Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 574537 |
| ensemblid | ENSG00000271271.6 |
| hgncid | 28183 |
| symbol | UGT2A2 |
| name | UDP glucuronosyltransferase family 2 member A2 |
| refseq_nuc | NM_001105677.2 |
| refseq_prot | NP_001099147.2 |
| ensembl_nuc | ENST00000604629.6 |
| ensembl_prot | ENSP00000475028.2 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 69588417 |
| end | 69639642 |
| strand | - |
| ver | v1.2 |
| region | chr4:69588417-69639642 |
| region5000 | chr4:69583417-69644642 |
| regionname0 | UGT2A2_chr4_69588417_69639642 |
| regionname5000 | UGT2A2_chr4_69583417_69644642 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 536 | 314 | 62 | 58 | 151 | 8 | 33 | 116 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | MVSIR others(531): Show |
chr4 | 69583417 | 69644642 |
| a0002 | 0/0 | 536 | 26 | 8 | 6 | 5 | 1 | 6 | 4 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | MVSIR others(531): Show |
chr4 | 69583417 | 69644642 |
| a0003 | 0/0 | 536 | 16 | 2 | 2 | 6 | 4 | 2 | 5 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | MVSIR others(531): Show |
chr4 | 69583417 | 69644642 |
| a0004 | 0/0 | 536 | 6 | 0 | 3 | 1 | 1 | 1 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | MVSIR others(531): Show |
chr4 | 69583417 | 69644642 |
| a0005 | 0/0 | 536 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | MVSIR others(531): Show |
chr4 | 69583417 | 69644642 |
| a0006 | 0/0 | 536 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | MVSIR others(531): Show |
chr4 | 69583417 | 69644642 |
| a0007 | 0/0 | 536 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | MISIR others(531): Show |
chr4 | 69583417 | 69644642 |
| a0008 | 0/0 | 536 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | MVSIR others(531): Show |
chr4 | 69583417 | 69644642 |
| a0009 | 0/0 | 536 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | MVSIR others(531): Show |
chr4 | 69583417 | 69644642 |
| a0010 | 0/0 | 536 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | MVSIR others(531): Show |
chr4 | 69583417 | 69644642 |
| a0011 | 0/0 | 536 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | MVSIR others(531): Show |
chr4 | 69583417 | 69644642 |
| a0012 | 0/0 | 536 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | MVSIR others(531): Show |
chr4 | 69583417 | 69644642 |
| a0013 | 0/0 | 536 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | MVSIR others(531): Show |
chr4 | 69583417 | 69644642 |
| a0014 | 0/0 | 536 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | MVSIR others(531): Show |
chr4 | 69583417 | 69644642 |
| a0015 | 0/0 | 536 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | MVSIR others(531): Show |
chr4 | 69583417 | 69644642 |
| a0016 | 0/0 | 536 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | MVSIR others(531): Show |
chr4 | 69583417 | 69644642 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1608 | 309 | 62 | 56 | 149 | 8 | 32 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | ATGGT others(1603): Show |
chr4 | 69583417 | 69644642 | ||
| a0001c0007 | 0/0 | 1608 | 2 | 0 | 2 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | ATGGT others(1603): Show |
chr4 | 69583417 | 69644642 | ||
| a0001c0009 | 0/0 | 1608 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | ATGGT others(1603): Show |
chr4 | 69583417 | 69644642 | ||
| a0001c0014 | 0/0 | 1608 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | ATGGT others(1603): Show |
chr4 | 69583417 | 69644642 | ||
| a0001c0017 | 0/0 | 1608 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | ATGGT others(1603): Show |
chr4 | 69583417 | 69644642 | ||
| a0002c0002 | 0/0 | 1608 | 26 | 8 | 6 | 5 | 1 | 6 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | ATGGT others(1603): Show |
chr4 | 69583417 | 69644642 | ||
| a0003c0003 | 0/0 | 1608 | 16 | 2 | 2 | 6 | 4 | 2 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | ATGGT others(1603): Show |
chr4 | 69583417 | 69644642 | ||
| a0004c0004 | 0/0 | 1608 | 6 | 0 | 3 | 1 | 1 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | ATGGT others(1603): Show |
chr4 | 69583417 | 69644642 | ||
| a0005c0005 | 0/0 | 1608 | 3 | 3 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | ATGGT others(1603): Show |
chr4 | 69583417 | 69644642 | ||
| a0006c0008 | 0/0 | 1608 | 2 | 0 | 0 | 2 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | ATGGT others(1603): Show |
chr4 | 69583417 | 69644642 | ||
| a0007c0006 | 0/0 | 1608 | 2 | 2 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | ATGAT others(1603): Show |
chr4 | 69583417 | 69644642 | ||
| a0008c0013 | 0/0 | 1608 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | ATGGT others(1603): Show |
chr4 | 69583417 | 69644642 | ||
| a0009c0012 | 0/0 | 1608 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | ATGGT others(1603): Show |
chr4 | 69583417 | 69644642 | ||
| a0010c0011 | 0/0 | 1608 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | ATGGT others(1603): Show |
chr4 | 69583417 | 69644642 | ||
| a0011c0018 | 0/0 | 1608 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | ATGGT others(1603): Show |
chr4 | 69583417 | 69644642 | ||
| a0012c0019 | 0/0 | 1608 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | ATGGT others(1603): Show |
chr4 | 69583417 | 69644642 | ||
| a0013c0010 | 0/0 | 1608 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | ATGGT others(1603): Show |
chr4 | 69583417 | 69644642 | ||
| a0014c0015 | 0/0 | 1608 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | ATGGT others(1603): Show |
chr4 | 69583417 | 69644642 | ||
| a0015c0016 | 0/0 | 1608 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | ATGGT others(1603): Show |
chr4 | 69583417 | 69644642 | ||
| a0016c0020 | 0/0 | 1608 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | ATGGT others(1603): Show |
chr4 | 69583417 | 69644642 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2568 | 209 | 37 | 42 | 103 | 4 | 23 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | GGATG others(2563): Show |
chr4 | 69583417 | 69644642 |
| a0001c0001t0002 | 1/1 | 2568 | 82 | 9 | 13 | 45 | 4 | 9 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | GGATG others(2563): Show |
chr4 | 69583417 | 69644642 |
| a0001c0001t0003 | 0/0 | 2568 | 15 | 15 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | GGATG others(2563): Show |
chr4 | 69583417 | 69644642 |
| a0001c0001t0008 | 0/0 | 2568 | 2 | 1 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | GGATG others(2563): Show |
chr4 | 69583417 | 69644642 |
| a0001c0001t0009 | 0/0 | 2568 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | GGATG others(2563): Show |
chr4 | 69583417 | 69644642 |
| a0001c0007t0002 | 0/0 | 2568 | 2 | 0 | 2 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | GGATG others(2563): Show |
chr4 | 69583417 | 69644642 |
| a0001c0009t0001 | 0/0 | 2568 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | GGATG others(2563): Show |
chr4 | 69583417 | 69644642 |
| a0001c0014t0001 | 0/0 | 2568 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | GGATG others(2563): Show |
chr4 | 69583417 | 69644642 |
| a0001c0017t0001 | 0/0 | 2568 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | GGATG others(2563): Show |
chr4 | 69583417 | 69644642 |
| a0002c0002t0002 | 0/0 | 2568 | 21 | 6 | 6 | 2 | 1 | 6 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | GGATG others(2563): Show |
chr4 | 69583417 | 69644642 |
| a0002c0002t0004 | 0/0 | 2568 | 3 | 0 | 0 | 3 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | GGATG others(2563): Show |
chr4 | 69583417 | 69644642 |
| a0002c0002t0005 | 0/0 | 2568 | 2 | 2 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | GGATG others(2563): Show |
chr4 | 69583417 | 69644642 |
| a0003c0003t0001 | 0/0 | 2568 | 14 | 0 | 2 | 6 | 4 | 2 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | GGATG others(2563): Show |
chr4 | 69583417 | 69644642 |
| a0003c0003t0006 | 0/0 | 2568 | 2 | 2 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | GGATG others(2563): Show |
chr4 | 69583417 | 69644642 |
| a0004c0004t0001 | 0/0 | 2568 | 6 | 0 | 3 | 1 | 1 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | GGATG others(2563): Show |
chr4 | 69583417 | 69644642 |
| a0005c0005t0001 | 0/0 | 2568 | 3 | 3 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | GGATG others(2563): Show |
chr4 | 69583417 | 69644642 |
| a0006c0008t0002 | 0/0 | 2568 | 2 | 0 | 0 | 2 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | GGATG others(2563): Show |
chr4 | 69583417 | 69644642 |
| a0007c0006t0001 | 0/0 | 2568 | 2 | 2 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | GGATG others(2563): Show |
chr4 | 69583417 | 69644642 |
| a0008c0013t0002 | 0/0 | 2568 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | GGATG others(2563): Show |
chr4 | 69583417 | 69644642 |
| a0009c0012t0001 | 0/0 | 2568 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | GGATG others(2563): Show |
chr4 | 69583417 | 69644642 |
| a0010c0011t0007 | 0/0 | 2568 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | GGATG others(2563): Show |
chr4 | 69583417 | 69644642 |
| a0011c0018t0001 | 0/0 | 2568 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | GGATG others(2563): Show |
chr4 | 69583417 | 69644642 |
| a0012c0019t0002 | 0/0 | 2568 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | GGATG others(2563): Show |
chr4 | 69583417 | 69644642 |
| a0013c0010t0007 | 0/0 | 2568 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | GGATG others(2563): Show |
chr4 | 69583417 | 69644642 |
| a0014c0015t0001 | 0/0 | 2568 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | GGATG others(2563): Show |
chr4 | 69583417 | 69644642 |
| a0015c0016t0010 | 0/0 | 2568 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | GGATG others(2563): Show |
chr4 | 69583417 | 69644642 |
| a0016c0020t0001 | 0/0 | 2568 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | GGATG others(2563): Show |
chr4 | 69583417 | 69644642 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0003 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0008 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0016 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0001 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0010 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0011 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0023 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0119 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0120 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0003g0006 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0003g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0003g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0003g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0003g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0003g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0008g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0008g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0009g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0007t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0007t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0009t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0014t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0017t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0002c0002t0002g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0002c0002t0002g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0002c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0002c0002t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0002c0002t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0002c0002t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0002c0002t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0002c0002t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0002c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0002c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0002c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0002c0002t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0002c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0002c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0002c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0002c0002t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0002c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0002c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0002c0002t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0002c0002t0004g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0002c0002t0004g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0002c0002t0004g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0002c0002t0005g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0002c0002t0005g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0003c0003t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0003c0003t0001g0020 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0003c0003t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0003c0003t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0003c0003t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0003c0003t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0003c0003t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0003c0003t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0003c0003t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0003c0003t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0003c0003t0006g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0003c0003t0006g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0004c0004t0001g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0004c0004t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0004c0004t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0004c0004t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0004c0004t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0005c0005t0001g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0005c0005t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0006c0008t0002g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0007c0006t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0007c0006t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0008c0013t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0009c0012t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0010c0011t0007g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0011c0018t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0012c0019t0002g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0013c0010t0007g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0014c0015t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0015c0016t0010g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0016c0020t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0164 | EUR | GBR | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0010 | EUR | GBR | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG00140 | hp1 | a0003 | c0003 | t0001 | g0295 | EUR | GBR | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0089 | EUR | GBR | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0090 | EUR | FIN | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0163 | EUR | FIN | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG00423 | hp1 | a0006 | c0008 | t0002 | g0049 | EAS | CHS | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | CHS | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | CHS | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | CHS | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | CHS | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | CHS | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | CHS | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | CHS | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | CHS | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | CHS | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0107 | AMR | PUR | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG00639 | hp2 | a0004 | c0004 | t0001 | g0042 | AMR | PUR | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0106 | AMR | PUR | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0024 | AMR | PUR | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG00741 | hp1 | a0004 | c0004 | t0001 | g0042 | AMR | PUR | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01071 | hp2 | a0008 | c0013 | t0002 | g0088 | AMR | PUR | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01099 | hp1 | a0003 | c0003 | t0001 | g0020 | AMR | PUR | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01106 | hp1 | a0003 | c0003 | t0001 | g0288 | AMR | PUR | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01109 | hp2 | a0001 | c0001 | t0008 | g0080 | AMR | PUR | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0160 | AMR | PUR | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | PUR | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01175 | hp1 | a0001 | c0007 | t0002 | g0081 | AMR | PUR | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0095 | AMR | PUR | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0281 | AMR | PUR | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01243 | hp1 | a0009 | c0012 | t0001 | g0191 | AMR | PUR | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0272 | AMR | PUR | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | CLM | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | CLM | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0024 | AMR | CLM | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | CLM | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01258 | hp2 | a0004 | c0004 | t0001 | g0177 | AMR | CLM | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | CLM | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01346 | hp2 | a0002 | c0002 | t0002 | g0208 | AMR | CLM | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01358 | hp1 | a0002 | c0002 | t0002 | g0261 | AMR | CLM | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0092 | AMR | CLM | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0023 | AMR | CLM | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | CLM | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | CLM | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | CLM | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0146 | EUR | IBS | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01516 | hp2 | a0003 | c0003 | t0001 | g0020 | EUR | IBS | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01517 | hp1 | a0003 | c0003 | t0001 | g0020 | EUR | IBS | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01517 | hp2 | a0002 | c0002 | t0002 | g0196 | EUR | IBS | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01884 | hp1 | a0010 | c0011 | t0007 | g0168 | AFR | ACB | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01891 | hp2 | a0011 | c0018 | t0001 | g0283 | AFR | ACB | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01928 | hp1 | a0002 | c0002 | t0002 | g0035 | AMR | PEL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PEL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0121 | AMR | PEL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | PEL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0104 | AMR | PEL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PEL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01952 | hp2 | a0002 | c0002 | t0002 | g0040 | AMR | PEL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PEL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01981 | hp1 | a0002 | c0002 | t0002 | g0035 | AMR | PEL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PEL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01993 | hp2 | a0012 | c0019 | t0002 | g0284 | AMR | PEL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | KHV | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | KHV | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | KHV | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | KHV | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | KHV | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | KHV | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | KHV | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | KHV | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02129 | hp1 | a0003 | c0003 | t0001 | g0290 | EAS | KHV | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | KHV | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | ACB | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0280 | AFR | ACB | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | CDX | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02165 | hp1 | a0002 | c0002 | t0002 | g0184 | EAS | CDX | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | CDX | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0149 | AFR | ACB | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | ACB | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PEL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PEL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ACB | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0150 | AFR | ACB | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02300 | hp2 | a0002 | c0002 | t0002 | g0040 | AMR | PEL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02451 | hp1 | a0002 | c0002 | t0002 | g0195 | AFR | ACB | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0270 | AFR | ACB | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0136 | AFR | GWD | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02572 | hp2 | a0003 | c0003 | t0006 | g0289 | AFR | GWD | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02602 | hp1 | a0001 | c0009 | t0001 | g0213 | SAS | PJL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02602 | hp2 | a0002 | c0002 | t0002 | g0064 | SAS | PJL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02615 | hp2 | a0002 | c0002 | t0002 | g0175 | AFR | GWD | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | GWD | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0148 | AFR | GWD | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0014 | AFR | GWD | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02630 | hp2 | a0013 | c0010 | t0007 | g0167 | AFR | GWD | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02698 | hp1 | a0002 | c0002 | t0002 | g0200 | SAS | PJL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02717 | hp1 | a0002 | c0002 | t0002 | g0171 | AFR | GWD | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0134 | AFR | GWD | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0023 | SAS | PJL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0244 | SAS | PJL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02738 | hp2 | a0002 | c0002 | t0002 | g0242 | SAS | PJL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02809 | hp1 | a0002 | c0002 | t0002 | g0170 | AFR | GWD | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | GWD | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0047 | AFR | GWD | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0014 | AFR | GWD | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02886 | hp2 | a0005 | c0005 | t0001 | g0048 | AFR | GWD | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0027 | AFR | GWD | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0027 | AFR | GWD | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | ESN | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | ESN | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | ESN | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02965 | hp2 | a0002 | c0002 | t0002 | g0172 | AFR | ESN | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | ESN | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | ESN | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0133 | AFR | ESN | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | ESN | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | MSL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0135 | AFR | MSL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | ESN | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | ESN | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03139 | hp1 | a0005 | c0005 | t0001 | g0048 | AFR | ESN | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03139 | hp2 | a0007 | c0006 | t0001 | g0050 | AFR | ESN | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0147 | AFR | ESN | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | ESN | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0138 | AFR | MSL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | MSL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | MSL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03225 | hp2 | a0005 | c0005 | t0001 | g0285 | AFR | MSL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03239 | hp2 | a0002 | c0002 | t0002 | g0186 | SAS | PJL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03453 | hp1 | a0002 | c0002 | t0002 | g0169 | AFR | MSL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | MSL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03486 | hp1 | a0003 | c0003 | t0006 | g0286 | AFR | MSL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03486 | hp2 | a0007 | c0006 | t0001 | g0051 | AFR | MSL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0254 | SAS | PJL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0010 | SAS | PJL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0010 | SAS | PJL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0198 | SAS | PJL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | ESN | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0047 | AFR | ESN | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | GWD | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03540 | hp2 | a0002 | c0002 | t0005 | g0140 | AFR | GWD | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | MSL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03579 | hp2 | a0002 | c0002 | t0005 | g0124 | AFR | MSL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0161 | SAS | PJL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03654 | hp2 | a0002 | c0002 | t0002 | g0199 | SAS | PJL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0264 | SAS | PJL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03669 | hp2 | a0003 | c0003 | t0001 | g0293 | SAS | PJL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | STU | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03688 | hp2 | a0003 | c0003 | t0001 | g0292 | SAS | STU | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0265 | SAS | PJL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | BEB | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0110 | SAS | BEB | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | BEB | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0188 | SAS | BEB | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03942 | hp2 | a0002 | c0002 | t0002 | g0187 | SAS | BEB | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0114 | SAS | STU | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | STU | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0025 | SAS | BEB | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0069 | SAS | BEB | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0210 | SAS | STU | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | STU | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | STU | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | STU | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | YRI | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0137 | AFR | YRI | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | CHB | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHB | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | CHB | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | CHB | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | YRI | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0276 | AFR | YRI | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18942 | hp1 | a0002 | c0002 | t0002 | g0209 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18965 | hp2 | a0001 | c0017 | t0001 | g0282 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18968 | hp2 | a0003 | c0003 | t0001 | g0294 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18969 | hp1 | a0002 | c0002 | t0004 | g0197 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18981 | hp2 | a0014 | c0015 | t0001 | g0216 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18988 | hp2 | a0003 | c0003 | t0001 | g0019 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18989 | hp2 | a0001 | c0014 | t0001 | g0218 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18997 | hp1 | a0002 | c0002 | t0004 | g0180 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19000 | hp1 | a0001 | c0001 | t0009 | g0256 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19006 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | LWK | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | LWK | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | LWK | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | LWK | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19056 | hp1 | a0006 | c0008 | t0002 | g0049 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19057 | hp2 | a0002 | c0002 | t0004 | g0212 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19067 | hp1 | a0004 | c0004 | t0001 | g0126 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19076 | hp2 | a0003 | c0003 | t0001 | g0291 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19081 | hp2 | a0003 | c0003 | t0001 | g0019 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19091 | hp2 | a0003 | c0003 | t0001 | g0019 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | YRI | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | YRI | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA20129 | hp1 | a0015 | c0016 | t0010 | g0082 | AFR | ASW | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | ASW | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA20752 | hp1 | a0004 | c0004 | t0001 | g0230 | EUR | TSI | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0158 | EUR | TSI | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA20805 | hp1 | a0003 | c0003 | t0001 | g0287 | EUR | TSI | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0083 | EUR | TSI | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA20905 | hp1 | a0004 | c0004 | t0001 | g0176 | SAS | GIH | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0025 | SAS | GIH | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01123 | hp1 | a0001 | c0007 | t0002 | g0094 | AMR | CLM | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | CLM | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03471 | hp1 | a0001 | c0001 | t0008 | g0079 | AFR | MSL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | MSL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0139 | AFR | USA | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | USA | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0125 | AFR | USA | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | USA | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | LWK | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA21309 | hp2 | a0016 | c0020 | t0001 | g0296 | AFR | LWK | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0119 | REF | REF | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0120 | REF | REF | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:69589433 | T | C | 1 | a0014 | 1 | NA18981.hp2 | missense_variant | MODERATE | c.1550A>G | p.Gln517Arg | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 6/6 | 1552/2568 | 1550/1611 | 517/536 | chr4 | 69589433 | |||
