | a0003c0034t0001g0142 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3094-19734A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76758474 | ||||||
| chr8:76758557
|
C | T | 1 | a0003c0037t0002g0024 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3094-19651C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76758557 | ||||||
| chr8:76758586
|
C | T | 5 | a0003c0002t0001g0032a0003c0002t0001g0145a0003c0002t0001g0147others(2): Show | 5 | HG01175.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.3094-19622C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76758586 | ||||||
| chr8:76758637
|
G | C | 121 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0012g0043others(118): Show | 123 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.3094-19571G>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76758637 | ||||||
| chr8:76758637
|
G | T | 1 | a0022c0075t0001g0089 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3094-19571G>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76758637 | ||||||
| chr8:76759028
|
A | T | 63 | a0001c0004t0002g0067a0001c0004t0002g0069a0001c0004t0002g0183others(60): Show | 64 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.3094-19180A>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76759028 | ||||||
| chr8:76759050
|
A | G | 9 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0197others(6): Show | 9 | HG02055.hp2 HG02572.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.3094-19158A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76759050 | ||||||
| chr8:76759053
|
T | C | 2 | a0001c0051t0002g0141a0017c0057t0001g0033 | 2 | HG02809.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.3094-19155T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76759053 | ||||||
| chr8:76759067
|
A | G | 1 | a0006c0009t0006g0151 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3094-19141A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76759067 | ||||||
| chr8:76759069
|
A | G | 1 | a0009c0011t0006g0065 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.3094-19139A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76759069 | ||||||
| chr8:76759402
|
C | G | 3 | a0002c0001t0001g0149a0003c0002t0001g0150a0006c0009t0006g0151 | 3 | HG02055.hp2 HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.3094-18806C>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76759402 | ||||||
| chr8:76759484
|
T | C | 118 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0012g0043others(115): Show | 120 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.3094-18724T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76759484 | ||||||
| chr8:76759641
|
G | T | 130 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0012g0043others(127): Show | 132 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.3094-18567G>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76759641 | ||||||
| chr8:76759737
|
A | G | 2 | a0001c0008t0005g0236a0004c0019t0005g0235 | 2 | HG00735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.3094-18471A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76759737 | ||||||
| chr8:76759858
|
T | C | 6 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0197others(3): Show | 6 | HG02572.hp1 HG02735.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.3094-18350T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76759858 | ||||||
| chr8:76760119
|
T | A | 2 | a0003c0007t0001g0090a0022c0075t0001g0089 | 2 | HG01891.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.3094-18089T>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76760119 | ||||||
| chr8:76760179
|
T | TG | 6 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0197others(3): Show | 6 | HG02572.hp1 HG02735.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.3094-18028dupG | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76760179 | |||||
| chr8:76760370
|
T | A | 1 | a0002c0001t0001g0149 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3094-17838T>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76760370 | ||||||
| chr8:76760515
|
C | T | 3 | a0002c0038t0002g0153a0016c0083t0001g0152a0019c0082t0014g0139 | 3 | HG01884.hp2 HG02976.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.3094-17693C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76760515 | ||||||
| chr8:76760568
|
G | C | 9 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0197others(6): Show | 9 | HG02055.hp2 HG02572.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.3094-17640G>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76760568 | ||||||
| chr8:76760690
|
G | A | 1 | a0001c0003t0002g0110 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.3094-17518G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76760690 | ||||||
| chr8:76760865
|
G | A | 3 | a0001c0015t0001g0003a0001c0015t0005g0005a0003c0002t0001g0004 | 3 | HG01109.hp1 HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.3094-17343G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76760865 | ||||||
| chr8:76760928
|
C | CA | 28 | a0001c0051t0002g0141a0001c0063t0001g0053a0002c0001t0001g0149others(25): Show | 29 | HG01081.hp1 HG01081.hp2 HG01167.hp2 others(26): Show |
intron_variant | MODIFIER | c.3094-17258dupA | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76760928 | |||||
| chr8:76760928
|
C | CAA | 93 | a0001c0003t0003g0035a0001c0003t0012g0043a0001c0004t0002g0040others(90): Show | 94 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.3094-17259_3094-17 others(8): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76760928 | |||||
| chr8:76760928
|
C | CAAA | 22 | a0001c0003t0003g0036a0001c0004t0005g0064a0001c0052t0001g0063others(19): Show | 22 | HG00597.hp2 HG00609.hp2 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.3094-17260_3094-17 others(9): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76760928 | |||||
| chr8:76760951
|
G | A | 3 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0197 | 3 | HG02735.hp1 HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.3094-17257G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76760951 | ||||||
| chr8:76760953
|
G | A | 1 | a0001c0004t0002g0197 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.3094-17255G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76760953 | ||||||
| chr8:76760953
|
GA | G | 6 | a0002c0001t0001g0149a0003c0002t0001g0150a0003c0045t0004g0136others(3): Show | 6 | HG02055.hp2 HG02572.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.3094-17247delA | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76760953 | |||||
| chr8:76761145
|
A | T | 1 | a0003c0034t0001g0142 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3094-17063A>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76761145 | ||||||
| chr8:76761430
|
A | C | 2 | a0002c0001t0001g0149a0006c0009t0006g0151 | 2 | HG02055.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3094-16778A>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76761430 | ||||||
| chr8:76761530
|
T | G | 4 | a0003c0002t0001g0007a0003c0002t0001g0009a0003c0002t0001g0081others(1): Show | 4 | HG02818.hp2 HG03209.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.3094-16678T>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76761530 | ||||||
| chr8:76761655
|
AC | A | 3 | a0002c0001t0001g0149a0003c0002t0001g0150a0006c0009t0006g0151 | 3 | HG02055.hp2 HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.3094-16552delC | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76761655 | ||||||
| chr8:76761796
|
C | G | 2 | a0001c0063t0001g0053a0003c0007t0005g0052 | 2 | HG02965.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.3094-16412C>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76761796 | ||||||
| chr8:76761848
|
T | C | 2 | a0001c0051t0002g0141a0017c0057t0001g0033 | 2 | HG02809.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.3094-16360T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76761848 | ||||||
| chr8:76761878
|
T | C | 5 | a0003c0002t0001g0032a0003c0002t0001g0145a0003c0002t0001g0147others(2): Show | 5 | HG01175.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.3094-16330T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76761878 | ||||||
| chr8:76762063
|
A | G | 5 | a0003c0002t0001g0032a0003c0002t0001g0145a0003c0002t0001g0147others(2): Show | 5 | HG01175.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.3094-16145A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76762063 | ||||||
| chr8:76762068
|
A | G | 118 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0012g0043others(115): Show | 120 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.3094-16140A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76762068 | ||||||
| chr8:76762339
|
G | A | 1 | a0005c0032t0004g0184 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.3094-15869G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76762339 | ||||||
| chr8:76762609
|
T | A | 9 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0197others(6): Show | 9 | HG02055.hp2 HG02572.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.3094-15599T>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76762609 | ||||||
| chr8:76762792
|
G | A | 1 | a0003c0002t0008g0012 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3094-15416G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76762792 | ||||||
| chr8:76762807
|
A | G | 1 | a0003c0045t0004g0136 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3094-15401A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76762807 | ||||||
| chr8:76762972
|
A | G | 1 | a0003c0037t0002g0024 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3094-15236A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76762972 | ||||||
| chr8:76763076
|
C | G | 132 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0012g0043others(129): Show | 134 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.3094-15132C>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76763076 | ||||||
| chr8:76763097
|
G | A | 2 | a0001c0051t0002g0141a0017c0057t0001g0033 | 2 | HG02809.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.3094-15111G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76763097 | ||||||
| chr8:76763106
|
T | C | 2 | a0002c0001t0001g0149a0006c0009t0006g0151 | 2 | HG02055.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3094-15102T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76763106 | ||||||
| chr8:76763138
|
G | A | 1 | a0026c0041t0005g0073 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3094-15070G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76763138 | ||||||
| chr8:76763215
|
G | A | 2 | a0002c0006t0002g0098a0002c0006t0010g0031 | 2 | HG02818.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3094-14993G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76763215 | ||||||
| chr8:76763233
|
TCTGATAG others(3): Show |
T | 121 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0012g0043others(118): Show | 123 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.3094-14973_3094-14 others(16): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76763233 | |||||
| chr8:76763572
|
G | A | 5 | a0001c0063t0001g0053a0003c0002t0001g0054a0003c0007t0005g0052others(2): Show | 5 | HG02965.hp2 HG02970.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.3094-14636G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76763572 | ||||||
| chr8:76763616
|
C | T | 1 | a0006c0048t0001g0022 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.3094-14592C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76763616 | ||||||
| chr8:76763729
|
T | G | 3 | a0003c0002t0001g0054a0003c0027t0001g0055a0003c0027t0001g0056 | 3 | HG02970.hp1 HG03486.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.3094-14479T>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76763729 | ||||||
| chr8:76763759
|
T | G | 132 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0012g0043others(129): Show | 134 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.3094-14449T>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76763759 | ||||||
| chr8:76763766
|
G | A | 2 | a0001c0078t0006g0159a0004c0022t0004g0161 | 2 | HG01261.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.3094-14442G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76763766 | ||||||
| chr8:76763883
|
G | A | 1 | a0002c0006t0010g0155 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3094-14325G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76763883 | ||||||
| chr8:76764062
|
T | C | 10 | a0001c0004t0005g0219a0001c0052t0001g0063a0004c0012t0002g0061others(7): Show | 10 | HG02486.hp2 HG02615.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.3094-14146T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76764062 | ||||||
| chr8:76764171
|
T | C | 1 | a0002c0021t0018g0133 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.3094-14037T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76764171 | ||||||
| chr8:76764183
|
A | G | 2 | a0001c0051t0002g0141a0017c0057t0001g0033 | 2 | HG02809.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.3094-14025A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76764183 | ||||||
| chr8:76764200
|
A | G | 1 | a0004c0026t0006g0019 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.3094-14008A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76764200 | ||||||
| chr8:76764202
|
A | C | 1 | a0004c0026t0006g0019 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.3094-14006A>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76764202 | ||||||
| chr8:76764218
|
A | T | 1 | a0004c0026t0006g0019 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.3094-13990A>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76764218 | ||||||
| chr8:76764219
|
G | A | 1 | a0004c0026t0006g0019 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.3094-13989G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76764219 | ||||||
| chr8:76764221
|
T | C | 1 | a0004c0026t0006g0019 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.3094-13987T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76764221 | ||||||
| chr8:76764222
|
T | A | 1 | a0004c0026t0006g0019 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.3094-13986T>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76764222 | ||||||
| chr8:76764226
|
T | A | 1 | a0004c0026t0006g0019 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.3094-13982T>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76764226 | ||||||
| chr8:76764231
|
T | C | 1 | a0004c0026t0006g0019 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.3094-13977T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76764231 | ||||||
| chr8:76764232
|
G | T | 1 | a0004c0026t0006g0019 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.3094-13976G>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76764232 | ||||||
| chr8:76764233
|
G | C | 1 | a0004c0026t0006g0019 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.3094-13975G>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76764233 | ||||||
| chr8:76764241
|
A | C | 1 | a0004c0026t0006g0019 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.3094-13967A>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76764241 | ||||||
| chr8:76764243
|
T | G | 1 | a0004c0026t0006g0019 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.3094-13965T>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76764243 | ||||||
| chr8:76764245
|
A | C | 1 | a0004c0026t0006g0019 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.3094-13963A>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76764245 | ||||||
| chr8:76764256
|
T | A | 1 | a0004c0026t0006g0019 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.3094-13952T>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76764256 | ||||||
| chr8:76764257
|
T | G | 1 | a0004c0026t0006g0019 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.3094-13951T>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76764257 | ||||||
| chr8:76764258
|
T | A | 1 | a0004c0026t0006g0019 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.3094-13950T>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76764258 | ||||||
| chr8:76764259
|
G | A | 1 | a0004c0026t0006g0019 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.3094-13949G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76764259 | ||||||
| chr8:76764261
|
C | A | 1 | a0004c0026t0006g0019 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.3094-13947C>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76764261 | ||||||
| chr8:76764264
|
G | A | 1 | a0004c0026t0006g0019 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.3094-13944G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76764264 | ||||||
| chr8:76764266
|
G | T | 1 | a0004c0026t0006g0019 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.3094-13942G>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76764266 | ||||||
| chr8:76764270
|
T | C | 1 | a0004c0026t0006g0019 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.3094-13938T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76764270 | ||||||
| chr8:76764271
|
A | G | 129 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0012g0043others(126): Show | 131 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.3094-13937A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76764271 | ||||||
| chr8:76764272
|
A | T | 1 | a0004c0026t0006g0019 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.3094-13936A>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76764272 | ||||||
| chr8:76764273
|
A | T | 1 | a0004c0026t0006g0019 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.3094-13935A>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76764273 | ||||||
| chr8:76764274
|
T | C | 1 | a0004c0026t0006g0019 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.3094-13934T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76764274 | ||||||
| chr8:76764278
|
A | G | 1 | a0004c0026t0006g0019 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.3094-13930A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76764278 | ||||||
| chr8:76764279
|
A | C | 1 | a0004c0026t0006g0019 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.3094-13929A>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76764279 | ||||||
| chr8:76764281
|
C | T | 1 | a0004c0026t0006g0019 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.3094-13927C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76764281 | ||||||
| chr8:76764282
|
C | G | 1 | a0004c0026t0006g0019 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.3094-13926C>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76764282 | ||||||
| chr8:76764283
|
A | T | 1 | a0004c0026t0006g0019 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.3094-13925A>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76764283 | ||||||
| chr8:76764285
|
A | T | 1 | a0004c0026t0006g0019 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.3094-13923A>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76764285 | ||||||
| chr8:76764286
|
A | T | 1 | a0004c0026t0006g0019 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.3094-13922A>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76764286 | ||||||
| chr8:76764287
|
A | C | 1 | a0004c0026t0006g0019 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.3094-13921A>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76764287 | ||||||
| chr8:76764289
|
A | T | 1 | a0004c0026t0006g0019 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.3094-13919A>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76764289 | ||||||
| chr8:76764296
|
C | T | 1 | a0004c0026t0006g0019 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.3094-13912C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76764296 | ||||||
| chr8:76764299
|
A | T | 1 | a0004c0026t0006g0019 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.3094-13909A>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76764299 | ||||||
| chr8:76764301
|
G | GTGTTTTT others(4): Show |
1 | a0004c0026t0006g0019 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.3094-13907_3094-13 others(17): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76764301 | ||||||
| chr8:76764302
|
A | T | 1 | a0004c0026t0006g0019 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.3094-13906A>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76764302 | ||||||
| chr8:76764308
|
C | T | 1 | a0004c0026t0006g0019 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.3094-13900C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76764308 | ||||||
| chr8:76764318
|
T | A | 1 | a0004c0026t0006g0019 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.3094-13890T>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76764318 | ||||||
| chr8:76764319
|
T | C | 1 | a0004c0026t0006g0019 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.3094-13889T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76764319 | ||||||
| chr8:76764321
|
G | T | 1 | a0004c0026t0006g0019 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.3094-13887G>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76764321 | ||||||
| chr8:76764328
|
T | A | 1 | a0004c0026t0006g0019 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.3094-13880T>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76764328 | ||||||
| chr8:76764331
|
T | A | 1 | a0004c0026t0006g0019 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.3094-13877T>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76764331 | ||||||
| chr8:76764333
|
A | T | 1 | a0004c0026t0006g0019 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.3094-13875A>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76764333 | ||||||
| chr8:76764336
|
A | T | 1 | a0004c0026t0006g0019 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.3094-13872A>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76764336 | ||||||
| chr8:76764403
|
A | G | 1 | a0016c0083t0001g0152 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3094-13805A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76764403 | ||||||
| chr8:76764535
|
G | A | 1 | a0003c0002t0001g0150 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3094-13673G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76764535 | ||||||
| chr8:76764582
|
A | G | 1 | a0003c0045t0004g0136 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3094-13626A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76764582 | ||||||
| chr8:76764662
|
C | A | 1 | a0003c0002t0005g0023 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.3094-13546C>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76764662 | ||||||
| chr8:76765213
|
A | G | 10 | a0003c0002t0001g0007a0003c0002t0001g0009a0003c0002t0001g0026others(7): Show | 10 | HG02055.hp1 HG02486.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.3094-12995A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76765213 | ||||||
| chr8:76765275
|
T | C | 3 | a0002c0001t0001g0149a0003c0002t0001g0150a0006c0009t0006g0151 | 3 | HG02055.hp2 HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.3094-12933T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76765275 | ||||||
| chr8:76765740
|
G | C | 1 | a0002c0001t0003g0037 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.3094-12468G>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76765740 | ||||||
| chr8:76765745
|
G | A | 3 | a0003c0002t0001g0054a0003c0027t0001g0055a0003c0027t0001g0056 | 3 | HG02970.hp1 HG03486.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.3094-12463G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76765745 | ||||||
| chr8:76765981
|
T | C | 9 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0197others(6): Show | 9 | HG02055.hp2 HG02572.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.3094-12227T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76765981 | ||||||
| chr8:76766041
|
G | A | 1 | a0005c0005t0004g0226 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.3094-12167G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76766041 | ||||||
| chr8:76766662
|
A | G | 1 | a0003c0034t0001g0142 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3094-11546A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76766662 | ||||||
| chr8:76766864
|
TG | T | 130 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0012g0043others(127): Show | 132 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.3094-11343delG | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76766864 | ||||||
| chr8:76766958
|
C | T | 33 | a0001c0004t0005g0064a0001c0004t0005g0219a0001c0004t0019g0050others(30): Show | 33 | HG00544.hp1 HG00597.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.3094-11250C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76766958 | ||||||
| chr8:76767044
|
G | GGT | 8 | a0001c0003t0002g0179a0001c0017t0003g0107a0001c0017t0003g0108others(5): Show | 8 | HG02809.hp1 HG03098.hp2 NA18983.hp2 others(5): Show |
intron_variant | MODIFIER | c.3094-11135_3094-11 others(8): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76767044 | |||||
| chr8:76767044
|
GGT | G | 118 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0012g0043others(115): Show | 120 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.3094-11135_3094-11 others(8): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76767044 | |||||
| chr8:76767044
|
GGTGT | G | 6 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0197others(3): Show | 6 | HG02572.hp1 HG02735.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.3094-11137_3094-11 others(10): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76767044 | |||||
| chr8:76767044
|
GGTGTGT | G | 3 | a0001c0003t0002g0216a0002c0001t0001g0149a0006c0009t0006g0151 | 3 | HG02055.hp2 HG02965.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.3094-11139_3094-11 others(12): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76767044 | |||||
| chr8:76767195
|
TAC | T | 3 | a0002c0001t0001g0149a0003c0002t0001g0150a0006c0009t0006g0151 | 3 | HG02055.hp2 HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.3094-11011_3094-11 others(8): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76767195 | |||||
| chr8:76767212
|
C | G | 1 | a0002c0038t0002g0153 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3094-10996C>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76767212 | ||||||
