| geneid | 10941 |
|---|---|
| ensemblid | ENSG00000173610.13 |
| hgncid | 12542 |
| symbol | UGT2A1 |
| name | UDP glucuronosyltransferase family 2 member A1 complex locus |
| refseq_nuc | NM_001252275.3 |
| refseq_prot | NP_001239204.2 |
| ensembl_nuc | ENST00000286604.9 |
| ensembl_prot | ENSP00000286604.4 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 69588417 |
| end | 69653247 |
| strand | - |
| ver | v1.2 |
| region | chr4:69588417-69653247 |
| region5000 | chr4:69583417-69658247 |
| regionname0 | UGT2A1_chr4_69588417_69653247 |
| regionname5000 | UGT2A1_chr4_69583417_69658247 |
| 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 | 527 | 289 | 47 | 48 | 156 | 9 | 27 | 119 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| a0002 | 0/0 | 527 | 33 | 23 | 4 | 4 | 1 | 1 | 4 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| a0003 | 0/0 | 527 | 21 | 2 | 7 | 5 | 1 | 6 | 4 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| a0004 | 0/0 | 527 | 18 | 1 | 10 | 0 | 3 | 4 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| a0005 | 0/0 | 527 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| a0006 | 0/0 | 191 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| a0007 | 0/0 | 527 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| a0008 | 0/0 | 527 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| a0009 | 0/0 | 527 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| a0010 | 0/0 | 527 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| a0011 | 0/0 | 527 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| a0012 | 0/0 | 527 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| 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 | 1584 | 285 | 47 | 48 | 155 | 9 | 24 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| c0002 | 0/0 | 1584 | 33 | 23 | 4 | 4 | 1 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| c0003 | 0/0 | 1584 | 19 | 2 | 7 | 4 | 1 | 5 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| c0004 | 0/0 | 1584 | 18 | 1 | 10 | 0 | 3 | 4 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| c0005 | 0/0 | 1584 | 6 | 6 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| c0006 | 0/0 | 1584 | 2 | 0 | 2 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| c0007 | 0/0 | 1584 | 2 | 0 | 0 | 0 | 0 | 2 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| c0008 | 0/0 | 1584 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| c0009 | 0/0 | 1584 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| c0010 | 0/0 | 1584 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| c0011 | 0/0 | 1584 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| c0012 | 0/0 | 1584 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| c0013 | 0/0 | 1584 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| c0014 | 0/0 | 1584 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| c0015 | 0/0 | 1584 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| c0016 | 0/0 | 1584 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| c0017 | 0/0 | 1584 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| c0018 | 0/0 | 1584 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| 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 | 1070 | 239 | 44 | 50 | 112 | 9 | 24 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| t0002 | 1/1 | 1070 | 107 | 15 | 22 | 49 | 5 | 14 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| t0003 | 0/0 | 1070 | 15 | 15 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| t0004 | 0/0 | 1070 | 3 | 0 | 0 | 3 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| t0005 | 0/0 | 1070 | 2 | 2 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| t0006 | 0/0 | 1070 | 2 | 2 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| t0007 | 0/0 | 1070 | 2 | 2 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| t0008 | 0/0 | 1070 | 2 | 1 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| t0009 | 0/0 | 1070 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| t0010 | 0/0 | 1070 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| t0011 | 0/0 | 1070 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| t0012 | 0/0 | 1070 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| 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 | 4 | 0 | 0 | 4 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0015 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0222 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0270 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0313 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0324 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| 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 | 1584 | 285 | 47 | 48 | 155 | 9 | 24 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| a0001c0007 | 0/0 | 1584 | 2 | 0 | 0 | 0 | 0 | 2 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| a0001c0011 | 0/0 | 1584 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| a0001c0017 | 0/0 | 1584 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| a0002c0002 | 0/0 | 1584 | 33 | 23 | 4 | 4 | 1 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| a0003c0003 | 0/0 | 1584 | 19 | 2 | 7 | 4 | 1 | 5 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| a0003c0009 | 0/0 | 1584 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| a0003c0010 | 0/0 | 1584 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| a0004c0004 | 0/0 | 1584 | 18 | 1 | 10 | 0 | 3 | 4 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| a0005c0005 | 0/0 | 1584 | 6 | 6 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| a0006c0006 | 0/0 | 1584 | 2 | 0 | 2 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| a0006c0008 | 0/0 | 1584 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| a0007c0016 | 0/0 | 1584 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| a0008c0013 | 0/0 | 1584 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| a0009c0012 | 0/0 | 1584 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| a0010c0018 | 0/0 | 1584 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| a0011c0014 | 0/0 | 1584 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| a0012c0015 | 0/0 | 1584 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2653 | 194 | 29 | 36 | 107 | 5 | 17 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| a0001c0001t0002 | 1/1 | 2653 | 80 | 9 | 11 | 47 | 4 | 7 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| a0001c0001t0003 | 0/0 | 2653 | 7 | 7 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| a0001c0001t0006 | 0/0 | 2653 | 2 | 2 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| a0001c0001t0009 | 0/0 | 2653 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| a0001c0001t0010 | 0/0 | 2653 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| a0001c0007t0001 | 0/0 | 2653 | 2 | 0 | 0 | 0 | 0 | 2 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| a0001c0011t0001 | 0/0 | 2653 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| a0001c0017t0001 | 0/0 | 2653 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| a0002c0002t0001 | 0/0 | 2653 | 22 | 14 | 3 | 3 | 1 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| a0002c0002t0003 | 0/0 | 2653 | 8 | 8 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| a0002c0002t0008 | 0/0 | 2653 | 2 | 1 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| a0002c0002t0012 | 0/0 | 2653 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| a0003c0003t0002 | 0/0 | 2653 | 16 | 2 | 7 | 1 | 1 | 5 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| a0003c0003t0004 | 0/0 | 2653 | 3 | 0 | 0 | 3 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| a0003c0009t0002 | 0/0 | 2653 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| a0003c0010t0002 | 0/0 | 2653 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| a0004c0004t0001 | 0/0 | 2653 | 16 | 1 | 9 | 0 | 3 | 3 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| a0004c0004t0002 | 0/0 | 2653 | 2 | 0 | 1 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| a0005c0005t0002 | 0/0 | 2653 | 4 | 4 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| a0005c0005t0005 | 0/0 | 2653 | 2 | 2 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| a0006c0006t0002 | 0/0 | 2653 | 2 | 0 | 2 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| a0006c0008t0001 | 0/0 | 2653 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| a0007c0016t0011 | 0/0 | 2653 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| a0008c0013t0007 | 0/0 | 2653 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| a0009c0012t0007 | 0/0 | 2653 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| a0010c0018t0001 | 0/0 | 2653 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| a0011c0014t0002 | 0/0 | 2653 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| a0012c0015t0001 | 0/0 | 2653 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | copy fasta | chr4 | 69583417 | 69658247 |
| 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 | 4 | 0 | 0 | 4 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0001g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0002g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0002g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0002g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0002g0222 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0002g0270 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0002g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0002g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0002g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0002g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0002g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0002g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0003g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0003g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0003g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0003g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0003g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0006g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0006g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0009g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0001t0010g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0007t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0007t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0011t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0001c0017t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0002c0002t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0002c0002t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0002c0002t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0002c0002t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0002c0002t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0002c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0002c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0002c0002t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0002c0002t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0002c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0002c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0002c0002t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0002c0002t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0002c0002t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0002c0002t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0002c0002t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0002c0002t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0002c0002t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0002c0002t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0002c0002t0001g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0002c0002t0001g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0002c0002t0003g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0002c0002t0003g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0002c0002t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0002c0002t0003g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0002c0002t0003g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0002c0002t0003g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0002c0002t0008g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0002c0002t0008g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0002c0002t0012g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0003c0003t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0003c0003t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0003c0003t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0003c0003t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0003c0003t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0003c0003t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0003c0003t0002g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0003c0003t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0003c0003t0002g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0003c0003t0002g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0003c0003t0002g0324 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0003c0003t0002g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0003c0003t0002g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0003c0003t0002g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0003c0003t0002g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0003c0003t0002g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0003c0003t0004g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0003c0003t0004g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0003c0009t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0003c0010t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0004c0004t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0004c0004t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0004c0004t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0004c0004t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0004c0004t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0004c0004t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0004c0004t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0004c0004t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0004c0004t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0004c0004t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0004c0004t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0004c0004t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0004c0004t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0004c0004t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0004c0004t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0004c0004t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0004c0004t0002g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0004c0004t0002g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0005c0005t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0005c0005t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0005c0005t0002g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0005c0005t0002g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0005c0005t0005g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0005c0005t0005g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0006c0006t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0006c0006t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0006c0008t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0007c0016t0011g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0008c0013t0007g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0009c0012t0007g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0010c0018t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0011c0014t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| a0012c0015t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0004 | c0004 | t0001 | g0306 | EUR | GBR | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0084 | EUR | GBR | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0305 | EUR | GBR | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0083 | EUR | GBR | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0101 | EUR | FIN | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG00280 | hp2 | a0004 | c0004 | t0001 | g0035 | EUR | FIN | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0303 | EAS | CHS | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | CHS | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | CHS | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | CHS | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | CHS | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0169 | EAS | CHS | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | CHS | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | CHS | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | CHS | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | CHS | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | CHS | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0104 | AMR | PUR | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0247 | AMR | PUR | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG00642 | hp1 | a0002 | c0002 | t0001 | g0178 | AMR | PUR | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0177 | AMR | PUR | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG00733 | hp1 | a0002 | c0002 | t0001 | g0320 | AMR | PUR | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG00733 | hp2 | a0004 | c0004 | t0001 | g0195 | AMR | PUR | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG00735 | hp1 | a0006 | c0008 | t0001 | g0060 | AMR | PUR | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0210 | AMR | PUR | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0226 | AMR | PUR | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG00738 | hp2 | a0004 | c0004 | t0001 | g0183 | AMR | PUR | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG00741 | hp2 | a0004 | c0004 | t0001 | g0070 | AMR | PUR | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG01070 | hp2 | a0004 | c0004 | t0001 | g0322 | AMR | PUR | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG01071 | hp2 | a0011 | c0014 | t0002 | g0082 | AMR | PUR | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG01081 | hp2 | a0004 | c0004 | t0001 | g0315 | AMR | PUR | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0311 | AMR | PUR | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG01109 | hp1 | a0004 | c0004 | t0001 | g0317 | AMR | PUR | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG01109 | hp2 | a0002 | c0002 | t0008 | g0354 | AMR | PUR | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG01168 | hp2 | a0004 | c0004 | t0002 | g0321 | AMR | PUR | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG01175 | hp1 | a0006 | c0006 | t0002 | g0076 | AMR | PUR | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0345 | AMR | PUR | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG01192 | hp1 | a0001 | c0001 | t0009 | g0016 | AMR | PUR | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0325 | AMR | PUR | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG01243 | hp1 | a0010 | c0018 | t0001 | g0275 | AMR | PUR | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0355 | AMR | PUR | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0327 | AMR | CLM | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | CLM | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | CLM | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0103 | AMR | CLM | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | CLM | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | CLM | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG01261 | hp2 | a0004 | c0004 | t0001 | g0221 | AMR | CLM | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | CLM | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG01346 | hp2 | a0003 | c0003 | t0002 | g0149 | AMR | CLM | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG01358 | hp1 | a0003 | c0003 | t0002 | g0302 | AMR | CLM | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0269 | AMR | CLM | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0271 | AMR | CLM | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0287 | AMR | CLM | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG01496 | hp1 | a0004 | c0004 | t0001 | g0057 | AMR | CLM | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | CLM | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG01516 | hp1 | a0002 | c0002 | t0001 | g0197 | EUR | IBS | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | IBS | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0015 | EUR | IBS | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG01517 | hp2 | a0003 | c0003 | t0002 | g0324 | EUR | IBS | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG01884 | hp1 | a0008 | c0013 | t0007 | g0351 | AFR | ACB | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG01884 | hp2 | a0002 | c0002 | t0001 | g0062 | AFR | ACB | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0336 | AFR | ACB | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG01891 | hp2 | a0002 | c0002 | t0001 | g0123 | AFR | ACB | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG01928 | hp1 | a0003 | c0003 | t0002 | g0150 | AMR | PEL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0286 | AMR | PEL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0212 | AMR | PEL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PEL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0282 | AMR | PEL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG01943 | hp2 | a0004 | c0004 | t0001 | g0059 | AMR | PEL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0350 | AMR | PEL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG01952 | hp2 | a0003 | c0003 | t0002 | g0284 | AMR | PEL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PEL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PEL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG01981 | hp1 | a0003 | c0003 | t0002 | g0344 | AMR | PEL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | PEL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG01993 | hp2 | a0003 | c0003 | t0002 | g0346 | AMR | PEL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0267 | AMR | PEL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG02004 | hp2 | a0002 | c0002 | t0001 | g0301 | AMR | PEL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | KHV | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | KHV | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | KHV | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | KHV | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | KHV | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | KHV | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | KHV | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | KHV | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | KHV | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | KHV | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | KHV | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0225 | EAS | KHV | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0335 | AFR | ACB | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | ACB | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | CDX | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | CDX | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG02165 | hp1 | a0003 | c0010 | t0002 | g0146 | EAS | CDX | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | CDX | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG02258 | hp1 | a0002 | c0002 | t0003 | g0196 | AFR | ACB | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0349 | AMR | PEL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | PEL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG02280 | hp2 | a0002 | c0002 | t0003 | g0063 | AFR | ACB | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0309 | AMR | PEL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG02300 | hp2 | a0003 | c0003 | t0002 | g0188 | AMR | PEL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG02451 | hp1 | a0003 | c0003 | t0002 | g0340 | AFR | ACB | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0333 | AFR | ACB | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0114 | AFR | GWD | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG02572 | hp2 | a0001 | c0001 | t0006 | g0174 | AFR | GWD | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG02602 | hp1 | a0001 | c0011 | t0001 | g0132 | SAS | PJL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG02602 | hp2 | a0003 | c0009 | t0002 | g0214 | SAS | PJL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG02615 | hp1 | a0002 | c0002 | t0001 | g0293 | AFR | GWD | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG02615 | hp2 | a0003 | c0003 | t0002 | g0218 | AFR | GWD | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | GWD | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG02622 | hp2 | a0002 | c0002 | t0003 | g0318 | AFR | GWD | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0291 | AFR | GWD | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG02630 | hp2 | a0009 | c0012 | t0007 | g0204 | AFR | GWD | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG02698 | hp1 | a0003 | c0003 | t0002 | g0241 | SAS | PJL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG02717 | hp1 | a0005 | c0005 | t0002 | g0208 | AFR | GWD | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0215 | AFR | GWD | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0279 | SAS | PJL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0299 | SAS | PJL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0245 | SAS | PJL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG02738 | hp2 | a0003 | c0003 | t0002 | g0133 | SAS | PJL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG02809 | hp1 | a0005 | c0005 | t0002 | g0297 | AFR | GWD | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG02809 | hp2 | a0002 | c0002 | t0001 | g0061 | AFR | GWD | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0338 | AFR | GWD | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0194 | AFR | GWD | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG02895 | hp1 | a0002 | c0002 | t0001 | g0216 | AFR | GWD | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0012 | AFR | GWD | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0012 | AFR | GWD | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG02897 | hp2 | a0002 | c0002 | t0001 | g0179 | AFR | GWD | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0308 | AFR | ESN | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0341 | AFR | ESN | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG02965 | hp1 | a0002 | c0002 | t0003 | g0072 | AFR | ESN | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG02965 | hp2 | a0005 | c0005 | t0002 | g0300 | AFR | ESN | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | ESN | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0290 | AFR | ESN | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0206 | AFR | ESN | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0356 | AFR | ESN | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | MSL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0328 | AFR | MSL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | ESN | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG03130 | hp2 | a0002 | c0002 | t0003 | g0002 | AFR | ESN | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | ESN | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG03139 | hp2 | a0002 | c0002 | t0001 | g0330 | AFR | ESN | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG03195 | hp1 | a0002 | c0002 | t0003 | g0064 | AFR | ESN | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0334 | AFR | ESN | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0219 | AFR | MSL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG03209 | hp2 | a0002 | c0002 | t0001 | g0329 | AFR | MSL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG03225 | hp1 | a0002 | c0002 | t0003 | g0002 | AFR | MSL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | MSL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0339 | SAS | PJL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG03239 | hp2 | a0003 | c0003 | t0002 | g0342 | SAS | PJL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG03453 | hp1 | a0005 | c0005 | t0002 | g0273 | AFR | MSL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG03453 | hp2 | a0002 | c0002 | t0001 | g0352 | AFR | MSL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG03486 | hp1 | a0001 | c0001 | t0006 | g0111 | AFR | MSL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG03486 | hp2 | a0002 | c0002 | t0001 | g0331 | AFR | MSL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0248 | SAS | PJL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0310 | SAS | PJL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG03516 | hp1 | a0002 | c0002 | t0001 | g0298 | AFR | ESN | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0229 | AFR | ESN | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG03540 | hp1 | a0002 | c0002 | t0003 | g0002 | AFR | GWD | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG03540 | hp2 | a0005 | c0005 | t0005 | g0288 | AFR | GWD | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0312 | AFR | MSL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG03579 | hp2 | a0005 | c0005 | t0005 | g0125 | AFR | MSL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG03654 | hp1 | a0004 | c0004 | t0002 | g0316 | SAS | PJL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG03654 | hp2 | a0003 | c0003 | t0002 | g0220 | SAS | PJL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG03688 | hp1 | a0004 | c0004 | t0001 | g0058 | SAS | STU | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | STU | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG03704 | hp1 | a0004 | c0004 | t0001 | g0289 | SAS | PJL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG03704 | hp2 | a0004 | c0004 | t0001 | g0319 | SAS | PJL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0236 | SAS | PJL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG03834 | hp1 | a0001 | c0007 | t0001 | g0213 | SAS | BEB | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0171 | SAS | BEB | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0323 | SAS | BEB | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG03942 | hp2 | a0003 | c0003 | t0002 | g0343 | SAS | BEB | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0193 | SAS | BEB | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0052 | SAS | BEB | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0175 | SAS | STU | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG04204 | hp2 | a0001 | c0007 | t0001 | g0107 | SAS | STU | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG04228 | hp1 | a0002 | c0002 | t0001 | g0200 | SAS | STU | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | STU | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA18522 | hp1 | a0002 | c0002 | t0001 | g0294 | AFR | YRI | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0115 | AFR | YRI | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | CHB | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | CHB | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | CHB | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | CHB | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA18906 | hp1 | a0002 | c0002 | t0001 | g0217 | AFR | YRI | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0337 | AFR | YRI | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0348 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA18942 | hp1 | a0003 | c0003 | t0002 | g0242 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA18965 | hp2 | a0001 | c0017 | t0001 | g0276 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA18967 | hp2 | a0002 | c0002 | t0001 | g0280 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA18970 | hp2 | a0003 | c0003 | t0004 | g0008 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0347 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA18981 | hp2 | a0012 | c0015 | t0001 | g0168 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA18986 | hp1 | a0002 | c0002 | t0001 | g0069 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0326 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA18997 | hp1 | a0003 | c0003 | t0004 | g0143 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA19000 | hp1 | a0001 | c0001 | t0010 | g0108 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA19006 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA19009 | hp1 | a0002 | c0002 | t0001 | g0281 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA19011 | hp2 | a0002 | c0002 | t0012 | g0357 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | LWK | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA19030 | hp2 | a0002 | c0002 | t0001 | g0353 | AFR | LWK | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | LWK | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | LWK | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA19057 | hp2 | a0003 | c0003 | t0004 | g0008 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | YRI | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | YRI | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA20129 | hp1 | a0007 | c0016 | t0011 | g0227 | AFR | ASW | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | ASW | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0243 | EUR | TSI | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA20752 | hp2 | a0004 | c0004 | t0001 | g0313 | EUR | TSI | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0304 | EUR | TSI | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0307 | EUR | TSI | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | GIH | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0041 | SAS | GIH | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG01123 | hp1 | a0006 | c0006 | t0002 | g0077 | AMR | CLM | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0285 | AMR | CLM | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG03471 | hp1 | a0002 | c0002 | t0008 | g0295 | AFR | MSL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | MSL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0332 | AFR | USA | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0296 | AFR | USA | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0292 | AFR | USA | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA20300 | hp2 | a0004 | c0004 | t0001 | g0314 | AFR | USA | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | LWK | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | LWK | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0270 | REF | REF | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0222 | REF | REF | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
