Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 25830 |
| ensemblid | ENSG00000130540.14 |
| hgncid | 14903 |
| symbol | SULT4A1 |
| name | sulfotransferase family 4A member 1 |
| refseq_nuc | NM_014351.4 |
| refseq_prot | NP_055166.1 |
| ensembl_nuc | ENST00000330884.9 |
| ensembl_prot | ENSP00000332565.4 |
| mane_status | MANE Select |
| chr | chr22 |
| start | 43824509 |
| end | 43862513 |
| strand | - |
| ver | v1.2 |
| region | chr22:43824509-43862513 |
| region5000 | chr22:43819509-43867513 |
| regionname0 | SULT4A1_chr22_43824509_43862513 |
| regionname5000 | SULT4A1_chr22_43819509_43867513 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 284 | 384 | 91 | 70 | 164 | 18 | 39 | 122 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | MAESE others(279): Show |
chr22 | 43819509 | 43867513 |
| a0002 | 0/0 | 284 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | MAESE others(279): Show |
chr22 | 43819509 | 43867513 |
| a0003 | 0/0 | 284 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | MAESE others(279): Show |
chr22 | 43819509 | 43867513 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 852 | 383 | 90 | 70 | 164 | 18 | 39 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | ATGGC others(847): Show |
chr22 | 43819509 | 43867513 | ||
| a0001c0003 | 0/0 | 852 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | ATGGC others(847): Show |
chr22 | 43819509 | 43867513 | ||
| a0002c0002 | 0/0 | 852 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | ATGGC others(847): Show |
chr22 | 43819509 | 43867513 | ||
| a0003c0004 | 0/0 | 852 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | ATGGC others(847): Show |
chr22 | 43819509 | 43867513 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2476 | 99 | 5 | 8 | 68 | 3 | 15 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | GTCAC others(2471): Show |
chr22 | 43819509 | 43867513 |
| a0001c0001t0002 | 0/0 | 2488 | 96 | 3 | 17 | 65 | 1 | 10 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | GTCAC others(2483): Show |
chr22 | 43819509 | 43867513 |
| a0001c0001t0003 | 0/0 | 2488 | 59 | 22 | 14 | 10 | 6 | 7 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | GTCAC others(2483): Show |
chr22 | 43819509 | 43867513 |
| a0001c0001t0004 | 0/1 | 2482 | 29 | 8 | 11 | 1 | 5 | 3 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | GTCAC others(2477): Show |
chr22 | 43819509 | 43867513 |
| a0001c0001t0005 | 1/0 | 2478 | 26 | 8 | 10 | 3 | 1 | 3 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | GTCAC others(2473): Show |
chr22 | 43819509 | 43867513 |
| a0001c0001t0006 | 0/0 | 2482 | 26 | 21 | 3 | 0 | 2 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | GTCAC others(2477): Show |
chr22 | 43819509 | 43867513 |
| a0001c0001t0007 | 0/0 | 2488 | 7 | 0 | 0 | 7 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | GTCAC others(2483): Show |
chr22 | 43819509 | 43867513 |
| a0001c0001t0008 | 0/0 | 2482 | 7 | 7 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | GTCAC others(2477): Show |
chr22 | 43819509 | 43867513 |
| a0001c0001t0009 | 0/0 | 2482 | 6 | 2 | 0 | 4 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | GTCAC others(2477): Show |
chr22 | 43819509 | 43867513 |
| a0001c0001t0010 | 0/0 | 2478 | 3 | 3 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | GTCAC others(2473): Show |
chr22 | 43819509 | 43867513 |
| a0001c0001t0011 | 0/0 | 2494 | 2 | 1 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | GTCAC others(2489): Show |
chr22 | 43819509 | 43867513 |
| a0001c0001t0012 | 0/0 | 2488 | 2 | 1 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | GTCAC others(2483): Show |
chr22 | 43819509 | 43867513 |
| a0001c0001t0013 | 0/0 | 2482 | 2 | 0 | 2 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | GTCAC others(2477): Show |
chr22 | 43819509 | 43867513 |
| a0001c0001t0014 | 0/0 | 2482 | 2 | 2 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | GTCAC others(2477): Show |
chr22 | 43819509 | 43867513 |
| a0001c0001t0015 | 0/0 | 2482 | 2 | 2 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | GTCAC others(2477): Show |
chr22 | 43819509 | 43867513 |
| a0001c0001t0016 | 0/0 | 2476 | 2 | 0 | 2 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | GTCAC others(2471): Show |
chr22 | 43819509 | 43867513 |
| a0001c0001t0017 | 0/0 | 2476 | 2 | 0 | 0 | 2 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | GTCAC others(2471): Show |
chr22 | 43819509 | 43867513 |
| a0001c0001t0018 | 0/0 | 2506 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | GTCAC others(2501): Show |
chr22 | 43819509 | 43867513 |
| a0001c0001t0019 | 0/0 | 2500 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | GTCAC others(2495): Show |
chr22 | 43819509 | 43867513 |
| a0001c0001t0021 | 0/0 | 2492 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | GTCAC others(2487): Show |
chr22 | 43819509 | 43867513 |
| a0001c0001t0022 | 0/0 | 2482 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | GTCAC others(2477): Show |
chr22 | 43819509 | 43867513 |
| a0001c0001t0023 | 0/0 | 2472 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | GTCAC others(2467): Show |
chr22 | 43819509 | 43867513 |
| a0001c0001t0024 | 0/0 | 2476 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | GTCAC others(2471): Show |
chr22 | 43819509 | 43867513 |
| a0001c0001t0025 | 0/0 | 2476 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | GTCAC others(2471): Show |
chr22 | 43819509 | 43867513 |
| a0001c0001t0026 | 0/0 | 2470 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | GTCAC others(2465): Show |
chr22 | 43819509 | 43867513 |
| a0001c0001t0027 | 0/0 | 2470 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | GTCAC others(2465): Show |
chr22 | 43819509 | 43867513 |
| a0001c0001t0028 | 0/0 | 2500 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | GTCAC others(2495): Show |
chr22 | 43819509 | 43867513 |
| a0001c0001t0029 | 0/0 | 2482 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | GTCAC others(2477): Show |
chr22 | 43819509 | 43867513 |
| a0001c0003t0005 | 0/0 | 2478 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | GTCAC others(2473): Show |
chr22 | 43819509 | 43867513 |
| a0002c0002t0020 | 0/0 | 2488 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | GTCAC others(2483): Show |
chr22 | 43819509 | 43867513 |
| a0003c0004t0003 | 0/0 | 2488 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | GTCAC others(2483): Show |
chr22 | 43819509 | 43867513 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 18 | 1 | 3 | 14 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0001g0004 | 0/0 | 7 | 2 | 1 | 3 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0001g0010 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0001g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0002g0003 | 0/0 | 9 | 0 | 2 | 7 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0002g0005 | 0/0 | 7 | 0 | 3 | 4 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0002g0011 | 0/0 | 5 | 1 | 0 | 0 | 1 | 3 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0002g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0002g0020 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0002g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0002g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0002g0041 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0002g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0002g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0002g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0002g0045 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0002g0046 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0003g0007 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0003g0008 | 0/0 | 5 | 0 | 3 | 0 | 2 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0003g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0003g0017 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0003g0018 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0003g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0003g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0003g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0003g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0003g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0003g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0003g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0003g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0003g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0003g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0003g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0003g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0004g0002 | 0/0 | 10 | 0 | 5 | 1 | 3 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0004g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0004g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0004g0029 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0004g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0004g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0004g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0004g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0004g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0004g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0004g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0004g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0004g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0004g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0004g0103 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0005g0031 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0005g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0005g0033 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0005g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0005g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0005g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0005g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0005g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0005g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0005g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0005g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0005g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0005g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0005g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0005g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0005g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0005g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0005g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0005g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0005g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0005g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0005g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0006g0009 | 0/0 | 5 | 3 | 2 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0006g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0006g0035 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0006g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0006g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0006g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0006g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0006g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0006g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0006g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0006g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0006g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0006g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0006g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0006g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0006g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0006g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0006g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0006g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0007g0006 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0007g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0008g0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0008g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0008g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0008g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0009g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0009g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0009g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0009g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0010g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0010g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0010g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0011g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0011g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0012g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0012g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0013g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0013g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0014g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0014g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0015g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0015g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0016g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0016g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0017g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0017g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0018g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0019g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0021g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0022g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0023g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0024g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0025g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0026g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0027g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0028g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0001t0029g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0001c0003t0005g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0002c0002t0020g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| a0003c0004t0003g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0008 | EUR | GBR | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0200 | EUR | GBR | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG00140 | hp1 | a0001 | c0001 | t0004 | g0002 | EUR | GBR | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0037 | EUR | GBR | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0011 | EUR | FIN | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0157 | EUR | FIN | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG00323 | hp1 | a0001 | c0001 | t0004 | g0093 | EUR | FIN | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0018 | EUR | FIN | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | CHS | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | CHS | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0235 | EAS | CHS | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG00438 | hp1 | a0001 | c0001 | t0009 | g0026 | EAS | CHS | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | CHS | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | CHS | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | CHS | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | CHS | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG00597 | hp1 | a0001 | c0001 | t0024 | g0168 | EAS | CHS | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | CHS | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG00621 | hp2 | a0001 | c0001 | t0009 | g0026 | EAS | CHS | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG00639 | hp2 | a0001 | c0001 | t0004 | g0095 | AMR | PUR | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG00733 | hp1 | a0001 | c0001 | t0005 | g0124 | AMR | PUR | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG00733 | hp2 | a0001 | c0001 | t0027 | g0211 | AMR | PUR | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG00738 | hp2 | a0001 | c0001 | t0005 | g0034 | AMR | PUR | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0045 | AMR | PUR | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG01069 | hp1 | a0001 | c0001 | t0013 | g0088 | AMR | PUR | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0043 | AMR | PUR | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0025 | AMR | PUR | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0220 | AMR | PUR | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0043 | AMR | PUR | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0025 | AMR | PUR | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG01074 | hp1 | a0001 | c0001 | t0005 | g0033 | AMR | PUR | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0080 | AMR | PUR | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0078 | AMR | PUR | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG01099 | hp1 | a0001 | c0001 | t0005 | g0034 | AMR | PUR | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG01099 | hp2 | a0001 | c0001 | t0016 | g0179 | AMR | PUR | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0082 | AMR | PUR | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG01106 | hp2 | a0001 | c0001 | t0016 | g0180 | AMR | PUR | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0077 | AMR | PUR | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0053 | AMR | PUR | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0008 | AMR | PUR | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0065 | AMR | PUR | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG01168 | hp2 | a0001 | c0001 | t0005 | g0122 | AMR | PUR | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0008 | AMR | PUR | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG01175 | hp1 | a0001 | c0001 | t0013 | g0087 | AMR | PUR | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG01175 | hp2 | a0001 | c0001 | t0004 | g0029 | AMR | PUR | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG01192 | hp1 | a0001 | c0001 | t0005 | g0108 | AMR | PUR | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG01192 | hp2 | a0001 | c0001 | t0004 | g0002 | AMR | PUR | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG01243 | hp1 | a0001 | c0001 | t0006 | g0009 | AMR | PUR | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG01243 | hp2 | a0001 | c0001 | t0012 | g0072 | AMR | PUR | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | CLM | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0217 | AMR | CLM | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0084 | AMR | CLM | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG01258 | hp1 | a0001 | c0001 | t0005 | g0123 | AMR | CLM | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0251 | AMR | CLM | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0046 | AMR | CLM | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG01261 | hp2 | a0001 | c0001 | t0026 | g0210 | AMR | CLM | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG01346 | hp1 | a0001 | c0001 | t0004 | g0099 | AMR | CLM | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG01346 | hp2 | a0001 | c0001 | t0005 | g0119 | AMR | CLM | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG01358 | hp1 | a0001 | c0001 | t0004 | g0028 | AMR | CLM | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG01358 | hp2 | a0001 | c0001 | t0005 | g0031 | AMR | CLM | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG01361 | hp1 | a0001 | c0001 | t0004 | g0002 | AMR | CLM | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0242 | AMR | CLM | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG01433 | hp1 | a0001 | c0001 | t0005 | g0125 | AMR | CLM | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG01433 | hp2 | a0001 | c0001 | t0006 | g0127 | AMR | CLM | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0008 | AMR | CLM | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG01496 | hp2 | a0001 | c0001 | t0006 | g0009 | AMR | CLM | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG01515 | hp1 | a0001 | c0001 | t0004 | g0002 | EUR | IBS | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG01515 | hp2 | a0001 | c0001 | t0005 | g0115 | EUR | IBS | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG01516 | hp1 | a0001 | c0001 | t0006 | g0035 | EUR | IBS | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0008 | EUR | IBS | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG01517 | hp1 | a0001 | c0001 | t0004 | g0002 | EUR | IBS | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG01517 | hp2 | a0001 | c0001 | t0006 | g0035 | EUR | IBS | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0052 | AFR | ACB | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0023 | AFR | ACB | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0236 | AMR | PEL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG01934 | hp2 | a0001 | c0001 | t0003 | g0017 | AMR | PEL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0018 | AMR | PEL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG01943 | hp2 | a0001 | c0001 | t0004 | g0094 | AMR | PEL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0239 | AMR | PEL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0255 | AMR | PEL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02004 | hp2 | a0001 | c0001 | t0004 | g0028 | AMR | PEL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | KHV | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | KHV | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02027 | hp2 | a0001 | c0001 | t0005 | g0121 | EAS | KHV | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02040 | hp2 | a0001 | c0001 | t0009 | g0027 | EAS | KHV | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02055 | hp1 | a0001 | c0001 | t0008 | g0131 | AFR | ACB | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02055 | hp2 | a0001 | c0001 | t0010 | g0139 | AFR | ACB | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02056 | hp2 | a0001 | c0001 | t0017 | g0197 | EAS | KHV | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | KHV | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02074 | hp1 | a0001 | c0001 | t0017 | g0191 | EAS | KHV | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0262 | EAS | KHV | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | KHV | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0252 | EAS | KHV | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02135 | hp2 | a0001 | c0001 | t0005 | g0092 | EAS | KHV | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0055 | AFR | ACB | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | CDX | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | CDX | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0237 | EAS | CDX | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | CDX | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02257 | hp1 | a0001 | c0001 | t0004 | g0013 | AFR | ACB | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0018 | AFR | ACB | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0097 | AFR | ACB | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0013 | AFR | ACB | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02273 | hp1 | a0001 | c0001 | t0004 | g0002 | AMR | PEL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0017 | AFR | ACB | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0023 | AFR | ACB | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02293 | hp1 | a0001 | c0001 | t0004 | g0002 | AMR | PEL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0020 | AMR | PEL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02300 | hp1 | a0001 | c0001 | t0004 | g0002 | AMR | PEL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0054 | AFR | ACB | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0260 | EAS | KHV | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02572 | hp1 | a0001 | c0001 | t0008 | g0134 | AFR | GWD | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02572 | hp2 | a0001 | c0001 | t0015 | g0107 | AFR | GWD | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0011 | SAS | PJL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02602 | hp2 | a0001 | c0001 | t0005 | g0118 | SAS | PJL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02615 | hp1 | a0001 | c0001 | t0008 | g0014 | AFR | GWD | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0070 | AFR | GWD | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0059 | AFR | GWD | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02622 | hp2 | a0001 | c0001 | t0005 | g0032 | AFR | GWD | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0079 | AFR | GWD | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02630 | hp2 | a0001 | c0001 | t0005 | g0141 | AFR | GWD | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02647 | hp1 | a0001 | c0001 | t0019 | g0048 | AFR | GWD | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0060 | AFR | GWD | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02683 | hp2 | a0001 | c0001 | t0004 | g0002 | SAS | PJL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0041 | SAS | PJL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0198 | SAS | PJL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02717 | hp1 | a0001 | c0001 | t0008 | g0133 | AFR | GWD | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02717 | hp2 | a0001 | c0001 | t0009 | g0089 | AFR | GWD | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02723 | hp1 | a0001 | c0001 | t0005 | g0116 | AFR | GWD | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02723 | hp2 | a0001 | c0001 | t0006 | g0009 | AFR | GWD | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0011 | SAS | PJL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0083 | SAS | PJL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0020 | SAS | PJL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02809 | hp1 | a0001 | c0001 | t0008 | g0014 | AFR | GWD | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0058 | AFR | GWD | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0020 | AFR | GWD | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02818 | hp2 | a0002 | c0002 | t0020 | g0051 | AFR | GWD | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0022 | AFR | GWD | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02886 | hp2 | a0001 | c0001 | t0029 | g0264 | AFR | GWD | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02895 | hp1 | a0001 | c0001 | t0006 | g0138 | AFR | GWD | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02895 | hp2 | a0001 | c0001 | t0006 | g0132 | AFR | GWD | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02896 | hp1 | a0001 | c0001 | t0006 | g0030 | AFR | GWD | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0061 | AFR | GWD | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02897 | hp1 | a0001 | c0001 | t0006 | g0126 | AFR | GWD | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02897 | hp2 | a0001 | c0001 | t0006 | g0030 | AFR | GWD | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02965 | hp1 | a0001 | c0001 | t0008 | g0014 | AFR | ESN | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02965 | hp2 | a0001 | c0001 | t0006 | g0009 | AFR | ESN | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02970 | hp1 | a0001 | c0001 | t0005 | g0109 | AFR | ESN | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02970 | hp2 | a0001 | c0001 | t0004 | g0102 | AFR | ESN | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02976 | hp1 | a0001 | c0001 | t0018 | g0047 | AFR | ESN | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02976 | hp2 | a0001 | c0001 | t0010 | g0110 | AFR | ESN | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG03041 | hp1 | a0001 | c0001 | t0006 | g0106 | AFR | GWD | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG03041 | hp2 | a0001 | c0001 | t0009 | g0090 | AFR | GWD | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG03098 | hp1 | a0001 | c0001 | t0006 | g0137 | AFR | MSL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0013 | AFR | MSL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG03139 | hp1 | a0001 | c0001 | t0008 | g0014 | AFR | ESN | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG03139 | hp2 | a0001 | c0001 | t0015 | g0128 | AFR | ESN | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | ESN | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG03195 | hp2 | a0001 | c0001 | t0006 | g0143 | AFR | ESN | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG03209 | hp1 | a0001 | c0001 | t0011 | g0049 | AFR | MSL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG03209 | hp2 | a0001 | c0001 | t0006 | g0144 | AFR | MSL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0022 | AFR | MSL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG03225 | hp2 | a0001 | c0001 | t0004 | g0098 | AFR | MSL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0263 | SAS | PJL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0041 | SAS | PJL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG03453 | hp1 | a0001 | c0001 | t0004 | g0100 | AFR | MSL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG03453 | hp2 | a0001 | c0001 | t0006 | g0009 | AFR | MSL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG03486 | hp1 | a0001 | c0001 | t0004 | g0013 | AFR | MSL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG03486 | hp2 | a0001 | c0001 | t0006 | g0111 | AFR | MSL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0046 | SAS | PJL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0068 | SAS | PJL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG03491 | hp2 | a0001 | c0001 | t0004 | g0096 | SAS | PJL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG03492 | hp1 | a0001 | c0001 | t0004 | g0101 | SAS | PJL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0011 | SAS | PJL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG03516 | hp1 | a0001 | c0001 | t0006 | g0136 | AFR | ESN | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG03516 | hp2 | a0001 | c0001 | t0006 | g0112 | AFR | ESN | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0017 | AFR | MSL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG03579 | hp2 | a0001 | c0001 | t0006 | g0146 | AFR | MSL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG03654 | hp2 | a0001 | c0001 | t0005 | g0117 | SAS | PJL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0069 | SAS | PJL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG03688 | hp1 | a0001 | c0001 | t0005 | g0033 | SAS | STU | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0024 | SAS | STU | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0063 | SAS | BEB | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0256 | SAS | BEB | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0024 | SAS | BEB | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | BEB | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0228 | SAS | STU | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG04115 | hp2 | a0003 | c0004 | t0003 | g0081 | SAS | STU | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0073 | SAS | STU | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0195 | SAS | STU | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG04204 | hp1 | a0001 | c0001 | t0028 | g0212 | SAS | STU | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0199 | SAS | STU | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | STU | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | STU | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0067 | AFR | YRI | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA18522 | hp2 | a0001 | c0001 | t0006 | g0140 | AFR | YRI | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0254 | EAS | CHB | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0238 | EAS | CHB | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0234 | EAS | CHB | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | CHB | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA18906 | hp1 | a0001 | c0001 | t0012 | g0074 | AFR | YRI | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA18906 | hp2 | a0001 | c0001 | t0006 | g0135 | AFR | YRI | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA18943 | hp2 | a0001 | c0001 | t0025 | g0152 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA18944 | hp2 | a0001 | c0001 | t0007 | g0006 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA18947 | hp1 | a0001 | c0001 | t0007 | g0006 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA18948 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA18954 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA18957 | hp2 | a0001 | c0001 | t0011 | g0050 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA18961 | hp2 | a0001 | c0001 | t0009 | g0027 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA18970 | hp1 | a0001 | c0001 | t0005 | g0120 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA18983 | hp1 | a0001 | c0001 | t0007 | g0006 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA18984 | hp1 | a0001 | c0001 | t0007 | g0076 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA18987 | hp2 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA18992 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA18993 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA18997 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA18999 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA19003 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA19030 | hp1 | a0001 | c0001 | t0014 | g0129 | AFR | LWK | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0066 | AFR | LWK | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA19043 | hp1 | a0001 | c0001 | t0006 | g0036 | AFR | LWK | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA19043 | hp2 | a0001 | c0001 | t0014 | g0130 | AFR | LWK | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA19058 | hp1 | a0001 | c0001 | t0023 | g0196 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0258 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA19064 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA19070 | hp1 | a0001 | c0001 | t0007 | g0006 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA19087 | hp2 | a0001 | c0001 | t0007 | g0006 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA19091 | hp2 | a0001 | c0001 | t0007 | g0006 | EAS | JPT | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0057 | AFR | YRI | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA19240 | hp2 | a0001 | c0001 | t0006 | g0036 | AFR | YRI | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA20129 | hp1 | a0001 | c0001 | t0010 | g0142 | AFR | ASW | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA20129 | hp2 | a0001 | c0001 | t0005 | g0105 | AFR | ASW | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0062 | EUR | TSI | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0064 | EUR | TSI | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0075 | EUR | TSI | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA20805 | hp2 | a0001 | c0001 | t0004 | g0029 | EUR | TSI | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | GIH | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | GIH | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02109 | hp2 | a0001 | c0001 | t0021 | g0086 | AFR | ACB | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02486 | hp1 | a0001 | c0001 | t0022 | g0091 | AFR | ACB | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0085 | AFR | ACB | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02559 | hp1 | a0001 | c0001 | t0005 | g0032 | AFR | ACB | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG02559 | hp2 | a0001 | c0003 | t0005 | g0104 | AFR | ACB | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0056 | AFR | MSL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | MSL | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | USA | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| HG06807 | hp2 | a0001 | c0001 | t0006 | g0145 | AFR | USA | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0241 | AFR | USA | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA20300 | hp2 | a0001 | c0001 | t0005 | g0113 | AFR | USA | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0071 | AFR | LWK | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| NA21309 | hp2 | a0001 | c0001 | t0005 | g0114 | AFR | LWK | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0004 | g0103 | REF | REF | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0005 | g0031 | REF | REF | SULT4A1_chr22_43819509_43867513 | SULT4A1 | chr22 | 43819509 | 43867513 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:43829188 | G | A | 1 | a0003 | 1 | HG04115.hp2 | missense_variant | MODERATE | c.614C>T | p.Thr205Met | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 6/7 | 745/2478 | 614/855 | 205/284 | chr22 | 43829188 | |||
| chr22:43833672 | C | T | 1 | a0002 | 1 | HG02818.hp2 | missense_variant | MODERATE | c.571G>A | p.Val191Met | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/7 | 702/2478 | 571/855 | 191/284 | chr22 | 43833672 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:43829073 | C | T | 1 | a0001c0003 | 1 | HG02559.hp2 | synonymous_variant | LOW | c.729G>A | p.Leu243Leu | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 6/7 | 860/2478 | 729/855 | 243/284 | chr22 | 43829073 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:43824789 | C | T | 1 | a0001c0001t0007 | 7 | NA18944.hp2 NA18947.hp1 NA18983.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1212G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 7/7 | 1212 | chr22 | 43824789 | ||||||
| chr22:43824793 | C | A | 10 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0009 others(7): Show |
82 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*1208G>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 7/7 | 1208 | chr22 | 43824793 | ||||||
| chr22:43824984 | C | G | 2 | a0001c0001t0004 a0001c0001t0027 |
29 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*1017G>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 7/7 | 1017 | chr22 | 43824984 | ||||||
| chr22:43824986 | C | T | 1 | a0001c0001t0024 | 1 | HG00597.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1015G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 7/7 | 1015 | chr22 | 43824986 | ||||||
| chr22:43825066 | G | C | 3 | a0001c0001t0014 a0001c0001t0015 a0001c0001t0021 |
5 | HG02109.hp2 HG02572.hp2 HG03139.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*935C>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 7/7 | 935 | chr22 | 43825066 | ||||||
| chr22:43825097 | G | A | 1 | a0001c0001t0025 | 1 | NA18943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*904C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 7/7 | 904 | chr22 | 43825097 | ||||||
| chr22:43825207 | G | A | 1 | a0001c0001t0012 | 2 | HG01243.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*794C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 7/7 | 794 | chr22 | 43825207 | ||||||
| chr22:43825231 | C | A | 1 | a0001c0001t0010 | 3 | HG02055.hp2 HG02976.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*770G>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 7/7 | 770 | chr22 | 43825231 | ||||||
| chr22:43825312 | C | T | 1 | a0001c0001t0014 | 2 | NA19030.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*689G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 7/7 | 689 | chr22 | 43825312 | ||||||
| chr22:43825367 | A | G | 11 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0009 others(8): Show |
82 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*634T>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 7/7 | 634 | chr22 | 43825367 | ||||||
| chr22:43825382 | A | G | 1 | a0001c0001t0016 | 2 | HG01099.hp2 HG01106.hp2 |
3_prime_UTR_variant | MODIFIER | c.*619T>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 7/7 | 619 | chr22 | 43825382 | ||||||
| chr22:43825608 | T | C | 1 | a0001c0001t0008 | 7 | HG02055.hp1 HG02572.hp1 HG02615.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*393A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 7/7 | 393 | chr22 | 43825608 | ||||||
| chr22:43825685 | C | CAATA | 27 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(24): Show |
354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
3_prime_UTR_variant | MODIFIER | c.*312_*315dupTATT | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 7/7 | 315 | chr22 | 43825685 | ||||||
| chr22:43825836 | G | A | 1 | a0002c0002t0020 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*165C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 7/7 | 165 | chr22 | 43825836 | ||||||
| chr22:43862403 | C | T | 1 | a0001c0001t0013 | 2 | HG01069.hp1 HG01175.hp1 |
5_prime_UTR_variant | MODIFIER | c.-21G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/7 | 21 | chr22 | 43862403 | ||||||
| chr22:43862424 | A | AGCCCGCA others(3): Show |
1 | a0001c0001t0021 | 1 | HG02109.hp2 | 5_prime_UTR_variant | MODIFIER | c.-52_-43dupGCGTGCGG others(2): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/7 | 43 | chr22 | 43862424 | ||||||
| chr22:43862431 | A | ACGCGCC | 5 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0012 others(2): Show |
70 | HG00099.hp1 HG00323.hp2 HG00558.hp1 others(67): Show |
5_prime_UTR_variant | MODIFIER | c.-55_-50dupGGCGCG | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/7 | 50 | chr22 | 43862431 | ||||||
| chr22:43862431 | A | ACGCGCCC others(5): Show |
1 | a0001c0001t0011 | 2 | HG03209.hp1 NA18957.hp2 |
5_prime_UTR_variant | MODIFIER | c.-61_-50dupGGCGCGGG others(4): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/7 | 50 | chr22 | 43862431 | ||||||
| chr22:43862431 | A | ACGCGCCC others(11): Show |
1 | a0001c0001t0019 | 1 | HG02647.hp1 | 5_prime_UTR_variant | MODIFIER | c.-67_-50dupGGCGCGGG others(10): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/7 | 50 | chr22 | 43862431 | ||||||
| chr22:43862431 | A | ACGCGCCC others(17): Show |
1 | a0001c0001t0018 | 1 | HG02976.hp1 | 5_prime_UTR_variant | MODIFIER | c.-73_-50dupGGCGCGGG others(16): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/7 | 50 | chr22 | 43862431 | ||||||
