Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 3174 |
| ensemblid | ENSG00000164749.13 |
| hgncid | 5026 |
| symbol | HNF4G |
| name | hepatocyte nuclear factor 4 gamma |
| refseq_nuc | NM_004133.5 |
| refseq_prot | NP_004124.5 |
| ensembl_nuc | ENST00000396423.4 |
| ensembl_prot | ENSP00000379701.3 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 75539869 |
| end | 75566834 |
| strand | + |
| ver | v1.2 |
| region | chr8:75539869-75566834 |
| region5000 | chr8:75534869-75571834 |
| regionname0 | HNF4G_chr8_75539869_75566834 |
| regionname5000 | HNF4G_chr8_75534869_75571834 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 455 | 238 | 78 | 31 | 99 | 9 | 21 | 83 | HNF4G_chr8_75534869_75571834 | HNF4G | MMRVS others(450): Show |
chr8 | 75534869 | 75571834 |
| a0002 | 1/1 | 455 | 152 | 6 | 29 | 85 | 9 | 21 | 63 | HNF4G_chr8_75534869_75571834 | HNF4G | MMRVS others(450): Show |
chr8 | 75534869 | 75571834 |
| a0003 | 0/0 | 455 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | MMRVS others(450): Show |
chr8 | 75534869 | 75571834 |
| a0004 | 0/0 | 455 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | MMRVS others(450): Show |
chr8 | 75534869 | 75571834 |
| a0005 | 0/0 | 455 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | MMRVS others(450): Show |
chr8 | 75534869 | 75571834 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1365 | 189 | 63 | 29 | 73 | 8 | 16 | HNF4G_chr8_75534869_75571834 | HNF4G | ATGAT others(1360): Show |
chr8 | 75534869 | 75571834 | ||
| a0001c0003 | 0/0 | 1365 | 43 | 9 | 2 | 26 | 1 | 5 | HNF4G_chr8_75534869_75571834 | HNF4G | ATGAT others(1360): Show |
chr8 | 75534869 | 75571834 | ||
| a0001c0004 | 0/0 | 1365 | 4 | 4 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | ATGAT others(1360): Show |
chr8 | 75534869 | 75571834 | ||
| a0001c0007 | 0/0 | 1365 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | ATGAT others(1360): Show |
chr8 | 75534869 | 75571834 | ||
| a0001c0009 | 0/0 | 1365 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | ATGAT others(1360): Show |
chr8 | 75534869 | 75571834 | ||
| a0002c0002 | 1/1 | 1365 | 152 | 6 | 29 | 85 | 9 | 21 | HNF4G_chr8_75534869_75571834 | HNF4G | ATGAT others(1360): Show |
chr8 | 75534869 | 75571834 | ||
| a0003c0005 | 0/0 | 1365 | 2 | 2 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | ATGAT others(1360): Show |
chr8 | 75534869 | 75571834 | ||
| a0004c0008 | 0/0 | 1365 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | ATGAT others(1360): Show |
chr8 | 75534869 | 75571834 | ||
| a0005c0006 | 0/0 | 1365 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | ATGAT others(1360): Show |
chr8 | 75534869 | 75571834 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4200 | 14 | 11 | 0 | 3 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | GGATT others(4195): Show |
chr8 | 75534869 | 75571834 |
| a0001c0001t0002 | 0/0 | 4198 | 51 | 12 | 7 | 21 | 4 | 7 | HNF4G_chr8_75534869_75571834 | HNF4G | GGATT others(4193): Show |
chr8 | 75534869 | 75571834 |
| a0001c0001t0003 | 0/0 | 4200 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | GGATT others(4195): Show |
chr8 | 75534869 | 75571834 |
| a0001c0001t0004 | 0/0 | 4199 | 28 | 0 | 1 | 27 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | GGATT others(4194): Show |
chr8 | 75534869 | 75571834 |
| a0001c0001t0005 | 0/0 | 4199 | 23 | 17 | 4 | 0 | 1 | 1 | HNF4G_chr8_75534869_75571834 | HNF4G | GGATT others(4194): Show |
chr8 | 75534869 | 75571834 |
| a0001c0001t0006 | 0/0 | 4199 | 18 | 11 | 4 | 0 | 1 | 2 | HNF4G_chr8_75534869_75571834 | HNF4G | GGATT others(4194): Show |
chr8 | 75534869 | 75571834 |
| a0001c0001t0007 | 0/0 | 4200 | 20 | 0 | 4 | 9 | 2 | 5 | HNF4G_chr8_75534869_75571834 | HNF4G | GGATT others(4195): Show |
chr8 | 75534869 | 75571834 |
| a0001c0001t0008 | 0/0 | 4200 | 13 | 0 | 6 | 7 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | GGATT others(4195): Show |
chr8 | 75534869 | 75571834 |
| a0001c0001t0009 | 0/0 | 4200 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | GGATT others(4195): Show |
chr8 | 75534869 | 75571834 |
| a0001c0001t0010 | 0/0 | 4200 | 3 | 3 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | GGATT others(4195): Show |
chr8 | 75534869 | 75571834 |
| a0001c0001t0011 | 0/0 | 4199 | 3 | 2 | 1 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | GGATT others(4194): Show |
chr8 | 75534869 | 75571834 |
| a0001c0001t0013 | 0/0 | 4199 | 2 | 0 | 0 | 2 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | GGATT others(4194): Show |
chr8 | 75534869 | 75571834 |
| a0001c0001t0014 | 0/0 | 4198 | 2 | 0 | 0 | 2 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | GGATT others(4193): Show |
chr8 | 75534869 | 75571834 |
| a0001c0001t0016 | 0/0 | 4200 | 2 | 2 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | GGATT others(4195): Show |
chr8 | 75534869 | 75571834 |
| a0001c0001t0017 | 0/0 | 4198 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | GGATT others(4193): Show |
chr8 | 75534869 | 75571834 |
| a0001c0001t0018 | 0/0 | 4201 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | GGATT others(4196): Show |
chr8 | 75534869 | 75571834 |
| a0001c0001t0019 | 0/0 | 4200 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | GGATT others(4195): Show |
chr8 | 75534869 | 75571834 |
| a0001c0001t0020 | 0/0 | 4198 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4G_chr8_75534869_75571834 | HNF4G | GGATT others(4193): Show |
chr8 | 75534869 | 75571834 |
| a0001c0001t0022 | 0/0 | 4199 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | GGATT others(4194): Show |
chr8 | 75534869 | 75571834 |
| a0001c0001t0023 | 0/0 | 4199 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | GGATT others(4194): Show |
chr8 | 75534869 | 75571834 |
| a0001c0001t0024 | 0/0 | 4199 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | GGATT others(4194): Show |
chr8 | 75534869 | 75571834 |
| a0001c0001t0025 | 0/0 | 4200 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | GGATT others(4195): Show |
chr8 | 75534869 | 75571834 |
| a0001c0003t0001 | 0/0 | 4200 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4G_chr8_75534869_75571834 | HNF4G | GGATT others(4195): Show |
chr8 | 75534869 | 75571834 |
| a0001c0003t0002 | 0/0 | 4198 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4G_chr8_75534869_75571834 | HNF4G | GGATT others(4193): Show |
chr8 | 75534869 | 75571834 |
| a0001c0003t0003 | 0/0 | 4200 | 40 | 9 | 2 | 25 | 1 | 3 | HNF4G_chr8_75534869_75571834 | HNF4G | GGATT others(4195): Show |
chr8 | 75534869 | 75571834 |
| a0001c0003t0021 | 0/0 | 4201 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | GGATT others(4196): Show |
chr8 | 75534869 | 75571834 |
| a0001c0004t0009 | 0/0 | 4200 | 4 | 4 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | GGATT others(4195): Show |
chr8 | 75534869 | 75571834 |
| a0001c0007t0006 | 0/0 | 4199 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | GGATT others(4194): Show |
chr8 | 75534869 | 75571834 |
| a0001c0009t0006 | 0/0 | 4199 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | GGATT others(4194): Show |
chr8 | 75534869 | 75571834 |
| a0002c0002t0001 | 1/1 | 4200 | 145 | 5 | 28 | 85 | 7 | 18 | HNF4G_chr8_75534869_75571834 | HNF4G | GGATT others(4195): Show |
chr8 | 75534869 | 75571834 |
| a0002c0002t0004 | 0/0 | 4199 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | GGATT others(4194): Show |
chr8 | 75534869 | 75571834 |
| a0002c0002t0005 | 0/0 | 4199 | 2 | 0 | 1 | 0 | 0 | 1 | HNF4G_chr8_75534869_75571834 | HNF4G | GGATT others(4194): Show |
chr8 | 75534869 | 75571834 |
| a0002c0002t0012 | 0/0 | 4200 | 2 | 0 | 0 | 0 | 0 | 2 | HNF4G_chr8_75534869_75571834 | HNF4G | GGATT others(4195): Show |
chr8 | 75534869 | 75571834 |
| a0002c0002t0015 | 0/0 | 4200 | 2 | 0 | 0 | 0 | 2 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | GGATT others(4195): Show |
chr8 | 75534869 | 75571834 |
| a0003c0005t0005 | 0/0 | 4199 | 2 | 2 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | GGATT others(4194): Show |
chr8 | 75534869 | 75571834 |
| a0004c0008t0001 | 0/0 | 4200 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | GGATT others(4195): Show |
chr8 | 75534869 | 75571834 |
| a0005c0006t0010 | 0/0 | 4200 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | GGATT others(4195): Show |
