| 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 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and 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 | copy fasta | chr4 | 69583417 | 69644642 |
| a0002 | 0/0 | 536 | 26 | 8 | 6 | 5 | 1 | 6 | 4 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| a0003 | 0/0 | 536 | 16 | 2 | 2 | 6 | 4 | 2 | 5 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| a0004 | 0/0 | 536 | 6 | 0 | 3 | 1 | 1 | 1 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| a0005 | 0/0 | 536 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| a0006 | 0/0 | 536 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| a0007 | 0/0 | 536 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| a0008 | 0/0 | 536 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| a0009 | 0/0 | 536 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| a0010 | 0/0 | 536 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| a0011 | 0/0 | 536 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| a0012 | 0/0 | 536 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| a0013 | 0/0 | 536 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| a0014 | 0/0 | 536 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| a0015 | 0/0 | 536 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| a0016 | 0/0 | 536 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1611 | 309 | 62 | 56 | 149 | 8 | 32 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| c0002 | 0/0 | 1611 | 26 | 8 | 6 | 5 | 1 | 6 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| c0003 | 0/0 | 1611 | 16 | 2 | 2 | 6 | 4 | 2 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| c0004 | 0/0 | 1611 | 6 | 0 | 3 | 1 | 1 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| c0005 | 0/0 | 1611 | 3 | 3 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| c0006 | 0/0 | 1611 | 2 | 2 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| c0007 | 0/0 | 1611 | 2 | 0 | 2 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| c0008 | 0/0 | 1611 | 2 | 0 | 0 | 2 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| c0009 | 0/0 | 1611 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| c0010 | 0/0 | 1611 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| c0011 | 0/0 | 1611 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| c0012 | 0/0 | 1611 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| c0013 | 0/0 | 1611 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| c0014 | 0/0 | 1611 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| c0015 | 0/0 | 1611 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| c0016 | 0/0 | 1611 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| c0017 | 0/0 | 1611 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| c0018 | 0/0 | 1611 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| c0019 | 0/0 | 1611 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| c0020 | 0/0 | 1611 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 958 | 241 | 44 | 48 | 113 | 9 | 27 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| t0002 | 1/1 | 958 | 109 | 15 | 23 | 49 | 5 | 15 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| t0003 | 0/0 | 958 | 15 | 15 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| t0004 | 0/0 | 958 | 3 | 0 | 0 | 3 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| t0005 | 0/0 | 958 | 2 | 2 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| t0006 | 0/0 | 958 | 2 | 2 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| t0007 | 0/0 | 958 | 2 | 2 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| t0008 | 0/0 | 958 | 2 | 1 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| t0009 | 0/0 | 958 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| t0010 | 0/0 | 958 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0002 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0003 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0006 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0011 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0013 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0015 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0017 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0029 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0031 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0097 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0119 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1611 | 309 | 62 | 56 | 149 | 8 | 32 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| a0001c0007 | 0/0 | 1611 | 2 | 0 | 2 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| a0001c0009 | 0/0 | 1611 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| a0001c0014 | 0/0 | 1611 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| a0001c0017 | 0/0 | 1611 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| a0002c0002 | 0/0 | 1611 | 26 | 8 | 6 | 5 | 1 | 6 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| a0003c0003 | 0/0 | 1611 | 16 | 2 | 2 | 6 | 4 | 2 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| a0004c0004 | 0/0 | 1611 | 6 | 0 | 3 | 1 | 1 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| a0005c0005 | 0/0 | 1611 | 3 | 3 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| a0006c0006 | 0/0 | 1611 | 2 | 2 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| a0007c0008 | 0/0 | 1611 | 2 | 0 | 0 | 2 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| a0008c0018 | 0/0 | 1611 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| a0009c0016 | 0/0 | 1611 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| a0010c0011 | 0/0 | 1611 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| a0011c0010 | 0/0 | 1611 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| a0012c0012 | 0/0 | 1611 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| a0013c0013 | 0/0 | 1611 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| a0014c0015 | 0/0 | 1611 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| a0015c0019 | 0/0 | 1611 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| a0016c0020 | 0/0 | 1611 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | 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 | copy fasta | chr4 | 69583417 | 69644642 |
| a0001c0001t0002 | 1/1 | 2568 | 82 | 9 | 13 | 45 | 4 | 9 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| a0001c0001t0003 | 0/0 | 2568 | 15 | 15 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| a0001c0001t0008 | 0/0 | 2568 | 2 | 1 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| a0001c0001t0009 | 0/0 | 2568 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| a0001c0007t0002 | 0/0 | 2568 | 2 | 0 | 2 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| a0001c0009t0001 | 0/0 | 2568 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| a0001c0014t0001 | 0/0 | 2568 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| a0001c0017t0001 | 0/0 | 2568 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| a0002c0002t0002 | 0/0 | 2568 | 21 | 6 | 6 | 2 | 1 | 6 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| a0002c0002t0004 | 0/0 | 2568 | 3 | 0 | 0 | 3 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| a0002c0002t0005 | 0/0 | 2568 | 2 | 2 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| a0003c0003t0001 | 0/0 | 2568 | 14 | 0 | 2 | 6 | 4 | 2 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| a0003c0003t0006 | 0/0 | 2568 | 2 | 2 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| a0004c0004t0001 | 0/0 | 2568 | 6 | 0 | 3 | 1 | 1 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| a0005c0005t0001 | 0/0 | 2568 | 3 | 3 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| a0006c0006t0001 | 0/0 | 2568 | 2 | 2 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| a0007c0008t0002 | 0/0 | 2568 | 2 | 0 | 0 | 2 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| a0008c0018t0001 | 0/0 | 2568 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| a0009c0016t0010 | 0/0 | 2568 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| a0010c0011t0007 | 0/0 | 2568 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| a0011c0010t0007 | 0/0 | 2568 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| a0012c0012t0001 | 0/0 | 2568 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| a0013c0013t0002 | 0/0 | 2568 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| a0014c0015t0001 | 0/0 | 2568 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| a0015c0019t0002 | 0/0 | 2568 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| a0016c0020t0001 | 0/0 | 2568 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | copy fasta | chr4 | 69583417 | 69644642 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0002 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 1 | 1 | 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 | 2 | 0 | 0 | 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 | 2 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0096 | 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 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 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 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0216 | 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 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| 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 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 0 | 1 | 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 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0006 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0015 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0017 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0081 | 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 | 0 | 1 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0089 | 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 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0097 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0098 | 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 | 1 | 0 | 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 | 0 | 1 | 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 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0002g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0003g0003 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0003g0023 | 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 |
| a0001c0001t0003g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0003g0146 | 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 |
| a0001c0001t0008g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0008g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0001t0009g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0007t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0007t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0009t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0014t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0001c0017t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0002c0002t0002g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0002c0002t0002g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0002c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0002c0002t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0002c0002t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0002c0002t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0002c0002t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0002c0002t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0002c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0002c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0002c0002t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0002c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0002c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0002c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0002c0002t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0002c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0002c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0002c0002t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0002c0002t0004g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0002c0002t0004g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0002c0002t0004g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0002c0002t0005g0123 | 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 |
| a0003c0003t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0003c0003t0001g0013 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0003c0003t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0003c0003t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0003c0003t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0003c0003t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0003c0003t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0003c0003t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0003c0003t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0003c0003t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0003c0003t0006g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0003c0003t0006g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0004c0004t0001g0035 | 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 |
