Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 6820 |
| ensemblid | ENSG00000088002.12 |
| hgncid | 11459 |
| symbol | SULT2B1 |
| name | sulfotransferase family 2B member 1 |
| refseq_nuc | NM_177973.2 |
| refseq_prot | NP_814444.1 |
| ensembl_nuc | ENST00000201586.7 |
| ensembl_prot | ENSP00000201586.2 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 48552172 |
| end | 48599423 |
| strand | + |
| ver | v1.2 |
| region | chr19:48552172-48599423 |
| region5000 | chr19:48547172-48604423 |
| regionname0 | SULT2B1_chr19_48552172_48599423 |
| regionname5000 | SULT2B1_chr19_48547172_48604423 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 365 | 356 | 92 | 81 | 131 | 11 | 39 | 91 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | MDGPA others(360): Show |
chr19 | 48547172 | 48604423 |
| a0002 | 0/0 | 365 | 9 | 0 | 0 | 9 | 0 | 0 | 4 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | MDGPA others(360): Show |
chr19 | 48547172 | 48604423 |
| a0003 | 0/0 | 365 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | MDGPA others(360): Show |
chr19 | 48547172 | 48604423 |
| a0004 | 0/0 | 365 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | MDGPA others(360): Show |
chr19 | 48547172 | 48604423 |
| a0005 | 0/0 | 365 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | MDGPA others(360): Show |
chr19 | 48547172 | 48604423 |
| a0006 | 0/0 | 365 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | MDGPA others(360): Show |
chr19 | 48547172 | 48604423 |
| a0007 | 0/0 | 365 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | MDGPA others(360): Show |
chr19 | 48547172 | 48604423 |
| a0008 | 0/0 | 359 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | MDGPA others(354): Show |
chr19 | 48547172 | 48604423 |
| a0009 | 0/0 | 365 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | MDGPA others(360): Show |
chr19 | 48547172 | 48604423 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1095 | 138 | 48 | 12 | 66 | 1 | 10 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | ATGGA others(1090): Show |
chr19 | 48547172 | 48604423 | ||
| a0001c0002 | 0/0 | 1095 | 78 | 8 | 26 | 26 | 4 | 14 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | ATGGA others(1090): Show |
chr19 | 48547172 | 48604423 | ||
| a0001c0003 | 0/0 | 1095 | 51 | 3 | 20 | 26 | 0 | 2 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | ATGGA others(1090): Show |
chr19 | 48547172 | 48604423 | ||
| a0001c0004 | 0/1 | 1095 | 41 | 13 | 8 | 13 | 3 | 3 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | ATGGA others(1090): Show |
chr19 | 48547172 | 48604423 | ||
| a0001c0005 | 0/0 | 1095 | 19 | 4 | 7 | 0 | 2 | 6 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | ATGGA others(1090): Show |
chr19 | 48547172 | 48604423 | ||
| a0001c0006 | 0/0 | 1095 | 9 | 7 | 1 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | ATGGA others(1090): Show |
chr19 | 48547172 | 48604423 | ||
| a0001c0007 | 0/0 | 1095 | 9 | 5 | 4 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | ATGGA others(1090): Show |
chr19 | 48547172 | 48604423 | ||
| a0001c0009 | 0/0 | 1095 | 6 | 0 | 2 | 0 | 1 | 3 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | ATGGA others(1090): Show |
chr19 | 48547172 | 48604423 | ||
| a0001c0010 | 0/0 | 1095 | 4 | 3 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | ATGGA others(1090): Show |
chr19 | 48547172 | 48604423 | ||
| a0001c0019 | 0/0 | 1095 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | ATGGA others(1090): Show |
chr19 | 48547172 | 48604423 | ||
| a0002c0008 | 0/0 | 1095 | 8 | 0 | 0 | 8 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | ATGGA others(1090): Show |
chr19 | 48547172 | 48604423 | ||
| a0002c0013 | 0/0 | 1095 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | ATGGA others(1090): Show |
chr19 | 48547172 | 48604423 | ||
| a0003c0011 | 0/0 | 1095 | 2 | 2 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | ATGGA others(1090): Show |
chr19 | 48547172 | 48604423 | ||
| a0003c0012 | 0/0 | 1095 | 2 | 2 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | ATGGA others(1090): Show |
chr19 | 48547172 | 48604423 | ||
| a0004c0016 | 0/0 | 1095 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | ATGGA others(1090): Show |
chr19 | 48547172 | 48604423 | ||
| a0004c0020 | 0/0 | 1095 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | ATGGA others(1090): Show |
chr19 | 48547172 | 48604423 | ||
| a0005c0018 | 0/0 | 1095 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | ATGGA others(1090): Show |
chr19 | 48547172 | 48604423 | ||
| a0006c0017 | 0/0 | 1095 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | ATGGA others(1090): Show |
chr19 | 48547172 | 48604423 | ||
| a0007c0021 | 0/0 | 1095 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | ATGGA others(1090): Show |
chr19 | 48547172 | 48604423 | ||
| a0008c0015 | 0/0 | 1077 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | ATGGA others(1072): Show |
chr19 | 48547172 | 48604423 | ||
| a0009c0014 | 0/0 | 1095 | 1 | 0 | 0 | 0 | 1 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | ATGGA others(1090): Show |
chr19 | 48547172 | 48604423 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 1196 | 138 | 48 | 12 | 66 | 1 | 10 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | AGACG others(1191): Show |
chr19 | 48547172 | 48604423 |
| a0001c0002t0001 | 0/0 | 1196 | 78 | 8 | 26 | 26 | 4 | 14 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | AGACG others(1191): Show |
chr19 | 48547172 | 48604423 |
| a0001c0003t0001 | 0/0 | 1196 | 51 | 3 | 20 | 26 | 0 | 2 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | AGACG others(1191): Show |
chr19 | 48547172 | 48604423 |
| a0001c0004t0001 | 0/1 | 1196 | 41 | 13 | 8 | 13 | 3 | 3 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | AGACG others(1191): Show |
chr19 | 48547172 | 48604423 |
| a0001c0005t0001 | 0/0 | 1196 | 19 | 4 | 7 | 0 | 2 | 6 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | AGACG others(1191): Show |
chr19 | 48547172 | 48604423 |
| a0001c0006t0001 | 0/0 | 1196 | 9 | 7 | 1 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | AGACG others(1191): Show |
chr19 | 48547172 | 48604423 |
| a0001c0007t0001 | 0/0 | 1196 | 9 | 5 | 4 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | AGACG others(1191): Show |
chr19 | 48547172 | 48604423 |
| a0001c0009t0001 | 0/0 | 1196 | 6 | 0 | 2 | 0 | 1 | 3 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | AGACG others(1191): Show |
chr19 | 48547172 | 48604423 |
| a0001c0010t0001 | 0/0 | 1196 | 4 | 3 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | AGACG others(1191): Show |
chr19 | 48547172 | 48604423 |
| a0001c0019t0001 | 0/0 | 1196 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | AGACG others(1191): Show |
chr19 | 48547172 | 48604423 |
| a0002c0008t0001 | 0/0 | 1196 | 8 | 0 | 0 | 8 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | AGACG others(1191): Show |
chr19 | 48547172 | 48604423 |
| a0002c0013t0001 | 0/0 | 1196 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | AGACG others(1191): Show |
chr19 | 48547172 | 48604423 |
| a0003c0011t0001 | 0/0 | 1196 | 2 | 2 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | AGACG others(1191): Show |
chr19 | 48547172 | 48604423 |
| a0003c0012t0001 | 0/0 | 1196 | 2 | 2 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | AGACG others(1191): Show |
chr19 | 48547172 | 48604423 |
| a0004c0016t0001 | 0/0 | 1196 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | AGACG others(1191): Show |
chr19 | 48547172 | 48604423 |
| a0004c0020t0001 | 0/0 | 1196 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | AGACG others(1191): Show |
chr19 | 48547172 | 48604423 |
| a0005c0018t0001 | 0/0 | 1196 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | AGACG others(1191): Show |
chr19 | 48547172 | 48604423 |
| a0006c0017t0001 | 0/0 | 1196 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | AGACG others(1191): Show |
chr19 | 48547172 | 48604423 |
| a0007c0021t0001 | 0/0 | 1196 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | AGACG others(1191): Show |
chr19 | 48547172 | 48604423 |
| a0008c0015t0001 | 0/0 | 1178 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | AGACG others(1173): Show |
chr19 | 48547172 | 48604423 |
| a0009c0014t0001 | 0/0 | 1196 | 1 | 0 | 0 | 0 | 1 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | AGACG others(1191): Show |
chr19 | 48547172 | 48604423 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 1/0 | 2 | 0 | 0 | 0 | 1 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0374 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0004t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0004t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0004t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0004t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0004t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0004t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0004t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0004t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0004t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0004t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0004t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0004t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0004t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0004t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0004t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0004t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0004t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0004t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0004t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0004t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0004t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0004t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0004t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0004t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0004t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0004t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0004t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0004t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0004t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0004t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0004t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0004t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0004t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0004t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0004t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0004t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0004t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0004t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0004t0001g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0004t0001g0346 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0004t0001g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0005t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0005t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0005t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0005t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0005t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0005t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0005t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0005t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0005t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0005t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0005t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0005t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0005t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0005t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0005t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0005t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0005t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0005t0001g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0006t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0006t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0006t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0006t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0006t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0006t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0006t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0006t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0006t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0007t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0007t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0007t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0007t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0007t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0007t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0007t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0007t0001g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0007t0001g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0009t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0009t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0009t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0009t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0009t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0009t0001g0337 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0010t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0010t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0010t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0010t0001g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0019t0001g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0002c0008t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0002c0008t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0002c0008t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0002c0008t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0002c0008t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0002c0008t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0002c0008t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0002c0008t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0002c0013t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0003c0011t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0003c0011t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0003c0012t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0003c0012t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0004c0016t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0004c0020t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0005c0018t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0006c0017t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0007c0021t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0008c0015t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0009c0014t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG00099 | hp2 | a0001 | c0005 | t0001 | g0114 | EUR | GBR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0307 | EUR | GBR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG00140 | hp2 | a0001 | c0005 | t0001 | g0072 | EUR | GBR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG00280 | hp1 | a0001 | c0004 | t0001 | g0096 | EUR | FIN | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG00280 | hp2 | a0001 | c0002 | t0001 | g0303 | EUR | FIN | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | CHS | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG00408 | hp2 | a0002 | c0008 | t0001 | g0152 | EAS | CHS | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG00423 | hp1 | a0001 | c0003 | t0001 | g0139 | EAS | CHS | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG00423 | hp2 | a0001 | c0002 | t0001 | g0292 | EAS | CHS | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG00438 | hp1 | a0002 | c0008 | t0001 | g0150 | EAS | CHS | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG00438 | hp2 | a0001 | c0003 | t0001 | g0136 | EAS | CHS | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG00558 | hp1 | a0001 | c0004 | t0001 | g0224 | EAS | CHS | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | CHS | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG00597 | hp1 | a0001 | c0003 | t0001 | g0273 | EAS | CHS | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG00597 | hp2 | a0001 | c0004 | t0001 | g0128 | EAS | CHS | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0329 | EAS | CHS | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0080 | EAS | CHS | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG00621 | hp1 | a0001 | c0002 | t0001 | g0208 | EAS | CHS | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG00621 | hp2 | a0001 | c0002 | t0001 | g0161 | EAS | CHS | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG00639 | hp1 | a0001 | c0009 | t0001 | g0183 | AMR | PUR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0084 | AMR | PUR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0206 | AMR | PUR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG00642 | hp2 | a0001 | c0003 | t0001 | g0374 | AMR | PUR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | CHS | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | CHS | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG00733 | hp1 | a0001 | c0002 | t0001 | g0035 | AMR | PUR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG00733 | hp2 | a0001 | c0003 | t0001 | g0102 | AMR | PUR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0305 | AMR | PUR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0068 | AMR | PUR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG00738 | hp1 | a0001 | c0004 | t0001 | g0063 | AMR | PUR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG00738 | hp2 | a0001 | c0002 | t0001 | g0064 | AMR | PUR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG00741 | hp1 | a0001 | c0004 | t0001 | g0243 | AMR | PUR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG00741 | hp2 | a0001 | c0005 | t0001 | g0109 | AMR | PUR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01069 | hp1 | a0001 | c0003 | t0001 | g0223 | AMR | PUR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0213 | AMR | PUR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01070 | hp1 | a0001 | c0002 | t0001 | g0181 | AMR | PUR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01070 | hp2 | a0001 | c0002 | t0001 | g0050 | AMR | PUR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0212 | AMR | PUR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0051 | AMR | PUR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01081 | hp1 | a0001 | c0005 | t0001 | g0168 | AMR | PUR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01081 | hp2 | a0001 | c0003 | t0001 | g0175 | AMR | PUR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01099 | hp1 | a0001 | c0005 | t0001 | g0237 | AMR | PUR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0313 | AMR | PUR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01106 | hp1 | a0001 | c0006 | t0001 | g0251 | AMR | PUR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0311 | AMR | PUR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01109 | hp1 | a0001 | c0003 | t0001 | g0262 | AMR | PUR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01109 | hp2 | a0001 | c0004 | t0001 | g0016 | AMR | PUR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01167 | hp2 | a0004 | c0016 | t0001 | g0154 | AMR | PUR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01168 | hp1 | a0001 | c0004 | t0001 | g0322 | AMR | PUR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01168 | hp2 | a0001 | c0002 | t0001 | g0357 | AMR | PUR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0358 | AMR | PUR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01175 | hp2 | a0001 | c0005 | t0001 | g0236 | AMR | PUR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01192 | hp1 | a0001 | c0005 | t0001 | g0256 | AMR | PUR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01192 | hp2 | a0001 | c0009 | t0001 | g0319 | AMR | PUR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0336 | AMR | PUR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01255 | hp1 | a0001 | c0004 | t0001 | g0314 | AMR | CLM | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0121 | AMR | CLM | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01256 | hp1 | a0001 | c0007 | t0001 | g0111 | AMR | CLM | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01256 | hp2 | a0001 | c0010 | t0001 | g0113 | AMR | CLM | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01257 | hp1 | a0001 | c0003 | t0001 | g0267 | AMR | CLM | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01257 | hp2 | a0001 | c0005 | t0001 | g0001 | AMR | CLM | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01258 | hp1 | a0001 | c0007 | t0001 | g0112 | AMR | CLM | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01258 | hp2 | a0001 | c0005 | t0001 | g0001 | AMR | CLM | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01261 | hp1 | a0001 | c0002 | t0001 | g0218 | AMR | CLM | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01261 | hp2 | a0001 | c0007 | t0001 | g0162 | AMR | CLM | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0253 | AMR | CLM | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01346 | hp2 | a0001 | c0007 | t0001 | g0034 | AMR | CLM | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | CLM | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01358 | hp2 | a0001 | c0002 | t0001 | g0301 | AMR | CLM | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0159 | AMR | CLM | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0326 | AMR | CLM | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01433 | hp2 | a0001 | c0004 | t0001 | g0142 | AMR | CLM | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | CLM | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0086 | AMR | CLM | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01515 | hp1 | a0001 | c0004 | t0001 | g0315 | EUR | IBS | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01515 | hp2 | a0001 | c0009 | t0001 | g0337 | EUR | IBS | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01884 | hp1 | a0003 | c0012 | t0001 | g0013 | AFR | ACB | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0364 | AFR | ACB | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01891 | hp1 | a0001 | c0004 | t0001 | g0017 | AFR | ACB | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01928 | hp1 | a0001 | c0003 | t0001 | g0166 | AMR | PEL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01928 | hp2 | a0001 | c0003 | t0001 | g0225 | AMR | PEL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01934 | hp1 | a0001 | c0002 | t0001 | g0209 | AMR | PEL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01934 | hp2 | a0001 | c0003 | t0001 | g0188 | AMR | PEL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01943 | hp1 | a0001 | c0003 | t0001 | g0165 | AMR | PEL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01943 | hp2 | a0001 | c0004 | t0001 | g0246 | AMR | PEL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01952 | hp1 | a0001 | c0002 | t0001 | g0049 | AMR | PEL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0261 | AMR | PEL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01975 | hp1 | a0001 | c0003 | t0001 | g0257 | AMR | PEL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01975 | hp2 | a0001 | c0003 | t0001 | g0106 | AMR | PEL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01978 | hp1 | a0001 | c0003 | t0001 | g0317 | AMR | PEL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PEL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01981 | hp1 | a0001 | c0003 | t0001 | g0226 | AMR | PEL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01981 | hp2 | a0001 | c0003 | t0001 | g0217 | AMR | PEL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01993 | hp1 | a0001 | c0003 | t0001 | g0145 | AMR | PEL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01993 | hp2 | a0001 | c0004 | t0001 | g0318 | AMR | PEL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02015 | hp1 | a0001 | c0003 | t0001 | g0287 | EAS | KHV | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | KHV | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02040 | hp1 | a0001 | c0002 | t0001 | g0331 | EAS | KHV | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0340 | EAS | KHV | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0300 | AFR | ACB | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | KHV | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0339 | EAS | KHV | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02071 | hp1 | a0005 | c0018 | t0001 | g0349 | EAS | KHV | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0344 | EAS | KHV | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0342 | EAS | KHV | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0327 | EAS | KHV | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02080 | hp2 | a0002 | c0008 | t0001 | g0244 | EAS | KHV | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | KHV | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0335 | EAS | KHV | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0078 | EAS | KHV | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | KHV | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02135 | hp2 | a0001 | c0004 | t0001 | g0135 | EAS | KHV | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | ACB | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02145 | hp2 | a0001 | c0006 | t0001 | g0061 | AFR | ACB | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02148 | hp1 | a0001 | c0003 | t0001 | g0177 | AMR | PEL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02148 | hp2 | a0001 | c0003 | t0001 | g0134 | AMR | PEL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | CDX | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02155 | hp2 | a0002 | c0008 | t0001 | g0151 | EAS | CDX | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | CDX | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | CDX | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | ACB | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02258 | hp1 | a0001 | c0004 | t0001 | g0031 | AFR | ACB | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02258 | hp2 | a0001 | c0004 | t0001 | g0090 | AFR | ACB | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02273 | hp1 | a0001 | c0002 | t0001 | g0160 | AMR | PEL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02273 | hp2 | a0001 | c0003 | t0001 | g0306 | AMR | PEL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0201 | AFR | ACB | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02280 | hp2 | a0001 | c0007 | t0001 | g0355 | AFR | ACB | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | ACB | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02523 | hp1 | a0001 | c0004 | t0001 | g0231 | EAS | KHV | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02523 | hp2 | a0001 | c0003 | t0001 | g0288 | EAS | KHV | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0359 | AFR | GWD | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02572 | hp2 | a0001 | c0004 | t0001 | g0196 | AFR | GWD | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02622 | hp2 | a0001 | c0002 | t0001 | g0036 | AFR | GWD | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | GWD | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0091 | AFR | GWD | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02647 | hp2 | a0001 | c0007 | t0001 | g0157 | AFR | GWD | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0104 | SAS | PJL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02698 | hp2 | a0001 | c0004 | t0001 | g0279 | SAS | PJL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02717 | hp2 | a0003 | c0011 | t0001 | g0060 | AFR | GWD | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02723 | hp1 | a0001 | c0004 | t0001 | g0370 | AFR | GWD | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02723 | hp2 | a0001 | c0006 | t0001 | g0045 | AFR | GWD | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02735 | hp1 | a0001 | c0006 | t0001 | g0021 | SAS | PJL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02735 | hp2 | a0001 | c0005 | t0001 | g0214 | SAS | PJL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0260 | SAS | PJL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0023 | SAS | PJL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0361 | AFR | GWD | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02818 | hp1 | a0001 | c0003 | t0001 | g0012 | AFR | GWD | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | GWD | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0360 | AFR | GWD | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02886 | hp2 | a0001 | c0004 | t0001 | g0058 | AFR | GWD | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | GWD | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02896 | hp1 | a0001 | c0004 | t0001 | g0046 | AFR | GWD | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02896 | hp2 | a0001 | c0005 | t0001 | g0010 | AFR | GWD | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02897 | hp1 | a0001 | c0005 | t0001 | g0009 | AFR | GWD | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ESN | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | ESN | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0119 | AFR | ESN | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | ESN | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0004 | AFR | ESN | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02970 | hp2 | a0001 | c0004 | t0001 | g0069 | AFR | ESN | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02976 | hp1 | a0001 | c0010 | t0001 | g0038 | AFR | ESN | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02976 | hp2 | a0003 | c0011 | t0001 | g0044 | AFR | ESN | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03017 | hp1 | a0001 | c0003 | t0001 | g0255 | SAS | PJL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0254 | SAS | PJL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03041 | hp1 | a0001 | c0010 | t0001 | g0367 | AFR | GWD | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03041 | hp2 | a0001 | c0006 | t0001 | g0094 | AFR | GWD | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | MSL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03098 | hp2 | a0001 | c0007 | t0001 | g0356 | AFR | MSL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03130 | hp1 | a0001 | c0007 | t0001 | g0057 | AFR | ESN | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | ESN | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03139 | hp2 | a0001 | c0004 | t0001 | g0053 | AFR | ESN | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03195 | hp1 | a0001 | c0003 | t0001 | g0047 | AFR | ESN | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ESN | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0368 | AFR | MSL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03209 | hp2 | a0006 | c0017 | t0001 | g0030 | AFR | MSL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03225 | hp1 | a0001 | c0006 | t0001 | g0029 | AFR | MSL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0366 | AFR | MSL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03453 | hp1 | a0001 | c0007 | t0001 | g0198 | AFR | MSL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0362 | AFR | MSL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0085 | SAS | PJL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03491 | hp2 | a0001 | c0009 | t0001 | g0320 | SAS | PJL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03492 | hp1 | a0001 | c0005 | t0001 | g0110 | SAS | PJL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03492 | hp2 | a0001 | c0009 | t0001 | g0321 | SAS | PJL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03516 | hp1 | a0001 | c0004 | t0001 | g0065 | AFR | ESN | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0363 | AFR | ESN | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03540 | hp1 | a0001 | c0005 | t0001 | g0011 | AFR | GWD | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03579 | hp1 | a0001 | c0006 | t0001 | g0039 | AFR | MSL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03579 | hp2 | a0001 | c0006 | t0001 | g0007 | AFR | MSL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0249 | SAS | PJL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03654 | hp2 | a0001 | c0002 | t0001 | g0250 | SAS | PJL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03669 | hp1 | a0001 | c0005 | t0001 | g0348 | SAS | PJL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0171 | SAS | PJL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | STU | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | STU | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0316 | SAS | PJL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03704 | hp2 | a0001 | c0005 | t0001 | g0312 | SAS | PJL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0153 | SAS | PJL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0189 | SAS | PJL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03831 | hp1 | a0001 | c0004 | t0001 | g0019 | SAS | BEB | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0309 | SAS | BEB | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03834 | hp1 | a0001 | c0004 | t0001 | g0341 | SAS | BEB | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03834 | hp2 | a0001 | c0003 | t0001 | g0191 | SAS | BEB | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03942 | hp1 | a0001 | c0002 | t0001 | g0347 | SAS | BEB | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0178 | SAS | BEB | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG04115 | hp1 | a0001 | c0009 | t0001 | g0120 | SAS | STU | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0269 | SAS | STU | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0310 | SAS | BEB | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0333 | SAS | BEB | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0239 | SAS | STU | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0289 | SAS | STU | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG04204 | hp1 | a0001 | c0002 | t0001 | g0082 | SAS | STU | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG04204 | hp2 | a0007 | c0021 | t0001 | g0304 | SAS | STU | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | STU | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | STU | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | YRI | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | CHB | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18612 | hp2 | a0002 | c0008 | t0001 | g0232 | EAS | CHB | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | CHB | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0345 | EAS | CHB | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0302 | AFR | YRI | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18906 | hp2 | a0001 | c0004 | t0001 | g0073 | AFR | YRI | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18942 | hp2 | a0001 | c0002 | t0001 | g0221 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18943 | hp2 | a0001 | c0004 | t0001 | g0129 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18944 | hp1 | a0001 | c0003 | t0001 | g0240 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18944 | hp2 | a0001 | c0003 | t0001 | g0124 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18947 | hp2 | a0001 | c0002 | t0001 | g0277 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18948 | hp2 | a0001 | c0004 | t0001 | g0265 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18949 | hp1 | a0001 | c0003 | t0001 | g0263 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18950 | hp1 | a0001 | c0003 | t0001 | g0133 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18950 | hp2 | a0001 | c0002 | t0001 | g0332 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18951 | hp1 | a0001 | c0003 | t0001 | g0146 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18952 | hp1 | a0002 | c0013 | t0001 | g0286 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18952 | hp2 | a0002 | c0008 | t0001 | g0158 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18954 | hp1 | a0001 | c0002 | t0001 | g0298 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18957 | hp1 | a0001 | c0002 | t0001 | g0272 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18959 | hp1 | a0001 | c0003 | t0001 | g0369 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18961 | hp2 | a0002 | c0008 | t0001 | g0343 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18964 | hp1 | a0001 | c0004 | t0001 | g0328 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18964 | hp2 | a0001 | c0003 | t0001 | g0193 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18966 | hp1 | a0001 | c0003 | t0001 | g0282 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0354 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18970 | hp1 | a0001 | c0003 | t0001 | g0222 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0278 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18971 | hp1 | a0001 | c0004 | t0001 | g0126 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18971 | hp2 | a0001 | c0003 | t0001 | g0079 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18974 | hp2 | a0001 | c0003 | t0001 | g0234 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18980 | hp1 | a0001 | c0003 | t0001 | g0127 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18982 | hp1 | a0001 | c0003 | t0001 | g0229 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18983 | hp1 | a0001 | c0002 | t0001 | g0264 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18983 | hp2 | a0001 | c0003 | t0001 | g0131 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18986 | hp1 | a0001 | c0003 | t0001 | g0115 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18986 | hp2 | a0001 | c0002 | t0001 | g0276 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18990 | hp1 | a0001 | c0002 | t0001 | g0350 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18990 | hp2 | a0001 | c0002 | t0001 | g0353 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18998 | hp1 | a0001 | c0002 | t0001 | g0103 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18998 | hp2 | a0001 | c0004 | t0001 | g0070 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18999 | hp1 | a0001 | c0002 | t0001 | g0169 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18999 | hp2 | a0001 | c0003 | t0001 | g0293 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19000 | hp2 | a0001 | c0003 | t0001 | g0323 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19003 | hp2 | a0001 | c0003 | t0001 | g0220 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19005 | hp1 | a0001 | c0003 | t0001 | g0294 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19009 | hp1 | a0001 | c0002 | t0001 | g0295 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0245 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19011 | hp1 | a0001 | c0003 | t0001 | g0140 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19012 | hp1 | a0001 | c0002 | t0001 | g0130 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19012 | hp2 | a0001 | c0002 | t0001 | g0123 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19030 | hp1 | a0003 | c0012 | t0001 | g0014 | AFR | LWK | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19030 | hp2 | a0001 | c0004 | t0001 | g0006 | AFR | LWK | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | LWK | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19043 | hp2 | a0001 | c0010 | t0001 | g0092 | AFR | LWK | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19056 | hp1 | a0001 | c0004 | t0001 | g0099 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19058 | hp1 | a0008 | c0015 | t0001 | g0351 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19058 | hp2 | a0001 | c0004 | t0001 | g0180 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19070 | hp1 | a0001 | c0003 | t0001 | g0202 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19070 | hp2 | a0001 | c0002 | t0001 | g0330 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19074 | hp1 | a0002 | c0008 | t0001 | g0270 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19079 | hp1 | a0001 | c0004 | t0001 | g0192 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19079 | hp2 | a0001 | c0004 | t0001 | g0138 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19080 | hp2 | a0001 | c0002 | t0001 | g0275 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0352 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19083 | hp2 | a0001 | c0002 | t0001 | g0100 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19085 | hp2 | a0001 | c0002 | t0001 | g0334 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0373 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | YRI | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | YRI | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ASW | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ASW | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA20752 | hp1 | a0009 | c0014 | t0001 | g0172 | EUR | TSI | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0097 | EUR | TSI | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA20805 | hp1 | a0001 | c0004 | t0001 | g0087 | EUR | TSI | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0077 | EUR | TSI | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA20905 | hp1 | a0001 | c0005 | t0001 | g0210 | SAS | GIH | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA20905 | hp2 | a0001 | c0005 | t0001 | g0195 | SAS | GIH | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01123 | hp1 | a0001 | c0003 | t0001 | g0215 | AMR | CLM | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01123 | hp2 | a0001 | c0002 | t0001 | g0143 | AMR | CLM | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02109 | hp1 | a0001 | c0006 | t0001 | g0095 | AFR | ACB | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0048 | AFR | ACB | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02486 | hp2 | a0001 | c0019 | t0001 | g0371 | AFR | ACB | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02559 | hp1 | a0001 | c0003 | t0001 | g0325 | AFR | ACB | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0372 | AFR | ACB | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03471 | hp1 | a0001 | c0005 | t0001 | g0020 | AFR | MSL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03471 | hp2 | a0001 | c0004 | t0001 | g0066 | AFR | MSL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG06807 | hp1 | a0004 | c0020 | t0001 | g0176 | AFR | USA | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0365 | AFR | USA | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | USA | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0156 | AFR | USA | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | LWK | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA21309 | hp2 | a0001 | c0002 | t0001 | g0083 | AFR | LWK | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| homoSapiens | chm13v2 | a0001 | c0004 | t0001 | g0346 | REF | REF | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0002 | REF | REF | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:48552281 | C | T | 1 | a0007 | 1 | HG04204.hp2 | missense_variant | MODERATE | c.29C>T | p.Pro10Leu | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/7 | 110/1196 | 29/1098 | 10/365 | chr19 | 48552281 | |||
