Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 27284 |
| ensemblid | ENSG00000173597.9 |
| hgncid | 17845 |
| symbol | SULT1B1 |
| name | sulfotransferase family 1B member 1 |
| refseq_nuc | NM_014465.4 |
| refseq_prot | NP_055280.2 |
| ensembl_nuc | ENST00000310613.8 |
| ensembl_prot | ENSP00000308770.2 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 69721167 |
| end | 69760620 |
| strand | - |
| ver | v1.2 |
| region | chr4:69721167-69760620 |
| region5000 | chr4:69716167-69765620 |
| regionname0 | SULT1B1_chr4_69721167_69760620 |
| regionname5000 | SULT1B1_chr4_69716167_69765620 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 296 | 397 | 75 | 71 | 197 | 16 | 36 | 147 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | MLSPK others(291): Show |
chr4 | 69716167 | 69765620 |
| a0002 | 0/0 | 296 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | MLSPK others(291): Show |
chr4 | 69716167 | 69765620 |
| a0003 | 0/0 | 296 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | MLSPK others(291): Show |
chr4 | 69716167 | 69765620 |
| a0004 | 0/0 | 296 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | MLSPK others(291): Show |
chr4 | 69716167 | 69765620 |
| a0005 | 0/0 | 296 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | MLSPK others(291): Show |
chr4 | 69716167 | 69765620 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 888 | 396 | 75 | 71 | 196 | 16 | 36 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | ATGCT others(883): Show |
chr4 | 69716167 | 69765620 | ||
| a0001c0006 | 0/0 | 888 | 1 | 0 | 0 | 1 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | ATGCT others(883): Show |
chr4 | 69716167 | 69765620 | ||
| a0002c0002 | 0/0 | 888 | 7 | 7 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | ATGCT others(883): Show |
chr4 | 69716167 | 69765620 | ||
| a0003c0003 | 0/0 | 888 | 2 | 1 | 1 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | ATGCT others(883): Show |
chr4 | 69716167 | 69765620 | ||
| a0004c0005 | 0/0 | 888 | 1 | 1 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | ATGCT others(883): Show |
chr4 | 69716167 | 69765620 | ||
| a0005c0004 | 0/0 | 888 | 1 | 0 | 0 | 1 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | ATGCT others(883): Show |
chr4 | 69716167 | 69765620 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 7018 | 75 | 1 | 15 | 49 | 1 | 9 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | GATTG others(7013): Show |
chr4 | 69716167 | 69765620 |
| a0001c0001t0002 | 0/0 | 7018 | 75 | 1 | 6 | 65 | 2 | 1 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | GATTG others(7013): Show |
chr4 | 69716167 | 69765620 |
| a0001c0001t0003 | 1/0 | 7018 | 68 | 18 | 7 | 33 | 4 | 5 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | GATTG others(7013): Show |
chr4 | 69716167 | 69765620 |
| a0001c0001t0004 | 0/0 | 7018 | 33 | 2 | 12 | 5 | 3 | 11 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | GATTG others(7013): Show |
chr4 | 69716167 | 69765620 |
| a0001c0001t0005 | 0/0 | 7018 | 14 | 0 | 10 | 0 | 0 | 4 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | GATTG others(7013): Show |
chr4 | 69716167 | 69765620 |
| a0001c0001t0006 | 0/0 | 6982 | 14 | 0 | 0 | 13 | 1 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | GATTG others(6977): Show |
chr4 | 69716167 | 69765620 |
| a0001c0001t0007 | 0/0 | 7018 | 12 | 0 | 3 | 9 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | GATTG others(7013): Show |
chr4 | 69716167 | 69765620 |
| a0001c0001t0008 | 0/0 | 6982 | 11 | 0 | 4 | 7 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | GATTG others(6977): Show |
chr4 | 69716167 | 69765620 |
| a0001c0001t0009 | 0/0 | 7017 | 10 | 5 | 3 | 0 | 1 | 1 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | GATTG others(7012): Show |
chr4 | 69716167 | 69765620 |
| a0001c0001t0010 | 0/0 | 7018 | 8 | 8 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | GATTG others(7013): Show |
chr4 | 69716167 | 69765620 |
| a0001c0001t0011 | 0/0 | 6991 | 8 | 7 | 1 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | GATTG others(6986): Show |
chr4 | 69716167 | 69765620 |
| a0001c0001t0012 | 0/0 | 7018 | 6 | 6 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | GATTG others(7013): Show |
chr4 | 69716167 | 69765620 |
| a0001c0001t0013 | 0/0 | 7018 | 6 | 0 | 3 | 3 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | GATTG others(7013): Show |
chr4 | 69716167 | 69765620 |
| a0001c0001t0015 | 0/0 | 7018 | 3 | 2 | 1 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | GATTG others(7013): Show |
chr4 | 69716167 | 69765620 |
| a0001c0001t0016 | 0/0 | 7018 | 3 | 2 | 1 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | GATTG others(7013): Show |
chr4 | 69716167 | 69765620 |
| a0001c0001t0017 | 0/0 | 7019 | 3 | 0 | 0 | 3 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | GATTG others(7014): Show |
chr4 | 69716167 | 69765620 |
| a0001c0001t0018 | 0/0 | 7018 | 3 | 3 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | GATTG others(7013): Show |
chr4 | 69716167 | 69765620 |
| a0001c0001t0019 | 0/0 | 7018 | 2 | 0 | 1 | 0 | 1 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | GATTG others(7013): Show |
chr4 | 69716167 | 69765620 |
| a0001c0001t0020 | 0/0 | 7018 | 2 | 0 | 2 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | GATTG others(7013): Show |
chr4 | 69716167 | 69765620 |
| a0001c0001t0021 | 0/0 | 6982 | 2 | 2 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | GATTG others(6977): Show |
chr4 | 69716167 | 69765620 |
| a0001c0001t0022 | 0/0 | 7018 | 2 | 0 | 0 | 0 | 2 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | GATTG others(7013): Show |
chr4 | 69716167 | 69765620 |
| a0001c0001t0023 | 0/0 | 7018 | 2 | 2 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | GATTG others(7013): Show |
chr4 | 69716167 | 69765620 |
| a0001c0001t0024 | 0/0 | 7018 | 1 | 0 | 1 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | GATTG others(7013): Show |
chr4 | 69716167 | 69765620 |
| a0001c0001t0025 | 0/0 | 7018 | 1 | 0 | 0 | 1 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | GATTG others(7013): Show |
chr4 | 69716167 | 69765620 |
| a0001c0001t0026 | 0/0 | 7018 | 1 | 0 | 1 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | GATTG others(7013): Show |
chr4 | 69716167 | 69765620 |
| a0001c0001t0030 | 0/0 | 7018 | 1 | 1 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | GATTG others(7013): Show |
chr4 | 69716167 | 69765620 |
| a0001c0001t0031 | 0/0 | 7018 | 1 | 1 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | GATTG others(7013): Show |
chr4 | 69716167 | 69765620 |
| a0001c0001t0032 | 0/0 | 7018 | 1 | 0 | 0 | 1 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | GATTG others(7013): Show |
chr4 | 69716167 | 69765620 |
| a0001c0001t0034 | 0/0 | 7018 | 1 | 1 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | GATTG others(7013): Show |
chr4 | 69716167 | 69765620 |
| a0001c0001t0036 | 0/0 | 6982 | 1 | 0 | 0 | 0 | 0 | 1 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | GATTG others(6977): Show |
chr4 | 69716167 | 69765620 |
| a0001c0001t0037 | 0/0 | 6982 | 1 | 0 | 0 | 1 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | GATTG others(6977): Show |
chr4 | 69716167 | 69765620 |
| a0001c0001t0038 | 0/0 | 6982 | 1 | 1 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | GATTG others(6977): Show |
chr4 | 69716167 | 69765620 |
| a0001c0001t0039 | 0/0 | 6982 | 1 | 0 | 0 | 0 | 1 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | GATTG others(6977): Show |
chr4 | 69716167 | 69765620 |
| a0001c0001t0040 | 0/0 | 7018 | 1 | 0 | 0 | 0 | 0 | 1 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | GATTG others(7013): Show |
chr4 | 69716167 | 69765620 |
| a0001c0001t0041 | 0/0 | 6982 | 1 | 1 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | GATTG others(6977): Show |
chr4 | 69716167 | 69765620 |
| a0001c0001t0042 | 0/0 | 6982 | 1 | 1 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | GATTG others(6977): Show |
chr4 | 69716167 | 69765620 |
| a0001c0001t0044 | 0/0 | 7018 | 1 | 1 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | GATTG others(7013): Show |
chr4 | 69716167 | 69765620 |
| a0001c0001t0045 | 0/0 | 7018 | 1 | 1 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | GATTG others(7013): Show |
chr4 | 69716167 | 69765620 |
| a0001c0001t0046 | 0/0 | 7018 | 1 | 1 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | GATTG others(7013): Show |
chr4 | 69716167 | 69765620 |
| a0001c0001t0047 | 0/0 | 7018 | 1 | 0 | 0 | 1 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | GATTG others(7013): Show |
chr4 | 69716167 | 69765620 |
| a0001c0001t0048 | 0/0 | 7018 | 1 | 0 | 0 | 1 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | GATTG others(7013): Show |
chr4 | 69716167 | 69765620 |
| a0001c0001t0049 | 0/0 | 7018 | 1 | 1 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | GATTG others(7013): Show |
chr4 | 69716167 | 69765620 |
| a0001c0001t0050 | 0/0 | 7018 | 1 | 0 | 0 | 0 | 0 | 1 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | GATTG others(7013): Show |
chr4 | 69716167 | 69765620 |
| a0001c0001t0051 | 0/0 | 7018 | 1 | 1 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | GATTG others(7013): Show |
chr4 | 69716167 | 69765620 |
| a0001c0001t0052 | 0/0 | 7018 | 1 | 0 | 0 | 0 | 0 | 1 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | GATTG others(7013): Show |
chr4 | 69716167 | 69765620 |
| a0001c0001t0053 | 0/0 | 7018 | 1 | 0 | 0 | 1 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | GATTG others(7013): Show |
chr4 | 69716167 | 69765620 |
| a0001c0001t0054 | 0/0 | 7018 | 1 | 0 | 0 | 1 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | GATTG others(7013): Show |
chr4 | 69716167 | 69765620 |
| a0001c0001t0055 | 0/0 | 7018 | 1 | 1 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | GATTG others(7013): Show |
chr4 | 69716167 | 69765620 |
| a0001c0001t0056 | 0/1 | 7008 | 1 | 0 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | GATTG others(7003): Show |
chr4 | 69716167 | 69765620 |
| a0001c0001t0057 | 0/0 | 7018 | 1 | 1 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | GATTG others(7013): Show |
chr4 | 69716167 | 69765620 |
| a0001c0001t0058 | 0/0 | 7018 | 1 | 1 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | GATTG others(7013): Show |
chr4 | 69716167 | 69765620 |
| a0001c0001t0059 | 0/0 | 7018 | 1 | 1 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | GATTG others(7013): Show |
chr4 | 69716167 | 69765620 |
| a0001c0001t0060 | 0/0 | 7018 | 1 | 1 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | GATTG others(7013): Show |
chr4 | 69716167 | 69765620 |
| a0001c0001t0061 | 0/0 | 6982 | 1 | 0 | 0 | 0 | 0 | 1 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | GATTG others(6977): Show |
chr4 | 69716167 | 69765620 |
| a0001c0001t0062 | 0/0 | 6982 | 1 | 0 | 0 | 1 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | GATTG others(6977): Show |
chr4 | 69716167 | 69765620 |
| a0001c0001t0063 | 0/0 | 6982 | 1 | 0 | 0 | 1 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | GATTG others(6977): Show |
chr4 | 69716167 | 69765620 |
| a0001c0006t0002 | 0/0 | 7018 | 1 | 0 | 0 | 1 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | GATTG others(7013): Show |
chr4 | 69716167 | 69765620 |
| a0002c0002t0014 | 0/0 | 7019 | 4 | 4 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | GATTG others(7014): Show |
chr4 | 69716167 | 69765620 |
| a0002c0002t0027 | 0/0 | 7019 | 1 | 1 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | GATTG others(7014): Show |
chr4 | 69716167 | 69765620 |
| a0002c0002t0028 | 0/0 | 7019 | 1 | 1 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | GATTG others(7014): Show |
chr4 | 69716167 | 69765620 |
| a0002c0002t0029 | 0/0 | 7019 | 1 | 1 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | GATTG others(7014): Show |
chr4 | 69716167 | 69765620 |
| a0003c0003t0033 | 0/0 | 7018 | 1 | 1 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | GATTG others(7013): Show |
chr4 | 69716167 | 69765620 |
| a0003c0003t0035 | 0/0 | 7018 | 1 | 0 | 1 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | GATTG others(7013): Show |
chr4 | 69716167 | 69765620 |
| a0004c0005t0043 | 0/0 | 7018 | 1 | 1 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | GATTG others(7013): Show |
chr4 | 69716167 | 69765620 |
| a0005c0004t0001 | 0/0 | 7018 | 1 | 0 | 0 | 1 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | GATTG others(7013): Show |
chr4 | 69716167 | 69765620 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 16 | 0 | 3 | 13 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0001g0004 | 0/0 | 12 | 1 | 1 | 9 | 1 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0001g0009 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0001g0024 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0002g0001 | 0/0 | 40 | 0 | 1 | 38 | 1 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0002g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0002g0017 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0002g0018 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0002g0023 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0002g0033 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0002g0050 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0003g0003 | 0/0 | 15 | 3 | 2 | 7 | 1 | 2 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0003g0010 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0003g0012 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0003g0013 | 1/0 | 5 | 4 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0003g0014 | 0/0 | 5 | 0 | 3 | 0 | 2 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0003g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0003g0028 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0003g0030 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0003g0031 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0003g0032 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0003g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0003g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0003g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0003g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0003g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0003g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0003g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0004g0007 | 0/0 | 7 | 0 | 2 | 0 | 1 | 4 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0004g0015 | 0/0 | 5 | 1 | 1 | 0 | 0 | 3 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0004g0016 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0004g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0004g0048 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0004g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0004g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0004g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0004g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0004g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0004g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0004g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0004g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0004g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0004g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0004g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0004g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0005g0006 | 0/0 | 8 | 0 | 7 | 0 | 0 | 1 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0005g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0005g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0005g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0005g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0005g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0005g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0006g0005 | 0/0 | 12 | 0 | 0 | 12 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0006g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0006g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0007g0022 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0007g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0007g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0007g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0007g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0007g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0007g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0007g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0008g0008 | 0/0 | 7 | 0 | 4 | 3 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0008g0034 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0008g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0009g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0009g0052 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0009g0053 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0009g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0009g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0009g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0009g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0010g0021 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0010g0027 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0010g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0011g0020 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0011g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0011g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0011g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0011g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0012g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0012g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0012g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0012g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0012g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0013g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0013g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0013g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0013g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0013g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0015g0049 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0015g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0016g0025 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0017g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0017g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0018g0029 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0019g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0019g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0020g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0021g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0022g0043 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0023g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0023g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0024g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0025g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0026g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0030g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0031g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0032g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0034g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0036g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0037g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0038g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0039g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0040g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0041g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0042g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0044g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0045g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0046g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0047g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0048g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0049g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0050g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0051g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0052g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0053g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0054g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0055g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0056g0140 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0057g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0058g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0059g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0060g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0061g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0062g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0001t0063g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0001c0006t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0002c0002t0014g0019 