| chr8:76767252
|
C | T | 127 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0012g0043others(124): Show | 129 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.3094-10956C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76767252 | ||||||
| chr8:76767554
|
A | G | 2 | a0003c0007t0001g0090a0022c0075t0001g0089 | 2 | HG01891.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.3094-10654A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76767554 | ||||||
| chr8:76767575
|
G | A | 1 | a0003c0002t0001g0054 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3094-10633G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76767575 | ||||||
| chr8:76767662
|
C | T | 2 | a0005c0005t0004g0047a0005c0032t0004g0046 | 2 | HG00438.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.3094-10546C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76767662 | ||||||
| chr8:76767774
|
C | T | 5 | a0001c0004t0005g0064a0003c0002t0001g0074a0003c0002t0001g0076others(2): Show | 5 | HG01069.hp1 HG01884.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.3094-10434C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76767774 | ||||||
| chr8:76768107
|
G | C | 2 | a0008c0010t0006g0018a0008c0010t0006g0021 | 2 | HG00438.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.3094-10101G>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76768107 | ||||||
| chr8:76768138
|
G | A | 120 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0040others(117): Show | 122 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.3094-10070G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76768138 | ||||||
| chr8:76768162
|
G | A | 1 | a0002c0001t0001g0149 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3094-10046G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76768162 | ||||||
| chr8:76768500
|
G | A | 1 | a0001c0003t0002g0168 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.3094-9708G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76768500 | ||||||
| chr8:76768576
|
G | A | 208 | a0001c0003t0002g0083a0001c0003t0002g0087a0001c0003t0002g0097others(205): Show | 210 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.3094-9632G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76768576 | ||||||
| chr8:76768583
|
T | C | 4 | a0001c0008t0005g0096a0001c0008t0005g0157a0001c0051t0002g0141others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.3094-9625T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76768583 | ||||||
| chr8:76768630
|
A | C | 3 | a0012c0024t0005g0001a0013c0023t0001g0143a0013c0023t0009g0144 | 4 | HG01168.hp2 HG02258.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.3094-9578A>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76768630 | ||||||
| chr8:76768857
|
G | T | 79 | a0001c0004t0002g0040a0001c0004t0002g0067a0001c0004t0002g0069others(76): Show | 81 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.3094-9351G>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76768857 | ||||||
| chr8:76768861
|
C | A | 89 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0040others(86): Show | 91 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.3094-9347C>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76768861 | ||||||
| chr8:76768862
|
G | A | 15 | a0001c0004t0005g0064a0001c0004t0019g0050a0001c0047t0016g0066others(12): Show | 15 | HG00544.hp1 HG00597.hp2 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.3094-9346G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76768862 | ||||||
| chr8:76768983
|
AGCTACTT others(5): Show |
A | 3 | a0002c0001t0001g0149a0003c0002t0001g0150a0006c0009t0006g0151 | 3 | HG02055.hp2 HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.3094-9221_3094-921 others(16): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76768983 | |||||
| chr8:76769214
|
A | T | 1 | a0002c0006t0003g0177 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.3094-8994A>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76769214 | ||||||
| chr8:76769307
|
T | C | 2 | a0002c0006t0002g0098a0002c0006t0010g0031 | 2 | HG02818.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3094-8901T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76769307 | ||||||
| chr8:76769441
|
C | T | 1 | a0010c0013t0004g0227 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.3094-8767C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76769441 | ||||||
| chr8:76769476
|
A | G | 1 | a0003c0045t0004g0136 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3094-8732A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76769476 | ||||||
| chr8:76769480
|
G | A | 4 | a0001c0004t0002g0206a0002c0001t0003g0191a0002c0001t0003g0214others(1): Show | 4 | HG00609.hp2 NA18981.hp2 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.3094-8728G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76769480 | ||||||
| chr8:76769632
|
G | A | 2 | a0001c0003t0003g0035a0001c0003t0003g0036 | 2 | NA18999.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.3094-8576G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76769632 | ||||||
| chr8:76769817
|
C | CTT | 120 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0040others(117): Show | 122 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.3094-8390_3094-838 others(6): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76769817 | |||||
| chr8:76769938
|
G | A | 62 | a0001c0004t0002g0067a0001c0004t0002g0069a0001c0004t0002g0183others(59): Show | 63 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.3094-8270G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76769938 | ||||||
| chr8:76770014
|
G | A | 1 | a0002c0001t0001g0149 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3094-8194G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76770014 | ||||||
| chr8:76770112
|
C | A | 1 | a0016c0083t0001g0152 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3094-8096C>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76770112 | ||||||
| chr8:76770234
|
T | C | 2 | a0015c0071t0002g0088a0032c0072t0002g0080 | 2 | HG00639.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.3094-7974T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76770234 | ||||||
| chr8:76770317
|
A | C | 122 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0040others(119): Show | 124 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.3094-7891A>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76770317 | ||||||
| chr8:76770321
|
C | A | 1 | a0012c0024t0005g0001 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.3094-7887C>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76770321 | ||||||
| chr8:76770360
|
C | T | 1 | a0002c0006t0003g0122 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.3094-7848C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76770360 | ||||||
| chr8:76770494
|
C | T | 1 | a0006c0074t0008g0166 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.3094-7714C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76770494 | ||||||
| chr8:76770500
|
T | C | 20 | a0001c0004t0005g0064a0001c0004t0019g0050a0001c0047t0016g0066others(17): Show | 20 | HG00544.hp1 HG00597.hp2 HG01069.hp1 others(17): Show |
intron_variant | MODIFIER | c.3094-7708T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76770500 | ||||||
| chr8:76770710
|
A | T | 125 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0040others(122): Show | 127 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.3094-7498A>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76770710 | ||||||
| chr8:76770781
|
G | A | 6 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0197others(3): Show | 6 | HG01884.hp2 HG02735.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.3094-7427G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76770781 | ||||||
| chr8:76770821
|
C | T | 5 | a0001c0015t0005g0213a0001c0025t0002g0210a0001c0055t0002g0201others(2): Show | 5 | HG02040.hp2 NA18968.hp2 NA19010.hp1 others(2): Show |
intron_variant | MODIFIER | c.3094-7387C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76770821 | ||||||
| chr8:76770854
|
A | C | 1 | a0002c0028t0003g0138 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3094-7354A>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76770854 | ||||||
| chr8:76770962
|
T | G | 1 | a0001c0080t0005g0006 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.3094-7246T>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76770962 | ||||||
| chr8:76771011
|
T | A | 1 | a0003c0034t0001g0142 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3094-7197T>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76771011 | ||||||
| chr8:76771040
|
A | G | 5 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0197others(2): Show | 5 | HG02735.hp1 HG03491.hp2 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.3094-7168A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76771040 | ||||||
| chr8:76771141
|
C | T | 1 | a0004c0022t0002g0242 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3094-7067C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76771141 | ||||||
| chr8:76771241
|
A | G | 3 | a0003c0007t0005g0086a0003c0059t0006g0085a0006c0016t0001g0084 | 3 | HG02258.hp2 HG02896.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.3094-6967A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76771241 | ||||||
| chr8:76771453
|
T | C | 2 | a0003c0002t0001g0068a0003c0045t0004g0136 | 2 | HG02572.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.3094-6755T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76771453 | ||||||
| chr8:76771563
|
C | T | 15 | a0001c0004t0005g0064a0001c0004t0019g0050a0001c0047t0016g0066others(12): Show | 15 | HG00544.hp1 HG00597.hp2 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.3094-6645C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76771563 | ||||||
| chr8:76771615
|
T | G | 1 | a0002c0006t0003g0177 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.3094-6593T>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76771615 | ||||||
| chr8:76771632
|
T | G | 125 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0040others(122): Show | 127 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.3094-6576T>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76771632 | ||||||
| chr8:76771770
|
A | G | 1 | a0019c0082t0014g0139 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3094-6438A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76771770 | ||||||
| chr8:76771812
|
T | C | 1 | a0001c0003t0002g0097 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.3094-6396T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76771812 | ||||||
| chr8:76771856
|
G | A | 2 | a0005c0005t0011g0095a0005c0005t0011g0099 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.3094-6352G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76771856 | ||||||
| chr8:76771861
|
T | A | 1 | a0003c0002t0005g0023 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.3094-6347T>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76771861 | ||||||
| chr8:76772115
|
C | A | 1 | a0003c0045t0004g0136 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3094-6093C>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76772115 | ||||||
| chr8:76772139
|
G | T | 4 | a0001c0003t0002g0179a0001c0003t0002g0216a0002c0006t0003g0165others(1): Show | 4 | NA18981.hp1 NA18989.hp2 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.3094-6069G>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76772139 | ||||||
| chr8:76772140
|
A | G | 7 | a0001c0004t0002g0040a0002c0001t0003g0034a0002c0001t0003g0037others(4): Show | 7 | HG00408.hp2 HG00639.hp1 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.3094-6068A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76772140 | ||||||
| chr8:76772238
|
G | A | 1 | a0016c0083t0001g0152 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3094-5970G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76772238 | ||||||
| chr8:76772268
|
A | G | 118 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0040others(115): Show | 120 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.3094-5940A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76772268 | ||||||
| chr8:76772375
|
A | G | 1 | a0003c0007t0001g0092 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3094-5833A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76772375 | ||||||
| chr8:76772460
|
G | C | 1 | a0001c0008t0005g0231 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.3094-5748G>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76772460 | ||||||
| chr8:76772538
|
A | G | 2 | a0001c0063t0001g0053a0003c0007t0005g0052 | 2 | HG02965.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.3094-5670A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76772538 | ||||||
| chr8:76772565
|
G | A | 2 | a0002c0038t0002g0153a0019c0082t0014g0139 | 2 | HG02976.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.3094-5643G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76772565 | ||||||
| chr8:76772597
|
C | T | 1 | a0023c0077t0002g0094 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.3094-5611C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76772597 | ||||||
| chr8:76773007
|
T | C | 7 | a0001c0004t0002g0040a0002c0001t0003g0034a0002c0001t0003g0037others(4): Show | 7 | HG00408.hp2 HG00639.hp1 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.3094-5201T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76773007 | ||||||
| chr8:76773064
|
T | G | 118 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0040others(115): Show | 120 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.3094-5144T>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76773064 | ||||||
| chr8:76773068
|
G | A | 1 | a0004c0022t0002g0242 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3094-5140G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76773068 | ||||||
| chr8:76773155
|
G | A | 1 | a0016c0083t0001g0152 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3094-5053G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76773155 | ||||||
| chr8:76773184
|
C | A | 118 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0040others(115): Show | 120 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.3094-5024C>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76773184 | ||||||
| chr8:76773185
|
A | G | 5 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0197others(2): Show | 5 | HG02735.hp1 HG03491.hp2 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.3094-5023A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76773185 | ||||||
| chr8:76773499
|
C | T | 1 | a0002c0028t0003g0138 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3094-4709C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76773499 | ||||||
| chr8:76773500
|
G | A | 5 | a0003c0002t0001g0032a0003c0002t0001g0145a0003c0002t0001g0147others(2): Show | 5 | HG01175.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.3094-4708G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76773500 | ||||||
| chr8:76773587
|
A | C | 1 | a0014c0050t0015g0220 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3094-4621A>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76773587 | ||||||
| chr8:76773855
|
C | T | 36 | a0001c0003t0002g0110a0001c0008t0005g0096a0001c0008t0005g0157others(33): Show | 36 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(33): Show |
intron_variant | MODIFIER | c.3094-4353C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76773855 | ||||||
| chr8:76773936
|
A | T | 3 | a0004c0012t0002g0061a0004c0012t0002g0062a0031c0049t0001g0060 | 3 | HG02615.hp2 HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.3094-4272A>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76773936 | ||||||
| chr8:76773939
|
C | T | 43 | a0001c0004t0002g0040a0001c0004t0005g0064a0001c0004t0005g0219others(40): Show | 43 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.3094-4269C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76773939 | ||||||
| chr8:76774035
|
A | G | 208 | a0001c0003t0002g0083a0001c0003t0002g0087a0001c0003t0002g0097others(205): Show | 210 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.3094-4173A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76774035 | ||||||
| chr8:76774045
|
G | A | 118 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0040others(115): Show | 120 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.3094-4163G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76774045 | ||||||
| chr8:76774049
|
C | T | 1 | a0001c0008t0005g0093 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.3094-4159C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76774049 | ||||||
| chr8:76774248
|
A | G | 1 | a0002c0021t0003g0171 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.3094-3960A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76774248 | ||||||
| chr8:76774287
|
C | T | 1 | a0002c0001t0003g0044 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.3094-3921C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76774287 | ||||||
| chr8:76774960
|
A | G | 7 | a0001c0004t0002g0040a0002c0001t0003g0034a0002c0001t0003g0037others(4): Show | 7 | HG00408.hp2 HG00639.hp1 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.3094-3248A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76774960 | ||||||
| chr8:76775770
|
T | A | 3 | a0003c0007t0001g0102a0006c0016t0001g0103a0006c0016t0008g0101 | 3 | HG02723.hp1 HG03098.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3094-2438T>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76775770 | ||||||
| chr8:76775895
|
C | CT | 37 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0197others(34): Show | 37 | HG00544.hp1 HG00597.hp2 HG01175.hp2 others(34): Show |
intron_variant | MODIFIER | c.3094-2296dupT | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76775895 | |||||
| chr8:76775895
|
CT | C | 10 | a0001c0008t0005g0157a0001c0031t0002g0127a0001c0051t0002g0141others(7): Show | 10 | HG01167.hp1 HG01168.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.3094-2296delT | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76775895 | |||||
| chr8:76776713
|
A | G | 2 | a0001c0051t0002g0141a0017c0057t0001g0033 | 2 | HG02809.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.3094-1495A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76776713 | ||||||
| chr8:76776810
|
G | C | 3 | a0002c0001t0001g0149a0003c0002t0001g0150a0006c0009t0006g0151 | 3 | HG02055.hp2 HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.3094-1398G>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76776810 | ||||||
| chr8:76777065
|
A | AT | 73 | a0001c0004t0002g0067a0001c0004t0002g0069a0001c0004t0002g0183others(70): Show | 75 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.3094-1137dupT | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76777065 | |||||
| chr8:76777559
|
A | G | 1 | a0006c0009t0001g0059 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3094-649A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76777559 | ||||||
| chr8:76777856
|
G | GT | 33 | a0001c0004t0005g0064a0001c0004t0005g0219a0001c0004t0019g0050others(30): Show | 33 | HG00544.hp1 HG00597.hp2 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.3094-341dupT | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76777856 | |||||
| chr8:76777856
|
G | GTT | 6 | a0003c0002t0001g0032a0003c0002t0001g0145a0003c0002t0001g0147others(3): Show | 6 | HG01175.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.3094-342_3094-341d others(4): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76777856 | |||||
| chr8:76777864
|
T | TG | 16 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0040others(13): Show | 16 | HG00408.hp2 HG00639.hp1 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.3094-344_3094-343i others(3): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76777864 | ||||||
| chr8:76777885
|
G | T | 1 | a0002c0006t0003g0177 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.3094-323G>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76777885 | ||||||
| chr8:76777885
|
GT | G | 10 | a0001c0003t0002g0164a0001c0031t0020g0163a0001c0063t0001g0053others(7): Show | 10 | HG01168.hp1 HG02056.hp1 HG02132.hp2 others(7): Show |
intron_variant | MODIFIER | c.3094-311delT | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 76777885 | |||||
| chr8:76777892
|
T | G | 1 | a0003c0045t0004g0136 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3094-316T>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76777892 | ||||||
| chr8:76777961
|
A | T | 1 | a0001c0003t0022g0135 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.3094-247A>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76777961 | ||||||
| chr8:76778101
|
G | A | 50 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0040others(47): Show | 50 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.3094-107G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76778101 | ||||||
| chr8:76778144
|
C | G | 120 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0040others(117): Show | 122 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.3094-64C>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76778144 | ||||||
| chr8:76778181
|
T | C | 3 | a0003c0002t0001g0054a0003c0027t0001g0055a0003c0027t0001g0056 | 3 | HG02970.hp1 HG03486.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.3094-27T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 3/10 | chr8 | 76778181 | ||||||
| chr8:76778720
|
T | A | 2 | a0001c0008t0005g0096a0001c0008t0005g0157 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.3325+281T>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76778720 | ||||||
| chr8:76778723
|
T | G | 1 | a0003c0002t0006g0058 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3325+284T>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76778723 | ||||||
| chr8:76778871
|
G | A | 1 | a0028c0043t0001g0140 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3325+432G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76778871 | ||||||
| chr8:76779331
|
G | C | 1 | a0008c0067t0003g0106 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3325+892G>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76779331 | ||||||
| chr8:76779382
|
G | T | 2 | a0001c0063t0001g0053a0003c0007t0005g0052 | 2 | HG02965.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.3325+943G>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76779382 | ||||||
| chr8:76779432
|
G | A | 123 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0040others(120): Show | 125 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.3325+993G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76779432 | ||||||
| chr8:76779492
|
A | G | 8 | a0001c0004t0002g0040a0002c0001t0003g0034a0002c0001t0003g0037others(5): Show | 8 | HG00408.hp2 HG00639.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.3325+1053A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76779492 | ||||||
| chr8:76779579
|
G | T | 1 | a0028c0043t0001g0140 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3325+1140G>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76779579 | ||||||
| chr8:76779930
|
T | C | 7 | a0003c0060t0001g0173a0005c0005t0004g0117a0005c0005t0004g0118others(4): Show | 7 | NA18957.hp2 NA18968.hp1 NA18975.hp2 others(4): Show |
intron_variant | MODIFIER | c.3325+1491T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76779930 | ||||||
| chr8:76779949
|
G | T | 1 | a0033c0073t0004g0132 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.3325+1510G>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76779949 | ||||||
| chr8:76780057
|
T | TA | 115 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0040others(112): Show | 116 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.3325+1629dupA | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr8 | 76780057 | |||||
| chr8:76780057
|
T | TAA | 6 | a0001c0051t0002g0141a0002c0001t0003g0044a0003c0002t0005g0023others(3): Show | 6 | HG01891.hp1 HG02056.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.3325+1628_3325+162 others(6): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr8 | 76780057 | |||||
| chr8:76780354
|
T | C | 123 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0040others(120): Show | 125 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.3325+1915T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76780354 | ||||||
| chr8:76780453
|
T | C | 65 | a0001c0004t0002g0067a0001c0004t0002g0069a0001c0004t0002g0183others(62): Show | 67 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.3325+2014T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76780453 | ||||||
| chr8:76780483
|
C | T | 5 | a0003c0002t0001g0032a0003c0002t0001g0145a0003c0002t0001g0147others(2): Show | 5 | HG01175.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.3325+2044C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76780483 | ||||||
| chr8:76780492
|
T | A | 9 | a0001c0008t0005g0230a0001c0008t0005g0231a0001c0008t0005g0232others(6): Show | 9 | HG00609.hp1 HG00735.hp2 HG02080.hp1 others(6): Show |
intron_variant | MODIFIER | c.3325+2053T>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76780492 | ||||||
| chr8:76780513
|
T | C | 208 | a0001c0003t0002g0083a0001c0003t0002g0087a0001c0003t0002g0097others(205): Show | 210 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.3325+2074T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76780513 | ||||||
| chr8:76780526
|
G | C | 1 | a0003c0034t0001g0142 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3325+2087G>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76780526 | ||||||
| chr8:76780649
|
C | T | 38 | a0001c0003t0002g0110a0001c0008t0005g0096a0001c0008t0005g0157others(35): Show | 38 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(35): Show |
intron_variant | MODIFIER | c.3325+2210C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76780649 | ||||||
| chr8:76780654
|
T | C | 1 | a0003c0034t0001g0142 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3325+2215T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76780654 | ||||||
| chr8:76780740
|
A | G | 1 | a0006c0009t0006g0151 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3325+2301A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76780740 | ||||||