| chr4:69589530 | C | T | 1 | a0008 | 1 | HG01071.hp2 | missense_variant | MODERATE | c.1453G>A | p.Val485Ile | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 6/6 | 1455/2568 | 1453/1611 | 485/536 | chr4 | 69589530 | |||
| chr4:69589581 | C | T | 1 | a0009 | 1 | HG01243.hp1 | missense_variant | MODERATE | c.1402G>A | p.Val468Ile | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 6/6 | 1404/2568 | 1402/1611 | 468/536 | chr4 | 69589581 | |||
| chr4:69589642 | C | A | 1 | a0010 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.1341G>T | p.Glu447Asp | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 6/6 | 1343/2568 | 1341/1611 | 447/536 | chr4 | 69589642 | |||
| chr4:69594602 | C | T | 2 | a0010 a0013 |
2 | HG01884.hp1 HG02630.hp2 |
missense_variant | MODERATE | c.1206G>A | p.Met402Ile | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 5/6 | 1208/2568 | 1206/1611 | 402/536 | chr4 | 69594602 | |||
| chr4:69594610 | C | T | 4 | a0002 a0010 a0012 others(1): Show |
29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
missense_variant | MODERATE | c.1198G>A | p.Val400Ile | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 5/6 | 1200/2568 | 1198/1611 | 400/536 | chr4 | 69594610 | |||
| chr4:69595221 | G | C | 1 | a0015 | 1 | NA20129.hp1 | missense_variant | MODERATE | c.1052C>G | p.Pro351Arg | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 4/6 | 1054/2568 | 1052/1611 | 351/536 | chr4 | 69595221 | |||
| chr4:69596324 | C | T | 3 | a0003 a0004 a0016 |
23 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(20): Show |
missense_variant | MODERATE | c.949G>A | p.Gly317Arg | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 3/6 | 951/2568 | 949/1611 | 317/536 | chr4 | 69596324 | |||
| chr4:69599287 | C | A | 1 | a0015 | 1 | NA20129.hp1 | missense_variant | MODERATE | c.850G>T | p.Val284Phe | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 2/6 | 852/2568 | 850/1611 | 284/536 | chr4 | 69599287 | |||
| chr4:69639033 | G | A | 1 | a0011 | 1 | HG01891.hp2 | missense_variant | MODERATE | c.608C>T | p.Pro203Leu | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/6 | 610/2568 | 608/1611 | 203/536 | chr4 | 69639033 | |||
| chr4:69639105 | G | C | 1 | a0016 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.536C>G | p.Thr179Arg | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/6 | 538/2568 | 536/1611 | 179/536 | chr4 | 69639105 | |||
| chr4:69639168 | G | A | 1 | a0012 | 1 | HG01993.hp2 | missense_variant | MODERATE | c.473C>T | p.Ala158Val | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/6 | 475/2568 | 473/1611 | 158/536 | chr4 | 69639168 | |||
| chr4:69639318 | G | A | 1 | a0005 | 3 | HG02886.hp2 HG03139.hp1 HG03225.hp2 |
missense_variant | MODERATE | c.323C>T | p.Pro108Leu | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/6 | 325/2568 | 323/1611 | 108/536 | chr4 | 69639318 | |||
| chr4:69639444 | G | A | 3 | a0003 a0006 a0016 |
19 | HG00140.hp1 HG00423.hp1 HG01099.hp1 others(16): Show |
missense_variant | MODERATE | c.197C>T | p.Ala66Val | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/6 | 199/2568 | 197/1611 | 66/536 | chr4 | 69639444 | |||
| chr4:69639637 | C | T | 1 | a0007 | 2 | HG03139.hp2 HG03486.hp2 |
missense_variant | MODERATE | c.4G>A | p.Val2Ile | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/6 | 6/2568 | 4/1611 | 2/536 | chr4 | 69639637 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:69589432 | T | C | 1 | a0001c0014 | 1 | NA18989.hp2 | synonymous_variant | LOW | c.1551A>G | p.Gln517Gln | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 6/6 | 1553/2568 | 1551/1611 | 517/536 | chr4 | 69589432 | |||
| chr4:69589513 | G | A | 1 | a0001c0007 | 2 | HG01123.hp1 HG01175.hp1 |
synonymous_variant | LOW | c.1470C>T | p.Leu490Leu | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 6/6 | 1472/2568 | 1470/1611 | 490/536 | chr4 | 69589513 | |||
| chr4:69599342 | G | A | 1 | a0001c0017 | 1 | NA18965.hp2 | synonymous_variant | LOW | c.795C>T | p.Ile265Ile | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 2/6 | 797/2568 | 795/1611 | 265/536 | chr4 | 69599342 | |||
| chr4:69599381 | C | T | 1 | a0001c0009 | 1 | HG02602.hp1 | synonymous_variant | LOW | c.756G>A | p.Thr252Thr | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 2/6 | 758/2568 | 756/1611 | 252/536 | chr4 | 69599381 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:69588503 | G | T | 1 | a0003c0003t0006 | 2 | HG02572.hp2 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*869C>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 6/6 | 869 | chr4 | 69588503 | ||||||
| chr4:69588571 | A | G | 15 | a0001c0001t0001 a0001c0001t0008 a0001c0009t0001 others(12): Show |
246 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(243): Show |
3_prime_UTR_variant | MODIFIER | c.*801T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 6/6 | 801 | chr4 | 69588571 | ||||||
| chr4:69588588 | G | T | 1 | a0001c0001t0003 | 15 | HG02258.hp1 HG02280.hp2 HG02572.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*784C>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 6/6 | 784 | chr4 | 69588588 | ||||||
| chr4:69588620 | C | A | 2 | a0010c0011t0007 a0013c0010t0007 |
2 | HG01884.hp1 HG02630.hp2 |
3_prime_UTR_variant | MODIFIER | c.*752G>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 6/6 | 752 | chr4 | 69588620 | ||||||
| chr4:69588682 | T | C | 2 | a0010c0011t0007 a0013c0010t0007 |
2 | HG01884.hp1 HG02630.hp2 |
3_prime_UTR_variant | MODIFIER | c.*690A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 6/6 | 690 | chr4 | 69588682 | ||||||
| chr4:69588811 | C | T | 1 | a0015c0016t0010 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*561G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 6/6 | 561 | chr4 | 69588811 | ||||||
| chr4:69588935 | C | T | 1 | a0002c0002t0005 | 2 | HG03540.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*437G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 6/6 | 437 | chr4 | 69588935 | ||||||
| chr4:69589006 | T | C | 1 | a0001c0001t0008 | 2 | HG01109.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*366A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 6/6 | 366 | chr4 | 69589006 | ||||||
| chr4:69589273 | C | T | 1 | a0002c0002t0004 | 3 | NA18969.hp1 NA18997.hp1 NA19057.hp2 |
3_prime_UTR_variant | MODIFIER | c.*99G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 6/6 | 99 | chr4 | 69589273 | ||||||
| chr4:69589280 | T | C | 1 | a0001c0001t0009 | 1 | NA19000.hp1 | 3_prime_UTR_variant | MODIFIER | c.*92A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 6/6 | 92 | chr4 | 69589280 | ||||||
| chr4:69589340 | T | G | 1 | a0015c0016t0010 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*32A>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 6/6 | 32 | chr4 | 69589340 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:69589760 | G | T | 224 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(221): Show |
275 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.1332-109C>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 5/5 | chr4 | 69589760 | |||||||
| chr4:69589857 | T | C | 7 | a0001c0001t0001g0059 a0001c0001t0001g0270 a0001c0001t0001g0271 others(4): Show |
7 | HG01243.hp2 HG02145.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1332-206A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 5/5 | chr4 | 69589857 | |||||||
| chr4:69589861 | C | G | 123 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(120): Show |
153 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(150): Show |
intron_variant | MODIFIER | c.1332-210G>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 5/5 | chr4 | 69589861 | |||||||
| chr4:69589881 | T | C | 1 | a0001c0001t0002g0089 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1332-230A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 5/5 | chr4 | 69589881 | |||||||
| chr4:69589932 | A | G | 123 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(120): Show |
153 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(150): Show |
intron_variant | MODIFIER | c.1332-281T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 5/5 | chr4 | 69589932 | |||||||
| chr4:69589946 | G | C | 3 | a0001c0001t0001g0281 a0009c0012t0001g0191 a0015c0016t0010g0082 |
3 | HG01192.hp2 HG01243.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1332-295C>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 5/5 | chr4 | 69589946 | |||||||
| chr4:69590001 | T | G | 1 | a0001c0001t0001g0065 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1332-350A>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 5/5 | chr4 | 69590001 | |||||||
| chr4:69590166 | C | T | 70 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(67): Show |
89 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.1332-515G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 5/5 | chr4 | 69590166 | |||||||
| chr4:69590468 | G | T | 197 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(194): Show |
246 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.1332-817C>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 5/5 | chr4 | 69590468 | |||||||
| chr4:69590526 | G | A | 2 | a0010c0011t0007g0168 a0013c0010t0007g0167 |
2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1332-875C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 5/5 | chr4 | 69590526 | |||||||
| chr4:69590559 | G | A | 1 | a0002c0002t0002g0175 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1332-908C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 5/5 | chr4 | 69590559 | |||||||
| chr4:69590597 | G | A | 7 | a0001c0001t0001g0059 a0001c0001t0001g0270 a0001c0001t0001g0271 others(4): Show |
7 | HG01243.hp2 HG02145.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1332-946C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 5/5 | chr4 | 69590597 | |||||||
| chr4:69590638 | A | AGT | 26 | a0001c0001t0001g0016 a0001c0001t0001g0031 a0001c0001t0001g0032 others(23): Show |
31 | HG00099.hp1 HG00280.hp2 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.1332-989_1332-988d others(4): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 5/5 | chr4 | 69590638 | |||||||
| chr4:69590638 | A | AGTGT | 90 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(87): Show |
115 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(112): Show |
intron_variant | MODIFIER | c.1332-991_1332-988d others(6): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 5/5 | chr4 | 69590638 | |||||||
| chr4:69590638 | AGT | A | 72 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(69): Show |
91 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.1332-989_1332-988d others(4): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 5/5 | chr4 | 69590638 | |||||||
| chr4:69590677 | C | A | 3 | a0001c0001t0001g0281 a0009c0012t0001g0191 a0015c0016t0010g0082 |
3 | HG01192.hp2 HG01243.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1332-1026G>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 5/5 | chr4 | 69590677 | |||||||
| chr4:69590710 | A | T | 18 | a0001c0001t0001g0016 a0001c0001t0001g0031 a0001c0001t0001g0032 others(15): Show |
22 | HG00099.hp1 HG00280.hp2 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.1332-1059T>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 5/5 | chr4 | 69590710 | |||||||
| chr4:69590771 | G | T | 3 | a0001c0001t0001g0281 a0009c0012t0001g0191 a0015c0016t0010g0082 |
3 | HG01192.hp2 HG01243.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1332-1120C>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 5/5 | chr4 | 69590771 | |||||||
| chr4:69590777 | G | T | 1 | a0001c0001t0002g0096 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1332-1126C>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 5/5 | chr4 | 69590777 | |||||||
| chr4:69590778 | A | G | 1 | a0009c0012t0001g0191 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1332-1127T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 5/5 | chr4 | 69590778 | |||||||
| chr4:69590793 | A | G | 2 | a0001c0001t0002g0012 a0001c0001t0002g0086 |
4 | NA18952.hp1 NA19055.hp2 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.1332-1142T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 5/5 | chr4 | 69590793 | |||||||
| chr4:69590856 | A | G | 1 | a0015c0016t0010g0082 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1332-1205T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 5/5 | chr4 | 69590856 | |||||||
| chr4:69590997 | T | G | 2 | a0001c0001t0001g0207 a0001c0001t0001g0243 |
2 | HG02622.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1332-1346A>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 5/5 | chr4 | 69590997 | |||||||
| chr4:69591195 | C | G | 1 | a0001c0001t0001g0194 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1332-1544G>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 5/5 | chr4 | 69591195 | |||||||
| chr4:69591303 | T | C | 224 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(221): Show |
275 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.1332-1652A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 5/5 | chr4 | 69591303 | |||||||
| chr4:69591319 | T | G | 1 | a0001c0001t0002g0092 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1332-1668A>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 5/5 | chr4 | 69591319 | |||||||
| chr4:69591607 | C | G | 1 | a0011c0018t0001g0283 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1332-1956G>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 5/5 | chr4 | 69591607 | |||||||
| chr4:69591749 | T | G | 123 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(120): Show |
153 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(150): Show |
intron_variant | MODIFIER | c.1332-2098A>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 5/5 | chr4 | 69591749 | |||||||
| chr4:69591838 | T | C | 74 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(71): Show |
93 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(90): Show |
intron_variant | MODIFIER | c.1332-2187A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 5/5 | chr4 | 69591838 | |||||||
| chr4:69591838 | T | G | 1 | a0001c0001t0001g0257 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1332-2187A>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 5/5 | chr4 | 69591838 | |||||||
| chr4:69591954 | T | C | 1 | a0001c0001t0001g0234 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1332-2303A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 5/5 | chr4 | 69591954 | |||||||
| chr4:69591972 | C | T | 126 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(123): Show |
156 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.1332-2321G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 5/5 | chr4 | 69591972 | |||||||
| chr4:69592159 | G | A | 197 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(194): Show |
246 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.1331+2318C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 5/5 | chr4 | 69592159 | |||||||
| chr4:69592214 | A | G | 7 | a0001c0001t0001g0059 a0001c0001t0001g0270 a0001c0001t0001g0271 others(4): Show |
7 | HG01243.hp2 HG02145.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1331+2263T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 5/5 | chr4 | 69592214 | |||||||
| chr4:69592345 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1331+2132G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 5/5 | chr4 | 69592345 | |||||||
| chr4:69592422 | G | T | 1 | a0001c0001t0002g0103 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1331+2055C>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 5/5 | chr4 | 69592422 | |||||||
| chr4:69592464 | C | A | 123 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(120): Show |
153 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(150): Show |
intron_variant | MODIFIER | c.1331+2013G>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 5/5 | chr4 | 69592464 | |||||||
| chr4:69592524 | G | C | 18 | a0001c0001t0001g0016 a0001c0001t0001g0031 a0001c0001t0001g0032 others(15): Show |
22 | HG00099.hp1 HG00280.hp2 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.1331+1953C>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 5/5 | chr4 | 69592524 | |||||||
| chr4:69592924 | C | T | 1 | a0001c0001t0002g0102 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1331+1553G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 5/5 | chr4 | 69592924 | |||||||
| chr4:69592930 | C | T | 197 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(194): Show |
246 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.1331+1547G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 5/5 | chr4 | 69592930 | |||||||
| chr4:69592931 | T | C | 66 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(63): Show |
85 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(82): Show |
intron_variant | MODIFIER | c.1331+1546A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 5/5 | chr4 | 69592931 | |||||||
| chr4:69592941 | A | C | 1 | a0011c0018t0001g0283 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1331+1536T>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 5/5 | chr4 | 69592941 | |||||||
| chr4:69593231 | C | A | 1 | a0002c0002t0002g0175 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1331+1246G>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 5/5 | chr4 | 69593231 | |||||||
| chr4:69593261 | T | C | 4 | a0001c0001t0001g0281 a0009c0012t0001g0191 a0011c0018t0001g0283 others(1): Show |
4 | HG01192.hp2 HG01243.hp1 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.1331+1216A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 5/5 | chr4 | 69593261 | |||||||
| chr4:69593265 | A | G | 1 | a0002c0002t0005g0124 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1331+1212T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 5/5 | chr4 | 69593265 | |||||||
| chr4:69593309 | G | A | 1 | a0015c0016t0010g0082 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1331+1168C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 5/5 | chr4 | 69593309 | |||||||
| chr4:69593313 | GA | G | 70 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(67): Show |
89 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.1331+1163delT | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 5/5 | chr4 | 69593313 | |||||||
| chr4:69593347 | T | A | 1 | a0001c0001t0001g0258 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1331+1130A>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 5/5 | chr4 | 69593347 | |||||||
| chr4:69593434 | T | C | 3 | a0001c0001t0001g0281 a0009c0012t0001g0191 a0015c0016t0010g0082 |
3 | HG01192.hp2 HG01243.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1331+1043A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 5/5 | chr4 | 69593434 | |||||||
| chr4:69593559 | CTT | C | 6 | a0001c0001t0001g0015 a0001c0001t0001g0068 a0001c0001t0001g0145 others(3): Show |
8 | HG00733.hp1 HG01516.hp1 HG02698.hp2 others(5): Show |
intron_variant | MODIFIER | c.1331+916_1331+917d others(4): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 5/5 | chr4 | 69593559 | |||||||
| chr4:69593649 | T | A | 1 | a0003c0003t0006g0289 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1331+828A>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 5/5 | chr4 | 69593649 | |||||||
| chr4:69593675 | A | T | 31 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0021 others(28): Show |
40 | HG00438.hp2 HG00609.hp2 HG01070.hp1 others(37): Show |
intron_variant | MODIFIER | c.1331+802T>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 5/5 | chr4 | 69593675 | |||||||
| chr4:69593742 | T | A | 1 | a0011c0018t0001g0283 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1331+735A>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 5/5 | chr4 | 69593742 | |||||||
| chr4:69593753 | G | A | 1 | a0001c0001t0001g0267 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1331+724C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 5/5 | chr4 | 69593753 | |||||||
| chr4:69593811 | G | A | 1 | a0007c0006t0001g0051 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1331+666C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 5/5 | chr4 | 69593811 | |||||||
| chr4:69593861 | A | G | 66 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(63): Show |
85 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(82): Show |
intron_variant | MODIFIER | c.1331+616T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 5/5 | chr4 | 69593861 | |||||||
| chr4:69593915 | A | C | 2 | a0002c0002t0005g0124 a0002c0002t0005g0140 |
2 | HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1331+562T>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 5/5 | chr4 | 69593915 | |||||||
| chr4:69593915 | A | T | 1 | a0001c0001t0001g0229 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1331+562T>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 5/5 | chr4 | 69593915 | |||||||
| chr4:69593964 | AGT | A | 4 | a0001c0001t0001g0281 a0009c0012t0001g0191 a0011c0018t0001g0283 others(1): Show |
4 | HG01192.hp2 HG01243.hp1 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.1331+511_1331+512d others(4): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 5/5 | chr4 | 69593964 | |||||||
| chr4:69593973 | T | G | 1 | a0002c0002t0002g0175 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1331+504A>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 5/5 | chr4 | 69593973 | |||||||
| chr4:69593975 | TTG | T | 7 | a0001c0001t0001g0130 a0001c0001t0001g0211 a0001c0001t0001g0221 others(4): Show |
7 | HG01891.hp2 HG03490.hp1 NA18747.hp1 others(4): Show |
intron_variant | MODIFIER | c.1331+500_1331+501d others(4): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 5/5 | chr4 | 69593975 | |||||||
| chr4:69593976 | TG | T | 158 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(155): Show |
198 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(195): Show |
intron_variant | MODIFIER | c.1331+500delC | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 5/5 | chr4 | 69593976 | |||||||
| chr4:69593977 | G | T | 38 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0015 others(35): Show |
42 | HG00099.hp1 HG00609.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.1331+500C>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 5/5 | chr4 | 69593977 | |||||||
| chr4:69593981 | G | T | 197 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(194): Show |
246 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.1331+496C>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 5/5 | chr4 | 69593981 | |||||||
| chr4:69593985 | T | G | 31 | a0001c0001t0002g0090 a0001c0001t0003g0135 a0001c0001t0003g0138 others(28): Show |
33 | HG00280.hp1 HG01346.hp2 HG01358.hp1 others(30): Show |
intron_variant | MODIFIER | c.1331+492A>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 5/5 | chr4 | 69593985 | |||||||
| chr4:69594067 | C | T | 123 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(120): Show |
153 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(150): Show |
intron_variant | MODIFIER | c.1331+410G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 5/5 | chr4 | 69594067 | |||||||
| chr4:69594119 | C | T | 1 | a0001c0001t0002g0025 | 2 | HG04184.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1331+358G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 5/5 | chr4 | 69594119 | |||||||
| chr4:69594458 | T | C | 1 | a0001c0001t0002g0111 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1331+19A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 5/5 | chr4 | 69594458 | |||||||
| chr4:69594981 | G | A | 1 | a0001c0001t0001g0098 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1111+181C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 4/5 | chr4 | 69594981 | |||||||
| chr4:69595095 | G | T | 1 | a0001c0001t0002g0101 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1111+67C>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 4/5 | chr4 | 69595095 | |||||||
| chr4:69595096 | C | T | 1 | a0001c0001t0002g0101 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1111+66G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 4/5 | chr4 | 69595096 | |||||||
| chr4:69595328 | A | G | 7 | a0001c0001t0001g0059 a0001c0001t0001g0270 a0001c0001t0001g0271 others(4): Show |
7 | HG01243.hp2 HG02145.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1024-79T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 3/5 | chr4 | 69595328 | |||||||
| chr4:69595345 | G | C | 1 | a0001c0001t0001g0069 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1024-96C>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 3/5 | chr4 | 69595345 | |||||||
| chr4:69595443 | C | T | 202 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(199): Show |
254 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(251): Show |
intron_variant | MODIFIER | c.1024-194G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 3/5 | chr4 | 69595443 | |||||||
| chr4:69595466 | A | G | 123 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(120): Show |
153 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(150): Show |
intron_variant | MODIFIER | c.1024-217T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 3/5 | chr4 | 69595466 | |||||||
| chr4:69595634 | G | A | 2 | a0007c0006t0001g0050 a0007c0006t0001g0051 |
2 | HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1024-385C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 3/5 | chr4 | 69595634 | |||||||
| chr4:69595727 | A | C | 1 | a0001c0001t0002g0025 | 2 | HG04184.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1024-478T>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 3/5 | chr4 | 69595727 | |||||||
| chr4:69595846 | G | C | 2 | a0002c0002t0005g0124 a0002c0002t0005g0140 |
2 | HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1023+404C>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 3/5 | chr4 | 69595846 | |||||||
| chr4:69596111 | A | C | 1 | a0001c0001t0001g0222 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1023+139T>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 3/5 | chr4 | 69596111 | |||||||
| chr4:69596532 | T | C | 98 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(95): Show |
124 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(121): Show |
intron_variant | MODIFIER | c.892-151A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 2/5 | chr4 | 69596532 | |||||||
| chr4:69596579 | G | A | 123 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(120): Show |
153 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(150): Show |
intron_variant | MODIFIER | c.892-198C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 2/5 | chr4 | 69596579 | |||||||
| chr4:69596674 | A | G | 2 | a0001c0001t0001g0108 a0001c0001t0001g0229 |
2 | NA18950.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.892-293T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 2/5 | chr4 | 69596674 | |||||||
| chr4:69596804 | G | A | 1 | a0001c0001t0001g0267 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.892-423C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 2/5 | chr4 | 69596804 | |||||||
| chr4:69596903 | A | G | 235 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(232): Show |
290 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(287): Show |
intron_variant | MODIFIER | c.892-522T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 2/5 | chr4 | 69596903 | |||||||
