Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 7364 |
| ensemblid | ENSG00000171234.14 |
| hgncid | 12554 |
| symbol | UGT2B7 |
| name | UDP glucuronosyltransferase family 2 member B7 |
| refseq_nuc | NM_001074.4 |
| refseq_prot | NP_001065.2 |
| ensembl_nuc | ENST00000305231.12 |
| ensembl_prot | ENSP00000304811.7 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 69096474 |
| end | 69112987 |
| strand | + |
| ver | v1.2 |
| region | chr4:69096474-69112987 |
| region5000 | chr4:69091474-69117987 |
| regionname0 | UGT2B7_chr4_69096474_69112987 |
| regionname5000 | UGT2B7_chr4_69091474_69117987 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 529 | 256 | 60 | 53 | 106 | 8 | 28 | 83 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | MSVKW others(524): Show |
chr4 | 69091474 | 69117987 |
| a0002 | 1/0 | 529 | 127 | 22 | 22 | 58 | 6 | 18 | 48 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | MSVKW others(524): Show |
chr4 | 69091474 | 69117987 |
| a0003 | 0/0 | 529 | 30 | 0 | 2 | 28 | 0 | 0 | 22 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | MSVKW others(524): Show |
chr4 | 69091474 | 69117987 |
| a0004 | 0/0 | 529 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | MSVKW others(524): Show |
chr4 | 69091474 | 69117987 |
| a0005 | 0/0 | 529 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | MSVKW others(524): Show |
chr4 | 69091474 | 69117987 |
| a0006 | 0/0 | 529 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | MSVKW others(524): Show |
chr4 | 69091474 | 69117987 |
| a0007 | 0/0 | 529 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | MSVKW others(524): Show |
chr4 | 69091474 | 69117987 |
| a0008 | 0/0 | 529 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | MSVKW others(524): Show |
chr4 | 69091474 | 69117987 |
| a0009 | 0/0 | 529 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | MSVKW others(524): Show |
chr4 | 69091474 | 69117987 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1587 | 161 | 36 | 25 | 85 | 2 | 13 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | ATGTC others(1582): Show |
chr4 | 69091474 | 69117987 | ||
| a0001c0003 | 0/0 | 1587 | 56 | 9 | 20 | 17 | 4 | 6 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | ATGTC others(1582): Show |
chr4 | 69091474 | 69117987 | ||
| a0001c0005 | 0/1 | 1587 | 25 | 7 | 7 | 4 | 2 | 4 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | ATGTC others(1582): Show |
chr4 | 69091474 | 69117987 | ||
| a0001c0008 | 0/0 | 1587 | 4 | 4 | 0 | 0 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | ATGTC others(1582): Show |
chr4 | 69091474 | 69117987 | ||
| a0001c0010 | 0/0 | 1587 | 3 | 0 | 0 | 0 | 0 | 3 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | ATGTC others(1582): Show |
chr4 | 69091474 | 69117987 | ||
| a0001c0011 | 0/0 | 1587 | 3 | 2 | 1 | 0 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | ATGTC others(1582): Show |
chr4 | 69091474 | 69117987 | ||
| a0001c0014 | 0/0 | 1587 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | ATGTC others(1582): Show |
chr4 | 69091474 | 69117987 | ||
| a0001c0016 | 0/0 | 1587 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | ATGTC others(1582): Show |
chr4 | 69091474 | 69117987 | ||
| a0001c0017 | 0/0 | 1587 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | ATGTC others(1582): Show |
chr4 | 69091474 | 69117987 | ||
| a0001c0018 | 0/0 | 1587 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | ATGTC others(1582): Show |
chr4 | 69091474 | 69117987 | ||
| a0002c0002 | 1/0 | 1587 | 116 | 15 | 18 | 58 | 6 | 18 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | ATGTC others(1582): Show |
chr4 | 69091474 | 69117987 | ||
| a0002c0006 | 0/0 | 1587 | 8 | 5 | 3 | 0 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | ATGTC others(1582): Show |
chr4 | 69091474 | 69117987 | ||
| a0002c0009 | 0/0 | 1587 | 3 | 2 | 1 | 0 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | ATGTC others(1582): Show |
chr4 | 69091474 | 69117987 | ||
| a0003c0004 | 0/0 | 1587 | 30 | 0 | 2 | 28 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | ATGTC others(1582): Show |
chr4 | 69091474 | 69117987 | ||
| a0004c0007 | 0/0 | 1587 | 5 | 5 | 0 | 0 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | ATGTC others(1582): Show |
chr4 | 69091474 | 69117987 | ||
| a0005c0012 | 0/0 | 1587 | 2 | 0 | 0 | 2 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | ATGTC others(1582): Show |
chr4 | 69091474 | 69117987 | ||
| a0006c0020 | 0/0 | 1587 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | ATGTC others(1582): Show |
chr4 | 69091474 | 69117987 | ||
| a0007c0015 | 0/0 | 1587 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | ATGTC others(1582): Show |
chr4 | 69091474 | 69117987 | ||
| a0008c0019 | 0/0 | 1587 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | ATGTC others(1582): Show |
chr4 | 69091474 | 69117987 | ||
| a0009c0013 | 0/0 | 1587 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | ATGTC others(1582): Show |
chr4 | 69091474 | 69117987 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1889 | 140 | 30 | 21 | 74 | 2 | 13 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | GACAG others(1884): Show |
chr4 | 69091474 | 69117987 |
| a0001c0001t0002 | 0/0 | 1888 | 17 | 4 | 4 | 9 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | GACAG others(1883): Show |
chr4 | 69091474 | 69117987 |
| a0001c0001t0005 | 0/0 | 1889 | 2 | 2 | 0 | 0 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | GACAG others(1884): Show |
chr4 | 69091474 | 69117987 |
| a0001c0001t0006 | 0/0 | 1889 | 2 | 0 | 0 | 2 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | GACAG others(1884): Show |
chr4 | 69091474 | 69117987 |
| a0001c0003t0001 | 0/0 | 1889 | 47 | 1 | 19 | 17 | 4 | 6 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | GACAG others(1884): Show |
chr4 | 69091474 | 69117987 |
| a0001c0003t0003 | 0/0 | 1890 | 7 | 6 | 1 | 0 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | GACAG others(1885): Show |
chr4 | 69091474 | 69117987 |
| a0001c0003t0004 | 0/0 | 1889 | 2 | 2 | 0 | 0 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | GACAG others(1884): Show |
chr4 | 69091474 | 69117987 |
| a0001c0005t0001 | 0/1 | 1889 | 24 | 6 | 7 | 4 | 2 | 4 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | GACAG others(1884): Show |
chr4 | 69091474 | 69117987 |
| a0001c0005t0002 | 0/0 | 1888 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | GACAG others(1883): Show |
chr4 | 69091474 | 69117987 |
| a0001c0008t0001 | 0/0 | 1889 | 4 | 4 | 0 | 0 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | GACAG others(1884): Show |
chr4 | 69091474 | 69117987 |
| a0001c0010t0002 | 0/0 | 1888 | 3 | 0 | 0 | 0 | 0 | 3 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | GACAG others(1883): Show |
chr4 | 69091474 | 69117987 |
| a0001c0011t0001 | 0/0 | 1889 | 3 | 2 | 1 | 0 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | GACAG others(1884): Show |
chr4 | 69091474 | 69117987 |
| a0001c0014t0002 | 0/0 | 1888 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | GACAG others(1883): Show |
chr4 | 69091474 | 69117987 |
| a0001c0016t0001 | 0/0 | 1889 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | GACAG others(1884): Show |
chr4 | 69091474 | 69117987 |
| a0001c0017t0008 | 0/0 | 1888 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | GACAG others(1883): Show |
chr4 | 69091474 | 69117987 |
| a0001c0018t0001 | 0/0 | 1889 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | GACAG others(1884): Show |
chr4 | 69091474 | 69117987 |
| a0002c0002t0001 | 0/0 | 1889 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | GACAG others(1884): Show |
chr4 | 69091474 | 69117987 |
| a0002c0002t0002 | 1/0 | 1888 | 114 | 15 | 18 | 56 | 6 | 18 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | GACAG others(1883): Show |
chr4 | 69091474 | 69117987 |
| a0002c0002t0007 | 0/0 | 1888 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | GACAG others(1883): Show |
chr4 | 69091474 | 69117987 |
| a0002c0006t0002 | 0/0 | 1888 | 8 | 5 | 3 | 0 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | GACAG others(1883): Show |
chr4 | 69091474 | 69117987 |
| a0002c0009t0003 | 0/0 | 1890 | 3 | 2 | 1 | 0 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | GACAG others(1885): Show |
chr4 | 69091474 | 69117987 |
| a0003c0004t0001 | 0/0 | 1889 | 30 | 0 | 2 | 28 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | GACAG others(1884): Show |
chr4 | 69091474 | 69117987 |
| a0004c0007t0004 | 0/0 | 1889 | 5 | 5 | 0 | 0 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | GACAG others(1884): Show |
chr4 | 69091474 | 69117987 |
| a0005c0012t0001 | 0/0 | 1889 | 2 | 0 | 0 | 2 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | GACAG others(1884): Show |
chr4 | 69091474 | 69117987 |
| a0006c0020t0001 | 0/0 | 1889 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | GACAG others(1884): Show |
chr4 | 69091474 | 69117987 |
| a0007c0015t0002 | 0/0 | 1888 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | GACAG others(1883): Show |
chr4 | 69091474 | 69117987 |
| a0008c0019t0005 | 0/0 | 1889 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | GACAG others(1884): Show |
chr4 | 69091474 | 69117987 |
| a0009c0013t0001 | 0/0 | 1889 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | GACAG others(1884): Show |
chr4 | 69091474 | 69117987 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 90 | 11 | 18 | 52 | 1 | 8 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0001c0001t0001g0004 | 0/0 | 7 | 2 | 0 | 5 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0001c0001t0001g0007 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0001c0001t0001g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0001c0001t0001g0020 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0001c0001t0001g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0001c0001t0002g0004 | 0/0 | 12 | 0 | 3 | 9 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0001c0001t0002g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0001c0001t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0001c0001t0005g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0001c0001t0005g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0001c0001t0006g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0001c0001t0006g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0001c0003t0001g0005 | 0/0 | 17 | 0 | 0 | 15 | 0 | 2 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0001c0003t0001g0008 | 0/0 | 10 | 0 | 5 | 0 | 4 | 1 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0001c0003t0001g0010 | 0/0 | 7 | 0 | 7 | 0 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0001c0003t0001g0017 | 0/0 | 5 | 0 | 4 | 0 | 0 | 1 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0001c0003t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0001c0003t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0001c0003t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0001c0003t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0001c0003t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0001c0003t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0001c0003t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0001c0003t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0001c0003t0003g0016 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0001c0003t0003g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0001c0003t0003g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0001c0003t0004g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0001c0005t0001g0003 | 0/0 | 5 | 0 | 0 | 3 | 0 | 2 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0001c0005t0001g0007 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0001c0005t0001g0009 | 0/1 | 8 | 1 | 4 | 0 | 1 | 1 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0001c0005t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0001c0005t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0001c0005t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0001c0005t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0001c0005t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0001c0005t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0001c0005t0002g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0001c0008t0001g0027 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0001c0008t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0001c0010t0002g0026 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0001c0011t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0001c0011t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0001c0011t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0001c0014t0002g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0001c0016t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0001c0017t0008g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0001c0018t0001g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0002c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0002c0002t0002g0002 | 0/0 | 47 | 5 | 7 | 30 | 1 | 4 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0002c0002t0002g0006 | 1/0 | 17 | 3 | 4 | 1 | 1 | 7 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0002c0002t0002g0011 | 0/0 | 7 | 4 | 3 | 0 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0002c0002t0002g0012 | 0/0 | 6 | 1 | 1 | 0 | 2 | 2 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0002c0002t0002g0018 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0002c0002t0002g0019 | 0/0 | 4 | 0 | 0 | 2 | 0 | 2 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0002c0002t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0002c0002t0002g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0002c0002t0002g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0002c0002t0002g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0002c0002t0002g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0002c0002t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0002c0002t0002g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0002c0002t0002g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0002c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0002c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0002c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0002c0002t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0002c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0002c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0002c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0002c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0002c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0002c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0002c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0002c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0002c0002t0007g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0002c0006t0002g0015 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0002c0006t0002g0024 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0002c0009t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0002c0009t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0002c0009t0003g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0003c0004t0001g0003 | 0/0 | 25 | 0 | 0 | 25 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0003c0004t0001g0021 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0003c0004t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0004c0007t0004g0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0004c0007t0004g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0005c0012t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0006c0020t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0007c0015t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0008c0019t0005g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| a0009c0013t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0002 | c0002 | t0002 | g0045 | EUR | GBR | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG00140 | hp2 | a0001 | c0003 | t0001 | g0008 | EUR | GBR | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG00280 | hp1 | a0002 | c0002 | t0002 | g0012 | EUR | FIN | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG00280 | hp2 | a0002 | c0002 | t0002 | g0002 | EUR | FIN | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG00323 | hp1 | a0001 | c0005 | t0001 | g0083 | EUR | FIN | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG00323 | hp2 | a0001 | c0005 | t0001 | g0009 | EUR | FIN | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG00408 | hp1 | a0002 | c0002 | t0002 | g0019 | EAS | CHS | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG00423 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | CHS | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | CHS | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG00544 | hp2 | a0001 | c0005 | t0001 | g0003 | EAS | CHS | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG00558 | hp1 | a0003 | c0004 | t0001 | g0003 | EAS | CHS | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | CHS | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG00621 | hp1 | a0002 | c0002 | t0007 | g0022 | EAS | CHS | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG00639 | hp1 | a0001 | c0005 | t0001 | g0009 | AMR | PUR | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG00639 | hp2 | a0003 | c0004 | t0001 | g0021 | AMR | PUR | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG00642 | hp1 | a0002 | c0006 | t0002 | g0024 | AMR | PUR | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG00642 | hp2 | a0001 | c0003 | t0001 | g0008 | AMR | PUR | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG00733 | hp1 | a0002 | c0002 | t0002 | g0006 | AMR | PUR | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG00735 | hp1 | a0002 | c0002 | t0002 | g0012 | AMR | PUR | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG00738 | hp1 | a0001 | c0005 | t0001 | g0009 | AMR | PUR | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG00738 | hp2 | a0002 | c0002 | t0002 | g0011 | AMR | PUR | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG00741 | hp1 | a0001 | c0003 | t0001 | g0008 | AMR | PUR | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG01069 | hp2 | a0002 | c0002 | t0002 | g0006 | AMR | PUR | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG01070 | hp1 | a0001 | c0005 | t0001 | g0034 | AMR | PUR | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG01070 | hp2 | a0001 | c0003 | t0001 | g0010 | AMR | PUR | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG01071 | hp2 | a0001 | c0003 | t0001 | g0010 | AMR | PUR | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG01081 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | PUR | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG01081 | hp2 | a0001 | c0005 | t0001 | g0034 | AMR | PUR | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG01099 | hp1 | a0002 | c0002 | t0002 | g0037 | AMR | PUR | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG01099 | hp2 | a0002 | c0002 | t0002 | g0011 | AMR | PUR | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG01106 | hp2 | a0002 | c0006 | t0002 | g0024 | AMR | PUR | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG01109 | hp1 | a0001 | c0005 | t0001 | g0009 | AMR | PUR | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG01109 | hp2 | a0002 | c0009 | t0003 | g0052 | AMR | PUR | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG01167 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | PUR | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG01168 | hp1 | a0002 | c0002 | t0002 | g0006 | AMR | PUR | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG01168 | hp2 | a0001 | c0003 | t0001 | g0070 | AMR | PUR | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG01169 | hp1 | a0001 | c0003 | t0001 | g0008 | AMR | PUR | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG01169 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | PUR | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG01175 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | PUR | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG01192 | hp1 | a0001 | c0003 | t0001 | g0008 | AMR | PUR | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG01243 | hp2 | a0001 | c0011 | t0001 | g0099 | AMR | PUR | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG01255 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | CLM | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG01255 | hp2 | a0002 | c0006 | t0002 | g0024 | AMR | CLM | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG01257 | hp2 | a0002 | c0002 | t0002 | g0011 | AMR | CLM | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG01258 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | CLM | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG01261 | hp1 | a0002 | c0002 | t0002 | g0006 | AMR | CLM | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG01261 | hp2 | a0001 | c0003 | t0003 | g0067 | AMR | CLM | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG01346 | hp1 | a0001 | c0003 | t0001 | g0017 | AMR | CLM | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG01346 | hp2 | a0003 | c0004 | t0001 | g0021 | AMR | CLM | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG01358 | hp1 | a0002 | c0002 | t0002 | g0037 | AMR | CLM | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG01358 | hp2 | a0001 | c0003 | t0001 | g0068 | AMR | CLM | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG01361 | hp2 | a0001 | c0005 | t0001 | g0082 | AMR | CLM | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG01433 | hp1 | a0001 | c0003 | t0001 | g0008 | AMR | CLM | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG01496 | hp1 | a0002 | c0002 | t0002 | g0041 | AMR | CLM | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG01516 | hp1 | a0002 | c0002 | t0002 | g0006 | EUR | IBS | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG01516 | hp2 | a0001 | c0003 | t0001 | g0008 | EUR | IBS | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG01517 | hp1 | a0001 | c0003 | t0001 | g0008 | EUR | IBS | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG01517 | hp2 | a0002 | c0002 | t0002 | g0012 | EUR | IBS | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG01884 | hp1 | a0002 | c0002 | t0002 | g0002 | AFR | ACB | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG01884 | hp2 | a0002 | c0002 | t0002 | g0006 | AFR | ACB | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG01891 | hp1 | a0001 | c0005 | t0001 | g0009 | AFR | ACB | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG01891 | hp2 | a0001 | c0001 | t0005 | g0097 | AFR | ACB | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG01928 | hp1 | a0001 | c0003 | t0001 | g0010 | AMR | PEL | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG01943 | hp1 | a0001 | c0005 | t0001 | g0009 | AMR | PEL | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG01952 | hp1 | a0001 | c0003 | t0001 | g0010 | AMR | PEL | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG01952 | hp2 | a0001 | c0003 | t0001 | g0017 | AMR | PEL | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG01975 | hp1 | a0001 | c0003 | t0001 | g0017 | AMR | PEL | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG01981 | hp1 | a0001 | c0003 | t0001 | g0010 | AMR | PEL | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0058 | AMR | PEL | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG01993 | hp2 | a0006 | c0020 | t0001 | g0010 | AMR | PEL | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02015 | hp1 | a0002 | c0002 | t0002 | g0022 | EAS | KHV | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02015 | hp2 | a0003 | c0004 | t0001 | g0003 | EAS | KHV | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02027 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | KHV | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02027 | hp2 | a0003 | c0004 | t0001 | g0003 | EAS | KHV | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02055 | hp1 | a0004 | c0007 | t0004 | g0014 | AFR | ACB | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02055 | hp2 | a0002 | c0002 | t0002 | g0029 | AFR | ACB | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02056 | hp1 | a0001 | c0003 | t0001 | g0005 | EAS | KHV | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02056 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | KHV | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02074 | hp2 | a0002 | c0002 | t0002 | g0023 | EAS | KHV | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02080 | hp2 | a0001 | c0005 | t0001 | g0003 | EAS | KHV | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02083 | hp2 | a0002 | c0002 | t0002 | g0023 | EAS | KHV | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | KHV | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02132 | hp1 | a0003 | c0004 | t0001 | g0003 | EAS | KHV | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02135 | hp1 | a0001 | c0003 | t0001 | g0005 | EAS | KHV | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02135 | hp2 | a0007 | c0015 | t0002 | g0046 | EAS | KHV | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02145 | hp1 | a0001 | c0003 | t0004 | g0014 | AFR | ACB | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02145 | hp2 | a0002 | c0006 | t0002 | g0015 | AFR | ACB | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02148 | hp2 | a0001 | c0003 | t0001 | g0010 | AMR | PEL | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02165 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | CDX | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02257 | hp1 | a0002 | c0002 | t0002 | g0029 | AFR | ACB | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02257 | hp2 | a0002 | c0002 | t0002 | g0012 | AFR | ACB | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02273 | hp1 | a0001 | c0003 | t0001 | g0017 | AMR | PEL | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02280 | hp2 | a0001 | c0005 | t0001 | g0007 | AFR | ACB | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02293 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | PEL | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02300 | hp1 | a0001 | c0003 | t0001 | g0010 | AMR | PEL | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | ACB | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02451 | hp2 | a0002 | c0002 | t0002 | g0002 | AFR | ACB | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02523 | hp2 | a0003 | c0004 | t0001 | g0074 | EAS | KHV | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02572 | hp1 | a0004 | c0007 | t0004 | g0014 | AFR | GWD | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02615 | hp2 | a0001 | c0008 | t0001 | g0027 | AFR | GWD | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02622 | hp1 | a0001 | c0003 | t0003 | g0016 | AFR | GWD | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02622 | hp2 | a0002 | c0002 | t0002 | g0011 | AFR | GWD | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02630 | hp1 | a0002 | c0002 | t0002 | g0006 | AFR | GWD | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02630 | hp2 | a0001 | c0003 | t0004 | g0014 | AFR | GWD | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02647 | hp2 | a0002 | c0002 | t0002 | g0011 | AFR | GWD | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02698 | hp1 | a0001 | c0003 | t0001 | g0091 | SAS | PJL | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02698 | hp2 | a0002 | c0002 | t0002 | g0002 | SAS | PJL | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02717 | hp1 | a0001 | c0003 | t0003 | g0016 | AFR | GWD | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02723 | hp2 | a0001 | c0005 | t0001 | g0007 | AFR | GWD | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02735 | hp1 | a0001 | c0003 | t0001 | g0071 | SAS | PJL | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02738 | hp1 | a0002 | c0002 | t0002 | g0006 | SAS | PJL | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02809 | hp2 | a0002 | c0009 | t0003 | g0050 | AFR | GWD | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02818 | hp1 | a0002 | c0006 | t0002 | g0015 | AFR | GWD | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02818 | hp2 | a0001 | c0005 | t0001 | g0007 | AFR | GWD | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02895 | hp2 | a0004 | c0007 | t0004 | g0014 | AFR | GWD | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02896 | hp1 | a0001 | c0005 | t0001 | g0007 | AFR | GWD | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02897 | hp1 | a0004 | c0007 | t0004 | g0096 | AFR | GWD | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02897 | hp2 | a0001 | c0005 | t0002 | g0007 | AFR | GWD | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02922 | hp1 | a0001 | c0003 | t0001 | g0090 | AFR | ESN | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02922 | hp2 | a0004 | c0007 | t0004 | g0014 | AFR | ESN | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | ESN | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02965 | hp2 | a0002 | c0002 | t0002 | g0002 | AFR | ESN | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | ESN | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02976 | hp2 | a0001 | c0016 | t0001 | g0094 | AFR | ESN | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG03017 | hp1 | a0001 | c0003 | t0001 | g0008 | SAS | PJL | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG03098 | hp1 | a0001 | c0003 | t0003 | g0095 | AFR | MSL | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG03098 | hp2 | a0001 | c0008 | t0001 | g0086 | AFR | MSL | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG03139 | hp2 | a0001 | c0011 | t0001 | g0089 | AFR | ESN | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG03195 | hp1 | a0002 | c0002 | t0002 | g0011 | AFR | ESN | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | MSL | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG03209 | hp2 | a0001 | c0011 | t0001 | g0085 | AFR | MSL | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG03225 | hp1 | a0001 | c0003 | t0003 | g0016 | AFR | MSL | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG03239 | hp1 | a0002 | c0002 | t0002 | g0012 | SAS | PJL | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG03239 | hp2 | a0002 | c0002 | t0002 | g0044 | SAS | PJL | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | MSL | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG03486 | hp2 | a0001 | c0005 | t0001 | g0077 | AFR | MSL | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG03490 | hp1 | a0002 | c0002 | t0002 | g0006 | SAS | PJL | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG03490 | hp2 | a0001 | c0003 | t0001 | g0017 | SAS | PJL | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG03491 | hp1 | a0002 | c0002 | t0002 | g0019 | SAS | PJL | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG03516 | hp1 | a0002 | c0006 | t0002 | g0015 | AFR | ESN | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG03516 | hp2 | a0008 | c0019 | t0005 | g0087 | AFR | ESN | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG03540 | hp1 | a0001 | c0008 | t0001 | g0027 | AFR | GWD | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG03540 | hp2 | a0002 | c0002 | t0002 | g0011 | AFR | GWD | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG03579 | hp1 | a0002 | c0009 | t0003 | g0051 | AFR | MSL | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | MSL | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG03654 | hp1 | a0001 | c0003 | t0001 | g0005 | SAS | PJL | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG03654 | hp2 | a0002 | c0002 | t0002 | g0012 | SAS | PJL | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG03669 | hp1 | a0002 | c0002 | t0002 | g0002 | SAS | PJL | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG03688 | hp1 | a0002 | c0002 | t0002 | g0040 | SAS | STU | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG03688 | hp2 | a0001 | c0005 | t0001 | g0081 | SAS | STU | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG03704 | hp1 | a0002 | c0002 | t0002 | g0006 | SAS | PJL | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG03704 | hp2 | a0002 | c0002 | t0002 | g0038 | SAS | PJL | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG03710 | hp2 | a0001 | c0018 | t0001 | g0005 | SAS | PJL | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG03831 | hp1 | a0001 | c0010 | t0002 | g0026 | SAS | BEB | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | BEB | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG03834 | hp2 | a0001 | c0010 | t0002 | g0026 | SAS | BEB | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG03927 | hp1 | a0002 | c0002 | t0002 | g0002 | SAS | BEB | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG03927 | hp2 | a0001 | c0005 | t0001 | g0003 | SAS | BEB | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG03942 | hp2 | a0002 | c0002 | t0002 | g0006 | SAS | BEB | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | STU | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG04115 | hp2 | a0001 | c0005 | t0001 | g0009 | SAS | STU | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG04184 | hp1 | a0002 | c0002 | t0002 | g0002 | SAS | BEB | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG04184 | hp2 | a0001 | c0017 | t0008 | g0093 | SAS | BEB | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG04199 | hp1 | a0001 | c0010 | t0002 | g0026 | SAS | STU | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG04199 | hp2 | a0002 | c0002 | t0002 | g0006 | SAS | STU | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG04204 | hp1 | a0002 | c0002 | t0002 | g0006 | SAS | STU | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG04204 | hp2 | a0001 | c0005 | t0001 | g0003 | SAS | STU | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG04228 | hp2 | a0002 | c0002 | t0002 | g0019 | SAS | STU | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | CHB | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18612 | hp2 | a0003 | c0004 | t0001 | g0003 | EAS | CHB | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18747 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | CHB | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0020 | AFR | YRI | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18906 | hp2 | a0002 | c0006 | t0002 | g0015 | AFR | YRI | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18940 | hp2 | a0002 | c0002 | t0002 | g0039 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18942 | hp1 | a0001 | c0005 | t0001 | g0075 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18943 | hp2 | a0002 | c0002 | t0002 | g0028 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18944 | hp2 | a0002 | c0002 | t0002 | g0035 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18945 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18946 | hp1 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18948 | hp1 | a0002 | c0002 | t0002 | g0036 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18948 | hp2 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18949 | hp1 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18949 | hp2 | a0002 | c0002 | t0002 | g0047 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18950 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18951 | hp2 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18952 | hp1 | a0001 | c0001 | t0006 | g0079 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18952 | hp2 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18953 | hp1 | a0001 | c0003 | t0001 | g0092 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18953 | hp2 | a0002 | c0002 | t0002 | g0030 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18957 | hp1 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18960 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18962 | hp1 | a0005 | c0012 | t0001 | g0013 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18963 | hp1 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18963 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18964 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18965 | hp1 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18966 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18967 | hp1 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18968 | hp1 | a0002 | c0002 | t0001 | g0042 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18972 | hp2 | a0001 | c0003 | t0001 | g0088 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18973 | hp2 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18974 | hp2 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18975 | hp1 | a0002 | c0002 | t0002 | g0049 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18975 | hp2 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18977 | hp1 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18977 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18979 | hp2 | a0002 | c0002 | t0002 | g0103 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18980 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18980 | hp2 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18981 | hp2 | a0001 | c0001 | t0006 | g0004 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18982 | hp1 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18983 | hp1 | a0002 | c0002 | t0002 | g0028 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18984 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18984 | hp2 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18986 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18987 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18988 | hp2 | a0002 | c0002 | t0002 | g0030 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18989 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18990 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18992 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18992 | hp2 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18993 | hp1 | a0002 | c0002 | t0002 | g0022 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18993 