| chr8:76780943
|
A | G | 1 | a0017c0057t0001g0033 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3325+2504A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76780943 | ||||||
| chr8:76781449
|
G | A | 8 | a0002c0001t0003g0020a0004c0026t0006g0019a0008c0010t0006g0015others(5): Show | 8 | HG00438.hp1 HG02040.hp1 NA18962.hp1 others(5): Show |
intron_variant | MODIFIER | c.3325+3010G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76781449 | ||||||
| chr8:76781574
|
A | C | 3 | a0011c0020t0004g0113a0011c0020t0004g0167a0033c0073t0004g0132 | 3 | HG02074.hp1 HG02165.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.3325+3135A>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76781574 | ||||||
| chr8:76781661
|
A | G | 1 | a0002c0006t0010g0031 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3325+3222A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76781661 | ||||||
| chr8:76781878
|
T | C | 1 | a0002c0021t0003g0171 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.3325+3439T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76781878 | ||||||
| chr8:76781904
|
A | C | 6 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0197others(3): Show | 6 | HG01070.hp1 HG02735.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.3325+3465A>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76781904 | ||||||
| chr8:76781919
|
T | C | 1 | a0002c0038t0002g0153 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3325+3480T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76781919 | ||||||
| chr8:76781930
|
A | G | 1 | a0022c0075t0001g0089 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3325+3491A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76781930 | ||||||
| chr8:76782100
|
A | AT | 42 | a0001c0003t0002g0176a0001c0017t0003g0107a0001c0017t0003g0108others(39): Show | 42 | HG00423.hp2 HG00438.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.3325+3685dupT | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr8 | 76782100 | |||||
| chr8:76782100
|
A | ATT | 5 | a0001c0008t0005g0096a0001c0051t0002g0141a0004c0018t0002g0105others(2): Show | 5 | HG00408.hp1 HG01169.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.3325+3684_3325+368 others(6): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr8 | 76782100 | |||||
| chr8:76782100
|
AT | A | 16 | a0001c0003t0002g0216a0001c0004t0002g0212a0002c0006t0003g0160others(13): Show | 16 | HG01175.hp2 HG01952.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.3325+3685delT | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr8 | 76782100 | |||||
| chr8:76782100
|
ATT | A | 51 | a0001c0004t0002g0067a0001c0004t0002g0069a0001c0004t0002g0183others(48): Show | 52 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.3325+3684_3325+368 others(6): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr8 | 76782100 | |||||
| chr8:76782100
|
ATTT | A | 29 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0040others(26): Show | 30 | HG00408.hp2 HG00438.hp1 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.3325+3683_3325+368 others(7): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr8 | 76782100 | |||||
| chr8:76782100
|
ATTTTT | A | 24 | a0001c0004t0005g0064a0001c0004t0005g0219a0001c0047t0016g0066others(21): Show | 24 | HG00597.hp2 HG01884.hp1 HG02132.hp1 others(21): Show |
intron_variant | MODIFIER | c.3325+3681_3325+368 others(9): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr8 | 76782100 | |||||
| chr8:76782394
|
G | T | 5 | a0001c0004t0002g0189a0002c0001t0003g0185a0002c0001t0003g0187others(2): Show | 5 | NA18939.hp2 NA18964.hp1 NA18980.hp2 others(2): Show |
intron_variant | MODIFIER | c.3325+3955G>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76782394 | ||||||
| chr8:76782406
|
C | T | 1 | a0002c0001t0003g0205 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.3325+3967C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76782406 | ||||||
| chr8:76782409
|
A | G | 64 | a0001c0004t0002g0067a0001c0004t0002g0069a0001c0004t0002g0183others(61): Show | 66 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.3325+3970A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76782409 | ||||||
| chr8:76782666
|
C | G | 122 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0040others(119): Show | 124 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.3325+4227C>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76782666 | ||||||
| chr8:76782790
|
C | T | 123 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0040others(120): Show | 125 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.3325+4351C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76782790 | ||||||
| chr8:76782851
|
G | A | 1 | a0003c0045t0004g0136 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3325+4412G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76782851 | ||||||
| chr8:76782901
|
G | A | 123 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0040others(120): Show | 125 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.3325+4462G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76782901 | ||||||
| chr8:76783061
|
G | T | 5 | a0003c0007t0001g0240a0003c0007t0001g0241a0003c0058t0001g0238others(2): Show | 5 | HG02109.hp2 HG02615.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.3325+4622G>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76783061 | ||||||
| chr8:76783152
|
T | C | 122 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0040others(119): Show | 124 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.3325+4713T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76783152 | ||||||
| chr8:76783273
|
G | A | 65 | a0001c0004t0002g0067a0001c0004t0002g0069a0001c0004t0002g0183others(62): Show | 67 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.3325+4834G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76783273 | ||||||
| chr8:76783304
|
T | A | 1 | a0003c0034t0001g0142 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3325+4865T>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76783304 | ||||||
| chr8:76783308
|
G | A | 122 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0040others(119): Show | 124 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.3325+4869G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76783308 | ||||||
| chr8:76783475
|
T | C | 2 | a0002c0038t0002g0153a0019c0082t0014g0139 | 2 | HG02976.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.3325+5036T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76783475 | ||||||
| chr8:76783496
|
C | T | 122 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0040others(119): Show | 124 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.3325+5057C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76783496 | ||||||
| chr8:76783582
|
A | G | 9 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0197others(6): Show | 9 | HG01070.hp1 HG01891.hp1 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.3325+5143A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76783582 | ||||||
| chr8:76783796
|
C | G | 8 | a0001c0004t0002g0040a0002c0001t0003g0034a0002c0001t0003g0037others(5): Show | 8 | HG00408.hp2 HG00639.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.3325+5357C>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76783796 | ||||||
| chr8:76783827
|
T | C | 5 | a0003c0002t0001g0032a0003c0002t0001g0145a0003c0002t0001g0147others(2): Show | 5 | HG01175.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.3325+5388T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76783827 | ||||||
| chr8:76783984
|
T | G | 6 | a0001c0004t0001g0203a0001c0004t0001g0204a0001c0004t0002g0197others(3): Show | 6 | HG01070.hp1 HG02735.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.3325+5545T>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76783984 | ||||||
| chr8:76784003
|
T | C | 2 | a0001c0003t0002g0083a0001c0003t0002g0097 | 2 | HG00280.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.3325+5564T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76784003 | ||||||
| chr8:76784144
|
G | A | 3 | a0002c0001t0001g0149a0006c0009t0006g0151a0009c0011t0007g0221 | 3 | HG02055.hp2 HG02717.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3325+5705G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76784144 | ||||||
| chr8:76784212
|
G | GTTTTA | 15 | a0001c0004t0002g0040a0001c0008t0005g0230a0001c0008t0005g0231others(12): Show | 15 | HG00609.hp1 HG00735.hp2 HG02080.hp1 others(12): Show |
intron_variant | MODIFIER | c.3325+5800_3325+580 others(9): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr8 | 76784212 | |||||
| chr8:76784222
|
A | C | 5 | a0002c0006t0010g0155a0003c0061t0001g0156a0006c0029t0001g0154others(2): Show | 5 | HG01081.hp1 HG01167.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.3325+5783A>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76784222 | ||||||
| chr8:76784327
|
T | C | 1 | a0002c0006t0003g0177 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.3325+5888T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76784327 | ||||||
| chr8:76784618
|
A | G | 2 | a0003c0040t0001g0049a0004c0026t0006g0048 | 2 | NA18953.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.3325+6179A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76784618 | ||||||
| chr8:76784889
|
G | A | 1 | a0003c0045t0004g0136 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3325+6450G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76784889 | ||||||
| chr8:76784956
|
A | G | 1 | a0028c0043t0001g0140 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3325+6517A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76784956 | ||||||
| chr8:76785456
|
T | C | 154 | a0001c0003t0002g0083a0001c0003t0002g0087a0001c0003t0002g0097others(151): Show | 154 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.3325+7017T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76785456 | ||||||
| chr8:76785464
|
G | T | 4 | a0003c0002t0001g0150a0003c0061t0001g0156a0006c0029t0001g0154others(1): Show | 4 | HG01081.hp1 HG02717.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.3325+7025G>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76785464 | ||||||
| chr8:76785470
|
A | G | 3 | a0003c0002t0001g0026a0009c0069t0007g0057a0030c0070t0007g0100 | 3 | HG01167.hp2 HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.3325+7031A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76785470 | ||||||
| chr8:76785477
|
A | C | 1 | a0002c0001t0003g0191 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.3325+7038A>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76785477 | ||||||
| chr8:76785478
|
C | A | 3 | a0003c0002t0001g0150a0003c0061t0001g0156a0006c0029t0001g0154 | 3 | HG01081.hp1 HG02717.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.3325+7039C>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76785478 | ||||||
| chr8:76785553
|
G | T | 49 | a0001c0031t0002g0127a0001c0051t0002g0141a0001c0063t0001g0053others(46): Show | 50 | HG00408.hp1 HG00423.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.3325+7114G>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76785553 | ||||||
| chr8:76785554
|
C | A | 49 | a0001c0031t0002g0127a0001c0051t0002g0141a0001c0063t0001g0053others(46): Show | 50 | HG00408.hp1 HG00423.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.3325+7115C>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76785554 | ||||||
| chr8:76785610
|
C | A | 1 | a0003c0058t0001g0238 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3325+7171C>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76785610 | ||||||
| chr8:76785808
|
C | T | 1 | a0002c0038t0002g0153 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3325+7369C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76785808 | ||||||
| chr8:76785868
|
G | A | 2 | a0003c0059t0006g0085a0006c0016t0001g0084 | 2 | HG02258.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.3325+7429G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76785868 | ||||||
| chr8:76785904
|
A | G | 3 | a0001c0004t0002g0197a0003c0027t0001g0056a0004c0012t0002g0196 | 3 | HG02735.hp1 HG03486.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.3325+7465A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76785904 | ||||||
| chr8:76785944
|
C | G | 1 | a0018c0064t0001g0137 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3325+7505C>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76785944 | ||||||
| chr8:76785950
|
A | G | 2 | a0003c0002t0001g0054a0006c0009t0006g0151 | 2 | HG02055.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.3325+7511A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76785950 | ||||||
| chr8:76785989
|
T | C | 1 | a0002c0038t0002g0153 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3325+7550T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76785989 | ||||||
| chr8:76786171
|
A | C | 1 | a0002c0028t0003g0138 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3325+7732A>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76786171 | ||||||
| chr8:76786208
|
G | A | 2 | a0003c0059t0006g0085a0006c0016t0001g0084 | 2 | HG02258.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.3325+7769G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76786208 | ||||||
| chr8:76786286
|
G | A | 1 | a0004c0019t0005g0234 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.3325+7847G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76786286 | ||||||
| chr8:76786625
|
C | A | 2 | a0006c0048t0001g0022a0008c0067t0003g0106 | 2 | HG03669.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3325+8186C>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76786625 | ||||||
| chr8:76786754
|
A | G | 48 | a0001c0004t0002g0197a0001c0031t0002g0127a0001c0051t0002g0141others(45): Show | 48 | HG00408.hp1 HG00423.hp2 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.3325+8315A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76786754 | ||||||
| chr8:76786955
|
A | C | 2 | a0001c0008t0005g0096a0001c0008t0005g0157 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.3325+8516A>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76786955 | ||||||
| chr8:76786988
|
A | G | 18 | a0001c0015t0001g0003a0001c0015t0005g0005a0001c0015t0005g0011others(15): Show | 18 | HG01109.hp1 HG01175.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.3325+8549A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76786988 | ||||||
| chr8:76787244
|
C | T | 1 | a0002c0028t0003g0138 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3325+8805C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76787244 | ||||||
| chr8:76787268
|
C | G | 27 | a0001c0031t0002g0127a0002c0006t0003g0122a0002c0006t0003g0170others(24): Show | 27 | HG00408.hp1 HG00423.hp2 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.3325+8829C>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76787268 | ||||||
| chr8:76787379
|
G | C | 1 | a0003c0007t0009g0082 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.3325+8940G>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76787379 | ||||||
| chr8:76787568
|
C | T | 1 | a0001c0003t0022g0135 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.3325+9129C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76787568 | ||||||
| chr8:76787638
|
T | TA | 27 | a0001c0003t0002g0087a0001c0003t0002g0164a0001c0003t0022g0135others(24): Show | 27 | HG00099.hp2 HG01109.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.3325+9224dupA | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr8 | 76787638 | |||||
| chr8:76787638
|
TA | T | 26 | a0002c0006t0003g0162a0002c0006t0003g0170a0003c0002t0001g0076others(23): Show | 26 | HG00408.hp1 HG00423.hp2 HG01175.hp1 others(23): Show |
intron_variant | MODIFIER | c.3325+9224delA | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr8 | 76787638 | |||||
| chr8:76787639
|
A | G | 2 | a0003c0061t0001g0156a0006c0029t0001g0154 | 2 | HG01081.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.3325+9200A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76787639 | ||||||
| chr8:76787807
|
T | C | 23 | a0001c0004t0002g0197a0001c0051t0002g0141a0002c0038t0002g0153others(20): Show | 23 | HG01081.hp1 HG01167.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.3325+9368T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76787807 | ||||||
| chr8:76787899
|
T | C | 2 | a0003c0002t0001g0054a0006c0009t0006g0151 | 2 | HG02055.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.3325+9460T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76787899 | ||||||
| chr8:76788037
|
A | G | 38 | a0001c0004t0002g0189a0001c0015t0005g0213a0001c0025t0002g0210others(35): Show | 39 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(36): Show |
intron_variant | MODIFIER | c.3325+9598A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76788037 | ||||||
| chr8:76788058
|
C | T | 21 | a0001c0004t0002g0197a0001c0051t0002g0141a0003c0002t0001g0007others(18): Show | 21 | HG01081.hp1 HG01167.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.3325+9619C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76788058 | ||||||
| chr8:76788201
|
A | G | 2 | a0006c0048t0001g0022a0008c0067t0003g0106 | 2 | HG03669.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3325+9762A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76788201 | ||||||
| chr8:76788696
|
A | G | 2 | a0006c0048t0001g0022a0008c0067t0003g0106 | 2 | HG03669.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3325+10257A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76788696 | ||||||
| chr8:76788718
|
C | G | 2 | a0006c0048t0001g0022a0008c0067t0003g0106 | 2 | HG03669.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3325+10279C>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76788718 | ||||||
| chr8:76788752
|
T | C | 1 | a0024c0079t0002g0169 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3325+10313T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76788752 | ||||||
| chr8:76788826
|
T | C | 2 | a0003c0007t0001g0102a0006c0016t0001g0103 | 2 | HG02723.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3325+10387T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76788826 | ||||||
| chr8:76789416
|
T | C | 2 | a0003c0002t0001g0054a0006c0009t0006g0151 | 2 | HG02055.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.3325+10977T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76789416 | ||||||
| chr8:76789512
|
T | C | 2 | a0001c0004t0002g0197a0004c0012t0002g0196 | 2 | HG02735.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.3325+11073T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76789512 | ||||||
| chr8:76789863
|
A | G | 1 | a0003c0002t0001g0032 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3325+11424A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76789863 | ||||||
| chr8:76789941
|
C | A | 2 | a0003c0061t0001g0156a0006c0029t0001g0154 | 2 | HG01081.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.3325+11502C>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76789941 | ||||||
| chr8:76790318
|
A | G | 1 | a0001c0008t0005g0233 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.3325+11879A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76790318 | ||||||
| chr8:76790425
|
A | G | 2 | a0003c0061t0001g0156a0006c0029t0001g0154 | 2 | HG01081.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.3325+11986A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76790425 | ||||||
| chr8:76790554
|
A | G | 68 | a0001c0004t0002g0197a0001c0015t0001g0003a0001c0015t0005g0005others(65): Show | 68 | HG00408.hp1 HG00423.hp2 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.3325+12115A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76790554 | ||||||
| chr8:76790607
|
G | A | 2 | a0003c0061t0001g0156a0006c0029t0001g0154 | 2 | HG01081.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.3325+12168G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76790607 | ||||||
| chr8:76790906
|
A | G | 68 | a0001c0004t0002g0197a0001c0015t0001g0003a0001c0015t0005g0005others(65): Show | 68 | HG00408.hp1 HG00423.hp2 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.3325+12467A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76790906 | ||||||
| chr8:76791029
|
T | C | 1 | a0003c0002t0008g0013 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.3325+12590T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76791029 | ||||||
| chr8:76791288
|
G | T | 2 | a0002c0006t0002g0098a0002c0006t0010g0031 | 2 | HG02818.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3325+12849G>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76791288 | ||||||
| chr8:76791299
|
G | A | 2 | a0003c0027t0001g0055a0003c0027t0001g0056 | 2 | HG03486.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.3325+12860G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76791299 | ||||||
| chr8:76791332
|
C | T | 1 | a0001c0008t0005g0093 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.3325+12893C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76791332 | ||||||
| chr8:76791467
|
G | A | 1 | a0005c0005t0004g0078 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3325+13028G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76791467 | ||||||
| chr8:76791892
|
C | T | 1 | a0002c0028t0003g0138 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3325+13453C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76791892 | ||||||
| chr8:76791907
|
T | C | 2 | a0003c0002t0001g0054a0006c0009t0006g0151 | 2 | HG02055.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.3325+13468T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76791907 | ||||||
| chr8:76791919
|
A | G | 1 | a0005c0005t0004g0078 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3325+13480A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76791919 | ||||||
| chr8:76792404
|
C | T | 3 | a0003c0027t0001g0055a0003c0027t0001g0056a0003c0034t0001g0142 | 3 | HG02109.hp1 HG03486.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.3325+13965C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76792404 | ||||||
| chr8:76792405
|
G | A | 1 | a0006c0009t0001g0059 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3325+13966G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76792405 | ||||||
| chr8:76792423
|
G | A | 3 | a0001c0017t0003g0107a0001c0017t0003g0108a0001c0017t0021g0129 | 3 | NA18983.hp2 NA19064.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.3325+13984G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76792423 | ||||||
| chr8:76792719
|
T | G | 3 | a0001c0004t0002g0197a0001c0051t0002g0141a0004c0012t0002g0196 | 3 | HG02735.hp1 HG02809.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.3325+14280T>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76792719 | ||||||
| chr8:76792746
|
T | C | 1 | a0006c0009t0006g0151 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3325+14307T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76792746 | ||||||
| chr8:76792974
|
C | T | 1 | a0001c0051t0002g0141 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3325+14535C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76792974 | ||||||
| chr8:76792975
|
C | T | 19 | a0001c0017t0003g0107a0001c0017t0003g0108a0001c0017t0021g0129others(16): Show | 19 | HG00597.hp2 HG00639.hp2 HG02132.hp1 others(16): Show |
intron_variant | MODIFIER | c.3325+14536C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76792975 | ||||||
| chr8:76793068
|
C | T | 21 | a0001c0031t0002g0127a0004c0018t0002g0105a0004c0018t0002g0116others(18): Show | 21 | HG00408.hp1 HG00423.hp2 HG00621.hp2 others(18): Show |
intron_variant | MODIFIER | c.3325+14629C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76793068 | ||||||
| chr8:76793323
|
A | AT | 87 | a0001c0004t0002g0197a0001c0015t0001g0003a0001c0015t0005g0005others(84): Show | 87 | HG00408.hp1 HG00423.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.3325+14887dupT | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr8 | 76793323 | |||||
| chr8:76793465
|
T | C | 68 | a0001c0004t0002g0197a0001c0015t0001g0003a0001c0015t0005g0005others(65): Show | 68 | HG00408.hp1 HG00423.hp2 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.3325+15026T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76793465 | ||||||
| chr8:76793762
|
C | A | 27 | a0001c0031t0002g0127a0002c0006t0003g0122a0002c0006t0003g0170others(24): Show | 27 | HG00408.hp1 HG00423.hp2 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.3325+15323C>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76793762 | ||||||
| chr8:76793881
|
C | G | 3 | a0001c0004t0002g0197a0001c0051t0002g0141a0004c0012t0002g0196 | 3 | HG02735.hp1 HG02809.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.3325+15442C>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76793881 | ||||||
| chr8:76793971
|
A | G | 3 | a0003c0002t0001g0074a0003c0002t0001g0076a0014c0039t0001g0072 | 3 | HG01069.hp1 HG02451.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.3325+15532A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76793971 | ||||||
| chr8:76794055
|
C | T | 2 | a0003c0002t0001g0054a0006c0009t0006g0151 | 2 | HG02055.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.3325+15616C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76794055 | ||||||
| chr8:76794058
|
A | G | 1 | a0005c0032t0004g0184 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.3325+15619A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76794058 | ||||||
| chr8:76794058
|
A | T | 2 | a0001c0004t0002g0197a0004c0012t0002g0196 | 2 | HG02735.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.3325+15619A>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76794058 | ||||||
| chr8:76794311
|
A | G | 1 | a0004c0018t0002g0125 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.3325+15872A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76794311 | ||||||
| chr8:76794578
|
A | G | 3 | a0002c0001t0003g0037a0002c0001t0003g0039a0002c0001t0003g0182 | 3 | NA18953.hp2 NA18992.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.3325+16139A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76794578 | ||||||
| chr8:76794873
|
T | TTG | 37 | a0001c0003t0002g0134a0001c0004t0002g0189a0001c0004t0002g0206others(34): Show | 38 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(35): Show |