| 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 | a0012 | 1 | NA18981.hp2 | missense_variant | MODERATE | c.1523A>G | p.Gln508Arg | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 7/7 | 1637/2653 | 1523/1584 | 508/527 | chr4 | 69589433 | ||
| chr4:69589530
|
C | T | 1 | a0011 | 1 | HG01071.hp2 | missense_variant | MODERATE | c.1426G>A | p.Val476Ile | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 7/7 | 1540/2653 | 1426/1584 | 476/527 | chr4 | 69589530 | ||
| chr4:69589581
|
C | T | 1 | a0010 | 1 | HG01243.hp1 | missense_variant | MODERATE | c.1375G>A | p.Val459Ile | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 7/7 | 1489/2653 | 1375/1584 | 459/527 | chr4 | 69589581 | ||
| chr4:69589642
|
C | A | 1 | a0008 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.1314G>T | p.Glu438Asp | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 7/7 | 1428/2653 | 1314/1584 | 438/527 | chr4 | 69589642 | ||
| chr4:69594602
|
C | T | 2 | a0008a0009 | 2 | HG01884.hp1 HG02630.hp2 |
missense_variant | MODERATE | c.1179G>A | p.Met393Ile | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/7 | 1293/2653 | 1179/1584 | 393/527 | chr4 | 69594602 | ||
| chr4:69594610
|
C | T | 4 | a0003a0005a0008others(1): Show | 29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
missense_variant | MODERATE | c.1171G>A | p.Val391Ile | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/7 | 1285/2653 | 1171/1584 | 391/527 | chr4 | 69594610 | ||
| chr4:69595221
|
G | C | 1 | a0007 | 1 | NA20129.hp1 | missense_variant | MODERATE | c.1025C>G | p.Pro342Arg | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 5/7 | 1139/2653 | 1025/1584 | 342/527 | chr4 | 69595221 | ||
| chr4:69599287
|
C | A | 1 | a0007 | 1 | NA20129.hp1 | missense_variant | MODERATE | c.955G>T | p.Val319Phe | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/7 | 1069/2653 | 955/1584 | 319/527 | chr4 | 69599287 | ||
| chr4:69635733
|
G | A | 3 | a0002a0004a0005 | 57 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(54): Show |
missense_variant | MODERATE | c.805C>T | p.Arg269Cys | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/7 | 919/2653 | 805/1584 | 269/527 | chr4 | 69635733 | ||
| chr4:69647055
|
A | G | 1 | a0004 | 18 | HG00099.hp1 HG00280.hp2 HG00733.hp2 others(15): Show |
missense_variant | MODERATE | c.590T>C | p.Leu197Ser | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/7 | 704/2653 | 590/1584 | 197/527 | chr4 | 69647055 | ||
| chr4:69647069
|
A | T | 1 | a0006 | 3 | HG00735.hp1 HG01123.hp1 HG01175.hp1 |
stop_gained | HIGH | c.576T>A | p.Tyr192* | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/7 | 690/2653 | 576/1584 | 192/527 | chr4 | 69647069 | ||
| chr4:69647083
|
A | G | 1 | a0004 | 18 | HG00099.hp1 HG00280.hp2 HG00733.hp2 others(15): Show |
missense_variant | MODERATE | c.562T>C | p.Tyr188His | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/7 | 676/2653 | 562/1584 | 188/527 | chr4 | 69647083 | ||
| chr4:69653188
|
C | T | 1 | a0001 | 1 | HG01192.hp1 | splice_region_variant | LOW | c.-55G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/7 | chr4 | 69653188 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:69589513
|
G | A | 1 | a0006c0006 | 2 | HG01123.hp1 HG01175.hp1 |
synonymous_variant | LOW | c.1443C>T | p.Leu481Leu | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 7/7 | 1557/2653 | 1443/1584 | 481/527 | chr4 | 69589513 | ||
| chr4:69599342
|
G | A | 1 | a0001c0017 | 1 | NA18965.hp2 | synonymous_variant | LOW | c.900C>T | p.Ile300Ile | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/7 | 1014/2653 | 900/1584 | 300/527 | chr4 | 69599342 | ||
| chr4:69599381
|
C | T | 1 | a0001c0011 | 1 | HG02602.hp1 | synonymous_variant | LOW | c.861G>A | p.Thr287Thr | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/7 | 975/2653 | 861/1584 | 287/527 | chr4 | 69599381 | ||
| chr4:69635782
|
C | T | 1 | a0003c0010 | 1 | HG02165.hp1 | synonymous_variant | LOW | c.756G>A | p.Ala252Ala | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/7 | 870/2653 | 756/1584 | 252/527 | chr4 | 69635782 | ||
| chr4:69647003
|
G | T | 2 | a0001c0007a0003c0009 | 3 | HG02602.hp2 HG03834.hp1 HG04204.hp2 |
synonymous_variant | LOW | c.642C>A | p.Ile214Ile | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/7 | 756/2653 | 642/1584 | 214/527 | chr4 | 69647003 | ||
| chr4:69647375
|
G | A | 1 | a0010c0018 | 1 | HG01243.hp1 | synonymous_variant | LOW | c.270C>T | p.Phe90Phe | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/7 | 384/2653 | 270/1584 | 90/527 | chr4 | 69647375 |
| 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 | a0001c0001t0006 | 2 | HG02572.hp2 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*869C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 7/7 | 869 | chr4 | 69588503 | |||||
| chr4:69588571
|
A | G | 13 | a0001c0001t0001a0001c0001t0006a0001c0007t0001others(10): Show | 245 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(242): Show |
3_prime_UTR_variant | MODIFIER | c.*801T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 7/7 | 801 | chr4 | 69588571 | |||||
| chr4:69588588
|
G | T | 2 | a0001c0001t0003a0002c0002t0003 | 15 | HG02258.hp1 HG02280.hp2 HG02572.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*784C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 7/7 | 784 | chr4 | 69588588 | |||||
| chr4:69588620
|
C | A | 2 | a0008c0013t0007a0009c0012t0007 | 2 | HG01884.hp1 HG02630.hp2 |
3_prime_UTR_variant | MODIFIER | c.*752G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 7/7 | 752 | chr4 | 69588620 | |||||
| chr4:69588682
|
T | C | 2 | a0008c0013t0007a0009c0012t0007 | 2 | HG01884.hp1 HG02630.hp2 |
3_prime_UTR_variant | MODIFIER | c.*690A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 7/7 | 690 | chr4 | 69588682 | |||||
| chr4:69588811
|
C | T | 1 | a0007c0016t0011 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*561G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 7/7 | 561 | chr4 | 69588811 | |||||
| chr4:69588935
|
C | T | 1 | a0005c0005t0005 | 2 | HG03540.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*437G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 7/7 | 437 | chr4 | 69588935 | |||||
| chr4:69589006
|
T | C | 1 | a0002c0002t0008 | 2 | HG01109.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*366A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 7/7 | 366 | chr4 | 69589006 | |||||
| chr4:69589273
|
C | T | 1 | a0003c0003t0004 | 3 | NA18970.hp2 NA18997.hp1 NA19057.hp2 |
3_prime_UTR_variant | MODIFIER | c.*99G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 7/7 | 99 | chr4 | 69589273 | |||||
| chr4:69589280
|
T | C | 1 | a0001c0001t0010 | 1 | NA19000.hp1 | 3_prime_UTR_variant | MODIFIER | c.*92A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 7/7 | 92 | chr4 | 69589280 | |||||
| chr4:69589340
|
T | G | 1 | a0007c0016t0011 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*32A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 7/7 | 32 | chr4 | 69589340 | |||||
| chr4:69653201
|
G | C | 1 | a0002c0002t0012 | 1 | NA19011.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-68C>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/7 | chr4 | 69653201 | ||||||
| chr4:69653205
|
A | T | 1 | a0001c0001t0009 | 1 | HG01192.hp1 | 5_prime_UTR_variant | MODIFIER | c.-72T>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/7 | 5561 | chr4 | 69653205 |
| 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 | 264 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(261): Show | 274 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(271): Show |
intron_variant | MODIFIER | c.1305-109C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69589760 | ||||||
| chr4:69589857
|
T | C | 8 | a0001c0001t0001g0124a0001c0001t0001g0223a0001c0001t0001g0224others(5): Show | 8 | HG01167.hp1 HG01243.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1305-206A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69589857 | ||||||
| chr4:69589861
|
C | G | 149 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(146): Show | 154 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.1305-210G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69589861 | ||||||
| chr4:69589881
|
T | C | 1 | a0001c0001t0002g0083 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1305-230A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69589881 | ||||||
| chr4:69589932
|
A | G | 149 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(146): Show | 154 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.1305-281T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69589932 | ||||||
| chr4:69589946
|
G | C | 3 | a0001c0001t0001g0325a0007c0016t0011g0227a0010c0018t0001g0275 | 3 | HG01192.hp2 HG01243.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1305-295C>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69589946 | ||||||
| chr4:69590001
|
T | G | 1 | a0001c0001t0001g0308 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1305-350A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69590001 | ||||||
| chr4:69590166
|
C | T | 83 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(80): Show | 87 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.1305-515G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69590166 | ||||||
| chr4:69590468
|
G | T | 236 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(233): Show | 245 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.1305-817C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69590468 | ||||||
| chr4:69590526
|
G | A | 2 | a0008c0013t0007g0351a0009c0012t0007g0204 | 2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1305-875C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69590526 | ||||||
| chr4:69590559
|
G | A | 1 | a0003c0003t0002g0218 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1305-908C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69590559 | ||||||
| chr4:69590597
|
G | A | 8 | a0001c0001t0001g0124a0001c0001t0001g0223a0001c0001t0001g0224others(5): Show | 8 | HG01167.hp1 HG01243.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1305-946C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69590597 | ||||||
| chr4:69590638
|
A | AGT | 30 | a0001c0001t0001g0021a0001c0001t0001g0128a0001c0001t0001g0186others(27): Show | 30 | HG00099.hp1 HG00280.hp2 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.1305-989_1305-988d others(4): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69590638 | ||||||
| chr4:69590638
|
A | AGTGT | 111 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(108): Show | 116 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(113): Show |
intron_variant | MODIFIER | c.1305-991_1305-988d others(6): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69590638 | ||||||
| chr4:69590638
|
AGT | A | 86 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(83): Show | 90 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(87): Show |
intron_variant | MODIFIER | c.1305-989_1305-988d others(4): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69590638 | ||||||
| chr4:69590677
|
C | A | 3 | a0001c0001t0001g0325a0007c0016t0011g0227a0010c0018t0001g0275 | 3 | HG01192.hp2 HG01243.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1305-1026G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69590677 | ||||||
| chr4:69590710
|
A | T | 21 | a0001c0001t0001g0113a0001c0001t0001g0128a0001c0001t0001g0186others(18): Show | 21 | HG00099.hp1 HG00280.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.1305-1059T>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69590710 | ||||||
| chr4:69590771
|
G | T | 3 | a0001c0001t0001g0325a0007c0016t0011g0227a0010c0018t0001g0275 | 3 | HG01192.hp2 HG01243.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1305-1120C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69590771 | ||||||
| chr4:69590777
|
G | T | 1 | a0001c0001t0002g0087 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1305-1126C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69590777 | ||||||
| chr4:69590778
|
A | G | 1 | a0010c0018t0001g0275 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1305-1127T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69590778 | ||||||
| chr4:69590793
|
A | G | 3 | a0001c0001t0002g0003a0001c0001t0002g0024a0001c0001t0002g0078 | 5 | NA18952.hp1 NA18984.hp1 NA19055.hp2 others(2): Show |
intron_variant | MODIFIER | c.1305-1142T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69590793 | ||||||
| chr4:69590856
|
A | G | 1 | a0007c0016t0011g0227 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1305-1205T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69590856 | ||||||
| chr4:69590997
|
T | G | 2 | a0001c0001t0001g0237a0001c0001t0001g0341 | 2 | HG02622.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1305-1346A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69590997 | ||||||
| chr4:69591195
|
C | G | 1 | a0001c0001t0001g0176 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1305-1544G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69591195 | ||||||
| chr4:69591303
|
T | C | 264 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(261): Show | 274 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(271): Show |
intron_variant | MODIFIER | c.1305-1652A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69591303 | ||||||
| chr4:69591319
|
T | G | 1 | a0001c0001t0002g0269 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1305-1668A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69591319 | ||||||
| chr4:69591607
|
C | G | 1 | a0002c0002t0001g0123 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1305-1956G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69591607 | ||||||
| chr4:69591749
|
T | G | 149 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(146): Show | 154 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.1305-2098A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69591749 | ||||||
| chr4:69591838
|
T | C | 87 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(84): Show | 91 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.1305-2187A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69591838 | ||||||
| chr4:69591838
|
T | G | 1 | a0001c0001t0001g0158 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1305-2187A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69591838 | ||||||
| chr4:69591954
|
T | C | 1 | a0001c0001t0001g0339 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1305-2303A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69591954 | ||||||
| chr4:69591972
|
C | T | 152 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(149): Show | 157 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(154): Show |
intron_variant | MODIFIER | c.1305-2321G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69591972 | ||||||
| chr4:69592159
|
G | A | 236 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(233): Show | 245 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.1304+2318C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69592159 | ||||||
| chr4:69592214
|
A | G | 8 | a0001c0001t0001g0124a0001c0001t0001g0223a0001c0001t0001g0224others(5): Show | 8 | HG01167.hp1 HG01243.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1304+2263T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69592214 | ||||||
| chr4:69592345
|
C | T | 1 | a0001c0001t0001g0308 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1304+2132G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69592345 | ||||||
| chr4:69592422
|
G | T | 1 | a0001c0001t0002g0089 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1304+2055C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69592422 | ||||||
| chr4:69592464
|
C | A | 149 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(146): Show | 154 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.1304+2013G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69592464 | ||||||
| chr4:69592524
|
G | C | 21 | a0001c0001t0001g0113a0001c0001t0001g0128a0001c0001t0001g0186others(18): Show | 21 | HG00099.hp1 HG00280.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.1304+1953C>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69592524 | ||||||
| chr4:69592924
|
C | T | 1 | a0001c0001t0002g0085 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1304+1553G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69592924 | ||||||
| chr4:69592930
|
C | T | 236 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(233): Show | 245 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.1304+1547G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69592930 | ||||||
| chr4:69592931
|
T | C | 79 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(76): Show | 83 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(80): Show |
intron_variant | MODIFIER | c.1304+1546A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69592931 | ||||||
| chr4:69592941
|
A | C | 1 | a0002c0002t0001g0123 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1304+1536T>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69592941 | ||||||
| chr4:69593231
|
C | A | 1 | a0003c0003t0002g0218 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1304+1246G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69593231 | ||||||
| chr4:69593261
|
T | C | 4 | a0001c0001t0001g0325a0002c0002t0001g0123a0007c0016t0011g0227others(1): Show | 4 | HG01192.hp2 HG01243.hp1 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.1304+1216A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69593261 | ||||||
| chr4:69593265
|
A | G | 1 | a0005c0005t0005g0125 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1304+1212T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69593265 | ||||||
| chr4:69593309
|
G | A | 1 | a0007c0016t0011g0227 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1304+1168C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69593309 | ||||||
| chr4:69593313
|
GA | G | 83 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(80): Show | 87 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.1304+1163delT | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69593313 | ||||||
| chr4:69593347
|
T | A | 1 | a0001c0001t0001g0250 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1304+1130A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69593347 | ||||||
| chr4:69593434
|
T | C | 3 | a0001c0001t0001g0325a0007c0016t0011g0227a0010c0018t0001g0275 | 3 | HG01192.hp2 HG01243.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1304+1043A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69593434 | ||||||
| chr4:69593559
|
CTT | C | 8 | a0001c0001t0001g0049a0001c0001t0002g0087a0002c0002t0001g0069others(5): Show | 8 | HG00733.hp1 HG01516.hp1 HG02698.hp2 others(5): Show |
intron_variant | MODIFIER | c.1304+916_1304+917d others(4): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69593559 | ||||||
| chr4:69593649
|
T | A | 1 | a0001c0001t0006g0174 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1304+828A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69593649 | ||||||
| chr4:69593675
|
A | T | 36 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0043others(33): Show | 38 | HG00438.hp2 HG00609.hp2 HG01070.hp1 others(35): Show |
intron_variant | MODIFIER | c.1304+802T>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69593675 | ||||||
| chr4:69593742
|
T | A | 1 | a0002c0002t0001g0123 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1304+735A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69593742 | ||||||
| chr4:69593753
|
G | A | 1 | a0001c0001t0001g0139 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1304+724C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69593753 | ||||||
| chr4:69593811
|
G | A | 1 | a0002c0002t0001g0331 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1304+666C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69593811 | ||||||
| chr4:69593861
|
A | G | 79 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(76): Show | 83 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(80): Show |
intron_variant | MODIFIER | c.1304+616T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69593861 | ||||||
| chr4:69593915
|
A | C | 2 | a0005c0005t0005g0125a0005c0005t0005g0288 | 2 | HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1304+562T>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69593915 | ||||||
| chr4:69593915
|
A | T | 1 | a0001c0001t0001g0116 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1304+562T>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69593915 | ||||||
| chr4:69593964
|
AGT | A | 4 | a0001c0001t0001g0325a0002c0002t0001g0123a0007c0016t0011g0227others(1): Show | 4 | HG01192.hp2 HG01243.hp1 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.1304+511_1304+512d others(4): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69593964 | ||||||
| chr4:69593973
|
T | G | 1 | a0003c0003t0002g0218 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1304+504A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69593973 | ||||||
| chr4:69593975
|
TTG | T | 8 | a0001c0001t0001g0030a0001c0001t0001g0036a0001c0001t0001g0068others(5): Show | 8 | HG01167.hp2 HG01891.hp2 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.1304+500_1304+501d others(4): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69593975 | ||||||
| chr4:69593976
|
TG | T | 187 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(184): Show | 195 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(192): Show |
intron_variant | MODIFIER | c.1304+500delC | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69593976 | ||||||
| chr4:69593977
|
G | T | 42 | a0001c0001t0001g0013a0001c0001t0001g0021a0001c0001t0001g0047others(39): Show | 43 | HG00099.hp1 HG00609.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.1304+500C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69593977 | ||||||
| chr4:69593981
|
G | T | 236 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(233): Show | 245 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.1304+496C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69593981 | ||||||
| chr4:69593985
|
T | G | 32 | a0001c0001t0002g0101a0001c0001t0003g0219a0001c0001t0003g0328others(29): Show | 33 | HG00280.hp1 HG01346.hp2 HG01358.hp1 others(30): Show |
intron_variant | MODIFIER | c.1304+492A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69593985 | ||||||
| chr4:69594067
|
C | T | 149 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(146): Show | 154 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.1304+410G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69594067 | ||||||
| chr4:69594119
|
C | T | 2 | a0001c0001t0002g0041a0001c0001t0002g0193 | 2 | HG04184.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1304+358G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69594119 | ||||||
| chr4:69594458
|
T | C | 1 | a0001c0001t0002g0110 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1304+19A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69594458 | ||||||
| chr4:69594981
|
G | A | 2 | a0001c0001t0001g0088a0001c0001t0001g0170 | 2 | NA18984.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.1084+181C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 5/6 | chr4 | 69594981 | ||||||
| chr4:69595095
|
G | T | 1 | a0001c0001t0002g0081 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1084+67C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 5/6 | chr4 | 69595095 | ||||||
| chr4:69595096
|
C | T | 1 | a0001c0001t0002g0081 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1084+66G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 5/6 | chr4 | 69595096 | ||||||
| chr4:69595328
|
A | G | 8 | a0001c0001t0001g0124a0001c0001t0001g0223a0001c0001t0001g0224others(5): Show | 8 | HG01167.hp1 HG01243.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.997-79T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/6 | chr4 | 69595328 | ||||||
| chr4:69595345
|
G | C | 1 | a0001c0001t0001g0052 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.997-96C>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/6 | chr4 | 69595345 | ||||||
| chr4:69595443
|
C | T | 242 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(239): Show | 253 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(250): Show |
intron_variant | MODIFIER | c.997-194G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/6 | chr4 | 69595443 | ||||||
| chr4:69595466
|
A | G | 149 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(146): Show | 154 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.997-217T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/6 | chr4 | 69595466 | ||||||
| chr4:69595553
|
A | G | 356 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(353): Show | 375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.997-304T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/6 | chr4 | 69595553 | ||||||
| chr4:69595634
|
G | A | 2 | a0002c0002t0001g0330a0002c0002t0001g0331 | 2 | HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.997-385C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/6 | chr4 | 69595634 | ||||||
| chr4:69595727
|
A | C | 2 | a0001c0001t0002g0041a0001c0001t0002g0193 | 2 | HG04184.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.997-478T>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/6 | chr4 | 69595727 | ||||||
| chr4:69595846
|
G | C | 2 | a0005c0005t0005g0125a0005c0005t0005g0288 | 2 | HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.997-597C>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/6 | chr4 | 69595846 | ||||||
| chr4:69596111
|
A | C | 1 | a0001c0001t0001g0258 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.997-862T>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/6 | chr4 | 69596111 | ||||||
| chr4:69596324
|
C | T | 21 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0027others(18): Show | 23 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.997-1075G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/6 | chr4 | 69596324 | ||||||
| chr4:69596532
|
T | C | 120 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(117): Show | 125 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(122): Show |
intron_variant | MODIFIER | c.997-1283A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/6 | chr4 | 69596532 | ||||||
| chr4:69596579
|
G | A | 149 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(146): Show | 154 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.997-1330C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/6 | chr4 | 69596579 | ||||||
| chr4:69596674
|
A | G | 2 | a0001c0001t0001g0094a0001c0001t0001g0116 | 2 | NA18950.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.997-1425T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/6 | chr4 | 69596674 | ||||||
| chr4:69596804
|
G | A | 1 | a0001c0001t0001g0139 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.997-1555C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/6 | chr4 | 69596804 | ||||||
| chr4:69596903
|
A | G | 276 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(273): Show | 289 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(286): Show |
intron_variant | MODIFIER | c.997-1654T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/6 | chr4 | 69596903 | ||||||
| chr4:69596950
|
C | T | 1 | a0001c0001t0001g0249 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.997-1701G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/6 | chr4 | 69596950 | ||||||
| chr4:69596951
|
T | G | 149 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(146): Show | 154 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.997-1702A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/6 | chr4 | 69596951 | ||||||
| chr4:69597085
|
T | G | 242 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(239): Show | 253 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(250): Show |
intron_variant | MODIFIER | c.997-1836A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/6 | chr4 | 69597085 | ||||||
| chr4:69597175
|
C | A | 242 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(239): Show | 253 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(250): Show |
intron_variant | MODIFIER | c.997-1926G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/6 | chr4 | 69597175 | ||||||
| chr4:69597299
|
C | T | 1 | a0004c0004t0001g0195 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.996+1947G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/6 | chr4 | 69597299 | ||||||
| chr4:69597422
|
C | T | 1 | a0001c0001t0001g0325 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.996+1824G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/6 | chr4 | 69597422 | ||||||
| chr4:69597466
|
T | C | 1 | a0004c0004t0001g0313 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.996+1780A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/6 | chr4 | 69597466 | ||||||
| chr4:69597500
|
C | T | 1 | a0001c0001t0002g0046 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.996+1746G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/6 | chr4 | 69597500 | ||||||
| chr4:69597606
|
G | T | 1 | a0001c0001t0001g0117 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.996+1640C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/6 | chr4 | 69597606 | ||||||
| chr4:69597715
|
A | AAC | 146 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(143): Show | 151 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(148): Show |
intron_variant | MODIFIER | c.996+1529_996+1530d others(4): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/6 | chr4 | 69597715 | ||||||
| chr4:69597715
|
A | AACACAC | 8 | a0001c0001t0001g0124a0001c0001t0001g0223a0001c0001t0001g0224others(5): Show | 8 | HG01167.hp1 HG01243.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.996+1525_996+1530d others(8): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/6 | chr4 | 69597715 | ||||||
| chr4:69597882
|
T | G | 120 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(117): Show | 125 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(122): Show |
intron_variant | MODIFIER | c.996+1364A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/6 | chr4 | 69597882 | ||||||
| chr4:69597908
|
T | A | 1 | a0001c0001t0001g0040 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.996+1338A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/6 | chr4 | 69597908 | ||||||
| chr4:69597944
|
T | C | 120 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(117): Show | 125 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(122): Show |
intron_variant | MODIFIER | c.996+1302A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/6 | chr4 | 69597944 | ||||||
| chr4:69597945
|
G | A | 120 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(117): Show | 125 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(122): Show |
intron_variant | MODIFIER | c.996+1301C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/6 | chr4 | 69597945 | ||||||
| chr4:69598136
|
T | A | 89 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(86): Show | 95 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.996+1110A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/6 | chr4 | 69598136 | ||||||
| chr4:69598149
|
G | T | 1 | a0005c0005t0002g0208 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.996+1097C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/6 | chr4 | 69598149 | ||||||
| chr4:69598154
|
C | A | 21 | a0001c0001t0001g0113a0001c0001t0001g0128a0001c0001t0001g0186others(18): Show | 21 | HG00099.hp1 HG00280.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.996+1092G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/6 | chr4 | 69598154 | ||||||
| chr4:69598406
|
C | T | 1 | a0001c0001t0001g0258 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.996+840G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/6 | chr4 | 69598406 | ||||||
| chr4:69598438
|
T | C | 1 | a0002c0002t0001g0352 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.996+808A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/6 | chr4 | 69598438 | ||||||
| chr4:69598631
|
C | A | 4 | a0001c0001t0001g0325a0002c0002t0001g0123a0007c0016t0011g0227others(1): Show | 4 | HG01192.hp2 HG01243.hp1 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.996+615G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/6 | chr4 | 69598631 | ||||||
| chr4:69598695
|
T | A | 149 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(146): Show | 154 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.996+551A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/6 | chr4 | 69598695 | ||||||
| chr4:69598793
|
C | G | 149 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(146): Show | 154 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.996+453G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/6 | chr4 | 69598793 | ||||||
| chr4:69598854
|
C | A | 8 | a0001c0001t0001g0124a0001c0001t0001g0223a0001c0001t0001g0224others(5): Show | 8 | HG01167.hp1 HG01243.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.996+392G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/6 | chr4 | 69598854 | ||||||
| chr4:69598983
|
A | G | 89 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(86): Show | 95 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.996+263T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/6 | chr4 | 69598983 | ||||||
| chr4:69599202
|
T | C | 2 | a0008c0013t0007g0351a0009c0012t0007g0204 | 2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.996+44A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/6 | chr4 | 69599202 | ||||||
| chr4:69599435
|
A | T | 149 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(146): Show | 154 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.848-41T>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69599435 | ||||||
| chr4:69599523
|
T | C | 1 | a0001c0001t0002g0110 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.848-129A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69599523 | ||||||
| chr4:69599689
|
TAAAG | T | 19 | a0003c0003t0002g0133a0003c0003t0002g0149a0003c0003t0002g0150others(16): Show | 20 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(17): Show |
intron_variant | MODIFIER | c.848-299_848-296del others(4): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69599689 | ||||||
| chr4:69599695
|
A | AAGAG | 74 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0026others(71): Show | 74 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.848-305_848-302dup others(4): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69599695 | ||||||
| chr4:69599695
|