| chr19:48575967 | G | A | 1 | a0002 | 9 | HG00408.hp2 HG00438.hp1 HG02080.hp2 others(6): Show |
missense_variant | MODERATE | c.98G>A | p.Arg33Gln | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/7 | 179/1196 | 98/1098 | 33/365 | chr19 | 48575967 | |||
| chr19:48576021 | T | C | 1 | a0009 | 1 | NA20752.hp1 | missense_variant | MODERATE | c.152T>C | p.Leu51Ser | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/7 | 233/1196 | 152/1098 | 51/365 | chr19 | 48576021 | |||
| chr19:48596811 | G | A | 1 | a0005 | 1 | HG02071.hp1 | missense_variant | MODERATE | c.718G>A | p.Val240Ile | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 6/7 | 799/1196 | 718/1098 | 240/365 | chr19 | 48596811 | |||
| chr19:48596827 | C | T | 1 | a0006 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.734C>T | p.Thr245Ile | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 6/7 | 815/1196 | 734/1098 | 245/365 | chr19 | 48596827 | |||
| chr19:48596853 | ATGTCCAA others(11): Show |
A | 1 | a0008 | 1 | NA19058.hp1 | conservative_inframe_deletion | MODERATE | c.763_780delTCCAACTA others(10): Show |
p.Ser255_Leu260del | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 6/7 | 844/1196 | 763/1098 | 255/365 | INFO_REALIGN_3_PRIME | chr19 | 48596853 | ||
| chr19:48599212 | C | G | 1 | a0003 | 4 | HG01884.hp1 HG02717.hp2 HG02976.hp2 others(1): Show |
missense_variant | MODERATE | c.904C>G | p.Arg302Gly | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 7/7 | 985/1196 | 904/1098 | 302/365 | chr19 | 48599212 | |||
| chr19:48599342 | C | T | 1 | a0004 | 2 | HG01167.hp2 HG06807.hp1 |
missense_variant | MODERATE | c.1034C>T | p.Pro345Leu | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 7/7 | 1115/1196 | 1034/1098 | 345/365 | chr19 | 48599342 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:48575989 | C | T | 6 | a0001c0005 a0001c0006 a0001c0007 others(3): Show |
44 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(41): Show |
synonymous_variant | LOW | c.120C>T | p.Pro40Pro | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/7 | 201/1196 | 120/1098 | 40/365 | chr19 | 48575989 | |||
| chr19:48592741 | C | T | 1 | a0001c0019 | 1 | HG02486.hp2 | synonymous_variant | LOW | c.570C>T | p.Phe190Phe | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/7 | 651/1196 | 570/1098 | 190/365 | chr19 | 48592741 | |||
| chr19:48592808 | C | T | 5 | a0001c0004 a0001c0007 a0001c0009 others(2): Show |
57 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(54): Show |
synonymous_variant | LOW | c.637C>T | p.Leu213Leu | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/7 | 718/1196 | 637/1098 | 213/365 | chr19 | 48592808 | |||
| chr19:48599142 | C | T | 5 | a0001c0002 a0001c0005 a0004c0016 others(2): Show |
100 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(97): Show |
synonymous_variant | LOW | c.834C>T | p.Cys278Cys | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 7/7 | 915/1196 | 834/1098 | 278/365 | chr19 | 48599142 | |||
| chr19:48599256 | C | T | 7 | a0001c0003 a0001c0009 a0001c0010 others(4): Show |
67 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(64): Show |
synonymous_variant | LOW | c.948C>T | p.Asp316Asp | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 7/7 | 1029/1196 | 948/1098 | 316/365 | chr19 | 48599256 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:48552421 | G | A | 6 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(3): Show |
6 | HG01433.hp1 HG02055.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.71+98G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48552421 | |||||||
| chr19:48552523 | C | T | 1 | a0001c0003t0001g0374 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.71+200C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48552523 | |||||||
| chr19:48552539 | T | C | 46 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(43): Show |
46 | HG00733.hp1 HG01109.hp2 HG01346.hp2 others(43): Show |
intron_variant | MODIFIER | c.71+216T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48552539 | |||||||
| chr19:48552564 | G | C | 6 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(3): Show |
6 | HG01433.hp1 HG02055.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.71+241G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48552564 | |||||||
| chr19:48552657 | C | A | 1 | a0001c0002t0001g0049 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.71+334C>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48552657 | |||||||
| chr19:48552745 | A | G | 1 | a0001c0001t0001g0373 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.71+422A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48552745 | |||||||
| chr19:48552913 | G | C | 6 | a0001c0003t0001g0012 a0001c0005t0001g0009 a0001c0005t0001g0010 others(3): Show |
6 | HG01884.hp1 HG02818.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.71+590G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48552913 | |||||||
| chr19:48553032 | G | A | 2 | a0001c0002t0001g0050 a0001c0002t0001g0051 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.71+709G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48553032 | |||||||
| chr19:48553456 | C | T | 1 | a0001c0001t0001g0372 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.71+1133C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48553456 | |||||||
| chr19:48553517 | C | T | 13 | a0001c0001t0001g0008 a0001c0001t0001g0040 a0001c0001t0001g0041 others(10): Show |
13 | HG01433.hp1 HG02486.hp1 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.71+1194C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48553517 | |||||||
| chr19:48553569 | T | C | 66 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(63): Show |
66 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(63): Show |
intron_variant | MODIFIER | c.71+1246T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48553569 | |||||||
| chr19:48553598 | C | G | 7 | a0001c0001t0001g0033 a0001c0001t0001g0037 a0001c0002t0001g0035 others(4): Show |
7 | HG00733.hp1 HG01346.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.71+1275C>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48553598 | |||||||
| chr19:48553638 | G | C | 1 | a0001c0002t0001g0097 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.71+1315G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48553638 | |||||||
| chr19:48553650 | C | T | 1 | a0001c0003t0001g0369 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.71+1327C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48553650 | |||||||
| chr19:48553655 | C | T | 9 | a0001c0001t0001g0360 a0001c0001t0001g0361 a0001c0001t0001g0362 others(6): Show |
9 | HG01884.hp2 HG02809.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.71+1332C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48553655 | |||||||
| chr19:48553657 | C | G | 1 | a0001c0001t0001g0359 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.71+1334C>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48553657 | |||||||
| chr19:48553675 | T | A | 21 | a0001c0001t0001g0015 a0001c0001t0001g0052 a0001c0001t0001g0054 others(18): Show |
21 | HG00735.hp2 HG00738.hp1 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.71+1352T>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48553675 | |||||||
| chr19:48553884 | C | T | 2 | a0001c0002t0001g0357 a0001c0002t0001g0358 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.71+1561C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48553884 | |||||||
| chr19:48553891 | T | G | 1 | a0001c0001t0001g0098 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.71+1568T>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48553891 | |||||||
| chr19:48553910 | G | T | 2 | a0001c0004t0001g0016 a0001c0004t0001g0096 |
2 | HG00280.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.71+1587G>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48553910 | |||||||
| chr19:48553962 | C | G | 1 | a0001c0019t0001g0371 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.71+1639C>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48553962 | |||||||
| chr19:48553971 | C | CT | 46 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(43): Show |
46 | HG00735.hp2 HG00738.hp1 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.71+1656dupT | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48553971 | ||||||
| chr19:48554066 | T | C | 8 | a0001c0001t0001g0032 a0001c0001t0001g0037 a0001c0001t0001g0040 others(5): Show |
8 | HG01891.hp2 HG02109.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.71+1743T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48554066 | |||||||
| chr19:48554173 | T | C | 2 | a0001c0006t0001g0045 a0003c0011t0001g0044 |
2 | HG02723.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.71+1850T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48554173 | |||||||
| chr19:48554411 | C | T | 2 | a0001c0007t0001g0355 a0001c0007t0001g0356 |
2 | HG02280.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.71+2088C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48554411 | |||||||
| chr19:48554461 | G | A | 2 | a0001c0001t0001g0071 a0001c0004t0001g0070 |
2 | HG00408.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.71+2138G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48554461 | |||||||
| chr19:48554532 | C | A | 7 | a0001c0001t0001g0008 a0001c0002t0001g0048 a0001c0003t0001g0047 others(4): Show |
7 | HG01433.hp1 HG02486.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.71+2209C>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48554532 | |||||||
| chr19:48554613 | G | GC | 22 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0037 others(19): Show |
22 | HG00642.hp2 HG01433.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.71+2297dupC | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48554613 | ||||||
| chr19:48554620 | C | A | 1 | a0001c0005t0001g0072 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.71+2297C>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48554620 | |||||||
| chr19:48554654 | CT | C | 93 | a0001c0001t0001g0003 a0001c0001t0001g0022 a0001c0001t0001g0032 others(90): Show |
93 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.71+2358delT | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48554654 | ||||||
| chr19:48554654 | CTT | C | 158 | a0001c0001t0001g0018 a0001c0001t0001g0067 a0001c0001t0001g0088 others(155): Show |
159 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.71+2357_71+2358del others(2): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48554654 | ||||||
| chr19:48554654 | CTTT | C | 36 | a0001c0001t0001g0008 a0001c0001t0001g0033 a0001c0001t0001g0062 others(33): Show |
36 | HG00280.hp1 HG00408.hp1 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.71+2356_71+2358del others(3): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48554654 | ||||||
| chr19:48554654 | CTTTT | C | 14 | a0001c0001t0001g0015 a0001c0001t0001g0052 a0001c0001t0001g0054 others(11): Show |
14 | HG02257.hp1 HG02258.hp2 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.71+2355_71+2358del others(4): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48554654 | ||||||
| chr19:48554681 | T | C | 9 | a0001c0002t0001g0347 a0001c0005t0001g0109 a0001c0005t0001g0110 others(6): Show |
9 | HG00099.hp2 HG00741.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.71+2358T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48554681 | |||||||
| chr19:48554749 | C | T | 1 | a0001c0006t0001g0021 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.71+2426C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48554749 | |||||||
| chr19:48554920 | C | T | 7 | a0001c0001t0001g0037 a0001c0001t0001g0040 a0001c0001t0001g0041 others(4): Show |
7 | HG02109.hp2 HG02895.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.71+2597C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48554920 | |||||||
| chr19:48555069 | G | A | 5 | a0001c0002t0001g0048 a0001c0003t0001g0047 a0001c0004t0001g0046 others(2): Show |
5 | HG02486.hp1 HG02723.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.71+2746G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48555069 | |||||||
| chr19:48555115 | G | A | 1 | a0001c0001t0001g0032 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.71+2792G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48555115 | |||||||
| chr19:48555136 | C | T | 1 | a0001c0001t0001g0235 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.71+2813C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48555136 | |||||||
| chr19:48555212 | C | T | 3 | a0001c0002t0001g0048 a0001c0003t0001g0047 a0001c0004t0001g0046 |
3 | HG02486.hp1 HG02896.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.71+2889C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48555212 | |||||||
| chr19:48555238 | C | T | 7 | a0001c0001t0001g0037 a0001c0001t0001g0040 a0001c0001t0001g0041 others(4): Show |
7 | HG02109.hp2 HG02895.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.71+2915C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48555238 | |||||||
| chr19:48555307 | T | G | 43 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(40): Show |
43 | HG00735.hp2 HG00738.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.71+2984T>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48555307 | |||||||
| chr19:48555488 | T | TTC | 6 | a0001c0001t0001g0037 a0001c0001t0001g0040 a0001c0001t0001g0041 others(3): Show |
6 | HG02109.hp2 HG02895.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.71+3185_71+3186dup others(2): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48555488 | ||||||
| chr19:48555544 | G | A | 4 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0002t0001g0004 others(1): Show |
4 | HG02055.hp1 HG02970.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.71+3221G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48555544 | |||||||
| chr19:48555549 | C | CCT | 37 | a0001c0001t0001g0022 a0001c0001t0001g0043 a0001c0001t0001g0052 others(34): Show |
37 | HG00733.hp2 HG00735.hp1 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.71+3265_71+3266dup others(2): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48555549 | ||||||
| chr19:48555549 | C | CCTCT | 38 | a0001c0001t0001g0093 a0001c0001t0001g0147 a0001c0001t0001g0148 others(35): Show |
39 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(36): Show |
intron_variant | MODIFIER | c.71+3263_71+3266dup others(4): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48555549 | ||||||
| chr19:48555549 | C | CCTCTCT | 32 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(29): Show |
32 | HG00423.hp1 HG00438.hp2 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.71+3261_71+3266dup others(6): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48555549 | ||||||
| chr19:48555549 | C | CCTCTCTC others(1): Show |
19 | a0001c0001t0001g0037 a0001c0001t0001g0122 a0001c0001t0001g0125 others(16): Show |
19 | HG01255.hp2 HG01884.hp2 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.71+3259_71+3266dup others(8): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48555549 | ||||||
| chr19:48555549 | C | CCTCTCTC others(3): Show |
5 | a0001c0001t0001g0025 a0001c0001t0001g0042 a0001c0001t0001g0118 others(2): Show |
5 | HG02622.hp1 HG02886.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.71+3257_71+3266dup others(10): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48555549 | ||||||
| chr19:48555549 | C | CCTCTCTC others(5): Show |
2 | a0001c0001t0001g0041 a0001c0001t0001g0117 |
2 | HG03540.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.71+3255_71+3266dup others(12): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48555549 | ||||||
| chr19:48555549 | C | CCTCTCTC others(7): Show |
6 | a0001c0001t0001g0024 a0001c0001t0001g0040 a0001c0004t0001g0017 others(3): Show |
6 | HG01099.hp1 HG01891.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.71+3253_71+3266dup others(14): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48555549 | ||||||
| chr19:48555549 | C | CCTCTCTC others(9): Show |
1 | a0001c0001t0001g0018 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.71+3251_71+3266dup others(16): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48555549 | ||||||
| chr19:48555549 | C | CCTCTCTC others(11): Show |
1 | a0001c0001t0001g0116 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.71+3249_71+3266dup others(18): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48555549 | ||||||
| chr19:48555549 | C | CCTCTCTC others(15): Show |
1 | a0001c0001t0001g0032 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.71+3245_71+3266dup others(22): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48555549 | ||||||
| chr19:48555549 | CCT | C | 9 | a0001c0001t0001g0003 a0001c0001t0001g0216 a0001c0001t0001g0260 others(6): Show |
9 | HG01123.hp1 HG01175.hp1 HG01981.hp2 others(6): Show |
intron_variant | MODIFIER | c.71+3265_71+3266del others(2): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48555549 | ||||||
| chr19:48555549 | CCTCT | C | 28 | a0001c0001t0001g0033 a0001c0001t0001g0108 a0001c0001t0001g0219 others(25): Show |
28 | HG00558.hp1 HG00642.hp2 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.71+3263_71+3266del others(4): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48555549 | ||||||
| chr19:48555549 | CCTCTCT | C | 10 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0002t0001g0048 others(7): Show |
10 | HG01433.hp1 HG02486.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.71+3261_71+3266del others(6): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48555549 | ||||||
| chr19:48555549 | CCTCTCTC others(1): Show |
C | 9 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 others(6): Show |
9 | HG00673.hp2 HG01257.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.71+3259_71+3266del others(8): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48555549 | ||||||
| chr19:48555549 | CCTCTCTC others(3): Show |
C | 90 | a0001c0001t0001g0071 a0001c0001t0001g0081 a0001c0001t0001g0088 others(87): Show |
90 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.71+3257_71+3266del others(10): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48555549 | ||||||
| chr19:48555549 | CCTCTCTC others(5): Show |
C | 1 | a0001c0003t0001g0234 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.71+3255_71+3266del others(12): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48555549 | ||||||
| chr19:48555549 | CCTCTCTC others(9): Show |
C | 1 | a0001c0004t0001g0087 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.71+3251_71+3266del others(16): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48555549 | ||||||
| chr19:48555589 | T | TC | 3 | a0001c0001t0001g0062 a0001c0001t0001g0199 a0001c0001t0001g0311 |
3 | HG01106.hp2 HG02809.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.71+3266_71+3267ins others(1): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48555589 | |||||||
| chr19:48555589 | T | TCTC | 4 | a0001c0001t0001g0059 a0001c0002t0001g0189 a0001c0002t0001g0307 others(1): Show |
4 | HG00140.hp1 HG01192.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.71+3266_71+3267ins others(3): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48555589 | |||||||
| chr19:48555589 | T | TCTCTC | 5 | a0001c0001t0001g0204 a0001c0002t0001g0103 a0001c0002t0001g0209 others(2): Show |
5 | HG01934.hp1 HG01934.hp2 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.71+3266_71+3267ins others(5): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48555589 | |||||||
| chr19:48555589 | T | TCTCTCTC others(4): Show |
1 | a0001c0001t0001g0368 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.71+3266_71+3267ins others(11): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48555589 | |||||||
| chr19:48555589 | T | TCTCTCTC others(14): Show |
1 | a0001c0006t0001g0021 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.71+3266_71+3267ins others(21): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48555589 | |||||||
| chr19:48555590 | T | C | 5 | a0001c0001t0001g0093 a0001c0002t0001g0091 a0001c0003t0001g0134 others(2): Show |
5 | HG01243.hp1 HG02109.hp1 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.71+3267T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48555590 | |||||||
| chr19:48555591 | T | C | 1 | a0001c0003t0001g0177 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.71+3268T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48555591 | |||||||
| chr19:48555592 | T | C | 5 | a0001c0001t0001g0093 a0001c0002t0001g0091 a0001c0006t0001g0094 others(2): Show |
5 | HG01243.hp1 HG02109.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.71+3269T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48555592 | |||||||
| chr19:48555733 | C | T | 4 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0002t0001g0004 others(1): Show |
4 | HG02055.hp1 HG02970.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.71+3410C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48555733 | |||||||
| chr19:48555747 | G | GT | 24 | a0001c0001t0001g0015 a0001c0001t0001g0052 a0001c0001t0001g0054 others(21): Show |
24 | HG00735.hp2 HG00738.hp1 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.71+3433dupT | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48555747 | ||||||
| chr19:48555825 | C | T | 17 | a0001c0001t0001g0037 a0001c0001t0001g0040 a0001c0001t0001g0041 others(14): Show |
17 | HG01243.hp1 HG01928.hp1 HG01943.hp1 others(14): Show |
intron_variant | MODIFIER | c.71+3502C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48555825 | |||||||
| chr19:48555906 | A | AT | 5 | a0001c0001t0001g0093 a0001c0002t0001g0091 a0001c0006t0001g0094 others(2): Show |
5 | HG01243.hp1 HG02109.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.71+3589dupT | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48555906 | ||||||
| chr19:48555941 | T | C | 20 | a0001c0001t0001g0015 a0001c0001t0001g0052 a0001c0001t0001g0054 others(17): Show |
20 | HG00735.hp2 HG00738.hp1 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.71+3618T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48555941 | |||||||
| chr19:48556181 | G | C | 4 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 others(1): Show |
4 | HG03098.hp1 HG03130.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.71+3858G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48556181 | |||||||
| chr19:48556228 | C | T | 4 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0002t0001g0004 others(1): Show |
4 | HG02055.hp1 HG02970.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.71+3905C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48556228 | |||||||
| chr19:48556268 | T | G | 140 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(137): Show |
140 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.71+3945T>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48556268 | |||||||
| chr19:48556272 | A | G | 2 | a0001c0002t0001g0212 a0001c0002t0001g0213 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.71+3949A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48556272 | |||||||
| chr19:48556339 | A | AAAGGACG others(5): Show |
1 | a0001c0001t0001g0268 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.71+4019_71+4030dup others(12): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48556339 | ||||||
| chr19:48556351 | G | C | 1 | a0001c0001t0001g0167 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.71+4028G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48556351 | |||||||
| chr19:48556377 | T | C | 1 | a0001c0001t0001g0117 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.71+4054T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48556377 | |||||||
| chr19:48556462 | G | A | 1 | a0001c0001t0001g0269 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.71+4139G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48556462 | |||||||
| chr19:48556480 | C | G | 30 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0022 others(27): Show |
30 | HG00733.hp1 HG01070.hp2 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.71+4157C>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48556480 | |||||||
| chr19:48556614 | G | A | 1 | a0001c0002t0001g0178 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.71+4291G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48556614 | |||||||
| chr19:48556652 | T | TA | 21 | a0001c0001t0001g0015 a0001c0001t0001g0033 a0001c0001t0001g0052 others(18): Show |
21 | HG00735.hp2 HG00738.hp1 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.71+4344dupA | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48556652 | ||||||
| chr19:48556652 | TA | T | 6 | a0001c0001t0001g0163 a0001c0001t0001g0211 a0001c0001t0001g0227 others(3): Show |
6 | HG01884.hp1 NA18747.hp1 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.71+4344delA | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48556652 | ||||||
| chr19:48556794 | T | TA | 7 | a0001c0001t0001g0037 a0001c0001t0001g0040 a0001c0001t0001g0041 others(4): Show |
7 | HG02109.hp2 HG02895.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.71+4478dupA | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48556794 | ||||||
| chr19:48556863 | T | A | 1 | a0001c0004t0001g0128 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.71+4540T>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48556863 | |||||||
| chr19:48556935 | A | G | 168 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(165): Show |
168 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.71+4612A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48556935 | |||||||
| chr19:48556936 | C | T | 1 | a0001c0005t0001g0210 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.71+4613C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48556936 | |||||||
| chr19:48556949 | C | CA | 103 | a0001c0001t0001g0071 a0001c0001t0001g0074 a0001c0001t0001g0075 others(100): Show |
103 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.71+4638dupA | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48556949 | ||||||
| chr19:48557019 | G | T | 21 | a0001c0001t0001g0071 a0001c0001t0001g0074 a0001c0001t0001g0075 others(18): Show |
21 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(18): Show |
intron_variant | MODIFIER | c.71+4696G>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48557019 | |||||||
| chr19:48557052 | C | A | 1 | a0001c0001t0001g0361 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.71+4729C>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48557052 | |||||||
| chr19:48557068 | A | G | 1 | a0001c0002t0001g0119 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.71+4745A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48557068 | |||||||
| chr19:48557228 | A | G | 20 | a0001c0001t0001g0015 a0001c0001t0001g0052 a0001c0001t0001g0054 others(17): Show |
20 | HG00735.hp2 HG00738.hp1 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.71+4905A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48557228 | |||||||
| chr19:48557240 | G | GCTTT | 20 | a0001c0001t0001g0015 a0001c0001t0001g0052 a0001c0001t0001g0054 others(17): Show |
20 | HG00735.hp2 HG00738.hp1 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.71+4917_71+4918ins others(4): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48557240 | |||||||
| chr19:48557278 | G | A | 7 | a0001c0001t0001g0015 a0001c0001t0001g0052 a0001c0001t0001g0054 others(4): Show |
7 | HG02257.hp1 HG02717.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.71+4955G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48557278 | |||||||
| chr19:48557539 | C | CA | 6 | a0001c0002t0001g0326 a0001c0004t0001g0058 a0001c0004t0001g0090 others(3): Show |
6 | HG01175.hp2 HG01361.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.71+5223dupA | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48557539 | ||||||
| chr19:48557547 | G | A | 124 | a0001c0001t0001g0015 a0001c0001t0001g0052 a0001c0001t0001g0054 others(121): Show |
124 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.71+5224G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48557547 | |||||||
| chr19:48557643 | A | C | 120 | a0001c0001t0001g0015 a0001c0001t0001g0052 a0001c0001t0001g0054 others(117): Show |
120 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.71+5320A>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48557643 | |||||||
| chr19:48557645 | G | A | 2 | a0001c0007t0001g0355 a0001c0007t0001g0356 |
2 | HG02280.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.71+5322G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48557645 | |||||||
| chr19:48557787 | T | C | 120 | a0001c0001t0001g0015 a0001c0001t0001g0052 a0001c0001t0001g0054 others(117): Show |
120 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.71+5464T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48557787 | |||||||
| chr19:48558050 | C | G | 2 | a0001c0001t0001g0344 a0001c0001t0001g0354 |
2 | HG02071.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.71+5727C>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48558050 | |||||||
| chr19:48558058 | C | A | 122 | a0001c0001t0001g0015 a0001c0001t0001g0052 a0001c0001t0001g0054 others(119): Show |
122 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.71+5735C>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48558058 | |||||||
| chr19:48558322 | C | T | 7 | a0001c0001t0001g0008 a0001c0002t0001g0048 a0001c0003t0001g0047 others(4): Show |
7 | HG01433.hp1 HG02486.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.71+5999C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48558322 | |||||||
| chr19:48558335 | GT | G | 121 | a0001c0001t0001g0015 a0001c0001t0001g0052 a0001c0001t0001g0054 others(118): Show |
121 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.71+6014delT | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48558335 | ||||||
| chr19:48558337 | T | G | 1 | a0002c0008t0001g0343 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.71+6014T>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48558337 | |||||||
| chr19:48558338 | A | C | 1 | a0002c0008t0001g0343 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.71+6015A>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48558338 | |||||||
| chr19:48558351 | C | T | 39 | a0001c0001t0001g0015 a0001c0001t0001g0052 a0001c0001t0001g0054 others(36): Show |
39 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(36): Show |
intron_variant | MODIFIER | c.71+6028C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48558351 | |||||||
| chr19:48558393 | G | A | 122 | a0001c0001t0001g0015 a0001c0001t0001g0052 a0001c0001t0001g0054 others(119): Show |
122 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.71+6070G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48558393 | |||||||
| chr19:48558467 | G | A | 161 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(158): Show |
161 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.71+6144G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48558467 | |||||||
| chr19:48558498 | G | T | 1 | a0001c0001t0001g0342 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.71+6175G>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48558498 | |||||||
| chr19:48558679 | C | CT | 25 | a0001c0001t0001g0118 a0001c0001t0001g0144 a0001c0001t0001g0207 others(22): Show |
25 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.71+6378dupT | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48558679 | ||||||
| chr19:48558679 | C | CTTT | 28 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(25): Show |
28 | HG00733.hp1 HG01243.hp1 HG01346.hp2 others(25): Show |
intron_variant | MODIFIER | c.71+6376_71+6378dup others(3): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48558679 | ||||||
| chr19:48558679 | C | CTTTT | 16 | a0001c0001t0001g0022 a0001c0001t0001g0040 a0001c0001t0001g0041 others(13): Show |
16 | HG01884.hp1 HG02257.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.71+6375_71+6378dup others(4): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48558679 | ||||||
| chr19:48558679 | CT | C | 12 | a0001c0001t0001g0018 a0001c0001t0001g0360 a0001c0001t0001g0361 others(9): Show |
12 | HG01255.hp2 HG01884.hp2 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.71+6378delT | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48558679 | ||||||
| chr19:48558679 | CTT | C | 20 | a0001c0001t0001g0062 a0001c0001t0001g0067 a0001c0001t0001g0268 others(17): Show |
20 | HG00423.hp2 HG00558.hp2 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.71+6377_71+6378del others(2): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48558679 | ||||||
| chr19:48558679 | CTTT | C | 93 | a0001c0001t0001g0071 a0001c0001t0001g0074 a0001c0001t0001g0075 others(90): Show |
93 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.71+6376_71+6378del others(3): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48558679 | ||||||
| chr19:48558683 | T | C | 1 | a0001c0002t0001g0103 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.71+6360T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48558683 | |||||||
| chr19:48558684 | T | C | 6 | a0001c0001t0001g0308 a0001c0001t0001g0309 a0001c0001t0001g0310 others(3): Show |
6 | HG00140.hp1 HG02165.hp1 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.71+6361T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48558684 | |||||||
| chr19:48558685 | T | C | 1 | a0001c0001t0001g0179 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.71+6362T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48558685 | |||||||
| chr19:48558771 | G | A | 1 | a0001c0002t0001g0078 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.71+6448G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48558771 | |||||||
| chr19:48558825 | C | T | 11 | a0001c0001t0001g0008 a0001c0002t0001g0048 a0001c0003t0001g0047 others(8): Show |
11 | HG01433.hp1 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.71+6502C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48558825 | |||||||
| chr19:48558900 | T | G | 157 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(154): Show |
157 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.71+6577T>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48558900 | |||||||
| chr19:48558906 | A | G | 157 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(154): Show |
157 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.71+6583A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48558906 | |||||||
| chr19:48558991 | C | T | 1 | a0001c0004t0001g0126 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.71+6668C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48558991 | |||||||
| chr19:48559007 | G | C | 7 | a0001c0001t0001g0037 a0001c0001t0001g0040 a0001c0001t0001g0041 others(4): Show |
7 | HG02109.hp2 HG02895.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.71+6684G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48559007 | |||||||
| chr19:48559065 | G | C | 1 | a0001c0001t0001g0239 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.71+6742G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48559065 | |||||||
| chr19:48559238 | C | T | 29 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0022 others(26): Show |
29 | HG00733.hp1 HG01243.hp1 HG01346.hp2 others(26): Show |
intron_variant | MODIFIER | c.71+6915C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48559238 | |||||||
| chr19:48559251 | G | C | 2 | a0001c0002t0001g0121 a0001c0009t0001g0120 |
2 | HG01255.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.71+6928G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48559251 | |||||||
| chr19:48559282 | G | C | 4 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0002t0001g0004 others(1): Show |
4 | HG02055.hp1 HG02970.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.71+6959G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48559282 | |||||||
| chr19:48559306 | G | A | 29 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0022 others(26): Show |
29 | HG00733.hp1 HG01243.hp1 HG01346.hp2 others(26): Show |
intron_variant | MODIFIER | c.71+6983G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48559306 | |||||||
| chr19:48559311 | T | A | 5 | a0001c0001t0001g0164 a0001c0002t0001g0100 a0001c0003t0001g0127 others(2): Show |
5 | HG01928.hp1 HG01943.hp1 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.71+6988T>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48559311 | |||||||