intron_variant | MODIFIER | c.3325+16471_3325+16 others(8): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr8 | 76794873 | |||||
| chr8:76794873
|
T | TTGTG | 36 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0008t0005g0096others(33): Show | 36 | HG00597.hp1 HG00639.hp2 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.3325+16469_3325+16 others(10): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr8 | 76794873 | |||||
| chr8:76794873
|
T | TTGTGTG | 3 | a0001c0017t0003g0107a0002c0001t0003g0039a0017c0057t0001g0033 | 3 | HG03486.hp1 NA18983.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.3325+16467_3325+16 others(12): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr8 | 76794873 | |||||
| chr8:76794873
|
T | TTGTGTGT others(1): Show |
2 | a0004c0046t0002g0075a0006c0016t0008g0101 | 2 | HG00597.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.3325+16465_3325+16 others(14): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr8 | 76794873 | |||||
| chr8:76794873
|
T | TTGTGTGT others(5): Show |
1 | a0006c0062t0001g0124 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.3325+16461_3325+16 others(18): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr8 | 76794873 | |||||
| chr8:76794873
|
TTG | T | 15 | a0001c0004t0005g0064a0001c0004t0005g0219a0001c0015t0005g0005others(12): Show | 15 | HG01884.hp1 HG02109.hp1 HG02132.hp2 others(12): Show |
intron_variant | MODIFIER | c.3325+16471_3325+16 others(8): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr8 | 76794873 | |||||
| chr8:76794873
|
TTGTG | T | 17 | a0001c0004t0002g0197a0003c0002t0001g0007a0003c0002t0001g0009others(14): Show | 17 | HG01081.hp1 HG01167.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.3325+16469_3325+16 others(10): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr8 | 76794873 | |||||
| chr8:76794876
|
T | C | 26 | a0001c0031t0002g0127a0002c0006t0003g0122a0002c0006t0003g0170others(23): Show | 26 | HG00408.hp1 HG00423.hp2 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.3325+16437T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76794876 | ||||||
| chr8:76794914
|
C | T | 1 | a0007c0030t0003g0175 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.3325+16475C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76794914 | ||||||
| chr8:76795075
|
T | C | 2 | a0002c0006t0002g0098a0002c0006t0010g0031 | 2 | HG02818.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3325+16636T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76795075 | ||||||
| chr8:76795286
|
T | C | 22 | a0001c0003t0002g0083a0001c0003t0002g0087a0001c0003t0002g0110others(19): Show | 22 | HG00099.hp2 HG00735.hp1 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.3325+16847T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76795286 | ||||||
| chr8:76795377
|
G | A | 26 | a0001c0003t0002g0097a0001c0008t0005g0093a0001c0008t0005g0230others(23): Show | 26 | HG00280.hp1 HG00438.hp1 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.3325+16938G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76795377 | ||||||
| chr8:76795426
|
A | G | 1 | a0005c0032t0004g0046 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.3325+16987A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76795426 | ||||||
| chr8:76795543
|
C | CT | 5 | a0001c0004t0002g0197a0002c0001t0010g0014a0003c0027t0001g0055others(2): Show | 5 | HG02735.hp1 HG02897.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.3325+17124dupT | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr8 | 76795543 | |||||
| chr8:76795543
|
CT | C | 8 | a0001c0003t0002g0179a0002c0001t0017g0194a0003c0059t0006g0085others(5): Show | 8 | HG01074.hp1 HG01081.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.3325+17124delT | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr8 | 76795543 | |||||
| chr8:76795568
|
C | T | 4 | a0001c0008t0005g0096a0001c0008t0005g0157a0001c0042t0002g0010others(1): Show | 4 | HG01070.hp1 HG01167.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.3325+17129C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76795568 | ||||||
| chr8:76795623
|
C | T | 19 | a0003c0002t0001g0007a0003c0002t0001g0009a0003c0002t0001g0054others(16): Show | 19 | HG01081.hp1 HG01167.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.3325+17184C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76795623 | ||||||
| chr8:76795705
|
G | C | 1 | a0002c0006t0010g0031 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3325+17266G>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76795705 | ||||||
| chr8:76795756
|
C | T | 2 | a0001c0004t0002g0197a0004c0012t0002g0196 | 2 | HG02735.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.3325+17317C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76795756 | ||||||
| chr8:76795832
|
A | C | 1 | a0026c0041t0005g0073 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3325+17393A>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76795832 | ||||||
| chr8:76796014
|
T | G | 3 | a0002c0006t0002g0098a0002c0038t0002g0153a0009c0011t0006g0065 | 3 | HG03041.hp2 HG03516.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.3325+17575T>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76796014 | ||||||
| chr8:76796198
|
G | GA | 21 | a0001c0004t0002g0197a0001c0051t0002g0141a0003c0002t0001g0007others(18): Show | 21 | HG01081.hp1 HG01167.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.3325+17763dupA | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr8 | 76796198 | |||||
| chr8:76796464
|
G | A | 8 | a0003c0002t0001g0026a0003c0002t0001g0027a0003c0002t0001g0029others(5): Show | 8 | HG01175.hp2 HG02486.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.3325+18025G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76796464 | ||||||
| chr8:76796473
|
G | A | 2 | a0001c0004t0002g0197a0004c0012t0002g0196 | 2 | HG02735.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.3325+18034G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76796473 | ||||||
| chr8:76796729
|
C | T | 1 | a0028c0043t0001g0140 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3325+18290C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76796729 | ||||||
| chr8:76796897
|
G | T | 2 | a0002c0038t0002g0153a0009c0011t0006g0065 | 2 | HG03041.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.3325+18458G>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76796897 | ||||||
| chr8:76796998
|
C | T | 1 | a0002c0006t0002g0098 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3325+18559C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76796998 | ||||||
| chr8:76797099
|
A | C | 2 | a0001c0004t0002g0197a0004c0012t0002g0196 | 2 | HG02735.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.3325+18660A>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76797099 | ||||||
| chr8:76797457
|
A | C | 27 | a0001c0031t0002g0127a0002c0006t0003g0122a0002c0006t0003g0170others(24): Show | 27 | HG00408.hp1 HG00423.hp2 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.3325+19018A>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76797457 | ||||||
| chr8:76797499
|
A | G | 3 | a0001c0004t0002g0197a0001c0051t0002g0141a0004c0012t0002g0196 | 3 | HG02735.hp1 HG02809.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.3325+19060A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76797499 | ||||||
| chr8:76797515
|
G | A | 9 | a0002c0028t0003g0138a0003c0002t0001g0026a0003c0002t0001g0027others(6): Show | 9 | HG01175.hp2 HG01891.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.3325+19076G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76797515 | ||||||
| chr8:76797882
|
C | CTATATG | 11 | a0003c0002t0001g0007a0003c0002t0001g0009a0003c0002t0001g0081others(8): Show | 11 | HG01891.hp1 HG02486.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.3325+19444_3325+19 others(12): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr8 | 76797882 | |||||
| chr8:76797882
|
C | CTATATGT others(3): Show |
1 | a0030c0070t0007g0100 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.3325+19444_3325+19 others(16): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr8 | 76797882 | |||||
| chr8:76797884
|
G | A | 2 | a0003c0061t0001g0156a0006c0029t0001g0154 | 2 | HG01081.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.3325+19445G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76797884 | ||||||
| chr8:76797886
|
A | ATG | 81 | a0001c0003t0002g0179a0001c0004t0001g0204a0001c0004t0002g0189others(78): Show | 83 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.3325+19479_3325+19 others(8): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr8 | 76797886 | |||||
| chr8:76797886
|
A | ATGTG | 29 | a0001c0004t0005g0064a0001c0004t0005g0219a0001c0031t0002g0127others(26): Show | 29 | HG00408.hp1 HG00423.hp2 HG01175.hp1 others(26): Show |
intron_variant | MODIFIER | c.3325+19477_3325+19 others(10): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr8 | 76797886 | |||||
| chr8:76797886
|
A | G | 14 | a0003c0002t0001g0007a0003c0002t0001g0009a0003c0002t0001g0081others(11): Show | 14 | HG01167.hp2 HG01891.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.3325+19447A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76797886 | ||||||
| chr8:76797886
|
ATG | A | 6 | a0001c0003t0002g0110a0001c0042t0002g0010a0001c0051t0002g0141others(3): Show | 6 | HG01070.hp1 HG02109.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.3325+19479_3325+19 others(8): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr8 | 76797886 | |||||
| chr8:76797886
|
ATGTG | A | 4 | a0002c0001t0001g0149a0002c0028t0003g0138a0003c0002t0001g0054others(1): Show | 4 | HG01891.hp2 HG02055.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.3325+19477_3325+19 others(10): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr8 | 76797886 | |||||
| chr8:76797886
|
ATGTGTG | A | 10 | a0002c0038t0002g0153a0003c0002t0001g0026a0003c0002t0001g0027others(7): Show | 10 | HG01175.hp2 HG02486.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.3325+19475_3325+19 others(12): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr8 | 76797886 | |||||
| chr8:76797994
|
C | T | 3 | a0003c0007t0001g0102a0006c0016t0001g0103a0006c0016t0008g0101 | 3 | HG02723.hp1 HG03098.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3325+19555C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76797994 | ||||||
| chr8:76798426
|
A | T | 3 | a0001c0004t0002g0197a0001c0051t0002g0141a0004c0012t0002g0196 | 3 | HG02735.hp1 HG02809.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.3325+19987A>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76798426 | ||||||
| chr8:76798531
|
C | CT | 8 | a0003c0002t0001g0026a0003c0002t0001g0027a0003c0002t0001g0029others(5): Show | 8 | HG01175.hp2 HG02486.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.3325+20093dupT | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr8 | 76798531 | |||||
| chr8:76798755
|
A | G | 3 | a0001c0004t0002g0197a0001c0051t0002g0141a0004c0012t0002g0196 | 3 | HG02735.hp1 HG02809.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.3325+20316A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76798755 | ||||||
| chr8:76798849
|
A | G | 3 | a0001c0004t0002g0197a0001c0051t0002g0141a0004c0012t0002g0196 | 3 | HG02735.hp1 HG02809.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.3325+20410A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76798849 | ||||||
| chr8:76798922
|
C | T | 3 | a0001c0004t0002g0197a0001c0051t0002g0141a0004c0012t0002g0196 | 3 | HG02735.hp1 HG02809.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.3325+20483C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76798922 | ||||||
| chr8:76799056
|
G | A | 1 | a0001c0033t0002g0224 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.3325+20617G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76799056 | ||||||
| chr8:76799166
|
G | T | 2 | a0001c0004t0002g0197a0004c0012t0002g0196 | 2 | HG02735.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.3325+20727G>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76799166 | ||||||
| chr8:76799327
|
C | CA | 23 | a0001c0004t0002g0197a0001c0051t0002g0141a0002c0038t0002g0153others(20): Show | 23 | HG01081.hp1 HG01167.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.3325+20888_3325+20 others(7): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76799327 | ||||||
| chr8:76799649
|
C | T | 2 | a0002c0038t0002g0153a0009c0011t0006g0065 | 2 | HG03041.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.3325+21210C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76799649 | ||||||
| chr8:76799658
|
A | C | 16 | a0003c0002t0001g0007a0003c0002t0001g0009a0003c0002t0001g0081others(13): Show | 16 | HG01081.hp1 HG01167.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.3325+21219A>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76799658 | ||||||
| chr8:76800042
|
G | A | 1 | a0001c0015t0005g0005 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3325+21603G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76800042 | ||||||
| chr8:76800058
|
G | A | 1 | a0004c0012t0002g0061 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3325+21619G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76800058 | ||||||
| chr8:76800108
|
A | T | 2 | a0005c0005t0004g0111a0005c0005t0004g0123 | 2 | NA18945.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.3325+21669A>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76800108 | ||||||
| chr8:76800151
|
G | A | 2 | a0005c0005t0011g0095a0005c0005t0011g0099 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.3325+21712G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76800151 | ||||||
| chr8:76800317
|
A | T | 1 | a0004c0012t0002g0190 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3325+21878A>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76800317 | ||||||
| chr8:76800408
|
C | T | 1 | a0001c0051t0002g0141 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3325+21969C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76800408 | ||||||
| chr8:76800425
|
A | G | 3 | a0001c0003t0002g0176a0001c0078t0006g0159a0005c0032t0004g0184 | 3 | HG01952.hp2 NA18946.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.3325+21986A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76800425 | ||||||
| chr8:76800677
|
C | T | 1 | a0003c0002t0001g0054 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3325+22238C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76800677 | ||||||
| chr8:76800838
|
C | T | 1 | a0003c0002t0001g0032 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3325+22399C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76800838 | ||||||
| chr8:76800900
|
G | A | 2 | a0002c0038t0002g0153a0009c0011t0006g0065 | 2 | HG03041.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.3325+22461G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76800900 | ||||||
| chr8:76800994
|
G | A | 1 | a0001c0003t0002g0168 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.3325+22555G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76800994 | ||||||
| chr8:76801114
|
G | A | 3 | a0001c0004t0002g0197a0001c0051t0002g0141a0004c0012t0002g0196 | 3 | HG02735.hp1 HG02809.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.3325+22675G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76801114 | ||||||
| chr8:76802086
|
T | C | 1 | a0004c0046t0002g0075 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.3325+23647T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76802086 | ||||||
| chr8:76802178
|
G | A | 1 | a0002c0038t0002g0153 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3325+23739G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76802178 | ||||||
| chr8:76802215
|
A | T | 2 | a0003c0002t0005g0023a0003c0007t0005g0086 | 2 | HG02896.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.3325+23776A>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76802215 | ||||||
| chr8:76802352
|
T | C | 1 | a0017c0057t0001g0033 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3325+23913T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76802352 | ||||||
| chr8:76803247
|
T | G | 8 | a0001c0008t0005g0096a0001c0008t0005g0157a0001c0042t0002g0010others(5): Show | 8 | HG01070.hp1 HG01167.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.3325+24808T>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76803247 | ||||||
| chr8:76803263
|
C | CGT | 5 | a0002c0006t0003g0160a0003c0002t0001g0054a0012c0024t0005g0001others(2): Show | 6 | HG01168.hp2 HG02258.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.3325+24844_3325+24 others(8): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr8 | 76803263 | |||||
| chr8:76803263
|
C | T | 22 | a0001c0031t0002g0127a0004c0018t0002g0105a0004c0018t0002g0116others(19): Show | 22 | HG00408.hp1 HG00423.hp2 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.3325+24824C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76803263 | ||||||
| chr8:76803263
|
CGT | C | 3 | a0001c0025t0002g0210a0002c0038t0002g0153a0009c0011t0006g0065 | 3 | HG03041.hp2 NA19011.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.3325+24844_3325+24 others(8): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr8 | 76803263 | |||||
| chr8:76803263
|
CGTGTGT | C | 3 | a0001c0004t0002g0197a0001c0051t0002g0141a0004c0012t0002g0196 | 3 | HG02735.hp1 HG02809.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.3325+24840_3325+24 others(12): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr8 | 76803263 | |||||
| chr8:76803265
|
T | C | 1 | a0019c0082t0014g0139 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3325+24826T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76803265 | ||||||
| chr8:76803510
|
T | C | 3 | a0001c0063t0001g0053a0003c0059t0006g0085a0006c0016t0001g0084 | 3 | HG02258.hp2 HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.3325+25071T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76803510 | ||||||
| chr8:76803976
|
G | A | 3 | a0001c0004t0002g0197a0001c0051t0002g0141a0004c0012t0002g0196 | 3 | HG02735.hp1 HG02809.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.3325+25537G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76803976 | ||||||
| chr8:76804164
|
T | C | 1 | a0001c0047t0016g0066 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.3325+25725T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76804164 | ||||||
| chr8:76804584
|
A | G | 17 | a0003c0002t0001g0007a0003c0002t0001g0009a0003c0002t0001g0054others(14): Show | 17 | HG01081.hp1 HG01167.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.3325+26145A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76804584 | ||||||
| chr8:76804703
|
T | A | 1 | a0003c0007t0009g0082 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.3325+26264T>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76804703 | ||||||
| chr8:76804750
|
C | CA | 241 | a0001c0003t0002g0083a0001c0003t0002g0087a0001c0003t0002g0097others(238): Show | 243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.3325+26312dupA | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr8 | 76804750 | |||||
| chr8:76805416
|
A | T | 2 | a0001c0008t0005g0236a0004c0019t0005g0235 | 2 | HG00735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.3325+26977A>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76805416 | ||||||
| chr8:76805544
|
A | G | 1 | a0001c0008t0005g0233 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.3325+27105A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76805544 | ||||||
| chr8:76805590
|
C | CT | 14 | a0001c0004t0002g0197a0003c0002t0001g0026a0003c0002t0001g0027others(11): Show | 14 | HG01175.hp2 HG02109.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.3325+27165dupT | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr8 | 76805590 | |||||
| chr8:76805820
|
A | G | 3 | a0003c0002t0001g0081a0003c0061t0001g0156a0006c0029t0001g0154 | 3 | HG01081.hp1 HG02818.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.3325+27381A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76805820 | ||||||
| chr8:76806011
|
A | G | 1 | a0003c0002t0001g0054 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3326-27327A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76806011 | ||||||
| chr8:76806148
|
A | G | 1 | a0001c0004t0002g0069 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.3326-27190A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76806148 | ||||||
| chr8:76806155
|
A | G | 1 | a0013c0023t0001g0143 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3326-27183A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76806155 | ||||||
| chr8:76806210
|
T | A | 27 | a0001c0031t0002g0127a0002c0006t0003g0122a0002c0006t0003g0170others(24): Show | 27 | HG00408.hp1 HG00423.hp2 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.3326-27128T>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76806210 | ||||||
| chr8:76806260
|
C | T | 2 | a0003c0007t0001g0102a0006c0016t0001g0103 | 2 | HG02723.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3326-27078C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76806260 | ||||||
| chr8:76806278
|
T | G | 1 | a0001c0004t0002g0067 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.3326-27060T>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76806278 | ||||||
| chr8:76806542
|
C | T | 3 | a0003c0002t0001g0081a0003c0061t0001g0156a0006c0029t0001g0154 | 3 | HG01081.hp1 HG02818.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.3326-26796C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76806542 | ||||||
| chr8:76806583
|
G | A | 67 | a0001c0004t0002g0197a0001c0015t0001g0003a0001c0015t0005g0005others(64): Show | 67 | HG00408.hp1 HG00423.hp2 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.3326-26755G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76806583 | ||||||
| chr8:76806612
|
G | C | 2 | a0006c0048t0001g0022a0008c0067t0003g0106 | 2 | HG03669.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3326-26726G>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76806612 | ||||||
| chr8:76807147
|
A | G | 3 | a0003c0002t0001g0081a0003c0061t0001g0156a0006c0029t0001g0154 | 3 | HG01081.hp1 HG02818.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.3326-26191A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76807147 | ||||||
| chr8:76807184
|
A | G | 17 | a0003c0002t0001g0007a0003c0002t0001g0009a0003c0002t0001g0054others(14): Show | 17 | HG01081.hp1 HG01167.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.3326-26154A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76807184 | ||||||
| chr8:76807498
|
T | C | 1 | a0004c0022t0002g0242 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3326-25840T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76807498 | ||||||
| chr8:76807579
|
G | C | 1 | a0003c0007t0009g0082 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.3326-25759G>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76807579 | ||||||
| chr8:76807857
|
A | G | 6 | a0001c0015t0001g0003a0001c0015t0005g0005a0001c0015t0005g0011others(3): Show | 6 | HG01109.hp1 HG01884.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.3326-25481A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76807857 | ||||||
| chr8:76807998
|
A | G | 1 | a0002c0001t0001g0149 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3326-25340A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76807998 | ||||||
| chr8:76808015
|
C | T | 1 | a0003c0007t0001g0092 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3326-25323C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76808015 | ||||||
| chr8:76808115
|
T | C | 1 | a0001c0031t0002g0127 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.3326-25223T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76808115 | ||||||
| chr8:76808191
|
A | G | 156 | a0001c0004t0002g0197a0001c0004t0002g0206a0001c0004t0005g0064others(153): Show | 158 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.3326-25147A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76808191 | ||||||
| chr8:76808205
|
A | G | 1 | a0004c0081t0002g0045 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.3326-25133A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76808205 | ||||||
| chr8:76808500
|
G | A | 2 | a0003c0059t0006g0085a0006c0016t0001g0084 | 2 | HG02258.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.3326-24838G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76808500 | ||||||
| chr8:76808528
|
A | C | 1 | a0004c0046t0002g0075 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.3326-24810A>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76808528 | ||||||
| chr8:76808910
|
GTC | G | 6 | a0002c0006t0004g0217a0003c0002t0001g0081a0003c0061t0001g0156others(3): Show | 6 | HG01081.hp1 HG02818.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.3326-24405_3326-24 others(8): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr8 | 76808910 | |||||
| chr8:76808910
|
GTCTCTC | G | 11 | a0003c0002t0001g0007a0003c0002t0001g0009a0003c0007t0001g0090others(8): Show | 11 | HG01167.hp2 HG01891.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.3326-24409_3326-24 others(12): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr8 | 76808910 | |||||
| chr8:76808916
|
C | G | 5 | a0001c0008t0005g0096a0001c0008t0005g0157a0001c0042t0002g0010others(2): Show | 5 | HG01070.hp1 HG01167.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.3326-24422C>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76808916 | ||||||
| chr8:76808933
|
T | A | 53 | a0001c0004t0005g0064a0001c0004t0005g0219a0001c0015t0001g0003others(50): Show | 54 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(51): Show |
intron_variant | MODIFIER | c.3326-24405T>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76808933 | ||||||
| chr8:76808935
|
A | T | 4 | a0003c0002t0001g0074a0003c0002t0001g0076a0004c0012t0002g0190others(1): Show | 4 | HG01069.hp1 HG01109.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.3326-24403A>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76808935 | ||||||
| chr8:76808948
|
C | A | 4 | a0001c0004t0005g0064a0001c0004t0005g0219a0004c0012t0002g0218others(1): Show | 4 | HG01884.hp1 HG03130.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.3326-24390C>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76808948 | ||||||
| chr8:76809300
|