| chr22:43862431 | ACGCGCC | A | 6 | a0001c0001t0001 a0001c0001t0016 a0001c0001t0017 others(3): Show |
106 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(103): Show |
5_prime_UTR_variant | MODIFIER | c.-55_-50delGGCGCG | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/7 | 50 | chr22 | 43862431 | ||||||
| chr22:43862431 | ACGCGCCC others(5): Show |
A | 2 | a0001c0001t0026 a0001c0001t0027 |
2 | HG00733.hp2 HG01261.hp2 |
5_prime_UTR_variant | MODIFIER | c.-61_-50delGGCGCGGG others(4): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/7 | 50 | chr22 | 43862431 | ||||||
| chr22:43862459 | G | A | 1 | a0001c0001t0029 | 1 | HG02886.hp2 | 5_prime_UTR_variant | MODIFIER | c.-77C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/7 | 77 | chr22 | 43862459 | ||||||
| chr22:43862459 | G | GCCCGCA | 1 | a0001c0001t0002 | 96 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(93): Show |
5_prime_UTR_variant | MODIFIER | c.-78_-77insTGCGGG | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/7 | 78 | chr22 | 43862459 | ||||||
| chr22:43862459 | G | GCCCGCGC others(11): Show |
1 | a0001c0001t0028 | 1 | HG04204.hp1 | 5_prime_UTR_variant | MODIFIER | c.-78_-77insTGCGGGCG others(10): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/7 | 78 | chr22 | 43862459 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:43826244 | G | T | 7 | a0001c0001t0005g0032 a0001c0001t0005g0109 a0001c0001t0005g0113 others(4): Show |
8 | HG02055.hp2 HG02559.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.743-131C>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 6/6 | chr22 | 43826244 | |||||||
| chr22:43826357 | A | T | 1 | a0001c0001t0004g0102 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.743-244T>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 6/6 | chr22 | 43826357 | |||||||
| chr22:43826465 | C | T | 85 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(82): Show |
124 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.743-352G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 6/6 | chr22 | 43826465 | |||||||
| chr22:43826487 | T | C | 31 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0037 others(28): Show |
54 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.743-374A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 6/6 | chr22 | 43826487 | |||||||
| chr22:43826536 | A | G | 55 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0012 others(52): Show |
82 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.743-423T>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 6/6 | chr22 | 43826536 | |||||||
| chr22:43826559 | C | T | 55 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0012 others(52): Show |
82 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.743-446G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 6/6 | chr22 | 43826559 | |||||||
| chr22:43826834 | G | T | 1 | a0001c0001t0002g0239 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.743-721C>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 6/6 | chr22 | 43826834 | |||||||
| chr22:43826864 | C | T | 3 | a0001c0001t0002g0020 a0001c0001t0002g0223 a0001c0001t0002g0227 |
5 | HG02293.hp2 HG02738.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.743-751G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 6/6 | chr22 | 43826864 | |||||||
| chr22:43826927 | A | C | 140 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(137): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.743-814T>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 6/6 | chr22 | 43826927 | |||||||
| chr22:43826960 | G | A | 53 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0012 others(50): Show |
80 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.743-847C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 6/6 | chr22 | 43826960 | |||||||
| chr22:43827140 | C | A | 2 | a0001c0001t0001g0169 a0001c0001t0024g0168 |
2 | HG00597.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.743-1027G>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 6/6 | chr22 | 43827140 | |||||||
| chr22:43827185 | T | C | 5 | a0001c0001t0014g0129 a0001c0001t0014g0130 a0001c0001t0015g0107 others(2): Show |
5 | HG02109.hp2 HG02572.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.743-1072A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 6/6 | chr22 | 43827185 | |||||||
| chr22:43827186 | T | C | 75 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(72): Show |
111 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.743-1073A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 6/6 | chr22 | 43827186 | |||||||
| chr22:43827328 | C | T | 5 | a0001c0001t0004g0013 a0001c0001t0004g0097 a0001c0001t0004g0098 others(2): Show |
8 | HG02257.hp1 HG02258.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.743-1215G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 6/6 | chr22 | 43827328 | |||||||
| chr22:43827335 | T | C | 2 | a0001c0001t0006g0135 a0001c0001t0006g0136 |
2 | HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.743-1222A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 6/6 | chr22 | 43827335 | |||||||
| chr22:43827342 | T | C | 1 | a0001c0001t0002g0245 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.743-1229A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 6/6 | chr22 | 43827342 | |||||||
| chr22:43827359 | T | C | 4 | a0001c0001t0001g0167 a0001c0001t0001g0184 a0001c0001t0001g0186 others(1): Show |
5 | HG01255.hp1 HG01516.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.743-1246A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 6/6 | chr22 | 43827359 | |||||||
| chr22:43827381 | GAAAAATT others(39): Show |
G | 1 | a0001c0001t0023g0196 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.743-1314_743-1269d others(48): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 6/6 | chr22 | 43827381 | |||||||
| chr22:43827755 | C | CCA | 68 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(65): Show |
103 | HG00280.hp2 HG00423.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.742+1303_742+1304d others(4): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 6/6 | chr22 | 43827755 | |||||||
| chr22:43827755 | C | CCACA | 74 | a0001c0001t0001g0037 a0001c0001t0001g0149 a0001c0001t0001g0161 others(71): Show |
112 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.742+1301_742+1304d others(6): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 6/6 | chr22 | 43827755 | |||||||
| chr22:43827755 | C | CCACACA | 56 | a0001c0001t0001g0170 a0001c0001t0002g0021 a0001c0001t0002g0234 others(53): Show |
83 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.742+1299_742+1304d others(8): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 6/6 | chr22 | 43827755 | |||||||
| chr22:43827755 | C | CCACACAC others(1): Show |
15 | a0001c0001t0002g0213 a0001c0001t0003g0008 a0001c0001t0003g0053 others(12): Show |
19 | HG00099.hp1 HG01106.hp1 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.742+1297_742+1304d others(10): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 6/6 | chr22 | 43827755 | |||||||
| chr22:43827755 | C | CCACACAC others(3): Show |
5 | a0001c0001t0003g0075 a0001c0001t0003g0080 a0001c0001t0003g0084 others(2): Show |
5 | HG01081.hp1 HG01256.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.742+1295_742+1304d others(12): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 6/6 | chr22 | 43827755 | |||||||
| chr22:43827755 | C | CCACACAC others(5): Show |
1 | a0001c0001t0006g0127 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.742+1293_742+1304d others(14): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 6/6 | chr22 | 43827755 | |||||||
| chr22:43827810 | G | C | 1 | a0001c0001t0014g0129 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.742+1250C>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 6/6 | chr22 | 43827810 | |||||||
| chr22:43828003 | G | A | 12 | a0001c0001t0006g0132 a0001c0001t0006g0135 a0001c0001t0006g0136 others(9): Show |
15 | HG02055.hp1 HG02109.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.742+1057C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 6/6 | chr22 | 43828003 | |||||||
| chr22:43828144 | C | T | 1 | a0001c0001t0006g0127 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.742+916G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 6/6 | chr22 | 43828144 | |||||||
| chr22:43828191 | G | A | 5 | a0001c0001t0006g0009 a0001c0001t0006g0126 a0001c0001t0006g0137 others(2): Show |
9 | HG01243.hp1 HG01496.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.742+869C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 6/6 | chr22 | 43828191 | |||||||
| chr22:43828366 | G | A | 2 | a0001c0001t0016g0179 a0001c0001t0016g0180 |
2 | HG01099.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.742+694C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 6/6 | chr22 | 43828366 | |||||||
| chr22:43828519 | C | T | 5 | a0001c0001t0014g0129 a0001c0001t0014g0130 a0001c0001t0015g0107 others(2): Show |
5 | HG02109.hp2 HG02572.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.742+541G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 6/6 | chr22 | 43828519 | |||||||
| chr22:43828608 | G | A | 1 | a0001c0001t0006g0035 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.742+452C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 6/6 | chr22 | 43828608 | |||||||
| chr22:43828631 | C | A | 1 | a0001c0001t0002g0237 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.742+429G>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 6/6 | chr22 | 43828631 | |||||||
| chr22:43828701 | T | C | 2 | a0001c0001t0006g0009 a0001c0001t0006g0137 |
6 | HG01243.hp1 HG01496.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.742+359A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 6/6 | chr22 | 43828701 | |||||||
| chr22:43828845 | C | T | 12 | a0001c0001t0006g0132 a0001c0001t0006g0135 a0001c0001t0006g0136 others(9): Show |
15 | HG02055.hp1 HG02109.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.742+215G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 6/6 | chr22 | 43828845 | |||||||
| chr22:43828862 | G | C | 1 | a0001c0001t0003g0082 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.742+198C>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 6/6 | chr22 | 43828862 | |||||||
| chr22:43828976 | C | G | 17 | a0001c0001t0004g0002 a0001c0001t0004g0028 a0001c0001t0004g0029 others(14): Show |
32 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.742+84G>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 6/6 | chr22 | 43828976 | |||||||
| chr22:43829037 | G | A | 5 | a0001c0001t0006g0036 a0001c0001t0006g0127 a0001c0001t0006g0143 others(2): Show |
6 | HG01433.hp2 HG03195.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.742+23C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 6/6 | chr22 | 43829037 | |||||||
| chr22:43829337 | TTGTCCAG others(13): Show |
T | 1 | a0001c0001t0023g0196 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.604-159_604-140del others(20): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43829337 | |||||||
| chr22:43829580 | T | C | 1 | a0001c0001t0001g0188 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.604-382A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43829580 | |||||||
| chr22:43829764 | A | G | 15 | a0001c0001t0004g0002 a0001c0001t0004g0013 a0001c0001t0004g0028 others(12): Show |
29 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.604-566T>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43829764 | |||||||
| chr22:43829914 | G | A | 206 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(203): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(301): Show |
intron_variant | MODIFIER | c.604-716C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43829914 | |||||||
| chr22:43829919 | A | C | 3 | a0001c0001t0006g0030 a0001c0001t0006g0111 a0001c0001t0006g0112 |
4 | HG02896.hp1 HG02897.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.604-721T>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43829919 | |||||||
| chr22:43829966 | T | A | 55 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0012 others(52): Show |
82 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.604-768A>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43829966 | |||||||
| chr22:43829978 | G | A | 73 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(70): Show |
109 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.604-780C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43829978 | |||||||
| chr22:43829993 | C | A | 247 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(244): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.604-795G>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43829993 | |||||||
| chr22:43830007 | C | A | 1 | a0001c0001t0003g0082 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.604-809G>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43830007 | |||||||
| chr22:43830008 | G | A | 66 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0011 others(63): Show |
98 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.604-810C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43830008 | |||||||
| chr22:43830346 | G | A | 1 | a0001c0001t0003g0071 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.604-1148C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43830346 | |||||||
| chr22:43830386 | C | T | 1 | a0001c0001t0001g0166 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.604-1188G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43830386 | |||||||
| chr22:43830552 | G | A | 1 | a0001c0001t0002g0256 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.604-1354C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43830552 | |||||||
| chr22:43830598 | C | T | 1 | a0001c0001t0002g0261 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.604-1400G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43830598 | |||||||
| chr22:43830722 | G | C | 1 | a0001c0001t0002g0262 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.604-1524C>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43830722 | |||||||
| chr22:43830768 | C | T | 1 | a0001c0001t0028g0212 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.604-1570G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43830768 | |||||||
| chr22:43830782 | G | A | 1 | a0001c0001t0022g0091 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.604-1584C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43830782 | |||||||
| chr22:43831010 | C | A | 1 | a0001c0001t0003g0080 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.604-1812G>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43831010 | |||||||
| chr22:43831107 | C | A | 54 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0012 others(51): Show |
81 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.604-1909G>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43831107 | |||||||
| chr22:43831126 | C | T | 1 | a0001c0001t0006g0106 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.604-1928G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43831126 | |||||||
| chr22:43831145 | C | T | 2 | a0001c0001t0013g0087 a0001c0001t0013g0088 |
2 | HG01069.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.604-1947G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43831145 | |||||||
| chr22:43831181 | AG | A | 73 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(70): Show |
109 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.604-1984delC | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43831181 | |||||||
| chr22:43831186 | G | A | 1 | a0001c0001t0001g0158 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.604-1988C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43831186 | |||||||
| chr22:43831226 | A | G | 1 | a0001c0001t0006g0145 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.604-2028T>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43831226 | |||||||
| chr22:43831252 | T | C | 1 | a0001c0001t0004g0100 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.604-2054A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43831252 | |||||||
| chr22:43831288 | C | CGGCAGCT others(17): Show |
1 | a0001c0001t0002g0230 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.604-2091_604-2090i others(26): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43831288 | |||||||
| chr22:43831288 | C | CGGCAGCT others(16): Show |
62 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0011 others(59): Show |
94 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.604-2113_604-2091d others(25): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43831288 | |||||||
| chr22:43831288 | C | CGGCAGCT others(39): Show |
1 | a0001c0001t0002g0256 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.604-2091_604-2090i others(48): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43831288 | |||||||
| chr22:43831468 | T | C | 54 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0012 others(51): Show |
81 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.603+2172A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43831468 | |||||||
| chr22:43831482 | A | C | 2 | a0001c0001t0004g0029 a0001c0001t0004g0099 |
3 | HG01175.hp2 HG01346.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.603+2158T>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43831482 | |||||||
| chr22:43831493 | C | T | 3 | a0001c0001t0003g0008 a0001c0001t0003g0083 a0001c0001t0003g0084 |
7 | HG00099.hp1 HG01167.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.603+2147G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43831493 | |||||||
| chr22:43831520 | G | A | 4 | a0001c0001t0006g0036 a0001c0001t0006g0143 a0001c0001t0006g0144 others(1): Show |
5 | HG03195.hp2 HG03209.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.603+2120C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43831520 | |||||||
| chr22:43831564 | G | A | 1 | a0001c0001t0005g0114 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.603+2076C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43831564 | |||||||
| chr22:43831589 | C | T | 1 | a0001c0001t0006g0140 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.603+2051G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43831589 | |||||||
| chr22:43831590 | G | A | 2 | a0001c0001t0006g0127 a0001c0001t0006g0144 |
2 | HG01433.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.603+2050C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43831590 | |||||||
| chr22:43831676 | A | G | 120 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0011 others(117): Show |
179 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.603+1964T>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43831676 | |||||||
| chr22:43831708 | C | G | 1 | a0001c0001t0001g0015 | 4 | HG00544.hp1 HG02132.hp2 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.603+1932G>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43831708 | |||||||
| chr22:43831772 | C | T | 3 | a0001c0001t0003g0007 a0001c0001t0003g0012 a0001c0001t0009g0026 |
12 | HG00438.hp1 HG00558.hp1 HG00621.hp2 others(9): Show |
intron_variant | MODIFIER | c.603+1868G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43831772 | |||||||
| chr22:43831906 | G | GAC | 54 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0012 others(51): Show |
81 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.603+1732_603+1733d others(4): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43831906 | |||||||
| chr22:43831925 | A | G | 1 | a0001c0001t0002g0233 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.603+1715T>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43831925 | |||||||
| chr22:43831996 | C | T | 2 | a0001c0001t0006g0135 a0001c0001t0006g0136 |
2 | HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.603+1644G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43831996 | |||||||
| chr22:43832110 | G | A | 3 | a0001c0001t0006g0036 a0001c0001t0006g0144 a0001c0001t0006g0145 |
4 | HG03209.hp2 HG06807.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.603+1530C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43832110 | |||||||
| chr22:43832131 | G | A | 1 | a0001c0001t0005g0108 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.603+1509C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43832131 | |||||||
| chr22:43832196 | T | G | 2 | a0001c0001t0003g0022 a0001c0001t0003g0053 |
3 | HG01109.hp2 HG02886.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.603+1444A>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43832196 | |||||||
| chr22:43832235 | T | C | 1 | a0001c0001t0001g0193 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.603+1405A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43832235 | |||||||
| chr22:43832304 | C | T | 1 | a0001c0001t0005g0114 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.603+1336G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43832304 | |||||||
| chr22:43832321 | C | T | 1 | a0001c0001t0001g0164 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.603+1319G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43832321 | |||||||
| chr22:43832389 | C | T | 3 | a0001c0001t0006g0030 a0001c0001t0006g0111 a0001c0001t0006g0112 |