A | AAGAGAG | 7 | a0001c0001t0001g0124a0001c0001t0001g0223a0001c0001t0001g0224others(4): Show | 7 | HG01167.hp1 HG02145.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.848-307_848-302dup others(6): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69599695 | ||||||
| chr4:69599695
|
A | G | 93 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(90): Show | 99 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.848-301T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69599695 | ||||||
| chr4:69599723
|
T | C | 238 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(235): Show | 249 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.848-329A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69599723 | ||||||
| chr4:69599775
|
G | A | 149 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(146): Show | 154 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.848-381C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69599775 | ||||||
| chr4:69599866
|
A | G | 120 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(117): Show | 125 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(122): Show |
intron_variant | MODIFIER | c.848-472T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69599866 | ||||||
| chr4:69599896
|
T | A | 1 | a0001c0001t0001g0308 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.848-502A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69599896 | ||||||
| chr4:69599908
|
G | A | 242 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(239): Show | 253 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(250): Show |
intron_variant | MODIFIER | c.848-514C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69599908 | ||||||
| chr4:69599974
|
A | T | 1 | a0001c0001t0003g0328 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.848-580T>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69599974 | ||||||
| chr4:69600019
|
G | T | 156 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(153): Show | 161 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(158): Show |
intron_variant | MODIFIER | c.848-625C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69600019 | ||||||
| chr4:69600087
|
G | A | 1 | a0005c0005t0002g0297 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.848-693C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69600087 | ||||||
| chr4:69600132
|
C | T | 1 | a0002c0002t0003g0318 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.848-738G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69600132 | ||||||
| chr4:69600261
|
C | T | 177 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(174): Show | 183 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.848-867G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69600261 | ||||||
| chr4:69600303
|
C | A | 1 | a0002c0002t0001g0123 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.848-909G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69600303 | ||||||
| chr4:69600321
|
C | A | 1 | a0001c0001t0002g0282 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.848-927G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69600321 | ||||||
| chr4:69600353
|
A | G | 5 | a0001c0001t0001g0029a0001c0001t0001g0142a0001c0001t0001g0156others(2): Show | 5 | HG00639.hp2 HG00741.hp1 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.848-959T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69600353 | ||||||
| chr4:69600502
|
G | A | 6 | a0001c0001t0003g0012a0001c0001t0003g0114a0001c0001t0003g0115others(3): Show | 7 | HG02572.hp1 HG02895.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.848-1108C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69600502 | ||||||
| chr4:69600519
|
C | G | 1 | a0004c0004t0002g0321 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.848-1125G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69600519 | ||||||
| chr4:69600527
|
T | C | 4 | a0002c0002t0001g0330a0002c0002t0001g0331a0002c0002t0008g0295others(1): Show | 4 | HG01109.hp2 HG03139.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.848-1133A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69600527 | ||||||
| chr4:69600539
|
G | A | 1 | a0001c0001t0001g0259 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.848-1145C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69600539 | ||||||
| chr4:69600561
|
C | A | 1 | a0001c0001t0001g0248 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.848-1167G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69600561 | ||||||
| chr4:69600562
|
T | C | 177 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(174): Show | 183 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.848-1168A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69600562 | ||||||
| chr4:69600566
|
T | C | 2 | a0001c0001t0001g0095a0001c0001t0001g0163 | 2 | NA18977.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.848-1172A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69600566 | ||||||
| chr4:69600568
|
G | A | 28 | a0003c0003t0002g0133a0003c0003t0002g0149a0003c0003t0002g0150others(25): Show | 29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.848-1174C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69600568 | ||||||
| chr4:69600620
|
A | T | 3 | a0001c0001t0001g0325a0007c0016t0011g0227a0010c0018t0001g0275 | 3 | HG01192.hp2 HG01243.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.848-1226T>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69600620 | ||||||
| chr4:69600631
|
T | A | 2 | a0001c0001t0001g0031a0001c0001t0001g0113 | 2 | NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.848-1237A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69600631 | ||||||
| chr4:69600649
|
G | T | 85 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(82): Show | 91 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.848-1255C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69600649 | ||||||
| chr4:69600658
|
C | T | 28 | a0003c0003t0002g0133a0003c0003t0002g0149a0003c0003t0002g0150others(25): Show | 29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.848-1264G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69600658 | ||||||
| chr4:69600809
|
T | TA | 119 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(116): Show | 124 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(121): Show |
intron_variant | MODIFIER | c.848-1416dupT | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69600809 | ||||||
| chr4:69600809
|
T | TAA | 27 | a0001c0001t0001g0151a0002c0002t0008g0295a0002c0002t0008g0354others(24): Show | 28 | HG01109.hp2 HG01346.hp2 HG01358.hp1 others(25): Show |
intron_variant | MODIFIER | c.848-1417_848-1416d others(4): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69600809 | ||||||
| chr4:69600875
|
C | T | 93 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(90): Show | 99 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.848-1481G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69600875 | ||||||
| chr4:69600916
|
C | T | 8 | a0001c0001t0001g0013a0001c0001t0001g0050a0001c0001t0001g0071others(5): Show | 9 | HG01070.hp1 HG01071.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.848-1522G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69600916 | ||||||
| chr4:69600924
|
T | C | 93 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(90): Show | 99 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.848-1530A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69600924 | ||||||
| chr4:69600996
|
C | A | 356 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(353): Show | 375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.848-1602G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69600996 | ||||||
| chr4:69601066
|
C | T | 1 | a0005c0005t0005g0125 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.848-1672G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69601066 | ||||||
| chr4:69601072
|
C | T | 2 | a0002c0002t0001g0330a0002c0002t0001g0331 | 2 | HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.848-1678G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69601072 | ||||||
| chr4:69601081
|
T | C | 121 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(118): Show | 128 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(125): Show |
intron_variant | MODIFIER | c.848-1687A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69601081 | ||||||
| chr4:69601092
|
T | G | 93 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(90): Show | 99 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.848-1698A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69601092 | ||||||
| chr4:69601187
|
G | A | 114 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(111): Show | 120 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.848-1793C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69601187 | ||||||
| chr4:69601191
|
G | A | 4 | a0005c0005t0002g0208a0005c0005t0002g0273a0005c0005t0002g0297others(1): Show | 4 | HG02717.hp1 HG02809.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.848-1797C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69601191 | ||||||
| chr4:69601218
|
C | T | 2 | a0008c0013t0007g0351a0009c0012t0007g0204 | 2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.848-1824G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69601218 | ||||||
| chr4:69601308
|
C | T | 1 | a0001c0001t0003g0114 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.848-1914G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69601308 | ||||||
| chr4:69601313
|
T | C | 93 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(90): Show | 99 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.848-1919A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69601313 | ||||||
| chr4:69601364
|
G | A | 2 | a0001c0001t0001g0223a0001c0001t0001g0355 | 2 | HG01243.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.848-1970C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69601364 | ||||||
| chr4:69601384
|
C | T | 85 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(82): Show | 91 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.848-1990G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69601384 | ||||||
| chr4:69601391
|
C | T | 120 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(117): Show | 125 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(122): Show |
intron_variant | MODIFIER | c.848-1997G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69601391 | ||||||
| chr4:69601392
|
G | A | 3 | a0001c0001t0001g0022a0001c0001t0001g0201a0001c0001t0001g0202 | 3 | HG02280.hp1 NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.848-1998C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69601392 | ||||||
| chr4:69601526
|
C | G | 8 | a0001c0001t0001g0124a0001c0001t0001g0223a0001c0001t0001g0224others(5): Show | 8 | HG01167.hp1 HG01243.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.848-2132G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69601526 | ||||||
| chr4:69601617
|
C | T | 2 | a0001c0001t0001g0073a0001c0001t0001g0145 | 2 | NA19003.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.848-2223G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69601617 | ||||||
| chr4:69601741
|
T | C | 93 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(90): Show | 99 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.848-2347A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69601741 | ||||||
| chr4:69601743
|
T | A | 93 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(90): Show | 99 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.848-2349A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69601743 | ||||||
| chr4:69601746
|
A | AG | 93 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(90): Show | 99 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.848-2353_848-2352i others(3): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69601746 | ||||||
| chr4:69601746
|
A | G | 28 | a0003c0003t0002g0133a0003c0003t0002g0149a0003c0003t0002g0150others(25): Show | 29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.848-2352T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69601746 | ||||||
| chr4:69601750
|
A | G | 93 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(90): Show | 99 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.848-2356T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69601750 | ||||||
| chr4:69601753
|
G | C | 93 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(90): Show | 99 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.848-2359C>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69601753 | ||||||
| chr4:69601754
|
G | T | 93 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(90): Show | 99 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.848-2360C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69601754 | ||||||
| chr4:69601755
|
AG | A | 93 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(90): Show | 99 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.848-2362delC | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69601755 | ||||||
| chr4:69601758
|
CTAGAGGA others(5319): Show |
C | 93 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(90): Show | 99 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.848-7690_848-2365d others(2): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69601758 | ||||||
| chr4:69602031
|
A | G | 1 | a0001c0001t0001g0175 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.848-2637T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69602031 | ||||||
| chr4:69602112
|
T | C | 4 | a0005c0005t0002g0208a0005c0005t0002g0273a0005c0005t0002g0297others(1): Show | 4 | HG02717.hp1 HG02809.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.848-2718A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69602112 | ||||||
| chr4:69602216
|
A | AAACTC | 28 | a0003c0003t0002g0133a0003c0003t0002g0149a0003c0003t0002g0150others(25): Show | 29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.848-2823_848-2822i others(7): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69602216 | ||||||
| chr4:69602359
|
C | T | 32 | a0001c0001t0001g0113a0001c0007t0001g0107a0001c0007t0001g0213others(29): Show | 33 | HG00735.hp1 HG01346.hp2 HG01358.hp1 others(30): Show |
intron_variant | MODIFIER | c.848-2965G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69602359 | ||||||
| chr4:69602459
|
G | T | 1 | a0001c0001t0001g0245 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.848-3065C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69602459 | ||||||
| chr4:69602462
|
TTTA | T | 4 | a0003c0003t0004g0008a0003c0010t0002g0146a0005c0005t0002g0273others(1): Show | 5 | HG02165.hp1 HG02809.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.848-3071_848-3069d others(5): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69602462 | ||||||
| chr4:69602462
|
TTTATCTA | T | 21 | a0003c0003t0002g0149a0003c0003t0002g0150a0003c0003t0002g0188others(18): Show | 21 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(18): Show |
intron_variant | MODIFIER | c.848-3075_848-3069d others(9): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69602462 | ||||||
| chr4:69602462
|
TTTATCTA others(4): Show |
T | 3 | a0003c0003t0002g0133a0008c0013t0007g0351a0009c0012t0007g0204 | 3 | HG01884.hp1 HG02630.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.848-3079_848-3069d others(13): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69602462 | ||||||
| chr4:69602463
|
T | TTATC | 11 | a0001c0001t0001g0026a0001c0001t0001g0135a0001c0001t0001g0175others(8): Show | 11 | HG00099.hp2 HG01167.hp1 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.848-3073_848-3070d others(6): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69602463 | ||||||
| chr4:69602463
|
TTATC | T | 37 | a0001c0001t0001g0006a0001c0001t0001g0094a0001c0001t0001g0119others(34): Show | 40 | HG01255.hp1 HG01255.hp2 HG01993.hp1 others(37): Show |
intron_variant | MODIFIER | c.848-3073_848-3070d others(6): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69602463 | ||||||
| chr4:69602463
|
TTATCTAT others(1): Show |
T | 44 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0019others(41): Show | 48 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.848-3077_848-3070d others(10): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69602463 | ||||||
| chr4:69602463
|
TTATCTAT others(5): Show |
T | 3 | a0001c0001t0001g0017a0001c0001t0001g0127a0001c0001t0001g0230 | 3 | HG02970.hp1 HG03130.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.848-3081_848-3070d others(14): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69602463 | ||||||
| chr4:69602587
|
G | A | 1 | a0005c0005t0005g0125 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.848-3193C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69602587 | ||||||
| chr4:69602594
|
A | G | 3 | a0001c0007t0001g0107a0001c0007t0001g0213a0006c0008t0001g0060 | 3 | HG00735.hp1 HG03834.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.848-3200T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69602594 | ||||||
| chr4:69602713
|
C | T | 2 | a0001c0001t0001g0154a0001c0001t0001g0159 | 2 | NA18992.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.848-3319G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69602713 | ||||||
| chr4:69602955
|
A | C | 28 | a0003c0003t0002g0133a0003c0003t0002g0149a0003c0003t0002g0150others(25): Show | 29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.848-3561T>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69602955 | ||||||
| chr4:69603038
|
C | G | 28 | a0003c0003t0002g0133a0003c0003t0002g0149a0003c0003t0002g0150others(25): Show | 29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.848-3644G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69603038 | ||||||
| chr4:69603065
|
T | G | 8 | a0001c0001t0001g0124a0001c0001t0001g0223a0001c0001t0001g0224others(5): Show | 8 | HG01167.hp1 HG01243.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.848-3671A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69603065 | ||||||
| chr4:69603183
|
G | A | 5 | a0001c0001t0001g0258a0005c0005t0002g0208a0005c0005t0002g0273others(2): Show | 5 | HG02717.hp1 HG02809.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.848-3789C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69603183 | ||||||
| chr4:69603196
|
G | C | 1 | a0001c0001t0001g0356 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.848-3802C>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69603196 | ||||||
| chr4:69603288
|
T | A | 3 | a0001c0001t0002g0092a0001c0001t0002g0093a0001c0001t0002g0326 | 3 | NA18965.hp1 NA18967.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.848-3894A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69603288 | ||||||
| chr4:69603352
|
C | T | 28 | a0003c0003t0002g0133a0003c0003t0002g0149a0003c0003t0002g0150others(25): Show | 29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.848-3958G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69603352 | ||||||
| chr4:69603535
|
T | G | 8 | a0001c0001t0001g0124a0001c0001t0001g0223a0001c0001t0001g0224others(5): Show | 8 | HG01167.hp1 HG01243.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.848-4141A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69603535 | ||||||
| chr4:69603542
|
A | C | 28 | a0003c0003t0002g0133a0003c0003t0002g0149a0003c0003t0002g0150others(25): Show | 29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.848-4148T>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69603542 | ||||||
| chr4:69603558
|
C | G | 28 | a0003c0003t0002g0133a0003c0003t0002g0149a0003c0003t0002g0150others(25): Show | 29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.848-4164G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69603558 | ||||||
| chr4:69603614
|
G | A | 28 | a0003c0003t0002g0133a0003c0003t0002g0149a0003c0003t0002g0150others(25): Show | 29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.848-4220C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69603614 | ||||||
| chr4:69603618
|
C | T | 8 | a0001c0001t0001g0124a0001c0001t0001g0223a0001c0001t0001g0224others(5): Show | 8 | HG01167.hp1 HG01243.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.848-4224G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69603618 | ||||||
| chr4:69603630
|
A | G | 28 | a0003c0003t0002g0133a0003c0003t0002g0149a0003c0003t0002g0150others(25): Show | 29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.848-4236T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69603630 | ||||||
| chr4:69603673
|
A | T | 28 | a0003c0003t0002g0133a0003c0003t0002g0149a0003c0003t0002g0150others(25): Show | 29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.848-4279T>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69603673 | ||||||
| chr4:69603699
|
C | A | 28 | a0003c0003t0002g0133a0003c0003t0002g0149a0003c0003t0002g0150others(25): Show | 29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.848-4305G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69603699 | ||||||
| chr4:69603847
|
C | T | 2 | a0005c0005t0005g0125a0005c0005t0005g0288 | 2 | HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.848-4453G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69603847 | ||||||
| chr4:69603935
|
G | A | 19 | a0003c0003t0002g0133a0003c0003t0002g0149a0003c0003t0002g0150others(16): Show | 20 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(17): Show |
intron_variant | MODIFIER | c.848-4541C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69603935 | ||||||
| chr4:69603979
|
T | C | 28 | a0003c0003t0002g0133a0003c0003t0002g0149a0003c0003t0002g0150others(25): Show | 29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.848-4585A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69603979 | ||||||
| chr4:69603983
|
A | G | 1 | a0004c0004t0001g0314 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.848-4589T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69603983 | ||||||
| chr4:69604131
|
A | T | 28 | a0003c0003t0002g0133a0003c0003t0002g0149a0003c0003t0002g0150others(25): Show | 29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.848-4737T>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69604131 | ||||||
| chr4:69604190
|
G | A | 120 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(117): Show | 125 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(122): Show |
intron_variant | MODIFIER | c.848-4796C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69604190 | ||||||
| chr4:69604320
|
C | T | 120 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(117): Show | 125 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(122): Show |
intron_variant | MODIFIER | c.848-4926G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69604320 | ||||||
| chr4:69604327
|
AGAG | A | 28 | a0003c0003t0002g0133a0003c0003t0002g0149a0003c0003t0002g0150others(25): Show | 29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.848-4936_848-4934d others(5): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69604327 | ||||||
| chr4:69604465
|
C | T | 1 | a0004c0004t0001g0314 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.848-5071G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69604465 | ||||||
| chr4:69604479
|
C | A | 28 | a0003c0003t0002g0133a0003c0003t0002g0149a0003c0003t0002g0150others(25): Show | 29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.848-5085G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69604479 | ||||||
| chr4:69604507
|
A | C | 2 | a0008c0013t0007g0351a0009c0012t0007g0204 | 2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.848-5113T>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69604507 | ||||||
| chr4:69604556
|
G | A | 28 | a0003c0003t0002g0133a0003c0003t0002g0149a0003c0003t0002g0150others(25): Show | 29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.848-5162C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69604556 | ||||||
| chr4:69604719
|
G | A | 28 | a0003c0003t0002g0133a0003c0003t0002g0149a0003c0003t0002g0150others(25): Show | 29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.848-5325C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69604719 | ||||||
| chr4:69604890
|
A | G | 1 | a0001c0001t0002g0212 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.848-5496T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69604890 | ||||||
| chr4:69604972
|
A | G | 1 | a0004c0004t0001g0070 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.848-5578T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69604972 | ||||||
| chr4:69604977
|
C | A | 6 | a0004c0004t0001g0035a0004c0004t0001g0183a0004c0004t0001g0221others(3): Show | 6 | HG00099.hp1 HG00280.hp2 HG00738.hp2 others(3): Show |
intron_variant | MODIFIER | c.848-5583G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69604977 | ||||||
| chr4:69604981
|
G | A | 29 | a0003c0003t0002g0133a0003c0003t0002g0149a0003c0003t0002g0150others(26): Show | 30 | HG00741.hp2 HG01346.hp2 HG01358.hp1 others(27): Show |
intron_variant | MODIFIER | c.848-5587C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69604981 | ||||||
| chr4:69604998
|
G | A | 29 | a0003c0003t0002g0133a0003c0003t0002g0149a0003c0003t0002g0150others(26): Show | 30 | HG00741.hp2 HG01346.hp2 HG01358.hp1 others(27): Show |
intron_variant | MODIFIER | c.848-5604C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69604998 | ||||||
| chr4:69605012
|
T | C | 1 | a0004c0004t0001g0070 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.848-5618A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69605012 | ||||||
| chr4:69605014
|
A | G | 1 | a0004c0004t0001g0070 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.848-5620T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69605014 | ||||||
| chr4:69605024
|
A | T | 1 | a0004c0004t0001g0070 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.848-5630T>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69605024 | ||||||
| chr4:69605032
|
T | G | 1 | a0004c0004t0001g0070 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.848-5638A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69605032 | ||||||
| chr4:69605036
|
T | C | 1 | a0004c0004t0001g0070 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.848-5642A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69605036 | ||||||
| chr4:69605265
|
A | T | 1 | a0001c0001t0001g0186 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.848-5871T>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69605265 | ||||||
| chr4:69605266
|
T | C | 1 | a0001c0001t0001g0186 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.848-5872A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69605266 | ||||||
| chr4:69605276
|
A | G | 1 | a0001c0001t0001g0186 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.848-5882T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69605276 | ||||||
| chr4:69605279
|
G | A | 2 | a0004c0004t0001g0070a0004c0004t0001g0314 | 2 | HG00741.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.848-5885C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69605279 | ||||||
| chr4:69605334
|
C | G | 28 | a0003c0003t0002g0133a0003c0003t0002g0149a0003c0003t0002g0150others(25): Show | 29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.848-5940G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69605334 | ||||||
| chr4:69605497
|
T | C | 120 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(117): Show | 125 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(122): Show |
intron_variant | MODIFIER | c.848-6103A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69605497 | ||||||
| chr4:69605560
|
A | G | 1 | a0001c0001t0002g0112 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.848-6166T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69605560 | ||||||
| chr4:69605802
|
C | A | 8 | a0001c0001t0001g0124a0001c0001t0001g0223a0001c0001t0001g0224others(5): Show | 8 | HG01167.hp1 HG01243.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.848-6408G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69605802 | ||||||
| chr4:69605848
|
G | A | 1 | a0001c0001t0002g0291 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.848-6454C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69605848 | ||||||
| chr4:69605991
|
A | T | 28 | a0003c0003t0002g0133a0003c0003t0002g0149a0003c0003t0002g0150others(25): Show | 29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.848-6597T>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69605991 | ||||||
| chr4:69606004
|
G | C | 1 | a0005c0005t0005g0288 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.848-6610C>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69606004 | ||||||
| chr4:69606035
|
G | T | 28 | a0003c0003t0002g0133a0003c0003t0002g0149a0003c0003t0002g0150others(25): Show | 29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.848-6641C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69606035 | ||||||
| chr4:69606047
|
G | C | 1 | a0006c0006t0002g0077 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.848-6653C>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69606047 | ||||||
| chr4:69606117
|
C | CA | 21 | a0001c0001t0001g0113a0001c0001t0001g0128a0001c0001t0001g0186others(18): Show | 21 | HG00099.hp1 HG00280.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.848-6724dupT | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69606117 | ||||||
| chr4:69606157
|
C | T | 28 | a0003c0003t0002g0133a0003c0003t0002g0149a0003c0003t0002g0150others(25): Show | 29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.848-6763G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69606157 | ||||||
| chr4:69606160
|
G | T | 28 | a0003c0003t0002g0133a0003c0003t0002g0149a0003c0003t0002g0150others(25): Show | 29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.848-6766C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69606160 | ||||||
| chr4:69606219
|
C | T | 28 | a0003c0003t0002g0133a0003c0003t0002g0149a0003c0003t0002g0150others(25): Show | 29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.848-6825G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69606219 | ||||||
| chr4:69606224
|
C | T | 2 | a0003c0003t0004g0008a0003c0003t0004g0143 | 3 | NA18970.hp2 NA18997.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.848-6830G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69606224 | ||||||
| chr4:69606247
|
T | G | 28 | a0003c0003t0002g0133a0003c0003t0002g0149a0003c0003t0002g0150others(25): Show | 29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.848-6853A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69606247 | ||||||
| chr4:69606416
|
T | C | 28 | a0003c0003t0002g0133a0003c0003t0002g0149a0003c0003t0002g0150others(25): Show | 29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.848-7022A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69606416 | ||||||
| chr4:69606421
|
C | T | 28 | a0003c0003t0002g0133a0003c0003t0002g0149a0003c0003t0002g0150others(25): Show | 29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.848-7027G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69606421 | ||||||
| chr4:69606440
|
T | C | 1 | a0003c0003t0002g0218 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.848-7046A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69606440 | ||||||
| chr4:69606500
|
T | C | 28 | a0003c0003t0002g0133a0003c0003t0002g0149a0003c0003t0002g0150others(25): Show | 29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.848-7106A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69606500 | ||||||
| chr4:69606573
|
T | G | 28 | a0003c0003t0002g0133a0003c0003t0002g0149a0003c0003t0002g0150others(25): Show | 29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.848-7179A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69606573 | ||||||
| chr4:69606592
|
G | A | 1 | a0003c0003t0002g0218 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.848-7198C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69606592 | ||||||
| chr4:69606601
|
G | C | 28 | a0003c0003t0002g0133a0003c0003t0002g0149a0003c0003t0002g0150others(25): Show | 29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.848-7207C>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69606601 | ||||||
| chr4:69606678
|
G | A | 1 | a0004c0004t0001g0313 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.848-7284C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69606678 | ||||||
| chr4:69606756
|
C | G | 1 | a0001c0001t0001g0308 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.848-7362G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69606756 | ||||||
| chr4:69606761
|
A | G | 2 | a0008c0013t0007g0351a0009c0012t0007g0204 | 2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.848-7367T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69606761 | ||||||
| chr4:69606869
|
C | T | 1 | a0001c0001t0001g0235 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.848-7475G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69606869 | ||||||
| chr4:69606874
|
G | A | 28 | a0003c0003t0002g0133a0003c0003t0002g0149a0003c0003t0002g0150others(25): Show | 29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.848-7480C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69606874 | ||||||
| chr4:69606932
|
T | C | 1 | a0001c0001t0001g0263 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.848-7538A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69606932 | ||||||
| chr4:69606973
|
C | T | 1 | a0001c0001t0001g0162 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.848-7579G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69606973 | ||||||
| chr4:69607055
|
T | C | 28 | a0003c0003t0002g0133a0003c0003t0002g0149a0003c0003t0002g0150others(25): Show | 29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.848-7661A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69607055 | ||||||
| chr4:69607101
|
G | A | 4 | a0002c0002t0001g0330a0002c0002t0001g0331a0002c0002t0008g0295others(1): Show | 4 | HG01109.hp2 HG03139.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.848-7707C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69607101 | ||||||
| chr4:69607122
|
GC | G | 28 | a0003c0003t0002g0133a0003c0003t0002g0149a0003c0003t0002g0150others(25): Show | 29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.848-7729delG | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69607122 | ||||||
| chr4:69607132
|
C | T | 1 | a0011c0014t0002g0082 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.848-7738G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69607132 | ||||||
| chr4:69607167
|
T | C | 1 | a0001c0001t0001g0038 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.848-7773A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69607167 | ||||||
| chr4:69607184
|
G | C | 28 | a0003c0003t0002g0133a0003c0003t0002g0149a0003c0003t0002g0150others(25): Show | 29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.848-7790C>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69607184 | ||||||
| chr4:69607186
|
A | AACCAAAA others(15): Show |