| chr19:48559322 | A | G | 4 | a0001c0001t0001g0062 a0001c0002t0001g0050 a0001c0002t0001g0051 others(1): Show |
4 | HG01070.hp2 HG01071.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.71+6999A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48559322 | |||||||
| chr19:48559348 | T | TTTTTG | 12 | a0001c0001t0001g0116 a0001c0001t0001g0118 a0001c0001t0001g0141 others(9): Show |
12 | HG00423.hp1 HG01069.hp2 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.71+7061_71+7065dup others(5): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48559348 | ||||||
| chr19:48559348 | TTTTTG | T | 140 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0022 others(137): Show |
140 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.71+7061_71+7065del others(5): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48559348 | ||||||
| chr19:48559348 | TTTTTGTT others(3): Show |
T | 11 | a0001c0001t0001g0008 a0001c0002t0001g0048 a0001c0003t0001g0047 others(8): Show |
11 | HG01433.hp1 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.71+7056_71+7065del others(10): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48559348 | ||||||
| chr19:48559348 | TTTTTGTT others(8): Show |
T | 1 | a0001c0002t0001g0119 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.71+7051_71+7065del others(15): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48559348 | ||||||
| chr19:48559388 | G | T | 1 | a0001c0002t0001g0326 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.71+7065G>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48559388 | |||||||
| chr19:48559551 | G | T | 2 | a0001c0001t0001g0204 a0001c0007t0001g0162 |
2 | HG01261.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.71+7228G>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48559551 | |||||||
| chr19:48559579 | C | A | 4 | a0001c0001t0001g0062 a0001c0002t0001g0050 a0001c0002t0001g0051 others(1): Show |
4 | HG01070.hp2 HG01071.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.71+7256C>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48559579 | |||||||
| chr19:48559722 | C | T | 77 | a0001c0001t0001g0228 a0001c0001t0001g0230 a0001c0001t0001g0233 others(74): Show |
77 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.71+7399C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48559722 | |||||||
| chr19:48559750 | AG | A | 18 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(15): Show |
18 | HG01433.hp1 HG02109.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.71+7429delG | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48559750 | ||||||
| chr19:48559849 | CA | C | 4 | a0001c0004t0001g0058 a0001c0004t0001g0090 a0001c0006t0001g0061 others(1): Show |
4 | HG02145.hp2 HG02258.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.71+7527delA | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48559849 | |||||||
| chr19:48559959 | T | TA | 6 | a0001c0001t0001g0108 a0001c0001t0001g0118 a0001c0001t0001g0311 others(3): Show |
6 | HG01070.hp1 HG01106.hp2 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.71+7654dupA | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48559959 | ||||||
| chr19:48559959 | TA | T | 14 | a0001c0001t0001g0015 a0001c0001t0001g0056 a0001c0001t0001g0067 others(11): Show |
14 | HG01081.hp2 HG01168.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.71+7654delA | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48559959 | ||||||
| chr19:48559959 | TAA | T | 22 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(19): Show |
22 | HG01243.hp1 HG01433.hp1 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.71+7653_71+7654del others(2): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48559959 | ||||||
| chr19:48559971 | A | C | 1 | a0001c0003t0001g0217 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.71+7648A>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48559971 | |||||||
| chr19:48560072 | C | G | 1 | a0001c0005t0001g0020 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.71+7749C>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48560072 | |||||||
| chr19:48560089 | C | T | 1 | a0001c0004t0001g0096 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.71+7766C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48560089 | |||||||
| chr19:48560135 | G | A | 7 | a0001c0001t0001g0037 a0001c0001t0001g0040 a0001c0001t0001g0041 others(4): Show |
7 | HG02109.hp2 HG02895.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.71+7812G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48560135 | |||||||
| chr19:48560361 | T | C | 1 | a0002c0008t0001g0158 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.71+8038T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48560361 | |||||||
| chr19:48560371 | A | G | 5 | a0001c0001t0001g0093 a0001c0002t0001g0091 a0001c0006t0001g0094 others(2): Show |
5 | HG01243.hp1 HG02109.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.71+8048A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48560371 | |||||||
| chr19:48560434 | C | A | 1 | a0001c0001t0001g0024 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.71+8111C>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48560434 | |||||||
| chr19:48560535 | A | G | 1 | a0001c0004t0001g0096 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.71+8212A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48560535 | |||||||
| chr19:48560579 | T | A | 1 | a0001c0005t0001g0009 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.71+8256T>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48560579 | |||||||
| chr19:48560579 | T | TA | 20 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0032 others(17): Show |
20 | HG00733.hp1 HG01346.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.71+8263dupA | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48560579 | ||||||
| chr19:48560651 | T | C | 5 | a0001c0001t0001g0093 a0001c0002t0001g0091 a0001c0006t0001g0094 others(2): Show |
5 | HG01243.hp1 HG02109.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.71+8328T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48560651 | |||||||
| chr19:48560657 | C | A | 2 | a0002c0008t0001g0270 a0002c0008t0001g0343 |
2 | NA18961.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.71+8334C>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48560657 | |||||||
| chr19:48560666 | A | AAATTGTC others(9): Show |
1 | a0001c0001t0001g0271 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.71+8345_71+8346ins others(16): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48560666 | ||||||
| chr19:48560669 | C | T | 155 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(152): Show |
155 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.71+8346C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48560669 | |||||||
| chr19:48560703 | ATAATCCC others(462): Show |
A | 2 | a0001c0006t0001g0045 a0003c0011t0001g0044 |
2 | HG02723.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.71+8392_71+8860del | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48560703 | ||||||
| chr19:48560863 | G | A | 4 | a0001c0004t0001g0058 a0001c0004t0001g0090 a0001c0006t0001g0061 others(1): Show |
4 | HG02145.hp2 HG02258.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.71+8540G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48560863 | |||||||
| chr19:48560899 | C | T | 5 | a0001c0001t0001g0093 a0001c0002t0001g0091 a0001c0006t0001g0094 others(2): Show |
5 | HG01243.hp1 HG02109.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.71+8576C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48560899 | |||||||
| chr19:48561004 | C | T | 3 | a0001c0002t0001g0050 a0001c0002t0001g0051 a0001c0006t0001g0095 |
3 | HG01070.hp2 HG01071.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.71+8681C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48561004 | |||||||
| chr19:48561063 | C | T | 1 | a0001c0005t0001g0020 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.71+8740C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48561063 | |||||||
| chr19:48561112 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.71+8789G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48561112 | |||||||
| chr19:48561146 | C | T | 3 | a0001c0001t0001g0008 a0001c0001t0001g0052 a0001c0006t0001g0007 |
3 | HG01433.hp1 HG03195.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.71+8823C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48561146 | |||||||
| chr19:48561152 | C | T | 2 | a0001c0002t0001g0050 a0001c0002t0001g0051 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.71+8829C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48561152 | |||||||
| chr19:48561195 | C | T | 10 | a0001c0001t0001g0015 a0001c0001t0001g0040 a0001c0001t0001g0041 others(7): Show |
10 | HG02257.hp1 HG02717.hp1 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.71+8872C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48561195 | |||||||
| chr19:48561227 | C | T | 1 | a0001c0006t0001g0095 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.71+8904C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48561227 | |||||||
| chr19:48561258 | C | T | 2 | a0001c0006t0001g0039 a0001c0010t0001g0038 |
2 | HG02976.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.71+8935C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48561258 | |||||||
| chr19:48561287 | T | G | 7 | a0001c0001t0001g0144 a0001c0001t0001g0147 a0001c0002t0001g0143 others(4): Show |
7 | HG01123.hp2 HG01361.hp1 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.71+8964T>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48561287 | |||||||
| chr19:48561288 | C | T | 7 | a0001c0001t0001g0144 a0001c0001t0001g0147 a0001c0002t0001g0143 others(4): Show |
7 | HG01123.hp2 HG01361.hp1 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.71+8965C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48561288 | |||||||
| chr19:48561296 | C | T | 7 | a0001c0001t0001g0144 a0001c0001t0001g0147 a0001c0002t0001g0143 others(4): Show |
7 | HG01123.hp2 HG01361.hp1 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.71+8973C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48561296 | |||||||
| chr19:48561353 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.71+9030C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48561353 | |||||||
| chr19:48561384 | G | A | 3 | a0001c0002t0001g0121 a0001c0002t0001g0253 a0001c0009t0001g0120 |
3 | HG01255.hp2 HG01346.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.71+9061G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48561384 | |||||||
| chr19:48561390 | T | C | 1 | a0001c0002t0001g0080 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.71+9067T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48561390 | |||||||
| chr19:48561416 | T | C | 99 | a0001c0001t0001g0122 a0001c0001t0001g0182 a0001c0001t0001g0228 others(96): Show |
99 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.71+9093T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48561416 | |||||||
| chr19:48561422 | A | T | 99 | a0001c0001t0001g0122 a0001c0001t0001g0182 a0001c0001t0001g0228 others(96): Show |
99 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.71+9099A>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48561422 | |||||||
| chr19:48561430 | A | AAAAT | 96 | a0001c0001t0001g0122 a0001c0001t0001g0182 a0001c0001t0001g0228 others(93): Show |
96 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.71+9121_71+9124dup others(4): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48561430 | ||||||
| chr19:48561448 | G | A | 3 | a0001c0002t0001g0050 a0001c0002t0001g0051 a0001c0006t0001g0095 |
3 | HG01070.hp2 HG01071.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.71+9125G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48561448 | |||||||
| chr19:48561456 | A | G | 3 | a0001c0002t0001g0050 a0001c0002t0001g0051 a0001c0006t0001g0095 |
3 | HG01070.hp2 HG01071.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.71+9133A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48561456 | |||||||
| chr19:48561458 | A | T | 3 | a0001c0002t0001g0050 a0001c0002t0001g0051 a0001c0006t0001g0095 |
3 | HG01070.hp2 HG01071.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.71+9135A>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48561458 | |||||||
| chr19:48561459 | T | A | 3 | a0001c0002t0001g0050 a0001c0002t0001g0051 a0001c0006t0001g0095 |
3 | HG01070.hp2 HG01071.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.71+9136T>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48561459 | |||||||
| chr19:48561462 | ATAAAT | A | 96 | a0001c0001t0001g0122 a0001c0001t0001g0182 a0001c0001t0001g0228 others(93): Show |
96 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.71+9143_71+9147del others(5): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48561462 | ||||||
| chr19:48561466 | AT | A | 3 | a0001c0002t0001g0050 a0001c0002t0001g0051 a0001c0006t0001g0095 |
3 | HG01070.hp2 HG01071.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.71+9145delT | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48561466 | ||||||
| chr19:48561547 | GA | G | 103 | a0001c0001t0001g0037 a0001c0001t0001g0122 a0001c0001t0001g0182 others(100): Show |
103 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.71+9231delA | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48561547 | ||||||
| chr19:48561597 | C | T | 100 | a0001c0001t0001g0117 a0001c0001t0001g0182 a0001c0001t0001g0228 others(97): Show |
100 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.71+9274C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48561597 | |||||||
| chr19:48561598 | A | G | 101 | a0001c0001t0001g0117 a0001c0001t0001g0182 a0001c0001t0001g0228 others(98): Show |
101 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.71+9275A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48561598 | |||||||
| chr19:48561702 | C | T | 105 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0015 others(102): Show |
105 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.71+9379C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48561702 | |||||||
| chr19:48561724 | G | A | 1 | a0001c0002t0001g0104 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.71+9401G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48561724 | |||||||
| chr19:48561752 | C | T | 36 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0015 others(33): Show |
36 | HG00733.hp1 HG01069.hp2 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.71+9429C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48561752 | |||||||
| chr19:48561795 | C | T | 2 | a0001c0002t0001g0048 a0006c0017t0001g0030 |
2 | HG02486.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.71+9472C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48561795 | |||||||
| chr19:48561802 | C | A | 84 | a0001c0001t0001g0122 a0001c0001t0001g0182 a0001c0001t0001g0228 others(81): Show |
84 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.71+9479C>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48561802 | |||||||
| chr19:48561905 | G | A | 80 | a0001c0001t0001g0122 a0001c0001t0001g0182 a0001c0001t0001g0228 others(77): Show |
80 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.71+9582G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48561905 | |||||||
| chr19:48561931 | A | G | 1 | a0001c0004t0001g0070 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.71+9608A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48561931 | |||||||
| chr19:48561988 | G | A | 84 | a0001c0001t0001g0098 a0001c0001t0001g0105 a0001c0001t0001g0122 others(81): Show |
84 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.71+9665G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48561988 | |||||||
| chr19:48562037 | A | G | 89 | a0001c0001t0001g0098 a0001c0001t0001g0105 a0001c0001t0001g0122 others(86): Show |
89 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.71+9714A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48562037 | |||||||
| chr19:48562157 | C | T | 2 | a0001c0002t0001g0050 a0001c0002t0001g0051 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.71+9834C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48562157 | |||||||
| chr19:48562218 | T | C | 25 | a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0026 others(22): Show |
25 | HG01243.hp1 HG02055.hp2 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.71+9895T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48562218 | |||||||
| chr19:48562249 | G | A | 2 | a0001c0001t0001g0197 a0001c0001t0001g0203 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.71+9926G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48562249 | |||||||
| chr19:48562269 | T | C | 2 | a0001c0001t0001g0101 a0001c0001t0001g0170 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.71+9946T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48562269 | |||||||
| chr19:48562335 | C | T | 1 | a0001c0001t0001g0117 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.71+10012C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48562335 | |||||||
| chr19:48562375 | A | G | 41 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0022 others(38): Show |
42 | HG00099.hp2 HG00140.hp2 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.71+10052A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48562375 | |||||||
| chr19:48562386 | C | CA | 14 | a0001c0001t0001g0116 a0001c0001t0001g0258 a0001c0001t0001g0362 others(11): Show |
14 | HG00423.hp1 HG01109.hp1 HG01515.hp1 others(11): Show |
intron_variant | MODIFIER | c.71+10078dupA | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48562386 | ||||||
| chr19:48562500 | C | T | 1 | a0001c0001t0001g0300 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.71+10177C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48562500 | |||||||
| chr19:48562534 | G | A | 110 | a0001c0001t0001g0032 a0001c0001t0001g0040 a0001c0001t0001g0041 others(107): Show |
110 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.71+10211G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48562534 | |||||||
| chr19:48562590 | T | C | 2 | a0001c0001t0001g0101 a0001c0001t0001g0170 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.71+10267T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48562590 | |||||||
| chr19:48562604 | T | A | 1 | a0001c0002t0001g0178 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.71+10281T>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48562604 | |||||||
| chr19:48562605 | T | A | 1 | a0001c0003t0001g0124 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.71+10282T>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48562605 | |||||||
| chr19:48562633 | T | C | 171 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0022 others(168): Show |
172 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.71+10310T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48562633 | |||||||
| chr19:48562666 | T | G | 39 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0025 others(36): Show |
39 | HG01070.hp2 HG01071.hp2 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.71+10343T>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48562666 | |||||||
| chr19:48562724 | A | G | 110 | a0001c0001t0001g0018 a0001c0001t0001g0032 a0001c0001t0001g0040 others(107): Show |
110 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.71+10401A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48562724 | |||||||
| chr19:48562741 | G | A | 6 | a0001c0005t0001g0009 a0001c0005t0001g0010 a0001c0005t0001g0011 others(3): Show |
6 | HG01884.hp1 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.71+10418G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48562741 | |||||||
| chr19:48562743 | G | A | 5 | a0001c0005t0001g0009 a0001c0005t0001g0010 a0001c0005t0001g0011 others(2): Show |
5 | HG01884.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.71+10420G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48562743 | |||||||
| chr19:48562780 | G | A | 204 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(201): Show |
205 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.71+10457G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48562780 | |||||||
| chr19:48563035 | C | G | 124 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0032 others(121): Show |
124 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.71+10712C>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48563035 | |||||||
| chr19:48563055 | T | A | 1 | a0001c0002t0001g0316 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.71+10732T>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48563055 | |||||||
| chr19:48563223 | CG | C | 25 | a0001c0001t0001g0018 a0001c0001t0001g0040 a0001c0001t0001g0041 others(22): Show |
25 | HG00642.hp1 HG00738.hp1 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.71+10902delG | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48563223 | ||||||
| chr19:48563415 | G | T | 1 | a0001c0001t0001g0372 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.71+11092G>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48563415 | |||||||
| chr19:48563461 | C | T | 5 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0052 others(2): Show |
5 | HG01433.hp1 HG01891.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.71+11138C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48563461 | |||||||
| chr19:48563473 | T | A | 20 | a0001c0002t0001g0347 a0001c0005t0001g0001 a0001c0005t0001g0072 others(17): Show |
21 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.71+11150T>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48563473 | |||||||
| chr19:48563586 | T | C | 1 | a0001c0005t0001g0312 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.71+11263T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48563586 | |||||||
| chr19:48563613 | C | T | 1 | a0001c0007t0001g0356 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.71+11290C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48563613 | |||||||
| chr19:48563623 | C | T | 1 | a0001c0006t0001g0095 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.71+11300C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48563623 | |||||||
| chr19:48563679 | T | C | 139 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0032 others(136): Show |
140 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.71+11356T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48563679 | |||||||
| chr19:48563680 | G | A | 20 | a0001c0002t0001g0347 a0001c0005t0001g0001 a0001c0005t0001g0072 others(17): Show |
21 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.71+11357G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48563680 | |||||||
| chr19:48563682 | G | A | 3 | a0001c0004t0001g0053 a0001c0004t0001g0090 a0001c0004t0001g0196 |
3 | HG02258.hp2 HG02572.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.71+11359G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48563682 | |||||||
| chr19:48563694 | G | A | 1 | a0002c0008t0001g0158 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.71+11371G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48563694 | |||||||
| chr19:48563792 | G | A | 9 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0033 others(6): Show |
9 | HG02055.hp1 HG02486.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.71+11469G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48563792 | |||||||
| chr19:48563797 | T | C | 1 | a0001c0006t0001g0094 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.71+11474T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48563797 | |||||||
| chr19:48563951 | C | T | 1 | a0001c0002t0001g0130 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.71+11628C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48563951 | |||||||
| chr19:48563959 | C | CA | 15 | a0001c0001t0001g0311 a0001c0001t0001g0338 a0001c0001t0001g0362 others(12): Show |
15 | HG01106.hp2 HG02015.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.71+11651dupA | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48563959 | ||||||
| chr19:48563959 | C | CAA | 14 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(11): Show |
14 | HG01243.hp1 HG02055.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.71+11650_71+11651d others(4): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48563959 | ||||||
| chr19:48563959 | CA | C | 126 | a0001c0001t0001g0018 a0001c0001t0001g0040 a0001c0001t0001g0041 others(123): Show |
127 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(124): Show |
intron_variant | MODIFIER | c.71+11651delA | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48563959 | ||||||
| chr19:48563959 | CAA | C | 7 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0052 others(4): Show |
7 | HG01433.hp1 HG01891.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.71+11650_71+11651d others(4): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48563959 | ||||||
| chr19:48563969 | A | C | 4 | a0001c0001t0001g0055 a0001c0001t0001g0101 a0001c0001t0001g0170 others(1): Show |
4 | HG00733.hp1 HG01167.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.71+11646A>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48563969 | |||||||
| chr19:48564107 | G | A | 20 | a0001c0002t0001g0347 a0001c0005t0001g0001 a0001c0005t0001g0072 others(17): Show |
21 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.71+11784G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48564107 | |||||||
| chr19:48564282 | A | G | 4 | a0001c0002t0001g0048 a0001c0002t0001g0119 a0001c0003t0001g0047 others(1): Show |
4 | HG02486.hp1 HG02965.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.72-11659A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48564282 | |||||||
| chr19:48564447 | G | A | 14 | a0001c0001t0001g0132 a0001c0001t0001g0148 a0001c0001t0001g0163 others(11): Show |
14 | HG00642.hp1 HG01168.hp2 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.72-11494G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48564447 | |||||||
| chr19:48564551 | C | CA | 54 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0040 others(51): Show |
54 | HG00642.hp1 HG00733.hp1 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.72-11366dupA | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48564551 | ||||||
| chr19:48564551 | C | CAA | 7 | a0001c0001t0001g0032 a0001c0001t0001g0041 a0001c0001t0001g0185 others(4): Show |
7 | HG01891.hp2 HG02738.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.72-11367_72-11366d others(4): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48564551 | ||||||
| chr19:48564551 | CA | C | 167 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0022 others(164): Show |
167 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.72-11366delA | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48564551 | ||||||
| chr19:48564551 | CAA | C | 8 | a0001c0001t0001g0037 a0001c0001t0001g0141 a0001c0001t0001g0197 others(5): Show |
8 | HG02109.hp2 HG02818.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.72-11367_72-11366d others(4): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48564551 | ||||||
| chr19:48564572 | A | AG | 4 | a0001c0001t0001g0081 a0001c0005t0001g0210 a0001c0005t0001g0214 others(1): Show |
4 | HG01192.hp1 HG01496.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-11369_72-11368i others(3): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48564572 | |||||||
| chr19:48564572 | A | G | 8 | a0001c0002t0001g0048 a0001c0002t0001g0119 a0001c0003t0001g0047 others(5): Show |
8 | HG01261.hp2 HG02109.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.72-11369A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48564572 | |||||||
| chr19:48564674 | A | T | 9 | a0001c0001t0001g0089 a0001c0001t0001g0216 a0001c0001t0001g0258 others(6): Show |
9 | HG00735.hp2 HG00738.hp2 HG01070.hp1 others(6): Show |
intron_variant | MODIFIER | c.72-11267A>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48564674 | |||||||
| chr19:48564677 | A | T | 4 | a0001c0001t0001g0362 a0001c0004t0001g0053 a0001c0004t0001g0090 others(1): Show |
4 | HG02258.hp2 HG02572.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-11264A>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48564677 | |||||||
| chr19:48564947 | C | T | 113 | a0001c0001t0001g0015 a0001c0001t0001g0037 a0001c0001t0001g0055 others(110): Show |
113 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(110): Show |
intron_variant | MODIFIER | c.72-10994C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48564947 | |||||||
| chr19:48564951 | C | T | 3 | a0001c0001t0001g0122 a0001c0001t0001g0186 a0001c0001t0001g0352 |
3 | NA18973.hp2 NA18982.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.72-10990C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48564951 | |||||||
| chr19:48565050 | A | T | 4 | a0001c0002t0001g0048 a0001c0002t0001g0119 a0001c0003t0001g0047 others(1): Show |
4 | HG02486.hp1 HG02965.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.72-10891A>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48565050 | |||||||
| chr19:48565097 | G | GT | 5 | a0001c0001t0001g0187 a0001c0001t0001g0268 a0001c0001t0001g0297 others(2): Show |
5 | HG02145.hp2 NA19011.hp2 NA19058.hp1 others(2): Show |
intron_variant | MODIFIER | c.72-10836dupT | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48565097 | ||||||
| chr19:48565333 | G | T | 5 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0052 others(2): Show |
5 | HG01433.hp1 HG01891.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.72-10608G>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48565333 | |||||||
| chr19:48565335 | G | T | 185 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(182): Show |
185 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(182): Show |
intron_variant | MODIFIER | c.72-10606G>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48565335 | |||||||
| chr19:48565355 | T | C | 171 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0015 others(168): Show |
171 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(168): Show |
intron_variant | MODIFIER | c.72-10586T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48565355 | |||||||
| chr19:48565357 | T | G | 1 | a0001c0001t0001g0211 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.72-10584T>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48565357 | |||||||
| chr19:48565481 | G | A | 1 | a0001c0004t0001g0135 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.72-10460G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48565481 | |||||||
| chr19:48565531 | C | T | 2 | a0001c0001t0001g0194 a0001c0002t0001g0104 |
2 | HG02698.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.72-10410C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48565531 | |||||||
| chr19:48565618 | G | A | 5 | a0001c0001t0001g0062 a0001c0002t0001g0048 a0001c0002t0001g0119 others(2): Show |
5 | HG02486.hp1 HG02809.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.72-10323G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48565618 | |||||||
| chr19:48565633 | G | A | 1 | a0001c0003t0001g0012 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.72-10308G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48565633 | |||||||
| chr19:48565736 | A | G | 1 | a0001c0002t0001g0156 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.72-10205A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48565736 | |||||||
| chr19:48565755 | TTTTG | T | 78 | a0001c0001t0001g0098 a0001c0001t0001g0118 a0001c0001t0001g0122 others(75): Show |
78 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.72-10166_72-10163d others(6): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48565755 | ||||||
| chr19:48565904 | A | G | 7 | a0001c0001t0001g0081 a0001c0005t0001g0020 a0001c0005t0001g0210 others(4): Show |
7 | HG01192.hp1 HG01261.hp2 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.72-10037A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48565904 | |||||||
| chr19:48565917 | A | AT | 187 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0015 others(184): Show |
188 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.72-10010dupT | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48565917 | ||||||
| chr19:48565934 | A | G | 176 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(173): Show |
176 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(173): Show |
intron_variant | MODIFIER | c.72-10007A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48565934 | |||||||
| chr19:48565935 | C | T | 1 | a0001c0001t0001g0018 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.72-10006C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48565935 | |||||||
| chr19:48566017 | A | G | 86 | a0001c0001t0001g0081 a0001c0001t0001g0098 a0001c0001t0001g0118 others(83): Show |
86 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.72-9924A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48566017 | |||||||
| chr19:48566019 | T | G | 1 | a0001c0002t0001g0316 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.72-9922T>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48566019 | |||||||
| chr19:48566061 | C | T | 30 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0052 others(27): Show |
31 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.72-9880C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48566061 | |||||||
| chr19:48566075 | G | A | 30 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0052 others(27): Show |
31 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.72-9866G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48566075 | |||||||
| chr19:48566100 | C | G | 1 | a0001c0002t0001g0249 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.72-9841C>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48566100 | |||||||
| chr19:48566100 | C | T | 170 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0015 others(167): Show |
170 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(167): Show |
intron_variant | MODIFIER | c.72-9841C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48566100 | |||||||
| chr19:48566102 | G | A | 30 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0052 others(27): Show |
31 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.72-9839G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48566102 | |||||||
| chr19:48566127 | G | C | 1 | a0001c0003t0001g0102 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.72-9814G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48566127 | |||||||
| chr19:48566146 | G | A | 5 | a0001c0001t0001g0062 a0001c0002t0001g0048 a0001c0002t0001g0119 others(2): Show |
5 | HG02486.hp1 HG02809.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.72-9795G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48566146 | |||||||
| chr19:48566151 | C | T | 5 | a0001c0001t0001g0062 a0001c0002t0001g0048 a0001c0002t0001g0119 others(2): Show |
5 | HG02486.hp1 HG02809.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.72-9790C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48566151 | |||||||
| chr19:48566159 | G | C | 30 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0052 others(27): Show |
31 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.72-9782G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48566159 | |||||||
| chr19:48566228 | A | T | 30 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0052 others(27): Show |
31 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.72-9713A>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48566228 | |||||||
| chr19:48566277 | G | A | 8 | a0001c0006t0001g0039 a0001c0006t0001g0061 a0001c0007t0001g0057 others(5): Show |
8 | HG02145.hp2 HG02280.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.72-9664G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48566277 | |||||||
| chr19:48566333 | T | C | 1 | a0001c0002t0001g0161 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.72-9608T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48566333 | |||||||
| chr19:48566366 | G | A | 25 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0052 others(22): Show |
26 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.72-9575G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48566366 | |||||||
| chr19:48566382 | G | C | 30 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0052 others(27): Show |
31 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.72-9559G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48566382 | |||||||
| chr19:48566420 | G | A | 3 | a0001c0001t0001g0185 a0001c0001t0001g0200 a0001c0002t0001g0123 |
3 | NA19002.hp2 NA19012.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.72-9521G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48566420 | |||||||
| chr19:48566631 | C | T | 11 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0054 others(8): Show |
11 | HG01884.hp2 HG02257.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.72-9310C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48566631 | |||||||
| chr19:48566659 | T | C | 2 | a0001c0001t0001g0008 a0001c0001t0001g0052 |
2 | HG01433.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.72-9282T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48566659 | |||||||
| chr19:48566670 | C | T | 1 | a0001c0003t0001g0374 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.72-9271C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48566670 | |||||||
| chr19:48566708 | A | G | 30 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0052 others(27): Show |
31 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.72-9233A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48566708 | |||||||
| chr19:48566791 | A | G | 30 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0052 others(27): Show |
31 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.72-9150A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48566791 | |||||||
| chr19:48566813 | G | T | 1 | a0001c0003t0001g0175 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.72-9128G>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48566813 | |||||||
| chr19:48566839 | CA | C | 29 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0052 others(26): Show |
30 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.72-9088delA | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48566839 | ||||||
| chr19:48566864 | G | A | 1 | a0002c0008t0001g0232 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.72-9077G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48566864 | |||||||
| chr19:48566877 | C | T | 30 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0052 others(27): Show |
31 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.72-9064C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48566877 | |||||||
| chr19:48566892 | T | A | 30 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0052 others(27): Show |
31 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.72-9049T>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48566892 | |||||||
| chr19:48566918 | A | G | 30 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0052 others(27): Show |
31 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.72-9023A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48566918 | |||||||
| chr19:48566981 | C | T | 1 | a0001c0005t0001g0312 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.72-8960C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48566981 | |||||||
| chr19:48566989 | C | G | 5 | a0001c0001t0001g0062 a0001c0002t0001g0048 a0001c0002t0001g0119 others(2): Show |
5 | HG02486.hp1 HG02809.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.72-8952C>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48566989 | |||||||
| chr19:48567002 | T | A | 2 | a0001c0001t0001g0296 a0001c0003t0001g0306 |
2 | HG00558.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.72-8939T>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48567002 | |||||||
| chr19:48567002 | T | C | 30 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0052 others(27): Show |
31 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.72-8939T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48567002 | |||||||