4 | HG02896.hp1 HG02897.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.603+1251G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43832389 | |||||||
| chr22:43832441 | G | A | 1 | a0001c0001t0003g0082 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.603+1199C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43832441 | |||||||
| chr22:43832447 | G | C | 1 | a0001c0001t0005g0108 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.603+1193C>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43832447 | |||||||
| chr22:43832487 | G | A | 62 | a0001c0001t0001g0177 a0001c0001t0002g0003 a0001c0001t0002g0005 others(59): Show |
92 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.603+1153C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43832487 | |||||||
| chr22:43832530 | G | A | 1 | a0001c0001t0022g0091 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.603+1110C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43832530 | |||||||
| chr22:43832567 | C | T | 1 | a0001c0001t0006g0127 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.603+1073G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43832567 | |||||||
| chr22:43832700 | C | T | 53 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0012 others(50): Show |
80 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.603+940G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43832700 | |||||||
| chr22:43832819 | C | T | 1 | a0001c0001t0006g0127 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.603+821G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43832819 | |||||||
| chr22:43832963 | G | C | 66 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0011 others(63): Show |
98 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.603+677C>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43832963 | |||||||
| chr22:43833034 | C | T | 2 | a0001c0001t0001g0154 a0001c0001t0001g0165 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.603+606G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43833034 | |||||||
| chr22:43833081 | G | A | 1 | a0001c0001t0001g0171 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.603+559C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43833081 | |||||||
| chr22:43833272 | C | A | 3 | a0001c0001t0006g0030 a0001c0001t0006g0111 a0001c0001t0006g0112 |
4 | HG02896.hp1 HG02897.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.603+368G>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43833272 | |||||||
| chr22:43833283 | C | T | 1 | a0001c0001t0002g0256 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.603+357G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43833283 | |||||||
| chr22:43833293 | G | A | 1 | a0001c0001t0002g0240 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.603+347C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43833293 | |||||||
| chr22:43833332 | T | A | 1 | a0001c0001t0001g0162 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.603+308A>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43833332 | |||||||
| chr22:43833352 | C | T | 1 | a0001c0001t0004g0097 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.603+288G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43833352 | |||||||
| chr22:43833612 | G | C | 246 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(243): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.603+28C>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43833612 | |||||||
| chr22:43833613 | G | A | 1 | a0001c0001t0023g0196 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.603+27C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43833613 | |||||||
| chr22:43833614 | A | G | 1 | a0001c0001t0023g0196 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.603+26T>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43833614 | |||||||
| chr22:43833626 | C | T | 1 | a0001c0001t0001g0164 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.603+14G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43833626 | |||||||
| chr22:43833628 | G | A | 54 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0012 others(51): Show |
81 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.603+12C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 5/6 | chr22 | 43833628 | |||||||
| chr22:43833765 | C | T | 1 | a0001c0001t0003g0054 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.509-31G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43833765 | |||||||
| chr22:43833846 | G | A | 1 | a0001c0001t0002g0227 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.509-112C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43833846 | |||||||
| chr22:43833913 | G | A | 66 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0011 others(63): Show |
98 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.509-179C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43833913 | |||||||
| chr22:43834002 | G | A | 1 | a0001c0001t0003g0064 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.509-268C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834002 | |||||||
| chr22:43834025 | C | T | 1 | a0001c0001t0002g0223 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.509-291G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834025 | |||||||
| chr22:43834249 | A | G | 1 | a0001c0001t0006g0140 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.509-515T>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834249 | |||||||
| chr22:43834263 | G | T | 66 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0012 others(63): Show |
96 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.509-529C>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834263 | |||||||
| chr22:43834285 | G | A | 4 | a0001c0001t0006g0036 a0001c0001t0006g0143 a0001c0001t0006g0144 others(1): Show |
5 | HG03195.hp2 HG03209.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.509-551C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834285 | |||||||
| chr22:43834292 | TGCTTCCC others(49): Show |
T | 3 | a0001c0001t0005g0105 a0001c0001t0005g0141 a0001c0003t0005g0104 |
3 | HG02559.hp2 HG02630.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.509-614_509-559del others(56): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834292 | |||||||
| chr22:43834303 | CCCCCACC others(20): Show |
C | 1 | a0001c0001t0001g0015 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.509-596_509-570del others(27): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834303 | |||||||
| chr22:43834310 | C | T | 53 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0012 others(50): Show |
80 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.509-576G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834310 | |||||||
| chr22:43834320 | TGCTTCCC others(21): Show |
T | 80 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(77): Show |
114 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.509-614_509-587del others(28): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834320 | |||||||
| chr22:43834331 | CCCCCACC others(20): Show |
C | 1 | a0001c0001t0001g0010 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.509-624_509-598del others(27): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834331 | |||||||
| chr22:43834334 | CCACCGCG others(497): Show |
C | 57 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0012 others(54): Show |
82 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.509-1104_509-601de others(1): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834334 | |||||||
| chr22:43834342 | G | T | 1 | a0001c0001t0001g0015 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.509-608C>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834342 | |||||||
| chr22:43834343 | CCCTGAGC others(20): Show |
C | 1 | a0001c0001t0001g0019 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.509-636_509-610del others(27): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834343 | |||||||
| chr22:43834348 | A | T | 1 | a0001c0001t0001g0015 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.509-614T>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834348 | |||||||
| chr22:43834348 | AGCTTCCC others(525): Show |
A | 2 | a0001c0001t0003g0008 a0001c0001t0006g0132 |
3 | HG00099.hp1 HG01496.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.509-1146_509-615de others(1): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834348 | |||||||
| chr22:43834356 | G | A | 2 | a0001c0001t0003g0073 a0001c0001t0022g0091 |
2 | HG02486.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.509-622C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834356 | |||||||
| chr22:43834362 | CCACCGCG others(357): Show |
C | 2 | a0001c0001t0006g0135 a0001c0001t0006g0136 |
2 | HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.509-992_509-629del | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834362 | |||||||
| chr22:43834362 | CCACCGCG others(637): Show |
C | 1 | a0001c0001t0003g0073 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.509-1272_509-629de others(1): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834362 | |||||||
| chr22:43834369 | GGCCCTGA others(441): Show |
G | 1 | a0001c0001t0005g0092 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.509-1083_509-636de others(1): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834369 | |||||||
| chr22:43834370 | G | T | 5 | a0001c0001t0008g0014 a0001c0001t0008g0131 a0001c0001t0008g0133 others(2): Show |
8 | HG02055.hp1 HG02486.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.509-636C>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834370 | |||||||
| chr22:43834376 | A | T | 5 | a0001c0001t0008g0014 a0001c0001t0008g0131 a0001c0001t0008g0133 others(2): Show |
8 | HG02055.hp1 HG02486.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.509-642T>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834376 | |||||||
| chr22:43834397 | T | G | 5 | a0001c0001t0008g0014 a0001c0001t0008g0131 a0001c0001t0008g0133 others(2): Show |
8 | HG02055.hp1 HG02486.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.509-663A>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834397 | |||||||
| chr22:43834398 | G | T | 4 | a0001c0001t0008g0014 a0001c0001t0008g0131 a0001c0001t0008g0133 others(1): Show |
7 | HG02055.hp1 HG02572.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.509-664C>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834398 | |||||||
| chr22:43834404 | A | T | 4 | a0001c0001t0008g0014 a0001c0001t0008g0131 a0001c0001t0008g0133 others(1): Show |
7 | HG02055.hp1 HG02572.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.509-670T>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834404 | |||||||
| chr22:43834411 | C | G | 4 | a0001c0001t0006g0036 a0001c0001t0006g0143 a0001c0001t0006g0144 others(1): Show |
5 | HG03195.hp2 HG03209.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.509-677G>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834411 | |||||||
| chr22:43834411 | C | T | 64 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0011 others(61): Show |
95 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.509-677G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834411 | |||||||
| chr22:43834414 | A | G | 5 | a0001c0001t0008g0014 a0001c0001t0008g0131 a0001c0001t0008g0133 others(2): Show |
8 | HG02055.hp1 HG02486.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.509-680T>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834414 | |||||||
| chr22:43834415 | G | C | 5 | a0001c0001t0008g0014 a0001c0001t0008g0131 a0001c0001t0008g0133 others(2): Show |
8 | HG02055.hp1 HG02486.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.509-681C>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834415 | |||||||
| chr22:43834418 | A | C | 5 | a0001c0001t0008g0014 a0001c0001t0008g0131 a0001c0001t0008g0133 others(2): Show |
8 | HG02055.hp1 HG02486.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.509-684T>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834418 | |||||||
| chr22:43834426 | G | T | 5 | a0001c0001t0001g0149 a0001c0001t0008g0014 a0001c0001t0008g0131 others(2): Show |
8 | HG02055.hp1 HG02572.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.509-692C>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834426 | |||||||
| chr22:43834453 | G | A | 1 | a0001c0001t0002g0011 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.509-719C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834453 | |||||||
| chr22:43834454 | T | G | 1 | a0001c0001t0022g0091 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.509-720A>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834454 | |||||||
| chr22:43834468 | GCGCCCCC others(21): Show |
G | 106 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(103): Show |
154 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.509-762_509-735del others(28): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834468 | |||||||
| chr22:43834471 | CCCCCACC others(20): Show |
C | 1 | a0001c0001t0001g0001 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.509-764_509-738del others(27): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834471 | |||||||
| chr22:43834474 | CCACCGCG others(77): Show |
C | 1 | a0001c0001t0002g0235 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.509-824_509-741del others(84): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834474 | |||||||
| chr22:43834482 | G | T | 1 | a0001c0001t0022g0091 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.509-748C>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834482 | |||||||
| chr22:43834488 | A | T | 1 | a0001c0001t0022g0091 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.509-754T>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834488 | |||||||
| chr22:43834488 | AGCTTCCC others(385): Show |
A | 31 | a0001c0001t0002g0005 a0001c0001t0002g0016 a0001c0001t0002g0020 others(28): Show |
47 | HG00438.hp2 HG00597.hp2 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.509-1146_509-755de others(1): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834488 | |||||||
| chr22:43834488 | AGCTTCCC others(413): Show |
A | 6 | a0001c0001t0002g0011 a0001c0001t0002g0232 a0001c0001t0008g0014 others(3): Show |
9 | HG02055.hp1 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.509-1174_509-755de others(1): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834488 | |||||||
| chr22:43834496 | A | G | 4 | a0001c0001t0002g0020 a0001c0001t0002g0040 a0001c0001t0004g0002 others(1): Show |
4 | HG01192.hp2 HG02486.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.509-762T>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834496 | |||||||
| chr22:43834496 | ACGCCCCC others(273): Show |
A | 1 | a0001c0001t0006g0127 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.509-1042_509-763de others(1): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834496 | |||||||
| chr22:43834496 | ACGCCCCC others(273): Show |
G | 19 | a0001c0001t0004g0002 a0001c0001t0004g0013 a0001c0001t0004g0028 others(16): Show |
33 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.509-1041_509-762de others(1): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834496 | |||||||
| chr22:43834499 | CCCCCACC others(384): Show |
C | 2 | a0001c0001t0002g0020 a0001c0001t0002g0040 |
2 | HG02738.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.509-1156_509-766de others(1): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834499 | |||||||
| chr22:43834502 | CCACCGCG others(329): Show |
C | 1 | a0001c0001t0022g0091 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.509-1104_509-769de others(1): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834502 | |||||||
| chr22:43834516 | AGCTTCCC others(385): Show |
A | 32 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0041 others(29): Show |
45 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(42): Show |
intron_variant | MODIFIER | c.509-1174_509-783de others(1): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834516 | |||||||
| chr22:43834527 | CCCCCACC others(272): Show |
C | 1 | a0001c0001t0004g0002 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.509-1072_509-794de others(1): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834527 | |||||||
| chr22:43834583 | CCCCCACC others(48): Show |
C | 1 | a0001c0001t0001g0001 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.509-904_509-850del others(55): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834583 | |||||||
| chr22:43834600 | TGCTTCCC others(49): Show |
T | 73 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(70): Show |
107 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.509-922_509-867del others(56): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834600 | |||||||
| chr22:43834600 | TGCTTCCC others(245): Show |
T | 5 | a0001c0001t0006g0009 a0001c0001t0006g0137 a0001c0001t0006g0146 others(2): Show |
9 | HG01069.hp1 HG01175.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.509-1118_509-867de others(1): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834600 | |||||||
| chr22:43834600 | TGCTTCCC others(329): Show |
T | 2 | a0001c0001t0006g0126 a0001c0001t0006g0138 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.509-1202_509-867de others(1): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834600 | |||||||
| chr22:43834611 | CCCCCACC others(48): Show |
C | 2 | a0001c0001t0001g0019 a0001c0001t0001g0173 |
2 | NA18977.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.509-932_509-878del others(55): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834611 | |||||||
| chr22:43834622 | T | G | 1 | a0001c0001t0002g0235 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.509-888A>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834622 | |||||||
| chr22:43834628 | T | A | 1 | a0001c0001t0002g0235 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.509-894A>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834628 | |||||||
| chr22:43834628 | TGCTTCCC others(21): Show |
T | 1 | a0001c0001t0010g0142 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.509-922_509-895del others(28): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834628 | |||||||
| chr22:43834650 | G | T | 1 | a0001c0001t0001g0001 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.509-916C>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834650 | |||||||
| chr22:43834656 | A | T | 1 | a0001c0001t0001g0001 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.509-922T>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834656 | |||||||
| chr22:43834705 | T | G | 1 | a0001c0001t0001g0163 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.509-971A>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834705 | |||||||
| chr22:43834719 | C | T | 1 | a0001c0001t0002g0235 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.509-985G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834719 | |||||||
| chr22:43834723 | C | G | 73 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(70): Show |
109 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.509-989G>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834723 | |||||||
| chr22:43834734 | T | G | 90 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(87): Show |
128 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.509-1000A>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834734 | |||||||
| chr22:43834758 | C | T | 1 | a0001c0001t0005g0033 | 2 | HG01074.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.509-1024G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834758 | |||||||
| chr22:43834762 | T | G | 2 | a0001c0001t0006g0135 a0001c0001t0006g0136 |
2 | HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.509-1028A>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834762 | |||||||
| chr22:43834796 | AGCTTCCC others(105): Show |
A | 1 | a0001c0001t0002g0235 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.509-1174_509-1063d others(2): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834796 | |||||||
| chr22:43834832 | G | A | 1 | a0001c0001t0006g0127 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.509-1098C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834832 | |||||||
| chr22:43834838 | ACACCGCG others(245): Show |
A | 2 | a0001c0001t0006g0135 a0001c0001t0006g0136 |
2 | HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.509-1356_509-1105d others(2): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834838 | |||||||
| chr22:43834845 | G | A | 74 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(71): Show |
110 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.509-1111C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834845 | |||||||
| chr22:43834860 | G | A | 52 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0012 others(49): Show |
77 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.509-1126C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834860 | |||||||
| chr22:43834874 | T | G | 6 | a0001c0001t0006g0009 a0001c0001t0006g0137 a0001c0001t0006g0146 others(3): Show |
10 | HG01069.hp1 HG01175.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.509-1140A>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834874 | |||||||