chr8 | 75534869 | 75571834 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0002g0003 | 0/0 | 17 | 1 | 3 | 11 | 0 | 2 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0002g0008 | 0/0 | 5 | 1 | 1 | 0 | 1 | 2 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0002g0033 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0004g0005 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0004g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0004g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0004g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0004g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0004g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0004g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0004g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0004g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0004g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0004g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0004g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0004g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0004g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0004g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0004g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0004g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0005g0019 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0005g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0005g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0005g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0005g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0005g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0005g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0005g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0005g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0005g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0005g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0005g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0005g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0005g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0005g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0005g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0006g0009 | 0/0 | 4 | 1 | 1 | 0 | 1 | 1 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0006g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0006g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0006g0036 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0006g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0006g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0006g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0006g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0006g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0006g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0007g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0007g0017 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0007g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0007g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0007g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0007g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0007g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0007g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0007g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0007g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0007g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0007g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0007g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0008g0007 | 0/0 | 7 | 0 | 5 | 2 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0008g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0008g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0008g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0008g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0009g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0010g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0010g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0010g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0011g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0011g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0013g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0014g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0016g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0016g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0017g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0018g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0019g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0020g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0022g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0023g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0024g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0001t0025g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0003t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0003t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0003t0003g0006 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0003t0003g0012 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0003t0003g0013 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0003t0003g0016 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0003t0003g0026 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0003t0003g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0003t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0003t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0003t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0003t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0003t0003g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0003t0003g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0003t0003g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0003t0003g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0003t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0003t0003g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0003t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0003t0003g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0003t0021g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0004t0009g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0004t0009g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0004t0009g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0007t0006g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0001c0009t0006g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0002c0002t0001g0001 | 1/0 | 44 | 0 | 10 | 29 | 1 | 3 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0002c0002t0001g0002 | 0/0 | 22 | 2 | 2 | 17 | 1 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0002c0002t0001g0004 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0002c0002t0001g0011 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0002c0002t0001g0015 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0002c0002t0001g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0002c0002t0001g0025 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0002c0002t0001g0040 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0002c0002t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0002c0002t0001g0042 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0002c0002t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0002c0002t0001g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0002c0002t0001g0045 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0002c0002t0001g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0002c0002t0001g0047 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0002c0002t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0002c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0002c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0002c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0002c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0002c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0002c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0002c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0002c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0002c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0002c0002t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0002c0002t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0002c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0002c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0002c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0002c0002t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0002c0002t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0002c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0002c0002t0001g0174 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0002c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0002c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0002c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0002c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0002c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0002c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0002c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0002c0002t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0002c0002t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0002c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0002c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0002c0002t0004g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0002c0002t0005g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0002c0002t0005g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0002c0002t0012g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0002c0002t0012g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0002c0002t0015g0001 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0003c0005t0005g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0003c0005t0005g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0004c0008t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| a0005c0006t0010g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0001 | g0177 | EUR | GBR | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG00099 | hp2 | a0001 | c0001 | t0005 | g0019 | EUR | GBR | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG00140 | hp1 | a0001 | c0001 | t0006 | g0009 | EUR | GBR | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG00140 | hp2 | a0002 | c0002 | t0001 | g0001 | EUR | GBR | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0088 | EUR | FIN | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG00280 | hp2 | a0002 | c0002 | t0001 | g0002 | EUR | FIN | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG00323 | hp1 | a0001 | c0003 | t0003 | g0196 | EUR | FIN | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG00323 | hp2 | a0001 | c0001 | t0007 | g0017 | EUR | FIN | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG00408 | hp1 | a0001 | c0001 | t0004 | g0109 | EAS | CHS | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG00408 