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18994 | hp1 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18995 | hp1 | a0002 | c0002 | t0002 | g0043 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18995 | hp2 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18997 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18997 | hp2 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18999 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA19001 | hp1 | a0002 | c0002 | t0002 | g0019 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA19002 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA19003 | hp2 | a0002 | c0002 | t0002 | g0036 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA19005 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA19007 | hp2 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA19010 | hp1 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA19012 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | LWK | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA19043 | hp1 | a0002 | c0002 | t0002 | g0002 | AFR | LWK | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA19043 | hp2 | a0001 | c0014 | t0002 | g0007 | AFR | LWK | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA19054 | hp1 | a0003 | c0004 | t0001 | g0021 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA19054 | hp2 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA19055 | hp1 | a0005 | c0012 | t0001 | g0013 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA19056 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA19056 | hp2 | a0002 | c0002 | t0002 | g0018 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA19057 | hp1 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA19058 | hp1 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA19060 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA19060 | hp2 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA19062 | hp1 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA19062 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA19064 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA19065 | hp1 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA19066 | hp1 | a0002 | c0002 | t0002 | g0048 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA19066 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA19074 | hp2 | a0009 | c0013 | t0001 | g0101 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA19076 | hp1 | a0001 | c0005 | t0001 | g0003 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA19077 | hp1 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA19080 | hp2 | a0003 | c0004 | t0001 | g0021 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA19082 | hp1 | a0002 | c0002 | t0002 | g0018 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA19082 | hp2 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA19083 | hp2 | a0002 | c0002 | t0002 | g0018 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA19085 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA19087 | hp1 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA19088 | hp1 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA19088 | hp2 | a0002 | c0002 | t0002 | g0023 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA19089 | hp1 | a0002 | c0002 | t0002 | g0018 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA19090 | hp1 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0057 | AFR | YRI | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ASW | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA20129 | hp2 | a0001 | c0001 | t0005 | g0098 | AFR | ASW | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA20752 | hp2 | a0001 | c0003 | t0001 | g0008 | EUR | TSI | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA20805 | hp1 | a0002 | c0002 | t0002 | g0104 | EUR | TSI | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0062 | EUR | TSI | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA20905 | hp1 | a0001 | c0003 | t0001 | g0005 | SAS | GIH | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA20905 | hp2 | a0002 | c0002 | t0002 | g0006 | SAS | GIH | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG01123 | hp2 | a0001 | c0003 | t0001 | g0069 | AMR | CLM | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02109 | hp2 | a0002 | c0002 | t0002 | g0002 | AFR | ACB | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02559 | hp1 | a0001 | c0003 | t0003 | g0016 | AFR | ACB | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG03471 | hp1 | a0001 | c0008 | t0001 | g0027 | AFR | MSL | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG03471 | hp2 | a0001 | c0003 | t0003 | g0016 | AFR | MSL | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | USA | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18955 | hp1 | a0002 | c0002 | t0002 | g0035 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | USA | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA21309 | hp1 | a0002 | c0006 | t0002 | g0015 | AFR | LWK | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| NA21309 | hp2 | a0002 | c0002 | t0002 | g0006 | AFR | LWK | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| homoSapiens | chm13v2 | a0001 | c0005 | t0001 | g0009 | REF | REF | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0002 | g0006 | REF | REF | UGT2B7_chr4_69091474_69117987 | UGT2B7 | chr4 | 69091474 | 69117987 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:69096644 | A | G | 1 | a0006 | 1 | HG01993.hp2 | missense_variant | MODERATE | c.124A>G | p.Ile42Val | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 1/6 | 171/1888 | 124/1590 | 42/529 | chr4 | 69096644 | |||
| chr4:69096690 | C | A | 1 | a0009 | 1 | NA19074.hp2 | missense_variant | MODERATE | c.170C>A | p.Ala57Glu | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 1/6 | 217/1888 | 170/1590 | 57/529 | chr4 | 69096690 | |||
| chr4:69096731 | G | T | 1 | a0003 | 30 | HG00558.hp1 HG00639.hp2 HG01346.hp2 others(27): Show |
missense_variant | MODERATE | c.211G>T | p.Ala71Ser | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 1/6 | 258/1888 | 211/1590 | 71/529 | chr4 | 69096731 | |||
| chr4:69096841 | A | T | 1 | a0008 | 1 | HG03516.hp2 | missense_variant | MODERATE | c.321A>T | p.Leu107Phe | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 1/6 | 368/1888 | 321/1590 | 107/529 | chr4 | 69096841 | |||
| chr4:69097056 | C | T | 1 | a0004 | 5 | HG02055.hp1 HG02572.hp1 HG02895.hp2 others(2): Show |
missense_variant | MODERATE | c.536C>T | p.Thr179Ile | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 1/6 | 583/1888 | 536/1590 | 179/529 | chr4 | 69097056 | |||
| chr4:69098620 | T | C | 7 | a0001 a0003 a0004 others(4): Show |
295 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(292): Show |
missense_variant | MODERATE | c.802T>C | p.Tyr268His | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 2/6 | 849/1888 | 802/1590 | 268/529 | chr4 | 69098620 | |||
| chr4:69098632 | C | T | 1 | a0007 | 1 | HG02135.hp2 | missense_variant | MODERATE | c.814C>T | p.Pro272Ser | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 2/6 | 861/1888 | 814/1590 | 272/529 | chr4 | 69098632 | |||
| chr4:69112470 | G | A | 1 | a0005 | 2 | NA18962.hp1 NA19055.hp1 |
missense_variant | MODERATE | c.1324G>A | p.Val442Ile | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 6/6 | 1371/1888 | 1324/1590 | 442/529 | chr4 | 69112470 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:69096892 | A | G | 2 | a0001c0005 a0003c0004 |
54 | HG00323.hp1 HG00323.hp2 HG00544.hp2 others(51): Show |
synonymous_variant | LOW | c.372A>G | p.Arg124Arg | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 1/6 | 419/1888 | 372/1590 | 124/529 | chr4 | 69096892 | |||
| chr4:69098553 | A | G | 6 | a0001c0003 a0001c0017 a0001c0018 others(3): Show |
65 | HG00140.hp2 HG00642.hp2 HG00741.hp1 others(62): Show |
synonymous_variant | LOW | c.735A>G | p.Thr245Thr | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 2/6 | 782/1888 | 735/1590 | 245/529 | chr4 | 69098553 | |||
| chr4:69098559 | T | C | 1 | a0001c0014 | 1 | NA19043.hp2 | synonymous_variant | LOW | c.741T>C | p.Ser247Ser | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 2/6 | 788/1888 | 741/1590 | 247/529 | chr4 | 69098559 | |||
| chr4:69098619 | A | T | 16 | a0001c0001 a0001c0003 a0001c0005 others(13): Show |
295 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(292): Show |
synonymous_variant | LOW | c.801A>T | p.Pro267Pro | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 2/6 | 848/1888 | 801/1590 | 267/529 | chr4 | 69098619 | |||
| chr4:69098673 | C | A | 1 | a0002c0006 | 8 | HG00642.hp1 HG01106.hp2 HG01255.hp2 others(5): Show |
synonymous_variant | LOW | c.855C>A | p.Ala285Ala | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 2/6 | 902/1888 | 855/1590 | 285/529 | chr4 | 69098673 | |||
| chr4:69107231 | C | G | 16 | a0001c0001 a0001c0003 a0001c0005 others(13): Show |
295 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(292): Show |
synonymous_variant | LOW | c.1059C>G | p.Leu353Leu | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 4/6 | 1106/1888 | 1059/1590 | 353/529 | chr4 | 69107231 | |||
| chr4:69107234 | C | T | 8 | a0001c0003 a0001c0011 a0001c0016 others(5): Show |
69 | HG00140.hp2 HG00642.hp2 HG00741.hp1 others(66): Show |
synonymous_variant | LOW | c.1062C>T | p.Tyr354Tyr | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 4/6 | 1109/1888 | 1062/1590 | 354/529 | chr4 | 69107234 | |||
| chr4:69108149 | C | A | 1 | a0001c0008 | 4 | HG02615.hp2 HG03098.hp2 HG03471.hp1 others(1): Show |
synonymous_variant | LOW | c.1137C>A | p.Gly379Gly | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 5/6 | 1184/1888 | 1137/1590 | 379/529 | chr4 | 69108149 | |||
| chr4:69108203 | C | T | 1 | a0002c0006 | 8 | HG00642.hp1 HG01106.hp2 HG01255.hp2 others(5): Show |
synonymous_variant | LOW | c.1191C>T | p.Ala397Ala | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 5/6 | 1238/1888 | 1191/1590 | 397/529 | chr4 | 69108203 | |||
| chr4:69108242 | A | T | 1 | a0001c0018 | 1 | HG03710.hp2 | synonymous_variant | LOW | c.1230A>T | p.Gly410Gly | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 5/6 | 1277/1888 | 1230/1590 | 410/529 | chr4 | 69108242 | |||
| chr4:69112472 | T | A | 1 | a0001c0017 | 1 | HG04184.hp2 | synonymous_variant | LOW | c.1326T>A | p.Val442Val | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 6/6 | 1373/1888 | 1326/1590 | 442/529 | chr4 | 69112472 | |||
| chr4:69112652 | A | G | 1 | a0001c0016 | 1 | HG02976.hp2 | synonymous_variant | LOW | c.1506A>G | p.Ala502Ala | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 6/6 | 1553/1888 | 1506/1590 | 502/529 | chr4 | 69112652 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:69096519 | G | A | 2 | a0001c0001t0005 a0008c0019t0005 |
3 | HG01891.hp2 HG03516.hp2 NA20129.hp2 |
5_prime_UTR_variant | MODIFIER | c.-2G>A | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 1/6 | 2 | chr4 | 69096519 | ||||||
| chr4:69112836 | C | CA | 17 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0006 others(14): Show |
266 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(263): Show |
3_prime_UTR_variant | MODIFIER | c.*113dupA | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 6/6 | 114 | INFO_REALIGN_3_PRIME | chr4 | 69112836 | |||||
| chr4:69112836 | C | CAA | 2 | a0001c0003t0003 a0002c0009t0003 |
10 | HG01109.hp2 HG01261.hp2 HG02559.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*112_*113dupAA | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 6/6 | 114 | INFO_REALIGN_3_PRIME | chr4 | 69112836 | |||||
| chr4:69112849 | A | G | 1 | a0001c0017t0008 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*113A>G | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 6/6 | 113 | chr4 | 69112849 | ||||||
| chr4:69112850 | G | A | 1 | a0001c0017t0008 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*114G>A | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 6/6 | 114 | chr4 | 69112850 | ||||||
| chr4:69112965 | A | G | 1 | a0001c0001t0006 | 2 | NA18952.hp1 NA18981.hp2 |
3_prime_UTR_variant | MODIFIER | c.*229A>G | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 6/6 | 229 | chr4 | 69112965 | ||||||
| chr4:69112967 | A | G | 1 | a0002c0002t0007 | 1 | HG00621.hp1 | 3_prime_UTR_variant | MODIFIER | c.*231A>G | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 6/6 | 231 | chr4 | 69112967 | ||||||
| chr4:69112983 | C | A | 2 | a0001c0003t0004 a0004c0007t0004 |
7 | HG02055.hp1 HG02145.hp1 HG02572.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*247C>A | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 6/6 | 247 | chr4 | 69112983 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:69097248 | A | AT | 3 | a0002c0002t0002g0011 a0002c0002t0002g0037 a0002c0002t0002g0104 |