| chr22:43834880 | T | A | 6 | a0001c0001t0006g0009 a0001c0001t0006g0137 a0001c0001t0006g0146 others(3): Show |
10 | HG01069.hp1 HG01175.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.509-1146A>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834880 | |||||||
| chr22:43834880 | TGCTTCCC others(49): Show |
T | 1 | a0001c0001t0001g0163 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.509-1202_509-1147d others(58): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834880 | |||||||
| chr22:43834888 | G | A | 1 | a0001c0001t0003g0008 | 2 | HG00099.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.509-1154C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834888 | |||||||
| chr22:43834894 | CCACCGCG others(105): Show |
C | 1 | a0001c0001t0001g0172 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.509-1272_509-1161d others(2): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834894 | |||||||
| chr22:43834900 | C | T | 2 | a0001c0001t0003g0023 a0001c0001t0003g0066 |
3 | HG01884.hp2 HG02280.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.509-1166G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834900 | |||||||
| chr22:43834902 | T | G | 149 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(146): Show |
225 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.509-1168A>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834902 | |||||||
| chr22:43834908 | T | A | 149 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(146): Show |
225 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.509-1174A>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834908 | |||||||
| chr22:43834908 | TGCTTCCC others(21): Show |
T | 37 | a0001c0001t0002g0005 a0001c0001t0002g0016 a0001c0001t0002g0020 others(34): Show |
59 | HG00438.hp2 HG00597.hp2 HG00741.hp2 others(56): Show |
intron_variant | MODIFIER | c.509-1202_509-1175d others(30): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834908 | |||||||
| chr22:43834930 | G | T | 129 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(126): Show |
197 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.509-1196C>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834930 | |||||||
| chr22:43834936 | A | T | 129 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(126): Show |
197 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.509-1202T>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834936 | |||||||
| chr22:43834943 | C | T | 3 | a0001c0001t0003g0018 a0001c0001t0003g0062 a0001c0001t0003g0078 |
5 | HG00323.hp2 HG01081.hp2 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.509-1209G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834943 | |||||||
| chr22:43834945 | C | T | 1 | a0001c0001t0003g0066 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.509-1211G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43834945 | |||||||
| chr22:43835002 | A | G | 1 | a0001c0001t0002g0232 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.509-1268T>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43835002 | |||||||
| chr22:43835003 | C | G | 59 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0012 others(56): Show |
86 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.509-1269G>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43835003 | |||||||
| chr22:43835006 | A | C | 2 | a0001c0001t0002g0232 a0001c0001t0006g0106 |
2 | HG03041.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.509-1272T>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43835006 | |||||||
| chr22:43835006 | ACACCGCG others(77): Show |
A | 59 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0012 others(56): Show |
86 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.509-1356_509-1273d others(86): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43835006 | |||||||
| chr22:43835014 | G | T | 1 | a0001c0001t0003g0073 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.509-1280C>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43835014 | |||||||
| chr22:43835020 | T | A | 5 | a0001c0001t0001g0172 a0001c0001t0008g0014 a0001c0001t0008g0131 others(2): Show |
8 | HG02055.hp1 HG02572.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.509-1286A>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43835020 | |||||||
| chr22:43835042 | T | G | 5 | a0001c0001t0003g0073 a0001c0001t0008g0014 a0001c0001t0008g0131 others(2): Show |
8 | HG02055.hp1 HG02572.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.509-1308A>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43835042 | |||||||
| chr22:43835048 | T | A | 5 | a0001c0001t0003g0073 a0001c0001t0008g0014 a0001c0001t0008g0131 others(2): Show |
8 | HG02055.hp1 HG02572.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.509-1314A>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43835048 | |||||||
| chr22:43835051 | T | C | 42 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0019 others(39): Show |
55 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.509-1317A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43835051 | |||||||
| chr22:43835069 | G | T | 4 | a0001c0001t0008g0014 a0001c0001t0008g0131 a0001c0001t0008g0133 others(1): Show |
7 | HG02055.hp1 HG02572.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.509-1335C>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43835069 | |||||||
| chr22:43835069 | GGCCCTGA others(21): Show |
G | 1 | a0001c0001t0004g0029 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.509-1363_509-1336d others(30): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43835069 | |||||||
| chr22:43835086 | G | A | 4 | a0001c0001t0008g0014 a0001c0001t0008g0131 a0001c0001t0008g0133 others(1): Show |
7 | HG02055.hp1 HG02572.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.509-1352C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43835086 | |||||||
| chr22:43835087 | C | G | 4 | a0001c0001t0008g0014 a0001c0001t0008g0131 a0001c0001t0008g0133 others(1): Show |
7 | HG02055.hp1 HG02572.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.509-1353G>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43835087 | |||||||
| chr22:43835090 | C | A | 4 | a0001c0001t0008g0014 a0001c0001t0008g0131 a0001c0001t0008g0133 others(1): Show |
7 | HG02055.hp1 HG02572.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.509-1356G>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43835090 | |||||||
| chr22:43835115 | G | C | 1 | a0001c0001t0001g0172 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.509-1381C>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43835115 | |||||||
| chr22:43835118 | ACACCGCA others(21): Show |
A | 2 | a0001c0001t0013g0087 a0001c0001t0013g0088 |
2 | HG01069.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.509-1412_509-1385d others(30): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43835118 | |||||||
| chr22:43835152 | C | G | 4 | a0001c0001t0002g0042 a0001c0001t0002g0231 a0001c0001t0002g0240 others(1): Show |
5 | NA18612.hp1 NA18952.hp1 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.509-1418G>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43835152 | |||||||
| chr22:43835443 | A | G | 7 | a0001c0001t0006g0009 a0001c0001t0006g0126 a0001c0001t0006g0137 others(4): Show |
11 | HG01069.hp1 HG01175.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.509-1709T>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43835443 | |||||||
| chr22:43835505 | C | T | 1 | a0001c0001t0022g0091 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.509-1771G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43835505 | |||||||
| chr22:43835929 | G | A | 2 | a0001c0001t0013g0087 a0001c0001t0013g0088 |
2 | HG01069.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.509-2195C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43835929 | |||||||
| chr22:43835963 | C | T | 1 | a0001c0001t0006g0135 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.509-2229G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43835963 | |||||||
| chr22:43836068 | C | T | 1 | a0001c0001t0001g0147 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.509-2334G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43836068 | |||||||
| chr22:43836089 | C | T | 2 | a0001c0001t0003g0024 a0001c0001t0003g0063 |
3 | HG03688.hp2 HG03834.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.509-2355G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43836089 | |||||||
| chr22:43836133 | C | T | 2 | a0001c0001t0006g0126 a0001c0001t0006g0138 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.509-2399G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43836133 | |||||||
| chr22:43836136 | T | C | 65 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0012 others(62): Show |
95 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.509-2402A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43836136 | |||||||
| chr22:43836153 | CACTGCAG others(119): Show |
C | 54 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0012 others(51): Show |
81 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.509-2545_509-2420d others(2): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43836153 | |||||||
| chr22:43836159 | A | G | 11 | a0001c0001t0006g0135 a0001c0001t0006g0136 a0001c0001t0008g0014 others(8): Show |
14 | HG02055.hp1 HG02109.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.509-2425T>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43836159 | |||||||
| chr22:43836173 | C | G | 183 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(180): Show |
272 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(269): Show |
intron_variant | MODIFIER | c.509-2439G>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43836173 | |||||||
| chr22:43836178 | T | C | 183 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(180): Show |
272 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(269): Show |
intron_variant | MODIFIER | c.509-2444A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43836178 | |||||||
| chr22:43836194 | C | A | 11 | a0001c0001t0006g0135 a0001c0001t0006g0136 a0001c0001t0008g0014 others(8): Show |
14 | HG02055.hp1 HG02109.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.509-2460G>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43836194 | |||||||
| chr22:43836195 | G | A | 1 | a0001c0001t0005g0114 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.509-2461C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43836195 | |||||||
| chr22:43836195 | G | C | 11 | a0001c0001t0006g0135 a0001c0001t0006g0136 a0001c0001t0008g0014 others(8): Show |
14 | HG02055.hp1 HG02109.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.509-2461C>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43836195 | |||||||
| chr22:43836222 | C | T | 11 | a0001c0001t0006g0135 a0001c0001t0006g0136 a0001c0001t0008g0014 others(8): Show |
14 | HG02055.hp1 HG02109.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.509-2488G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43836222 | |||||||
| chr22:43836257 | G | C | 11 | a0001c0001t0006g0135 a0001c0001t0006g0136 a0001c0001t0008g0014 others(8): Show |
14 | HG02055.hp1 HG02109.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.509-2523C>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43836257 | |||||||
| chr22:43836285 | A | G | 54 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0012 others(51): Show |
81 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.509-2551T>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43836285 | |||||||
| chr22:43836341 | C | T | 11 | a0001c0001t0006g0135 a0001c0001t0006g0136 a0001c0001t0008g0014 others(8): Show |
14 | HG02055.hp1 HG02109.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.508+2526G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43836341 | |||||||
| chr22:43836349 | A | T | 2 | a0001c0001t0013g0087 a0001c0001t0013g0088 |
2 | HG01069.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.508+2518T>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43836349 | |||||||
| chr22:43836383 | C | G | 13 | a0001c0001t0006g0135 a0001c0001t0006g0136 a0001c0001t0008g0014 others(10): Show |
16 | HG01069.hp1 HG01175.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.508+2484G>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43836383 | |||||||
| chr22:43836388 | T | C | 11 | a0001c0001t0006g0135 a0001c0001t0006g0136 a0001c0001t0008g0014 others(8): Show |
14 | HG02055.hp1 HG02109.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.508+2479A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43836388 | |||||||
| chr22:43836397 | C | T | 43 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0019 others(40): Show |
56 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.508+2470G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43836397 | |||||||
| chr22:43836404 | A | C | 54 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0012 others(51): Show |
81 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.508+2463T>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43836404 | |||||||
| chr22:43836405 | C | A | 54 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0012 others(51): Show |
81 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.508+2462G>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43836405 | |||||||
| chr22:43836413 | G | A | 1 | a0001c0001t0006g0137 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.508+2454C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43836413 | |||||||
| chr22:43836425 | C | T | 11 | a0001c0001t0006g0135 a0001c0001t0006g0136 a0001c0001t0008g0014 others(8): Show |
14 | HG02055.hp1 HG02109.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.508+2442G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43836425 | |||||||
| chr22:43836440 | G | A | 1 | a0001c0001t0003g0085 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.508+2427C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43836440 | |||||||
| chr22:43836446 | A | C | 11 | a0001c0001t0006g0135 a0001c0001t0006g0136 a0001c0001t0008g0014 others(8): Show |
14 | HG02055.hp1 HG02109.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.508+2421T>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43836446 | |||||||
| chr22:43836447 | C | A | 11 | a0001c0001t0006g0135 a0001c0001t0006g0136 a0001c0001t0008g0014 others(8): Show |
14 | HG02055.hp1 HG02109.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.508+2420G>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43836447 | |||||||
| chr22:43836467 | T | C | 11 | a0001c0001t0006g0135 a0001c0001t0006g0136 a0001c0001t0008g0014 others(8): Show |
14 | HG02055.hp1 HG02109.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.508+2400A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43836467 | |||||||
| chr22:43836488 | C | A | 11 | a0001c0001t0006g0135 a0001c0001t0006g0136 a0001c0001t0008g0014 others(8): Show |
14 | HG02055.hp1 HG02109.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.508+2379G>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43836488 | |||||||
| chr22:43836489 | A | C | 11 | a0001c0001t0006g0135 a0001c0001t0006g0136 a0001c0001t0008g0014 others(8): Show |
14 | HG02055.hp1 HG02109.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.508+2378T>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43836489 | |||||||
| chr22:43836514 | CCTACACA others(77): Show |
C | 65 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0012 others(62): Show |
95 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.508+2269_508+2352d others(86): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43836514 | |||||||
| chr22:43836613 | C | G | 65 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0012 others(62): Show |
95 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.508+2254G>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43836613 | |||||||
| chr22:43836635 | T | G | 66 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0012 others(63): Show |
96 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.508+2232A>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43836635 | |||||||
| chr22:43836800 | A | T | 6 | a0001c0001t0006g0135 a0001c0001t0006g0136 a0001c0001t0008g0014 others(3): Show |
9 | HG02055.hp1 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.508+2067T>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43836800 | |||||||
| chr22:43836854 | G | A | 2 | a0001c0001t0003g0065 a0001c0001t0003g0077 |
2 | HG01109.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.508+2013C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43836854 | |||||||
| chr22:43837007 | G | C | 176 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(173): Show |
266 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.508+1860C>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43837007 | |||||||
| chr22:43837164 | T | G | 16 | a0001c0001t0005g0032 a0001c0001t0005g0109 a0001c0001t0005g0113 others(13): Show |
18 | HG01069.hp1 HG01175.hp1 HG01433.hp2 others(15): Show |
intron_variant | MODIFIER | c.508+1703A>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43837164 | |||||||
| chr22:43837169 | G | A | 1 | a0001c0001t0006g0143 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.508+1698C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43837169 | |||||||
| chr22:43837200 | G | A | 1 | a0001c0001t0003g0078 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.508+1667C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43837200 | |||||||
| chr22:43837495 | G | C | 1 | a0001c0001t0005g0114 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.508+1372C>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43837495 | |||||||
| chr22:43837546 | A | G | 28 | a0001c0001t0004g0002 a0001c0001t0004g0013 a0001c0001t0004g0028 others(25): Show |
49 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.508+1321T>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43837546 | |||||||
| chr22:43837560 | G | C | 1 | a0001c0001t0002g0240 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.508+1307C>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43837560 | |||||||
| chr22:43838143 | C | T | 1 | a0001c0001t0008g0134 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.508+724G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43838143 | |||||||
| chr22:43838159 | G | A | 15 | a0001c0001t0004g0002 a0001c0001t0004g0013 a0001c0001t0004g0028 others(12): Show |
29 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.508+708C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43838159 | |||||||
| chr22:43838167 | G | A | 8 | a0001c0001t0006g0009 a0001c0001t0006g0111 a0001c0001t0006g0126 others(5): Show |
12 | HG01069.hp1 HG01175.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.508+700C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43838167 | |||||||
| chr22:43838203 | A | G | 261 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(258): Show |
382 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(379): Show |
intron_variant | MODIFIER | c.508+664T>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43838203 | |||||||
| chr22:43838265 | C | T | 1 | a0001c0001t0006g0143 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.508+602G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43838265 | |||||||
| chr22:43838406 | G | A | 1 | a0001c0001t0006g0112 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.508+461C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43838406 | |||||||
| chr22:43838446 | G | C | 2 | a0001c0001t0006g0135 a0001c0001t0006g0136 |
2 | HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.508+421C>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43838446 | |||||||
| chr22:43838504 | T | C | 2 | a0001c0001t0003g0022 a0001c0001t0003g0053 |
3 | HG01109.hp2 HG02886.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.508+363A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43838504 | |||||||
| chr22:43838619 | G | A | 1 | a0001c0001t0006g0106 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.508+248C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43838619 | |||||||
| chr22:43838848 | G | T | 1 | a0001c0001t0002g0044 | 2 | HG00408.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.508+19C>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | 43838848 | |||||||
| chr22:43839053 | C | T | 54 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0012 others(51): Show |
81 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.382-60G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 3/6 | chr22 | 43839053 | |||||||
| chr22:43839106 | G | C | 1 | a0001c0001t0006g0146 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.382-113C>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 3/6 | chr22 | 43839106 | |||||||
| chr22:43839321 | C | T | 1 | a0001c0001t0003g0079 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.382-328G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 3/6 | chr22 | 43839321 | |||||||
| chr22:43839566 | C | T | 1 | a0001c0001t0005g0121 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.381+379G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 3/6 | chr22 | 43839566 | |||||||