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG00423 | hp1 | a0001 | c0003 | t0003 | g0048 | EAS | CHS | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG00423 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG00438 | hp1 | a0001 | c0001 | t0004 | g0120 | EAS | CHS | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG00438 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG00558 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG00558 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG00597 | hp1 | a0001 | c0001 | t0004 | g0010 | EAS | CHS | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG00597 | hp2 | a0001 | c0003 | t0003 | g0191 | EAS | CHS | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG00609 | hp1 | a0002 | c0002 | t0001 | g0152 | EAS | CHS | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG00609 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | CHS | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0166 | EAS | CHS | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG00639 | hp1 | a0001 | c0001 | t0024 | g0142 | AMR | PUR | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG00639 | hp2 | a0002 | c0002 | t0001 | g0047 | AMR | PUR | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG00673 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG00673 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | CHS | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG00733 | hp1 | a0001 | c0001 | t0007 | g0067 | AMR | PUR | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG00733 | hp2 | a0002 | c0002 | t0001 | g0044 | AMR | PUR | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG00735 | hp1 | a0002 | c0002 | t0001 | g0170 | AMR | PUR | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG00735 | hp2 | a0001 | c0001 | t0005 | g0148 | AMR | PUR | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG00738 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG00741 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG00741 | hp2 | a0002 | c0002 | t0001 | g0046 | AMR | PUR | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG01070 | hp1 | a0001 | c0001 | t0005 | g0019 | AMR | PUR | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG01070 | hp2 | a0001 | c0001 | t0006 | g0036 | AMR | PUR | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG01071 | hp1 | a0001 | c0001 | t0006 | g0009 | AMR | PUR | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG01071 | hp2 | a0001 | c0001 | t0005 | g0019 | AMR | PUR | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG01074 | hp1 | a0002 | c0002 | t0001 | g0045 | AMR | PUR | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG01074 | hp2 | a0001 | c0001 | t0025 | g0145 | AMR | PUR | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG01099 | hp1 | a0002 | c0002 | t0005 | g0165 | AMR | PUR | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG01099 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG01109 | hp1 | a0002 | c0002 | t0001 | g0011 | AMR | PUR | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG01109 | hp2 | a0001 | c0001 | t0006 | g0104 | AMR | PUR | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG01167 | hp1 | a0001 | c0001 | t0011 | g0027 | AMR | PUR | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG01167 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG01168 | hp2 | a0001 | c0001 | t0007 | g0065 | AMR | PUR | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG01169 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG01175 | hp1 | a0001 | c0003 | t0003 | g0026 | AMR | PUR | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG01175 | hp2 | a0002 | c0002 | t0001 | g0044 | AMR | PUR | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG01192 | hp2 | a0001 | c0001 | t0008 | g0007 | AMR | PUR | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG01258 | hp1 | a0001 | c0001 | t0006 | g0141 | AMR | CLM | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG01258 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG01261 | hp1 | a0001 | c0001 | t0004 | g0112 | AMR | CLM | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG01261 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG01346 | hp2 | a0001 | c0001 | t0007 | g0066 | AMR | CLM | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG01433 | hp1 | a0002 | c0002 | t0001 | g0046 | AMR | CLM | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0076 | AMR | CLM | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0033 | EUR | IBS | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG01515 | hp2 | a0002 | c0002 | t0001 | g0015 | EUR | IBS | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0008 | EUR | IBS | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG01516 | hp2 | a0002 | c0002 | t0015 | g0001 | EUR | IBS | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0033 | EUR | IBS | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG01517 | hp2 | a0002 | c0002 | t0015 | g0001 | EUR | IBS | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG01884 | hp1 | a0001 | c0003 | t0003 | g0202 | AFR | ACB | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG01884 | hp2 | a0001 | c0001 | t0005 | g0020 | AFR | ACB | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG01891 | hp1 | a0001 | c0001 | t0018 | g0050 | AFR | ACB | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG01891 | hp2 | a0004 | c0008 | t0001 | g0071 | AFR | ACB | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG01934 | hp1 | a0001 | c0003 | t0003 | g0026 | AMR | PEL | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG01934 | hp2 | a0001 | c0001 | t0008 | g0007 | AMR | PEL | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG01952 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG01975 | hp1 | a0002 | c0002 | t0001 | g0162 | AMR | PEL | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG01975 | hp2 | a0001 | c0001 | t0008 | g0007 | AMR | PEL | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG01978 | hp1 | a0002 | c0002 | t0001 | g0011 | AMR | PEL | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG01978 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG01981 | hp1 | a0002 | c0002 | t0001 | g0011 | AMR | PEL | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG01981 | hp2 | a0002 | c0002 | t0001 | g0163 | AMR | PEL | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG01993 | hp1 | a0001 | c0001 | t0008 | g0007 | AMR | PEL | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG01993 | hp2 | a0002 | c0002 | t0001 | g0011 | AMR | PEL | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG02004 | hp1 | a0001 | c0001 | t0007 | g0057 | AMR | PEL | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG02004 | hp2 | a0002 | c0002 | t0001 | g0040 | AMR | PEL | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG02015 | hp1 | a0002 | c0002 | t0001 | g0167 | EAS | KHV | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG02027 | hp1 | a0002 | c0002 | t0001 | g0182 | EAS | KHV | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG02027 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | KHV | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG02040 | hp1 | a0002 | c0002 | t0001 | g0168 | EAS | KHV | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG02040 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG02055 | hp1 | a0001 | c0001 | t0016 | g0099 | AFR | ACB | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG02055 | hp2 | a0001 | c0001 | t0009 | g0072 | AFR | ACB | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG02056 | hp1 | a0001 | c0001 | t0013 | g0005 | EAS | KHV | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG02056 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG02071 | hp1 | a0002 | c0002 | t0001 | g0186 | EAS | KHV | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG02071 | hp2 | a0001 | c0003 | t0003 | g0193 | EAS | KHV | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG02074 | hp2 | a0002 | c0002 | t0001 | g0025 | EAS | KHV | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG02129 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | KHV | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | KHV | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG02135 | hp1 | a0001 | c0001 | t0007 | g0030 | EAS | KHV | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG02135 | hp2 | a0002 | c0002 | t0001 | g0181 | EAS | KHV | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG02145 | hp1 | a0001 | c0001 | t0005 | g0021 | AFR | ACB | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG02145 | hp2 | a0001 | c0004 | t0009 | g0031 | AFR | ACB | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0063 | AMR | PEL | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG02148 | hp2 | a0001 | c0001 | t0008 | g0124 | AMR | PEL | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | CDX | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG02165 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | CDX | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG02257 | hp1 | a0001 | c0003 | t0003 | g0026 | AFR | ACB | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG02257 | hp2 | a0001 | c0001 | t0006 | g0022 | AFR | ACB | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG02258 | hp1 | a0002 | c0002 | t0001 | g0002 | AFR | ACB | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | ACB | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG02273 | hp1 | a0002 | c0002 | t0001 | g0171 | AMR | PEL | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG02273 | hp2 | a0001 | c0001 | t0008 | g0007 | AMR | PEL | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0079 | AFR | ACB | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG02280 | hp2 | a0002 | c0002 | t0001 | g0002 | AFR | ACB | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0100 | AMR | PEL | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG02293 | hp2 | a0002 | c0002 | t0001 | g0011 | AMR | PEL | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG02523 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG02523 | hp2 | a0001 | c0003 | t0003 | g0192 | EAS | KHV | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG02572 | hp1 | a0001 | c0001 | t0005 | g0139 | AFR | GWD | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG02572 | hp2 | a0001 | c0001 | t0010 | g0094 | AFR | GWD | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0034 | SAS | PJL | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG02602 | hp2 | a0002 | c0002 | t0001 | g0172 | SAS | PJL | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG02615 | hp1 | a0001 | c0003 | t0003 | g0012 | AFR | GWD | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG02615 | hp2 | a0001 | c0001 | t0005 | g0039 | AFR | GWD | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0096 | AFR | GWD | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG02622 | hp2 | a0002 | c0002 | t0004 | g0146 | AFR | GWD | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG02630 | hp1 | a0001 | c0001 | t0005 | g0020 | AFR | GWD | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0084 | AFR | GWD | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0053 | AFR | GWD | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0183 | SAS | PJL | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG02698 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG02717 | hp1 | a0001 | c0001 | t0006 | g0103 | AFR | GWD | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0097 | AFR | GWD | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0095 | AFR | GWD | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG02723 | hp2 | a0001 | c0001 | t0005 | g0132 | AFR | GWD | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG02735 | hp1 | a0001 | c0001 | t0020 | g0034 | SAS | PJL | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG02735 | hp2 | a0001 | c0001 | t0007 | g0029 | SAS | PJL | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG02738 | hp1 | a0001 | c0001 | t0007 | g0060 | SAS | PJL | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG02738 | hp2 | a0002 | c0002 | t0001 | g0015 | SAS | PJL | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0082 | AFR | GWD | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG02818 | hp2 | a0001 | c0001 | t0005 | g0143 | AFR | GWD | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG02886 | hp1 | a0001 | c0001 | t0005 | g0137 | AFR | GWD | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG02886 | hp2 | a0001 | c0001 | t0023 | g0133 | AFR | GWD | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG02895 | hp1 | a0001 | c0004 | t0009 | g0078 | AFR | GWD | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG02895 | hp2 | a0001 | c0001 | t0005 | g0035 | AFR | GWD | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG02897 | hp1 | a0001 | c0001 | t0005 | g0035 | AFR | GWD | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG02897 | hp2 | a0001 | c0003 | t0003 | g0197 | AFR | GWD | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG02965 | hp1 | a0003 | c0005 | t0005 | g0020 | AFR | ESN | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG02965 | hp2 | a0002 | c0002 | t0001 | g0184 | AFR | ESN | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG02970 | hp1 | a0001 | c0003 | t0003 | g0012 | AFR | ESN | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | ESN | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG02976 | hp1 | a0001 | c0003 | t0003 | g0012 | AFR | ESN | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG02976 | hp2 | a0001 | c0001 | t0006 | g0022 | AFR | ESN | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG03017 | hp1 | a0002 | c0002 | t0001 | g0015 | SAS | PJL | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG03017 | hp2 | a0002 | c0002 | t0001 | g0047 | SAS | PJL | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0051 | AFR | GWD | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG03041 | hp2 | a0001 | c0001 | t0005 | g0131 | AFR | GWD | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG03098 | hp1 | a0001 | c0001 | t0006 | g0102 | AFR | MSL | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG03098 | hp2 | a0001 | c0001 | t0005 | g0021 | AFR | MSL | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | ESN | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG03130 | hp2 | a0001 | c0003 | t0003 | g0194 | AFR | ESN | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG03139 | hp1 | a0001 | c0001 | t0010 | g0074 | AFR | ESN | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG03139 | hp2 | a0001 | c0001 | t0006 | g0144 | AFR | ESN | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | ESN | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG03195 | hp2 | a0001 | c0001 | t0006 | g0023 | AFR | ESN | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG03209 | hp1 | a0001 | c0003 | t0003 | g0012 | AFR | MSL | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | MSL | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG03239 | hp1 | a0001 | c0001 | t0007 | g0017 | SAS | PJL | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG03239 | hp2 | a0001 | c0001 | t0007 | g0054 | SAS | PJL | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG03453 | hp1 | a0001 | c0001 | t0005 | g0021 | AFR | MSL | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | MSL | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG03486 | hp1 | a0003 | c0005 | t0005 | g0134 | AFR | MSL | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG03486 | hp2 | a0001 | c0001 | t0005 | g0125 | AFR | MSL | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG03490 | hp1 | a0001 | c0001 | t0006 | g0009 | SAS | PJL | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG03491 | hp1 | a0002 | c0002 | t0001 | g0042 | SAS | PJL | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0008 | SAS | PJL | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG03516 | hp1 | a0001 | c0001 | t0005 | g0140 | AFR | ESN | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG03516 | hp2 | a0001 | c0007 | t0006 | g0059 | AFR | ESN | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG03540 | hp2 | a0001 | c0009 | t0006 | g0009 | AFR | GWD | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG03579 | hp1 | a0001 | c0001 | t0005 | g0039 | AFR | MSL | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG03579 | hp2 | a0001 | c0001 | t0006 | g0022 | AFR | MSL | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG03669 | hp1 | a0001 | c0003 | t0003 | g0016 | SAS | PJL | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG03669 | hp2 | a0002 | c0002 | t0001 | g0151 | SAS | PJL | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG03688 | hp1 | a0002 | c0002 | t0005 | g0015 | SAS | STU | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG03688 | hp2 | a0002 | c0002 | t0012 | g0002 | SAS | STU | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG03704 | hp1 | a0001 | c0001 | t0005 | g0128 | SAS | PJL | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG03704 | hp2 | a0002 | c0002 | t0001 | g0179 | SAS | PJL | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG03710 | hp1 | a0001 | c0001 | t0007 | g0029 | SAS | PJL | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG03710 | hp2 | a0001 | c0003 | t0003 | g0195 | SAS | PJL | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG03834 | hp1 | a0002 | c0002 | t0001 | g0040 | SAS | BEB | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG03834 | hp2 | a0001 | c0001 | t0006 | g0101 | SAS | BEB | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0064 | SAS | BEB | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG03927 | hp2 | a0002 | c0002 | t0001 | g0025 | SAS | BEB | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG03942 | hp1 | a0002 | c0002 | t0001 | g0149 | SAS | BEB | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | BEB | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG04115 | hp1 | a0002 | c0002 | t0001 | g0150 | SAS | STU | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG04115 | hp2 | a0001 | c0003 | t0003 | g0199 | SAS | STU | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG04184 | hp1 | a0001 | c0003 | t0001 | g0190 | SAS | BEB | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG04184 | hp2 | a0002 | c0002 | t0012 | g0178 | SAS | BEB | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0008 | SAS | STU | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG04199 | hp2 | a0002 | c0002 | t0001 | g0161 | SAS | STU | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG04204 | hp1 | a0002 | c0002 | t0001 | g0156 | SAS | STU | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG04204 | hp2 | a0001 | c0003 | t0002 | g0122 | SAS | STU | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG04228 | hp1 | a0002 | c0002 | t0001 | g0001 | SAS | STU | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG04228 | hp2 | a0002 | c0002 | t0001 | g0187 | SAS | STU | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | YRI | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18522 | hp2 | a0001 | c0001 | t0006 | g0023 | AFR | YRI | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18747 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | CHB | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18747 | hp2 | a0001 | c0001 | t0008 | g0007 | EAS | CHB | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0080 | AFR | YRI | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18906 | hp2 | a0002 | c0002 | t0001 | g0147 | AFR | YRI | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18939 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18939 | hp2 | a0001 | c0003 | t0003 | g0013 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18940 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18941 | hp1 | a0001 | c0001 | t0004 | g0118 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18941 | hp2 | a0001 | c0001 | t0014 | g0032 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18942 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18944 | hp1 | a0001 | c0001 | t0004 | g0116 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18945 | hp1 | a0001 | c0003 | t0003 | g0048 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18945 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18946 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18947 | hp1 | a0001 | c0001 | t0004 | g0108 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18947 | hp2 | a0001 | c0003 | t0003 | g0006 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18948 | hp1 | a0001 | c0001 | t0007 | g0014 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18948 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18949 | hp1 | a0001 | c0001 | t0004 | g0111 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18949 | hp2 | a0002 | c0002 | t0001 | g0154 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18950 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18950 | hp2 | a0001 | c0003 | t0003 | g0013 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18951 | hp1 | a0001 | c0001 | t0014 | g0032 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18951 | hp2 | a0002 | c0002 | t0001 | g0043 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18952 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18953 | hp1 | a0001 | c0003 | t0003 | g0006 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18953 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18954 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18954 | hp2 | a0001 | c0001 | t0004 | g0119 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18956 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18956 | hp2 | a0001 | c0001 | t0004 | g0117 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18957 | hp1 | a0001 | c0003 | t0003 | g0006 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18957 | hp2 | a0002 | c0002 | t0001 | g0155 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18961 | hp1 | a0002 | c0002 | t0001 | g0164 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18961 | hp2 | a0001 | c0001 | t0004 | g0115 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18963 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18963 | hp2 | a0001 | c0001 | t0008 | g0018 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18964 | hp2 | a0001 | c0003 | t0003 | g0006 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18966 | hp1 | a0002 | c0002 | t0001 | g0041 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18966 | hp2 | a0002 | c0002 | t0001 | g0024 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18967 | hp1 | a0001 | c0001 | t0007 | g0030 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18967 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18968 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18968 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18969 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18969 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18972 | hp1 | a0001 | c0003 | t0003 | g0016 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18972 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18973 | hp2 | a0002 | c0002 | t0001 | g0160 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18975 | hp1 | a0001 | c0001 | t0008 | g0007 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18977 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18977 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18978 | hp1 | a0001 | c0003 | t0003 | g0198 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18978 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18979 | hp1 | a0002 | c0002 | t0001 | g0176 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18979 | hp2 | a0001 | c0001 | t0013 | g0005 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18980 | hp1 | a0001 | c0003 | t0003 | g0013 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18980 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18982 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18982 | hp2 | a0001 | c0003 | t0003 | g0006 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18983 | hp1 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18983 | hp2 | a0001 | c0003 | t0003 | g0006 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18984 | hp1 | a0001 | c0003 | t0003 | g0006 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18984 | hp2 | a0001 | c0001 | t0008 | g0018 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18989 | hp1 | a0002 | c0002 | t0001 | g0041 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18989 | hp2 | a0001 | c0001 | t0007 | g0014 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18990 | hp1 | a0001 | c0001 | t0004 | g0038 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18990 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18992 | hp1 | a0001 | c0003 | t0003 | g0189 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18992 | hp2 | a0001 | c0001 | t0007 | g0014 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18993 | hp1 | a0002 | c0002 | t0001 | g0158 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18993 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18997 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18997 | hp2 | a0002 | c0002 | t0001 | g0159 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18998 | hp1 | a0002 | c0002 | t0001 | g0043 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18998 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA19000 | hp1 | a0001 | c0001 | t0007 | g0014 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA19000 | hp2 | a0001 | c0001 | t0019 | g0003 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA19003 | hp2 | a0002 | c0002 | t0001 | g0157 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA19005 | hp1 | a0002 | c0002 | t0001 | g0153 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA19006 | hp1 | a0001 | c0001 | t0007 | g0058 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA19006 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA19007 | hp1 | a0001 | c0001 | t0007 | g0062 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA19007 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA19009 | hp1 | a0001 | c0003 | t0003 | g0016 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA19011 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA19012 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA19012 | hp2 | a0001 | c0003 | t0003 | g0016 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | LWK | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA19030 | hp2 | a0001 | c0004 | t0009 | g0077 | AFR | LWK | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0083 | AFR | LWK | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA19043 | hp2 | a0001 | c0001 | t0016 | g0070 | AFR | LWK | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA19054 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA19054 | hp2 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA19055 | hp1 | a0002 | c0002 | t0001 | g0024 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA19055 | hp2 | a0001 | c0001 | t0004 | g0038 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA19056 | hp1 | a0002 | c0002 | t0001 | g0188 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA19056 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA19057 | hp1 | a0001 | c0001 | t0008 | g0018 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA19057 | hp2 | a0001 | c0001 | t0004 | g0110 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA19060 | hp1 | a0001 | c0001 | t0004 | g0114 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA19060 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA19062 | hp1 | a0001 | c0001 | t0022 | g0010 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA19062 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA19064 | hp1 | a0001 | c0001 | t0004 | g0037 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA19064 | hp2 | a0001 | c0003 | t0003 | g0013 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA19065 | hp1 | a0001 | c0003 | t0003 | g0006 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA19065 | hp2 | a0002 | c0002 | t0001 | g0173 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA19066 | hp1 | a0001 | c0001 | t0004 | g0037 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA19066 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA19067 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA19067 | hp2 | a0001 | c0001 | t0008 | g0138 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA19068 | hp1 | a0002 | c0002 | t0001 | g0175 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA19068 | hp2 | a0001 | c0003 | t0021 | g0201 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA19072 | hp1 | a0001 | c0003 | t0003 | g0013 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA19072 | hp2 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA19074 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA19075 | hp1 | a0002 | c0002 | t0001 | g0025 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA19075 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA19076 