C | T | 1 | a0002c0001t0003g0051 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.3326-24038C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76809300 | ||||||
| chr8:76809368
|
C | T | 1 | a0004c0012t0002g0218 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3326-23970C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76809368 | ||||||
| chr8:76809423
|
A | C | 1 | a0002c0021t0018g0133 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.3326-23915A>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76809423 | ||||||
| chr8:76809428
|
G | A | 16 | a0003c0002t0001g0007a0003c0002t0001g0009a0003c0002t0001g0081others(13): Show | 16 | HG01081.hp1 HG01167.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.3326-23910G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76809428 | ||||||
| chr8:76809590
|
A | C | 11 | a0003c0002t0001g0007a0003c0002t0001g0009a0003c0007t0001g0090others(8): Show | 11 | HG01167.hp2 HG01891.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.3326-23748A>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76809590 | ||||||
| chr8:76809738
|
T | A | 3 | a0003c0002t0001g0081a0003c0061t0001g0156a0006c0029t0001g0154 | 3 | HG01081.hp1 HG02818.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.3326-23600T>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76809738 | ||||||
| chr8:76810018
|
AT | A | 5 | a0003c0002t0001g0026a0003c0002t0001g0027a0003c0002t0001g0029others(2): Show | 5 | HG02486.hp1 HG02572.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.3326-23313delT | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr8 | 76810018 | |||||
| chr8:76810725
|
G | T | 1 | a0002c0028t0002g0202 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.3326-22613G>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76810725 | ||||||
| chr8:76810924
|
C | T | 1 | a0017c0057t0001g0033 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3326-22414C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76810924 | ||||||
| chr8:76811018
|
C | T | 13 | a0003c0002t0001g0007a0003c0002t0001g0009a0003c0007t0001g0090others(10): Show | 13 | HG01167.hp2 HG01891.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.3326-22320C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76811018 | ||||||
| chr8:76811107
|
C | A | 1 | a0014c0039t0001g0072 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.3326-22231C>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76811107 | ||||||
| chr8:76811141
|
G | A | 2 | a0003c0027t0001g0055a0003c0027t0001g0056 | 2 | HG03486.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.3326-22197G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76811141 | ||||||
| chr8:76811231
|
G | A | 2 | a0001c0004t0002g0197a0004c0012t0002g0196 | 2 | HG02735.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.3326-22107G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76811231 | ||||||
| chr8:76811420
|
T | G | 5 | a0001c0003t0002g0087a0001c0003t0002g0110a0001c0004t0002g0212others(2): Show | 5 | HG01109.hp2 HG01952.hp1 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.3326-21918T>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76811420 | ||||||
| chr8:76811579
|
C | T | 2 | a0003c0002t0008g0012a0003c0002t0008g0013 | 2 | HG02723.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.3326-21759C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76811579 | ||||||
| chr8:76811738
|
T | C | 3 | a0001c0004t0002g0197a0001c0051t0002g0141a0004c0012t0002g0196 | 3 | HG02735.hp1 HG02809.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.3326-21600T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76811738 | ||||||
| chr8:76811818
|
G | C | 1 | a0005c0005t0004g0121 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.3326-21520G>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76811818 | ||||||
| chr8:76811872
|
T | C | 15 | a0002c0006t0002g0098a0002c0006t0010g0031a0003c0002t0001g0007others(12): Show | 15 | HG01167.hp2 HG01891.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.3326-21466T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76811872 | ||||||
| chr8:76811929
|
A | G | 1 | a0003c0002t0001g0054 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3326-21409A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76811929 | ||||||
| chr8:76811991
|
T | C | 15 | a0002c0006t0002g0098a0002c0006t0010g0031a0003c0002t0001g0007others(12): Show | 15 | HG01167.hp2 HG01891.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.3326-21347T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76811991 | ||||||
| chr8:76812202
|
G | A | 30 | a0001c0004t0002g0197a0001c0031t0002g0127a0002c0006t0003g0122others(27): Show | 30 | HG00408.hp1 HG00423.hp2 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.3326-21136G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76812202 | ||||||
| chr8:76812271
|
C | G | 1 | a0006c0009t0006g0151 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3326-21067C>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76812271 | ||||||
| chr8:76812324
|
G | A | 1 | a0002c0001t0003g0205 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.3326-21014G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76812324 | ||||||
| chr8:76812342
|
G | A | 1 | a0002c0028t0003g0138 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3326-20996G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76812342 | ||||||
| chr8:76812354
|
G | T | 1 | a0005c0032t0004g0184 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.3326-20984G>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76812354 | ||||||
| chr8:76812521
|
T | C | 18 | a0001c0004t0002g0197a0001c0051t0002g0141a0002c0006t0002g0098others(15): Show | 18 | HG01167.hp2 HG01891.hp1 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.3326-20817T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76812521 | ||||||
| chr8:76812627
|
A | G | 1 | a0002c0001t0001g0149 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3326-20711A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76812627 | ||||||
| chr8:76812699
|
C | T | 9 | a0003c0002t0001g0026a0003c0002t0001g0027a0003c0002t0001g0029others(6): Show | 9 | HG01175.hp2 HG02486.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.3326-20639C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76812699 | ||||||
| chr8:76812756
|
C | T | 2 | a0003c0002t0006g0058a0017c0057t0001g0033 | 2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.3326-20582C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76812756 | ||||||
| chr8:76812849
|
G | GT | 15 | a0002c0006t0002g0098a0002c0006t0010g0031a0003c0002t0001g0007others(12): Show | 15 | HG01167.hp2 HG01891.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.3326-20483dupT | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr8 | 76812849 | |||||
| chr8:76813000
|
T | G | 1 | a0001c0031t0020g0163 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.3326-20338T>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76813000 | ||||||
| chr8:76813207
|
C | T | 28 | a0001c0031t0002g0127a0002c0006t0003g0122a0002c0006t0003g0170others(25): Show | 28 | HG00408.hp1 HG00423.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.3326-20131C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76813207 | ||||||
| chr8:76813219
|
A | C | 15 | a0002c0006t0002g0098a0002c0006t0010g0031a0003c0002t0001g0007others(12): Show | 15 | HG01167.hp2 HG01891.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.3326-20119A>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76813219 | ||||||
| chr8:76813270
|
T | C | 15 | a0002c0006t0002g0098a0002c0006t0010g0031a0003c0002t0001g0007others(12): Show | 15 | HG01167.hp2 HG01891.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.3326-20068T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76813270 | ||||||
| chr8:76813289
|
G | A | 6 | a0001c0008t0005g0231a0001c0008t0005g0232a0001c0008t0005g0233others(3): Show | 6 | HG02080.hp1 HG02723.hp2 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.3326-20049G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76813289 | ||||||
| chr8:76813471
|
T | C | 9 | a0003c0002t0001g0026a0003c0002t0001g0027a0003c0002t0001g0029others(6): Show | 9 | HG01175.hp2 HG02486.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.3326-19867T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76813471 | ||||||
| chr8:76813936
|
C | G | 1 | a0002c0006t0003g0160 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.3326-19402C>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76813936 | ||||||
| chr8:76814053
|
G | A | 1 | a0001c0004t0002g0183 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.3326-19285G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76814053 | ||||||
| chr8:76814232
|
T | C | 4 | a0001c0008t0005g0231a0001c0008t0005g0232a0001c0008t0005g0233others(1): Show | 4 | HG02080.hp1 NA19062.hp1 NA19077.hp1 others(1): Show |
intron_variant | MODIFIER | c.3326-19106T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76814232 | ||||||
| chr8:76814257
|
T | A | 1 | a0004c0012t0002g0190 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3326-19081T>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76814257 | ||||||
| chr8:76814263
|
C | T | 2 | a0005c0005t0004g0111a0005c0005t0004g0123 | 2 | NA18945.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.3326-19075C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76814263 | ||||||
| chr8:76814405
|
G | C | 13 | a0002c0028t0003g0138a0003c0002t0001g0026a0003c0002t0001g0027others(10): Show | 13 | HG01175.hp2 HG01891.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.3326-18933G>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76814405 | ||||||
| chr8:76814497
|
G | A | 1 | a0001c0003t0002g0097 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.3326-18841G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76814497 | ||||||
| chr8:76814614
|
C | T | 2 | a0003c0002t0006g0058a0017c0057t0001g0033 | 2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.3326-18724C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76814614 | ||||||
| chr8:76814691
|
A | G | 1 | a0003c0002t0001g0081 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3326-18647A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76814691 | ||||||
| chr8:76814726
|
G | T | 2 | a0003c0002t0006g0058a0017c0057t0001g0033 | 2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.3326-18612G>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76814726 | ||||||
| chr8:76814751
|
G | A | 7 | a0001c0015t0001g0003a0001c0015t0005g0005a0001c0015t0005g0011others(4): Show | 8 | HG01109.hp1 HG01884.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.3326-18587G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76814751 | ||||||
| chr8:76814891
|
G | C | 18 | a0001c0017t0003g0107a0001c0017t0003g0108a0001c0017t0021g0129others(15): Show | 18 | HG00597.hp2 HG00639.hp2 HG02132.hp1 others(15): Show |
intron_variant | MODIFIER | c.3326-18447G>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76814891 | ||||||
| chr8:76815165
|
TA | T | 3 | a0001c0004t0002g0197a0001c0051t0002g0141a0004c0012t0002g0196 | 3 | HG02735.hp1 HG02809.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.3326-18171delA | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr8 | 76815165 | |||||
| chr8:76815280
|
G | A | 18 | a0001c0017t0003g0107a0001c0017t0003g0108a0001c0017t0021g0129others(15): Show | 18 | HG00597.hp2 HG00639.hp2 HG02132.hp1 others(15): Show |
intron_variant | MODIFIER | c.3326-18058G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76815280 | ||||||
| chr8:76815360
|
T | G | 10 | a0002c0028t0003g0138a0003c0002t0001g0026a0003c0002t0001g0027others(7): Show | 10 | HG01175.hp2 HG01891.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.3326-17978T>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76815360 | ||||||
| chr8:76815428
|
A | G | 4 | a0001c0004t0002g0197a0001c0051t0002g0141a0004c0012t0002g0196others(1): Show | 4 | HG02735.hp1 HG02809.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.3326-17910A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76815428 | ||||||
| chr8:76815569
|
G | A | 17 | a0001c0004t0002g0197a0001c0051t0002g0141a0002c0006t0002g0098others(14): Show | 17 | HG01167.hp2 HG01891.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.3326-17769G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76815569 | ||||||
| chr8:76815648
|
C | T | 1 | a0001c0015t0005g0005 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3326-17690C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76815648 | ||||||
| chr8:76815693
|
G | T | 1 | a0001c0015t0005g0011 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3326-17645G>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76815693 | ||||||
| chr8:76815703
|
A | G | 14 | a0002c0006t0002g0098a0002c0006t0010g0031a0003c0002t0001g0007others(11): Show | 14 | HG01167.hp2 HG01891.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.3326-17635A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76815703 | ||||||
| chr8:76815743
|
C | T | 2 | a0003c0002t0001g0004a0003c0007t0001g0240 | 2 | HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.3326-17595C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76815743 | ||||||
| chr8:76815747
|
C | T | 1 | a0002c0006t0010g0031 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3326-17591C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76815747 | ||||||
| chr8:76815803
|
C | T | 2 | a0005c0005t0004g0226a0010c0013t0004g0227 | 2 | HG00621.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.3326-17535C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76815803 | ||||||
| chr8:76815893
|
G | C | 14 | a0002c0006t0002g0098a0002c0006t0010g0031a0003c0002t0001g0007others(11): Show | 14 | HG01167.hp2 HG01891.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.3326-17445G>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76815893 | ||||||
| chr8:76816488
|
C | A | 3 | a0001c0017t0003g0107a0001c0017t0003g0108a0001c0017t0021g0129 | 3 | NA18983.hp2 NA19064.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.3326-16850C>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76816488 | ||||||
| chr8:76816526
|
T | C | 7 | a0002c0001t0003g0185a0002c0001t0003g0187a0003c0027t0001g0055others(4): Show | 7 | HG02109.hp1 HG03486.hp2 HG06807.hp2 others(4): Show |
intron_variant | MODIFIER | c.3326-16812T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76816526 | ||||||
| chr8:76816590
|
C | CT | 35 | a0002c0001t0003g0185a0002c0006t0002g0098a0002c0006t0004g0217others(32): Show | 35 | HG01081.hp1 HG01109.hp2 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.3326-16726dupT | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr8 | 76816590 | |||||
| chr8:76816752
|
T | A | 3 | a0001c0004t0002g0197a0001c0051t0002g0141a0004c0012t0002g0196 | 3 | HG02735.hp1 HG02809.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.3326-16586T>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76816752 | ||||||
| chr8:76816754
|
C | T | 1 | a0001c0004t0019g0050 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.3326-16584C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76816754 | ||||||
| chr8:76816904
|
C | A | 1 | a0001c0003t0002g0176 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.3326-16434C>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76816904 | ||||||
| chr8:76817099
|
G | A | 2 | a0001c0042t0002g0010a0002c0001t0010g0014 | 2 | HG01070.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3326-16239G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76817099 | ||||||
| chr8:76817140
|
G | T | 2 | a0008c0010t0006g0015a0008c0010t0006g0017 | 2 | HG02040.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.3326-16198G>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76817140 | ||||||
| chr8:76817269
|
G | A | 1 | a0003c0002t0001g0004 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3326-16069G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76817269 | ||||||
| chr8:76817478
|
C | T | 21 | a0001c0004t0002g0197a0001c0051t0002g0141a0002c0006t0002g0098others(18): Show | 21 | HG01167.hp2 HG01891.hp1 HG02486.hp2 others(18): Show |
intron_variant | MODIFIER | c.3326-15860C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76817478 | ||||||
| chr8:76817700
|
C | G | 1 | a0006c0009t0001g0028 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3326-15638C>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76817700 | ||||||
| chr8:76817716
|
A | G | 1 | a0002c0028t0003g0138 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3326-15622A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76817716 | ||||||
| chr8:76817912
|
A | G | 19 | a0001c0004t0002g0197a0001c0051t0002g0141a0002c0006t0002g0098others(16): Show | 19 | HG01167.hp2 HG01891.hp1 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.3326-15426A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76817912 | ||||||
| chr8:76817979
|
G | C | 2 | a0003c0002t0001g0054a0008c0067t0003g0106 | 2 | HG02970.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3326-15359G>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76817979 | ||||||
| chr8:76818050
|
A | G | 1 | a0002c0006t0010g0155 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3326-15288A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76818050 | ||||||
| chr8:76818077
|
C | T | 14 | a0002c0006t0002g0098a0002c0006t0010g0031a0003c0002t0001g0007others(11): Show | 14 | HG01167.hp2 HG01891.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.3326-15261C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76818077 | ||||||
| chr8:76818452
|
A | G | 1 | a0002c0001t0002g0198 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.3326-14886A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76818452 | ||||||
| chr8:76818640
|
G | A | 1 | a0001c0015t0001g0003 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3326-14698G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76818640 | ||||||
| chr8:76818963
|
G | A | 2 | a0003c0002t0001g0054a0008c0067t0003g0106 | 2 | HG02970.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3326-14375G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76818963 | ||||||
| chr8:76819051
|
G | A | 24 | a0002c0006t0002g0098a0002c0006t0010g0031a0002c0028t0003g0138others(21): Show | 24 | HG01167.hp2 HG01175.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.3326-14287G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76819051 | ||||||
| chr8:76819142
|
GT | G | 141 | a0001c0003t0002g0097a0001c0003t0002g0110a0001c0003t0002g0134others(138): Show | 143 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.3326-14175delT | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr8 | 76819142 | |||||
| chr8:76819142
|
GTT | G | 23 | a0001c0008t0005g0231a0001c0008t0005g0232a0001c0008t0005g0233others(20): Show | 23 | HG00609.hp1 HG00609.hp2 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.3326-14176_3326-14 others(8): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr8 | 76819142 | |||||
| chr8:76819560
|
G | C | 2 | a0003c0002t0001g0074a0003c0002t0001g0076 | 2 | HG02451.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.3326-13778G>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76819560 | ||||||
| chr8:76819681
|
T | C | 5 | a0001c0004t0002g0197a0001c0051t0002g0141a0002c0038t0002g0153others(2): Show | 5 | HG02735.hp1 HG02809.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.3326-13657T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76819681 | ||||||
| chr8:76820210
|
A | G | 1 | a0003c0002t0001g0071 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.3326-13128A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76820210 | ||||||
| chr8:76820272
|
G | A | 1 | a0031c0049t0001g0060 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.3326-13066G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76820272 | ||||||
| chr8:76820498
|
G | A | 2 | a0005c0005t0004g0226a0010c0013t0004g0227 | 2 | HG00621.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.3326-12840G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76820498 | ||||||
| chr8:76820520
|
G | A | 4 | a0002c0006t0002g0098a0002c0006t0010g0031a0003c0002t0001g0054others(1): Show | 4 | HG02818.hp1 HG02970.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.3326-12818G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76820520 | ||||||
| chr8:76820566
|
T | C | 1 | a0001c0080t0005g0006 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.3326-12772T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76820566 | ||||||
| chr8:76821108
|
A | G | 1 | a0001c0025t0002g0200 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.3326-12230A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76821108 | ||||||
| chr8:76821260
|
A | G | 1 | a0008c0010t0006g0016 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.3326-12078A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76821260 | ||||||
| chr8:76821369
|
C | T | 1 | a0002c0001t0004g0199 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.3326-11969C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76821369 | ||||||
| chr8:76821496
|
T | TGGAAAGG others(1296): Show |
1 | a0001c0078t0006g0159 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.3326-11842_3326-11 others(1309): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76821496 | ||||||
| chr8:76821497
|
T | A | 1 | a0001c0078t0006g0159 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.3326-11841T>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76821497 | ||||||
| chr8:76821527
|
A | AT | 17 | a0001c0004t0002g0197a0001c0004t0005g0064a0001c0004t0005g0219others(14): Show | 17 | HG01081.hp1 HG01081.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.3326-11797dupT | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr8 | 76821527 | |||||
| chr8:76821527
|
AT | A | 18 | a0003c0002t0001g0007a0003c0002t0001g0009a0003c0002t0005g0023others(15): Show | 18 | HG01167.hp2 HG01891.hp1 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.3326-11797delT | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr8 | 76821527 | |||||
| chr8:76821609
|
T | C | 4 | a0002c0006t0002g0098a0002c0006t0010g0031a0003c0002t0001g0054others(1): Show | 4 | HG02818.hp1 HG02970.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.3326-11729T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76821609 | ||||||
| chr8:76821881
|
G | A | 2 | a0002c0038t0002g0153a0009c0011t0006g0065 | 2 | HG03041.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.3326-11457G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76821881 | ||||||
| chr8:76822067
|
T | A | 1 | a0004c0046t0002g0075 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.3326-11271T>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76822067 | ||||||
| chr8:76822127
|
C | T | 12 | a0003c0002t0001g0007a0003c0002t0001g0009a0003c0007t0001g0090others(9): Show | 12 | HG01167.hp2 HG01891.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.3326-11211C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76822127 | ||||||
| chr8:76822213
|
G | A | 2 | a0002c0006t0002g0098a0002c0006t0010g0031 | 2 | HG02818.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3326-11125G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76822213 | ||||||
| chr8:76822411
|
G | C | 10 | a0001c0004t0002g0197a0001c0004t0005g0064a0001c0004t0005g0219others(7): Show | 10 | HG01884.hp1 HG02615.hp2 HG02735.hp1 others(7): Show |
intron_variant | MODIFIER | c.3326-10927G>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76822411 | ||||||
| chr8:76822416
|
T | C | 1 | a0002c0001t0001g0149 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3326-10922T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76822416 | ||||||
| chr8:76822426
|
A | G | 1 | a0004c0022t0002g0180 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.3326-10912A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76822426 | ||||||
| chr8:76822450
|
C | CTG | 3 | a0001c0031t0002g0127a0010c0013t0004g0104a0011c0020t0004g0041 | 3 | HG01261.hp2 NA18967.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.3326-10887_3326-10 others(8): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr8 | 76822450 | |||||
| chr8:76822451
|
T | TG | 20 | a0004c0018t0002g0105a0005c0005t0004g0047a0005c0005t0004g0078others(17): Show | 20 | HG00408.hp1 HG00621.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.3326-10887_3326-10 others(7): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76822451 | ||||||
| chr8:76822452
|
C | CT | 13 | a0001c0004t0002g0197a0001c0004t0005g0064a0001c0004t0005g0219others(10): Show | 13 | HG01884.hp1 HG02615.hp2 HG02735.hp1 others(10): Show |
intron_variant | MODIFIER | c.3326-10864dupT | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr8 | 76822452 | |||||
| chr8:76822452
|
C | CTT | 5 | a0001c0003t0003g0120a0002c0006t0002g0098a0002c0006t0010g0031others(2): Show | 5 | HG02074.hp2 HG02818.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.3326-10865_3326-10 others(8): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr8 | 76822452 | |||||
| chr8:76822452
|
C | CTTT | 14 | a0003c0002t0001g0007a0003c0002t0001g0009a0003c0002t0001g0054others(11): Show | 14 | HG01167.hp2 HG01891.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.3326-10866_3326-10 others(9): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr8 | 76822452 | |||||
| chr8:76822452
|
C | G | 3 | a0004c0018t0002g0116a0004c0068t0006g0109a0027c0066t0003g0115 | 3 | HG00423.hp2 NA19076.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.3326-10886C>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76822452 | ||||||
| chr8:76822452
|
C | T | 23 | a0001c0031t0002g0127a0004c0018t0002g0105a0005c0005t0004g0047others(20): Show | 23 | HG00408.hp1 HG00621.hp2 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.3326-10886C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76822452 | ||||||
| chr8:76822452
|
CT | C | 11 | a0001c0003t0002g0097a0002c0001t0003g0205a0002c0001t0003g0207others(8): Show | 11 | HG00280.hp1 HG02886.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.3326-10864delT | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr8 | 76822452 | |||||
| chr8:76822656
|