| chr22:43839815 | G | A | 1 | a0001c0001t0005g0114 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.381+130C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 3/6 | chr22 | 43839815 | |||||||
| chr22:43839895 | C | T | 1 | a0001c0001t0002g0218 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.381+50G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 3/6 | chr22 | 43839895 | |||||||
| chr22:43840123 | G | C | 1 | a0001c0001t0005g0120 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.301-98C>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 2/6 | chr22 | 43840123 | |||||||
| chr22:43840125 | G | A | 74 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(71): Show |
110 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.301-100C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 2/6 | chr22 | 43840125 | |||||||
| chr22:43840159 | G | A | 54 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0012 others(51): Show |
81 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.301-134C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 2/6 | chr22 | 43840159 | |||||||
| chr22:43840261 | G | A | 4 | a0001c0001t0006g0036 a0001c0001t0006g0143 a0001c0001t0006g0144 others(1): Show |
5 | HG03195.hp2 HG03209.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.301-236C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 2/6 | chr22 | 43840261 | |||||||
| chr22:43840288 | G | A | 6 | a0001c0001t0001g0019 a0001c0001t0001g0155 a0001c0001t0001g0161 others(3): Show |
8 | NA18940.hp1 NA18950.hp1 NA18979.hp1 others(5): Show |
intron_variant | MODIFIER | c.301-263C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 2/6 | chr22 | 43840288 | |||||||
| chr22:43840382 | G | A | 3 | a0001c0001t0005g0105 a0001c0001t0005g0141 a0001c0003t0005g0104 |
3 | HG02559.hp2 HG02630.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.301-357C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 2/6 | chr22 | 43840382 | |||||||
| chr22:43840527 | G | A | 1 | a0001c0001t0003g0082 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.301-502C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 2/6 | chr22 | 43840527 | |||||||
| chr22:43840540 | G | T | 2 | a0001c0001t0002g0229 a0001c0001t0002g0230 |
2 | NA18946.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.301-515C>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 2/6 | chr22 | 43840540 | |||||||
| chr22:43840561 | G | A | 54 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0012 others(51): Show |
81 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.301-536C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 2/6 | chr22 | 43840561 | |||||||
| chr22:43840580 | G | A | 3 | a0001c0001t0003g0008 a0001c0001t0003g0083 a0001c0001t0003g0084 |
7 | HG00099.hp1 HG01167.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.301-555C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 2/6 | chr22 | 43840580 | |||||||
| chr22:43840601 | G | A | 6 | a0001c0001t0006g0132 a0001c0001t0006g0135 a0001c0001t0006g0136 others(3): Show |
9 | HG02055.hp1 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.301-576C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 2/6 | chr22 | 43840601 | |||||||
| chr22:43840753 | C | G | 4 | a0001c0001t0006g0036 a0001c0001t0006g0143 a0001c0001t0006g0144 others(1): Show |
5 | HG03195.hp2 HG03209.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.301-728G>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 2/6 | chr22 | 43840753 | |||||||
| chr22:43840805 | C | T | 2 | a0001c0001t0003g0022 a0001c0001t0003g0053 |
3 | HG01109.hp2 HG02886.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.301-780G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 2/6 | chr22 | 43840805 | |||||||
| chr22:43840920 | GC | G | 30 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0037 others(27): Show |
53 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.300+881delG | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 2/6 | chr22 | 43840920 | |||||||
| chr22:43840936 | G | C | 54 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0012 others(51): Show |
81 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.300+866C>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 2/6 | chr22 | 43840936 | |||||||
| chr22:43840984 | C | T | 70 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0011 others(67): Show |
102 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.300+818G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 2/6 | chr22 | 43840984 | |||||||
| chr22:43841029 | A | G | 1 | a0001c0001t0002g0248 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.300+773T>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 2/6 | chr22 | 43841029 | |||||||
| chr22:43841084 | C | T | 5 | a0001c0001t0014g0129 a0001c0001t0014g0130 a0001c0001t0015g0107 others(2): Show |
5 | HG02109.hp2 HG02572.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.300+718G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 2/6 | chr22 | 43841084 | |||||||
| chr22:43841101 | C | A | 1 | a0001c0001t0005g0123 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.300+701G>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 2/6 | chr22 | 43841101 | |||||||
| chr22:43841102 | G | A | 54 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0012 others(51): Show |
81 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.300+700C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 2/6 | chr22 | 43841102 | |||||||
| chr22:43841160 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.300+642C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 2/6 | chr22 | 43841160 | |||||||
| chr22:43841371 | C | T | 1 | a0001c0001t0002g0253 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.300+431G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 2/6 | chr22 | 43841371 | |||||||
| chr22:43841447 | T | C | 1 | a0001c0001t0001g0192 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.300+355A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 2/6 | chr22 | 43841447 | |||||||
| chr22:43841522 | C | A | 54 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0012 others(51): Show |
81 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.300+280G>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 2/6 | chr22 | 43841522 | |||||||
| chr22:43841580 | C | T | 2 | a0001c0001t0013g0087 a0001c0001t0013g0088 |
2 | HG01069.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.300+222G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 2/6 | chr22 | 43841580 | |||||||
| chr22:43841752 | T | C | 1 | a0001c0001t0011g0050 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.300+50A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 2/6 | chr22 | 43841752 | |||||||
| chr22:43842218 | G | A | 5 | a0001c0001t0006g0009 a0001c0001t0006g0126 a0001c0001t0006g0137 others(2): Show |
9 | HG01243.hp1 HG01496.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.170-286C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43842218 | |||||||
| chr22:43842290 | G | C | 1 | a0001c0001t0001g0189 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.170-358C>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43842290 | |||||||
| chr22:43842296 | A | T | 3 | a0001c0001t0005g0105 a0001c0001t0005g0141 a0001c0003t0005g0104 |
3 | HG02559.hp2 HG02630.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.170-364T>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43842296 | |||||||
| chr22:43842386 | G | A | 10 | a0001c0001t0005g0032 a0001c0001t0005g0109 a0001c0001t0005g0113 others(7): Show |
12 | HG02055.hp2 HG02559.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.170-454C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43842386 | |||||||
| chr22:43842416 | C | T | 74 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(71): Show |
110 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.170-484G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43842416 | |||||||
| chr22:43842425 | G | A | 2 | a0001c0001t0001g0173 a0001c0001t0001g0174 |
2 | NA18974.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.170-493C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43842425 | |||||||
| chr22:43842443 | T | C | 3 | a0001c0001t0001g0037 a0001c0001t0001g0189 a0001c0001t0001g0200 |
4 | HG00099.hp2 HG00140.hp2 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.170-511A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43842443 | |||||||
| chr22:43842525 | T | G | 129 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(126): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.170-593A>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43842525 | |||||||
| chr22:43842568 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.170-636G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43842568 | |||||||
| chr22:43842641 | C | A | 55 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0012 others(52): Show |
82 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.170-709G>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43842641 | |||||||
| chr22:43842924 | G | C | 1 | a0001c0001t0004g0095 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.170-992C>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43842924 | |||||||
| chr22:43842948 | C | T | 1 | a0001c0001t0002g0227 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.170-1016G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43842948 | |||||||
| chr22:43842975 | A | ATC | 52 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0037 others(49): Show |
92 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(89): Show |
intron_variant | MODIFIER | c.170-1045_170-1044d others(4): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43842975 | |||||||
| chr22:43842975 | A | ATCTC | 59 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0039 others(56): Show |
74 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.170-1047_170-1044d others(6): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43842975 | |||||||
| chr22:43842975 | A | ATCTCTC | 18 | a0001c0001t0001g0019 a0001c0001t0001g0175 a0001c0001t0001g0181 others(15): Show |
29 | HG00280.hp1 HG01069.hp2 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.170-1049_170-1044d others(8): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43842975 | |||||||
| chr22:43842975 | A | ATCTCTCT others(1): Show |
20 | a0001c0001t0002g0222 a0001c0001t0003g0007 a0001c0001t0003g0023 others(17): Show |
28 | HG01884.hp2 HG02055.hp2 HG02280.hp2 others(25): Show |
intron_variant | MODIFIER | c.170-1051_170-1044d others(10): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43842975 | |||||||
| chr22:43842975 | A | ATCTCTCT others(3): Show |
4 | a0001c0001t0003g0067 a0001c0001t0003g0085 a0001c0001t0009g0089 others(1): Show |
4 | HG02486.hp2 HG02647.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.170-1053_170-1044d others(12): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43842975 | |||||||
| chr22:43842975 | A | ATCTCTCT others(5): Show |
35 | a0001c0001t0003g0008 a0001c0001t0003g0012 a0001c0001t0003g0017 others(32): Show |
56 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.170-1055_170-1044d others(14): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43842975 | |||||||
| chr22:43842975 | A | ATCTCTCT others(7): Show |
3 | a0001c0001t0003g0061 a0001c0001t0003g0083 a0001c0001t0018g0047 |
3 | HG02738.hp1 HG02896.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.170-1057_170-1044d others(16): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43842975 | |||||||
| chr22:43842975 | A | ATCTCTCT others(9): Show |
2 | a0001c0001t0003g0064 a0001c0001t0012g0072 |
2 | HG01243.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.170-1059_170-1044d others(18): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43842975 | |||||||
| chr22:43842975 | A | ATCTCTCT others(11): Show |
2 | a0001c0001t0003g0052 a0001c0001t0003g0059 |
2 | HG01884.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.170-1061_170-1044d others(20): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43842975 | |||||||
| chr22:43842975 | A | ATCTCTCT others(13): Show |
1 | a0001c0001t0003g0058 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.170-1063_170-1044d others(22): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43842975 | |||||||
| chr22:43843094 | G | A | 1 | a0001c0001t0005g0034 | 2 | HG00738.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.170-1162C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43843094 | |||||||
| chr22:43843177 | G | A | 7 | a0001c0001t0006g0009 a0001c0001t0006g0126 a0001c0001t0006g0137 others(4): Show |
11 | HG01069.hp1 HG01175.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.170-1245C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43843177 | |||||||
| chr22:43843197 | T | C | 1 | a0001c0001t0013g0088 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.170-1265A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43843197 | |||||||
| chr22:43843212 | C | T | 1 | a0002c0002t0020g0051 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.170-1280G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43843212 | |||||||
| chr22:43843311 | A | G | 1 | a0001c0001t0001g0037 | 2 | HG00140.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.170-1379T>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43843311 | |||||||
| chr22:43843316 | A | G | 55 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0012 others(52): Show |
82 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.170-1384T>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43843316 | |||||||
| chr22:43843415 | C | A | 1 | a0001c0001t0005g0118 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.170-1483G>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43843415 | |||||||
| chr22:43843619 | T | C | 247 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(244): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.170-1687A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43843619 | |||||||
| chr22:43843690 | G | A | 1 | a0001c0001t0003g0080 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.170-1758C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43843690 | |||||||
| chr22:43843721 | C | T | 6 | a0001c0001t0001g0019 a0001c0001t0001g0155 a0001c0001t0001g0161 others(3): Show |
8 | NA18940.hp1 NA18950.hp1 NA18979.hp1 others(5): Show |
intron_variant | MODIFIER | c.170-1789G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43843721 | |||||||
| chr22:43843870 | G | T | 15 | a0001c0001t0004g0002 a0001c0001t0004g0013 a0001c0001t0004g0028 others(12): Show |
29 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.170-1938C>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43843870 | |||||||
| chr22:43843982 | G | A | 2 | a0001c0001t0004g0096 a0001c0001t0004g0101 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.170-2050C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43843982 | |||||||
| chr22:43844188 | T | G | 2 | a0001c0001t0001g0175 a0001c0001t0001g0181 |
2 | NA18940.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.170-2256A>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43844188 | |||||||
| chr22:43844282 | T | C | 54 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0012 others(51): Show |
79 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.170-2350A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43844282 | |||||||
| chr22:43844334 | G | A | 2 | a0001c0001t0004g0013 a0001c0001t0004g0102 |
5 | HG02257.hp1 HG02258.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.170-2402C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43844334 | |||||||
| chr22:43844342 | C | T | 1 | a0001c0001t0002g0226 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.170-2410G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43844342 | |||||||
| chr22:43844425 | G | C | 4 | a0001c0001t0006g0036 a0001c0001t0006g0143 a0001c0001t0006g0144 others(1): Show |
5 | HG03195.hp2 HG03209.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.170-2493C>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43844425 | |||||||
| chr22:43844547 | A | C | 1 | a0001c0001t0001g0192 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.170-2615T>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43844547 | |||||||
| chr22:43844685 | C | T | 2 | a0001c0001t0006g0009 a0001c0001t0006g0137 |
6 | HG01243.hp1 HG01496.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.170-2753G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43844685 | |||||||
| chr22:43844805 | C | T | 247 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(244): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.170-2873G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43844805 | |||||||
| chr22:43844831 | C | T | 1 | a0001c0001t0002g0221 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.170-2899G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43844831 | |||||||
| chr22:43844832 | G | A | 1 | a0001c0001t0006g0132 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.170-2900C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43844832 | |||||||
| chr22:43844879 | A | G | 2 | a0001c0001t0003g0070 a0001c0001t0003g0071 |
2 | HG02615.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.170-2947T>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43844879 | |||||||
| chr22:43844983 | C | T | 1 | a0001c0001t0003g0069 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.170-3051G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43844983 | |||||||
| chr22:43845095 | T | C | 261 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(258): Show |
382 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(379): Show |
intron_variant | MODIFIER | c.170-3163A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43845095 | |||||||
| chr22:43845230 | G | A | 1 | a0001c0001t0001g0185 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.170-3298C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43845230 | |||||||
| chr22:43845396 | T | C | 54 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0012 others(51): Show |
81 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.170-3464A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43845396 | |||||||
| chr22:43845405 | C | T | 44 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0019 others(41): Show |
57 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.170-3473G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43845405 | |||||||
| chr22:43845509 | G | A | 7 | a0001c0001t0006g0009 a0001c0001t0006g0126 a0001c0001t0006g0137 others(4): Show |
11 | HG01069.hp1 HG01175.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.170-3577C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43845509 | |||||||
| chr22:43845521 | G | A | 54 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0012 others(51): Show |
81 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.170-3589C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43845521 | |||||||
| chr22:43845550 | CT | C | 15 | a0001c0001t0004g0002 a0001c0001t0004g0013 a0001c0001t0004g0028 others(12): Show |
29 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.170-3619delA | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43845550 | |||||||
| chr22:43845562 | G | A | 44 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0019 others(41): Show |
57 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.170-3630C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43845562 | |||||||
| chr22:43845599 | C | T | 1 | a0001c0001t0006g0106 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.170-3667G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43845599 | |||||||
| chr22:43845646 | G | T | 15 | a0001c0001t0004g0002 a0001c0001t0004g0013 a0001c0001t0004g0028 others(12): Show |
29 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.170-3714C>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43845646 | |||||||
| chr22:43845689 | G | A | 1 | a0001c0001t0003g0057 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.170-3757C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43845689 | |||||||
| chr22:43845693 | C | T | 54 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0012 others(51): Show |
81 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.170-3761G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43845693 | |||||||
| chr22:43845694 | G | A | 1 | a0001c0001t0001g0192 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.170-3762C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43845694 | |||||||
| chr22:43845719 | G | A | 1 | a0001c0001t0002g0238 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.170-3787C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43845719 | |||||||
| chr22:43845759 | A | G | 1 | a0001c0001t0006g0106 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.170-3827T>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43845759 | |||||||
| chr22:43845780 | T | C | 2 | a0001c0001t0003g0023 a0001c0001t0003g0066 |
3 | HG01884.hp2 HG02280.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.170-3848A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43845780 | |||||||
| chr22:43845938 | C | T | 14 | a0001c0001t0005g0032 a0001c0001t0005g0105 a0001c0001t0005g0109 others(11): Show |