10 | HG00738.hp2 HG01099.hp1 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.721+14dupT | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 69097248 | ||||||
| chr4:69097347 | GA | G | 3 | a0002c0002t0002g0035 a0002c0002t0002g0036 a0002c0002t0002g0103 |
5 | NA18944.hp2 NA18948.hp1 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.721+108delA | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 69097347 | ||||||
| chr4:69097382 | A | T | 1 | a0001c0001t0001g0102 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.721+141A>T | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 1/5 | chr4 | 69097382 | |||||||
| chr4:69097410 | A | T | 1 | a0001c0001t0001g0102 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.721+169A>T | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 1/5 | chr4 | 69097410 | |||||||
| chr4:69097442 | A | C | 83 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(80): Show |
295 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(292): Show |
intron_variant | MODIFIER | c.721+201A>C | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 1/5 | chr4 | 69097442 | |||||||
| chr4:69097450 | A | G | 83 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(80): Show |
295 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(292): Show |
intron_variant | MODIFIER | c.721+209A>G | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 1/5 | chr4 | 69097450 | |||||||
| chr4:69097513 | T | C | 21 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0020 others(18): Show |
119 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.721+272T>C | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 1/5 | chr4 | 69097513 | |||||||
| chr4:69097538 | A | G | 2 | a0002c0009t0003g0051 a0002c0009t0003g0052 |
2 | HG01109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.721+297A>G | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 1/5 | chr4 | 69097538 | |||||||
| chr4:69097548 | C | T | 1 | a0009c0013t0001g0101 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.721+307C>T | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 1/5 | chr4 | 69097548 | |||||||
| chr4:69097653 | G | C | 1 | a0001c0001t0001g0066 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.721+412G>C | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 1/5 | chr4 | 69097653 | |||||||
| chr4:69097706 | G | A | 6 | a0001c0003t0001g0008 a0001c0003t0001g0068 a0001c0003t0001g0069 others(3): Show |
15 | HG00140.hp2 HG00642.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.721+465G>A | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 1/5 | chr4 | 69097706 | |||||||
| chr4:69097740 | C | A | 83 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(80): Show |
295 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(292): Show |
intron_variant | MODIFIER | c.721+499C>A | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 1/5 | chr4 | 69097740 | |||||||
| chr4:69097825 | A | G | 1 | a0001c0001t0001g0100 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.721+584A>G | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 1/5 | chr4 | 69097825 | |||||||
| chr4:69097873 | T | C | 1 | a0001c0001t0001g0072 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.721+632T>C | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 1/5 | chr4 | 69097873 | |||||||
| chr4:69098070 | C | T | 88 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(85): Show |
306 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(303): Show |
intron_variant | MODIFIER | c.722-470C>T | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 1/5 | chr4 | 69098070 | |||||||
| chr4:69098201 | C | T | 2 | a0002c0009t0003g0051 a0002c0009t0003g0052 |
2 | HG01109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.722-339C>T | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 1/5 | chr4 | 69098201 | |||||||
| chr4:69098226 | A | G | 32 | a0001c0001t0001g0084 a0001c0001t0005g0097 a0001c0001t0005g0098 others(29): Show |
77 | HG00140.hp2 HG00642.hp2 HG00741.hp1 others(74): Show |
intron_variant | MODIFIER | c.722-314A>G | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 1/5 | chr4 | 69098226 | |||||||
| chr4:69098240 | C | A | 2 | a0002c0002t0002g0012 a0002c0002t0002g0038 |
7 | HG00280.hp1 HG00735.hp1 HG01517.hp2 others(4): Show |
intron_variant | MODIFIER | c.722-300C>A | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 1/5 | chr4 | 69098240 | |||||||
| chr4:69098248 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.722-292C>T | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 1/5 | chr4 | 69098248 | |||||||
| chr4:69098359 | C | T | 2 | a0002c0006t0002g0015 a0002c0006t0002g0024 |
8 | HG00642.hp1 HG01106.hp2 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.722-181C>T | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 1/5 | chr4 | 69098359 | |||||||
| chr4:69098405 | A | G | 1 | a0001c0003t0001g0017 | 5 | HG01346.hp1 HG01952.hp2 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.722-135A>G | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 1/5 | chr4 | 69098405 | |||||||
| chr4:69098462 | T | C | 83 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(80): Show |
295 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(292): Show |
intron_variant | MODIFIER | c.722-78T>C | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 1/5 | chr4 | 69098462 | |||||||
| chr4:69098473 | C | T | 2 | a0002c0009t0003g0051 a0002c0009t0003g0052 |
2 | HG01109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.722-67C>T | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 1/5 | chr4 | 69098473 | |||||||
| chr4:69098491 | A | G | 83 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(80): Show |
295 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(292): Show |
intron_variant | MODIFIER | c.722-49A>G | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 1/5 | chr4 | 69098491 | |||||||
| chr4:69098516 | C | CT | 83 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(80): Show |
294 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(291): Show |
intron_variant | MODIFIER | c.722-14dupT | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 69098516 | ||||||
| chr4:69098516 | C | CTT | 5 | a0001c0005t0001g0009 a0001c0005t0001g0034 a0001c0005t0001g0081 others(2): Show |
12 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.722-15_722-14dupTT | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 69098516 | ||||||
| chr4:69098755 | T | C | 2 | a0001c0001t0001g0066 a0001c0001t0001g0073 |
2 | HG02572.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.870+67T>C | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 2/5 | chr4 | 69098755 | |||||||
| chr4:69098803 | G | A | 83 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(80): Show |
295 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(292): Show |
intron_variant | MODIFIER | c.870+115G>A | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 2/5 | chr4 | 69098803 | |||||||
| chr4:69098836 | G | A | 83 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(80): Show |
295 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(292): Show |
intron_variant | MODIFIER | c.870+148G>A | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 2/5 | chr4 | 69098836 | |||||||
| chr4:69099017 | G | T | 1 | a0003c0004t0001g0021 | 4 | HG00639.hp2 HG01346.hp2 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.870+329G>T | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 2/5 | chr4 | 69099017 | |||||||
| chr4:69099052 | T | C | 1 | a0002c0002t0002g0039 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.870+364T>C | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 2/5 | chr4 | 69099052 | |||||||
| chr4:69099090 | A | C | 2 | a0002c0006t0002g0015 a0002c0006t0002g0024 |
8 | HG00642.hp1 HG01106.hp2 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.870+402A>C | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 2/5 | chr4 | 69099090 | |||||||
| chr4:69099137 | A | T | 1 | a0001c0011t0001g0099 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.870+449A>T | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 2/5 | chr4 | 69099137 | |||||||
| chr4:69099141 | G | C | 83 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(80): Show |
295 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(292): Show |
intron_variant | MODIFIER | c.870+453G>C | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 2/5 | chr4 | 69099141 | |||||||
| chr4:69099243 | C | T | 21 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0020 others(18): Show |
119 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.870+555C>T | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 2/5 | chr4 | 69099243 | |||||||
| chr4:69099257 | CA | C | 3 | a0002c0002t0002g0023 a0002c0002t0002g0036 a0002c0002t0002g0038 |
6 | HG02074.hp2 HG02083.hp2 HG03704.hp2 others(3): Show |
intron_variant | MODIFIER | c.870+590delA | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 69099257 | ||||||
| chr4:69099257 | CAAAA | C | 26 | a0001c0001t0001g0031 a0001c0001t0001g0066 a0001c0001t0001g0073 others(23): Show |
72 | HG00140.hp2 HG00642.hp2 HG00741.hp1 others(69): Show |
intron_variant | MODIFIER | c.870+587_870+590del others(4): Show |
UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 69099257 | ||||||
| chr4:69099257 | CAAAAA | C | 50 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(47): Show |
216 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(213): Show |
intron_variant | MODIFIER | c.870+586_870+590del others(5): Show |
UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 69099257 | ||||||
| chr4:69099478 | C | A | 1 | a0001c0001t0001g0084 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.870+790C>A | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 2/5 | chr4 | 69099478 | |||||||
| chr4:69099705 | T | C | 3 | a0001c0011t0001g0085 a0001c0011t0001g0089 a0001c0011t0001g0099 |
3 | HG01243.hp2 HG03139.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.870+1017T>C | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 2/5 | chr4 | 69099705 | |||||||
| chr4:69099784 | T | C | 82 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(79): Show |
294 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(291): Show |
intron_variant | MODIFIER | c.870+1096T>C | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 2/5 | chr4 | 69099784 | |||||||
| chr4:69099987 | A | G | 1 | a0001c0001t0001g0064 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.870+1299A>G | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 2/5 | chr4 | 69099987 | |||||||
| chr4:69100057 | T | C | 2 | a0002c0002t0002g0018 a0002c0002t0002g0028 |
6 | NA18943.hp2 NA18983.hp1 NA19056.hp2 others(3): Show |
intron_variant | MODIFIER | c.870+1369T>C | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 2/5 | chr4 | 69100057 | |||||||
| chr4:69100087 | GACCCCAG others(3): Show |
G | 1 | a0001c0016t0001g0094 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.870+1400_870+1409d others(12): Show |
UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 2/5 | chr4 | 69100087 | |||||||
| chr4:69100098 | T | C | 1 | a0001c0016t0001g0094 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.870+1410T>C | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 2/5 | chr4 | 69100098 | |||||||
| chr4:69100212 | C | G | 83 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(80): Show |
295 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(292): Show |
intron_variant | MODIFIER | c.870+1524C>G | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 2/5 | chr4 | 69100212 | |||||||
| chr4:69100306 | G | A | 83 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(80): Show |
295 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(292): Show |
intron_variant | MODIFIER | c.870+1618G>A | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 2/5 | chr4 | 69100306 | |||||||
| chr4:69100332 | AT | A | 83 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(80): Show |
295 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(292): Show |
intron_variant | MODIFIER | c.870+1650delT | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 69100332 | ||||||
| chr4:69100380 | A | G | 2 | a0001c0011t0001g0085 a0001c0011t0001g0089 |
2 | HG03139.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.870+1692A>G | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 2/5 | chr4 | 69100380 | |||||||
| chr4:69100403 | A | G | 6 | a0001c0003t0001g0005 a0001c0003t0001g0088 a0001c0003t0001g0092 others(3): Show |
22 | HG02056.hp1 HG02135.hp1 HG03654.hp1 others(19): Show |
