Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 7368 |
| ensemblid | ENSG00000174607.11 |
| hgncid | 12555 |
| symbol | UGT8 |
| name | UDP glycosyltransferase 8 |
| refseq_nuc | NM_001128174.3 |
| refseq_prot | NP_001121646.2 |
| ensembl_nuc | ENST00000310836.11 |
| ensembl_prot | ENSP00000311648.6 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 114598807 |
| end | 114678225 |
| strand | + |
| ver | v1.2 |
| region | chr4:114598807-114678225 |
| region5000 | chr4:114593807-114683225 |
| regionname0 | UGT8_chr4_114598807_114678225 |
| regionname5000 | UGT8_chr4_114593807_114683225 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 541 | 233 | 81 | 48 | 72 | 12 | 19 | 51 | UGT8_chr4_114593807_114683225 | UGT8 | MKSYT others(536): Show |
chr4 | 114593807 | 114683225 |
| a0002 | 0/0 | 541 | 36 | 0 | 4 | 26 | 2 | 4 | 15 | UGT8_chr4_114593807_114683225 | UGT8 | MKSYT others(536): Show |
chr4 | 114593807 | 114683225 |
| a0003 | 0/0 | 541 | 4 | 0 | 4 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | MKSYT others(536): Show |
chr4 | 114593807 | 114683225 |
| a0004 | 1/0 | 541 | 3 | 2 | 0 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | MKSYT others(536): Show |
chr4 | 114593807 | 114683225 |
| a0005 | 0/0 | 541 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | MKSYT others(536): Show |
chr4 | 114593807 | 114683225 |
| a0006 | 0/0 | 541 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | MKSYT others(536): Show |
chr4 | 114593807 | 114683225 |
| a0007 | 0/0 | 541 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | MKSYT others(536): Show |
chr4 | 114593807 | 114683225 |
| a0008 | 0/0 | 541 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | MKSYT others(536): Show |
chr4 | 114593807 | 114683225 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1623 | 214 | 77 | 42 | 65 | 11 | 18 | UGT8_chr4_114593807_114683225 | UGT8 | ATGAA others(1618): Show |
chr4 | 114593807 | 114683225 | ||
| a0001c0003 | 0/0 | 1623 | 11 | 0 | 3 | 7 | 1 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | ATGAA others(1618): Show |
chr4 | 114593807 | 114683225 | ||
| a0001c0006 | 0/0 | 1623 | 2 | 1 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | ATGAA others(1618): Show |
chr4 | 114593807 | 114683225 | ||
| a0001c0007 | 0/0 | 1623 | 2 | 1 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | ATGAA others(1618): Show |
chr4 | 114593807 | 114683225 | ||
| a0001c0011 | 0/0 | 1623 | 1 | 0 | 0 | 0 | 0 | 1 | UGT8_chr4_114593807_114683225 | UGT8 | ATGAA others(1618): Show |
chr4 | 114593807 | 114683225 | ||
| a0001c0013 | 0/0 | 1623 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | ATGAA others(1618): Show |
chr4 | 114593807 | 114683225 | ||
| a0001c0014 | 0/0 | 1623 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | ATGAA others(1618): Show |
chr4 | 114593807 | 114683225 | ||
| a0001c0015 | 0/0 | 1623 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | ATGAA others(1618): Show |
chr4 | 114593807 | 114683225 | ||
| a0002c0002 | 0/0 | 1623 | 36 | 0 | 4 | 26 | 2 | 4 | UGT8_chr4_114593807_114683225 | UGT8 | ATGAA others(1618): Show |
chr4 | 114593807 | 114683225 | ||
| a0003c0004 | 0/0 | 1623 | 4 | 0 | 4 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | ATGAA others(1618): Show |
chr4 | 114593807 | 114683225 | ||
| a0004c0005 | 1/0 | 1623 | 3 | 2 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | ATGAA others(1618): Show |
chr4 | 114593807 | 114683225 | ||
| a0005c0008 | 0/0 | 1623 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | ATGAA others(1618): Show |
chr4 | 114593807 | 114683225 | ||
| a0006c0012 | 0/0 | 1623 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | ATGAA others(1618): Show |
chr4 | 114593807 | 114683225 | ||
| a0007c0009 | 0/0 | 1623 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | ATGAA others(1618): Show |
chr4 | 114593807 | 114683225 | ||
| a0008c0010 | 0/0 | 1623 | 1 | 0 | 0 | 0 | 0 | 1 | UGT8_chr4_114593807_114683225 | UGT8 | ATGAA others(1618): Show |
chr4 | 114593807 | 114683225 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3733 | 108 | 19 | 21 | 52 | 6 | 9 | UGT8_chr4_114593807_114683225 | UGT8 | AGAGA others(3728): Show |
chr4 | 114593807 | 114683225 |
| a0001c0001t0002 | 0/0 | 3733 | 33 | 5 | 8 | 13 | 3 | 4 | UGT8_chr4_114593807_114683225 | UGT8 | AGAGA others(3728): Show |
chr4 | 114593807 | 114683225 |
| a0001c0001t0003 | 0/0 | 3733 | 37 | 30 | 7 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | AGAGA others(3728): Show |
chr4 | 114593807 | 114683225 |
| a0001c0001t0004 | 0/0 | 3733 | 9 | 8 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | AGAGA others(3728): Show |
chr4 | 114593807 | 114683225 |
| a0001c0001t0005 | 0/0 | 3733 | 6 | 0 | 2 | 0 | 2 | 2 | UGT8_chr4_114593807_114683225 | UGT8 | AGAGA others(3728): Show |
chr4 | 114593807 | 114683225 |
| a0001c0001t0006 | 0/0 | 3733 | 6 | 6 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | AGAGA others(3728): Show |
chr4 | 114593807 | 114683225 |
| a0001c0001t0007 | 0/0 | 3731 | 4 | 3 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | AGAGA others(3726): Show |
chr4 | 114593807 | 114683225 |
| a0001c0001t0008 | 0/0 | 3733 | 3 | 3 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | AGAGA others(3728): Show |
chr4 | 114593807 | 114683225 |
| a0001c0001t0009 | 0/0 | 3733 | 2 | 1 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | AGAGA others(3728): Show |
chr4 | 114593807 | 114683225 |
| a0001c0001t0010 | 0/0 | 3733 | 2 | 0 | 0 | 0 | 0 | 2 | UGT8_chr4_114593807_114683225 | UGT8 | AGAGA others(3728): Show |
chr4 | 114593807 | 114683225 |
| a0001c0001t0012 | 0/0 | 3733 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | AGAGA others(3728): Show |
chr4 | 114593807 | 114683225 |
| a0001c0001t0016 | 0/0 | 3733 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | AGAGA others(3728): Show |
chr4 | 114593807 | 114683225 |
| a0001c0001t0017 | 0/0 | 3733 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | AGAGA others(3728): Show |
chr4 | 114593807 | 114683225 |
| a0001c0001t0018 | 0/0 | 3733 | 1 | 0 | 0 | 0 | 0 | 1 | UGT8_chr4_114593807_114683225 | UGT8 | AGAGA others(3728): Show |
chr4 | 114593807 | 114683225 |
| a0001c0003t0001 | 0/0 | 3733 | 11 | 0 | 3 | 7 | 1 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | AGAGA others(3728): Show |
chr4 | 114593807 | 114683225 |
| a0001c0006t0003 | 0/0 | 3733 | 2 | 1 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | AGAGA others(3728): Show |
chr4 | 114593807 | 114683225 |
| a0001c0007t0011 | 0/0 | 3733 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | AGAGA others(3728): Show |
chr4 | 114593807 | 114683225 |
| a0001c0007t0015 | 0/0 | 3733 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | AGAGA others(3728): Show |
chr4 | 114593807 | 114683225 |
| a0001c0011t0001 | 0/0 | 3733 | 1 | 0 | 0 | 0 | 0 | 1 | UGT8_chr4_114593807_114683225 | UGT8 | AGAGA others(3728): Show |
chr4 | 114593807 | 114683225 |
| a0001c0013t0003 | 0/0 | 3733 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | AGAGA others(3728): Show |
chr4 | 114593807 | 114683225 |
| a0001c0014t0013 | 0/0 | 3733 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | AGAGA others(3728): Show |
chr4 | 114593807 | 114683225 |
| a0001c0015t0014 | 0/0 | 3733 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | AGAGA others(3728): Show |
chr4 | 114593807 | 114683225 |
| a0002c0002t0002 | 0/0 | 3733 | 36 | 0 | 4 | 26 | 2 | 4 | UGT8_chr4_114593807_114683225 | UGT8 | AGAGA others(3728): Show |
chr4 | 114593807 | 114683225 |
| a0003c0004t0001 | 0/0 | 3733 | 4 | 0 | 4 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | AGAGA others(3728): Show |
chr4 | 114593807 | 114683225 |
| a0004c0005t0003 | 1/0 | 3733 | 3 | 2 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | AGAGA others(3728): Show |
chr4 | 114593807 | 114683225 |
| a0005c0008t0001 | 0/0 | 3733 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | AGAGA others(3728): Show |
chr4 | 114593807 | 114683225 |
| a0006c0012t0004 | 0/0 | 3733 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | AGAGA others(3728): Show |
chr4 | 114593807 | 114683225 |
| a0007c0009t0003 | 0/0 | 3733 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | AGAGA others(3728): Show |
chr4 | 114593807 | 114683225 |
| a0008c0010t0002 | 0/0 | 3733 | 1 | 0 | 0 | 0 | 0 | 1 | UGT8_chr4_114593807_114683225 | UGT8 | AGAGA others(3728): Show |
chr4 | 114593807 | 114683225 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0008 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0101 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0002g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0003g0005 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0003g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0003g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0003g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0003g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0003g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0003g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0003g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0003g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0003g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0003g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0003g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0003g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0003g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0003g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0003g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0003g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0003g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0003g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0003g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0003g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0003g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0003g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0003g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0003g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0003g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0003g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0003g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0003g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0003g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0004g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0004g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0004g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0004g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0004g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0004g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0004g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0004g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0004g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0005g0012 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0005g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0005g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0005g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0006g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0006g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0006g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0006g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0006g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0007g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0007g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0007g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0007g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0008g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0008g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0008g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0009g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0009g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0010g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0010g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0012g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0016g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0017g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0001t0018g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0003t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0003t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0003t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0003t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0003t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0003t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0003t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0003t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0003t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0003t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0003t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0006t0003g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0006t0003g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0007t0011g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0007t0015g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0011t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0013t0003g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0014t0013g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0001c0015t0014g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0002c0002t0002g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0002c0002t0002g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0002c0002t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0002c0002t0002g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0002c0002t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0002c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0002c0002t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0002c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0002c0002t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0002c0002t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0002c0002t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0002c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0002c0002t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0002c0002t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0002c0002t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0002c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0002c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0002c0002t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0002c0002t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0002c0002t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0002c0002t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0002c0002t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0002c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0002c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0002c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0002c0002t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0002c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0002c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0002c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0003c0004t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0003c0004t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0003c0004t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0004c0005t0003g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0004c0005t0003g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0004c0005t0003g0237 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0005c0008t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0006c0012t0004g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0007c0009t0003g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| a0008c0010t0002g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0002 | c0002 | t0002 | g0231 | EUR | GBR | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG00140 | hp2 | a0001 | c0001 | t0005 | g0012 | EUR | GBR | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0038 | EUR | FIN | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG00280 | hp2 | a0001 | c0003 | t0001 | g0192 | EUR | FIN | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0112 | EUR | FIN | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0133 | EUR | FIN | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG00423 | hp1 | a0001 | c0003 | t0001 | g0184 | EAS | CHS | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | CHS | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | CHS | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | CHS | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG00558 | hp1 | a0002 | c0002 | t0002 | g0010 | EAS | CHS | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | CHS | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | CHS | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG00597 | hp2 | a0002 | c0002 | t0002 | g0180 | EAS | CHS | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | CHS | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG00621 | hp2 | a0002 | c0002 | t0002 | g0162 | EAS | CHS | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG00639 | hp1 | a0001 | c0001 | t0009 | g0255 | AMR | PUR | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG00733 | hp1 | a0002 | c0002 | t0002 | g0146 | AMR | PUR | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG00733 | hp2 | a0003 | c0004 | t0001 | g0007 | AMR | PUR | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0179 | AMR | PUR | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG00738 | hp2 | a0001 | c0006 | t0003 | g0233 | AMR | PUR | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG00741 | hp1 | a0003 | c0004 | t0001 | g0007 | AMR | PUR | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0119 | AMR | PUR | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG01069 | hp1 | a0001 | c0001 | t0005 | g0013 | AMR | PUR | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG01071 | hp1 | a0001 | c0001 | t0005 | g0013 | AMR | PUR | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG01074 | hp1 | a0002 | c0002 | t0002 | g0014 | AMR | PUR | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0118 | AMR | PUR | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0219 | AMR | PUR | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG01109 | hp2 | a0001 | c0015 | t0014 | g0168 | AMR | PUR | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0220 | AMR | PUR | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0218 | AMR | PUR | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0131 | AMR | PUR | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG01192 | hp2 | a0001 | c0001 | t0004 | g0140 | AMR | PUR | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG01243 | hp1 | a0001 | c0001 | t0007 | g0224 | AMR | PUR | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0130 | AMR | PUR | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0251 | AMR | CLM | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0005 | AMR | CLM | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | CLM | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG01257 | hp2 | a0001 | c0007 | t0015 | g0253 | AMR | CLM | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0005 | AMR | CLM | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | CLM | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG01361 | hp1 | a0002 | c0002 | t0002 | g0139 | AMR | CLM | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG01361 | hp2 | a0001 | c0001 | t0016 | g0122 | AMR | CLM | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0109 | EUR | IBS | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0171 | EUR | IBS | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0170 | EUR | IBS | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0081 | EUR | IBS | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0227 | AFR | ACB | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | ACB | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0247 | AFR | ACB | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG01928 | hp1 | a0001 | c0003 | t0001 | g0195 | AMR | PEL | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG01928 | hp2 | a0003 | c0004 | t0001 | g0095 | AMR | PEL | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG01934 | hp1 | a0002 | c0002 | t0002 | g0014 | AMR | PEL | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0126 | AMR | PEL | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0238 | AMR | PEL | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG01981 | hp1 | a0001 | c0003 | t0001 | g0186 | AMR | PEL | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG01981 | hp2 | a0003 | c0004 | t0001 | g0047 | AMR | PEL | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG02004 | hp2 | a0001 | c0003 | t0001 | g0193 | AMR | PEL | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG02015 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | KHV | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | KHV | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG02040 | hp1 | a0002 | c0002 | t0002 | g0158 | EAS | KHV | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG02055 | hp1 | a0001 | c0001 | t0004 | g0141 | AFR | ACB | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG02055 | hp2 | a0001 | c0001 | t0008 | g0205 | AFR | ACB | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG02056 | hp1 | a0002 | c0002 | t0002 | g0157 | EAS | KHV | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | KHV | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | KHV | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG02074 | hp2 | a0001 | c0003 | t0001 | g0198 | EAS | KHV | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | KHV | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | KHV | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG02083 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | KHV | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG02132 | hp2 | a0002 | c0002 | t0002 | g0147 | EAS | KHV | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0215 | AFR | ACB | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0174 | AFR | ACB | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | CDX | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | CDX | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG02165 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | CDX | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CDX | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0173 | AFR | ACB | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0155 | AFR | ACB | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0016 | AFR | ACB | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0116 | AFR | ACB | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0246 | AFR | ACB | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0016 | AFR | ACB | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG02523 | hp2 | a0002 | c0002 | t0002 | g0142 | EAS | KHV | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG02572 | hp2 | a0001 | c0001 | t0006 | g0208 | AFR | GWD | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG02602 | hp2 | a0001 | c0001 | t0005 | g0176 | SAS | PJL | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG02615 | hp1 | a0001 | c0001 | t0017 | g0211 | AFR | GWD | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0257 | AFR | GWD | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG02698 | hp1 | a0002 | c0002 | t0002 | g0137 | SAS | PJL | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0243 | AFR | GWD | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG02723 | hp1 | a0004 | c0005 | t0003 | g0235 | AFR | GWD | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG02723 | hp2 | a0001 | c0001 | t0004 | g0161 | AFR | GWD | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG02738 | hp1 | a0001 | c0011 | t0001 | g0048 | SAS | PJL | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0121 | SAS | PJL | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0228 | AFR | GWD | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0232 | AFR | GWD | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0149 | AFR | GWD | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0249 | AFR | GWD | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0225 | AFR | GWD | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG02895 | hp1 | a0001 | c0001 | t0006 | g0015 | AFR | GWD | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG02895 | hp2 | a0001 | c0001 | t0008 | g0206 | AFR | GWD | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG02896 | hp1 | a0001 | c0001 | t0008 | g0204 | AFR | GWD | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG02896 | hp2 | a0001 | c0001 | t0007 | g0222 | AFR | GWD | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG02897 | hp1 | a0001 | c0001 | t0006 | g0015 | AFR | GWD | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG02897 | hp2 | a0001 | c0001 | t0007 | g0223 | AFR | GWD | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0216 | AFR | ESN | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | ESN | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG02976 | hp1 | a0005 | c0008 | t0001 | g0097 | AFR | ESN | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG02976 | hp2 | a0001 | c0001 | t0004 | g0148 | AFR | ESN | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG03017 | hp2 | a0001 | c0001 | t0018 | g0128 | SAS | PJL | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0242 | AFR | GWD | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG03041 | hp2 | a0001 | c0001 | t0004 | g0160 | AFR | GWD | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0214 | AFR | MSL | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG03098 | hp2 | a0004 | c0005 | t0003 | g0236 | AFR | MSL | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0250 | AFR | ESN | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0244 | AFR | ESN | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG03195 | hp2 | a0001 | c0013 | t0003 | g0212 | AFR | ESN | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG03209 | hp1 | a0001 | c0001 | t0009 | g0203 | AFR | MSL | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0240 | AFR | MSL | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG03225 | hp1 | a0001 | c0001 | t0007 | g0221 | AFR | MSL | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG03225 | hp2 | a0006 | c0012 | t0004 | g0153 | AFR | MSL | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0009 | SAS | PJL | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0213 | AFR | MSL | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | MSL | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0256 | AFR | ESN | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0159 | AFR | ESN | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG03540 | hp1 | a0001 | c0007 | t0011 | g0254 | AFR | GWD | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0017 | AFR | MSL | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG03579 | hp2 | a0001 | c0001 | t0004 | g0165 | AFR | MSL | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG03669 | hp1 | a0001 | c0001 | t0010 | g0052 | SAS | PJL | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0009 | SAS | PJL | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG03704 | hp2 | a0008 | c0010 | t0002 | g0024 | SAS | PJL | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG03710 | hp1 | a0001 | c0001 | t0005 | g0177 | SAS | PJL | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG03710 | hp2 | a0001 | c0001 | t0010 | g0003 | SAS | PJL | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG03927 | hp1 | a0002 | c0002 | t0002 | g0154 | SAS | BEB | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | BEB | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | BEB | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | BEB | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG04204 | hp1 | a0002 | c0002 | t0002 | g0138 | SAS | STU | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | STU | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG04228 | hp1 | a0002 | c0002 | t0002 | g0164 | SAS | STU | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0129 | SAS | STU | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0248 | AFR | YRI | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | YRI | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA18612 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | CHB | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | YRI | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0017 | AFR | YRI | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA18939 | hp2 | a0002 | c0002 | t0002 | g0144 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA18948 | hp2 | a0002 | c0002 | t0002 | g0156 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA18953 | hp2 | a0002 | c0002 | t0002 | g0229 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA18957 | hp2 | a0002 | c0002 | t0002 | g0163 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA18986 | hp2 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA18992 | hp1 | a0001 | c0003 | t0001 | g0042 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA18993 | hp2 | a0002 | c0002 | t0002 | g0143 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA18999 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA19001 | hp2 | a0002 | c0002 | t0002 | g0150 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA19005 | hp2 | a0002 | c0002 | t0002 | g0136 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA19006 | hp1 | a0002 | c0002 | t0002 | g0151 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | LWK | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0252 | AFR | LWK | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0230 | AFR | LWK | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0172 | AFR | LWK | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA19054 | hp2 | a0001 | c0003 | t0001 | g0188 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA19063 | hp1 | a0001 | c0003 | t0001 | g0199 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA19064 | hp1 | a0001 | c0003 | t0001 | g0196 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA19064 | hp2 | a0002 | c0002 | t0002 | g0178 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA19067 | hp2 | a0002 | c0002 | t0002 | g0152 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA19075 | hp1 | a0002 | c0002 | t0002 | g0135 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA19077 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA19086 | hp2 | a0001 | c0003 | t0001 | g0185 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA19088 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA19240 | hp1 | a0001 | c0006 | t0003 | g0239 | AFR | YRI | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0241 | AFR | YRI | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA20129 | hp1 | a0001 | c0014 | t0013 | g0169 | AFR | ASW | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA20129 | hp2 | a0001 | c0001 | t0012 | g0226 | AFR | ASW | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA20752 | hp1 | a0002 | c0002 | t0002 | g0145 | EUR | TSI | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0035 | EUR | TSI | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0044 | EUR | TSI | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA20805 | hp2 | a0001 | c0001 | t0005 | g0012 | EUR | TSI | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG02109 | hp1 | a0001 | c0001 | t0006 | g0210 | AFR | ACB | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | ACB | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | ACB | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG03471 | hp1 | a0001 | c0001 | t0006 | g0207 | AFR | MSL | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG03471 | hp2 | a0007 | c0009 | t0003 | g0234 | AFR | MSL | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0245 | AFR | USA | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0217 | AFR | USA | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | USA | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0175 | AFR | USA | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0120 | AFR | LWK | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| NA21309 | hp2 | a0001 | c0001 | t0006 | g0209 | AFR | LWK | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0101 | REF | REF | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| homoSapiens | grch38p0 | a0004 | c0005 | t0003 | g0237 | REF | REF | UGT8_chr4_114593807_114683225 | UGT8 | chr4 | 114593807 | 114683225 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:114623334 | G | A | 1 | a0005 | 1 | HG02976.hp1 | missense_variant | MODERATE | c.454G>A | p.Gly152Arg | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/6 | 624/3733 | 454/1626 | 152/541 | chr4 | 114623334 | |||
| chr4:114623440 | G | A | 1 | a0007 | 1 | HG03471.hp2 | missense_variant | MODERATE | c.560G>A | p.Arg187His | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/6 | 730/3733 | 560/1626 | 187/541 | chr4 | 114623440 | |||
| chr4:114623540 | G | C | 1 | a0008 | 1 | HG03704.hp2 | missense_variant | MODERATE | c.660G>C | p.Gln220His | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/6 | 830/3733 | 660/1626 | 220/541 | chr4 | 114623540 | |||
| chr4:114623557 | C | T | 2 | a0002 a0008 |
37 | HG00140.hp1 HG00558.hp1 HG00597.hp2 others(34): Show |
missense_variant | MODERATE | c.677C>T | p.Pro226Leu | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/6 | 847/3733 | 677/1626 | 226/541 | chr4 | 114623557 | |||
| chr4:114668146 | A | G | 7 | a0001 a0002 a0003 others(4): Show |
276 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(273): Show |
missense_variant | MODERATE | c.1104A>G | p.Ile368Met | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/6 | 1274/3733 | 1104/1626 | 368/541 | chr4 | 114668146 | |||
| chr4:114668285 | A | G | 1 | a0003 | 4 | HG00733.hp2 HG00741.hp1 HG01928.hp2 others(1): Show |
missense_variant | MODERATE | c.1243A>G | p.Lys415Glu | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/6 | 1413/3733 | 1243/1626 | 415/541 | chr4 | 114668285 | |||
| chr4:114676026 | A | G | 1 | a0006 | 1 | HG03225.hp2 | missense_variant | MODERATE | c.1364A>G | p.Asn455Ser | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 6/6 | 1534/3733 | 1364/1626 | 455/541 | chr4 | 114676026 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:114623408 | C | T | 1 | a0001c0015 | 1 | HG01109.hp2 | synonymous_variant | LOW | c.528C>T | p.Tyr176Tyr | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/6 | 698/3733 | 528/1626 | 176/541 | chr4 | 114623408 | |||
| chr4:114623498 | G | T | 1 | a0001c0007 | 2 | HG01257.hp2 HG03540.hp1 |
synonymous_variant | LOW | c.618G>T | p.Gly206Gly | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/6 | 788/3733 | 618/1626 | 206/541 | chr4 | 114623498 | |||
| chr4:114623558 | A | G | 13 | a0001c0001 a0001c0003 a0001c0007 others(10): Show |
274 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(271): Show |
synonymous_variant | LOW | c.678A>G | p.Pro226Pro | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/6 | 848/3733 | 678/1626 | 226/541 | chr4 | 114623558 | |||
| chr4:114623615 | C | T | 1 | a0001c0014 | 1 | NA20129.hp1 | synonymous_variant | LOW | c.735C>T | p.Asp245Asp | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/6 | 905/3733 | 735/1626 | 245/541 | chr4 | 114623615 | |||
| chr4:114623621 | A | G | 1 | a0001c0003 | 11 | HG00280.hp2 HG00423.hp1 HG01928.hp1 others(8): Show |
synonymous_variant | LOW | c.741A>G | p.Ala247Ala | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/6 | 911/3733 | 741/1626 | 247/541 | chr4 | 114623621 | |||
| chr4:114665716 | C | T | 1 | a0001c0013 | 1 | HG03195.hp2 | synonymous_variant | LOW | c.1002C>T | p.Asn334Asn | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 4/6 | 1172/3733 | 1002/1626 | 334/541 | chr4 | 114665716 | |||
| chr4:114676270 | T | C | 1 | a0001c0011 | 1 | HG02738.hp1 | synonymous_variant | LOW | c.1608T>C | p.His536His | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 6/6 | 1778/3733 | 1608/1626 | 536/541 | chr4 | 114676270 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:114598933 | C | T | 1 | a0001c0001t0018 | 1 | HG03017.hp2 | 5_prime_UTR_variant | MODIFIER | c.-44C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/6 | 23948 | chr4 | 114598933 | ||||||
| chr4:114598947 | A | G | 20 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(17): Show |
227 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(224): Show |
5_prime_UTR_variant | MODIFIER | c.-30A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/6 | 23934 | chr4 | 114598947 | ||||||
| chr4:114676297 | C | T | 2 | a0001c0001t0006 a0001c0001t0017 |
7 | HG02109.hp1 HG02572.hp2 HG02615.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*9C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 6/6 | 9 | chr4 | 114676297 | ||||||
| chr4:114676590 | G | A | 2 | a0001c0001t0008 a0001c0001t0009 |
5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*302G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 6/6 | 302 | chr4 | 114676590 | ||||||
| chr4:114676639 | GTA | G | 1 | a0001c0001t0007 | 4 | HG01243.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*353_*354delAT | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 6/6 | 353 | INFO_REALIGN_3_PRIME | chr4 | 114676639 | |||||
| chr4:114676641 | A | ATG | 5 | a0001c0001t0001 a0001c0001t0003 a0001c0003t0001 others(2): Show |
26 | HG00280.hp2 HG00423.hp1 HG01255.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*375_*376dupGT | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 6/6 | 377 | INFO_REALIGN_3_PRIME | chr4 | 114676641 | |||||
| chr4:114676641 | ATG | A | 4 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0012 others(1): Show |
4 | HG01109.hp2 NA19043.hp1 NA20129.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*375_*376delGT | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 6/6 | 375 | INFO_REALIGN_3_PRIME | chr4 | 114676641 | |||||
| chr4:114676665 | T | TTGTGTG | 2 | a0001c0001t0001 a0001c0003t0001 |
7 | NA18957.hp1 NA18961.hp2 NA18983.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*391_*396dupGTGTGT | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 6/6 | 397 | INFO_REALIGN_3_PRIME | chr4 | 114676665 | |||||
| chr4:114676797 | A | C | 1 | a0001c0001t0016 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*509A>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 6/6 | 509 | chr4 | 114676797 | ||||||
| chr4:114676799 | G | A | 2 | a0001c0001t0004 a0006c0012t0004 |
10 | HG01192.hp2 HG02055.hp1 HG02257.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*511G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 6/6 | 511 | chr4 | 114676799 | ||||||
| chr4:114676939 | T | C | 8 | a0001c0001t0001 a0001c0001t0010 a0001c0003t0001 others(5): Show |
128 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
3_prime_UTR_variant | MODIFIER | c.*651T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 6/6 | 651 | chr4 | 114676939 | ||||||
| chr4:114677109 | A | G | 1 | a0001c0015t0014 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*821A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 6/6 | 821 | chr4 | 114677109 | ||||||
| chr4:114677165 | C | T | 1 | a0001c0001t0010 | 2 | HG03669.hp1 HG03710.hp2 |
3_prime_UTR_variant | MODIFIER | c.*877C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 6/6 | 877 | chr4 | 114677165 | ||||||
| chr4:114677248 | G | A | 1 | a0001c0007t0015 | 1 | HG01257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*960G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 6/6 | 960 | chr4 | 114677248 | ||||||
| chr4:114677304 | T | G | 2 | a0001c0007t0011 a0001c0007t0015 |
2 | HG01257.hp2 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1016T>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 6/6 | 1016 | chr4 | 114677304 | ||||||
| chr4:114677421 | G | A | 2 | a0001c0007t0011 a0001c0007t0015 |
2 | HG01257.hp2 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1133G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 6/6 | 1133 | chr4 | 114677421 | ||||||
| chr4:114677554 | T | C | 1 | a0001c0001t0017 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1266T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 6/6 | 1266 | chr4 | 114677554 | ||||||
| chr4:114678003 | T | G | 1 | a0001c0001t0005 | 6 | HG00140.hp2 HG01069.hp1 HG01071.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1715T>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 6/6 | 1715 | chr4 | 114678003 | ||||||
| chr4:114678046 | A | G | 1 | a0001c0001t0012 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1758A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 6/6 | 1758 | chr4 | 114678046 | ||||||
| chr4:114678116 | T | C | 1 | a0001c0014t0013 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1828T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 6/6 | 1828 | chr4 | 114678116 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:114599013 | G | A | 103 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(100): Show |
109 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.-3+39G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114599013 | |||||||
| chr4:114599249 | G | C | 231 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(228): Show |
253 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.-3+275G>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114599249 | |||||||
| chr4:114599383 | C | T | 1 | a0002c0002t0002g0231 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-3+409C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114599383 | |||||||
| chr4:114599430 | C | G | 1 | a0001c0001t0003g0230 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-3+456C>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114599430 | |||||||
| chr4:114599438 | C | T | 1 | a0001c0001t0001g0115 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-3+464C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114599438 | |||||||
| chr4:114599581 | A | G | 2 | a0001c0001t0001g0113 a0001c0001t0001g0114 |
2 | HG00642.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.-3+607A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114599581 | |||||||
| chr4:114599608 | G | T | 1 | a0002c0002t0002g0229 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-3+634G>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114599608 | |||||||
| chr4:114599615 | C | T | 1 | a0001c0001t0003g0257 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-3+641C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114599615 | |||||||
| chr4:114599675 | G | A | 1 | a0001c0001t0003g0116 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-3+701G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114599675 | |||||||
| chr4:114599833 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-3+859C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114599833 | |||||||
| chr4:114599884 | G | A | 1 | a0001c0001t0003g0232 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-3+910G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114599884 | |||||||
| chr4:114599943 | C | T | 22 | a0001c0001t0003g0005 a0001c0001t0003g0016 a0001c0001t0003g0017 others(19): Show |
26 | HG01106.hp1 HG01168.hp1 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.-3+969C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114599943 | |||||||
| chr4:114599954 | C | T | 1 | a0001c0001t0001g0111 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-3+980C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114599954 | |||||||
| chr4:114599988 | C | T | 6 | a0001c0001t0006g0015 a0001c0001t0006g0207 a0001c0001t0006g0208 others(3): Show |
7 | HG02109.hp1 HG02572.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.-3+1014C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114599988 | |||||||
| chr4:114600413 | G | A | 1 | a0001c0001t0001g0018 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-3+1439G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114600413 | |||||||
| chr4:114600417 | A | G | 1 | a0001c0001t0003g0256 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-3+1443A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114600417 | |||||||
| chr4:114600442 | C | T | 5 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(2): Show |
5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3+1468C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114600442 | |||||||
| chr4:114600451 | C | A | 1 | a0001c0001t0001g0019 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-3+1477C>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114600451 | |||||||
| chr4:114600640 | A | C | 22 | a0001c0001t0003g0005 a0001c0001t0003g0016 a0001c0001t0003g0017 others(19): Show |
26 | HG01106.hp1 HG01168.hp1 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.-3+1666A>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114600640 | |||||||
| chr4:114600648 | C | G | 122 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(119): Show |
128 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.-3+1674C>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114600648 | |||||||
| chr4:114600811 | T | C | 1 | a0001c0001t0003g0257 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-3+1837T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114600811 | |||||||
| chr4:114600872 | A | G | 1 | a0002c0002t0002g0178 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-3+1898A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114600872 | |||||||
| chr4:114600971 | A | G | 1 | a0001c0001t0001g0110 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-3+1997A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114600971 | |||||||
| chr4:114601150 | G | A | 24 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0020 others(21): Show |
26 | HG00323.hp2 HG00438.hp2 HG00558.hp2 others(23): Show |
intron_variant | MODIFIER | c.-3+2176G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114601150 | |||||||
| chr4:114601232 | G | T | 22 | a0001c0001t0003g0005 a0001c0001t0003g0016 a0001c0001t0003g0017 others(19): Show |
26 | HG01106.hp1 HG01168.hp1 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.-3+2258G>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114601232 | |||||||
| chr4:114601262 | T | G | 1 | a0001c0001t0003g0116 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-3+2288T>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114601262 | |||||||
| chr4:114601589 | TA | T | 28 | a0001c0001t0001g0109 a0001c0001t0002g0006 a0001c0001t0002g0009 others(25): Show |
32 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.-3+2624delA | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114601589 | ||||||
| chr4:114601744 | G | C | 1 | a0001c0001t0001g0025 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-3+2770G>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114601744 | |||||||
| chr4:114601829 | G | GT | 25 | a0001c0001t0001g0108 a0001c0001t0003g0005 a0001c0001t0003g0016 others(22): Show |
29 | HG00639.hp1 HG01106.hp1 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.-3+2869dupT | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114601829 | ||||||
| chr4:114601833 | T | G | 35 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0020 others(32): Show |
40 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.-3+2859T>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114601833 | |||||||
| chr4:114602107 | G | A | 1 | a0001c0001t0001g0026 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-3+3133G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114602107 | |||||||
| chr4:114602153 | T | C | 2 | a0001c0001t0003g0016 a0001c0013t0003g0212 |
3 | HG02258.hp1 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-3+3179T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114602153 | |||||||
| chr4:114602254 | C | T | 2 | a0001c0007t0011g0254 a0001c0007t0015g0253 |
2 | HG01257.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-3+3280C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114602254 | |||||||
| chr4:114602332 | G | A | 201 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(198): Show |
219 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.-3+3358G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114602332 | |||||||
| chr4:114602529 | A | G | 1 | a0001c0001t0003g0116 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-3+3555A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114602529 | |||||||
| chr4:114602711 | G | GAT | 7 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(4): Show |
7 | HG00639.hp1 HG01257.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-3+3739_-3+3740dup others(2): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114602711 | ||||||
| chr4:114602742 | G | A | 22 | a0001c0001t0003g0005 a0001c0001t0003g0016 a0001c0001t0003g0017 others(19): Show |
26 | HG01106.hp1 HG01168.hp1 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.-3+3768G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114602742 | |||||||
| chr4:114602786 | T | A | 40 | a0001c0001t0004g0140 a0001c0001t0004g0141 a0001c0001t0004g0148 others(37): Show |
47 | HG00140.hp1 HG00558.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.-3+3812T>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114602786 | |||||||
| chr4:114603052 | A | G | 3 | a0001c0001t0002g0011 a0001c0001t0002g0170 a0001c0001t0002g0171 |
4 | HG01257.hp1 HG01258.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.-3+4078A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114603052 | |||||||
| chr4:114603054 | A | C | 1 | a0001c0001t0001g0109 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-3+4080A>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114603054 | |||||||
| chr4:114603271 | T | C | 1 | a0001c0001t0001g0027 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-3+4297T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114603271 | |||||||
| chr4:114603489 | A | G | 3 | a0001c0001t0002g0011 a0001c0001t0002g0170 a0001c0001t0002g0171 |
4 | HG01257.hp1 HG01258.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.-3+4515A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114603489 | |||||||
| chr4:114603665 | G | A | 1 | a0001c0001t0002g0117 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-3+4691G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114603665 | |||||||
| chr4:114603708 | T | C | 5 | a0001c0001t0002g0009 a0001c0001t0002g0118 a0001c0001t0002g0119 others(2): Show |
6 | HG00741.hp2 HG01099.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.-3+4734T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114603708 | |||||||
| chr4:114603855 | T | C | 7 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(4): Show |
7 | HG00639.hp1 HG01257.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-3+4881T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114603855 | |||||||
| chr4:114603918 | G | C | 1 | a0001c0001t0002g0172 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-3+4944G>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114603918 | |||||||
| chr4:114603963 | T | C | 3 | a0001c0001t0002g0011 a0001c0001t0002g0170 a0001c0001t0002g0171 |
4 | HG01257.hp1 HG01258.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.-3+4989T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114603963 | |||||||
| chr4:114603964 | TA | T | 3 | a0001c0001t0002g0011 a0001c0001t0002g0170 a0001c0001t0002g0171 |
4 | HG01257.hp1 HG01258.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.-3+4992delA | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114603964 | ||||||
| chr4:114604196 | C | G | 2 | a0001c0007t0011g0254 a0001c0007t0015g0253 |
2 | HG01257.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-3+5222C>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114604196 | |||||||
| chr4:114604293 | C | T | 2 | a0001c0001t0003g0016 a0001c0013t0003g0212 |
3 | HG02258.hp1 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-3+5319C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114604293 | |||||||
| chr4:114604318 | A | G | 4 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(1): Show |
4 | HG02055.hp2 HG02895.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3+5344A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114604318 | |||||||
| chr4:114604457 | C | CT | 69 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0104 others(66): Show |
75 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.-3+5498dupT | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114604457 | ||||||
