Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 391365 |
| ensemblid | ENSG00000138068.12 |
| hgncid | 33433 |
| symbol | SULT6B1 |
| name | sulfotransferase family 6B member 1 |
| refseq_nuc | NM_001367551.1 |
| refseq_prot | NP_001354480.1 |
| ensembl_nuc | ENST00000535679.6 |
| ensembl_prot | ENSP00000444081.1 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 37167820 |
| end | 37188670 |
| strand | - |
| ver | v1.2 |
| region | chr2:37167820-37188670 |
| region5000 | chr2:37162820-37193670 |
| regionname0 | SULT6B1_chr2_37167820_37188670 |
| regionname5000 | SULT6B1_chr2_37162820_37193670 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 303 | 169 | 60 | 43 | 46 | 9 | 9 | 38 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | MADKS others(298): Show |
chr2 | 37162820 | 37193670 |
| a0002 | 0/0 | 303 | 164 | 13 | 28 | 103 | 2 | 18 | 77 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | MADKS others(298): Show |
chr2 | 37162820 | 37193670 |
| a0003 | 0/0 | 303 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | MADKS others(298): Show |
chr2 | 37162820 | 37193670 |
| a0004 | 0/0 | 303 | 3 | 1 | 0 | 0 | 1 | 1 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | MADKS others(298): Show |
chr2 | 37162820 | 37193670 |
| a0005 | 0/0 | 303 | 2 | 0 | 0 | 0 | 1 | 1 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | MADKS others(298): Show |
chr2 | 37162820 | 37193670 |
| a0006 | 0/0 | 303 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | MADKS others(298): Show |
chr2 | 37162820 | 37193670 |
| a0007 | 0/0 | 303 | 2 | 0 | 0 | 0 | 1 | 1 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | MADKS others(298): Show |
chr2 | 37162820 | 37193670 |
| a0008 | 0/0 | 303 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | MADKS others(298): Show |
chr2 | 37162820 | 37193670 |
| a0009 | 0/0 | 303 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | MADKS others(298): Show |
chr2 | 37162820 | 37193670 |
| a0010 | 0/0 | 303 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | MADKS others(298): Show |
chr2 | 37162820 | 37193670 |
| a0011 | 0/0 | 303 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | MADKS others(298): Show |
chr2 | 37162820 | 37193670 |
| a0012 | 0/0 | 303 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | MADKS others(298): Show |
chr2 | 37162820 | 37193670 |
| a0013 | 0/0 | 303 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | MADKS others(298): Show |
chr2 | 37162820 | 37193670 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 909 | 168 | 60 | 42 | 46 | 9 | 9 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | ATGGC others(904): Show |
chr2 | 37162820 | 37193670 | ||
| a0001c0015 | 0/0 | 909 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | ATGGC others(904): Show |
chr2 | 37162820 | 37193670 | ||
| a0002c0002 | 0/0 | 909 | 160 | 12 | 25 | 103 | 2 | 18 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | ATGGC others(904): Show |
chr2 | 37162820 | 37193670 | ||
| a0002c0009 | 0/0 | 909 | 2 | 0 | 2 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | ATGGC others(904): Show |
chr2 | 37162820 | 37193670 | ||
| a0002c0012 | 0/0 | 909 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | ATGGC others(904): Show |
chr2 | 37162820 | 37193670 | ||
| a0002c0013 | 0/0 | 909 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | ATGGC others(904): Show |
chr2 | 37162820 | 37193670 | ||
| a0003c0003 | 0/0 | 909 | 5 | 4 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | ATGGC others(904): Show |
chr2 | 37162820 | 37193670 | ||
| a0004c0004 | 0/0 | 909 | 3 | 1 | 0 | 0 | 1 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | ATGGC others(904): Show |
chr2 | 37162820 | 37193670 | ||
| a0005c0005 | 0/0 | 909 | 2 | 0 | 0 | 0 | 1 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | ATGGC others(904): Show |
chr2 | 37162820 | 37193670 | ||
| a0006c0008 | 0/0 | 909 | 2 | 2 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | ATGGC others(904): Show |
chr2 | 37162820 | 37193670 | ||
| a0007c0007 | 0/0 | 909 | 2 | 0 | 0 | 0 | 1 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | ATGGC others(904): Show |
chr2 | 37162820 | 37193670 | ||
| a0008c0006 | 0/0 | 909 | 2 | 0 | 0 | 2 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | ATGGC others(904): Show |
chr2 | 37162820 | 37193670 | ||
| a0009c0011 | 0/0 | 909 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | ATGGC others(904): Show |
chr2 | 37162820 | 37193670 | ||
| a0010c0016 | 0/0 | 909 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | ATGGC others(904): Show |
chr2 | 37162820 | 37193670 | ||
| a0011c0017 | 0/0 | 909 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | ATGGC others(904): Show |
chr2 | 37162820 | 37193670 | ||
| a0012c0014 | 0/0 | 909 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | ATGGC others(904): Show |
chr2 | 37162820 | 37193670 | ||
| a0013c0010 | 0/0 | 909 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | ATGGC others(904): Show |
chr2 | 37162820 | 37193670 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1057 | 158 | 50 | 42 | 46 | 9 | 9 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | ACAGA others(1052): Show |
chr2 | 37162820 | 37193670 |
| a0001c0001t0002 | 0/0 | 1053 | 10 | 10 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | ACAGA others(1048): Show |
chr2 | 37162820 | 37193670 |
| a0001c0015t0001 | 0/0 | 1057 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | ACAGA others(1052): Show |
chr2 | 37162820 | 37193670 |
| a0002c0002t0001 | 0/0 | 1057 | 160 | 12 | 25 | 103 | 2 | 18 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | ACAGA others(1052): Show |
chr2 | 37162820 | 37193670 |
| a0002c0009t0001 | 0/0 | 1057 | 2 | 0 | 2 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | ACAGA others(1052): Show |
chr2 | 37162820 | 37193670 |
| a0002c0012t0001 | 0/0 | 1057 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | ACAGA others(1052): Show |
chr2 | 37162820 | 37193670 |
| a0002c0013t0001 | 0/0 | 1057 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | ACAGA others(1052): Show |
chr2 | 37162820 | 37193670 |
| a0003c0003t0001 | 0/0 | 1057 | 5 | 4 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | ACAGA others(1052): Show |
chr2 | 37162820 | 37193670 |
| a0004c0004t0001 | 0/0 | 1057 | 3 | 1 | 0 | 0 | 1 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | ACAGA others(1052): Show |
chr2 | 37162820 | 37193670 |
| a0005c0005t0001 | 0/0 | 1057 | 2 | 0 | 0 | 0 | 1 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | ACAGA others(1052): Show |
chr2 | 37162820 | 37193670 |
| a0006c0008t0001 | 0/0 | 1057 | 2 | 2 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | ACAGA others(1052): Show |
chr2 | 37162820 | 37193670 |
| a0007c0007t0001 | 0/0 | 1057 | 2 | 0 | 0 | 0 | 1 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | ACAGA others(1052): Show |
chr2 | 37162820 | 37193670 |
| a0008c0006t0001 | 0/0 | 1057 | 2 | 0 | 0 | 2 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | ACAGA others(1052): Show |
chr2 | 37162820 | 37193670 |
| a0009c0011t0001 | 0/0 | 1057 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | ACAGA others(1052): Show |
chr2 | 37162820 | 37193670 |
| a0010c0016t0001 | 0/0 | 1057 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | ACAGA others(1052): Show |
chr2 | 37162820 | 37193670 |
| a0011c0017t0001 | 0/0 | 1057 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | ACAGA others(1052): Show |
chr2 | 37162820 | 37193670 |
| a0012c0014t0001 | 0/0 | 1057 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | ACAGA others(1052): Show |
chr2 | 37162820 | 37193670 |
| a0013c0010t0001 | 0/0 | 1057 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | ACAGA others(1052): Show |
chr2 | 37162820 | 37193670 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 27 | 2 | 7 | 14 | 3 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0003 | 0/0 | 7 | 1 | 2 | 4 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0004 | 0/0 | 7 | 4 | 3 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0005 | 0/0 | 7 | 0 | 3 | 2 | 1 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0007 | 0/0 | 5 | 2 | 2 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0008 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0009 | 1/0 | 4 | 3 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0018 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0031 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0154 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0002g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0002g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0001t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0001c0015t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0002 | 0/0 | 20 | 0 | 1 | 19 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0006 | 0/0 | 7 | 0 | 0 | 5 | 0 | 2 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0010 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0011 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0012 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0014 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0033 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0036 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0044 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0009t0001g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0012t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0002c0013t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0003c0003t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0003c0003t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0003c0003t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0003c0003t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0003c0003t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0004c0004t0001g0025 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0004c0004t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0005c0005t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0005c0005t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0006c0008t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0007c0007t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0007c0007t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0008c0006t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0009c0011t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0010c0016t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0011c0017t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0012c0014t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| a0013c0010t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0001 | g0197 | EUR | GBR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG00099 | hp2 | a0005 | c0005 | t0001 | g0106 | EUR | GBR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | GBR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0152 | EUR | GBR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0153 | EUR | FIN | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG00280 | hp2 | a0004 | c0004 | t0001 | g0025 | EUR | FIN | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0026 | EUR | FIN | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0158 | EUR | FIN | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG00408 | hp1 | a0002 | c0002 | t0001 | g0014 | EAS | CHS | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG00408 | hp2 | a0002 | c0002 | t0001 | g0020 | EAS | CHS | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG00438 | hp1 | a0002 | c0002 | t0001 | g0014 | EAS | CHS | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG00438 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | CHS | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG00558 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG00597 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG00597 | hp2 | a0002 | c0002 | t0001 | g0119 | EAS | CHS | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0041 | EAS | CHS | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | CHS | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0012 | AMR | PUR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG00642 | hp1 | a0002 | c0002 | t0001 | g0044 | AMR | PUR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0010 | AMR | PUR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG00735 | hp1 | a0002 | c0002 | t0001 | g0194 | AMR | PUR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG00735 | hp2 | a0002 | c0002 | t0001 | g0193 | AMR | PUR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG00738 | hp2 | a0003 | c0003 | t0001 | g0096 | AMR | PUR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG00741 | hp2 | a0002 | c0002 | t0001 | g0104 | AMR | PUR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG01069 | hp2 | a0002 | c0009 | t0001 | g0037 | AMR | PUR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG01071 | hp2 | a0002 | c0009 | t0001 | g0037 | AMR | PUR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG01168 | hp2 | a0002 | c0002 | t0001 | g0196 | AMR | PUR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0014 | AMR | PUR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG01243 | hp1 | a0001 | c0015 | t0001 | g0076 | AMR | PUR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | CLM | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | CLM | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG01433 | hp1 | a0002 | c0002 | t0001 | g0012 | AMR | CLM | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | CLM | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0201 | EUR | IBS | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | ACB | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | ACB | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG01928 | hp1 | a0002 | c0002 | t0001 | g0121 | AMR | PEL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG01928 | hp2 | a0002 | c0002 | t0001 | g0010 | AMR | PEL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG01934 | hp1 | a0002 | c0002 | t0001 | g0134 | AMR | PEL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PEL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG01943 | hp2 | a0002 | c0002 | t0001 | g0011 | AMR | PEL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG01952 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG01975 | hp1 | a0002 | c0002 | t0001 | g0046 | AMR | PEL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG01975 | hp2 | a0002 | c0002 | t0001 | g0033 | AMR | PEL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG01978 | hp1 | a0002 | c0002 | t0001 | g0191 | AMR | PEL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG01978 | hp2 | a0002 | c0002 | t0001 | g0046 | AMR | PEL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PEL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG01993 | hp1 | a0002 | c0012 | t0001 | g0165 | AMR | PEL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG01993 | hp2 | a0002 | c0002 | t0001 | g0117 | AMR | PEL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG02004 | hp1 | a0002 | c0002 | t0001 | g0124 | AMR | PEL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG02004 | hp2 | a0002 | c0002 | t0001 | g0012 | AMR | PEL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG02015 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG02040 | hp1 | a0002 | c0002 | t0001 | g0108 | EAS | KHV | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | KHV | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0203 | AFR | ACB | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | ACB | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG02074 | hp1 | a0002 | c0002 | t0001 | g0172 | EAS | KHV | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG02074 | hp2 | a0002 | c0002 | t0001 | g0163 | EAS | KHV | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG02083 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG02083 | hp2 | a0002 | c0002 | t0001 | g0067 | EAS | KHV | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | KHV | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG02129 | hp2 | a0002 | c0002 | t0001 | g0192 | EAS | KHV | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG02132 | hp1 | a0002 | c0002 | t0001 | g0019 | EAS | KHV | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG02132 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG02135 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG02145 | hp2 | a0003 | c0003 | t0001 | g0098 | AFR | ACB | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG02165 | hp1 | a0002 | c0002 | t0001 | g0115 | EAS | CDX | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG02165 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | CDX | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG02257 | hp1 | a0006 | c0008 | t0001 | g0027 | AFR | ACB | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG02257 | hp2 | a0010 | c0016 | t0001 | g0085 | AFR | ACB | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG02273 | hp2 | a0002 | c0002 | t0001 | g0127 | AMR | PEL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG02280 | hp2 | a0011 | c0017 | t0001 | g0215 | AFR | ACB | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG02293 | hp1 | a0002 | c0002 | t0001 | g0166 | AMR | PEL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PEL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG02300 | hp1 | a0002 | c0002 | t0001 | g0010 | AMR | PEL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG02300 | hp2 | a0002 | c0002 | t0001 | g0012 | AMR | PEL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG02523 | hp2 | a0002 | c0002 | t0001 | g0181 | EAS | KHV | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG02602 | hp1 | a0004 | c0004 | t0001 | g0049 | SAS | PJL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG02602 | hp2 | a0002 | c0002 | t0001 | g0120 | SAS | PJL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0131 | AFR | GWD | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG02683 | hp1 | a0002 | c0002 | t0001 | g0036 | SAS | PJL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG02698 | hp2 | a0002 | c0002 | t0001 | g0173 | SAS | PJL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | GWD | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG02735 | hp1 | a0002 | c0002 | t0001 | g0011 | SAS | PJL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0024 | AFR | GWD | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | GWD | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG02886 | hp1 | a0003 | c0003 | t0001 | g0095 | AFR | GWD | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG02886 | hp2 | a0002 | c0002 | t0001 | g0058 | AFR | GWD | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | GWD | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | ESN | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG02922 | hp2 | a0002 | c0002 | t0001 | g0060 | AFR | ESN | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0213 | AFR | ESN | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG02970 | hp2 | a0002 | c0002 | t0001 | g0065 | AFR | ESN | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG02976 | hp1 | a0002 | c0002 | t0001 | g0064 | AFR | ESN | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG02976 | hp2 | a0002 | c0002 | t0001 | g0066 | AFR | ESN | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG03098 | hp1 | a0002 | c0013 | t0001 | g0062 | AFR | MSL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0024 | AFR | ESN | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | ESN | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG03209 | hp1 | a0003 | c0003 | t0001 | g0057 | AFR | MSL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG03209 | hp2 | a0002 | c0002 | t0001 | g0028 | AFR | MSL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG03225 | hp2 | a0002 | c0002 | t0001 | g0114 | AFR | MSL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | MSL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0047 | AFR | MSL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG03492 | hp1 | a0002 | c0002 | t0001 | g0006 | SAS | PJL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0024 | AFR | GWD | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG03579 | hp1 | a0002 | c0002 | t0001 | g0028 | AFR | MSL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | MSL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG03669 | hp1 | a0007 | c0007 | t0001 | g0072 | SAS | PJL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG03669 | hp2 | a0002 | c0002 | t0001 | g0006 | SAS | PJL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG03710 | hp1 | a0002 | c0002 | t0001 | g0112 | SAS | PJL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG03831 | hp1 | a0002 | c0002 | t0001 | g0164 | SAS | BEB | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0128 | SAS | BEB | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG03834 | hp1 | a0005 | c0005 | t0001 | g0105 | SAS | BEB | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG03834 | hp2 | a0002 | c0002 | t0001 | g0044 | SAS | BEB | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG03927 | hp1 | a0002 | c0002 | t0001 | g0123 | SAS | BEB | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG03927 | hp2 | a0002 | c0002 | t0001 | g0186 | SAS | BEB | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | BEB | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG03942 | hp2 | a0002 | c0002 | t0001 | g0189 | SAS | BEB | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG04184 | hp1 | a0002 | c0002 | t0001 | g0010 | SAS | BEB | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG04184 | hp2 | a0002 | c0002 | t0001 | g0176 | SAS | BEB | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG04199 | hp1 | a0002 | c0002 | t0001 | g0178 | SAS | STU | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | STU | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG04204 | hp1 | a0002 | c0002 | t0001 | g0122 | SAS | STU | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG04204 | hp2 | a0002 | c0002 | t0001 | g0111 | SAS | STU | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA18522 | hp1 | a0002 | c0002 | t0001 | g0061 | AFR | YRI | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0047 | AFR | YRI | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA18612 | hp1 | a0002 | c0002 | t0001 | g0015 | EAS | CHB | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA18612 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | CHB | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA18747 | hp1 | a0002 | c0002 | t0001 | g0022 | EAS | CHB | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA18747 | hp2 | a0002 | c0002 | t0001 | g0171 | EAS | CHB | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA18906 | hp1 | a0002 | c0002 | t0001 | g0100 | AFR | YRI | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA18906 | hp2 | a0012 | c0014 | t0001 | g0199 | AFR | YRI | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA18939 | hp1 | a0002 | c0002 | t0001 | g0170 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA18939 | hp2 | a0002 | c0002 | t0001 | g0159 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA18940 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA18941 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA18942 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA18944 | hp1 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA18944 | hp2 | a0002 | c0002 | t0001 | g0043 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA18945 | hp1 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA18945 | hp2 | a0008 | c0006 | t0001 | g0035 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA18946 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA18950 | hp2 | a0002 | c0002 | t0001 | g0020 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA18952 | hp1 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA18952 | hp2 | a0002 | c0002 | t0001 | g0034 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA18954 | hp2 | a0002 | c0002 | t0001 | g0118 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA18959 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA18960 | hp2 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA18961 | hp1 | a0002 | c0002 | t0001 | g0043 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA18961 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA18963 | hp2 | a0002 | c0002 | t0001 | g0200 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA18964 | hp1 | a0002 | c0002 | t0001 | g0168 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA18964 | hp2 | a0002 | c0002 | t0001 | g0126 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA18966 | hp1 | a0002 | c0002 | t0001 | g0045 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA18966 | hp2 | a0002 | c0002 | t0001 | g0110 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA18968 | hp1 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA18969 | hp1 | a0002 | c0002 | t0001 | g0045 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA18971 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA18971 | hp2 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA18977 | hp1 | a0002 | c0002 | t0001 | g0103 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA18977 | hp2 | a0002 | c0002 | t0001 | g0182 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA18979 | hp1 | a0002 | c0002 | t0001 | g0132 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA18979 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA18980 | hp2 | a0002 | c0002 | t0001 | g0183 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA18983 | hp2 | a0002 | c0002 | t0001 | g0212 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA18984 | hp1 | a0002 | c0002 | t0001 | g0033 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA18984 | hp2 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA18985 | hp1 | a0002 | c0002 | t0001 | g0174 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA18986 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA18987 | hp1 | a0002 | c0002 | t0001 | g0188 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA18991 | hp1 | a0002 | c0002 | t0001 | g0190 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA18995 | hp1 | a0002 | c0002 | t0001 | g0022 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA18998 | hp1 | a0002 | c0002 | t0001 | g0169 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA19002 | hp1 | a0002 | c0002 | t0001 | g0022 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA19005 | hp1 | a0002 | c0002 | t0001 | g0167 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA19005 | hp2 | a0002 | c0002 | t0001 | g0021 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA19007 | hp1 | a0002 | c0002 | t0001 | g0042 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA19007 | hp2 | a0013 | c0010 | t0001 | g0048 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA19010 | hp1 | a0002 | c0002 | t0001 | g0162 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA19010 | hp2 | a0002 | c0002 | t0001 | g0180 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA19011 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA19011 | hp2 | a0002 | c0002 | t0001 | g0021 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA19012 | hp1 | a0002 | c0002 | t0001 | g0113 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA19012 | hp2 | a0002 | c0002 | t0001 | g0161 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | LWK | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0130 | AFR | LWK | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | LWK | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA19056 | hp1 | a0002 | c0002 | t0001 | g0177 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA19057 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA19063 | hp2 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA19064 | hp1 | a0002 | c0002 | t0001 | g0116 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA19064 | hp2 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0185 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA19065 | hp2 | a0002 | c0002 | t0001 | g0034 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA19066 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA19067 | hp2 | a0002 | c0002 | t0001 | g0101 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA19068 | hp1 | a0002 | c0002 | t0001 | g0042 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA19068 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA19070 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA19072 | hp1 | a0002 | c0002 | t0001 | g0109 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA19072 | hp2 | a0002 | c0002 | t0001 | g0179 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA19076 | hp1 | a0002 | c0002 | t0001 | g0175 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA19076 | hp2 | a0002 | c0002 | t0001 | g0187 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA19077 | hp1 | a0002 | c0002 | t0001 | g0041 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA19080 | hp1 | a0002 | c0002 | t0001 | g0102 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA19080 | hp2 | a0008 | c0006 | t0001 | g0035 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA19082 | hp1 | a0002 | c0002 | t0001 | g0160 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA19082 | hp2 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA19084 | hp1 | a0002 | c0002 | t0001 | g0020 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA19086 | hp1 | a0002 | c0002 | t0001 | g0036 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA19087 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA19088 | hp2 | a0002 | c0002 | t0001 | g0021 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA19089 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA19090 | hp1 | a0002 | c0002 | t0001 | g0198 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA19090 | hp2 | a0002 | c0002 | t0001 | g0184 | EAS | JPT | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA19240 | hp1 | a0003 | c0003 | t0001 | g0097 | AFR | YRI | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA19240 | hp2 | a0002 | c0002 | t0001 | g0059 | AFR | YRI | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ASW | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | ASW | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA20752 | hp1 | a0007 | c0007 | t0001 | g0205 | EUR | TSI | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA20752 | hp2 | a0002 | c0002 | t0001 | g0195 | EUR | TSI | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | CLM | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG02109 | hp1 | a0009 | c0011 | t0001 | g0107 | AFR | ACB | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0211 | AFR | ACB | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | ACB | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG02486 | hp2 | a0002 | c0002 | t0001 | g0125 | AFR | ACB | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | ACB | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | ACB | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | MSL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | MSL | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | USA | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | USA | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA20300 | hp1 | a0006 | c0008 | t0001 | g0027 | AFR | USA | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | USA | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA21309 | hp1 | a0004 | c0004 | t0001 | g0025 | AFR | LWK | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | LWK | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0154 | REF | REF | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0009 | REF | REF | SULT6B1_chr2_37162820_37193670 | SULT6B1 | chr2 | 37162820 | 37193670 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:37167960 | T | C | 1 | a0007 | 2 | HG03669.hp1 NA20752.hp1 |
missense_variant | MODERATE | c.887A>G | p.Lys296Arg | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 7/7 | 917/1057 | 887/912 | 296/303 | chr2 | 37167960 | |||
| chr2:37168029 | A | G | 1 | a0008 | 2 | NA18945.hp2 NA19080.hp2 |
missense_variant | MODERATE | c.818T>C | p.Ile273Thr | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 7/7 | 848/1057 | 818/912 | 273/303 | chr2 | 37168029 | |||
| chr2:37171439 | C | A | 2 | a0003 a0011 |
6 | HG00738.hp2 HG02145.hp2 HG02280.hp2 others(3): Show |
missense_variant | MODERATE | c.776G>T | p.Arg259Leu | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/7 | 806/1057 | 776/912 | 259/303 | chr2 | 37171439 | |||
| chr2:37175213 | C | G | 2 | a0004 a0012 |
4 | HG00280.hp2 HG02602.hp1 NA18906.hp2 others(1): Show |
missense_variant | MODERATE | c.543G>C | p.Arg181Ser | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/7 | 573/1057 | 543/912 | 181/303 | chr2 | 37175213 | |||
| chr2:37179500 | C | T | 1 | a0005 | 2 | HG00099.hp2 HG03834.hp1 |
missense_variant | MODERATE | c.487G>A | p.Gly163Ser | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/7 | 517/1057 | 487/912 | 163/303 | chr2 | 37179500 | |||
| chr2:37179502 | T | C | 1 | a0006 | 2 | HG02257.hp1 NA20300.hp1 |
missense_variant | MODERATE | c.485A>G | p.Tyr162Cys | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/7 | 515/1057 | 485/912 | 162/303 | chr2 | 37179502 | |||
| chr2:37179518 | G | C | 1 | a0010 | 1 | HG02257.hp2 | missense_variant | MODERATE | c.469C>G | p.Pro157Ala | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/7 | 499/1057 | 469/912 | 157/303 | chr2 | 37179518 | |||
| chr2:37179537 | C | G | 6 | a0002 a0004 a0005 others(3): Show |
173 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(170): Show |