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0002c0002t0027g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0002c0002t0028g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0002c0002t0029g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0003c0003t0033g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0003c0003t0035g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0004c0005t0043g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| a0005c0004t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0004 | g0115 | EUR | GBR | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG00099 | hp2 | a0001 | c0001 | t0009 | g0053 | EUR | GBR | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG00140 | hp1 | a0001 | c0001 | t0006 | g0171 | EUR | GBR | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0132 | EUR | GBR | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG00280 | hp1 | a0001 | c0001 | t0039 | g0175 | EUR | FIN | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG00280 | hp2 | a0001 | c0001 | t0019 | g0084 | EUR | FIN | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG00323 | hp1 | a0001 | c0001 | t0004 | g0114 | EUR | FIN | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | FIN | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | CHS | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0165 | EAS | CHS | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG00423 | hp2 | a0001 | c0001 | t0006 | g0172 | EAS | CHS | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG00438 | hp1 | a0001 | c0001 | t0025 | g0099 | EAS | CHS | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG00438 | hp2 | a0001 | c0001 | t0004 | g0047 | EAS | CHS | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG00544 | hp2 | a0001 | c0001 | t0037 | g0173 | EAS | CHS | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | CHS | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0163 | EAS | CHS | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG00609 | hp1 | a0001 | c0001 | t0007 | g0022 | EAS | CHS | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG00621 | hp1 | a0001 | c0001 | t0006 | g0005 | EAS | CHS | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG00639 | hp1 | a0001 | c0001 | t0005 | g0006 | AMR | PUR | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG00639 | hp2 | a0001 | c0001 | t0007 | g0137 | AMR | PUR | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | CHS | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG00733 | hp1 | a0001 | c0001 | t0004 | g0143 | AMR | PUR | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0014 | AMR | PUR | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG00735 | hp1 | a0001 | c0001 | t0020 | g0037 | AMR | PUR | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG00735 | hp2 | a0001 | c0001 | t0004 | g0007 | AMR | PUR | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG00738 | hp2 | a0001 | c0001 | t0005 | g0178 | AMR | PUR | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0014 | AMR | PUR | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0017 | AMR | PUR | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG01069 | hp1 | a0001 | c0001 | t0004 | g0015 | AMR | PUR | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG01070 | hp1 | a0001 | c0001 | t0007 | g0046 | AMR | PUR | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG01070 | hp2 | a0001 | c0001 | t0004 | g0048 | AMR | PUR | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG01071 | hp1 | a0001 | c0001 | t0007 | g0046 | AMR | PUR | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0018 | AMR | PUR | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG01081 | hp2 | a0001 | c0001 | t0004 | g0048 | AMR | PUR | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG01109 | hp1 | a0001 | c0001 | t0015 | g0049 | AMR | PUR | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG01109 | hp2 | a0001 | c0001 | t0004 | g0117 | AMR | PUR | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG01168 | hp1 | a0001 | c0001 | t0009 | g0052 | AMR | PUR | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0014 | AMR | PUR | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG01175 | hp1 | a0001 | c0001 | t0024 | g0068 | AMR | PUR | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG01175 | hp2 | a0001 | c0001 | t0026 | g0090 | AMR | PUR | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG01192 | hp1 | a0001 | c0001 | t0004 | g0177 | AMR | PUR | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG01243 | hp1 | a0001 | c0001 | t0011 | g0020 | AMR | PUR | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG01243 | hp2 | a0003 | c0003 | t0035 | g0108 | AMR | PUR | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG01255 | hp1 | a0001 | c0001 | t0004 | g0145 | AMR | CLM | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG01255 | hp2 | a0001 | c0001 | t0004 | g0007 | AMR | CLM | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG01256 | hp1 | a0001 | c0001 | t0004 | g0116 | AMR | CLM | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG01256 | hp2 | a0001 | c0001 | t0019 | g0080 | AMR | CLM | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0119 | AMR | CLM | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0018 | AMR | CLM | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG01346 | hp1 | a0001 | c0001 | t0005 | g0006 | AMR | CLM | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG01346 | hp2 | a0001 | c0001 | t0004 | g0016 | AMR | CLM | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0050 | AMR | CLM | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG01358 | hp2 | a0001 | c0001 | t0009 | g0052 | AMR | CLM | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0018 | AMR | CLM | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG01361 | hp2 | a0001 | c0001 | t0008 | g0008 | AMR | CLM | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG01433 | hp1 | a0001 | c0001 | t0009 | g0182 | AMR | CLM | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG01433 | hp2 | a0001 | c0001 | t0013 | g0134 | AMR | CLM | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0003 | EUR | IBS | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG01515 | hp2 | a0001 | c0001 | t0022 | g0043 | EUR | IBS | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0001 | EUR | IBS | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0014 | EUR | IBS | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG01517 | hp1 | a0001 | c0001 | t0022 | g0043 | EUR | IBS | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0014 | EUR | IBS | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG01884 | hp1 | a0001 | c0001 | t0055 | g0120 | AFR | ACB | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG01884 | hp2 | a0004 | c0005 | t0043 | g0191 | AFR | ACB | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG01891 | hp1 | a0001 | c0001 | t0010 | g0021 | AFR | ACB | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG01891 | hp2 | a0001 | c0001 | t0011 | g0020 | AFR | ACB | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG01928 | hp1 | a0001 | c0001 | t0008 | g0008 | AMR | PEL | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG01928 | hp2 | a0001 | c0001 | t0005 | g0058 | AMR | PEL | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PEL | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG01943 | hp2 | a0001 | c0001 | t0016 | g0025 | AMR | PEL | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG01952 | hp1 | a0001 | c0001 | t0008 | g0008 | AMR | PEL | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG01952 | hp2 | a0001 | c0001 | t0005 | g0006 | AMR | PEL | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG01975 | hp1 | a0001 | c0001 | t0008 | g0008 | AMR | PEL | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG01975 | hp2 | a0001 | c0001 | t0005 | g0006 | AMR | PEL | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PEL | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG01978 | hp2 | a0001 | c0001 | t0005 | g0006 | AMR | PEL | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG01981 | hp1 | a0001 | c0001 | t0005 | g0065 | AMR | PEL | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PEL | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02027 | hp2 | a0001 | c0001 | t0004 | g0016 | EAS | KHV | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02055 | hp1 | a0001 | c0001 | t0010 | g0021 | AFR | ACB | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0170 | AFR | ACB | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0161 | EAS | KHV | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02071 | hp1 | a0001 | c0001 | t0054 | g0131 | EAS | KHV | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02074 | hp1 | a0001 | c0001 | t0006 | g0005 | EAS | KHV | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | KHV | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02080 | hp1 | a0001 | c0001 | t0006 | g0005 | EAS | KHV | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02083 | hp1 | a0001 | c0001 | t0006 | g0005 | EAS | KHV | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02083 | hp2 | a0001 | c0006 | t0002 | g0057 | EAS | KHV | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02129 | hp1 | a0001 | c0001 | t0007 | g0196 | EAS | KHV | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02132 | hp1 | a0001 | c0001 | t0004 | g0016 | EAS | KHV | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02135 | hp1 | a0001 | c0001 | t0063 | g0200 | EAS | KHV | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0032 | AFR | ACB | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02145 | hp2 | a0001 | c0001 | t0011 | g0020 | AFR | ACB | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0123 | EAS | CDX | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | CDX | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02165 | hp1 | a0001 | c0001 | t0013 | g0151 | EAS | CDX | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | CDX | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02258 | hp1 | a0001 | c0001 | t0018 | g0029 | AFR | ACB | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02258 | hp2 | a0001 | c0001 | t0021 | g0040 | AFR | ACB | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02273 | hp1 | a0001 | c0001 | t0005 | g0006 | AMR | PEL | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02273 | hp2 | a0001 | c0001 | t0003 | g0066 | AMR | PEL | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02280 | hp1 | a0001 | c0001 | t0049 | g0153 | AFR | ACB | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0013 | AFR | ACB | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02293 | hp1 | a0001 | c0001 | t0013 | g0063 | AMR | PEL | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02300 | hp1 | a0001 | c0001 | t0004 | g0016 | AMR | PEL | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02300 | hp2 | a0001 | c0001 | t0005 | g0006 | AMR | PEL | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02451 | hp2 | a0001 | c0001 | t0015 | g0078 | AFR | ACB | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02523 | hp2 | a0001 | c0001 | t0007 | g0148 | EAS | KHV | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02572 | hp1 | a0001 | c0001 | t0012 | g0190 | AFR | GWD | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02572 | hp2 | a0001 | c0001 | t0045 | g0188 | AFR | GWD | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02602 | hp2 | a0001 | c0001 | t0004 | g0007 | SAS | PJL | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02615 | hp1 | a0002 | c0002 | t0014 | g0019 | AFR | GWD | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02615 | hp2 | a0001 | c0001 | t0010 | g0021 | AFR | GWD | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02622 | hp1 | a0001 | c0001 | t0042 | g0107 | AFR | GWD | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02622 | hp2 | a0001 | c0001 | t0031 | g0076 | AFR | GWD | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02630 | hp1 | a0001 | c0001 | t0046 | g0189 | AFR | GWD | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02630 | hp2 | a0001 | c0001 | t0010 | g0027 | AFR | GWD | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02698 | hp1 | a0001 | c0001 | t0040 | g0118 | SAS | PJL | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02698 | hp2 | a0001 | c0001 | t0061 | g0199 | SAS | PJL | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02717 | hp1 | a0001 | c0001 | t0011 | g0129 | AFR | GWD | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02717 | hp2 | a0001 | c0001 | t0010 | g0027 | AFR | GWD | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0197 | SAS | PJL | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02738 | hp1 | a0001 | c0001 | t0004 | g0126 | SAS | PJL | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0055 | SAS | PJL | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0124 | AFR | GWD | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0030 | AFR | GWD | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | GWD | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02818 | hp2 | a0001 | c0001 | t0034 | g0106 | AFR | GWD | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02886 | hp1 | a0001 | c0001 | t0060 | g0186 | AFR | GWD | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0121 | AFR | GWD | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02896 | hp1 | a0001 | c0001 | t0030 | g0075 | AFR | GWD | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02896 | hp2 | a0001 | c0001 | t0018 | g0029 | AFR | GWD | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | GWD | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02897 | hp2 | a0001 | c0001 | t0018 | g0029 | AFR | GWD | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0146 | AFR | ESN | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02922 | hp2 | a0001 | c0001 | t0010 | g0021 | AFR | ESN | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0152 | AFR | ESN | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02965 | hp2 | a0001 | c0001 | t0059 | g0185 | AFR | ESN | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02970 | hp1 | a0002 | c0002 | t0014 | g0019 | AFR | ESN | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02970 | hp2 | a0001 | c0001 | t0021 | g0040 | AFR | ESN | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02976 | hp1 | a0001 | c0001 | t0015 | g0049 | AFR | ESN | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02976 | hp2 | a0001 | c0001 | t0011 | g0192 | AFR | ESN | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG03041 | hp1 | a0001 | c0001 | t0010 | g0155 | AFR | GWD | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG03041 | hp2 | a0001 | c0001 | t0016 | g0025 | AFR | GWD | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG03098 | hp1 | a0001 | c0001 | t0009 | g0183 | AFR | MSL | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG03098 | hp2 | a0001 | c0001 | t0010 | g0027 | AFR | MSL | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG03130 | hp1 | a0001 | c0001 | t0016 | g0025 | AFR | ESN | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0013 | AFR | ESN | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG03139 | hp1 | a0002 | c0002 | t0028 | g0110 | AFR | ESN | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG03139 | hp2 | a0001 | c0001 | t0012 | g0195 | AFR | ESN | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG03195 | hp1 | a0001 | c0001 | t0011 | g0020 | AFR | ESN | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG03195 | hp2 | a0001 | c0001 | t0004 | g0059 | AFR | ESN | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0032 | AFR | MSL | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG03209 | hp2 | a0001 | c0001 | t0041 | g0109 | AFR | MSL | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG03239 | hp1 | a0001 | c0001 | t0004 | g0150 | SAS | PJL | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG03239 | hp2 | a0001 | c0001 | t0005 | g0006 | SAS | PJL | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG03453 | hp1 | a0001 | c0001 | t0009 | g0051 | AFR | MSL | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG03453 | hp2 | a0002 | c0002 | t0027 | g0111 | AFR | MSL | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0013 | AFR | MSL | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG03486 | hp2 | a0002 | c0002 | t0029 | g0112 | AFR | MSL | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG03491 | hp2 | a0001 | c0001 | t0004 | g0007 | SAS | PJL | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0013 | AFR | GWD | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG03540 | hp2 | a0002 | c0002 | t0014 | g0019 | AFR | GWD | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG03579 | hp1 | a0001 | c0001 | t0012 | g0193 | AFR | MSL | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG03579 | hp2 | a0001 | c0001 | t0023 | g0184 | AFR | MSL | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG03654 | hp1 | a0001 | c0001 | t0004 | g0007 | SAS | PJL | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG03654 | hp2 | a0001 | c0001 | t0050 | g0138 | SAS | PJL | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG03688 | hp1 | a0001 | c0001 | t0005 | g0103 | SAS | STU | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG03688 | hp2 | a0001 | c0001 | t0004 | g0007 | SAS | STU | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG03704 | hp1 | a0001 | c0001 | t0009 | g0053 | SAS | PJL | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG03704 | hp2 | a0001 | c0001 | t0004 | g0015 | SAS | PJL | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG03710 | hp1 | a0001 | c0001 | t0052 | g0139 | SAS | PJL | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0003 | SAS | BEB | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | BEB | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG03834 | hp1 | a0001 | c0001 | t0005 | g0064 | SAS | BEB | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | BEB | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG03942 | hp1 | a0001 | c0001 | t0004 | g0127 | SAS | BEB | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | BEB | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG04115 | hp1 | a0001 | c0001 | t0004 | g0144 | SAS | STU | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | STU | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0028 | SAS | BEB | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG04184 | hp2 | a0001 | c0001 | t0004 | g0015 | SAS | BEB | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | STU | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG04199 | hp2 | a0001 | c0001 | t0004 | g0015 | SAS | STU | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG04204 | hp1 | a0001 | c0001 | t0005 | g0062 | SAS | STU | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | STU | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0128 | SAS | STU | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG04228 | hp2 | a0001 | c0001 | t0036 | g0174 | SAS | STU | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18522 | hp1 | a0001 | c0001 | t0044 | g0194 | AFR | YRI | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18522 | hp2 | a0001 | c0001 | t0011 | g0113 | AFR | YRI | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18612 | hp1 | a0001 | c0001 | t0003 | g0028 | EAS | CHB | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18612 | hp2 | a0001 | c0001 | t0008 | g0034 | EAS | CHB | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0160 | EAS | CHB | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0028 | EAS | CHB | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18946 | hp2 | a0001 | c0001 | t0003 | g0133 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18947 | hp1 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18948 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18949 | hp2 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18952 | hp2 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18953 | hp2 | a0001 | c0001 | t0008 | g0034 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18957 | hp1 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18960 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18960 | hp2 | a0001 | c0001 | t0006 | g0005 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18962 | hp1 | a0001 | c0001 | t0007 | g0022 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18962 | hp2 | a0001 | c0001 | t0013 | g0044 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18965 | hp1 | a0001 | c0001 | t0006 | g0005 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18965 | hp2 | a0001 | c0001 | t0004 | g0016 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18967 | hp1 | a0001 | c0001 | t0006 | g0005 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18979 | hp1 | a0001 | c0001 | t0008 | g0201 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18980 | hp2 | a0001 | c0001 | t0017 | g0041 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18981 | hp2 | a0001 | c0001 | t0007 | g0142 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18982 | hp1 | a0001 | c0001 | t0062 | g0202 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18983 | hp1 | a0001 | c0001 | t0008 | g0008 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18984 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18988 | hp1 | a0001 | c0001 | t0006 | g0005 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18989 | hp1 | a0001 | c0001 | t0008 | g0008 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18989 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18995 | hp1 | a0001 | c0001 | t0004 | g0047 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0147 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18999 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA19000 | hp2 | a0001 | c0001 | t0008 | g0034 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA19001 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA19004 | hp2 | a0001 | c0001 | t0008 | g0008 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA19007 | hp1 | a0001 | c0001 | t0007 | g0022 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA19009 | hp1 | a0001 | c0001 | t0006 | g0005 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA19009 | hp2 | a0001 | c0001 | t0048 | g0198 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA19010 | hp1 | a0001 | c0001 | t0047 | g0141 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA19012 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0032 | AFR | LWK | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA19030 | hp2 | a0001 | c0001 | t0038 | g0176 | AFR | LWK | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0030 | AFR | LWK | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | LWK | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA19054 | hp1 | a0001 | c0001 | t0007 | g0086 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA19058 | hp2 | a0005 | c0004 | t0001 | g0060 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA19060 | hp2 | a0001 | c0001 | t0017 | g0041 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA19063 | hp1 | a0001 | c0001 | t0032 | g0157 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA19064 | hp1 | a0001 | c0001 | t0006 | g0005 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA19066 | hp1 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA19066 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA19070 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA19074 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA19076 | hp1 | a0001 | c0001 | t0007 | g0022 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA19076 | hp2 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA19083 | hp1 | a0001 | c0001 | t0007 | g0122 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA19086 | hp1 | a0001 | c0001 | t0006 | g0005 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA19086 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA19087 | hp2 | a0001 | c0001 | t0053 | g0136 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA19088 | hp1 | a0001 | c0001 | t0017 | g0130 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA19089 | hp2 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA19091 | hp2 | a0001 | c0001 | t0006 | g0005 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0077 | AFR | YRI | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA19240 | hp2 | a0001 | c0001 | t0051 | g0135 | AFR | YRI | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA20752 | hp1 | a0001 | c0001 | t0004 | g0007 | EUR | TSI | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0018 | EUR | TSI | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG01123 | hp1 | a0001 | c0001 | t0020 | g0037 | AMR | CLM | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG01123 | hp2 | a0001 | c0001 | t0013 | g0149 | AMR | CLM | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0015 | AFR | ACB | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02109 | hp2 | a0001 | c0001 | t0012 | g0054 | AFR | ACB | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02486 | hp1 | a0001 | c0001 | t0058 | g0074 | AFR | ACB | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0030 | AFR | ACB | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02559 | hp1 | a0001 | c0001 | t0057 | g0187 | AFR | ACB | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG02559 | hp2 | a0002 | c0002 | t0014 | g0019 | AFR | ACB | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG03471 | hp1 | a0001 | c0001 | t0012 | g0105 | AFR | MSL | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG03471 | hp2 | a0001 | c0001 | t0011 | g0125 | AFR | MSL | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG06807 | hp1 | a0001 | c0001 | t0012 | g0054 | AFR | USA | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| HG06807 | hp2 | a0001 | c0001 | t0023 | g0179 | AFR | USA | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18955 | hp1 | a0001 | c0001 | t0013 | g0044 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA20300 | hp1 | a0001 | c0001 | t0009 | g0051 | AFR | USA | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA20300 | hp2 | a0001 | c0001 | t0009 | g0181 | AFR | USA | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA21309 | hp1 | a0003 | c0003 | t0033 | g0104 | AFR | LWK | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| NA21309 | hp2 | a0001 | c0001 | t0009 | g0180 | AFR | LWK | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0056 | g0140 | REF | REF | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0013 | REF | REF | SULT1B1_chr4_69716167_69765620 | SULT1B1 | chr4 | 69716167 | 69765620 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:69727197 | G | A | 1 | a0003 | 2 | HG01243.hp2 NA21309.hp1 |
missense_variant | MODERATE | c.782C>T | p.Thr261Met | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 988/7018 | 782/891 | 261/296 | chr4 | 69727197 | |||
| chr4:69730649 | T | A | 1 | a0004 | 1 | HG01884.hp2 | missense_variant | MODERATE | c.630A>T | p.Arg210Ser | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 7/8 | 836/7018 | 630/891 | 210/296 | chr4 | 69730649 | |||
| chr4:69734207 | A | C | 1 | a0002 | 7 | HG02559.hp2 HG02615.hp1 HG02970.hp1 others(4): Show |
missense_variant | MODERATE | c.433T>G | p.Leu145Val | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 5/8 | 639/7018 | 433/891 | 145/296 | chr4 | 69734207 | |||
| chr4:69754730 | C | T | 1 | a0005 | 1 | NA19058.hp2 | missense_variant | MODERATE | c.217G>A | p.Gly73Ser | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 3/8 | 423/7018 | 217/891 | 73/296 | chr4 | 69754730 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:69755206 | T | C | 1 | a0001c0006 | 1 | HG02083.hp2 | synonymous_variant | LOW | c.12A>G | p.Pro4Pro | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 2/8 | 218/7018 | 12/891 | 4/296 | chr4 | 69755206 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:69721295 | A | G | 4 | a0001c0001t0045 a0001c0001t0046 a0003c0003t0033 others(1): Show |
4 | HG01243.hp2 HG02572.hp2 HG02630.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5793T>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 5793 | chr4 | 69721295 | ||||||
| chr4:69721348 | G | T | 12 | a0001c0001t0002 a0001c0001t0032 a0001c0001t0034 others(9): Show |
89 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*5740C>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 5740 | chr4 | 69721348 | ||||||
| chr4:69721412 | C | T | 6 | a0001c0001t0009 a0001c0001t0023 a0001c0001t0057 others(3): Show |
16 | HG00099.hp2 HG01168.hp1 HG01358.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*5676G>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 5676 | chr4 | 69721412 | ||||||
| chr4:69721561 | C | A | 9 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0015 others(6): Show |
100 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*5527G>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 5527 | chr4 | 69721561 | ||||||
| chr4:69721578 | G | T | 1 | a0001c0001t0034 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5510C>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 5510 | chr4 | 69721578 | ||||||
| chr4:69721620 | A | G | 6 | a0001c0001t0009 a0001c0001t0023 a0001c0001t0057 others(3): Show |
16 | HG00099.hp2 HG01168.hp1 HG01358.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*5468T>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 5468 | chr4 | 69721620 | ||||||
| chr4:69721934 | A | T | 1 | a0001c0001t0061 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5154T>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 5154 | chr4 | 69721934 | ||||||
| chr4:69721966 | T | A | 1 | a0001c0001t0051 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5122A>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 5122 | chr4 | 69721966 | ||||||
| chr4:69721988 | G | C | 1 | a0001c0001t0054 | 1 | HG02071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5100C>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 5100 | chr4 | 69721988 | ||||||
| chr4:69722024 | A | G | 1 | a0001c0001t0045 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5064T>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 5064 | chr4 | 69722024 | ||||||
| chr4:69722035 | A | G | 1 | a0001c0001t0022 | 2 | HG01515.hp2 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5053T>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 5053 | chr4 | 69722035 | ||||||
| chr4:69722108 | T | C | 1 | a0001c0001t0039 | 1 | HG00280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4980A>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 4980 | chr4 | 69722108 | ||||||
| chr4:69722154 | C | T | 1 | a0001c0001t0032 | 1 | NA19063.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4934G>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 4934 | chr4 | 69722154 | ||||||
| chr4:69722176 | C | G | 1 | a0001c0001t0058 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4912G>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 4912 | chr4 | 69722176 | ||||||
| chr4:69722196 | C | G | 1 | a0001c0001t0034 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4892G>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 4892 | chr4 | 69722196 | ||||||
| chr4:69722285 | A | G | 1 | a0001c0001t0044 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4803T>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 4803 | chr4 | 69722285 | ||||||
| chr4:69722483 | G | T | 3 | a0001c0001t0007 a0001c0001t0047 a0001c0001t0048 |
14 | HG00609.hp1 HG00639.hp2 HG01070.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*4605C>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 4605 | chr4 | 69722483 | ||||||
| chr4:69722518 | T | A | 4 | a0001c0001t0045 a0001c0001t0046 a0003c0003t0033 others(1): Show |
4 | HG01243.hp2 HG02572.hp2 HG02630.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4570A>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 4570 | chr4 | 69722518 | ||||||
| chr4:69722591 | C | T | 8 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0022 others(5): Show |
52 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*4497G>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 4497 | chr4 | 69722591 | ||||||
| chr4:69722715 | G | A | 1 | a0001c0001t0062 | 1 | NA18982.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4373C>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 4373 | chr4 | 69722715 | ||||||
| chr4:69722728 | G | A | 1 | a0001c0001t0052 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4360C>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 4360 | chr4 | 69722728 | ||||||
| chr4:69722743 | T | C | 1 | a0001c0001t0016 | 3 | HG01943.hp2 HG03041.hp2 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4345A>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 4345 | chr4 | 69722743 | ||||||
| chr4:69722746 | C | T | 1 | a0004c0005t0043 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4342G>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 4342 | chr4 | 69722746 | ||||||
| chr4:69723007 | G | C | 7 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0019 others(4): Show |
96 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*4081C>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 4081 | chr4 | 69723007 | ||||||
| chr4:69723007 | G | T | 1 | a0001c0001t0025 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4081C>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 4081 | chr4 | 69723007 | ||||||
| chr4:69723023 | G | T | 12 | a0001c0001t0002 a0001c0001t0032 a0001c0001t0034 others(9): Show |
89 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*4065C>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 4065 | chr4 | 69723023 | ||||||
| chr4:69723027 | A | G | 1 | a0001c0001t0049 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4061T>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 4061 | chr4 | 69723027 | ||||||
| chr4:69723084 | C | G | 1 | a0004c0005t0043 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4004G>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 4004 | chr4 | 69723084 | ||||||
| chr4:69723112 | G | T | 4 | a0001c0001t0045 a0001c0001t0046 a0003c0003t0033 others(1): Show |
4 | HG01243.hp2 HG02572.hp2 HG02630.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3976C>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 3976 | chr4 | 69723112 | ||||||
| chr4:69723127 | A | G | 3 | a0001c0001t0021 a0001c0001t0041 a0001c0001t0042 |
4 | HG02258.hp2 HG02622.hp1 HG02970.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3961T>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 3961 | chr4 | 69723127 | ||||||
| chr4:69723205 | C | A | 6 | a0001c0001t0009 a0001c0001t0023 a0001c0001t0057 others(3): Show |
16 | HG00099.hp2 HG01168.hp1 HG01358.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*3883G>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 3883 | chr4 | 69723205 | ||||||
| chr4:69723324 | G | C | 7 | a0001c0001t0002 a0001c0001t0032 a0001c0006t0002 others(4): Show |
84 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*3764C>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 3764 | chr4 | 69723324 | ||||||
| chr4:69723338 | C | A | 1 | a0001c0001t0060 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3750G>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 3750 | chr4 | 69723338 | ||||||
| chr4:69723386 | G | T | 1 | a0001c0001t0050 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3702C>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 3702 | chr4 | 69723386 | ||||||
| chr4:69723492 | A | G | 1 | a0001c0001t0049 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3596T>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 3596 | chr4 | 69723492 | ||||||
| chr4:69723691 | T | C | 6 | a0001c0001t0009 a0001c0001t0023 a0001c0001t0057 others(3): Show |
16 | HG00099.hp2 HG01168.hp1 HG01358.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*3397A>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 3397 | chr4 | 69723691 | ||||||
| chr4:69723705 | T | G | 11 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0015 others(8): Show |
102 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*3383A>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 3383 | chr4 | 69723705 | ||||||
| chr4:69723716 | T | G | 1 | a0001c0001t0031 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3372A>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 3372 | chr4 | 69723716 | ||||||
| chr4:69723979 | G | A | 4 | a0001c0001t0045 a0001c0001t0046 a0003c0003t0033 others(1): Show |
4 | HG01243.hp2 HG02572.hp2 HG02630.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3109C>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 3109 | chr4 | 69723979 | ||||||
| chr4:69723979 | G | C | 3 | a0001c0001t0021 a0001c0001t0026 a0001c0001t0042 |
4 | HG01175.hp2 HG02258.hp2 HG02622.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3109C>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 3109 | chr4 | 69723979 | ||||||
| chr4:69724409 | A | G | 1 | a0003c0003t0033 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2679T>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 2679 | chr4 | 69724409 | ||||||
| chr4:69724420 | C | T | 1 | a0001c0001t0005 | 14 | HG00639.hp1 HG00738.hp2 HG01346.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2668G>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 2668 | chr4 | 69724420 | ||||||
| chr4:69724478 | A | G | 3 | a0001c0001t0012 a0001c0001t0044 a0004c0005t0043 |
8 | HG01884.hp2 HG02109.hp2 HG02572.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2610T>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 2610 | chr4 | 69724478 | ||||||
| chr4:69724519 | T | C | 1 | a0001c0001t0013 | 6 | HG01123.hp2 HG01433.hp2 HG02165.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2569A>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 2569 | chr4 | 69724519 | ||||||
| chr4:69724660 | G | A | 8 | a0001c0001t0006 a0001c0001t0008 a0001c0001t0036 others(5): Show |
31 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*2428C>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 2428 | chr4 | 69724660 | ||||||
| chr4:69724691 | G | C | 1 | a0001c0001t0053 | 1 | NA19087.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2397C>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 2397 | chr4 | 69724691 | ||||||
| chr4:69724697 | A | C | 7 | a0001c0001t0002 a0001c0001t0032 a0001c0006t0002 others(4): Show |
84 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*2391T>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 2391 | chr4 | 69724697 | ||||||
| chr4:69724704 | A | C | 1 | a0001c0001t0011 | 8 | HG01243.hp1 HG01891.hp2 HG02145.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2384T>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 2384 | chr4 | 69724704 | ||||||
| chr4:69724715 | T | C | 1 | a0001c0001t0054 | 1 | HG02071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2373A>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 2373 | chr4 | 69724715 | ||||||
| chr4:69724764 | A | G | 6 | a0001c0001t0009 a0001c0001t0023 a0001c0001t0057 others(3): Show |
16 | HG00099.hp2 HG01168.hp1 HG01358.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*2324T>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 2324 | chr4 | 69724764 | ||||||
| chr4:69724856 | A | G | 9 | a0001c0001t0006 a0001c0001t0008 a0001c0001t0036 others(6): Show |
32 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*2232T>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 2232 | chr4 | 69724856 | ||||||
| chr4:69725006 | C | A | 11 | a0001c0001t0002 a0001c0001t0032 a0001c0001t0034 others(8): Show |
88 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*2082G>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 2082 | chr4 | 69725006 | ||||||
| chr4:69725061 | AACTACCA others(20): Show |
A | 1 | a0001c0001t0011 | 8 | HG01243.hp1 HG01891.hp2 HG02145.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2000_*2026delAGGT others(23): Show |
SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 2000 | chr4 | 69725061 | ||||||
| chr4:69725073 | C | A | 3 | a0001c0001t0001 a0001c0001t0009 a0001c0001t0026 |
24 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*2015G>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 2015 | chr4 | 69725073 | ||||||
| chr4:69725089 | A | G | 1 | a0001c0001t0011 | 8 | HG01243.hp1 HG01891.hp2 HG02145.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1999T>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 1999 | chr4 | 69725089 | ||||||
| chr4:69725097 | G | A | 1 | a0001c0001t0010 | 8 | HG01891.hp1 HG02055.hp1 HG02615.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1991C>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 1991 | chr4 | 69725097 | ||||||
| chr4:69725154 | A | T | 1 | a0001c0001t0048 | 1 | NA19009.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1934T>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 1934 | chr4 | 69725154 | ||||||
| chr4:69725165 | A | T | 6 | a0001c0001t0009 a0001c0001t0023 a0001c0001t0057 others(3): Show |
16 | HG00099.hp2 HG01168.hp1 HG01358.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1923T>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 1923 | chr4 | 69725165 | ||||||
| chr4:69725166 | A | T | 6 | a0001c0001t0009 a0001c0001t0023 a0001c0001t0057 others(3): Show |
16 | HG00099.hp2 HG01168.hp1 HG01358.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1922T>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 1922 | chr4 | 69725166 | ||||||
| chr4:69725173 | A | C | 1 | a0001c0001t0019 | 2 | HG00280.hp2 HG01256.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1915T>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 1915 | chr4 | 69725173 | ||||||
| chr4:69725175 | G | GA | 5 | a0001c0001t0017 a0002c0002t0014 a0002c0002t0027 others(2): Show |
10 | HG02559.hp2 HG02615.hp1 HG02970.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1912dupT | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 1912 | chr4 | 69725175 | ||||||
| chr4:69725175 | GA | G | 1 | a0001c0001t0009 | 10 | HG00099.hp2 HG01168.hp1 HG01358.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1912delT | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 1912 | chr4 | 69725175 | ||||||
| chr4:69725192 | C | T | 12 | a0001c0001t0006 a0001c0001t0008 a0001c0001t0021 others(9): Show |
36 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*1896G>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 1896 | chr4 | 69725192 | ||||||