T | G | 28 | a0001c0004t0002g0197a0001c0004t0005g0064a0001c0004t0005g0219others(25): Show | 28 | HG01167.hp2 HG01884.hp1 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.3326-10682T>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76822656 | ||||||
| chr8:76822708
|
T | C | 1 | a0003c0007t0005g0052 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3326-10630T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76822708 | ||||||
| chr8:76822834
|
G | A | 26 | a0001c0031t0002g0127a0004c0018t0002g0105a0004c0018t0002g0116others(23): Show | 26 | HG00408.hp1 HG00423.hp2 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.3326-10504G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76822834 | ||||||
| chr8:76822842
|
T | G | 1 | a0029c0065t0003g0114 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.3326-10496T>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76822842 | ||||||
| chr8:76822870
|
T | C | 1 | a0002c0001t0003g0077 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.3326-10468T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76822870 | ||||||
| chr8:76822974
|
A | G | 2 | a0003c0002t0006g0058a0017c0057t0001g0033 | 2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.3326-10364A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76822974 | ||||||
| chr8:76823130
|
CT | C | 49 | a0001c0004t0002g0197a0001c0004t0005g0064a0001c0004t0005g0219others(46): Show | 49 | HG00408.hp1 HG00423.hp2 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.3326-10191delT | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr8 | 76823130 | |||||
| chr8:76823130
|
CTTT | C | 12 | a0003c0002t0001g0007a0003c0002t0001g0009a0003c0007t0001g0090others(9): Show | 12 | HG01167.hp2 HG01891.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.3326-10193_3326-10 others(9): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr8 | 76823130 | |||||
| chr8:76823339
|
C | T | 1 | a0001c0003t0002g0083 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.3326-9999C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76823339 | ||||||
| chr8:76823598
|
A | G | 1 | a0028c0043t0001g0140 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3326-9740A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76823598 | ||||||
| chr8:76823832
|
G | A | 2 | a0001c0004t0002g0197a0004c0012t0002g0196 | 2 | HG02735.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.3326-9506G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76823832 | ||||||
| chr8:76823892
|
C | T | 2 | a0002c0038t0002g0153a0031c0049t0001g0060 | 2 | HG02615.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.3326-9446C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76823892 | ||||||
| chr8:76824318
|
A | G | 1 | a0002c0006t0010g0155 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3326-9020A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76824318 | ||||||
| chr8:76824368
|
A | T | 1 | a0002c0001t0003g0195 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.3326-8970A>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76824368 | ||||||
| chr8:76824410
|
T | A | 12 | a0003c0002t0001g0007a0003c0002t0001g0009a0003c0007t0001g0090others(9): Show | 12 | HG01167.hp2 HG01891.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.3326-8928T>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76824410 | ||||||
| chr8:76824448
|
G | A | 1 | a0006c0029t0001g0158 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3326-8890G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76824448 | ||||||
| chr8:76824673
|
A | G | 13 | a0002c0028t0003g0138a0003c0002t0001g0026a0003c0002t0001g0027others(10): Show | 13 | HG01175.hp2 HG01891.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.3326-8665A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76824673 | ||||||
| chr8:76824895
|
C | T | 14 | a0001c0017t0003g0107a0001c0017t0003g0108a0001c0017t0021g0129others(11): Show | 14 | HG00597.hp2 HG00639.hp2 HG02132.hp1 others(11): Show |
intron_variant | MODIFIER | c.3326-8443C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76824895 | ||||||
| chr8:76824968
|
A | G | 1 | a0005c0005t0004g0078 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3326-8370A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76824968 | ||||||
| chr8:76825125
|
A | G | 1 | a0011c0020t0004g0113 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.3326-8213A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76825125 | ||||||
| chr8:76825131
|
A | G | 2 | a0002c0006t0002g0098a0002c0006t0010g0031 | 2 | HG02818.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3326-8207A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76825131 | ||||||
| chr8:76825143
|
T | C | 2 | a0002c0038t0002g0153a0009c0011t0006g0065 | 2 | HG03041.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.3326-8195T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76825143 | ||||||
| chr8:76825226
|
C | T | 2 | a0003c0002t0005g0023a0003c0007t0005g0086 | 2 | HG02896.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.3326-8112C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76825226 | ||||||
| chr8:76825282
|
C | T | 2 | a0001c0004t0001g0203a0001c0004t0001g0204 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.3326-8056C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76825282 | ||||||
| chr8:76825322
|
A | C | 1 | a0001c0003t0022g0135 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.3326-8016A>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76825322 | ||||||
| chr8:76825388
|
A | G | 12 | a0003c0002t0001g0007a0003c0002t0001g0009a0003c0007t0001g0090others(9): Show | 12 | HG01167.hp2 HG01891.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.3326-7950A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76825388 | ||||||
| chr8:76825426
|
C | T | 1 | a0003c0002t0006g0058 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3326-7912C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76825426 | ||||||
| chr8:76825441
|
C | T | 1 | a0006c0048t0001g0022 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.3326-7897C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76825441 | ||||||
| chr8:76825530
|
T | C | 1 | a0001c0051t0002g0141 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3326-7808T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76825530 | ||||||
| chr8:76825538
|
A | G | 12 | a0003c0002t0001g0007a0003c0002t0001g0009a0003c0007t0001g0090others(9): Show | 12 | HG01167.hp2 HG01891.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.3326-7800A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76825538 | ||||||
| chr8:76825676
|
T | C | 2 | a0002c0001t0003g0002a0002c0001t0003g0193 | 3 | HG00280.hp2 NA18945.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.3326-7662T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76825676 | ||||||
| chr8:76826375
|
C | T | 26 | a0001c0031t0002g0127a0004c0018t0002g0105a0004c0018t0002g0116others(23): Show | 26 | HG00408.hp1 HG00423.hp2 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.3326-6963C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76826375 | ||||||
| chr8:76826391
|
G | C | 2 | a0001c0004t0001g0203a0001c0004t0001g0204 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.3326-6947G>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76826391 | ||||||
| chr8:76826518
|
G | A | 1 | a0001c0078t0006g0159 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.3326-6820G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76826518 | ||||||
| chr8:76826616
|
T | A | 12 | a0003c0002t0001g0007a0003c0002t0001g0009a0003c0007t0001g0090others(9): Show | 12 | HG01167.hp2 HG01891.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.3326-6722T>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76826616 | ||||||
| chr8:76826928
|
C | T | 9 | a0001c0004t0002g0197a0001c0004t0005g0064a0001c0004t0005g0219others(6): Show | 9 | HG01884.hp1 HG02615.hp2 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.3326-6410C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76826928 | ||||||
| chr8:76826990
|
C | G | 2 | a0009c0011t0007g0222a0009c0011t0007g0223 | 2 | HG02486.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.3326-6348C>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76826990 | ||||||
| chr8:76827148
|
C | T | 3 | a0003c0027t0001g0055a0003c0027t0001g0056a0003c0034t0001g0142 | 3 | HG02109.hp1 HG03486.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.3326-6190C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76827148 | ||||||
| chr8:76827331
|
G | A | 26 | a0001c0031t0002g0127a0004c0018t0002g0105a0004c0018t0002g0116others(23): Show | 26 | HG00408.hp1 HG00423.hp2 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.3326-6007G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76827331 | ||||||
| chr8:76827369
|
G | A | 2 | a0002c0038t0002g0153a0009c0011t0006g0065 | 2 | HG03041.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.3326-5969G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76827369 | ||||||
| chr8:76827407
|
G | A | 1 | a0003c0034t0001g0142 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3326-5931G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76827407 | ||||||
| chr8:76827676
|
C | T | 2 | a0002c0038t0002g0153a0009c0011t0006g0065 | 2 | HG03041.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.3326-5662C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76827676 | ||||||
| chr8:76827796
|
A | G | 21 | a0003c0002t0001g0007a0003c0002t0001g0009a0003c0002t0001g0026others(18): Show | 21 | HG01167.hp2 HG01175.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.3326-5542A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76827796 | ||||||
| chr8:76827951
|
G | T | 2 | a0003c0002t0001g0054a0008c0067t0003g0106 | 2 | HG02970.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3326-5387G>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76827951 | ||||||
| chr8:76828025
|
G | A | 1 | a0006c0074t0008g0166 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.3326-5313G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76828025 | ||||||
| chr8:76828197
|
T | C | 2 | a0003c0002t0001g0054a0008c0067t0003g0106 | 2 | HG02970.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3326-5141T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76828197 | ||||||
| chr8:76828314
|
G | A | 2 | a0003c0059t0006g0085a0006c0016t0001g0084 | 2 | HG02258.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.3326-5024G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76828314 | ||||||
| chr8:76828360
|
G | A | 1 | a0014c0050t0015g0220 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3326-4978G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76828360 | ||||||
| chr8:76828432
|
A | G | 2 | a0004c0019t0005g0091a0012c0024t0005g0001 | 3 | HG03239.hp2 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.3326-4906A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76828432 | ||||||
| chr8:76828533
|
C | A | 9 | a0003c0002t0001g0026a0003c0002t0001g0027a0003c0002t0001g0029others(6): Show | 9 | HG01175.hp2 HG02486.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.3326-4805C>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76828533 | ||||||
| chr8:76828545
|
C | T | 26 | a0001c0031t0002g0127a0004c0018t0002g0105a0004c0018t0002g0116others(23): Show | 26 | HG00408.hp1 HG00423.hp2 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.3326-4793C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76828545 | ||||||
| chr8:76828569
|
T | C | 5 | a0001c0003t0002g0216a0001c0003t0012g0043a0001c0004t0002g0067others(2): Show | 5 | HG00597.hp1 HG02080.hp2 HG02165.hp2 others(2): Show |
intron_variant | MODIFIER | c.3326-4769T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76828569 | ||||||
| chr8:76828629
|
T | C | 1 | a0003c0007t0009g0082 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.3326-4709T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76828629 | ||||||
| chr8:76828833
|
T | C | 1 | a0002c0028t0003g0138 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3326-4505T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76828833 | ||||||
| chr8:76828872
|
A | T | 1 | a0002c0006t0010g0155 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3326-4466A>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76828872 | ||||||
| chr8:76828943
|
ATACTT | A | 6 | a0003c0002t0001g0007a0003c0002t0001g0009a0003c0007t0001g0090others(3): Show | 6 | HG01891.hp1 HG02622.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.3326-4392_3326-438 others(9): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr8 | 76828943 | |||||
| chr8:76829224
|
C | T | 6 | a0003c0002t0001g0007a0003c0002t0001g0009a0003c0007t0001g0090others(3): Show | 6 | HG01891.hp1 HG02622.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.3326-4114C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76829224 | ||||||
| chr8:76829275
|
C | T | 1 | a0004c0019t0005g0234 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.3326-4063C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76829275 | ||||||
| chr8:76829280
|
C | T | 14 | a0001c0004t0002g0197a0001c0004t0005g0064a0001c0004t0005g0219others(11): Show | 14 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.3326-4058C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76829280 | ||||||
| chr8:76829680
|
G | A | 50 | a0001c0003t0002g0216a0001c0004t0002g0067a0001c0004t0002g0189others(47): Show | 51 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.3326-3658G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76829680 | ||||||
| chr8:76829729
|
A | T | 175 | a0001c0003t0003g0120a0001c0008t0005g0093a0001c0008t0005g0096others(172): Show | 177 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.3326-3609A>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76829729 | ||||||
| chr8:76829776
|
G | A | 1 | a0001c0003t0002g0168 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.3326-3562G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76829776 | ||||||
| chr8:76829829
|
A | T | 26 | a0001c0031t0002g0127a0004c0018t0002g0105a0004c0018t0002g0116others(23): Show | 26 | HG00408.hp1 HG00423.hp2 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.3326-3509A>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76829829 | ||||||
| chr8:76830014
|
A | G | 183 | a0001c0003t0003g0120a0001c0008t0005g0093a0001c0008t0005g0096others(180): Show | 185 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.3326-3324A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76830014 | ||||||
| chr8:76830110
|
C | G | 2 | a0003c0002t0001g0076a0014c0039t0001g0072 | 2 | HG01069.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.3326-3228C>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76830110 | ||||||
| chr8:76830176
|
G | A | 2 | a0002c0038t0002g0153a0009c0011t0006g0065 | 2 | HG03041.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.3326-3162G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76830176 | ||||||
| chr8:76830399
|
A | G | 26 | a0001c0031t0002g0127a0004c0018t0002g0105a0004c0018t0002g0116others(23): Show | 26 | HG00408.hp1 HG00423.hp2 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.3326-2939A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76830399 | ||||||
| chr8:76830546
|
C | A | 175 | a0001c0008t0005g0093a0001c0008t0005g0096a0001c0008t0005g0157others(172): Show | 177 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.3326-2792C>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76830546 | ||||||
| chr8:76830556
|
T | C | 2 | a0003c0002t0001g0068a0006c0009t0001g0028 | 2 | HG02055.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.3326-2782T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76830556 | ||||||
| chr8:76830604
|
G | A | 6 | a0003c0002t0001g0007a0003c0002t0001g0009a0003c0007t0001g0090others(3): Show | 6 | HG01891.hp1 HG02622.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.3326-2734G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76830604 | ||||||
| chr8:76830655
|
T | C | 6 | a0003c0002t0001g0007a0003c0002t0001g0009a0003c0007t0001g0090others(3): Show | 6 | HG01891.hp1 HG02622.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.3326-2683T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76830655 | ||||||
| chr8:76830687
|
T | G | 140 | a0001c0003t0003g0120a0001c0008t0005g0093a0001c0008t0005g0096others(137): Show | 142 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.3326-2651T>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76830687 | ||||||
| chr8:76830795
|
A | G | 5 | a0003c0002t0001g0007a0003c0002t0001g0009a0003c0007t0001g0090others(2): Show | 5 | HG01891.hp1 HG02622.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.3326-2543A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76830795 | ||||||
| chr8:76830912
|
C | G | 4 | a0001c0004t0005g0064a0001c0004t0005g0219a0004c0012t0002g0218others(1): Show | 4 | HG01884.hp1 HG03130.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.3326-2426C>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76830912 | ||||||
| chr8:76830933
|
C | T | 2 | a0005c0005t0004g0111a0005c0005t0004g0123 | 2 | NA18945.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.3326-2405C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76830933 | ||||||
| chr8:76830973
|
T | C | 1 | a0001c0078t0006g0159 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.3326-2365T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76830973 | ||||||
| chr8:76830974
|
G | C | 1 | a0002c0001t0010g0014 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.3326-2364G>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76830974 | ||||||
| chr8:76831313
|
G | A | 178 | a0001c0003t0003g0120a0001c0008t0005g0093a0001c0008t0005g0096others(175): Show | 180 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.3326-2025G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76831313 | ||||||
| chr8:76831319
|
A | G | 1 | a0001c0003t0002g0216 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.3326-2019A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76831319 | ||||||
| chr8:76831390
|
A | G | 1 | a0017c0057t0001g0033 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3326-1948A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76831390 | ||||||
| chr8:76831395
|
T | C | 2 | a0015c0071t0002g0088a0032c0072t0002g0080 | 2 | HG00639.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.3326-1943T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76831395 | ||||||
| chr8:76831468
|
A | G | 2 | a0002c0038t0002g0153a0009c0011t0006g0065 | 2 | HG03041.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.3326-1870A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76831468 | ||||||
| chr8:76831518
|
A | G | 1 | a0002c0038t0002g0153 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3326-1820A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76831518 | ||||||
| chr8:76831535
|
G | A | 2 | a0001c0004t0005g0064a0001c0004t0005g0219 | 2 | HG01884.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.3326-1803G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76831535 | ||||||
| chr8:76831747
|
C | A | 2 | a0002c0038t0002g0153a0009c0011t0006g0065 | 2 | HG03041.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.3326-1591C>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76831747 | ||||||
| chr8:76831748
|
G | A | 1 | a0022c0075t0001g0089 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3326-1590G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76831748 | ||||||
| chr8:76831984
|
A | C | 1 | a0004c0022t0002g0180 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.3326-1354A>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76831984 | ||||||
| chr8:76832002
|
T | TG | 131 | a0001c0004t0002g0189a0001c0008t0005g0093a0001c0008t0005g0096others(128): Show | 133 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.3326-1327dupG | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr8 | 76832002 | |||||
| chr8:76832002
|
T | TGG | 37 | a0001c0003t0003g0120a0001c0031t0002g0127a0002c0001t0003g0020others(34): Show | 37 | HG00408.hp1 HG00423.hp2 HG00597.hp2 others(34): Show |
intron_variant | MODIFIER | c.3326-1328_3326-132 others(6): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr8 | 76832002 | |||||
| chr8:76832475
|
T | C | 1 | a0002c0006t0002g0098 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3326-863T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76832475 | ||||||
| chr8:76832538
|
G | A | 2 | a0005c0005t0011g0095a0005c0005t0011g0099 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.3326-800G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76832538 | ||||||
| chr8:76832538
|
G | T | 2 | a0002c0038t0002g0153a0009c0011t0006g0065 | 2 | HG03041.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.3326-800G>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76832538 | ||||||
| chr8:76832549
|
C | T | 1 | a0002c0028t0002g0202 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.3326-789C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76832549 | ||||||
| chr8:76832559
|
A | G | 64 | a0001c0008t0005g0093a0001c0008t0005g0230a0001c0008t0005g0231others(61): Show | 65 | HG00099.hp1 HG00438.hp1 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.3326-779A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76832559 | ||||||
| chr8:76832591
|
A | G | 6 | a0009c0011t0007g0025a0009c0011t0007g0221a0009c0011t0007g0222others(3): Show | 6 | HG01167.hp2 HG02486.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.3326-747A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76832591 | ||||||
| chr8:76833031
|
C | A | 1 | a0001c0008t0005g0230 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3326-307C>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 4/10 | chr8 | 76833031 | ||||||
| chr8:76833683
|
T | A | 1 | a0005c0005t0004g0117 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.3394+277T>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | chr8 | 76833683 | ||||||
| chr8:76833721
|
A | G | 177 | a0001c0003t0002g0110a0001c0003t0003g0120a0001c0008t0005g0093others(174): Show | 179 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.3394+315A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | chr8 | 76833721 | ||||||
| chr8:76834015
|
T | C | 1 | a0006c0009t0001g0059 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3394+609T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | chr8 | 76834015 | ||||||
| chr8:76834091
|
T | C | 1 | a0005c0032t0004g0046 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.3394+685T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | chr8 | 76834091 | ||||||
| chr8:76834175
|
C | T | 2 | a0003c0002t0006g0058a0017c0057t0001g0033 | 2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.3394+769C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | chr8 | 76834175 | ||||||
| chr8:76834197
|
C | T | 1 | a0018c0064t0001g0137 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3394+791C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | chr8 | 76834197 | ||||||
| chr8:76834243
|
T | A | 1 | a0006c0009t0006g0151 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3394+837T>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | chr8 | 76834243 | ||||||
| chr8:76834276
|
G | C | 1 | a0006c0009t0006g0151 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3394+870G>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | chr8 | 76834276 | ||||||
| chr8:76834466
|
T | TTTCATAA others(26): Show |
1 | a0004c0046t0002g0075 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.3394+1061_3394+106 others(37): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 76834466 | |||||
| chr8:76834469
|
C | T | 1 | a0004c0046t0002g0075 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.3394+1063C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | chr8 | 76834469 | ||||||
| chr8:76834724
|
C | A | 1 | a0006c0074t0008g0166 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.3394+1318C>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | chr8 | 76834724 | ||||||
| chr8:76834924
|
G | A | 4 | a0001c0004t0005g0064a0001c0004t0005g0219a0004c0012t0002g0218others(1): Show | 4 | HG01884.hp1 HG03130.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.3394+1518G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | chr8 | 76834924 | ||||||
| chr8:76835207
|
G | T | 2 | a0002c0038t0002g0153a0009c0011t0006g0065 | 2 | HG03041.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.3394+1801G>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | chr8 | 76835207 | ||||||
| chr8:76835209
|
GTATATAT others(15): Show |
G | 1 | a0031c0049t0001g0060 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.3394+1833_3394+185 others(26): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 76835209 | |||||
| chr8:76835219
|
G | GTA | 33 | a0001c0004t0002g0212a0001c0004t0005g0219a0001c0017t0003g0107others(30): Show | 33 | HG00597.hp2 HG00639.hp2 HG01167.hp2 others(30): Show |
intron_variant | MODIFIER | c.3394+1833_3394+183 others(6): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 76835219 | |||||
| chr8:76835227
|
A | ATATATAT others(43): Show |
1 | a0010c0013t0004g0172 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3394+1829_3394+183 others(54): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 76835227 | |||||
| chr8:76835227
|
A | ATATATAT others(43): Show |
3 | a0004c0018t0002g0105a0005c0005t0004g0078a0005c0005t0004g0121 | 3 | HG00408.hp1 NA18994.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3394+1834_3394+183 others(54): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 76835227 | |||||
| chr8:76835227
|
A | ATATATAT others(35): Show |
1 | a0006c0016t0001g0084 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3394+1832_3394+183 others(46): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 76835227 | |||||
| chr8:76835227
|
A | ATATATAT others(15): Show |
1 | a0001c0008t0005g0232 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.3394+1832_3394+183 others(26): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 76835227 | |||||
| chr8:76835227
|
A | ATATATAT others(41): Show |
1 | a0003c0002t0006g0058 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3394+1832_3394+183 others(52): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 76835227 | |||||
| chr8:76835227
|
A | ATATATAT others(39): Show |