missense_variant | MODERATE | c.450G>C | p.Leu150Phe | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/7 | 480/1057 | 450/912 | 150/303 | chr2 | 37179537 | |||
| chr2:37179568 | C | T | 1 | a0009 | 1 | HG02109.hp1 | missense_variant | MODERATE | c.419G>A | p.Arg140Gln | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/7 | 449/1057 | 419/912 | 140/303 | chr2 | 37179568 | |||
| chr2:37187405 | T | C | 1 | a0004 | 3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
missense_variant | MODERATE | c.262A>G | p.Lys88Glu | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/7 | 292/1057 | 262/912 | 88/303 | chr2 | 37187405 | |||
| chr2:37187443 | A | T | 1 | a0004 | 3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
missense_variant | MODERATE | c.224T>A | p.Val75Asp | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/7 | 254/1057 | 224/912 | 75/303 | chr2 | 37187443 | |||
| chr2:37188460 | C | T | 1 | a0004 | 3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
missense_variant | MODERATE | c.181G>A | p.Ala61Thr | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 1/7 | 211/1057 | 181/912 | 61/303 | chr2 | 37188460 | |||
| chr2:37188523 | A | C | 1 | a0013 | 1 | NA19007.hp2 | missense_variant | MODERATE | c.118T>G | p.Cys40Gly | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 1/7 | 148/1057 | 118/912 | 40/303 | chr2 | 37188523 | |||
| chr2:37188607 | C | A | 1 | a0011 | 1 | HG02280.hp2 | missense_variant | MODERATE | c.34G>T | p.Asp12Tyr | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 1/7 | 64/1057 | 34/912 | 12/303 | chr2 | 37188607 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:37167962 | C | T | 1 | a0002c0013 | 1 | HG03098.hp1 | synonymous_variant | LOW | c.885G>A | p.Leu295Leu | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 7/7 | 915/1057 | 885/912 | 295/303 | chr2 | 37167962 | |||
| chr2:37171483 | C | T | 1 | a0002c0012 | 1 | HG01993.hp1 | synonymous_variant | LOW | c.732G>A | p.Ala244Ala | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/7 | 762/1057 | 732/912 | 244/303 | chr2 | 37171483 | |||
| chr2:37171585 | C | T | 1 | a0001c0015 | 1 | HG01243.hp1 | synonymous_variant | LOW | c.630G>A | p.Leu210Leu | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/7 | 660/1057 | 630/912 | 210/303 | chr2 | 37171585 | |||
| chr2:37179501 | A | G | 10 | a0002c0002 a0002c0009 a0002c0012 others(7): Show |
174 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(171): Show |
synonymous_variant | LOW | c.486T>C | p.Tyr162Tyr | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/7 | 516/1057 | 486/912 | 162/303 | chr2 | 37179501 | |||
| chr2:37183440 | G | A | 1 | a0002c0009 | 2 | HG01069.hp2 HG01071.hp2 |
synonymous_variant | LOW | c.387C>T | p.Phe129Phe | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/7 | 417/1057 | 387/912 | 129/303 | chr2 | 37183440 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:37167836 | TTTAA | T | 1 | a0001c0001t0002 | 10 | HG02055.hp1 HG02109.hp2 HG02622.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*95_*98delTTAA | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 7/7 | 95 | chr2 | 37167836 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:37168124 | T | A | 1 | a0002c0002t0001g0181 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.782-59A>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37168124 | |||||||
| chr2:37168174 | G | C | 1 | a0001c0001t0001g0070 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.782-109C>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37168174 | |||||||
| chr2:37168217 | T | C | 7 | a0001c0001t0001g0069 a0002c0002t0001g0028 a0002c0002t0001g0058 others(4): Show |
9 | HG02257.hp1 HG02886.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.782-152A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37168217 | |||||||
| chr2:37168246 | G | A | 2 | a0004c0004t0001g0025 a0004c0004t0001g0049 |
3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.782-181C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37168246 | |||||||
| chr2:37168287 | G | A | 7 | a0001c0001t0001g0069 a0002c0002t0001g0028 a0002c0002t0001g0058 others(4): Show |
9 | HG02257.hp1 HG02886.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.782-222C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37168287 | |||||||
| chr2:37168400 | C | G | 1 | a0001c0001t0001g0206 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.782-335G>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37168400 | |||||||
| chr2:37168426 | A | G | 191 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(188): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(311): Show |
intron_variant | MODIFIER | c.782-361T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37168426 | |||||||
| chr2:37168445 | T | C | 133 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(130): Show |
212 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.782-380A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37168445 | |||||||
| chr2:37168495 | G | A | 34 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0026 others(31): Show |
66 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.782-430C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37168495 | |||||||
| chr2:37168881 | G | A | 62 | a0001c0001t0001g0016 a0001c0001t0001g0075 a0001c0001t0001g0077 others(59): Show |
84 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.782-816C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37168881 | |||||||
| chr2:37168892 | C | T | 61 | a0001c0001t0001g0016 a0001c0001t0001g0075 a0001c0001t0001g0077 others(58): Show |
83 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.782-827G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37168892 | |||||||
| chr2:37168911 | G | A | 7 | a0001c0001t0001g0077 a0002c0013t0001g0062 a0003c0003t0001g0057 others(4): Show |
7 | HG00738.hp2 HG02055.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.782-846C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37168911 | |||||||
| chr2:37168912 | A | T | 7 | a0001c0001t0001g0077 a0002c0013t0001g0062 a0003c0003t0001g0057 others(4): Show |
7 | HG00738.hp2 HG02055.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.782-847T>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37168912 | |||||||
| chr2:37168959 | A | G | 1 | a0002c0002t0001g0175 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.782-894T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37168959 | |||||||
| chr2:37168964 | G | C | 1 | a0002c0002t0001g0178 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.782-899C>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37168964 | |||||||
| chr2:37168993 | G | A | 1 | a0002c0002t0001g0108 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.782-928C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37168993 | |||||||
| chr2:37169006 | G | A | 61 | a0001c0001t0001g0016 a0001c0001t0001g0075 a0001c0001t0001g0077 others(58): Show |
83 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.782-941C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37169006 | |||||||
| chr2:37169025 | G | A | 61 | a0001c0001t0001g0016 a0001c0001t0001g0075 a0001c0001t0001g0077 others(58): Show |
83 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.782-960C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37169025 | |||||||
| chr2:37169173 | A | G | 61 | a0001c0001t0001g0016 a0001c0001t0001g0075 a0001c0001t0001g0077 others(58): Show |
83 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.782-1108T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37169173 | |||||||
| chr2:37169210 | T | C | 61 | a0001c0001t0001g0016 a0001c0001t0001g0075 a0001c0001t0001g0077 others(58): Show |
83 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.782-1145A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37169210 | |||||||
| chr2:37169218 | G | T | 169 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(166): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.782-1153C>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37169218 | |||||||
| chr2:37169219 | A | T | 1 | a0002c0002t0001g0179 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.782-1154T>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37169219 | |||||||
| chr2:37169361 | C | T | 170 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(167): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(280): Show |
intron_variant | MODIFIER | c.782-1296G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37169361 | |||||||
| chr2:37169370 | T | C | 10 | a0002c0002t0001g0012 a0002c0002t0001g0022 a0002c0002t0001g0101 others(7): Show |
15 | HG00639.hp1 HG01433.hp1 HG01978.hp1 others(12): Show |
intron_variant | MODIFIER | c.782-1305A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37169370 | |||||||
| chr2:37169465 | T | C | 61 | a0001c0001t0001g0016 a0001c0001t0001g0075 a0001c0001t0001g0077 others(58): Show |
83 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.782-1400A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37169465 | |||||||
| chr2:37169494 | T | G | 1 | a0002c0002t0001g0186 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.782-1429A>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37169494 | |||||||
| chr2:37169520 | G | T | 1 | a0001c0001t0001g0214 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.782-1455C>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37169520 | |||||||
| chr2:37169605 | C | A | 1 | a0001c0001t0001g0031 | 2 | HG01109.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.782-1540G>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37169605 | |||||||
| chr2:37169605 | C | G | 4 | a0001c0001t0001g0007 a0001c0001t0001g0032 a0001c0001t0001g0081 others(1): Show |
9 | HG00639.hp2 HG01175.hp2 HG02015.hp2 others(6): Show |
intron_variant | MODIFIER | c.782-1540G>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37169605 | |||||||
| chr2:37169615 | A | G | 8 | a0001c0001t0001g0077 a0001c0001t0002g0211 a0002c0013t0001g0062 others(5): Show |
8 | HG00738.hp2 HG02055.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.782-1550T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37169615 | |||||||
| chr2:37169637 | C | T | 71 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(68): Show |
126 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(123): Show |
intron_variant | MODIFIER | c.782-1572G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37169637 | |||||||
| chr2:37169638 | G | A | 2 | a0004c0004t0001g0025 a0004c0004t0001g0049 |
3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.782-1573C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37169638 | |||||||
| chr2:37169654 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.782-1589G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37169654 | |||||||
| chr2:37169681 | G | C | 1 | a0002c0002t0001g0058 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.782-1616C>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37169681 | |||||||
| chr2:37169700 | C | T | 70 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(67): Show |
125 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(122): Show |
intron_variant | MODIFIER | c.782-1635G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37169700 | |||||||
| chr2:37169744 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.782-1679G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37169744 | |||||||
| chr2:37169778 | C | A | 1 | a0003c0003t0001g0057 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.781+1656G>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37169778 | |||||||
| chr2:37169783 | A | G | 62 | a0001c0001t0001g0016 a0001c0001t0001g0075 a0001c0001t0001g0077 others(59): Show |
86 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.781+1651T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37169783 | |||||||
| chr2:37169806 | G | GT | 4 | a0002c0002t0001g0064 a0002c0002t0001g0065 a0002c0002t0001g0100 others(1): Show |
4 | HG02970.hp2 HG02976.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.781+1627dupA | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37169806 | |||||||
| chr2:37170038 | A | T | 2 | a0002c0002t0001g0021 a0002c0002t0001g0170 |
4 | NA18939.hp1 NA19005.hp2 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.781+1396T>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37170038 | |||||||
| chr2:37170049 | C | T | 3 | a0002c0002t0001g0160 a0002c0002t0001g0198 a0002c0002t0001g0212 |
3 | NA18983.hp2 NA19082.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.781+1385G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37170049 | |||||||
| chr2:37170100 | T | G | 1 | a0011c0017t0001g0215 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.781+1334A>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37170100 | |||||||
| chr2:37170170 | T | C | 1 | a0006c0008t0001g0027 | 2 | HG02257.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.781+1264A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37170170 | |||||||
| chr2:37170231 | C | T | 1 | a0002c0002t0001g0115 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.781+1203G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37170231 | |||||||
| chr2:37170271 | A | G | 1 | a0002c0002t0001g0173 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.781+1163T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37170271 | |||||||
| chr2:37170327 | T | C | 62 | a0001c0001t0001g0016 a0001c0001t0001g0075 a0001c0001t0001g0077 others(59): Show |
86 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.781+1107A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37170327 | |||||||
| chr2:37170340 | A | G | 62 | a0001c0001t0001g0016 a0001c0001t0001g0075 a0001c0001t0001g0077 others(59): Show |
86 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.781+1094T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37170340 | |||||||
| chr2:37170452 | G | T | 1 | a0002c0002t0001g0113 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.781+982C>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37170452 | |||||||
| chr2:37170473 | A | G | 1 | a0009c0011t0001g0107 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.781+961T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37170473 | |||||||
| chr2:37170473 | A | T | 60 | a0001c0001t0001g0016 a0001c0001t0001g0075 a0001c0001t0001g0077 others(57): Show |
84 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.781+961T>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37170473 | |||||||
| chr2:37170550 | C | T | 32 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0038 others(29): Show |
63 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.781+884G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37170550 | |||||||
| chr2:37170586 | T | C | 59 | a0001c0001t0001g0016 a0001c0001t0001g0075 a0001c0001t0001g0077 others(56): Show |
83 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.781+848A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37170586 | |||||||
| chr2:37170635 | G | A | 59 | a0001c0001t0001g0016 a0001c0001t0001g0075 a0001c0001t0001g0077 others(56): Show |
83 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.781+799C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37170635 | |||||||
| chr2:37170667 | A | G | 60 | a0001c0001t0001g0016 a0001c0001t0001g0075 a0001c0001t0001g0077 others(57): Show |
84 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.781+767T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37170667 | |||||||
| chr2:37170737 | C | CA | 16 | a0001c0001t0001g0093 a0001c0001t0001g0206 a0001c0001t0001g0210 others(13): Show |
20 | HG00735.hp1 HG00735.hp2 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.781+696dupT | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37170737 | |||||||
| chr2:37170737 | CA | C | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(100): Show |
195 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.781+696delT | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37170737 | |||||||
| chr2:37170737 | CAA | C | 15 | a0001c0001t0001g0038 a0001c0001t0001g0081 a0001c0001t0001g0094 others(12): Show |
16 | HG00738.hp1 HG01074.hp2 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.781+695_781+696del others(2): Show |
SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37170737 | |||||||
| chr2:37170737 | CAAA | C | 25 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0039 others(22): Show |
55 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.781+694_781+696del others(3): Show |
SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37170737 | |||||||
| chr2:37170914 | G | A | 54 | a0001c0001t0001g0016 a0001c0001t0001g0075 a0001c0001t0001g0077 others(51): Show |
75 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.781+520C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37170914 | |||||||
| chr2:37170945 | A | T | 30 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0038 others(27): Show |