| chr4:69596950 | C | T | 1 | a0001c0001t0001g0259 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.892-569G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 2/5 | chr4 | 69596950 | |||||||
| chr4:69596951 | T | G | 123 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(120): Show |
153 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(150): Show |
intron_variant | MODIFIER | c.892-570A>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 2/5 | chr4 | 69596951 | |||||||
| chr4:69597085 | T | G | 202 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(199): Show |
254 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(251): Show |
intron_variant | MODIFIER | c.892-704A>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 2/5 | chr4 | 69597085 | |||||||
| chr4:69597175 | C | A | 202 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(199): Show |
254 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(251): Show |
intron_variant | MODIFIER | c.892-794G>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 2/5 | chr4 | 69597175 | |||||||
| chr4:69597299 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.892-918G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 2/5 | chr4 | 69597299 | |||||||
| chr4:69597422 | C | T | 1 | a0001c0001t0001g0281 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.892-1041G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 2/5 | chr4 | 69597422 | |||||||
| chr4:69597466 | T | C | 1 | a0001c0001t0001g0158 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.892-1085A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 2/5 | chr4 | 69597466 | |||||||
| chr4:69597500 | C | T | 1 | a0001c0001t0002g0053 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.892-1119G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 2/5 | chr4 | 69597500 | |||||||
| chr4:69597606 | G | T | 1 | a0001c0001t0001g0225 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.892-1225C>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 2/5 | chr4 | 69597606 | |||||||
| chr4:69597715 | A | AAC | 120 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(117): Show |
150 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(147): Show |
intron_variant | MODIFIER | c.892-1336_892-1335d others(4): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 2/5 | chr4 | 69597715 | |||||||
| chr4:69597715 | A | AACACAC | 7 | a0001c0001t0001g0059 a0001c0001t0001g0270 a0001c0001t0001g0271 others(4): Show |
7 | HG01243.hp2 HG02145.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.892-1340_892-1335d others(8): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 2/5 | chr4 | 69597715 | |||||||
| chr4:69597882 | T | G | 98 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(95): Show |
124 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(121): Show |
intron_variant | MODIFIER | c.891+1364A>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 2/5 | chr4 | 69597882 | |||||||
| chr4:69597908 | T | A | 1 | a0001c0001t0001g0264 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.891+1338A>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 2/5 | chr4 | 69597908 | |||||||
| chr4:69597944 | T | C | 98 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(95): Show |
124 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(121): Show |
intron_variant | MODIFIER | c.891+1302A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 2/5 | chr4 | 69597944 | |||||||
| chr4:69597945 | G | A | 98 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(95): Show |
124 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(121): Show |
intron_variant | MODIFIER | c.891+1301C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 2/5 | chr4 | 69597945 | |||||||
| chr4:69598136 | T | A | 75 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(72): Show |
97 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(94): Show |
intron_variant | MODIFIER | c.891+1110A>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 2/5 | chr4 | 69598136 | |||||||
| chr4:69598149 | G | T | 1 | a0002c0002t0002g0171 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.891+1097C>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 2/5 | chr4 | 69598149 | |||||||
| chr4:69598154 | C | A | 18 | a0001c0001t0001g0016 a0001c0001t0001g0031 a0001c0001t0001g0032 others(15): Show |
22 | HG00099.hp1 HG00280.hp2 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.891+1092G>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 2/5 | chr4 | 69598154 | |||||||
| chr4:69598406 | C | T | 1 | a0001c0001t0001g0222 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.891+840G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 2/5 | chr4 | 69598406 | |||||||
| chr4:69598438 | T | C | 1 | a0001c0001t0001g0156 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.891+808A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 2/5 | chr4 | 69598438 | |||||||
| chr4:69598631 | C | A | 4 | a0001c0001t0001g0281 a0009c0012t0001g0191 a0011c0018t0001g0283 others(1): Show |
4 | HG01192.hp2 HG01243.hp1 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.891+615G>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 2/5 | chr4 | 69598631 | |||||||
| chr4:69598695 | T | A | 123 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(120): Show |
153 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(150): Show |
intron_variant | MODIFIER | c.891+551A>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 2/5 | chr4 | 69598695 | |||||||
| chr4:69598793 | C | G | 123 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(120): Show |
153 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(150): Show |
intron_variant | MODIFIER | c.891+453G>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 2/5 | chr4 | 69598793 | |||||||
| chr4:69598854 | C | A | 7 | a0001c0001t0001g0059 a0001c0001t0001g0270 a0001c0001t0001g0271 others(4): Show |
7 | HG01243.hp2 HG02145.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.891+392G>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 2/5 | chr4 | 69598854 | |||||||
| chr4:69598983 | A | G | 75 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(72): Show |
97 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(94): Show |
intron_variant | MODIFIER | c.891+263T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 2/5 | chr4 | 69598983 | |||||||
| chr4:69599152 | G | A | 1 | a0001c0001t0001g0203 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.891+94C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 2/5 | chr4 | 69599152 | |||||||
| chr4:69599202 | T | C | 2 | a0010c0011t0007g0168 a0013c0010t0007g0167 |
2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.891+44A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 2/5 | chr4 | 69599202 | |||||||
| chr4:69599435 | A | T | 123 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(120): Show |
153 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(150): Show |
intron_variant | MODIFIER | c.743-41T>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69599435 | |||||||
| chr4:69599523 | T | C | 1 | a0001c0001t0002g0111 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.743-129A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69599523 | |||||||
| chr4:69599689 | TAAAG | T | 18 | a0002c0002t0002g0035 a0002c0002t0002g0040 a0002c0002t0002g0064 others(15): Show |
20 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(17): Show |
intron_variant | MODIFIER | c.743-299_743-296del others(4): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69599689 | |||||||
| chr4:69599695 | A | AAGAG | 61 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0031 others(58): Show |
72 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.743-305_743-302dup others(4): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69599695 | |||||||
| chr4:69599695 | A | AAGAGAG | 6 | a0001c0001t0001g0059 a0001c0001t0001g0270 a0001c0001t0001g0271 others(3): Show |
6 | HG02145.hp1 HG02451.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.743-307_743-302dup others(6): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69599695 | |||||||
| chr4:69599695 | A | G | 79 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(76): Show |
101 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(98): Show |
intron_variant | MODIFIER | c.743-301T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69599695 | |||||||
| chr4:69599723 | T | C | 198 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(195): Show |
250 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.743-329A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69599723 | |||||||
| chr4:69599775 | G | A | 123 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(120): Show |
153 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(150): Show |
intron_variant | MODIFIER | c.743-381C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69599775 | |||||||
| chr4:69599866 | A | G | 98 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(95): Show |
124 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(121): Show |
intron_variant | MODIFIER | c.743-472T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69599866 | |||||||
| chr4:69599896 | T | A | 1 | a0001c0001t0001g0065 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.743-502A>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69599896 | |||||||
| chr4:69599908 | G | A | 202 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(199): Show |
254 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(251): Show |
intron_variant | MODIFIER | c.743-514C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69599908 | |||||||
| chr4:69599974 | A | T | 1 | a0001c0001t0003g0135 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.743-580T>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69599974 | |||||||
| chr4:69600019 | G | T | 130 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(127): Show |
160 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(157): Show |
intron_variant | MODIFIER | c.743-625C>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69600019 | |||||||
| chr4:69600087 | G | A | 1 | a0002c0002t0002g0170 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.743-693C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69600087 | |||||||
| chr4:69600132 | C | T | 1 | a0001c0001t0003g0148 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.743-738G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69600132 | |||||||
| chr4:69600261 | C | T | 150 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(147): Show |
182 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(179): Show |
intron_variant | MODIFIER | c.743-867G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69600261 | |||||||
| chr4:69600303 | C | A | 1 | a0011c0018t0001g0283 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.743-909G>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69600303 | |||||||
| chr4:69600321 | C | A | 1 | a0001c0001t0002g0104 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.743-927G>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69600321 | |||||||
| chr4:69600353 | A | G | 4 | a0003c0003t0001g0288 a0004c0004t0001g0042 a0004c0004t0001g0177 others(1): Show |
5 | HG00639.hp2 HG00741.hp1 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.743-959T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69600353 | |||||||
| chr4:69600502 | G | A | 6 | a0001c0001t0003g0027 a0001c0001t0003g0135 a0001c0001t0003g0136 others(3): Show |
7 | HG02572.hp1 HG02895.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.743-1108C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69600502 | |||||||
| chr4:69600519 | C | G | 1 | a0001c0001t0002g0160 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.743-1125G>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69600519 | |||||||
| chr4:69600527 | T | C | 4 | a0001c0001t0008g0079 a0001c0001t0008g0080 a0007c0006t0001g0050 others(1): Show |
4 | HG01109.hp2 HG03139.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.743-1133A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69600527 | |||||||
| chr4:69600539 | G | A | 1 | a0001c0001t0001g0223 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.743-1145C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69600539 | |||||||
| chr4:69600561 | C | A | 1 | a0001c0001t0001g0254 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.743-1167G>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69600561 | |||||||
| chr4:69600562 | T | C | 150 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(147): Show |
182 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(179): Show |
intron_variant | MODIFIER | c.743-1168A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69600562 | |||||||
| chr4:69600566 | T | C | 2 | a0001c0001t0001g0112 a0001c0001t0001g0248 |
2 | NA18977.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.743-1172A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69600566 | |||||||
| chr4:69600568 | G | A | 27 | a0002c0002t0002g0035 a0002c0002t0002g0040 a0002c0002t0002g0064 others(24): Show |
29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.743-1174C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69600568 | |||||||
| chr4:69600620 | A | T | 3 | a0001c0001t0001g0281 a0009c0012t0001g0191 a0015c0016t0010g0082 |
3 | HG01192.hp2 HG01243.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.743-1226T>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69600620 | |||||||
| chr4:69600631 | T | A | 2 | a0001c0001t0001g0055 a0016c0020t0001g0296 |
2 | NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.743-1237A>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69600631 | |||||||
| chr4:69600649 | G | T | 71 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(68): Show |
93 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(90): Show |
intron_variant | MODIFIER | c.743-1255C>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69600649 | |||||||
| chr4:69600658 | C | T | 27 | a0002c0002t0002g0035 a0002c0002t0002g0040 a0002c0002t0002g0064 others(24): Show |
29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.743-1264G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69600658 | |||||||
| chr4:69600809 | T | TA | 97 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(94): Show |
123 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(120): Show |
intron_variant | MODIFIER | c.743-1416dupT | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69600809 | |||||||
| chr4:69600809 | T | TAA | 26 | a0001c0001t0001g0227 a0001c0001t0008g0079 a0001c0001t0008g0080 others(23): Show |
28 | HG01109.hp2 HG01346.hp2 HG01358.hp1 others(25): Show |
intron_variant | MODIFIER | c.743-1417_743-1416d others(4): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69600809 | |||||||
| chr4:69600875 | C | T | 79 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(76): Show |
101 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(98): Show |
intron_variant | MODIFIER | c.743-1481G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69600875 | |||||||
| chr4:69600916 | C | T | 5 | a0001c0001t0001g0003 a0001c0001t0001g0070 a0001c0001t0001g0073 others(2): Show |
9 | HG01070.hp1 HG01071.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.743-1522G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69600916 | |||||||
| chr4:69600924 | T | C | 79 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(76): Show |
101 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(98): Show |
intron_variant | MODIFIER | c.743-1530A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69600924 | |||||||
| chr4:69601066 | C | T | 1 | a0002c0002t0005g0124 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.743-1672G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69601066 | |||||||
| chr4:69601072 | C | T | 2 | a0007c0006t0001g0050 a0007c0006t0001g0051 |
2 | HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.743-1678G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69601072 | |||||||
| chr4:69601081 | T | C | 106 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(103): Show |
130 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(127): Show |
intron_variant | MODIFIER | c.743-1687A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69601081 | |||||||
| chr4:69601092 | T | G | 79 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(76): Show |
101 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(98): Show |
intron_variant | MODIFIER | c.743-1698A>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69601092 | |||||||
| chr4:69601187 | G | A | 97 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(94): Show |
123 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.743-1793C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69601187 | |||||||
| chr4:69601191 | G | A | 4 | a0002c0002t0002g0169 a0002c0002t0002g0170 a0002c0002t0002g0171 others(1): Show |
4 | HG02717.hp1 HG02809.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.743-1797C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69601191 | |||||||
| chr4:69601218 | C | T | 2 | a0010c0011t0007g0168 a0013c0010t0007g0167 |
2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.743-1824G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69601218 | |||||||
| chr4:69601308 | C | T | 1 | a0001c0001t0003g0136 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.743-1914G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69601308 | |||||||
| chr4:69601313 | T | C | 79 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(76): Show |
101 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(98): Show |
intron_variant | MODIFIER | c.743-1919A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69601313 | |||||||
| chr4:69601364 | G | A | 2 | a0001c0001t0001g0271 a0001c0001t0001g0272 |
2 | HG01243.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.743-1970C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69601364 | |||||||
| chr4:69601384 | C | T | 71 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(68): Show |
93 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(90): Show |
intron_variant | MODIFIER | c.743-1990G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69601384 | |||||||
| chr4:69601391 | C | T | 98 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(95): Show |
124 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(121): Show |
intron_variant | MODIFIER | c.743-1997G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69601391 | |||||||
| chr4:69601392 | G | A | 2 | a0001c0001t0001g0043 a0001c0001t0001g0232 |
3 | HG02280.hp1 NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.743-1998C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69601392 | |||||||
| chr4:69601526 | C | G | 7 | a0001c0001t0001g0059 a0001c0001t0001g0270 a0001c0001t0001g0271 others(4): Show |
7 | HG01243.hp2 HG02145.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.743-2132G>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69601526 | |||||||
| chr4:69601617 | C | T | 2 | a0001c0001t0001g0182 a0001c0001t0001g0219 |
2 | NA19003.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.743-2223G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69601617 | |||||||
| chr4:69601741 | T | C | 79 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(76): Show |
101 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(98): Show |
intron_variant | MODIFIER | c.743-2347A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69601741 | |||||||
| chr4:69601743 | T | A | 79 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(76): Show |
101 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(98): Show |
intron_variant | MODIFIER | c.743-2349A>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69601743 | |||||||
| chr4:69601746 | A | AG | 79 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(76): Show |
101 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(98): Show |
intron_variant | MODIFIER | c.743-2353_743-2352i others(3): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69601746 | |||||||
| chr4:69601746 | A | G | 27 | a0002c0002t0002g0035 a0002c0002t0002g0040 a0002c0002t0002g0064 others(24): Show |
29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.743-2352T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69601746 | |||||||
| chr4:69601750 | A | G | 79 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(76): Show |
101 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(98): Show |
intron_variant | MODIFIER | c.743-2356T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69601750 | |||||||
| chr4:69601753 | G | C | 79 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(76): Show |
101 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(98): Show |
intron_variant | MODIFIER | c.743-2359C>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69601753 | |||||||
| chr4:69601754 | G | T | 79 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(76): Show |
101 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(98): Show |
intron_variant | MODIFIER | c.743-2360C>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69601754 | |||||||
| chr4:69601755 | AG | A | 79 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(76): Show |
101 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(98): Show |
intron_variant | MODIFIER | c.743-2362delC | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69601755 | |||||||
| chr4:69601758 | CTAGAGGA others(5319): Show |
C | 79 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(76): Show |
101 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(98): Show |
intron_variant | MODIFIER | c.743-7690_743-2365d others(2): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69601758 | |||||||
| chr4:69602031 | A | G | 1 | a0001c0001t0001g0210 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.743-2637T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69602031 | |||||||
| chr4:69602112 | T | C | 4 | a0002c0002t0002g0169 a0002c0002t0002g0170 a0002c0002t0002g0171 others(1): Show |
4 | HG02717.hp1 HG02809.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.743-2718A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69602112 | |||||||
| chr4:69602216 | A | AAACTC | 27 | a0002c0002t0002g0035 a0002c0002t0002g0040 a0002c0002t0002g0064 others(24): Show |
29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.743-2823_743-2822i others(7): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69602216 | |||||||
| chr4:69602359 | C | T | 32 | a0001c0001t0001g0055 a0001c0001t0001g0061 a0001c0001t0001g0062 others(29): Show |
34 | HG00735.hp1 HG01346.hp2 HG01358.hp1 others(31): Show |
intron_variant | MODIFIER | c.743-2965G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69602359 | |||||||
| chr4:69602459 | G | T | 1 | a0001c0001t0001g0244 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.743-3065C>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69602459 | |||||||
| chr4:69602462 | TTTA | T | 4 | a0002c0002t0002g0169 a0002c0002t0002g0170 a0002c0002t0002g0184 others(1): Show |
4 | HG02165.hp1 HG02809.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.743-3071_743-3069d others(5): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69602462 | |||||||
| chr4:69602462 | TTTATCTA | T | 20 | a0002c0002t0002g0035 a0002c0002t0002g0040 a0002c0002t0002g0064 others(17): Show |
22 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(19): Show |
intron_variant | MODIFIER | c.743-3075_743-3069d others(9): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69602462 | |||||||
| chr4:69602462 | TTTATCTA others(4): Show |
T | 3 | a0002c0002t0002g0242 a0010c0011t0007g0168 a0013c0010t0007g0167 |
3 | HG01884.hp1 HG02630.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.743-3079_743-3069d others(13): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69602462 | |||||||
| chr4:69602463 | T | TTATC | 10 | a0001c0001t0001g0007 a0001c0001t0001g0210 a0001c0001t0001g0221 others(7): Show |
10 | HG00099.hp2 HG01261.hp1 HG01934.hp1 others(7): Show |
intron_variant | MODIFIER | c.743-3073_743-3070d others(6): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69602463 | |||||||
| chr4:69602463 | TTATC | T | 30 | a0001c0001t0001g0017 a0001c0001t0001g0038 a0001c0001t0001g0045 others(27): Show |
39 | HG01255.hp1 HG01255.hp2 HG01993.hp1 others(36): Show |
intron_variant | MODIFIER | c.743-3073_743-3070d others(6): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69602463 | |||||||
| chr4:69602463 | TTATCTAT others(1): Show |
T | 35 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0018 others(32): Show |
50 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.743-3077_743-3070d others(10): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69602463 | |||||||
| chr4:69602463 | TTATCTAT others(5): Show |
T | 2 | a0001c0001t0001g0046 a0001c0001t0001g0279 |
3 | HG02970.hp1 HG03130.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.743-3081_743-3070d others(14): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69602463 | |||||||
| chr4:69602587 | G | A | 1 | a0002c0002t0005g0124 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.743-3193C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69602587 | |||||||
| chr4:69602594 | A | G | 4 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(1): Show |
4 | HG00735.hp1 HG03834.hp1 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.743-3200T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69602594 | |||||||
| chr4:69602713 | C | T | 2 | a0001c0001t0001g0018 a0001c0001t0001g0236 |
2 | NA18992.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.743-3319G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69602713 | |||||||
| chr4:69602831 | T | C | 1 | a0001c0001t0002g0001 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.743-3437A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69602831 | |||||||
| chr4:69602955 | A | C | 27 | a0002c0002t0002g0035 a0002c0002t0002g0040 a0002c0002t0002g0064 others(24): Show |
29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.743-3561T>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69602955 | |||||||
| chr4:69603038 | C | G | 27 | a0002c0002t0002g0035 a0002c0002t0002g0040 a0002c0002t0002g0064 others(24): Show |
29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.743-3644G>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69603038 | |||||||
| chr4:69603065 | T | G | 7 | a0001c0001t0001g0059 a0001c0001t0001g0270 a0001c0001t0001g0271 others(4): Show |
7 | HG01243.hp2 HG02145.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.743-3671A>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69603065 | |||||||
| chr4:69603183 | G | A | 5 | a0001c0001t0001g0222 a0002c0002t0002g0169 a0002c0002t0002g0170 others(2): Show |
5 | HG02717.hp1 HG02809.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.743-3789C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69603183 | |||||||
| chr4:69603196 | G | C | 1 | a0001c0001t0001g0066 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.743-3802C>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69603196 | |||||||
| chr4:69603288 | T | A | 1 | a0001c0001t0002g0005 | 3 | NA18965.hp1 NA18967.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.743-3894A>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69603288 | |||||||
| chr4:69603352 | C | T | 27 | a0002c0002t0002g0035 a0002c0002t0002g0040 a0002c0002t0002g0064 others(24): Show |
29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.743-3958G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69603352 | |||||||
| chr4:69603535 | T | G | 7 | a0001c0001t0001g0059 a0001c0001t0001g0270 a0001c0001t0001g0271 others(4): Show |
7 | HG01243.hp2 HG02145.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.743-4141A>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69603535 | |||||||
| chr4:69603542 | A | C | 27 | a0002c0002t0002g0035 a0002c0002t0002g0040 a0002c0002t0002g0064 others(24): Show |
29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.743-4148T>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69603542 | |||||||
| chr4:69603558 | C | G | 27 | a0002c0002t0002g0035 a0002c0002t0002g0040 a0002c0002t0002g0064 others(24): Show |
29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.743-4164G>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69603558 | |||||||
| chr4:69603614 | G | A | 27 | a0002c0002t0002g0035 a0002c0002t0002g0040 a0002c0002t0002g0064 others(24): Show |
29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.743-4220C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69603614 | |||||||
| chr4:69603618 | C | T | 7 | a0001c0001t0001g0059 a0001c0001t0001g0270 a0001c0001t0001g0271 others(4): Show |
7 | HG01243.hp2 HG02145.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.743-4224G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69603618 | |||||||
| chr4:69603630 | A | G | 27 | a0002c0002t0002g0035 a0002c0002t0002g0040 a0002c0002t0002g0064 others(24): Show |
29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.743-4236T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69603630 | |||||||
| chr4:69603673 | A | T | 27 | a0002c0002t0002g0035 a0002c0002t0002g0040 a0002c0002t0002g0064 others(24): Show |
29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.743-4279T>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69603673 | |||||||
| chr4:69603699 | C | A | 27 | a0002c0002t0002g0035 a0002c0002t0002g0040 a0002c0002t0002g0064 others(24): Show |