intron_variant | MODIFIER | c.870+1715A>G | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 2/5 | chr4 | 69100403 | |||||||
| chr4:69100421 | C | T | 5 | a0001c0005t0001g0003 a0001c0005t0001g0075 a0003c0004t0001g0003 others(2): Show |
36 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.870+1733C>T | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 2/5 | chr4 | 69100421 | |||||||
| chr4:69100490 | A | T | 1 | a0001c0016t0001g0094 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.870+1802A>T | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 2/5 | chr4 | 69100490 | |||||||
| chr4:69100517 | G | T | 1 | a0001c0001t0001g0063 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.870+1829G>T | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 2/5 | chr4 | 69100517 | |||||||
| chr4:69100645 | A | G | 1 | a0002c0002t0002g0028 | 2 | NA18943.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.870+1957A>G | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 2/5 | chr4 | 69100645 | |||||||
| chr4:69100700 | T | C | 83 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(80): Show |
295 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(292): Show |
intron_variant | MODIFIER | c.870+2012T>C | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 2/5 | chr4 | 69100700 | |||||||
| chr4:69100837 | A | G | 83 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(80): Show |
295 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(292): Show |
intron_variant | MODIFIER | c.871-1970A>G | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 2/5 | chr4 | 69100837 | |||||||
| chr4:69100876 | A | T | 83 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(80): Show |
295 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(292): Show |
intron_variant | MODIFIER | c.871-1931A>T | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 2/5 | chr4 | 69100876 | |||||||
| chr4:69100940 | G | A | 82 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(79): Show |
294 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(291): Show |
intron_variant | MODIFIER | c.871-1867G>A | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 2/5 | chr4 | 69100940 | |||||||
| chr4:69100940 | G | T | 1 | a0001c0001t0001g0080 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.871-1867G>T | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 2/5 | chr4 | 69100940 | |||||||
| chr4:69101135 | T | A | 83 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(80): Show |
295 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(292): Show |
intron_variant | MODIFIER | c.871-1672T>A | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 2/5 | chr4 | 69101135 | |||||||
| chr4:69101208 | T | C | 83 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(80): Show |
295 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(292): Show |
intron_variant | MODIFIER | c.871-1599T>C | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 2/5 | chr4 | 69101208 | |||||||
| chr4:69101312 | C | A | 1 | a0002c0002t0002g0040 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.871-1495C>A | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 2/5 | chr4 | 69101312 | |||||||
| chr4:69101522 | A | C | 1 | a0001c0001t0001g0063 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.871-1285A>C | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 2/5 | chr4 | 69101522 | |||||||
| chr4:69101571 | G | A | 3 | a0001c0003t0001g0090 a0001c0003t0003g0016 a0001c0003t0003g0095 |
7 | HG02559.hp1 HG02622.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.871-1236G>A | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 2/5 | chr4 | 69101571 | |||||||
| chr4:69101631 | A | C | 16 | a0001c0003t0001g0005 a0001c0003t0001g0008 a0001c0003t0001g0010 others(13): Show |
51 | HG00140.hp2 HG00642.hp2 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.871-1176A>C | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 2/5 | chr4 | 69101631 | |||||||
| chr4:69101647 | TA | T | 83 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(80): Show |
295 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(292): Show |
intron_variant | MODIFIER | c.871-1153delA | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 69101647 | ||||||
| chr4:69101657 | C | T | 28 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0032 others(25): Show |
97 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.871-1150C>T | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 2/5 | chr4 | 69101657 | |||||||
| chr4:69101661 | G | A | 55 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0020 others(52): Show |
198 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(195): Show |
intron_variant | MODIFIER | c.871-1146G>A | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 2/5 | chr4 | 69101661 | |||||||
| chr4:69101807 | A | G | 1 | a0002c0002t0002g0049 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.871-1000A>G | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 2/5 | chr4 | 69101807 | |||||||
| chr4:69101866 | G | A | 2 | a0001c0001t0001g0066 a0001c0001t0001g0073 |
2 | HG02572.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.871-941G>A | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 2/5 | chr4 | 69101866 | |||||||
| chr4:69101921 | G | A | 83 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(80): Show |
295 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(292): Show |
intron_variant | MODIFIER | c.871-886G>A | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 2/5 | chr4 | 69101921 | |||||||
| chr4:69102032 | T | G | 1 | a0001c0005t0001g0082 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.871-775T>G | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 2/5 | chr4 | 69102032 | |||||||
| chr4:69102209 | T | C | 28 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0032 others(25): Show |
97 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.871-598T>C | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 2/5 | chr4 | 69102209 | |||||||
| chr4:69102221 | A | G | 21 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0020 others(18): Show |
119 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.871-586A>G | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 2/5 | chr4 | 69102221 | |||||||
| chr4:69102348 | T | G | 88 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(85): Show |
306 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(303): Show |
intron_variant | MODIFIER | c.871-459T>G | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 2/5 | chr4 | 69102348 | |||||||
| chr4:69102440 | C | G | 2 | a0002c0006t0002g0015 a0002c0006t0002g0024 |
8 | HG00642.hp1 HG01106.hp2 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.871-367C>G | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 2/5 | chr4 | 69102440 | |||||||
| chr4:69103107 | A | AT | 88 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(85): Show |
306 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(303): Show |
intron_variant | MODIFIER | c.1002+178dupT | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr4 | 69103107 | ||||||
| chr4:69103125 | TTAAG | T | 10 | a0001c0001t0001g0004 a0001c0001t0001g0032 a0001c0001t0001g0033 others(7): Show |
31 | HG00423.hp1 HG00673.hp2 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.1002+190_1002+193d others(6): Show |
UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr4 | 69103125 | ||||||
| chr4:69103141 | C | A | 1 | a0001c0005t0001g0034 | 2 | HG01070.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.1002+203C>A | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 3/5 | chr4 | 69103141 | |||||||
| chr4:69103250 | A | G | 1 | a0002c0002t0002g0048 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1002+312A>G | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 3/5 | chr4 | 69103250 | |||||||
| chr4:69103288 | G | T | 86 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(83): Show |
298 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(295): Show |
intron_variant | MODIFIER | c.1002+350G>T | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 3/5 | chr4 | 69103288 | |||||||
| chr4:69103462 | C | T | 86 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(83): Show |
298 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(295): Show |
intron_variant | MODIFIER | c.1002+524C>T | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 3/5 | chr4 | 69103462 | |||||||
| chr4:69103586 | G | T | 1 | a0008c0019t0005g0087 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1002+648G>T | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 3/5 | chr4 | 69103586 | |||||||
| chr4:69103593 | C | T | 2 | a0001c0001t0001g0013 a0005c0012t0001g0013 |
6 | NA18944.hp1 NA18962.hp1 NA18973.hp1 others(3): Show |
intron_variant | MODIFIER | c.1002+655C>T | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 3/5 | chr4 | 69103593 | |||||||
| chr4:69103825 | C | T | 86 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(83): Show |
298 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(295): Show |
intron_variant | MODIFIER | c.1002+887C>T | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 3/5 | chr4 | 69103825 | |||||||
| chr4:69103949 | A | G | 86 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(83): Show |
298 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(295): Show |
intron_variant | MODIFIER | c.1002+1011A>G | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 3/5 | chr4 | 69103949 | |||||||
| chr4:69103961 | C | A | 86 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(83): Show |
298 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(295): Show |
intron_variant | MODIFIER | c.1002+1023C>A | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 3/5 | chr4 | 69103961 | |||||||
| chr4:69103991 | A | C | 1 | a0001c0003t0001g0069 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1002+1053A>C | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 3/5 | chr4 | 69103991 | |||||||
| chr4:69104017 | G | A | 86 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(83): Show |
298 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(295): Show |
intron_variant | MODIFIER | c.1002+1079G>A | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 3/5 | chr4 | 69104017 | |||||||
| chr4:69104054 | C | T | 29 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0032 others(26): Show |
98 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.1002+1116C>T | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 3/5 | chr4 | 69104054 | |||||||
| chr4:69104057 | G | C | 1 | a0002c0002t0002g0041 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1002+1119G>C | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 3/5 | chr4 | 69104057 | |||||||
| chr4:69104070 | C | T | 86 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(83): Show |
298 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(295): Show |
intron_variant | MODIFIER | c.1002+1132C>T | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 3/5 | chr4 | 69104070 | |||||||
| chr4:69104141 | C | T | 86 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(83): Show |
298 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(295): Show |
intron_variant | MODIFIER | c.1002+1203C>T | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 3/5 | chr4 | 69104141 | |||||||
| chr4:69104180 | G | A | 86 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(83): Show |
298 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(295): Show |
intron_variant | MODIFIER | c.1002+1242G>A | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 3/5 | chr4 | 69104180 | |||||||
| chr4:69104248 | A | T | 86 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(83): Show |
298 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(295): Show |
intron_variant | MODIFIER | c.1002+1310A>T | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 3/5 | chr4 | 69104248 | |||||||
| chr4:69104272 | C | T | 1 | a0001c0005t0001g0077 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1002+1334C>T | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 3/5 | chr4 | 69104272 | |||||||
| chr4:69104767 | A | G | 3 | a0001c0003t0001g0090 a0001c0003t0003g0016 a0001c0003t0003g0095 |
7 | HG02559.hp1 HG02622.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1002+1829A>G | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 3/5 | chr4 | 69104767 | |||||||
| chr4:69104908 | A | G | 1 | a0002c0002t0002g0018 | 4 | NA19056.hp2 NA19082.hp1 NA19083.hp2 others(1): Show |
intron_variant | MODIFIER | c.1002+1970A>G | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 3/5 | chr4 | 69104908 | |||||||
| chr4:69104984 | T | A | 29 | a0001c0001t0001g0084 a0001c0003t0001g0005 a0001c0003t0001g0008 others(26): Show |