| chr19:48567002 | T | TA | 12 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0054 others(9): Show |
12 | HG01884.hp2 HG02257.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.72-8930dupA | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48567002 | ||||||
| chr19:48567003 | A | T | 1 | a0001c0001t0001g0296 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.72-8938A>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48567003 | |||||||
| chr19:48567128 | G | A | 2 | a0001c0001t0001g0026 a0001c0004t0001g0142 |
2 | HG01433.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.72-8813G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48567128 | |||||||
| chr19:48567135 | G | A | 30 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0052 others(27): Show |
31 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.72-8806G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48567135 | |||||||
| chr19:48567148 | T | C | 30 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0052 others(27): Show |
31 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.72-8793T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48567148 | |||||||
| chr19:48567195 | C | T | 1 | a0001c0002t0001g0085 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.72-8746C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48567195 | |||||||
| chr19:48567269 | G | GAA | 5 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0052 others(2): Show |
5 | HG01433.hp1 HG01891.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.72-8671_72-8670dup others(2): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48567269 | ||||||
| chr19:48567335 | G | A | 170 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0015 others(167): Show |
170 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(167): Show |
intron_variant | MODIFIER | c.72-8606G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48567335 | |||||||
| chr19:48567391 | G | C | 31 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0052 others(28): Show |
32 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.72-8550G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48567391 | |||||||
| chr19:48567423 | G | A | 4 | a0001c0001t0001g0055 a0001c0001t0001g0101 a0001c0001t0001g0170 others(1): Show |
4 | HG00733.hp1 HG01167.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.72-8518G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48567423 | |||||||
| chr19:48567425 | G | A | 31 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0052 others(28): Show |
32 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.72-8516G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48567425 | |||||||
| chr19:48567434 | C | T | 20 | a0001c0002t0001g0347 a0001c0005t0001g0001 a0001c0005t0001g0072 others(17): Show |
21 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.72-8507C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48567434 | |||||||
| chr19:48567526 | C | T | 1 | a0001c0001t0001g0329 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.72-8415C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48567526 | |||||||
| chr19:48567542 | T | C | 31 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0052 others(28): Show |
32 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.72-8399T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48567542 | |||||||
| chr19:48567557 | A | C | 110 | a0001c0001t0001g0015 a0001c0001t0001g0037 a0001c0001t0001g0089 others(107): Show |
110 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(107): Show |
intron_variant | MODIFIER | c.72-8384A>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48567557 | |||||||
| chr19:48567611 | G | A | 5 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0052 others(2): Show |
5 | HG01433.hp1 HG01891.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.72-8330G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48567611 | |||||||
| chr19:48567617 | A | G | 31 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0052 others(28): Show |
32 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.72-8324A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48567617 | |||||||
| chr19:48567707 | C | T | 19 | a0001c0001t0001g0247 a0001c0002t0001g0082 a0001c0002t0001g0083 others(16): Show |
19 | HG00639.hp2 HG00735.hp1 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.72-8234C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48567707 | |||||||
| chr19:48567788 | G | A | 171 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0015 others(168): Show |
171 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(168): Show |
intron_variant | MODIFIER | c.72-8153G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48567788 | |||||||
| chr19:48567861 | T | C | 171 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0015 others(168): Show |
171 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(168): Show |
intron_variant | MODIFIER | c.72-8080T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48567861 | |||||||
| chr19:48567918 | T | G | 5 | a0001c0001t0001g0081 a0001c0005t0001g0210 a0001c0005t0001g0214 others(2): Show |
5 | HG01192.hp1 HG01261.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.72-8023T>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48567918 | |||||||
| chr19:48567956 | C | T | 110 | a0001c0001t0001g0015 a0001c0001t0001g0037 a0001c0001t0001g0089 others(107): Show |
110 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(107): Show |
intron_variant | MODIFIER | c.72-7985C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48567956 | |||||||
| chr19:48568132 | G | T | 1 | a0001c0004t0001g0128 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.72-7809G>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48568132 | |||||||
| chr19:48568145 | CA | C | 6 | a0001c0001t0001g0141 a0001c0001t0001g0179 a0001c0001t0001g0242 others(3): Show |
6 | HG00423.hp1 NA18945.hp1 NA18954.hp2 others(3): Show |
intron_variant | MODIFIER | c.72-7795delA | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48568145 | |||||||
| chr19:48568213 | G | A | 1 | a0001c0005t0001g0195 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.72-7728G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48568213 | |||||||
| chr19:48568281 | A | G | 171 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0015 others(168): Show |
171 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(168): Show |
intron_variant | MODIFIER | c.72-7660A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48568281 | |||||||
| chr19:48568285 | C | CA | 62 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0025 others(59): Show |
62 | HG00438.hp2 HG00597.hp1 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.72-7639dupA | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48568285 | ||||||
| chr19:48568285 | C | CAA | 9 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0033 others(6): Show |
9 | HG02055.hp1 HG02486.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.72-7640_72-7639dup others(2): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48568285 | ||||||
| chr19:48568311 | A | T | 171 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0015 others(168): Show |
171 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(168): Show |
intron_variant | MODIFIER | c.72-7630A>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48568311 | |||||||
| chr19:48568499 | A | G | 176 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0015 others(173): Show |
176 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(173): Show |
intron_variant | MODIFIER | c.72-7442A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48568499 | |||||||
| chr19:48568514 | C | T | 5 | a0001c0001t0001g0149 a0001c0003t0001g0215 a0001c0003t0001g0257 others(2): Show |
5 | HG01123.hp1 HG01975.hp1 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.72-7427C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48568514 | |||||||
| chr19:48568520 | G | A | 18 | a0001c0001t0001g0147 a0001c0001t0001g0155 a0001c0001t0001g0173 others(15): Show |
18 | HG01074.hp1 HG01167.hp2 HG01358.hp1 others(15): Show |
intron_variant | MODIFIER | c.72-7421G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48568520 | |||||||
| chr19:48568559 | G | A | 1 | a0001c0006t0001g0095 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.72-7382G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48568559 | |||||||
| chr19:48568617 | C | G | 5 | a0001c0001t0001g0062 a0001c0002t0001g0048 a0001c0002t0001g0119 others(2): Show |
5 | HG02486.hp1 HG02809.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.72-7324C>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48568617 | |||||||
| chr19:48568628 | C | G | 2 | a0001c0006t0001g0061 a0001c0007t0001g0057 |
2 | HG02145.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.72-7313C>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48568628 | |||||||
| chr19:48568758 | T | C | 9 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0033 others(6): Show |
9 | HG02055.hp1 HG02486.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.72-7183T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48568758 | |||||||
| chr19:48568768 | C | T | 9 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0033 others(6): Show |
9 | HG02055.hp1 HG02486.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.72-7173C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48568768 | |||||||
| chr19:48568849 | T | C | 4 | a0001c0001t0001g0055 a0001c0001t0001g0101 a0001c0001t0001g0170 others(1): Show |
4 | HG00733.hp1 HG01167.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.72-7092T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48568849 | |||||||
| chr19:48568852 | C | A | 21 | a0001c0002t0001g0347 a0001c0005t0001g0001 a0001c0005t0001g0072 others(18): Show |
22 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.72-7089C>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48568852 | |||||||
| chr19:48568854 | C | A | 1 | a0001c0001t0001g0155 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.72-7087C>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48568854 | |||||||
| chr19:48568859 | G | A | 372 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(369): Show |
373 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(370): Show |
intron_variant | MODIFIER | c.72-7082G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48568859 | |||||||
| chr19:48568890 | T | TC | 119 | a0001c0001t0001g0015 a0001c0001t0001g0037 a0001c0001t0001g0055 others(116): Show |
119 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(116): Show |
intron_variant | MODIFIER | c.72-7050dupC | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48568890 | ||||||
| chr19:48568899 | T | G | 114 | a0001c0001t0001g0015 a0001c0001t0001g0037 a0001c0001t0001g0055 others(111): Show |
114 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(111): Show |
intron_variant | MODIFIER | c.72-7042T>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48568899 | |||||||
| chr19:48568982 | C | A | 8 | a0001c0001t0001g0238 a0001c0002t0001g0218 a0001c0003t0001g0188 others(5): Show |
8 | HG01168.hp1 HG01261.hp1 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.72-6959C>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48568982 | |||||||
| chr19:48569008 | A | G | 114 | a0001c0001t0001g0015 a0001c0001t0001g0037 a0001c0001t0001g0055 others(111): Show |
114 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(111): Show |
intron_variant | MODIFIER | c.72-6933A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569008 | |||||||
| chr19:48569020 | G | A | 114 | a0001c0001t0001g0015 a0001c0001t0001g0037 a0001c0001t0001g0055 others(111): Show |
114 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(111): Show |
intron_variant | MODIFIER | c.72-6921G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569020 | |||||||
| chr19:48569101 | A | G | 114 | a0001c0001t0001g0015 a0001c0001t0001g0037 a0001c0001t0001g0055 others(111): Show |
114 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(111): Show |
intron_variant | MODIFIER | c.72-6840A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569101 | |||||||
| chr19:48569135 | G | A | 1 | a0001c0003t0001g0220 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.72-6806G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569135 | |||||||
| chr19:48569148 | C | T | 2 | a0001c0002t0001g0050 a0001c0002t0001g0051 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.72-6793C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569148 | |||||||
| chr19:48569192 | A | C | 1 | a0001c0001t0001g0362 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.72-6749A>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569192 | |||||||
| chr19:48569203 | G | A | 114 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0032 others(111): Show |
114 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(111): Show |
intron_variant | MODIFIER | c.72-6738G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569203 | |||||||
| chr19:48569210 | C | T | 114 | a0001c0001t0001g0015 a0001c0001t0001g0037 a0001c0001t0001g0055 others(111): Show |
114 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(111): Show |
intron_variant | MODIFIER | c.72-6731C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569210 | |||||||
| chr19:48569264 | T | C | 21 | a0001c0002t0001g0347 a0001c0005t0001g0001 a0001c0005t0001g0072 others(18): Show |
22 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.72-6677T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569264 | |||||||
| chr19:48569298 | C | T | 11 | a0001c0001t0001g0233 a0001c0001t0001g0266 a0001c0001t0001g0280 others(8): Show |
11 | HG00673.hp2 HG01257.hp1 HG01952.hp2 others(8): Show |
intron_variant | MODIFIER | c.72-6643C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569298 | |||||||
| chr19:48569299 | G | C | 140 | a0001c0001t0001g0015 a0001c0001t0001g0037 a0001c0001t0001g0055 others(137): Show |
141 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.72-6642G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569299 | |||||||
| chr19:48569300 | C | A | 140 | a0001c0001t0001g0015 a0001c0001t0001g0037 a0001c0001t0001g0055 others(137): Show |
141 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.72-6641C>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569300 | |||||||
| chr19:48569328 | A | C | 192 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0015 others(189): Show |
193 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.72-6613A>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569328 | |||||||
| chr19:48569329 | G | A | 1 | a0001c0001t0001g0259 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.72-6612G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569329 | |||||||
| chr19:48569341 | CA | C | 6 | a0001c0001t0001g0032 a0001c0001t0001g0365 a0001c0005t0001g0009 others(3): Show |
6 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.72-6579delA | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48569341 | ||||||
| chr19:48569347 | A | G | 192 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0015 others(189): Show |
193 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.72-6594A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569347 | |||||||
| chr19:48569352 | A | G | 192 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0015 others(189): Show |
193 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.72-6589A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569352 | |||||||
| chr19:48569357 | A | G | 192 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0015 others(189): Show |
193 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.72-6584A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569357 | |||||||
| chr19:48569361 | A | AAAACATA others(3): Show |
3 | a0001c0001t0001g0238 a0001c0003t0001g0188 a0001c0003t0001g0225 |
3 | HG01928.hp2 HG01934.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.72-6579_72-6578ins others(10): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48569361 | ||||||
| chr19:48569361 | A | AAAC | 8 | a0001c0001t0001g0290 a0001c0001t0001g0342 a0001c0002t0001g0023 others(5): Show |
8 | HG00423.hp2 HG00673.hp1 HG02074.hp1 others(5): Show |
intron_variant | MODIFIER | c.72-6579_72-6578ins others(3): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48569361 | ||||||
| chr19:48569361 | A | AAACAT | 10 | a0001c0001t0001g0118 a0001c0001t0001g0164 a0001c0001t0001g0291 others(7): Show |
10 | HG00140.hp1 HG00738.hp1 HG01943.hp2 others(7): Show |
intron_variant | MODIFIER | c.72-6579_72-6578ins others(5): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48569361 | ||||||
| chr19:48569361 | A | AAACATAT | 10 | a0001c0001t0001g0163 a0001c0001t0001g0241 a0001c0001t0001g0268 others(7): Show |
10 | HG02896.hp1 HG02970.hp2 HG03516.hp1 others(7): Show |
intron_variant | MODIFIER | c.72-6579_72-6578ins others(7): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48569361 | ||||||
| chr19:48569361 | A | T | 2 | a0001c0005t0001g0020 a0001c0006t0001g0029 |
2 | HG03225.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.72-6580A>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569361 | |||||||
| chr19:48569361 | AACATATA others(11): Show |
A | 14 | a0001c0001t0001g0043 a0001c0001t0001g0074 a0001c0001t0001g0075 others(11): Show |
14 | HG02145.hp2 HG02280.hp2 HG02647.hp2 others(11): Show |
intron_variant | MODIFIER | c.72-6578_72-6561del others(18): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48569361 | ||||||
| chr19:48569361 | AACATATA others(13): Show |
A | 177 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0015 others(174): Show |
178 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.72-6578_72-6559del others(20): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48569361 | ||||||
| chr19:48569361 | AACATATA others(15): Show |
A | 1 | a0001c0003t0001g0047 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.72-6578_72-6557del others(22): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48569361 | ||||||
| chr19:48569362 | AC | A | 10 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0137 others(7): Show |
10 | HG00280.hp2 HG00597.hp2 HG00639.hp1 others(7): Show |
intron_variant | MODIFIER | c.72-6578delC | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569362 | |||||||
| chr19:48569363 | C | A | 2 | a0001c0001t0001g0204 a0001c0003t0001g0293 |
2 | HG02647.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.72-6578C>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569363 | |||||||
| chr19:48569363 | C | CAT | 16 | a0001c0001t0001g0081 a0001c0001t0001g0167 a0001c0001t0001g0233 others(13): Show |
16 | HG00558.hp2 HG01243.hp2 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.72-6543_72-6542dup others(2): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48569363 | ||||||
| chr19:48569363 | C | CATAT | 18 | a0001c0001t0001g0008 a0001c0001t0001g0052 a0001c0001t0001g0098 others(15): Show |
18 | HG00733.hp2 HG01361.hp1 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.72-6545_72-6542dup others(4): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48569363 | ||||||
| chr19:48569363 | C | CATATAT | 18 | a0001c0001t0001g0018 a0001c0001t0001g0067 a0001c0001t0001g0117 others(15): Show |
18 | HG00423.hp1 HG00609.hp1 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.72-6547_72-6542dup others(6): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48569363 | ||||||
| chr19:48569363 | C | CATATATA others(1): Show |
32 | a0001c0001t0001g0032 a0001c0001t0001g0071 a0001c0001t0001g0088 others(29): Show |
32 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(29): Show |
intron_variant | MODIFIER | c.72-6549_72-6542dup others(8): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48569363 | ||||||
| chr19:48569363 | C | CATATATA others(3): Show |
1 | a0001c0001t0001g0365 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.72-6551_72-6542dup others(10): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48569363 | ||||||
| chr19:48569363 | C | T | 39 | a0001c0001t0001g0118 a0001c0001t0001g0163 a0001c0001t0001g0164 others(36): Show |
39 | HG00140.hp1 HG00423.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.72-6578C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569363 | |||||||
| chr19:48569363 | CAT | C | 15 | a0001c0001t0001g0122 a0001c0001t0001g0327 a0001c0001t0001g0352 others(12): Show |
15 | HG00621.hp2 HG01123.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.72-6543_72-6542del others(2): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48569363 | ||||||
| chr19:48569363 | CATATATA others(3): Show |
C | 4 | a0001c0002t0001g0272 a0001c0003t0001g0229 a0001c0003t0001g0294 others(1): Show |
4 | NA18957.hp1 NA18982.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.72-6551_72-6542del others(10): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48569363 | ||||||
| chr19:48569365 | T | A | 1 | a0001c0005t0001g0256 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.72-6576T>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569365 | |||||||
| chr19:48569365 | T | C | 11 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0137 others(8): Show |
11 | HG00280.hp2 HG00597.hp2 HG00639.hp1 others(8): Show |
intron_variant | MODIFIER | c.72-6576T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569365 | |||||||
| chr19:48569365 | T | TATATATA others(5335): Show |
1 | a0003c0012t0001g0014 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.72-6544_72-6543ins others(5342): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48569365 | ||||||
| chr19:48569365 | T | TATATATA others(5334): Show |
1 | a0003c0012t0001g0013 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.72-6544_72-6543ins others(5341): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48569365 | ||||||
| chr19:48569365 | T | TATATATA others(5333): Show |
3 | a0001c0005t0001g0009 a0001c0005t0001g0010 a0001c0005t0001g0011 |
3 | HG02896.hp2 HG02897.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.72-6544_72-6543ins others(5340): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48569365 | ||||||
| chr19:48569367 | T | A | 1 | a0001c0005t0001g0256 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.72-6574T>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569367 | |||||||
| chr19:48569367 | T | C | 1 | a0001c0003t0001g0374 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.72-6574T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569367 | |||||||
| chr19:48569369 | T | A | 4 | a0001c0005t0001g0210 a0001c0005t0001g0214 a0001c0005t0001g0256 others(1): Show |
4 | HG01192.hp1 HG01261.hp2 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-6572T>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569369 | |||||||
| chr19:48569371 | T | A | 3 | a0001c0005t0001g0210 a0001c0005t0001g0214 a0001c0007t0001g0162 |
3 | HG01261.hp2 HG02735.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.72-6570T>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569371 | |||||||
| chr19:48569373 | T | A | 4 | a0001c0005t0001g0210 a0001c0005t0001g0214 a0001c0006t0001g0095 others(1): Show |
4 | HG01261.hp2 HG02109.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-6568T>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569373 | |||||||
| chr19:48569373 | T | C | 1 | a0001c0002t0001g0295 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.72-6568T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569373 | |||||||
| chr19:48569375 | T | A | 1 | a0001c0005t0001g0214 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.72-6566T>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569375 | |||||||
| chr19:48569381 | T | A | 14 | a0001c0001t0001g0043 a0001c0001t0001g0074 a0001c0001t0001g0075 others(11): Show |
14 | HG02145.hp2 HG02280.hp2 HG02647.hp2 others(11): Show |
intron_variant | MODIFIER | c.72-6560T>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569381 | |||||||
| chr19:48569383 | T | A | 181 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0015 others(178): Show |
182 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.72-6558T>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569383 | |||||||
| chr19:48569385 | T | A | 93 | a0001c0001t0001g0022 a0001c0001t0001g0025 a0001c0001t0001g0026 others(90): Show |
94 | HG00140.hp2 HG00280.hp1 HG00621.hp1 others(91): Show |
intron_variant | MODIFIER | c.72-6556T>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569385 | |||||||
| chr19:48569387 | T | A | 1 | a0001c0003t0001g0369 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.72-6554T>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569387 | |||||||
| chr19:48569398 | A | G | 192 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0015 others(189): Show |
193 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.72-6543A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569398 | |||||||
| chr19:48569399 | T | A | 192 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0015 others(189): Show |
193 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.72-6542T>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569399 | |||||||
| chr19:48569433 | T | C | 192 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0015 others(189): Show |
193 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.72-6508T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569433 | |||||||
| chr19:48569453 | CATCT | C | 192 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0015 others(189): Show |
193 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.72-6483_72-6480del others(4): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48569453 | ||||||
| chr19:48569459 | T | C | 192 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0015 others(189): Show |
193 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.72-6482T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569459 | |||||||
| chr19:48569535 | A | T | 2 | a0001c0001t0001g0032 a0001c0001t0001g0365 |
2 | HG01891.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.72-6406A>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569535 | |||||||
| chr19:48569537 | T | C | 192 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0015 others(189): Show |
193 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.72-6404T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569537 | |||||||
| chr19:48569554 | T | G | 192 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0015 others(189): Show |
193 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.72-6387T>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569554 | |||||||
| chr19:48569559 | A | G | 192 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0015 others(189): Show |
193 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.72-6382A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569559 | |||||||
| chr19:48569569 | G | C | 192 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0015 others(189): Show |
193 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.72-6372G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569569 | |||||||
| chr19:48569645 | T | C | 192 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0015 others(189): Show |
193 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.72-6296T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569645 | |||||||
| chr19:48569654 | A | G | 192 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0015 others(189): Show |
193 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.72-6287A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569654 | |||||||
| chr19:48569656 | G | A | 192 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0015 others(189): Show |
193 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.72-6285G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569656 | |||||||
| chr19:48569672 | G | T | 192 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0015 others(189): Show |
193 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.72-6269G>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569672 | |||||||
| chr19:48569673 | G | T | 192 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0015 others(189): Show |
193 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.72-6268G>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569673 | |||||||
| chr19:48569680 | G | T | 192 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0015 others(189): Show |
193 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.72-6261G>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569680 | |||||||
| chr19:48569744 | A | G | 192 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0015 others(189): Show |
193 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.72-6197A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569744 | |||||||
| chr19:48569753 | G | A | 192 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0015 others(189): Show |
193 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.72-6188G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569753 | |||||||
| chr19:48569769 | T | G | 5 | a0001c0001t0001g0062 a0001c0002t0001g0048 a0001c0002t0001g0119 others(2): Show |
5 | HG02486.hp1 HG02809.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.72-6172T>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569769 | |||||||
| chr19:48569792 | G | C | 11 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0054 others(8): Show |
11 | HG01884.hp2 HG02257.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.72-6149G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569792 | |||||||
| chr19:48569816 | G | A | 4 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0052 others(1): Show |
4 | HG01433.hp1 HG01891.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-6125G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569816 | |||||||
| chr19:48569912 | T | C | 192 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0015 others(189): Show |
193 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.72-6029T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569912 | |||||||
| chr19:48569948 | G | A | 21 | a0001c0002t0001g0347 a0001c0005t0001g0001 a0001c0005t0001g0072 others(18): Show |
22 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.72-5993G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569948 | |||||||
| chr19:48569958 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.72-5983G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569958 | |||||||
| chr19:48570027 | A | G | 1 | a0001c0002t0001g0104 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.72-5914A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48570027 | |||||||
| chr19:48570179 | CTTT | C | 192 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0015 others(189): Show |
193 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.72-5749_72-5747del others(3): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48570179 | ||||||
| chr19:48570380 | T | C | 53 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0022 others(50): Show |
53 | HG01070.hp2 HG01071.hp2 HG01243.hp1 others(50): Show |
intron_variant | MODIFIER | c.72-5561T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48570380 | |||||||
| chr19:48570422 | G | C | 192 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0015 others(189): Show |
193 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.72-5519G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48570422 | |||||||
| chr19:48570537 | T | C | 1 | a0001c0005t0001g0109 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.72-5404T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48570537 | |||||||
| chr19:48570542 | A | G | 192 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0015 others(189): Show |
193 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.72-5399A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48570542 | |||||||
| chr19:48570717 | C | T | 192 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0015 others(189): Show |
193 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.72-5224C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48570717 | |||||||
| chr19:48570718 | G | GTTTC | 192 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0015 others(189): Show |
193 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.72-5220_72-5219ins others(4): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48570718 | ||||||
| chr19:48570727 | T | G | 192 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0015 others(189): Show |
193 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.72-5214T>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48570727 | |||||||
| chr19:48570730 | GT | G | 192 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0015 others(189): Show |
193 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.72-5201delT | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48570730 | ||||||
| chr19:48570734 | T | G | 2 | a0001c0007t0001g0111 a0001c0007t0001g0112 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.72-5207T>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48570734 | |||||||
| chr19:48570788 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.72-5153G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48570788 | |||||||
| chr19:48570798 | C | T | 1 | a0001c0006t0001g0095 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.72-5143C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48570798 | |||||||
| chr19:48570839 | G | C | 192 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0015 others(189): Show |
193 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.72-5102G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48570839 | |||||||
| chr19:48570847 | C | T | 192 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0015 others(189): Show |
193 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.72-5094C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48570847 | |||||||
| chr19:48570914 | G | C | 1 | a0001c0003t0001g0139 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.72-5027G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48570914 | |||||||
| chr19:48570916 | G | T | 4 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0052 others(1): Show |
4 | HG01433.hp1 HG01891.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-5025G>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48570916 | |||||||
| chr19:48570943 | C | T | 1 | a0001c0002t0001g0218 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.72-4998C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48570943 | |||||||
| chr19:48570966 | C | T | 1 | a0001c0004t0001g0129 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.72-4975C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48570966 | |||||||
| chr19:48570999 | T | C | 2 | a0001c0009t0001g0320 a0001c0009t0001g0321 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.72-4942T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48570999 | |||||||
| chr19:48571004 | A | G | 2 | a0001c0009t0001g0320 a0001c0009t0001g0321 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.72-4937A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48571004 | |||||||
| chr19:48571207 | A | TTTTTTTT others(3139): Show |
2 | a0001c0001t0001g0008 a0001c0001t0001g0052 |
2 | HG01433.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.72-4735_72-4734ins others(3146): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48571207 | |||||||
| chr19:48571207 | A | TTTTTTTT others(3139): Show |
2 | a0001c0001t0001g0032 a0001c0001t0001g0365 |
2 | HG01891.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.72-4735_72-4734ins others(3146): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48571207 | |||||||
| chr19:48571211 | A | ATTTATTT others(2): Show |
156 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0015 others(153): Show |
156 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(153): Show |
intron_variant | MODIFIER | c.72-4727_72-4726ins others(9): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48571211 | ||||||
| chr19:48571211 | A | ATTTATTT others(6): Show |
31 | a0001c0001t0001g0043 a0001c0001t0001g0074 a0001c0001t0001g0075 others(28): Show |
32 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.72-4727_72-4726ins others(13): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48571211 | ||||||
| chr19:48571211 | A | ATTTATTT others(10): Show |
5 | a0001c0002t0001g0048 a0001c0002t0001g0119 a0001c0003t0001g0047 others(2): Show |
5 | HG02486.hp1 HG02723.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.72-4727_72-4726ins others(17): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48571211 | ||||||
| chr19:48571211 | A | T | 4 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0052 others(1): Show |
4 | HG01433.hp1 HG01891.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-4730A>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48571211 | |||||||
| chr19:48571321 | C | T | 4 | a0001c0002t0001g0048 a0001c0002t0001g0119 a0001c0003t0001g0047 others(1): Show |
4 | HG02486.hp1 HG02965.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.72-4620C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48571321 | |||||||
| chr19:48571357 | C | T | 192 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0015 others(189): Show |
193 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.72-4584C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48571357 | |||||||
| chr19:48571378 | G | C | 5 | a0001c0001t0001g0067 a0001c0004t0001g0063 a0001c0004t0001g0065 others(2): Show |
5 | HG00738.hp1 HG02451.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.72-4563G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48571378 | |||||||
| chr19:48571439 | C | T | 1 | a0001c0004t0001g0322 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.72-4502C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48571439 | |||||||
| chr19:48571507 | G | A | 192 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0015 others(189): Show |
193 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.72-4434G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48571507 | |||||||
| chr19:48571636 | C | CA | 98 | a0001c0001t0001g0054 a0001c0001t0001g0089 a0001c0001t0001g0105 others(95): Show |
99 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.72-4301dupA | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48571636 | ||||||
| chr19:48571636 | C | CAA | 5 | a0001c0001t0001g0125 a0001c0001t0001g0155 a0001c0001t0001g0271 others(2): Show |
5 | HG02071.hp2 HG02074.hp2 NA18612.hp1 others(2): Show |
intron_variant | MODIFIER | c.72-4302_72-4301dup others(2): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48571636 | ||||||
| chr19:48571640 | AG | A | 5 | a0001c0002t0001g0048 a0001c0002t0001g0119 a0001c0003t0001g0047 others(2): Show |
5 | HG02486.hp1 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.72-4300delG | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48571640 | |||||||
| chr19:48571641 | G | A | 187 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0015 others(184): Show |
188 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.72-4300G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48571641 | |||||||
| chr19:48571648 | A | C | 1 | a0001c0004t0001g0031 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.72-4293A>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48571648 | |||||||
| chr19:48571649 | C | A | 192 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0015 others(189): Show |
193 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.72-4292C>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48571649 | |||||||
| chr19:48571655 | AT | A | 192 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0015 others(189): Show |
193 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.72-4279delT | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48571655 | ||||||