29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.743-4305G>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69603699 | |||||||
| chr4:69603847 | C | T | 2 | a0002c0002t0005g0124 a0002c0002t0005g0140 |
2 | HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.743-4453G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69603847 | |||||||
| chr4:69603935 | G | A | 18 | a0002c0002t0002g0035 a0002c0002t0002g0040 a0002c0002t0002g0064 others(15): Show |
20 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(17): Show |
intron_variant | MODIFIER | c.743-4541C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69603935 | |||||||
| chr4:69603979 | T | C | 27 | a0002c0002t0002g0035 a0002c0002t0002g0040 a0002c0002t0002g0064 others(24): Show |
29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.743-4585A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69603979 | |||||||
| chr4:69603983 | A | G | 1 | a0001c0001t0001g0016 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.743-4589T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69603983 | |||||||
| chr4:69604131 | A | T | 27 | a0002c0002t0002g0035 a0002c0002t0002g0040 a0002c0002t0002g0064 others(24): Show |
29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.743-4737T>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69604131 | |||||||
| chr4:69604190 | G | A | 98 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(95): Show |
124 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(121): Show |
intron_variant | MODIFIER | c.743-4796C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69604190 | |||||||
| chr4:69604320 | C | T | 98 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(95): Show |
124 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(121): Show |
intron_variant | MODIFIER | c.743-4926G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69604320 | |||||||
| chr4:69604327 | AGAG | A | 27 | a0002c0002t0002g0035 a0002c0002t0002g0040 a0002c0002t0002g0064 others(24): Show |
29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.743-4936_743-4934d others(5): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69604327 | |||||||
| chr4:69604465 | C | T | 1 | a0001c0001t0001g0016 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.743-5071G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69604465 | |||||||
| chr4:69604479 | C | A | 27 | a0002c0002t0002g0035 a0002c0002t0002g0040 a0002c0002t0002g0064 others(24): Show |
29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.743-5085G>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69604479 | |||||||
| chr4:69604507 | A | C | 2 | a0010c0011t0007g0168 a0013c0010t0007g0167 |
2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.743-5113T>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69604507 | |||||||
| chr4:69604556 | G | A | 27 | a0002c0002t0002g0035 a0002c0002t0002g0040 a0002c0002t0002g0064 others(24): Show |
29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.743-5162C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69604556 | |||||||
| chr4:69604719 | G | A | 27 | a0002c0002t0002g0035 a0002c0002t0002g0040 a0002c0002t0002g0064 others(24): Show |
29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.743-5325C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69604719 | |||||||
| chr4:69604890 | A | G | 1 | a0001c0001t0002g0121 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.743-5496T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69604890 | |||||||
| chr4:69604972 | A | G | 1 | a0001c0001t0001g0016 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.743-5578T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69604972 | |||||||
| chr4:69604977 | C | A | 5 | a0001c0001t0001g0032 a0001c0001t0001g0162 a0001c0001t0001g0163 others(2): Show |
6 | HG00099.hp1 HG00280.hp2 HG00738.hp2 others(3): Show |
intron_variant | MODIFIER | c.743-5583G>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69604977 | |||||||
| chr4:69604981 | G | A | 28 | a0001c0001t0001g0016 a0002c0002t0002g0035 a0002c0002t0002g0040 others(25): Show |
30 | HG00741.hp2 HG01346.hp2 HG01358.hp1 others(27): Show |
intron_variant | MODIFIER | c.743-5587C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69604981 | |||||||
| chr4:69604998 | G | A | 28 | a0001c0001t0001g0016 a0002c0002t0002g0035 a0002c0002t0002g0040 others(25): Show |
30 | HG00741.hp2 HG01346.hp2 HG01358.hp1 others(27): Show |
intron_variant | MODIFIER | c.743-5604C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69604998 | |||||||
| chr4:69605012 | T | C | 1 | a0001c0001t0001g0016 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.743-5618A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69605012 | |||||||
| chr4:69605014 | A | G | 1 | a0001c0001t0001g0016 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.743-5620T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69605014 | |||||||
| chr4:69605024 | A | T | 1 | a0001c0001t0001g0016 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.743-5630T>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69605024 | |||||||
| chr4:69605032 | T | G | 1 | a0001c0001t0001g0016 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.743-5638A>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69605032 | |||||||
| chr4:69605036 | T | C | 1 | a0001c0001t0001g0016 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.743-5642A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69605036 | |||||||
| chr4:69605077 | C | G | 1 | a0001c0014t0001g0218 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.743-5683G>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69605077 | |||||||
| chr4:69605092 | A | C | 1 | a0001c0014t0001g0218 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.743-5698T>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69605092 | |||||||
| chr4:69605265 | A | T | 1 | a0001c0001t0001g0174 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.743-5871T>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69605265 | |||||||
| chr4:69605266 | T | C | 1 | a0001c0001t0001g0174 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.743-5872A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69605266 | |||||||
| chr4:69605276 | A | G | 1 | a0001c0001t0001g0174 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.743-5882T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69605276 | |||||||
| chr4:69605279 | G | A | 1 | a0001c0001t0001g0016 | 2 | HG00741.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.743-5885C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69605279 | |||||||
| chr4:69605334 | C | G | 27 | a0002c0002t0002g0035 a0002c0002t0002g0040 a0002c0002t0002g0064 others(24): Show |
29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.743-5940G>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69605334 | |||||||
| chr4:69605497 | T | C | 98 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(95): Show |
124 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(121): Show |
intron_variant | MODIFIER | c.743-6103A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69605497 | |||||||
| chr4:69605560 | A | G | 1 | a0001c0001t0002g0100 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.743-6166T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69605560 | |||||||
| chr4:69605802 | C | A | 7 | a0001c0001t0001g0059 a0001c0001t0001g0270 a0001c0001t0001g0271 others(4): Show |
7 | HG01243.hp2 HG02145.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.743-6408G>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69605802 | |||||||
| chr4:69605848 | G | A | 1 | a0001c0001t0002g0014 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.743-6454C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69605848 | |||||||
| chr4:69605991 | A | T | 27 | a0002c0002t0002g0035 a0002c0002t0002g0040 a0002c0002t0002g0064 others(24): Show |
29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.743-6597T>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69605991 | |||||||
| chr4:69606004 | G | C | 1 | a0002c0002t0005g0140 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.743-6610C>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69606004 | |||||||
| chr4:69606035 | G | T | 27 | a0002c0002t0002g0035 a0002c0002t0002g0040 a0002c0002t0002g0064 others(24): Show |
29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.743-6641C>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69606035 | |||||||
| chr4:69606047 | G | C | 1 | a0001c0007t0002g0094 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.743-6653C>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69606047 | |||||||
| chr4:69606117 | C | CA | 18 | a0001c0001t0001g0016 a0001c0001t0001g0031 a0001c0001t0001g0032 others(15): Show |
22 | HG00099.hp1 HG00280.hp2 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.743-6724dupT | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69606117 | |||||||
| chr4:69606157 | C | T | 27 | a0002c0002t0002g0035 a0002c0002t0002g0040 a0002c0002t0002g0064 others(24): Show |
29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.743-6763G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69606157 | |||||||
| chr4:69606160 | G | T | 27 | a0002c0002t0002g0035 a0002c0002t0002g0040 a0002c0002t0002g0064 others(24): Show |
29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.743-6766C>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69606160 | |||||||
| chr4:69606219 | C | T | 27 | a0002c0002t0002g0035 a0002c0002t0002g0040 a0002c0002t0002g0064 others(24): Show |
29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.743-6825G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69606219 | |||||||
| chr4:69606224 | C | T | 3 | a0002c0002t0004g0180 a0002c0002t0004g0197 a0002c0002t0004g0212 |
3 | NA18969.hp1 NA18997.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.743-6830G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69606224 | |||||||
| chr4:69606247 | T | G | 27 | a0002c0002t0002g0035 a0002c0002t0002g0040 a0002c0002t0002g0064 others(24): Show |
29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.743-6853A>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69606247 | |||||||
| chr4:69606416 | T | C | 27 | a0002c0002t0002g0035 a0002c0002t0002g0040 a0002c0002t0002g0064 others(24): Show |
29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.743-7022A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69606416 | |||||||
| chr4:69606421 | C | T | 27 | a0002c0002t0002g0035 a0002c0002t0002g0040 a0002c0002t0002g0064 others(24): Show |
29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.743-7027G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69606421 | |||||||
| chr4:69606440 | T | C | 1 | a0002c0002t0002g0175 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.743-7046A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69606440 | |||||||
| chr4:69606500 | T | C | 27 | a0002c0002t0002g0035 a0002c0002t0002g0040 a0002c0002t0002g0064 others(24): Show |
29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.743-7106A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69606500 | |||||||
| chr4:69606573 | T | G | 27 | a0002c0002t0002g0035 a0002c0002t0002g0040 a0002c0002t0002g0064 others(24): Show |
29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.743-7179A>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69606573 | |||||||
| chr4:69606592 | G | A | 1 | a0002c0002t0002g0175 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.743-7198C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69606592 | |||||||
| chr4:69606601 | G | C | 27 | a0002c0002t0002g0035 a0002c0002t0002g0040 a0002c0002t0002g0064 others(24): Show |
29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.743-7207C>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69606601 | |||||||
| chr4:69606678 | G | A | 1 | a0001c0001t0001g0158 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.743-7284C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69606678 | |||||||
| chr4:69606756 | C | G | 1 | a0001c0001t0001g0065 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.743-7362G>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69606756 | |||||||
| chr4:69606761 | A | G | 2 | a0010c0011t0007g0168 a0013c0010t0007g0167 |
2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.743-7367T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69606761 | |||||||
| chr4:69606869 | C | T | 1 | a0001c0001t0001g0206 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.743-7475G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69606869 | |||||||
| chr4:69606874 | G | A | 27 | a0002c0002t0002g0035 a0002c0002t0002g0040 a0002c0002t0002g0064 others(24): Show |
29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.743-7480C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69606874 | |||||||
| chr4:69606932 | T | C | 1 | a0001c0001t0001g0251 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.743-7538A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69606932 | |||||||
| chr4:69606973 | C | T | 1 | a0001c0001t0001g0007 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.743-7579G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69606973 | |||||||
| chr4:69607055 | T | C | 27 | a0002c0002t0002g0035 a0002c0002t0002g0040 a0002c0002t0002g0064 others(24): Show |
29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.743-7661A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69607055 | |||||||
| chr4:69607101 | G | A | 4 | a0001c0001t0008g0079 a0001c0001t0008g0080 a0007c0006t0001g0050 others(1): Show |
4 | HG01109.hp2 HG03139.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.743-7707C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69607101 | |||||||
| chr4:69607122 | GC | G | 27 | a0002c0002t0002g0035 a0002c0002t0002g0040 a0002c0002t0002g0064 others(24): Show |
29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.743-7729delG | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69607122 | |||||||
| chr4:69607132 | C | T | 1 | a0008c0013t0002g0088 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.743-7738G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69607132 | |||||||
| chr4:69607167 | T | C | 1 | a0001c0001t0001g0224 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.743-7773A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69607167 | |||||||
| chr4:69607184 | G | C | 27 | a0002c0002t0002g0035 a0002c0002t0002g0040 a0002c0002t0002g0064 others(24): Show |
29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.743-7790C>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69607184 | |||||||
| chr4:69607186 | A | AACCAAAA others(15): Show |
35 | a0001c0001t0001g0281 a0001c0001t0008g0079 a0001c0001t0008g0080 others(32): Show |
37 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.743-7814_743-7793d others(24): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69607186 | |||||||
| chr4:69607194 | C | T | 1 | a0001c0001t0002g0011 | 3 | HG00642.hp2 HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.743-7800G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69607194 | |||||||
| chr4:69607223 | A | G | 4 | a0001c0001t0001g0281 a0009c0012t0001g0191 a0011c0018t0001g0283 others(1): Show |
4 | HG01192.hp2 HG01243.hp1 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.743-7829T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69607223 | |||||||
| chr4:69607224 | A | T | 1 | a0001c0001t0002g0024 | 2 | HG00738.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.743-7830T>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69607224 | |||||||
| chr4:69607228 | C | T | 1 | a0001c0001t0002g0024 | 2 | HG00738.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.743-7834G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69607228 | |||||||
| chr4:69607248 | C | T | 4 | a0001c0001t0008g0079 a0001c0001t0008g0080 a0007c0006t0001g0050 others(1): Show |
4 | HG01109.hp2 HG03139.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.743-7854G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69607248 | |||||||
| chr4:69607265 | C | T | 27 | a0002c0002t0002g0035 a0002c0002t0002g0040 a0002c0002t0002g0064 others(24): Show |
29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.743-7871G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69607265 | |||||||
| chr4:69607266 | G | A | 235 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(232): Show |
290 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(287): Show |
intron_variant | MODIFIER | c.743-7872C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69607266 | |||||||
| chr4:69607286 | T | G | 79 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(76): Show |
101 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(98): Show |
intron_variant | MODIFIER | c.743-7892A>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69607286 | |||||||
| chr4:69607309 | G | T | 2 | a0001c0001t0002g0091 a0001c0001t0002g0099 |
2 | NA18980.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.743-7915C>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69607309 | |||||||
| chr4:69607367 | T | C | 79 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(76): Show |
101 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(98): Show |
intron_variant | MODIFIER | c.743-7973A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69607367 | |||||||
| chr4:69607368 | G | A | 71 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(68): Show |
93 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(90): Show |
intron_variant | MODIFIER | c.743-7974C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69607368 | |||||||
| chr4:69607381 | C | A | 79 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(76): Show |
101 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(98): Show |
intron_variant | MODIFIER | c.743-7987G>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69607381 | |||||||
| chr4:69607386 | A | G | 4 | a0001c0001t0008g0079 a0001c0001t0008g0080 a0007c0006t0001g0050 others(1): Show |
4 | HG01109.hp2 HG03139.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.743-7992T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69607386 | |||||||
| chr4:69607403 | T | A | 1 | a0001c0001t0001g0277 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.743-8009A>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69607403 | |||||||
| chr4:69607444 | T | G | 2 | a0003c0003t0001g0292 a0003c0003t0001g0293 |
2 | HG03669.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.743-8050A>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69607444 | |||||||
| chr4:69607488 | C | T | 1 | a0001c0007t0002g0081 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.743-8094G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69607488 | |||||||
| chr4:69607521 | T | C | 27 | a0002c0002t0002g0035 a0002c0002t0002g0040 a0002c0002t0002g0064 others(24): Show |
29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.743-8127A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69607521 | |||||||
| chr4:69607522 | G | C | 27 | a0002c0002t0002g0035 a0002c0002t0002g0040 a0002c0002t0002g0064 others(24): Show |
29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.743-8128C>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69607522 | |||||||
| chr4:69607530 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.743-8136G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69607530 | |||||||
| chr4:69607598 | A | G | 1 | a0001c0001t0001g0257 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.743-8204T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69607598 | |||||||
| chr4:69607610 | A | C | 27 | a0002c0002t0002g0035 a0002c0002t0002g0040 a0002c0002t0002g0064 others(24): Show |
29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.743-8216T>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69607610 | |||||||
| chr4:69607644 | G | A | 71 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(68): Show |
93 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(90): Show |
intron_variant | MODIFIER | c.743-8250C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69607644 | |||||||
| chr4:69607824 | C | T | 79 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(76): Show |
101 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(98): Show |
intron_variant | MODIFIER | c.743-8430G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69607824 | |||||||
| chr4:69607835 | G | T | 79 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(76): Show |
101 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(98): Show |
intron_variant | MODIFIER | c.743-8441C>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69607835 | |||||||
| chr4:69607897 | G | A | 29 | a0002c0002t0002g0035 a0002c0002t0002g0040 a0002c0002t0002g0064 others(26): Show |
31 | HG01258.hp2 HG01346.hp2 HG01358.hp1 others(28): Show |
intron_variant | MODIFIER | c.743-8503C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69607897 | |||||||
| chr4:69607976 | T | G | 4 | a0001c0001t0001g0281 a0009c0012t0001g0191 a0011c0018t0001g0283 others(1): Show |
4 | HG01192.hp2 HG01243.hp1 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.743-8582A>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69607976 | |||||||
| chr4:69608070 | G | A | 79 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(76): Show |
101 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(98): Show |
intron_variant | MODIFIER | c.743-8676C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69608070 | |||||||
| chr4:69608137 | G | A | 1 | a0001c0001t0002g0105 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.743-8743C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69608137 | |||||||
| chr4:69608141 | T | G | 79 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(76): Show |
101 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(98): Show |
intron_variant | MODIFIER | c.743-8747A>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69608141 | |||||||
| chr4:69608143 | C | A | 79 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(76): Show |
101 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(98): Show |
intron_variant | MODIFIER | c.743-8749G>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69608143 | |||||||
| chr4:69608145 | C | G | 1 | a0001c0001t0001g0270 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.743-8751G>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69608145 | |||||||
| chr4:69608168 | C | G | 1 | a0001c0001t0001g0057 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.743-8774G>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69608168 | |||||||
| chr4:69608263 | C | G | 1 | a0002c0002t0005g0140 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.743-8869G>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69608263 | |||||||
| chr4:69608321 | CA | C | 79 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(76): Show |
101 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(98): Show |
intron_variant | MODIFIER | c.743-8928delT | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69608321 | |||||||
| chr4:69608362 | T | C | 1 | a0001c0001t0001g0255 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.743-8968A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69608362 | |||||||
| chr4:69608379 | A | G | 79 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(76): Show |
101 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(98): Show |
intron_variant | MODIFIER | c.743-8985T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69608379 | |||||||
| chr4:69608409 | G | A | 27 | a0002c0002t0002g0035 a0002c0002t0002g0040 a0002c0002t0002g0064 others(24): Show |
29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.743-9015C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69608409 | |||||||
| chr4:69608431 | G | A | 79 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(76): Show |
101 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(98): Show |
intron_variant | MODIFIER | c.743-9037C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69608431 | |||||||
| chr4:69608434 | G | T | 4 | a0001c0001t0001g0281 a0009c0012t0001g0191 a0011c0018t0001g0283 others(1): Show |
4 | HG01192.hp2 HG01243.hp1 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.743-9040C>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69608434 | |||||||
| chr4:69608451 | G | A | 106 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(103): Show |
130 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(127): Show |
intron_variant | MODIFIER | c.743-9057C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69608451 | |||||||
| chr4:69608529 | C | T | 2 | a0001c0001t0001g0029 a0001c0001t0001g0155 |
3 | HG02895.hp1 HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.743-9135G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69608529 | |||||||
| chr4:69608530 | G | A | 1 | a0002c0002t0002g0171 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.743-9136C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69608530 | |||||||
| chr4:69608592 | G | A | 229 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(226): Show |
283 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.743-9198C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69608592 | |||||||
| chr4:69608756 | C | T | 1 | a0001c0001t0001g0206 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.743-9362G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69608756 | |||||||
| chr4:69608767 | C | T | 3 | a0001c0001t0002g0091 a0001c0001t0002g0099 a0001c0001t0002g0100 |
3 | NA18980.hp2 NA19058.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.743-9373G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69608767 | |||||||
| chr4:69608989 | A | T | 1 | a0001c0001t0008g0080 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.743-9595T>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69608989 | |||||||
| chr4:69608992 | T | C | 3 | a0001c0001t0001g0281 a0009c0012t0001g0191 a0015c0016t0010g0082 |
3 | HG01192.hp2 HG01243.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.743-9598A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69608992 | |||||||
| chr4:69609051 | C | T | 1 | a0002c0002t0005g0140 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.743-9657G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69609051 | |||||||
| chr4:69609052 | G | A | 71 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(68): Show |
93 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(90): Show |
intron_variant | MODIFIER | c.743-9658C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69609052 | |||||||
| chr4:69609080 | G | A | 71 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(68): Show |
93 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(90): Show |
intron_variant | MODIFIER | c.743-9686C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69609080 | |||||||
| chr4:69609099 | G | T | 2 | a0010c0011t0007g0168 a0013c0010t0007g0167 |
2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.743-9705C>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69609099 | |||||||
| chr4:69609155 | A | AT | 105 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(102): Show |
132 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(129): Show |
intron_variant | MODIFIER | c.743-9762dupA | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69609155 | |||||||
| chr4:69609155 | A | ATT | 11 | a0001c0001t0001g0057 a0001c0001t0001g0077 a0001c0001t0001g0203 others(8): Show |
11 | HG01261.hp1 HG01496.hp2 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.743-9763_743-9762d others(4): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69609155 | |||||||
| chr4:69609155 | A | ATTT | 84 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(81): Show |
110 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.743-9764_743-9762d others(5): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69609155 | |||||||
| chr4:69609155 | AT | A | 26 | a0002c0002t0002g0035 a0002c0002t0002g0040 a0002c0002t0002g0064 others(23): Show |
28 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(25): Show |
intron_variant | MODIFIER | c.743-9762delA | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69609155 | |||||||
| chr4:69609232 | A | G | 98 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(95): Show |
124 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(121): Show |
intron_variant | MODIFIER | c.743-9838T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69609232 | |||||||
| chr4:69609290 | C | G | 2 | a0010c0011t0007g0168 a0013c0010t0007g0167 |
2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.743-9896G>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69609290 | |||||||
| chr4:69609338 | C | T | 235 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(232): Show |
290 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(287): Show |
intron_variant | MODIFIER | c.743-9944G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69609338 | |||||||
| chr4:69609378 | G | T | 2 | a0010c0011t0007g0168 a0013c0010t0007g0167 |
2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.743-9984C>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69609378 | |||||||
| chr4:69609382 | T | C | 1 | a0001c0001t0001g0130 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.743-9988A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69609382 | |||||||
| chr4:69609412 | C | G | 18 | a0001c0001t0001g0016 a0001c0001t0001g0031 a0001c0001t0001g0032 others(15): Show |