| a0004c0004t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0004c0004t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0004c0004t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0005c0005t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0005c0005t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0006c0006t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0006c0006t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0007c0008t0002g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0008c0018t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0009c0016t0010g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0010c0011t0007g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0011c0010t0007g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0012c0012t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0013c0013t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0014c0015t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0015c0019t0002g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| a0016c0020t0001g0318 | 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 | g0170 | EUR | GBR | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0084 | EUR | GBR | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG00140 | hp1 | a0003 | c0003 | t0001 | g0317 | EUR | GBR | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0083 | EUR | GBR | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0085 | EUR | FIN | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0169 | EUR | FIN | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG00423 | hp1 | a0007 | c0008 | t0002 | g0041 | EAS | CHS | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | CHS | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | CHS | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | CHS | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0288 | 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 | g0276 | EAS | CHS | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | CHS | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | CHS | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | CHS | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | CHS | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0267 | 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 | g0035 | AMR | PUR | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0090 | 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 | g0018 | AMR | PUR | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG00741 | hp1 | a0004 | c0004 | t0001 | g0035 | AMR | PUR | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01071 | hp2 | a0013 | c0013 | t0002 | g0082 | AMR | PUR | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01099 | hp1 | a0003 | c0003 | t0001 | g0013 | AMR | PUR | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01106 | hp1 | a0003 | c0003 | t0001 | g0310 | AMR | PUR | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01109 | hp2 | a0001 | c0001 | t0008 | g0074 | AMR | PUR | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0166 | AMR | PUR | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01175 | hp1 | a0001 | c0007 | t0002 | g0075 | AMR | PUR | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0092 | AMR | PUR | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0303 | AMR | PUR | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01243 | hp1 | a0012 | c0012 | t0001 | g0203 | AMR | PUR | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0292 | 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 | g0274 | AMR | CLM | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0018 | AMR | CLM | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01258 | hp2 | a0004 | c0004 | t0001 | g0189 | AMR | CLM | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0280 | AMR | CLM | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0270 | AMR | CLM | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01346 | hp2 | a0002 | c0002 | t0002 | g0220 | AMR | CLM | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01358 | hp1 | a0002 | c0002 | t0002 | g0279 | AMR | CLM | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0087 | AMR | CLM | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0017 | AMR | CLM | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | CLM | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0247 | AMR | CLM | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0177 | EUR | IBS | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01516 | hp2 | a0003 | c0003 | t0001 | g0013 | EUR | IBS | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01517 | hp1 | a0003 | c0003 | t0001 | g0013 | EUR | IBS | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01517 | hp2 | a0002 | c0002 | t0002 | g0208 | EUR | IBS | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01884 | hp1 | a0010 | c0011 | t0007 | g0180 | 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 | g0044 | AFR | ACB | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01891 | hp2 | a0008 | c0018 | t0001 | g0305 | AFR | ACB | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01928 | hp1 | a0002 | c0002 | t0002 | g0028 | AMR | PEL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0253 | AMR | PEL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0120 | AMR | PEL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0272 | AMR | PEL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0101 | AMR | PEL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01952 | hp2 | a0002 | c0002 | t0002 | g0032 | AMR | PEL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01981 | hp1 | a0002 | c0002 | t0002 | g0028 | AMR | PEL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | PEL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01993 | hp2 | a0015 | c0019 | t0002 | g0306 | AMR | PEL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PEL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | KHV | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | KHV | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | KHV | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | KHV | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | KHV | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0103 | EAS | KHV | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0254 | 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 | g0191 | EAS | KHV | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | KHV | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | KHV | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02129 | hp1 | a0003 | c0003 | t0001 | g0313 | EAS | KHV | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | KHV | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | KHV | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | KHV | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0295 | AFR | ACB | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0302 | AFR | ACB | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | CDX | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02165 | hp1 | a0002 | c0002 | t0002 | g0196 | EAS | CDX | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | CDX | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0147 | AFR | ACB | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | ACB | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | PEL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PEL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0148 | AFR | ACB | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02300 | hp2 | a0002 | c0002 | t0002 | g0032 | AMR | PEL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02451 | hp1 | a0002 | c0002 | t0002 | g0207 | AFR | ACB | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0290 | 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 | g0311 | AFR | GWD | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02602 | hp1 | a0001 | c0009 | t0001 | g0225 | SAS | PJL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02602 | hp2 | a0002 | c0002 | t0002 | g0056 | SAS | PJL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02615 | hp2 | a0002 | c0002 | t0002 | g0187 | AFR | GWD | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | GWD | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0146 | AFR | GWD | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0124 | AFR | GWD | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02630 | hp2 | a0011 | c0010 | t0007 | g0179 | AFR | GWD | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02698 | hp1 | a0002 | c0002 | t0002 | g0212 | SAS | PJL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02717 | hp1 | a0002 | c0002 | t0002 | g0183 | 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 | g0050 | SAS | PJL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0017 | SAS | PJL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0258 | SAS | PJL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02738 | hp2 | a0002 | c0002 | t0002 | g0256 | SAS | PJL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02809 | hp1 | a0002 | c0002 | t0002 | g0182 | 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 | g0287 | AFR | GWD | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0300 | AFR | GWD | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | GWD | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02886 | hp2 | a0005 | c0005 | t0001 | g0040 | AFR | GWD | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0023 | AFR | GWD | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0023 | 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 | g0057 | AFR | ESN | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | ESN | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | ESN | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02965 | hp2 | a0002 | c0002 | t0002 | g0184 | AFR | ESN | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0301 | AFR | ESN | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0022 | 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 | g0058 | AFR | ESN | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0291 | 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 | g0039 | AFR | ESN | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | ESN | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03139 | hp1 | a0005 | c0005 | t0001 | g0040 | AFR | ESN | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03139 | hp2 | a0006 | c0006 | t0001 | g0042 | AFR | ESN | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0145 | AFR | ESN | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0294 | 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 | g0155 | AFR | MSL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | MSL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03225 | hp2 | a0005 | c0005 | t0001 | g0307 | AFR | MSL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0248 | SAS | PJL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03239 | hp2 | a0002 | c0002 | t0002 | g0198 | SAS | PJL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03453 | hp1 | a0002 | c0002 | t0002 | g0181 | 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 | g0308 | AFR | MSL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03486 | hp2 | a0006 | c0006 | t0001 | g0043 | AFR | MSL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0271 | SAS | PJL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0015 | SAS | PJL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | PJL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0015 | SAS | PJL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0210 | 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 | g0299 | AFR | ESN | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0003 | 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 | g0048 | AFR | MSL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03579 | hp2 | a0002 | c0002 | t0005 | g0123 | AFR | MSL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0167 | SAS | PJL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03654 | hp2 | a0002 | c0002 | t0002 | g0211 | SAS | PJL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0284 | SAS | PJL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03669 | hp2 | a0003 | c0003 | t0001 | g0315 | SAS | PJL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | STU | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03688 | hp2 | a0003 | c0003 | t0001 | g0314 | SAS | STU | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0285 | SAS | PJL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0055 | 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 | g0054 | SAS | BEB | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0200 | SAS | BEB | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03942 | hp2 | a0002 | c0002 | t0002 | g0199 | 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 | g0175 | SAS | STU | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0019 | SAS | BEB | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | BEB | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0222 | SAS | STU | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0053 | SAS | STU | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0154 | SAS | STU | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | STU | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0149 | 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 | g0216 | EAS | CHB | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | CHB | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | CHB | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | CHB | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | YRI | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0296 | AFR | YRI | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0233 | 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 | g0007 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18942 | hp1 | a0002 | c0002 | t0002 | g0221 | 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 | g0241 | 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 | g0227 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0255 | 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 | g0065 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0031 | 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 | g0030 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18965 | hp2 | a0001 | c0017 | t0001 | g0304 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18968 | hp2 | a0003 | c0003 | t0001 | g0316 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18969 | hp1 | a0002 | c0002 | t0004 | g0209 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0121 | 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 | g0264 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0010 | 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 | g0033 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18981 | hp2 | a0014 | c0015 | t0001 | g0228 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18988 | hp2 | a0003 | c0003 | t0001 | g0012 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18989 | hp2 | a0001 | c0014 | t0001 | g0230 | 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 | g0190 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18997 | hp1 | a0002 | c0002 | t0004 | g0192 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19000 | hp1 | a0001 | c0001 | t0009 | g0273 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19006 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | LWK | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | LWK | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | LWK | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | LWK | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19056 | hp1 | a0007 | c0008 | t0002 | g0041 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19057 | hp2 | a0002 | c0002 | t0004 | g0224 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0275 | 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 | g0037 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0229 | 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 | g0027 | 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 | g0312 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0102 | 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 | g0238 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19081 | hp2 | a0003 | c0003 | t0001 | g0012 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19091 | hp2 | a0003 | c0003 | t0001 | g0012 | EAS | JPT | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0293 | AFR | YRI | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | YRI | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA20129 | hp1 | a0009 | c0016 | t0010 | g0076 | AFR | ASW | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | ASW | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA20752 | hp1 | a0004 | c0004 | t0001 | g0244 | EUR | TSI | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0160 | EUR | TSI | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA20805 | hp1 | a0003 | c0003 | t0001 | g0309 | EUR | TSI | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0077 | EUR | TSI | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA20905 | hp1 | a0004 | c0004 | t0001 | g0188 | SAS | GIH | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0019 | SAS | GIH | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01123 | hp1 | a0001 | c0007 | t0002 | g0091 | AMR | CLM | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | CLM | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03471 | hp1 | a0001 | c0001 | t0008 | g0073 | AFR | MSL | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0195 | 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 | g0163 | AFR | USA | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | LWK | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| NA21309 | hp2 | a0016 | c0020 | t0001 | g0318 | AFR | LWK | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0097 | REF | REF | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0119 | REF | REF | UGT2A2_chr4_69583417_69644642 | UGT2A2 | chr4 | 69583417 | 69644642 |