| chr4:114604457 | C | CTT | 44 | a0001c0001t0002g0121 a0001c0001t0002g0173 a0001c0001t0002g0174 others(41): Show |
51 | HG00140.hp1 HG00558.hp1 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.-3+5497_-3+5498dup others(2): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114604457 | ||||||
| chr4:114604472 | TC | T | 4 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(1): Show |
4 | HG02055.hp2 HG02895.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3+5503delC | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114604472 | ||||||
| chr4:114604473 | C | T | 229 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(226): Show |
251 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.-3+5499C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114604473 | |||||||
| chr4:114604474 | C | T | 29 | a0001c0001t0003g0005 a0001c0001t0003g0016 a0001c0001t0003g0017 others(26): Show |
33 | HG00639.hp1 HG01106.hp1 HG01168.hp1 others(30): Show |
intron_variant | MODIFIER | c.-3+5500C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114604474 | |||||||
| chr4:114604545 | G | T | 3 | a0001c0001t0002g0011 a0001c0001t0002g0170 a0001c0001t0002g0171 |
4 | HG01257.hp1 HG01258.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.-3+5571G>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114604545 | |||||||
| chr4:114604748 | C | T | 1 | a0001c0001t0004g0165 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-3+5774C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114604748 | |||||||
| chr4:114604769 | A | G | 42 | a0001c0001t0002g0174 a0001c0001t0002g0175 a0001c0001t0004g0140 others(39): Show |
49 | HG00140.hp1 HG00558.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.-3+5795A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114604769 | |||||||
| chr4:114604887 | T | C | 1 | a0001c0001t0001g0102 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-3+5913T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114604887 | |||||||
| chr4:114604888 | C | T | 1 | a0001c0001t0001g0102 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-3+5914C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114604888 | |||||||
| chr4:114605205 | A | G | 1 | a0001c0001t0001g0100 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-3+6231A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114605205 | |||||||
| chr4:114605540 | A | G | 1 | a0001c0014t0013g0169 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-3+6566A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114605540 | |||||||
| chr4:114605935 | A | C | 1 | a0001c0001t0002g0117 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-3+6961A>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114605935 | |||||||
| chr4:114606104 | C | A | 1 | a0002c0002t0002g0136 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-3+7130C>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114606104 | |||||||
| chr4:114606130 | C | T | 24 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0020 others(21): Show |
26 | HG00323.hp2 HG00438.hp2 HG00558.hp2 others(23): Show |
intron_variant | MODIFIER | c.-3+7156C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114606130 | |||||||
| chr4:114606152 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-3+7178C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114606152 | |||||||
| chr4:114606327 | A | C | 1 | a0001c0001t0001g0098 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-3+7353A>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114606327 | |||||||
| chr4:114606433 | T | C | 7 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(4): Show |
7 | HG00639.hp1 HG01257.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-3+7459T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114606433 | |||||||
| chr4:114606734 | A | T | 7 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(4): Show |
7 | HG00639.hp1 HG01257.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-3+7760A>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114606734 | |||||||
| chr4:114606738 | G | A | 1 | a0001c0001t0001g0028 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-3+7764G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114606738 | |||||||
| chr4:114606826 | T | C | 5 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(2): Show |
5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3+7852T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114606826 | |||||||
| chr4:114607233 | G | A | 2 | a0001c0007t0011g0254 a0001c0007t0015g0253 |
2 | HG01257.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-3+8259G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114607233 | |||||||
| chr4:114607486 | G | A | 1 | a0001c0001t0003g0213 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-3+8512G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114607486 | |||||||
| chr4:114607728 | A | G | 3 | a0001c0001t0002g0011 a0001c0001t0002g0170 a0001c0001t0002g0171 |
4 | HG01257.hp1 HG01258.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.-3+8754A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114607728 | |||||||
| chr4:114608093 | G | A | 6 | a0001c0001t0006g0015 a0001c0001t0006g0207 a0001c0001t0006g0208 others(3): Show |
7 | HG02109.hp1 HG02572.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.-3+9119G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114608093 | |||||||
| chr4:114608098 | T | C | 7 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(4): Show |
7 | HG00639.hp1 HG01257.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-3+9124T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114608098 | |||||||
| chr4:114608291 | G | T | 6 | a0001c0001t0006g0015 a0001c0001t0006g0207 a0001c0001t0006g0208 others(3): Show |
7 | HG02109.hp1 HG02572.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.-3+9317G>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114608291 | |||||||
| chr4:114608520 | C | A | 24 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0020 others(21): Show |
26 | HG00323.hp2 HG00438.hp2 HG00558.hp2 others(23): Show |
intron_variant | MODIFIER | c.-3+9546C>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114608520 | |||||||
| chr4:114608561 | A | C | 1 | a0001c0001t0003g0116 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-3+9587A>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114608561 | |||||||
| chr4:114608708 | A | G | 7 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(4): Show |
7 | HG00639.hp1 HG01257.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-3+9734A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114608708 | |||||||
| chr4:114608771 | A | T | 1 | a0001c0001t0001g0110 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-3+9797A>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114608771 | |||||||
| chr4:114608867 | G | C | 2 | a0001c0001t0006g0207 a0001c0001t0006g0208 |
2 | HG02572.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-3+9893G>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114608867 | |||||||
| chr4:114608935 | A | G | 7 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(4): Show |
7 | HG00639.hp1 HG01257.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-3+9961A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114608935 | |||||||
| chr4:114609179 | G | A | 1 | a0001c0001t0003g0213 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-3+10205G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114609179 | |||||||
| chr4:114609194 | C | A | 2 | a0001c0007t0011g0254 a0001c0007t0015g0253 |
2 | HG01257.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-3+10220C>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114609194 | |||||||
| chr4:114609253 | A | G | 6 | a0001c0001t0002g0020 a0001c0001t0002g0022 a0001c0001t0002g0023 others(3): Show |
6 | HG00323.hp2 HG00438.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.-3+10279A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114609253 | |||||||
| chr4:114609299 | A | G | 1 | a0002c0002t0002g0164 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-3+10325A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114609299 | |||||||
| chr4:114609479 | A | G | 35 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0020 others(32): Show |
40 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.-3+10505A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114609479 | |||||||
| chr4:114609801 | C | T | 1 | a0002c0002t0002g0163 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-3+10827C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114609801 | |||||||
| chr4:114609876 | A | G | 1 | a0001c0001t0001g0109 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-3+10902A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114609876 | |||||||
| chr4:114610043 | G | A | 2 | a0001c0001t0002g0006 a0001c0001t0002g0021 |
3 | NA18947.hp1 NA18961.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.-3+11069G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114610043 | |||||||
| chr4:114610074 | A | G | 1 | a0001c0001t0003g0257 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-3+11100A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114610074 | |||||||
| chr4:114610144 | A | T | 1 | a0002c0002t0002g0162 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-3+11170A>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114610144 | |||||||
| chr4:114610189 | T | C | 7 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(4): Show |
7 | HG00639.hp1 HG01257.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-3+11215T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114610189 | |||||||
| chr4:114610466 | C | T | 1 | a0001c0001t0003g0257 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-3+11492C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114610466 | |||||||
| chr4:114610549 | A | G | 1 | a0001c0001t0003g0230 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-3+11575A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114610549 | |||||||
| chr4:114610616 | T | G | 7 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(4): Show |
7 | HG00639.hp1 HG01257.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-3+11642T>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114610616 | |||||||
| chr4:114610699 | G | A | 41 | a0001c0001t0001g0019 a0001c0001t0001g0025 a0001c0001t0001g0029 others(38): Show |
41 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(38): Show |
intron_variant | MODIFIER | c.-3+11725G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114610699 | |||||||
| chr4:114610801 | C | T | 3 | a0001c0001t0002g0011 a0001c0001t0002g0170 a0001c0001t0002g0171 |
4 | HG01257.hp1 HG01258.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.-3+11827C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114610801 | |||||||
| chr4:114610859 | G | A | 1 | a0001c0001t0001g0029 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-3+11885G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114610859 | |||||||
| chr4:114610870 | A | T | 1 | a0002c0002t0002g0178 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-3+11896A>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114610870 | |||||||
| chr4:114610978 | T | G | 3 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0014t0013g0169 |
3 | HG02615.hp2 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-2-11901T>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114610978 | |||||||
| chr4:114611064 | T | C | 1 | a0001c0001t0001g0181 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-2-11815T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114611064 | |||||||
| chr4:114611278 | ATT | A | 3 | a0001c0001t0003g0017 a0001c0001t0003g0214 a0001c0001t0003g0215 |
4 | HG02145.hp1 HG03098.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-11600_-2-11599d others(4): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114611278 | |||||||
| chr4:114611403 | C | CAT | 11 | a0001c0001t0002g0006 a0001c0001t0002g0021 a0001c0001t0002g0023 others(8): Show |
12 | HG00558.hp2 HG01175.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.-2-11434_-2-11433d others(4): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114611403 | ||||||
| chr4:114611403 | CAT | C | 14 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0183 others(11): Show |
15 | HG00741.hp2 HG01099.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.-2-11434_-2-11433d others(4): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114611403 | ||||||
| chr4:114611403 | CATAT | C | 14 | a0001c0001t0001g0030 a0001c0001t0001g0166 a0001c0001t0001g0167 others(11): Show |
14 | HG02040.hp1 HG02559.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.-2-11436_-2-11433d others(6): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114611403 | ||||||
| chr4:114611403 | CATATAT | C | 10 | a0001c0001t0003g0005 a0001c0001t0003g0016 a0001c0001t0003g0116 others(7): Show |
13 | HG01106.hp1 HG01168.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.-2-11438_-2-11433d others(8): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114611403 | ||||||
| chr4:114611403 | CATATATA others(1): Show |
C | 11 | a0001c0001t0003g0213 a0001c0001t0003g0216 a0001c0001t0003g0217 others(8): Show |
13 | HG00738.hp2 HG02015.hp1 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.-2-11440_-2-11433d others(10): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114611403 | ||||||
| chr4:114611403 | CATATATA others(3): Show |
C | 33 | a0001c0001t0002g0011 a0001c0001t0002g0170 a0001c0001t0002g0171 others(30): Show |
39 | HG00140.hp1 HG00558.hp1 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.-2-11442_-2-11433d others(12): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114611403 | ||||||
| chr4:114611403 | CATATATA others(5): Show |
C | 1 | a0001c0015t0014g0168 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-2-11444_-2-11433d others(14): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114611403 | ||||||
| chr4:114611403 | CATATATA others(9): Show |
C | 3 | a0002c0002t0002g0137 a0002c0002t0002g0138 a0002c0002t0002g0164 |
3 | HG02698.hp1 HG04204.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.-2-11448_-2-11433d others(18): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114611403 | ||||||
| chr4:114611403 | CATATATA others(15): Show |
C | 2 | a0001c0001t0001g0099 a0001c0001t0003g0238 |
2 | HG01975.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.-2-11454_-2-11433d others(24): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114611403 | ||||||
| chr4:114611403 | CATATATA others(17): Show |
C | 76 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(73): Show |
81 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.-2-11456_-2-11433d others(26): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114611403 | ||||||
| chr4:114611415 | TATATATA others(25): Show |
T | 6 | a0001c0001t0006g0015 a0001c0001t0006g0207 a0001c0001t0006g0208 others(3): Show |
7 | HG02109.hp1 HG02572.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.-2-11462_-2-11431d others(34): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114611415 | ||||||
| chr4:114611423 | T | C | 1 | a0002c0002t0002g0180 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-2-11456T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114611423 | |||||||
| chr4:114611427 | TATATATA others(13): Show |
T | 4 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(1): Show |
4 | HG02055.hp2 HG02895.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-11450_-2-11431d others(22): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114611427 | ||||||
| chr4:114611431 | T | TATACATA others(27): Show |
2 | a0001c0007t0011g0254 a0001c0007t0015g0253 |
2 | HG01257.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-2-11445_-2-11444i others(36): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114611431 | ||||||
| chr4:114611441 | T | TATAC | 2 | a0001c0001t0003g0017 a0001c0001t0003g0214 |
3 | HG03098.hp1 HG03579.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-2-11435_-2-11434i others(6): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114611441 | ||||||
| chr4:114611442 | A | G | 1 | a0001c0015t0014g0168 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-2-11437A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114611442 | |||||||
| chr4:114611443 | T | C | 5 | a0001c0001t0003g0016 a0001c0001t0003g0217 a0001c0001t0005g0012 others(2): Show |
6 | HG00140.hp2 HG02451.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.-2-11436T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114611443 | |||||||
| chr4:114611443 | T | TAC | 3 | a0001c0001t0003g0241 a0001c0001t0003g0242 a0001c0001t0009g0255 |
3 | HG00639.hp1 HG03041.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-2-11435_-2-11434i others(4): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114611443 | ||||||
| chr4:114611445 | T | C | 114 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(111): Show |
123 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.-2-11434T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114611445 | |||||||
| chr4:114611445 | T | TACAC | 3 | a0001c0001t0007g0222 a0001c0001t0007g0223 a0001c0001t0007g0224 |
3 | HG01243.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-2-11424_-2-11421d others(6): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114611445 | ||||||
| chr4:114611445 | T | TATAC | 11 | a0001c0001t0001g0029 a0001c0001t0001g0041 a0001c0001t0001g0043 others(8): Show |
11 | HG01099.hp2 HG01255.hp1 HG01928.hp1 others(8): Show |
intron_variant | MODIFIER | c.-2-11433_-2-11432i others(6): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114611445 | ||||||
| chr4:114611445 | T | TATATAC | 3 | a0001c0001t0001g0045 a0001c0003t0001g0198 a0001c0003t0001g0199 |
3 | HG02074.hp2 HG02280.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.-2-11433_-2-11432i others(8): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114611445 | ||||||
| chr4:114611457 | C | CAG | 16 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(13): Show |
16 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(13): Show |
intron_variant | MODIFIER | c.-2-11418_-2-11417d others(4): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114611457 | ||||||
| chr4:114611457 | C | G | 103 | a0001c0001t0001g0019 a0001c0001t0001g0025 a0001c0001t0001g0029 others(100): Show |
116 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.-2-11422C>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114611457 | |||||||
| chr4:114611460 | A | C | 2 | a0002c0002t0002g0014 a0002c0002t0002g0180 |
3 | HG00597.hp2 HG01074.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.-2-11419A>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114611460 | |||||||
| chr4:114611516 | G | A | 1 | a0001c0003t0001g0184 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-2-11363G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114611516 | |||||||
| chr4:114611528 | C | CAT | 14 | a0001c0001t0003g0005 a0001c0001t0003g0016 a0001c0001t0003g0216 others(11): Show |
17 | HG01106.hp1 HG01168.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.-2-11333_-2-11332d others(4): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114611528 | ||||||
| chr4:114611528 | CAT | C | 7 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(4): Show |
7 | HG00639.hp1 HG01257.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-2-11333_-2-11332d others(4): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114611528 | ||||||
| chr4:114611546 | T | C | 8 | a0001c0001t0001g0112 a0001c0001t0001g0181 a0001c0001t0001g0202 others(5): Show |
8 | HG00323.hp1 HG01109.hp2 HG02698.hp1 others(5): Show |
intron_variant | MODIFIER | c.-2-11333T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114611546 | |||||||
| chr4:114611546 | T | TAC | 166 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(163): Show |
182 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.-2-11323_-2-11322d others(4): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114611546 | ||||||
| chr4:114611546 | T | TATAC | 29 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0183 others(26): Show |
31 | HG00323.hp2 HG00438.hp2 HG00558.hp2 others(28): Show |
intron_variant | MODIFIER | c.-2-11332_-2-11331i others(6): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114611546 | ||||||
| chr4:114611746 | G | T | 2 | a0001c0007t0011g0254 a0001c0007t0015g0253 |
2 | HG01257.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-2-11133G>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114611746 | |||||||
| chr4:114611949 | T | C | 3 | a0001c0001t0003g0017 a0001c0001t0003g0214 a0001c0001t0003g0215 |
4 | HG02145.hp1 HG03098.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-10930T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114611949 | |||||||
| chr4:114611970 | T | C | 1 | a0001c0001t0002g0179 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-2-10909T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114611970 | |||||||
| chr4:114611981 | G | T | 4 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 others(1): Show |
4 | HG00423.hp2 NA18983.hp1 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2-10898G>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114611981 | |||||||
| chr4:114612482 | C | T | 1 | a0001c0001t0001g0044 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-2-10397C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114612482 | |||||||
| chr4:114612619 | G | A | 22 | a0001c0001t0003g0005 a0001c0001t0003g0016 a0001c0001t0003g0017 others(19): Show |
26 | HG01106.hp1 HG01168.hp1 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.-2-10260G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114612619 | |||||||
| chr4:114612732 | A | G | 3 | a0001c0001t0004g0159 a0001c0001t0004g0160 a0001c0001t0004g0161 |
3 | HG02723.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-2-10147A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114612732 | |||||||
| chr4:114612871 | A | C | 3 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0014t0013g0169 |
3 | HG02615.hp2 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-2-10008A>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114612871 | |||||||
| chr4:114612966 | T | A | 7 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(4): Show |
7 | HG00639.hp1 HG01257.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-2-9913T>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114612966 | |||||||
| chr4:114613169 | T | G | 1 | a0001c0001t0003g0245 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-2-9710T>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114613169 | |||||||
| chr4:114613406 | A | G | 3 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0014t0013g0169 |
3 | HG02615.hp2 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-2-9473A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114613406 | |||||||
| chr4:114613543 | G | A | 7 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(4): Show |
7 | HG00639.hp1 HG01257.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-2-9336G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114613543 | |||||||
| chr4:114613573 | T | C | 40 | a0001c0001t0004g0140 a0001c0001t0004g0141 a0001c0001t0004g0148 others(37): Show |
47 | HG00140.hp1 HG00558.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.-2-9306T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114613573 | |||||||
| chr4:114613660 | T | G | 119 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(116): Show |
124 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.-2-9219T>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114613660 | |||||||
| chr4:114613678 | A | G | 1 | a0001c0001t0003g0116 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-2-9201A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114613678 | |||||||
| chr4:114613749 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-2-9130C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114613749 | |||||||
| chr4:114613788 | A | G | 120 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(117): Show |
125 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.-2-9091A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114613788 | |||||||
| chr4:114614102 | G | A | 126 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(123): Show |
132 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.-2-8777G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114614102 | |||||||
| chr4:114614235 | G | T | 235 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(232): Show |
257 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.-2-8644G>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114614235 | |||||||
| chr4:114614659 | G | T | 3 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0014t0013g0169 |
3 | HG02615.hp2 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-2-8220G>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114614659 | |||||||
| chr4:114614666 | C | T | 201 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(198): Show |
219 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.-2-8213C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114614666 | |||||||
| chr4:114614675 | CT | C | 201 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(198): Show |
219 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.-2-8203delT | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114614675 | |||||||
| chr4:114614794 | C | G | 7 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(4): Show |
7 | HG00639.hp1 HG01257.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-2-8085C>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114614794 | |||||||
| chr4:114614838 | GA | G | 5 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(2): Show |
5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-2-8040delA | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114614838 | |||||||
| chr4:114614839 | A | C | 2 | a0001c0007t0011g0254 a0001c0007t0015g0253 |
2 | HG01257.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-2-8040A>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114614839 | |||||||
| chr4:114614840 | C | CT | 8 | a0001c0001t0002g0117 a0001c0001t0002g0121 a0001c0001t0003g0005 others(5): Show |
10 | HG01106.hp1 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.-2-8019dupT | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114614840 | ||||||