36 | a0001c0001t0001g0325a0002c0002t0001g0123a0002c0002t0001g0330others(33): Show | 37 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.848-7814_848-7793d others(24): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69607186 | ||||||
| chr4:69607194
|
C | T | 2 | a0001c0001t0002g0010a0001c0001t0002g0177 | 3 | HG00642.hp2 HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.848-7800G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69607194 | ||||||
| chr4:69607223
|
A | G | 4 | a0001c0001t0001g0325a0002c0002t0001g0123a0007c0016t0011g0227others(1): Show | 4 | HG01192.hp2 HG01243.hp1 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.848-7829T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69607223 | ||||||
| chr4:69607224
|
A | T | 2 | a0001c0001t0002g0103a0001c0001t0002g0226 | 2 | HG00738.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.848-7830T>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69607224 | ||||||
| chr4:69607228
|
C | T | 2 | a0001c0001t0002g0103a0001c0001t0002g0226 | 2 | HG00738.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.848-7834G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69607228 | ||||||
| chr4:69607248
|
C | T | 4 | a0002c0002t0001g0330a0002c0002t0001g0331a0002c0002t0008g0295others(1): Show | 4 | HG01109.hp2 HG03139.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.848-7854G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69607248 | ||||||
| chr4:69607265
|
C | T | 28 | a0003c0003t0002g0133a0003c0003t0002g0149a0003c0003t0002g0150others(25): Show | 29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.848-7871G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69607265 | ||||||
| chr4:69607266
|
G | A | 276 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(273): Show | 289 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(286): Show |
intron_variant | MODIFIER | c.848-7872C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69607266 | ||||||
| chr4:69607286
|
T | G | 93 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(90): Show | 99 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.848-7892A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69607286 | ||||||
| chr4:69607309
|
G | T | 2 | a0001c0001t0002g0198a0001c0001t0002g0199 | 2 | NA18980.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.848-7915C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69607309 | ||||||
| chr4:69607367
|
T | C | 93 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(90): Show | 99 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.848-7973A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69607367 | ||||||
| chr4:69607368
|
G | A | 85 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(82): Show | 91 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.848-7974C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69607368 | ||||||
| chr4:69607381
|
C | A | 93 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(90): Show | 99 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.848-7987G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69607381 | ||||||
| chr4:69607386
|
A | G | 4 | a0002c0002t0001g0330a0002c0002t0001g0331a0002c0002t0008g0295others(1): Show | 4 | HG01109.hp2 HG03139.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.848-7992T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69607386 | ||||||
| chr4:69607403
|
T | A | 1 | a0001c0001t0001g0160 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.848-8009A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69607403 | ||||||
| chr4:69607444
|
T | G | 2 | a0001c0001t0001g0032a0001c0001t0001g0033 | 2 | HG03669.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.848-8050A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69607444 | ||||||
| chr4:69607488
|
C | T | 1 | a0006c0006t0002g0076 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.848-8094G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69607488 | ||||||
| chr4:69607521
|
T | C | 28 | a0003c0003t0002g0133a0003c0003t0002g0149a0003c0003t0002g0150others(25): Show | 29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.848-8127A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69607521 | ||||||
| chr4:69607522
|
G | C | 28 | a0003c0003t0002g0133a0003c0003t0002g0149a0003c0003t0002g0150others(25): Show | 29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.848-8128C>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69607522 | ||||||
| chr4:69607530
|
C | T | 1 | a0001c0001t0001g0327 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.848-8136G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69607530 | ||||||
| chr4:69607598
|
A | G | 1 | a0001c0001t0001g0158 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.848-8204T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69607598 | ||||||
| chr4:69607610
|
A | C | 28 | a0003c0003t0002g0133a0003c0003t0002g0149a0003c0003t0002g0150others(25): Show | 29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.848-8216T>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69607610 | ||||||
| chr4:69607644
|
G | A | 85 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(82): Show | 91 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.848-8250C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69607644 | ||||||
| chr4:69607824
|
C | T | 93 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(90): Show | 99 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.848-8430G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69607824 | ||||||
| chr4:69607835
|
G | T | 93 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(90): Show | 99 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.848-8441C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69607835 | ||||||
| chr4:69607897
|
G | A | 30 | a0001c0001t0001g0142a0001c0001t0001g0243a0003c0003t0002g0133others(27): Show | 31 | HG01258.hp2 HG01346.hp2 HG01358.hp1 others(28): Show |
intron_variant | MODIFIER | c.848-8503C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69607897 | ||||||
| chr4:69607976
|
T | G | 4 | a0001c0001t0001g0325a0002c0002t0001g0123a0007c0016t0011g0227others(1): Show | 4 | HG01192.hp2 HG01243.hp1 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.848-8582A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69607976 | ||||||
| chr4:69608070
|
G | A | 93 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(90): Show | 99 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.848-8676C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69608070 | ||||||
| chr4:69608137
|
G | A | 1 | a0001c0001t0002g0091 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.848-8743C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69608137 | ||||||
| chr4:69608141
|
T | G | 93 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(90): Show | 99 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.848-8747A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69608141 | ||||||
| chr4:69608143
|
C | A | 93 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(90): Show | 99 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.848-8749G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69608143 | ||||||
| chr4:69608145
|
C | G | 1 | a0001c0001t0001g0333 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.848-8751G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69608145 | ||||||
| chr4:69608168
|
C | G | 1 | a0001c0001t0001g0279 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.848-8774G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69608168 | ||||||
| chr4:69608263
|
C | G | 1 | a0005c0005t0005g0288 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.848-8869G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69608263 | ||||||
| chr4:69608321
|
CA | C | 93 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(90): Show | 99 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.848-8928delT | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69608321 | ||||||
| chr4:69608362
|
T | C | 1 | a0001c0001t0001g0190 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.848-8968A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69608362 | ||||||
| chr4:69608379
|
A | G | 93 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(90): Show | 99 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.848-8985T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69608379 | ||||||
| chr4:69608409
|
G | A | 28 | a0003c0003t0002g0133a0003c0003t0002g0149a0003c0003t0002g0150others(25): Show | 29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.848-9015C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69608409 | ||||||
| chr4:69608431
|
G | A | 93 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(90): Show | 99 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.848-9037C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69608431 | ||||||
| chr4:69608434
|
G | T | 4 | a0001c0001t0001g0325a0002c0002t0001g0123a0007c0016t0011g0227others(1): Show | 4 | HG01192.hp2 HG01243.hp1 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.848-9040C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69608434 | ||||||
| chr4:69608451
|
G | A | 121 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(118): Show | 128 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(125): Show |
intron_variant | MODIFIER | c.848-9057C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69608451 | ||||||
| chr4:69608529
|
C | T | 3 | a0002c0002t0001g0216a0002c0002t0001g0217a0002c0002t0001g0329 | 3 | HG02895.hp1 HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.848-9135G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69608529 | ||||||
| chr4:69608530
|
G | A | 1 | a0005c0005t0002g0208 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.848-9136C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69608530 | ||||||
| chr4:69608592
|
G | A | 270 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(267): Show | 282 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.848-9198C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69608592 | ||||||
| chr4:69608756
|
C | T | 1 | a0001c0001t0001g0235 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.848-9362G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69608756 | ||||||
| chr4:69608767
|
C | T | 3 | a0001c0001t0002g0112a0001c0001t0002g0198a0001c0001t0002g0199 | 3 | NA18980.hp2 NA19058.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.848-9373G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69608767 | ||||||
| chr4:69608989
|
A | T | 1 | a0002c0002t0008g0354 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.848-9595T>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69608989 | ||||||
| chr4:69608992
|
T | C | 3 | a0001c0001t0001g0325a0007c0016t0011g0227a0010c0018t0001g0275 | 3 | HG01192.hp2 HG01243.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.848-9598A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69608992 | ||||||
| chr4:69609051
|
C | T | 1 | a0005c0005t0005g0288 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.848-9657G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69609051 | ||||||
| chr4:69609052
|
G | A | 85 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(82): Show | 91 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.848-9658C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69609052 | ||||||
| chr4:69609080
|
G | A | 85 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(82): Show | 91 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.848-9686C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69609080 | ||||||
| chr4:69609099
|
G | T | 2 | a0008c0013t0007g0351a0009c0012t0007g0204 | 2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.848-9705C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69609099 | ||||||
| chr4:69609155
|
A | AT | 131 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(128): Show | 136 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(133): Show |
intron_variant | MODIFIER | c.848-9762dupA | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69609155 | ||||||
| chr4:69609155
|
A | ATT | 10 | a0001c0001t0001g0018a0001c0001t0001g0026a0001c0001t0001g0106others(7): Show | 10 | HG01261.hp1 HG01496.hp2 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.848-9763_848-9762d others(4): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69609155 | ||||||
| chr4:69609155
|
A | ATTT | 101 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(98): Show | 107 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.848-9764_848-9762d others(5): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69609155 | ||||||
| chr4:69609155
|
AT | A | 27 | a0003c0003t0002g0133a0003c0003t0002g0149a0003c0003t0002g0150others(24): Show | 28 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(25): Show |
intron_variant | MODIFIER | c.848-9762delA | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69609155 | ||||||
| chr4:69609232
|
A | G | 120 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(117): Show | 125 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(122): Show |
intron_variant | MODIFIER | c.848-9838T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69609232 | ||||||
| chr4:69609290
|
C | G | 2 | a0008c0013t0007g0351a0009c0012t0007g0204 | 2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.848-9896G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69609290 | ||||||
| chr4:69609338
|
C | T | 276 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(273): Show | 289 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(286): Show |
intron_variant | MODIFIER | c.848-9944G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69609338 | ||||||
| chr4:69609378
|
G | T | 2 | a0008c0013t0007g0351a0009c0012t0007g0204 | 2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.848-9984C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69609378 | ||||||
| chr4:69609382
|
T | C | 1 | a0001c0001t0001g0068 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.848-9988A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69609382 | ||||||
| chr4:69609412
|
C | G | 21 | a0001c0001t0001g0113a0001c0001t0001g0128a0001c0001t0001g0186others(18): Show | 21 | HG00099.hp1 HG00280.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.848-10018G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69609412 | ||||||
| chr4:69609555
|
G | A | 1 | a0004c0004t0001g0195 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.848-10161C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69609555 | ||||||
| chr4:69609610
|
G | A | 117 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(114): Show | 124 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(121): Show |
intron_variant | MODIFIER | c.848-10216C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69609610 | ||||||
| chr4:69609657
|
C | G | 120 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(117): Show | 125 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(122): Show |
intron_variant | MODIFIER | c.848-10263G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69609657 | ||||||
| chr4:69609658
|
C | G | 1 | a0010c0018t0001g0275 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.848-10264G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69609658 | ||||||
| chr4:69609685
|
CACCTAT | C | 122 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(119): Show | 129 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.848-10297_848-1029 others(10): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69609685 | ||||||
| chr4:69609750
|
C | A | 30 | a0001c0001t0001g0325a0002c0002t0001g0123a0003c0003t0002g0133others(27): Show | 31 | HG01192.hp2 HG01243.hp1 HG01346.hp2 others(28): Show |
intron_variant | MODIFIER | c.848-10356G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69609750 | ||||||
| chr4:69609800
|
A | C | 4 | a0005c0005t0002g0208a0005c0005t0002g0273a0005c0005t0002g0297others(1): Show | 4 | HG02717.hp1 HG02809.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.848-10406T>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69609800 | ||||||
| chr4:69609929
|
A | G | 4 | a0002c0002t0001g0330a0002c0002t0001g0331a0002c0002t0008g0295others(1): Show | 4 | HG01109.hp2 HG03139.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.848-10535T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69609929 | ||||||
| chr4:69610015
|
C | A | 2 | a0002c0002t0008g0295a0002c0002t0008g0354 | 2 | HG01109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.848-10621G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69610015 | ||||||
| chr4:69610070
|
G | A | 1 | a0001c0001t0001g0068 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.848-10676C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69610070 | ||||||
| chr4:69610148
|
A | C | 115 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(112): Show | 122 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(119): Show |
intron_variant | MODIFIER | c.848-10754T>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69610148 | ||||||
| chr4:69610170
|
G | A | 2 | a0008c0013t0007g0351a0009c0012t0007g0204 | 2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.848-10776C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69610170 | ||||||
| chr4:69610246
|
C | CA | 116 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(113): Show | 123 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(120): Show |
intron_variant | MODIFIER | c.848-10853dupT | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69610246 | ||||||
| chr4:69610246
|
C | T | 1 | a0001c0001t0002g0100 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.848-10852G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69610246 | ||||||
| chr4:69610328
|
C | T | 1 | a0001c0001t0002g0110 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.848-10934G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69610328 | ||||||
| chr4:69610481
|
C | A | 6 | a0001c0001t0003g0012a0001c0001t0003g0114a0001c0001t0003g0115others(3): Show | 7 | HG02572.hp1 HG02895.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.848-11087G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69610481 | ||||||
| chr4:69610590
|
C | G | 1 | a0001c0001t0001g0336 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.848-11196G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69610590 | ||||||
| chr4:69610591
|
C | G | 2 | a0002c0002t0001g0330a0002c0002t0001g0331 | 2 | HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.848-11197G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69610591 | ||||||
| chr4:69610591
|
C | T | 2 | a0002c0002t0008g0295a0002c0002t0008g0354 | 2 | HG01109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.848-11197G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69610591 | ||||||
| chr4:69610651
|
G | A | 2 | a0001c0001t0001g0007a0001c0001t0001g0140 | 3 | NA18985.hp1 NA18999.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.848-11257C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69610651 | ||||||
| chr4:69610675
|
T | C | 2 | a0001c0001t0001g0253a0001c0001t0001g0258 | 2 | NA18747.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.848-11281A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69610675 | ||||||
| chr4:69610762
|
T | C | 1 | a0002c0002t0001g0123 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.848-11368A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69610762 | ||||||
| chr4:69610817
|
G | C | 85 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(82): Show | 91 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.848-11423C>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69610817 | ||||||
| chr4:69610847
|
T | C | 6 | a0001c0001t0002g0194a0001c0001t0002g0206a0001c0001t0002g0215others(3): Show | 6 | HG02630.hp1 HG02717.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.848-11453A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69610847 | ||||||
| chr4:69610870
|
G | A | 120 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(117): Show | 125 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(122): Show |
intron_variant | MODIFIER | c.848-11476C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69610870 | ||||||
| chr4:69610877
|
C | T | 30 | a0001c0001t0001g0325a0002c0002t0001g0123a0003c0003t0002g0133others(27): Show | 31 | HG01192.hp2 HG01243.hp1 HG01346.hp2 others(28): Show |
intron_variant | MODIFIER | c.848-11483G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69610877 | ||||||
| chr4:69611005
|
C | G | 121 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(118): Show | 128 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(125): Show |
intron_variant | MODIFIER | c.848-11611G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69611005 | ||||||
| chr4:69611025
|
G | A | 1 | a0001c0001t0003g0219 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.848-11631C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69611025 | ||||||
| chr4:69611113
|
T | TA | 121 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(118): Show | 128 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(125): Show |
intron_variant | MODIFIER | c.848-11720dupT | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69611113 | ||||||
| chr4:69611208
|
C | A | 2 | a0008c0013t0007g0351a0009c0012t0007g0204 | 2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.848-11814G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69611208 | ||||||
| chr4:69611264
|
A | G | 1 | a0001c0001t0001g0278 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.848-11870T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69611264 | ||||||
| chr4:69611265
|
T | C | 2 | a0008c0013t0007g0351a0009c0012t0007g0204 | 2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.848-11871A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69611265 | ||||||
| chr4:69611287
|
G | T | 85 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(82): Show | 91 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.848-11893C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69611287 | ||||||
| chr4:69611288
|
T | TCCAGCTA others(302): Show |
2 | a0001c0001t0001g0054a0001c0001t0001g0283 | 2 | HG03710.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.848-11895_848-1189 others(313): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69611288 | ||||||
| chr4:69611288
|
T | TCCAGCTA others(303): Show |
5 | a0001c0001t0001g0029a0001c0001t0001g0142a0001c0001t0001g0156others(2): Show | 5 | HG00639.hp2 HG00741.hp1 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.848-11895_848-1189 others(314): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69611288 | ||||||
| chr4:69611288
|
T | TCCAGCTA others(303): Show |
73 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(70): Show | 79 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(76): Show |
intron_variant | MODIFIER | c.848-11895_848-1189 others(314): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69611288 | ||||||
| chr4:69611288
|
T | TCCAGCTA others(304): Show |
2 | a0001c0001t0001g0056a0001c0001t0001g0140 | 2 | NA18982.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.848-11895_848-1189 others(315): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69611288 | ||||||
| chr4:69611288
|
T | TCCAGCTA others(323): Show |
1 | a0002c0002t0001g0298 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.848-11895_848-1189 others(334): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69611288 | ||||||
| chr4:69611288
|
T | TCCAGCTA others(324): Show |
1 | a0002c0002t0001g0301 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.848-11895_848-1189 others(335): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69611288 | ||||||
| chr4:69611288
|
T | TCCAGCTA others(342): Show |
1 | a0002c0002t0001g0061 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.848-11895_848-1189 others(353): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69611288 | ||||||
| chr4:69611290
|
C | T | 1 | a0010c0018t0001g0275 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.848-11896G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69611290 | ||||||
| chr4:69611390
|
C | A | 1 | a0005c0005t0005g0125 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.848-11996G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69611390 | ||||||
| chr4:69611398
|
T | C | 1 | a0001c0001t0002g0091 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.848-12004A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69611398 | ||||||
| chr4:69611610
|
G | T | 121 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(118): Show | 128 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(125): Show |
intron_variant | MODIFIER | c.848-12216C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69611610 | ||||||
| chr4:69611854
|
G | T | 121 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(118): Show | 128 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(125): Show |
intron_variant | MODIFIER | c.848-12460C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69611854 | ||||||
| chr4:69611860
|
G | C | 1 | a0002c0002t0001g0330 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.848-12466C>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69611860 | ||||||
| chr4:69611879
|
C | T | 1 | a0001c0001t0001g0336 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.848-12485G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69611879 | ||||||
| chr4:69611940
|
A | G | 8 | a0001c0001t0001g0124a0001c0001t0001g0223a0001c0001t0001g0224others(5): Show | 8 | HG01167.hp1 HG01243.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.848-12546T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69611940 | ||||||
| chr4:69611949
|
T | C | 2 | a0008c0013t0007g0351a0009c0012t0007g0204 | 2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.848-12555A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69611949 | ||||||
| chr4:69611972
|
T | C | 1 | a0001c0001t0001g0266 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.848-12578A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69611972 | ||||||
| chr4:69612147
|
G | A | 121 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(118): Show | 128 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(125): Show |
intron_variant | MODIFIER | c.848-12753C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69612147 | ||||||
| chr4:69612192
|
C | G | 1 | a0002c0002t0001g0123 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.848-12798G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69612192 | ||||||
| chr4:69612266
|
C | T | 121 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(118): Show | 128 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(125): Show |
intron_variant | MODIFIER | c.848-12872G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69612266 | ||||||
| chr4:69612408
|
T | G | 40 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0043others(37): Show | 42 | HG00438.hp2 HG00609.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.848-13014A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69612408 | ||||||
| chr4:69612451
|
C | T | 121 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(118): Show | 128 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(125): Show |
intron_variant | MODIFIER | c.848-13057G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69612451 | ||||||
| chr4:69612465
|
C | T | 30 | a0001c0001t0001g0325a0002c0002t0001g0123a0003c0003t0002g0133others(27): Show | 31 | HG01192.hp2 HG01243.hp1 HG01346.hp2 others(28): Show |
intron_variant | MODIFIER | c.848-13071G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69612465 | ||||||
| chr4:69612486
|
T | G | 1 | a0001c0001t0001g0287 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.848-13092A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69612486 | ||||||
| chr4:69612498
|
G | T | 1 | a0001c0001t0001g0153 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.848-13104C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69612498 | ||||||
| chr4:69612534
|
CAGAT | C | 85 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(82): Show | 91 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.848-13144_848-1314 others(8): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69612534 | ||||||
| chr4:69612592
|
G | C | 8 | a0001c0001t0001g0124a0001c0001t0001g0223a0001c0001t0001g0224others(5): Show | 8 | HG01167.hp1 HG01243.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.848-13198C>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69612592 | ||||||
| chr4:69612673
|
C | T | 1 | a0002c0002t0001g0123 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.848-13279G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69612673 | ||||||
| chr4:69612677
|
T | C | 2 | a0004c0004t0001g0315a0004c0004t0001g0322 | 2 | HG01070.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.848-13283A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69612677 | ||||||
| chr4:69612715
|
T | C | 2 | a0008c0013t0007g0351a0009c0012t0007g0204 | 2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.848-13321A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69612715 | ||||||
| chr4:69612857
|
C | T | 21 | a0001c0001t0001g0113a0001c0001t0001g0128a0001c0001t0001g0186others(18): Show | 21 | HG00099.hp1 HG00280.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.848-13463G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69612857 | ||||||
| chr4:69612869
|
T | A | 2 | a0008c0013t0007g0351a0009c0012t0007g0204 | 2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.848-13475A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69612869 | ||||||
| chr4:69612874
|
A | G | 2 | a0008c0013t0007g0351a0009c0012t0007g0204 | 2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.848-13480T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69612874 | ||||||
| chr4:69612907
|
G | GA | 236 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(233): Show | 249 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.848-13514dupT | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69612907 | ||||||
| chr4:69612907
|
G | GAA | 17 | a0001c0001t0001g0014a0001c0001t0001g0030a0001c0001t0001g0128others(14): Show | 18 | HG01192.hp2 HG01257.hp1 HG01258.hp1 others(15): Show |
intron_variant | MODIFIER | c.848-13515_848-1351 others(6): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69612907 | ||||||
| chr4:69612907
|
G | GAAA | 25 | a0002c0002t0001g0123a0003c0003t0002g0149a0003c0003t0002g0150others(22): Show | 26 | HG01243.hp1 HG01346.hp2 HG01358.hp1 others(23): Show |
intron_variant | MODIFIER | c.848-13516_848-1351 others(7): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69612907 | ||||||
| chr4:69612950
|
T | G | 123 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(120): Show | 130 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.848-13556A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69612950 | ||||||
| chr4:69612961
|
A | T | 123 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(120): Show | 130 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.848-13567T>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69612961 | ||||||
| chr4:69613054
|
TA | T | 121 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(118): Show | 128 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(125): Show |
intron_variant | MODIFIER | c.848-13661delT | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69613054 | ||||||
| chr4:69613066
|
G | A | 84 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(81): Show | 90 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(87): Show |
intron_variant | MODIFIER | c.848-13672C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69613066 | ||||||
| chr4:69613090
|
A | G | 3 | a0001c0001t0001g0325a0007c0016t0011g0227a0010c0018t0001g0275 | 3 | HG01192.hp2 HG01243.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.848-13696T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69613090 | ||||||
| chr4:69613095
|
A | G | 121 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(118): Show | 128 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(125): Show |
intron_variant | MODIFIER | c.848-13701T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69613095 | ||||||
| chr4:69613194
|
T | C | 19 | a0003c0003t0002g0133a0003c0003t0002g0149a0003c0003t0002g0150others(16): Show | 20 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(17): Show |
intron_variant | MODIFIER | c.848-13800A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69613194 | ||||||
| chr4:69613253
|
T | C | 21 | a0001c0001t0001g0113a0001c0001t0001g0128a0001c0001t0001g0186others(18): Show | 21 | HG00099.hp1 HG00280.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.848-13859A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69613253 | ||||||
| chr4:69613304
|
C | T | 1 | a0001c0001t0001g0119 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.848-13910G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69613304 | ||||||
| chr4:69613355
|
A | C | 1 | a0001c0001t0001g0356 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.848-13961T>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69613355 | ||||||
| chr4:69613507
|
CACA | C | 21 | a0001c0001t0001g0113a0001c0001t0001g0128a0001c0001t0001g0186others(18): Show | 21 | HG00099.hp1 HG00280.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.848-14116_848-1411 others(7): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69613507 | ||||||
| chr4:69613693
|
T | C | 29 | a0001c0001t0001g0325a0003c0003t0002g0133a0003c0003t0002g0149others(26): Show | 30 | HG01192.hp2 HG01243.hp1 HG01346.hp2 others(27): Show |
intron_variant | MODIFIER | c.848-14299A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69613693 | ||||||
| chr4:69613829
|
A | G | 6 | a0001c0001t0003g0012a0001c0001t0003g0114a0001c0001t0003g0115others(3): Show | 7 | HG02572.hp1 HG02895.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.848-14435T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69613829 | ||||||
| chr4:69613900
|
C | A | 2 | a0008c0013t0007g0351a0009c0012t0007g0204 | 2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.848-14506G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69613900 | ||||||
| chr4:69613948
|
C | T | 2 | a0002c0002t0008g0295a0002c0002t0008g0354 | 2 | HG01109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.848-14554G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69613948 | ||||||
| chr4:69613967
|
T | C | 1 | a0005c0005t0002g0208 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.848-14573A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69613967 | ||||||
| chr4:69614065
|
G | A | 278 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(275): Show | 291 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(288): Show |
intron_variant | MODIFIER | c.848-14671C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69614065 | ||||||