| chr19:48571697 | GAGA | G | 192 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0015 others(189): Show |
193 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.72-4240_72-4238del others(3): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48571697 | ||||||
| chr19:48571706 | G | T | 192 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0015 others(189): Show |
193 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.72-4235G>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48571706 | |||||||
| chr19:48571825 | G | C | 192 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0015 others(189): Show |
193 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.72-4116G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48571825 | |||||||
| chr19:48571904 | T | C | 192 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0015 others(189): Show |
193 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.72-4037T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48571904 | |||||||
| chr19:48572020 | T | C | 192 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0015 others(189): Show |
193 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.72-3921T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48572020 | |||||||
| chr19:48572080 | G | C | 39 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0025 others(36): Show |
39 | HG01070.hp2 HG01071.hp2 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.72-3861G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48572080 | |||||||
| chr19:48572084 | G | A | 192 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0015 others(189): Show |
193 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.72-3857G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48572084 | |||||||
| chr19:48572099 | T | G | 4 | a0001c0001t0001g0055 a0001c0001t0001g0101 a0001c0001t0001g0170 others(1): Show |
4 | HG00733.hp1 HG01167.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.72-3842T>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48572099 | |||||||
| chr19:48572123 | T | C | 2 | a0001c0004t0001g0090 a0001c0004t0001g0196 |
2 | HG02258.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.72-3818T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48572123 | |||||||
| chr19:48572197 | T | G | 192 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0015 others(189): Show |
193 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.72-3744T>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48572197 | |||||||
| chr19:48572208 | G | A | 11 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0054 others(8): Show |
11 | HG01884.hp2 HG02257.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.72-3733G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48572208 | |||||||
| chr19:48572255 | C | T | 2 | a0001c0001t0001g0042 a0001c0001t0001g0300 |
2 | HG02055.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.72-3686C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48572255 | |||||||
| chr19:48572281 | G | A | 192 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0015 others(189): Show |
193 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.72-3660G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48572281 | |||||||
| chr19:48572289 | C | T | 192 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0015 others(189): Show |
193 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.72-3652C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48572289 | |||||||
| chr19:48572299 | G | A | 192 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0015 others(189): Show |
193 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.72-3642G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48572299 | |||||||
| chr19:48572317 | A | T | 1 | a0001c0001t0001g0354 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.72-3624A>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48572317 | |||||||
| chr19:48572374 | A | G | 192 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0015 others(189): Show |
193 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.72-3567A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48572374 | |||||||
| chr19:48572388 | C | A | 139 | a0001c0001t0001g0015 a0001c0001t0001g0037 a0001c0001t0001g0055 others(136): Show |
140 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.72-3553C>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48572388 | |||||||
| chr19:48572396 | C | T | 1 | a0001c0004t0001g0058 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.72-3545C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48572396 | |||||||
| chr19:48572414 | G | A | 1 | a0001c0001t0001g0132 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.72-3527G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48572414 | |||||||
| chr19:48572437 | C | G | 139 | a0001c0001t0001g0015 a0001c0001t0001g0037 a0001c0001t0001g0055 others(136): Show |
140 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.72-3504C>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48572437 | |||||||
| chr19:48572446 | G | A | 1 | a0001c0002t0001g0189 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.72-3495G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48572446 | |||||||
| chr19:48572455 | A | T | 139 | a0001c0001t0001g0015 a0001c0001t0001g0037 a0001c0001t0001g0055 others(136): Show |
140 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.72-3486A>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48572455 | |||||||
| chr19:48572485 | G | A | 2 | a0001c0001t0001g0125 a0001c0001t0001g0339 |
2 | HG02056.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.72-3456G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48572485 | |||||||
| chr19:48572509 | A | G | 143 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0032 others(140): Show |
144 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.72-3432A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48572509 | |||||||
| chr19:48572513 | C | CA | 142 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0032 others(139): Show |
143 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.72-3420dupA | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48572513 | ||||||
| chr19:48572524 | A | G | 183 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0024 others(180): Show |
184 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.72-3417A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48572524 | |||||||
| chr19:48572554 | C | G | 187 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0022 others(184): Show |
188 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.72-3387C>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48572554 | |||||||
| chr19:48572579 | G | A | 1 | a0001c0002t0001g0303 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.72-3362G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48572579 | |||||||
| chr19:48572617 | G | T | 1 | a0001c0001t0001g0147 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.72-3324G>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48572617 | |||||||
| chr19:48572827 | G | C | 1 | a0001c0004t0001g0053 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.72-3114G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48572827 | |||||||
| chr19:48573018 | G | A | 4 | a0001c0001t0001g0055 a0001c0001t0001g0101 a0001c0001t0001g0170 others(1): Show |
4 | HG00733.hp1 HG01167.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.72-2923G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48573018 | |||||||
| chr19:48573080 | T | C | 4 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0052 others(1): Show |
4 | HG01433.hp1 HG01891.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-2861T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48573080 | |||||||
| chr19:48573112 | G | A | 4 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0052 others(1): Show |
4 | HG01433.hp1 HG01891.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-2829G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48573112 | |||||||
| chr19:48573123 | C | T | 10 | a0001c0001t0001g0105 a0001c0001t0001g0184 a0001c0001t0001g0230 others(7): Show |
10 | HG02071.hp2 NA18948.hp1 NA18959.hp2 others(7): Show |
intron_variant | MODIFIER | c.72-2818C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48573123 | |||||||
| chr19:48573128 | G | C | 4 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0052 others(1): Show |
4 | HG01433.hp1 HG01891.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-2813G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48573128 | |||||||
| chr19:48573155 | C | CA | 10 | a0001c0001t0001g0032 a0001c0001t0001g0088 a0001c0001t0001g0373 others(7): Show |
10 | HG00438.hp1 HG00738.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.72-2767dupA | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48573155 | ||||||
| chr19:48573155 | CA | C | 170 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0015 others(167): Show |
170 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(167): Show |
intron_variant | MODIFIER | c.72-2767delA | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48573155 | ||||||
| chr19:48573155 | CAA | C | 21 | a0001c0001t0001g0194 a0001c0002t0001g0347 a0001c0005t0001g0001 others(18): Show |
22 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.72-2768_72-2767del others(2): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48573155 | ||||||
| chr19:48573177 | T | C | 4 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0052 others(1): Show |
4 | HG01433.hp1 HG01891.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-2764T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48573177 | |||||||
| chr19:48573181 | T | C | 5 | a0001c0001t0001g0062 a0001c0002t0001g0048 a0001c0002t0001g0119 others(2): Show |
5 | HG02486.hp1 HG02809.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.72-2760T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48573181 | |||||||
| chr19:48573204 | A | G | 290 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(287): Show |
291 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(288): Show |
intron_variant | MODIFIER | c.72-2737A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48573204 | |||||||
| chr19:48573345 | G | A | 118 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0032 others(115): Show |
118 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(115): Show |
intron_variant | MODIFIER | c.72-2596G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48573345 | |||||||
| chr19:48573374 | G | A | 4 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0052 others(1): Show |
4 | HG01433.hp1 HG01891.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-2567G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48573374 | |||||||
| chr19:48573430 | G | A | 126 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(123): Show |
126 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(123): Show |
intron_variant | MODIFIER | c.72-2511G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48573430 | |||||||
| chr19:48573493 | C | T | 1 | a0001c0002t0001g0353 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.72-2448C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48573493 | |||||||
| chr19:48573498 | A | G | 3 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0002t0001g0004 |
3 | HG02055.hp1 HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.72-2443A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48573498 | |||||||
| chr19:48573528 | C | T | 117 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0032 others(114): Show |
117 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(114): Show |
intron_variant | MODIFIER | c.72-2413C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48573528 | |||||||
| chr19:48573565 | G | A | 43 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0025 others(40): Show |
43 | HG01070.hp2 HG01071.hp2 HG01243.hp1 others(40): Show |
intron_variant | MODIFIER | c.72-2376G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48573565 | |||||||
| chr19:48573574 | G | A | 1 | a0001c0007t0001g0162 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.72-2367G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48573574 | |||||||
| chr19:48573653 | G | C | 1 | a0001c0001t0001g0354 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.72-2288G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48573653 | |||||||
| chr19:48573654 | G | A | 1 | a0001c0001t0001g0354 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.72-2287G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48573654 | |||||||
| chr19:48573657 | G | A | 1 | a0001c0001t0001g0354 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.72-2284G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48573657 | |||||||
| chr19:48573664 | G | C | 1 | a0001c0001t0001g0354 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.72-2277G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48573664 | |||||||
| chr19:48573666 | C | G | 116 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0032 others(113): Show |
116 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(113): Show |
intron_variant | MODIFIER | c.72-2275C>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48573666 | |||||||
| chr19:48573671 | A | G | 1 | a0001c0001t0001g0354 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.72-2270A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48573671 | |||||||
| chr19:48573672 | T | G | 116 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0032 others(113): Show |
116 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(113): Show |
intron_variant | MODIFIER | c.72-2269T>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48573672 | |||||||
| chr19:48573673 | G | T | 1 | a0001c0001t0001g0354 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.72-2268G>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48573673 | |||||||
| chr19:48573769 | G | C | 117 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0032 others(114): Show |
117 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(114): Show |
intron_variant | MODIFIER | c.72-2172G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48573769 | |||||||
| chr19:48573800 | G | A | 235 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0032 others(232): Show |
236 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.72-2141G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48573800 | |||||||
| chr19:48573807 | T | C | 119 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0032 others(116): Show |
119 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(116): Show |
intron_variant | MODIFIER | c.72-2134T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48573807 | |||||||
| chr19:48573848 | C | T | 3 | a0001c0005t0001g0210 a0001c0005t0001g0214 a0001c0005t0001g0256 |
3 | HG01192.hp1 HG02735.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.72-2093C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48573848 | |||||||
| chr19:48573856 | G | A | 1 | a0001c0004t0001g0053 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.72-2085G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48573856 | |||||||
| chr19:48573865 | C | G | 235 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0032 others(232): Show |
236 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.72-2076C>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48573865 | |||||||
| chr19:48573921 | G | A | 9 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0033 others(6): Show |
9 | HG02055.hp1 HG02486.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.72-2020G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48573921 | |||||||
| chr19:48573922 | C | T | 1 | a0001c0002t0001g0169 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.72-2019C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48573922 | |||||||
| chr19:48573974 | C | T | 94 | a0001c0001t0001g0081 a0001c0001t0001g0098 a0001c0001t0001g0118 others(91): Show |
94 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.72-1967C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48573974 | |||||||
| chr19:48573991 | G | A | 1 | a0001c0001t0001g0041 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.72-1950G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48573991 | |||||||
| chr19:48574019 | G | C | 125 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0052 others(122): Show |
126 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.72-1922G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48574019 | |||||||
| chr19:48574139 | G | A | 1 | a0001c0002t0001g0303 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.72-1802G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48574139 | |||||||
| chr19:48574195 | A | G | 289 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(286): Show |
290 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(287): Show |
intron_variant | MODIFIER | c.72-1746A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48574195 | |||||||
| chr19:48574264 | CTTCA | C | 4 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0052 others(1): Show |
4 | HG01433.hp1 HG01891.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-1673_72-1670del others(4): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48574264 | ||||||
| chr19:48574268 | A | C | 6 | a0001c0001t0001g0055 a0001c0001t0001g0101 a0001c0001t0001g0170 others(3): Show |
6 | HG00733.hp1 HG01070.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.72-1673A>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48574268 | |||||||
| chr19:48574374 | G | A | 1 | a0001c0001t0001g0032 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.72-1567G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48574374 | |||||||
| chr19:48574410 | C | T | 124 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0052 others(121): Show |
125 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.72-1531C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48574410 | |||||||
| chr19:48574781 | C | A | 1 | a0001c0007t0001g0034 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.72-1160C>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48574781 | |||||||
| chr19:48574876 | C | A | 1 | a0001c0006t0001g0007 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.72-1065C>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48574876 | |||||||
| chr19:48574884 | G | A | 137 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0043 others(134): Show |
138 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.72-1057G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48574884 | |||||||
| chr19:48574950 | T | C | 10 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0033 others(7): Show |
10 | HG01243.hp1 HG02055.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.72-991T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48574950 | |||||||
| chr19:48575054 | A | G | 10 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0052 others(7): Show |
10 | HG00733.hp1 HG01070.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.72-887A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48575054 | |||||||
| chr19:48575100 | C | CT | 63 | a0001c0001t0001g0018 a0001c0001t0001g0041 a0001c0001t0001g0067 others(60): Show |
63 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.72-815dupT | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48575100 | ||||||
| chr19:48575100 | C | CTT | 10 | a0001c0001t0001g0241 a0001c0001t0001g0327 a0001c0001t0001g0336 others(7): Show |
10 | HG00423.hp2 HG01243.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.72-816_72-815dupTT | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48575100 | ||||||
| chr19:48575100 | CT | C | 7 | a0001c0001t0001g0043 a0001c0001t0001g0074 a0001c0001t0001g0302 others(4): Show |
7 | HG02280.hp2 HG02572.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.72-815delT | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48575100 | ||||||
| chr19:48575100 | CTT | C | 24 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(21): Show |
24 | HG00735.hp2 HG00738.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.72-816_72-815delTT | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48575100 | ||||||
| chr19:48575100 | CTTT | C | 127 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0015 others(124): Show |
127 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.72-817_72-815delTT others(1): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48575100 | ||||||
| chr19:48575100 | CTTTT | C | 8 | a0001c0001t0001g0037 a0001c0001t0001g0197 a0001c0001t0001g0199 others(5): Show |
8 | HG02109.hp2 HG02818.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.72-818_72-815delTT others(2): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48575100 | ||||||
| chr19:48575170 | A | G | 171 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(168): Show |
171 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(168): Show |
intron_variant | MODIFIER | c.72-771A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48575170 | |||||||
| chr19:48575436 | G | T | 298 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(295): Show |
299 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(296): Show |
intron_variant | MODIFIER | c.72-505G>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48575436 | |||||||
| chr19:48575447 | A | G | 1 | a0001c0004t0001g0017 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.72-494A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48575447 | |||||||
| chr19:48575461 | AAAAT | A | 13 | a0001c0005t0001g0009 a0001c0005t0001g0010 a0001c0005t0001g0011 others(10): Show |
13 | HG01192.hp1 HG01261.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.72-478_72-475delAA others(2): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48575461 | ||||||
| chr19:48575463 | A | T | 33 | a0001c0001t0001g0043 a0001c0001t0001g0074 a0001c0001t0001g0075 others(30): Show |
34 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.72-478A>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48575463 | |||||||
| chr19:48575463 | AAT | A | 5 | a0001c0001t0001g0042 a0001c0001t0001g0296 a0001c0001t0001g0300 others(2): Show |
5 | HG00558.hp2 HG02055.hp2 HG02129.hp1 others(2): Show |
intron_variant | MODIFIER | c.72-461_72-460delAT | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48575463 | ||||||
| chr19:48575463 | AATAT | A | 237 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0015 others(234): Show |
237 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(234): Show |
intron_variant | MODIFIER | c.72-463_72-460delAT others(2): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48575463 | ||||||
| chr19:48575465 | T | A | 1 | a0001c0004t0001g0231 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.72-476T>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48575465 | |||||||
| chr19:48575469 | T | A | 11 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0033 others(8): Show |
11 | HG01243.hp1 HG02055.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.72-472T>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48575469 | |||||||
| chr19:48575513 | T | C | 10 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0052 others(7): Show |
10 | HG00733.hp1 HG01070.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.72-428T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48575513 | |||||||
| chr19:48575516 | C | T | 10 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0052 others(7): Show |
10 | HG00733.hp1 HG01070.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.72-425C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48575516 | |||||||
| chr19:48575582 | A | G | 252 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(249): Show |
252 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.72-359A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48575582 | |||||||
| chr19:48575640 | C | T | 101 | a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0026 others(98): Show |
101 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.72-301C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48575640 | |||||||
| chr19:48575652 | T | C | 1 | a0001c0004t0001g0053 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.72-289T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48575652 | |||||||
| chr19:48576107 | G | A | 6 | a0001c0003t0001g0166 a0001c0003t0001g0177 a0001c0003t0001g0223 others(3): Show |
6 | HG01069.hp1 HG01109.hp1 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.214+24G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48576107 | |||||||
| chr19:48576162 | G | A | 1 | a0001c0001t0001g0324 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.214+79G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48576162 | |||||||
| chr19:48576205 | G | A | 48 | a0001c0001t0001g0043 a0001c0001t0001g0074 a0001c0001t0001g0075 others(45): Show |
49 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(46): Show |
intron_variant | MODIFIER | c.214+122G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48576205 | |||||||
| chr19:48576344 | T | C | 1 | a0001c0006t0001g0029 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.214+261T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48576344 | |||||||
| chr19:48576346 | A | C | 49 | a0001c0001t0001g0043 a0001c0001t0001g0074 a0001c0001t0001g0075 others(46): Show |
50 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(47): Show |
intron_variant | MODIFIER | c.214+263A>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48576346 | |||||||
| chr19:48576347 | C | CTTTTCTT others(5): Show |
1 | a0001c0006t0001g0029 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.214+264_214+265ins others(12): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48576347 | |||||||
| chr19:48576348 | C | T | 1 | a0001c0006t0001g0029 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.214+265C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48576348 | |||||||
| chr19:48576351 | C | T | 1 | a0001c0006t0001g0029 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.214+268C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48576351 | |||||||
| chr19:48576353 | A | ACTTTT | 4 | a0001c0001t0001g0336 a0001c0002t0001g0307 a0001c0004t0001g0279 others(1): Show |
4 | HG00140.hp1 HG01243.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.214+273_214+274ins others(5): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48576353 | ||||||
| chr19:48576353 | A | T | 1 | a0001c0006t0001g0029 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.214+270A>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48576353 | |||||||
| chr19:48576354 | C | CTTTTCTT others(6): Show |
1 | a0001c0002t0001g0077 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.214+273_214+274ins others(13): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48576354 | ||||||
| chr19:48576354 | C | CTTTTTTT | 26 | a0001c0001t0001g0037 a0001c0001t0001g0197 a0001c0001t0001g0199 others(23): Show |
26 | HG00639.hp2 HG00735.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.214+273_214+274ins others(7): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48576354 | ||||||
| chr19:48576354 | C | CTTTTTTT others(1): Show |
24 | a0001c0001t0001g0015 a0001c0001t0001g0089 a0001c0001t0001g0107 others(21): Show |
24 | HG00280.hp1 HG00735.hp2 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.214+273_214+274ins others(8): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48576354 | ||||||
| chr19:48576354 | C | CTTTTTTT others(2): Show |
43 | a0001c0001t0001g0022 a0001c0001t0001g0088 a0001c0001t0001g0105 others(40): Show |
43 | HG00558.hp1 HG00621.hp1 HG01074.hp1 others(40): Show |
intron_variant | MODIFIER | c.214+273_214+274ins others(9): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48576354 | ||||||
| chr19:48576354 | C | CTTTTTTT others(3): Show |
14 | a0001c0001t0001g0184 a0001c0001t0001g0187 a0001c0001t0001g0260 others(11): Show |
14 | HG00438.hp1 HG00558.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.214+273_214+274ins others(10): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48576354 | ||||||
| chr19:48576354 | C | CTTTTTTT others(4): Show |
17 | a0001c0001t0001g0024 a0001c0001t0001g0054 a0001c0001t0001g0056 others(14): Show |
17 | HG00408.hp2 HG01070.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.214+273_214+274ins others(11): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48576354 | ||||||
| chr19:48576354 | C | CTTTTTTT others(5): Show |
2 | a0001c0001t0001g0344 a0001c0001t0001g0362 |
2 | HG02071.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.214+273_214+274ins others(12): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48576354 | ||||||
| chr19:48576354 | C | CTTTTTTT others(6): Show |
1 | a0001c0001t0001g0194 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.214+273_214+274ins others(13): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48576354 | ||||||
| chr19:48576354 | C | CTTTTTTT others(7): Show |
1 | a0001c0002t0001g0250 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.214+273_214+274ins others(14): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48576354 | ||||||
| chr19:48576354 | C | T | 1 | a0001c0006t0001g0029 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.214+271C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48576354 | |||||||
| chr19:48576356 | TCTC | T | 4 | a0001c0003t0001g0166 a0001c0003t0001g0223 a0001c0003t0001g0226 others(1): Show |
4 | HG01069.hp1 HG01109.hp1 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.214+274_214+276del others(3): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48576356 | |||||||
| chr19:48576357 | C | T | 292 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(289): Show |
293 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.214+274C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48576357 | |||||||
| chr19:48576359 | C | CT | 15 | a0001c0001t0001g0149 a0001c0001t0001g0207 a0001c0001t0001g0238 others(12): Show |
15 | HG01123.hp1 HG01975.hp1 HG01975.hp2 others(12): Show |
intron_variant | MODIFIER | c.214+294dupT | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48576359 | ||||||
| chr19:48576359 | C | CTTTTCTT others(10): Show |
1 | a0001c0005t0001g0214 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.214+280_214+281ins others(17): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48576359 | ||||||
| chr19:48576359 | C | CTTTTCTT others(11): Show |
3 | a0001c0005t0001g0210 a0001c0005t0001g0256 a0001c0007t0001g0162 |
3 | HG01192.hp1 HG01261.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.214+280_214+281ins others(18): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48576359 | ||||||
| chr19:48576359 | C | CTTTTCTT others(12): Show |
5 | a0001c0001t0001g0043 a0001c0001t0001g0074 a0001c0001t0001g0075 others(2): Show |
5 | HG03041.hp2 HG03130.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.214+280_214+281ins others(19): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48576359 | ||||||
| chr19:48576359 | C | CTTTTCTT others(13): Show |
2 | a0001c0001t0001g0076 a0001c0004t0001g0073 |
2 | HG03098.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.214+280_214+281ins others(20): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48576359 | ||||||
| chr19:48576359 | C | CTTTTCTT others(14): Show |
3 | a0001c0006t0001g0095 a0001c0007t0001g0198 a0001c0010t0001g0038 |
3 | HG02109.hp1 HG02976.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.214+280_214+281ins others(21): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48576359 | ||||||
| chr19:48576359 | C | CTTTTCTT others(15): Show |
4 | a0001c0006t0001g0039 a0001c0007t0001g0157 a0001c0007t0001g0355 others(1): Show |
4 | HG02280.hp2 HG02647.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.214+280_214+281ins others(22): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48576359 | ||||||
| chr19:48576359 | C | CTTTTCTT others(16): Show |
5 | a0001c0005t0001g0009 a0001c0005t0001g0010 a0001c0005t0001g0011 others(2): Show |
5 | HG01884.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.214+280_214+281ins others(23): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48576359 | ||||||
| chr19:48576359 | C | CTTTTCTT others(17): Show |
6 | a0001c0006t0001g0045 a0001c0006t0001g0061 a0001c0007t0001g0057 others(3): Show |
6 | HG01256.hp2 HG02145.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.214+280_214+281ins others(24): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48576359 | ||||||
| chr19:48576359 | C | CTTTTCTT others(18): Show |
7 | a0001c0005t0001g0109 a0001c0005t0001g0168 a0001c0005t0001g0195 others(4): Show |
7 | HG00741.hp2 HG01081.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.214+280_214+281ins others(25): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48576359 | ||||||
| chr19:48576359 | C | CTTTTCTT others(19): Show |
7 | a0001c0005t0001g0001 a0001c0005t0001g0072 a0001c0005t0001g0110 others(4): Show |
8 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.214+280_214+281ins others(26): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48576359 | ||||||
| chr19:48576359 | C | CTTTTCTT others(20): Show |
2 | a0001c0006t0001g0021 a0004c0020t0001g0176 |
2 | HG02735.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.214+280_214+281ins others(27): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48576359 | ||||||
| chr19:48576359 | C | CTTTTCTT others(23): Show |
2 | a0001c0006t0001g0007 a0001c0007t0001g0034 |
2 | HG01346.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.214+280_214+281ins others(30): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48576359 | ||||||
| chr19:48576359 | C | CTTTTCTT others(19): Show |
1 | a0001c0001t0001g0032 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.214+280_214+281ins others(26): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48576359 | ||||||
| chr19:48576359 | C | CTTTTCTT others(4): Show |
8 | a0001c0001t0001g0137 a0001c0001t0001g0342 a0001c0002t0001g0050 others(5): Show |
8 | HG01070.hp2 HG01071.hp2 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.214+280_214+281ins others(11): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48576359 | ||||||
| chr19:48576359 | C | CTTTTCTT others(5): Show |
65 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(62): Show |
65 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.214+280_214+281ins others(12): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48576359 | ||||||
| chr19:48576359 | C | CTTTTCTT others(6): Show |
12 | a0001c0001t0001g0164 a0001c0001t0001g0228 a0001c0001t0001g0281 others(9): Show |
12 | HG00597.hp1 HG00597.hp2 HG02027.hp2 others(9): Show |
intron_variant | MODIFIER | c.214+280_214+281ins others(13): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48576359 | ||||||
| chr19:48576359 | C | CTTTTCTT others(7): Show |
2 | a0001c0002t0001g0353 a0001c0003t0001g0293 |
2 | NA18990.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.214+280_214+281ins others(14): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48576359 | ||||||
| chr19:48576359 | C | CTTTTCTT others(11): Show |
1 | a0001c0002t0001g0035 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.214+280_214+281ins others(18): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48576359 | ||||||
| chr19:48576359 | C | CTTTTCTT others(12): Show |
1 | a0001c0001t0001g0055 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.214+280_214+281ins others(19): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48576359 | ||||||
| chr19:48576359 | C | CTTTTCTT others(20): Show |
1 | a0001c0001t0001g0365 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.214+280_214+281ins others(27): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48576359 | ||||||
| chr19:48576359 | C | CTTTTCTT others(24): Show |
2 | a0001c0001t0001g0101 a0001c0001t0001g0170 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.214+280_214+281ins others(31): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48576359 | ||||||
| chr19:48576359 | C | CTTTTCTT others(27): Show |
1 | a0001c0001t0001g0008 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.214+280_214+281ins others(34): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48576359 | ||||||
| chr19:48576359 | C | CTTTTCTT others(31): Show |
1 | a0001c0001t0001g0052 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.214+280_214+281ins others(38): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48576359 | ||||||
| chr19:48576359 | C | T | 135 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0024 others(132): Show |
135 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(132): Show |
intron_variant | MODIFIER | c.214+276C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48576359 | |||||||
| chr19:48576360 | T | TTTTCTTT others(5): Show |
1 | a0001c0002t0001g0326 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.214+280_214+281ins others(12): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48576360 | ||||||
| chr19:48576364 | T | C | 1 | a0001c0001t0001g0182 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.214+281T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48576364 | |||||||
| chr19:48576394 | G | A | 139 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0024 others(136): Show |
139 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.214+311G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48576394 | |||||||
| chr19:48576453 | T | TC | 139 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0024 others(136): Show |
139 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.214+373dupC | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48576453 | ||||||
| chr19:48576460 | G | A | 19 | a0001c0005t0001g0001 a0001c0005t0001g0072 a0001c0005t0001g0109 others(16): Show |
20 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.214+377G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48576460 | |||||||
| chr19:48576533 | T | C | 1 | a0001c0006t0001g0045 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.214+450T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48576533 | |||||||
| chr19:48576640 | C | CT | 24 | a0001c0001t0001g0043 a0001c0001t0001g0074 a0001c0001t0001g0075 others(21): Show |
24 | HG00140.hp2 HG00741.hp2 HG01192.hp1 others(21): Show |
intron_variant | MODIFIER | c.214+578dupT | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48576640 | ||||||
| chr19:48576640 | CT | C | 6 | a0001c0002t0001g0080 a0001c0003t0001g0079 a0001c0004t0001g0126 others(3): Show |
6 | HG00609.hp2 HG03041.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.214+578delT | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48576640 | ||||||
| chr19:48576640 | CTTT | C | 18 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0033 others(15): Show |
18 | HG00438.hp2 HG01175.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.214+576_214+578del others(3): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48576640 | ||||||
| chr19:48576640 | CTTTT | C | 138 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0022 others(135): Show |
138 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.214+575_214+578del others(4): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48576640 | ||||||
| chr19:48576640 | CTTTTT | C | 89 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(86): Show |
89 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.214+574_214+578del others(5): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48576640 | ||||||
| chr19:48576665 | G | A | 4 | a0001c0001t0001g0362 a0001c0004t0001g0053 a0001c0004t0001g0090 others(1): Show |
4 | HG02258.hp2 HG02572.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.214+582G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48576665 | |||||||
| chr19:48576686 | C | T | 1 | a0001c0003t0001g0374 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.214+603C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48576686 | |||||||