| chr4:114614840 | CT | C | 178 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(175): Show |
193 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.-2-8019delT | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114614840 | ||||||
| chr4:114614841 | T | C | 5 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(2): Show |
5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-2-8038T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114614841 | |||||||
| chr4:114614852 | T | C | 1 | a0001c0003t0001g0195 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-2-8027T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114614852 | |||||||
| chr4:114614872 | A | G | 2 | a0001c0001t0002g0006 a0001c0001t0002g0021 |
3 | NA18947.hp1 NA18961.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.-2-8007A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114614872 | |||||||
| chr4:114614891 | T | A | 3 | a0001c0003t0001g0184 a0001c0003t0001g0185 a0001c0003t0001g0186 |
3 | HG00423.hp1 HG01981.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.-2-7988T>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114614891 | |||||||
| chr4:114615411 | T | C | 1 | a0001c0014t0013g0169 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-2-7468T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114615411 | |||||||
| chr4:114615452 | T | A | 1 | a0002c0002t0002g0164 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-2-7427T>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114615452 | |||||||
| chr4:114615466 | C | T | 1 | a0001c0001t0001g0115 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-2-7413C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114615466 | |||||||
| chr4:114615659 | G | A | 1 | a0001c0015t0014g0168 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-2-7220G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114615659 | |||||||
| chr4:114615862 | T | TAGTGGGC others(6747): Show |
1 | a0001c0001t0009g0255 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-2-7016_-2-7015ins others(6754): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114615862 | ||||||
| chr4:114615862 | T | TAGTGGGC others(6727): Show |
2 | a0001c0001t0008g0204 a0001c0001t0009g0203 |
2 | HG02896.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-2-7016_-2-7015ins others(6734): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114615862 | ||||||
| chr4:114615862 | T | TAGTGGGC others(6727): Show |
2 | a0001c0001t0008g0205 a0001c0001t0008g0206 |
2 | HG02055.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.-2-7016_-2-7015ins others(6734): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114615862 | ||||||
| chr4:114615862 | T | TAGTGGGC others(6726): Show |
2 | a0001c0007t0011g0254 a0001c0007t0015g0253 |
2 | HG01257.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-2-7016_-2-7015ins others(6733): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114615862 | ||||||
| chr4:114615890 | AG | A | 7 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(4): Show |
7 | HG00639.hp1 HG01257.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-2-6987delG | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114615890 | ||||||
| chr4:114615891 | GGCAGCAG others(7): Show |
G | 119 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(116): Show |
124 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.-2-6987_-2-6974del others(14): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114615891 | |||||||
| chr4:114615987 | A | G | 7 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(4): Show |
7 | HG00639.hp1 HG01257.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-2-6892A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114615987 | |||||||
| chr4:114616051 | A | T | 1 | a0001c0001t0003g0240 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-2-6828A>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114616051 | |||||||
| chr4:114616095 | C | T | 7 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(4): Show |
7 | HG00639.hp1 HG01257.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-2-6784C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114616095 | |||||||
| chr4:114616144 | T | C | 7 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(4): Show |
7 | HG00639.hp1 HG01257.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-2-6735T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114616144 | |||||||
| chr4:114616254 | C | T | 2 | a0001c0007t0011g0254 a0001c0007t0015g0253 |
2 | HG01257.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-2-6625C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114616254 | |||||||
| chr4:114616267 | C | T | 2 | a0001c0007t0011g0254 a0001c0007t0015g0253 |
2 | HG01257.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-2-6612C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114616267 | |||||||
| chr4:114616292 | G | A | 7 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(4): Show |
7 | HG00639.hp1 HG01257.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-2-6587G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114616292 | |||||||
| chr4:114616312 | C | T | 1 | a0001c0001t0002g0172 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-2-6567C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114616312 | |||||||
| chr4:114616404 | G | A | 1 | a0001c0001t0005g0176 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-2-6475G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114616404 | |||||||
| chr4:114616567 | C | T | 40 | a0001c0001t0004g0140 a0001c0001t0004g0141 a0001c0001t0004g0148 others(37): Show |
47 | HG00140.hp1 HG00558.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.-2-6312C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114616567 | |||||||
| chr4:114616575 | C | T | 1 | a0001c0001t0003g0240 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-2-6304C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114616575 | |||||||
| chr4:114616586 | C | T | 1 | a0001c0001t0003g0213 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-2-6293C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114616586 | |||||||
| chr4:114616677 | G | A | 1 | a0001c0001t0003g0241 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-2-6202G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114616677 | |||||||
| chr4:114616747 | T | C | 4 | a0001c0001t0003g0017 a0001c0001t0003g0214 a0001c0001t0003g0215 others(1): Show |
5 | HG02145.hp1 HG02886.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-2-6132T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114616747 | |||||||
| chr4:114616846 | T | C | 7 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(4): Show |
7 | HG00639.hp1 HG01257.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-2-6033T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114616846 | |||||||
| chr4:114616890 | C | T | 1 | a0001c0001t0001g0088 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-2-5989C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114616890 | |||||||
| chr4:114616986 | C | T | 29 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0020 others(26): Show |
33 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.-2-5893C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114616986 | |||||||
| chr4:114616989 | A | G | 7 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(4): Show |
7 | HG00639.hp1 HG01257.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-2-5890A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114616989 | |||||||
| chr4:114617024 | A | G | 7 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(4): Show |
7 | HG00639.hp1 HG01257.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-2-5855A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114617024 | |||||||
| chr4:114617123 | A | G | 254 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(251): Show |
276 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.-2-5756A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114617123 | |||||||
| chr4:114617140 | G | A | 1 | a0002c0002t0002g0164 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-2-5739G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114617140 | |||||||
| chr4:114617264 | A | G | 1 | a0002c0002t0002g0152 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-2-5615A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114617264 | |||||||
| chr4:114617270 | C | A | 1 | a0001c0001t0002g0117 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-2-5609C>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114617270 | |||||||
| chr4:114617314 | C | T | 7 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(4): Show |
7 | HG00639.hp1 HG01257.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-2-5565C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114617314 | |||||||
| chr4:114617357 | A | G | 113 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0002g0006 others(110): Show |
130 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.-2-5522A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114617357 | |||||||
| chr4:114617415 | A | T | 1 | a0001c0001t0001g0091 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-2-5464A>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114617415 | |||||||
| chr4:114617501 | G | A | 1 | a0001c0015t0014g0168 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-2-5378G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114617501 | |||||||
| chr4:114617504 | G | A | 1 | a0001c0001t0004g0165 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-2-5375G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114617504 | |||||||
| chr4:114617728 | G | A | 1 | a0001c0001t0003g0247 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-2-5151G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114617728 | |||||||
| chr4:114617883 | G | A | 3 | a0001c0001t0002g0011 a0001c0001t0002g0170 a0001c0001t0002g0171 |
4 | HG01257.hp1 HG01258.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2-4996G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114617883 | |||||||
| chr4:114618077 | A | G | 1 | a0001c0001t0001g0202 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-2-4802A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114618077 | |||||||
| chr4:114618077 | ATCT | A | 16 | a0001c0001t0002g0172 a0001c0001t0002g0173 a0001c0001t0003g0232 others(13): Show |
16 | HG01255.hp1 HG01891.hp1 HG01975.hp1 others(13): Show |
intron_variant | MODIFIER | c.-2-4797_-2-4795del others(3): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114618077 | ||||||
| chr4:114618148 | A | G | 1 | a0001c0001t0009g0255 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-2-4731A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114618148 | |||||||
| chr4:114618241 | A | G | 2 | a0001c0001t0001g0087 a0001c0001t0001g0099 |
2 | HG03927.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-2-4638A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114618241 | |||||||
| chr4:114618354 | C | T | 1 | a0001c0001t0001g0036 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-2-4525C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114618354 | |||||||
| chr4:114618672 | A | C | 1 | a0001c0001t0001g0094 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-2-4207A>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114618672 | |||||||
| chr4:114618710 | T | C | 1 | a0001c0001t0003g0116 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-2-4169T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114618710 | |||||||
| chr4:114618772 | G | A | 2 | a0001c0007t0011g0254 a0001c0007t0015g0253 |
2 | HG01257.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-2-4107G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114618772 | |||||||
| chr4:114619264 | T | A | 7 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(4): Show |
7 | HG00639.hp1 HG01257.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-2-3615T>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114619264 | |||||||
| chr4:114619275 | A | T | 2 | a0001c0006t0003g0233 a0001c0006t0003g0239 |
2 | HG00738.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-2-3604A>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114619275 | |||||||
| chr4:114619375 | A | G | 1 | a0001c0001t0002g0179 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-2-3504A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114619375 | |||||||
| chr4:114619420 | C | T | 2 | a0001c0007t0011g0254 a0001c0007t0015g0253 |
2 | HG01257.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-2-3459C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114619420 | |||||||
| chr4:114619438 | C | T | 3 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0014t0013g0169 |
3 | HG02615.hp2 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-2-3441C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114619438 | |||||||
| chr4:114619496 | C | T | 4 | a0001c0001t0003g0005 a0001c0001t0003g0218 a0001c0001t0003g0219 others(1): Show |
6 | HG01106.hp1 HG01168.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.-2-3383C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114619496 | |||||||
| chr4:114619599 | A | G | 1 | a0001c0015t0014g0168 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-2-3280A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114619599 | |||||||
| chr4:114619641 | C | T | 4 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(1): Show |
4 | HG02055.hp2 HG02895.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-3238C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114619641 | |||||||
| chr4:114619696 | G | C | 7 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(4): Show |
7 | HG00639.hp1 HG01257.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-2-3183G>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114619696 | |||||||
| chr4:114620100 | TA | T | 3 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0014t0013g0169 |
3 | HG02615.hp2 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-2-2774delA | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114620100 | ||||||
| chr4:114620195 | C | T | 4 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(1): Show |
4 | HG02055.hp2 HG02895.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-2684C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114620195 | |||||||
| chr4:114620229 | A | G | 1 | a0007c0009t0003g0234 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-2-2650A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114620229 | |||||||
| chr4:114620444 | C | T | 7 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(4): Show |
7 | HG00639.hp1 HG01257.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-2-2435C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114620444 | |||||||
| chr4:114620589 | G | A | 3 | a0001c0001t0002g0011 a0001c0001t0002g0170 a0001c0001t0002g0171 |
4 | HG01257.hp1 HG01258.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2-2290G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114620589 | |||||||
| chr4:114620633 | G | A | 21 | a0001c0001t0003g0005 a0001c0001t0003g0016 a0001c0001t0003g0017 others(18): Show |
25 | HG01106.hp1 HG01168.hp1 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.-2-2246G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114620633 | |||||||
| chr4:114620675 | T | C | 2 | a0001c0001t0001g0111 a0001c0001t0001g0200 |
2 | NA18948.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.-2-2204T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114620675 | |||||||
| chr4:114620748 | A | G | 2 | a0001c0007t0011g0254 a0001c0007t0015g0253 |
2 | HG01257.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-2-2131A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114620748 | |||||||
| chr4:114620805 | T | C | 28 | a0001c0001t0003g0005 a0001c0001t0003g0016 a0001c0001t0003g0017 others(25): Show |
32 | HG00639.hp1 HG01106.hp1 HG01168.hp1 others(29): Show |
intron_variant | MODIFIER | c.-2-2074T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114620805 | |||||||
| chr4:114620905 | G | T | 4 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(1): Show |
4 | HG02055.hp2 HG02895.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-1974G>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114620905 | |||||||
| chr4:114620912 | A | G | 1 | a0001c0001t0003g0257 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-2-1967A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114620912 | |||||||
| chr4:114621056 | G | T | 3 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0014t0013g0169 |
3 | HG02615.hp2 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-2-1823G>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114621056 | |||||||
| chr4:114621060 | G | T | 1 | a0001c0001t0001g0086 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-2-1819G>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114621060 | |||||||
| chr4:114621085 | TC | T | 4 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(1): Show |
4 | HG02055.hp2 HG02895.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-1790delC | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114621085 | ||||||
| chr4:114621243 | T | A | 1 | a0001c0001t0001g0046 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-2-1636T>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114621243 | |||||||
| chr4:114621831 | T | C | 1 | a0001c0001t0001g0089 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-2-1048T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114621831 | |||||||
| chr4:114621913 | A | G | 119 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(116): Show |
124 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.-2-966A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114621913 | |||||||
| chr4:114621954 | CT | C | 21 | a0001c0001t0003g0005 a0001c0001t0003g0016 a0001c0001t0003g0017 others(18): Show |
25 | HG01106.hp1 HG01168.hp1 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.-2-916delT | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114621954 | ||||||
| chr4:114622049 | G | A | 7 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(4): Show |
7 | HG00639.hp1 HG01257.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-2-830G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114622049 | |||||||
| chr4:114622088 | A | G | 21 | a0001c0001t0003g0005 a0001c0001t0003g0016 a0001c0001t0003g0017 others(18): Show |
25 | HG01106.hp1 HG01168.hp1 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.-2-791A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114622088 | |||||||
| chr4:114622105 | T | C | 1 | a0001c0001t0002g0126 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-2-774T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114622105 | |||||||
| chr4:114622111 | C | G | 1 | a0001c0001t0003g0213 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-2-768C>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114622111 | |||||||
| chr4:114622200 | C | T | 21 | a0001c0001t0003g0005 a0001c0001t0003g0016 a0001c0001t0003g0017 others(18): Show |
25 | HG01106.hp1 HG01168.hp1 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.-2-679C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114622200 | |||||||
| chr4:114622201 | G | A | 15 | a0001c0001t0001g0025 a0001c0001t0001g0029 a0001c0001t0001g0031 others(12): Show |
15 | HG00280.hp1 HG00642.hp2 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.-2-678G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114622201 | |||||||
| chr4:114622369 | G | C | 76 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(73): Show |
81 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.-2-510G>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114622369 | |||||||
| chr4:114622403 | C | T | 41 | a0001c0001t0003g0217 a0001c0001t0004g0140 a0001c0001t0004g0141 others(38): Show |
48 | HG00140.hp1 HG00558.hp1 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.-2-476C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114622403 | |||||||
| chr4:114622615 | T | G | 5 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(2): Show |
5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-2-264T>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114622615 | |||||||
| chr4:114622674 | T | C | 6 | a0001c0001t0001g0049 a0001c0001t0001g0090 a0001c0011t0001g0048 others(3): Show |
7 | HG00733.hp2 HG00741.hp1 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.-2-205T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114622674 | |||||||
| chr4:114622752 | G | A | 3 | a0001c0001t0002g0011 a0001c0001t0002g0170 a0001c0001t0002g0171 |
4 | HG01257.hp1 HG01258.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2-127G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | chr4 | 114622752 | |||||||
| chr4:114622759 | A | AT | 220 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(217): Show |
239 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.-2-110dupT | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114622759 | ||||||
| chr4:114622759 | A | ATT | 11 | a0001c0001t0003g0016 a0001c0001t0003g0216 a0001c0001t0003g0227 others(8): Show |
14 | HG00140.hp2 HG01069.hp1 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.-2-111_-2-110dupTT | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 114622759 | ||||||
| chr4:114623769 | G | T | 1 | a0001c0001t0009g0255 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.822+67G>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114623769 | |||||||
| chr4:114623836 | C | T | 1 | a0001c0001t0009g0255 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.822+134C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114623836 | |||||||
| chr4:114624205 | T | G | 3 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0014t0013g0169 |
3 | HG02615.hp2 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.822+503T>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114624205 | |||||||
| chr4:114624206 | T | C | 7 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(4): Show |
7 | HG00639.hp1 HG01257.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.822+504T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114624206 | |||||||
| chr4:114624315 | A | G | 42 | a0001c0001t0002g0174 a0001c0001t0002g0175 a0001c0001t0004g0140 others(39): Show |
49 | HG00140.hp1 HG00558.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.822+613A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114624315 | |||||||
| chr4:114624730 | C | T | 3 | a0001c0001t0002g0011 a0001c0001t0002g0170 a0001c0001t0002g0171 |
4 | HG01257.hp1 HG01258.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.822+1028C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114624730 | |||||||
| chr4:114624787 | G | A | 1 | a0001c0001t0003g0250 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.822+1085G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114624787 | |||||||
| chr4:114624891 | G | A | 1 | a0001c0001t0002g0124 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.822+1189G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114624891 | |||||||
| chr4:114624907 | A | G | 1 | a0001c0001t0001g0085 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.822+1205A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114624907 | |||||||
| chr4:114625069 | C | CACACCTT others(7): Show |
5 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(2): Show |
5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.822+1367_822+1368i others(16): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114625069 | |||||||
| chr4:114625142 | C | G | 4 | a0001c0001t0003g0017 a0001c0001t0003g0214 a0001c0001t0003g0215 others(1): Show |
5 | HG02145.hp1 HG02886.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.822+1440C>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114625142 | |||||||
| chr4:114625204 | T | C | 1 | a0004c0005t0003g0236 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.822+1502T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114625204 | |||||||
| chr4:114625338 | C | T | 21 | a0001c0001t0003g0005 a0001c0001t0003g0016 a0001c0001t0003g0017 others(18): Show |
25 | HG01106.hp1 HG01168.hp1 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.822+1636C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114625338 | |||||||
| chr4:114625368 | G | A | 5 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(2): Show |
5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.822+1666G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114625368 | |||||||
| chr4:114625449 | C | T | 5 | a0001c0001t0001g0046 a0001c0001t0008g0204 a0001c0001t0008g0205 others(2): Show |
5 | HG01074.hp2 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.822+1747C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114625449 | |||||||
| chr4:114625466 | A | G | 1 | a0001c0001t0001g0084 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.822+1764A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114625466 | |||||||
| chr4:114625483 | C | CCTAGGTG others(11): Show |
7 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(4): Show |
7 | HG00639.hp1 HG01257.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.822+1783_822+1800d others(20): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114625483 | ||||||
| chr4:114625509 | T | TA | 62 | a0001c0001t0001g0019 a0001c0001t0001g0025 a0001c0001t0001g0026 others(59): Show |
63 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.822+1832dupA | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114625509 | ||||||
| chr4:114625509 | T | TAA | 67 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0018 others(64): Show |
71 | HG00323.hp1 HG00423.hp2 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.822+1831_822+1832d others(4): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114625509 | ||||||
| chr4:114625509 | T | TAAA | 9 | a0001c0001t0001g0008 a0001c0001t0001g0050 a0001c0001t0001g0051 others(6): Show |
10 | HG00438.hp1 HG01109.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.822+1830_822+1832d others(5): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114625509 | ||||||
| chr4:114625509 | TA | T | 29 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0020 others(26): Show |
33 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.822+1832delA | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114625509 | ||||||
| chr4:114625509 | TAA | T | 20 | a0001c0001t0002g0179 a0001c0001t0003g0005 a0001c0001t0003g0016 others(17): Show |