22 | HG00099.hp1 HG00280.hp2 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.743-10018G>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69609412 | |||||||
| chr4:69609555 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.743-10161C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69609555 | |||||||
| chr4:69609610 | G | A | 102 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(99): Show |
126 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(123): Show |
intron_variant | MODIFIER | c.743-10216C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69609610 | |||||||
| chr4:69609657 | C | G | 98 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(95): Show |
124 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(121): Show |
intron_variant | MODIFIER | c.743-10263G>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69609657 | |||||||
| chr4:69609658 | C | G | 1 | a0009c0012t0001g0191 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.743-10264G>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69609658 | |||||||
| chr4:69609685 | CACCTAT | C | 107 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(104): Show |
131 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.743-10297_743-1029 others(10): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69609685 | |||||||
| chr4:69609750 | C | A | 29 | a0001c0001t0001g0281 a0002c0002t0002g0035 a0002c0002t0002g0040 others(26): Show |
31 | HG01192.hp2 HG01243.hp1 HG01346.hp2 others(28): Show |
intron_variant | MODIFIER | c.743-10356G>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69609750 | |||||||
| chr4:69609800 | A | C | 4 | a0002c0002t0002g0169 a0002c0002t0002g0170 a0002c0002t0002g0171 others(1): Show |
4 | HG02717.hp1 HG02809.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.743-10406T>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69609800 | |||||||
| chr4:69609929 | A | G | 4 | a0001c0001t0008g0079 a0001c0001t0008g0080 a0007c0006t0001g0050 others(1): Show |
4 | HG01109.hp2 HG03139.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.743-10535T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69609929 | |||||||
| chr4:69610015 | C | A | 2 | a0001c0001t0008g0079 a0001c0001t0008g0080 |
2 | HG01109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.743-10621G>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69610015 | |||||||
| chr4:69610070 | G | A | 1 | a0001c0001t0001g0130 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.743-10676C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69610070 | |||||||
| chr4:69610148 | A | C | 100 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(97): Show |
124 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(121): Show |
intron_variant | MODIFIER | c.743-10754T>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69610148 | |||||||
| chr4:69610170 | G | A | 2 | a0010c0011t0007g0168 a0013c0010t0007g0167 |
2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.743-10776C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69610170 | |||||||
| chr4:69610246 | C | CA | 101 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(98): Show |
125 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(122): Show |
intron_variant | MODIFIER | c.743-10853dupT | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69610246 | |||||||
| chr4:69610246 | C | T | 1 | a0001c0001t0002g0084 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.743-10852G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69610246 | |||||||
| chr4:69610328 | C | T | 1 | a0001c0001t0002g0111 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.743-10934G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69610328 | |||||||
| chr4:69610481 | C | A | 6 | a0001c0001t0003g0027 a0001c0001t0003g0135 a0001c0001t0003g0136 others(3): Show |
7 | HG02572.hp1 HG02895.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.743-11087G>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69610481 | |||||||
| chr4:69610590 | C | G | 1 | a0001c0001t0001g0052 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.743-11196G>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69610590 | |||||||
| chr4:69610591 | C | G | 2 | a0007c0006t0001g0050 a0007c0006t0001g0051 |
2 | HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.743-11197G>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69610591 | |||||||
| chr4:69610591 | C | T | 2 | a0001c0001t0008g0079 a0001c0001t0008g0080 |
2 | HG01109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.743-11197G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69610591 | |||||||
| chr4:69610651 | G | A | 2 | a0001c0001t0001g0009 a0001c0001t0001g0054 |
4 | NA18985.hp1 NA18989.hp1 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.743-11257C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69610651 | |||||||
| chr4:69610675 | T | C | 2 | a0001c0001t0001g0211 a0001c0001t0001g0222 |
2 | NA18747.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.743-11281A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69610675 | |||||||
| chr4:69610762 | T | C | 1 | a0011c0018t0001g0283 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.743-11368A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69610762 | |||||||
| chr4:69610817 | G | C | 71 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(68): Show |
93 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(90): Show |
intron_variant | MODIFIER | c.743-11423C>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69610817 | |||||||
| chr4:69610847 | T | C | 4 | a0001c0001t0002g0014 a0001c0001t0002g0125 a0001c0001t0002g0133 others(1): Show |
6 | HG02630.hp1 HG02717.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.743-11453A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69610847 | |||||||
| chr4:69610870 | G | A | 98 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(95): Show |
124 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(121): Show |
intron_variant | MODIFIER | c.743-11476C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69610870 | |||||||
| chr4:69610877 | C | T | 29 | a0001c0001t0001g0281 a0002c0002t0002g0035 a0002c0002t0002g0040 others(26): Show |
31 | HG01192.hp2 HG01243.hp1 HG01346.hp2 others(28): Show |
intron_variant | MODIFIER | c.743-11483G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69610877 | |||||||
| chr4:69611005 | C | G | 106 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(103): Show |
130 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(127): Show |
intron_variant | MODIFIER | c.743-11611G>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69611005 | |||||||
| chr4:69611025 | G | A | 1 | a0001c0001t0003g0138 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.743-11631C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69611025 | |||||||
| chr4:69611113 | T | TA | 106 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(103): Show |
130 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(127): Show |
intron_variant | MODIFIER | c.743-11720dupT | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69611113 | |||||||
| chr4:69611208 | C | A | 2 | a0010c0011t0007g0168 a0013c0010t0007g0167 |
2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.743-11814G>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69611208 | |||||||
| chr4:69611264 | A | G | 1 | a0003c0003t0001g0290 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.743-11870T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69611264 | |||||||
| chr4:69611265 | T | C | 2 | a0010c0011t0007g0168 a0013c0010t0007g0167 |
2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.743-11871A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69611265 | |||||||
| chr4:69611287 | G | T | 71 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(68): Show |
93 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(90): Show |
intron_variant | MODIFIER | c.743-11893C>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69611287 | |||||||
| chr4:69611288 | T | TCCAGCTA others(302): Show |
2 | a0001c0001t0001g0058 a0001c0001t0001g0072 |
2 | HG03710.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.743-11895_743-1189 others(313): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69611288 | |||||||
| chr4:69611288 | T | TCCAGCTA others(303): Show |
4 | a0003c0003t0001g0288 a0004c0004t0001g0042 a0004c0004t0001g0177 others(1): Show |
5 | HG00639.hp2 HG00741.hp1 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.743-11895_743-1189 others(314): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69611288 | |||||||
| chr4:69611288 | T | TCCAGCTA others(303): Show |
60 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(57): Show |
81 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(78): Show |
intron_variant | MODIFIER | c.743-11895_743-1189 others(314): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69611288 | |||||||
| chr4:69611288 | T | TCCAGCTA others(304): Show |
2 | a0001c0001t0001g0054 a0001c0001t0001g0078 |
2 | NA18982.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.743-11895_743-1189 others(315): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69611288 | |||||||
| chr4:69611288 | T | TCCAGCTA others(323): Show |
1 | a0001c0001t0001g0142 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.743-11895_743-1189 others(334): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69611288 | |||||||
| chr4:69611288 | T | TCCAGCTA others(324): Show |
1 | a0001c0001t0001g0166 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.743-11895_743-1189 others(335): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69611288 | |||||||
| chr4:69611288 | T | TCCAGCTA others(342): Show |
1 | a0001c0001t0001g0141 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.743-11895_743-1189 others(353): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69611288 | |||||||
| chr4:69611290 | C | T | 1 | a0009c0012t0001g0191 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.743-11896G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69611290 | |||||||
| chr4:69611390 | C | A | 1 | a0002c0002t0005g0124 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.743-11996G>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69611390 | |||||||
| chr4:69611398 | T | C | 1 | a0001c0001t0002g0105 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.743-12004A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69611398 | |||||||
| chr4:69611610 | G | T | 106 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(103): Show |
130 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(127): Show |
intron_variant | MODIFIER | c.743-12216C>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69611610 | |||||||
| chr4:69611854 | G | T | 106 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(103): Show |
130 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(127): Show |
intron_variant | MODIFIER | c.743-12460C>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69611854 | |||||||
| chr4:69611860 | G | C | 1 | a0007c0006t0001g0050 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.743-12466C>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69611860 | |||||||
| chr4:69611879 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.743-12485G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69611879 | |||||||
| chr4:69611940 | A | G | 7 | a0001c0001t0001g0059 a0001c0001t0001g0270 a0001c0001t0001g0271 others(4): Show |
7 | HG01243.hp2 HG02145.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.743-12546T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69611940 | |||||||
| chr4:69611949 | T | C | 2 | a0010c0011t0007g0168 a0013c0010t0007g0167 |
2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.743-12555A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69611949 | |||||||
| chr4:69611972 | T | C | 1 | a0001c0001t0001g0247 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.743-12578A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69611972 | |||||||
| chr4:69612147 | G | A | 106 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(103): Show |
130 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(127): Show |
intron_variant | MODIFIER | c.743-12753C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69612147 | |||||||
| chr4:69612192 | C | G | 1 | a0011c0018t0001g0283 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.743-12798G>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69612192 | |||||||
| chr4:69612266 | C | T | 106 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(103): Show |
130 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(127): Show |
intron_variant | MODIFIER | c.743-12872G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69612266 | |||||||
| chr4:69612408 | T | G | 34 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0021 others(31): Show |
44 | HG00438.hp2 HG00609.hp2 HG01070.hp1 others(41): Show |
intron_variant | MODIFIER | c.743-13014A>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69612408 | |||||||
| chr4:69612451 | C | T | 106 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(103): Show |
130 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(127): Show |
intron_variant | MODIFIER | c.743-13057G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69612451 | |||||||
| chr4:69612465 | C | T | 29 | a0001c0001t0001g0281 a0002c0002t0002g0035 a0002c0002t0002g0040 others(26): Show |
31 | HG01192.hp2 HG01243.hp1 HG01346.hp2 others(28): Show |
intron_variant | MODIFIER | c.743-13071G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69612465 | |||||||
| chr4:69612486 | T | G | 1 | a0001c0001t0001g0075 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.743-13092A>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69612486 | |||||||
| chr4:69612498 | G | T | 1 | a0001c0001t0001g0235 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.743-13104C>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69612498 | |||||||
| chr4:69612534 | CAGAT | C | 71 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(68): Show |
93 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(90): Show |
intron_variant | MODIFIER | c.743-13144_743-1314 others(8): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69612534 | |||||||
| chr4:69612592 | G | C | 7 | a0001c0001t0001g0059 a0001c0001t0001g0270 a0001c0001t0001g0271 others(4): Show |
7 | HG01243.hp2 HG02145.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.743-13198C>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69612592 | |||||||
| chr4:69612673 | C | T | 1 | a0011c0018t0001g0283 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.743-13279G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69612673 | |||||||
| chr4:69612677 | T | C | 1 | a0001c0001t0001g0031 | 2 | HG01070.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.743-13283A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69612677 | |||||||
| chr4:69612715 | T | C | 2 | a0010c0011t0007g0168 a0013c0010t0007g0167 |
2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.743-13321A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69612715 | |||||||
| chr4:69612857 | C | T | 18 | a0001c0001t0001g0016 a0001c0001t0001g0031 a0001c0001t0001g0032 others(15): Show |
22 | HG00099.hp1 HG00280.hp2 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.743-13463G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69612857 | |||||||
| chr4:69612869 | T | A | 2 | a0010c0011t0007g0168 a0013c0010t0007g0167 |
2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.743-13475A>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69612869 | |||||||
| chr4:69612874 | A | G | 2 | a0010c0011t0007g0168 a0013c0010t0007g0167 |
2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.743-13480T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69612874 | |||||||
| chr4:69612907 | G | GA | 190 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(187): Show |
250 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.743-13514dupT | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69612907 | |||||||
| chr4:69612907 | G | GAA | 15 | a0001c0001t0001g0044 a0001c0001t0001g0065 a0001c0001t0001g0146 others(12): Show |
18 | HG01192.hp2 HG01257.hp1 HG01258.hp1 others(15): Show |
intron_variant | MODIFIER | c.743-13515_743-1351 others(6): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69612907 | |||||||
| chr4:69612907 | G | GAAA | 24 | a0002c0002t0002g0035 a0002c0002t0002g0040 a0002c0002t0002g0064 others(21): Show |
26 | HG01243.hp1 HG01346.hp2 HG01358.hp1 others(23): Show |
intron_variant | MODIFIER | c.743-13516_743-1351 others(7): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69612907 | |||||||
| chr4:69612950 | T | G | 107 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(104): Show |
132 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.743-13556A>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69612950 | |||||||
| chr4:69612961 | A | T | 107 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(104): Show |
132 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.743-13567T>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69612961 | |||||||
| chr4:69613054 | TA | T | 106 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(103): Show |
130 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(127): Show |
intron_variant | MODIFIER | c.743-13661delT | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69613054 | |||||||
| chr4:69613066 | G | A | 70 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(67): Show |
92 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.743-13672C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69613066 | |||||||
| chr4:69613090 | A | G | 3 | a0001c0001t0001g0281 a0009c0012t0001g0191 a0015c0016t0010g0082 |
3 | HG01192.hp2 HG01243.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.743-13696T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69613090 | |||||||
| chr4:69613095 | A | G | 106 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(103): Show |
130 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(127): Show |
intron_variant | MODIFIER | c.743-13701T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69613095 | |||||||
| chr4:69613194 | T | C | 18 | a0002c0002t0002g0035 a0002c0002t0002g0040 a0002c0002t0002g0064 others(15): Show |
20 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(17): Show |
intron_variant | MODIFIER | c.743-13800A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69613194 | |||||||
| chr4:69613253 | T | C | 18 | a0001c0001t0001g0016 a0001c0001t0001g0031 a0001c0001t0001g0032 others(15): Show |
22 | HG00099.hp1 HG00280.hp2 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.743-13859A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69613253 | |||||||
| chr4:69613304 | C | T | 1 | a0001c0001t0001g0226 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.743-13910G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69613304 | |||||||
| chr4:69613355 | A | C | 1 | a0001c0001t0001g0066 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.743-13961T>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69613355 | |||||||
| chr4:69613507 | CACA | C | 18 | a0001c0001t0001g0016 a0001c0001t0001g0031 a0001c0001t0001g0032 others(15): Show |
22 | HG00099.hp1 HG00280.hp2 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.743-14116_743-1411 others(7): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69613507 | |||||||
| chr4:69613693 | T | C | 28 | a0001c0001t0001g0281 a0002c0002t0002g0035 a0002c0002t0002g0040 others(25): Show |
30 | HG01192.hp2 HG01243.hp1 HG01346.hp2 others(27): Show |
intron_variant | MODIFIER | c.743-14299A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69613693 | |||||||
| chr4:69613829 | A | G | 6 | a0001c0001t0003g0027 a0001c0001t0003g0135 a0001c0001t0003g0136 others(3): Show |
7 | HG02572.hp1 HG02895.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.743-14435T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69613829 | |||||||
| chr4:69613900 | C | A | 2 | a0010c0011t0007g0168 a0013c0010t0007g0167 |
2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.743-14506G>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69613900 | |||||||
| chr4:69613948 | C | T | 2 | a0001c0001t0008g0079 a0001c0001t0008g0080 |
2 | HG01109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.743-14554G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69613948 | |||||||
| chr4:69613967 | T | C | 1 | a0002c0002t0002g0171 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.743-14573A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69613967 | |||||||
| chr4:69614065 | G | A | 236 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(233): Show |
292 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(289): Show |
intron_variant | MODIFIER | c.743-14671C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69614065 | |||||||
| chr4:69614112 | T | A | 78 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(75): Show |
101 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.743-14718A>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69614112 | |||||||
| chr4:69614113 | A | C | 78 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(75): Show |
101 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.743-14719T>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69614113 | |||||||
| chr4:69614114 | A | T | 78 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(75): Show |
101 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.743-14720T>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69614114 | |||||||
| chr4:69614116 | C | CTGAATGG others(2): Show |
78 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(75): Show |
101 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.743-14723_743-1472 others(13): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69614116 | |||||||
| chr4:69614117 | C | T | 78 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(75): Show |
101 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.743-14723G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69614117 | |||||||
| chr4:69614118 | C | T | 78 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(75): Show |
101 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.743-14724G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69614118 | |||||||
| chr4:69614149 | T | C | 1 | a0001c0001t0001g0063 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.743-14755A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69614149 | |||||||
| chr4:69614410 | A | G | 18 | a0001c0001t0001g0016 a0001c0001t0001g0031 a0001c0001t0001g0032 others(15): Show |
22 | HG00099.hp1 HG00280.hp2 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.743-15016T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69614410 | |||||||
| chr4:69614415 | T | A | 107 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(104): Show |
132 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.743-15021A>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69614415 | |||||||
| chr4:69614418 | C | T | 78 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(75): Show |
101 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.743-15024G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69614418 | |||||||
| chr4:69614436 | C | T | 2 | a0010c0011t0007g0168 a0013c0010t0007g0167 |
2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.743-15042G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69614436 | |||||||
| chr4:69614461 | A | AT | 107 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(104): Show |
132 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.743-15068_743-1506 others(5): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69614461 | |||||||
| chr4:69614501 | C | G | 1 | a0003c0003t0006g0289 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.743-15107G>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69614501 | |||||||
| chr4:69614609 | T | C | 230 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(227): Show |
285 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(282): Show |
intron_variant | MODIFIER | c.743-15215A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69614609 | |||||||
| chr4:69614617 | A | C | 230 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(227): Show |
285 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(282): Show |
intron_variant | MODIFIER | c.743-15223T>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69614617 | |||||||
| chr4:69614630 | C | A | 2 | a0010c0011t0007g0168 a0013c0010t0007g0167 |
2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.743-15236G>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69614630 | |||||||
| chr4:69614760 | T | C | 1 | a0001c0001t0001g0072 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.743-15366A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69614760 | |||||||
| chr4:69614836 | T | C | 2 | a0010c0011t0007g0168 a0013c0010t0007g0167 |
2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.743-15442A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69614836 | |||||||
| chr4:69615039 | C | A | 26 | a0002c0002t0002g0035 a0002c0002t0002g0040 a0002c0002t0002g0064 others(23): Show |
28 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(25): Show |
intron_variant | MODIFIER | c.743-15645G>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69615039 | |||||||
| chr4:69615107 | T | G | 1 | a0001c0001t0002g0106 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.743-15713A>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69615107 | |||||||
| chr4:69615157 | C | T | 7 | a0001c0001t0001g0059 a0001c0001t0001g0270 a0001c0001t0001g0271 others(4): Show |
7 | HG01243.hp2 HG02145.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.743-15763G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69615157 | |||||||
| chr4:69615174 | C | A | 1 | a0001c0001t0002g0107 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.743-15780G>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69615174 | |||||||
| chr4:69615199 | C | A | 3 | a0010c0011t0007g0168 a0013c0010t0007g0167 a0015c0016t0010g0082 |
3 | HG01884.hp1 HG02630.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.743-15805G>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69615199 | |||||||
| chr4:69615208 | A | G | 107 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(104): Show |
132 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.743-15814T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69615208 | |||||||
| chr4:69615275 | G | A | 3 | a0010c0011t0007g0168 a0013c0010t0007g0167 a0015c0016t0010g0082 |
3 | HG01884.hp1 HG02630.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.743-15881C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69615275 | |||||||
| chr4:69615484 | G | A | 1 | a0001c0001t0001g0281 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.743-16090C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69615484 | |||||||
| chr4:69615564 | T | C | 2 | a0001c0001t0001g0281 a0009c0012t0001g0191 |
2 | HG01192.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.743-16170A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69615564 | |||||||
| chr4:69615702 | A | C | 1 | a0001c0001t0001g0201 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.743-16308T>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69615702 | |||||||
| chr4:69615724 | G | A | 108 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(105): Show |
133 | HG00140.hp1 HG00423.hp1 HG00597.hp2 others(130): Show |
intron_variant | MODIFIER | c.743-16330C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69615724 | |||||||
| chr4:69615731 | A | G | 2 | a0001c0001t0008g0079 a0001c0001t0008g0080 |
2 | HG01109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.743-16337T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69615731 | |||||||
| chr4:69615786 | G | A | 3 | a0001c0001t0001g0215 a0001c0001t0001g0221 a0014c0015t0001g0216 |
3 | NA18939.hp1 NA18946.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.743-16392C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69615786 | |||||||
| chr4:69615858 | C | CA | 55 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0017 others(52): Show |
74 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.743-16465dupT | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69615858 | |||||||
| chr4:69615890 | C | T | 2 | a0001c0001t0008g0079 a0001c0001t0008g0080 |
2 | HG01109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.743-16496G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69615890 | |||||||
| chr4:69615935 | T | C | 1 | a0001c0001t0001g0281 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.743-16541A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69615935 | |||||||
| chr4:69615969 | C | T | 1 | a0001c0001t0003g0147 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.743-16575G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69615969 | |||||||
| chr4:69615987 | C | T | 83 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(80): Show |
110 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.743-16593G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69615987 | |||||||
| chr4:69616115 | C | T | 25 | a0002c0002t0002g0035 a0002c0002t0002g0040 a0002c0002t0002g0169 others(22): Show |
27 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(24): Show |
intron_variant | MODIFIER | c.743-16721G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69616115 | |||||||
| chr4:69616118 | G | A | 2 | a0010c0011t0007g0168 a0013c0010t0007g0167 |