| chr4:69614112
|
T | A | 93 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(90): Show | 99 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.848-14718A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69614112 | ||||||
| chr4:69614113
|
A | C | 93 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(90): Show | 99 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.848-14719T>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69614113 | ||||||
| chr4:69614114
|
A | T | 93 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(90): Show | 99 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.848-14720T>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69614114 | ||||||
| chr4:69614116
|
C | CTGAATGG others(2): Show |
93 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(90): Show | 99 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.848-14723_848-1472 others(13): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69614116 | ||||||
| chr4:69614117
|
C | T | 93 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(90): Show | 99 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.848-14723G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69614117 | ||||||
| chr4:69614118
|
C | T | 93 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(90): Show | 99 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.848-14724G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69614118 | ||||||
| chr4:69614149
|
T | C | 1 | a0001c0007t0001g0213 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.848-14755A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69614149 | ||||||
| chr4:69614410
|
A | G | 21 | a0001c0001t0001g0113a0001c0001t0001g0128a0001c0001t0001g0186others(18): Show | 21 | HG00099.hp1 HG00280.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.848-15016T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69614410 | ||||||
| chr4:69614415
|
T | A | 123 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(120): Show | 130 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.848-15021A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69614415 | ||||||
| chr4:69614418
|
C | T | 93 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(90): Show | 99 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.848-15024G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69614418 | ||||||
| chr4:69614436
|
C | T | 2 | a0008c0013t0007g0351a0009c0012t0007g0204 | 2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.848-15042G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69614436 | ||||||
| chr4:69614461
|
A | AT | 123 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(120): Show | 130 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.848-15068_848-1506 others(5): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69614461 | ||||||
| chr4:69614501
|
C | G | 1 | a0001c0001t0006g0174 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.848-15107G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69614501 | ||||||
| chr4:69614609
|
T | C | 272 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(269): Show | 284 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(281): Show |
intron_variant | MODIFIER | c.848-15215A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69614609 | ||||||
| chr4:69614617
|
A | C | 272 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(269): Show | 284 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(281): Show |
intron_variant | MODIFIER | c.848-15223T>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69614617 | ||||||
| chr4:69614630
|
C | A | 2 | a0008c0013t0007g0351a0009c0012t0007g0204 | 2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.848-15236G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69614630 | ||||||
| chr4:69614760
|
T | C | 1 | a0001c0001t0001g0054 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.848-15366A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69614760 | ||||||
| chr4:69614836
|
T | C | 2 | a0008c0013t0007g0351a0009c0012t0007g0204 | 2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.848-15442A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69614836 | ||||||
| chr4:69615039
|
C | A | 27 | a0003c0003t0002g0133a0003c0003t0002g0149a0003c0003t0002g0150others(24): Show | 28 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(25): Show |
intron_variant | MODIFIER | c.848-15645G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69615039 | ||||||
| chr4:69615107
|
T | G | 1 | a0001c0001t0002g0210 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.848-15713A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69615107 | ||||||
| chr4:69615157
|
C | T | 8 | a0001c0001t0001g0124a0001c0001t0001g0223a0001c0001t0001g0224others(5): Show | 8 | HG01167.hp1 HG01243.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.848-15763G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69615157 | ||||||
| chr4:69615174
|
C | A | 1 | a0001c0001t0002g0104 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.848-15780G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69615174 | ||||||
| chr4:69615199
|
C | A | 3 | a0007c0016t0011g0227a0008c0013t0007g0351a0009c0012t0007g0204 | 3 | HG01884.hp1 HG02630.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.848-15805G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69615199 | ||||||
| chr4:69615208
|
A | G | 123 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(120): Show | 130 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.848-15814T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69615208 | ||||||
| chr4:69615275
|
G | A | 3 | a0007c0016t0011g0227a0008c0013t0007g0351a0009c0012t0007g0204 | 3 | HG01884.hp1 HG02630.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.848-15881C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69615275 | ||||||
| chr4:69615484
|
G | A | 1 | a0001c0001t0001g0325 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.848-16090C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69615484 | ||||||
| chr4:69615564
|
T | C | 2 | a0001c0001t0001g0325a0010c0018t0001g0275 | 2 | HG01192.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.848-16170A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69615564 | ||||||
| chr4:69615702
|
A | C | 1 | a0001c0001t0001g0141 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.848-16308T>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69615702 | ||||||
| chr4:69615724
|
G | A | 124 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(121): Show | 131 | HG00140.hp1 HG00423.hp1 HG00597.hp2 others(128): Show |
intron_variant | MODIFIER | c.848-16330C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69615724 | ||||||
| chr4:69615731
|
A | G | 2 | a0002c0002t0008g0295a0002c0002t0008g0354 | 2 | HG01109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.848-16337T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69615731 | ||||||
| chr4:69615786
|
G | A | 3 | a0001c0001t0001g0109a0001c0001t0001g0348a0012c0015t0001g0168 | 3 | NA18939.hp1 NA18946.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.848-16392C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69615786 | ||||||
| chr4:69615858
|
C | CA | 68 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(65): Show | 73 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.848-16465dupT | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69615858 | ||||||
| chr4:69615890
|
C | T | 2 | a0002c0002t0008g0295a0002c0002t0008g0354 | 2 | HG01109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.848-16496G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69615890 | ||||||
| chr4:69615935
|
T | C | 1 | a0001c0001t0001g0325 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.848-16541A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69615935 | ||||||
| chr4:69615969
|
C | T | 1 | a0002c0002t0003g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.848-16575G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69615969 | ||||||
| chr4:69615987
|
C | T | 102 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(99): Show | 108 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.848-16593G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69615987 | ||||||
| chr4:69616115
|
C | T | 26 | a0002c0002t0001g0123a0003c0003t0002g0133a0003c0003t0002g0149others(23): Show | 27 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(24): Show |
intron_variant | MODIFIER | c.848-16721G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69616115 | ||||||
| chr4:69616118
|
G | A | 2 | a0008c0013t0007g0351a0009c0012t0007g0204 | 2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.848-16724C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69616118 | ||||||
| chr4:69616119
|
G | A | 1 | a0003c0003t0002g0343 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.848-16725C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69616119 | ||||||
| chr4:69616162
|
A | G | 137 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(134): Show | 144 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.848-16768T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69616162 | ||||||
| chr4:69616292
|
A | G | 4 | a0001c0001t0001g0142a0001c0001t0001g0156a0001c0001t0001g0243others(1): Show | 4 | HG00639.hp2 HG00741.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.848-16898T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69616292 | ||||||
| chr4:69616379
|
T | C | 116 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(113): Show | 122 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.848-16985A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69616379 | ||||||
| chr4:69616382
|
G | C | 1 | a0001c0001t0001g0339 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.848-16988C>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69616382 | ||||||
| chr4:69616604
|
A | G | 1 | a0001c0001t0001g0176 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.848-17210T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69616604 | ||||||
| chr4:69616667
|
T | C | 6 | a0001c0001t0002g0194a0001c0001t0002g0206a0001c0001t0002g0215others(3): Show | 6 | HG02630.hp1 HG02717.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.848-17273A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69616667 | ||||||
| chr4:69616698
|
G | A | 356 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(353): Show | 375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.848-17304C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69616698 | ||||||
| chr4:69616751
|
A | G | 1 | a0001c0001t0002g0066 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.848-17357T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69616751 | ||||||
| chr4:69616833
|
C | CT | 18 | a0001c0001t0001g0154a0001c0001t0002g0011a0001c0001t0002g0023others(15): Show | 19 | HG01243.hp1 HG01934.hp1 HG02630.hp1 others(16): Show |
intron_variant | MODIFIER | c.848-17440dupA | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69616833 | ||||||
| chr4:69616833
|
C | CTT | 35 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0019others(32): Show | 39 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.848-17441_848-1744 others(6): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69616833 | ||||||
| chr4:69616833
|
C | CTTT | 108 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0018others(105): Show | 109 | HG00544.hp1 HG00609.hp1 HG00621.hp2 others(106): Show |
intron_variant | MODIFIER | c.848-17442_848-1744 others(7): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69616833 | ||||||
| chr4:69616833
|
CT | C | 23 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0027others(20): Show | 25 | HG00140.hp1 HG00423.hp1 HG00544.hp2 others(22): Show |
intron_variant | MODIFIER | c.848-17440delA | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69616833 | ||||||
| chr4:69616833
|
CTT | C | 78 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0043others(75): Show | 82 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.848-17441_848-1744 others(6): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69616833 | ||||||
| chr4:69616850
|
T | G | 2 | a0002c0002t0001g0330a0002c0002t0001g0331 | 2 | HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.848-17456A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69616850 | ||||||
| chr4:69617324
|
G | A | 112 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(109): Show | 118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.848-17930C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69617324 | ||||||
| chr4:69617448
|
T | C | 6 | a0001c0001t0003g0012a0001c0001t0003g0114a0001c0001t0003g0115others(3): Show | 7 | HG02572.hp1 HG02895.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.848-18054A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69617448 | ||||||
| chr4:69617469
|
G | A | 1 | a0002c0002t0001g0352 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.848-18075C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69617469 | ||||||
| chr4:69617482
|
C | T | 1 | a0001c0001t0001g0155 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.848-18088G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69617482 | ||||||
| chr4:69617511
|
A | C | 1 | a0002c0002t0001g0179 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.848-18117T>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69617511 | ||||||
| chr4:69617532
|
A | G | 1 | a0003c0003t0002g0218 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.848-18138T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69617532 | ||||||
| chr4:69617605
|
A | C | 112 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(109): Show | 118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.847+18086T>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69617605 | ||||||
| chr4:69617630
|
C | T | 9 | a0002c0002t0001g0330a0002c0002t0001g0331a0002c0002t0008g0295others(6): Show | 9 | HG01109.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.847+18061G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69617630 | ||||||
| chr4:69617733
|
C | T | 112 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(109): Show | 118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.847+17958G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69617733 | ||||||
| chr4:69617771
|
C | G | 6 | a0001c0001t0002g0194a0001c0001t0002g0206a0001c0001t0002g0215others(3): Show | 6 | HG02630.hp1 HG02717.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.847+17920G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69617771 | ||||||
| chr4:69617969
|
T | C | 2 | a0008c0013t0007g0351a0009c0012t0007g0204 | 2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.847+17722A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69617969 | ||||||
| chr4:69618187
|
A | ATG | 199 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(196): Show | 210 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.847+17502_847+1750 others(6): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69618187 | ||||||
| chr4:69618187
|
A | ATGTG | 17 | a0001c0001t0001g0116a0001c0001t0001g0130a0001c0001t0001g0131others(14): Show | 17 | HG00423.hp2 HG01192.hp1 HG01192.hp2 others(14): Show |
intron_variant | MODIFIER | c.847+17500_847+1750 others(8): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69618187 | ||||||
| chr4:69618187
|
ATGTGTG | A | 3 | a0002c0002t0008g0295a0002c0002t0008g0354a0003c0009t0002g0214 | 3 | HG01109.hp2 HG02602.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.847+17498_847+1750 others(10): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69618187 | ||||||
| chr4:69618201
|
G | GTGTGTGT others(5): Show |
8 | a0001c0001t0001g0014a0001c0001t0001g0030a0001c0001t0001g0167others(5): Show | 9 | HG00423.hp1 HG02615.hp2 NA18968.hp2 others(6): Show |
intron_variant | MODIFIER | c.847+17489_847+1749 others(16): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69618201 | ||||||
| chr4:69618203
|
G | GTGTGTAT others(3): Show |
4 | a0001c0001t0001g0029a0001c0001t0001g0278a0001c0001t0006g0174others(1): Show | 4 | HG01106.hp1 HG01891.hp2 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.847+17487_847+1748 others(14): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69618203 | ||||||
| chr4:69618205
|
G | GTGTATGT others(1): Show |
8 | a0001c0001t0001g0015a0001c0001t0001g0027a0001c0001t0001g0031others(5): Show | 9 | HG01099.hp1 HG01516.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.847+17485_847+1748 others(12): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69618205 | ||||||
| chr4:69618205
|
G | GTGTGTGT others(5): Show |
1 | a0002c0002t0003g0063 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.847+17485_847+1748 others(16): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69618205 | ||||||
| chr4:69618207
|
G | GTGTA | 24 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0054others(21): Show | 24 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.847+17483_847+1748 others(8): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69618207 | ||||||
| chr4:69618207
|
G | GTGTATGT others(1): Show |
12 | a0001c0001t0001g0007a0001c0001t0001g0052a0001c0001t0001g0053others(9): Show | 13 | HG01884.hp1 HG02258.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.847+17483_847+1748 others(12): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69618207 | ||||||
| chr4:69618209
|
G | GTA | 9 | a0001c0001t0001g0045a0002c0002t0001g0179a0004c0004t0001g0057others(6): Show | 9 | HG01496.hp1 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.847+17481_847+1748 others(6): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69618209 | ||||||
| chr4:69618209
|
G | GTATGTT | 40 | a0001c0001t0001g0013a0001c0001t0001g0047a0001c0001t0001g0048others(37): Show | 43 | HG00597.hp2 HG00609.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.847+17481_847+1748 others(10): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69618209 | ||||||
| chr4:69618209
|
G | T | 1 | a0001c0001t0001g0305 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.847+17482C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69618209 | ||||||
| chr4:69618211
|
G | A | 7 | a0001c0001t0001g0113a0001c0001t0001g0128a0001c0001t0001g0186others(4): Show | 7 | HG02922.hp1 HG02976.hp2 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.847+17480C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69618211 | ||||||
| chr4:69618211
|
G | T | 24 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0054others(21): Show | 24 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.847+17480C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69618211 | ||||||
| chr4:69618213
|
G | A | 2 | a0002c0002t0001g0330a0002c0002t0001g0331 | 2 | HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.847+17478C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69618213 | ||||||
| chr4:69618213
|
G | T | 9 | a0001c0001t0001g0045a0002c0002t0001g0179a0004c0004t0001g0057others(6): Show | 9 | HG01496.hp1 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.847+17478C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69618213 | ||||||
| chr4:69618213
|
GTGTA | G | 7 | a0001c0001t0001g0113a0001c0001t0001g0128a0001c0001t0001g0186others(4): Show | 7 | HG02922.hp1 HG02976.hp2 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.847+17474_847+1747 others(8): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69618213 | ||||||
| chr4:69618217
|
A | G | 108 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(105): Show | 114 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.847+17474T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69618217 | ||||||
| chr4:69618217
|
A | T | 2 | a0002c0002t0001g0330a0002c0002t0001g0331 | 2 | HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.847+17474T>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69618217 | ||||||
| chr4:69618219
|
G | T | 7 | a0001c0001t0001g0113a0001c0001t0001g0128a0001c0001t0001g0186others(4): Show | 7 | HG02922.hp1 HG02976.hp2 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.847+17472C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69618219 | ||||||
| chr4:69618221
|
T | G | 117 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(114): Show | 123 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.847+17470A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69618221 | ||||||
| chr4:69618221
|
T | TTG | 91 | a0001c0001t0001g0088a0001c0001t0001g0094a0001c0001t0001g0095others(88): Show | 98 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.847+17468_847+1746 others(6): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69618221 | ||||||
| chr4:69618221
|
T | TTGTG | 146 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(143): Show | 152 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(149): Show |
intron_variant | MODIFIER | c.847+17466_847+1746 others(8): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69618221 | ||||||
| chr4:69618239
|
A | G | 112 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(109): Show | 118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.847+17452T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69618239 | ||||||
| chr4:69618328
|
C | A | 112 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(109): Show | 118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.847+17363G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69618328 | ||||||
| chr4:69618350
|
CATA | C | 79 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0043others(76): Show | 83 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.847+17338_847+1734 others(7): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69618350 | ||||||
| chr4:69618471
|
T | G | 112 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(109): Show | 118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.847+17220A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69618471 | ||||||
| chr4:69618512
|
T | A | 2 | a0001c0001t0001g0245a0001c0011t0001g0132 | 2 | HG02602.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.847+17179A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69618512 | ||||||
| chr4:69618512
|
T | C | 1 | a0001c0001t0001g0235 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.847+17179A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69618512 | ||||||
| chr4:69618532
|
G | A | 21 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0027others(18): Show | 23 | HG00140.hp1 HG00423.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.847+17159C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69618532 | ||||||
| chr4:69618674
|
G | T | 1 | a0010c0018t0001g0275 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.847+17017C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69618674 | ||||||
| chr4:69618777
|
A | G | 1 | a0001c0001t0002g0212 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.847+16914T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69618777 | ||||||
| chr4:69618915
|
T | A | 9 | a0001c0001t0001g0007a0001c0001t0001g0053a0001c0001t0001g0055others(6): Show | 10 | NA18950.hp2 NA18964.hp1 NA18982.hp1 others(7): Show |
intron_variant | MODIFIER | c.847+16776A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69618915 | ||||||
| chr4:69618960
|
T | G | 1 | a0001c0001t0001g0186 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.847+16731A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69618960 | ||||||
| chr4:69618993
|
T | C | 1 | a0001c0001t0002g0097 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.847+16698A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69618993 | ||||||
| chr4:69619079
|
A | T | 1 | a0001c0001t0001g0096 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.847+16612T>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69619079 | ||||||
| chr4:69619122
|
C | T | 21 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0027others(18): Show | 23 | HG00140.hp1 HG00423.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.847+16569G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69619122 | ||||||
| chr4:69619395
|
G | A | 5 | a0001c0001t0001g0014a0001c0001t0001g0030a0001c0001t0001g0167others(2): Show | 6 | NA18968.hp2 NA18988.hp2 NA19067.hp1 others(3): Show |
intron_variant | MODIFIER | c.847+16296C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69619395 | ||||||
| chr4:69619420
|
C | CATAAA | 99 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(96): Show | 105 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.847+16266_847+1627 others(9): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69619420 | ||||||
| chr4:69619420
|
C | CATAAAAT others(3): Show |
5 | a0001c0001t0002g0046a0002c0002t0008g0295a0002c0002t0008g0354others(2): Show | 5 | HG00597.hp2 HG01109.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.847+16261_847+1627 others(14): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69619420 | ||||||
| chr4:69619420
|
C | CATAAAAT others(8): Show |
5 | a0002c0002t0001g0330a0002c0002t0001g0331a0005c0005t0002g0208others(2): Show | 5 | HG02717.hp1 HG02809.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.847+16256_847+1627 others(19): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69619420 | ||||||
| chr4:69619470
|
T | C | 110 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(107): Show | 116 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.847+16221A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69619470 | ||||||
| chr4:69619517
|
C | T | 5 | a0001c0001t0001g0325a0001c0001t0002g0229a0001c0001t0002g0337others(2): Show | 5 | HG01192.hp2 HG01243.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.847+16174G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69619517 | ||||||
| chr4:69619518
|
G | T | 1 | a0003c0003t0002g0218 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.847+16173C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69619518 | ||||||
| chr4:69619551
|
A | T | 1 | a0005c0005t0002g0297 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.847+16140T>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69619551 | ||||||
| chr4:69619909
|
C | T | 267 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(264): Show | 279 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(276): Show |
intron_variant | MODIFIER | c.847+15782G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69619909 | ||||||
| chr4:69619945
|
T | C | 79 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0043others(76): Show | 83 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.847+15746A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69619945 | ||||||
| chr4:69619990
|
T | C | 112 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(109): Show | 118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.847+15701A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69619990 | ||||||
| chr4:69620125
|
C | T | 112 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(109): Show | 118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.847+15566G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69620125 | ||||||
| chr4:69620189
|
A | G | 1 | a0010c0018t0001g0275 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.847+15502T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69620189 | ||||||
| chr4:69620221
|
T | C | 1 | a0002c0002t0001g0178 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.847+15470A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69620221 | ||||||
| chr4:69620288
|
C | G | 1 | a0003c0003t0002g0218 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.847+15403G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69620288 | ||||||
| chr4:69620291
|
G | GA | 111 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(108): Show | 117 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.847+15399dupT | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69620291 | ||||||
| chr4:69620341
|
G | A | 1 | a0005c0005t0005g0288 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.847+15350C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69620341 | ||||||
| chr4:69620379
|
A | AAAATGCC others(37): Show |
8 | a0001c0001t0001g0113a0001c0001t0001g0128a0001c0001t0001g0186others(5): Show | 8 | HG02602.hp2 HG02922.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.847+15311_847+1531 others(48): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69620379 | ||||||
| chr4:69620381
|
T | A | 8 | a0001c0001t0001g0113a0001c0001t0001g0128a0001c0001t0001g0186others(5): Show | 8 | HG02602.hp2 HG02922.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.847+15310A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69620381 | ||||||
| chr4:69620655
|
CA | C | 81 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0037others(78): Show | 85 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.847+15035delT | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69620655 | ||||||
| chr4:69620655
|
CAA | C | 9 | a0002c0002t0001g0330a0002c0002t0001g0331a0002c0002t0008g0295others(6): Show | 9 | HG01109.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.847+15034_847+1503 others(6): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69620655 | ||||||
| chr4:69620772
|
T | C | 1 | a0002c0002t0001g0179 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.847+14919A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69620772 | ||||||
| chr4:69620794
|
A | G | 9 | a0002c0002t0001g0330a0002c0002t0001g0331a0002c0002t0008g0295others(6): Show | 9 | HG01109.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.847+14897T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69620794 | ||||||
| chr4:69620932
|
C | G | 112 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(109): Show | 118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.847+14759G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69620932 | ||||||
| chr4:69621091
|
G | T | 21 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0027others(18): Show | 23 | HG00140.hp1 HG00423.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.847+14600C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69621091 | ||||||
| chr4:69621114
|
C | T | 5 | a0001c0001t0002g0323a0003c0003t0002g0302a0003c0003t0002g0340others(2): Show | 5 | HG01358.hp1 HG02451.hp1 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.847+14577G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69621114 | ||||||
| chr4:69621291
|
C | G | 1 | a0003c0003t0002g0218 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.847+14400G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69621291 | ||||||
| chr4:69621371
|
G | A | 1 | a0001c0001t0002g0171 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.847+14320C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69621371 | ||||||
| chr4:69621384
|
A | T | 1 | a0004c0004t0001g0057 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.847+14307T>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69621384 | ||||||
| chr4:69621491
|
A | T | 112 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(109): Show | 118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.847+14200T>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69621491 | ||||||
| chr4:69621585
|
C | T | 4 | a0001c0001t0001g0113a0001c0007t0001g0107a0001c0007t0001g0213others(1): Show | 4 | HG02602.hp2 HG03834.hp1 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.847+14106G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69621585 | ||||||
| chr4:69621621
|
T | A | 147 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(144): Show | 153 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(150): Show |
intron_variant | MODIFIER | c.847+14070A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69621621 | ||||||
| chr4:69621656
|
C | T | 112 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(109): Show | 118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.847+14035G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69621656 | ||||||
| chr4:69621679
|
C | T | 20 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0027others(17): Show | 22 | HG00140.hp1 HG00423.hp1 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.847+14012G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69621679 | ||||||
| chr4:69621711
|
T | C | 2 | a0002c0002t0001g0061a0005c0005t0005g0288 | 2 | HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.847+13980A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69621711 | ||||||
| chr4:69621894
|
A | G | 2 | a0004c0004t0001g0059a0004c0004t0001g0313 | 2 | HG01943.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.847+13797T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69621894 | ||||||
| chr4:69622043
|
T | C | 112 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(109): Show | 118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.847+13648A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69622043 | ||||||
| chr4:69622044
|
A | C | 80 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0043others(77): Show | 84 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.847+13647T>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69622044 | ||||||
| chr4:69622244
|
A | T | 112 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(109): Show | 118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.847+13447T>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69622244 | ||||||
| chr4:69622271
|
GTAA | G | 3 | a0001c0007t0001g0107a0001c0007t0001g0213a0003c0009t0002g0214 | 3 | HG02602.hp2 HG03834.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.847+13417_847+1341 others(7): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69622271 | ||||||
| chr4:69622304
|
G | C | 101 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(98): Show | 107 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.847+13387C>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69622304 | ||||||
| chr4:69622389
|
A | G | 11 | a0002c0002t0001g0330a0002c0002t0001g0331a0002c0002t0008g0295others(8): Show | 11 | HG01109.hp2 HG01884.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.847+13302T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69622389 | ||||||
| chr4:69622559
|
A | G | 1 | a0007c0016t0011g0227 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.847+13132T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69622559 | ||||||
| chr4:69622642
|
C | A | 112 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(109): Show | 118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.847+13049G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69622642 | ||||||
| chr4:69622662
|
G | C | 11 | a0002c0002t0001g0330a0002c0002t0001g0331a0002c0002t0008g0295others(8): Show | 11 | HG01109.hp2 HG01884.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.847+13029C>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69622662 | ||||||
| chr4:69622689
|