24 | HG00738.hp1 HG01106.hp1 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.822+1831_822+1832d others(4): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114625509 | ||||||
| chr4:114625849 | C | A | 7 | a0001c0001t0003g0016 a0001c0001t0003g0216 a0001c0001t0003g0227 others(4): Show |
8 | HG01884.hp1 HG02258.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.822+2147C>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114625849 | |||||||
| chr4:114626003 | A | C | 1 | a0001c0001t0017g0211 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.822+2301A>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114626003 | |||||||
| chr4:114626033 | A | C | 1 | a0001c0001t0004g0149 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.822+2331A>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114626033 | |||||||
| chr4:114626296 | T | C | 1 | a0001c0001t0003g0249 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.822+2594T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114626296 | |||||||
| chr4:114626394 | G | A | 4 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0014t0013g0169 others(1): Show |
4 | HG01109.hp2 HG02615.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.822+2692G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114626394 | |||||||
| chr4:114626414 | A | G | 4 | a0001c0001t0007g0221 a0001c0001t0007g0222 a0001c0001t0007g0223 others(1): Show |
4 | HG01243.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.822+2712A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114626414 | |||||||
| chr4:114626452 | G | A | 1 | a0001c0015t0014g0168 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.822+2750G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114626452 | |||||||
| chr4:114626515 | G | C | 42 | a0001c0001t0002g0174 a0001c0001t0002g0175 a0001c0001t0004g0140 others(39): Show |
49 | HG00140.hp1 HG00558.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.822+2813G>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114626515 | |||||||
| chr4:114626880 | T | A | 6 | a0001c0001t0006g0015 a0001c0001t0006g0207 a0001c0001t0006g0208 others(3): Show |
7 | HG02109.hp1 HG02572.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.822+3178T>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114626880 | |||||||
| chr4:114627255 | C | CT | 6 | a0001c0001t0001g0049 a0001c0001t0001g0082 a0001c0001t0001g0106 others(3): Show |
6 | HG01168.hp2 HG01175.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.822+3572dupT | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114627255 | ||||||
| chr4:114627255 | CT | C | 45 | a0001c0001t0001g0115 a0001c0001t0002g0011 a0001c0001t0002g0170 others(42): Show |
50 | HG01106.hp1 HG01168.hp1 HG01169.hp1 others(47): Show |
intron_variant | MODIFIER | c.822+3572delT | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114627255 | ||||||
| chr4:114627255 | CTT | C | 6 | a0001c0001t0002g0172 a0001c0001t0008g0204 a0001c0001t0008g0205 others(3): Show |
6 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.822+3571_822+3572d others(4): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114627255 | ||||||
| chr4:114627451 | A | G | 7 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(4): Show |
7 | HG00639.hp1 HG01257.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.822+3749A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114627451 | |||||||
| chr4:114627509 | C | T | 1 | a0001c0001t0003g0230 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.822+3807C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114627509 | |||||||
| chr4:114627582 | G | A | 1 | a0001c0001t0016g0122 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.822+3880G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114627582 | |||||||
| chr4:114627667 | T | G | 4 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0176 others(1): Show |
6 | HG00140.hp2 HG01069.hp1 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.822+3965T>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114627667 | |||||||
| chr4:114627881 | A | G | 2 | a0001c0001t0006g0015 a0001c0001t0006g0210 |
3 | HG02109.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.822+4179A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114627881 | |||||||
| chr4:114628208 | T | C | 5 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(2): Show |
5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.822+4506T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114628208 | |||||||
| chr4:114628218 | T | C | 5 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(2): Show |
5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.822+4516T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114628218 | |||||||
| chr4:114628382 | C | A | 40 | a0001c0001t0004g0140 a0001c0001t0004g0141 a0001c0001t0004g0148 others(37): Show |
47 | HG00140.hp1 HG00558.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.822+4680C>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114628382 | |||||||
| chr4:114628383 | A | G | 232 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(229): Show |
254 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.822+4681A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114628383 | |||||||
| chr4:114628406 | C | T | 1 | a0001c0001t0004g0165 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.822+4704C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114628406 | |||||||
| chr4:114628574 | G | A | 28 | a0001c0001t0003g0005 a0001c0001t0003g0016 a0001c0001t0003g0017 others(25): Show |
32 | HG00639.hp1 HG01106.hp1 HG01168.hp1 others(29): Show |
intron_variant | MODIFIER | c.822+4872G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114628574 | |||||||
| chr4:114628661 | A | G | 204 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(201): Show |
222 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.822+4959A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114628661 | |||||||
| chr4:114628767 | T | TAAGAAAG others(316): Show |
3 | a0001c0001t0002g0011 a0001c0001t0002g0170 a0001c0001t0002g0171 |
4 | HG01257.hp1 HG01258.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.822+5072_822+5073i others(325): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114628767 | ||||||
| chr4:114628767 | T | TAAGAAAG others(313): Show |
4 | a0001c0001t0001g0046 a0001c0001t0001g0080 a0001c0001t0001g0081 others(1): Show |
4 | HG01074.hp2 HG01496.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.822+5072_822+5073i others(322): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114628767 | ||||||
| chr4:114628767 | T | TAAGAAAG others(314): Show |
99 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(96): Show |
104 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.822+5072_822+5073i others(323): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114628767 | ||||||
| chr4:114628767 | T | TAAGAAAG others(315): Show |
17 | a0001c0001t0001g0025 a0001c0001t0001g0053 a0001c0001t0001g0054 others(14): Show |
17 | HG00423.hp2 HG00621.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.822+5072_822+5073i others(324): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114628767 | ||||||
| chr4:114628767 | T | TAAGAAAG others(316): Show |
1 | a0001c0014t0013g0169 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.822+5072_822+5073i others(325): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114628767 | ||||||
| chr4:114628767 | T | TAAGAAAG others(319): Show |
1 | a0001c0015t0014g0168 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.822+5072_822+5073i others(328): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114628767 | ||||||
| chr4:114628767 | T | TAAGAAAG others(314): Show |
1 | a0003c0004t0001g0047 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.822+5072_822+5073i others(323): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114628767 | ||||||
| chr4:114628769 | A | AGAAAGTG others(317): Show |
12 | a0001c0001t0004g0149 a0001c0001t0004g0159 a0002c0002t0002g0136 others(9): Show |
12 | HG00597.hp2 HG00621.hp2 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.822+5072_822+5073i others(326): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114628769 | ||||||
| chr4:114628769 | A | AGAAAGTG others(316): Show |
26 | a0001c0001t0003g0217 a0001c0001t0004g0140 a0001c0001t0004g0141 others(23): Show |
33 | HG00140.hp1 HG00558.hp1 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.822+5072_822+5073i others(325): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114628769 | ||||||
| chr4:114628769 | A | AGAAAGTG others(315): Show |
1 | a0001c0001t0004g0148 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.822+5072_822+5073i others(324): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114628769 | ||||||
| chr4:114628769 | A | AGAAAGTG others(316): Show |
1 | a0001c0001t0004g0165 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.822+5072_822+5073i others(325): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114628769 | ||||||
| chr4:114628769 | A | AGAAAGTG others(317): Show |
1 | a0002c0002t0002g0154 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.822+5072_822+5073i others(326): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114628769 | ||||||
| chr4:114628778 | A | G | 1 | a0001c0003t0001g0192 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.822+5076A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114628778 | |||||||
| chr4:114628873 | T | C | 3 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0086 |
3 | NA18947.hp2 NA18955.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.822+5171T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114628873 | |||||||
| chr4:114628956 | A | G | 230 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(227): Show |
252 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.822+5254A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114628956 | |||||||
| chr4:114629112 | C | T | 1 | a0001c0001t0003g0256 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.822+5410C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114629112 | |||||||
| chr4:114629240 | G | A | 5 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(2): Show |
5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.822+5538G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114629240 | |||||||
| chr4:114629264 | A | G | 2 | a0001c0001t0003g0230 a0001c0001t0012g0226 |
2 | NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.822+5562A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114629264 | |||||||
| chr4:114629320 | T | G | 5 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(2): Show |
5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.822+5618T>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114629320 | |||||||
| chr4:114629358 | C | G | 40 | a0001c0001t0004g0140 a0001c0001t0004g0141 a0001c0001t0004g0148 others(37): Show |
47 | HG00140.hp1 HG00558.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.822+5656C>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114629358 | |||||||
| chr4:114629442 | T | C | 1 | a0001c0015t0014g0168 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.822+5740T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114629442 | |||||||
| chr4:114629688 | C | G | 202 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(199): Show |
220 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.822+5986C>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114629688 | |||||||
| chr4:114629888 | A | G | 40 | a0001c0001t0004g0140 a0001c0001t0004g0141 a0001c0001t0004g0148 others(37): Show |
47 | HG00140.hp1 HG00558.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.822+6186A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114629888 | |||||||
| chr4:114630017 | G | A | 3 | a0001c0001t0002g0174 a0001c0001t0002g0175 a0001c0001t0003g0250 |
3 | HG02145.hp2 HG03139.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.822+6315G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114630017 | |||||||
| chr4:114630144 | CT | C | 77 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(74): Show |
82 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.822+6444delT | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114630144 | ||||||
| chr4:114630286 | C | T | 1 | a0001c0001t0017g0211 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.822+6584C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114630286 | |||||||
| chr4:114630310 | C | T | 6 | a0001c0001t0003g0217 a0001c0001t0008g0204 a0001c0001t0008g0205 others(3): Show |
6 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.822+6608C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114630310 | |||||||
| chr4:114630311 | G | C | 3 | a0001c0001t0002g0011 a0001c0001t0002g0170 a0001c0001t0002g0171 |
4 | HG01257.hp1 HG01258.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.822+6609G>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114630311 | |||||||
| chr4:114630360 | C | T | 202 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(199): Show |
220 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.822+6658C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114630360 | |||||||
| chr4:114630395 | G | A | 11 | a0001c0003t0001g0042 a0001c0003t0001g0184 a0001c0003t0001g0185 others(8): Show |
11 | HG00280.hp2 HG00423.hp1 HG01928.hp1 others(8): Show |
intron_variant | MODIFIER | c.822+6693G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114630395 | |||||||
| chr4:114630431 | A | G | 1 | a0001c0001t0009g0255 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.822+6729A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114630431 | |||||||
| chr4:114630639 | A | ATT | 5 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(2): Show |
5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.822+6948_822+6949d others(4): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114630639 | ||||||
| chr4:114630639 | AT | A | 5 | a0001c0001t0002g0126 a0001c0001t0002g0174 a0001c0001t0002g0175 others(2): Show |
5 | HG01934.hp2 HG02145.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.822+6949delT | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114630639 | ||||||
| chr4:114630739 | A | C | 1 | a0001c0001t0001g0183 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.822+7037A>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114630739 | |||||||
| chr4:114630867 | A | C | 4 | a0001c0001t0003g0240 a0001c0001t0003g0243 a0001c0001t0003g0252 others(1): Show |
4 | HG02717.hp1 HG03209.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.822+7165A>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114630867 | |||||||
| chr4:114630894 | G | A | 4 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(1): Show |
4 | HG02055.hp2 HG02895.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.822+7192G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114630894 | |||||||
| chr4:114630937 | T | G | 1 | a0001c0001t0002g0125 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.822+7235T>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114630937 | |||||||
| chr4:114631210 | A | G | 5 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(2): Show |
5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.822+7508A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114631210 | |||||||
| chr4:114631741 | T | A | 4 | a0001c0001t0003g0005 a0001c0001t0003g0218 a0001c0001t0003g0219 others(1): Show |
6 | HG01106.hp1 HG01168.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.822+8039T>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114631741 | |||||||
| chr4:114631796 | G | A | 2 | a0002c0002t0002g0137 a0002c0002t0002g0138 |
2 | HG02698.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.822+8094G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114631796 | |||||||
| chr4:114631939 | C | T | 5 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(2): Show |
5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.822+8237C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114631939 | |||||||
| chr4:114632027 | G | A | 207 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(204): Show |
225 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.822+8325G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114632027 | |||||||
| chr4:114632109 | C | T | 1 | a0001c0001t0005g0176 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.822+8407C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114632109 | |||||||
| chr4:114632200 | G | A | 1 | a0001c0001t0003g0225 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.822+8498G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114632200 | |||||||
| chr4:114632419 | G | C | 1 | a0001c0001t0001g0094 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.822+8717G>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114632419 | |||||||
| chr4:114632439 | C | T | 3 | a0001c0001t0002g0011 a0001c0001t0002g0170 a0001c0001t0002g0171 |
4 | HG01257.hp1 HG01258.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.822+8737C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114632439 | |||||||
| chr4:114632518 | C | A | 35 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0020 others(32): Show |
40 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.822+8816C>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114632518 | |||||||
| chr4:114632758 | C | A | 2 | a0001c0001t0001g0058 a0001c0001t0001g0059 |
2 | NA18983.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.822+9056C>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114632758 | |||||||
| chr4:114632825 | C | T | 41 | a0001c0001t0003g0217 a0001c0001t0004g0140 a0001c0001t0004g0141 others(38): Show |
48 | HG00140.hp1 HG00558.hp1 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.822+9123C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114632825 | |||||||
| chr4:114632831 | C | T | 1 | a0001c0001t0001g0040 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.822+9129C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114632831 | |||||||
| chr4:114632833 | G | A | 202 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(199): Show |
220 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.822+9131G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114632833 | |||||||
| chr4:114632920 | A | C | 1 | a0001c0001t0001g0034 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.822+9218A>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114632920 | |||||||
| chr4:114632934 | A | G | 5 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(2): Show |
5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.822+9232A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114632934 | |||||||
| chr4:114632969 | G | A | 5 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(2): Show |
5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.822+9267G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114632969 | |||||||
| chr4:114633051 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.822+9349G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114633051 | |||||||
| chr4:114633122 | A | T | 6 | a0001c0001t0006g0015 a0001c0001t0006g0207 a0001c0001t0006g0208 others(3): Show |
7 | HG02109.hp1 HG02572.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.822+9420A>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114633122 | |||||||
| chr4:114633181 | T | G | 2 | a0001c0006t0003g0233 a0001c0006t0003g0239 |
2 | HG00738.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.822+9479T>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114633181 | |||||||
| chr4:114633283 | A | G | 29 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0020 others(26): Show |
33 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.822+9581A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114633283 | |||||||
| chr4:114633292 | A | C | 6 | a0001c0001t0006g0015 a0001c0001t0006g0207 a0001c0001t0006g0208 others(3): Show |
7 | HG02109.hp1 HG02572.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.822+9590A>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114633292 | |||||||
| chr4:114633409 | A | AG | 3 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0107 |
3 | NA18983.hp1 NA19006.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.822+9709dupG | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114633409 | ||||||
| chr4:114633520 | T | C | 1 | a0002c0002t0002g0162 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.822+9818T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114633520 | |||||||
| chr4:114633799 | C | A | 1 | a0001c0001t0001g0041 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.822+10097C>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114633799 | |||||||
| chr4:114633805 | G | A | 35 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0020 others(32): Show |
40 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.822+10103G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114633805 | |||||||
| chr4:114634223 | T | A | 5 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(2): Show |
5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.822+10521T>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114634223 | |||||||
| chr4:114634226 | A | G | 4 | a0001c0001t0003g0017 a0001c0001t0003g0214 a0001c0001t0003g0215 others(1): Show |
5 | HG02145.hp1 HG02886.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.822+10524A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114634226 | |||||||
| chr4:114634257 | T | G | 2 | a0001c0001t0001g0182 a0001c0001t0001g0189 |
2 | HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.822+10555T>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114634257 | |||||||
| chr4:114634303 | T | C | 3 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0014t0013g0169 |
3 | HG02615.hp2 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.822+10601T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114634303 | |||||||
| chr4:114634422 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.822+10720C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114634422 | |||||||
| chr4:114634426 | T | C | 1 | a0001c0001t0001g0080 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.822+10724T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114634426 | |||||||
| chr4:114634463 | G | A | 2 | a0001c0001t0001g0181 a0001c0001t0001g0202 |
2 | NA18906.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.822+10761G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114634463 | |||||||
| chr4:114634539 | G | A | 1 | a0001c0001t0009g0255 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.822+10837G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114634539 | |||||||
| chr4:114634577 | AT | A | 22 | a0001c0001t0001g0083 a0001c0001t0001g0086 a0001c0001t0001g0111 others(19): Show |
22 | HG00280.hp2 HG00423.hp1 HG01928.hp1 others(19): Show |
intron_variant | MODIFIER | c.822+10876delT | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114634577 | |||||||
| chr4:114634767 | C | CT | 5 | a0001c0001t0002g0174 a0001c0001t0002g0175 a0001c0001t0003g0250 others(2): Show |
5 | HG02145.hp2 HG02630.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.822+11072dupT | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114634767 | ||||||
| chr4:114635028 | C | CT | 19 | a0001c0001t0001g0083 a0001c0001t0001g0111 a0001c0001t0001g0181 others(16): Show |
19 | HG00280.hp2 HG00423.hp1 HG01928.hp1 others(16): Show |
intron_variant | MODIFIER | c.822+11339dupT | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114635028 | ||||||
| chr4:114635028 | C | CTGTT | 5 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(2): Show |
5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.822+11327_822+1132 others(8): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114635028 | ||||||
| chr4:114635328 | G | T | 40 | a0001c0001t0004g0140 a0001c0001t0004g0141 a0001c0001t0004g0148 others(37): Show |
47 | HG00140.hp1 HG00558.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.822+11626G>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114635328 | |||||||
| chr4:114635417 | C | G | 2 | a0001c0001t0001g0103 a0001c0001t0001g0187 |
2 | HG02080.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.822+11715C>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114635417 | |||||||
| chr4:114635497 | G | A | 1 | a0001c0015t0014g0168 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.822+11795G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114635497 | |||||||
| chr4:114635682 | C | T | 4 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(1): Show |
4 | HG02055.hp2 HG02895.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.822+11980C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114635682 | |||||||
| chr4:114635719 | T | A | 119 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(116): Show |
124 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.822+12017T>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114635719 | |||||||
| chr4:114635841 | A | G | 5 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(2): Show |
5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.822+12139A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114635841 | |||||||
| chr4:114635869 | A | G | 21 | a0001c0001t0003g0005 a0001c0001t0003g0016 a0001c0001t0003g0017 others(18): Show |
25 | HG01106.hp1 HG01168.hp1 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.822+12167A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114635869 | |||||||
| chr4:114636002 | T | A | 5 | a0001c0001t0001g0002 a0001c0001t0001g0060 a0001c0001t0001g0061 others(2): Show |
7 | HG00597.hp1 HG01169.hp2 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.822+12300T>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114636002 | |||||||
| chr4:114636089 | G | A | 1 | a0001c0001t0001g0035 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.822+12387G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114636089 | |||||||
| chr4:114636184 | C | T | 1 | a0001c0001t0003g0232 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.822+12482C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114636184 | |||||||
| chr4:114636264 | G | A | 1 | a0001c0001t0001g0063 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.822+12562G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114636264 | |||||||