61 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.781+489T>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37170945 | |||||||
| chr2:37171002 | G | C | 1 | a0001c0001t0001g0052 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.781+432C>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37171002 | |||||||
| chr2:37171093 | A | G | 1 | a0001c0001t0001g0094 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.781+341T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37171093 | |||||||
| chr2:37171111 | C | T | 3 | a0002c0002t0001g0102 a0002c0002t0001g0132 a0002c0002t0001g0174 |
3 | NA18979.hp1 NA18985.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.781+323G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37171111 | |||||||
| chr2:37171130 | C | G | 1 | a0002c0002t0001g0134 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.781+304G>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37171130 | |||||||
| chr2:37171226 | C | T | 1 | a0002c0002t0001g0108 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.781+208G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37171226 | |||||||
| chr2:37171345 | C | G | 1 | a0001c0001t0001g0008 | 5 | HG02572.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.781+89G>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 6/6 | chr2 | 37171345 | |||||||
| chr2:37171603 | T | G | 1 | a0001c0001t0001g0075 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.625-13A>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37171603 | |||||||
| chr2:37171618 | T | C | 1 | a0002c0002t0001g0192 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.625-28A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37171618 | |||||||
| chr2:37172013 | A | C | 2 | a0002c0002t0001g0045 a0002c0002t0001g0188 |
3 | NA18966.hp1 NA18969.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.625-423T>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37172013 | |||||||
| chr2:37172041 | A | G | 8 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(5): Show |
20 | HG01074.hp1 HG01099.hp1 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.625-451T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37172041 | |||||||
| chr2:37172050 | AT | A | 158 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(155): Show |
266 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.625-461delA | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37172050 | |||||||
| chr2:37172050 | ATT | A | 20 | a0001c0001t0001g0157 a0002c0002t0001g0010 a0002c0002t0001g0011 others(17): Show |
30 | HG00099.hp2 HG00621.hp2 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.625-462_625-461del others(2): Show |
SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37172050 | |||||||
| chr2:37172073 | G | C | 1 | a0002c0002t0001g0116 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.625-483C>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37172073 | |||||||
| chr2:37172115 | A | G | 47 | a0001c0001t0001g0075 a0001c0001t0001g0078 a0001c0001t0001g0139 others(44): Show |
66 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.625-525T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37172115 | |||||||
| chr2:37172137 | A | C | 2 | a0004c0004t0001g0025 a0004c0004t0001g0049 |
3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.625-547T>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37172137 | |||||||
| chr2:37172179 | T | C | 2 | a0004c0004t0001g0025 a0004c0004t0001g0049 |
3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.625-589A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37172179 | |||||||
| chr2:37172208 | A | G | 176 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(173): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(292): Show |
intron_variant | MODIFIER | c.625-618T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37172208 | |||||||
| chr2:37172251 | T | G | 4 | a0003c0003t0001g0095 a0003c0003t0001g0096 a0003c0003t0001g0097 others(1): Show |
4 | HG00738.hp2 HG02145.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.625-661A>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37172251 | |||||||
| chr2:37172484 | T | C | 27 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0023 others(24): Show |
39 | HG01070.hp1 HG01071.hp1 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.625-894A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37172484 | |||||||
| chr2:37172513 | CT | C | 9 | a0001c0001t0001g0078 a0001c0001t0001g0099 a0002c0002t0001g0110 others(6): Show |
9 | HG00738.hp2 HG02145.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.625-924delA | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37172513 | |||||||
| chr2:37172593 | C | T | 1 | a0002c0002t0001g0012 | 4 | HG00639.hp1 HG01433.hp1 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.625-1003G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37172593 | |||||||
| chr2:37172624 | C | G | 2 | a0001c0001t0001g0026 a0001c0001t0001g0053 |
3 | HG00323.hp1 HG01081.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.625-1034G>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37172624 | |||||||
| chr2:37172662 | C | T | 14 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(11): Show |
27 | HG01074.hp1 HG01099.hp1 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.625-1072G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37172662 | |||||||
| chr2:37172664 | C | T | 8 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(5): Show |
20 | HG01074.hp1 HG01099.hp1 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.625-1074G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37172664 | |||||||
| chr2:37172668 | T | C | 175 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(172): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(292): Show |
intron_variant | MODIFIER | c.625-1078A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37172668 | |||||||
| chr2:37172707 | C | T | 3 | a0004c0004t0001g0025 a0004c0004t0001g0049 a0012c0014t0001g0199 |
4 | HG00280.hp2 HG02602.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.625-1117G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37172707 | |||||||
| chr2:37172755 | G | A | 3 | a0004c0004t0001g0025 a0004c0004t0001g0049 a0012c0014t0001g0199 |
4 | HG00280.hp2 HG02602.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.625-1165C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37172755 | |||||||
| chr2:37172778 | G | T | 1 | a0003c0003t0001g0057 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.625-1188C>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37172778 | |||||||
| chr2:37172787 | C | T | 3 | a0004c0004t0001g0025 a0004c0004t0001g0049 a0012c0014t0001g0199 |
4 | HG00280.hp2 HG02602.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.625-1197G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37172787 | |||||||
| chr2:37172823 | C | CTTGT | 166 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(163): Show |
284 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.625-1237_625-1234d others(6): Show |
SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37172823 | |||||||
| chr2:37172823 | C | CTTGTTTG others(1): Show |
7 | a0002c0002t0001g0028 a0002c0002t0001g0058 a0002c0002t0001g0059 others(4): Show |
8 | HG00099.hp1 HG02886.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.625-1241_625-1234d others(10): Show |
SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37172823 | |||||||
| chr2:37172876 | G | A | 1 | a0001c0001t0001g0207 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.625-1286C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37172876 | |||||||
| chr2:37172962 | C | T | 1 | a0002c0002t0001g0191 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.625-1372G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37172962 | |||||||
| chr2:37173010 | A | G | 10 | a0002c0002t0001g0104 a0002c0002t0001g0124 a0003c0003t0001g0057 others(7): Show |
10 | HG00099.hp2 HG00738.hp2 HG00741.hp2 others(7): Show |
intron_variant | MODIFIER | c.625-1420T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37173010 | |||||||
| chr2:37173035 | T | C | 5 | a0001c0001t0001g0023 a0001c0001t0001g0071 a0001c0001t0001g0073 others(2): Show |
7 | HG01070.hp1 HG01071.hp1 HG01123.hp1 others(4): Show |
intron_variant | MODIFIER | c.625-1445A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37173035 | |||||||
| chr2:37173081 | G | C | 1 | a0010c0016t0001g0085 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.625-1491C>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37173081 | |||||||
| chr2:37173179 | T | C | 3 | a0004c0004t0001g0025 a0004c0004t0001g0049 a0012c0014t0001g0199 |
4 | HG00280.hp2 HG02602.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.625-1589A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37173179 | |||||||
| chr2:37173306 | T | C | 1 | a0001c0001t0001g0090 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.625-1716A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37173306 | |||||||
| chr2:37173376 | T | C | 3 | a0004c0004t0001g0025 a0004c0004t0001g0049 a0012c0014t0001g0199 |
4 | HG00280.hp2 HG02602.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.624+1756A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37173376 | |||||||
| chr2:37173392 | C | G | 3 | a0004c0004t0001g0025 a0004c0004t0001g0049 a0012c0014t0001g0199 |
4 | HG00280.hp2 HG02602.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.624+1740G>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37173392 | |||||||
| chr2:37173420 | G | A | 3 | a0004c0004t0001g0025 a0004c0004t0001g0049 a0012c0014t0001g0199 |
4 | HG00280.hp2 HG02602.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.624+1712C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37173420 | |||||||
| chr2:37173551 | C | G | 37 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(34): Show |
81 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.624+1581G>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37173551 | |||||||
| chr2:37173721 | C | G | 3 | a0004c0004t0001g0025 a0004c0004t0001g0049 a0012c0014t0001g0199 |
4 | HG00280.hp2 HG02602.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.624+1411G>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37173721 | |||||||
| chr2:37173730 | T | C | 3 | a0004c0004t0001g0025 a0004c0004t0001g0049 a0012c0014t0001g0199 |
4 | HG00280.hp2 HG02602.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.624+1402A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37173730 | |||||||
| chr2:37173758 | C | T | 3 | a0004c0004t0001g0025 a0004c0004t0001g0049 a0012c0014t0001g0199 |
4 | HG00280.hp2 HG02602.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.624+1374G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37173758 | |||||||
| chr2:37173805 | TCCTTTGC others(17): Show |
T | 1 | a0002c0002t0001g0118 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.624+1303_624+1326d others(26): Show |
SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37173805 | |||||||
| chr2:37173824 | C | T | 8 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(5): Show |
19 | HG01074.hp1 HG01099.hp1 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.624+1308G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37173824 | |||||||
| chr2:37174021 | G | A | 1 | a0001c0001t0001g0039 | 2 | HG01081.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.624+1111C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37174021 | |||||||
| chr2:37174033 | C | T | 1 | a0003c0003t0001g0097 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.624+1099G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37174033 | |||||||
| chr2:37174071 | C | A | 1 | a0001c0001t0001g0140 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.624+1061G>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37174071 | |||||||
| chr2:37174092 | C | A | 106 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0010 others(103): Show |
169 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.624+1040G>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37174092 | |||||||
| chr2:37174163 | C | G | 6 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0206 others(3): Show |
6 | HG01106.hp1 HG01891.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.624+969G>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37174163 | |||||||
| chr2:37174227 | CT | C | 112 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(109): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.624+904delA | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37174227 | |||||||
| chr2:37174227 | CTT | C | 83 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(80): Show |
133 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.624+903_624+904del others(2): Show |
SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37174227 | |||||||
| chr2:37174227 | CTTT | C | 17 | a0001c0001t0001g0008 a0001c0001t0001g0084 a0001c0001t0001g0092 others(14): Show |
21 | HG00639.hp1 HG01106.hp1 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.624+902_624+904del others(3): Show |
SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37174227 | |||||||
| chr2:37174283 | G | A | 2 | a0001c0001t0001g0004 a0001c0001t0001g0055 |
8 | HG01074.hp1 HG01099.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.624+849C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37174283 | |||||||
| chr2:37174380 | A | G | 3 | a0004c0004t0001g0025 a0004c0004t0001g0049 a0012c0014t0001g0199 |
4 | HG00280.hp2 HG02602.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.624+752T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37174380 | |||||||
| chr2:37174456 | T | C | 3 | a0004c0004t0001g0025 a0004c0004t0001g0049 a0012c0014t0001g0199 |
4 | HG00280.hp2 HG02602.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.624+676A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37174456 | |||||||
| chr2:37174465 | T | C | 1 | a0001c0001t0001g0078 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.624+667A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37174465 | |||||||
| chr2:37174529 | A | G | 1 | a0012c0014t0001g0199 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.624+603T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37174529 | |||||||
| chr2:37174538 | C | T | 1 | a0002c0002t0001g0112 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.624+594G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37174538 | |||||||
| chr2:37174738 | T | C | 2 | a0004c0004t0001g0025 a0004c0004t0001g0049 |
3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.624+394A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37174738 | |||||||
| chr2:37174793 | A | ATAACT | 181 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(178): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(298): Show |
intron_variant | MODIFIER | c.624+338_624+339ins others(5): Show |
SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37174793 | |||||||
| chr2:37174881 | A | G | 173 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(170): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(289): Show |
intron_variant | MODIFIER | c.624+251T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37174881 | |||||||
| chr2:37174885 | A | C | 3 | a0004c0004t0001g0025 a0004c0004t0001g0049 a0012c0014t0001g0199 |
4 | HG00280.hp2 HG02602.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.624+247T>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37174885 | |||||||
| chr2:37174895 | G | A | 1 | a0002c0002t0001g0118 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.624+237C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37174895 | |||||||
| chr2:37174950 | T | C | 1 | a0001c0001t0001g0083 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.624+182A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37174950 | |||||||
| chr2:37174996 | C | T | 3 | a0004c0004t0001g0025 a0004c0004t0001g0049 a0012c0014t0001g0199 |
4 | HG00280.hp2 HG02602.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.624+136G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37174996 | |||||||
| chr2:37175012 | A | G | 1 | a0002c0002t0001g0034 | 2 | NA18952.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.624+120T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37175012 | |||||||
| chr2:37175082 | C | T | 3 | a0004c0004t0001g0025 a0004c0004t0001g0049 a0012c0014t0001g0199 |
4 | HG00280.hp2 HG02602.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.624+50G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37175082 | |||||||
| chr2:37175089 | G | C | 3 | a0004c0004t0001g0025 a0004c0004t0001g0049 a0012c0014t0001g0199 |
4 | HG00280.hp2 HG02602.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.624+43C>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37175089 | |||||||
| chr2:37175094 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.624+38G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37175094 | |||||||