1 | a0028c0043t0001g0140 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3394+1832_3394+183 others(50): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 76835227 | |||||
| chr8:76835227
|
A | ATATATAT others(35): Show |
2 | a0002c0006t0002g0098a0002c0006t0010g0031 | 2 | HG02818.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3394+1828_3394+182 others(46): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 76835227 | |||||
| chr8:76835229
|
A | ATATATAT others(39): Show |
35 | a0001c0031t0020g0163a0002c0001t0002g0198a0002c0001t0003g0020others(32): Show | 35 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(32): Show |
intron_variant | MODIFIER | c.3394+1832_3394+183 others(50): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 76835229 | |||||
| chr8:76835229
|
A | ATATATAT others(79): Show |
1 | a0002c0006t0003g0177 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.3394+1832_3394+183 others(90): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 76835229 | |||||
| chr8:76835229
|
A | ATATATAT others(77): Show |
1 | a0017c0057t0001g0033 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3394+1832_3394+183 others(88): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 76835229 | |||||
| chr8:76835229
|
A | ATATATAT others(37): Show |
2 | a0001c0015t0001g0003a0001c0015t0005g0005 | 2 | HG01109.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3394+1832_3394+183 others(48): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 76835229 | |||||
| chr8:76835229
|
A | ATATATAT others(35): Show |
2 | a0001c0015t0005g0011a0016c0083t0001g0152 | 2 | HG01884.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.3394+1832_3394+183 others(46): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 76835229 | |||||
| chr8:76835229
|
A | ATATATAT others(15): Show |
1 | a0003c0002t0008g0013 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.3394+1832_3394+183 others(26): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 76835229 | |||||
| chr8:76835229
|
A | ATATATAT others(39): Show |
2 | a0003c0002t0001g0054a0008c0067t0003g0106 | 2 | HG02970.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3394+1830_3394+183 others(50): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 76835229 | |||||
| chr8:76835231
|
A | ATATATAT others(1): Show |
43 | a0001c0008t0005g0093a0001c0008t0005g0230a0001c0008t0005g0231others(40): Show | 43 | HG00099.hp1 HG00438.hp1 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.3394+1832_3394+183 others(12): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 76835231 | |||||
| chr8:76835231
|
A | ATATATAT others(37): Show |
3 | a0001c0025t0002g0210a0002c0001t0003g0002a0002c0001t0003g0191 | 4 | HG00609.hp2 NA18945.hp2 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.3394+1832_3394+183 others(48): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 76835231 | |||||
| chr8:76835231
|
A | ATATATG | 3 | a0002c0006t0010g0155a0003c0027t0001g0055a0003c0027t0001g0056 | 3 | HG03486.hp2 HG03540.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.3394+1830_3394+183 others(10): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 76835231 | |||||
| chr8:76835233
|
A | ATATATGT others(19): Show |
1 | a0003c0059t0006g0085 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3394+1832_3394+183 others(30): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 76835233 | |||||
| chr8:76835235
|
ATATATG | A | 8 | a0002c0001t0001g0149a0002c0028t0003g0138a0003c0002t0001g0007others(5): Show | 8 | HG01891.hp1 HG01891.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.3394+1835_3394+184 others(10): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 76835235 | |||||
| chr8:76835239
|
A | ATATGTAT others(45): Show |
19 | a0001c0031t0002g0127a0004c0018t0002g0116a0005c0005t0004g0111others(16): Show | 19 | HG00438.hp2 HG00621.hp2 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.3394+1834_3394+183 others(56): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 76835239 | |||||
| chr8:76835239
|
A | G | 1 | a0002c0001t0004g0199 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.3394+1833A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | chr8 | 76835239 | ||||||
| chr8:76835241
|
G | A | 77 | a0001c0008t0005g0232a0001c0015t0001g0003a0001c0015t0005g0005others(74): Show | 78 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.3394+1835G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | chr8 | 76835241 | ||||||
| chr8:76835241
|
G | GTATATAT others(43): Show |
2 | a0004c0068t0006g0109a0005c0005t0004g0047 | 2 | HG00423.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.3394+1844_3394+184 others(54): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 76835241 | |||||
| chr8:76835241
|
G | GTATATAT others(41): Show |
1 | a0027c0066t0003g0115 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.3394+1844_3394+184 others(52): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 76835241 | |||||
| chr8:76835241
|
GTA | G | 3 | a0001c0051t0002g0141a0002c0038t0002g0153a0009c0011t0006g0065 | 3 | HG02809.hp1 HG03041.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.3394+1853_3394+185 others(6): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 76835241 | |||||
| chr8:76835243
|
A | ATATATAT others(7): Show |
44 | a0001c0008t0005g0093a0001c0008t0005g0230a0001c0008t0005g0231others(41): Show | 44 | HG00099.hp1 HG00438.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.3394+1850_3394+185 others(18): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 76835243 | |||||
| chr8:76835243
|
A | ATATATAT others(101): Show |
1 | a0006c0009t0006g0151 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3394+1844_3394+184 others(112): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 76835243 | |||||
| chr8:76835243
|
A | ATATATAT others(71): Show |
1 | a0012c0024t0005g0001 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.3394+1844_3394+184 others(82): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 76835243 | |||||
| chr8:76835243
|
A | ATATATAT others(41): Show |
2 | a0002c0001t0003g0039a0002c0001t0017g0194 | 2 | HG01074.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.3394+1844_3394+184 others(52): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 76835243 | |||||
| chr8:76835243
|
A | ATATATAT others(39): Show |
4 | a0001c0042t0002g0010a0002c0001t0010g0014a0004c0019t0005g0091others(1): Show | 4 | HG01070.hp1 HG02258.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.3394+1844_3394+184 others(50): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 76835243 | |||||
| chr8:76835243
|
A | ATGTATAT others(77): Show |
1 | a0006c0009t0001g0059 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3394+1838_3394+183 others(88): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 76835243 | |||||
| chr8:76835243
|
A | ATGTATAT others(41): Show |
2 | a0009c0011t0007g0222a0009c0011t0007g0223 | 2 | HG02486.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.3394+1838_3394+183 others(52): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 76835243 | |||||
| chr8:76835243
|
A | G | 52 | a0001c0031t0020g0163a0002c0001t0001g0149a0002c0001t0002g0198others(49): Show | 52 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.3394+1837A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | chr8 | 76835243 | ||||||
| chr8:76835245
|
A | ATATATGT others(73): Show |
9 | a0001c0017t0003g0107a0001c0017t0003g0108a0001c0017t0021g0129others(6): Show | 9 | HG03491.hp1 HG04115.hp1 NA18946.hp1 others(6): Show |
intron_variant | MODIFIER | c.3394+1844_3394+184 others(84): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 76835245 | |||||
| chr8:76835245
|
A | ATATATGT others(73): Show |
1 | a0001c0047t0016g0066 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.3394+1844_3394+184 others(84): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 76835245 | |||||
| chr8:76835245
|
A | ATATATGT others(71): Show |
1 | a0004c0046t0002g0075 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.3394+1844_3394+184 others(82): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 76835245 | |||||
| chr8:76835245
|
A | ATATATGT others(41): Show |
1 | a0018c0064t0001g0137 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3394+1844_3394+184 others(52): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 76835245 | |||||
| chr8:76835245
|
A | ATATATGT others(71): Show |
3 | a0006c0016t0008g0101a0015c0071t0002g0088a0032c0072t0002g0080 | 3 | HG00639.hp2 HG02735.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.3394+1844_3394+184 others(82): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 76835245 | |||||
| chr8:76835245
|
A | ATATATGT others(69): Show |
2 | a0003c0007t0001g0102a0006c0016t0001g0103 | 2 | HG02723.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3394+1844_3394+184 others(80): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 76835245 | |||||
| chr8:76835245
|
A | ATATATGT others(39): Show |
1 | a0003c0045t0004g0136 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3394+1844_3394+184 others(50): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 76835245 | |||||
| chr8:76835245
|
A | ATATATGT others(37): Show |
2 | a0001c0008t0005g0096a0001c0008t0005g0157 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.3394+1844_3394+184 others(48): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 76835245 | |||||
| chr8:76835245
|
A | ATATATGT others(37): Show |
4 | a0009c0011t0007g0025a0009c0011t0007g0221a0009c0069t0007g0057others(1): Show | 4 | HG01167.hp2 HG02717.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.3394+1844_3394+184 others(48): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 76835245 | |||||
| chr8:76835245
|
A | ATATGTAT others(39): Show |
1 | a0002c0001t0004g0199 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.3394+1842_3394+184 others(50): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 76835245 | |||||
| chr8:76835245
|
A | G | 17 | a0001c0015t0001g0003a0001c0015t0005g0005a0001c0015t0005g0011others(14): Show | 18 | HG00609.hp2 HG01109.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.3394+1839A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | chr8 | 76835245 | ||||||
| chr8:76835247
|
A | ATATGTAT others(67): Show |
1 | a0003c0002t0001g0032 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3394+1844_3394+184 others(78): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 76835247 | |||||
| chr8:76835247
|
A | ATATGTAT others(39): Show |
1 | a0019c0082t0014g0139 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3394+1844_3394+184 others(50): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 76835247 | |||||
| chr8:76835247
|
A | ATATGTAT others(35): Show |
7 | a0003c0002t0001g0026a0003c0002t0001g0027a0003c0002t0001g0029others(4): Show | 7 | HG02486.hp1 HG02572.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.3394+1844_3394+184 others(46): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 76835247 | |||||
| chr8:76835247
|
A | ATATGTAT others(33): Show |
1 | a0006c0009t0001g0146 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3394+1844_3394+184 others(44): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 76835247 | |||||
| chr8:76835253
|
A | ATATGTAT others(7): Show |
1 | a0002c0006t0010g0155 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3394+1850_3394+185 others(18): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 76835253 | |||||
| chr8:76835253
|
A | ATATGTAT others(31): Show |
1 | a0002c0006t0003g0162 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.3394+1850_3394+185 others(42): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 76835253 | |||||
| chr8:76835288
|
G | A | 93 | a0001c0008t0005g0096a0001c0008t0005g0157a0001c0015t0001g0003others(90): Show | 95 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.3394+1882G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | chr8 | 76835288 | ||||||
| chr8:76835399
|
C | A | 1 | a0005c0032t0004g0046 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.3394+1993C>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | chr8 | 76835399 | ||||||
| chr8:76835439
|
T | A | 1 | a0003c0007t0005g0052 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3394+2033T>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | chr8 | 76835439 | ||||||
| chr8:76835505
|
T | C | 2 | a0001c0004t0001g0203a0001c0004t0001g0204 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.3394+2099T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | chr8 | 76835505 | ||||||
| chr8:76835587
|
G | C | 1 | a0002c0001t0003g0214 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.3394+2181G>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | chr8 | 76835587 | ||||||
| chr8:76835691
|
C | T | 4 | a0001c0008t0005g0231a0001c0008t0005g0232a0001c0008t0005g0233others(1): Show | 4 | HG02080.hp1 NA19062.hp1 NA19077.hp1 others(1): Show |
intron_variant | MODIFIER | c.3394+2285C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | chr8 | 76835691 | ||||||
| chr8:76835723
|
A | G | 26 | a0001c0031t0002g0127a0004c0018t0002g0105a0004c0018t0002g0116others(23): Show | 26 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(23): Show |
intron_variant | MODIFIER | c.3394+2317A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | chr8 | 76835723 | ||||||
| chr8:76835962
|
T | C | 1 | a0001c0008t0005g0093 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.3394+2556T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | chr8 | 76835962 | ||||||
| chr8:76836197
|
C | T | 1 | a0002c0006t0010g0031 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3394+2791C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | chr8 | 76836197 | ||||||
| chr8:76836356
|
T | C | 2 | a0003c0002t0001g0054a0008c0067t0003g0106 | 2 | HG02970.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3394+2950T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | chr8 | 76836356 | ||||||
| chr8:76836390
|
T | C | 1 | a0003c0002t0001g0032 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3394+2984T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | chr8 | 76836390 | ||||||
| chr8:76836527
|
C | G | 178 | a0001c0008t0005g0093a0001c0008t0005g0096a0001c0008t0005g0157others(175): Show | 180 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.3394+3121C>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | chr8 | 76836527 | ||||||
| chr8:76836537
|
C | T | 4 | a0001c0003t0002g0087a0001c0003t0002g0110a0001c0004t0002g0212others(1): Show | 4 | HG01109.hp2 HG01952.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.3394+3131C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | chr8 | 76836537 | ||||||
| chr8:76836771
|
A | C | 178 | a0001c0008t0005g0093a0001c0008t0005g0096a0001c0008t0005g0157others(175): Show | 180 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.3394+3365A>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | chr8 | 76836771 | ||||||
| chr8:76837251
|
A | G | 192 | a0001c0004t0002g0197a0001c0004t0005g0064a0001c0004t0005g0219others(189): Show | 194 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.3394+3845A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | chr8 | 76837251 | ||||||
| chr8:76837488
|
A | G | 1 | a0004c0026t0006g0048 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.3394+4082A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | chr8 | 76837488 | ||||||
| chr8:76837493
|
GA | G | 57 | a0001c0004t0005g0064a0001c0008t0005g0093a0001c0008t0005g0230others(54): Show | 57 | HG00099.hp1 HG00438.hp1 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.3394+4101delA | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 76837493 | |||||
| chr8:76837584
|
T | C | 178 | a0001c0008t0005g0093a0001c0008t0005g0096a0001c0008t0005g0157others(175): Show | 180 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.3394+4178T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | chr8 | 76837584 | ||||||
| chr8:76837797
|
T | C | 1 | a0001c0051t0002g0141 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3394+4391T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | chr8 | 76837797 | ||||||
| chr8:76837896
|
A | G | 2 | a0005c0005t0011g0095a0005c0005t0011g0099 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.3394+4490A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | chr8 | 76837896 | ||||||
| chr8:76837957
|
C | T | 1 | a0018c0064t0001g0137 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3394+4551C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | chr8 | 76837957 | ||||||
| chr8:76838067
|
G | A | 2 | a0001c0025t0002g0210a0007c0030t0003g0229 | 2 | NA19011.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.3395-4588G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | chr8 | 76838067 | ||||||
| chr8:76838096
|
G | A | 2 | a0002c0038t0002g0153a0009c0011t0006g0065 | 2 | HG03041.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.3395-4559G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | chr8 | 76838096 | ||||||
| chr8:76838232
|
C | G | 1 | a0003c0002t0006g0058 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3395-4423C>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | chr8 | 76838232 | ||||||
| chr8:76838323
|
A | G | 6 | a0003c0002t0001g0007a0003c0002t0001g0009a0003c0007t0001g0090others(3): Show | 6 | HG01891.hp1 HG02622.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.3395-4332A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | chr8 | 76838323 | ||||||
| chr8:76838424
|
C | T | 28 | a0001c0031t0002g0127a0004c0018t0002g0105a0004c0018t0002g0116others(25): Show | 28 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.3395-4231C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | chr8 | 76838424 | ||||||
| chr8:76838433
|
G | A | 1 | a0002c0001t0004g0199 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.3395-4222G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | chr8 | 76838433 | ||||||
| chr8:76838590
|
C | T | 2 | a0002c0006t0002g0098a0002c0006t0010g0031 | 2 | HG02818.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3395-4065C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | chr8 | 76838590 | ||||||
| chr8:76838778
|
A | G | 180 | a0001c0008t0005g0093a0001c0008t0005g0096a0001c0008t0005g0157others(177): Show | 182 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.3395-3877A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | chr8 | 76838778 | ||||||
| chr8:76838821
|
T | C | 6 | a0009c0011t0007g0025a0009c0011t0007g0221a0009c0011t0007g0222others(3): Show | 6 | HG01167.hp2 HG02486.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.3395-3834T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | chr8 | 76838821 | ||||||
| chr8:76838867
|
C | A | 6 | a0003c0002t0001g0007a0003c0002t0001g0009a0003c0007t0001g0090others(3): Show | 6 | HG01891.hp1 HG02622.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.3395-3788C>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | chr8 | 76838867 | ||||||
| chr8:76839000
|
G | A | 1 | a0003c0034t0001g0142 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3395-3655G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | chr8 | 76839000 | ||||||
| chr8:76839024
|
G | C | 180 | a0001c0008t0005g0093a0001c0008t0005g0096a0001c0008t0005g0157others(177): Show | 182 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.3395-3631G>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | chr8 | 76839024 | ||||||
| chr8:76839051
|
GA | G | 4 | a0002c0001t0003g0039a0003c0002t0001g0147a0006c0009t0006g0151others(1): Show | 4 | HG02055.hp2 HG02897.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.3395-3601delA | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 76839051 | |||||
| chr8:76839053
|
A | AAG | 12 | a0001c0003t0002g0174a0001c0003t0002g0179a0001c0003t0022g0135others(9): Show | 12 | HG00099.hp2 HG01167.hp1 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.3395-3556_3395-355 others(6): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 76839053 | |||||
| chr8:76839053
|
A | AAGAG | 21 | a0001c0003t0002g0134a0001c0003t0002g0176a0001c0003t0002g0216others(18): Show | 21 | HG00408.hp2 HG00735.hp1 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.3395-3558_3395-355 others(8): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 76839053 | |||||
| chr8:76839053
|
A | AAGAGAG | 11 | a0001c0003t0003g0120a0001c0004t0002g0040a0001c0004t0002g0067others(8): Show | 11 | HG00597.hp1 HG01109.hp2 HG01952.hp1 others(8): Show |
intron_variant | MODIFIER | c.3395-3560_3395-355 others(10): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 76839053 | |||||
| chr8:76839053
|
A | AAGAGAGA others(5): Show |
1 | a0001c0004t0002g0206 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.3395-3566_3395-355 others(16): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 76839053 | |||||
| chr8:76839053
|
AAG | A | 53 | a0001c0003t0002g0168a0001c0004t0002g0197a0001c0015t0005g0005others(50): Show | 54 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.3395-3556_3395-355 others(6): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 76839053 | |||||
| chr8:76839053
|
AAGAG | A | 33 | a0001c0015t0005g0011a0001c0025t0002g0200a0001c0042t0002g0010others(30): Show | 34 | HG00099.hp1 HG00621.hp1 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.3395-3558_3395-355 others(8): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 76839053 | |||||
| chr8:76839053
|
AAGAGAG | A | 24 | a0001c0008t0005g0231a0001c0008t0005g0232a0001c0008t0005g0233others(21): Show | 24 | HG00280.hp2 HG01261.hp2 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.3395-3560_3395-355 others(10): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 76839053 | |||||
| chr8:76839053
|
AAGAGAGA others(1): Show |
A | 20 | a0001c0008t0005g0093a0001c0008t0005g0230a0001c0008t0005g0236others(17): Show | 20 | HG00609.hp1 HG00639.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.3395-3562_3395-355 others(12): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 76839053 | |||||
| chr8:76839053
|
AAGAGAGA others(3): Show |
A | 3 | a0002c0028t0003g0138a0008c0010t0006g0021a0026c0041t0005g0073 | 3 | HG00438.hp1 HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.3395-3564_3395-355 others(14): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 76839053 | |||||
| chr8:76839053
|
AAGAGAGA others(5): Show |
A | 5 | a0002c0001t0001g0149a0003c0002t0001g0074a0003c0002t0001g0081others(2): Show | 5 | HG01081.hp1 HG02818.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.3395-3566_3395-355 others(16): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 76839053 | |||||
| chr8:76839053
|
AAGAGAGA others(7): Show |
A | 19 | a0001c0017t0003g0107a0001c0017t0003g0108a0001c0017t0021g0129others(16): Show | 19 | HG00597.hp2 HG00639.hp2 HG02132.hp1 others(16): Show |
intron_variant | MODIFIER | c.3395-3568_3395-355 others(18): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 76839053 | |||||
| chr8:76839053
|
AAGAGAGA others(9): Show |
A | 2 | a0004c0018t0002g0116a0034c0084t0002g0131 | 2 | NA18940.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.3395-3570_3395-355 others(20): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 76839053 | |||||
| chr8:76839053
|
AAGAGAGA others(15): Show |
A | 6 | a0001c0004t0005g0064a0001c0004t0005g0219a0001c0052t0001g0063others(3): Show | 6 | HG01884.hp1 HG02886.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.3395-3576_3395-355 others(26): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 76839053 | |||||
| chr8:76839079
|
G | T | 4 | a0001c0008t0005g0231a0001c0008t0005g0232a0001c0008t0005g0233others(1): Show | 4 | HG02080.hp1 NA19062.hp1 NA19077.hp1 others(1): Show |
intron_variant | MODIFIER | c.3395-3576G>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | chr8 | 76839079 | ||||||
| chr8:76839253
|
G | A | 1 | a0003c0002t0001g0009 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3395-3402G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | chr8 | 76839253 | ||||||
| chr8:76839339
|
A | G | 180 | a0001c0008t0005g0093a0001c0008t0005g0096a0001c0008t0005g0157others(177): Show | 182 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.3395-3316A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | chr8 | 76839339 | ||||||
| chr8:76839760
|
A | G | 53 | a0001c0008t0005g0093a0001c0008t0005g0230a0001c0008t0005g0231others(50): Show | 53 | HG00099.hp1 HG00438.hp1 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.3395-2895A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | chr8 | 76839760 | ||||||
| chr8:76839799
|
A | G | 65 | a0001c0008t0005g0096a0001c0008t0005g0157a0001c0015t0001g0003others(62): Show | 67 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.3395-2856A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | chr8 | 76839799 | ||||||
| chr8:76839838
|
C | T | 1 | a0004c0019t0005g0234 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.3395-2817C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | chr8 | 76839838 | ||||||
| chr8:76840095
|
G | C | 119 | a0001c0008t0005g0096a0001c0008t0005g0157a0001c0015t0001g0003others(116): Show | 121 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.3395-2560G>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | chr8 | 76840095 | ||||||
| chr8:76840142
|
C | G | 9 | a0003c0002t0001g0026a0003c0002t0001g0027a0003c0002t0001g0029others(6): Show | 9 | HG01175.hp2 HG02486.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.3395-2513C>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | chr8 | 76840142 | ||||||
| chr8:76840199
|
G | A | 1 | a0006c0029t0001g0158 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3395-2456G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | chr8 | 76840199 | ||||||
| chr8:76840617
|
C | T | 1 | a0002c0038t0002g0153 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3395-2038C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | chr8 | 76840617 | ||||||
| chr8:76840745
|
T | C | 1 | a0014c0039t0001g0072 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.3395-1910T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | chr8 | 76840745 | ||||||
| chr8:76841016
|
T | C | 1 | a0006c0009t0001g0028 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3395-1639T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | chr8 | 76841016 | ||||||
| chr8:76841224
|