T | C | 1 | a0002c0002t0008g0354 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.847+13002A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69622689 | ||||||
| chr4:69622735
|
T | A | 7 | a0001c0001t0001g0113a0001c0001t0001g0128a0001c0001t0001g0308others(4): Show | 7 | HG02602.hp2 HG02922.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.847+12956A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69622735 | ||||||
| chr4:69622823
|
C | G | 9 | a0002c0002t0001g0330a0002c0002t0001g0331a0002c0002t0008g0295others(6): Show | 9 | HG01109.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.847+12868G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69622823 | ||||||
| chr4:69622860
|
T | A | 1 | a0001c0001t0002g0078 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.847+12831A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69622860 | ||||||
| chr4:69623025
|
T | G | 1 | a0003c0003t0002g0302 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.847+12666A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69623025 | ||||||
| chr4:69623068
|
T | G | 79 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0043others(76): Show | 83 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.847+12623A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69623068 | ||||||
| chr4:69623086
|
A | C | 279 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(276): Show | 292 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(289): Show |
intron_variant | MODIFIER | c.847+12605T>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69623086 | ||||||
| chr4:69623131
|
T | C | 112 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(109): Show | 118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.847+12560A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69623131 | ||||||
| chr4:69623168
|
C | T | 1 | a0001c0001t0009g0016 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.847+12523G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69623168 | ||||||
| chr4:69623324
|
T | A | 1 | a0001c0001t0002g0078 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.847+12367A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69623324 | ||||||
| chr4:69623421
|
A | G | 112 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(109): Show | 118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.847+12270T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69623421 | ||||||
| chr4:69623434
|
A | G | 79 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0043others(76): Show | 83 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.847+12257T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69623434 | ||||||
| chr4:69623436
|
A | C | 1 | a0002c0002t0001g0331 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.847+12255T>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69623436 | ||||||
| chr4:69623534
|
A | G | 16 | a0002c0002t0001g0062a0002c0002t0001g0178a0002c0002t0001g0179others(13): Show | 18 | HG00642.hp1 HG01884.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.847+12157T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69623534 | ||||||
| chr4:69623563
|
C | T | 112 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(109): Show | 118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.847+12128G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69623563 | ||||||
| chr4:69623564
|
A | G | 112 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(109): Show | 118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.847+12127T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69623564 | ||||||
| chr4:69623667
|
C | G | 112 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(109): Show | 118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.847+12024G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69623667 | ||||||
| chr4:69623701
|
A | G | 80 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0043others(77): Show | 84 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.847+11990T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69623701 | ||||||
| chr4:69623728
|
G | A | 79 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0043others(76): Show | 83 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.847+11963C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69623728 | ||||||
| chr4:69624013
|
A | C | 112 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(109): Show | 118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.847+11678T>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69624013 | ||||||
| chr4:69624075
|
G | A | 1 | a0001c0001t0001g0141 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.847+11616C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69624075 | ||||||
| chr4:69624231
|
C | T | 20 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0027others(17): Show | 22 | HG00140.hp1 HG00423.hp1 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.847+11460G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69624231 | ||||||
| chr4:69624399
|
T | A | 112 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(109): Show | 118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.847+11292A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69624399 | ||||||
| chr4:69624488
|
A | G | 1 | a0010c0018t0001g0275 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.847+11203T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69624488 | ||||||
| chr4:69624514
|
G | T | 112 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(109): Show | 118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.847+11177C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69624514 | ||||||
| chr4:69624588
|
T | C | 3 | a0002c0002t0001g0069a0002c0002t0001g0280a0002c0002t0001g0281 | 3 | NA18967.hp2 NA18986.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.847+11103A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69624588 | ||||||
| chr4:69624620
|
T | C | 1 | a0001c0001t0001g0038 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.847+11071A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69624620 | ||||||
| chr4:69624803
|
G | T | 79 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0043others(76): Show | 83 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.847+10888C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69624803 | ||||||
| chr4:69624867
|
T | C | 112 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(109): Show | 118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.847+10824A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69624867 | ||||||
| chr4:69624908
|
G | A | 2 | a0002c0002t0001g0298a0002c0002t0001g0301 | 2 | HG02004.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.847+10783C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69624908 | ||||||
| chr4:69624971
|
T | C | 1 | a0001c0001t0002g0323 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.847+10720A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69624971 | ||||||
| chr4:69625003
|
C | CA | 111 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(108): Show | 117 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.847+10687dupT | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69625003 | ||||||
| chr4:69625022
|
T | A | 1 | a0001c0001t0001g0074 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.847+10669A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69625022 | ||||||
| chr4:69625074
|
A | G | 4 | a0002c0002t0001g0330a0002c0002t0001g0331a0002c0002t0008g0295others(1): Show | 4 | HG01109.hp2 HG03139.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.847+10617T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69625074 | ||||||
| chr4:69625165
|
CT | C | 112 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(109): Show | 118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.847+10525delA | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69625165 | ||||||
| chr4:69625185
|
T | G | 5 | a0005c0005t0002g0208a0005c0005t0002g0273a0005c0005t0002g0297others(2): Show | 5 | HG02717.hp1 HG02809.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.847+10506A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69625185 | ||||||
| chr4:69625220
|
T | A | 9 | a0002c0002t0001g0330a0002c0002t0001g0331a0002c0002t0008g0295others(6): Show | 9 | HG01109.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.847+10471A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69625220 | ||||||
| chr4:69625236
|
C | G | 112 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(109): Show | 118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.847+10455G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69625236 | ||||||
| chr4:69625551
|
A | G | 9 | a0002c0002t0001g0330a0002c0002t0001g0331a0002c0002t0008g0295others(6): Show | 9 | HG01109.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.847+10140T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69625551 | ||||||
| chr4:69625613
|
T | C | 1 | a0001c0001t0002g0110 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.847+10078A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69625613 | ||||||
| chr4:69625661
|
C | T | 1 | a0001c0001t0001g0333 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.847+10030G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69625661 | ||||||
| chr4:69625790
|
C | G | 112 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(109): Show | 118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.847+9901G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69625790 | ||||||
| chr4:69625896
|
T | C | 112 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(109): Show | 118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.847+9795A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69625896 | ||||||
| chr4:69626039
|
T | G | 1 | a0001c0001t0002g0215 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.847+9652A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69626039 | ||||||
| chr4:69626077
|
C | G | 112 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(109): Show | 118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.847+9614G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69626077 | ||||||
| chr4:69626090
|
T | G | 112 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(109): Show | 118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.847+9601A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69626090 | ||||||
| chr4:69626155
|
T | G | 1 | a0001c0001t0001g0026 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.847+9536A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69626155 | ||||||
| chr4:69626173
|
A | G | 147 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(144): Show | 153 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(150): Show |
intron_variant | MODIFIER | c.847+9518T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69626173 | ||||||
| chr4:69626252
|
C | T | 112 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(109): Show | 118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.847+9439G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69626252 | ||||||
| chr4:69626267
|
T | G | 1 | a0001c0001t0006g0174 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.847+9424A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69626267 | ||||||
| chr4:69626303
|
C | T | 8 | a0001c0001t0001g0113a0001c0001t0001g0128a0001c0001t0001g0186others(5): Show | 8 | HG02602.hp2 HG02922.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.847+9388G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69626303 | ||||||
| chr4:69626313
|
G | T | 21 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0027others(18): Show | 23 | HG00140.hp1 HG00423.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.847+9378C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69626313 | ||||||
| chr4:69626323
|
G | T | 112 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(109): Show | 118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.847+9368C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69626323 | ||||||
| chr4:69626337
|
G | A | 21 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0027others(18): Show | 23 | HG00140.hp1 HG00423.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.847+9354C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69626337 | ||||||
| chr4:69626424
|
A | G | 9 | a0002c0002t0001g0330a0002c0002t0001g0331a0002c0002t0008g0295others(6): Show | 9 | HG01109.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.847+9267T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69626424 | ||||||
| chr4:69626587
|
G | A | 112 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(109): Show | 118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.847+9104C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69626587 | ||||||
| chr4:69626669
|
TA | T | 112 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(109): Show | 118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.847+9021delT | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69626669 | ||||||
| chr4:69626714
|
A | C | 1 | a0002c0002t0001g0062 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.847+8977T>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69626714 | ||||||
| chr4:69626760
|
T | C | 7 | a0001c0001t0001g0021a0001c0001t0001g0117a0001c0001t0001g0254others(4): Show | 7 | HG00621.hp2 HG02165.hp2 NA18961.hp1 others(4): Show |
intron_variant | MODIFIER | c.847+8931A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69626760 | ||||||
| chr4:69626827
|
T | C | 1 | a0001c0001t0002g0110 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.847+8864A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69626827 | ||||||
| chr4:69626861
|
C | A | 267 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(264): Show | 279 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(276): Show |
intron_variant | MODIFIER | c.847+8830G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69626861 | ||||||
| chr4:69626988
|
A | G | 3 | a0006c0006t0002g0076a0006c0006t0002g0077a0006c0008t0001g0060 | 3 | HG00735.hp1 HG01123.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.847+8703T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69626988 | ||||||
| chr4:69627004
|
C | T | 113 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(110): Show | 119 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.847+8687G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69627004 | ||||||
| chr4:69627095
|
T | C | 2 | a0001c0001t0002g0206a0001c0001t0002g0215 | 2 | HG02717.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.847+8596A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69627095 | ||||||
| chr4:69627215
|
A | C | 20 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0027others(17): Show | 22 | HG00140.hp1 HG00423.hp1 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.847+8476T>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69627215 | ||||||
| chr4:69627254
|
A | C | 1 | a0002c0002t0001g0123 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.847+8437T>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69627254 | ||||||
| chr4:69627361
|
T | C | 112 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(109): Show | 118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.847+8330A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69627361 | ||||||
| chr4:69627456
|
ACAGGCAA others(13): Show |
A | 112 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(109): Show | 118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.847+8215_847+8234d others(22): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69627456 | ||||||
| chr4:69627486
|
A | G | 3 | a0001c0001t0001g0126a0001c0001t0001g0129a0001c0001t0001g0228 | 3 | NA18954.hp2 NA19009.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.847+8205T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69627486 | ||||||
| chr4:69627534
|
A | AAG | 87 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0043others(84): Show | 91 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.847+8155_847+8156d others(4): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69627534 | ||||||
| chr4:69627538
|
GAGAGAGA others(3): Show |
G | 1 | a0001c0001t0002g0292 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.847+8143_847+8152d others(12): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69627538 | ||||||
| chr4:69627540
|
GAGAGAGA others(1): Show |
G | 67 | a0001c0001t0001g0088a0001c0001t0001g0094a0001c0001t0001g0095others(64): Show | 73 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.847+8143_847+8150d others(10): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69627540 | ||||||
| chr4:69627542
|
G | A | 19 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0027others(16): Show | 21 | HG00140.hp1 HG00423.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.847+8149C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69627542 | ||||||
| chr4:69627542
|
GAGAGAA | G | 5 | a0001c0001t0002g0194a0001c0001t0002g0206a0001c0001t0002g0215others(2): Show | 5 | HG02630.hp1 HG02717.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.847+8143_847+8148d others(8): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69627542 | ||||||
| chr4:69627544
|
GAGAA | G | 4 | a0001c0001t0002g0085a0001c0001t0002g0086a0001c0001t0002g0097others(1): Show | 4 | NA18963.hp1 NA18968.hp1 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.847+8143_847+8146d others(6): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69627544 | ||||||
| chr4:69627546
|
GAA | G | 18 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0027others(15): Show | 20 | HG00140.hp1 HG01099.hp1 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.847+8143_847+8144d others(4): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69627546 | ||||||
| chr4:69627548
|
A | G | 5 | a0001c0001t0001g0277a0001c0001t0002g0028a0001c0001t0002g0303others(2): Show | 5 | HG00423.hp1 HG02004.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.847+8143T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69627548 | ||||||
| chr4:69627550
|
G | A | 1 | a0002c0002t0001g0298 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.847+8141C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69627550 | ||||||
| chr4:69627552
|
G | A | 1 | a0005c0005t0002g0273 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.847+8139C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69627552 | ||||||
| chr4:69627566
|
G | A | 6 | a0004c0004t0001g0035a0004c0004t0001g0183a0004c0004t0001g0221others(3): Show | 6 | HG00099.hp1 HG00280.hp2 HG00738.hp2 others(3): Show |
intron_variant | MODIFIER | c.847+8125C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69627566 | ||||||
| chr4:69627568
|
A | G | 22 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0027others(19): Show | 24 | HG00140.hp1 HG00423.hp1 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.847+8123T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69627568 | ||||||
| chr4:69627572
|
A | G | 1 | a0002c0002t0001g0123 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.847+8119T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69627572 | ||||||
| chr4:69627581
|
A | T | 1 | a0001c0001t0001g0345 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.847+8110T>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69627581 | ||||||
| chr4:69627597
|
G | GGAAA | 3 | a0002c0002t0001g0293a0002c0002t0001g0294a0002c0002t0001g0353 | 3 | HG02615.hp1 NA18522.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.847+8093_847+8094i others(6): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69627597 | ||||||
| chr4:69627598
|
A | AAAAG | 82 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0043others(79): Show | 86 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.847+8089_847+8092d others(6): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69627598 | ||||||
| chr4:69627598
|
A | AAAAGAAA others(5): Show |
2 | a0008c0013t0007g0351a0009c0012t0007g0204 | 2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.847+8081_847+8092d others(14): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69627598 | ||||||
| chr4:69627598
|
A | G | 3 | a0002c0002t0001g0293a0002c0002t0001g0294a0002c0002t0001g0353 | 3 | HG02615.hp1 NA18522.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.847+8093T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69627598 | ||||||
| chr4:69627868
|
A | G | 91 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0043others(88): Show | 95 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.847+7823T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69627868 | ||||||
| chr4:69627912
|
T | C | 6 | a0002c0002t0003g0002a0002c0002t0003g0063a0002c0002t0003g0064others(3): Show | 8 | HG02258.hp1 HG02280.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.847+7779A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69627912 | ||||||
| chr4:69627949
|
C | T | 112 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(109): Show | 118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.847+7742G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69627949 | ||||||
| chr4:69627960
|
C | A | 2 | a0002c0002t0001g0298a0002c0002t0001g0301 | 2 | HG02004.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.847+7731G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69627960 | ||||||
| chr4:69627997
|
G | T | 1 | a0002c0002t0001g0123 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.847+7694C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69627997 | ||||||
| chr4:69628009
|
C | A | 1 | a0002c0002t0001g0123 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.847+7682G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69628009 | ||||||
| chr4:69628108
|
C | A | 1 | a0001c0001t0002g0099 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.847+7583G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69628108 | ||||||
| chr4:69628108
|
C | T | 112 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(109): Show | 118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.847+7583G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69628108 | ||||||
| chr4:69628275
|
T | G | 32 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0043others(29): Show | 34 | HG00597.hp2 HG00609.hp2 HG01070.hp1 others(31): Show |
intron_variant | MODIFIER | c.847+7416A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69628275 | ||||||
| chr4:69628283
|
C | CA | 113 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(110): Show | 119 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.847+7407dupT | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69628283 | ||||||
| chr4:69628369
|
G | A | 1 | a0001c0001t0002g0005 | 2 | NA18941.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.847+7322C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69628369 | ||||||
| chr4:69628401
|
G | A | 2 | a0002c0002t0001g0298a0002c0002t0001g0301 | 2 | HG02004.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.847+7290C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69628401 | ||||||
| chr4:69628521
|
G | T | 1 | a0002c0002t0001g0123 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.847+7170C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69628521 | ||||||
| chr4:69628617
|
A | T | 21 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0027others(18): Show | 23 | HG00140.hp1 HG00423.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.847+7074T>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69628617 | ||||||
| chr4:69628653
|
G | A | 1 | a0001c0001t0001g0095 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.847+7038C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69628653 | ||||||
| chr4:69628691
|
T | C | 3 | a0001c0001t0002g0075a0001c0001t0002g0080a0001c0001t0002g0100 | 3 | NA18945.hp2 NA18968.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.847+7000A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69628691 | ||||||
| chr4:69628696
|
G | C | 1 | a0001c0001t0001g0155 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.847+6995C>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69628696 | ||||||
| chr4:69628745
|
A | G | 1 | a0010c0018t0001g0275 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.847+6946T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69628745 | ||||||
| chr4:69628757
|
A | C | 1 | a0003c0003t0002g0218 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.847+6934T>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69628757 | ||||||
| chr4:69628796
|
C | T | 1 | a0002c0002t0001g0123 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.847+6895G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69628796 | ||||||
| chr4:69628913
|
T | G | 21 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0027others(18): Show | 23 | HG00140.hp1 HG00423.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.847+6778A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69628913 | ||||||
| chr4:69629006
|
G | T | 12 | a0002c0002t0001g0330a0002c0002t0001g0331a0002c0002t0008g0295others(9): Show | 12 | HG01109.hp2 HG01884.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.847+6685C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69629006 | ||||||
| chr4:69629015
|
T | A | 1 | a0002c0002t0001g0123 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.847+6676A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69629015 | ||||||
| chr4:69629123
|
T | C | 113 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(110): Show | 119 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.847+6568A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69629123 | ||||||
| chr4:69629183
|
G | A | 91 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0043others(88): Show | 95 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.847+6508C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69629183 | ||||||
| chr4:69629215
|
G | A | 77 | a0001c0001t0001g0088a0001c0001t0001g0094a0001c0001t0001g0095others(74): Show | 83 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.847+6476C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69629215 | ||||||
| chr4:69629266
|
C | T | 21 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0027others(18): Show | 23 | HG00140.hp1 HG00423.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.847+6425G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69629266 | ||||||
| chr4:69629476
|
T | C | 3 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0274 | 3 | HG02886.hp2 HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.847+6215A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69629476 | ||||||
| chr4:69629635
|
T | C | 18 | a0004c0004t0001g0035a0004c0004t0001g0057a0004c0004t0001g0058others(15): Show | 18 | HG00099.hp1 HG00280.hp2 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.847+6056A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69629635 | ||||||
| chr4:69629656
|
A | T | 43 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0043others(40): Show | 45 | HG00597.hp2 HG00609.hp2 HG01070.hp1 others(42): Show |
intron_variant | MODIFIER | c.847+6035T>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69629656 | ||||||
| chr4:69629694
|
T | A | 1 | a0001c0001t0001g0119 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.847+5997A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69629694 | ||||||
| chr4:69629704
|
C | A | 2 | a0008c0013t0007g0351a0009c0012t0007g0204 | 2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.847+5987G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69629704 | ||||||
| chr4:69629776
|
G | C | 16 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0027others(13): Show | 18 | HG00140.hp1 HG00423.hp1 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.847+5915C>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69629776 | ||||||
| chr4:69629801
|
G | C | 76 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0027others(73): Show | 80 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.847+5890C>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69629801 | ||||||
| chr4:69629934
|
C | A | 19 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0027others(16): Show | 21 | HG00140.hp1 HG00423.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.847+5757G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69629934 | ||||||
| chr4:69630021
|
A | G | 5 | a0005c0005t0002g0208a0005c0005t0002g0273a0005c0005t0002g0297others(2): Show | 5 | HG02717.hp1 HG02809.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.847+5670T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69630021 | ||||||
| chr4:69630022
|
A | G | 1 | a0007c0016t0011g0227 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.847+5669T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69630022 | ||||||
| chr4:69630243
|
C | T | 56 | a0002c0002t0001g0061a0002c0002t0001g0062a0002c0002t0001g0069others(53): Show | 58 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.847+5448G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69630243 | ||||||
| chr4:69630254
|
C | T | 6 | a0003c0003t0002g0149a0003c0003t0002g0150a0003c0003t0002g0188others(3): Show | 6 | HG01346.hp2 HG01928.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.847+5437G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69630254 | ||||||
| chr4:69630269
|
G | A | 2 | a0001c0001t0001g0238a0001c0001t0001g0239 | 2 | NA18612.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.847+5422C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69630269 | ||||||
| chr4:69630339
|
G | A | 78 | a0001c0001t0001g0088a0001c0001t0001g0094a0001c0001t0001g0095others(75): Show | 84 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.847+5352C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69630339 | ||||||
| chr4:69630400
|
T | C | 1 | a0010c0018t0001g0275 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.847+5291A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69630400 | ||||||
| chr4:69630464
|
T | C | 1 | a0005c0005t0005g0125 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.847+5227A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69630464 | ||||||
| chr4:69630525
|
A | T | 1 | a0001c0001t0001g0176 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.847+5166T>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69630525 | ||||||
| chr4:69630544
|
C | T | 56 | a0002c0002t0001g0061a0002c0002t0001g0062a0002c0002t0001g0069others(53): Show | 58 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.847+5147G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69630544 | ||||||
| chr4:69630558
|
A | G | 2 | a0001c0001t0001g0109a0012c0015t0001g0168 | 2 | NA18946.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.847+5133T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69630558 | ||||||
| chr4:69630591
|
G | C | 1 | a0004c0004t0001g0289 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.847+5100C>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69630591 | ||||||
| chr4:69630922
|
AAAG | A | 9 | a0002c0002t0001g0330a0002c0002t0001g0331a0002c0002t0008g0295others(6): Show | 9 | HG01109.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.847+4766_847+4768d others(5): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69630922 | ||||||
| chr4:69631077
|
T | G | 1 | a0002c0002t0001g0123 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.847+4614A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69631077 | ||||||
| chr4:69631157
|
T | C | 2 | a0008c0013t0007g0351a0009c0012t0007g0204 | 2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.847+4534A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69631157 | ||||||
| chr4:69631318
|
A | ATC | 271 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(268): Show | 283 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.847+4372_847+4373i others(4): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69631318 | ||||||
| chr4:69631435
|
A | C | 9 | a0002c0002t0001g0330a0002c0002t0001g0331a0002c0002t0008g0295others(6): Show | 9 | HG01109.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.847+4256T>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69631435 | ||||||
| chr4:69631468
|
G | A | 2 | a0001c0001t0001g0032a0001c0001t0001g0033 | 2 | HG03669.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.847+4223C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69631468 | ||||||
| chr4:69631517
|
T | A | 44 | a0002c0002t0001g0061a0002c0002t0001g0062a0002c0002t0001g0069others(41): Show | 46 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.847+4174A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69631517 | ||||||
| chr4:69631666
|
G | A | 3 | a0001c0001t0001g0124a0001c0001t0001g0334a0001c0001t0001g0335 | 3 | HG02145.hp1 HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.847+4025C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69631666 | ||||||
| chr4:69631873
|
T | C | 1 | a0001c0001t0001g0096 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.847+3818A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69631873 | ||||||
| chr4:69631883
|
C | T | 44 | a0002c0002t0001g0061a0002c0002t0001g0062a0002c0002t0001g0069others(41): Show | 46 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.847+3808G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69631883 | ||||||
| chr4:69631895
|
T | G | 1 | a0002c0002t0001g0294 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.847+3796A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69631895 | ||||||
| chr4:69632188
|
G | A | 37 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0047others(34): Show | 39 | HG00597.hp2 HG00609.hp2 HG01070.hp1 others(36): Show |
intron_variant | MODIFIER | c.847+3503C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69632188 | ||||||
| chr4:69632194
|
T | C | 37 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0047others(34): Show | 39 | HG00597.hp2 HG00609.hp2 HG01070.hp1 others(36): Show |
intron_variant | MODIFIER | c.847+3497A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69632194 | ||||||
| chr4:69632196
|
G | A | 1 | a0002c0002t0001g0123 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.847+3495C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69632196 | ||||||
| chr4:69632315
|
C | G | 1 | a0002c0002t0001g0123 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.847+3376G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69632315 | ||||||
| chr4:69632430
|
T | C | 10 | a0002c0002t0001g0123a0002c0002t0001g0330a0002c0002t0001g0331others(7): Show | 10 | HG01109.hp2 HG01891.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.847+3261A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69632430 | ||||||
| chr4:69632447
|
C | T | 37 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0047others(34): Show | 39 | HG00597.hp2 HG00609.hp2 HG01070.hp1 others(36): Show |