| 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 | a0013 | 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 | a0012 | 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 | a0010a0011 | 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 | a0002a0010a0011others(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 | a0009 | 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 | a0003a0004a0016 | 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 | a0009 | 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 | a0008 | 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 | a0015 | 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 | a0003a0007a0016 | 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 | a0006 | 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 |
| 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 |
| 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 | a0001c0001t0001a0001c0001t0008a0001c0009t0001others(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 | a0010c0011t0007a0011c0010t0007 | 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 | a0010c0011t0007a0011c0010t0007 | 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 | a0009c0016t0010 | 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 | a0009c0016t0010 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*32A>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 6/6 | 32 | chr4 | 69589340 |
| 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 | 238 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(235): 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 | a0001c0001t0001g0048a0001c0001t0001g0290a0001c0001t0001g0291others(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 | 132 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(129): 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 | a0001c0001t0002g0083 | 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 | 132 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(129): 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 | a0001c0001t0001g0303a0009c0016t0010g0076a0012c0012t0001g0203 | 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 | a0001c0001t0001g0057 | 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 | 75 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(72): 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 | 211 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(208): 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 | a0010c0011t0007g0180a0011c0010t0007g0179 | 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 | a0002c0002t0002g0187 | 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 | a0001c0001t0001g0048a0001c0001t0001g0290a0001c0001t0001g0291others(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 | 30 | a0001c0001t0001g0025a0001c0001t0001g0053a0001c0001t0001g0054others(27): 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 | 95 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(92): 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 | 78 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(75): Show | 92 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(89): 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 | a0001c0001t0001g0303a0009c0016t0010g0076a0012c0012t0001g0203 | 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 | 21 | a0001c0001t0001g0025a0001c0001t0001g0047a0001c0001t0001g0053others(18): 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 | a0001c0001t0001g0303a0009c0016t0010g0076a0012c0012t0001g0203 | 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 | a0001c0001t0002g0093 | 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 | a0012c0012t0001g0203 | 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 | a0001c0001t0002g0008a0001c0001t0002g0080 | 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 | a0009c0016t0010g0076 | 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 | a0001c0001t0001g0219a0001c0001t0001g0257 | 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 | a0001c0001t0001g0206 | 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 | 238 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(235): 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 | a0001c0001t0002g0087 | 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 | a0008c0018t0001g0305 | 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 | 132 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(129): 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 | 79 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(76): 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 | a0001c0001t0001g0274 | 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 | a0001c0001t0001g0248 | 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 | 135 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(132): 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 | 211 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(208): 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 | a0001c0001t0001g0048a0001c0001t0001g0290a0001c0001t0001g0291others(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 | a0001c0001t0001g0057 | 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 | a0001c0001t0002g0100 | 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 | 132 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(129): 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 | 21 | a0001c0001t0001g0025a0001c0001t0001g0047a0001c0001t0001g0053others(18): 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 | a0001c0001t0002g0088 | 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 | 211 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(208): 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 | 71 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(68): 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 | a0008c0018t0001g0305 | 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 | a0002c0002t0002g0187 | 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 | a0001c0001t0001g0303a0008c0018t0001g0305a0009c0016t0010g0076others(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 | a0002c0002t0005g0123 | 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 | a0009c0016t0010g0076 | 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 | 75 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(72): 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 | a0001c0001t0001g0277 | 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 | a0001c0001t0001g0303a0009c0016t0010g0076a0012c0012t0001g0203 | 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 | 8 | a0001c0001t0001g0060a0001c0001t0001g0156a0001c0001t0001g0157others(5): 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 | a0003c0003t0006g0311 | 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 | 33 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(30): 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 | a0008c0018t0001g0305 | 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 | a0001c0001t0001g0287 | 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 | a0006c0006t0001g0043 | 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 | 71 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(68): 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 | a0002c0002t0005g0123a0002c0002t0005g0140 | 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 | a0001c0001t0001g0243 | 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 | a0001c0001t0001g0303a0008c0018t0001g0305a0009c0016t0010g0076others(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 | a0002c0002t0002g0187 | 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 | a0001c0001t0001g0130a0001c0001t0001g0223a0001c0001t0001g0233others(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 | 167 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(164): 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 | a0001c0001t0001g0002a0001c0001t0001g0044a0001c0001t0001g0048others(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 | 211 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(208): 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 | a0001c0001t0002g0085a0001c0001t0003g0135a0001c0001t0003g0138others(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 | 132 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(129): 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 | a0001c0001t0002g0019 | 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 | a0001c0001t0001g0096 | 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 | a0001c0001t0002g0102 | 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 | a0001c0001t0002g0102 | 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 | a0001c0001t0001g0048a0001c0001t0001g0290a0001c0001t0001g0291others(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 | a0001c0001t0001g0063 | 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 | 216 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(213): 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 | 132 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(129): 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 | ||||||
| chr4:69595553
|
A | G | 317 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(314): Show | 377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.1024-304T>C | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 3/5 | chr4 | 69595553 | ||||||
| chr4:69595634
|
G | A | 2 | a0006c0006t0001g0042a0006c0006t0001g0043 | 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 | a0001c0001t0002g0019 | 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 | a0002c0002t0005g0123a0002c0002t0005g0140 | 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 | a0001c0001t0001g0234 | 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 | 104 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(101): 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 | 132 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(129): 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 | a0001c0001t0001g0108a0001c0001t0001g0243 | 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 | a0001c0001t0001g0287 | 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 | 249 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(246): 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 | a0001c0001t0001g0276 | 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 | 132 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(129): 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 | 216 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(213): 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 | 216 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(213): 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 | a0001c0001t0001g0153 | 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 | a0001c0001t0001g0303 | 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 | a0001c0001t0001g0160 | 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 | a0001c0001t0002g0045 | 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 | a0001c0001t0001g0237 | 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 | 129 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(126): 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 | a0001c0001t0001g0048a0001c0001t0001g0290a0001c0001t0001g0291others(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 | 104 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(101): 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 | a0001c0001t0001g0284 | 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 | 104 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(101): 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 | 104 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(101): 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 | 80 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(77): 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 | a0002c0002t0002g0183 | 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 | 21 | a0001c0001t0001g0025a0001c0001t0001g0047a0001c0001t0001g0053others(18): 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 | a0001c0001t0001g0234 | 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 | a0001c0001t0001g0303a0008c0018t0001g0305a0009c0016t0010g0076others(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 | 132 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(129): 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 | 132 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(129): 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 | a0001c0001t0001g0048a0001c0001t0001g0290a0001c0001t0001g0291others(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 | 80 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(77): 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 | a0001c0001t0001g0215 | 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 | a0010c0011t0007g0180a0011c0010t0007g0179 | 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 | 132 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(129): 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 | a0002c0002t0002g0028a0002c0002t0002g0032a0002c0002t0002g0056others(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 | 68 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0029others(65): 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 | a0001c0001t0001g0048a0001c0001t0001g0290a0001c0001t0001g0291others(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 | 84 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(81): 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 | 212 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(209): 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 | 132 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(129): 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 | 104 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(101): 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 | a0001c0001t0001g0057 | 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 | 216 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(213): 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 | 139 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(136): 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 | a0002c0002t0002g0182 | 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 | a0001c0001t0003g0146 | 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 | 159 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(156): 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 | a0008c0018t0001g0305 | 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 | a0001c0001t0002g0101 | 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 | a0003c0003t0001g0310a0004c0004t0001g0035a0004c0004t0001g0189others(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 | a0001c0001t0003g0023a0001c0001t0003g0135a0001c0001t0003g0136others(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 | a0001c0001t0002g0166 | 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 | a0001c0001t0008g0073a0001c0001t0008g0074a0006c0006t0001g0042others(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 | a0001c0001t0001g0235 | 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 | a0001c0001t0001g0271 | 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 | 159 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(156): 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 | a0001c0001t0001g0112a0001c0001t0001g0263 | 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 | a0002c0002t0002g0028a0002c0002t0002g0032a0002c0002t0002g0056others(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 | a0001c0001t0001g0303a0009c0016t0010g0076a0012c0012t0001g0203 | 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 | a0001c0001t0001g0047a0016c0020t0001g0318 | 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 | 76 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(73): 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 | a0002c0002t0002g0028a0002c0002t0002g0032a0002c0002t0002g0056others(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 | 103 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(100): 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 | a0001c0001t0001g0241a0001c0001t0008g0073a0001c0001t0008g0074others(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 | 84 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(81): 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 | a0001c0001t0001g0002a0001c0001t0001g0064a0001c0001t0001g0067others(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 | 84 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(81): 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 | ||||||
| chr4:69600996
|
C | A | 317 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(314): Show | 377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.743-1602G>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69600996 | ||||||
| chr4:69601066
|
C | T | 1 | a0002c0002t0005g0123 | 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 | a0006c0006t0001g0042a0006c0006t0001g0043 | 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 | 111 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(108): 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 | 84 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(81): 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 | 105 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(102): 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 | a0002c0002t0002g0181a0002c0002t0002g0182a0002c0002t0002g0183others(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 | a0010c0011t0007g0180a0011c0010t0007g0179 | 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 | 84 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(81): 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 | a0001c0001t0001g0291a0001c0001t0001g0292 | 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 | 76 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(73): 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 | 104 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(101): 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 | a0001c0001t0001g0036a0001c0001t0001g0246 | 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 | a0001c0001t0001g0048a0001c0001t0001g0290a0001c0001t0001g0291others(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 | a0001c0001t0001g0194a0001c0001t0001g0231 | 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 | 84 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(81): 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 | 84 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(81): 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 | 84 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(81): 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 | a0002c0002t0002g0028a0002c0002t0002g0032a0002c0002t0002g0056others(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 | 84 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(81): 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 | 84 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(81): 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 | 84 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(81): 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 | 84 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(81): 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 | 84 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(81): 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 | a0001c0001t0001g0222 | 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 | a0002c0002t0002g0181a0002c0002t0002g0182a0002c0002t0002g0183others(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 | a0002c0002t0002g0028a0002c0002t0002g0032a0002c0002t0002g0056others(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 | a0001c0001t0001g0047a0001c0001t0001g0053a0001c0001t0001g0054others(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 | a0001c0001t0001g0258 | 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 | a0002c0002t0002g0181a0002c0002t0002g0182a0002c0002t0002g0196others(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 | a0002c0002t0002g0028a0002c0002t0002g0032a0002c0002t0002g0056others(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 | a0002c0002t0002g0256a0010c0011t0007g0180a0011c0010t0007g0179 | 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 | a0001c0001t0001g0222a0001c0001t0001g0233a0001c0001t0001g0264others(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 | 33 | a0001c0001t0001g0010a0001c0001t0001g0030a0001c0001t0001g0108others(30): Show | 40 | HG01255.hp1 HG01255.hp2 HG01993.hp1 others(37): 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 | 37 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0027others(34): 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 | a0001c0001t0001g0039a0001c0001t0001g0301 | 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 | a0002c0002t0005g0123 | 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 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(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 | a0001c0001t0001g0250a0001c0001t0001g0275 | 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 | a0001c0001t0002g0094 | 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 | a0002c0002t0002g0028a0002c0002t0002g0032a0002c0002t0002g0056others(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 | a0002c0002t0002g0028a0002c0002t0002g0032a0002c0002t0002g0056others(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 | a0001c0001t0001g0048a0001c0001t0001g0290a0001c0001t0001g0291others(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 | a0001c0001t0001g0234a0002c0002t0002g0181a0002c0002t0002g0182others(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 | a0001c0001t0001g0058 | 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 | 2 | a0001c0001t0002g0020a0001c0001t0002g0105 | 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 | a0002c0002t0002g0028a0002c0002t0002g0032a0002c0002t0002g0056others(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 | a0001c0001t0001g0048a0001c0001t0001g0290a0001c0001t0001g0291others(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 | a0002c0002t0002g0028a0002c0002t0002g0032a0002c0002t0002g0056others(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 | a0002c0002t0002g0028a0002c0002t0002g0032a0002c0002t0002g0056others(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 | a0002c0002t0002g0028a0002c0002t0002g0032a0002c0002t0002g0056others(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 | a0001c0001t0001g0048a0001c0001t0001g0290a0001c0001t0001g0291others(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 | a0002c0002t0002g0028a0002c0002t0002g0032a0002c0002t0002g0056others(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 | a0002c0002t0002g0028a0002c0002t0002g0032a0002c0002t0002g0056others(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 | a0002c0002t0002g0028a0002c0002t0002g0032a0002c0002t0002g0056others(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 | a0002c0002t0005g0123a0002c0002t0005g0140 | 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 | a0002c0002t0002g0028a0002c0002t0002g0032a0002c0002t0002g0056others(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 | a0002c0002t0002g0028a0002c0002t0002g0032a0002c0002t0002g0056others(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 | a0001c0001t0001g0163 | 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 | a0002c0002t0002g0028a0002c0002t0002g0032a0002c0002t0002g0056others(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 | 104 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(101): 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 | 104 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(101): 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 | a0002c0002t0002g0028a0002c0002t0002g0032a0002c0002t0002g0056others(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 | a0001c0001t0001g0163 | 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 | a0002c0002t0002g0028a0002c0002t0002g0032a0002c0002t0002g0056others(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 | a0010c0011t0007g0180a0011c0010t0007g0179 | 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 | a0002c0002t0002g0028a0002c0002t0002g0032a0002c0002t0002g0056others(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 | a0002c0002t0002g0028a0002c0002t0002g0032a0002c0002t0002g0056others(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 | a0001c0001t0002g0120 | 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 | a0001c0001t0001g0164 | 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 | a0001c0001t0001g0025a0001c0001t0001g0168a0001c0001t0001g0169others(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 | a0001c0001t0001g0164a0002c0002t0002g0028a0002c0002t0002g0032others(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 | a0001c0001t0001g0164a0002c0002t0002g0028a0002c0002t0002g0032others(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 | a0001c0001t0001g0164 | 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 | a0001c0001t0001g0164 | 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 | a0001c0001t0001g0164 | 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 | a0001c0001t0001g0164 | 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 | a0001c0001t0001g0164 | 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 | a0001c0014t0001g0230 | 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 | a0001c0014t0001g0230 | 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 | a0001c0001t0001g0186 | 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 | a0001c0001t0001g0186 | 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 | a0001c0001t0001g0186 | 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 | 2 | a0001c0001t0001g0163a0001c0001t0001g0164 | 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 | a0002c0002t0002g0028a0002c0002t0002g0032a0002c0002t0002g0056others(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 | 104 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(101): 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 | a0001c0001t0002g0099 | 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 | a0001c0001t0001g0048a0001c0001t0001g0290a0001c0001t0001g0291others(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 | a0001c0001t0002g0124 | 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 | a0002c0002t0002g0028a0002c0002t0002g0032a0002c0002t0002g0056others(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 | a0002c0002t0002g0028a0002c0002t0002g0032a0002c0002t0002g0056others(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 | a0001c0007t0002g0091 | 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 | 21 | a0001c0001t0001g0025a0001c0001t0001g0047a0001c0001t0001g0053others(18): 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 | a0002c0002t0002g0028a0002c0002t0002g0032a0002c0002t0002g0056others(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 | a0002c0002t0002g0028a0002c0002t0002g0032a0002c0002t0002g0056others(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 | a0002c0002t0002g0028a0002c0002t0002g0032a0002c0002t0002g0056others(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 | a0002c0002t0004g0192a0002c0002t0004g0209a0002c0002t0004g0224 | 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 | a0002c0002t0002g0028a0002c0002t0002g0032a0002c0002t0002g0056others(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 | a0002c0002t0002g0028a0002c0002t0002g0032a0002c0002t0002g0056others(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 | a0002c0002t0002g0028a0002c0002t0002g0032a0002c0002t0002g0056others(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 | a0002c0002t0002g0187 | 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 | a0002c0002t0002g0028a0002c0002t0002g0032a0002c0002t0002g0056others(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 | a0002c0002t0002g0028a0002c0002t0002g0032a0002c0002t0002g0056others(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 | a0002c0002t0002g0187 | 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 | a0002c0002t0002g0028a0002c0002t0002g0032a0002c0002t0002g0056others(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 | a0001c0001t0001g0160 | 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 | a0001c0001t0001g0057 | 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 | a0010c0011t0007g0180a0011c0010t0007g0179 | 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 | a0001c0001t0001g0218 | 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 | a0002c0002t0002g0028a0002c0002t0002g0032a0002c0002t0002g0056others(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 | a0001c0001t0001g0267 | 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 | a0001c0001t0001g0262 | 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 | a0002c0002t0002g0028a0002c0002t0002g0032a0002c0002t0002g0056others(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 | a0001c0001t0008g0073a0001c0001t0008g0074a0006c0006t0001g0042others(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 | a0002c0002t0002g0028a0002c0002t0002g0032a0002c0002t0002g0056others(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 | a0013c0013t0002g0082 | 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 | a0001c0001t0001g0236 | 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 | a0002c0002t0002g0028a0002c0002t0002g0032a0002c0002t0002g0056others(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 | a0001c0001t0001g0303a0001c0001t0008g0073a0001c0001t0008g0074others(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 | a0001c0001t0002g0006 | 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 | a0001c0001t0001g0303a0008c0018t0001g0305a0009c0016t0010g0076others(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 | a0001c0001t0002g0018 | 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 | a0001c0001t0002g0018 | 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 | a0001c0001t0008g0073a0001c0001t0008g0074a0006c0006t0001g0042others(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 | a0002c0002t0002g0028a0002c0002t0002g0032a0002c0002t0002g0056others(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 | 249 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(246): 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 | 84 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(81): 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 | a0001c0001t0002g0086a0001c0001t0002g0098 | 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 | 84 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(81): 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 | 76 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(73): 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 | 84 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(81): 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 | a0001c0001t0008g0073a0001c0001t0008g0074a0006c0006t0001g0042others(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 | a0001c0001t0001g0297 | 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 | a0003c0003t0001g0314a0003c0003t0001g0315 | 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 | a0001c0007t0002g0075 | 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 | a0002c0002t0002g0028a0002c0002t0002g0032a0002c0002t0002g0056others(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 | a0002c0002t0002g0028a0002c0002t0002g0032a0002c0002t0002g0056others(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 | a0001c0001t0001g0274 | 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 | a0002c0002t0002g0028a0002c0002t0002g0032a0002c0002t0002g0056others(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 | 76 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(73): 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 | 84 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(81): 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 | 84 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(81): 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 | a0002c0002t0002g0028a0002c0002t0002g0032a0002c0002t0002g0056others(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 | a0001c0001t0001g0303a0008c0018t0001g0305a0009c0016t0010g0076others(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 | 84 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(81): 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 | a0001c0001t0002g0103 | 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 | 84 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(81): 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 | 84 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(81): 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 | a0001c0001t0001g0290 | 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 | a0001c0001t0001g0050 | 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 | 84 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(81): 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 | a0001c0001t0001g0272 | 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 | 84 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(81): 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 | a0002c0002t0002g0028a0002c0002t0002g0032a0002c0002t0002g0056others(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 | 84 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(81): 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 | a0001c0001t0001g0303a0008c0018t0001g0305a0009c0016t0010g0076others(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 | 111 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(108): 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 | 3 | a0001c0001t0001g0155a0001c0001t0001g0172a0001c0001t0001g0173 | 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 | a0002c0002t0002g0183 | 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 | 243 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(240): 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 | a0001c0001t0001g0218 | 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 | a0001c0001t0002g0086a0001c0001t0002g0098a0001c0001t0002g0099 | 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 | a0001c0001t0008g0074 | 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 | a0001c0001t0001g0303a0009c0016t0010g0076a0012c0012t0001g0203 | 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 | 76 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(73): 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 | 76 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(73): 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 | a0010c0011t0007g0180a0011c0010t0007g0179 | 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 | 112 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(109): Show | 133 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(130): Show |
intron_variant | MODIFIER | c.743-9762dupA | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69609155 | ||||||
| chr4:69609155
|
A | ATT | 11 | a0001c0001t0001g0050a0001c0001t0001g0071a0001c0001t0001g0215others(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 | 92 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(89): 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 | a0002c0002t0002g0028a0002c0002t0002g0032a0002c0002t0002g0056others(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 | 104 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(101): 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 | a0010c0011t0007g0180a0011c0010t0007g0179 | 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 | 249 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(246): 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 | a0010c0011t0007g0180a0011c0010t0007g0179 | 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 | 21 | a0001c0001t0001g0025a0001c0001t0001g0047a0001c0001t0001g0053others(18): 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 | a0001c0001t0001g0153 | 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 | 107 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(104): 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 | 104 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(101): 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 | a0012c0012t0001g0203 | 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 | 112 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(109): 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 | a0001c0001t0001g0303a0002c0002t0002g0028a0002c0002t0002g0032others(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 | a0002c0002t0002g0181a0002c0002t0002g0182a0002c0002t0002g0183others(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 | a0001c0001t0008g0073a0001c0001t0008g0074a0006c0006t0001g0042others(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 | a0001c0001t0008g0073a0001c0001t0008g0074 | 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 | 105 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(102): 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 | a0010c0011t0007g0180a0011c0010t0007g0179 | 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 | 106 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(103): 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 | a0001c0001t0002g0078 | 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 | a0001c0001t0003g0023a0001c0001t0003g0135a0001c0001t0003g0136others(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 | a0001c0001t0001g0044 | 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 | a0006c0006t0001g0042a0006c0006t0001g0043 | 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 | a0001c0001t0008g0073a0001c0001t0008g0074 | 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 | a0001c0001t0001g0004a0001c0001t0001g0046 | 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 | a0001c0001t0001g0223a0001c0001t0001g0234 | 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 | a0008c0018t0001g0305 | 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 | 76 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(73): 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 | 5 | a0001c0001t0002g0022a0001c0001t0002g0124a0001c0001t0002g0125others(2): 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 | 104 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(101): 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 | a0001c0001t0001g0303a0002c0002t0002g0028a0002c0002t0002g0032others(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 | 111 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(108): 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 | 111 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(108): 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 | a0010c0011t0007g0180a0011c0010t0007g0179 | 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 | a0003c0003t0001g0313 | 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 | a0010c0011t0007g0180a0011c0010t0007g0179 | 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 | 76 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(73): 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 | a0001c0001t0001g0051a0001c0001t0001g0066 | 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 | a0003c0003t0001g0310a0004c0004t0001g0035a0004c0004t0001g0189others(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 |
65 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(62): 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 | a0001c0001t0001g0046a0001c0001t0001g0072 | 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 | a0001c0001t0001g0178 | 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 | a0012c0012t0001g0203 | 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 | a0002c0002t0005g0123 | 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 | a0001c0001t0002g0103 | 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 | 111 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(108): 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 | 111 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(108): 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 | a0006c0006t0001g0042 | 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 | a0001c0001t0001g0044 | 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 | a0001c0001t0001g0048a0001c0001t0001g0290a0001c0001t0001g0291others(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 | a0010c0011t0007g0180a0011c0010t0007g0179 | 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 | a0001c0001t0001g0261 | 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 | 111 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(108): 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 | a0008c0018t0001g0305 | 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 | 111 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(108): 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 | 36 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(33): 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 | 111 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(108): 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 | a0001c0001t0001g0303a0002c0002t0002g0028a0002c0002t0002g0032others(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 | a0001c0001t0001g0069 | 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 | a0001c0001t0001g0249 | 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 | 76 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(73): 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 | a0001c0001t0001g0048a0001c0001t0001g0290a0001c0001t0001g0291others(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 | a0008c0018t0001g0305 | 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 | 2 | a0001c0001t0001g0152a0001c0001t0001g0165 | 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 | a0010c0011t0007g0180a0011c0010t0007g0179 | 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 | 21 | a0001c0001t0001g0025a0001c0001t0001g0047a0001c0001t0001g0053others(18): 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 | a0010c0011t0007g0180a0011c0010t0007g0179 | 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 | a0010c0011t0007g0180a0011c0010t0007g0179 | 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 | 208 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(205): 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 | a0001c0001t0001g0038a0001c0001t0001g0057a0001c0001t0001g0177others(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 | a0002c0002t0002g0028a0002c0002t0002g0032a0002c0002t0002g0056others(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 | 112 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(109): 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 | 112 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(109): 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 | 111 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(108): 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 | 75 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(72): 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 | a0001c0001t0001g0303a0009c0016t0010g0076a0012c0012t0001g0203 | 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 | 111 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(108): 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 | a0002c0002t0002g0028a0002c0002t0002g0032a0002c0002t0002g0056others(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 | 21 | a0001c0001t0001g0025a0001c0001t0001g0047a0001c0001t0001g0053others(18): 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 | a0001c0001t0001g0240 | 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 | a0001c0001t0001g0058 | 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 | 21 | a0001c0001t0001g0025a0001c0001t0001g0047a0001c0001t0001g0053others(18): 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 | a0001c0001t0001g0303a0002c0002t0002g0028a0002c0002t0002g0032others(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 | a0001c0001t0003g0023a0001c0001t0003g0135a0001c0001t0003g0136others(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 | a0010c0011t0007g0180a0011c0010t0007g0179 | 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 | a0001c0001t0008g0073a0001c0001t0008g0074 | 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 | a0002c0002t0002g0183 | 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 | 250 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(247): 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 | 83 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(80): 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 | 83 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(80): 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 | 83 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(80): 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 |