| chr4:69725242 | T | A | 2 | a0001c0001t0059 a0001c0001t0060 |
2 | HG02886.hp1 HG02965.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1846A>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 1846 | chr4 | 69725242 | ||||||
| chr4:69725292 | A | C | 1 | a0001c0001t0037 | 1 | HG00544.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1796T>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 1796 | chr4 | 69725292 | ||||||
| chr4:69725465 | A | G | 1 | a0001c0001t0047 | 1 | NA19010.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1623T>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 1623 | chr4 | 69725465 | ||||||
| chr4:69725539 | A | G | 1 | a0001c0001t0036 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1549T>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 1549 | chr4 | 69725539 | ||||||
| chr4:69725544 | T | A | 1 | a0001c0001t0042 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1544A>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 1544 | chr4 | 69725544 | ||||||
| chr4:69725626 | G | A | 1 | a0001c0001t0055 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1462C>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 1462 | chr4 | 69725626 | ||||||
| chr4:69725683 | G | C | 24 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(21): Show |
199 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(196): Show |
3_prime_UTR_variant | MODIFIER | c.*1405C>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 1405 | chr4 | 69725683 | ||||||
| chr4:69725711 | G | T | 4 | a0002c0002t0014 a0002c0002t0027 a0002c0002t0028 others(1): Show |
7 | HG02559.hp2 HG02615.hp1 HG02970.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1377C>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 1377 | chr4 | 69725711 | ||||||
| chr4:69725831 | T | C | 1 | a0001c0001t0018 | 3 | HG02258.hp1 HG02896.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1257A>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 1257 | chr4 | 69725831 | ||||||
| chr4:69725886 | G | T | 3 | a0001c0001t0012 a0001c0001t0044 a0004c0005t0043 |
8 | HG01884.hp2 HG02109.hp2 HG02572.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1202C>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 1202 | chr4 | 69725886 | ||||||
| chr4:69725927 | C | T | 1 | a0001c0001t0024 | 1 | HG01175.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1161G>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 1161 | chr4 | 69725927 | ||||||
| chr4:69725987 | A | G | 45 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(42): Show |
259 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(256): Show |
3_prime_UTR_variant | MODIFIER | c.*1101T>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 1101 | chr4 | 69725987 | ||||||
| chr4:69726030 | GTACATAT others(29): Show |
G | 12 | a0001c0001t0006 a0001c0001t0008 a0001c0001t0021 others(9): Show |
36 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*1022_*1057delTATA others(32): Show |
SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 1022 | chr4 | 69726030 | ||||||
| chr4:69726033 | C | CAT | 14 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(11): Show |
41 | HG00323.hp2 HG00438.hp1 HG00673.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*1053_*1054dupAT | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 1054 | chr4 | 69726033 | ||||||
| chr4:69726033 | C | CATAT | 11 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(8): Show |
38 | HG00099.hp1 HG00408.hp1 HG01123.hp2 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*1051_*1054dupATAT | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 1054 | chr4 | 69726033 | ||||||
| chr4:69726033 | C | CATATAT | 9 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(6): Show |
30 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*1049_*1054dupATAT others(2): Show |
SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 1054 | chr4 | 69726033 | ||||||
| chr4:69726033 | C | CATATATA others(1): Show |
7 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(4): Show |
23 | HG01081.hp1 HG01261.hp2 HG01496.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1047_*1054dupATAT others(4): Show |
SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 1054 | chr4 | 69726033 | ||||||
| chr4:69726033 | C | CATATATA others(3): Show |
4 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(1): Show |
8 | HG00735.hp2 HG02040.hp2 HG02145.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1045_*1054dupATAT others(6): Show |
SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 1054 | chr4 | 69726033 | ||||||
| chr4:69726033 | C | CATATATA others(5): Show |
4 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(1): Show |
6 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1043_*1054dupATAT others(8): Show |
SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 1054 | chr4 | 69726033 | ||||||
| chr4:69726033 | C | CATATATA others(9): Show |
1 | a0001c0001t0003 | 1 | HG02004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1039_*1054dupATAT others(12): Show |
SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 1054 | chr4 | 69726033 | ||||||
| chr4:69726033 | C | CATATATA others(11): Show |
2 | a0001c0001t0002 a0001c0001t0003 |
3 | HG02965.hp1 NA18983.hp2 NA19089.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1037_*1054dupATAT others(14): Show |
SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 1054 | chr4 | 69726033 | ||||||
| chr4:69726033 | C | T | 1 | a0001c0001t0003 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1055G>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 1055 | chr4 | 69726033 | ||||||
| chr4:69726033 | CAT | C | 8 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(5): Show |
35 | HG00597.hp2 HG00639.hp1 HG00738.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*1053_*1054delAT | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 1053 | chr4 | 69726033 | ||||||
| chr4:69726033 | CATAT | C | 9 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(6): Show |
26 | HG00423.hp1 HG00558.hp1 HG01109.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*1051_*1054delATAT | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 1051 | chr4 | 69726033 | ||||||
| chr4:69726033 | CATATAT | C | 7 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(4): Show |
8 | HG02055.hp2 HG02109.hp2 HG02132.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1049_*1054delATAT others(2): Show |
SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 1049 | chr4 | 69726033 | ||||||
| chr4:69726033 | CATATATA others(1): Show |
C | 5 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0007 others(2): Show |
12 | HG00099.hp2 HG00140.hp2 HG00741.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1047_*1054delATAT others(4): Show |
SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 1047 | chr4 | 69726033 | ||||||
| chr4:69726033 | CATATATA others(3): Show |
C | 4 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0007 others(1): Show |
12 | HG00438.hp2 HG00639.hp2 HG01069.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1045_*1054delATAT others(6): Show |
SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 1045 | chr4 | 69726033 | ||||||
| chr4:69726033 | CATATATA others(5): Show |
C | 5 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0007 others(2): Show |
13 | HG01070.hp2 HG01081.hp2 HG01192.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1043_*1054delATAT others(8): Show |
SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 1043 | chr4 | 69726033 | ||||||
| chr4:69726033 | CATATATA others(7): Show |
C | 3 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0007 |
3 | HG00609.hp1 HG04184.hp2 NA19085.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1041_*1054delATAT others(10): Show |
SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 1041 | chr4 | 69726033 | ||||||
| chr4:69726033 | CATATATA others(9): Show |
C | 2 | a0001c0001t0004 a0001c0001t0016 |
2 | HG03041.hp2 NA18965.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1039_*1054delATAT others(12): Show |
SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 1039 | chr4 | 69726033 | ||||||
| chr4:69726033 | CATATATA others(11): Show |
C | 2 | a0001c0001t0012 a0001c0001t0016 |
3 | HG01943.hp2 HG02572.hp1 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1037_*1054delATAT others(14): Show |
SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 1037 | chr4 | 69726033 | ||||||
| chr4:69726033 | CATATATA others(13): Show |
C | 3 | a0001c0001t0003 a0001c0001t0040 a0002c0002t0028 |
3 | HG02698.hp1 HG03139.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1035_*1054delATAT others(16): Show |
SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 1035 | chr4 | 69726033 | ||||||
| chr4:69726033 | CATATATA others(15): Show |
C | 4 | a0001c0001t0002 a0002c0002t0014 a0002c0002t0027 others(1): Show |
8 | HG00609.hp2 HG02015.hp1 HG02559.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1033_*1054delATAT others(18): Show |
SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 1033 | chr4 | 69726033 | ||||||
| chr4:69726033 | CATATATA others(17): Show |
C | 2 | a0001c0001t0003 a0001c0001t0011 |
7 | HG02976.hp2 NA18971.hp1 NA18979.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1031_*1054delATAT others(20): Show |
SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 1031 | chr4 | 69726033 | ||||||
| chr4:69726033 | CATATATA others(19): Show |
C | 1 | a0001c0001t0011 | 7 | HG01243.hp1 HG01891.hp2 HG02145.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1029_*1054delATAT others(22): Show |
SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 1029 | chr4 | 69726033 | ||||||
| chr4:69726033 | CATATATA others(21): Show |
C | 4 | a0001c0001t0045 a0001c0001t0046 a0003c0003t0033 others(1): Show |
4 | HG01243.hp2 HG02572.hp2 HG02630.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1027_*1054delATAT others(24): Show |
SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 1027 | chr4 | 69726033 | ||||||
| chr4:69726033 | CATATATA others(25): Show |
C | 1 | a0001c0001t0004 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1023_*1054delATAT others(28): Show |
SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 1023 | chr4 | 69726033 | ||||||
| chr4:69726082 | A | ATATATAT others(6): Show |
1 | a0001c0001t0013 | 1 | HG02293.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1005_*1006insATAT others(9): Show |
SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 1005 | chr4 | 69726082 | ||||||
| chr4:69726083 | A | T | 1 | a0001c0001t0057 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1005T>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 1005 | chr4 | 69726083 | ||||||
| chr4:69726116 | C | T | 2 | a0001c0001t0019 a0001c0001t0020 |
4 | HG00280.hp2 HG00735.hp1 HG01123.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*972G>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 972 | chr4 | 69726116 | ||||||
| chr4:69726234 | T | C | 1 | a0001c0001t0011 | 8 | HG01243.hp1 HG01891.hp2 HG02145.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*854A>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 854 | chr4 | 69726234 | ||||||
| chr4:69726238 | A | T | 1 | a0002c0002t0014 | 4 | HG02559.hp2 HG02615.hp1 HG02970.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*850T>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 850 | chr4 | 69726238 | ||||||
| chr4:69726264 | A | G | 1 | a0001c0001t0040 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*824T>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 824 | chr4 | 69726264 | ||||||
| chr4:69726509 | A | T | 1 | a0002c0002t0027 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*579T>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 579 | chr4 | 69726509 | ||||||
| chr4:69726524 | G | T | 8 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0019 others(5): Show |
97 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*564C>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 564 | chr4 | 69726524 | ||||||
| chr4:69726642 | A | C | 9 | a0001c0001t0006 a0001c0001t0008 a0001c0001t0036 others(6): Show |
32 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*446T>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 446 | chr4 | 69726642 | ||||||
| chr4:69726886 | T | A | 6 | a0001c0001t0009 a0001c0001t0023 a0001c0001t0057 others(3): Show |
16 | HG00099.hp2 HG01168.hp1 HG01358.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*202A>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 202 | chr4 | 69726886 | ||||||
| chr4:69726920 | A | C | 9 | a0001c0001t0006 a0001c0001t0008 a0001c0001t0036 others(6): Show |
32 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*168T>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 168 | chr4 | 69726920 | ||||||
| chr4:69726939 | G | A | 1 | a0001c0001t0063 | 1 | HG02135.hp1 | 3_prime_UTR_variant | MODIFIER | c.*149C>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 149 | chr4 | 69726939 | ||||||
| chr4:69727072 | G | T | 21 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(18): Show |
189 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(186): Show |
3_prime_UTR_variant | MODIFIER | c.*16C>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 8/8 | 16 | chr4 | 69727072 | ||||||
| chr4:69760484 | T | C | 4 | a0001c0001t0008 a0001c0001t0061 a0001c0001t0062 others(1): Show |
14 | HG01361.hp2 HG01928.hp1 HG01952.hp1 others(11): Show |
5_prime_UTR_variant | MODIFIER | c.-70A>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 1/8 | 5267 | chr4 | 69760484 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:69727236 | A | G | 2 | a0001c0001t0011g0125 a0001c0001t0011g0129 |
2 | HG02717.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.779-36T>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 7/7 | chr4 | 69727236 | |||||||
| chr4:69727270 | G | A | 2 | a0003c0003t0033g0104 a0003c0003t0035g0108 |
2 | HG01243.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.779-70C>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 7/7 | chr4 | 69727270 | |||||||
| chr4:69727371 | T | A | 90 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(87): Show |
197 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.779-171A>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 7/7 | chr4 | 69727371 | |||||||
| chr4:69727560 | TAGTC | T | 29 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0017 others(26): Show |
87 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.779-364_779-361del others(4): Show |
SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 7/7 | chr4 | 69727560 | |||||||
| chr4:69727622 | G | A | 3 | a0001c0001t0034g0106 a0003c0003t0033g0104 a0003c0003t0035g0108 |
3 | HG01243.hp2 HG02818.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.779-422C>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 7/7 | chr4 | 69727622 | |||||||
| chr4:69727699 | G | A | 1 | a0004c0005t0043g0191 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.779-499C>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 7/7 | chr4 | 69727699 | |||||||
| chr4:69727829 | A | G | 2 | a0001c0001t0001g0082 a0005c0004t0001g0060 |
2 | NA19010.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.779-629T>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 7/7 | chr4 | 69727829 | |||||||
| chr4:69727875 | T | C | 10 | a0001c0001t0009g0051 a0001c0001t0009g0183 a0001c0001t0023g0179 others(7): Show |
11 | HG02486.hp1 HG02559.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.779-675A>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 7/7 | chr4 | 69727875 | |||||||
| chr4:69727899 | T | C | 1 | a0001c0001t0001g0085 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.779-699A>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 7/7 | chr4 | 69727899 | |||||||
| chr4:69727987 | T | A | 7 | a0001c0001t0012g0054 a0001c0001t0012g0105 a0001c0001t0012g0190 others(4): Show |
8 | HG01884.hp2 HG02109.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.779-787A>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 7/7 | chr4 | 69727987 | |||||||
| chr4:69728358 | A | T | 56 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(53): Show |
102 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.779-1158T>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 7/7 | chr4 | 69728358 | |||||||
| chr4:69728366 | T | G | 1 | a0001c0001t0055g0120 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.779-1166A>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 7/7 | chr4 | 69728366 | |||||||
| chr4:69728600 | C | T | 3 | a0001c0001t0034g0106 a0003c0003t0033g0104 a0003c0003t0035g0108 |
3 | HG01243.hp2 HG02818.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.779-1400G>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 7/7 | chr4 | 69728600 | |||||||
| chr4:69728635 | G | GGGAA | 23 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0017 others(20): Show |
78 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(75): Show |
intron_variant | MODIFIER | c.779-1439_779-1436d others(6): Show |
SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 7/7 | chr4 | 69728635 | |||||||
| chr4:69728635 | G | GGGAAGGA others(5): Show |
4 | a0001c0001t0010g0021 a0001c0001t0010g0027 a0001c0001t0010g0155 others(1): Show |
9 | HG01891.hp1 HG02055.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.779-1447_779-1436d others(14): Show |
SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 7/7 | chr4 | 69728635 | |||||||
| chr4:69728700 | T | C | 1 | a0001c0001t0001g0094 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.779-1500A>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 7/7 | chr4 | 69728700 | |||||||
| chr4:69728703 | T | G | 1 | a0001c0001t0001g0092 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.779-1503A>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 7/7 | chr4 | 69728703 | |||||||
| chr4:69728752 | G | C | 1 | a0001c0001t0058g0074 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.779-1552C>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 7/7 | chr4 | 69728752 | |||||||
| chr4:69728802 | T | C | 1 | a0001c0001t0005g0062 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.779-1602A>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 7/7 | chr4 | 69728802 | |||||||
| chr4:69728802 | T | G | 55 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(52): Show |
101 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.779-1602A>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 7/7 | chr4 | 69728802 | |||||||
| chr4:69728807 | A | G | 1 | a0001c0001t0037g0173 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.779-1607T>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 7/7 | chr4 | 69728807 | |||||||
| chr4:69728889 | C | A | 1 | a0001c0001t0016g0025 | 3 | HG01943.hp2 HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.778+1612G>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 7/7 | chr4 | 69728889 | |||||||
| chr4:69728913 | G | A | 1 | a0001c0001t0009g0051 | 2 | HG03453.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.778+1588C>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 7/7 | chr4 | 69728913 | |||||||
| chr4:69728944 | A | G | 5 | a0001c0001t0034g0106 a0001c0001t0045g0188 a0001c0001t0046g0189 others(2): Show |
5 | HG01243.hp2 HG02572.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.778+1557T>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 7/7 | chr4 | 69728944 | |||||||
| chr4:69729112 | A | G | 26 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0017 others(23): Show |
84 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.778+1389T>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 7/7 | chr4 | 69729112 | |||||||
| chr4:69729141 | C | T | 2 | a0001c0001t0021g0040 a0001c0001t0042g0107 |
3 | HG02258.hp2 HG02622.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.778+1360G>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 7/7 | chr4 | 69729141 | |||||||
| chr4:69729289 | A | G | 4 | a0001c0001t0015g0049 a0001c0001t0015g0078 a0001c0001t0030g0075 others(1): Show |
5 | HG01109.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.778+1212T>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 7/7 | chr4 | 69729289 | |||||||
| chr4:69729349 | G | C | 1 | a0003c0003t0033g0104 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.778+1152C>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 7/7 | chr4 | 69729349 | |||||||
| chr4:69729435 | C | T | 1 | a0001c0001t0003g0124 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.778+1066G>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 7/7 | chr4 | 69729435 | |||||||
| chr4:69729466 | T | C | 56 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(53): Show |
102 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.778+1035A>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 7/7 | chr4 | 69729466 | |||||||
| chr4:69729662 | A | G | 1 | a0001c0001t0001g0069 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.778+839T>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 7/7 | chr4 | 69729662 | |||||||
| chr4:69729727 | C | A | 1 | a0001c0001t0001g0038 | 2 | NA18987.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.778+774G>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 7/7 | chr4 | 69729727 | |||||||