16 | HG02055.hp2 HG02559.hp1 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.170-4006G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43845938 | |||||||
| chr22:43846187 | C | T | 247 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(244): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.170-4255G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43846187 | |||||||
| chr22:43846222 | C | T | 15 | a0001c0001t0004g0002 a0001c0001t0004g0013 a0001c0001t0004g0028 others(12): Show |
29 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.170-4290G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43846222 | |||||||
| chr22:43846311 | C | T | 1 | a0001c0001t0003g0068 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.170-4379G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43846311 | |||||||
| chr22:43846396 | G | T | 1 | a0001c0001t0004g0099 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.170-4464C>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43846396 | |||||||
| chr22:43846807 | G | C | 4 | a0001c0001t0008g0014 a0001c0001t0008g0131 a0001c0001t0008g0133 others(1): Show |
7 | HG02055.hp1 HG02572.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.170-4875C>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43846807 | |||||||
| chr22:43847212 | C | T | 1 | a0001c0001t0006g0127 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.170-5280G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43847212 | |||||||
| chr22:43847590 | T | C | 15 | a0001c0001t0004g0002 a0001c0001t0004g0013 a0001c0001t0004g0028 others(12): Show |
29 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.170-5658A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43847590 | |||||||
| chr22:43847704 | G | A | 2 | a0001c0001t0003g0056 a0001c0001t0003g0057 |
2 | HG03471.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.170-5772C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43847704 | |||||||
| chr22:43847799 | G | A | 5 | a0001c0001t0014g0129 a0001c0001t0014g0130 a0001c0001t0015g0107 others(2): Show |
5 | HG02109.hp2 HG02572.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.170-5867C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43847799 | |||||||
| chr22:43847809 | G | A | 7 | a0001c0001t0006g0132 a0001c0001t0006g0135 a0001c0001t0006g0136 others(4): Show |
10 | HG02055.hp1 HG02572.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.170-5877C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43847809 | |||||||
| chr22:43847894 | C | G | 232 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(229): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.170-5962G>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43847894 | |||||||
| chr22:43848119 | G | A | 73 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(70): Show |
109 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.170-6187C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43848119 | |||||||
| chr22:43848149 | C | T | 1 | a0001c0001t0022g0091 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.170-6217G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43848149 | |||||||
| chr22:43848226 | A | G | 48 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0012 others(45): Show |
74 | HG00099.hp1 HG00323.hp2 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.170-6294T>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43848226 | |||||||
| chr22:43848253 | G | A | 1 | a0001c0001t0002g0239 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.170-6321C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43848253 | |||||||
| chr22:43848403 | C | G | 2 | a0001c0001t0002g0224 a0001c0001t0002g0225 |
2 | NA18979.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.170-6471G>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43848403 | |||||||
| chr22:43848422 | C | A | 232 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(229): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.170-6490G>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43848422 | |||||||
| chr22:43848580 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.170-6648G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43848580 | |||||||
| chr22:43848719 | G | A | 1 | a0001c0001t0005g0114 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.170-6787C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43848719 | |||||||
| chr22:43848741 | A | G | 247 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(244): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.170-6809T>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43848741 | |||||||
| chr22:43849106 | C | T | 54 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0012 others(51): Show |
81 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.170-7174G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43849106 | |||||||
| chr22:43849107 | C | T | 4 | a0001c0001t0006g0036 a0001c0001t0006g0143 a0001c0001t0006g0144 others(1): Show |
5 | HG03195.hp2 HG03209.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.170-7175G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43849107 | |||||||
| chr22:43849129 | G | T | 74 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(71): Show |
110 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.170-7197C>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43849129 | |||||||
| chr22:43849201 | T | C | 231 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(228): Show |
348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.170-7269A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43849201 | |||||||
| chr22:43849258 | T | A | 1 | a0001c0001t0008g0131 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.170-7326A>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43849258 | |||||||
| chr22:43849299 | G | T | 248 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(245): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.170-7367C>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43849299 | |||||||
| chr22:43849314 | G | A | 2 | a0001c0001t0006g0126 a0001c0001t0006g0138 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.170-7382C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43849314 | |||||||
| chr22:43849391 | G | A | 52 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0012 others(49): Show |
79 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.170-7459C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43849391 | |||||||
| chr22:43849509 | C | T | 1 | a0001c0001t0001g0158 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.170-7577G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43849509 | |||||||
| chr22:43849545 | G | A | 1 | a0001c0001t0002g0240 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.170-7613C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43849545 | |||||||
| chr22:43849837 | C | T | 3 | a0001c0001t0005g0105 a0001c0001t0005g0141 a0001c0003t0005g0104 |
3 | HG02559.hp2 HG02630.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.170-7905G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43849837 | |||||||
| chr22:43850227 | A | G | 74 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(71): Show |
110 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.170-8295T>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43850227 | |||||||
| chr22:43850252 | C | T | 54 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0012 others(51): Show |
81 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.170-8320G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43850252 | |||||||
| chr22:43850562 | C | T | 7 | a0001c0001t0006g0132 a0001c0001t0006g0135 a0001c0001t0006g0136 others(4): Show |
10 | HG02055.hp1 HG02572.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.170-8630G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43850562 | |||||||
| chr22:43850596 | T | C | 261 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(258): Show |
382 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(379): Show |
intron_variant | MODIFIER | c.170-8664A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43850596 | |||||||
| chr22:43850860 | C | T | 53 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0012 others(50): Show |
80 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.170-8928G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43850860 | |||||||
| chr22:43850877 | C | A | 54 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0012 others(51): Show |
81 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.170-8945G>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43850877 | |||||||
| chr22:43850989 | T | C | 2 | a0001c0001t0002g0252 a0001c0001t0002g0257 |
2 | HG02135.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.170-9057A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43850989 | |||||||
| chr22:43851205 | G | T | 7 | a0001c0001t0006g0009 a0001c0001t0006g0126 a0001c0001t0006g0137 others(4): Show |
11 | HG01069.hp1 HG01175.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.170-9273C>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43851205 | |||||||
| chr22:43851208 | G | C | 4 | a0001c0001t0006g0036 a0001c0001t0006g0143 a0001c0001t0006g0144 others(1): Show |
5 | HG03195.hp2 HG03209.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.170-9276C>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43851208 | |||||||
| chr22:43851494 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.170-9562C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43851494 | |||||||
| chr22:43851624 | G | A | 3 | a0001c0001t0005g0105 a0001c0001t0005g0141 a0001c0003t0005g0104 |
3 | HG02559.hp2 HG02630.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.170-9692C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43851624 | |||||||
| chr22:43851900 | A | C | 55 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0012 others(52): Show |
82 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.170-9968T>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43851900 | |||||||
| chr22:43851905 | T | C | 2 | a0001c0001t0009g0089 a0001c0001t0009g0090 |
2 | HG02717.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.170-9973A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43851905 | |||||||
| chr22:43851908 | G | A | 74 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(71): Show |
110 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.170-9976C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43851908 | |||||||
| chr22:43851988 | C | T | 2 | a0001c0001t0004g0097 a0001c0001t0004g0098 |
2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.170-10056G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43851988 | |||||||
| chr22:43852137 | C | T | 1 | a0001c0001t0002g0252 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.169+10077G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43852137 | |||||||
| chr22:43852345 | G | T | 1 | a0001c0001t0003g0082 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.169+9869C>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43852345 | |||||||
| chr22:43852348 | G | GT | 128 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(125): Show |
191 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(188): Show |
intron_variant | MODIFIER | c.169+9865dupA | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43852348 | |||||||
| chr22:43852348 | G | GTT | 9 | a0001c0001t0001g0157 a0001c0001t0001g0194 a0001c0001t0001g0205 others(6): Show |
14 | HG00280.hp1 HG00280.hp2 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.169+9864_169+9865d others(4): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43852348 | |||||||
| chr22:43852351 | T | G | 15 | a0001c0001t0004g0002 a0001c0001t0004g0013 a0001c0001t0004g0028 others(12): Show |
29 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.169+9863A>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43852351 | |||||||
| chr22:43852391 | C | T | 1 | a0001c0001t0001g0193 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.169+9823G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43852391 | |||||||
| chr22:43852406 | A | C | 1 | a0001c0001t0006g0132 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.169+9808T>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43852406 | |||||||
| chr22:43852597 | C | T | 5 | a0001c0001t0006g0009 a0001c0001t0006g0126 a0001c0001t0006g0137 others(2): Show |
9 | HG01243.hp1 HG01496.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.169+9617G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43852597 | |||||||
| chr22:43852624 | G | A | 53 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0012 others(50): Show |
80 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.169+9590C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43852624 | |||||||
| chr22:43852637 | C | T | 2 | a0001c0001t0002g0222 a0001c0001t0002g0223 |
2 | NA19004.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.169+9577G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43852637 | |||||||
| chr22:43852663 | T | C | 4 | a0001c0001t0001g0010 a0001c0001t0001g0177 a0001c0001t0001g0182 others(1): Show |
8 | HG02040.hp1 HG02071.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.169+9551A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43852663 | |||||||
| chr22:43852721 | C | T | 65 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0011 others(62): Show |
97 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.169+9493G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43852721 | |||||||
| chr22:43852747 | G | C | 53 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0012 others(50): Show |
80 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.169+9467C>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43852747 | |||||||
| chr22:43852760 | C | T | 2 | a0001c0001t0003g0024 a0001c0001t0003g0063 |
3 | HG03688.hp2 HG03834.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.169+9454G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43852760 | |||||||
| chr22:43852996 | G | T | 2 | a0001c0001t0002g0217 a0001c0001t0002g0251 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.169+9218C>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43852996 | |||||||
| chr22:43852999 | C | A | 3 | a0001c0001t0002g0011 a0001c0001t0002g0046 a0001c0001t0002g0263 |
8 | HG00280.hp1 HG01261.hp1 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.169+9215G>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43852999 | |||||||
| chr22:43853140 | T | A | 1 | a0001c0001t0001g0178 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.169+9074A>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43853140 | |||||||
| chr22:43853222 | C | T | 2 | a0001c0001t0003g0023 a0001c0001t0003g0066 |
3 | HG01884.hp2 HG02280.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.169+8992G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43853222 | |||||||
| chr22:43853389 | G | A | 54 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0012 others(51): Show |
81 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.169+8825C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43853389 | |||||||
| chr22:43853397 | G | C | 1 | a0001c0001t0001g0203 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.169+8817C>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43853397 | |||||||
| chr22:43853402 | G | C | 1 | a0001c0001t0001g0183 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.169+8812C>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43853402 | |||||||
| chr22:43853477 | C | T | 1 | a0001c0001t0005g0119 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.169+8737G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43853477 | |||||||
| chr22:43853500 | C | T | 1 | a0001c0001t0002g0221 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.169+8714G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43853500 | |||||||
| chr22:43853583 | C | A | 74 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(71): Show |
110 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.169+8631G>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43853583 | |||||||
| chr22:43853593 | C | G | 1 | a0001c0001t0005g0114 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.169+8621G>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43853593 | |||||||
| chr22:43853597 | G | A | 74 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(71): Show |
110 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.169+8617C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43853597 | |||||||
| chr22:43853819 | A | C | 2 | a0001c0001t0003g0023 a0001c0001t0003g0066 |
3 | HG01884.hp2 HG02280.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.169+8395T>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43853819 | |||||||
| chr22:43853898 | G | C | 74 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(71): Show |
110 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.169+8316C>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43853898 | |||||||
| chr22:43853971 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.169+8243C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43853971 | |||||||
| chr22:43853975 | A | AG | 54 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0012 others(51): Show |
81 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.169+8238dupC | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43853975 | |||||||
| chr22:43854021 | G | A | 2 | a0001c0001t0014g0129 a0001c0001t0014g0130 |
2 | NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.169+8193C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43854021 | |||||||
| chr22:43854024 | C | T | 1 | a0001c0001t0003g0065 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.169+8190G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43854024 | |||||||
| chr22:43854025 | G | A | 75 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(72): Show |
111 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.169+8189C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43854025 | |||||||
| chr22:43854129 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.169+8085G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43854129 | |||||||
| chr22:43854138 | A | G | 1 | a0001c0001t0006g0127 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.169+8076T>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43854138 | |||||||
| chr22:43854187 | C | T | 54 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0012 others(51): Show |
81 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.169+8027G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43854187 | |||||||
| chr22:43854267 | C | T | 1 | a0001c0001t0003g0064 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.169+7947G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43854267 | |||||||
| chr22:43854274 | C | A | 2 | a0001c0001t0005g0113 a0001c0001t0010g0142 |
2 | NA20129.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.169+7940G>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43854274 | |||||||
| chr22:43854381 | C | T | 73 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(70): Show |
109 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.169+7833G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43854381 | |||||||
| chr22:43854616 | C | T | 1 | a0001c0001t0003g0063 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.169+7598G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43854616 | |||||||
| chr22:43854641 | G | A | 1 | a0001c0001t0002g0044 | 2 | HG00408.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.169+7573C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43854641 | |||||||
| chr22:43854690 | A | G | 193 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(190): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(285): Show |
intron_variant | MODIFIER | c.169+7524T>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43854690 | |||||||
| chr22:43854750 | C | T | 74 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(71): Show |
110 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.169+7464G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43854750 | |||||||
| chr22:43854789 | C | T | 2 | a0001c0001t0005g0117 a0001c0001t0005g0118 |
2 | HG02602.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.169+7425G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43854789 | |||||||
| chr22:43854801 | C | T | 1 | a0001c0001t0017g0191 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.169+7413G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43854801 | |||||||
| chr22:43854939 | G | A | 2 | a0001c0001t0016g0179 a0001c0001t0016g0180 |
2 | HG01099.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.169+7275C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43854939 | |||||||
| chr22:43855073 | G | T | 2 | a0001c0001t0013g0087 a0001c0001t0013g0088 |
2 | HG01069.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.169+7141C>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43855073 | |||||||
| chr22:43855269 | C | G | 12 | a0001c0001t0005g0032 a0001c0001t0005g0109 a0001c0001t0005g0113 others(9): Show |