| chr19:48576797 | T | C | 5 | a0001c0001t0001g0043 a0001c0001t0001g0074 a0001c0001t0001g0075 others(2): Show |
5 | HG03098.hp1 HG03130.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.214+714T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48576797 | |||||||
| chr19:48576841 | A | G | 1 | a0001c0004t0001g0046 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.214+758A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48576841 | |||||||
| chr19:48576919 | G | A | 138 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0024 others(135): Show |
138 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.214+836G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48576919 | |||||||
| chr19:48577028 | A | AT | 27 | a0001c0001t0001g0018 a0001c0001t0001g0040 a0001c0001t0001g0041 others(24): Show |
27 | HG01168.hp2 HG01169.hp2 HG01978.hp1 others(24): Show |
intron_variant | MODIFIER | c.214+970dupT | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48577028 | ||||||
| chr19:48577028 | A | ATT | 8 | a0001c0001t0001g0043 a0001c0001t0001g0074 a0001c0001t0001g0075 others(5): Show |
8 | HG03130.hp2 HG03942.hp1 NA18522.hp1 others(5): Show |
intron_variant | MODIFIER | c.214+969_214+970dup others(2): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48577028 | ||||||
| chr19:48577028 | AT | A | 17 | a0001c0001t0001g0239 a0001c0002t0001g0218 a0001c0003t0001g0106 others(14): Show |
17 | HG01168.hp1 HG01261.hp1 HG01928.hp2 others(14): Show |
intron_variant | MODIFIER | c.214+970delT | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48577028 | ||||||
| chr19:48577028 | ATTT | A | 34 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0022 others(31): Show |
34 | HG01243.hp1 HG01358.hp1 HG01358.hp2 others(31): Show |
intron_variant | MODIFIER | c.214+968_214+970del others(3): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48577028 | ||||||
| chr19:48577028 | ATTTT | A | 109 | a0001c0001t0001g0015 a0001c0001t0001g0037 a0001c0001t0001g0062 others(106): Show |
109 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.214+967_214+970del others(4): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48577028 | ||||||
| chr19:48577028 | ATTTTT | A | 12 | a0001c0001t0001g0101 a0001c0001t0001g0108 a0001c0001t0001g0170 others(9): Show |
12 | HG00673.hp2 HG01167.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.214+966_214+970del others(5): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48577028 | ||||||
| chr19:48577028 | ATTTTTT | A | 99 | a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0026 others(96): Show |
99 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.214+965_214+970del others(6): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48577028 | ||||||
| chr19:48577028 | ATTTTTTT others(3): Show |
A | 18 | a0001c0005t0001g0001 a0001c0005t0001g0072 a0001c0005t0001g0109 others(15): Show |
19 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.214+961_214+970del others(10): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48577028 | ||||||
| chr19:48577128 | G | A | 3 | a0001c0001t0001g0290 a0001c0001t0001g0291 a0001c0004t0001g0231 |
3 | HG00673.hp1 HG02056.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.214+1045G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48577128 | |||||||
| chr19:48577149 | C | A | 23 | a0001c0001t0001g0018 a0001c0001t0001g0040 a0001c0001t0001g0041 others(20): Show |
23 | HG00738.hp1 HG01168.hp2 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.214+1066C>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48577149 | |||||||
| chr19:48577176 | G | A | 3 | a0001c0001t0001g0290 a0001c0001t0001g0291 a0001c0004t0001g0231 |
3 | HG00673.hp1 HG02056.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.214+1093G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48577176 | |||||||
| chr19:48577352 | C | CT | 76 | a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0026 others(73): Show |
76 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.214+1299dupT | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48577352 | ||||||
| chr19:48577352 | C | CTT | 44 | a0001c0001t0001g0081 a0001c0001t0001g0098 a0001c0001t0001g0122 others(41): Show |
44 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.214+1298_214+1299d others(4): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48577352 | ||||||
| chr19:48577352 | C | CTTT | 8 | a0001c0001t0001g0324 a0001c0002t0001g0206 a0001c0002t0001g0264 others(5): Show |
8 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(5): Show |
intron_variant | MODIFIER | c.214+1297_214+1299d others(5): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48577352 | ||||||
| chr19:48577352 | C | CTTTT | 7 | a0001c0001t0001g0108 a0001c0001t0001g0241 a0001c0001t0001g0247 others(4): Show |
7 | HG02109.hp1 HG02630.hp1 HG04204.hp2 others(4): Show |
intron_variant | MODIFIER | c.214+1296_214+1299d others(6): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48577352 | ||||||
| chr19:48577352 | C | CTTTTT | 18 | a0001c0001t0001g0155 a0001c0001t0001g0205 a0001c0001t0001g0230 others(15): Show |
18 | HG00558.hp1 HG02965.hp1 HG03017.hp1 others(15): Show |
intron_variant | MODIFIER | c.214+1295_214+1299d others(7): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48577352 | ||||||
| chr19:48577352 | C | CTTTTTT | 49 | a0001c0001t0001g0024 a0001c0001t0001g0032 a0001c0001t0001g0037 others(46): Show |
49 | HG00408.hp2 HG00438.hp1 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.214+1294_214+1299d others(8): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48577352 | ||||||
| chr19:48577352 | C | CTTTTTTT | 42 | a0001c0001t0001g0022 a0001c0001t0001g0052 a0001c0001t0001g0056 others(39): Show |
42 | HG00280.hp1 HG00558.hp2 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.214+1293_214+1299d others(9): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48577352 | ||||||
| chr19:48577352 | C | CTTTTTTT others(1): Show |
28 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0089 others(25): Show |
28 | HG00735.hp1 HG00735.hp2 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.214+1292_214+1299d others(10): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48577352 | ||||||
| chr19:48577352 | C | CTTTTTTT others(2): Show |
9 | a0001c0001t0001g0033 a0001c0001t0001g0309 a0001c0002t0001g0084 others(6): Show |
9 | HG00621.hp1 HG00639.hp2 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.214+1291_214+1299d others(11): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48577352 | ||||||
| chr19:48577352 | C | CTTTTTTT others(3): Show |
8 | a0001c0002t0001g0091 a0001c0002t0001g0171 a0001c0004t0001g0090 others(5): Show |
8 | HG01167.hp2 HG01192.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.214+1290_214+1299d others(12): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48577352 | ||||||
| chr19:48577352 | C | CTTTTTTT others(4): Show |
2 | a0001c0002t0001g0036 a0001c0019t0001g0371 |
2 | HG02486.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.214+1289_214+1299d others(13): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48577352 | ||||||
| chr19:48577352 | CT | C | 10 | a0001c0001t0001g0242 a0001c0003t0001g0234 a0001c0006t0001g0039 others(7): Show |
10 | HG02280.hp2 HG02647.hp2 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.214+1299delT | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48577352 | ||||||
| chr19:48577352 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0186 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.214+1290_214+1299d others(12): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48577352 | ||||||
| chr19:48577352 | CTTTTTTT others(5): Show |
C | 1 | a0001c0007t0001g0034 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.214+1288_214+1299d others(14): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48577352 | ||||||
| chr19:48577390 | G | T | 4 | a0001c0002t0001g0218 a0001c0003t0001g0257 a0001c0004t0001g0318 others(1): Show |
4 | HG01168.hp1 HG01261.hp1 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.214+1307G>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48577390 | |||||||
| chr19:48577475 | C | T | 151 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0015 others(148): Show |
151 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.214+1392C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48577475 | |||||||
| chr19:48577511 | G | T | 105 | a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0026 others(102): Show |
105 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.214+1428G>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48577511 | |||||||
| chr19:48577569 | C | T | 105 | a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0026 others(102): Show |
105 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.214+1486C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48577569 | |||||||
| chr19:48577629 | G | C | 1 | a0001c0002t0001g0119 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.214+1546G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48577629 | |||||||
| chr19:48577674 | G | A | 1 | a0001c0001t0001g0186 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.214+1591G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48577674 | |||||||
| chr19:48577971 | C | T | 1 | a0001c0003t0001g0202 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.214+1888C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48577971 | |||||||
| chr19:48578051 | TA | T | 228 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0025 others(225): Show |
228 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.214+1980delA | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48578051 | ||||||
| chr19:48578071 | G | A | 19 | a0001c0005t0001g0001 a0001c0005t0001g0072 a0001c0005t0001g0109 others(16): Show |
20 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.214+1988G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48578071 | |||||||
| chr19:48578138 | G | T | 105 | a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0026 others(102): Show |
105 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.214+2055G>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48578138 | |||||||
| chr19:48578227 | G | C | 140 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0024 others(137): Show |
140 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(137): Show |
intron_variant | MODIFIER | c.214+2144G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48578227 | |||||||
| chr19:48578255 | G | A | 10 | a0001c0006t0001g0039 a0001c0006t0001g0061 a0001c0007t0001g0057 others(7): Show |
10 | HG02145.hp2 HG02280.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.214+2172G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48578255 | |||||||
| chr19:48578379 | C | T | 2 | a0001c0002t0001g0082 a0001c0003t0001g0175 |
2 | HG01081.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.214+2296C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48578379 | |||||||
| chr19:48578490 | G | A | 5 | a0001c0001t0001g0043 a0001c0001t0001g0074 a0001c0001t0001g0075 others(2): Show |
5 | HG03098.hp1 HG03130.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.214+2407G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48578490 | |||||||
| chr19:48578494 | A | T | 8 | a0001c0005t0001g0020 a0001c0005t0001g0210 a0001c0005t0001g0214 others(5): Show |
8 | HG01192.hp1 HG01261.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.214+2411A>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48578494 | |||||||
| chr19:48578513 | T | C | 1 | a0001c0001t0001g0291 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.214+2430T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48578513 | |||||||
| chr19:48578530 | C | T | 96 | a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0026 others(93): Show |
96 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.214+2447C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48578530 | |||||||
| chr19:48578531 | G | A | 2 | a0001c0005t0001g0009 a0001c0005t0001g0010 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.214+2448G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48578531 | |||||||
| chr19:48578647 | C | T | 1 | a0001c0001t0001g0187 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.214+2564C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48578647 | |||||||
| chr19:48578705 | C | T | 1 | a0001c0004t0001g0315 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.214+2622C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48578705 | |||||||
| chr19:48578732 | C | A | 1 | a0001c0002t0001g0330 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.214+2649C>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48578732 | |||||||
| chr19:48578769 | G | A | 99 | a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0026 others(96): Show |
99 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.214+2686G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48578769 | |||||||
| chr19:48578801 | G | C | 2 | a0001c0005t0001g0020 a0001c0006t0001g0029 |
2 | HG03225.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.214+2718G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48578801 | |||||||
| chr19:48578834 | C | T | 1 | a0001c0001t0001g0296 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.214+2751C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48578834 | |||||||
| chr19:48579008 | G | A | 105 | a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0026 others(102): Show |
105 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.214+2925G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48579008 | |||||||
| chr19:48579010 | T | C | 1 | a0001c0006t0001g0095 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.214+2927T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48579010 | |||||||
| chr19:48579149 | A | T | 105 | a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0026 others(102): Show |
105 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.214+3066A>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48579149 | |||||||
| chr19:48579172 | T | C | 10 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0033 others(7): Show |
10 | HG01243.hp1 HG02055.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.214+3089T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48579172 | |||||||
| chr19:48579283 | C | CT | 7 | a0001c0001t0001g0116 a0001c0001t0001g0205 a0001c0001t0001g0241 others(4): Show |
7 | HG00408.hp2 HG00738.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.214+3217dupT | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48579283 | ||||||
| chr19:48579283 | CT | C | 108 | a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0026 others(105): Show |
108 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.214+3217delT | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48579283 | ||||||
| chr19:48579314 | G | A | 1 | a0001c0001t0001g0015 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.214+3231G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48579314 | |||||||
| chr19:48579343 | C | A | 140 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0024 others(137): Show |
140 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(137): Show |
intron_variant | MODIFIER | c.214+3260C>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48579343 | |||||||
| chr19:48579393 | T | C | 105 | a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0026 others(102): Show |
105 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.214+3310T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48579393 | |||||||
| chr19:48579430 | C | T | 1 | a0001c0001t0001g0269 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.214+3347C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48579430 | |||||||
| chr19:48579432 | A | G | 3 | a0001c0005t0001g0210 a0001c0005t0001g0214 a0001c0005t0001g0256 |
3 | HG01192.hp1 HG02735.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.214+3349A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48579432 | |||||||
| chr19:48579442 | C | T | 10 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0033 others(7): Show |
10 | HG01243.hp1 HG02055.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.214+3359C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48579442 | |||||||
| chr19:48579455 | TG | T | 10 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0033 others(7): Show |
10 | HG01243.hp1 HG02055.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.214+3373delG | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48579455 | |||||||
| chr19:48579529 | G | A | 1 | a0001c0005t0001g0020 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.214+3446G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48579529 | |||||||
| chr19:48579563 | C | G | 4 | a0001c0001t0001g0055 a0001c0002t0001g0035 a0001c0002t0001g0050 others(1): Show |
4 | HG00733.hp1 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.214+3480C>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48579563 | |||||||
| chr19:48579593 | T | TTTC | 10 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(7): Show |
10 | HG02055.hp2 HG02258.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.214+3512_214+3513i others(5): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48579593 | ||||||
| chr19:48579593 | T | TTTTCTTT others(2): Show |
6 | a0001c0001t0001g0037 a0001c0001t0001g0197 a0001c0001t0001g0199 others(3): Show |
6 | HG01891.hp1 HG02109.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.214+3517_214+3518i others(11): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48579593 | ||||||
| chr19:48579605 | C | CT | 44 | a0001c0001t0001g0043 a0001c0001t0001g0074 a0001c0001t0001g0075 others(41): Show |
45 | HG00099.hp2 HG00140.hp2 HG01081.hp1 others(42): Show |
intron_variant | MODIFIER | c.214+3540dupT | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48579605 | ||||||
| chr19:48579605 | C | CTTT | 7 | a0001c0001t0001g0037 a0001c0001t0001g0197 a0001c0001t0001g0199 others(4): Show |
7 | HG01346.hp2 HG01891.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.214+3538_214+3540d others(5): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48579605 | ||||||
| chr19:48579605 | C | CTTTCTTT others(3): Show |
4 | a0001c0001t0001g0227 a0001c0002t0001g0086 a0001c0002t0001g0316 others(1): Show |
4 | HG01496.hp2 HG03195.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.214+3525_214+3526i others(12): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48579605 | ||||||
| chr19:48579605 | C | CTTTCTTT others(4): Show |
83 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0024 others(80): Show |
83 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(80): Show |
intron_variant | MODIFIER | c.214+3525_214+3526i others(13): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48579605 | ||||||
| chr19:48579605 | C | CTTTCTTT others(5): Show |
39 | a0001c0001t0001g0088 a0001c0001t0001g0105 a0001c0001t0001g0155 others(36): Show |
39 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.214+3525_214+3526i others(14): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48579605 | ||||||
| chr19:48579605 | C | CTTTCTTT others(6): Show |
5 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0001g0310 others(2): Show |
5 | HG02056.hp2 HG02080.hp2 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.214+3525_214+3526i others(15): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48579605 | ||||||
| chr19:48579605 | C | CTTTCTTT others(1): Show |
65 | a0001c0001t0001g0081 a0001c0001t0001g0122 a0001c0001t0001g0137 others(62): Show |
65 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.214+3525_214+3526i others(10): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48579605 | ||||||
| chr19:48579605 | C | CTTTCTTT others(2): Show |
18 | a0001c0001t0001g0055 a0001c0001t0001g0098 a0001c0001t0001g0170 others(15): Show |
18 | HG00140.hp1 HG00609.hp1 HG00642.hp2 others(15): Show |
intron_variant | MODIFIER | c.214+3525_214+3526i others(11): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48579605 | ||||||
| chr19:48579605 | C | CTTTCTTT others(3): Show |
7 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0052 others(4): Show |
7 | HG01169.hp1 HG01433.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.214+3525_214+3526i others(12): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48579605 | ||||||
| chr19:48579605 | C | T | 10 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(7): Show |
10 | HG02055.hp2 HG02258.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.214+3522C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48579605 | |||||||
| chr19:48579607 | T | TTC | 10 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0033 others(7): Show |
10 | HG01243.hp1 HG02055.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.214+3525_214+3526i others(4): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48579607 | ||||||
| chr19:48579611 | T | C | 10 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0033 others(7): Show |
10 | HG01243.hp1 HG02055.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.214+3528T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48579611 | |||||||
| chr19:48579726 | C | T | 4 | a0001c0001t0001g0055 a0001c0002t0001g0035 a0001c0002t0001g0050 others(1): Show |
4 | HG00733.hp1 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.214+3643C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48579726 | |||||||
| chr19:48579738 | T | C | 4 | a0001c0001t0001g0055 a0001c0002t0001g0035 a0001c0002t0001g0050 others(1): Show |
4 | HG00733.hp1 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.214+3655T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48579738 | |||||||
| chr19:48579740 | G | A | 1 | a0001c0002t0001g0249 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.214+3657G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48579740 | |||||||
| chr19:48579742 | A | G | 4 | a0001c0001t0001g0055 a0001c0002t0001g0035 a0001c0002t0001g0050 others(1): Show |
4 | HG00733.hp1 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.214+3659A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48579742 | |||||||
| chr19:48579745 | T | C | 4 | a0001c0001t0001g0055 a0001c0002t0001g0035 a0001c0002t0001g0050 others(1): Show |
4 | HG00733.hp1 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.214+3662T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48579745 | |||||||
| chr19:48579760 | C | T | 5 | a0001c0005t0001g0009 a0001c0005t0001g0010 a0001c0005t0001g0011 others(2): Show |
5 | HG01884.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.214+3677C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48579760 | |||||||
| chr19:48579795 | C | T | 1 | a0001c0002t0001g0091 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.214+3712C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48579795 | |||||||
| chr19:48580066 | A | G | 290 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(287): Show |
291 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(288): Show |
intron_variant | MODIFIER | c.214+3983A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48580066 | |||||||
| chr19:48580081 | G | T | 1 | a0002c0008t0001g0150 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.214+3998G>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48580081 | |||||||
| chr19:48580100 | C | CT | 150 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0024 others(147): Show |
150 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.214+4030dupT | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48580100 | ||||||
| chr19:48580236 | A | G | 141 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0037 others(138): Show |
141 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.214+4153A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48580236 | |||||||
| chr19:48580249 | C | T | 4 | a0001c0001t0001g0024 a0001c0001t0001g0054 a0001c0001t0001g0056 others(1): Show |
4 | HG02257.hp1 HG02717.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.214+4166C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48580249 | |||||||
| chr19:48580372 | GC | G | 121 | a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0026 others(118): Show |
121 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.214+4291delC | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48580372 | ||||||
| chr19:48580799 | G | A | 162 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0022 others(159): Show |
162 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(159): Show |
intron_variant | MODIFIER | c.214+4716G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48580799 | |||||||
| chr19:48580831 | G | A | 2 | a0001c0004t0001g0090 a0001c0004t0001g0196 |
2 | HG02258.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.214+4748G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48580831 | |||||||
| chr19:48580857 | C | T | 105 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(102): Show |
105 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.214+4774C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48580857 | |||||||
| chr19:48580992 | C | T | 4 | a0001c0001t0001g0137 a0001c0001t0001g0340 a0001c0001t0001g0342 others(1): Show |
4 | HG02040.hp2 HG02074.hp1 HG02129.hp2 others(1): Show |
intron_variant | MODIFIER | c.214+4909C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48580992 | |||||||
| chr19:48581029 | C | CT | 113 | a0001c0001t0001g0015 a0001c0001t0001g0037 a0001c0001t0001g0059 others(110): Show |
113 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.214+4970dupT | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48581029 | ||||||
| chr19:48581029 | C | CTT | 98 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(95): Show |
98 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.214+4969_214+4970d others(4): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48581029 | ||||||
| chr19:48581029 | C | CTTT | 15 | a0001c0001t0001g0147 a0001c0001t0001g0329 a0001c0001t0001g0336 others(12): Show |
15 | HG00438.hp2 HG00609.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.214+4968_214+4970d others(5): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48581029 | ||||||
| chr19:48581029 | CTT | C | 12 | a0001c0001t0001g0022 a0001c0001t0001g0043 a0001c0001t0001g0074 others(9): Show |
12 | HG01884.hp2 HG02257.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.214+4969_214+4970d others(4): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48581029 | ||||||
| chr19:48581029 | CTTTT | C | 35 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(32): Show |
35 | HG00733.hp1 HG00738.hp1 HG01167.hp1 others(32): Show |
intron_variant | MODIFIER | c.214+4967_214+4970d others(6): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48581029 | ||||||
| chr19:48581029 | CTTTTTTT | C | 21 | a0001c0005t0001g0001 a0001c0005t0001g0072 a0001c0005t0001g0109 others(18): Show |
22 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.214+4964_214+4970d others(9): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48581029 | ||||||
| chr19:48581099 | C | T | 50 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(47): Show |
50 | HG00733.hp1 HG00738.hp1 HG01167.hp1 others(47): Show |
intron_variant | MODIFIER | c.214+5016C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48581099 | |||||||
| chr19:48581207 | AT | A | 152 | a0001c0001t0001g0015 a0001c0001t0001g0037 a0001c0001t0001g0088 others(149): Show |
153 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.214+5140delT | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48581207 | ||||||
| chr19:48581207 | ATT | A | 108 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(105): Show |
108 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.214+5139_214+5140d others(4): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48581207 | ||||||
| chr19:48581207 | ATTT | A | 49 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(46): Show |
49 | HG00733.hp1 HG00738.hp1 HG01167.hp1 others(46): Show |
intron_variant | MODIFIER | c.214+5138_214+5140d others(5): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48581207 | ||||||
| chr19:48581223 | T | C | 1 | a0001c0001t0001g0260 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.214+5140T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48581223 | |||||||
| chr19:48581264 | G | A | 3 | a0001c0001t0001g0238 a0001c0003t0001g0188 a0001c0003t0001g0225 |
3 | HG01928.hp2 HG01934.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.214+5181G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48581264 | |||||||
| chr19:48581274 | T | C | 50 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(47): Show |
50 | HG00733.hp1 HG00738.hp1 HG01167.hp1 others(47): Show |
intron_variant | MODIFIER | c.214+5191T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48581274 | |||||||
| chr19:48581296 | G | A | 1 | a0002c0008t0001g0244 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.214+5213G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48581296 | |||||||
| chr19:48581299 | C | T | 105 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(102): Show |
105 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.214+5216C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48581299 | |||||||
| chr19:48581334 | G | A | 4 | a0001c0001t0001g0024 a0001c0001t0001g0054 a0001c0001t0001g0056 others(1): Show |
4 | HG02257.hp1 HG02717.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.214+5251G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48581334 | |||||||
| chr19:48581339 | T | C | 309 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(306): Show |
310 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(307): Show |
intron_variant | MODIFIER | c.214+5256T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48581339 | |||||||
| chr19:48581346 | A | G | 1 | a0001c0001t0001g0242 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.214+5263A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48581346 | |||||||
| chr19:48581398 | G | A | 311 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(308): Show |
312 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(309): Show |
intron_variant | MODIFIER | c.214+5315G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48581398 | |||||||
| chr19:48581418 | G | A | 86 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(83): Show |
87 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(84): Show |
intron_variant | MODIFIER | c.214+5335G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48581418 | |||||||
| chr19:48581455 | A | G | 86 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(83): Show |
87 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(84): Show |
intron_variant | MODIFIER | c.214+5372A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48581455 | |||||||
| chr19:48581470 | G | GTTT | 6 | a0001c0001t0001g0022 a0001c0001t0001g0360 a0001c0001t0001g0363 others(3): Show |
6 | HG01884.hp2 HG02257.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.214+5387_214+5388i others(5): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48581470 | |||||||
| chr19:48581471 | A | T | 7 | a0001c0001t0001g0022 a0001c0001t0001g0360 a0001c0001t0001g0363 others(4): Show |
7 | HG01884.hp2 HG02257.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.214+5388A>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48581471 | |||||||
| chr19:48581472 | G | GT | 7 | a0001c0001t0001g0271 a0001c0001t0001g0284 a0001c0001t0001g0285 others(4): Show |
7 | HG03139.hp2 NA18973.hp1 NA18974.hp1 others(4): Show |
intron_variant | MODIFIER | c.214+5405dupT | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48581472 | ||||||
| chr19:48581472 | G | GTT | 86 | a0001c0001t0001g0037 a0001c0001t0001g0088 a0001c0001t0001g0089 others(83): Show |
86 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.214+5404_214+5405d others(4): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48581472 | ||||||
| chr19:48581472 | G | GTTT | 152 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(149): Show |
152 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(149): Show |
intron_variant | MODIFIER | c.214+5403_214+5405d others(5): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48581472 | ||||||
| chr19:48581472 | G | GTTTT | 25 | a0001c0001t0001g0033 a0001c0001t0001g0074 a0001c0001t0001g0076 others(22): Show |
25 | HG00423.hp1 HG01243.hp1 HG01261.hp1 others(22): Show |
intron_variant | MODIFIER | c.214+5402_214+5405d others(6): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48581472 | ||||||
| chr19:48581472 | G | GTTTTT | 32 | a0001c0001t0001g0043 a0001c0001t0001g0075 a0001c0002t0001g0353 others(29): Show |
33 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.214+5401_214+5405d others(7): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48581472 | ||||||
| chr19:48581472 | G | GTTTTTT | 7 | a0001c0001t0001g0015 a0001c0001t0001g0259 a0001c0005t0001g0020 others(4): Show |
7 | HG02818.hp2 HG03041.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.214+5400_214+5405d others(8): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48581472 | ||||||
| chr19:48581472 | G | T | 7 | a0001c0001t0001g0022 a0001c0001t0001g0360 a0001c0001t0001g0363 others(4): Show |
7 | HG01884.hp2 HG02257.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.214+5389G>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48581472 | |||||||
| chr19:48581582 | C | T | 86 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(83): Show |
87 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(84): Show |
intron_variant | MODIFIER | c.214+5499C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48581582 | |||||||
| chr19:48581875 | TTTA | T | 33 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0018 others(30): Show |
33 | HG00733.hp1 HG01081.hp2 HG01346.hp2 others(30): Show |
intron_variant | MODIFIER | c.215-5340_215-5338d others(5): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48581875 | ||||||
| chr19:48581882 | T | TTATTA | 6 | a0001c0001t0001g0360 a0001c0001t0001g0363 a0001c0001t0001g0364 others(3): Show |
6 | HG01884.hp2 HG02559.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.215-5345_215-5341d others(7): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48581882 | ||||||
| chr19:48581885 | T | TTA | 3 | a0001c0005t0001g0072 a0001c0006t0001g0021 a0001c0006t0001g0045 |
3 | HG00140.hp2 HG02723.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.215-5342_215-5341d others(4): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48581885 | ||||||
| chr19:48581887 | A | T | 13 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0052 others(10): Show |
13 | HG00738.hp1 HG01167.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.215-5342A>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48581887 | |||||||
| chr19:48581887 | ATTATATT others(2): Show |
A | 5 | a0001c0005t0001g0210 a0001c0005t0001g0214 a0001c0005t0001g0256 others(2): Show |
5 | HG01192.hp1 HG01261.hp2 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.215-5340_215-5332d others(11): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48581887 | ||||||
| chr19:48581889 | T | A | 38 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0043 others(35): Show |
39 | HG00099.hp2 HG00738.hp1 HG00741.hp2 others(36): Show |
intron_variant | MODIFIER | c.215-5340T>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48581889 | |||||||
| chr19:48581890 | A | AT | 10 | a0001c0001t0001g0022 a0001c0001t0001g0360 a0001c0001t0001g0363 others(7): Show |
10 | HG00140.hp2 HG01884.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.215-5338dupT | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48581890 | ||||||
| chr19:48581890 | A | T | 63 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(60): Show |
64 | HG00099.hp2 HG00733.hp1 HG00738.hp1 others(61): Show |
intron_variant | MODIFIER | c.215-5339A>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48581890 | |||||||
| chr19:48581890 | ATAT | A | 216 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(213): Show |
216 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.215-5309_215-5307d others(5): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48581890 | ||||||
| chr19:48581924 | A | G | 6 | a0001c0001t0001g0022 a0001c0001t0001g0360 a0001c0001t0001g0363 others(3): Show |
6 | HG01884.hp2 HG02257.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.215-5305A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48581924 | |||||||
| chr19:48581943 | C | T | 86 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(83): Show |
87 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(84): Show |
intron_variant | MODIFIER | c.215-5286C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48581943 | |||||||
| chr19:48581944 | G | A | 1 | a0001c0003t0001g0047 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.215-5285G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48581944 | |||||||
| chr19:48581951 | C | G | 1 | a0001c0001t0001g0284 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.215-5278C>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48581951 | |||||||
| chr19:48581952 | T | C | 1 | a0001c0001t0001g0284 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.215-5277T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48581952 | |||||||
| chr19:48581990 | C | T | 2 | a0001c0001t0001g0268 a0001c0003t0001g0323 |
2 | NA19000.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.215-5239C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48581990 | |||||||
| chr19:48582145 | T | A | 1 | a0001c0002t0001g0156 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.215-5084T>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48582145 | |||||||
| chr19:48582168 | G | C | 86 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(83): Show |
87 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(84): Show |
intron_variant | MODIFIER | c.215-5061G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48582168 | |||||||
| chr19:48582184 | C | T | 1 | a0001c0001t0001g0372 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.215-5045C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48582184 | |||||||
| chr19:48582387 | GTA | G | 86 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(83): Show |
87 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(84): Show |
intron_variant | MODIFIER | c.215-4837_215-4836d others(4): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48582387 | ||||||
| chr19:48582453 | C | T | 86 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(83): Show |
87 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(84): Show |
intron_variant | MODIFIER | c.215-4776C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48582453 | |||||||
| chr19:48582476 | A | T | 86 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(83): Show |
87 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(84): Show |
intron_variant | MODIFIER | c.215-4753A>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48582476 | |||||||
| chr19:48582583 | A | C | 86 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(83): Show |
87 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(84): Show |
intron_variant | MODIFIER | c.215-4646A>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48582583 | |||||||
| chr19:48582642 | A | G | 86 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(83): Show |
87 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(84): Show |
intron_variant | MODIFIER | c.215-4587A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48582642 | |||||||
| chr19:48582654 | A | C | 86 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(83): Show |
87 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(84): Show |
intron_variant | MODIFIER | c.215-4575A>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48582654 | |||||||