| chr4:69729768 | C | G | 16 | a0001c0001t0003g0028 a0001c0001t0003g0031 a0001c0001t0003g0032 others(13): Show |
26 | HG01123.hp2 HG01433.hp2 HG02145.hp1 others(23): Show |
intron_variant | MODIFIER | c.778+733G>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 7/7 | chr4 | 69729768 | |||||||
| chr4:69729797 | C | A | 1 | a0001c0001t0003g0132 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.778+704G>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 7/7 | chr4 | 69729797 | |||||||
| chr4:69729799 | T | C | 1 | a0004c0005t0043g0191 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.778+702A>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 7/7 | chr4 | 69729799 | |||||||
| chr4:69729896 | A | G | 1 | a0001c0001t0046g0189 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.778+605T>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 7/7 | chr4 | 69729896 | |||||||
| chr4:69729919 | C | T | 16 | a0001c0001t0002g0001 a0001c0001t0002g0023 a0001c0001t0002g0033 others(13): Show |
61 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.778+582G>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 7/7 | chr4 | 69729919 | |||||||
| chr4:69730191 | G | C | 1 | a0001c0001t0003g0123 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.778+310C>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 7/7 | chr4 | 69730191 | |||||||
| chr4:69730371 | T | C | 1 | a0001c0001t0003g0042 | 2 | NA18957.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.778+130A>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 7/7 | chr4 | 69730371 | |||||||
| chr4:69730468 | C | T | 3 | a0001c0001t0012g0054 a0001c0001t0012g0105 a0001c0001t0044g0194 |
4 | HG02109.hp2 HG03471.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.778+33G>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 7/7 | chr4 | 69730468 | |||||||
| chr4:69730475 | G | A | 1 | a0001c0001t0004g0117 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.778+26C>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 7/7 | chr4 | 69730475 | |||||||
| chr4:69730496 | T | G | 2 | a0001c0001t0001g0082 a0005c0004t0001g0060 |
2 | NA19010.hp2 NA19058.hp2 |
splice_region_variant&intron_variant | LOW | c.778+5A>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 7/7 | chr4 | 69730496 | |||||||
| chr4:69730938 | A | G | 8 | a0001c0001t0009g0051 a0001c0001t0009g0183 a0001c0001t0023g0179 others(5): Show |
9 | HG02486.hp1 HG02559.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.598-257T>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 6/7 | chr4 | 69730938 | |||||||
| chr4:69730945 | G | A | 56 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(53): Show |
102 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.598-264C>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 6/7 | chr4 | 69730945 | |||||||
| chr4:69730965 | G | A | 2 | a0001c0001t0045g0188 a0001c0001t0046g0189 |
2 | HG02572.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.598-284C>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 6/7 | chr4 | 69730965 | |||||||
| chr4:69730967 | G | A | 1 | a0001c0001t0057g0187 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.598-286C>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 6/7 | chr4 | 69730967 | |||||||
| chr4:69731009 | T | C | 199 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(196): Show |
401 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(398): Show |
intron_variant | MODIFIER | c.598-328A>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 6/7 | chr4 | 69731009 | |||||||
| chr4:69731116 | G | A | 8 | a0001c0001t0009g0051 a0001c0001t0009g0183 a0001c0001t0023g0179 others(5): Show |
9 | HG02486.hp1 HG02559.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.598-435C>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 6/7 | chr4 | 69731116 | |||||||
| chr4:69731148 | A | G | 2 | a0001c0001t0005g0064 a0001c0001t0005g0178 |
2 | HG00738.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.598-467T>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 6/7 | chr4 | 69731148 | |||||||
| chr4:69731159 | A | G | 1 | a0001c0001t0001g0089 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.598-478T>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 6/7 | chr4 | 69731159 | |||||||
| chr4:69731259 | G | A | 55 | a0001c0001t0003g0003 a0001c0001t0003g0010 a0001c0001t0003g0012 others(52): Show |
116 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(113): Show |
intron_variant | MODIFIER | c.598-578C>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 6/7 | chr4 | 69731259 | |||||||
| chr4:69731313 | C | T | 1 | a0001c0001t0002g0161 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.598-632G>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 6/7 | chr4 | 69731313 | |||||||
| chr4:69731363 | G | A | 26 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0017 others(23): Show |
84 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.598-682C>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 6/7 | chr4 | 69731363 | |||||||
| chr4:69731423 | T | C | 56 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(53): Show |
102 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.598-742A>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 6/7 | chr4 | 69731423 | |||||||
| chr4:69731468 | A | G | 1 | a0001c0001t0041g0109 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.598-787T>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 6/7 | chr4 | 69731468 | |||||||
| chr4:69731483 | T | C | 1 | a0001c0001t0001g0083 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.598-802A>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 6/7 | chr4 | 69731483 | |||||||
| chr4:69731662 | C | T | 56 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(53): Show |
102 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.598-981G>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 6/7 | chr4 | 69731662 | |||||||
| chr4:69731663 | T | C | 2 | a0001c0001t0045g0188 a0001c0001t0046g0189 |
2 | HG02572.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.598-982A>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 6/7 | chr4 | 69731663 | |||||||
| chr4:69732021 | G | T | 1 | a0001c0001t0003g0197 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.598-1340C>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 6/7 | chr4 | 69732021 | |||||||
| chr4:69732084 | C | T | 1 | a0001c0001t0012g0190 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.597+1329G>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 6/7 | chr4 | 69732084 | |||||||
| chr4:69732393 | T | C | 1 | a0003c0003t0033g0104 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.597+1020A>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 6/7 | chr4 | 69732393 | |||||||
| chr4:69732400 | G | A | 1 | a0001c0001t0034g0106 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.597+1013C>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 6/7 | chr4 | 69732400 | |||||||
| chr4:69732418 | T | G | 1 | a0001c0001t0058g0074 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.597+995A>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 6/7 | chr4 | 69732418 | |||||||
| chr4:69732487 | CCT | C | 7 | a0001c0001t0012g0054 a0001c0001t0012g0105 a0001c0001t0012g0190 others(4): Show |
8 | HG01884.hp2 HG02109.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.597+924_597+925del others(2): Show |
SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 6/7 | chr4 | 69732487 | |||||||
| chr4:69732534 | A | G | 10 | a0001c0001t0009g0051 a0001c0001t0009g0183 a0001c0001t0023g0179 others(7): Show |
11 | HG02486.hp1 HG02559.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.597+879T>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 6/7 | chr4 | 69732534 | |||||||
| chr4:69732668 | A | G | 5 | a0001c0001t0011g0020 a0001c0001t0011g0113 a0001c0001t0011g0125 others(2): Show |
8 | HG01243.hp1 HG01891.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.597+745T>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 6/7 | chr4 | 69732668 | |||||||
| chr4:69732803 | A | T | 1 | a0001c0001t0002g0160 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.597+610T>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 6/7 | chr4 | 69732803 | |||||||
| chr4:69732876 | T | C | 1 | a0001c0001t0063g0200 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.597+537A>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 6/7 | chr4 | 69732876 | |||||||
| chr4:69733211 | G | C | 1 | a0001c0001t0007g0142 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.597+202C>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 6/7 | chr4 | 69733211 | |||||||
| chr4:69733329 | A | G | 1 | a0001c0001t0008g0034 | 3 | NA18612.hp2 NA18953.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.597+84T>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 6/7 | chr4 | 69733329 | |||||||
| chr4:69733355 | C | T | 88 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(85): Show |
193 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.597+58G>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 6/7 | chr4 | 69733355 | |||||||
| chr4:69733522 | A | G | 13 | a0001c0001t0006g0005 a0001c0001t0006g0171 a0001c0001t0006g0172 others(10): Show |
32 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(29): Show |
intron_variant | MODIFIER | c.503-15T>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 5/7 | chr4 | 69733522 | |||||||
| chr4:69733526 | C | A | 1 | a0001c0001t0001g0091 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.503-19G>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 5/7 | chr4 | 69733526 | |||||||
| chr4:69733563 | T | C | 1 | a0001c0001t0003g0045 | 2 | NA18954.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.503-56A>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 5/7 | chr4 | 69733563 | |||||||
| chr4:69733668 | T | C | 57 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(54): Show |
103 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.503-161A>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 5/7 | chr4 | 69733668 | |||||||
| chr4:69733678 | A | G | 57 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(54): Show |
103 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.503-171T>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 5/7 | chr4 | 69733678 | |||||||
| chr4:69733708 | A | G | 2 | a0001c0001t0011g0125 a0001c0001t0011g0129 |
2 | HG02717.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.503-201T>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 5/7 | chr4 | 69733708 | |||||||
| chr4:69733720 | A | G | 1 | a0001c0001t0001g0092 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.503-213T>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 5/7 | chr4 | 69733720 | |||||||
| chr4:69733793 | C | A | 1 | a0001c0001t0010g0027 | 3 | HG02630.hp2 HG02717.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.503-286G>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 5/7 | chr4 | 69733793 | |||||||
| chr4:69733902 | C | T | 1 | a0001c0001t0023g0184 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.502+236G>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 5/7 | chr4 | 69733902 | |||||||
| chr4:69733927 | A | C | 1 | a0001c0001t0002g0167 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.502+211T>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 5/7 | chr4 | 69733927 | |||||||
| chr4:69734059 | T | G | 5 | a0001c0001t0011g0020 a0001c0001t0011g0113 a0001c0001t0011g0125 others(2): Show |
8 | HG01243.hp1 HG01891.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.502+79A>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 5/7 | chr4 | 69734059 | |||||||
| chr4:69734449 | C | T | 3 | a0001c0001t0011g0020 a0001c0001t0011g0113 a0001c0001t0011g0192 |
6 | HG01243.hp1 HG01891.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.376-185G>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69734449 | |||||||
| chr4:69734481 | C | G | 122 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(119): Show |
251 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.376-217G>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69734481 | |||||||
| chr4:69734494 | A | T | 1 | a0001c0001t0003g0121 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.376-230T>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69734494 | |||||||
| chr4:69734538 | C | T | 4 | a0001c0001t0009g0052 a0001c0001t0009g0053 a0001c0001t0009g0180 others(1): Show |
6 | HG00099.hp2 HG01168.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.376-274G>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69734538 | |||||||
| chr4:69734657 | A | T | 14 | a0001c0001t0006g0005 a0001c0001t0006g0171 a0001c0001t0006g0172 others(11): Show |
33 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(30): Show |
intron_variant | MODIFIER | c.376-393T>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69734657 | |||||||
| chr4:69734828 | C | CT | 40 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0002g0001 others(37): Show |
113 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.376-565dupA | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69734828 | |||||||
| chr4:69734828 | C | CTT | 63 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0024 others(60): Show |
109 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.376-566_376-565dup others(2): Show |
SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69734828 | |||||||
| chr4:69734828 | C | CTTT | 19 | a0001c0001t0001g0009 a0001c0001t0001g0071 a0001c0001t0001g0073 others(16): Show |
28 | HG00558.hp1 HG01243.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.376-567_376-565dup others(3): Show |
SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69734828 | |||||||
| chr4:69734879 | T | C | 1 | a0001c0001t0003g0026 | 3 | NA18947.hp1 NA18949.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.376-615A>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69734879 | |||||||
| chr4:69734953 | T | G | 1 | a0001c0001t0003g0146 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.376-689A>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69734953 | |||||||
| chr4:69734964 | G | A | 6 | a0001c0001t0009g0052 a0001c0001t0009g0053 a0001c0001t0009g0180 others(3): Show |
8 | HG00099.hp2 HG01168.hp1 HG01358.hp2 others(5): Show |
intron_variant | MODIFIER | c.376-700C>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69734964 | |||||||
| chr4:69734974 | A | G | 1 | a0001c0001t0003g0119 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.376-710T>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69734974 | |||||||
| chr4:69734991 | T | C | 1 | a0001c0001t0015g0078 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.376-727A>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69734991 | |||||||
| chr4:69735020 | A | G | 123 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(120): Show |
252 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.376-756T>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69735020 | |||||||
| chr4:69735061 | G | A | 1 | a0001c0001t0003g0152 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.376-797C>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69735061 | |||||||
| chr4:69735125 | T | A | 3 | a0001c0001t0021g0040 a0001c0001t0034g0106 a0001c0001t0042g0107 |
4 | HG02258.hp2 HG02622.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.376-861A>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69735125 | |||||||
| chr4:69735156 | T | C | 1 | a0001c0001t0038g0176 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.376-892A>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69735156 | |||||||
| chr4:69735264 | G | C | 1 | a0001c0001t0044g0194 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.376-1000C>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69735264 | |||||||
| chr4:69735430 | T | G | 1 | a0001c0001t0001g0038 | 2 | NA18987.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.376-1166A>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69735430 | |||||||
| chr4:69735474 | A | C | 180 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(177): Show |
370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.376-1210T>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69735474 | |||||||
| chr4:69735489 | C | T | 2 | a0001c0001t0011g0020 a0001c0001t0011g0113 |
5 | HG01243.hp1 HG01891.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.376-1225G>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69735489 | |||||||
| chr4:69735566 | C | T | 32 | a0001c0001t0003g0128 a0001c0001t0004g0007 a0001c0001t0004g0015 others(29): Show |
53 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.376-1302G>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69735566 | |||||||
| chr4:69735572 | C | T | 7 | a0001c0001t0012g0054 a0001c0001t0012g0105 a0001c0001t0012g0190 others(4): Show |
8 | HG01884.hp2 HG02109.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.376-1308G>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69735572 | |||||||
| chr4:69735608 | T | C | 101 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(98): Show |
210 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.376-1344A>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69735608 | |||||||
| chr4:69736032 | T | C | 13 | a0001c0001t0004g0016 a0001c0001t0004g0047 a0001c0001t0004g0145 others(10): Show |
22 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.376-1768A>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69736032 | |||||||
| chr4:69736352 | C | T | 1 | a0003c0003t0033g0104 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.376-2088G>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69736352 | |||||||
| chr4:69736443 | C | G | 1 | a0001c0001t0004g0126 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.376-2179G>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69736443 | |||||||
| chr4:69736482 | G | A | 2 | a0003c0003t0033g0104 a0003c0003t0035g0108 |
2 | HG01243.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.376-2218C>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69736482 | |||||||
| chr4:69736508 | C | T | 12 | a0001c0001t0006g0005 a0001c0001t0006g0171 a0001c0001t0006g0172 others(9): Show |
31 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(28): Show |
intron_variant | MODIFIER | c.376-2244G>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69736508 | |||||||
| chr4:69736626 | A | C | 1 | a0001c0001t0003g0133 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.376-2362T>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69736626 | |||||||
| chr4:69736670 | G | C | 13 | a0001c0001t0006g0005 a0001c0001t0006g0171 a0001c0001t0006g0172 others(10): Show |
32 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(29): Show |
intron_variant | MODIFIER | c.376-2406C>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69736670 | |||||||
| chr4:69736855 | G | A | 1 | a0001c0001t0057g0187 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.376-2591C>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69736855 | |||||||
| chr4:69737024 | GA | G | 6 | a0001c0001t0006g0005 a0001c0001t0006g0171 a0001c0001t0006g0172 others(3): Show |
17 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(14): Show |
intron_variant | MODIFIER | c.376-2761delT | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69737024 | |||||||
| chr4:69737122 | C | T | 59 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(56): Show |
105 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.376-2858G>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69737122 | |||||||
| chr4:69737158 | C | T | 6 | a0001c0001t0006g0005 a0001c0001t0006g0171 a0001c0001t0006g0172 others(3): Show |
17 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(14): Show |
intron_variant | MODIFIER | c.376-2894G>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69737158 | |||||||
| chr4:69737160 | T | A | 1 | a0001c0001t0041g0109 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.376-2896A>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69737160 | |||||||
| chr4:69737250 | A | G | 1 | a0001c0001t0001g0081 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.376-2986T>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69737250 | |||||||
| chr4:69737309 | A | T | 1 | a0001c0001t0004g0047 | 2 | HG00438.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.376-3045T>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69737309 | |||||||
| chr4:69737439 | A | G | 1 | a0001c0001t0002g0159 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.376-3175T>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69737439 | |||||||
| chr4:69737511 | C | G | 1 | a0001c0001t0038g0176 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.376-3247G>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69737511 | |||||||
| chr4:69737800 | T | C | 129 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(126): Show |
260 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.376-3536A>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69737800 | |||||||
| chr4:69737801 | G | A | 60 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(57): Show |