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA19076 | hp2 | a0001 | c0001 | t0004 | g0113 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA19077 | hp2 | a0001 | c0001 | t0008 | g0121 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA19078 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA19079 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA19079 | hp2 | a0002 | c0002 | t0001 | g0024 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA19080 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA19080 | hp2 | a0001 | c0003 | t0003 | g0006 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA19081 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA19081 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA19084 | hp1 | a0001 | c0001 | t0007 | g0073 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA19087 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA19088 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA19091 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA19240 | hp1 | a0001 | c0001 | t0010 | g0049 | AFR | YRI | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA19240 | hp2 | a0001 | c0003 | t0003 | g0012 | AFR | YRI | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA20752 | hp1 | a0002 | c0002 | t0001 | g0045 | EUR | TSI | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA20752 | hp2 | a0001 | c0001 | t0007 | g0017 | EUR | TSI | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA20805 | hp1 | a0002 | c0002 | t0001 | g0180 | EUR | TSI | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA20805 | hp2 | a0002 | c0002 | t0001 | g0042 | EUR | TSI | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0001 | SAS | GIH | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0093 | SAS | GIH | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG01123 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG01123 | hp2 | a0001 | c0001 | t0005 | g0127 | AMR | CLM | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG02109 | hp1 | a0005 | c0006 | t0010 | g0068 | AFR | ACB | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG02486 | hp1 | a0001 | c0004 | t0009 | g0031 | AFR | ACB | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0098 | AFR | ACB | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG02559 | hp1 | a0001 | c0001 | t0017 | g0008 | AFR | ACB | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG02559 | hp2 | a0001 | c0001 | t0006 | g0009 | AFR | ACB | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG03471 | hp1 | a0002 | c0002 | t0001 | g0185 | AFR | MSL | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | MSL | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG06807 | hp1 | a0001 | c0001 | t0011 | g0052 | AFR | USA | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| HG06807 | hp2 | a0001 | c0001 | t0005 | g0105 | AFR | USA | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18955 | hp1 | a0002 | c0002 | t0001 | g0169 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA18955 | hp2 | a0001 | c0003 | t0003 | g0200 | EAS | JPT | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA20300 | hp1 | a0001 | c0001 | t0006 | g0036 | AFR | USA | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | USA | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA21309 | hp1 | a0001 | c0001 | t0006 | g0023 | AFR | LWK | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| NA21309 | hp2 | a0001 | c0001 | t0011 | g0027 | AFR | LWK | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0174 | REF | REF | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0001 | REF | REF | HNF4G_chr8_75534869_75571834 | HNF4G | chr8 | 75534869 | 75571834 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:75540078 | G | A | 4 | a0001 a0003 a0004 others(1): Show |
242 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(239): Show |
missense_variant&splice_region_variant | MODERATE | c.116G>A | p.Ser39Asn | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 1/10 | 210/4200 | 116/1368 | 39/455 | chr8 | 75540078 | |||
| chr8:75556047 | G | A | 3 | a0001 a0003 a0005 |
241 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(238): Show |
missense_variant | MODERATE | c.711G>A | p.Met237Ile | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 6/10 | 805/4200 | 711/1368 | 237/455 | chr8 | 75556047 | |||
| chr8:75560399 | A | T | 1 | a0003 | 2 | HG02965.hp1 HG03486.hp1 |
missense_variant | MODERATE | c.1179A>T | p.Gln393His | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 9/10 | 1273/4200 | 1179/1368 | 393/455 | chr8 | 75560399 | |||
| chr8:75564065 | A | C | 1 | a0005 | 1 | HG02109.hp1 | missense_variant | MODERATE | c.1337A>C | p.His446Pro | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 10/10 | 1431/4200 | 1337/1368 | 446/455 | chr8 | 75564065 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:75553107 | T | C | 1 | a0001c0004 | 4 | HG02145.hp2 HG02486.hp1 HG02895.hp1 others(1): Show |
synonymous_variant | LOW | c.555T>C | p.Asp185Asp | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 5/10 | 649/4200 | 555/1368 | 185/455 | chr8 | 75553107 | |||
| chr8:75553125 | A | G | 1 | a0001c0003 | 43 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(40): Show |
synonymous_variant | LOW | c.573A>G | p.Lys191Lys | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 5/10 | 667/4200 | 573/1368 | 191/455 | chr8 | 75553125 | |||
| chr8:75553149 | A | G | 1 | a0001c0009 | 1 | HG03540.hp2 | synonymous_variant | LOW | c.597A>G | p.Glu199Glu | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 5/10 | 691/4200 | 597/1368 | 199/455 | chr8 | 75553149 | |||
| chr8:75563994 | C | T | 1 | a0001c0007 | 1 | HG03516.hp2 | synonymous_variant | LOW | c.1266C>T | p.Leu422Leu | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 10/10 | 1360/4200 | 1266/1368 | 422/455 | chr8 | 75563994 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:75539948 | T | C | 1 | a0002c0002t0012 | 2 | HG03688.hp2 HG04184.hp2 |
5_prime_UTR_variant | MODIFIER | c.-15T>C | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 1/10 | 15 | chr8 | 75539948 | ||||||
| chr8:75564117 | G | A | 1 | a0001c0001t0013 | 2 | HG02056.hp1 NA18979.hp2 |
3_prime_UTR_variant | MODIFIER | c.*21G>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 10/10 | 21 | chr8 | 75564117 | ||||||
| chr8:75564161 | G | A | 23 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(20): Show |
184 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(181): Show |
3_prime_UTR_variant | MODIFIER | c.*65G>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 10/10 | 65 | chr8 | 75564161 | ||||||
| chr8:75564222 | G | A | 23 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(20): Show |
184 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(181): Show |
3_prime_UTR_variant | MODIFIER | c.*126G>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 10/10 | 126 | chr8 | 75564222 | ||||||
| chr8:75564304 | G | A | 1 | a0001c0001t0017 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*208G>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 10/10 | 208 | chr8 | 75564304 | ||||||
| chr8:75564435 | G | A | 23 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(20): Show |
184 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(181): Show |
3_prime_UTR_variant | MODIFIER | c.*339G>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 10/10 | 339 | chr8 | 75564435 | ||||||
| chr8:75564449 | C | A | 1 | a0002c0002t0015 | 2 | HG01516.hp2 HG01517.hp2 |
3_prime_UTR_variant | MODIFIER | c.*353C>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 10/10 | 353 | chr8 | 75564449 | ||||||
| chr8:75564458 | C | A | 2 | a0001c0001t0011 a0001c0001t0018 |
4 | HG01167.hp1 HG01891.hp1 HG06807.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*362C>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 10/10 | 362 | chr8 | 75564458 | ||||||
| chr8:75564502 | A | C | 5 | a0001c0001t0005 a0001c0001t0023 a0001c0001t0024 others(2): Show |
29 | HG00099.hp2 HG00639.hp1 HG00735.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*406A>C | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 10/10 | 406 | chr8 | 75564502 | ||||||
| chr8:75564578 | G | C | 1 | a0001c0001t0023 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*482G>C | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 10/10 | 482 | chr8 | 75564578 | ||||||
| chr8:75564604 | T | C | 5 | a0001c0001t0009 a0001c0001t0010 a0001c0001t0025 others(2): Show |
10 | HG01074.hp2 HG02055.hp2 HG02109.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*508T>C | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 10/10 | 508 | chr8 | 75564604 | ||||||
| chr8:75564634 | T | C | 2 | a0001c0001t0007 a0001c0001t0016 |
22 | HG00323.hp2 HG00733.hp1 HG01168.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*538T>C | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 10/10 | 538 | chr8 | 75564634 | ||||||
| chr8:75564670 | A | G | 1 | a0001c0001t0008 | 13 | HG01192.hp2 HG01934.hp2 HG01975.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*574A>G | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 10/10 | 574 | chr8 | 75564670 | ||||||
| chr8:75564724 | C | A | 30 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(27): Show |
216 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(213): Show |
3_prime_UTR_variant | MODIFIER | c.*628C>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 10/10 | 628 | chr8 | 75564724 | ||||||
| chr8:75564736 | A | G | 1 | a0001c0001t0014 | 2 | NA18941.hp2 NA18951.hp1 |
3_prime_UTR_variant | MODIFIER | c.*640A>G | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 10/10 | 640 | chr8 | 75564736 | ||||||
| chr8:75564887 | T | C | 30 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(27): Show |