2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.743-16724C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69616118 | |||||||
| chr4:69616119 | G | A | 1 | a0002c0002t0002g0187 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.743-16725C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69616119 | |||||||
| chr4:69616162 | A | G | 117 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(114): Show |
146 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.743-16768T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69616162 | |||||||
| chr4:69616292 | A | G | 3 | a0004c0004t0001g0042 a0004c0004t0001g0177 a0004c0004t0001g0230 |
4 | HG00639.hp2 HG00741.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.743-16898T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69616292 | |||||||
| chr4:69616379 | T | C | 97 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(94): Show |
124 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.743-16985A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69616379 | |||||||
| chr4:69616382 | G | C | 1 | a0001c0001t0001g0234 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.743-16988C>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69616382 | |||||||
| chr4:69616604 | A | G | 1 | a0001c0001t0001g0194 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.743-17210T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69616604 | |||||||
| chr4:69616667 | T | C | 4 | a0001c0001t0002g0014 a0001c0001t0002g0125 a0001c0001t0002g0133 others(1): Show |
6 | HG02630.hp1 HG02717.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.743-17273A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69616667 | |||||||
| chr4:69616751 | A | G | 1 | a0001c0001t0002g0097 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.743-17357T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69616751 | |||||||
| chr4:69616833 | C | CT | 13 | a0001c0001t0001g0236 a0001c0001t0002g0001 a0001c0001t0002g0014 others(10): Show |
20 | HG01243.hp1 HG01934.hp1 HG02630.hp1 others(17): Show |
intron_variant | MODIFIER | c.743-17440dupA | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69616833 | |||||||
| chr4:69616833 | C | CTT | 30 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0034 others(27): Show |
41 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.743-17441_743-1744 others(6): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69616833 | |||||||
| chr4:69616833 | C | CTTT | 89 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0017 others(86): Show |
107 | HG00544.hp1 HG00609.hp1 HG00621.hp2 others(104): Show |
intron_variant | MODIFIER | c.743-17442_743-1744 others(7): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69616833 | |||||||
| chr4:69616833 | CT | C | 20 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0002g0109 others(17): Show |
25 | HG00140.hp1 HG00423.hp1 HG00544.hp2 others(22): Show |
intron_variant | MODIFIER | c.743-17440delA | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69616833 | |||||||
| chr4:69616833 | CTT | C | 63 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(60): Show |
84 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.743-17441_743-1744 others(6): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69616833 | |||||||
| chr4:69616850 | T | G | 2 | a0007c0006t0001g0050 a0007c0006t0001g0051 |
2 | HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.743-17456A>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69616850 | |||||||
| chr4:69617324 | G | A | 94 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(91): Show |
120 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.743-17930C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69617324 | |||||||
| chr4:69617448 | T | C | 6 | a0001c0001t0003g0027 a0001c0001t0003g0135 a0001c0001t0003g0136 others(3): Show |
7 | HG02572.hp1 HG02895.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.743-18054A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69617448 | |||||||
| chr4:69617469 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.743-18075C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69617469 | |||||||
| chr4:69617482 | C | T | 1 | a0001c0001t0001g0238 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.743-18088G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69617482 | |||||||
| chr4:69617511 | A | C | 1 | a0001c0001t0001g0144 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.743-18117T>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69617511 | |||||||
| chr4:69617532 | A | G | 1 | a0002c0002t0002g0175 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.743-18138T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69617532 | |||||||
| chr4:69617605 | A | C | 94 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(91): Show |
120 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.743-18211T>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69617605 | |||||||
| chr4:69617630 | C | T | 9 | a0001c0001t0008g0079 a0001c0001t0008g0080 a0002c0002t0002g0169 others(6): Show |
9 | HG01109.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.743-18236G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69617630 | |||||||
| chr4:69617733 | C | T | 94 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(91): Show |
120 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.743-18339G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69617733 | |||||||
| chr4:69617771 | C | G | 4 | a0001c0001t0002g0014 a0001c0001t0002g0125 a0001c0001t0002g0133 others(1): Show |
6 | HG02630.hp1 HG02717.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.743-18377G>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69617771 | |||||||
| chr4:69617969 | T | C | 2 | a0010c0011t0007g0168 a0013c0010t0007g0167 |
2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.743-18575A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69617969 | |||||||
| chr4:69618187 | A | ATG | 156 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(153): Show |
207 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.743-18795_743-1879 others(6): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69618187 | |||||||
| chr4:69618187 | A | ATGTG | 17 | a0001c0001t0001g0041 a0001c0001t0001g0052 a0001c0001t0001g0181 others(14): Show |
19 | HG00423.hp2 HG01192.hp1 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.743-18797_743-1879 others(8): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69618187 | |||||||
| chr4:69618187 | ATGTGTG | A | 3 | a0001c0001t0008g0079 a0001c0001t0008g0080 a0002c0002t0002g0064 |
3 | HG01109.hp2 HG02602.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.743-18799_743-1879 others(10): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69618187 | |||||||
| chr4:69618201 | G | GTGTGTGT others(5): Show |
6 | a0002c0002t0002g0175 a0003c0003t0001g0019 a0003c0003t0001g0287 others(3): Show |
9 | HG00423.hp1 HG02615.hp2 NA18968.hp2 others(6): Show |
intron_variant | MODIFIER | c.743-18808_743-1880 others(16): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69618201 | |||||||
| chr4:69618203 | G | GTGTGTAT others(3): Show |
4 | a0003c0003t0001g0288 a0003c0003t0001g0290 a0003c0003t0006g0289 others(1): Show |
4 | HG01106.hp1 HG01891.hp2 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.743-18810_743-1880 others(14): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69618203 | |||||||
| chr4:69618205 | G | GTGTATGT others(1): Show |
7 | a0001c0001t0001g0132 a0003c0003t0001g0020 a0003c0003t0001g0291 others(4): Show |
9 | HG01099.hp1 HG01516.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.743-18812_743-1881 others(12): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69618205 | |||||||
| chr4:69618205 | G | GTGTGTGT others(5): Show |
1 | a0001c0001t0003g0150 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.743-18812_743-1881 others(16): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69618205 | |||||||
| chr4:69618207 | G | GTGTA | 20 | a0001c0001t0001g0016 a0001c0001t0001g0031 a0001c0001t0001g0032 others(17): Show |
24 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.743-18814_743-1881 others(8): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69618207 | |||||||
| chr4:69618207 | G | GTGTATGT others(1): Show |
11 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0054 others(8): Show |
14 | HG01884.hp1 HG02258.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.743-18814_743-1881 others(12): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69618207 | |||||||
| chr4:69618209 | G | GTA | 9 | a0001c0001t0001g0030 a0001c0001t0001g0131 a0001c0001t0001g0144 others(6): Show |
10 | HG01496.hp1 HG02717.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.743-18816_743-1881 others(6): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69618209 | |||||||
| chr4:69618209 | G | GTATGTT | 30 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0021 others(27): Show |
43 | HG00597.hp2 HG00609.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.743-18816_743-1881 others(10): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69618209 | |||||||
| chr4:69618209 | G | T | 1 | a0003c0003t0001g0295 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.743-18815C>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69618209 | |||||||
| chr4:69618211 | G | A | 8 | a0001c0001t0001g0055 a0001c0001t0001g0061 a0001c0001t0001g0062 others(5): Show |
8 | HG02922.hp1 HG02976.hp2 HG03834.hp1 others(5): Show |
intron_variant | MODIFIER | c.743-18817C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69618211 | |||||||
| chr4:69618211 | G | T | 20 | a0001c0001t0001g0016 a0001c0001t0001g0031 a0001c0001t0001g0032 others(17): Show |
24 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.743-18817C>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69618211 | |||||||
| chr4:69618213 | G | A | 2 | a0007c0006t0001g0050 a0007c0006t0001g0051 |
2 | HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.743-18819C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69618213 | |||||||
| chr4:69618213 | G | T | 9 | a0001c0001t0001g0030 a0001c0001t0001g0131 a0001c0001t0001g0144 others(6): Show |
10 | HG01496.hp1 HG02717.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.743-18819C>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69618213 | |||||||
| chr4:69618213 | GTGTA | G | 8 | a0001c0001t0001g0055 a0001c0001t0001g0061 a0001c0001t0001g0062 others(5): Show |
8 | HG02922.hp1 HG02976.hp2 HG03834.hp1 others(5): Show |
intron_variant | MODIFIER | c.743-18823_743-1882 others(8): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69618213 | |||||||
| chr4:69618217 | A | G | 90 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(87): Show |
116 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.743-18823T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69618217 | |||||||
| chr4:69618217 | A | T | 2 | a0007c0006t0001g0050 a0007c0006t0001g0051 |
2 | HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.743-18823T>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69618217 | |||||||
| chr4:69618219 | G | T | 8 | a0001c0001t0001g0055 a0001c0001t0001g0061 a0001c0001t0001g0062 others(5): Show |
8 | HG02922.hp1 HG02976.hp2 HG03834.hp1 others(5): Show |
intron_variant | MODIFIER | c.743-18825C>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69618219 | |||||||
| chr4:69618221 | T | G | 100 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(97): Show |
126 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.743-18827A>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69618221 | |||||||
| chr4:69618221 | T | TTG | 70 | a0001c0001t0001g0093 a0001c0001t0001g0098 a0001c0001t0001g0108 others(67): Show |
97 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.743-18829_743-1882 others(6): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69618221 | |||||||
| chr4:69618221 | T | TTGTG | 122 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(119): Show |
151 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(148): Show |
intron_variant | MODIFIER | c.743-18831_743-1882 others(8): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69618221 | |||||||
| chr4:69618239 | A | G | 94 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(91): Show |
120 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.743-18845T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69618239 | |||||||
| chr4:69618328 | C | A | 94 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(91): Show |
120 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.743-18934G>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69618328 | |||||||
| chr4:69618350 | CATA | C | 64 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(61): Show |
85 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.743-18959_743-1895 others(7): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69618350 | |||||||
| chr4:69618471 | T | G | 94 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(91): Show |
120 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.743-19077A>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69618471 | |||||||
| chr4:69618512 | T | A | 2 | a0001c0001t0001g0244 a0001c0009t0001g0213 |
2 | HG02602.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.743-19118A>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69618512 | |||||||
| chr4:69618512 | T | C | 1 | a0001c0001t0001g0206 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.743-19118A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69618512 | |||||||
| chr4:69618532 | G | A | 18 | a0001c0001t0001g0132 a0003c0003t0001g0019 a0003c0003t0001g0020 others(15): Show |
23 | HG00140.hp1 HG00423.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.743-19138C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69618532 | |||||||
| chr4:69618674 | G | T | 1 | a0009c0012t0001g0191 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.743-19280C>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69618674 | |||||||
| chr4:69618777 | A | G | 1 | a0001c0001t0002g0121 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.743-19383T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69618777 | |||||||
| chr4:69618915 | T | A | 8 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0054 others(5): Show |
11 | NA18950.hp2 NA18964.hp1 NA18982.hp1 others(8): Show |
intron_variant | MODIFIER | c.743-19521A>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69618915 | |||||||
| chr4:69618960 | T | G | 1 | a0001c0001t0001g0174 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.743-19566A>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69618960 | |||||||
| chr4:69618993 | T | C | 1 | a0001c0001t0002g0117 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.743-19599A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69618993 | |||||||
| chr4:69619079 | A | T | 1 | a0001c0001t0001g0115 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.743-19685T>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69619079 | |||||||
| chr4:69619122 | C | T | 18 | a0001c0001t0001g0132 a0003c0003t0001g0019 a0003c0003t0001g0020 others(15): Show |
23 | HG00140.hp1 HG00423.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.743-19728G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69619122 | |||||||
| chr4:69619395 | G | A | 4 | a0003c0003t0001g0019 a0003c0003t0001g0291 a0003c0003t0001g0294 others(1): Show |
6 | NA18968.hp2 NA18988.hp2 NA19067.hp1 others(3): Show |
intron_variant | MODIFIER | c.742+19504C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69619395 | |||||||
| chr4:69619420 | C | CATAAA | 81 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(78): Show |
107 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.742+19474_742+1947 others(9): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69619420 | |||||||
| chr4:69619420 | C | CATAAAAT others(3): Show |
5 | a0001c0001t0002g0053 a0001c0001t0008g0079 a0001c0001t0008g0080 others(2): Show |
5 | HG00597.hp2 HG01109.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.742+19469_742+1947 others(14): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69619420 | |||||||
| chr4:69619420 | C | CATAAAAT others(8): Show |
5 | a0002c0002t0002g0170 a0002c0002t0002g0171 a0002c0002t0002g0172 others(2): Show |
5 | HG02717.hp1 HG02809.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.742+19464_742+1947 others(19): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69619420 | |||||||
| chr4:69619470 | T | C | 92 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(89): Show |
118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.742+19429A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69619470 | |||||||
| chr4:69619517 | C | T | 4 | a0001c0001t0001g0281 a0001c0001t0002g0047 a0001c0001t0002g0276 others(1): Show |
5 | HG01192.hp2 HG01243.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.742+19382G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69619517 | |||||||
| chr4:69619518 | G | T | 1 | a0002c0002t0002g0175 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.742+19381C>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69619518 | |||||||
| chr4:69619551 | A | T | 1 | a0002c0002t0002g0170 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.742+19348T>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69619551 | |||||||
| chr4:69619909 | C | T | 226 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(223): Show |
281 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(278): Show |
intron_variant | MODIFIER | c.742+18990G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69619909 | |||||||
| chr4:69619945 | T | C | 64 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(61): Show |
85 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.742+18954A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69619945 | |||||||
| chr4:69619990 | T | C | 94 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(91): Show |
120 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.742+18909A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69619990 | |||||||
| chr4:69620125 | C | T | 94 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(91): Show |
120 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.742+18774G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69620125 | |||||||
| chr4:69620189 | A | G | 1 | a0009c0012t0001g0191 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.742+18710T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69620189 | |||||||
| chr4:69620221 | T | C | 1 | a0001c0001t0001g0154 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.742+18678A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69620221 | |||||||
| chr4:69620288 | C | G | 1 | a0002c0002t0002g0175 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.742+18611G>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69620288 | |||||||
| chr4:69620291 | G | GA | 93 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(90): Show |
119 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.742+18607dupT | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69620291 | |||||||
| chr4:69620341 | G | A | 1 | a0002c0002t0005g0140 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.742+18558C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69620341 | |||||||
| chr4:69620379 | A | AAAATGCC others(37): Show |
9 | a0001c0001t0001g0055 a0001c0001t0001g0061 a0001c0001t0001g0062 others(6): Show |
9 | HG02602.hp2 HG02922.hp1 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.742+18519_742+1852 others(48): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69620379 | |||||||
| chr4:69620381 | T | A | 9 | a0001c0001t0001g0055 a0001c0001t0001g0061 a0001c0001t0001g0062 others(6): Show |
9 | HG02602.hp2 HG02922.hp1 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.742+18518A>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69620381 | |||||||
| chr4:69620655 | CA | C | 66 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(63): Show |
87 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.742+18243delT | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69620655 | |||||||
| chr4:69620655 | CAA | C | 9 | a0001c0001t0008g0079 a0001c0001t0008g0080 a0002c0002t0002g0169 others(6): Show |
9 | HG01109.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.742+18242_742+1824 others(6): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69620655 | |||||||
| chr4:69620772 | T | C | 1 | a0001c0001t0001g0144 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.742+18127A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69620772 | |||||||
| chr4:69620794 | A | G | 9 | a0001c0001t0008g0079 a0001c0001t0008g0080 a0002c0002t0002g0169 others(6): Show |
9 | HG01109.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.742+18105T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69620794 | |||||||
| chr4:69620932 | C | G | 94 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(91): Show |
120 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.742+17967G>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69620932 | |||||||
| chr4:69621091 | G | T | 18 | a0001c0001t0001g0132 a0003c0003t0001g0019 a0003c0003t0001g0020 others(15): Show |
23 | HG00140.hp1 HG00423.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.742+17808C>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69621091 | |||||||
| chr4:69621114 | C | T | 5 | a0001c0001t0002g0188 a0002c0002t0002g0186 a0002c0002t0002g0187 others(2): Show |
5 | HG01358.hp1 HG02451.hp1 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.742+17785G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69621114 | |||||||
| chr4:69621291 | C | G | 1 | a0002c0002t0002g0175 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.742+17608G>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69621291 | |||||||
| chr4:69621371 | G | A | 1 | a0001c0001t0002g0110 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.742+17528C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69621371 | |||||||
| chr4:69621384 | A | T | 1 | a0001c0001t0001g0159 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.742+17515T>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69621384 | |||||||
| chr4:69621491 | A | T | 94 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(91): Show |
120 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.742+17408T>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69621491 | |||||||
| chr4:69621585 | C | T | 5 | a0001c0001t0001g0055 a0001c0001t0001g0061 a0001c0001t0001g0062 others(2): Show |
5 | HG02602.hp2 HG03834.hp1 HG03927.hp1 others(2): Show |
intron_variant | MODIFIER | c.742+17314G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69621585 | |||||||
| chr4:69621621 | T | A | 123 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(120): Show |
152 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(149): Show |
intron_variant | MODIFIER | c.742+17278A>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69621621 | |||||||
| chr4:69621656 | C | T | 94 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(91): Show |
120 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.742+17243G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69621656 | |||||||
| chr4:69621679 | C | T | 17 | a0001c0001t0001g0132 a0003c0003t0001g0019 a0003c0003t0001g0020 others(14): Show |
22 | HG00140.hp1 HG00423.hp1 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.742+17220G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69621679 | |||||||
| chr4:69621711 | T | C | 2 | a0001c0001t0001g0141 a0002c0002t0005g0140 |
2 | HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.742+17188A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69621711 | |||||||
| chr4:69621894 | A | G | 2 | a0001c0001t0001g0157 a0001c0001t0001g0158 |
2 | HG01943.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.742+17005T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69621894 | |||||||
| chr4:69622043 | T | C | 94 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(91): Show |
120 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.742+16856A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69622043 | |||||||
| chr4:69622044 | A | C | 65 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(62): Show |
86 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.742+16855T>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69622044 | |||||||
| chr4:69622244 | A | T | 94 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(91): Show |
120 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.742+16655T>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69622244 | |||||||
| chr4:69622271 | GTAA | G | 4 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(1): Show |
4 | HG02602.hp2 HG03834.hp1 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.742+16625_742+1662 others(7): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69622271 | |||||||
| chr4:69622304 | G | C | 83 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(80): Show |
109 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.742+16595C>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69622304 | |||||||
| chr4:69622389 | A | G | 11 | a0001c0001t0008g0079 a0001c0001t0008g0080 a0002c0002t0002g0169 others(8): Show |
11 | HG01109.hp2 HG01884.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.742+16510T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69622389 | |||||||
| chr4:69622559 | A | G | 1 | a0015c0016t0010g0082 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.742+16340T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69622559 | |||||||
| chr4:69622642 | C | A | 94 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(91): Show |
120 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.742+16257G>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69622642 | |||||||
| chr4:69622662 | G | C | 11 | a0001c0001t0008g0079 a0001c0001t0008g0080 a0002c0002t0002g0169 others(8): Show |
11 | HG01109.hp2 HG01884.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.742+16237C>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69622662 | |||||||
| chr4:69622689 | T | C | 1 | a0001c0001t0008g0080 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.742+16210A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69622689 | |||||||
| chr4:69622735 | T | A | 8 | a0001c0001t0001g0055 a0001c0001t0001g0061 a0001c0001t0001g0062 others(5): Show |
8 | HG02602.hp2 HG02922.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.742+16164A>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69622735 | |||||||
| chr4:69622823 | C | G | 9 | a0001c0001t0008g0079 a0001c0001t0008g0080 a0002c0002t0002g0169 others(6): Show |
9 | HG01109.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.742+16076G>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69622823 | |||||||
| chr4:69622860 | T | A | 1 | a0001c0001t0002g0086 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.742+16039A>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69622860 | |||||||
| chr4:69623025 | T | G | 1 | a0002c0002t0002g0261 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.742+15874A>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69623025 | |||||||
| chr4:69623068 | T | G | 64 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(61): Show |
85 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.742+15831A>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69623068 | |||||||
| chr4:69623086 | A | C | 237 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(234): Show |
294 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(291): Show |
intron_variant | MODIFIER | c.742+15813T>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69623086 | |||||||
| chr4:69623131 | T | C | 94 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(91): Show |
120 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.742+15768A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69623131 | |||||||
| chr4:69623168 | C | T | 1 | a0001c0001t0002g0095 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.742+15731G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69623168 | |||||||
| chr4:69623324 | T | A | 1 | a0001c0001t0002g0086 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.742+15575A>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69623324 | |||||||
| chr4:69623421 | A | G | 94 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(91): Show |
120 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.742+15478T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69623421 | |||||||
| chr4:69623434 | A | G | 64 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(61): Show |
85 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.742+15465T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69623434 | |||||||
| chr4:69623436 | A | C | 1 | a0007c0006t0001g0051 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.742+15463T>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69623436 | |||||||
| chr4:69623534 | A | G | 13 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0143 others(10): Show |
18 | HG00642.hp1 HG01884.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.742+15365T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69623534 | |||||||
| chr4:69623563 | C | T | 94 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(91): Show |
120 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.742+15336G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69623563 | |||||||