106 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.376-3537C>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69737801 | |||||||
| chr4:69737909 | G | A | 8 | a0001c0001t0003g0003 a0001c0001t0003g0010 a0001c0001t0003g0026 others(5): Show |
31 | HG01106.hp2 HG01261.hp1 HG01515.hp1 others(28): Show |
intron_variant | MODIFIER | c.376-3645C>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69737909 | |||||||
| chr4:69737909 | G | C | 1 | a0001c0001t0049g0153 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.376-3645C>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69737909 | |||||||
| chr4:69737933 | G | T | 1 | a0001c0001t0034g0106 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.376-3669C>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69737933 | |||||||
| chr4:69737983 | T | C | 1 | a0001c0001t0001g0087 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.376-3719A>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69737983 | |||||||
| chr4:69738156 | C | T | 1 | a0001c0001t0011g0125 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.376-3892G>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69738156 | |||||||
| chr4:69738201 | C | T | 1 | a0001c0001t0007g0046 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.376-3937G>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69738201 | |||||||
| chr4:69738254 | C | T | 1 | a0001c0001t0002g0158 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.376-3990G>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69738254 | |||||||
| chr4:69738261 | A | G | 4 | a0002c0002t0014g0019 a0002c0002t0027g0111 a0002c0002t0028g0110 others(1): Show |
7 | HG02559.hp2 HG02615.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.376-3997T>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69738261 | |||||||
| chr4:69738390 | C | A | 1 | a0001c0001t0005g0178 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.376-4126G>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69738390 | |||||||
| chr4:69738620 | A | G | 129 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(126): Show |
260 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.376-4356T>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69738620 | |||||||
| chr4:69738633 | T | C | 129 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(126): Show |
260 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.376-4369A>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69738633 | |||||||
| chr4:69738649 | T | G | 180 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(177): Show |
370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.376-4385A>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69738649 | |||||||
| chr4:69738652 | A | G | 1 | a0001c0001t0019g0080 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.376-4388T>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69738652 | |||||||
| chr4:69738721 | G | A | 1 | a0001c0001t0017g0130 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.376-4457C>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69738721 | |||||||
| chr4:69738798 | G | A | 115 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(112): Show |
243 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.376-4534C>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69738798 | |||||||
| chr4:69738808 | A | G | 21 | a0001c0001t0006g0005 a0001c0001t0006g0171 a0001c0001t0006g0172 others(18): Show |
41 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(38): Show |
intron_variant | MODIFIER | c.376-4544T>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69738808 | |||||||
| chr4:69738895 | T | C | 2 | a0001c0001t0002g0023 a0001c0001t0002g0163 |
5 | HG00597.hp2 HG02074.hp2 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.376-4631A>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69738895 | |||||||
| chr4:69738900 | A | G | 60 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(57): Show |
106 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.376-4636T>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69738900 | |||||||
| chr4:69738914 | A | G | 1 | a0001c0001t0013g0134 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.376-4650T>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69738914 | |||||||
| chr4:69738929 | C | A | 8 | a0001c0001t0001g0002 a0001c0001t0001g0079 a0001c0001t0001g0088 others(5): Show |
23 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(20): Show |
intron_variant | MODIFIER | c.376-4665G>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69738929 | |||||||
| chr4:69738993 | C | T | 1 | a0001c0001t0003g0123 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.376-4729G>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69738993 | |||||||
| chr4:69739007 | G | A | 2 | a0001c0001t0004g0116 a0001c0001t0004g0117 |
2 | HG01109.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.376-4743C>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69739007 | |||||||
| chr4:69739031 | C | T | 1 | a0001c0001t0006g0172 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.376-4767G>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69739031 | |||||||
| chr4:69739072 | G | A | 1 | a0001c0001t0012g0195 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.376-4808C>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69739072 | |||||||
| chr4:69739163 | G | T | 1 | a0001c0001t0011g0192 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.376-4899C>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69739163 | |||||||
| chr4:69739166 | C | G | 60 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(57): Show |
106 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.376-4902G>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69739166 | |||||||
| chr4:69739179 | G | C | 1 | a0001c0001t0001g0094 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.376-4915C>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69739179 | |||||||
| chr4:69739208 | G | T | 4 | a0002c0002t0014g0019 a0002c0002t0027g0111 a0002c0002t0028g0110 others(1): Show |
7 | HG02559.hp2 HG02615.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.376-4944C>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69739208 | |||||||
| chr4:69739288 | C | G | 54 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(51): Show |
99 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.376-5024G>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69739288 | |||||||
| chr4:69739327 | G | A | 2 | a0001c0001t0005g0064 a0001c0001t0005g0178 |
2 | HG00738.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.376-5063C>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69739327 | |||||||
| chr4:69739357 | A | C | 2 | a0001c0001t0011g0020 a0001c0001t0011g0113 |
5 | HG01243.hp1 HG01891.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.376-5093T>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69739357 | |||||||
| chr4:69739528 | T | G | 1 | a0001c0001t0038g0176 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.376-5264A>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69739528 | |||||||
| chr4:69739657 | A | G | 1 | a0001c0001t0010g0027 | 3 | HG02630.hp2 HG02717.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.376-5393T>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69739657 | |||||||
| chr4:69739918 | T | A | 3 | a0001c0001t0011g0020 a0001c0001t0011g0113 a0001c0001t0011g0192 |
6 | HG01243.hp1 HG01891.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.376-5654A>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69739918 | |||||||
| chr4:69740094 | G | A | 1 | a0001c0001t0041g0109 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.376-5830C>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69740094 | |||||||
| chr4:69740308 | A | G | 129 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(126): Show |
260 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.376-6044T>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69740308 | |||||||
| chr4:69740316 | A | G | 3 | a0001c0001t0011g0020 a0001c0001t0011g0113 a0001c0001t0011g0192 |
6 | HG01243.hp1 HG01891.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.376-6052T>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69740316 | |||||||
| chr4:69740650 | T | G | 1 | a0001c0001t0001g0093 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.376-6386A>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69740650 | |||||||
| chr4:69740662 | T | G | 2 | a0001c0001t0003g0014 a0001c0001t0003g0132 |
6 | HG00140.hp2 HG00733.hp2 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.376-6398A>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69740662 | |||||||
| chr4:69740805 | T | C | 129 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(126): Show |
260 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.376-6541A>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69740805 | |||||||
| chr4:69740860 | C | T | 2 | a0001c0001t0059g0185 a0001c0001t0060g0186 |
2 | HG02886.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.376-6596G>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69740860 | |||||||
| chr4:69740932 | C | G | 7 | a0001c0001t0012g0054 a0001c0001t0012g0105 a0001c0001t0012g0190 others(4): Show |
8 | HG01884.hp2 HG02109.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.376-6668G>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69740932 | |||||||
| chr4:69740972 | T | G | 60 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(57): Show |
106 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.376-6708A>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69740972 | |||||||
| chr4:69741363 | G | T | 1 | a0001c0001t0007g0122 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.376-7099C>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69741363 | |||||||
| chr4:69741413 | G | A | 20 | a0001c0001t0006g0005 a0001c0001t0006g0171 a0001c0001t0006g0172 others(17): Show |
40 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(37): Show |
intron_variant | MODIFIER | c.376-7149C>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69741413 | |||||||
| chr4:69741643 | T | G | 1 | a0001c0001t0038g0176 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.376-7379A>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69741643 | |||||||
| chr4:69741653 | G | A | 1 | a0001c0001t0007g0122 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.376-7389C>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69741653 | |||||||
| chr4:69741800 | C | G | 2 | a0001c0001t0001g0168 a0001c0001t0001g0169 |
2 | NA19005.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.376-7536G>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69741800 | |||||||
| chr4:69741805 | T | TA | 7 | a0001c0001t0012g0054 a0001c0001t0012g0105 a0001c0001t0012g0190 others(4): Show |
8 | HG01884.hp2 HG02109.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.376-7542dupT | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69741805 | |||||||
| chr4:69741933 | T | A | 1 | a0001c0001t0001g0095 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.376-7669A>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69741933 | |||||||
| chr4:69741977 | C | T | 12 | a0001c0001t0009g0051 a0001c0001t0009g0052 a0001c0001t0009g0053 others(9): Show |
15 | HG00099.hp2 HG01168.hp1 HG01358.hp2 others(12): Show |
intron_variant | MODIFIER | c.376-7713G>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69741977 | |||||||
| chr4:69742325 | G | A | 13 | a0001c0001t0006g0005 a0001c0001t0006g0171 a0001c0001t0006g0172 others(10): Show |
32 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(29): Show |
intron_variant | MODIFIER | c.375+7396C>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69742325 | |||||||
| chr4:69742425 | T | G | 2 | a0001c0001t0002g0011 a0001c0006t0002g0057 |
6 | HG00597.hp1 HG00673.hp2 HG02083.hp2 others(3): Show |
intron_variant | MODIFIER | c.375+7296A>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69742425 | |||||||
| chr4:69742727 | A | G | 1 | a0001c0001t0001g0079 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.375+6994T>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69742727 | |||||||
| chr4:69742728 | T | G | 16 | a0001c0001t0009g0051 a0001c0001t0009g0052 a0001c0001t0009g0053 others(13): Show |
19 | HG00099.hp2 HG01168.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.375+6993A>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69742728 | |||||||
| chr4:69742759 | G | A | 3 | a0001c0001t0021g0040 a0001c0001t0034g0106 a0001c0001t0042g0107 |
4 | HG02258.hp2 HG02622.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.375+6962C>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69742759 | |||||||
| chr4:69742816 | G | A | 1 | a0001c0001t0005g0065 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.375+6905C>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69742816 | |||||||
| chr4:69743061 | G | A | 2 | a0001c0001t0059g0185 a0001c0001t0060g0186 |
2 | HG02886.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.375+6660C>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69743061 | |||||||
| chr4:69743154 | C | T | 104 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(101): Show |
179 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.375+6567G>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69743154 | |||||||
| chr4:69743167 | C | T | 1 | a0001c0001t0003g0032 | 3 | HG02145.hp1 HG03209.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.375+6554G>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69743167 | |||||||
| chr4:69743188 | C | A | 3 | a0001c0001t0021g0040 a0001c0001t0034g0106 a0001c0001t0042g0107 |
4 | HG02258.hp2 HG02622.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.375+6533G>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69743188 | |||||||
| chr4:69743322 | T | C | 60 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(57): Show |
106 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.375+6399A>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69743322 | |||||||
| chr4:69743388 | G | A | 1 | a0001c0001t0001g0094 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.375+6333C>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69743388 | |||||||
| chr4:69743407 | G | T | 7 | a0001c0001t0012g0054 a0001c0001t0012g0105 a0001c0001t0012g0190 others(4): Show |
8 | HG01884.hp2 HG02109.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.375+6314C>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69743407 | |||||||
| chr4:69743471 | T | C | 14 | a0001c0001t0009g0051 a0001c0001t0009g0052 a0001c0001t0009g0053 others(11): Show |
17 | HG00099.hp2 HG01168.hp1 HG01358.hp2 others(14): Show |
intron_variant | MODIFIER | c.375+6250A>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69743471 | |||||||
| chr4:69743796 | G | A | 1 | a0001c0001t0004g0143 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.375+5925C>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69743796 | |||||||
| chr4:69743812 | G | A | 2 | a0003c0003t0033g0104 a0003c0003t0035g0108 |
2 | HG01243.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.375+5909C>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69743812 | |||||||
| chr4:69743857 | T | C | 1 | a0001c0001t0012g0195 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.375+5864A>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69743857 | |||||||
| chr4:69744071 | C | T | 2 | a0003c0003t0033g0104 a0003c0003t0035g0108 |
2 | HG01243.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.375+5650G>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69744071 | |||||||
| chr4:69744072 | G | A | 60 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(57): Show |
106 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.375+5649C>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69744072 | |||||||
| chr4:69744086 | G | C | 1 | a0001c0001t0009g0182 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.375+5635C>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69744086 | |||||||
| chr4:69744196 | C | T | 6 | a0001c0001t0006g0005 a0001c0001t0006g0171 a0001c0001t0006g0172 others(3): Show |
17 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(14): Show |
intron_variant | MODIFIER | c.375+5525G>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69744196 | |||||||
| chr4:69744229 | C | T | 13 | a0001c0001t0006g0005 a0001c0001t0006g0171 a0001c0001t0006g0172 others(10): Show |
32 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(29): Show |
intron_variant | MODIFIER | c.375+5492G>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69744229 | |||||||
| chr4:69744232 | G | A | 13 | a0001c0001t0006g0005 a0001c0001t0006g0171 a0001c0001t0006g0172 others(10): Show |
32 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(29): Show |
intron_variant | MODIFIER | c.375+5489C>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69744232 | |||||||
| chr4:69744291 | G | A | 2 | a0001c0001t0001g0095 a0001c0001t0001g0100 |
2 | HG03834.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.375+5430C>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69744291 | |||||||
| chr4:69744296 | C | T | 1 | a0004c0005t0043g0191 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.375+5425G>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69744296 | |||||||
| chr4:69744297 | G | C | 3 | a0001c0001t0021g0040 a0001c0001t0034g0106 a0001c0001t0042g0107 |
4 | HG02258.hp2 HG02622.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.375+5424C>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69744297 | |||||||
| chr4:69744374 | C | A | 1 | a0001c0001t0051g0135 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.375+5347G>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69744374 | |||||||
| chr4:69744439 | C | T | 1 | a0001c0001t0032g0157 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.375+5282G>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69744439 | |||||||
| chr4:69744464 | C | T | 6 | a0001c0001t0006g0005 a0001c0001t0006g0171 a0001c0001t0006g0172 others(3): Show |
17 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(14): Show |
intron_variant | MODIFIER | c.375+5257G>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69744464 | |||||||
| chr4:69744467 | G | T | 3 | a0001c0001t0021g0040 a0001c0001t0034g0106 a0001c0001t0042g0107 |
4 | HG02258.hp2 HG02622.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.375+5254C>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69744467 | |||||||
| chr4:69744522 | G | A | 12 | a0001c0001t0009g0051 a0001c0001t0009g0052 a0001c0001t0009g0053 others(9): Show |
15 | HG00099.hp2 HG01168.hp1 HG01358.hp2 others(12): Show |
intron_variant | MODIFIER | c.375+5199C>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69744522 | |||||||
| chr4:69744703 | G | A | 1 | a0001c0001t0009g0181 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.375+5018C>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69744703 | |||||||
| chr4:69744718 | G | A | 104 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(101): Show |
179 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.375+5003C>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69744718 | |||||||
| chr4:69744827 | T | C | 1 | a0001c0001t0011g0192 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.375+4894A>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69744827 | |||||||
| chr4:69744873 | C | A | 1 | a0001c0001t0003g0147 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.375+4848G>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69744873 | |||||||
| chr4:69744922 | T | C | 2 | a0003c0003t0033g0104 a0003c0003t0035g0108 |
2 | HG01243.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.375+4799A>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69744922 | |||||||
| chr4:69744946 | T | C | 5 | a0001c0001t0012g0054 a0001c0001t0012g0105 a0001c0001t0012g0193 others(2): Show |
6 | HG02109.hp2 HG03139.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.375+4775A>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69744946 | |||||||
| chr4:69744992 | A | G | 2 | a0001c0001t0007g0046 a0001c0001t0007g0137 |
3 | HG00639.hp2 HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.375+4729T>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69744992 | |||||||
| chr4:69745016 | ACTTCTGT others(23): Show |
A | 1 | a0001c0001t0004g0144 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.375+4675_375+4704d others(32): Show |
SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69745016 | |||||||
| chr4:69745051 | T | A | 1 | a0001c0001t0054g0131 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.375+4670A>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69745051 | |||||||
| chr4:69745070 | C | A | 54 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(51): Show |
99 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.375+4651G>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69745070 | |||||||
| chr4:69745126 | T | C | 22 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0017 others(19): Show |
77 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.375+4595A>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69745126 | |||||||