| chr2:37175127 | C | G | 38 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(35): Show |
82 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(79): Show |
splice_region_variant&intron_variant | LOW | c.624+5G>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 5/6 | chr2 | 37175127 | |||||||
| chr2:37175230 | A | G | 38 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(35): Show |
82 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(79): Show |
splice_region_variant&intron_variant | LOW | c.530-4T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37175230 | |||||||
| chr2:37175391 | A | G | 1 | a0002c0002t0001g0118 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.530-165T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37175391 | |||||||
| chr2:37175519 | A | C | 3 | a0004c0004t0001g0025 a0004c0004t0001g0049 a0012c0014t0001g0199 |
4 | HG00280.hp2 HG02602.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.530-293T>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37175519 | |||||||
| chr2:37175549 | T | C | 3 | a0004c0004t0001g0025 a0004c0004t0001g0049 a0012c0014t0001g0199 |
4 | HG00280.hp2 HG02602.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.530-323A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37175549 | |||||||
| chr2:37175625 | G | C | 1 | a0002c0002t0001g0181 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.530-399C>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37175625 | |||||||
| chr2:37175659 | A | G | 3 | a0004c0004t0001g0025 a0004c0004t0001g0049 a0012c0014t0001g0199 |
4 | HG00280.hp2 HG02602.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.530-433T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37175659 | |||||||
| chr2:37175730 | A | G | 173 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(170): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(289): Show |
intron_variant | MODIFIER | c.530-504T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37175730 | |||||||
| chr2:37175752 | C | T | 1 | a0002c0009t0001g0037 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.530-526G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37175752 | |||||||
| chr2:37175753 | A | C | 3 | a0004c0004t0001g0025 a0004c0004t0001g0049 a0012c0014t0001g0199 |
4 | HG00280.hp2 HG02602.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.530-527T>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37175753 | |||||||
| chr2:37175771 | G | T | 3 | a0004c0004t0001g0025 a0004c0004t0001g0049 a0012c0014t0001g0199 |
4 | HG00280.hp2 HG02602.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.530-545C>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37175771 | |||||||
| chr2:37175812 | A | G | 176 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(173): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(293): Show |
intron_variant | MODIFIER | c.530-586T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37175812 | |||||||
| chr2:37175956 | C | A | 3 | a0004c0004t0001g0025 a0004c0004t0001g0049 a0012c0014t0001g0199 |
4 | HG00280.hp2 HG02602.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.530-730G>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37175956 | |||||||
| chr2:37176101 | G | A | 3 | a0004c0004t0001g0025 a0004c0004t0001g0049 a0012c0014t0001g0199 |
4 | HG00280.hp2 HG02602.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.530-875C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37176101 | |||||||
| chr2:37176102 | T | C | 3 | a0004c0004t0001g0025 a0004c0004t0001g0049 a0012c0014t0001g0199 |
4 | HG00280.hp2 HG02602.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.530-876A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37176102 | |||||||
| chr2:37176114 | G | T | 3 | a0004c0004t0001g0025 a0004c0004t0001g0049 a0012c0014t0001g0199 |
4 | HG00280.hp2 HG02602.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.530-888C>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37176114 | |||||||
| chr2:37176260 | C | CT | 160 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(157): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.530-1035dupA | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37176260 | |||||||
| chr2:37176260 | C | CTT | 15 | a0001c0001t0001g0056 a0001c0001t0001g0071 a0001c0001t0001g0087 others(12): Show |
15 | HG01934.hp2 HG02055.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.530-1036_530-1035d others(4): Show |
SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37176260 | |||||||
| chr2:37176356 | G | A | 3 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0150 |
3 | NA18974.hp1 NA18983.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.530-1130C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37176356 | |||||||
| chr2:37176356 | G | C | 2 | a0002c0002t0001g0058 a0002c0002t0001g0059 |
2 | HG02886.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.530-1130C>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37176356 | |||||||
| chr2:37176394 | G | A | 2 | a0004c0004t0001g0025 a0004c0004t0001g0049 |
3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.530-1168C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37176394 | |||||||
| chr2:37176443 | A | G | 6 | a0002c0002t0001g0028 a0002c0002t0001g0058 a0002c0002t0001g0059 others(3): Show |
7 | HG02886.hp2 HG02922.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.530-1217T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37176443 | |||||||
| chr2:37176491 | T | G | 27 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0023 others(24): Show |
39 | HG01070.hp1 HG01071.hp1 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.530-1265A>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37176491 | |||||||
| chr2:37176556 | G | A | 1 | a0002c0013t0001g0062 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.530-1330C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37176556 | |||||||
| chr2:37176676 | C | T | 1 | a0012c0014t0001g0199 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.530-1450G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37176676 | |||||||
| chr2:37176694 | C | T | 1 | a0002c0002t0001g0171 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.530-1468G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37176694 | |||||||
| chr2:37176872 | T | C | 3 | a0002c0002t0001g0028 a0002c0002t0001g0060 a0002c0002t0001g0061 |
4 | HG02922.hp2 HG03209.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.530-1646A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37176872 | |||||||
| chr2:37176936 | A | G | 3 | a0004c0004t0001g0025 a0004c0004t0001g0049 a0012c0014t0001g0199 |
4 | HG00280.hp2 HG02602.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.530-1710T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37176936 | |||||||
| chr2:37176971 | G | A | 1 | a0012c0014t0001g0199 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.530-1745C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37176971 | |||||||
| chr2:37177028 | G | C | 1 | a0001c0001t0001g0156 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.530-1802C>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37177028 | |||||||
| chr2:37177151 | CTCA | C | 27 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0023 others(24): Show |
39 | HG01070.hp1 HG01071.hp1 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.530-1928_530-1926d others(5): Show |
SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37177151 | |||||||
| chr2:37177155 | T | A | 4 | a0001c0001t0001g0026 a0001c0001t0001g0039 a0001c0001t0001g0053 others(1): Show |
6 | HG00323.hp1 HG01081.hp1 HG01081.hp2 others(3): Show |
intron_variant | MODIFIER | c.530-1929A>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37177155 | |||||||
| chr2:37177184 | C | G | 39 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(36): Show |
83 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.530-1958G>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37177184 | |||||||
| chr2:37177226 | C | T | 3 | a0004c0004t0001g0025 a0004c0004t0001g0049 a0012c0014t0001g0199 |
4 | HG00280.hp2 HG02602.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.530-2000G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37177226 | |||||||
| chr2:37177284 | G | A | 1 | a0002c0002t0001g0183 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.530-2058C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37177284 | |||||||
| chr2:37177345 | A | G | 3 | a0004c0004t0001g0025 a0004c0004t0001g0049 a0012c0014t0001g0199 |
4 | HG00280.hp2 HG02602.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.529+2113T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37177345 | |||||||
| chr2:37177368 | T | C | 3 | a0004c0004t0001g0025 a0004c0004t0001g0049 a0012c0014t0001g0199 |
4 | HG00280.hp2 HG02602.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.529+2090A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37177368 | |||||||
| chr2:37177371 | C | T | 3 | a0004c0004t0001g0025 a0004c0004t0001g0049 a0012c0014t0001g0199 |
4 | HG00280.hp2 HG02602.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.529+2087G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37177371 | |||||||
| chr2:37177409 | C | A | 6 | a0003c0003t0001g0057 a0003c0003t0001g0095 a0003c0003t0001g0096 others(3): Show |
6 | HG00738.hp2 HG02145.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.529+2049G>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37177409 | |||||||
| chr2:37177411 | CA | C | 146 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(143): Show |
256 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.529+2046delT | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37177411 | |||||||
| chr2:37177411 | CAA | C | 27 | a0001c0001t0001g0008 a0001c0001t0001g0092 a0001c0001t0001g0093 others(24): Show |
35 | HG00738.hp2 HG01106.hp1 HG01515.hp1 others(32): Show |
intron_variant | MODIFIER | c.529+2045_529+2046d others(4): Show |
SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37177411 | |||||||
| chr2:37177430 | A | G | 3 | a0004c0004t0001g0025 a0004c0004t0001g0049 a0012c0014t0001g0199 |
4 | HG00280.hp2 HG02602.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.529+2028T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37177430 | |||||||
| chr2:37177447 | A | G | 1 | a0002c0002t0001g0168 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.529+2011T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37177447 | |||||||
| chr2:37177448 | A | G | 3 | a0004c0004t0001g0025 a0004c0004t0001g0049 a0012c0014t0001g0199 |
4 | HG00280.hp2 HG02602.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.529+2010T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37177448 | |||||||
| chr2:37177450 | A | G | 3 | a0004c0004t0001g0025 a0004c0004t0001g0049 a0012c0014t0001g0199 |
4 | HG00280.hp2 HG02602.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.529+2008T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37177450 | |||||||
| chr2:37177457 | A | AATACAGC | 107 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0010 others(104): Show |
170 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.529+1994_529+2000d others(9): Show |
SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37177457 | |||||||
| chr2:37177556 | G | A | 3 | a0004c0004t0001g0025 a0004c0004t0001g0049 a0012c0014t0001g0199 |
4 | HG00280.hp2 HG02602.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.529+1902C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37177556 | |||||||
| chr2:37177571 | A | G | 27 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0023 others(24): Show |
39 | HG01070.hp1 HG01071.hp1 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.529+1887T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37177571 | |||||||
| chr2:37177591 | A | T | 3 | a0004c0004t0001g0025 a0004c0004t0001g0049 a0012c0014t0001g0199 |
4 | HG00280.hp2 HG02602.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.529+1867T>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37177591 | |||||||
| chr2:37177703 | A | G | 1 | a0002c0002t0001g0167 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.529+1755T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37177703 | |||||||
| chr2:37177717 | C | G | 1 | a0002c0013t0001g0062 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.529+1741G>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37177717 | |||||||
| chr2:37177860 | T | A | 3 | a0004c0004t0001g0025 a0004c0004t0001g0049 a0012c0014t0001g0199 |
4 | HG00280.hp2 HG02602.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.529+1598A>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37177860 | |||||||
| chr2:37177944 | C | G | 3 | a0004c0004t0001g0025 a0004c0004t0001g0049 a0012c0014t0001g0199 |
4 | HG00280.hp2 HG02602.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.529+1514G>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37177944 | |||||||
| chr2:37177979 | T | A | 1 | a0003c0003t0001g0097 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.529+1479A>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37177979 | |||||||
| chr2:37178065 | G | A | 28 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0023 others(25): Show |
40 | HG01070.hp1 HG01071.hp1 HG01074.hp2 others(37): Show |
intron_variant | MODIFIER | c.529+1393C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37178065 | |||||||
| chr2:37178148 | A | C | 2 | a0002c0002t0001g0044 a0002c0002t0001g0189 |
3 | HG00642.hp1 HG03834.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.529+1310T>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37178148 | |||||||
| chr2:37178250 | T | G | 39 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(36): Show |
83 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.529+1208A>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37178250 | |||||||
| chr2:37178290 | T | G | 1 | a0001c0001t0001g0068 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.529+1168A>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37178290 | |||||||
| chr2:37178306 | C | T | 1 | a0013c0010t0001g0048 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.529+1152G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37178306 | |||||||
| chr2:37178354 | G | C | 6 | a0003c0003t0001g0057 a0003c0003t0001g0095 a0003c0003t0001g0096 others(3): Show |
6 | HG00738.hp2 HG02145.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.529+1104C>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37178354 | |||||||
| chr2:37178388 | A | G | 43 | a0002c0002t0001g0006 a0002c0002t0001g0010 a0002c0002t0001g0011 others(40): Show |
60 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.529+1070T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37178388 | |||||||
| chr2:37178450 | G | C | 1 | a0001c0001t0001g0087 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.529+1008C>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37178450 | |||||||
| chr2:37178481 | C | T | 2 | a0004c0004t0001g0025 a0004c0004t0001g0049 |
3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.529+977G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37178481 | |||||||
| chr2:37178512 | A | G | 176 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(173): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(293): Show |
intron_variant | MODIFIER | c.529+946T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37178512 | |||||||
| chr2:37178545 | T | A | 1 | a0002c0013t0001g0062 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.529+913A>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37178545 | |||||||
| chr2:37178614 | AT | A | 110 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0010 others(107): Show |
174 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.529+843delA | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37178614 | |||||||
| chr2:37178637 | C | T | 4 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0206 others(1): Show |
4 | HG01106.hp1 HG01891.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.529+821G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37178637 | |||||||
| chr2:37178714 | A | G | 1 | a0001c0001t0001g0050 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.529+744T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37178714 | |||||||
| chr2:37178768 | G | T | 1 | a0002c0002t0001g0066 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.529+690C>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37178768 | |||||||
| chr2:37178953 | T | TTTTG | 105 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0010 others(102): Show |
166 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.529+501_529+504dup others(4): Show |
SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37178953 | |||||||
| chr2:37178953 | TTTTG | T | 2 | a0002c0002t0001g0012 a0002c0012t0001g0165 |
5 | HG00639.hp1 HG01433.hp1 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.529+501_529+504del others(4): Show |
SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37178953 | |||||||
| chr2:37178977 | T | C | 16 | a0001c0001t0001g0017 a0001c0001t0001g0023 a0001c0001t0001g0090 others(13): Show |
24 | HG01070.hp1 HG01071.hp1 HG01346.hp1 others(21): Show |
intron_variant | MODIFIER | c.529+481A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37178977 | |||||||
| chr2:37179000 | C | T | 108 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0010 others(105): Show |
171 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.529+458G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37179000 | |||||||
| chr2:37179019 | C | T | 110 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0010 others(107): Show |
174 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.529+439G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37179019 | |||||||
| chr2:37179040 | T | C | 110 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0010 others(107): Show |
174 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.529+418A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37179040 | |||||||
| chr2:37179119 | A | T | 110 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0010 others(107): Show |
174 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.529+339T>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37179119 | |||||||
| chr2:37179131 | T | C | 1 | a0012c0014t0001g0199 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.529+327A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37179131 | |||||||
| chr2:37179141 | G | A | 110 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0010 others(107): Show |
174 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.529+317C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37179141 | |||||||
| chr2:37179144 | G | C | 108 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0010 others(105): Show |
171 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.529+314C>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37179144 | |||||||
| chr2:37179160 | G | A | 1 | a0002c0002t0001g0185 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.529+298C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37179160 | |||||||
| chr2:37179173 | C | T | 1 | a0012c0014t0001g0199 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.529+285G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37179173 | |||||||
| chr2:37179174 | A | G | 111 | a0001c0001t0001g0087 a0002c0002t0001g0002 a0002c0002t0001g0006 others(108): Show |
175 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.529+284T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37179174 | |||||||
| chr2:37179204 | C | T | 1 | a0012c0014t0001g0199 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.529+254G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37179204 | |||||||
| chr2:37179225 | T | C | 1 | a0001c0001t0001g0040 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.529+233A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37179225 | |||||||
| chr2:37179271 | T | C | 2 | a0003c0003t0001g0057 a0011c0017t0001g0215 |
2 | HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.529+187A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37179271 | |||||||
| chr2:37179276 | C | T | 110 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0010 others(107): Show |
174 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.529+182G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 4/6 | chr2 | 37179276 | |||||||
| chr2:37179618 | T | C | 110 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0010 others(107): Show |
174 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.403-34A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37179618 | |||||||
| chr2:37179622 | T | C | 1 | a0002c0002t0001g0186 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.403-38A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37179622 | |||||||
| chr2:37179657 | T | C | 1 | a0001c0001t0001g0031 | 2 | HG01109.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.403-73A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37179657 | |||||||
| chr2:37179664 | A | G | 110 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0010 others(107): Show |
174 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.403-80T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37179664 | |||||||
| chr2:37179666 | G | C | 1 | a0003c0003t0001g0098 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.403-82C>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37179666 | |||||||
| chr2:37179682 | C | T | 6 | a0003c0003t0001g0057 a0003c0003t0001g0095 a0003c0003t0001g0096 others(3): Show |
6 | HG00738.hp2 HG02145.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.403-98G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37179682 | |||||||
| chr2:37179689 | G | A | 2 | a0001c0001t0001g0004 a0001c0001t0001g0055 |
8 | HG01074.hp1 HG01099.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.403-105C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37179689 | |||||||
| chr2:37179723 | A | G | 108 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0010 others(105): Show |
171 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.403-139T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37179723 | |||||||
| chr2:37179795 | G | T | 3 | a0002c0002t0001g0195 a0002c0002t0001g0196 a0002c0002t0001g0197 |
3 | HG00099.hp1 HG01168.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.403-211C>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37179795 | |||||||
| chr2:37179893 | T | C | 2 | a0004c0004t0001g0025 a0004c0004t0001g0049 |
3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.403-309A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37179893 | |||||||
| chr2:37179947 | A | T | 1 | a0012c0014t0001g0199 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.403-363T>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37179947 | |||||||
| chr2:37179961 | A | G | 3 | a0003c0003t0001g0096 a0003c0003t0001g0097 a0003c0003t0001g0098 |
3 | HG00738.hp2 HG02145.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.403-377T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37179961 | |||||||
| chr2:37180035 | A | G | 111 | a0001c0001t0001g0139 a0002c0002t0001g0002 a0002c0002t0001g0006 others(108): Show |
175 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.403-451T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37180035 | |||||||
| chr2:37180078 | A | C | 1 | a0003c0003t0001g0057 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.403-494T>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37180078 | |||||||
| chr2:37180079 | G | T | 1 | a0003c0003t0001g0057 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.403-495C>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37180079 | |||||||
| chr2:37180080 | T | G | 1 | a0003c0003t0001g0057 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.403-496A>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37180080 | |||||||
| chr2:37180109 | A | C | 6 | a0003c0003t0001g0057 a0003c0003t0001g0095 a0003c0003t0001g0096 others(3): Show |
6 | HG00738.hp2 HG02145.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.403-525T>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37180109 | |||||||
| chr2:37180160 | T | A | 107 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0010 others(104): Show |
170 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.403-576A>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37180160 | |||||||
| chr2:37180199 | C | A | 6 | a0003c0003t0001g0057 a0003c0003t0001g0095 a0003c0003t0001g0096 others(3): Show |
6 | HG00738.hp2 HG02145.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.403-615G>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37180199 | |||||||
| chr2:37180406 | G | C | 1 | a0011c0017t0001g0215 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.403-822C>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37180406 | |||||||
| chr2:37180487 | G | C | 111 | a0001c0001t0001g0133 a0002c0002t0001g0002 a0002c0002t0001g0006 others(108): Show |
175 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.403-903C>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37180487 | |||||||
| chr2:37180576 | C | T | 2 | a0004c0004t0001g0025 a0004c0004t0001g0049 |
3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.403-992G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37180576 | |||||||
| chr2:37180609 | C | T | 1 | a0002c0002t0001g0043 | 2 | NA18944.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.403-1025G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37180609 | |||||||
| chr2:37180691 | C | T | 3 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0148 |
3 | NA19003.hp1 NA19056.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.403-1107G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37180691 | |||||||
| chr2:37180694 | G | C | 107 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0010 others(104): Show |
170 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.403-1110C>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37180694 | |||||||
| chr2:37180715 | T | C | 118 | a0001c0001t0001g0007 a0001c0001t0001g0032 a0001c0001t0001g0079 others(115): Show |
187 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.403-1131A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37180715 | |||||||
| chr2:37180754 | T | C | 1 | a0002c0002t0001g0119 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.403-1170A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37180754 | |||||||
| chr2:37180777 | G | T | 1 | a0002c0002t0001g0120 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.403-1193C>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37180777 | |||||||
| chr2:37180815 | C | T | 1 | a0002c0002t0001g0195 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.403-1231G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37180815 | |||||||
| chr2:37180833 | A | G | 111 | a0001c0001t0001g0133 a0002c0002t0001g0002 a0002c0002t0001g0006 others(108): Show |
175 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.403-1249T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37180833 | |||||||
| chr2:37180867 | G | C | 109 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0010 others(106): Show |
173 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.403-1283C>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37180867 | |||||||
| chr2:37180873 | G | A | 1 | a0002c0002t0001g0120 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.403-1289C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37180873 | |||||||
| chr2:37180988 | A | G | 1 | a0002c0002t0001g0164 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.403-1404T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37180988 | |||||||
| chr2:37181000 | T | C | 1 | a0002c0002t0001g0100 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.403-1416A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37181000 | |||||||
| chr2:37181005 | T | A | 1 | a0001c0001t0001g0210 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.403-1421A>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37181005 | |||||||
| chr2:37181086 | A | C | 1 | a0001c0001t0001g0136 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.403-1502T>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37181086 | |||||||
| chr2:37181148 | A | G | 1 | a0011c0017t0001g0215 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.403-1564T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37181148 | |||||||
| chr2:37181155 | T | G | 108 | a0001c0001t0001g0133 a0002c0002t0001g0002 a0002c0002t0001g0006 others(105): Show |
171 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.403-1571A>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37181155 | |||||||
| chr2:37181170 | A | G | 182 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(179): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(299): Show |
intron_variant | MODIFIER | c.403-1586T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37181170 | |||||||
| chr2:37181247 | C | T | 1 | a0002c0002t0001g0104 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.403-1663G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37181247 | |||||||
| chr2:37181345 | T | C | 1 | a0002c0002t0001g0121 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.403-1761A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37181345 | |||||||
| chr2:37181405 | C | T | 107 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0010 others(104): Show |
170 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.403-1821G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37181405 | |||||||
| chr2:37181443 | G | A | 39 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(36): Show |
83 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.403-1859C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37181443 | |||||||
| chr2:37181461 | A | G | 1 | a0002c0013t0001g0062 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.403-1877T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37181461 | |||||||
| chr2:37181504 | C | A | 2 | a0004c0004t0001g0025 a0004c0004t0001g0049 |
3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.403-1920G>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37181504 | |||||||
| chr2:37181532 | A | G | 106 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0010 others(103): Show |
169 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.402+1893T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37181532 | |||||||
| chr2:37181554 | A | G | 1 | a0002c0002t0001g0163 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.402+1871T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37181554 | |||||||
| chr2:37181563 | A | G | 2 | a0004c0004t0001g0025 a0004c0004t0001g0049 |
3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.402+1862T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37181563 | |||||||
| chr2:37181568 | C | CG | 2 | a0004c0004t0001g0025 a0004c0004t0001g0049 |
3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.402+1856_402+1857i others(3): Show |
SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37181568 | |||||||
| chr2:37181569 | A | G | 108 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0010 others(105): Show |
172 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.402+1856T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37181569 | |||||||
| chr2:37181621 | TC | T | 109 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0010 others(106): Show |
173 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.402+1803delG | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37181621 | |||||||
| chr2:37181627 | C | T | 2 | a0002c0002t0001g0042 a0002c0002t0001g0162 |
3 | NA19007.hp1 NA19010.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.402+1798G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37181627 | |||||||
| chr2:37181631 | T | C | 109 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0010 others(106): Show |
173 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.402+1794A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37181631 | |||||||
| chr2:37181681 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.402+1744G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37181681 | |||||||
| chr2:37181717 | A | G | 2 | a0004c0004t0001g0025 a0004c0004t0001g0049 |
3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.402+1708T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37181717 | |||||||
| chr2:37181815 | A | G | 43 | a0002c0002t0001g0006 a0002c0002t0001g0010 a0002c0002t0001g0011 others(40): Show |
60 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.402+1610T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37181815 | |||||||
| chr2:37181826 | A | G | 5 | a0001c0001t0001g0094 a0001c0001t0001g0152 a0001c0001t0001g0204 others(2): Show |
5 | HG00140.hp2 HG01074.hp2 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.402+1599T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37181826 | |||||||
| chr2:37182005 | A | G | 108 | a0001c0001t0001g0063 a0002c0002t0001g0002 a0002c0002t0001g0006 others(105): Show |
171 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.402+1420T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37182005 | |||||||
| chr2:37182145 | C | T | 4 | a0001c0001t0001g0094 a0001c0001t0001g0204 a0001c0001t0001g0214 others(1): Show |
4 | HG01074.hp2 HG01106.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.402+1280G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37182145 | |||||||
| chr2:37182167 | C | T | 110 | a0001c0001t0001g0063 a0002c0002t0001g0002 a0002c0002t0001g0006 others(107): Show |
174 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.402+1258G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37182167 | |||||||