T | C | 1 | a0001c0025t0002g0210 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.3395-1431T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | chr8 | 76841224 | ||||||
| chr8:76841496
|
C | T | 4 | a0001c0015t0001g0003a0001c0015t0005g0005a0001c0015t0005g0011others(1): Show | 4 | HG01109.hp1 HG01884.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.3395-1159C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | chr8 | 76841496 | ||||||
| chr8:76841546
|
A | G | 1 | a0001c0003t0002g0174 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.3395-1109A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | chr8 | 76841546 | ||||||
| chr8:76842090
|
G | A | 172 | a0001c0004t0019g0050a0001c0008t0005g0093a0001c0008t0005g0096others(169): Show | 174 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(171): Show |
intron_variant | MODIFIER | c.3395-565G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | chr8 | 76842090 | ||||||
| chr8:76842108
|
T | C | 176 | a0001c0004t0019g0050a0001c0008t0005g0093a0001c0008t0005g0096others(173): Show | 178 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(175): Show |
intron_variant | MODIFIER | c.3395-547T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | chr8 | 76842108 | ||||||
| chr8:76842330
|
G | T | 24 | a0001c0008t0005g0096a0001c0008t0005g0157a0001c0042t0002g0010others(21): Show | 24 | HG01070.hp1 HG01167.hp1 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.3395-325G>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | chr8 | 76842330 | ||||||
| chr8:76842342
|
G | A | 2 | a0003c0002t0001g0074a0003c0002t0001g0081 | 2 | HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.3395-313G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | chr8 | 76842342 | ||||||
| chr8:76842623
|
A | C | 6 | a0009c0011t0007g0025a0009c0011t0007g0221a0009c0011t0007g0222others(3): Show | 6 | HG01167.hp2 HG02486.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.3395-32A>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 5/10 | chr8 | 76842623 | ||||||
| chr8:76842797
|
G | A | 2 | a0001c0051t0002g0141a0018c0064t0001g0137 | 2 | HG02809.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.3511+26G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 6/10 | chr8 | 76842797 | ||||||
| chr8:76842822
|
C | A | 1 | a0001c0015t0005g0011 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3511+51C>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 6/10 | chr8 | 76842822 | ||||||
| chr8:76842916
|
T | C | 18 | a0001c0008t0005g0093a0001c0008t0005g0096a0001c0008t0005g0157others(15): Show | 19 | HG00609.hp1 HG00735.hp1 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.3511+145T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 6/10 | chr8 | 76842916 | ||||||
| chr8:76843205
|
G | A | 1 | a0001c0078t0006g0159 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.3511+434G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 6/10 | chr8 | 76843205 | ||||||
| chr8:76843283
|
A | C | 1 | a0027c0066t0003g0115 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.3511+512A>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 6/10 | chr8 | 76843283 | ||||||
| chr8:76843410
|
G | A | 9 | a0004c0026t0006g0019a0004c0026t0006g0048a0004c0068t0006g0109others(6): Show | 9 | HG00423.hp2 HG00438.hp1 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.3511+639G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 6/10 | chr8 | 76843410 | ||||||
| chr8:76843817
|
A | T | 2 | a0003c0002t0008g0012a0003c0002t0008g0013 | 2 | HG02723.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.3511+1046A>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 6/10 | chr8 | 76843817 | ||||||
| chr8:76844087
|
T | C | 18 | a0001c0008t0005g0093a0001c0008t0005g0096a0001c0008t0005g0157others(15): Show | 19 | HG00609.hp1 HG00735.hp1 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.3511+1316T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 6/10 | chr8 | 76844087 | ||||||
| chr8:76844270
|
G | C | 1 | a0001c0078t0006g0159 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.3511+1499G>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 6/10 | chr8 | 76844270 | ||||||
| chr8:76844399
|
A | C | 18 | a0001c0008t0005g0093a0001c0008t0005g0096a0001c0008t0005g0157others(15): Show | 19 | HG00609.hp1 HG00735.hp1 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.3511+1628A>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 6/10 | chr8 | 76844399 | ||||||
| chr8:76844503
|
G | A | 1 | a0002c0001t0001g0149 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3511+1732G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 6/10 | chr8 | 76844503 | ||||||
| chr8:76844738
|
G | A | 181 | a0001c0008t0005g0093a0001c0008t0005g0096a0001c0008t0005g0157others(178): Show | 183 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(180): Show |
intron_variant | MODIFIER | c.3511+1967G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 6/10 | chr8 | 76844738 | ||||||
| chr8:76844745
|
T | C | 1 | a0003c0002t0001g0054 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3511+1974T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 6/10 | chr8 | 76844745 | ||||||
| chr8:76845199
|
T | C | 1 | a0003c0007t0001g0102 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3511+2428T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 6/10 | chr8 | 76845199 | ||||||
| chr8:76845594
|
T | G | 56 | a0002c0001t0001g0149a0002c0001t0002g0198a0002c0001t0003g0002others(53): Show | 57 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.3511+2823T>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 6/10 | chr8 | 76845594 | ||||||
| chr8:76845659
|
G | A | 73 | a0001c0017t0003g0107a0001c0017t0003g0108a0001c0017t0021g0129others(70): Show | 73 | HG00099.hp1 HG00639.hp1 HG01069.hp1 others(70): Show |
intron_variant | MODIFIER | c.3511+2888G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 6/10 | chr8 | 76845659 | ||||||
| chr8:76845705
|
C | T | 2 | a0001c0008t0005g0236a0004c0019t0005g0235 | 2 | HG00735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.3511+2934C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 6/10 | chr8 | 76845705 | ||||||
| chr8:76845722
|
T | A | 1 | a0027c0066t0003g0115 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.3511+2951T>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 6/10 | chr8 | 76845722 | ||||||
| chr8:76845722
|
T | C | 1 | a0001c0003t0002g0174 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.3511+2951T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 6/10 | chr8 | 76845722 | ||||||
| chr8:76845809
|
A | G | 9 | a0003c0002t0001g0026a0003c0002t0001g0027a0003c0002t0001g0029others(6): Show | 9 | HG01175.hp2 HG02486.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.3511+3038A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 6/10 | chr8 | 76845809 | ||||||
| chr8:76845838
|
T | C | 1 | a0001c0004t0005g0064 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3511+3067T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 6/10 | chr8 | 76845838 | ||||||
| chr8:76846093
|
A | G | 1 | a0003c0058t0001g0238 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3512-2902A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 6/10 | chr8 | 76846093 | ||||||
| chr8:76846198
|
A | G | 3 | a0001c0017t0003g0107a0001c0017t0003g0108a0001c0017t0021g0129 | 3 | NA18983.hp2 NA19064.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.3512-2797A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 6/10 | chr8 | 76846198 | ||||||
| chr8:76846397
|
C | A | 1 | a0013c0023t0009g0144 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.3512-2598C>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 6/10 | chr8 | 76846397 | ||||||
| chr8:76846508
|
C | T | 3 | a0002c0038t0002g0153a0006c0016t0008g0101a0006c0074t0008g0166 | 3 | HG03041.hp2 HG03098.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.3512-2487C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 6/10 | chr8 | 76846508 | ||||||
| chr8:76846827
|
T | G | 1 | a0018c0064t0001g0137 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3512-2168T>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 6/10 | chr8 | 76846827 | ||||||
| chr8:76846875
|
G | T | 2 | a0003c0002t0001g0004a0003c0007t0001g0240 | 2 | HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.3512-2120G>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 6/10 | chr8 | 76846875 | ||||||
| chr8:76846929
|
C | T | 1 | a0015c0056t0002g0042 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.3512-2066C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 6/10 | chr8 | 76846929 | ||||||
| chr8:76846936
|
T | A | 1 | a0001c0063t0001g0053 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3512-2059T>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 6/10 | chr8 | 76846936 | ||||||
| chr8:76847116
|
G | T | 9 | a0004c0026t0006g0019a0004c0026t0006g0048a0004c0068t0006g0109others(6): Show | 9 | HG00423.hp2 HG00438.hp1 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.3512-1879G>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 6/10 | chr8 | 76847116 | ||||||
| chr8:76847218
|
A | G | 1 | a0004c0046t0002g0075 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.3512-1777A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 6/10 | chr8 | 76847218 | ||||||
| chr8:76847273
|
G | A | 1 | a0001c0063t0001g0053 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3512-1722G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 6/10 | chr8 | 76847273 | ||||||
| chr8:76847443
|
C | T | 1 | a0001c0003t0002g0134 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.3512-1552C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 6/10 | chr8 | 76847443 | ||||||
| chr8:76847660
|
T | C | 1 | a0003c0034t0001g0142 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3512-1335T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 6/10 | chr8 | 76847660 | ||||||
| chr8:76847702
|
A | C | 1 | a0001c0042t0002g0010 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.3512-1293A>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 6/10 | chr8 | 76847702 | ||||||
| chr8:76847736
|
A | AT | 25 | a0003c0045t0004g0136a0005c0005t0004g0047a0005c0005t0004g0078others(22): Show | 25 | HG00438.hp2 HG00621.hp2 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.3512-1251dupT | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr8 | 76847736 | |||||
| chr8:76847834
|
C | T | 163 | a0001c0017t0003g0107a0001c0017t0003g0108a0001c0017t0021g0129others(160): Show | 164 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(161): Show |
intron_variant | MODIFIER | c.3512-1161C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 6/10 | chr8 | 76847834 | ||||||
| chr8:76847843
|
C | T | 129 | a0001c0017t0003g0107a0001c0017t0003g0108a0001c0017t0021g0129others(126): Show | 130 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.3512-1152C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 6/10 | chr8 | 76847843 | ||||||
| chr8:76847906
|
T | C | 7 | a0001c0003t0002g0179a0001c0003t0003g0035a0001c0003t0003g0036others(4): Show | 7 | HG02074.hp2 NA18962.hp1 NA18989.hp2 others(4): Show |
intron_variant | MODIFIER | c.3512-1089T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 6/10 | chr8 | 76847906 | ||||||
| chr8:76848504
|
C | T | 9 | a0004c0026t0006g0019a0004c0026t0006g0048a0004c0068t0006g0109others(6): Show | 9 | HG00423.hp2 HG00438.hp1 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.3512-491C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 6/10 | chr8 | 76848504 | ||||||
| chr8:76848581
|
C | A | 9 | a0004c0026t0006g0019a0004c0026t0006g0048a0004c0068t0006g0109others(6): Show | 9 | HG00423.hp2 HG00438.hp1 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.3512-414C>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 6/10 | chr8 | 76848581 | ||||||
| chr8:76848582
|
G | T | 23 | a0005c0005t0004g0047a0005c0005t0004g0078a0005c0005t0004g0111others(20): Show | 23 | HG00438.hp2 HG00621.hp2 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.3512-413G>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 6/10 | chr8 | 76848582 | ||||||
| chr8:76848913
|
C | T | 4 | a0002c0001t0003g0191a0002c0001t0003g0205a0002c0001t0003g0214others(1): Show | 4 | HG00609.hp2 NA18747.hp1 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.3512-82C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 6/10 | chr8 | 76848913 | ||||||
| chr8:76849189
|
T | C | 73 | a0001c0017t0003g0107a0001c0017t0003g0108a0001c0017t0021g0129others(70): Show | 73 | HG00099.hp1 HG00639.hp1 HG01069.hp1 others(70): Show |
intron_variant | MODIFIER | c.3645+61T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 7/10 | chr8 | 76849189 | ||||||
| chr8:76849280
|
T | C | 9 | a0004c0026t0006g0019a0004c0026t0006g0048a0004c0068t0006g0109others(6): Show | 9 | HG00423.hp2 HG00438.hp1 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.3645+152T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 7/10 | chr8 | 76849280 | ||||||
| chr8:76849350
|
A | G | 57 | a0002c0001t0001g0149a0002c0001t0002g0198a0002c0001t0003g0002others(54): Show | 58 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.3646-162A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 7/10 | chr8 | 76849350 | ||||||
| chr8:76849424
|
A | C | 1 | a0008c0010t0006g0015 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.3646-88A>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 7/10 | chr8 | 76849424 | ||||||
| chr8:76849487
|
G | A | 3 | a0002c0038t0002g0153a0006c0016t0008g0101a0006c0074t0008g0166 | 3 | HG03041.hp2 HG03098.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.3646-25G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 7/10 | chr8 | 76849487 | ||||||
| chr8:76850203
|
T | G | 24 | a0003c0045t0004g0136a0005c0005t0004g0047a0005c0005t0004g0078others(21): Show | 24 | HG00438.hp2 HG00621.hp2 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.3847-42T>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 8/10 | chr8 | 76850203 | ||||||
| chr8:76850538
|
G | T | 10 | a0003c0002t0001g0026a0003c0002t0001g0027a0003c0002t0001g0029others(7): Show | 10 | HG01175.hp2 HG02486.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.3964+176G>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 9/10 | chr8 | 76850538 | ||||||
| chr8:76850767
|
A | G | 2 | a0003c0002t0005g0023a0003c0007t0005g0086 | 2 | HG02896.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.3965-119A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 9/10 | chr8 | 76850767 | ||||||
| chr8:76850839
|
G | T | 1 | a0002c0038t0002g0153 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3965-47G>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 9/10 | chr8 | 76850839 | ||||||
| chr8:76856541
|
A | G | 2 | a0005c0005t0004g0111a0005c0005t0004g0123 | 2 | NA18945.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.9379+241A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 10/10 | chr8 | 76856541 | ||||||
| chr8:76856789
|
C | T | 3 | a0002c0001t0010g0014a0002c0006t0010g0031a0002c0006t0010g0155 | 3 | HG02818.hp1 HG02897.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.9379+489C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 10/10 | chr8 | 76856789 | ||||||
| chr8:76856981
|
A | T | 1 | a0003c0007t0005g0052 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.9379+681A>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 10/10 | chr8 | 76856981 | ||||||
| chr8:76857176
|
T | A | 2 | a0002c0006t0003g0122a0002c0006t0003g0170 | 2 | NA18962.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.9379+876T>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 10/10 | chr8 | 76857176 | ||||||
| chr8:76857309
|
A | G | 1 | a0001c0003t0002g0097 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.9379+1009A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 10/10 | chr8 | 76857309 | ||||||
| chr8:76857354
|
T | TTA | 15 | a0001c0003t0002g0097a0001c0003t0002g0174a0001c0004t0002g0206others(12): Show | 15 | HG00280.hp1 HG01175.hp2 HG01975.hp1 others(12): Show |
intron_variant | MODIFIER | c.9379+1080_9379+108 others(6): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr8 | 76857354 | |||||
| chr8:76857354
|
T | TTATA | 6 | a0001c0003t0002g0168a0001c0031t0020g0163a0001c0033t0002g0224others(3): Show | 6 | HG00639.hp2 HG02132.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.9379+1078_9379+108 others(8): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr8 | 76857354 | |||||
| chr8:76857354
|
TTA | T | 14 | a0001c0004t0002g0069a0001c0004t0002g0197a0001c0004t0005g0064others(11): Show | 14 | HG01081.hp2 HG01884.hp1 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.9379+1080_9379+108 others(6): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr8 | 76857354 | |||||
| chr8:76857354
|
TTATA | T | 41 | a0001c0052t0001g0063a0001c0063t0001g0053a0003c0002t0001g0004others(38): Show | 41 | HG00099.hp1 HG00639.hp1 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.9379+1078_9379+108 others(8): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr8 | 76857354 | |||||
| chr8:76857354
|
TTATATA | T | 28 | a0002c0006t0004g0217a0003c0002t0008g0013a0003c0027t0001g0055others(25): Show | 28 | HG00438.hp2 HG00621.hp2 HG01168.hp1 others(25): Show |
intron_variant | MODIFIER | c.9379+1076_9379+108 others(10): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr8 | 76857354 | |||||
| chr8:76857354
|
TTATATAT others(1): Show |
T | 28 | a0001c0008t0005g0093a0001c0008t0005g0096a0001c0008t0005g0157others(25): Show | 29 | HG00423.hp2 HG00438.hp1 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.9379+1074_9379+108 others(12): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr8 | 76857354 | |||||
| chr8:76857354
|
TTATATAT others(3): Show |
T | 63 | a0001c0003t0003g0120a0001c0015t0005g0011a0001c0017t0003g0107others(60): Show | 64 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.9379+1072_9379+108 others(14): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr8 | 76857354 | |||||
| chr8:76857574
|
G | A | 9 | a0004c0026t0006g0019a0004c0026t0006g0048a0004c0068t0006g0109others(6): Show | 9 | HG00423.hp2 HG00438.hp1 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.9379+1274G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 10/10 | chr8 | 76857574 | ||||||
| chr8:76857583
|
C | T | 90 | a0001c0003t0003g0120a0001c0008t0005g0093a0001c0008t0005g0096others(87): Show | 92 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.9379+1283C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 10/10 | chr8 | 76857583 | ||||||
| chr8:76857738
|
G | A | 1 | a0003c0002t0001g0009 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.9379+1438G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 10/10 | chr8 | 76857738 | ||||||
| chr8:76857839
|
A | AT | 5 | a0001c0003t0002g0097a0002c0006t0010g0155a0003c0058t0001g0238others(2): Show | 5 | HG00280.hp1 HG03195.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.9379+1554dupT | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr8 | 76857839 | |||||
| chr8:76857839
|
AT | A | 20 | a0001c0008t0005g0093a0001c0008t0005g0096a0001c0008t0005g0157others(17): Show | 21 | HG00609.hp1 HG00735.hp1 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.9379+1554delT | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr8 | 76857839 | |||||
| chr8:76858100
|
A | G | 1 | a0006c0009t0001g0059 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.9379+1800A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 10/10 | chr8 | 76858100 | ||||||
| chr8:76858217
|
G | A | 1 | a0001c0031t0020g0163 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.9379+1917G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 10/10 | chr8 | 76858217 | ||||||
| chr8:76859101
|
G | T | 4 | a0002c0001t0002g0198a0002c0001t0003g0051a0002c0001t0003g0077others(1): Show | 4 | HG00423.hp1 HG02040.hp2 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.9379+2801G>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 10/10 | chr8 | 76859101 | ||||||
| chr8:76859349
|
AT | A | 9 | a0004c0026t0006g0019a0004c0026t0006g0048a0004c0068t0006g0109others(6): Show | 9 | HG00423.hp2 HG00438.hp1 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.9379+3056delT | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr8 | 76859349 | |||||
| chr8:76859585
|
T | C | 1 | a0001c0017t0003g0107 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.9379+3285T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 10/10 | chr8 | 76859585 | ||||||
| chr8:76859809
|
G | A | 1 | a0001c0003t0002g0134 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.9380-3285G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 10/10 | chr8 | 76859809 | ||||||
| chr8:76859857
|
G | A | 1 | a0002c0001t0001g0149 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.9380-3237G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 10/10 | chr8 | 76859857 | ||||||
| chr8:76860152
|
T | C | 1 | a0025c0076t0002g0178 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.9380-2942T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 10/10 | chr8 | 76860152 | ||||||
| chr8:76860879
|
A | C | 6 | a0001c0003t0002g0179a0001c0003t0003g0035a0001c0003t0003g0036others(3): Show | 6 | NA18986.hp1 NA18989.hp2 NA18999.hp2 others(3): Show |
intron_variant | MODIFIER | c.9380-2215A>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 10/10 | chr8 | 76860879 | ||||||
| chr8:76860946
|
A | G | 10 | a0003c0002t0006g0058a0004c0026t0006g0019a0004c0026t0006g0048others(7): Show | 10 | HG00423.hp2 HG00438.hp1 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.9380-2148A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 10/10 | chr8 | 76860946 | ||||||
| chr8:76861155
|
G | A | 1 | a0004c0046t0002g0075 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.9380-1939G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 10/10 | chr8 | 76861155 | ||||||
| chr8:76861215
|
ACAT | A | 26 | a0002c0001t0004g0199a0002c0006t0004g0217a0003c0045t0004g0136others(23): Show | 26 | HG00438.hp2 HG00621.hp2 HG01168.hp1 others(23): Show |
intron_variant | MODIFIER | c.9380-1878_9380-187 others(7): Show |
ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 10/10 | chr8 | 76861215 | ||||||
| chr8:76861216
|
C | T | 105 | a0001c0008t0005g0093a0001c0008t0005g0096a0001c0008t0005g0157others(102): Show | 106 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.9380-1878C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 10/10 | chr8 | 76861216 | ||||||
| chr8:76861406
|
A | G | 3 | a0001c0003t0003g0035a0001c0003t0003g0036a0002c0001t0003g0187 | 3 | NA18986.hp1 NA18999.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.9380-1688A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 10/10 | chr8 | 76861406 | ||||||
| chr8:76861455
|
C | T | 45 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0003g0120others(42): Show | 46 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.9380-1639C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 10/10 | chr8 | 76861455 | ||||||
| chr8:76861691
|
T | G | 1 | a0019c0082t0014g0139 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.9380-1403T>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 10/10 | chr8 | 76861691 | ||||||
| chr8:76861748
|
A | G | 215 | a0001c0003t0002g0083a0001c0003t0002g0087a0001c0003t0002g0097others(212): Show | 216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.9380-1346A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 10/10 | chr8 | 76861748 | ||||||
| chr8:76861923
|
G | A | 1 | a0002c0038t0002g0153 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.9380-1171G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 10/10 | chr8 | 76861923 | ||||||
| chr8:76861984
|
C | A | 2 | a0006c0009t0006g0151a0009c0011t0006g0065 | 2 | HG02055.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.9380-1110C>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 10/10 | chr8 | 76861984 | ||||||
| chr8:76862027
|
T | C | 63 | a0001c0015t0001g0003a0001c0052t0001g0063a0001c0063t0001g0053others(60): Show | 63 | HG00099.hp1 HG00639.hp1 HG01069.hp1 others(60): Show |
intron_variant | MODIFIER | c.9380-1067T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 10/10 | chr8 | 76862027 | ||||||
| chr8:76862146
|
T | C | 1 | a0003c0002t0006g0058 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.9380-948T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 10/10 | chr8 | 76862146 | ||||||
| chr8:76862248
|
C | T | 1 | a0003c0059t0006g0085 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.9380-846C>T | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 10/10 | chr8 | 76862248 | ||||||
| chr8:76862311
|
G | A | 57 | a0001c0015t0001g0003a0001c0052t0001g0063a0001c0063t0001g0053others(54): Show | 57 | HG00099.hp1 HG00639.hp1 HG01069.hp1 others(54): Show |
intron_variant | MODIFIER | c.9380-783G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 10/10 | chr8 | 76862311 | ||||||
| chr8:76862347
|
G | A | 41 | a0001c0015t0001g0003a0001c0063t0001g0053a0003c0002t0001g0004others(38): Show | 41 | HG00099.hp1 HG00639.hp1 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.9380-747G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 10/10 | chr8 | 76862347 | ||||||
| chr8:76862498
|
G | A | 1 | a0005c0005t0004g0078 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.9380-596G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 10/10 | chr8 | 76862498 | ||||||
| chr8:76862817
|
G | A | 229 | a0001c0003t0002g0083a0001c0003t0002g0087a0001c0003t0002g0097others(226): Show | 230 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.9380-277G>A | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 10/10 | chr8 | 76862817 | ||||||
| chr8:76862822
|
A | G | 2 | a0005c0005t0011g0095a0005c0005t0011g0099 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.9380-272A>G | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 10/10 | chr8 | 76862822 | ||||||
| chr8:76862973
|
T | C | 1 | a0011c0020t0004g0113 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.9380-121T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 10/10 | chr8 | 76862973 | ||||||
| chr8:76862994
|
T | C | 1 | a0006c0048t0001g0022 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.9380-100T>C | ZFHX4 | ENSG00000091656.19 | transcript | ENST00000651372.2 | protein_coding | 10/10 | chr8 | 76862994 |