| chr19:48582677 | T | C | 86 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(83): Show |
87 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(84): Show |
intron_variant | MODIFIER | c.215-4552T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48582677 | |||||||
| chr19:48582711 | T | C | 86 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(83): Show |
87 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(84): Show |
intron_variant | MODIFIER | c.215-4518T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48582711 | |||||||
| chr19:48582712 | G | A | 86 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(83): Show |
87 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(84): Show |
intron_variant | MODIFIER | c.215-4517G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48582712 | |||||||
| chr19:48582736 | G | A | 106 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(103): Show |
106 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.215-4493G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48582736 | |||||||
| chr19:48582779 | G | A | 1 | a0001c0004t0001g0224 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.215-4450G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48582779 | |||||||
| chr19:48582797 | C | T | 1 | a0001c0004t0001g0129 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.215-4432C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48582797 | |||||||
| chr19:48582798 | G | A | 85 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(82): Show |
86 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(83): Show |
intron_variant | MODIFIER | c.215-4431G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48582798 | |||||||
| chr19:48582869 | G | T | 2 | a0001c0001t0001g0190 a0001c0001t0001g0311 |
2 | HG01074.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.215-4360G>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48582869 | |||||||
| chr19:48582881 | G | A | 1 | a0001c0001t0001g0117 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.215-4348G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48582881 | |||||||
| chr19:48582961 | T | A | 86 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(83): Show |
87 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(84): Show |
intron_variant | MODIFIER | c.215-4268T>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48582961 | |||||||
| chr19:48582979 | C | T | 3 | a0001c0002t0001g0077 a0001c0002t0001g0326 a0001c0004t0001g0129 |
3 | HG01361.hp2 NA18943.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.215-4250C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48582979 | |||||||
| chr19:48582989 | C | CA | 108 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(105): Show |
108 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.215-4228dupA | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48582989 | ||||||
| chr19:48582989 | C | CAAA | 48 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0043 others(45): Show |
49 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(46): Show |
intron_variant | MODIFIER | c.215-4230_215-4228d others(5): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48582989 | ||||||
| chr19:48582989 | C | CAAAA | 38 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(35): Show |
38 | HG00733.hp1 HG00738.hp1 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.215-4231_215-4228d others(6): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48582989 | ||||||
| chr19:48583017 | C | CGTGCGTG others(700): Show |
3 | a0001c0001t0001g0032 a0001c0001t0001g0067 a0001c0001t0001g0365 |
3 | HG01891.hp2 HG02451.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.215-4208_215-4207i others(709): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48583017 | ||||||
| chr19:48583017 | C | CGTGCGTG others(681): Show |
3 | a0001c0001t0001g0015 a0001c0010t0001g0092 a0001c0010t0001g0367 |
3 | HG03041.hp1 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.215-4208_215-4207i others(690): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48583017 | ||||||
| chr19:48583017 | C | CGTGCGTG others(695): Show |
79 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(76): Show |
80 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(77): Show |
intron_variant | MODIFIER | c.215-4208_215-4207i others(704): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48583017 | ||||||
| chr19:48583031 | G | A | 85 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(82): Show |
86 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(83): Show |
intron_variant | MODIFIER | c.215-4198G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48583031 | |||||||
| chr19:48583031 | G | GTCCCAGC others(695): Show |
1 | a0001c0006t0001g0095 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.215-4174_215-4173i others(704): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48583031 | ||||||
| chr19:48583046 | G | A | 7 | a0001c0001t0001g0238 a0001c0003t0001g0188 a0001c0003t0001g0225 others(4): Show |
7 | HG01168.hp1 HG01928.hp2 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.215-4183G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48583046 | |||||||
| chr19:48583108 | T | G | 86 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(83): Show |
87 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(84): Show |
intron_variant | MODIFIER | c.215-4121T>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48583108 | |||||||
| chr19:48583176 | C | CAGAAT | 86 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(83): Show |
87 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(84): Show |
intron_variant | MODIFIER | c.215-4049_215-4048i others(7): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48583176 | ||||||
| chr19:48583540 | G | A | 85 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(82): Show |
86 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(83): Show |
intron_variant | MODIFIER | c.215-3689G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48583540 | |||||||
| chr19:48583588 | C | G | 1 | a0008c0015t0001g0351 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.215-3641C>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48583588 | |||||||
| chr19:48583589 | G | C | 1 | a0008c0015t0001g0351 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.215-3640G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48583589 | |||||||
| chr19:48583670 | T | A | 1 | a0001c0004t0001g0180 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.215-3559T>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48583670 | |||||||
| chr19:48583689 | G | A | 6 | a0001c0005t0001g0020 a0001c0005t0001g0210 a0001c0005t0001g0214 others(3): Show |
6 | HG01192.hp1 HG01261.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.215-3540G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48583689 | |||||||
| chr19:48583690 | C | G | 1 | a0001c0001t0001g0118 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.215-3539C>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48583690 | |||||||
| chr19:48583691 | G | C | 1 | a0001c0001t0001g0118 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.215-3538G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48583691 | |||||||
| chr19:48583737 | G | C | 1 | a0001c0001t0001g0067 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.215-3492G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48583737 | |||||||
| chr19:48583738 | A | G | 1 | a0001c0004t0001g0180 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.215-3491A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48583738 | |||||||
| chr19:48583740 | C | A | 1 | a0001c0004t0001g0180 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.215-3489C>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48583740 | |||||||
| chr19:48583807 | G | C | 3 | a0001c0001t0001g0211 a0001c0001t0001g0344 a0001c0001t0001g0354 |
3 | HG02071.hp2 NA18966.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.215-3422G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48583807 | |||||||
| chr19:48583814 | TCAAA | T | 82 | a0001c0001t0001g0081 a0001c0001t0001g0098 a0001c0001t0001g0118 others(79): Show |
82 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.215-3402_215-3399d others(6): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48583814 | ||||||
| chr19:48583830 | A | G | 1 | a0001c0007t0001g0034 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.215-3399A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48583830 | |||||||
| chr19:48583844 | T | A | 1 | a0008c0015t0001g0351 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.215-3385T>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48583844 | |||||||
| chr19:48583940 | T | C | 85 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(82): Show |
86 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(83): Show |
intron_variant | MODIFIER | c.215-3289T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48583940 | |||||||
| chr19:48584035 | C | T | 85 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(82): Show |
86 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(83): Show |
intron_variant | MODIFIER | c.215-3194C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48584035 | |||||||
| chr19:48584277 | G | A | 8 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(5): Show |
8 | HG02055.hp2 HG02572.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.215-2952G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48584277 | |||||||
| chr19:48584313 | A | T | 3 | a0001c0001t0001g0363 a0001c0001t0001g0364 a0001c0001t0001g0366 |
3 | HG01884.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.215-2916A>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48584313 | |||||||
| chr19:48584314 | C | A | 1 | a0001c0001t0001g0118 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.215-2915C>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48584314 | |||||||
| chr19:48584315 | A | C | 1 | a0001c0001t0001g0118 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.215-2914A>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48584315 | |||||||
| chr19:48584316 | G | A | 1 | a0001c0001t0001g0118 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.215-2913G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48584316 | |||||||
| chr19:48584373 | T | A | 1 | a0001c0001t0001g0283 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.215-2856T>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48584373 | |||||||
| chr19:48584410 | T | C | 315 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(312): Show |
316 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(313): Show |
intron_variant | MODIFIER | c.215-2819T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48584410 | |||||||
| chr19:48584499 | G | A | 5 | a0001c0001t0001g0043 a0001c0001t0001g0074 a0001c0001t0001g0075 others(2): Show |
5 | HG03098.hp1 HG03130.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.215-2730G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48584499 | |||||||
| chr19:48584527 | T | C | 1 | a0001c0005t0001g0195 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.215-2702T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48584527 | |||||||
| chr19:48584532 | CA | C | 88 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(85): Show |
89 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(86): Show |
intron_variant | MODIFIER | c.215-2692delA | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48584532 | ||||||
| chr19:48584541 | C | G | 88 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(85): Show |
89 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(86): Show |
intron_variant | MODIFIER | c.215-2688C>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48584541 | |||||||
| chr19:48584638 | C | T | 3 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0204 |
3 | HG02647.hp1 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.215-2591C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48584638 | |||||||
| chr19:48584685 | G | T | 1 | a0007c0021t0001g0304 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.215-2544G>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48584685 | |||||||
| chr19:48584789 | G | A | 2 | a0001c0006t0001g0061 a0001c0007t0001g0057 |
2 | HG02145.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.215-2440G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48584789 | |||||||
| chr19:48584808 | T | C | 109 | a0001c0001t0001g0037 a0001c0001t0001g0088 a0001c0001t0001g0089 others(106): Show |
109 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.215-2421T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48584808 | |||||||
| chr19:48584827 | G | T | 2 | a0001c0002t0001g0050 a0001c0002t0001g0051 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.215-2402G>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48584827 | |||||||
| chr19:48584911 | C | T | 107 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(104): Show |
107 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.215-2318C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48584911 | |||||||
| chr19:48584912 | G | A | 6 | a0001c0001t0001g0308 a0001c0001t0001g0309 a0001c0002t0001g0189 others(3): Show |
6 | HG00621.hp1 HG02165.hp1 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.215-2317G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48584912 | |||||||
| chr19:48584959 | G | A | 1 | a0001c0001t0001g0324 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.215-2270G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48584959 | |||||||
| chr19:48585048 | C | CA | 146 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(143): Show |
146 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.215-2157dupA | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48585048 | ||||||
| chr19:48585048 | C | CAA | 39 | a0001c0001t0001g0015 a0001c0001t0001g0025 a0001c0001t0001g0027 others(36): Show |
40 | HG00140.hp2 HG00597.hp1 HG01081.hp1 others(37): Show |
intron_variant | MODIFIER | c.215-2158_215-2157d others(4): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48585048 | ||||||
| chr19:48585048 | C | CAAA | 17 | a0001c0001t0001g0043 a0001c0001t0001g0074 a0001c0001t0001g0075 others(14): Show |
17 | HG00741.hp2 HG01106.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.215-2159_215-2157d others(5): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48585048 | ||||||
| chr19:48585048 | CA | C | 69 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0107 others(66): Show |
69 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.215-2157delA | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48585048 | ||||||
| chr19:48585048 | CAA | C | 36 | a0001c0001t0001g0037 a0001c0001t0001g0197 a0001c0001t0001g0199 others(33): Show |
36 | HG00621.hp1 HG00639.hp2 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.215-2158_215-2157d others(4): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48585048 | ||||||
| chr19:48585073 | G | A | 1 | a0001c0001t0001g0118 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.215-2156G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48585073 | |||||||
| chr19:48585074 | C | G | 1 | a0001c0001t0001g0118 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.215-2155C>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48585074 | |||||||
| chr19:48585096 | C | T | 1 | a0001c0003t0001g0047 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.215-2133C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48585096 | |||||||
| chr19:48585142 | G | C | 4 | a0001c0001t0001g0008 a0001c0001t0001g0052 a0001c0001t0001g0101 others(1): Show |
4 | HG01167.hp1 HG01169.hp1 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.215-2087G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48585142 | |||||||
| chr19:48585142 | G | T | 14 | a0001c0001t0001g0118 a0001c0001t0001g0147 a0001c0001t0001g0274 others(11): Show |
14 | HG00423.hp2 HG02040.hp1 NA18949.hp1 others(11): Show |
intron_variant | MODIFIER | c.215-2087G>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48585142 | |||||||
| chr19:48585389 | C | T | 3 | a0001c0002t0001g0023 a0001c0002t0001g0357 a0001c0002t0001g0358 |
3 | HG01168.hp2 HG01169.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.215-1840C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48585389 | |||||||
| chr19:48585433 | T | C | 46 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0033 others(43): Show |
47 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.215-1796T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48585433 | |||||||
| chr19:48585624 | G | C | 1 | a0001c0001t0001g0118 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.215-1605G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48585624 | |||||||
| chr19:48585665 | G | A | 38 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0033 others(35): Show |
39 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(36): Show |
intron_variant | MODIFIER | c.215-1564G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48585665 | |||||||
| chr19:48585684 | T | G | 45 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0033 others(42): Show |
46 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(43): Show |
intron_variant | MODIFIER | c.215-1545T>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48585684 | |||||||
| chr19:48585691 | A | AG | 22 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0018 others(19): Show |
22 | HG02055.hp1 HG02071.hp2 HG02165.hp2 others(19): Show |
intron_variant | MODIFIER | c.215-1532dupG | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48585691 | ||||||
| chr19:48585735 | T | C | 128 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0033 others(125): Show |
129 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.215-1494T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48585735 | |||||||
| chr19:48585817 | C | T | 1 | a0001c0004t0001g0279 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.215-1412C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48585817 | |||||||
| chr19:48585829 | TA | T | 5 | a0001c0001t0001g0043 a0001c0001t0001g0074 a0001c0001t0001g0075 others(2): Show |
5 | HG03098.hp1 HG03130.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.215-1393delA | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48585829 | ||||||
| chr19:48585947 | G | A | 2 | a0001c0005t0001g0072 a0001c0006t0001g0021 |
2 | HG00140.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.215-1282G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48585947 | |||||||
| chr19:48585948 | G | A | 100 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(97): Show |
100 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.215-1281G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48585948 | |||||||
| chr19:48585975 | G | A | 1 | a0001c0006t0001g0045 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.215-1254G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48585975 | |||||||
| chr19:48586052 | T | A | 304 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(301): Show |
305 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(302): Show |
intron_variant | MODIFIER | c.215-1177T>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48586052 | |||||||
| chr19:48586061 | A | G | 1 | a0001c0006t0001g0029 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.215-1168A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48586061 | |||||||
| chr19:48586120 | G | T | 2 | a0001c0001t0001g0028 a0001c0002t0001g0156 |
2 | NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.215-1109G>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48586120 | |||||||
| chr19:48586229 | A | G | 5 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0365 others(2): Show |
5 | HG01891.hp2 HG02486.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.215-1000A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48586229 | |||||||
| chr19:48586269 | C | G | 1 | a0001c0001t0001g0028 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.215-960C>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48586269 | |||||||
| chr19:48586307 | T | G | 56 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0032 others(53): Show |
57 | HG00099.hp2 HG00140.hp2 HG00738.hp1 others(54): Show |
intron_variant | MODIFIER | c.215-922T>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48586307 | |||||||
| chr19:48586330 | C | A | 1 | a0001c0007t0001g0162 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.215-899C>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48586330 | |||||||
| chr19:48586348 | G | T | 5 | a0001c0005t0001g0009 a0001c0005t0001g0010 a0001c0005t0001g0011 others(2): Show |
5 | HG01884.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.215-881G>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48586348 | |||||||
| chr19:48586364 | C | T | 1 | a0001c0006t0001g0094 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.215-865C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48586364 | |||||||
| chr19:48586454 | A | G | 56 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0032 others(53): Show |
57 | HG00099.hp2 HG00140.hp2 HG00738.hp1 others(54): Show |
intron_variant | MODIFIER | c.215-775A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48586454 | |||||||
| chr19:48586538 | T | C | 310 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(307): Show |
311 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(308): Show |
intron_variant | MODIFIER | c.215-691T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48586538 | |||||||
| chr19:48586640 | T | G | 1 | a0001c0004t0001g0129 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.215-589T>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48586640 | |||||||
| chr19:48586672 | C | T | 1 | a0001c0004t0001g0090 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.215-557C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48586672 | |||||||
| chr19:48586675 | C | G | 56 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0032 others(53): Show |
57 | HG00099.hp2 HG00140.hp2 HG00738.hp1 others(54): Show |
intron_variant | MODIFIER | c.215-554C>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48586675 | |||||||
| chr19:48586908 | C | T | 56 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0032 others(53): Show |
57 | HG00099.hp2 HG00140.hp2 HG00738.hp1 others(54): Show |
intron_variant | MODIFIER | c.215-321C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48586908 | |||||||
| chr19:48586967 | A | G | 50 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0032 others(47): Show |
51 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(48): Show |
intron_variant | MODIFIER | c.215-262A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48586967 | |||||||
| chr19:48586996 | G | C | 50 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0032 others(47): Show |
51 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(48): Show |
intron_variant | MODIFIER | c.215-233G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48586996 | |||||||
| chr19:48587041 | G | A | 4 | a0001c0001t0001g0008 a0001c0001t0001g0052 a0001c0001t0001g0101 others(1): Show |
4 | HG01167.hp1 HG01169.hp1 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.215-188G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48587041 | |||||||
| chr19:48587049 | T | C | 50 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0032 others(47): Show |
51 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(48): Show |
intron_variant | MODIFIER | c.215-180T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48587049 | |||||||
| chr19:48587085 | G | C | 50 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0032 others(47): Show |
51 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(48): Show |
intron_variant | MODIFIER | c.215-144G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48587085 | |||||||
| chr19:48587091 | A | G | 50 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0032 others(47): Show |
51 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(48): Show |
intron_variant | MODIFIER | c.215-138A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48587091 | |||||||
| chr19:48587111 | T | TA | 205 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(202): Show |
205 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(202): Show |
intron_variant | MODIFIER | c.215-109dupA | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48587111 | ||||||
| chr19:48587111 | T | TAA | 33 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(30): Show |
33 | HG00733.hp1 HG01167.hp1 HG01169.hp1 others(30): Show |
intron_variant | MODIFIER | c.215-110_215-109dup others(2): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48587111 | ||||||
| chr19:48587111 | TA | T | 50 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0032 others(47): Show |
51 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(48): Show |
intron_variant | MODIFIER | c.215-109delA | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48587111 | ||||||
| chr19:48587118 | A | AAT | 12 | a0001c0001t0001g0040 a0001c0001t0001g0043 a0001c0001t0001g0067 others(9): Show |
12 | HG00738.hp1 HG02451.hp1 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.215-110_215-109ins others(2): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48587118 | ||||||
| chr19:48587118 | A | AT | 4 | a0001c0002t0001g0050 a0001c0002t0001g0051 a0001c0002t0001g0303 others(1): Show |
4 | HG00280.hp2 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.215-111_215-110ins others(1): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48587118 | |||||||
| chr19:48587190 | C | T | 1 | a0001c0001t0001g0242 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.215-39C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48587190 | |||||||
| chr19:48587191 | T | C | 1 | a0001c0001t0001g0242 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.215-38T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48587191 | |||||||
| chr19:48587474 | G | A | 1 | a0001c0004t0001g0180 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.423+37G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48587474 | |||||||
| chr19:48587552 | T | A | 52 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0032 others(49): Show |
53 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(50): Show |
intron_variant | MODIFIER | c.423+115T>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48587552 | |||||||
| chr19:48587725 | T | C | 150 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0025 others(147): Show |
151 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.423+288T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48587725 | |||||||
| chr19:48587754 | G | A | 41 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(38): Show |
41 | HG00733.hp1 HG00738.hp1 HG01167.hp1 others(38): Show |
intron_variant | MODIFIER | c.423+317G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48587754 | |||||||
| chr19:48587890 | CA | C | 31 | a0001c0001t0001g0062 a0001c0001t0001g0105 a0001c0001t0001g0125 others(28): Show |
31 | HG00733.hp2 HG01168.hp1 HG01928.hp2 others(28): Show |
intron_variant | MODIFIER | c.423+486delA | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 48587890 | ||||||
| chr19:48587890 | CAA | C | 17 | a0001c0001t0001g0071 a0001c0001t0001g0117 a0001c0001t0001g0149 others(14): Show |
17 | HG00408.hp1 HG00609.hp2 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.423+485_423+486del others(2): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 48587890 | ||||||
| chr19:48587890 | CAAA | C | 11 | a0001c0001t0001g0040 a0001c0001t0001g0055 a0001c0001t0001g0076 others(8): Show |
11 | HG00733.hp1 HG00738.hp1 HG02015.hp2 others(8): Show |
intron_variant | MODIFIER | c.423+484_423+486del others(3): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 48587890 | ||||||
| chr19:48587890 | CAAAA | C | 29 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(26): Show |
29 | HG01167.hp1 HG01169.hp1 HG01433.hp1 others(26): Show |
intron_variant | MODIFIER | c.423+483_423+486del others(4): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 48587890 | ||||||
| chr19:48587890 | CAAAAA | C | 23 | a0001c0001t0001g0088 a0001c0001t0001g0093 a0001c0001t0001g0137 others(20): Show |
23 | HG00558.hp2 HG00621.hp2 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.423+482_423+486del others(5): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 48587890 | ||||||
| chr19:48587890 | CAAAAAA | C | 108 | a0001c0001t0001g0089 a0001c0001t0001g0107 a0001c0001t0001g0108 others(105): Show |
108 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.423+481_423+486del others(6): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 48587890 | ||||||
| chr19:48587890 | CAAAAAAA | C | 88 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(85): Show |
88 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.423+480_423+486del others(7): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 48587890 | ||||||
| chr19:48587890 | CAAAAAAA others(1): Show |
C | 32 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0033 others(29): Show |
32 | HG00741.hp2 HG01081.hp1 HG01175.hp2 others(29): Show |
intron_variant | MODIFIER | c.423+479_423+486del others(8): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 48587890 | ||||||
| chr19:48587890 | CAAAAAAA others(2): Show |
C | 15 | a0001c0005t0001g0001 a0001c0005t0001g0072 a0001c0005t0001g0114 others(12): Show |
16 | HG00099.hp2 HG00140.hp2 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.423+478_423+486del others(9): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 48587890 | ||||||
| chr19:48587890 | CAAAAAAA others(4): Show |
C | 4 | a0001c0001t0001g0024 a0001c0001t0001g0054 a0001c0001t0001g0056 others(1): Show |
4 | HG02257.hp1 HG02717.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.423+476_423+486del others(11): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 48587890 | ||||||
| chr19:48587890 | CAAAAAAA others(7): Show |
C | 1 | a0001c0003t0001g0079 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.423+473_423+486del others(14): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 48587890 | ||||||
| chr19:48587890 | CAAAAAAA others(12): Show |
C | 1 | a0001c0004t0001g0053 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.423+468_423+486del others(19): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 48587890 | ||||||
| chr19:48588017 | T | C | 306 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(303): Show |
307 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(304): Show |
intron_variant | MODIFIER | c.423+580T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48588017 | |||||||
| chr19:48588096 | G | C | 1 | a0001c0004t0001g0180 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.423+659G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48588096 | |||||||
| chr19:48588209 | C | CA | 48 | a0001c0001t0001g0015 a0001c0001t0001g0025 a0001c0001t0001g0026 others(45): Show |
49 | HG00099.hp2 HG00140.hp2 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.423+789dupA | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 48588209 | ||||||
| chr19:48588209 | C | CAA | 13 | a0001c0001t0001g0022 a0001c0001t0001g0259 a0001c0001t0001g0363 others(10): Show |
13 | HG01884.hp2 HG02257.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.423+788_423+789dup others(2): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 48588209 | ||||||
| chr19:48588209 | C | CAAAAA | 6 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0365 others(3): Show |
6 | HG01891.hp2 HG02258.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.423+785_423+789dup others(5): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 48588209 | ||||||
| chr19:48588209 | CA | C | 132 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(129): Show |
132 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.423+789delA | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 48588209 | ||||||
| chr19:48588238 | C | T | 3 | a0001c0001t0001g0093 a0001c0001t0001g0361 a0001c0002t0001g0091 |
3 | HG01243.hp1 HG02630.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.423+801C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48588238 | |||||||
| chr19:48588250 | C | G | 1 | a0001c0001t0001g0368 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.423+813C>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48588250 | |||||||
| chr19:48588258 | C | A | 14 | a0001c0001t0001g0024 a0001c0001t0001g0032 a0001c0001t0001g0033 others(11): Show |
14 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.423+821C>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48588258 | |||||||
| chr19:48588487 | G | A | 20 | a0001c0001t0001g0024 a0001c0001t0001g0032 a0001c0001t0001g0033 others(17): Show |
20 | HG01346.hp2 HG01891.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.423+1050G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48588487 | |||||||
| chr19:48588490 | CA | C | 20 | a0001c0001t0001g0024 a0001c0001t0001g0032 a0001c0001t0001g0033 others(17): Show |
20 | HG01346.hp2 HG01891.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.423+1055delA | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 48588490 | ||||||
| chr19:48588496 | A | G | 36 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0025 others(33): Show |
36 | HG01243.hp1 HG01346.hp2 HG01891.hp2 others(33): Show |
intron_variant | MODIFIER | c.423+1059A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48588496 | |||||||
| chr19:48588500 | A | G | 36 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0025 others(33): Show |
36 | HG01243.hp1 HG01346.hp2 HG01891.hp2 others(33): Show |
intron_variant | MODIFIER | c.423+1063A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48588500 | |||||||
| chr19:48588507 | C | T | 4 | a0001c0001t0001g0101 a0001c0001t0001g0170 a0001c0001t0001g0362 others(1): Show |
4 | HG01167.hp1 HG01169.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.423+1070C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48588507 | |||||||
| chr19:48588512 | C | CA | 9 | a0001c0001t0001g0149 a0001c0001t0001g0163 a0001c0002t0001g0301 others(6): Show |
9 | HG00438.hp2 HG01192.hp1 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.423+1085dupA | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 48588512 | ||||||
| chr19:48588512 | CA | C | 17 | a0001c0001t0001g0015 a0001c0001t0001g0025 a0001c0001t0001g0026 others(14): Show |
17 | HG01243.hp1 HG02055.hp2 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.423+1085delA | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 48588512 | ||||||
| chr19:48588523 | C | A | 20 | a0001c0001t0001g0022 a0001c0001t0001g0259 a0001c0001t0001g0363 others(17): Show |
20 | HG00642.hp1 HG01070.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.423+1086C>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48588523 | |||||||
| chr19:48588526 | CCATAT | C | 20 | a0001c0001t0001g0024 a0001c0001t0001g0032 a0001c0001t0001g0033 others(17): Show |
20 | HG01346.hp2 HG01891.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.423+1090_423+1094d others(7): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48588526 | |||||||
| chr19:48588595 | A | G | 4 | a0001c0001t0001g0308 a0001c0001t0001g0309 a0001c0002t0001g0208 others(1): Show |
4 | HG00621.hp1 HG02165.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.423+1158A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48588595 | |||||||
| chr19:48588605 | C | T | 35 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0025 others(32): Show |
35 | HG01243.hp1 HG01346.hp2 HG01891.hp2 others(32): Show |
intron_variant | MODIFIER | c.423+1168C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48588605 | |||||||
| chr19:48588607 | TATA | T | 4 | a0001c0001t0001g0362 a0001c0002t0001g0156 a0001c0003t0001g0047 others(1): Show |
4 | HG03139.hp2 HG03195.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.423+1175_423+1177d others(5): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 48588607 | ||||||
| chr19:48588621 | G | A | 372 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(369): Show |
373 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(370): Show |
intron_variant | MODIFIER | c.423+1184G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48588621 | |||||||
| chr19:48588637 | C | T | 19 | a0001c0001t0001g0024 a0001c0001t0001g0032 a0001c0001t0001g0043 others(16): Show |
19 | HG01346.hp2 HG01891.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.423+1200C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48588637 | |||||||
| chr19:48588672 | G | A | 2 | a0001c0001t0001g0360 a0001c0007t0001g0034 |
2 | HG01346.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.423+1235G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48588672 | |||||||
| chr19:48588683 | G | A | 3 | a0001c0001t0001g0362 a0001c0003t0001g0047 a0001c0004t0001g0053 |
3 | HG03139.hp2 HG03195.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.423+1246G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48588683 | |||||||
| chr19:48588855 | G | A | 91 | a0001c0001t0001g0071 a0001c0001t0001g0081 a0001c0001t0001g0098 others(88): Show |
91 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.423+1418G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48588855 | |||||||
| chr19:48588885 | A | G | 6 | a0001c0001t0001g0043 a0001c0001t0001g0074 a0001c0001t0001g0075 others(3): Show |
6 | HG02486.hp2 HG03098.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.423+1448A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48588885 | |||||||
| chr19:48588977 | C | A | 128 | a0001c0001t0001g0033 a0001c0001t0001g0037 a0001c0001t0001g0043 others(125): Show |
128 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.423+1540C>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48588977 | |||||||
| chr19:48589173 | A | G | 240 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(237): Show |
241 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(238): Show |
intron_variant | MODIFIER | c.423+1736A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48589173 | |||||||
| chr19:48589234 | T | C | 38 | a0001c0001t0001g0055 a0001c0001t0001g0059 a0001c0001t0001g0067 others(35): Show |
38 | HG00438.hp1 HG00735.hp2 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.423+1797T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48589234 | |||||||
| chr19:48589268 | A | C | 3 | a0001c0001t0001g0062 a0001c0001t0001g0093 a0001c0004t0001g0058 |
3 | HG01243.hp1 HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.423+1831A>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48589268 | |||||||
| chr19:48589280 | A | C | 1 | a0001c0001t0001g0033 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.423+1843A>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48589280 | |||||||
| chr19:48589294 | G | A | 223 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(220): Show |
224 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.423+1857G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48589294 | |||||||
| chr19:48589319 | G | A | 1 | a0001c0010t0001g0038 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.423+1882G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48589319 | |||||||
| chr19:48589322 | G | A | 1 | a0001c0002t0001g0278 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.423+1885G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48589322 | |||||||
| chr19:48589370 | A | T | 46 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0015 others(43): Show |
47 | HG00597.hp2 HG00639.hp1 HG01074.hp2 others(44): Show |
intron_variant | MODIFIER | c.423+1933A>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48589370 | |||||||
| chr19:48589644 | A | G | 8 | a0001c0001t0001g0025 a0001c0001t0001g0043 a0001c0001t0001g0075 others(5): Show |