| chr4:114636384 | T | A | 1 | a0001c0001t0003g0217 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.822+12682T>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114636384 | |||||||
| chr4:114636525 | T | TGTAAAGC others(1): Show |
5 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(2): Show |
5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.822+12824_822+1282 others(12): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114636525 | ||||||
| chr4:114636536 | A | G | 1 | a0001c0001t0003g0256 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.822+12834A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114636536 | |||||||
| chr4:114636549 | A | C | 1 | a0001c0001t0009g0255 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.822+12847A>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114636549 | |||||||
| chr4:114636954 | T | C | 5 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(2): Show |
5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.822+13252T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114636954 | |||||||
| chr4:114636987 | T | C | 1 | a0001c0003t0001g0198 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.822+13285T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114636987 | |||||||
| chr4:114637033 | A | G | 5 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(2): Show |
5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.822+13331A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114637033 | |||||||
| chr4:114637085 | T | C | 35 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0020 others(32): Show |
40 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.822+13383T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114637085 | |||||||
| chr4:114637290 | T | C | 1 | a0001c0001t0001g0046 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.822+13588T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114637290 | |||||||
| chr4:114637341 | G | A | 6 | a0001c0001t0003g0005 a0001c0001t0003g0116 a0001c0001t0003g0213 others(3): Show |
8 | HG01106.hp1 HG01168.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.822+13639G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114637341 | |||||||
| chr4:114637388 | T | G | 5 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(2): Show |
5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.822+13686T>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114637388 | |||||||
| chr4:114637487 | A | G | 3 | a0001c0001t0002g0011 a0001c0001t0002g0170 a0001c0001t0002g0171 |
4 | HG01257.hp1 HG01258.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.822+13785A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114637487 | |||||||
| chr4:114637758 | T | G | 35 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0020 others(32): Show |
40 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.822+14056T>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114637758 | |||||||
| chr4:114637932 | C | T | 1 | a0001c0015t0014g0168 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.822+14230C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114637932 | |||||||
| chr4:114637981 | T | G | 5 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(2): Show |
5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.822+14279T>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114637981 | |||||||
| chr4:114638290 | A | G | 4 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(1): Show |
4 | HG02055.hp2 HG02895.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.822+14588A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114638290 | |||||||
| chr4:114638567 | T | A | 5 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(2): Show |
5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.822+14865T>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114638567 | |||||||
| chr4:114638668 | C | T | 16 | a0002c0002t0002g0001 a0002c0002t0002g0004 a0002c0002t0002g0135 others(13): Show |
21 | HG00621.hp2 HG02015.hp1 HG02040.hp1 others(18): Show |
intron_variant | MODIFIER | c.822+14966C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114638668 | |||||||
| chr4:114638987 | C | T | 2 | a0001c0007t0011g0254 a0001c0007t0015g0253 |
2 | HG01257.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.822+15285C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114638987 | |||||||
| chr4:114639152 | T | C | 4 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0014t0013g0169 others(1): Show |
4 | HG01109.hp2 HG02615.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.822+15450T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114639152 | |||||||
| chr4:114639255 | A | G | 1 | a0001c0001t0003g0256 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.822+15553A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114639255 | |||||||
| chr4:114639584 | A | T | 119 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(116): Show |
124 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.822+15882A>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114639584 | |||||||
| chr4:114640033 | G | GT | 162 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(159): Show |
175 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.822+16346dupT | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114640033 | ||||||
| chr4:114640033 | G | GTT | 5 | a0001c0001t0001g0062 a0001c0001t0001g0098 a0001c0001t0001g0200 others(2): Show |
5 | HG00597.hp1 HG01109.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.822+16345_822+1634 others(6): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114640033 | ||||||
| chr4:114640033 | GT | G | 5 | a0001c0001t0002g0133 a0001c0001t0007g0221 a0001c0001t0007g0222 others(2): Show |
5 | HG00323.hp2 HG01243.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.822+16346delT | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114640033 | ||||||
| chr4:114640069 | C | T | 5 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(2): Show |
5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.822+16367C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114640069 | |||||||
| chr4:114640199 | T | A | 1 | a0001c0001t0004g0160 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.822+16497T>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114640199 | |||||||
| chr4:114640240 | C | T | 2 | a0001c0007t0011g0254 a0001c0007t0015g0253 |
2 | HG01257.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.822+16538C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114640240 | |||||||
| chr4:114640282 | G | A | 1 | a0005c0008t0001g0097 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.822+16580G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114640282 | |||||||
| chr4:114640438 | C | A | 1 | a0001c0006t0003g0233 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.822+16736C>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114640438 | |||||||
| chr4:114640455 | A | AT | 24 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0020 others(21): Show |
26 | HG00323.hp2 HG00438.hp2 HG00558.hp2 others(23): Show |
intron_variant | MODIFIER | c.822+16760dupT | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114640455 | ||||||
| chr4:114640717 | A | G | 207 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(204): Show |
225 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.822+17015A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114640717 | |||||||
| chr4:114640765 | T | A | 4 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(1): Show |
4 | HG02055.hp2 HG02895.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.822+17063T>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114640765 | |||||||
| chr4:114640914 | C | G | 3 | a0001c0001t0002g0011 a0001c0001t0002g0170 a0001c0001t0002g0171 |
4 | HG01257.hp1 HG01258.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.822+17212C>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114640914 | |||||||
| chr4:114641011 | G | A | 6 | a0001c0001t0003g0241 a0001c0001t0003g0242 a0001c0001t0005g0012 others(3): Show |
8 | HG00140.hp2 HG01069.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.822+17309G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114641011 | |||||||
| chr4:114641285 | C | G | 5 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(2): Show |
5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.822+17583C>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114641285 | |||||||
| chr4:114641536 | G | A | 1 | a0001c0001t0001g0064 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.822+17834G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114641536 | |||||||
| chr4:114642053 | G | C | 4 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(1): Show |
4 | HG02055.hp2 HG02895.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.822+18351G>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114642053 | |||||||
| chr4:114642195 | G | A | 35 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0020 others(32): Show |
40 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.822+18493G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114642195 | |||||||
| chr4:114642214 | C | CT | 5 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(2): Show |
5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.822+18523dupT | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114642214 | ||||||
| chr4:114642234 | A | G | 1 | a0001c0001t0001g0078 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.822+18532A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114642234 | |||||||
| chr4:114642290 | G | A | 1 | a0001c0015t0014g0168 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.822+18588G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114642290 | |||||||
| chr4:114642383 | A | G | 1 | a0001c0001t0001g0029 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.822+18681A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114642383 | |||||||
| chr4:114642457 | A | T | 2 | a0001c0007t0011g0254 a0001c0007t0015g0253 |
2 | HG01257.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.822+18755A>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114642457 | |||||||
| chr4:114642666 | T | G | 4 | a0001c0001t0007g0221 a0001c0001t0007g0222 a0001c0001t0007g0223 others(1): Show |
4 | HG01243.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.822+18964T>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114642666 | |||||||
| chr4:114642903 | T | C | 1 | a0001c0001t0001g0037 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.822+19201T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114642903 | |||||||
| chr4:114642937 | G | T | 1 | a0001c0015t0014g0168 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.822+19235G>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114642937 | |||||||
| chr4:114642998 | T | A | 1 | a0001c0001t0003g0217 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.822+19296T>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114642998 | |||||||
| chr4:114643113 | G | C | 3 | a0001c0001t0002g0011 a0001c0001t0002g0170 a0001c0001t0002g0171 |
4 | HG01257.hp1 HG01258.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.822+19411G>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114643113 | |||||||
| chr4:114643204 | GT | G | 4 | a0001c0001t0007g0221 a0001c0001t0007g0222 a0001c0001t0007g0223 others(1): Show |
4 | HG01243.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.822+19503delT | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114643204 | |||||||
| chr4:114643256 | A | G | 1 | a0005c0008t0001g0097 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.822+19554A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114643256 | |||||||
| chr4:114643274 | T | G | 1 | a0001c0001t0003g0256 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.822+19572T>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114643274 | |||||||
| chr4:114643513 | A | G | 255 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(252): Show |
277 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.822+19811A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114643513 | |||||||
| chr4:114643741 | G | C | 5 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(2): Show |
5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.822+20039G>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114643741 | |||||||
| chr4:114643924 | C | T | 1 | a0001c0001t0001g0111 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.823-20071C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114643924 | |||||||
| chr4:114644083 | A | G | 1 | a0001c0015t0014g0168 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.823-19912A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114644083 | |||||||
| chr4:114644111 | C | T | 1 | a0001c0001t0003g0249 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.823-19884C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114644111 | |||||||
| chr4:114644266 | C | T | 5 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(2): Show |
5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.823-19729C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114644266 | |||||||
| chr4:114644306 | A | T | 1 | a0001c0001t0003g0217 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.823-19689A>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114644306 | |||||||
| chr4:114644503 | A | G | 119 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(116): Show |
124 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.823-19492A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114644503 | |||||||
| chr4:114644657 | A | G | 1 | a0001c0001t0009g0255 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.823-19338A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114644657 | |||||||
| chr4:114644723 | T | C | 2 | a0001c0001t0008g0205 a0001c0001t0008g0206 |
2 | HG02055.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.823-19272T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114644723 | |||||||
| chr4:114644733 | A | C | 5 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(2): Show |
5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.823-19262A>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114644733 | |||||||
| chr4:114644740 | T | G | 2 | a0001c0003t0001g0193 a0001c0003t0001g0195 |
2 | HG01928.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.823-19255T>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114644740 | |||||||
| chr4:114644934 | A | G | 6 | a0001c0001t0006g0015 a0001c0001t0006g0207 a0001c0001t0006g0208 others(3): Show |
7 | HG02109.hp1 HG02572.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.823-19061A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114644934 | |||||||
| chr4:114644955 | A | C | 5 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(2): Show |
5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.823-19040A>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114644955 | |||||||
| chr4:114645039 | C | CACAG | 207 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(204): Show |
225 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.823-18949_823-1894 others(8): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114645039 | ||||||
| chr4:114645057 | C | A | 4 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(1): Show |
4 | HG02055.hp2 HG02895.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.823-18938C>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114645057 | |||||||
| chr4:114645246 | C | A | 4 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(1): Show |
4 | HG02055.hp2 HG02895.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.823-18749C>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114645246 | |||||||
| chr4:114645573 | G | C | 5 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(2): Show |
5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.823-18422G>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114645573 | |||||||
| chr4:114645598 | T | C | 202 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(199): Show |
220 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.823-18397T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114645598 | |||||||
| chr4:114645687 | G | A | 1 | a0001c0001t0002g0134 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.823-18308G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114645687 | |||||||
| chr4:114645805 | G | A | 3 | a0001c0001t0002g0011 a0001c0001t0002g0170 a0001c0001t0002g0171 |
4 | HG01257.hp1 HG01258.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.823-18190G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114645805 | |||||||
| chr4:114645835 | A | G | 1 | a0001c0001t0001g0098 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.823-18160A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114645835 | |||||||
| chr4:114645869 | C | T | 6 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0064 others(3): Show |
6 | NA18957.hp1 NA18961.hp2 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.823-18126C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114645869 | |||||||
| chr4:114646049 | T | G | 1 | a0001c0001t0002g0124 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.823-17946T>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114646049 | |||||||
| chr4:114646127 | A | G | 4 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(1): Show |
4 | HG02055.hp2 HG02895.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.823-17868A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114646127 | |||||||
| chr4:114646277 | A | G | 1 | a0001c0001t0001g0096 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.823-17718A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114646277 | |||||||
| chr4:114646391 | A | C | 1 | a0001c0001t0003g0225 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.823-17604A>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114646391 | |||||||
| chr4:114646474 | T | A | 3 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0014t0013g0169 |
3 | HG02615.hp2 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.823-17521T>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114646474 | |||||||
| chr4:114646856 | A | G | 5 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(2): Show |
5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.823-17139A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114646856 | |||||||
| chr4:114647356 | T | TTG | 51 | a0001c0001t0001g0050 a0001c0001t0001g0063 a0001c0001t0001g0065 others(48): Show |
59 | HG00140.hp1 HG00280.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.823-16603_823-1660 others(6): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114647356 | ||||||
| chr4:114647356 | T | TTGTG | 110 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(107): Show |
118 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.823-16605_823-1660 others(8): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114647356 | ||||||
| chr4:114647356 | T | TTGTGTG | 31 | a0001c0001t0001g0031 a0001c0001t0001g0051 a0001c0001t0001g0061 others(28): Show |
33 | HG00323.hp2 HG00438.hp2 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.823-16607_823-1660 others(10): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114647356 | ||||||
| chr4:114647356 | T | TTGTGTGT others(1): Show |
5 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0107 others(2): Show |
5 | HG00738.hp1 HG01109.hp2 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.823-16609_823-1660 others(12): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114647356 | ||||||
| chr4:114647356 | TTG | T | 3 | a0001c0001t0003g0232 a0001c0001t0006g0207 a0001c0001t0006g0208 |
3 | HG02572.hp2 HG02818.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.823-16603_823-1660 others(6): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114647356 | ||||||
| chr4:114647356 | TTGTG | T | 6 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(3): Show |
6 | HG01257.hp2 HG02055.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.823-16605_823-1660 others(8): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114647356 | ||||||
| chr4:114647516 | A | G | 1 | a0001c0001t0006g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.823-16479A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114647516 | |||||||
| chr4:114647657 | G | A | 1 | a0001c0001t0003g0256 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.823-16338G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114647657 | |||||||
| chr4:114647690 | G | A | 1 | a0001c0001t0001g0066 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.823-16305G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114647690 | |||||||
| chr4:114647874 | T | G | 40 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0020 others(37): Show |
45 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.823-16121T>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114647874 | |||||||
| chr4:114647914 | G | A | 1 | a0001c0001t0002g0123 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.823-16081G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114647914 | |||||||
| chr4:114648371 | GT | G | 10 | a0001c0001t0001g0102 a0001c0001t0001g0104 a0001c0001t0001g0107 others(7): Show |
11 | HG00621.hp1 HG00741.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.823-15603delT | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114648371 | ||||||
| chr4:114648371 | GTT | G | 195 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(192): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.823-15604_823-1560 others(6): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114648371 | ||||||
| chr4:114648433 | G | A | 5 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(2): Show |
5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.823-15562G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114648433 | |||||||
| chr4:114648451 | T | TG | 5 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(2): Show |
5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.823-15541dupG | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114648451 | ||||||
| chr4:114648505 | A | C | 1 | a0001c0001t0001g0071 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.823-15490A>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114648505 | |||||||
| chr4:114648506 | G | A | 1 | a0001c0001t0001g0049 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.823-15489G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114648506 | |||||||
| chr4:114648658 | A | G | 3 | a0001c0001t0002g0011 a0001c0001t0002g0170 a0001c0001t0002g0171 |
4 | HG01257.hp1 HG01258.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.823-15337A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114648658 | |||||||
| chr4:114649082 | C | T | 207 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(204): Show |
225 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.823-14913C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114649082 | |||||||
| chr4:114649114 | G | T | 1 | a0001c0001t0002g0127 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.823-14881G>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114649114 | |||||||
| chr4:114649537 | A | G | 4 | a0001c0001t0001g0033 a0001c0001t0001g0039 a0001c0001t0001g0041 others(1): Show |
4 | HG01081.hp2 HG01975.hp2 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.823-14458A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114649537 | |||||||
| chr4:114649552 | A | G | 5 | a0001c0001t0003g0016 a0001c0001t0003g0216 a0001c0001t0003g0227 others(2): Show |
6 | HG01884.hp1 HG02258.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.823-14443A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114649552 | |||||||
| chr4:114649718 | C | T | 4 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(1): Show |
4 | HG02055.hp2 HG02895.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.823-14277C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114649718 | |||||||
| chr4:114649811 | T | TA | 38 | a0001c0001t0001g0075 a0001c0001t0004g0140 a0001c0001t0004g0141 others(35): Show |
45 | HG00140.hp1 HG00558.hp1 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.823-14175dupA | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114649811 | ||||||
| chr4:114649812 | A | T | 1 | a0001c0001t0001g0194 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.823-14183A>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114649812 | |||||||
| chr4:114649863 | CT | C | 5 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(2): Show |
5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.823-14128delT | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114649863 | ||||||
| chr4:114650125 | T | C | 5 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(2): Show |
5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.823-13870T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114650125 | |||||||
| chr4:114650189 | C | G | 35 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0020 others(32): Show |
40 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.823-13806C>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114650189 | |||||||
| chr4:114650219 | G | C | 4 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(1): Show |
4 | HG02055.hp2 HG02895.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.823-13776G>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114650219 | |||||||
| chr4:114650269 | C | T | 5 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(2): Show |
5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.823-13726C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114650269 | |||||||
| chr4:114650270 | C | G | 5 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(2): Show |
5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.823-13725C>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114650270 | |||||||
| chr4:114650390 | C | T | 5 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(2): Show |
5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.823-13605C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114650390 | |||||||
| chr4:114650424 | A | G | 207 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(204): Show |
225 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.823-13571A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114650424 | |||||||