intron_variant | MODIFIER | c.847+3244G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69632447 | ||||||
| chr4:69632574
|
T | C | 1 | a0002c0002t0001g0123 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.847+3117A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69632574 | ||||||
| chr4:69632672
|
A | G | 10 | a0002c0002t0001g0123a0002c0002t0001g0330a0002c0002t0001g0331others(7): Show | 10 | HG01109.hp2 HG01891.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.847+3019T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69632672 | ||||||
| chr4:69632705
|
G | T | 1 | a0001c0001t0002g0269 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.847+2986C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69632705 | ||||||
| chr4:69632885
|
C | CA | 47 | a0001c0001t0001g0021a0001c0001t0001g0036a0001c0001t0001g0037others(44): Show | 47 | HG00544.hp1 HG00609.hp1 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.847+2805dupT | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69632885 | ||||||
| chr4:69632885
|
CA | C | 7 | a0001c0001t0001g0341a0001c0001t0002g0078a0001c0001t0002g0198others(4): Show | 7 | HG00642.hp1 HG02004.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.847+2805delT | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69632885 | ||||||
| chr4:69632888
|
A | C | 2 | a0008c0013t0007g0351a0009c0012t0007g0204 | 2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.847+2803T>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69632888 | ||||||
| chr4:69632889
|
A | G | 1 | a0005c0005t0005g0288 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.847+2802T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69632889 | ||||||
| chr4:69632921
|
C | G | 2 | a0001c0001t0001g0251a0001c0001t0001g0347 | 2 | NA18963.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.847+2770G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69632921 | ||||||
| chr4:69633058
|
T | C | 1 | a0001c0001t0001g0327 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.847+2633A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69633058 | ||||||
| chr4:69633221
|
C | T | 2 | a0008c0013t0007g0351a0009c0012t0007g0204 | 2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.847+2470G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69633221 | ||||||
| chr4:69633260
|
A | T | 20 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0027others(17): Show | 22 | HG00140.hp1 HG00423.hp1 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.847+2431T>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69633260 | ||||||
| chr4:69633268
|
T | C | 4 | a0005c0005t0002g0208a0005c0005t0002g0273a0005c0005t0002g0297others(1): Show | 4 | HG02717.hp1 HG02809.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.847+2423A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69633268 | ||||||
| chr4:69633307
|
A | T | 9 | a0002c0002t0001g0330a0002c0002t0001g0331a0002c0002t0008g0295others(6): Show | 9 | HG01109.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.847+2384T>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69633307 | ||||||
| chr4:69633485
|
T | C | 9 | a0002c0002t0001g0330a0002c0002t0001g0331a0002c0002t0008g0295others(6): Show | 9 | HG01109.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.847+2206A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69633485 | ||||||
| chr4:69633516
|
T | C | 59 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(56): Show | 64 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.847+2175A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69633516 | ||||||
| chr4:69633578
|
T | C | 1 | a0001c0001t0001g0054 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.847+2113A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69633578 | ||||||
| chr4:69633630
|
T | C | 44 | a0002c0002t0001g0061a0002c0002t0001g0062a0002c0002t0001g0069others(41): Show | 46 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.847+2061A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69633630 | ||||||
| chr4:69633723
|
T | C | 2 | a0001c0001t0001g0018a0001c0001t0001g0121 | 2 | HG02056.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.847+1968A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69633723 | ||||||
| chr4:69633747
|
T | G | 8 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(5): Show | 8 | HG00438.hp1 HG02015.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.847+1944A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69633747 | ||||||
| chr4:69634031
|
C | T | 2 | a0008c0013t0007g0351a0009c0012t0007g0204 | 2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.847+1660G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69634031 | ||||||
| chr4:69634032
|
T | G | 16 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0027others(13): Show | 18 | HG00140.hp1 HG00423.hp1 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.847+1659A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69634032 | ||||||
| chr4:69634106
|
T | G | 63 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0027others(60): Show | 67 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.847+1585A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69634106 | ||||||
| chr4:69634145
|
T | C | 2 | a0002c0002t0001g0298a0002c0002t0001g0301 | 2 | HG02004.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.847+1546A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69634145 | ||||||
| chr4:69634153
|
G | A | 1 | a0001c0001t0001g0074 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.847+1538C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69634153 | ||||||
| chr4:69634172
|
G | A | 1 | a0002c0002t0001g0123 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.847+1519C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69634172 | ||||||
| chr4:69634251
|
CAAACAAA others(3): Show |
C | 54 | a0002c0002t0001g0061a0002c0002t0001g0062a0002c0002t0001g0069others(51): Show | 56 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.847+1430_847+1439d others(12): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69634251 | ||||||
| chr4:69634335
|
T | C | 1 | a0003c0003t0002g0218 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.847+1356A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69634335 | ||||||
| chr4:69634589
|
C | T | 1 | a0001c0001t0001g0304 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.847+1102G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69634589 | ||||||
| chr4:69634662
|
G | T | 2 | a0001c0001t0002g0028a0001c0001t0002g0303 | 2 | HG00423.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.847+1029C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69634662 | ||||||
| chr4:69634802
|
A | G | 1 | a0001c0001t0002g0101 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.847+889T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69634802 | ||||||
| chr4:69634809
|
A | T | 44 | a0002c0002t0001g0061a0002c0002t0001g0062a0002c0002t0001g0069others(41): Show | 46 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.847+882T>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69634809 | ||||||
| chr4:69634843
|
G | A | 1 | a0001c0001t0002g0097 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.847+848C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69634843 | ||||||
| chr4:69635112
|
T | C | 61 | a0001c0001t0001g0296a0001c0001t0002g0194a0001c0001t0002g0206others(58): Show | 63 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.847+579A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69635112 | ||||||
| chr4:69635130
|
A | T | 2 | a0001c0001t0002g0075a0001c0001t0002g0100 | 2 | NA18968.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.847+561T>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69635130 | ||||||
| chr4:69635131
|
A | C | 1 | a0004c0004t0001g0195 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.847+560T>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69635131 | ||||||
| chr4:69635131
|
A | T | 2 | a0001c0001t0002g0075a0001c0001t0002g0100 | 2 | NA18968.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.847+560T>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69635131 | ||||||
| chr4:69635268
|
T | A | 61 | a0001c0001t0001g0296a0001c0001t0002g0194a0001c0001t0002g0206others(58): Show | 63 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.847+423A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69635268 | ||||||
| chr4:69635443
|
C | T | 6 | a0001c0001t0001g0006a0001c0001t0001g0137a0001c0001t0001g0138others(3): Show | 7 | HG01993.hp1 HG02027.hp1 HG02135.hp2 others(4): Show |
intron_variant | MODIFIER | c.847+248G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69635443 | ||||||
| chr4:69635555
|
T | C | 1 | a0001c0001t0002g0098 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.847+136A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69635555 | ||||||
| chr4:69635656
|
C | T | 4 | a0001c0001t0002g0004a0001c0001t0002g0083a0001c0001t0002g0084others(1): Show | 5 | HG00099.hp2 HG00140.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.847+35G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69635656 | ||||||
| chr4:69635825
|
C | CA | 26 | a0001c0001t0001g0144a0002c0002t0001g0061a0002c0002t0001g0069others(23): Show | 26 | HG00099.hp1 HG00280.hp2 HG00733.hp2 others(23): Show |
splice_region_variant&intron_variant | LOW | c.716-4dupT | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69635825 | ||||||
| chr4:69635825
|
C | CAA | 3 | a0002c0002t0001g0216a0002c0002t0001g0217a0002c0002t0001g0281 | 3 | HG02895.hp1 NA18906.hp1 NA19009.hp1 |
splice_region_variant&intron_variant | LOW | c.716-4_716-3insTT | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69635825 | ||||||
| chr4:69635825
|
CACCAAAA others(4): Show |
C | 11 | a0002c0002t0001g0062a0002c0002t0001g0179a0002c0002t0001g0293others(8): Show | 13 | HG01884.hp2 HG02258.hp1 HG02280.hp2 others(10): Show |
splice_region_variant&intron_variant | LOW | c.716-14_716-4delTTT others(8): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69635825 | ||||||
| chr4:69635826
|
ACC | A | 6 | a0001c0001t0002g0065a0001c0001t0002g0075a0001c0001t0002g0078others(3): Show | 6 | HG01516.hp1 HG03239.hp2 NA18968.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.716-6_716-5delGG | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69635826 | ||||||
| chr4:69635827
|
C | A | 334 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(331): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
splice_region_variant&intron_variant | LOW | c.716-5G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69635827 | ||||||
| chr4:69635828
|
C | A | 41 | a0001c0001t0001g0144a0002c0002t0001g0061a0002c0002t0001g0069others(38): Show | 41 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(38): Show |
splice_region_variant&intron_variant | LOW | c.716-6G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69635828 | ||||||
| chr4:69635828
|
C | CAAAAAAA | 27 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0043others(24): Show | 29 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(26): Show |
splice_region_variant&intron_variant | LOW | c.716-13_716-7dupTTT others(4): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69635828 | ||||||
| chr4:69635828
|
C | CAAAAAAA others(1): Show |
7 | a0001c0001t0001g0045a0001c0001t0001g0055a0001c0001t0001g0106others(4): Show | 7 | HG00597.hp2 HG01106.hp2 HG01361.hp2 others(4): Show |
splice_region_variant&intron_variant | LOW | c.716-14_716-7dupTTT others(5): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69635828 | ||||||
| chr4:69635828
|
C | CAAAAAAA others(2): Show |
5 | a0001c0001t0001g0056a0001c0001t0003g0012a0001c0001t0003g0219others(2): Show | 6 | HG01884.hp1 HG02630.hp2 HG02895.hp2 others(3): Show |
splice_region_variant&intron_variant | LOW | c.716-15_716-7dupTTT others(6): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69635828 | ||||||
| chr4:69635828
|
C | CAAAAAAA others(3): Show |
2 | a0001c0001t0003g0332a0007c0016t0011g0227 | 2 | HG06807.hp1 NA20129.hp1 |
splice_region_variant&intron_variant | LOW | c.716-16_716-7dupTTT others(7): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69635828 | ||||||
| chr4:69635828
|
C | CAAAAAAA others(6): Show |
1 | a0001c0001t0001g0336 | 1 | HG01891.hp1 | splice_region_variant&intron_variant | LOW | c.716-19_716-7dupTTT others(10): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69635828 | ||||||
| chr4:69635828
|
C | CAAAAAAA others(7): Show |
4 | a0001c0001t0001g0130a0001c0001t0001g0223a0001c0001t0001g0333others(1): Show | 4 | HG01243.hp2 HG02451.hp2 HG03098.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.716-20_716-7dupTTT others(11): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69635828 | ||||||
| chr4:69635828
|
C | CAAAAAAA others(8): Show |
17 | a0001c0001t0001g0019a0001c0001t0001g0027a0001c0001t0001g0124others(14): Show | 17 | HG01167.hp1 HG01517.hp2 HG02258.hp2 others(14): Show |
splice_region_variant&intron_variant | LOW | c.716-21_716-7dupTTT others(12): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69635828 | ||||||
| chr4:69635828
|
C | CAAAAAAA others(9): Show |
59 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0020others(56): Show | 63 | HG00438.hp2 HG01167.hp2 HG01258.hp1 others(60): Show |
splice_region_variant&intron_variant | LOW | c.716-22_716-7dupTTT others(13): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69635828 | ||||||
| chr4:69635828
|
C | CAAAAAAA others(10): Show |
45 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0022others(42): Show | 46 | HG00423.hp2 HG00597.hp1 HG00609.hp1 others(43): Show |
splice_region_variant&intron_variant | LOW | c.716-23_716-7dupTTT others(14): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69635828 | ||||||
| chr4:69635828
|
C | CAAAAAAA others(11): Show |
10 | a0001c0001t0001g0026a0001c0001t0001g0040a0001c0001t0001g0120others(7): Show | 10 | HG01261.hp1 HG01358.hp1 HG02818.hp2 others(7): Show |
splice_region_variant&intron_variant | LOW | c.716-24_716-7dupTTT others(15): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69635828 | ||||||
| chr4:69635828
|
C | CAAAAAAA others(12): Show |
4 | a0001c0001t0001g0139a0001c0001t0001g0231a0001c0001t0001g0236others(1): Show | 4 | HG02145.hp2 HG02818.hp1 HG03710.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.716-25_716-7dupTTT others(16): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69635828 | ||||||
| chr4:69635828
|
C | CAAAAAAA others(13): Show |
1 | a0001c0001t0001g0265 | 1 | HG00544.hp1 | splice_region_variant&intron_variant | LOW | c.716-26_716-7dupTTT others(17): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69635828 | ||||||
| chr4:69635828
|
C | CAAAAAAA others(14): Show |
1 | a0001c0001t0001g0325 | 1 | HG01192.hp2 | splice_region_variant&intron_variant | LOW | c.716-27_716-7dupTTT others(18): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69635828 | ||||||
| chr4:69635828
|
CA | C | 71 | a0001c0001t0001g0088a0001c0001t0001g0094a0001c0001t0001g0095others(68): Show | 77 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(74): Show |
splice_region_variant&intron_variant | LOW | c.716-7delT | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69635828 | ||||||
| chr4:69635830
|
A | C | 5 | a0001c0001t0002g0065a0001c0001t0002g0075a0001c0001t0002g0078others(2): Show | 5 | HG03239.hp2 NA18968.hp1 NA18982.hp2 others(2): Show |
splice_region_variant&intron_variant | LOW | c.716-8T>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69635830 | ||||||
| chr4:69635831
|
A | C | 1 | a0001c0001t0002g0307 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.716-9T>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69635831 | ||||||
| chr4:69635835
|
A | C | 1 | a0001c0001t0006g0111 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.716-13T>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69635835 | ||||||
| chr4:69635849
|
A | AAAAAAAA others(9): Show |
2 | a0001c0001t0001g0147a0003c0010t0002g0146 | 2 | HG02165.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.716-28_716-27insCT others(14): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69635849 | ||||||
| chr4:69635849
|
A | AAAAAAAA others(4): Show |
2 | a0001c0001t0001g0030a0001c0001t0001g0167 | 2 | NA18968.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.716-28_716-27insCT others(9): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69635849 | ||||||
| chr4:69635849
|
A | AAAAAAAA others(3): Show |
1 | a0001c0001t0003g0328 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.716-28_716-27insGT others(8): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69635849 | ||||||
| chr4:69635849
|
A | AAAAAAAA others(3): Show |
13 | a0001c0001t0001g0014a0001c0001t0001g0029a0001c0001t0001g0031others(10): Show | 14 | HG00423.hp1 HG01106.hp1 HG02129.hp1 others(11): Show |
intron_variant | MODIFIER | c.716-28_716-27insCT others(8): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69635849 | ||||||
| chr4:69635849
|
A | G | 1 | a0001c0001t0006g0111 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.716-27T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69635849 | ||||||
| chr4:69635849
|
AAGAGAG | A | 8 | a0002c0002t0001g0330a0002c0002t0001g0331a0002c0002t0008g0354others(5): Show | 8 | HG01109.hp2 HG02717.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.716-33_716-28delCT others(4): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69635849 | ||||||
| chr4:69635851
|
G | A | 84 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0043others(81): Show | 88 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.716-29C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69635851 | ||||||
| chr4:69635853
|
G | A | 2 | a0002c0002t0001g0197a0002c0002t0001g0320 | 2 | HG00733.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.716-31C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69635853 | ||||||
| chr4:69635855
|
G | A | 2 | a0002c0002t0001g0197a0002c0002t0001g0320 | 2 | HG00733.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.716-33C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69635855 | ||||||
| chr4:69635960
|
A | T | 1 | a0001c0001t0001g0240 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.716-138T>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69635960 | ||||||
| chr4:69636038
|
T | C | 12 | a0002c0002t0001g0123a0002c0002t0001g0330a0002c0002t0001g0331others(9): Show | 12 | HG01109.hp2 HG01884.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.716-216A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69636038 | ||||||
| chr4:69636043
|
A | G | 44 | a0002c0002t0001g0061a0002c0002t0001g0062a0002c0002t0001g0069others(41): Show | 46 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.716-221T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69636043 | ||||||
| chr4:69636069
|
A | G | 9 | a0002c0002t0001g0330a0002c0002t0001g0331a0002c0002t0008g0295others(6): Show | 9 | HG01109.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.716-247T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69636069 | ||||||
| chr4:69636262
|
C | T | 273 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(270): Show | 286 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(283): Show |
intron_variant | MODIFIER | c.716-440G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69636262 | ||||||
| chr4:69636278
|
C | T | 1 | a0001c0001t0001g0145 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.716-456G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69636278 | ||||||
| chr4:69636375
|
G | A | 1 | a0002c0002t0001g0331 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.716-553C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69636375 | ||||||
| chr4:69636396
|
A | G | 4 | a0002c0002t0001g0330a0002c0002t0001g0331a0002c0002t0008g0295others(1): Show | 4 | HG01109.hp2 HG03139.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.716-574T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69636396 | ||||||
| chr4:69636527
|
GATT | G | 44 | a0002c0002t0001g0061a0002c0002t0001g0062a0002c0002t0001g0069others(41): Show | 46 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.716-708_716-706del others(3): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69636527 | ||||||
| chr4:69636564
|
C | A | 40 | a0002c0002t0001g0062a0002c0002t0001g0069a0002c0002t0001g0178others(37): Show | 42 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.716-742G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69636564 | ||||||
| chr4:69636577
|
C | A | 5 | a0005c0005t0002g0208a0005c0005t0002g0273a0005c0005t0002g0297others(2): Show | 5 | HG02717.hp1 HG02809.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.716-755G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69636577 | ||||||
| chr4:69636668
|
T | G | 52 | a0001c0001t0001g0296a0001c0001t0002g0194a0001c0001t0002g0206others(49): Show | 54 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.716-846A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69636668 | ||||||
| chr4:69636755
|
T | A | 43 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0043others(40): Show | 45 | HG00597.hp2 HG00609.hp2 HG01070.hp1 others(42): Show |
intron_variant | MODIFIER | c.716-933A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69636755 | ||||||
| chr4:69636949
|
C | G | 1 | a0001c0001t0001g0144 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.716-1127G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69636949 | ||||||
| chr4:69637061
|
G | A | 88 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0043others(85): Show | 92 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(89): Show |
intron_variant | MODIFIER | c.716-1239C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69637061 | ||||||
| chr4:69637231
|
A | G | 1 | a0003c0003t0004g0143 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.716-1409T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69637231 | ||||||
| chr4:69637537
|
C | A | 1 | a0003c0003t0002g0218 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.716-1715G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69637537 | ||||||
| chr4:69637657
|
C | T | 5 | a0001c0001t0001g0074a0001c0001t0001g0251a0001c0001t0001g0252others(2): Show | 5 | HG02071.hp2 NA18963.hp2 NA18972.hp1 others(2): Show |
intron_variant | MODIFIER | c.716-1835G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69637657 | ||||||
| chr4:69637671
|
A | G | 1 | a0001c0001t0006g0111 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.716-1849T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69637671 | ||||||
| chr4:69637678
|
A | G | 2 | a0002c0002t0008g0295a0002c0002t0008g0354 | 2 | HG01109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.716-1856T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69637678 | ||||||
| chr4:69637710
|
T | G | 1 | a0002c0002t0001g0331 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.716-1888A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69637710 | ||||||
| chr4:69637729
|
C | T | 4 | a0002c0002t0001g0330a0002c0002t0001g0331a0002c0002t0008g0295others(1): Show | 4 | HG01109.hp2 HG03139.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.716-1907G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69637729 | ||||||
| chr4:69637757
|
G | C | 7 | a0001c0001t0001g0124a0001c0001t0001g0223a0001c0001t0001g0224others(4): Show | 7 | HG01167.hp1 HG01243.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.716-1935C>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69637757 | ||||||
| chr4:69637891
|
G | A | 1 | a0001c0001t0001g0027 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.716-2069C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69637891 | ||||||
| chr4:69637908
|
AAGGC | A | 28 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(25): Show | 30 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(27): Show |
intron_variant | MODIFIER | c.716-2090_716-2087d others(6): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69637908 | ||||||
| chr4:69637908
|
AAGGCAGG others(5): Show |
A | 3 | a0001c0001t0001g0296a0001c0001t0002g0206a0001c0001t0002g0215 | 3 | HG02717.hp2 HG02976.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.716-2098_716-2087d others(14): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69637908 | ||||||
| chr4:69637997
|
C | CAGGA | 6 | a0001c0001t0003g0012a0001c0001t0003g0114a0001c0001t0003g0115others(3): Show | 7 | HG02572.hp1 HG02895.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.716-2179_716-2176d others(6): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69637997 | ||||||
| chr4:69637997
|
CAGGA | C | 4 | a0002c0002t0001g0123a0002c0002t0008g0295a0002c0002t0008g0354others(1): Show | 4 | HG01109.hp2 HG01175.hp1 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.716-2179_716-2176d others(6): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69637997 | ||||||
| chr4:69638001
|
A | C | 1 | a0001c0001t0001g0142 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.716-2179T>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69638001 | ||||||
| chr4:69638076
|
G | T | 82 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0047others(79): Show | 86 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.716-2254C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69638076 | ||||||
| chr4:69638184
|
G | A | 1 | a0002c0002t0001g0301 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.716-2362C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69638184 | ||||||
| chr4:69638260
|
G | C | 44 | a0002c0002t0001g0061a0002c0002t0001g0062a0002c0002t0001g0069others(41): Show | 46 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.716-2438C>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69638260 | ||||||
| chr4:69638305
|
G | T | 2 | a0001c0001t0001g0007a0001c0001t0001g0140 | 3 | NA18985.hp1 NA18999.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.716-2483C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69638305 | ||||||
| chr4:69638309
|
A | G | 1 | a0001c0001t0002g0046 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.716-2487T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69638309 | ||||||
| chr4:69638402
|
T | C | 6 | a0005c0005t0002g0208a0005c0005t0002g0273a0005c0005t0002g0297others(3): Show | 6 | HG01884.hp1 HG02630.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.716-2580A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69638402 | ||||||
| chr4:69638488
|
T | C | 1 | a0001c0001t0002g0172 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.716-2666A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69638488 | ||||||
| chr4:69638571
|
T | C | 21 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0027others(18): Show | 23 | HG00140.hp1 HG00423.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.716-2749A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69638571 | ||||||
| chr4:69638595
|
T | C | 153 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(150): Show | 159 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(156): Show |
intron_variant | MODIFIER | c.716-2773A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69638595 | ||||||
| chr4:69638640
|
G | T | 1 | a0001c0001t0001g0336 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.716-2818C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69638640 | ||||||
| chr4:69638910
|
C | T | 1 | a0001c0001t0002g0081 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.716-3088G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69638910 | ||||||
| chr4:69639033
|
G | A | 1 | a0002c0002t0001g0123 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.716-3211C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69639033 | ||||||
| chr4:69639105
|
G | C | 1 | a0001c0001t0001g0031 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.716-3283C>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69639105 | ||||||
| chr4:69639168
|
G | A | 1 | a0003c0003t0002g0346 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.716-3346C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69639168 | ||||||
| chr4:69639318
|
G | A | 3 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0274 | 3 | HG02886.hp2 HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.716-3496C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69639318 | ||||||
| chr4:69639444
|
G | A | 17 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0029others(14): Show | 19 | HG00140.hp1 HG00423.hp1 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.716-3622C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69639444 | ||||||
| chr4:69639637
|
C | T | 2 | a0002c0002t0001g0330a0002c0002t0001g0331 | 2 | HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.716-3815G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69639637 | ||||||
| chr4:69639722
|
G | A | 2 | a0008c0013t0007g0351a0009c0012t0007g0204 | 2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.716-3900C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69639722 | ||||||
| chr4:69639747
|
A | G | 2 | a0002c0002t0001g0061a0005c0005t0005g0288 | 2 | HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.716-3925T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69639747 | ||||||
| chr4:69639829
|
A | G | 2 | a0008c0013t0007g0351a0009c0012t0007g0204 | 2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.716-4007T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69639829 | ||||||
| chr4:69639861
|
G | A | 2 | a0001c0001t0001g0191a0001c0001t0001g0192 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.716-4039C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69639861 | ||||||
| chr4:69640139
|
C | A | 48 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0043others(45): Show | 50 | HG00597.hp2 HG00609.hp2 HG01070.hp1 others(47): Show |
intron_variant | MODIFIER | c.716-4317G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69640139 | ||||||
| chr4:69640186
|
T | C | 50 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0043others(47): Show | 52 | HG00597.hp2 HG00609.hp2 HG01070.hp1 others(49): Show |
intron_variant | MODIFIER | c.716-4364A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69640186 | ||||||
| chr4:69640303
|
A | AT | 277 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(274): Show | 289 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(286): Show |
intron_variant | MODIFIER | c.716-4482_716-4481i others(3): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69640303 | ||||||
| chr4:69640308
|
T | C | 3 | a0001c0001t0002g0075a0001c0001t0002g0080a0001c0001t0002g0100 | 3 | NA18945.hp2 NA18968.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.716-4486A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69640308 | ||||||
| chr4:69640340
|
T | C | 52 | a0001c0001t0001g0296a0001c0001t0002g0194a0001c0001t0002g0206others(49): Show | 54 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.716-4518A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69640340 | ||||||
| chr4:69640348
|
G | T | 1 | a0002c0002t0001g0123 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.716-4526C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69640348 | ||||||
| chr4:69640388
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.716-4566C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69640388 | ||||||
| chr4:69640402
|
G | A | 44 | a0002c0002t0001g0061a0002c0002t0001g0062a0002c0002t0001g0069others(41): Show | 46 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.716-4580C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69640402 | ||||||
| chr4:69640454
|
G | A | 1 | a0002c0002t0001g0178 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.716-4632C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69640454 | ||||||
| chr4:69640665
|
G | A | 277 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(274): Show | 289 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(286): Show |
intron_variant | MODIFIER | c.716-4843C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69640665 | ||||||
| chr4:69640722
|
C | T | 1 | a0001c0001t0002g0104 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.716-4900G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69640722 | ||||||
| chr4:69640761
|
G | C | 1 | a0001c0001t0009g0016 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.716-4939C>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69640761 | ||||||
| chr4:69640800
|
T | C | 101 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0043others(98): Show | 105 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(102): Show |
intron_variant | MODIFIER | c.716-4978A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69640800 | ||||||
| chr4:69640804
|
C | A | 1 | a0001c0001t0002g0101 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.716-4982G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69640804 | ||||||
| chr4:69640825
|
A | T | 1 | a0005c0005t0005g0125 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.716-5003T>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69640825 | ||||||
| chr4:69641110
|
A | G | 51 | a0001c0001t0001g0296a0001c0001t0002g0194a0001c0001t0002g0206others(48): Show | 53 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.716-5288T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69641110 | ||||||
| chr4:69641160
|
C | T | 2 | a0001c0001t0001g0038a0001c0001t0001g0232 | 2 | HG00609.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.716-5338G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69641160 | ||||||
| chr4:69641169
|
C | A | 1 | a0005c0005t0005g0125 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.716-5347G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69641169 | ||||||
| chr4:69641197
|
A | G | 1 | a0001c0001t0001g0126 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.716-5375T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69641197 | ||||||
| chr4:69641215
|
C | T | 14 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(11): Show | 14 | HG01099.hp1 HG01109.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.716-5393G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69641215 | ||||||
| chr4:69641238
|
A | T | 1 | a0001c0001t0001g0285 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.716-5416T>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69641238 | ||||||
| chr4:69641301
|
T | C | 40 | a0001c0001t0001g0021a0001c0001t0001g0038a0001c0001t0001g0073others(37): Show | 40 | HG00544.hp1 HG00609.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.716-5479A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69641301 | ||||||
| chr4:69641340
|
C | G | 98 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0043others(95): Show | 102 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(99): Show |
intron_variant | MODIFIER | c.716-5518G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69641340 | ||||||
| chr4:69641438
|