8 | HG01346.hp2 HG02486.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.424-1965A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48589644 | |||||||
| chr19:48589855 | G | A | 1 | a0002c0013t0001g0286 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.424-1754G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48589855 | |||||||
| chr19:48589868 | G | A | 1 | a0001c0004t0001g0180 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.424-1741G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48589868 | |||||||
| chr19:48589978 | C | CTTTATTT | 4 | a0001c0001t0001g0033 a0001c0001t0001g0040 a0001c0001t0001g0041 others(1): Show |
4 | HG02615.hp2 HG02647.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.424-1628_424-1627i others(9): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 48589978 | ||||||
| chr19:48590136 | C | T | 210 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0022 others(207): Show |
210 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.424-1473C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48590136 | |||||||
| chr19:48590367 | C | T | 48 | a0001c0001t0001g0071 a0001c0001t0001g0088 a0001c0001t0001g0105 others(45): Show |
48 | HG00408.hp1 HG00597.hp1 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.424-1242C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48590367 | |||||||
| chr19:48590368 | G | A | 3 | a0001c0001t0001g0247 a0001c0001t0001g0259 a0001c0001t0001g0362 |
3 | HG02630.hp1 HG02818.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.424-1241G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48590368 | |||||||
| chr19:48590394 | G | T | 56 | a0001c0001t0001g0042 a0001c0004t0001g0006 a0001c0004t0001g0016 others(53): Show |
56 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.424-1215G>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48590394 | |||||||
| chr19:48590590 | A | G | 7 | a0001c0001t0001g0024 a0001c0001t0001g0054 a0001c0001t0001g0056 others(4): Show |
7 | HG02145.hp1 HG02257.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.424-1019A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48590590 | |||||||
| chr19:48590838 | GTTTA | G | 27 | a0001c0001t0001g0025 a0001c0001t0001g0032 a0001c0001t0001g0033 others(24): Show |
27 | HG00558.hp2 HG01074.hp1 HG01257.hp1 others(24): Show |
intron_variant | MODIFIER | c.424-767_424-764del others(4): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 48590838 | ||||||
| chr19:48590887 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.424-722G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48590887 | |||||||
| chr19:48590918 | C | T | 1 | a0001c0006t0001g0007 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.424-691C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48590918 | |||||||
| chr19:48591025 | G | C | 1 | a0001c0003t0001g0134 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.424-584G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48591025 | |||||||
| chr19:48591213 | T | C | 23 | a0001c0001t0001g0025 a0001c0001t0001g0032 a0001c0001t0001g0033 others(20): Show |
23 | HG00558.hp2 HG01074.hp1 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.424-396T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48591213 | |||||||
| chr19:48591513 | G | A | 3 | a0001c0001t0001g0247 a0001c0001t0001g0259 a0001c0001t0001g0362 |
3 | HG02630.hp1 HG02818.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.424-96G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48591513 | |||||||
| chr19:48591599 | C | T | 49 | a0001c0001t0001g0071 a0001c0001t0001g0088 a0001c0001t0001g0105 others(46): Show |
49 | HG00408.hp1 HG00597.hp1 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.424-10C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48591599 | |||||||
| chr19:48591754 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.550+19G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 4/6 | chr19 | 48591754 | |||||||
| chr19:48591843 | G | A | 1 | a0002c0008t0001g0150 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.550+108G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 4/6 | chr19 | 48591843 | |||||||
| chr19:48591885 | G | GAGA | 330 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(327): Show |
330 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(327): Show |
intron_variant | MODIFIER | c.550+154_550+156dup others(3): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 48591885 | ||||||
| chr19:48591918 | G | A | 2 | a0001c0001t0001g0197 a0001c0001t0001g0203 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.550+183G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 4/6 | chr19 | 48591918 | |||||||
| chr19:48592017 | G | A | 2 | a0001c0002t0001g0153 a0001c0005t0001g0256 |
2 | HG01192.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.550+282G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 4/6 | chr19 | 48592017 | |||||||
| chr19:48592021 | T | C | 315 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0018 others(312): Show |
315 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(312): Show |
intron_variant | MODIFIER | c.550+286T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 4/6 | chr19 | 48592021 | |||||||
| chr19:48592109 | T | C | 1 | a0001c0001t0001g0042 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.550+374T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 4/6 | chr19 | 48592109 | |||||||
| chr19:48592117 | CCCCGTCT others(8): Show |
C | 1 | a0001c0001t0001g0271 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.550+383_550+397del others(15): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 4/6 | chr19 | 48592117 | |||||||
| chr19:48592162 | G | A | 1 | a0001c0002t0001g0091 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.550+427G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 4/6 | chr19 | 48592162 | |||||||
| chr19:48592206 | G | C | 57 | a0001c0004t0001g0006 a0001c0004t0001g0016 a0001c0004t0001g0017 others(54): Show |
57 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.550+471G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 4/6 | chr19 | 48592206 | |||||||
| chr19:48592257 | A | C | 3 | a0001c0001t0001g0247 a0001c0001t0001g0259 a0001c0001t0001g0362 |
3 | HG02630.hp1 HG02818.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.551-465A>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 4/6 | chr19 | 48592257 | |||||||
| chr19:48592307 | TAA | T | 16 | a0001c0001t0001g0033 a0001c0001t0001g0040 a0001c0001t0001g0041 others(13): Show |
16 | HG00558.hp2 HG01074.hp1 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.551-411_551-410del others(2): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 48592307 | ||||||
| chr19:48592354 | A | G | 1 | a0001c0001t0001g0042 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.551-368A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 4/6 | chr19 | 48592354 | |||||||
| chr19:48592383 | G | A | 8 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0055 others(5): Show |
8 | HG01884.hp2 HG02055.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.551-339G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 4/6 | chr19 | 48592383 | |||||||
| chr19:48592388 | AGGCCCCT | A | 6 | a0001c0001t0001g0144 a0001c0001t0001g0185 a0001c0001t0001g0186 others(3): Show |
6 | NA18945.hp2 NA18957.hp2 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.551-331_551-325del others(7): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 48592388 | ||||||
| chr19:48592389 | GGCCCCTG others(3): Show |
G | 1 | a0001c0002t0001g0049 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.551-332_551-323del others(10): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 4/6 | chr19 | 48592389 | |||||||
| chr19:48592506 | A | C | 1 | a0001c0002t0001g0209 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.551-216A>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 4/6 | chr19 | 48592506 | |||||||
| chr19:48592507 | T | A | 1 | a0001c0002t0001g0209 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.551-215T>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 4/6 | chr19 | 48592507 | |||||||
| chr19:48592508 | A | C | 1 | a0001c0002t0001g0209 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.551-214A>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 4/6 | chr19 | 48592508 | |||||||
| chr19:48592513 | A | C | 1 | a0001c0002t0001g0209 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.551-209A>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 4/6 | chr19 | 48592513 | |||||||
| chr19:48592514 | A | G | 1 | a0001c0002t0001g0209 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.551-208A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 4/6 | chr19 | 48592514 | |||||||
| chr19:48592515 | G | A | 1 | a0001c0002t0001g0209 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.551-207G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 4/6 | chr19 | 48592515 | |||||||
| chr19:48592516 | G | C | 1 | a0001c0002t0001g0209 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.551-206G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 4/6 | chr19 | 48592516 | |||||||
| chr19:48592517 | C | G | 1 | a0001c0002t0001g0209 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.551-205C>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 4/6 | chr19 | 48592517 | |||||||
| chr19:48592517 | C | T | 1 | a0001c0001t0001g0163 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.551-205C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 4/6 | chr19 | 48592517 | |||||||
| chr19:48592518 | C | A | 49 | a0001c0001t0001g0116 a0001c0001t0001g0141 a0001c0001t0001g0164 others(46): Show |
49 | HG00423.hp1 HG00438.hp2 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.551-204C>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 4/6 | chr19 | 48592518 | |||||||
| chr19:48592519 | C | T | 1 | a0001c0002t0001g0209 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.551-203C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 4/6 | chr19 | 48592519 | |||||||
| chr19:48592520 | C | G | 1 | a0001c0002t0001g0209 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.551-202C>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 4/6 | chr19 | 48592520 | |||||||
| chr19:48592521 | C | T | 1 | a0001c0002t0001g0209 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.551-201C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 4/6 | chr19 | 48592521 | |||||||
| chr19:48592522 | C | T | 1 | a0001c0002t0001g0209 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.551-200C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 4/6 | chr19 | 48592522 | |||||||
| chr19:48592548 | G | C | 24 | a0001c0001t0001g0025 a0001c0001t0001g0032 a0001c0001t0001g0033 others(21): Show |
24 | HG00558.hp2 HG01074.hp1 HG01358.hp1 others(21): Show |
intron_variant | MODIFIER | c.551-174G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 4/6 | chr19 | 48592548 | |||||||
| chr19:48592614 | G | A | 48 | a0001c0001t0001g0116 a0001c0001t0001g0141 a0001c0001t0001g0164 others(45): Show |
48 | HG00423.hp1 HG00438.hp2 HG00733.hp2 others(45): Show |
intron_variant | MODIFIER | c.551-108G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 4/6 | chr19 | 48592614 | |||||||
| chr19:48592641 | G | A | 15 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0037 others(12): Show |
15 | HG01243.hp1 HG01884.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.551-81G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 4/6 | chr19 | 48592641 | |||||||
| chr19:48592651 | C | T | 5 | a0003c0011t0001g0044 a0003c0011t0001g0060 a0003c0012t0001g0013 others(2): Show |
5 | HG01884.hp1 HG02717.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.551-71C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 4/6 | chr19 | 48592651 | |||||||
| chr19:48592682 | C | T | 1 | a0001c0006t0001g0095 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.551-40C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 4/6 | chr19 | 48592682 | |||||||
| chr19:48592701 | C | T | 1 | a0001c0006t0001g0095 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.551-21C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 4/6 | chr19 | 48592701 | |||||||
| chr19:48592904 | C | A | 23 | a0001c0001t0001g0025 a0001c0001t0001g0032 a0001c0001t0001g0033 others(20): Show |
23 | HG00558.hp2 HG01074.hp1 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.645+88C>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48592904 | |||||||
| chr19:48592910 | G | A | 50 | a0001c0001t0001g0071 a0001c0001t0001g0088 a0001c0001t0001g0105 others(47): Show |
50 | HG00408.hp1 HG00597.hp1 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.645+94G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48592910 | |||||||
| chr19:48592957 | A | G | 1 | a0001c0001t0001g0067 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.645+141A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48592957 | |||||||
| chr19:48593020 | C | T | 2 | a0001c0001t0001g0197 a0001c0001t0001g0203 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.645+204C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48593020 | |||||||
| chr19:48593035 | G | A | 245 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0018 others(242): Show |
245 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.645+219G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48593035 | |||||||
| chr19:48593054 | G | A | 50 | a0001c0001t0001g0071 a0001c0001t0001g0088 a0001c0001t0001g0105 others(47): Show |
50 | HG00408.hp1 HG00597.hp1 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.645+238G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48593054 | |||||||
| chr19:48593279 | T | C | 1 | a0001c0003t0001g0323 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.645+463T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48593279 | |||||||
| chr19:48593569 | A | T | 1 | a0001c0001t0001g0067 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.645+753A>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48593569 | |||||||
| chr19:48593594 | C | T | 297 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0018 others(294): Show |
297 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(294): Show |
intron_variant | MODIFIER | c.645+778C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48593594 | |||||||
| chr19:48593641 | T | A | 185 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0018 others(182): Show |
186 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(183): Show |
intron_variant | MODIFIER | c.645+825T>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48593641 | |||||||
| chr19:48593869 | G | A | 50 | a0001c0001t0001g0018 a0001c0001t0001g0190 a0001c0001t0001g0311 others(47): Show |
50 | HG00558.hp1 HG00597.hp2 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.645+1053G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48593869 | |||||||
| chr19:48593943 | C | T | 1 | a0001c0003t0001g0140 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.645+1127C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48593943 | |||||||
| chr19:48593963 | A | C | 1 | a0001c0001t0001g0302 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.645+1147A>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48593963 | |||||||
| chr19:48593964 | A | G | 1 | a0001c0001t0001g0302 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.645+1148A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48593964 | |||||||
| chr19:48593972 | A | G | 2 | a0001c0001t0001g0032 a0001c0001t0001g0365 |
2 | HG01891.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.645+1156A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48593972 | |||||||
| chr19:48593980 | T | C | 1 | a0001c0001t0001g0302 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.645+1164T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48593980 | |||||||
| chr19:48593982 | G | A | 1 | a0001c0001t0001g0302 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.645+1166G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48593982 | |||||||
| chr19:48593983 | G | C | 1 | a0001c0001t0001g0302 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.645+1167G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48593983 | |||||||
| chr19:48593983 | G | T | 3 | a0001c0003t0001g0102 a0001c0003t0001g0175 a0001c0010t0001g0113 |
3 | HG00733.hp2 HG01081.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.645+1167G>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48593983 | |||||||
| chr19:48593990 | G | T | 1 | a0001c0001t0001g0302 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.645+1174G>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48593990 | |||||||
| chr19:48593991 | G | A | 1 | a0001c0001t0001g0302 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.645+1175G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48593991 | |||||||
| chr19:48593992 | C | T | 1 | a0001c0001t0001g0302 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.645+1176C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48593992 | |||||||
| chr19:48593993 | T | A | 1 | a0001c0001t0001g0302 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.645+1177T>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48593993 | |||||||
| chr19:48593994 | C | T | 1 | a0001c0001t0001g0302 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.645+1178C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48593994 | |||||||
| chr19:48593996 | C | A | 1 | a0001c0001t0001g0302 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.645+1180C>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48593996 | |||||||
| chr19:48593997 | G | A | 63 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0037 others(60): Show |
64 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.645+1181G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48593997 | |||||||
| chr19:48593998 | C | T | 1 | a0001c0001t0001g0302 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.645+1182C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48593998 | |||||||
| chr19:48593999 | C | A | 1 | a0001c0001t0001g0302 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.645+1183C>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48593999 | |||||||
| chr19:48594001 | G | A | 1 | a0001c0001t0001g0302 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.645+1185G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48594001 | |||||||
| chr19:48594008 | C | T | 1 | a0001c0001t0001g0302 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.645+1192C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48594008 | |||||||
| chr19:48594011 | C | A | 1 | a0001c0001t0001g0302 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.645+1195C>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48594011 | |||||||
| chr19:48594033 | C | T | 1 | a0001c0001t0001g0302 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.645+1217C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48594033 | |||||||
| chr19:48594034 | A | G | 1 | a0001c0001t0001g0302 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.645+1218A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48594034 | |||||||
| chr19:48594178 | T | C | 1 | a0001c0002t0001g0261 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.645+1362T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48594178 | |||||||
| chr19:48594406 | C | T | 62 | a0001c0003t0001g0012 a0001c0003t0001g0047 a0001c0003t0001g0079 others(59): Show |
62 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.645+1590C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48594406 | |||||||
| chr19:48594490 | C | T | 3 | a0001c0001t0001g0052 a0001c0001t0001g0300 a0001c0001t0001g0360 |
3 | HG02055.hp2 HG02886.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.645+1674C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48594490 | |||||||
| chr19:48594538 | G | A | 1 | a0001c0003t0001g0293 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.645+1722G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48594538 | |||||||
| chr19:48594630 | A | T | 347 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(344): Show |
348 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(345): Show |
intron_variant | MODIFIER | c.645+1814A>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48594630 | |||||||
| chr19:48594692 | C | T | 63 | a0001c0003t0001g0012 a0001c0003t0001g0047 a0001c0003t0001g0079 others(60): Show |
63 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.645+1876C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48594692 | |||||||
| chr19:48594902 | CCAG | C | 273 | a0001c0001t0001g0018 a0001c0001t0001g0024 a0001c0001t0001g0042 others(270): Show |
274 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(271): Show |
intron_variant | MODIFIER | c.646-1832_646-1830d others(5): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr19 | 48594902 | ||||||
| chr19:48594997 | G | C | 1 | a0001c0003t0001g0325 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.646-1742G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48594997 | |||||||
| chr19:48595079 | T | C | 1 | a0007c0021t0001g0304 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.646-1660T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48595079 | |||||||
| chr19:48595099 | A | G | 96 | a0001c0001t0001g0018 a0001c0001t0001g0042 a0001c0001t0001g0098 others(93): Show |
97 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.646-1640A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48595099 | |||||||
| chr19:48595151 | A | G | 1 | a0001c0006t0001g0045 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.646-1588A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48595151 | |||||||
| chr19:48595154 | T | C | 4 | a0003c0011t0001g0044 a0003c0011t0001g0060 a0003c0012t0001g0013 others(1): Show |
4 | HG01884.hp1 HG02717.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.646-1585T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48595154 | |||||||
| chr19:48595222 | C | T | 1 | a0001c0003t0001g0217 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.646-1517C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48595222 | |||||||
| chr19:48595269 | C | T | 63 | a0001c0003t0001g0012 a0001c0003t0001g0047 a0001c0003t0001g0079 others(60): Show |
63 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.646-1470C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48595269 | |||||||
| chr19:48595278 | G | A | 4 | a0003c0011t0001g0044 a0003c0011t0001g0060 a0003c0012t0001g0013 others(1): Show |
4 | HG01884.hp1 HG02717.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.646-1461G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48595278 | |||||||
| chr19:48595281 | TA | T | 345 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(342): Show |
346 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(343): Show |
intron_variant | MODIFIER | c.646-1447delA | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr19 | 48595281 | ||||||
| chr19:48595305 | CA | C | 273 | a0001c0001t0001g0018 a0001c0001t0001g0024 a0001c0001t0001g0042 others(270): Show |
274 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(271): Show |
intron_variant | MODIFIER | c.646-1433delA | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48595305 | |||||||
| chr19:48595359 | T | C | 1 | a0001c0001t0001g0269 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.646-1380T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48595359 | |||||||
| chr19:48595450 | G | A | 1 | a0006c0017t0001g0030 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.646-1289G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48595450 | |||||||
| chr19:48595493 | A | G | 173 | a0001c0001t0001g0024 a0001c0001t0001g0052 a0001c0001t0001g0054 others(170): Show |
173 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.646-1246A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48595493 | |||||||
| chr19:48595518 | C | T | 273 | a0001c0001t0001g0018 a0001c0001t0001g0024 a0001c0001t0001g0042 others(270): Show |
274 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(271): Show |
intron_variant | MODIFIER | c.646-1221C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48595518 | |||||||
| chr19:48595522 | C | T | 96 | a0001c0001t0001g0018 a0001c0001t0001g0042 a0001c0001t0001g0098 others(93): Show |
97 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.646-1217C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48595522 | |||||||
| chr19:48595654 | GGTTTTTT others(8): Show |
G | 15 | a0001c0001t0001g0118 a0001c0001t0001g0300 a0001c0001t0001g0354 others(12): Show |
15 | HG01106.hp1 HG01192.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.646-1084_646-1070d others(17): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48595654 | |||||||
| chr19:48595654 | GGTTTTTT others(9): Show |
G | 247 | a0001c0001t0001g0018 a0001c0001t0001g0042 a0001c0001t0001g0052 others(244): Show |
248 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.646-1084_646-1069d others(18): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48595654 | |||||||
| chr19:48595654 | GGTTTTTT others(10): Show |
G | 2 | a0001c0003t0001g0115 a0008c0015t0001g0351 |
2 | NA18986.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.646-1084_646-1068d others(19): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48595654 | |||||||
| chr19:48595655 | GTTTTTTT others(9): Show |
G | 9 | a0001c0001t0001g0024 a0001c0001t0001g0054 a0001c0001t0001g0056 others(6): Show |
9 | HG02145.hp1 HG02257.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.646-1074_646-1059d others(18): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr19 | 48595655 | ||||||
| chr19:48595668 | G | GTT | 66 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(63): Show |
66 | HG00408.hp1 HG01167.hp1 HG01169.hp1 others(63): Show |
intron_variant | MODIFIER | c.646-1055_646-1054d others(4): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr19 | 48595668 | ||||||
| chr19:48595668 | G | GTTT | 8 | a0001c0001t0001g0062 a0001c0001t0001g0093 a0001c0001t0001g0216 others(5): Show |
8 | HG01175.hp1 HG01243.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.646-1056_646-1054d others(5): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr19 | 48595668 | ||||||
| chr19:48595668 | G | T | 1 | a0001c0001t0001g0040 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.646-1071G>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48595668 | |||||||
| chr19:48595675 | T | G | 1 | a0001c0004t0001g0138 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.646-1064T>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48595675 | |||||||
| chr19:48595677 | T | A | 1 | a0001c0001t0001g0118 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.646-1062T>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48595677 | |||||||
| chr19:48595749 | A | C | 264 | a0001c0001t0001g0018 a0001c0001t0001g0042 a0001c0001t0001g0052 others(261): Show |
265 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.646-990A>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48595749 | |||||||
| chr19:48595895 | G | A | 1 | a0001c0002t0001g0316 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.646-844G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48595895 | |||||||
| chr19:48595933 | A | G | 282 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0018 others(279): Show |
283 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(280): Show |
intron_variant | MODIFIER | c.646-806A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48595933 | |||||||
| chr19:48596055 | G | C | 4 | a0003c0011t0001g0044 a0003c0011t0001g0060 a0003c0012t0001g0013 others(1): Show |
4 | HG01884.hp1 HG02717.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.646-684G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48596055 | |||||||
| chr19:48596093 | G | T | 1 | a0001c0001t0001g0040 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.646-646G>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48596093 | |||||||
| chr19:48596124 | A | G | 346 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(343): Show |
347 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(344): Show |
intron_variant | MODIFIER | c.646-615A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48596124 | |||||||
| chr19:48596190 | G | A | 18 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0055 others(15): Show |
18 | HG01243.hp1 HG01884.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.646-549G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48596190 | |||||||
| chr19:48596234 | T | C | 281 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0018 others(278): Show |
282 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.646-505T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48596234 | |||||||
| chr19:48596249 | G | A | 1 | a0001c0002t0001g0301 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.646-490G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48596249 | |||||||
| chr19:48596325 | G | A | 1 | a0008c0015t0001g0351 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.646-414G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48596325 | |||||||
| chr19:48596376 | G | A | 1 | a0001c0002t0001g0249 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.646-363G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48596376 | |||||||
| chr19:48596408 | C | G | 98 | a0001c0001t0001g0372 a0001c0002t0001g0004 a0001c0002t0001g0023 others(95): Show |
98 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.646-331C>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48596408 | |||||||
| chr19:48596436 | A | ACTGTGAC others(12): Show |
19 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0055 others(16): Show |
19 | HG01243.hp1 HG01884.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.646-285_646-267dup others(19): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr19 | 48596436 | ||||||
| chr19:48596454 | GGCTGTGA others(12): Show |
G | 6 | a0001c0001t0001g0118 a0001c0001t0001g0141 a0001c0001t0001g0211 others(3): Show |
6 | HG02071.hp2 HG02738.hp1 NA18945.hp1 others(3): Show |
intron_variant | MODIFIER | c.646-248_646-230del others(19): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr19 | 48596454 | ||||||
| chr19:48596470 | C | G | 98 | a0001c0001t0001g0372 a0001c0002t0001g0004 a0001c0002t0001g0023 others(95): Show |
98 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.646-269C>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48596470 | |||||||
| chr19:48596473 | T | G | 257 | a0001c0001t0001g0018 a0001c0001t0001g0042 a0001c0001t0001g0052 others(254): Show |
258 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(255): Show |
intron_variant | MODIFIER | c.646-266T>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48596473 | |||||||
| chr19:48596492 | T | G | 5 | a0001c0001t0001g0132 a0001c0001t0001g0207 a0001c0001t0001g0260 others(2): Show |
5 | HG02738.hp1 HG03041.hp1 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.646-247T>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48596492 | |||||||
| chr19:48596569 | T | C | 1 | a0001c0006t0001g0251 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.646-170T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48596569 | |||||||
| chr19:48596577 | G | A | 1 | a0001c0002t0001g0130 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.646-162G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48596577 | |||||||
| chr19:48596698 | C | T | 66 | a0001c0003t0001g0012 a0001c0003t0001g0047 a0001c0003t0001g0079 others(63): Show |
66 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.646-41C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48596698 | |||||||
| chr19:48596922 | G | A | 2 | a0001c0001t0001g0302 a0001c0006t0001g0061 |
2 | HG02145.hp2 NA18906.hp1 |
splice_region_variant&intron_variant | LOW | c.826+3G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 6/6 | chr19 | 48596922 | |||||||
| chr19:48597135 | C | T | 1 | a0001c0001t0001g0327 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.826+216C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 6/6 | chr19 | 48597135 | |||||||
| chr19:48597139 | A | G | 1 | a0001c0010t0001g0038 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.826+220A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 6/6 | chr19 | 48597139 | |||||||
| chr19:48597166 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.826+247G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 6/6 | chr19 | 48597166 | |||||||
| chr19:48597337 | CT | C | 99 | a0001c0001t0001g0018 a0001c0001t0001g0032 a0001c0001t0001g0040 others(96): Show |
100 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.826+438delT | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr19 | 48597337 | ||||||
| chr19:48597337 | CTT | C | 221 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(218): Show |
221 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(218): Show |
intron_variant | MODIFIER | c.826+437_826+438del others(2): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr19 | 48597337 | ||||||
| chr19:48597337 | CTTT | C | 26 | a0001c0001t0001g0024 a0001c0001t0001g0054 a0001c0001t0001g0056 others(23): Show |
26 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(23): Show |
intron_variant | MODIFIER | c.826+436_826+438del others(3): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr19 | 48597337 | ||||||
| chr19:48597338 | T | G | 1 | a0001c0006t0001g0251 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.826+419T>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 6/6 | chr19 | 48597338 | |||||||
| chr19:48597339 | T | C | 1 | a0001c0003t0001g0263 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.826+420T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 6/6 | chr19 | 48597339 | |||||||
| chr19:48597369 | G | A | 1 | a0003c0011t0001g0060 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.826+450G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 6/6 | chr19 | 48597369 | |||||||
| chr19:48597395 | T | TTGCAG | 56 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0022 others(53): Show |
56 | HG00408.hp1 HG01167.hp1 HG01169.hp1 others(53): Show |
intron_variant | MODIFIER | c.826+479_826+483dup others(5): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr19 | 48597395 | ||||||
| chr19:48597406 | C | T | 290 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0018 others(287): Show |
291 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(288): Show |
intron_variant | MODIFIER | c.826+487C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 6/6 | chr19 | 48597406 | |||||||
| chr19:48597446 | T | C | 334 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0018 others(331): Show |
335 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(332): Show |
intron_variant | MODIFIER | c.826+527T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 6/6 | chr19 | 48597446 | |||||||
| chr19:48597512 | T | C | 1 | a0006c0017t0001g0030 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.826+593T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 6/6 | chr19 | 48597512 | |||||||
| chr19:48597595 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.826+676G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 6/6 | chr19 | 48597595 | |||||||
| chr19:48597647 | C | CTTTTTTT others(3): Show |
1 | a0001c0001t0001g0271 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.826+734_826+735ins others(10): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr19 | 48597647 | ||||||
| chr19:48597654 | C | CTTTTTTT others(2): Show |
55 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0022 others(52): Show |
55 | HG00408.hp1 HG01167.hp1 HG01169.hp1 others(52): Show |
intron_variant | MODIFIER | c.826+741_826+742ins others(9): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr19 | 48597654 | ||||||
| chr19:48597654 | C | CTTTTTTT others(3): Show |
194 | a0001c0001t0001g0018 a0001c0001t0001g0024 a0001c0001t0001g0042 others(191): Show |
194 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.826+741_826+742ins others(10): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr19 | 48597654 | ||||||
| chr19:48597654 | C | CTTTTTTT others(4): Show |
97 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0055 others(94): Show |
98 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.826+741_826+742ins others(11): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr19 | 48597654 | ||||||
| chr19:48597654 | C | T | 1 | a0001c0001t0001g0271 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.826+735C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 6/6 | chr19 | 48597654 | |||||||
| chr19:48597919 | C | T | 2 | a0001c0002t0001g0130 a0001c0002t0001g0278 |
2 | NA18970.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.826+1000C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 6/6 | chr19 | 48597919 | |||||||
| chr19:48597964 | C | T | 1 | a0001c0002t0001g0161 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.826+1045C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 6/6 | chr19 | 48597964 | |||||||
| chr19:48598079 | A | G | 9 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0054 others(6): Show |
9 | HG02145.hp1 HG02257.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.827-1056A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 6/6 | chr19 | 48598079 | |||||||
| chr19:48598145 | C | T | 4 | a0003c0011t0001g0044 a0003c0011t0001g0060 a0003c0012t0001g0013 others(1): Show |
4 | HG01884.hp1 HG02717.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.827-990C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 6/6 | chr19 | 48598145 | |||||||
| chr19:48598291 | A | G | 62 | a0001c0003t0001g0012 a0001c0003t0001g0047 a0001c0003t0001g0079 others(59): Show |
62 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.827-844A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 6/6 | chr19 | 48598291 | |||||||
| chr19:48598320 | C | T | 41 | a0001c0001t0001g0042 a0001c0001t0001g0098 a0001c0001t0001g0117 others(38): Show |
41 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.827-815C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 6/6 | chr19 | 48598320 | |||||||
| chr19:48598417 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.827-718C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 6/6 | chr19 | 48598417 | |||||||
| chr19:48598570 | C | T | 7 | a0001c0009t0001g0120 a0001c0009t0001g0183 a0001c0009t0001g0319 others(4): Show |
7 | HG00639.hp1 HG01192.hp2 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.827-565C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 6/6 | chr19 | 48598570 | |||||||
| chr19:48598571 | G | A | 4 | a0001c0002t0001g0078 a0001c0002t0001g0189 a0001c0002t0001g0254 others(1): Show |
4 | HG02129.hp1 HG03017.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.827-564G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 6/6 | chr19 | 48598571 | |||||||
| chr19:48598699 | C | T | 186 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0018 others(183): Show |
186 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.827-436C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 6/6 | chr19 | 48598699 | |||||||
| chr19:48598733 | G | A | 93 | a0001c0001t0001g0018 a0001c0001t0001g0042 a0001c0001t0001g0098 others(90): Show |
93 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.827-402G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 6/6 | chr19 | 48598733 | |||||||
| chr19:48598777 | G | A | 1 | a0001c0001t0001g0105 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.827-358G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 6/6 | chr19 | 48598777 | |||||||
| chr19:48598937 | C | T | 1 | a0001c0001t0001g0194 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.827-198C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 6/6 | chr19 | 48598937 | |||||||
| chr19:48598940 | C | T | 1 | a0006c0017t0001g0030 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.827-195C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 6/6 | chr19 | 48598940 |