| chr4:114650495 | A | C | 1 | a0001c0015t0014g0168 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.823-13500A>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114650495 | |||||||
| chr4:114650549 | T | C | 202 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(199): Show |
220 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.823-13446T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114650549 | |||||||
| chr4:114650667 | A | G | 39 | a0001c0001t0003g0217 a0001c0001t0004g0140 a0001c0001t0004g0141 others(36): Show |
46 | HG00140.hp1 HG00558.hp1 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.823-13328A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114650667 | |||||||
| chr4:114650870 | A | T | 1 | a0001c0001t0002g0117 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.823-13125A>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114650870 | |||||||
| chr4:114650928 | G | A | 1 | a0001c0001t0005g0176 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.823-13067G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114650928 | |||||||
| chr4:114650975 | T | C | 1 | a0008c0010t0002g0024 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.823-13020T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114650975 | |||||||
| chr4:114651169 | C | A | 1 | a0001c0001t0001g0183 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.823-12826C>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114651169 | |||||||
| chr4:114651169 | C | T | 206 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(203): Show |
224 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.823-12826C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114651169 | |||||||
| chr4:114651235 | A | G | 230 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(227): Show |
252 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.823-12760A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114651235 | |||||||
| chr4:114651492 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.823-12503C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114651492 | |||||||
| chr4:114651574 | A | G | 1 | a0002c0002t0002g0162 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.823-12421A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114651574 | |||||||
| chr4:114651766 | T | C | 1 | a0001c0001t0001g0038 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.823-12229T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114651766 | |||||||
| chr4:114652219 | G | T | 1 | a0001c0003t0001g0184 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.823-11776G>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114652219 | |||||||
| chr4:114652396 | A | AT | 5 | a0001c0001t0002g0126 a0001c0001t0002g0174 a0001c0001t0002g0175 others(2): Show |
5 | HG01934.hp2 HG02145.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.823-11585dupT | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114652396 | ||||||
| chr4:114652396 | AT | A | 7 | a0001c0001t0006g0015 a0001c0001t0006g0207 a0001c0001t0006g0208 others(4): Show |
8 | HG02109.hp1 HG02572.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.823-11585delT | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114652396 | ||||||
| chr4:114652412 | A | G | 1 | a0001c0001t0009g0255 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.823-11583A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114652412 | |||||||
| chr4:114652469 | C | A | 1 | a0001c0001t0002g0134 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.823-11526C>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114652469 | |||||||
| chr4:114652513 | T | C | 2 | a0001c0001t0002g0011 a0001c0001t0002g0171 |
3 | HG01257.hp1 HG01258.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.823-11482T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114652513 | |||||||
| chr4:114652516 | G | A | 6 | a0001c0001t0006g0015 a0001c0001t0006g0207 a0001c0001t0006g0208 others(3): Show |
7 | HG02109.hp1 HG02572.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.823-11479G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114652516 | |||||||
| chr4:114652811 | A | G | 1 | a0001c0001t0001g0187 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.823-11184A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114652811 | |||||||
| chr4:114652815 | T | G | 5 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(2): Show |
5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.823-11180T>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114652815 | |||||||
| chr4:114652827 | C | G | 39 | a0001c0001t0003g0217 a0001c0001t0004g0140 a0001c0001t0004g0141 others(36): Show |
46 | HG00140.hp1 HG00558.hp1 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.823-11168C>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114652827 | |||||||
| chr4:114652891 | A | T | 235 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(232): Show |
257 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.823-11104A>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114652891 | |||||||
| chr4:114653017 | C | T | 1 | a0001c0001t0001g0075 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.823-10978C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114653017 | |||||||
| chr4:114653291 | A | G | 5 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(2): Show |
5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.823-10704A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114653291 | |||||||
| chr4:114653334 | C | T | 1 | a0003c0004t0001g0047 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.823-10661C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114653334 | |||||||
| chr4:114654071 | G | A | 6 | a0001c0001t0006g0015 a0001c0001t0006g0207 a0001c0001t0006g0208 others(3): Show |
7 | HG02109.hp1 HG02572.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.823-9924G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114654071 | |||||||
| chr4:114654112 | C | T | 207 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(204): Show |
225 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.823-9883C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114654112 | |||||||
| chr4:114654255 | T | G | 2 | a0001c0001t0001g0166 a0001c0001t0001g0167 |
2 | HG02615.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.823-9740T>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114654255 | |||||||
| chr4:114654273 | C | T | 2 | a0001c0001t0001g0031 a0001c0001t0001g0037 |
2 | HG00642.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.823-9722C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114654273 | |||||||
| chr4:114654322 | C | A | 1 | a0002c0002t0002g0154 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.823-9673C>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114654322 | |||||||
| chr4:114654379 | T | A | 1 | a0001c0001t0003g0249 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.823-9616T>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114654379 | |||||||
| chr4:114654706 | A | AAG | 3 | a0002c0002t0002g0010 a0002c0002t0002g0136 a0002c0002t0002g0178 |
4 | HG00558.hp1 NA18986.hp2 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.823-9279_823-9278d others(4): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114654706 | ||||||
| chr4:114654823 | C | T | 1 | a0002c0002t0002g0137 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.823-9172C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114654823 | |||||||
| chr4:114655066 | G | GT | 5 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(2): Show |
5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.823-8918dupT | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114655066 | ||||||
| chr4:114655139 | AT | A | 3 | a0001c0001t0002g0011 a0001c0001t0002g0170 a0001c0001t0002g0171 |
4 | HG01257.hp1 HG01258.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.823-8853delT | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114655139 | ||||||
| chr4:114655155 | C | T | 1 | a0001c0001t0008g0206 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.823-8840C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114655155 | |||||||
| chr4:114655186 | T | C | 2 | a0001c0007t0011g0254 a0001c0007t0015g0253 |
2 | HG01257.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.823-8809T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114655186 | |||||||
| chr4:114655202 | A | G | 1 | a0001c0001t0001g0037 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.823-8793A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114655202 | |||||||
| chr4:114655205 | A | G | 4 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(1): Show |
4 | HG02055.hp2 HG02895.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.823-8790A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114655205 | |||||||
| chr4:114655281 | G | T | 1 | a0006c0012t0004g0153 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.823-8714G>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114655281 | |||||||
| chr4:114655828 | A | G | 3 | a0001c0001t0001g0111 a0001c0003t0001g0196 a0001c0003t0001g0198 |
3 | HG02074.hp2 NA18948.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.823-8167A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114655828 | |||||||
| chr4:114656041 | G | A | 1 | a0001c0001t0009g0255 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.823-7954G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114656041 | |||||||
| chr4:114656225 | C | T | 35 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0020 others(32): Show |
40 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.823-7770C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114656225 | |||||||
| chr4:114656668 | G | A | 5 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(2): Show |
5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.823-7327G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114656668 | |||||||
| chr4:114656697 | T | C | 5 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(2): Show |
5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.823-7298T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114656697 | |||||||
| chr4:114656748 | C | T | 1 | a0001c0001t0001g0044 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.823-7247C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114656748 | |||||||
| chr4:114656841 | C | G | 29 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0020 others(26): Show |
33 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.823-7154C>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114656841 | |||||||
| chr4:114656953 | G | C | 1 | a0001c0001t0009g0255 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.823-7042G>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114656953 | |||||||
| chr4:114657125 | C | A | 4 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(1): Show |
4 | HG02055.hp2 HG02895.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.823-6870C>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114657125 | |||||||
| chr4:114657364 | G | C | 1 | a0001c0003t0001g0198 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.823-6631G>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114657364 | |||||||
| chr4:114657607 | A | G | 1 | a0001c0001t0003g0116 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.823-6388A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114657607 | |||||||
| chr4:114657609 | T | C | 4 | a0001c0001t0003g0017 a0001c0001t0003g0214 a0001c0001t0003g0215 others(1): Show |
5 | HG02145.hp1 HG02886.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.823-6386T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114657609 | |||||||
| chr4:114657617 | A | G | 5 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(2): Show |
5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.823-6378A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114657617 | |||||||
| chr4:114657632 | G | A | 1 | a0001c0001t0003g0217 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.823-6363G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114657632 | |||||||
| chr4:114657873 | G | A | 3 | a0001c0001t0003g0017 a0001c0001t0003g0214 a0001c0001t0003g0215 |
4 | HG02145.hp1 HG03098.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.823-6122G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114657873 | |||||||
| chr4:114657878 | C | T | 1 | a0001c0001t0002g0174 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.823-6117C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114657878 | |||||||
| chr4:114658072 | G | A | 1 | a0001c0001t0002g0172 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.823-5923G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114658072 | |||||||
| chr4:114658247 | G | C | 3 | a0001c0001t0002g0011 a0001c0001t0002g0170 a0001c0001t0002g0171 |
4 | HG01257.hp1 HG01258.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.823-5748G>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114658247 | |||||||
| chr4:114658285 | C | A | 164 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(161): Show |
176 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.823-5710C>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114658285 | |||||||
| chr4:114658499 | C | T | 2 | a0001c0014t0013g0169 a0001c0015t0014g0168 |
2 | HG01109.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.823-5496C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114658499 | |||||||
| chr4:114658605 | T | C | 5 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(2): Show |
5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.823-5390T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114658605 | |||||||
| chr4:114658706 | T | TA | 123 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(120): Show |
128 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.823-5280dupA | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114658706 | ||||||
| chr4:114658983 | TA | T | 3 | a0001c0001t0002g0011 a0001c0001t0002g0170 a0001c0001t0002g0171 |
4 | HG01257.hp1 HG01258.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.823-5011delA | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114658983 | |||||||
| chr4:114659132 | A | C | 1 | a0002c0002t0002g0146 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.823-4863A>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114659132 | |||||||
| chr4:114659160 | C | G | 1 | a0001c0001t0001g0036 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.823-4835C>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114659160 | |||||||
| chr4:114659174 | A | G | 1 | a0001c0001t0001g0055 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.823-4821A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114659174 | |||||||
| chr4:114659290 | A | C | 2 | a0001c0001t0001g0080 a0001c0001t0001g0112 |
2 | HG00323.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.823-4705A>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114659290 | |||||||
| chr4:114659367 | T | C | 1 | a0001c0001t0003g0240 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.823-4628T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114659367 | |||||||
| chr4:114659402 | A | G | 1 | a0002c0002t0002g0150 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.823-4593A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114659402 | |||||||
| chr4:114659524 | A | G | 211 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(208): Show |
229 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.823-4471A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114659524 | |||||||
| chr4:114659545 | T | C | 2 | a0001c0014t0013g0169 a0001c0015t0014g0168 |
2 | HG01109.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.823-4450T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114659545 | |||||||
| chr4:114659650 | C | T | 1 | a0001c0001t0002g0011 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.823-4345C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114659650 | |||||||
| chr4:114659777 | A | G | 1 | a0001c0001t0001g0066 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.823-4218A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114659777 | |||||||
| chr4:114659801 | A | C | 1 | a0001c0001t0002g0117 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.823-4194A>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114659801 | |||||||
| chr4:114660209 | A | G | 7 | a0001c0001t0003g0016 a0001c0001t0003g0216 a0001c0001t0003g0227 others(4): Show |
8 | HG01884.hp1 HG02258.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.823-3786A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114660209 | |||||||
| chr4:114660224 | T | C | 237 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(234): Show |
259 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.823-3771T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114660224 | |||||||
| chr4:114660242 | AT | A | 3 | a0001c0001t0002g0174 a0001c0001t0002g0175 a0001c0001t0003g0250 |
3 | HG02145.hp2 HG03139.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.823-3752delT | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114660242 | |||||||
| chr4:114660313 | C | T | 1 | a0001c0001t0003g0257 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.823-3682C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114660313 | |||||||
| chr4:114660316 | CAG | C | 3 | a0001c0001t0002g0174 a0001c0001t0002g0175 a0001c0001t0003g0250 |
3 | HG02145.hp2 HG03139.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.823-3676_823-3675d others(4): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114660316 | ||||||
| chr4:114660546 | G | C | 1 | a0001c0001t0001g0029 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.823-3449G>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114660546 | |||||||
| chr4:114660692 | A | G | 2 | a0001c0006t0003g0233 a0001c0006t0003g0239 |
2 | HG00738.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.823-3303A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114660692 | |||||||
| chr4:114660710 | G | A | 1 | a0001c0001t0009g0255 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.823-3285G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114660710 | |||||||
| chr4:114660753 | G | A | 1 | a0001c0001t0001g0019 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.823-3242G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114660753 | |||||||
| chr4:114660890 | C | CA | 20 | a0001c0001t0002g0172 a0001c0001t0002g0173 a0001c0001t0003g0017 others(17): Show |
21 | HG00639.hp1 HG01255.hp1 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.823-3085dupA | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114660890 | ||||||
| chr4:114660890 | C | CAA | 10 | a0001c0001t0003g0238 a0001c0001t0003g0240 a0001c0001t0003g0241 others(7): Show |
10 | HG01109.hp2 HG01975.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.823-3086_823-3085d others(4): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114660890 | ||||||
| chr4:114660890 | CA | C | 11 | a0001c0001t0001g0189 a0001c0001t0002g0011 a0001c0001t0002g0170 others(8): Show |
13 | HG01257.hp1 HG01258.hp2 HG01515.hp2 others(10): Show |
intron_variant | MODIFIER | c.823-3085delA | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114660890 | ||||||
| chr4:114660906 | A | G | 120 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(117): Show |
125 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.823-3089A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114660906 | |||||||
| chr4:114660958 | A | G | 1 | a0001c0001t0001g0070 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.823-3037A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114660958 | |||||||
| chr4:114661002 | T | C | 1 | a0001c0001t0001g0038 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.823-2993T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114661002 | |||||||
| chr4:114661138 | A | G | 1 | a0001c0001t0002g0172 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.823-2857A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114661138 | |||||||
| chr4:114661153 | A | G | 29 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0020 others(26): Show |
33 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.823-2842A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114661153 | |||||||
| chr4:114661360 | T | C | 1 | a0001c0001t0001g0187 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.823-2635T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114661360 | |||||||
| chr4:114661484 | C | T | 1 | a0001c0001t0003g0217 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.823-2511C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114661484 | |||||||
| chr4:114661718 | C | T | 2 | a0001c0001t0003g0227 a0001c0001t0003g0228 |
2 | HG01884.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.823-2277C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114661718 | |||||||
| chr4:114661850 | C | G | 1 | a0001c0001t0003g0257 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.823-2145C>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114661850 | |||||||
| chr4:114662002 | C | G | 3 | a0001c0001t0002g0011 a0001c0001t0002g0170 a0001c0001t0002g0171 |
4 | HG01257.hp1 HG01258.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.823-1993C>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114662002 | |||||||
| chr4:114662005 | C | T | 4 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(1): Show |
4 | HG02055.hp2 HG02895.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.823-1990C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114662005 | |||||||
| chr4:114662008 | A | G | 1 | a0001c0001t0001g0030 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.823-1987A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114662008 | |||||||
| chr4:114662048 | A | G | 1 | a0001c0001t0001g0110 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.823-1947A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114662048 | |||||||
| chr4:114662334 | G | A | 1 | a0005c0008t0001g0097 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.823-1661G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114662334 | |||||||
| chr4:114662414 | G | T | 1 | a0001c0001t0001g0039 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.823-1581G>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114662414 | |||||||
| chr4:114662448 | A | G | 1 | a0002c0002t0002g0142 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.823-1547A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114662448 | |||||||
| chr4:114662567 | C | T | 209 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(206): Show |
227 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.823-1428C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114662567 | |||||||
| chr4:114662779 | CTTAA | C | 4 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(1): Show |
4 | HG02055.hp2 HG02895.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.823-1211_823-1208d others(6): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114662779 | ||||||
| chr4:114662816 | CTT | C | 43 | a0001c0001t0001g0025 a0001c0001t0001g0028 a0001c0001t0001g0029 others(40): Show |
44 | HG00597.hp2 HG01168.hp1 HG01169.hp1 others(41): Show |
intron_variant | MODIFIER | c.823-1153_823-1152d others(4): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114662816 | ||||||
| chr4:114662816 | CTTT | C | 186 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(183): Show |
205 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.823-1154_823-1152d others(5): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114662816 | ||||||
| chr4:114662816 | CTTTT | C | 15 | a0001c0001t0001g0026 a0001c0001t0001g0049 a0001c0001t0002g0011 others(12): Show |
17 | HG01109.hp2 HG01168.hp2 HG01256.hp2 others(14): Show |
intron_variant | MODIFIER | c.823-1155_823-1152d others(6): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 114662816 | ||||||
| chr4:114662865 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.823-1130G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114662865 | |||||||
| chr4:114662889 | A | G | 16 | a0001c0001t0002g0172 a0001c0001t0002g0173 a0001c0001t0003g0232 others(13): Show |
16 | HG01255.hp1 HG01891.hp1 HG01975.hp1 others(13): Show |
intron_variant | MODIFIER | c.823-1106A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114662889 | |||||||
| chr4:114662899 | C | T | 5 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(2): Show |
5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.823-1096C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114662899 | |||||||
| chr4:114662990 | T | C | 40 | a0001c0001t0004g0140 a0001c0001t0004g0141 a0001c0001t0004g0148 others(37): Show |
47 | HG00140.hp1 HG00558.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.823-1005T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114662990 | |||||||
| chr4:114663066 | A | G | 209 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(206): Show |
227 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.823-929A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114663066 | |||||||
| chr4:114663122 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.823-873C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114663122 | |||||||
| chr4:114663214 | G | C | 5 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(2): Show |
5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.823-781G>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114663214 | |||||||
| chr4:114663401 | C | T | 1 | a0001c0001t0003g0217 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.823-594C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114663401 | |||||||
| chr4:114663407 | G | A | 1 | a0001c0001t0007g0221 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.823-588G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114663407 | |||||||
| chr4:114663465 | T | C | 1 | a0001c0001t0002g0125 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.823-530T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114663465 | |||||||
| chr4:114663650 | C | A | 3 | a0001c0001t0002g0174 a0001c0001t0002g0175 a0001c0001t0003g0250 |
3 | HG02145.hp2 HG03139.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.823-345C>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114663650 | |||||||
| chr4:114663707 | A | G | 7 | a0001c0001t0001g0059 a0001c0001t0001g0064 a0001c0001t0001g0069 others(4): Show |
7 | NA18957.hp1 NA18961.hp2 NA18983.hp2 others(4): Show |