216 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(213): Show |
3_prime_UTR_variant | MODIFIER | c.*791T>C | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 10/10 | 791 | chr8 | 75564887 | ||||||
| chr8:75564932 | T | C | 5 | a0001c0001t0009 a0001c0001t0010 a0001c0001t0025 others(2): Show |
10 | HG01074.hp2 HG02055.hp2 HG02109.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*836T>C | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 10/10 | 836 | chr8 | 75564932 | ||||||
| chr8:75564981 | A | G | 1 | a0001c0001t0018 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*885A>G | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 10/10 | 885 | chr8 | 75564981 | ||||||
| chr8:75564983 | T | C | 1 | a0001c0001t0016 | 2 | HG02055.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*887T>C | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 10/10 | 887 | chr8 | 75564983 | ||||||
| chr8:75565133 | G | A | 23 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(20): Show |
184 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(181): Show |
3_prime_UTR_variant | MODIFIER | c.*1037G>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 10/10 | 1037 | chr8 | 75565133 | ||||||
| chr8:75565294 | C | T | 2 | a0001c0001t0007 a0001c0001t0016 |
22 | HG00323.hp2 HG00733.hp1 HG01168.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1198C>T | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 10/10 | 1198 | chr8 | 75565294 | ||||||
| chr8:75565345 | G | T | 5 | a0001c0001t0009 a0001c0001t0010 a0001c0001t0025 others(2): Show |
10 | HG01074.hp2 HG02055.hp2 HG02109.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1249G>T | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 10/10 | 1249 | chr8 | 75565345 | ||||||
| chr8:75565348 | GT | G | 6 | a0001c0001t0002 a0001c0001t0014 a0001c0001t0017 others(3): Show |
57 | HG00280.hp1 HG00738.hp1 HG01168.hp1 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*1256delT | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 10/10 | 1256 | INFO_REALIGN_3_PRIME | chr8 | 75565348 | |||||
| chr8:75565355 | C | T | 23 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(20): Show |
184 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(181): Show |
3_prime_UTR_variant | MODIFIER | c.*1259C>T | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 10/10 | 1259 | chr8 | 75565355 | ||||||
| chr8:75565393 | T | C | 2 | a0001c0001t0007 a0001c0001t0016 |
22 | HG00323.hp2 HG00733.hp1 HG01168.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1297T>C | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 10/10 | 1297 | chr8 | 75565393 | ||||||
| chr8:75565617 | G | C | 2 | a0001c0001t0010 a0005c0006t0010 |
4 | HG02109.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1521G>C | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 10/10 | 1521 | chr8 | 75565617 | ||||||
| chr8:75565760 | T | G | 3 | a0001c0001t0003 a0001c0003t0003 a0001c0003t0021 |
42 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*1664T>G | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 10/10 | 1664 | chr8 | 75565760 | ||||||
| chr8:75565826 | C | G | 1 | a0001c0001t0020 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1730C>G | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 10/10 | 1730 | chr8 | 75565826 | ||||||
| chr8:75565873 | C | A | 2 | a0001c0001t0010 a0005c0006t0010 |
4 | HG02109.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1777C>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 10/10 | 1777 | chr8 | 75565873 | ||||||
| chr8:75566016 | T | TG | 4 | a0001c0001t0003 a0001c0001t0018 a0001c0003t0003 others(1): Show |
43 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*1927dupG | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 10/10 | 1928 | INFO_REALIGN_3_PRIME | chr8 | 75566016 | |||||
| chr8:75566017 | GGGGGGGT others(22): Show |
G | 1 | a0001c0001t0019 | 1 | NA19000.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1922_*1950delGGGG others(25): Show |
HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 10/10 | 1922 | chr8 | 75566017 | ||||||
| chr8:75566018 | G | A | 2 | a0001c0001t0010 a0005c0006t0010 |
4 | HG02109.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1922G>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 10/10 | 1922 | chr8 | 75566018 | ||||||
| chr8:75566057 | T | A | 1 | a0001c0001t0019 | 1 | NA19000.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1961T>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 10/10 | 1961 | chr8 | 75566057 | ||||||
| chr8:75566060 | G | A | 1 | a0001c0001t0019 | 1 | NA19000.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1964G>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 10/10 | 1964 | chr8 | 75566060 | ||||||
| chr8:75566061 | T | A | 1 | a0001c0001t0019 | 1 | NA19000.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1965T>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 10/10 | 1965 | chr8 | 75566061 | ||||||
| chr8:75566064 | G | T | 1 | a0001c0001t0019 | 1 | NA19000.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1968G>T | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 10/10 | 1968 | chr8 | 75566064 | ||||||
| chr8:75566065 | T | G | 1 | a0001c0001t0019 | 1 | NA19000.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1969T>G | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 10/10 | 1969 | chr8 | 75566065 | ||||||
| chr8:75566069 | G | GCTTATTT others(24): Show |
1 | a0001c0001t0019 | 1 | NA19000.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1973_*1974insCTTA others(27): Show |
HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 10/10 | 1974 | chr8 | 75566069 | ||||||
| chr8:75566070 | G | T | 1 | a0001c0001t0019 | 1 | NA19000.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1974G>T | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 10/10 | 1974 | chr8 | 75566070 | ||||||
| chr8:75566071 | C | T | 1 | a0001c0001t0019 | 1 | NA19000.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1975C>T | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 10/10 | 1975 | chr8 | 75566071 | ||||||
| chr8:75566073 | G | T | 1 | a0001c0001t0019 | 1 | NA19000.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1977G>T | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 10/10 | 1977 | chr8 | 75566073 | ||||||
| chr8:75566074 | C | T | 1 | a0001c0001t0019 | 1 | NA19000.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1978C>T | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 10/10 | 1978 | chr8 | 75566074 | ||||||
| chr8:75566076 | G | T | 1 | a0001c0001t0019 | 1 | NA19000.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1980G>T | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 10/10 | 1980 | chr8 | 75566076 | ||||||
| chr8:75566086 | A | T | 1 | a0001c0001t0019 | 1 | NA19000.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1990A>T | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 10/10 | 1990 | chr8 | 75566086 | ||||||
| chr8:75566087 | C | T | 1 | a0001c0001t0019 | 1 | NA19000.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1991C>T | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 10/10 | 1991 | chr8 | 75566087 | ||||||
| chr8:75566089 | A | T | 1 | a0001c0001t0019 | 1 | NA19000.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1993A>T | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 10/10 | 1993 | chr8 | 75566089 | ||||||
| chr8:75566211 | T | C | 2 | a0001c0001t0007 a0001c0001t0016 |
22 | HG00323.hp2 HG00733.hp1 HG01168.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*2115T>C | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 10/10 | 2115 | chr8 | 75566211 | ||||||
| chr8:75566381 | A | G | 27 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(24): Show |
211 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(208): Show |
3_prime_UTR_variant | MODIFIER | c.*2285A>G | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 10/10 | 2285 | chr8 | 75566381 | ||||||
| chr8:75566435 | G | A | 30 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(27): Show |
216 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(213): Show |
3_prime_UTR_variant | MODIFIER | c.*2339G>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 10/10 | 2339 | chr8 | 75566435 | ||||||
| chr8:75566533 | C | T | 22 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(19): Show |
183 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(180): Show |
3_prime_UTR_variant | MODIFIER | c.*2437C>T | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 10/10 | 2437 | chr8 | 75566533 | ||||||
| chr8:75566595 | A | G | 1 | a0001c0001t0022 | 1 | NA19062.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2499A>G | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 10/10 | 2499 | chr8 | 75566595 | ||||||
| chr8:75566756 | G | A | 3 | a0001c0001t0006 a0001c0007t0006 a0001c0009t0006 |
20 | HG00140.hp1 HG01070.hp2 HG01071.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*2660G>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 10/10 | 2660 | chr8 | 75566756 | ||||||
| chr8:75566824 | GA | G | 21 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(18): Show |
182 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(179): Show |
3_prime_UTR_variant | MODIFIER | c.*2727delA | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 10/10 | 2727 | INFO_REALIGN_3_PRIME | chr8 | 75566824 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:75540137 | G | C | 5 | a0001c0001t0003g0051 a0001c0001t0010g0049 a0001c0001t0011g0027 others(2): Show |
6 | HG01167.hp1 HG01891.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.118+57G>C | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 1/9 | chr8 | 75540137 | |||||||