14 | HG02055.hp2 HG02559.hp1 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.169+6945G>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43855269 | |||||||
| chr22:43855309 | G | A | 43 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0019 others(40): Show |
56 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.169+6905C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43855309 | |||||||
| chr22:43855446 | G | A | 65 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0011 others(62): Show |
97 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.169+6768C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43855446 | |||||||
| chr22:43855613 | G | A | 65 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0011 others(62): Show |
97 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.169+6601C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43855613 | |||||||
| chr22:43855711 | T | A | 1 | a0001c0001t0001g0147 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.169+6503A>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43855711 | |||||||
| chr22:43855711 | T | G | 1 | a0001c0001t0009g0027 | 2 | HG02040.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.169+6503A>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43855711 | |||||||
| chr22:43855735 | G | A | 1 | a0001c0001t0002g0244 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.169+6479C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43855735 | |||||||
| chr22:43855768 | C | T | 54 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0012 others(51): Show |
81 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.169+6446G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43855768 | |||||||
| chr22:43855795 | GC | G | 54 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0012 others(51): Show |
81 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.169+6418delG | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43855795 | |||||||
| chr22:43855802 | C | T | 7 | a0001c0001t0006g0132 a0001c0001t0006g0135 a0001c0001t0006g0136 others(4): Show |
10 | HG02055.hp1 HG02572.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.169+6412G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43855802 | |||||||
| chr22:43855911 | C | G | 1 | a0001c0001t0001g0190 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.169+6303G>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43855911 | |||||||
| chr22:43855972 | T | C | 54 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0012 others(51): Show |
81 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.169+6242A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43855972 | |||||||
| chr22:43856090 | A | C | 53 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0012 others(50): Show |
80 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.169+6124T>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43856090 | |||||||
| chr22:43856155 | T | C | 1 | a0001c0001t0002g0245 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.169+6059A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43856155 | |||||||
| chr22:43856184 | T | C | 1 | a0001c0001t0005g0116 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.169+6030A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43856184 | |||||||
| chr22:43856253 | C | T | 1 | a0001c0001t0001g0156 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.169+5961G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43856253 | |||||||
| chr22:43856266 | G | GAAGA | 4 | a0001c0001t0006g0036 a0001c0001t0006g0143 a0001c0001t0006g0144 others(1): Show |
5 | HG03195.hp2 HG03209.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.169+5944_169+5947d others(6): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43856266 | |||||||
| chr22:43856319 | T | C | 1 | a0001c0001t0002g0246 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.169+5895A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43856319 | |||||||
| chr22:43856522 | A | C | 1 | a0001c0001t0008g0131 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.169+5692T>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43856522 | |||||||
| chr22:43856553 | C | T | 1 | a0001c0001t0001g0155 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.169+5661G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43856553 | |||||||
| chr22:43856594 | G | A | 1 | a0001c0001t0001g0205 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.169+5620C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43856594 | |||||||
| chr22:43856683 | C | A | 1 | a0001c0001t0003g0061 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.169+5531G>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43856683 | |||||||
| chr22:43856797 | G | A | 1 | a0001c0001t0003g0061 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.169+5417C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43856797 | |||||||
| chr22:43856945 | C | T | 54 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0012 others(51): Show |
81 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.169+5269G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43856945 | |||||||
| chr22:43857016 | C | CTGATTA | 4 | a0001c0001t0006g0036 a0001c0001t0006g0143 a0001c0001t0006g0144 others(1): Show |
5 | HG03195.hp2 HG03209.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.169+5192_169+5197d others(8): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43857016 | |||||||
| chr22:43857033 | G | C | 1 | a0001c0001t0002g0044 | 2 | HG00408.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.169+5181C>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43857033 | |||||||
| chr22:43857209 | C | T | 54 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0012 others(51): Show |
81 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.169+5005G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43857209 | |||||||
| chr22:43857210 | G | A | 2 | a0001c0001t0006g0135 a0001c0001t0006g0136 |
2 | HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.169+5004C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43857210 | |||||||
| chr22:43857234 | G | A | 1 | a0001c0001t0005g0124 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.169+4980C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43857234 | |||||||
| chr22:43857370 | CA | C | 31 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0183 others(28): Show |
37 | HG00597.hp2 HG00741.hp2 HG01255.hp1 others(34): Show |
intron_variant | MODIFIER | c.169+4843delT | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43857370 | |||||||
| chr22:43857370 | CAA | C | 149 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(146): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.169+4842_169+4843d others(4): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43857370 | |||||||
| chr22:43857370 | CAAA | C | 67 | a0001c0001t0001g0187 a0001c0001t0001g0189 a0001c0001t0002g0217 others(64): Show |
94 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.169+4841_169+4843d others(5): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43857370 | |||||||
| chr22:43857788 | G | A | 54 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0012 others(51): Show |
81 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.169+4426C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43857788 | |||||||
| chr22:43857816 | G | T | 1 | a0001c0001t0002g0248 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.169+4398C>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43857816 | |||||||
| chr22:43857891 | A | C | 1 | a0001c0001t0003g0062 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.169+4323T>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43857891 | |||||||
| chr22:43857926 | T | C | 1 | a0001c0001t0001g0184 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.169+4288A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43857926 | |||||||
| chr22:43858003 | T | A | 54 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0012 others(51): Show |
81 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.169+4211A>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43858003 | |||||||
| chr22:43858035 | G | A | 7 | a0001c0001t0006g0009 a0001c0001t0006g0126 a0001c0001t0006g0137 others(4): Show |
11 | HG01069.hp1 HG01175.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.169+4179C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43858035 | |||||||
| chr22:43858049 | C | CA | 120 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(117): Show |
181 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.169+4164dupT | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43858049 | |||||||
| chr22:43858049 | C | CAA | 52 | a0001c0001t0001g0038 a0001c0001t0001g0151 a0001c0001t0001g0185 others(49): Show |
79 | HG00140.hp1 HG00438.hp2 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.169+4163_169+4164d others(4): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43858049 | |||||||
| chr22:43858049 | CA | C | 53 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0012 others(50): Show |
80 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.169+4164delT | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43858049 | |||||||
| chr22:43858072 | A | G | 1 | a0001c0001t0002g0215 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.169+4142T>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43858072 | |||||||
| chr22:43858084 | A | C | 65 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0011 others(62): Show |
97 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.169+4130T>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43858084 | |||||||
| chr22:43858142 | T | C | 261 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(258): Show |
382 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(379): Show |
intron_variant | MODIFIER | c.169+4072A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43858142 | |||||||
| chr22:43858147 | T | C | 1 | a0001c0001t0002g0258 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.169+4067A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43858147 | |||||||
| chr22:43858223 | G | A | 2 | a0001c0001t0013g0087 a0001c0001t0013g0088 |
2 | HG01069.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.169+3991C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43858223 | |||||||
| chr22:43858479 | G | A | 3 | a0001c0001t0005g0105 a0001c0001t0005g0141 a0001c0003t0005g0104 |
3 | HG02559.hp2 HG02630.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.169+3735C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43858479 | |||||||
| chr22:43858583 | C | T | 1 | a0001c0001t0002g0216 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.169+3631G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43858583 | |||||||
| chr22:43858605 | T | C | 1 | a0001c0001t0010g0139 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.169+3609A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43858605 | |||||||
| chr22:43858629 | T | C | 2 | a0001c0001t0001g0186 a0001c0001t0006g0035 |
3 | HG01516.hp1 HG01517.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.169+3585A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43858629 | |||||||
| chr22:43858649 | C | T | 1 | a0001c0001t0029g0264 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.169+3565G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43858649 | |||||||
| chr22:43858719 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.169+3495G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43858719 | |||||||
| chr22:43858797 | C | T | 13 | a0001c0001t0003g0017 a0001c0001t0003g0022 a0001c0001t0003g0052 others(10): Show |
16 | HG01109.hp2 HG01884.hp1 HG01934.hp2 others(13): Show |
intron_variant | MODIFIER | c.169+3417G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43858797 | |||||||
| chr22:43858804 | G | A | 3 | a0001c0001t0001g0039 a0001c0001t0001g0207 a0001c0001t0001g0208 |
4 | NA18940.hp2 NA18948.hp1 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.169+3410C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43858804 | |||||||
| chr22:43859238 | G | A | 3 | a0001c0001t0002g0259 a0001c0001t0002g0260 a0001c0001t0002g0261 |
3 | HG02523.hp1 NA18954.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.169+2976C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43859238 | |||||||
| chr22:43859296 | G | T | 1 | a0001c0001t0001g0153 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.169+2918C>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43859296 | |||||||
| chr22:43859342 | C | T | 43 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0019 others(40): Show |
56 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.169+2872G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43859342 | |||||||
| chr22:43859384 | C | T | 1 | a0001c0001t0015g0107 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.169+2830G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43859384 | |||||||
| chr22:43859441 | G | A | 1 | a0001c0001t0025g0152 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.169+2773C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43859441 | |||||||
| chr22:43859452 | C | T | 15 | a0001c0001t0004g0002 a0001c0001t0004g0013 a0001c0001t0004g0028 others(12): Show |
29 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.169+2762G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43859452 | |||||||
| chr22:43859647 | C | T | 1 | a0001c0001t0006g0030 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.169+2567G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43859647 | |||||||
| chr22:43859673 | A | G | 1 | a0001c0001t0025g0152 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.169+2541T>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43859673 | |||||||
| chr22:43859767 | G | A | 4 | a0001c0001t0006g0036 a0001c0001t0006g0143 a0001c0001t0006g0144 others(1): Show |
5 | HG03195.hp2 HG03209.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.169+2447C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43859767 | |||||||
| chr22:43859779 | G | A | 1 | a0001c0001t0002g0262 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.169+2435C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43859779 | |||||||
| chr22:43859829 | T | G | 1 | a0001c0001t0006g0140 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.169+2385A>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43859829 | |||||||
| chr22:43859838 | A | G | 1 | a0001c0001t0002g0215 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.169+2376T>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43859838 | |||||||
| chr22:43859948 | T | C | 64 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0011 others(61): Show |
96 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.169+2266A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43859948 | |||||||
| chr22:43859952 | G | A | 194 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(191): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.169+2262C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43859952 | |||||||
| chr22:43859984 | G | C | 1 | a0001c0001t0006g0106 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.169+2230C>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43859984 | |||||||
| chr22:43860016 | G | A | 2 | a0001c0001t0013g0087 a0001c0001t0013g0088 |
2 | HG01069.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.169+2198C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43860016 | |||||||
| chr22:43860046 | C | T | 1 | a0001c0001t0006g0106 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.169+2168G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43860046 | |||||||
| chr22:43860071 | T | C | 1 | a0001c0001t0001g0209 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.169+2143A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43860071 | |||||||
| chr22:43860080 | A | C | 1 | a0001c0001t0001g0151 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.169+2134T>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43860080 | |||||||
| chr22:43860254 | C | T | 1 | a0001c0001t0001g0150 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.169+1960G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43860254 | |||||||
| chr22:43860352 | A | G | 3 | a0001c0001t0005g0105 a0001c0001t0005g0141 a0001c0003t0005g0104 |
3 | HG02559.hp2 HG02630.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.169+1862T>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43860352 | |||||||
| chr22:43860428 | G | C | 54 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0012 others(51): Show |
81 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.169+1786C>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43860428 | |||||||
| chr22:43860568 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.169+1646G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43860568 | |||||||
| chr22:43860587 | C | T | 1 | a0001c0001t0002g0213 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.169+1627G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43860587 | |||||||
| chr22:43860620 | T | C | 1 | a0001c0001t0005g0141 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.169+1594A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43860620 | |||||||
| chr22:43860701 | CA | C | 66 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0011 others(63): Show |
98 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.169+1512delT | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43860701 | |||||||
| chr22:43860847 | A | G | 1 | a0001c0001t0001g0148 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.169+1367T>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43860847 | |||||||
| chr22:43861047 | C | T | 1 | a0001c0001t0001g0147 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.169+1167G>A | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43861047 | |||||||
| chr22:43861171 | C | A | 4 | a0001c0001t0006g0036 a0001c0001t0006g0143 a0001c0001t0006g0144 others(1): Show |
5 | HG03195.hp2 HG03209.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.169+1043G>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43861171 | |||||||
| chr22:43861176 | A | G | 15 | a0001c0001t0004g0002 a0001c0001t0004g0013 a0001c0001t0004g0028 others(12): Show |
29 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.169+1038T>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43861176 | |||||||
| chr22:43861364 | T | C | 55 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0012 others(52): Show |
82 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.169+850A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43861364 | |||||||
| chr22:43861547 | A | G | 15 | a0001c0001t0004g0002 a0001c0001t0004g0013 a0001c0001t0004g0028 others(12): Show |
29 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.169+667T>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43861547 | |||||||
| chr22:43861651 | G | A | 1 | a0001c0001t0010g0142 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.169+563C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43861651 | |||||||
| chr22:43861694 | G | A | 3 | a0001c0001t0002g0011 a0001c0001t0002g0046 a0001c0001t0002g0263 |
8 | HG00280.hp1 HG01261.hp1 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.169+520C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43861694 | |||||||
| chr22:43861713 | C | G | 1 | a0001c0001t0005g0092 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.169+501G>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43861713 | |||||||
| chr22:43861882 | C | A | 66 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0011 others(63): Show |
98 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.169+332G>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43861882 | |||||||
| chr22:43861953 | T | C | 55 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0012 others(52): Show |
82 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.169+261A>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43861953 | |||||||
| chr22:43862091 | A | G | 55 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0012 others(52): Show |
82 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.169+123T>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43862091 | |||||||
| chr22:43862123 | A | G | 55 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0012 others(52): Show |
82 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.169+91T>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43862123 | |||||||
| chr22:43862134 | C | G | 55 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0012 others(52): Show |
82 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.169+80G>C | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43862134 | |||||||
| chr22:43862156 | G | C | 70 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0011 others(67): Show |
103 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.169+58C>G | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43862156 | |||||||
| chr22:43862196 | G | A | 1 | a0001c0001t0006g0146 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.169+18C>T | SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 1/6 | chr22 | 43862196 |