| chr2:37182241 | G | A | 108 | a0001c0001t0001g0063 a0002c0002t0001g0002 a0002c0002t0001g0006 others(105): Show |
171 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.402+1184C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37182241 | |||||||
| chr2:37182251 | A | AACTATGC others(13): Show |
1 | a0001c0001t0001g0151 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.402+1173_402+1174i others(22): Show |
SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37182251 | |||||||
| chr2:37182253 | AT | A | 60 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(57): Show |
116 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.402+1171delA | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37182253 | |||||||
| chr2:37182253 | ATT | A | 7 | a0001c0001t0001g0063 a0001c0001t0001g0148 a0001c0001t0001g0149 others(4): Show |
7 | HG02647.hp1 HG02970.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.402+1170_402+1171d others(4): Show |
SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37182253 | |||||||
| chr2:37182253 | ATTT | A | 105 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0010 others(102): Show |
169 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.402+1169_402+1171d others(5): Show |
SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37182253 | |||||||
| chr2:37182254 | T | A | 1 | a0001c0001t0001g0151 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.402+1171A>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37182254 | |||||||
| chr2:37182255 | T | A | 1 | a0001c0001t0001g0151 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.402+1170A>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37182255 | |||||||
| chr2:37182270 | T | A | 1 | a0001c0001t0001g0151 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.402+1155A>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37182270 | |||||||
| chr2:37182279 | G | A | 110 | a0001c0001t0001g0063 a0002c0002t0001g0002 a0002c0002t0001g0006 others(107): Show |
174 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.402+1146C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37182279 | |||||||
| chr2:37182285 | G | A | 66 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(63): Show |
122 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.402+1140C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37182285 | |||||||
| chr2:37182312 | G | C | 1 | a0003c0003t0001g0057 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.402+1113C>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37182312 | |||||||
| chr2:37182314 | C | A | 1 | a0001c0001t0001g0151 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.402+1111G>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37182314 | |||||||
| chr2:37182315 | G | T | 1 | a0001c0001t0001g0151 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.402+1110C>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37182315 | |||||||
| chr2:37182336 | G | C | 2 | a0004c0004t0001g0025 a0004c0004t0001g0049 |
3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.402+1089C>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37182336 | |||||||
| chr2:37182339 | C | A | 1 | a0001c0001t0001g0151 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.402+1086G>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37182339 | |||||||
| chr2:37182341 | C | G | 1 | a0001c0001t0001g0151 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.402+1084G>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37182341 | |||||||
| chr2:37182343 | T | G | 1 | a0001c0001t0001g0151 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.402+1082A>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37182343 | |||||||
| chr2:37182356 | C | G | 39 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(36): Show |
83 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.402+1069G>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37182356 | |||||||
| chr2:37182365 | T | C | 108 | a0001c0001t0001g0063 a0002c0002t0001g0002 a0002c0002t0001g0006 others(105): Show |
171 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.402+1060A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37182365 | |||||||
| chr2:37182400 | C | T | 1 | a0004c0004t0001g0025 | 2 | HG00280.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.402+1025G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37182400 | |||||||
| chr2:37182429 | G | C | 108 | a0001c0001t0001g0063 a0002c0002t0001g0002 a0002c0002t0001g0006 others(105): Show |
171 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.402+996C>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37182429 | |||||||
| chr2:37182549 | G | C | 1 | a0003c0003t0001g0098 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.402+876C>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37182549 | |||||||
| chr2:37182607 | G | A | 108 | a0001c0001t0001g0063 a0002c0002t0001g0002 a0002c0002t0001g0006 others(105): Show |
171 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.402+818C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37182607 | |||||||
| chr2:37182658 | A | G | 4 | a0002c0002t0001g0193 a0002c0002t0001g0195 a0002c0002t0001g0196 others(1): Show |
4 | HG00099.hp1 HG00735.hp2 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.402+767T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37182658 | |||||||
| chr2:37182665 | A | C | 2 | a0004c0004t0001g0025 a0004c0004t0001g0049 |
3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.402+760T>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37182665 | |||||||
| chr2:37182710 | C | T | 2 | a0004c0004t0001g0025 a0004c0004t0001g0049 |
3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.402+715G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37182710 | |||||||
| chr2:37182711 | A | G | 110 | a0001c0001t0001g0063 a0002c0002t0001g0002 a0002c0002t0001g0006 others(107): Show |
174 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.402+714T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37182711 | |||||||
| chr2:37182743 | G | T | 43 | a0002c0002t0001g0006 a0002c0002t0001g0010 a0002c0002t0001g0011 others(40): Show |
60 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.402+682C>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37182743 | |||||||
| chr2:37182873 | T | C | 2 | a0002c0002t0001g0060 a0002c0002t0001g0061 |
2 | HG02922.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.402+552A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37182873 | |||||||
| chr2:37182894 | A | G | 110 | a0001c0001t0001g0063 a0002c0002t0001g0002 a0002c0002t0001g0006 others(107): Show |
174 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.402+531T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37182894 | |||||||
| chr2:37182899 | C | T | 110 | a0001c0001t0001g0063 a0002c0002t0001g0002 a0002c0002t0001g0006 others(107): Show |
174 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.402+526G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37182899 | |||||||
| chr2:37182914 | T | G | 110 | a0001c0001t0001g0063 a0002c0002t0001g0002 a0002c0002t0001g0006 others(107): Show |
174 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.402+511A>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37182914 | |||||||
| chr2:37182972 | G | C | 2 | a0002c0002t0001g0045 a0002c0002t0001g0188 |
3 | NA18966.hp1 NA18969.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.402+453C>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37182972 | |||||||
| chr2:37183088 | A | C | 43 | a0002c0002t0001g0006 a0002c0002t0001g0010 a0002c0002t0001g0011 others(40): Show |
60 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.402+337T>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37183088 | |||||||
| chr2:37183173 | T | G | 111 | a0001c0001t0001g0023 a0001c0001t0001g0063 a0001c0001t0001g0201 others(108): Show |
176 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.402+252A>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37183173 | |||||||
| chr2:37183214 | T | C | 66 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(63): Show |
122 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.402+211A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37183214 | |||||||
| chr2:37183323 | T | G | 1 | a0002c0002t0001g0122 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.402+102A>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37183323 | |||||||
| chr2:37183372 | T | G | 1 | a0010c0016t0001g0085 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.402+53A>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37183372 | |||||||
| chr2:37183394 | C | T | 66 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(63): Show |
122 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.402+31G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37183394 | |||||||
| chr2:37183411 | G | A | 2 | a0004c0004t0001g0025 a0004c0004t0001g0049 |
3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.402+14C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 3/6 | chr2 | 37183411 | |||||||
| chr2:37183550 | G | A | 2 | a0004c0004t0001g0025 a0004c0004t0001g0049 |
3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.313-36C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37183550 | |||||||
| chr2:37183662 | G | T | 2 | a0004c0004t0001g0025 a0004c0004t0001g0049 |
3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.313-148C>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37183662 | |||||||
| chr2:37183675 | A | G | 4 | a0003c0003t0001g0095 a0003c0003t0001g0096 a0003c0003t0001g0097 others(1): Show |
4 | HG00738.hp2 HG02145.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.313-161T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37183675 | |||||||
| chr2:37183720 | C | T | 2 | a0004c0004t0001g0025 a0004c0004t0001g0049 |
3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.313-206G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37183720 | |||||||
| chr2:37183721 | G | A | 112 | a0001c0001t0001g0023 a0001c0001t0001g0063 a0001c0001t0001g0133 others(109): Show |
177 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.313-207C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37183721 | |||||||
| chr2:37183743 | A | T | 3 | a0001c0001t0001g0023 a0001c0001t0001g0201 a0001c0001t0001g0202 |
5 | HG01070.hp1 HG01071.hp1 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.313-229T>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37183743 | |||||||
| chr2:37183812 | T | A | 2 | a0004c0004t0001g0025 a0004c0004t0001g0049 |
3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.313-298A>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37183812 | |||||||
| chr2:37183820 | T | G | 108 | a0001c0001t0001g0063 a0002c0002t0001g0002 a0002c0002t0001g0006 others(105): Show |
171 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.313-306A>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37183820 | |||||||
| chr2:37183853 | T | A | 183 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(180): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(300): Show |
intron_variant | MODIFIER | c.313-339A>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37183853 | |||||||
| chr2:37183871 | T | C | 3 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0158 |
3 | HG00140.hp2 HG00280.hp1 HG00323.hp2 |
intron_variant | MODIFIER | c.313-357A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37183871 | |||||||
| chr2:37183913 | C | G | 2 | a0004c0004t0001g0025 a0004c0004t0001g0049 |
3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.313-399G>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37183913 | |||||||
| chr2:37183933 | T | C | 111 | a0001c0001t0001g0063 a0001c0001t0001g0133 a0002c0002t0001g0002 others(108): Show |
175 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.313-419A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37183933 | |||||||
| chr2:37183939 | C | T | 43 | a0002c0002t0001g0006 a0002c0002t0001g0010 a0002c0002t0001g0011 others(40): Show |
60 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.313-425G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37183939 | |||||||
| chr2:37184009 | A | G | 2 | a0004c0004t0001g0025 a0004c0004t0001g0049 |
3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.313-495T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37184009 | |||||||
| chr2:37184079 | T | A | 44 | a0002c0002t0001g0006 a0002c0002t0001g0010 a0002c0002t0001g0011 others(41): Show |
61 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.313-565A>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37184079 | |||||||
| chr2:37184156 | A | G | 2 | a0004c0004t0001g0025 a0004c0004t0001g0049 |
3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.313-642T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37184156 | |||||||
| chr2:37184299 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.313-785G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37184299 | |||||||
| chr2:37184309 | A | G | 6 | a0003c0003t0001g0057 a0003c0003t0001g0095 a0003c0003t0001g0096 others(3): Show |
6 | HG00738.hp2 HG02145.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.313-795T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37184309 | |||||||
| chr2:37184327 | G | A | 2 | a0004c0004t0001g0025 a0004c0004t0001g0049 |
3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.313-813C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37184327 | |||||||
| chr2:37184339 | A | T | 10 | a0001c0001t0001g0017 a0001c0001t0001g0090 a0001c0001t0001g0091 others(7): Show |
12 | HG01106.hp1 HG01891.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.313-825T>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37184339 | |||||||
| chr2:37184594 | T | C | 1 | a0002c0002t0001g0028 | 2 | HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.313-1080A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37184594 | |||||||
| chr2:37184622 | G | T | 1 | a0011c0017t0001g0215 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.313-1108C>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37184622 | |||||||
| chr2:37184637 | C | G | 4 | a0002c0002t0001g0041 a0002c0002t0001g0159 a0002c0002t0001g0160 others(1): Show |
5 | HG00621.hp1 NA18939.hp2 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.313-1123G>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37184637 | |||||||
| chr2:37184647 | A | G | 10 | a0001c0001t0001g0017 a0001c0001t0001g0090 a0001c0001t0001g0091 others(7): Show |
12 | HG01106.hp1 HG01891.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.313-1133T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37184647 | |||||||
| chr2:37184660 | A | G | 111 | a0001c0001t0001g0063 a0001c0001t0001g0133 a0002c0002t0001g0002 others(108): Show |
175 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.313-1146T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37184660 | |||||||
| chr2:37184692 | C | T | 2 | a0002c0002t0001g0123 a0002c0002t0001g0125 |
2 | HG02486.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.313-1178G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37184692 | |||||||
| chr2:37184693 | G | C | 2 | a0003c0003t0001g0057 a0011c0017t0001g0215 |
2 | HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.313-1179C>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37184693 | |||||||
| chr2:37184730 | G | A | 2 | a0004c0004t0001g0025 a0004c0004t0001g0049 |
3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.313-1216C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37184730 | |||||||
| chr2:37184756 | C | T | 2 | a0004c0004t0001g0025 a0004c0004t0001g0049 |
3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.313-1242G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37184756 | |||||||
| chr2:37184767 | T | C | 2 | a0004c0004t0001g0025 a0004c0004t0001g0049 |
3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.313-1253A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37184767 | |||||||
| chr2:37184788 | C | T | 2 | a0004c0004t0001g0025 a0004c0004t0001g0049 |
3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.313-1274G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37184788 | |||||||
| chr2:37184811 | G | A | 3 | a0003c0003t0001g0096 a0003c0003t0001g0097 a0003c0003t0001g0098 |
3 | HG00738.hp2 HG02145.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.313-1297C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37184811 | |||||||
| chr2:37184826 | C | T | 2 | a0004c0004t0001g0025 a0004c0004t0001g0049 |
3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.313-1312G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37184826 | |||||||
| chr2:37184827 | A | G | 181 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(178): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(294): Show |
intron_variant | MODIFIER | c.313-1313T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37184827 | |||||||