intron_variant | MODIFIER | c.823-288A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114663707 | |||||||
| chr4:114663873 | C | G | 167 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(164): Show |
180 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.823-122C>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114663873 | |||||||
| chr4:114663886 | T | C | 4 | a0002c0002t0002g0139 a0002c0002t0002g0145 a0002c0002t0002g0146 others(1): Show |
4 | HG00140.hp1 HG00733.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.823-109T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 2/5 | chr4 | 114663886 | |||||||
| chr4:114664251 | G | A | 3 | a0001c0001t0002g0011 a0001c0001t0002g0170 a0001c0001t0002g0171 |
4 | HG01257.hp1 HG01258.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.965+114G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 3/5 | chr4 | 114664251 | |||||||
| chr4:114664359 | A | G | 2 | a0001c0007t0011g0254 a0001c0007t0015g0253 |
2 | HG01257.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.965+222A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 3/5 | chr4 | 114664359 | |||||||
| chr4:114664680 | C | T | 1 | a0001c0001t0009g0255 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.965+543C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 3/5 | chr4 | 114664680 | |||||||
| chr4:114664755 | C | T | 4 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(1): Show |
4 | HG02055.hp2 HG02895.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.965+618C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 3/5 | chr4 | 114664755 | |||||||
| chr4:114664791 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.965+654G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 3/5 | chr4 | 114664791 | |||||||
| chr4:114664943 | C | T | 6 | a0001c0001t0006g0015 a0001c0001t0006g0207 a0001c0001t0006g0208 others(3): Show |
7 | HG02109.hp1 HG02572.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.966-737C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 3/5 | chr4 | 114664943 | |||||||
| chr4:114665137 | T | G | 123 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(120): Show |
128 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.966-543T>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 3/5 | chr4 | 114665137 | |||||||
| chr4:114665320 | T | C | 209 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(206): Show |
227 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.966-360T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 3/5 | chr4 | 114665320 | |||||||
| chr4:114665419 | A | G | 1 | a0001c0001t0003g0256 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.966-261A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 3/5 | chr4 | 114665419 | |||||||
| chr4:114665540 | A | G | 204 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(201): Show |
222 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.966-140A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 3/5 | chr4 | 114665540 | |||||||
| chr4:114665548 | A | G | 1 | a0001c0001t0006g0015 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.966-132A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 3/5 | chr4 | 114665548 | |||||||
| chr4:114665586 | A | C | 1 | a0001c0001t0017g0211 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.966-94A>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 3/5 | chr4 | 114665586 | |||||||
| chr4:114665623 | C | T | 1 | a0001c0001t0001g0074 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.966-57C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 3/5 | chr4 | 114665623 | |||||||
| chr4:114665640 | T | C | 6 | a0001c0001t0003g0005 a0001c0001t0003g0116 a0001c0001t0003g0213 others(3): Show |
8 | HG01106.hp1 HG01168.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.966-40T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 3/5 | chr4 | 114665640 | |||||||
| chr4:114665786 | G | C | 1 | a0001c0001t0001g0025 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1042+30G>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 4/5 | chr4 | 114665786 | |||||||
| chr4:114665816 | C | CT | 12 | a0001c0001t0002g0172 a0001c0001t0002g0173 a0001c0001t0002g0179 others(9): Show |
12 | HG00639.hp1 HG00738.hp1 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.1042+75dupT | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 114665816 | ||||||
| chr4:114666275 | C | G | 1 | a0001c0001t0001g0038 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1042+519C>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 4/5 | chr4 | 114666275 | |||||||
| chr4:114666658 | G | A | 4 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(1): Show |
4 | HG02055.hp2 HG02895.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1042+902G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 4/5 | chr4 | 114666658 | |||||||
| chr4:114666914 | G | C | 1 | a0001c0001t0003g0249 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1042+1158G>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 4/5 | chr4 | 114666914 | |||||||
| chr4:114666993 | A | G | 1 | a0003c0004t0001g0047 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1043-1092A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 4/5 | chr4 | 114666993 | |||||||
| chr4:114667067 | T | A | 3 | a0001c0001t0002g0174 a0001c0001t0002g0175 a0001c0001t0003g0250 |
3 | HG02145.hp2 HG03139.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1043-1018T>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 4/5 | chr4 | 114667067 | |||||||
| chr4:114667081 | C | A | 2 | a0001c0007t0011g0254 a0001c0007t0015g0253 |
2 | HG01257.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1043-1004C>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 4/5 | chr4 | 114667081 | |||||||
| chr4:114667118 | A | C | 1 | a0003c0004t0001g0047 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1043-967A>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 4/5 | chr4 | 114667118 | |||||||
| chr4:114667120 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1043-965G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 4/5 | chr4 | 114667120 | |||||||
| chr4:114667131 | G | A | 1 | a0001c0001t0003g0249 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1043-954G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 4/5 | chr4 | 114667131 | |||||||
| chr4:114667219 | C | G | 2 | a0001c0001t0001g0166 a0001c0001t0001g0167 |
2 | HG02615.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1043-866C>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 4/5 | chr4 | 114667219 | |||||||
| chr4:114667355 | A | G | 1 | a0001c0001t0002g0134 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1043-730A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 4/5 | chr4 | 114667355 | |||||||
| chr4:114667471 | T | A | 5 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(2): Show |
5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1043-614T>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 4/5 | chr4 | 114667471 | |||||||
| chr4:114667531 | A | G | 2 | a0001c0007t0011g0254 a0001c0007t0015g0253 |
2 | HG01257.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1043-554A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 4/5 | chr4 | 114667531 | |||||||
| chr4:114667805 | T | A | 166 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(163): Show |
178 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.1043-280T>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 4/5 | chr4 | 114667805 | |||||||
| chr4:114668003 | C | T | 211 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(208): Show |
229 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.1043-82C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 4/5 | chr4 | 114668003 | |||||||
| chr4:114668584 | T | C | 2 | a0001c0007t0011g0254 a0001c0007t0015g0253 |
2 | HG01257.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1262+280T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114668584 | |||||||
| chr4:114668587 | T | C | 1 | a0001c0001t0001g0046 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1262+283T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114668587 | |||||||
| chr4:114668819 | C | T | 1 | a0001c0001t0002g0175 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1262+515C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114668819 | |||||||
| chr4:114669067 | C | G | 16 | a0001c0001t0002g0172 a0001c0001t0002g0173 a0001c0001t0003g0232 others(13): Show |
16 | HG01255.hp1 HG01891.hp1 HG01975.hp1 others(13): Show |
intron_variant | MODIFIER | c.1262+763C>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114669067 | |||||||
| chr4:114669381 | C | CAT | 8 | a0001c0001t0003g0016 a0001c0001t0003g0213 a0001c0001t0003g0216 others(5): Show |
9 | HG01243.hp1 HG02258.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1262+1102_1262+110 others(6): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr4 | 114669381 | ||||||
| chr4:114669381 | CAT | C | 12 | a0001c0001t0002g0174 a0001c0001t0002g0175 a0001c0001t0003g0249 others(9): Show |
12 | HG00738.hp2 HG02055.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.1262+1102_1262+110 others(6): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr4 | 114669381 | ||||||
| chr4:114669381 | CATAT | C | 28 | a0001c0001t0002g0006 a0001c0001t0002g0021 a0001c0001t0002g0134 others(25): Show |
32 | HG00438.hp2 HG01106.hp1 HG01168.hp1 others(29): Show |
intron_variant | MODIFIER | c.1262+1100_1262+110 others(8): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr4 | 114669381 | ||||||
| chr4:114669381 | CATATAT | C | 71 | a0001c0001t0002g0009 a0001c0001t0002g0020 a0001c0001t0002g0022 others(68): Show |
82 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.1262+1098_1262+110 others(10): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr4 | 114669381 | ||||||
| chr4:114669381 | CATATATA others(3): Show |
C | 1 | a0001c0001t0001g0036 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1262+1094_1262+110 others(14): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr4 | 114669381 | ||||||
| chr4:114669381 | CATATATA others(5): Show |
C | 120 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(117): Show |
124 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.1262+1092_1262+110 others(16): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr4 | 114669381 | ||||||
| chr4:114669381 | CATATATA others(7): Show |
C | 1 | a0003c0004t0001g0007 | 2 | HG00733.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.1262+1090_1262+110 others(18): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr4 | 114669381 | ||||||
| chr4:114669387 | T | C | 2 | a0001c0001t0002g0006 a0001c0001t0002g0021 |
3 | NA18947.hp1 NA18961.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.1262+1083T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114669387 | |||||||
| chr4:114669467 | T | G | 1 | a0002c0002t0002g0156 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1262+1163T>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114669467 | |||||||
| chr4:114669633 | C | T | 1 | a0001c0001t0003g0257 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1262+1329C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114669633 | |||||||
| chr4:114669653 | A | G | 2 | a0001c0001t0001g0182 a0001c0001t0001g0189 |
2 | HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1262+1349A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114669653 | |||||||
| chr4:114669665 | A | G | 2 | a0001c0007t0011g0254 a0001c0007t0015g0253 |
2 | HG01257.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1262+1361A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114669665 | |||||||
| chr4:114669693 | T | C | 1 | a0002c0002t0002g0229 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1262+1389T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114669693 | |||||||
| chr4:114670073 | G | T | 1 | a0001c0001t0003g0243 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1262+1769G>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114670073 | |||||||
| chr4:114670088 | T | C | 5 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(2): Show |
5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1262+1784T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114670088 | |||||||
| chr4:114670115 | A | G | 1 | a0001c0001t0001g0028 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1262+1811A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114670115 | |||||||
| chr4:114670348 | G | A | 6 | a0001c0001t0006g0015 a0001c0001t0006g0207 a0001c0001t0006g0208 others(3): Show |
7 | HG02109.hp1 HG02572.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1262+2044G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114670348 | |||||||
| chr4:114670430 | C | CA | 150 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(147): Show |
163 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.1262+2151dupA | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr4 | 114670430 | ||||||
| chr4:114670430 | C | CAA | 38 | a0001c0001t0001g0036 a0001c0001t0001g0039 a0001c0001t0001g0057 others(35): Show |
40 | HG01081.hp1 HG01081.hp2 HG01175.hp1 others(37): Show |
intron_variant | MODIFIER | c.1262+2150_1262+215 others(6): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr4 | 114670430 | ||||||
| chr4:114670430 | CA | C | 6 | a0001c0001t0003g0217 a0001c0001t0003g0252 a0001c0001t0003g0257 others(3): Show |
6 | HG01109.hp2 HG01257.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1262+2151delA | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr4 | 114670430 | ||||||
| chr4:114670479 | G | A | 1 | a0001c0001t0001g0066 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1262+2175G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114670479 | |||||||
| chr4:114670587 | C | T | 125 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(122): Show |
130 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.1262+2283C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114670587 | |||||||
| chr4:114670801 | C | G | 5 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(2): Show |
5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1262+2497C>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114670801 | |||||||
| chr4:114671101 | C | G | 1 | a0001c0015t0014g0168 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1262+2797C>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114671101 | |||||||
| chr4:114671127 | G | T | 1 | a0001c0001t0001g0191 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1262+2823G>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114671127 | |||||||
| chr4:114671186 | C | G | 1 | a0001c0001t0003g0217 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1262+2882C>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114671186 | |||||||
| chr4:114671363 | A | G | 1 | a0001c0001t0001g0073 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1262+3059A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114671363 | |||||||
| chr4:114671570 | T | C | 1 | a0001c0001t0004g0148 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1262+3266T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114671570 | |||||||
| chr4:114671591 | A | G | 24 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0020 others(21): Show |
26 | HG00323.hp2 HG00438.hp2 HG00558.hp2 others(23): Show |
intron_variant | MODIFIER | c.1262+3287A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114671591 | |||||||
| chr4:114671715 | T | TA | 3 | a0001c0001t0002g0011 a0001c0001t0002g0170 a0001c0001t0002g0171 |
4 | HG01257.hp1 HG01258.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.1262+3416dupA | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr4 | 114671715 | ||||||
| chr4:114671856 | G | T | 1 | a0001c0001t0001g0068 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1262+3552G>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114671856 | |||||||
| chr4:114672054 | C | A | 1 | a0001c0001t0005g0177 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1262+3750C>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114672054 | |||||||
| chr4:114672384 | A | G | 7 | a0001c0001t0001g0059 a0001c0001t0001g0064 a0001c0001t0001g0069 others(4): Show |
7 | NA18957.hp1 NA18961.hp2 NA18983.hp2 others(4): Show |
intron_variant | MODIFIER | c.1263-3541A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114672384 | |||||||
| chr4:114672386 | A | C | 5 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(2): Show |
5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1263-3539A>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114672386 | |||||||
| chr4:114672508 | G | C | 254 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(251): Show |
276 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.1263-3417G>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114672508 | |||||||
| chr4:114672548 | C | T | 6 | a0001c0001t0002g0009 a0001c0001t0002g0118 a0001c0001t0002g0119 others(3): Show |
7 | HG00741.hp2 HG01099.hp1 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.1263-3377C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114672548 | |||||||
| chr4:114672622 | G | A | 164 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(161): Show |
176 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.1263-3303G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114672622 | |||||||
| chr4:114672666 | G | T | 4 | a0001c0001t0004g0140 a0001c0001t0004g0141 a0001c0001t0004g0149 others(1): Show |
4 | HG01192.hp2 HG02055.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.1263-3259G>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114672666 | |||||||
| chr4:114672701 | G | A | 35 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0020 others(32): Show |
40 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.1263-3224G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114672701 | |||||||
| chr4:114672737 | T | G | 1 | a0001c0001t0003g0116 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1263-3188T>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114672737 | |||||||
| chr4:114672781 | T | C | 1 | a0001c0014t0013g0169 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1263-3144T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114672781 | |||||||
| chr4:114672838 | T | A | 1 | a0001c0014t0013g0169 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1263-3087T>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114672838 | |||||||
| chr4:114672909 | C | T | 2 | a0001c0007t0011g0254 a0001c0007t0015g0253 |
2 | HG01257.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1263-3016C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114672909 | |||||||
| chr4:114673035 | A | G | 2 | a0001c0014t0013g0169 a0001c0015t0014g0168 |
2 | HG01109.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1263-2890A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114673035 | |||||||
| chr4:114673168 | AT | A | 234 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(231): Show |
256 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.1263-2752delT | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr4 | 114673168 | ||||||
| chr4:114673217 | A | G | 3 | a0001c0001t0002g0011 a0001c0001t0002g0170 a0001c0001t0002g0171 |
4 | HG01257.hp1 HG01258.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.1263-2708A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114673217 | |||||||
| chr4:114673260 | C | T | 76 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(73): Show |
81 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.1263-2665C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114673260 | |||||||
| chr4:114673296 | T | TAAAAAAA others(26): Show |
1 | a0001c0001t0001g0028 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1263-2628_1263-262 others(37): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr4 | 114673296 | ||||||
| chr4:114673298 | C | A | 1 | a0001c0001t0001g0028 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1263-2627C>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114673298 | |||||||
| chr4:114673300 | T | A | 1 | a0001c0001t0001g0028 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1263-2625T>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114673300 | |||||||
| chr4:114673332 | A | G | 1 | a0001c0001t0003g0217 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1263-2593A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114673332 | |||||||
| chr4:114673424 | A | T | 1 | a0001c0015t0014g0168 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1263-2501A>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114673424 | |||||||
| chr4:114673444 | G | T | 1 | a0001c0001t0003g0230 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1263-2481G>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114673444 | |||||||
| chr4:114674020 | C | T | 2 | a0001c0007t0011g0254 a0001c0007t0015g0253 |
2 | HG01257.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1263-1905C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114674020 | |||||||
| chr4:114674073 | G | T | 1 | a0002c0002t0002g0162 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1263-1852G>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114674073 | |||||||
| chr4:114674113 | A | G | 5 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(2): Show |
5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1263-1812A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114674113 | |||||||
| chr4:114674201 | G | T | 1 | a0001c0001t0009g0255 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1263-1724G>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114674201 | |||||||
| chr4:114674241 | TAATCATT others(9): Show |
T | 4 | a0001c0001t0001g0026 a0001c0001t0001g0054 a0001c0001t0001g0081 others(1): Show |
4 | HG01256.hp2 HG01516.hp2 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.1263-1682_1263-166 others(20): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr4 | 114674241 | ||||||
| chr4:114674243 | A | G | 1 | a0001c0001t0002g0179 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1263-1682A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114674243 | |||||||
| chr4:114674378 | T | C | 1 | a0001c0001t0002g0121 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1263-1547T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114674378 | |||||||
| chr4:114674491 | T | C | 209 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(206): Show |
227 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.1263-1434T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114674491 | |||||||
| chr4:114674545 | A | G | 5 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(2): Show |
5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1263-1380A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114674545 | |||||||
| chr4:114674589 | A | C | 5 | a0001c0001t0002g0174 a0001c0001t0002g0175 a0001c0001t0003g0250 others(2): Show |
5 | HG02145.hp2 HG02630.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1263-1336A>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114674589 | |||||||
| chr4:114674866 | T | C | 1 | a0001c0001t0003g0217 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1263-1059T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114674866 | |||||||
| chr4:114674879 | G | C | 1 | a0001c0001t0001g0037 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1263-1046G>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114674879 | |||||||
| chr4:114674936 | G | A | 202 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(199): Show |
220 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.1263-989G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114674936 | |||||||
| chr4:114675190 | A | G | 209 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(206): Show |
227 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.1263-735A>G | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114675190 | |||||||
| chr4:114675469 | G | A | 1 | a0001c0001t0012g0226 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1263-456G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114675469 | |||||||
| chr4:114675490 | C | T | 5 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(2): Show |
5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1263-435C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114675490 | |||||||
| chr4:114675515 | C | T | 5 | a0001c0001t0008g0204 a0001c0001t0008g0205 a0001c0001t0008g0206 others(2): Show |
5 | HG00639.hp1 HG02055.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1263-410C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114675515 | |||||||
| chr4:114675536 | T | C | 211 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(208): Show |
229 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.1263-389T>C | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114675536 | |||||||
| chr4:114675556 | C | T | 1 | a0002c0002t0002g0135 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1263-369C>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114675556 | |||||||
| chr4:114675568 | G | A | 3 | a0001c0001t0003g0240 a0001c0001t0003g0252 a0007c0009t0003g0234 |
3 | HG03209.hp2 HG03471.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1263-357G>A | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114675568 | |||||||
| chr4:114675735 | G | T | 1 | a0001c0013t0003g0212 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1263-190G>T | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | chr4 | 114675735 | |||||||
| chr4:114675739 | C | CA | 116 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(113): Show |
126 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.1263-159dupA | UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr4 | 114675739 | ||||||
| chr4:114675739 | C | CAA | 43 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0057 others(40): Show |
46 | HG00323.hp2 HG00558.hp2 HG00741.hp2 others(43): Show |
intron_variant | MODIFIER | c.1263-160_1263-159d others(4): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr4 | 114675739 | ||||||
| chr4:114675739 | C | CAAA | 9 | a0001c0001t0002g0021 a0001c0001t0002g0117 a0001c0001t0002g0118 others(6): Show |
9 | HG00438.hp2 HG01099.hp1 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.1263-161_1263-159d others(5): Show |
UGT8 | ENSG00000174607.11 | transcript | ENST00000310836.11 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr4 | 114675739 |