74 | HG00140.hp2 HG00642.hp2 HG00741.hp1 others(71): Show |
intron_variant | MODIFIER | c.1002+2046T>A | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 3/5 | chr4 | 69104984 | |||||||
| chr4:69105219 | A | C | 19 | a0002c0002t0001g0042 a0002c0002t0002g0002 a0002c0002t0002g0011 others(16): Show |
78 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.1003-1956A>C | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 3/5 | chr4 | 69105219 | |||||||
| chr4:69105246 | A | G | 86 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(83): Show |
298 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(295): Show |
intron_variant | MODIFIER | c.1003-1929A>G | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 3/5 | chr4 | 69105246 | |||||||
| chr4:69105255 | ATAAAATA others(14): Show |
A | 28 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0032 others(25): Show |
97 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.1003-1917_1003-189 others(25): Show |
UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr4 | 69105255 | ||||||
| chr4:69105273 | A | T | 58 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0020 others(55): Show |
201 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(198): Show |
intron_variant | MODIFIER | c.1003-1902A>T | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 3/5 | chr4 | 69105273 | |||||||
| chr4:69105356 | T | C | 1 | a0002c0002t0001g0042 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1003-1819T>C | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 3/5 | chr4 | 69105356 | |||||||
| chr4:69105374 | C | G | 2 | a0002c0002t0002g0012 a0002c0002t0002g0038 |
7 | HG00280.hp1 HG00735.hp1 HG01517.hp2 others(4): Show |
intron_variant | MODIFIER | c.1003-1801C>G | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 3/5 | chr4 | 69105374 | |||||||
| chr4:69105451 | T | A | 1 | a0002c0009t0003g0050 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1003-1724T>A | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 3/5 | chr4 | 69105451 | |||||||
| chr4:69105553 | T | A | 1 | a0001c0003t0001g0090 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1003-1622T>A | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 3/5 | chr4 | 69105553 | |||||||
| chr4:69105617 | G | A | 28 | a0001c0003t0001g0005 a0001c0003t0001g0008 a0001c0003t0001g0010 others(25): Show |
73 | HG00140.hp2 HG00642.hp2 HG00741.hp1 others(70): Show |
intron_variant | MODIFIER | c.1003-1558G>A | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 3/5 | chr4 | 69105617 | |||||||
| chr4:69105764 | A | G | 1 | a0002c0002t0002g0047 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1003-1411A>G | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 3/5 | chr4 | 69105764 | |||||||
| chr4:69105768 | A | C | 1 | a0001c0001t0001g0084 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1003-1407A>C | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 3/5 | chr4 | 69105768 | |||||||
| chr4:69105792 | A | T | 3 | a0002c0002t0002g0022 a0002c0002t0002g0039 a0002c0002t0007g0022 |
4 | HG00621.hp1 HG02015.hp1 NA18940.hp2 others(1): Show |
intron_variant | MODIFIER | c.1003-1383A>T | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 3/5 | chr4 | 69105792 | |||||||
| chr4:69105858 | C | T | 2 | a0002c0006t0002g0015 a0002c0006t0002g0024 |
8 | HG00642.hp1 HG01106.hp2 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.1003-1317C>T | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 3/5 | chr4 | 69105858 | |||||||
| chr4:69105878 | C | T | 85 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(82): Show |
295 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(292): Show |
intron_variant | MODIFIER | c.1003-1297C>T | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 3/5 | chr4 | 69105878 | |||||||
| chr4:69105906 | C | A | 85 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(82): Show |
295 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(292): Show |
intron_variant | MODIFIER | c.1003-1269C>A | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 3/5 | chr4 | 69105906 | |||||||
| chr4:69105971 | A | G | 1 | a0001c0001t0001g0061 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1003-1204A>G | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 3/5 | chr4 | 69105971 | |||||||
| chr4:69105990 | C | T | 1 | a0002c0002t0002g0037 | 2 | HG01099.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.1003-1185C>T | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 3/5 | chr4 | 69105990 | |||||||
| chr4:69106024 | A | G | 2 | a0002c0009t0003g0051 a0002c0009t0003g0052 |
2 | HG01109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1003-1151A>G | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 3/5 | chr4 | 69106024 | |||||||
| chr4:69106078 | T | A | 85 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(82): Show |
295 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(292): Show |
intron_variant | MODIFIER | c.1003-1097T>A | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 3/5 | chr4 | 69106078 | |||||||
| chr4:69106113 | A | G | 2 | a0001c0003t0001g0068 a0001c0003t0001g0071 |
2 | HG01358.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.1003-1062A>G | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 3/5 | chr4 | 69106113 | |||||||
| chr4:69106116 | T | G | 2 | a0001c0001t0001g0066 a0001c0001t0001g0073 |
2 | HG02572.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1003-1059T>G | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 3/5 | chr4 | 69106116 | |||||||
| chr4:69106140 | T | C | 1 | a0001c0001t0001g0055 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1003-1035T>C | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 3/5 | chr4 | 69106140 | |||||||
| chr4:69106148 | T | G | 3 | a0001c0011t0001g0085 a0001c0011t0001g0089 a0001c0011t0001g0099 |
3 | HG01243.hp2 HG03139.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1003-1027T>G | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 3/5 | chr4 | 69106148 | |||||||
| chr4:69106192 | T | A | 85 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(82): Show |
295 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(292): Show |
intron_variant | MODIFIER | c.1003-983T>A | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 3/5 | chr4 | 69106192 | |||||||
| chr4:69106278 | T | C | 85 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(82): Show |
295 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(292): Show |
intron_variant | MODIFIER | c.1003-897T>C | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 3/5 | chr4 | 69106278 | |||||||
| chr4:69106368 | T | G | 85 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(82): Show |
295 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(292): Show |
intron_variant | MODIFIER | c.1003-807T>G | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 3/5 | chr4 | 69106368 | |||||||
| chr4:69106413 | C | T | 1 | a0001c0001t0006g0079 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1003-762C>T | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 3/5 | chr4 | 69106413 | |||||||
| chr4:69106467 | T | G | 1 | a0001c0011t0001g0099 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1003-708T>G | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 3/5 | chr4 | 69106467 | |||||||
| chr4:69106521 | T | C | 1 | a0001c0001t0001g0062 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1003-654T>C | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 3/5 | chr4 | 69106521 | |||||||
| chr4:69106554 | A | G | 85 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(82): Show |
295 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(292): Show |
intron_variant | MODIFIER | c.1003-621A>G | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 3/5 | chr4 | 69106554 | |||||||
| chr4:69106601 | C | T | 85 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(82): Show |
295 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(292): Show |
intron_variant | MODIFIER | c.1003-574C>T | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 3/5 | chr4 | 69106601 | |||||||
| chr4:69106641 | G | A | 1 | a0002c0002t0002g0043 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1003-534G>A | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 3/5 | chr4 | 69106641 | |||||||
| chr4:69106672 | G | A | 2 | a0001c0001t0001g0025 a0001c0001t0001g0056 |
4 | NA18979.hp1 NA18989.hp1 NA19074.hp1 others(1): Show |
intron_variant | MODIFIER | c.1003-503G>A | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 3/5 | chr4 | 69106672 | |||||||
| chr4:69106696 | A | T | 85 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(82): Show |
295 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(292): Show |
intron_variant | MODIFIER | c.1003-479A>T | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 3/5 | chr4 | 69106696 | |||||||
| chr4:69106745 | C | T | 49 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(46): Show |
214 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(211): Show |
intron_variant | MODIFIER | c.1003-430C>T | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 3/5 | chr4 | 69106745 | |||||||
| chr4:69106769 | G | A | 1 | a0001c0001t0001g0032 | 2 | HG02602.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1003-406G>A | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 3/5 | chr4 | 69106769 | |||||||
| chr4:69106838 | C | G | 1 | a0007c0015t0002g0046 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1003-337C>G | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 3/5 | chr4 | 69106838 | |||||||
| chr4:69106859 | C | CT | 30 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0032 others(27): Show |
97 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.1003-305dupT | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr4 | 69106859 | ||||||
| chr4:69106914 | A | T | 1 | a0001c0016t0001g0094 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1003-261A>T | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 3/5 | chr4 | 69106914 | |||||||
| chr4:69107059 | G | A | 85 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(82): Show |
295 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(292): Show |
intron_variant | MODIFIER | c.1003-116G>A | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 3/5 | chr4 | 69107059 | |||||||
| chr4:69107061 | G | A | 19 | a0002c0002t0001g0042 a0002c0002t0002g0002 a0002c0002t0002g0011 others(16): Show |
78 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.1003-114G>A | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 3/5 | chr4 | 69107061 | |||||||
| chr4:69107326 | A | T | 85 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(82): Show |
295 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(292): Show |
intron_variant | MODIFIER | c.1090+64A>T | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 4/5 | chr4 | 69107326 | |||||||
| chr4:69107374 | A | T | 1 | a0001c0003t0003g0067 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1090+112A>T | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 4/5 | chr4 | 69107374 | |||||||
| chr4:69107416 | CA | C | 85 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(82): Show |
295 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(292): Show |
intron_variant | MODIFIER | c.1090+155delA | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 4/5 | chr4 | 69107416 | |||||||
| chr4:69107448 | C | A | 21 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0020 others(18): Show |
119 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.1090+186C>A | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 4/5 | chr4 | 69107448 | |||||||
| chr4:69107521 | A | T | 28 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0032 others(25): Show |
95 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.1090+259A>T | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 4/5 | chr4 | 69107521 | |||||||
| chr4:69107807 | C | A | 85 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(82): Show |
295 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(292): Show |
intron_variant | MODIFIER | c.1091-296C>A | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 4/5 | chr4 | 69107807 | |||||||
| chr4:69107809 | C | T | 1 | a0002c0002t0002g0103 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1091-294C>T | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 4/5 | chr4 | 69107809 | |||||||
| chr4:69107921 | C | T | 1 | a0001c0001t0001g0060 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1091-182C>T | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 4/5 | chr4 | 69107921 | |||||||
| chr4:69107922 | A | G | 85 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(82): Show |