| chr2:37184830 | T | TA | 8 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0204 others(5): Show |
8 | HG01070.hp2 HG01074.hp2 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.313-1317dupT | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37184830 | |||||||
| chr2:37184841 | A | AC | 2 | a0004c0004t0001g0025 a0004c0004t0001g0049 |
3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.313-1328_313-1327i others(3): Show |
SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37184841 | |||||||
| chr2:37184844 | C | A | 1 | a0011c0017t0001g0215 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.313-1330G>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37184844 | |||||||
| chr2:37184889 | A | T | 2 | a0004c0004t0001g0025 a0004c0004t0001g0049 |
3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.313-1375T>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37184889 | |||||||
| chr2:37184910 | G | A | 1 | a0003c0003t0001g0057 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.313-1396C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37184910 | |||||||
| chr2:37185006 | G | A | 111 | a0001c0001t0001g0063 a0001c0001t0001g0133 a0002c0002t0001g0002 others(108): Show |
175 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.313-1492C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37185006 | |||||||
| chr2:37185044 | C | A | 1 | a0002c0002t0001g0124 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.313-1530G>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37185044 | |||||||
| chr2:37185049 | T | C | 1 | a0003c0003t0001g0057 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.313-1535A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37185049 | |||||||
| chr2:37185057 | A | AT | 2 | a0004c0004t0001g0025 a0004c0004t0001g0049 |
3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.313-1544dupA | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37185057 | |||||||
| chr2:37185060 | A | G | 1 | a0001c0001t0001g0135 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.313-1546T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37185060 | |||||||
| chr2:37185186 | A | G | 5 | a0002c0002t0001g0028 a0002c0002t0001g0058 a0002c0002t0001g0059 others(2): Show |
6 | HG02886.hp2 HG02922.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.313-1672T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37185186 | |||||||
| chr2:37185352 | C | T | 6 | a0003c0003t0001g0057 a0003c0003t0001g0095 a0003c0003t0001g0096 others(3): Show |
6 | HG00738.hp2 HG02145.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.313-1838G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37185352 | |||||||
| chr2:37185443 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.312+1912C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37185443 | |||||||
| chr2:37185444 | T | C | 110 | a0001c0001t0001g0063 a0002c0002t0001g0002 a0002c0002t0001g0006 others(107): Show |
174 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.312+1911A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37185444 | |||||||
| chr2:37185459 | G | C | 1 | a0002c0013t0001g0062 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.312+1896C>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37185459 | |||||||
| chr2:37185464 | C | A | 2 | a0004c0004t0001g0025 a0004c0004t0001g0049 |
3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.312+1891G>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37185464 | |||||||
| chr2:37185517 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.312+1838C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37185517 | |||||||
| chr2:37185518 | A | T | 1 | a0001c0001t0001g0135 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.312+1837T>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37185518 | |||||||
| chr2:37185537 | C | T | 4 | a0001c0001t0002g0024 a0001c0001t0002g0047 a0001c0001t0002g0203 others(1): Show |
7 | HG02055.hp1 HG02818.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.312+1818G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37185537 | |||||||
| chr2:37185543 | C | G | 1 | a0002c0002t0001g0125 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.312+1812G>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37185543 | |||||||
| chr2:37185583 | T | C | 1 | a0001c0001t0001g0157 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.312+1772A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37185583 | |||||||
| chr2:37185610 | C | T | 1 | a0002c0002t0001g0159 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.312+1745G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37185610 | |||||||
| chr2:37185717 | C | CA | 28 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0040 others(25): Show |
34 | HG00280.hp2 HG00323.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.312+1637dupT | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37185717 | |||||||
| chr2:37185717 | C | CAAAAAAA others(1): Show |
8 | a0002c0002t0001g0065 a0002c0002t0001g0066 a0002c0002t0001g0103 others(5): Show |
8 | HG00099.hp2 HG00735.hp1 HG00735.hp2 others(5): Show |
intron_variant | MODIFIER | c.312+1630_312+1637d others(10): Show |
SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37185717 | |||||||
| chr2:37185717 | C | CAAAAAAA others(2): Show |
31 | a0002c0002t0001g0006 a0002c0002t0001g0010 a0002c0002t0001g0033 others(28): Show |
45 | HG00099.hp1 HG00438.hp2 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.312+1629_312+1637d others(11): Show |
SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37185717 | |||||||
| chr2:37185717 | C | CAAAAAAA others(3): Show |
4 | a0002c0002t0001g0011 a0002c0002t0001g0125 a0002c0002t0001g0126 others(1): Show |
7 | HG00621.hp2 HG01943.hp2 HG02273.hp2 others(4): Show |
intron_variant | MODIFIER | c.312+1628_312+1637d others(12): Show |
SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37185717 | |||||||
| chr2:37185717 | C | CAAAAAAA others(4): Show |
1 | a0002c0002t0001g0128 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.312+1627_312+1637d others(13): Show |
SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37185717 | |||||||
| chr2:37185717 | CAAAAAAA | C | 5 | a0002c0002t0001g0015 a0002c0002t0001g0046 a0002c0002t0001g0102 others(2): Show |
9 | HG01975.hp1 HG01978.hp1 HG01978.hp2 others(6): Show |
intron_variant | MODIFIER | c.312+1631_312+1637d others(9): Show |
SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37185717 | |||||||
| chr2:37185717 | CAAAAAAA others(1): Show |
C | 52 | a0001c0001t0001g0133 a0002c0002t0001g0002 a0002c0002t0001g0012 others(49): Show |
93 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.312+1630_312+1637d others(10): Show |
SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37185717 | |||||||
| chr2:37185727 | A | AAAAAAAA others(1): Show |
6 | a0002c0002t0001g0028 a0002c0002t0001g0058 a0002c0002t0001g0059 others(3): Show |
7 | HG02886.hp2 HG02922.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.312+1627_312+1628i others(10): Show |
SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37185727 | |||||||
| chr2:37185752 | T | G | 2 | a0004c0004t0001g0025 a0004c0004t0001g0049 |
3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.312+1603A>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37185752 | |||||||
| chr2:37185792 | T | G | 109 | a0001c0001t0001g0063 a0001c0001t0001g0133 a0002c0002t0001g0002 others(106): Show |
172 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.312+1563A>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37185792 | |||||||
| chr2:37185918 | T | C | 2 | a0004c0004t0001g0025 a0004c0004t0001g0049 |
3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.312+1437A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37185918 | |||||||
| chr2:37185923 | C | G | 2 | a0004c0004t0001g0025 a0004c0004t0001g0049 |
3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.312+1432G>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37185923 | |||||||
| chr2:37185990 | A | G | 2 | a0004c0004t0001g0025 a0004c0004t0001g0049 |
3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.312+1365T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37185990 | |||||||
| chr2:37186002 | G | A | 182 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(179): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(295): Show |
intron_variant | MODIFIER | c.312+1353C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37186002 | |||||||
| chr2:37186099 | C | G | 40 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(37): Show |
84 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.312+1256G>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37186099 | |||||||
| chr2:37186227 | T | A | 109 | a0001c0001t0001g0063 a0001c0001t0001g0133 a0002c0002t0001g0002 others(106): Show |
172 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.312+1128A>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37186227 | |||||||
| chr2:37186327 | G | A | 3 | a0001c0001t0001g0129 a0001c0001t0002g0130 a0001c0001t0002g0131 |
3 | HG02622.hp1 HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.312+1028C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37186327 | |||||||
| chr2:37186384 | A | C | 111 | a0001c0001t0001g0063 a0001c0001t0001g0133 a0002c0002t0001g0002 others(108): Show |
175 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.312+971T>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37186384 | |||||||
| chr2:37186526 | C | T | 2 | a0004c0004t0001g0025 a0004c0004t0001g0049 |
3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.312+829G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37186526 | |||||||
| chr2:37186532 | G | T | 2 | a0004c0004t0001g0025 a0004c0004t0001g0049 |
3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.312+823C>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37186532 | |||||||
| chr2:37186569 | C | T | 2 | a0004c0004t0001g0025 a0004c0004t0001g0049 |
3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.312+786G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37186569 | |||||||
| chr2:37186611 | G | C | 1 | a0003c0003t0001g0057 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.312+744C>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37186611 | |||||||
| chr2:37186634 | A | G | 2 | a0004c0004t0001g0025 a0004c0004t0001g0049 |
3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.312+721T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37186634 | |||||||
| chr2:37186717 | C | A | 62 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(59): Show |
112 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.312+638G>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37186717 | |||||||
| chr2:37186722 | C | T | 2 | a0004c0004t0001g0025 a0004c0004t0001g0049 |
3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.312+633G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37186722 | |||||||
| chr2:37186728 | C | CA | 5 | a0002c0002t0001g0200 a0003c0003t0001g0095 a0003c0003t0001g0096 others(2): Show |
5 | HG00738.hp2 HG02145.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.312+626dupT | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37186728 | |||||||
| chr2:37186759 | A | C | 2 | a0004c0004t0001g0025 a0004c0004t0001g0049 |
3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.312+596T>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37186759 | |||||||
| chr2:37186770 | C | G | 1 | a0002c0002t0001g0100 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.312+585G>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37186770 | |||||||
| chr2:37186842 | G | A | 2 | a0004c0004t0001g0025 a0004c0004t0001g0049 |
3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.312+513C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37186842 | |||||||
| chr2:37186897 | A | T | 2 | a0004c0004t0001g0025 a0004c0004t0001g0049 |
3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.312+458T>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37186897 | |||||||
| chr2:37186901 | G | A | 2 | a0004c0004t0001g0025 a0004c0004t0001g0049 |
3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.312+454C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37186901 | |||||||
| chr2:37186935 | C | T | 2 | a0004c0004t0001g0025 a0004c0004t0001g0049 |
3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.312+420G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37186935 | |||||||
| chr2:37186976 | A | G | 2 | a0004c0004t0001g0025 a0004c0004t0001g0049 |
3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.312+379T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37186976 | |||||||
| chr2:37187074 | G | A | 6 | a0003c0003t0001g0057 a0003c0003t0001g0095 a0003c0003t0001g0096 others(3): Show |
6 | HG00738.hp2 HG02145.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.312+281C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37187074 | |||||||
| chr2:37187083 | G | A | 2 | a0004c0004t0001g0025 a0004c0004t0001g0049 |
3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.312+272C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37187083 | |||||||
| chr2:37187084 | G | A | 65 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(62): Show |
117 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.312+271C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37187084 | |||||||
| chr2:37187176 | A | G | 6 | a0003c0003t0001g0057 a0003c0003t0001g0095 a0003c0003t0001g0096 others(3): Show |
6 | HG00738.hp2 HG02145.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.312+179T>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37187176 | |||||||
| chr2:37187180 | T | C | 2 | a0004c0004t0001g0025 a0004c0004t0001g0049 |
3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.312+175A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37187180 | |||||||
| chr2:37187288 | A | C | 42 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(39): Show |
87 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.312+67T>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37187288 | |||||||
| chr2:37187334 | T | G | 1 | a0001c0001t0002g0211 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.312+21A>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 2/6 | chr2 | 37187334 | |||||||
| chr2:37187614 | G | A | 2 | a0004c0004t0001g0025 a0004c0004t0001g0049 |
3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.200-147C>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 1/6 | chr2 | 37187614 | |||||||
| chr2:37187782 | T | G | 1 | a0002c0002t0001g0212 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.200-315A>C | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 1/6 | chr2 | 37187782 | |||||||
| chr2:37187805 | A | T | 1 | a0002c0002t0001g0132 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.200-338T>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 1/6 | chr2 | 37187805 | |||||||
| chr2:37187865 | GA | G | 40 | a0001c0001t0001g0129 a0001c0001t0002g0130 a0001c0001t0002g0131 others(37): Show |
57 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.200-399delT | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 1/6 | chr2 | 37187865 | |||||||
| chr2:37188179 | C | T | 2 | a0004c0004t0001g0025 a0004c0004t0001g0049 |
3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.199+263G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 1/6 | chr2 | 37188179 | |||||||
| chr2:37188191 | C | A | 1 | a0001c0001t0002g0213 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.199+251G>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 1/6 | chr2 | 37188191 | |||||||
| chr2:37188206 | C | T | 2 | a0004c0004t0001g0025 a0004c0004t0001g0049 |
3 | HG00280.hp2 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.199+236G>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 1/6 | chr2 | 37188206 | |||||||
| chr2:37188212 | T | C | 5 | a0003c0003t0001g0095 a0003c0003t0001g0096 a0003c0003t0001g0097 others(2): Show |
5 | HG00738.hp2 HG02145.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.199+230A>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 1/6 | chr2 | 37188212 | |||||||
| chr2:37188267 | C | A | 1 | a0001c0001t0001g0214 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.199+175G>T | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 1/6 | chr2 | 37188267 | |||||||
| chr2:37188290 | A | T | 1 | a0002c0002t0001g0100 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.199+152T>A | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 1/6 | chr2 | 37188290 | |||||||
| chr2:37188328 | A | C | 1 | a0001c0001t0001g0099 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.199+114T>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 1/6 | chr2 | 37188328 | |||||||
| chr2:37188353 | G | C | 147 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0023 others(144): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.199+89C>G | SULT6B1 | ENSG00000138068.12 | transcript | ENST00000535679.6 | protein_coding | 1/6 | chr2 | 37188353 |