83 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(80): 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 | 83 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(80): 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 | 83 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(80): 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 | a0001c0001t0001g0055 | 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 | 21 | a0001c0001t0001g0025a0001c0001t0001g0047a0001c0001t0001g0053others(18): 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 | 112 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(109): 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 | 83 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(80): 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 | a0010c0011t0007g0180a0011c0010t0007g0179 | 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 | 112 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(109): 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 | a0003c0003t0006g0311 | 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 | 244 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(241): 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 | 244 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(241): 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 | a0010c0011t0007g0180a0011c0010t0007g0179 | 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 | a0001c0001t0001g0066 | 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 | a0010c0011t0007g0180a0011c0010t0007g0179 | 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 | a0002c0002t0002g0028a0002c0002t0002g0032a0002c0002t0002g0056others(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 | a0001c0001t0001g0048a0001c0001t0001g0290a0001c0001t0001g0291others(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 | a0009c0016t0010g0076a0010c0011t0007g0180a0011c0010t0007g0179 | 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 | 112 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(109): 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 | a0009c0016t0010g0076a0010c0011t0007g0180a0011c0010t0007g0179 | 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 | a0001c0001t0001g0303 | 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 | a0001c0001t0001g0303a0012c0012t0001g0203 | 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 | a0001c0001t0001g0213 | 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 | 113 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(110): 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 | a0001c0001t0008g0073a0001c0001t0008g0074 | 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 | a0001c0001t0001g0227a0001c0001t0001g0233a0014c0015t0001g0228 | 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 | 57 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(54): 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 | a0001c0001t0008g0073a0001c0001t0008g0074 | 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 | a0001c0001t0001g0303 | 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 | a0001c0001t0003g0145 | 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 | 91 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(88): 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 | a0002c0002t0002g0028a0002c0002t0002g0032a0002c0002t0002g0181others(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 | a0010c0011t0007g0180a0011c0010t0007g0179 | 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 | a0002c0002t0002g0199 | 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 | 125 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(122): 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 | a0004c0004t0001g0035a0004c0004t0001g0189a0004c0004t0001g0244 | 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 | 106 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(103): 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 | a0001c0001t0001g0248 | 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 | a0001c0001t0001g0206 | 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 | 5 | a0001c0001t0002g0022a0001c0001t0002g0124a0001c0001t0002g0125others(2): 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 | ||||||
| chr4:69616698
|
G | A | 317 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(314): Show | 377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.743-17304C>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69616698 | ||||||
| chr4:69616751
|
A | G | 1 | a0001c0001t0002g0095 | 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 | 16 | a0001c0001t0001g0250a0001c0001t0002g0005a0001c0001t0002g0016others(13): 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 | 31 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0030others(28): 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 | 94 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0026others(91): 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 | a0001c0001t0001g0150a0001c0001t0001g0154a0001c0001t0002g0109others(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 | 71 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(68): 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 | a0006c0006t0001g0042a0006c0006t0001g0043 | 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 | 102 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(99): 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 | a0001c0001t0003g0023a0001c0001t0003g0135a0001c0001t0003g0136others(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 | a0001c0001t0001g0252 | 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 | a0002c0002t0002g0187 | 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 | 102 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(99): 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 | a0001c0001t0008g0073a0001c0001t0008g0074a0002c0002t0002g0181others(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 | 102 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(99): 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 | 5 | a0001c0001t0002g0022a0001c0001t0002g0124a0001c0001t0002g0125others(2): 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 | a0010c0011t0007g0180a0011c0010t0007g0179 | 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 | 169 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(166): Show | 208 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(205): 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 | 18 | a0001c0001t0001g0034a0001c0001t0001g0044a0001c0001t0001g0193others(15): 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 | a0001c0001t0008g0073a0001c0001t0008g0074a0002c0002t0002g0056 | 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 | a0002c0002t0002g0187a0003c0003t0001g0012a0003c0003t0001g0309others(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 | a0003c0003t0001g0310a0003c0003t0001g0313a0003c0003t0006g0311others(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 | a0001c0001t0001g0132a0003c0003t0001g0013a0003c0003t0001g0312others(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 | a0001c0001t0003g0148 | 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 | 23 | a0001c0001t0001g0025a0001c0001t0001g0059a0001c0001t0001g0066others(20): 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 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0046others(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 | 10 | a0001c0001t0001g0131a0001c0001t0001g0144a0001c0001t0001g0151others(7): 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 | 34 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0049others(31): 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 | a0003c0003t0001g0317 | 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 | a0001c0001t0001g0047a0001c0001t0001g0053a0001c0001t0001g0054others(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 | 23 | a0001c0001t0001g0025a0001c0001t0001g0059a0001c0001t0001g0066others(20): 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 | a0006c0006t0001g0042a0006c0006t0001g0043 | 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 | 10 | a0001c0001t0001g0131a0001c0001t0001g0144a0001c0001t0001g0151others(7): 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 | a0001c0001t0001g0047a0001c0001t0001g0053a0001c0001t0001g0054others(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 | 98 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(95): 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 | a0006c0006t0001g0042a0006c0006t0001g0043 | 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 | a0001c0001t0001g0047a0001c0001t0001g0053a0001c0001t0001g0054others(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 | 108 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(105): 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 | 79 | a0001c0001t0001g0090a0001c0001t0001g0096a0001c0001t0001g0108others(76): Show | 98 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(95): 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 | 128 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(125): 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 | 102 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(99): 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 | 102 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(99): 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 | 72 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(69): 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 | 102 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(99): 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 | a0001c0001t0001g0258a0001c0009t0001g0225 | 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 | a0001c0001t0001g0218 | 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 | a0001c0001t0001g0132a0003c0003t0001g0012a0003c0003t0001g0013others(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 | a0012c0012t0001g0203 | 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 | a0001c0001t0002g0120 | 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 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0046others(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 | a0001c0001t0001g0186 | 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 | a0001c0001t0001g0132a0003c0003t0001g0012a0003c0003t0001g0013others(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 | a0003c0003t0001g0012a0003c0003t0001g0312a0003c0003t0001g0316others(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 | 89 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(86): 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 | a0001c0001t0002g0045a0001c0001t0008g0073a0001c0001t0008g0074others(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 | a0002c0002t0002g0182a0002c0002t0002g0183a0002c0002t0002g0184others(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 | 100 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(97): 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 | 5 | a0001c0001t0001g0303a0001c0001t0002g0296a0001c0001t0002g0299others(2): 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 | a0002c0002t0002g0187 | 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 | a0002c0002t0002g0182 | 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 | 240 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(237): 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 | 72 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(69): 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 | 102 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(99): 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 | 102 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(99): 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 | a0012c0012t0001g0203 | 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 | a0001c0001t0001g0150 | 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 | a0002c0002t0002g0187 | 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 | 101 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(98): 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 | a0001c0001t0001g0047a0001c0001t0001g0053a0001c0001t0001g0054others(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 | a0001c0001t0001g0047a0001c0001t0001g0053a0001c0001t0001g0054others(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 | 74 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(71): 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 | a0001c0001t0008g0073a0001c0001t0008g0074a0002c0002t0002g0181others(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 | a0001c0001t0008g0073a0001c0001t0008g0074a0002c0002t0002g0181others(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 | 102 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(99): 