295 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(292): Show |
intron_variant | MODIFIER | c.1091-181A>G | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 4/5 | chr4 | 69107922 | |||||||
| chr4:69107926 | C | T | 1 | a0001c0005t0001g0083 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1091-177C>T | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 4/5 | chr4 | 69107926 | |||||||
| chr4:69107929 | A | G | 3 | a0002c0002t0002g0022 a0002c0002t0002g0039 a0002c0002t0007g0022 |
4 | HG00621.hp1 HG02015.hp1 NA18940.hp2 others(1): Show |
intron_variant | MODIFIER | c.1091-174A>G | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 4/5 | chr4 | 69107929 | |||||||
| chr4:69107930 | T | C | 6 | a0002c0002t0002g0018 a0002c0002t0002g0019 a0002c0002t0002g0022 others(3): Show |
14 | HG00408.hp1 HG00621.hp1 HG02015.hp1 others(11): Show |
intron_variant | MODIFIER | c.1091-173T>C | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 4/5 | chr4 | 69107930 | |||||||
| chr4:69107949 | C | G | 85 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(82): Show |
295 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(292): Show |
intron_variant | MODIFIER | c.1091-154C>G | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 4/5 | chr4 | 69107949 | |||||||
| chr4:69107951 | G | A | 3 | a0001c0003t0004g0014 a0004c0007t0004g0014 a0004c0007t0004g0096 |
7 | HG02055.hp1 HG02145.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1091-152G>A | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 4/5 | chr4 | 69107951 | |||||||
| chr4:69107974 | C | T | 85 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(82): Show |
295 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(292): Show |
intron_variant | MODIFIER | c.1091-129C>T | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 4/5 | chr4 | 69107974 | |||||||
| chr4:69108008 | G | A | 4 | a0002c0002t0002g0011 a0002c0002t0002g0029 a0002c0002t0002g0037 others(1): Show |
12 | HG00738.hp2 HG01099.hp1 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.1091-95G>A | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 4/5 | chr4 | 69108008 | |||||||
| chr4:69108353 | T | C | 1 | a0001c0001t0001g0033 | 2 | HG03834.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1310+31T>C | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 5/5 | chr4 | 69108353 | |||||||
| chr4:69108363 | T | C | 2 | a0001c0001t0001g0066 a0001c0001t0001g0073 |
2 | HG02572.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1310+41T>C | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 5/5 | chr4 | 69108363 | |||||||
| chr4:69108506 | TA | T | 2 | a0002c0006t0002g0015 a0002c0006t0002g0024 |
8 | HG00642.hp1 HG01106.hp2 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.1310+187delA | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr4 | 69108506 | ||||||
| chr4:69108549 | A | T | 85 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(82): Show |
295 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(292): Show |
intron_variant | MODIFIER | c.1310+227A>T | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 5/5 | chr4 | 69108549 | |||||||
| chr4:69108594 | T | A | 1 | a0001c0003t0001g0071 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1310+272T>A | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 5/5 | chr4 | 69108594 | |||||||
| chr4:69108762 | G | T | 80 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(77): Show |
290 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(287): Show |
intron_variant | MODIFIER | c.1310+440G>T | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 5/5 | chr4 | 69108762 | |||||||
| chr4:69109040 | G | T | 1 | a0001c0001t0005g0098 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1310+718G>T | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 5/5 | chr4 | 69109040 | |||||||
| chr4:69109109 | A | G | 2 | a0002c0009t0003g0051 a0002c0009t0003g0052 |
2 | HG01109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1310+787A>G | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 5/5 | chr4 | 69109109 | |||||||
| chr4:69109344 | A | G | 3 | a0001c0001t0001g0020 a0001c0001t0001g0054 a0001c0001t0002g0020 |
5 | HG01192.hp2 HG02895.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1310+1022A>G | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 5/5 | chr4 | 69109344 | |||||||
| chr4:69109420 | C | T | 1 | a0001c0001t0001g0056 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1310+1098C>T | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 5/5 | chr4 | 69109420 | |||||||
| chr4:69109444 | G | A | 28 | a0001c0003t0001g0005 a0001c0003t0001g0008 a0001c0003t0001g0010 others(25): Show |
73 | HG00140.hp2 HG00642.hp2 HG00741.hp1 others(70): Show |
intron_variant | MODIFIER | c.1310+1122G>A | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 5/5 | chr4 | 69109444 | |||||||
| chr4:69109508 | G | A | 1 | a0002c0002t0002g0044 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1310+1186G>A | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 5/5 | chr4 | 69109508 | |||||||
| chr4:69109542 | A | G | 1 | a0002c0002t0002g0030 | 2 | NA18953.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.1310+1220A>G | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 5/5 | chr4 | 69109542 | |||||||
| chr4:69109610 | T | C | 1 | a0002c0006t0002g0024 | 3 | HG00642.hp1 HG01106.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.1310+1288T>C | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 5/5 | chr4 | 69109610 | |||||||
| chr4:69109629 | G | A | 27 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0032 others(24): Show |
94 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.1310+1307G>A | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 5/5 | chr4 | 69109629 | |||||||
| chr4:69109723 | TAA | T | 6 | a0001c0003t0001g0008 a0001c0003t0001g0068 a0001c0003t0001g0069 others(3): Show |
15 | HG00140.hp2 HG00642.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1310+1402_1310+140 others(6): Show |
UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 5/5 | chr4 | 69109723 | |||||||
| chr4:69109749 | T | C | 1 | a0002c0002t0002g0104 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1310+1427T>C | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 5/5 | chr4 | 69109749 | |||||||
| chr4:69109775 | A | C | 1 | a0001c0017t0008g0093 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1310+1453A>C | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 5/5 | chr4 | 69109775 | |||||||
| chr4:69109886 | A | T | 1 | a0001c0001t0001g0078 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1310+1564A>T | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 5/5 | chr4 | 69109886 | |||||||
| chr4:69109887 | T | C | 1 | a0001c0003t0001g0092 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1310+1565T>C | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 5/5 | chr4 | 69109887 | |||||||
| chr4:69109978 | GA | G | 2 | a0001c0003t0001g0010 a0006c0020t0001g0010 |
8 | HG01070.hp2 HG01071.hp2 HG01928.hp1 others(5): Show |
intron_variant | MODIFIER | c.1310+1664delA | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr4 | 69109978 | ||||||
| chr4:69110031 | T | A | 1 | a0007c0015t0002g0046 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1310+1709T>A | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 5/5 | chr4 | 69110031 | |||||||
| chr4:69110141 | C | T | 85 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(82): Show |
295 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(292): Show |
intron_variant | MODIFIER | c.1310+1819C>T | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 5/5 | chr4 | 69110141 | |||||||
| chr4:69110227 | T | A | 1 | a0001c0017t0008g0093 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1310+1905T>A | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 5/5 | chr4 | 69110227 | |||||||
| chr4:69110230 | G | C | 2 | a0002c0009t0003g0051 a0002c0009t0003g0052 |
2 | HG01109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1310+1908G>C | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 5/5 | chr4 | 69110230 | |||||||
| chr4:69110274 | A | G | 1 | a0001c0011t0001g0099 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1310+1952A>G | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 5/5 | chr4 | 69110274 | |||||||
| chr4:69110468 | TAGA | T | 85 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(82): Show |
295 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(292): Show |
intron_variant | MODIFIER | c.1311-1984_1311-198 others(7): Show |
UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr4 | 69110468 | ||||||
| chr4:69110473 | G | C | 1 | a0001c0001t0001g0073 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1311-1984G>C | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 5/5 | chr4 | 69110473 | |||||||
| chr4:69110499 | T | C | 85 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(82): Show |
295 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(292): Show |
intron_variant | MODIFIER | c.1311-1958T>C | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 5/5 | chr4 | 69110499 | |||||||
| chr4:69110574 | C | A | 2 | a0001c0001t0001g0066 a0001c0001t0001g0073 |
2 | HG02572.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1311-1883C>A | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 5/5 | chr4 | 69110574 | |||||||
| chr4:69110645 | A | G | 1 | a0001c0001t0005g0097 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1311-1812A>G | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 5/5 | chr4 | 69110645 | |||||||
| chr4:69110688 | C | T | 2 | a0001c0008t0001g0027 a0001c0008t0001g0086 |
4 | HG02615.hp2 HG03098.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1311-1769C>T | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 5/5 | chr4 | 69110688 | |||||||
| chr4:69110945 | C | A | 2 | a0002c0006t0002g0015 a0002c0006t0002g0024 |
8 | HG00642.hp1 HG01106.hp2 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.1311-1512C>A | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 5/5 | chr4 | 69110945 | |||||||
| chr4:69110955 | A | AAAATAAG others(3): Show |
1 | a0001c0001t0005g0098 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1311-1500_1311-149 others(14): Show |
UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr4 | 69110955 | ||||||
| chr4:69111281 | T | A | 2 | a0001c0001t0001g0066 a0001c0001t0001g0073 |
2 | HG02572.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1311-1176T>A | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 5/5 | chr4 | 69111281 | |||||||
| chr4:69111652 | A | G | 7 | a0001c0001t0001g0059 a0001c0003t0001g0005 a0001c0003t0001g0088 others(4): Show |
23 | HG00438.hp1 HG02056.hp1 HG02135.hp1 others(20): Show |
intron_variant | MODIFIER | c.1311-805A>G | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 5/5 | chr4 | 69111652 | |||||||
| chr4:69111884 | A | G | 2 | a0001c0003t0001g0090 a0008c0019t0005g0087 |
2 | HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1311-573A>G | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 5/5 | chr4 | 69111884 | |||||||
| chr4:69111891 | G | C | 1 | a0001c0001t0001g0076 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1311-566G>C | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 5/5 | chr4 | 69111891 | |||||||
| chr4:69111957 | A | T | 2 | a0001c0003t0003g0016 a0001c0003t0003g0095 |
6 | HG02559.hp1 HG02622.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1311-500A>T | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 5/5 | chr4 | 69111957 | |||||||
| chr4:69112090 | T | C | 87 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(84): Show |
303 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(300): Show |
intron_variant | MODIFIER | c.1311-367T>C | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 5/5 | chr4 | 69112090 | |||||||
| chr4:69112190 | T | C | 3 | a0001c0001t0002g0057 a0002c0006t0002g0015 a0002c0006t0002g0024 |
9 | HG00642.hp1 HG01106.hp2 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.1311-267T>C | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 5/5 | chr4 | 69112190 | |||||||
| chr4:69112302 | G | C | 2 | a0001c0008t0001g0027 a0001c0008t0001g0086 |
4 | HG02615.hp2 HG03098.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1311-155G>C | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 5/5 | chr4 | 69112302 | |||||||
| chr4:69112350 | G | A | 84 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(81): Show |
294 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(291): Show |
intron_variant | MODIFIER | c.1311-107G>A | UGT2B7 | ENSG00000171234.14 | transcript | ENST00000305231.12 | protein_coding | 5/5 | chr4 | 69112350 |