| chr4:69623564 | A | G | 94 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(91): Show |
120 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.742+15335T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69623564 | |||||||
| chr4:69623667 | C | G | 94 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(91): Show |
120 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.742+15232G>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69623667 | |||||||
| chr4:69623701 | A | G | 65 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(62): Show |
86 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.742+15198T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69623701 | |||||||
| chr4:69623728 | G | A | 64 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(61): Show |
85 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.742+15171C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69623728 | |||||||
| chr4:69624013 | A | C | 94 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(91): Show |
120 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.742+14886T>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69624013 | |||||||
| chr4:69624075 | G | A | 1 | a0001c0001t0001g0201 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.742+14824C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69624075 | |||||||
| chr4:69624231 | C | T | 17 | a0001c0001t0001g0132 a0003c0003t0001g0019 a0003c0003t0001g0020 others(14): Show |
22 | HG00140.hp1 HG00423.hp1 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.742+14668G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69624231 | |||||||
| chr4:69624399 | T | A | 94 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(91): Show |
120 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.742+14500A>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69624399 | |||||||
| chr4:69624488 | A | G | 1 | a0009c0012t0001g0191 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.742+14411T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69624488 | |||||||
| chr4:69624514 | G | T | 94 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(91): Show |
120 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.742+14385C>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69624514 | |||||||
| chr4:69624588 | T | C | 1 | a0001c0001t0001g0015 | 3 | NA18967.hp2 NA18986.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.742+14311A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69624588 | |||||||
| chr4:69624620 | T | C | 1 | a0001c0001t0001g0224 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.742+14279A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69624620 | |||||||
| chr4:69624803 | G | T | 64 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(61): Show |
85 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.742+14096C>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69624803 | |||||||
| chr4:69624867 | T | C | 94 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(91): Show |
120 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.742+14032A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69624867 | |||||||
| chr4:69624908 | G | A | 2 | a0001c0001t0001g0142 a0001c0001t0001g0166 |
2 | HG02004.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.742+13991C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69624908 | |||||||
| chr4:69624971 | T | C | 1 | a0001c0001t0002g0188 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.742+13928A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69624971 | |||||||
| chr4:69625003 | C | CA | 93 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(90): Show |
119 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.742+13895dupT | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69625003 | |||||||
| chr4:69625074 | A | G | 4 | a0001c0001t0008g0079 a0001c0001t0008g0080 a0007c0006t0001g0050 others(1): Show |
4 | HG01109.hp2 HG03139.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.742+13825T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69625074 | |||||||
| chr4:69625165 | CT | C | 94 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(91): Show |
120 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.742+13733delA | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69625165 | |||||||
| chr4:69625185 | T | G | 5 | a0002c0002t0002g0169 a0002c0002t0002g0170 a0002c0002t0002g0171 others(2): Show |
5 | HG02717.hp1 HG02809.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.742+13714A>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69625185 | |||||||
| chr4:69625220 | T | A | 9 | a0001c0001t0008g0079 a0001c0001t0008g0080 a0002c0002t0002g0169 others(6): Show |
9 | HG01109.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.742+13679A>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69625220 | |||||||
| chr4:69625236 | C | G | 94 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(91): Show |
120 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.742+13663G>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69625236 | |||||||
| chr4:69625551 | A | G | 9 | a0001c0001t0008g0079 a0001c0001t0008g0080 a0002c0002t0002g0169 others(6): Show |
9 | HG01109.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.742+13348T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69625551 | |||||||
| chr4:69625613 | T | C | 1 | a0001c0001t0002g0111 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.742+13286A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69625613 | |||||||
| chr4:69625661 | C | T | 1 | a0001c0001t0001g0270 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.742+13238G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69625661 | |||||||
| chr4:69625790 | C | G | 94 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(91): Show |
120 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.742+13109G>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69625790 | |||||||
| chr4:69625896 | T | C | 94 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(91): Show |
120 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.742+13003A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69625896 | |||||||
| chr4:69626039 | T | G | 1 | a0001c0001t0002g0134 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.742+12860A>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69626039 | |||||||
| chr4:69626077 | C | G | 94 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(91): Show |
120 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.742+12822G>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69626077 | |||||||
| chr4:69626090 | T | G | 94 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(91): Show |
120 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.742+12809A>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69626090 | |||||||
| chr4:69626155 | T | G | 1 | a0001c0001t0001g0262 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.742+12744A>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69626155 | |||||||
| chr4:69626173 | A | G | 123 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(120): Show |
152 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(149): Show |
intron_variant | MODIFIER | c.742+12726T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69626173 | |||||||
| chr4:69626252 | C | T | 94 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(91): Show |
120 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.742+12647G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69626252 | |||||||
| chr4:69626267 | T | G | 1 | a0003c0003t0006g0289 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.742+12632A>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69626267 | |||||||
| chr4:69626303 | C | T | 9 | a0001c0001t0001g0055 a0001c0001t0001g0061 a0001c0001t0001g0062 others(6): Show |
9 | HG02602.hp2 HG02922.hp1 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.742+12596G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69626303 | |||||||
| chr4:69626313 | G | T | 18 | a0001c0001t0001g0132 a0003c0003t0001g0019 a0003c0003t0001g0020 others(15): Show |
23 | HG00140.hp1 HG00423.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.742+12586C>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69626313 | |||||||
| chr4:69626323 | G | T | 94 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(91): Show |
120 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.742+12576C>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69626323 | |||||||
| chr4:69626337 | G | A | 18 | a0001c0001t0001g0132 a0003c0003t0001g0019 a0003c0003t0001g0020 others(15): Show |
23 | HG00140.hp1 HG00423.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.742+12562C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69626337 | |||||||
| chr4:69626424 | A | G | 9 | a0001c0001t0008g0079 a0001c0001t0008g0080 a0002c0002t0002g0169 others(6): Show |
9 | HG01109.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.742+12475T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69626424 | |||||||
| chr4:69626587 | G | A | 94 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(91): Show |
120 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.742+12312C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69626587 | |||||||
| chr4:69626669 | TA | T | 94 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(91): Show |
120 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.742+12229delT | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69626669 | |||||||
| chr4:69626714 | A | C | 1 | a0001c0001t0001g0143 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.742+12185T>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69626714 | |||||||
| chr4:69626760 | T | C | 6 | a0001c0001t0001g0037 a0001c0001t0001g0214 a0001c0001t0001g0225 others(3): Show |
7 | HG00621.hp2 HG02165.hp2 NA18961.hp1 others(4): Show |
intron_variant | MODIFIER | c.742+12139A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69626760 | |||||||
| chr4:69626827 | T | C | 1 | a0001c0001t0002g0111 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.742+12072A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69626827 | |||||||
| chr4:69626861 | C | A | 226 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(223): Show |
281 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(278): Show |
intron_variant | MODIFIER | c.742+12038G>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69626861 | |||||||
| chr4:69626877 | TC | T | 2 | a0001c0001t0001g0041 a0001c0001t0001g0227 |
3 | NA18945.hp1 NA18993.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.742+12021delG | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69626877 | |||||||
| chr4:69626988 | A | G | 3 | a0001c0001t0001g0093 a0001c0007t0002g0081 a0001c0007t0002g0094 |
3 | HG00735.hp1 HG01123.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.742+11911T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69626988 | |||||||
| chr4:69627004 | C | T | 95 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(92): Show |
121 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.742+11895G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69627004 | |||||||
| chr4:69627095 | T | C | 2 | a0001c0001t0002g0133 a0001c0001t0002g0134 |
2 | HG02717.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.742+11804A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69627095 | |||||||
| chr4:69627215 | A | C | 17 | a0001c0001t0001g0132 a0003c0003t0001g0019 a0003c0003t0001g0020 others(14): Show |
22 | HG00140.hp1 HG00423.hp1 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.742+11684T>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69627215 | |||||||
| chr4:69627254 | A | C | 1 | a0011c0018t0001g0283 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.742+11645T>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69627254 | |||||||
| chr4:69627361 | T | C | 94 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(91): Show |
120 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.742+11538A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69627361 | |||||||
| chr4:69627456 | ACAGGCAA others(13): Show |
A | 94 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(91): Show |
120 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.742+11423_742+1144 others(24): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69627456 | |||||||
| chr4:69627486 | A | G | 2 | a0001c0001t0001g0038 a0001c0001t0001g0253 |
3 | NA18954.hp2 NA19009.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.742+11413T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69627486 | |||||||
| chr4:69627534 | A | AAG | 72 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(69): Show |
93 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.742+11363_742+1136 others(6): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69627534 | |||||||
| chr4:69627538 | GAGAGAGA others(3): Show |
G | 1 | a0001c0001t0002g0125 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.742+11351_742+1136 others(14): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69627538 | |||||||
| chr4:69627540 | GAGAGAGA others(1): Show |
G | 50 | a0001c0001t0001g0093 a0001c0001t0001g0098 a0001c0001t0001g0108 others(47): Show |
72 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.742+11351_742+1135 others(12): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69627540 | |||||||
| chr4:69627542 | G | A | 16 | a0001c0001t0001g0132 a0003c0003t0001g0019 a0003c0003t0001g0020 others(13): Show |
21 | HG00140.hp1 HG00423.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.742+11357C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69627542 | |||||||
| chr4:69627542 | GAGAGAA | G | 3 | a0001c0001t0002g0014 a0001c0001t0002g0133 a0001c0001t0002g0134 |
5 | HG02630.hp1 HG02717.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.742+11351_742+1135 others(10): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69627542 | |||||||
| chr4:69627544 | GAGAA | G | 4 | a0001c0001t0002g0004 a0001c0001t0002g0084 a0001c0001t0002g0102 others(1): Show |
4 | NA18963.hp1 NA18968.hp1 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.742+11351_742+1135 others(8): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69627544 | |||||||
| chr4:69627546 | GAA | G | 16 | a0001c0001t0001g0132 a0002c0002t0002g0169 a0003c0003t0001g0019 others(13): Show |
20 | HG00140.hp1 HG01099.hp1 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.742+11351_742+1135 others(6): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69627546 | |||||||
| chr4:69627548 | A | G | 4 | a0001c0001t0001g0142 a0001c0001t0001g0166 a0003c0003t0001g0291 others(1): Show |
5 | HG00423.hp1 HG02004.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.742+11351T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69627548 | |||||||
| chr4:69627550 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.742+11349C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69627550 | |||||||
| chr4:69627552 | G | A | 1 | a0002c0002t0002g0169 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.742+11347C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69627552 | |||||||
| chr4:69627566 | G | A | 5 | a0001c0001t0001g0032 a0001c0001t0001g0162 a0001c0001t0001g0163 others(2): Show |
6 | HG00099.hp1 HG00280.hp2 HG00738.hp2 others(3): Show |
intron_variant | MODIFIER | c.742+11333C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69627566 | |||||||
| chr4:69627568 | A | G | 19 | a0001c0001t0001g0132 a0002c0002t0002g0169 a0003c0003t0001g0019 others(16): Show |
24 | HG00140.hp1 HG00423.hp1 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.742+11331T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69627568 | |||||||
| chr4:69627572 | A | G | 1 | a0011c0018t0001g0283 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.742+11327T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69627572 | |||||||
| chr4:69627581 | A | T | 1 | a0001c0001t0001g0252 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.742+11318T>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69627581 | |||||||
| chr4:69627597 | G | GGAAA | 2 | a0001c0001t0001g0028 a0001c0001t0001g0151 |
3 | HG02615.hp1 NA18522.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.742+11301_742+1130 others(8): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69627597 | |||||||
| chr4:69627598 | A | AAAAG | 68 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(65): Show |
88 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.742+11297_742+1130 others(8): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69627598 | |||||||
| chr4:69627598 | A | AAAAGAAA others(5): Show |
2 | a0010c0011t0007g0168 a0013c0010t0007g0167 |
2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.742+11289_742+1130 others(16): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69627598 | |||||||
| chr4:69627598 | A | G | 2 | a0001c0001t0001g0028 a0001c0001t0001g0151 |
3 | HG02615.hp1 NA18522.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.742+11301T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69627598 | |||||||
| chr4:69627868 | A | G | 76 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(73): Show |
97 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.742+11031T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69627868 | |||||||
| chr4:69627912 | T | C | 5 | a0001c0001t0003g0006 a0001c0001t0003g0147 a0001c0001t0003g0148 others(2): Show |
8 | HG02258.hp1 HG02280.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.742+10987A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69627912 | |||||||
| chr4:69627949 | C | T | 94 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(91): Show |
120 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.742+10950G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69627949 | |||||||
| chr4:69627960 | C | A | 2 | a0001c0001t0001g0142 a0001c0001t0001g0166 |
2 | HG02004.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.742+10939G>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69627960 | |||||||
| chr4:69627997 | G | T | 1 | a0011c0018t0001g0283 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.742+10902C>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69627997 | |||||||
| chr4:69628009 | C | A | 1 | a0011c0018t0001g0283 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.742+10890G>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69628009 | |||||||
| chr4:69628108 | C | A | 1 | a0001c0001t0002g0123 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.742+10791G>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69628108 | |||||||
| chr4:69628108 | C | T | 94 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(91): Show |
120 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.742+10791G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69628108 | |||||||
| chr4:69628275 | T | G | 27 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0021 others(24): Show |
35 | HG00597.hp2 HG00609.hp2 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.742+10624A>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69628275 | |||||||
| chr4:69628283 | C | CA | 95 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(92): Show |
121 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.742+10615dupT | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69628283 | |||||||
| chr4:69628369 | G | A | 1 | a0001c0001t0002g0026 | 2 | NA18941.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.742+10530C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69628369 | |||||||
| chr4:69628401 | G | A | 2 | a0001c0001t0001g0142 a0001c0001t0001g0166 |
2 | HG02004.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.742+10498C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69628401 | |||||||
| chr4:69628521 | G | T | 1 | a0011c0018t0001g0283 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.742+10378C>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69628521 | |||||||
| chr4:69628617 | A | T | 18 | a0001c0001t0001g0132 a0001c0001t0001g0174 a0003c0003t0001g0019 others(15): Show |
23 | HG00140.hp1 HG00423.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.742+10282T>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69628617 | |||||||
| chr4:69628653 | G | A | 1 | a0001c0001t0001g0112 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.742+10246C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69628653 | |||||||
| chr4:69628691 | T | C | 3 | a0001c0001t0002g0084 a0001c0001t0002g0085 a0001c0001t0002g0113 |
3 | NA18945.hp2 NA18968.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.742+10208A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69628691 | |||||||
| chr4:69628696 | G | C | 1 | a0001c0001t0001g0238 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.742+10203C>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69628696 | |||||||
| chr4:69628745 | A | G | 1 | a0009c0012t0001g0191 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.742+10154T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69628745 | |||||||
| chr4:69628757 | A | C | 1 | a0002c0002t0002g0175 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.742+10142T>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69628757 | |||||||
| chr4:69628796 | C | T | 1 | a0011c0018t0001g0283 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.742+10103G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69628796 | |||||||
| chr4:69628913 | T | G | 18 | a0001c0001t0001g0132 a0001c0001t0001g0174 a0003c0003t0001g0019 others(15): Show |
23 | HG00140.hp1 HG00423.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.742+9986A>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69628913 | |||||||
| chr4:69629006 | G | T | 12 | a0001c0001t0008g0079 a0001c0001t0008g0080 a0002c0002t0002g0169 others(9): Show |
12 | HG01109.hp2 HG01884.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.742+9893C>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69629006 | |||||||
| chr4:69629015 | T | A | 1 | a0011c0018t0001g0283 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.742+9884A>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69629015 | |||||||
| chr4:69629123 | T | C | 95 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(92): Show |
121 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.742+9776A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69629123 | |||||||
| chr4:69629183 | G | A | 76 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(73): Show |
97 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.742+9716C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69629183 | |||||||
| chr4:69629215 | G | A | 57 | a0001c0001t0001g0093 a0001c0001t0001g0098 a0001c0001t0001g0108 others(54): Show |
82 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.742+9684C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69629215 | |||||||
| chr4:69629266 | C | T | 18 | a0001c0001t0001g0132 a0003c0003t0001g0019 a0003c0003t0001g0020 others(15): Show |
23 | HG00140.hp1 HG00423.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.742+9633G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69629266 | |||||||
| chr4:69629476 | T | C | 2 | a0005c0005t0001g0048 a0005c0005t0001g0285 |
3 | HG02886.hp2 HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.742+9423A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69629476 | |||||||
| chr4:69629635 | T | C | 14 | a0001c0001t0001g0016 a0001c0001t0001g0030 a0001c0001t0001g0031 others(11): Show |
19 | HG00099.hp1 HG00280.hp2 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.742+9264A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69629635 | |||||||
| chr4:69629656 | A | T | 38 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0021 others(35): Show |
47 | HG00597.hp2 HG00609.hp2 HG01070.hp1 others(44): Show |
intron_variant | MODIFIER | c.742+9243T>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69629656 | |||||||
| chr4:69629694 | T | A | 1 | a0001c0001t0001g0226 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.742+9205A>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69629694 | |||||||
| chr4:69629704 | C | A | 2 | a0010c0011t0007g0168 a0013c0010t0007g0167 |
2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.742+9195G>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69629704 | |||||||
| chr4:69629776 | G | C | 13 | a0003c0003t0001g0019 a0003c0003t0001g0020 a0003c0003t0001g0287 others(10): Show |
18 | HG00140.hp1 HG00423.hp1 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.742+9123C>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69629776 | |||||||
| chr4:69629801 | G | C | 64 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0028 others(61): Show |
81 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.742+9098C>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69629801 | |||||||
| chr4:69629934 | C | A | 16 | a0003c0003t0001g0019 a0003c0003t0001g0020 a0003c0003t0001g0287 others(13): Show |
21 | HG00140.hp1 HG00423.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.742+8965G>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69629934 | |||||||
| chr4:69630021 | A | G | 5 | a0002c0002t0002g0169 a0002c0002t0002g0170 a0002c0002t0002g0171 others(2): Show |
5 | HG02717.hp1 HG02809.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.742+8878T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69630021 | |||||||
| chr4:69630022 | A | G | 1 | a0015c0016t0010g0082 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.742+8877T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69630022 | |||||||
| chr4:69630243 | C | T | 47 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0028 others(44): Show |
59 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.742+8656G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69630243 | |||||||
| chr4:69630254 | C | T | 4 | a0002c0002t0002g0035 a0002c0002t0002g0040 a0002c0002t0002g0208 others(1): Show |
6 | HG01346.hp2 HG01928.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.742+8645G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69630254 | |||||||
| chr4:69630269 | G | A | 2 | a0001c0001t0001g0204 a0001c0001t0001g0260 |
2 | NA18612.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.742+8630C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69630269 | |||||||
| chr4:69630339 | G | A | 58 | a0001c0001t0001g0093 a0001c0001t0001g0098 a0001c0001t0001g0108 others(55): Show |
83 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.742+8560C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69630339 | |||||||
| chr4:69630400 | T | C | 1 | a0009c0012t0001g0191 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.742+8499A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69630400 | |||||||
| chr4:69630464 | T | C | 1 | a0002c0002t0005g0124 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.742+8435A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69630464 | |||||||
| chr4:69630525 | A | T | 1 | a0001c0001t0001g0194 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.742+8374T>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69630525 | |||||||
| chr4:69630544 | C | T | 47 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0028 others(44): Show |
59 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.742+8355G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69630544 | |||||||
| chr4:69630558 | A | G | 2 | a0001c0001t0001g0215 a0014c0015t0001g0216 |
2 | NA18946.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.742+8341T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69630558 | |||||||
| chr4:69630591 | G | C | 1 | a0001c0001t0001g0165 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.742+8308C>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69630591 | |||||||
| chr4:69630643 | G | A | 1 | a0001c0001t0002g0114 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.742+8256C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69630643 | |||||||
| chr4:69630922 | AAAG | A | 9 | a0001c0001t0008g0079 a0001c0001t0008g0080 a0002c0002t0002g0169 others(6): Show |
9 | HG01109.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.742+7974_742+7976d others(5): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69630922 | |||||||
| chr4:69631077 | T | G | 1 | a0011c0018t0001g0283 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.742+7822A>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69631077 | |||||||
| chr4:69631157 | T | C | 2 | a0010c0011t0007g0168 a0013c0010t0007g0167 |
2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.742+7742A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69631157 | |||||||
| chr4:69631318 | A | ATC | 229 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(226): Show |
285 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(282): Show |
intron_variant | MODIFIER | c.742+7580_742+7581i others(4): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69631318 | |||||||
| chr4:69631435 | A | C | 9 | a0001c0001t0008g0079 a0001c0001t0008g0080 a0002c0002t0002g0169 others(6): Show |
9 | HG01109.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.742+7464T>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69631435 | |||||||
| chr4:69631468 | G | A | 2 | a0003c0003t0001g0292 a0003c0003t0001g0293 |
2 | HG03669.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.742+7431C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69631468 | |||||||
| chr4:69631517 | T | A | 35 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0028 others(32): Show |