| chr4:69745401 | A | G | 84 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(81): Show |
139 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.375+4320T>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69745401 | |||||||
| chr4:69745405 | A | C | 1 | a0001c0001t0001g0072 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.375+4316T>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69745405 | |||||||
| chr4:69745520 | C | G | 1 | a0001c0001t0051g0135 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.375+4201G>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69745520 | |||||||
| chr4:69745597 | T | C | 60 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(57): Show |
106 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.375+4124A>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69745597 | |||||||
| chr4:69745741 | T | A | 2 | a0001c0001t0009g0053 a0001c0001t0009g0182 |
3 | HG00099.hp2 HG01433.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.375+3980A>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69745741 | |||||||
| chr4:69745754 | CT | C | 3 | a0001c0001t0008g0008 a0001c0001t0008g0034 a0001c0001t0062g0202 |
11 | HG01361.hp2 HG01928.hp1 HG01952.hp1 others(8): Show |
intron_variant | MODIFIER | c.375+3966delA | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69745754 | |||||||
| chr4:69745802 | G | C | 1 | a0001c0001t0001g0096 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.375+3919C>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69745802 | |||||||
| chr4:69746060 | C | G | 4 | a0002c0002t0014g0019 a0002c0002t0027g0111 a0002c0002t0028g0110 others(1): Show |
7 | HG02559.hp2 HG02615.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.375+3661G>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69746060 | |||||||
| chr4:69746082 | C | T | 1 | a0001c0001t0002g0170 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.375+3639G>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69746082 | |||||||
| chr4:69746104 | A | ATGTGTGG others(23): Show |
1 | a0001c0001t0004g0144 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.375+3616_375+3617i others(32): Show |
SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69746104 | |||||||
| chr4:69746107 | A | G | 1 | a0001c0001t0004g0144 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.375+3614T>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69746107 | |||||||
| chr4:69746108 | C | T | 1 | a0001c0001t0004g0144 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.375+3613G>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69746108 | |||||||
| chr4:69746109 | C | G | 1 | a0001c0001t0004g0144 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.375+3612G>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69746109 | |||||||
| chr4:69746112 | C | G | 1 | a0001c0001t0004g0144 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.375+3609G>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69746112 | |||||||
| chr4:69746113 | C | T | 1 | a0001c0001t0004g0144 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.375+3608G>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69746113 | |||||||
| chr4:69746114 | C | G | 1 | a0001c0001t0004g0144 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.375+3607G>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69746114 | |||||||
| chr4:69746115 | C | G | 1 | a0001c0001t0004g0144 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.375+3606G>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69746115 | |||||||
| chr4:69746117 | T | G | 1 | a0001c0001t0004g0144 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.375+3604A>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69746117 | |||||||
| chr4:69746119 | C | G | 1 | a0001c0001t0004g0144 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.375+3602G>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69746119 | |||||||
| chr4:69746121 | C | T | 1 | a0001c0001t0004g0144 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.375+3600G>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69746121 | |||||||
| chr4:69746122 | T | A | 1 | a0001c0001t0004g0144 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.375+3599A>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69746122 | |||||||
| chr4:69746242 | A | G | 104 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(101): Show |
179 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.375+3479T>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69746242 | |||||||
| chr4:69746450 | A | G | 1 | a0001c0001t0003g0133 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.375+3271T>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69746450 | |||||||
| chr4:69746574 | C | T | 60 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(57): Show |
106 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.375+3147G>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69746574 | |||||||
| chr4:69746587 | T | C | 1 | a0001c0001t0003g0121 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.375+3134A>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69746587 | |||||||
| chr4:69746589 | T | C | 1 | a0003c0003t0033g0104 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.375+3132A>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69746589 | |||||||
| chr4:69746611 | C | T | 3 | a0001c0001t0021g0040 a0001c0001t0034g0106 a0001c0001t0042g0107 |
4 | HG02258.hp2 HG02622.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.375+3110G>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69746611 | |||||||
| chr4:69746854 | T | C | 1 | a0001c0001t0003g0010 | 6 | NA18971.hp1 NA18979.hp2 NA19001.hp1 others(3): Show |
intron_variant | MODIFIER | c.375+2867A>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69746854 | |||||||
| chr4:69746928 | A | G | 1 | a0001c0001t0041g0109 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.375+2793T>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69746928 | |||||||
| chr4:69746994 | G | A | 60 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(57): Show |
106 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.375+2727C>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69746994 | |||||||
| chr4:69747144 | G | A | 1 | a0001c0001t0004g0145 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.375+2577C>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69747144 | |||||||
| chr4:69747257 | G | A | 14 | a0001c0001t0006g0005 a0001c0001t0006g0171 a0001c0001t0006g0172 others(11): Show |
33 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(30): Show |
intron_variant | MODIFIER | c.375+2464C>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69747257 | |||||||
| chr4:69747401 | G | A | 5 | a0001c0001t0003g0012 a0001c0001t0003g0014 a0001c0001t0003g0123 others(2): Show |
13 | HG00140.hp2 HG00733.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.375+2320C>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69747401 | |||||||
| chr4:69747412 | G | A | 4 | a0002c0002t0014g0019 a0002c0002t0027g0111 a0002c0002t0028g0110 others(1): Show |
7 | HG02559.hp2 HG02615.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.375+2309C>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69747412 | |||||||
| chr4:69747446 | T | C | 1 | a0001c0001t0012g0190 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.375+2275A>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69747446 | |||||||
| chr4:69747587 | A | C | 1 | a0001c0001t0001g0070 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.375+2134T>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69747587 | |||||||
| chr4:69747597 | G | A | 2 | a0001c0001t0001g0071 a0001c0001t0024g0068 |
2 | HG01175.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.375+2124C>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69747597 | |||||||
| chr4:69747600 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.375+2121C>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69747600 | |||||||
| chr4:69747662 | G | A | 3 | a0002c0002t0014g0019 a0002c0002t0028g0110 a0002c0002t0029g0112 |
6 | HG02559.hp2 HG02615.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.375+2059C>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69747662 | |||||||
| chr4:69747664 | G | A | 6 | a0001c0001t0011g0192 a0001c0001t0012g0054 a0001c0001t0012g0105 others(3): Show |
7 | HG02109.hp2 HG02976.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.375+2057C>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69747664 | |||||||
| chr4:69747709 | G | A | 1 | a0001c0001t0001g0097 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.375+2012C>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69747709 | |||||||
| chr4:69747816 | C | T | 1 | a0001c0001t0049g0153 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.375+1905G>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69747816 | |||||||
| chr4:69747837 | T | C | 13 | a0001c0001t0006g0005 a0001c0001t0006g0171 a0001c0001t0006g0172 others(10): Show |
32 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(29): Show |
intron_variant | MODIFIER | c.375+1884A>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69747837 | |||||||
| chr4:69747840 | T | A | 2 | a0001c0001t0002g0033 a0001c0001t0032g0157 |
4 | HG02155.hp2 NA19007.hp2 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.375+1881A>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69747840 | |||||||
| chr4:69747861 | A | G | 60 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(57): Show |
106 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.375+1860T>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69747861 | |||||||
| chr4:69747895 | G | T | 16 | a0001c0001t0009g0051 a0001c0001t0009g0052 a0001c0001t0009g0053 others(13): Show |
19 | HG00099.hp2 HG01168.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.375+1826C>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69747895 | |||||||
| chr4:69747987 | G | T | 6 | a0001c0001t0003g0077 a0001c0001t0015g0049 a0001c0001t0015g0078 others(3): Show |
7 | HG01109.hp1 HG02451.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.375+1734C>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69747987 | |||||||
| chr4:69748136 | A | G | 1 | a0001c0001t0001g0073 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.375+1585T>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69748136 | |||||||
| chr4:69748467 | C | A | 1 | a0003c0003t0033g0104 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.375+1254G>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69748467 | |||||||
| chr4:69748541 | G | A | 104 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(101): Show |
179 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.375+1180C>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69748541 | |||||||
| chr4:69748675 | C | T | 2 | a0001c0001t0001g0036 a0001c0001t0001g0072 |
3 | HG02135.hp2 NA18977.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.375+1046G>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69748675 | |||||||
| chr4:69748887 | A | G | 1 | a0001c0001t0009g0182 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.375+834T>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69748887 | |||||||
| chr4:69749065 | C | T | 1 | a0001c0001t0001g0071 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.375+656G>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69749065 | |||||||
| chr4:69749080 | A | C | 2 | a0001c0001t0003g0012 a0001c0001t0003g0123 |
6 | HG02155.hp1 NA18960.hp1 NA18984.hp1 others(3): Show |
intron_variant | MODIFIER | c.375+641T>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69749080 | |||||||
| chr4:69749104 | C | T | 1 | a0001c0001t0001g0070 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.375+617G>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69749104 | |||||||
| chr4:69749327 | T | G | 21 | a0001c0001t0006g0005 a0001c0001t0006g0171 a0001c0001t0006g0172 others(18): Show |
41 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(38): Show |
intron_variant | MODIFIER | c.375+394A>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69749327 | |||||||
| chr4:69749358 | A | G | 2 | a0001c0001t0001g0024 a0001c0001t0001g0069 |
4 | HG01978.hp1 HG01981.hp2 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.375+363T>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69749358 | |||||||
| chr4:69749584 | T | C | 8 | a0001c0001t0003g0031 a0001c0001t0003g0045 a0001c0001t0003g0133 others(5): Show |
12 | HG01123.hp2 HG01433.hp2 HG02165.hp1 others(9): Show |
intron_variant | MODIFIER | c.375+137A>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69749584 | |||||||
| chr4:69749590 | G | A | 60 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(57): Show |
106 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.375+131C>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 4/7 | chr4 | 69749590 | |||||||
| chr4:69749903 | C | T | 22 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0017 others(19): Show |
77 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.278-85G>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 3/7 | chr4 | 69749903 | |||||||
| chr4:69749919 | G | C | 1 | a0001c0001t0051g0135 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.278-101C>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 3/7 | chr4 | 69749919 | |||||||
| chr4:69750015 | C | T | 1 | a0003c0003t0033g0104 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.278-197G>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 3/7 | chr4 | 69750015 | |||||||
| chr4:69750131 | C | A | 1 | a0001c0001t0001g0098 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.278-313G>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 3/7 | chr4 | 69750131 | |||||||
| chr4:69750170 | A | G | 13 | a0001c0001t0006g0005 a0001c0001t0006g0171 a0001c0001t0006g0172 others(10): Show |
32 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(29): Show |
intron_variant | MODIFIER | c.278-352T>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 3/7 | chr4 | 69750170 | |||||||
| chr4:69750376 | C | A | 1 | a0001c0001t0053g0136 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.278-558G>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 3/7 | chr4 | 69750376 | |||||||
| chr4:69750516 | T | C | 2 | a0001c0001t0011g0020 a0001c0001t0011g0113 |
5 | HG01243.hp1 HG01891.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.278-698A>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 3/7 | chr4 | 69750516 | |||||||
| chr4:69750520 | C | T | 1 | a0001c0001t0009g0183 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.278-702G>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 3/7 | chr4 | 69750520 | |||||||
| chr4:69750577 | C | A | 1 | a0001c0001t0025g0099 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.278-759G>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 3/7 | chr4 | 69750577 | |||||||
| chr4:69750597 | C | A | 1 | a0001c0001t0038g0176 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.278-779G>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 3/7 | chr4 | 69750597 | |||||||
| chr4:69750601 | C | G | 1 | a0001c0001t0024g0068 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.278-783G>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 3/7 | chr4 | 69750601 | |||||||
| chr4:69750604 | A | G | 60 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(57): Show |
106 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.278-786T>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 3/7 | chr4 | 69750604 | |||||||
| chr4:69750861 | G | A | 13 | a0001c0001t0006g0005 a0001c0001t0006g0171 a0001c0001t0006g0172 others(10): Show |
32 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(29): Show |
intron_variant | MODIFIER | c.278-1043C>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 3/7 | chr4 | 69750861 | |||||||
| chr4:69751052 | C | G | 1 | a0001c0001t0041g0109 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.278-1234G>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 3/7 | chr4 | 69751052 | |||||||
| chr4:69751237 | T | C | 21 | a0001c0001t0006g0005 a0001c0001t0006g0171 a0001c0001t0006g0172 others(18): Show |
41 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(38): Show |
intron_variant | MODIFIER | c.278-1419A>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 3/7 | chr4 | 69751237 | |||||||
| chr4:69751445 | C | T | 1 | a0001c0001t0038g0176 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.278-1627G>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 3/7 | chr4 | 69751445 | |||||||
| chr4:69751462 | G | A | 6 | a0001c0001t0011g0192 a0001c0001t0012g0054 a0001c0001t0012g0105 others(3): Show |
7 | HG02109.hp2 HG02976.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.278-1644C>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 3/7 | chr4 | 69751462 | |||||||
| chr4:69751475 | G | A | 2 | a0003c0003t0033g0104 a0003c0003t0035g0108 |
2 | HG01243.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.278-1657C>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 3/7 | chr4 | 69751475 | |||||||
| chr4:69751483 | A | G | 124 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(121): Show |
253 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(250): Show |
intron_variant | MODIFIER | c.278-1665T>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 3/7 | chr4 | 69751483 | |||||||
| chr4:69751491 | G | A | 4 | a0001c0001t0008g0008 a0001c0001t0008g0034 a0001c0001t0008g0201 others(1): Show |
12 | HG01361.hp2 HG01928.hp1 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.278-1673C>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 3/7 | chr4 | 69751491 | |||||||
| chr4:69751597 | G | T | 2 | a0001c0001t0011g0020 a0001c0001t0011g0113 |
5 | HG01243.hp1 HG01891.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.278-1779C>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 3/7 | chr4 | 69751597 | |||||||
| chr4:69751601 | G | A | 23 | a0001c0001t0004g0015 a0001c0001t0004g0016 a0001c0001t0004g0047 others(20): Show |
37 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.278-1783C>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 3/7 | chr4 | 69751601 | |||||||
| chr4:69751633 | T | C | 1 | a0001c0001t0001g0100 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.278-1815A>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 3/7 | chr4 | 69751633 | |||||||
| chr4:69751674 | G | A | 22 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0017 others(19): Show |
77 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.278-1856C>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 3/7 | chr4 | 69751674 | |||||||
| chr4:69751748 | G | A | 13 | a0001c0001t0006g0005 a0001c0001t0006g0171 a0001c0001t0006g0172 others(10): Show |
32 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(29): Show |
intron_variant | MODIFIER | c.278-1930C>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 3/7 | chr4 | 69751748 | |||||||
| chr4:69751834 | T | C | 1 | a0001c0001t0004g0048 | 2 | HG01070.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.278-2016A>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 3/7 | chr4 | 69751834 | |||||||
| chr4:69751843 | A | C | 1 | a0001c0001t0006g0171 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.278-2025T>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 3/7 | chr4 | 69751843 | |||||||
| chr4:69751951 | C | T | 1 | a0001c0001t0002g0167 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.278-2133G>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 3/7 | chr4 | 69751951 | |||||||
| chr4:69751967 | T | C | 1 | a0001c0001t0023g0179 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.278-2149A>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 3/7 | chr4 | 69751967 | |||||||
| chr4:69751974 | T | C | 2 | a0003c0003t0033g0104 a0003c0003t0035g0108 |
2 | HG01243.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.278-2156A>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 3/7 | chr4 | 69751974 | |||||||
| chr4:69752010 | A | C | 1 | a0001c0001t0012g0190 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.278-2192T>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 3/7 | chr4 | 69752010 | |||||||
| chr4:69752124 | G | C | 1 | a0001c0001t0003g0146 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.278-2306C>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 3/7 | chr4 | 69752124 | |||||||
| chr4:69752191 | T | C | 1 | a0001c0001t0003g0147 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.278-2373A>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 3/7 | chr4 | 69752191 | |||||||
| chr4:69752195 | A | G | 2 | a0001c0001t0011g0020 a0001c0001t0011g0113 |
5 | HG01243.hp1 HG01891.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.278-2377T>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 3/7 | chr4 | 69752195 | |||||||
| chr4:69752274 | C | T | 1 | a0001c0001t0009g0182 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.277+2396G>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 3/7 | chr4 | 69752274 | |||||||