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 | a0001c0001t0001g0132a0003c0003t0001g0012a0003c0003t0001g0013others(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 | a0001c0001t0002g0200a0002c0002t0002g0198a0002c0002t0002g0199others(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 | a0002c0002t0002g0187 | 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 | a0001c0001t0001g0151 | 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 | 102 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(99): 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 | a0001c0001t0001g0047a0001c0001t0001g0053a0001c0001t0001g0054others(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 | 129 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(126): 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 | 102 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(99): 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 | a0001c0001t0001g0132a0003c0003t0001g0012a0003c0003t0001g0013others(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 | a0001c0001t0001g0141a0002c0002t0005g0140 | 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 | a0001c0001t0001g0159a0001c0001t0001g0160 | 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 | 102 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(99): 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 | 73 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(70): 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 | 102 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(99): 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 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(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 | 91 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(88): 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 | a0001c0001t0008g0073a0001c0001t0008g0074a0002c0002t0002g0181others(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 | a0009c0016t0010g0076 | 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 | 102 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(99): 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 | a0001c0001t0008g0073a0001c0001t0008g0074a0002c0002t0002g0181others(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 | a0001c0001t0008g0074 | 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 | a0001c0001t0001g0047a0001c0001t0001g0053a0001c0001t0001g0054others(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 | a0001c0001t0008g0073a0001c0001t0008g0074a0002c0002t0002g0181others(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 | a0001c0001t0002g0080 | 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 | a0002c0002t0002g0279 | 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 | 72 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(69): 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 | 252 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(249): 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 | 102 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(99): 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 | a0001c0001t0002g0092 | 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 | a0001c0001t0002g0080 | 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 | 102 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(99): 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 | 72 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(69): 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 | a0006c0006t0001g0043 | 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 | 14 | a0001c0001t0001g0024a0001c0001t0001g0143a0001c0001t0001g0144others(11): 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 | 102 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(99): 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 | 102 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(99): 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 | 102 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(99): 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 | 73 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(70): 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 | 72 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(69): 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 | 102 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(99): 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 | a0001c0001t0001g0213 | 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 | a0001c0001t0001g0132a0003c0003t0001g0012a0003c0003t0001g0013others(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 | 102 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(99): 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 | a0012c0012t0001g0203 | 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 | 102 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(99): 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 | 3 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0174 | 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 | a0001c0001t0001g0236 | 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 | 72 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(69): 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 | 102 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(99): 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 | a0001c0001t0001g0142a0001c0001t0001g0178 | 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 | a0001c0001t0002g0200 | 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 | 101 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(98): 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 | a0001c0001t0008g0073a0001c0001t0008g0074a0006c0006t0001g0042others(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 | 102 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(99): 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 | a0002c0002t0002g0181a0002c0002t0002g0182a0002c0002t0002g0183others(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 | a0001c0001t0008g0073a0001c0001t0008g0074a0002c0002t0002g0181others(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 | 102 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(99): 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 | a0001c0001t0008g0073a0001c0001t0008g0074a0002c0002t0002g0181others(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 | a0001c0001t0001g0290 | 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 | 102 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(99): 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 | 102 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(99): 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 | 102 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(99): 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 | 102 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(99): 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 | a0001c0001t0001g0280 | 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 | 129 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(126): 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 | 102 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(99): 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 | a0003c0003t0006g0311 | 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 | a0001c0001t0001g0047a0001c0001t0001g0053a0001c0001t0001g0054others(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 | a0001c0001t0001g0132a0003c0003t0001g0012a0003c0003t0001g0013others(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 | 102 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(99): 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 | a0001c0001t0001g0132a0003c0003t0001g0012a0003c0003t0001g0013others(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 | a0001c0001t0008g0073a0001c0001t0008g0074a0002c0002t0002g0181others(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 | 102 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(99): 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 | 102 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(99): 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 | 7 | a0001c0001t0001g0226a0001c0001t0001g0237a0001c0001t0001g0238others(4): 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 | 240 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(237): 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 | a0001c0001t0001g0034a0001c0001t0001g0241 | 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 | a0001c0001t0001g0090a0001c0007t0002g0075a0001c0007t0002g0091 | 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 | 103 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(100): 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 | a0001c0001t0002g0133a0001c0001t0002g0134 | 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 | a0001c0001t0001g0132a0003c0003t0001g0012a0003c0003t0001g0013others(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 | a0008c0018t0001g0305 | 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 | 102 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(99): 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 | 102 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(99): 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 | a0001c0001t0001g0030a0001c0001t0001g0269 | 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 | 80 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(77): 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 | 56 | a0001c0001t0001g0090a0001c0001t0001g0096a0001c0001t0001g0108others(53): Show | 73 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(70): 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 | a0001c0001t0001g0132a0003c0003t0001g0012a0003c0003t0001g0013others(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 | 4 | a0001c0001t0002g0022a0001c0001t0002g0124a0001c0001t0002g0133others(1): Show | 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 | a0001c0001t0002g0078a0001c0001t0002g0088a0001c0001t0002g0089others(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 | a0001c0001t0001g0132a0002c0002t0002g0181a0003c0003t0001g0012others(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 | a0001c0001t0001g0142a0001c0001t0001g0178a0003c0003t0001g0312others(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 | a0002c0002t0002g0181 | 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 | a0001c0001t0001g0025a0001c0001t0001g0168a0001c0001t0001g0169others(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 | a0001c0001t0001g0132a0002c0002t0002g0181a0003c0003t0001g0012others(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 | a0008c0018t0001g0305 | 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 | a0001c0001t0001g0268 | 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 | a0001c0001t0001g0024a0001c0001t0001g0149 | 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 | 76 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(73): 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 | a0010c0011t0007g0180a0011c0010t0007g0179 | 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 | a0001c0001t0001g0024a0001c0001t0001g0149 | 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 | 84 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(81): 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 | a0001c0001t0003g0003a0001c0001t0003g0145a0001c0001t0003g0146others(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 | 102 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(99): 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 | a0001c0001t0001g0142a0001c0001t0001g0178 | 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 | a0008c0018t0001g0305 | 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 | a0008c0018t0001g0305 | 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 | a0001c0001t0002g0122 | 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 | 102 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(99): 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 | 28 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(25): 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 | 103 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(100): 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 | a0001c0001t0002g0021 | 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 | a0001c0001t0001g0142a0001c0001t0001g0178 | 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 | a0008c0018t0001g0305 | 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 | a0001c0001t0001g0132a0001c0001t0001g0186a0003c0003t0001g0012others(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 | a0001c0001t0002g0078a0001c0001t0002g0079a0001c0001t0002g0113 | 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 | a0001c0001t0001g0252 | 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 | a0012c0012t0001g0203 | 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 | a0002c0002t0002g0187 | 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 | a0008c0018t0001g0305 | 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 | a0001c0001t0001g0132a0001c0001t0001g0186a0003c0003t0001g0012others(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 | a0001c0001t0008g0073a0001c0001t0008g0074a0002c0002t0002g0181others(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 | a0008c0018t0001g0305 | 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 | 103 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(100): 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 | 84 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(81): 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 | 65 | a0001c0001t0001g0090a0001c0001t0001g0096a0001c0001t0001g0108others(62): Show | 83 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(80): 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 | a0001c0001t0001g0132a0003c0003t0001g0012a0003c0003t0001g0013others(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 | a0005c0005t0001g0040a0005c0005t0001g0307 | 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 | 18 | a0001c0001t0001g0025a0001c0001t0001g0151a0001c0001t0001g0152others(15): 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 | 39 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(36): 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 | a0001c0001t0001g0240 | 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 | a0010c0011t0007g0180a0011c0010t0007g0179 | 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 | a0003c0003t0001g0012a0003c0003t0001g0013a0003c0003t0001g0309others(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 | 71 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0141others(68): 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 | a0003c0003t0001g0012a0003c0003t0001g0013a0003c0003t0001g0309others(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 | a0002c0002t0002g0181a0002c0002t0002g0182a0002c0002t0002g0183others(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 | a0009c0016t0010g0076 | 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 | 54 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0141others(51): 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 | a0002c0002t0002g0028a0002c0002t0002g0032a0002c0002t0002g0220others(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 | a0001c0001t0001g0216a0001c0001t0001g0278 | 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 | 66 | a0001c0001t0001g0090a0001c0001t0001g0096a0001c0001t0001g0108others(63): Show | 84 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(81): 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 | a0012c0012t0001g0203 | 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 | a0002c0002t0005g0123 | 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 | a0001c0001t0001g0206 | 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 | 54 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0141others(51): 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 | a0001c0001t0001g0227a0014c0015t0001g0228 | 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 | a0001c0001t0001g0171 | 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 | a0001c0001t0008g0073a0001c0001t0008g0074a0002c0002t0002g0181others(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 | a0008c0018t0001g0305 | 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 | a0010c0011t0007g0180a0011c0010t0007g0179 | 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 | 244 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(241): 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 | a0001c0001t0008g0073a0001c0001t0008g0074a0002c0002t0002g0181others(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 | a0003c0003t0001g0314a0003c0003t0001g0315 | 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 | 42 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0141others(39): 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 | a0001c0001t0001g0293a0001c0001t0001g0294a0001c0001t0001g0295 | 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 | 42 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0141others(39): 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 | a0001c0001t0001g0149 | 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 | 33 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(30): 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 | 33 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(30): 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 | a0008c0018t0001g0305 | 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 | a0008c0018t0001g0305 | 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 | a0001c0001t0008g0073a0001c0001t0008g0074a0002c0002t0002g0181others(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 | 33 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(30): 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 | a0008c0018t0001g0305 | 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 | a0001c0001t0008g0073a0001c0001t0008g0074a0002c0002t0002g0181others(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 | a0001c0001t0002g0087 | 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 | 42 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0033others(39): 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 | a0001c0001t0001g0142a0001c0001t0001g0150a0001c0001t0001g0154others(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 | a0010c0011t0007g0180a0011c0010t0007g0179 | 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 | a0001c0001t0001g0026 | 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 | a0010c0011t0007g0180a0011c0010t0007g0179 | 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 | a0001c0001t0001g0186a0003c0003t0001g0012a0003c0003t0001g0013others(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 | a0002c0002t0002g0181a0002c0002t0002g0182a0002c0002t0002g0183others(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 | a0001c0001t0008g0073a0001c0001t0008g0074a0002c0002t0002g0181others(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 | a0001c0001t0008g0073a0001c0001t0008g0074a0002c0002t0002g0181others(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 | 49 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(46): 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 | a0001c0001t0001g0066 | 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 | 42 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0141others(39): 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 | a0001c0001t0001g0254a0001c0001t0001g0255 | 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 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(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 | a0010c0011t0007g0180a0011c0010t0007g0179 | 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 | a0003c0003t0001g0012a0003c0003t0001g0013a0003c0003t0001g0309others(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 | 58 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0141others(55): 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 | a0001c0001t0001g0142a0001c0001t0001g0178 | 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 | a0008c0018t0001g0305 | 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 | 52 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0141others(49): 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 | a0002c0002t0002g0187 | 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 | a0003c0003t0001g0309 | 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 | a0007c0008t0002g0041 | 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 | a0001c0001t0002g0085 | 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 | 42 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0141others(39): 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 | 58 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0132others(55): 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 | a0001c0001t0002g0078a0001c0001t0002g0079 | 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 | a0001c0001t0001g0153 | 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 | a0001c0001t0002g0078a0001c0001t0002g0079 | 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 | 58 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0132others(55): 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 | a0001c0001t0001g0010a0001c0001t0001g0202a0001c0001t0001g0217others(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 | 4 | a0001c0001t0002g0015a0001c0001t0002g0083a0001c0001t0002g0084others(1): Show | 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 | 53 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0067others(50): 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 | a0002c0002t0002g0196 | 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 | 25 | a0001c0001t0001g0025a0001c0001t0001g0141a0001c0001t0001g0142others(22): 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 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0174others(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 | a0001c0001t0001g0024a0001c0001t0001g0143a0001c0001t0001g0144others(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 | a0001c0001t0001g0177a0001c0001t0002g0078a0001c0001t0002g0079others(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 | 297 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(294): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.742+3072G>T | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69635827 | ||||||
| chr4:69635828
|
C | A | 41 | a0001c0001t0001g0025a0001c0001t0001g0141a0001c0001t0001g0142others(38): 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 | 23 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(20): 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 | a0001c0001t0001g0046a0001c0001t0001g0068a0001c0001t0001g0069others(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 | a0001c0001t0001g0072a0001c0001t0003g0023a0001c0001t0003g0138others(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 | a0001c0001t0003g0139a0009c0016t0010g0076 | 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 | a0001c0001t0001g0044 | 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 | a0001c0001t0001g0205a0001c0001t0001g0290a0001c0001t0001g0291others(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 | a0001c0001t0001g0027a0001c0001t0001g0194a0001c0001t0001g0195others(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 |
49 | a0001c0001t0001g0001a0001c0001t0001g0026a0001c0001t0001g0029others(46): 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 |
38 | a0001c0001t0001g0011a0001c0001t0001g0033a0001c0001t0001g0034others(35): 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 |
10 | a0001c0001t0001g0280a0001c0001t0001g0281a0001c0001t0001g0282others(7): 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 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0287others(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 | a0001c0001t0001g0288 | 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 | a0001c0001t0001g0303 | 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 | 60 | a0001c0001t0001g0090a0001c0001t0001g0096a0001c0001t0001g0108others(57): Show | 78 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.742+3070delT | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69635828 | ||||||
| chr4:69635830
|
A | C | 5 | a0001c0001t0002g0078a0001c0001t0002g0079a0001c0001t0002g0080others(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 | a0001c0001t0002g0077 | 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 | a0003c0003t0006g0308 | 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 | a0001c0001t0001g0197a0002c0002t0002g0196 | 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 | a0003c0003t0001g0316a0004c0004t0001g0126 | 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 | a0001c0001t0001g0186a0003c0003t0001g0012a0003c0003t0001g0309others(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 | a0003c0003t0006g0308 | 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 | a0001c0001t0008g0074a0002c0002t0002g0181a0002c0002t0002g0182others(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 | 78 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(75): 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 | a0001c0001t0001g0176a0001c0001t0001g0177 | 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 | a0001c0001t0001g0176a0001c0001t0001g0177 | 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 | a0001c0001t0001g0195 | 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 | a0001c0001t0008g0073a0001c0001t0008g0074a0002c0002t0002g0181others(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 | 42 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0141others(39): 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 | a0001c0001t0008g0073a0001c0001t0008g0074a0002c0002t0002g0181others(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 | 246 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(243): 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 | a0001c0001t0001g0194 | 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 | a0006c0006t0001g0043 | 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 | a0001c0001t0008g0073a0001c0001t0008g0074a0006c0006t0001g0042others(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 | 42 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0141others(39): 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 | 38 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0143others(35): 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 | a0002c0002t0002g0181a0002c0002t0002g0182a0002c0002t0002g0183others(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 | 49 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0132others(46): 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 | 39 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(36): 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 | a0001c0001t0001g0193 | 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 | 82 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(79): 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 | a0002c0002t0004g0192 | 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 | a0002c0002t0002g0187 | 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 | a0001c0001t0001g0026a0001c0001t0001g0190a0001c0001t0001g0191 | 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 | a0003c0003t0006g0308 | 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 | a0001c0001t0008g0073a0001c0001t0008g0074 | 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 | a0006c0006t0001g0043 | 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 | a0001c0001t0008g0073a0001c0001t0008g0074a0006c0006t0001g0042others(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 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0001g0292others(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 | a0004c0004t0001g0188 | 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 | 24 | a0001c0001t0001g0039a0001c0001t0001g0044a0001c0001t0001g0297others(21): 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 | a0001c0001t0001g0132a0001c0001t0002g0133a0001c0001t0002g0134 | 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 | a0001c0001t0003g0023a0001c0001t0003g0135a0001c0001t0003g0136others(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 | a0001c0001t0008g0073a0001c0001t0008g0074a0001c0007t0002g0075others(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 | a0004c0004t0001g0189 | 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 | 76 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(73): 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 | a0001c0001t0001g0178 | 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 | 42 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0141others(39): 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 | a0001c0001t0001g0004a0001c0001t0001g0046 | 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 | a0001c0001t0002g0045 | 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 | a0002c0002t0002g0181a0002c0002t0002g0182a0002c0002t0002g0183others(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 | a0001c0001t0002g0185 | 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 | a0001c0001t0001g0186a0001c0017t0001g0304a0002c0002t0002g0187others(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 | 135 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(132): 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 | a0001c0001t0001g0044 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.742+259C>A | UGT2A2 | ENSG00000271271.6 | transcript | ENST00000604629.6 | protein_coding | 1/5 | chr4 | 69638640 |