47 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.742+7382A>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69631517 | |||||||
| chr4:69631666 | G | A | 3 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0001g0275 |
3 | HG02145.hp1 HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.742+7233C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69631666 | |||||||
| chr4:69631873 | T | C | 1 | a0001c0001t0001g0115 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.742+7026A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69631873 | |||||||
| chr4:69631883 | C | T | 35 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0028 others(32): Show |
47 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.742+7016G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69631883 | |||||||
| chr4:69631895 | T | G | 1 | a0001c0001t0001g0151 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.742+7004A>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69631895 | |||||||
| chr4:69632188 | G | A | 32 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0021 others(29): Show |
41 | HG00597.hp2 HG00609.hp2 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.742+6711C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69632188 | |||||||
| chr4:69632194 | T | C | 32 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0021 others(29): Show |
41 | HG00597.hp2 HG00609.hp2 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.742+6705A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69632194 | |||||||
| chr4:69632196 | G | A | 1 | a0011c0018t0001g0283 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.742+6703C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69632196 | |||||||
| chr4:69632315 | C | G | 1 | a0011c0018t0001g0283 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.742+6584G>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69632315 | |||||||
| chr4:69632430 | T | C | 10 | a0001c0001t0008g0079 a0001c0001t0008g0080 a0002c0002t0002g0169 others(7): Show |
10 | HG01109.hp2 HG01891.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.742+6469A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69632430 | |||||||
| chr4:69632447 | C | T | 32 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0021 others(29): Show |
41 | HG00597.hp2 HG00609.hp2 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.742+6452G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69632447 | |||||||
| chr4:69632574 | T | C | 1 | a0011c0018t0001g0283 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.742+6325A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69632574 | |||||||
| chr4:69632672 | A | G | 10 | a0001c0001t0008g0079 a0001c0001t0008g0080 a0002c0002t0002g0169 others(7): Show |
10 | HG01109.hp2 HG01891.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.742+6227T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69632672 | |||||||
| chr4:69632705 | G | T | 1 | a0001c0001t0002g0092 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.742+6194C>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69632705 | |||||||
| chr4:69632885 | C | CA | 38 | a0001c0001t0001g0007 a0001c0001t0001g0033 a0001c0001t0001g0036 others(35): Show |
45 | HG00544.hp1 HG00609.hp1 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.742+6013dupT | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69632885 | |||||||
| chr4:69632885 | CA | C | 7 | a0001c0001t0001g0142 a0001c0001t0001g0153 a0001c0001t0001g0154 others(4): Show |
7 | HG00642.hp1 HG02004.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.742+6013delT | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69632885 | |||||||
| chr4:69632888 | A | C | 2 | a0010c0011t0007g0168 a0013c0010t0007g0167 |
2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.742+6011T>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69632888 | |||||||
| chr4:69632889 | A | G | 1 | a0002c0002t0005g0140 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.742+6010T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69632889 | |||||||
| chr4:69632921 | C | G | 1 | a0001c0001t0001g0033 | 2 | NA18963.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.742+5978G>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69632921 | |||||||
| chr4:69633058 | T | C | 1 | a0001c0001t0001g0116 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.742+5841A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69633058 | |||||||
| chr4:69633221 | C | T | 2 | a0010c0011t0007g0168 a0013c0010t0007g0167 |
2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.742+5678G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69633221 | |||||||
| chr4:69633260 | A | T | 17 | a0001c0001t0001g0174 a0003c0003t0001g0019 a0003c0003t0001g0020 others(14): Show |
22 | HG00140.hp1 HG00423.hp1 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.742+5639T>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69633260 | |||||||
| chr4:69633268 | T | C | 4 | a0002c0002t0002g0169 a0002c0002t0002g0170 a0002c0002t0002g0171 others(1): Show |
4 | HG02717.hp1 HG02809.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.742+5631A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69633268 | |||||||
| chr4:69633307 | A | T | 9 | a0001c0001t0008g0079 a0001c0001t0008g0080 a0002c0002t0002g0169 others(6): Show |
9 | HG01109.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.742+5592T>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69633307 | |||||||
| chr4:69633485 | T | C | 9 | a0001c0001t0008g0079 a0001c0001t0008g0080 a0002c0002t0002g0169 others(6): Show |
9 | HG01109.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.742+5414A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69633485 | |||||||
| chr4:69633516 | T | C | 47 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0017 others(44): Show |
66 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.742+5383A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69633516 | |||||||
| chr4:69633578 | T | C | 1 | a0001c0001t0001g0072 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.742+5321A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69633578 | |||||||
| chr4:69633630 | T | C | 35 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0028 others(32): Show |
47 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.742+5269A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69633630 | |||||||
| chr4:69633723 | T | C | 2 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
2 | HG02056.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.742+5176A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69633723 | |||||||
| chr4:69633747 | T | G | 6 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(3): Show |
8 | HG00438.hp1 HG02015.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.742+5152A>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69633747 | |||||||
| chr4:69634031 | C | T | 2 | a0010c0011t0007g0168 a0013c0010t0007g0167 |
2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.742+4868G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69634031 | |||||||
| chr4:69634032 | T | G | 13 | a0003c0003t0001g0019 a0003c0003t0001g0020 a0003c0003t0001g0287 others(10): Show |
18 | HG00140.hp1 HG00423.hp1 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.742+4867A>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69634032 | |||||||
| chr4:69634106 | T | G | 51 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0028 others(48): Show |
68 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.742+4793A>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69634106 | |||||||
| chr4:69634145 | T | C | 2 | a0001c0001t0001g0142 a0001c0001t0001g0166 |
2 | HG02004.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.742+4754A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69634145 | |||||||
| chr4:69634172 | G | A | 1 | a0011c0018t0001g0283 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.742+4727C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69634172 | |||||||
| chr4:69634251 | CAAACAAA others(3): Show |
C | 45 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0028 others(42): Show |
57 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.742+4638_742+4647d others(12): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69634251 | |||||||
| chr4:69634335 | T | C | 1 | a0002c0002t0002g0175 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.742+4564A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69634335 | |||||||
| chr4:69634589 | C | T | 1 | a0003c0003t0001g0287 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.742+4310G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69634589 | |||||||
| chr4:69634662 | G | T | 1 | a0006c0008t0002g0049 | 2 | HG00423.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.742+4237C>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69634662 | |||||||
| chr4:69634802 | A | G | 1 | a0001c0001t0002g0090 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.742+4097T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69634802 | |||||||
| chr4:69634809 | A | T | 35 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0028 others(32): Show |
47 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.742+4090T>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69634809 | |||||||
| chr4:69634843 | G | A | 1 | a0001c0001t0002g0117 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.742+4056C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69634843 | |||||||
| chr4:69635112 | T | C | 50 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0028 others(47): Show |
64 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.742+3787A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69635112 | |||||||
| chr4:69635130 | A | T | 2 | a0001c0001t0002g0084 a0001c0001t0002g0085 |
2 | NA18968.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.742+3769T>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69635130 | |||||||
| chr4:69635131 | A | C | 1 | a0001c0001t0001g0152 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.742+3768T>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69635131 | |||||||
| chr4:69635131 | A | T | 2 | a0001c0001t0002g0084 a0001c0001t0002g0085 |
2 | NA18968.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.742+3768T>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69635131 | |||||||
| chr4:69635268 | T | A | 50 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0028 others(47): Show |
64 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.742+3631A>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69635268 | |||||||
| chr4:69635443 | C | T | 5 | a0001c0001t0001g0017 a0001c0001t0001g0190 a0001c0001t0001g0205 others(2): Show |
7 | HG01993.hp1 HG02027.hp1 HG02135.hp2 others(4): Show |
intron_variant | MODIFIER | c.742+3456G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69635443 | |||||||
| chr4:69635555 | T | C | 1 | a0001c0001t0002g0118 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.742+3344A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69635555 | |||||||
| chr4:69635656 | C | T | 3 | a0001c0001t0002g0010 a0001c0001t0002g0089 a0008c0013t0002g0088 |
5 | HG00099.hp2 HG00140.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.742+3243G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69635656 | |||||||
| chr4:69635733 | G | A | 46 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0028 others(43): Show |
58 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.742+3166C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69635733 | |||||||
| chr4:69635782 | C | T | 1 | a0002c0002t0002g0184 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.742+3117G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69635782 | |||||||
| chr4:69635825 | C | CA | 22 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0029 others(19): Show |
26 | HG00099.hp1 HG00280.hp2 HG00733.hp2 others(23): Show |
intron_variant | MODIFIER | c.742+3073dupT | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69635825 | |||||||
| chr4:69635825 | C | CAA | 4 | a0001c0001t0001g0015 a0001c0001t0001g0029 a0001c0001t0001g0030 others(1): Show |
4 | HG02895.hp1 HG04115.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.742+3073_742+3074i others(4): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69635825 | |||||||
| chr4:69635825 | CACCAAAA others(4): Show |
C | 9 | a0001c0001t0001g0028 a0001c0001t0001g0143 a0001c0001t0001g0144 others(6): Show |
13 | HG01884.hp2 HG02258.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.742+3063_742+3073d others(13): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69635825 | |||||||
| chr4:69635826 | ACC | A | 6 | a0001c0001t0001g0146 a0001c0001t0002g0084 a0001c0001t0002g0085 others(3): Show |
6 | HG01516.hp1 HG03239.hp2 NA18968.hp1 others(3): Show |
intron_variant | MODIFIER | c.742+3071_742+3072d others(4): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69635826 | |||||||
| chr4:69635827 | C | A | 274 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(271): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.742+3072G>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69635827 | |||||||
| chr4:69635828 | C | A | 34 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0029 others(31): Show |
42 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.742+3071G>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69635828 | |||||||
| chr4:69635828 | C | CAAAAAAA | 22 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0021 others(19): Show |
31 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.742+3064_742+3070d others(9): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69635828 | |||||||
| chr4:69635828 | C | CAAAAAAA others(1): Show |
7 | a0001c0001t0001g0054 a0001c0001t0001g0074 a0001c0001t0001g0075 others(4): Show |
7 | HG00597.hp2 HG01106.hp2 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.742+3063_742+3070d others(10): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69635828 | |||||||
| chr4:69635828 | C | CAAAAAAA others(2): Show |
5 | a0001c0001t0001g0078 a0001c0001t0003g0027 a0001c0001t0003g0138 others(2): Show |
6 | HG01884.hp1 HG02630.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.742+3062_742+3070d others(11): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69635828 | |||||||
| chr4:69635828 | C | CAAAAAAA others(3): Show |
2 | a0001c0001t0003g0139 a0015c0016t0010g0082 |
2 | HG06807.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.742+3061_742+3070d others(12): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69635828 | |||||||
| chr4:69635828 | C | CAAAAAAA others(6): Show |
1 | a0001c0001t0001g0052 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.742+3058_742+3070d others(15): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69635828 | |||||||
| chr4:69635828 | C | CAAAAAAA others(7): Show |
4 | a0001c0001t0001g0193 a0001c0001t0001g0270 a0001c0001t0001g0271 others(1): Show |
4 | HG01243.hp2 HG02451.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.742+3057_742+3070d others(16): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69635828 | |||||||
| chr4:69635828 | C | CAAAAAAA others(8): Show |
17 | a0001c0001t0001g0034 a0001c0001t0001g0182 a0001c0001t0001g0183 others(14): Show |
18 | HG01517.hp2 HG02258.hp2 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.742+3056_742+3070d others(17): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69635828 | |||||||
| chr4:69635828 | C | CAAAAAAA others(9): Show |
48 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0036 others(45): Show |
59 | HG00438.hp2 HG01258.hp2 HG01346.hp2 others(56): Show |
intron_variant | MODIFIER | c.742+3055_742+3070d others(18): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69635828 | |||||||
| chr4:69635828 | C | CAAAAAAA others(10): Show |
34 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0018 others(31): Show |
48 | HG00423.hp2 HG00597.hp1 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.742+3054_742+3070d others(19): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69635828 | |||||||
| chr4:69635828 | C | CAAAAAAA others(11): Show |
8 | a0001c0001t0001g0045 a0001c0001t0001g0262 a0001c0001t0001g0263 others(5): Show |
10 | HG01261.hp1 HG01358.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.742+3053_742+3070d others(20): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69635828 | |||||||
| chr4:69635828 | C | CAAAAAAA others(12): Show |
4 | a0001c0001t0001g0265 a0001c0001t0001g0266 a0001c0001t0001g0267 others(1): Show |
4 | HG02145.hp2 HG02818.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.742+3052_742+3070d others(21): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69635828 | |||||||
| chr4:69635828 | C | CAAAAAAA others(13): Show |
1 | a0001c0001t0001g0268 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.742+3051_742+3070d others(22): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69635828 | |||||||
| chr4:69635828 | C | CAAAAAAA others(14): Show |
1 | a0001c0001t0001g0281 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.742+3050_742+3070d others(23): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69635828 | |||||||
| chr4:69635828 | CA | C | 52 | a0001c0001t0001g0093 a0001c0001t0001g0098 a0001c0001t0001g0108 others(49): Show |
77 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.742+3070delT | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69635828 | |||||||
| chr4:69635830 | A | C | 5 | a0001c0001t0002g0084 a0001c0001t0002g0085 a0001c0001t0002g0086 others(2): Show |
5 | HG03239.hp2 NA18968.hp1 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.742+3069T>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69635830 | |||||||
| chr4:69635831 | A | C | 1 | a0001c0001t0002g0083 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.742+3068T>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69635831 | |||||||
| chr4:69635835 | A | C | 1 | a0003c0003t0006g0286 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.742+3064T>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69635835 | |||||||
| chr4:69635849 | A | AAAAAAAA others(9): Show |
2 | a0001c0001t0001g0185 a0002c0002t0002g0184 |
2 | HG02165.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.742+3049_742+3050i others(18): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69635849 | |||||||
| chr4:69635849 | A | AAAAAAAA others(4): Show |
2 | a0003c0003t0001g0294 a0004c0004t0001g0126 |
2 | NA18968.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.742+3049_742+3050i others(13): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69635849 | |||||||
| chr4:69635849 | A | AAAAAAAA others(3): Show |
1 | a0001c0001t0003g0135 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.742+3049_742+3050i others(12): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69635849 | |||||||
| chr4:69635849 | A | AAAAAAAA others(3): Show |
11 | a0001c0001t0001g0174 a0003c0003t0001g0019 a0003c0003t0001g0287 others(8): Show |
14 | HG00423.hp1 HG01106.hp1 HG02129.hp1 others(11): Show |
intron_variant | MODIFIER | c.742+3049_742+3050i others(12): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69635849 | |||||||
| chr4:69635849 | A | G | 1 | a0003c0003t0006g0286 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.742+3050T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69635849 | |||||||
| chr4:69635849 | AAGAGAG | A | 8 | a0001c0001t0008g0080 a0002c0002t0002g0169 a0002c0002t0002g0170 others(5): Show |
8 | HG01109.hp2 HG02717.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.742+3044_742+3049d others(8): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69635849 | |||||||
| chr4:69635851 | G | A | 70 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(67): Show |
91 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.742+3048C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69635851 | |||||||
| chr4:69635853 | G | A | 2 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
2 | HG00733.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.742+3046C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69635853 | |||||||
| chr4:69635855 | G | A | 2 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
2 | HG00733.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.742+3044C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69635855 | |||||||
| chr4:69635960 | A | T | 1 | a0001c0001t0001g0183 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.742+2939T>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69635960 | |||||||
| chr4:69636038 | T | C | 12 | a0001c0001t0008g0079 a0001c0001t0008g0080 a0002c0002t0002g0169 others(9): Show |
12 | HG01109.hp2 HG01884.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.742+2861A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69636038 | |||||||
| chr4:69636043 | A | G | 35 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0028 others(32): Show |
47 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.742+2856T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69636043 | |||||||
| chr4:69636069 | A | G | 9 | a0001c0001t0008g0079 a0001c0001t0008g0080 a0002c0002t0002g0169 others(6): Show |
9 | HG01109.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.742+2830T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69636069 | |||||||
| chr4:69636262 | C | T | 231 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(228): Show |
288 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(285): Show |
intron_variant | MODIFIER | c.742+2637G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69636262 | |||||||
| chr4:69636278 | C | T | 1 | a0001c0001t0001g0182 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.742+2621G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69636278 | |||||||
| chr4:69636375 | G | A | 1 | a0007c0006t0001g0051 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.742+2524C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69636375 | |||||||
| chr4:69636396 | A | G | 4 | a0001c0001t0008g0079 a0001c0001t0008g0080 a0007c0006t0001g0050 others(1): Show |
4 | HG01109.hp2 HG03139.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.742+2503T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69636396 | |||||||
| chr4:69636527 | GATT | G | 35 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0028 others(32): Show |
47 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.742+2369_742+2371d others(5): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69636527 | |||||||
| chr4:69636564 | C | A | 31 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0028 others(28): Show |
43 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.742+2335G>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69636564 | |||||||
| chr4:69636577 | C | A | 5 | a0002c0002t0002g0169 a0002c0002t0002g0170 a0002c0002t0002g0171 others(2): Show |
5 | HG02717.hp1 HG02809.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.742+2322G>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69636577 | |||||||
| chr4:69636668 | T | G | 41 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0028 others(38): Show |
55 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.742+2231A>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69636668 | |||||||
| chr4:69636755 | T | A | 38 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0021 others(35): Show |
47 | HG00597.hp2 HG00609.hp2 HG01070.hp1 others(44): Show |
intron_variant | MODIFIER | c.742+2144A>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69636755 | |||||||
| chr4:69636949 | C | G | 1 | a0001c0001t0001g0181 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.742+1950G>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69636949 | |||||||
| chr4:69637061 | G | A | 74 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(71): Show |
95 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.742+1838C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69637061 | |||||||
| chr4:69637231 | A | G | 1 | a0002c0002t0004g0180 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.742+1668T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69637231 | |||||||
| chr4:69637537 | C | A | 1 | a0002c0002t0002g0175 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.742+1362G>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69637537 | |||||||
| chr4:69637657 | C | T | 3 | a0001c0001t0001g0033 a0001c0001t0001g0178 a0001c0001t0001g0179 |
4 | HG02071.hp2 NA18963.hp2 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.742+1242G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69637657 | |||||||
| chr4:69637671 | A | G | 1 | a0003c0003t0006g0286 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.742+1228T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69637671 | |||||||
| chr4:69637678 | A | G | 2 | a0001c0001t0008g0079 a0001c0001t0008g0080 |
2 | HG01109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.742+1221T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69637678 | |||||||
| chr4:69637710 | T | G | 1 | a0007c0006t0001g0051 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.742+1189A>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69637710 | |||||||
| chr4:69637729 | C | T | 4 | a0001c0001t0008g0079 a0001c0001t0008g0080 a0007c0006t0001g0050 others(1): Show |
4 | HG01109.hp2 HG03139.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.742+1170G>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69637729 | |||||||
| chr4:69637757 | G | C | 6 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 others(3): Show |
6 | HG01243.hp2 HG02145.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.742+1142C>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69637757 | |||||||
| chr4:69637891 | G | A | 1 | a0004c0004t0001g0176 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.742+1008C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69637891 | |||||||
| chr4:69637908 | AAGGC | A | 23 | a0001c0001t0001g0046 a0001c0001t0001g0052 a0001c0001t0001g0277 others(20): Show |
30 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(27): Show |
intron_variant | MODIFIER | c.742+987_742+990del others(4): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69637908 | |||||||
| chr4:69637908 | AAGGCAGG others(5): Show |
A | 3 | a0001c0001t0001g0132 a0001c0001t0002g0133 a0001c0001t0002g0134 |
3 | HG02717.hp2 HG02976.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.742+979_742+990del others(12): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69637908 | |||||||
| chr4:69637997 | C | CAGGA | 6 | a0001c0001t0003g0027 a0001c0001t0003g0135 a0001c0001t0003g0136 others(3): Show |
7 | HG02572.hp1 HG02895.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.742+898_742+901dup others(4): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69637997 | |||||||
| chr4:69637997 | CAGGA | C | 4 | a0001c0001t0008g0079 a0001c0001t0008g0080 a0001c0007t0002g0081 others(1): Show |
4 | HG01109.hp2 HG01175.hp1 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.742+898_742+901del others(4): Show |
UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69637997 | |||||||
| chr4:69638001 | A | C | 1 | a0004c0004t0001g0177 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.742+898T>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69638001 | |||||||
| chr4:69638076 | G | T | 68 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(65): Show |
89 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.742+823C>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69638076 | |||||||
| chr4:69638184 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.742+715C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69638184 | |||||||
| chr4:69638260 | G | C | 35 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0028 others(32): Show |
47 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.742+639C>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69638260 | |||||||
| chr4:69638305 | G | T | 2 | a0001c0001t0001g0009 a0001c0001t0001g0054 |
4 | NA18985.hp1 NA18989.hp1 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.742+594C>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69638305 | |||||||
| chr4:69638309 | A | G | 1 | a0001c0001t0002g0053 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.742+590T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69638309 | |||||||
| chr4:69638402 | T | C | 6 | a0002c0002t0002g0169 a0002c0002t0002g0170 a0002c0002t0002g0171 others(3): Show |
6 | HG01884.hp1 HG02630.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.742+497A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69638402 | |||||||
| chr4:69638488 | T | C | 1 | a0001c0001t0002g0173 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.742+411A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69638488 | |||||||
| chr4:69638571 | T | C | 18 | a0001c0001t0001g0174 a0001c0017t0001g0282 a0002c0002t0002g0175 others(15): Show |
23 | HG00140.hp1 HG00423.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.742+328A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69638571 | |||||||
| chr4:69638595 | T | C | 128 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(125): Show |
158 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(155): Show |
intron_variant | MODIFIER | c.742+304A>G | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69638595 | |||||||
| chr4:69638640 | G | T | 1 | a0001c0001t0001g0052 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.742+259C>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69638640 |