G | T | 97 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0043others(94): Show | 101 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(98): Show |
intron_variant | MODIFIER | c.715+5492C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69641438 | ||||||
| chr4:69641461
|
C | G | 152 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(149): Show | 158 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(155): Show |
intron_variant | MODIFIER | c.715+5469G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69641461 | ||||||
| chr4:69641702
|
C | T | 3 | a0001c0007t0001g0107a0001c0007t0001g0213a0003c0009t0002g0214 | 3 | HG02602.hp2 HG03834.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.715+5228G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69641702 | ||||||
| chr4:69641824
|
A | C | 1 | a0001c0001t0002g0080 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.715+5106T>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69641824 | ||||||
| chr4:69641827
|
C | G | 6 | a0002c0002t0001g0069a0002c0002t0001g0197a0002c0002t0001g0280others(3): Show | 6 | HG00733.hp1 HG01516.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.715+5103G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69641827 | ||||||
| chr4:69642076
|
C | T | 91 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0047others(88): Show | 95 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.715+4854G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69642076 | ||||||
| chr4:69642143
|
C | T | 1 | a0001c0001t0003g0328 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.715+4787G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69642143 | ||||||
| chr4:69642346
|
T | G | 1 | a0001c0001t0001g0266 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.715+4584A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69642346 | ||||||
| chr4:69642434
|
A | G | 2 | a0001c0001t0001g0238a0001c0001t0001g0239 | 2 | NA18612.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.715+4496T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69642434 | ||||||
| chr4:69642610
|
T | C | 1 | a0001c0001t0002g0102 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.715+4320A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69642610 | ||||||
| chr4:69642752
|
A | G | 1 | a0006c0008t0001g0060 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.715+4178T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69642752 | ||||||
| chr4:69642953
|
T | A | 1 | a0005c0005t0005g0125 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.715+3977A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69642953 | ||||||
| chr4:69643151
|
T | C | 64 | a0001c0001t0001g0296a0001c0001t0001g0312a0001c0001t0002g0194others(61): Show | 66 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(63): Show |
intron_variant | MODIFIER | c.715+3779A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69643151 | ||||||
| chr4:69643160
|
G | A | 254 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(251): Show | 264 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(261): Show |
intron_variant | MODIFIER | c.715+3770C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69643160 | ||||||
| chr4:69643171
|
A | T | 1 | a0002c0002t0001g0123 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.715+3759T>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69643171 | ||||||
| chr4:69643189
|
C | T | 2 | a0001c0001t0001g0073a0001c0001t0001g0207 | 2 | NA19003.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.715+3741G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69643189 | ||||||
| chr4:69643414
|
A | G | 5 | a0004c0004t0001g0035a0004c0004t0001g0183a0004c0004t0001g0221others(2): Show | 5 | HG00099.hp1 HG00280.hp2 HG00738.hp2 others(2): Show |
intron_variant | MODIFIER | c.715+3516T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69643414 | ||||||
| chr4:69643468
|
T | C | 11 | a0002c0002t0001g0330a0002c0002t0001g0331a0002c0002t0008g0295others(8): Show | 11 | HG01109.hp2 HG01884.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.715+3462A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69643468 | ||||||
| chr4:69643519
|
T | G | 63 | a0001c0001t0001g0296a0001c0001t0001g0312a0001c0001t0002g0194others(60): Show | 65 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(62): Show |
intron_variant | MODIFIER | c.715+3411A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69643519 | ||||||
| chr4:69643739
|
T | A | 36 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0043others(33): Show | 38 | HG00597.hp2 HG00609.hp2 HG01070.hp1 others(35): Show |
intron_variant | MODIFIER | c.715+3191A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69643739 | ||||||
| chr4:69643812
|
A | C | 21 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0027others(18): Show | 23 | HG00140.hp1 HG00423.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.715+3118T>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69643812 | ||||||
| chr4:69643996
|
T | C | 2 | a0001c0001t0002g0103a0001c0001t0002g0226 | 2 | HG00738.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.715+2934A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69643996 | ||||||
| chr4:69644284
|
T | G | 1 | a0001c0001t0001g0348 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.715+2646A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69644284 | ||||||
| chr4:69644360
|
T | C | 1 | a0001c0001t0001g0128 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.715+2570A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69644360 | ||||||
| chr4:69644440
|
T | C | 1 | a0002c0002t0001g0123 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.715+2490A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69644440 | ||||||
| chr4:69644446
|
C | T | 2 | a0002c0002t0008g0295a0002c0002t0008g0354 | 2 | HG01109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.715+2484G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69644446 | ||||||
| chr4:69644457
|
C | T | 1 | a0001c0001t0002g0079 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.715+2473G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69644457 | ||||||
| chr4:69644570
|
T | G | 1 | a0002c0002t0001g0123 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.715+2360A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69644570 | ||||||
| chr4:69644607
|
C | T | 1 | a0001c0001t0002g0079 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.715+2323G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69644607 | ||||||
| chr4:69644691
|
CTCT | C | 7 | a0002c0002t0001g0330a0002c0002t0001g0331a0005c0005t0002g0208others(4): Show | 7 | HG02717.hp1 HG02809.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.715+2236_715+2238d others(5): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69644691 | ||||||
| chr4:69644799
|
G | A | 1 | a0001c0001t0002g0104 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.715+2131C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69644799 | ||||||
| chr4:69644847
|
C | T | 4 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0333others(1): Show | 4 | HG01167.hp1 HG01243.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.715+2083G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69644847 | ||||||
| chr4:69644911
|
G | A | 1 | a0002c0002t0001g0123 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.715+2019C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69644911 | ||||||
| chr4:69644930
|
T | C | 20 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0027others(17): Show | 22 | HG00140.hp1 HG00423.hp1 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.715+2000A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69644930 | ||||||
| chr4:69645000
|
C | T | 1 | a0002c0002t0001g0123 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.715+1930G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69645000 | ||||||
| chr4:69645034
|
T | C | 1 | a0002c0002t0001g0123 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.715+1896A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69645034 | ||||||
| chr4:69645072
|
C | T | 2 | a0001c0001t0002g0198a0001c0001t0002g0199 | 2 | NA18980.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.715+1858G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69645072 | ||||||
| chr4:69645166
|
G | A | 1 | a0002c0002t0001g0179 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.715+1764C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69645166 | ||||||
| chr4:69645482
|
G | A | 17 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0029others(14): Show | 19 | HG00140.hp1 HG00423.hp1 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.715+1448C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69645482 | ||||||
| chr4:69645628
|
TCTCAA | T | 7 | a0002c0002t0001g0330a0002c0002t0001g0331a0005c0005t0002g0208others(4): Show | 7 | HG02717.hp1 HG02809.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.715+1297_715+1301d others(7): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69645628 | ||||||
| chr4:69645709
|
G | C | 278 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(275): Show | 290 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(287): Show |
intron_variant | MODIFIER | c.715+1221C>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69645709 | ||||||
| chr4:69645842
|
G | C | 1 | a0001c0001t0001g0138 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.715+1088C>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69645842 | ||||||
| chr4:69645907
|
T | C | 18 | a0004c0004t0001g0035a0004c0004t0001g0057a0004c0004t0001g0058others(15): Show | 18 | HG00099.hp1 HG00280.hp2 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.715+1023A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69645907 | ||||||
| chr4:69645928
|
A | C | 1 | a0003c0003t0002g0218 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.715+1002T>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69645928 | ||||||
| chr4:69646075
|
T | A | 1 | a0001c0001t0002g0078 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.715+855A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69646075 | ||||||
| chr4:69646078
|
A | T | 1 | a0001c0001t0002g0078 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.715+852T>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69646078 | ||||||
| chr4:69646288
|
T | G | 49 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0043others(46): Show | 51 | HG00597.hp2 HG00609.hp2 HG01070.hp1 others(48): Show |
intron_variant | MODIFIER | c.715+642A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69646288 | ||||||
| chr4:69646347
|
C | T | 1 | a0005c0005t0005g0125 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.715+583G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69646347 | ||||||
| chr4:69646354
|
A | G | 1 | a0006c0006t0002g0076 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.715+576T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69646354 | ||||||
| chr4:69646382
|
T | C | 2 | a0002c0002t0008g0295a0002c0002t0008g0354 | 2 | HG01109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.715+548A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69646382 | ||||||
| chr4:69646395
|
G | A | 51 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0026others(48): Show | 51 | HG00544.hp1 HG00609.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.715+535C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69646395 | ||||||
| chr4:69646430
|
C | T | 3 | a0001c0001t0001g0141a0001c0001t0001g0237a0001c0001t0001g0341 | 3 | HG02258.hp2 HG02622.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.715+500G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69646430 | ||||||
| chr4:69646590
|
C | T | 1 | a0005c0005t0005g0288 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.715+340G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69646590 | ||||||
| chr4:69646816
|
A | G | 2 | a0002c0002t0008g0295a0002c0002t0008g0354 | 2 | HG01109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.715+114T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69646816 | ||||||
| chr4:69646892
|
T | G | 2 | a0001c0001t0003g0114a0001c0001t0003g0115 | 2 | HG02572.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.715+38A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69646892 | ||||||
| chr4:69647833
|
G | A | 150 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(147): Show | 156 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(153): Show |
intron_variant | MODIFIER | c.-54-135C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69647833 | ||||||
| chr4:69647875
|
G | A | 8 | a0001c0001t0001g0113a0001c0001t0003g0012a0001c0001t0003g0114others(5): Show | 9 | HG02572.hp1 HG02895.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.-54-177C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69647875 | ||||||
| chr4:69647979
|
T | C | 3 | a0001c0001t0001g0022a0001c0001t0001g0201a0001c0001t0001g0202 | 3 | HG02280.hp1 NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-54-281A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69647979 | ||||||
| chr4:69647992
|
C | T | 244 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(241): Show | 254 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(251): Show |
intron_variant | MODIFIER | c.-54-294G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69647992 | ||||||
| chr4:69648129
|
A | C | 2 | a0004c0004t0001g0057a0004c0004t0001g0058 | 2 | HG01496.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.-54-431T>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69648129 | ||||||
| chr4:69648170
|
T | G | 1 | a0002c0002t0001g0123 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-54-472A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69648170 | ||||||
| chr4:69648174
|
T | C | 45 | a0001c0001t0001g0312a0002c0002t0001g0061a0002c0002t0001g0062others(42): Show | 47 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(44): Show |
intron_variant | MODIFIER | c.-54-476A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69648174 | ||||||
| chr4:69648251
|
C | T | 1 | a0001c0001t0001g0236 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-54-553G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69648251 | ||||||
| chr4:69648268
|
C | T | 1 | a0001c0017t0001g0276 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-54-570G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69648268 | ||||||
| chr4:69648298
|
T | TTA | 356 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(353): Show | 375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.-54-601_-54-600ins others(2): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69648298 | ||||||
| chr4:69648307
|
C | A | 273 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(270): Show | 286 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(283): Show |
intron_variant | MODIFIER | c.-54-609G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69648307 | ||||||
| chr4:69648505
|
G | A | 2 | a0001c0001t0001g0036a0001c0001t0001g0037 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-54-807C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69648505 | ||||||
| chr4:69648524
|
T | C | 1 | a0001c0001t0001g0165 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-54-826A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69648524 | ||||||
| chr4:69648553
|
G | A | 4 | a0001c0001t0001g0166a0001c0001t0001g0267a0001c0001t0001g0349others(1): Show | 4 | HG01952.hp1 HG01981.hp2 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.-54-855C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69648553 | ||||||
| chr4:69648640
|
C | T | 153 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(150): Show | 160 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(157): Show |
intron_variant | MODIFIER | c.-54-942G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69648640 | ||||||
| chr4:69648650
|
T | C | 1 | a0001c0001t0002g0169 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-54-952A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69648650 | ||||||
| chr4:69648770
|
A | G | 6 | a0005c0005t0002g0208a0005c0005t0002g0273a0005c0005t0002g0297others(3): Show | 6 | HG01884.hp1 HG02630.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-54-1072T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69648770 | ||||||
| chr4:69648995
|
A | G | 1 | a0001c0001t0001g0139 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-54-1297T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69648995 | ||||||
| chr4:69649047
|
G | A | 1 | a0001c0001t0001g0268 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-54-1349C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69649047 | ||||||
| chr4:69649047
|
G | T | 1 | a0001c0001t0002g0075 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-54-1349C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69649047 | ||||||
| chr4:69649093
|
G | A | 66 | a0001c0001t0001g0088a0001c0001t0001g0094a0001c0001t0001g0095others(63): Show | 72 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.-54-1395C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69649093 | ||||||
| chr4:69649094
|
C | T | 6 | a0001c0001t0001g0006a0001c0001t0001g0137a0001c0001t0001g0138others(3): Show | 7 | HG01993.hp1 HG02027.hp1 HG02135.hp2 others(4): Show |
intron_variant | MODIFIER | c.-54-1396G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69649094 | ||||||
| chr4:69649111
|
T | A | 154 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(151): Show | 161 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(158): Show |
intron_variant | MODIFIER | c.-54-1413A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69649111 | ||||||
| chr4:69649185
|
C | G | 45 | a0001c0001t0001g0312a0002c0002t0001g0061a0002c0002t0001g0062others(42): Show | 47 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(44): Show |
intron_variant | MODIFIER | c.-54-1487G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69649185 | ||||||
| chr4:69649243
|
A | G | 4 | a0002c0002t0001g0330a0002c0002t0001g0331a0002c0002t0008g0295others(1): Show | 4 | HG01109.hp2 HG03139.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-54-1545T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69649243 | ||||||
| chr4:69649290
|
G | A | 1 | a0002c0002t0001g0123 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-54-1592C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69649290 | ||||||
| chr4:69649307
|
T | G | 79 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0027others(76): Show | 83 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.-54-1609A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69649307 | ||||||
| chr4:69649423
|
A | G | 5 | a0001c0001t0001g0038a0001c0001t0001g0134a0001c0001t0001g0135others(2): Show | 5 | HG00609.hp1 HG02155.hp1 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.-54-1725T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69649423 | ||||||
| chr4:69649448
|
T | A | 1 | a0002c0002t0001g0123 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-54-1750A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69649448 | ||||||
| chr4:69649449
|
A | T | 1 | a0002c0002t0001g0123 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-54-1751T>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69649449 | ||||||
| chr4:69649589
|
A | G | 2 | a0001c0001t0001g0036a0001c0001t0001g0037 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-54-1891T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69649589 | ||||||
| chr4:69649620
|
T | G | 1 | a0003c0003t0002g0218 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-54-1922A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69649620 | ||||||
| chr4:69649646
|
G | A | 1 | a0002c0002t0001g0123 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-54-1948C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69649646 | ||||||
| chr4:69649685
|
C | T | 7 | a0005c0005t0002g0208a0005c0005t0002g0273a0005c0005t0002g0297others(4): Show | 7 | HG01884.hp1 HG02630.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-54-1987G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69649685 | ||||||
| chr4:69649705
|
T | C | 356 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(353): Show | 375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.-54-2007A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69649705 | ||||||
| chr4:69649793
|
C | A | 1 | a0004c0004t0001g0319 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-54-2095G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69649793 | ||||||
| chr4:69649871
|
G | A | 10 | a0001c0001t0001g0017a0001c0001t0001g0127a0001c0001t0001g0128others(7): Show | 10 | HG01192.hp2 HG01891.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.-54-2173C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69649871 | ||||||
| chr4:69650070
|
T | C | 65 | a0001c0001t0001g0296a0001c0001t0001g0312a0001c0001t0002g0194others(62): Show | 67 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(64): Show |
intron_variant | MODIFIER | c.-54-2372A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69650070 | ||||||
| chr4:69650242
|
G | A | 1 | a0012c0015t0001g0168 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.-54-2544C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69650242 | ||||||
| chr4:69650390
|
T | A | 1 | a0002c0002t0003g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-54-2692A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69650390 | ||||||
| chr4:69650395
|
T | A | 1 | a0001c0007t0001g0107 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-54-2697A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69650395 | ||||||
| chr4:69650507
|
A | G | 9 | a0001c0001t0001g0018a0001c0001t0001g0026a0001c0001t0001g0121others(6): Show | 9 | HG01261.hp1 HG02056.hp2 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.-55+2681T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69650507 | ||||||
| chr4:69650609
|
A | T | 66 | a0001c0001t0001g0088a0001c0001t0001g0094a0001c0001t0001g0095others(63): Show | 72 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.-55+2579T>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69650609 | ||||||
| chr4:69650683
|
C | T | 1 | a0004c0004t0001g0195 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-55+2505G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69650683 | ||||||
| chr4:69650713
|
C | T | 210 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(207): Show | 219 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(216): Show |
intron_variant | MODIFIER | c.-55+2475G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69650713 | ||||||
| chr4:69650790
|
T | C | 176 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(173): Show | 185 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(182): Show |
intron_variant | MODIFIER | c.-55+2398A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69650790 | ||||||
| chr4:69650791
|
G | A | 3 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0120 | 3 | NA18960.hp1 NA18970.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.-55+2397C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69650791 | ||||||
| chr4:69650802
|
G | A | 155 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(152): Show | 162 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(159): Show |
intron_variant | MODIFIER | c.-55+2386C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69650802 | ||||||
| chr4:69650805
|
A | G | 1 | a0003c0003t0002g0302 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-55+2383T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69650805 | ||||||
| chr4:69650953
|
C | T | 153 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(150): Show | 160 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(157): Show |
intron_variant | MODIFIER | c.-55+2235G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69650953 | ||||||
| chr4:69651018
|
A | G | 1 | a0003c0003t0002g0218 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-55+2170T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69651018 | ||||||
| chr4:69651042
|
G | A | 45 | a0001c0001t0001g0312a0002c0002t0001g0061a0002c0002t0001g0062others(42): Show | 47 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(44): Show |
intron_variant | MODIFIER | c.-55+2146C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69651042 | ||||||
| chr4:69651088
|
C | T | 1 | a0002c0002t0001g0123 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-55+2100G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69651088 | ||||||
| chr4:69651160
|
C | T | 1 | a0001c0001t0001g0014 | 2 | NA18988.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.-55+2028G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69651160 | ||||||
| chr4:69651390
|
C | T | 155 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(152): Show | 163 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(160): Show |
intron_variant | MODIFIER | c.-55+1798G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69651390 | ||||||
| chr4:69651425
|
G | A | 44 | a0002c0002t0001g0061a0002c0002t0001g0062a0002c0002t0001g0069others(41): Show | 46 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.-55+1763C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69651425 | ||||||
| chr4:69651430
|
A | T | 2 | a0002c0002t0001g0330a0002c0002t0001g0331 | 2 | HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-55+1758T>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69651430 | ||||||
| chr4:69651480
|
C | T | 2 | a0001c0001t0001g0339a0003c0003t0002g0340 | 2 | HG02451.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.-55+1708G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69651480 | ||||||
| chr4:69651744
|
C | G | 2 | a0002c0002t0001g0197a0002c0002t0001g0320 | 2 | HG00733.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.-55+1444G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69651744 | ||||||
| chr4:69651794
|
T | C | 2 | a0002c0002t0008g0295a0002c0002t0008g0354 | 2 | HG01109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-55+1394A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69651794 | ||||||
| chr4:69651823
|
A | C | 9 | a0001c0001t0001g0017a0001c0001t0001g0127a0001c0001t0001g0128others(6): Show | 9 | HG01891.hp1 HG02145.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.-55+1365T>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69651823 | ||||||
| chr4:69651932
|
C | T | 2 | a0001c0001t0001g0126a0001c0001t0001g0228 | 2 | NA18954.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.-55+1256G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69651932 | ||||||
| chr4:69652003
|
C | A | 356 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(353): Show | 375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.-55+1185G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69652003 | ||||||
| chr4:69652074
|
C | G | 4 | a0004c0004t0001g0035a0004c0004t0001g0183a0004c0004t0001g0289others(1): Show | 4 | HG00099.hp1 HG00280.hp2 HG00738.hp2 others(1): Show |
intron_variant | MODIFIER | c.-55+1114G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69652074 | ||||||
| chr4:69652184
|
G | GT | 243 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(240): Show | 256 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(253): Show |
intron_variant | MODIFIER | c.-55+1003dupA | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69652184 | ||||||
| chr4:69652234
|
T | C | 170 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(167): Show | 181 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(178): Show |
intron_variant | MODIFIER | c.-55+954A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69652234 | ||||||
| chr4:69652282
|
C | CT | 18 | a0001c0001t0001g0113a0001c0001t0001g0116a0001c0001t0001g0117others(15): Show | 18 | HG01109.hp2 HG01243.hp1 HG02004.hp2 others(15): Show |
intron_variant | MODIFIER | c.-55+905dupA | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69652282 | ||||||
| chr4:69652282
|
C | CTT | 80 | a0001c0001t0001g0071a0001c0001t0001g0073a0001c0001t0001g0074others(77): Show | 86 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.-55+904_-55+905dup others(2): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69652282 | ||||||
| chr4:69652282
|
C | CTTT | 88 | a0001c0001t0001g0022a0001c0001t0001g0036a0001c0001t0001g0037others(85): Show | 90 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.-55+903_-55+905dup others(3): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69652282 | ||||||
| chr4:69652282
|
C | CTTTTT | 19 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0027others(16): Show | 21 | HG00140.hp1 HG00423.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.-55+901_-55+905dup others(5): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69652282 | ||||||
| chr4:69652368
|
C | G | 1 | a0003c0003t0002g0302 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-55+820G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69652368 | ||||||
| chr4:69652388
|
A | G | 1 | a0001c0001t0001g0026 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-55+800T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69652388 | ||||||
| chr4:69652441
|
A | T | 1 | a0001c0001t0002g0303 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-55+747T>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69652441 | ||||||
| chr4:69652452
|
T | C | 1 | a0001c0001t0001g0272 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-55+736A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69652452 | ||||||
| chr4:69652466
|
T | C | 1 | a0001c0001t0001g0356 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-55+722A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69652466 | ||||||
| chr4:69652542
|
A | G | 3 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025 | 3 | NA18951.hp2 NA18984.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.-55+646T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69652542 | ||||||
| chr4:69652562
|
C | T | 2 | a0003c0003t0002g0302a0004c0004t0001g0183 | 2 | HG00738.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.-55+626G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69652562 | ||||||
| chr4:69652626
|
A | G | 3 | a0001c0001t0001g0022a0002c0002t0001g0301a0005c0005t0005g0288 | 3 | HG02004.hp2 HG02280.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-55+562T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69652626 | ||||||
| chr4:69652667
|
T | G | 6 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0274others(3): Show | 6 | HG01243.hp1 HG02886.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-55+521A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69652667 | ||||||
| chr4:69652741
|
C | T | 1 | a0001c0001t0001g0021 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-55+447G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69652741 | ||||||
| chr4:69652767
|
A | G | 1 | a0005c0005t0002g0300 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-55+421T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69652767 | ||||||
| chr4:69652881
|
A | G | 3 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020 | 3 | HG02155.hp2 NA18948.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.-55+307T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69652881 | ||||||
| chr4:69652976
|
G | A | 4 | a0001c0001t0001g0355a0001c0001t0001g0356a0002c0002t0001g0353others(1): Show | 4 | HG01109.hp2 HG01243.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-55+212C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69652976 | ||||||
| chr4:69652994
|
T | C | 14 | a0001c0001t0001g0014a0001c0001t0001g0182a0001c0001t0001g0277others(11): Show | 15 | HG01123.hp2 HG01361.hp2 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.-55+194A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69652994 | ||||||
| chr4:69653025
|
C | G | 189 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(186): Show | 203 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.-55+163G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69653025 | ||||||
| chr4:69653036
|
G | A | 70 | a0001c0001t0001g0015a0001c0001t0001g0296a0001c0001t0001g0304others(67): Show | 71 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.-55+152C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69653036 | ||||||
| chr4:69653130
|
A | C | 1 | a0001c0001t0001g0017 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-55+58T>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69653130 | ||||||
| chr4:69653133
|
A | T | 1 | a0001c0001t0009g0016 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-55+55T>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69653133 | ||||||
| chr4:69653138
|
T | A | 1 | a0001c0001t0009g0016 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-55+50A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69653138 | ||||||
| chr4:69653155
|
T | A | 1 | a0001c0001t0009g0016 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-55+33A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69653155 | ||||||
| chr4:69653159
|
G | T | 1 | a0001c0001t0009g0016 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-55+29C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69653159 | ||||||
| chr4:69653161
|
T | A | 1 | a0001c0001t0009g0016 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-55+27A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69653161 | ||||||
| chr4:69653162
|
T | A | 1 | a0001c0001t0009g0016 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-55+26A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69653162 | ||||||
| chr4:69653175
|
T | C | 1 | a0001c0001t0009g0016 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-55+13A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69653175 | ||||||
| chr4:69653176
|
C | T | 1 | a0001c0001t0009g0016 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-55+12G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69653176 | ||||||
| chr4:69653180
|
T | C | 1 | a0001c0001t0009g0016 | 1 | HG01192.hp1 | splice_region_variant&intron_variant | LOW | c.-55+8A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69653180 | ||||||
| chr4:69653181
|
T | A | 1 | a0001c0001t0009g0016 | 1 | HG01192.hp1 | splice_region_variant&intron_variant | LOW | c.-55+7A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69653181 | ||||||
| chr4:69653185
|
T | A | 1 | a0001c0001t0009g0016 | 1 | HG01192.hp1 | splice_region_variant&intron_variant | LOW | c.-55+3A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69653185 | ||||||
| chr4:69653186
|
A | C | 1 | a0001c0001t0009g0016 | 1 | HG01192.hp1 | splice_donor_variant&intron_variant | HIGH | c.-55+2T>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69653186 | ||||||
| chr4:69653187
|
C | A | 1 | a0001c0001t0009g0016 | 1 | HG01192.hp1 | splice_donor_variant&intron_variant | HIGH | c.-55+1G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69653187 |