| chr4:69752281 | G | C | 1 | a0001c0001t0002g0164 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.277+2389C>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 3/7 | chr4 | 69752281 | |||||||
| chr4:69752320 | T | C | 1 | a0001c0001t0011g0113 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.277+2350A>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 3/7 | chr4 | 69752320 | |||||||
| chr4:69752354 | T | A | 1 | a0001c0001t0001g0169 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.277+2316A>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 3/7 | chr4 | 69752354 | |||||||
| chr4:69752355 | G | A | 1 | a0001c0001t0001g0056 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.277+2315C>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 3/7 | chr4 | 69752355 | |||||||
| chr4:69752424 | A | G | 1 | a0001c0001t0012g0190 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.277+2246T>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 3/7 | chr4 | 69752424 | |||||||
| chr4:69752690 | T | C | 8 | a0001c0001t0011g0192 a0001c0001t0012g0054 a0001c0001t0012g0105 others(5): Show |
9 | HG01884.hp2 HG02109.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.277+1980A>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 3/7 | chr4 | 69752690 | |||||||
| chr4:69752754 | C | A | 1 | a0001c0001t0038g0176 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.277+1916G>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 3/7 | chr4 | 69752754 | |||||||
| chr4:69753260 | A | G | 1 | a0002c0002t0028g0110 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.277+1410T>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 3/7 | chr4 | 69753260 | |||||||
| chr4:69753320 | G | C | 84 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(81): Show |
139 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.277+1350C>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 3/7 | chr4 | 69753320 | |||||||
| chr4:69753324 | C | A | 105 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(102): Show |
180 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.277+1346G>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 3/7 | chr4 | 69753324 | |||||||
| chr4:69753427 | T | C | 9 | a0001c0001t0003g0066 a0001c0001t0005g0006 a0001c0001t0005g0058 others(6): Show |
16 | HG00639.hp1 HG00738.hp2 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.277+1243A>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 3/7 | chr4 | 69753427 | |||||||
| chr4:69753441 | C | T | 1 | a0001c0001t0007g0122 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.277+1229G>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 3/7 | chr4 | 69753441 | |||||||
| chr4:69753488 | T | A | 1 | a0001c0001t0007g0148 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.277+1182A>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 3/7 | chr4 | 69753488 | |||||||
| chr4:69753583 | G | A | 1 | a0001c0001t0002g0165 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.277+1087C>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 3/7 | chr4 | 69753583 | |||||||
| chr4:69753652 | T | C | 1 | a0001c0001t0001g0101 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.277+1018A>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 3/7 | chr4 | 69753652 | |||||||
| chr4:69753721 | T | C | 1 | a0001c0001t0004g0177 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.277+949A>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 3/7 | chr4 | 69753721 | |||||||
| chr4:69753838 | C | G | 8 | a0001c0001t0003g0003 a0001c0001t0003g0010 a0001c0001t0003g0026 others(5): Show |
31 | HG01106.hp2 HG01261.hp1 HG01515.hp1 others(28): Show |
intron_variant | MODIFIER | c.277+832G>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 3/7 | chr4 | 69753838 | |||||||
| chr4:69753897 | A | G | 105 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(102): Show |
180 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.277+773T>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 3/7 | chr4 | 69753897 | |||||||
| chr4:69754102 | C | T | 1 | a0003c0003t0033g0104 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.277+568G>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 3/7 | chr4 | 69754102 | |||||||
| chr4:69754173 | C | T | 3 | a0001c0001t0001g0035 a0001c0001t0001g0067 a0001c0001t0005g0103 |
4 | HG01069.hp2 HG01071.hp2 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.277+497G>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 3/7 | chr4 | 69754173 | |||||||
| chr4:69754365 | A | C | 9 | a0001c0001t0003g0066 a0001c0001t0005g0006 a0001c0001t0005g0058 others(6): Show |
16 | HG00639.hp1 HG00738.hp2 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.277+305T>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 3/7 | chr4 | 69754365 | |||||||
| chr4:69754425 | G | T | 1 | a0001c0001t0001g0061 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.277+245C>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 3/7 | chr4 | 69754425 | |||||||
| chr4:69754584 | G | A | 1 | a0001c0001t0001g0102 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.277+86C>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 3/7 | chr4 | 69754584 | |||||||
| chr4:69754603 | C | T | 2 | a0001c0001t0009g0180 a0001c0001t0009g0181 |
2 | NA20300.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.277+67G>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 3/7 | chr4 | 69754603 | |||||||
| chr4:69754646 | T | C | 1 | a0001c0001t0001g0039 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.277+24A>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 3/7 | chr4 | 69754646 | |||||||
| chr4:69754844 | G | A | 1 | a0001c0001t0013g0149 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.149-46C>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 2/7 | chr4 | 69754844 | |||||||
| chr4:69754850 | G | A | 1 | a0003c0003t0035g0108 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.149-52C>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 2/7 | chr4 | 69754850 | |||||||
| chr4:69754990 | G | A | 130 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(127): Show |
261 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.148+80C>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 2/7 | chr4 | 69754990 | |||||||
| chr4:69755313 | T | G | 1 | a0001c0001t0057g0187 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-44-52A>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 1/7 | chr4 | 69755313 | |||||||
| chr4:69755356 | A | G | 8 | a0001c0001t0003g0003 a0001c0001t0003g0010 a0001c0001t0003g0026 others(5): Show |
31 | HG01106.hp2 HG01261.hp1 HG01515.hp1 others(28): Show |
intron_variant | MODIFIER | c.-44-95T>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 1/7 | chr4 | 69755356 | |||||||
| chr4:69755782 | G | A | 1 | a0001c0001t0002g0166 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-44-521C>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 1/7 | chr4 | 69755782 | |||||||
| chr4:69755827 | G | A | 1 | a0001c0001t0004g0150 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-44-566C>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 1/7 | chr4 | 69755827 | |||||||
| chr4:69755874 | T | C | 1 | a0001c0001t0003g0032 | 3 | HG02145.hp1 HG03209.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-44-613A>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 1/7 | chr4 | 69755874 | |||||||
| chr4:69755969 | TA | T | 3 | a0001c0001t0002g0033 a0001c0001t0002g0156 a0001c0001t0032g0157 |
5 | HG02155.hp2 NA19007.hp2 NA19063.hp1 others(2): Show |
intron_variant | MODIFIER | c.-44-709delT | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 1/7 | chr4 | 69755969 | |||||||
| chr4:69755970 | A | T | 1 | a0001c0001t0009g0052 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-44-709T>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 1/7 | chr4 | 69755970 | |||||||
| chr4:69756069 | C | A | 1 | a0001c0001t0002g0018 | 4 | HG01081.hp1 HG01261.hp2 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.-44-808G>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 1/7 | chr4 | 69756069 | |||||||
| chr4:69756097 | C | T | 12 | a0001c0001t0006g0005 a0001c0001t0006g0171 a0001c0001t0006g0172 others(9): Show |
31 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(28): Show |
intron_variant | MODIFIER | c.-44-836G>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 1/7 | chr4 | 69756097 | |||||||
| chr4:69756208 | T | G | 13 | a0001c0001t0006g0005 a0001c0001t0006g0171 a0001c0001t0006g0172 others(10): Show |
32 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(29): Show |
intron_variant | MODIFIER | c.-44-947A>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 1/7 | chr4 | 69756208 | |||||||
| chr4:69756276 | T | G | 4 | a0001c0001t0011g0192 a0001c0001t0012g0054 a0001c0001t0012g0193 others(1): Show |
5 | HG02109.hp2 HG02976.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.-44-1015A>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 1/7 | chr4 | 69756276 | |||||||
| chr4:69756278 | C | G | 1 | a0001c0001t0004g0114 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-44-1017G>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 1/7 | chr4 | 69756278 | |||||||
| chr4:69756278 | CAT | C | 13 | a0001c0001t0006g0005 a0001c0001t0006g0171 a0001c0001t0006g0172 others(10): Show |
32 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(29): Show |
intron_variant | MODIFIER | c.-44-1019_-44-1018d others(4): Show |
SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 1/7 | chr4 | 69756278 | |||||||
| chr4:69756297 | T | C | 2 | a0001c0001t0011g0020 a0001c0001t0011g0113 |
5 | HG01243.hp1 HG01891.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.-44-1036A>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 1/7 | chr4 | 69756297 | |||||||
| chr4:69756358 | G | C | 7 | a0001c0001t0011g0192 a0001c0001t0012g0054 a0001c0001t0012g0190 others(4): Show |
8 | HG01884.hp2 HG02109.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.-44-1097C>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 1/7 | chr4 | 69756358 | |||||||
| chr4:69756391 | C | T | 1 | a0001c0001t0040g0118 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-44-1130G>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 1/7 | chr4 | 69756391 | |||||||
| chr4:69756426 | T | C | 1 | a0001c0001t0005g0103 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-44-1165A>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 1/7 | chr4 | 69756426 | |||||||
| chr4:69756450 | T | C | 1 | a0001c0001t0013g0151 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-44-1189A>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 1/7 | chr4 | 69756450 | |||||||
| chr4:69756499 | G | T | 20 | a0001c0001t0006g0005 a0001c0001t0006g0171 a0001c0001t0006g0172 others(17): Show |
40 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(37): Show |
intron_variant | MODIFIER | c.-44-1238C>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 1/7 | chr4 | 69756499 | |||||||
| chr4:69756534 | T | C | 4 | a0002c0002t0014g0019 a0002c0002t0027g0111 a0002c0002t0028g0110 others(1): Show |
7 | HG02559.hp2 HG02615.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.-44-1273A>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 1/7 | chr4 | 69756534 | |||||||
| chr4:69756813 | A | G | 1 | a0001c0001t0023g0179 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-44-1552T>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 1/7 | chr4 | 69756813 | |||||||
| chr4:69756833 | G | T | 1 | a0004c0005t0043g0191 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-44-1572C>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 1/7 | chr4 | 69756833 | |||||||
| chr4:69756960 | G | GAC | 62 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(59): Show |
108 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.-44-1701_-44-1700d others(4): Show |
SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 1/7 | chr4 | 69756960 | |||||||
| chr4:69756974 | C | G | 2 | a0001c0001t0011g0020 a0001c0001t0011g0113 |
5 | HG01243.hp1 HG01891.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.-44-1713G>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 1/7 | chr4 | 69756974 | |||||||
| chr4:69756976 | CACAG | C | 2 | a0001c0001t0011g0020 a0001c0001t0011g0113 |
5 | HG01243.hp1 HG01891.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.-44-1719_-44-1716d others(6): Show |
SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 1/7 | chr4 | 69756976 | |||||||
| chr4:69756978 | C | CACACAG | 2 | a0001c0001t0009g0051 a0001c0001t0009g0183 |
3 | HG03098.hp1 HG03453.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-44-1718_-44-1717i others(8): Show |
SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 1/7 | chr4 | 69756978 | |||||||
| chr4:69756980 | G | C | 2 | a0001c0001t0009g0051 a0001c0001t0009g0183 |
3 | HG03098.hp1 HG03453.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-44-1719C>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 1/7 | chr4 | 69756980 | |||||||
| chr4:69756980 | G | GAC | 16 | a0001c0001t0002g0001 a0001c0001t0002g0017 a0001c0001t0002g0023 others(13): Show |
19 | HG00099.hp2 HG00741.hp2 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.-44-1721_-44-1720d others(4): Show |
SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 1/7 | chr4 | 69756980 | |||||||
| chr4:69757206 | G | A | 1 | a0001c0001t0002g0167 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-44-1945C>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 1/7 | chr4 | 69757206 | |||||||
| chr4:69757210 | T | C | 1 | a0001c0001t0041g0109 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-44-1949A>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 1/7 | chr4 | 69757210 | |||||||
| chr4:69757309 | T | A | 13 | a0001c0001t0006g0005 a0001c0001t0006g0171 a0001c0001t0006g0172 others(10): Show |
32 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(29): Show |
intron_variant | MODIFIER | c.-44-2048A>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 1/7 | chr4 | 69757309 | |||||||
| chr4:69757494 | T | C | 4 | a0002c0002t0014g0019 a0002c0002t0027g0111 a0002c0002t0028g0110 others(1): Show |
7 | HG02559.hp2 HG02615.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.-44-2233A>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 1/7 | chr4 | 69757494 | |||||||
| chr4:69757501 | A | T | 1 | a0001c0001t0012g0190 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-44-2240T>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 1/7 | chr4 | 69757501 | |||||||
| chr4:69757585 | T | TAC | 7 | a0001c0001t0011g0192 a0001c0001t0012g0054 a0001c0001t0012g0190 others(4): Show |
8 | HG01884.hp2 HG02109.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.-44-2326_-44-2325d others(4): Show |
SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 1/7 | chr4 | 69757585 | |||||||
| chr4:69757664 | G | A | 2 | a0001c0001t0011g0020 a0001c0001t0011g0113 |
5 | HG01243.hp1 HG01891.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.-44-2403C>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 1/7 | chr4 | 69757664 | |||||||
| chr4:69757703 | G | T | 61 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(58): Show |
107 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.-44-2442C>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 1/7 | chr4 | 69757703 | |||||||
| chr4:69757756 | G | A | 1 | a0001c0001t0049g0153 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-44-2495C>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 1/7 | chr4 | 69757756 | |||||||
| chr4:69757876 | A | G | 4 | a0001c0001t0004g0114 a0001c0001t0004g0115 a0001c0001t0004g0116 others(1): Show |
4 | HG00099.hp1 HG00323.hp1 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.-45+2583T>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 1/7 | chr4 | 69757876 | |||||||
| chr4:69757878 | A | G | 13 | a0001c0001t0006g0005 a0001c0001t0006g0171 a0001c0001t0006g0172 others(10): Show |
32 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(29): Show |
intron_variant | MODIFIER | c.-45+2581T>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 1/7 | chr4 | 69757878 | |||||||
| chr4:69757897 | A | G | 130 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(127): Show |
261 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.-45+2562T>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 1/7 | chr4 | 69757897 | |||||||
| chr4:69758051 | T | C | 1 | a0001c0001t0001g0154 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-45+2408A>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 1/7 | chr4 | 69758051 | |||||||
| chr4:69758136 | T | C | 1 | a0001c0001t0015g0049 | 2 | HG01109.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-45+2323A>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 1/7 | chr4 | 69758136 | |||||||
| chr4:69758370 | A | G | 1 | a0001c0001t0004g0059 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-45+2089T>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 1/7 | chr4 | 69758370 | |||||||
| chr4:69758944 | T | C | 13 | a0001c0001t0006g0005 a0001c0001t0006g0171 a0001c0001t0006g0172 others(10): Show |
32 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(29): Show |
intron_variant | MODIFIER | c.-45+1515A>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 1/7 | chr4 | 69758944 | |||||||
| chr4:69758950 | G | A | 1 | a0001c0001t0010g0155 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-45+1509C>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 1/7 | chr4 | 69758950 | |||||||
| chr4:69758993 | A | G | 1 | a0001c0001t0005g0058 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-45+1466T>C | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 1/7 | chr4 | 69758993 | |||||||
| chr4:69759046 | T | C | 18 | a0001c0001t0002g0001 a0001c0001t0002g0023 a0001c0001t0002g0033 others(15): Show |
63 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.-45+1413A>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 1/7 | chr4 | 69759046 | |||||||
| chr4:69759118 | T | C | 2 | a0001c0001t0001g0168 a0001c0001t0001g0169 |
2 | NA19005.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.-45+1341A>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 1/7 | chr4 | 69759118 | |||||||
| chr4:69759180 | G | T | 2 | a0001c0001t0002g0011 a0001c0006t0002g0057 |
6 | HG00597.hp1 HG00673.hp2 HG02083.hp2 others(3): Show |
intron_variant | MODIFIER | c.-45+1279C>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 1/7 | chr4 | 69759180 | |||||||
| chr4:69759187 | G | C | 1 | a0001c0001t0002g0170 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-45+1272C>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 1/7 | chr4 | 69759187 | |||||||
| chr4:69759209 | T | A | 1 | a0001c0001t0012g0195 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-45+1250A>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 1/7 | chr4 | 69759209 | |||||||
| chr4:69759408 | C | T | 12 | a0001c0001t0009g0051 a0001c0001t0009g0052 a0001c0001t0009g0053 others(9): Show |
15 | HG00099.hp2 HG01168.hp1 HG01358.hp2 others(12): Show |
intron_variant | MODIFIER | c.-45+1051G>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 1/7 | chr4 | 69759408 | |||||||
| chr4:69759481 | T | C | 20 | a0001c0001t0006g0005 a0001c0001t0006g0171 a0001c0001t0006g0172 others(17): Show |
40 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(37): Show |
intron_variant | MODIFIER | c.-45+978A>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 1/7 | chr4 | 69759481 | |||||||
| chr4:69759519 | C | A | 1 | a0001c0001t0004g0177 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-45+940G>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 1/7 | chr4 | 69759519 | |||||||
| chr4:69759533 | G | C | 1 | a0001c0001t0005g0178 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-45+926C>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 1/7 | chr4 | 69759533 | |||||||
| chr4:69759635 | G | A | 14 | a0001c0001t0009g0051 a0001c0001t0009g0052 a0001c0001t0009g0053 others(11): Show |
17 | HG00099.hp2 HG01168.hp1 HG01358.hp2 others(14): Show |
intron_variant | MODIFIER | c.-45+824C>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 1/7 | chr4 | 69759635 | |||||||
| chr4:69760168 | G | A | 7 | a0001c0001t0011g0192 a0001c0001t0012g0054 a0001c0001t0012g0190 others(4): Show |
8 | HG01884.hp2 HG02109.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.-45+291C>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 1/7 | chr4 | 69760168 | |||||||
| chr4:69760278 | T | C | 1 | a0001c0001t0007g0196 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-45+181A>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 1/7 | chr4 | 69760278 | |||||||
| chr4:69760332 | A | C | 1 | a0001c0001t0001g0056 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-45+127T>G | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 1/7 | chr4 | 69760332 | |||||||
| chr4:69760410 | C | T | 1 | a0001c0001t0002g0055 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-45+49G>A | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 1/7 | chr4 | 69760410 | |||||||
| chr4:69760411 | G | A | 2 | a0001c0001t0003g0197 a0001c0001t0048g0198 |
2 | HG02735.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.-45+48C>T | SULT1B1 | ENSG00000173597.9 | transcript | ENST00000310613.8 | protein_coding | 1/7 | chr4 | 69760411 |