| chr8:75540167 | A | G | 20 | a0001c0003t0001g0190 a0001c0003t0003g0006 a0001c0003t0003g0012 others(17): Show |
42 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.118+87A>G | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 1/9 | chr8 | 75540167 | |||||||
| chr8:75540186 | G | A | 155 | a0001c0001t0001g0007 a0001c0001t0001g0028 a0001c0001t0001g0055 others(152): Show |
244 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.118+106G>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 1/9 | chr8 | 75540186 | |||||||
| chr8:75540379 | G | A | 1 | a0001c0001t0002g0053 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.118+299G>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 1/9 | chr8 | 75540379 | |||||||
| chr8:75540483 | G | A | 1 | a0002c0002t0001g0149 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.118+403G>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 1/9 | chr8 | 75540483 | |||||||
| chr8:75540494 | A | C | 1 | a0002c0002t0001g0188 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.118+414A>C | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 1/9 | chr8 | 75540494 | |||||||
| chr8:75540544 | A | G | 1 | a0001c0001t0005g0148 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.118+464A>G | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 1/9 | chr8 | 75540544 | |||||||
| chr8:75540655 | G | C | 1 | a0001c0001t0007g0054 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.118+575G>C | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 1/9 | chr8 | 75540655 | |||||||
| chr8:75540704 | T | G | 153 | a0001c0001t0001g0007 a0001c0001t0001g0028 a0001c0001t0001g0055 others(150): Show |
242 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.118+624T>G | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 1/9 | chr8 | 75540704 | |||||||
| chr8:75540729 | T | C | 1 | a0001c0003t0003g0189 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.118+649T>C | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 1/9 | chr8 | 75540729 | |||||||
| chr8:75540845 | A | ATGTGTGT others(1): Show |
3 | a0001c0001t0006g0023 a0001c0001t0006g0144 a0001c0001t0025g0145 |
5 | HG01074.hp2 HG03139.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.118+770_118+771ins others(8): Show |
HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 75540845 | ||||||
| chr8:75540845 | A | ATGTGTGT others(3): Show |
1 | a0001c0001t0006g0022 | 3 | HG02257.hp2 HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.118+770_118+771ins others(10): Show |
HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 75540845 | ||||||
| chr8:75540851 | A | ATG | 51 | a0001c0001t0001g0007 a0001c0001t0001g0123 a0001c0001t0001g0126 others(48): Show |
76 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.118+801_118+802dup others(2): Show |
HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 75540851 | ||||||
| chr8:75540851 | A | ATGTG | 16 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0002g0100 others(13): Show |
23 | HG00140.hp1 HG01070.hp2 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.118+799_118+802dup others(4): Show |
HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 75540851 | ||||||
| chr8:75540851 | A | ATGTGTG | 7 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(4): Show |
9 | HG00423.hp1 HG01167.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.118+797_118+802dup others(6): Show |
HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 75540851 | ||||||
| chr8:75540851 | A | ATGTGTGT others(1): Show |
51 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0033 others(48): Show |
92 | HG00280.hp1 HG00323.hp1 HG00597.hp2 others(89): Show |
intron_variant | MODIFIER | c.118+795_118+802dup others(8): Show |
HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 75540851 | ||||||
| chr8:75540851 | A | ATGTGTGT others(3): Show |
12 | a0001c0001t0002g0069 a0001c0001t0003g0051 a0001c0001t0007g0029 others(9): Show |
17 | HG00733.hp1 HG01168.hp2 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.118+793_118+802dup others(10): Show |
HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 75540851 | ||||||
| chr8:75540851 | A | ATGTGTGT others(5): Show |
8 | a0001c0001t0001g0061 a0001c0001t0002g0063 a0001c0001t0002g0064 others(5): Show |
13 | HG00323.hp2 HG02148.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.118+791_118+802dup others(12): Show |
HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 75540851 | ||||||
| chr8:75540851 | A | ATGTGTGT others(7): Show |
6 | a0001c0001t0001g0028 a0001c0001t0001g0055 a0001c0001t0001g0056 others(3): Show |
7 | HG02004.hp1 HG02109.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.118+789_118+802dup others(14): Show |
HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 75540851 | ||||||
| chr8:75540851 | A | G | 4 | a0001c0001t0006g0022 a0001c0001t0006g0023 a0001c0001t0006g0144 others(1): Show |
8 | HG01074.hp2 HG02257.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.118+771A>G | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 1/9 | chr8 | 75540851 | |||||||
| chr8:75540991 | T | G | 9 | a0001c0001t0007g0017 a0001c0001t0007g0029 a0001c0001t0007g0054 others(6): Show |
12 | HG00323.hp2 HG00733.hp1 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.118+911T>G | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 1/9 | chr8 | 75540991 | |||||||
| chr8:75541001 | G | A | 3 | a0001c0001t0001g0028 a0001c0001t0001g0055 a0001c0001t0001g0056 |
4 | HG02109.hp2 HG02258.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.118+921G>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 1/9 | chr8 | 75541001 | |||||||
| chr8:75541073 | C | A | 25 | a0001c0001t0001g0028 a0001c0001t0001g0055 a0001c0001t0001g0056 others(22): Show |
38 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.118+993C>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 1/9 | chr8 | 75541073 | |||||||
| chr8:75541153 | C | A | 6 | a0001c0001t0007g0014 a0001c0001t0007g0030 a0001c0001t0007g0057 others(3): Show |
10 | HG02004.hp1 HG02135.hp1 NA18948.hp1 others(7): Show |
intron_variant | MODIFIER | c.118+1073C>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 1/9 | chr8 | 75541153 | |||||||
| chr8:75541242 | G | A | 1 | a0001c0001t0006g0022 | 3 | HG02257.hp2 HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.118+1162G>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 1/9 | chr8 | 75541242 | |||||||
| chr8:75541245 | C | G | 1 | a0001c0001t0010g0094 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.118+1165C>G | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 1/9 | chr8 | 75541245 | |||||||
| chr8:75541257 | T | A | 155 | a0001c0001t0001g0007 a0001c0001t0001g0028 a0001c0001t0001g0055 others(152): Show |
244 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.118+1177T>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 1/9 | chr8 | 75541257 | |||||||
| chr8:75541346 | C | G | 19 | a0001c0001t0004g0005 a0001c0001t0004g0010 a0001c0001t0004g0037 others(16): Show |
31 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.118+1266C>G | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 1/9 | chr8 | 75541346 | |||||||
| chr8:75541465 | G | A | 1 | a0002c0002t0001g0152 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.118+1385G>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 1/9 | chr8 | 75541465 | |||||||
| chr8:75541519 | T | C | 1 | a0002c0002t0001g0153 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.118+1439T>C | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 1/9 | chr8 | 75541519 | |||||||
| chr8:75541557 | TACTCAGA | T | 7 | a0001c0001t0007g0017 a0001c0001t0007g0029 a0001c0001t0007g0054 others(4): Show |
10 | HG00323.hp2 HG00733.hp1 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.118+1479_118+1485d others(9): Show |
HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 75541557 | ||||||
| chr8:75541790 | C | T | 34 | a0001c0001t0001g0007 a0001c0001t0001g0106 a0001c0001t0001g0107 others(31): Show |
48 | HG00099.hp2 HG00639.hp1 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.118+1710C>T | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 1/9 | chr8 | 75541790 | |||||||
| chr8:75541905 | A | G | 1 | a0002c0002t0001g0187 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.118+1825A>G | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 1/9 | chr8 | 75541905 | |||||||
| chr8:75542080 | C | T | 2 | a0002c0002t0001g0015 a0002c0002t0005g0015 |
4 | HG01515.hp2 HG02738.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.119-1731C>T | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 1/9 | chr8 | 75542080 | |||||||
| chr8:75542149 | A | T | 9 | a0001c0001t0005g0035 a0001c0001t0006g0009 a0001c0001t0006g0036 others(6): Show |
14 | HG00140.hp1 HG01070.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.119-1662A>T | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 1/9 | chr8 | 75542149 | |||||||
| chr8:75542304 | CA | C | 88 | a0001c0001t0001g0028 a0001c0001t0001g0055 a0001c0001t0001g0056 others(85): Show |
150 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.119-1501delA | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 75542304 | ||||||
| chr8:75542532 | G | A | 3 | a0001c0001t0010g0074 a0001c0001t0010g0094 a0005c0006t0010g0068 |
3 | HG02109.hp1 HG02572.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.119-1279G>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 1/9 | chr8 | 75542532 | |||||||
| chr8:75542535 | G | GA | 9 | a0001c0001t0002g0075 a0001c0001t0002g0095 a0001c0001t0010g0094 others(6): Show |
10 | HG02572.hp2 HG02622.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.119-1256dupA | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 75542535 | ||||||
| chr8:75542535 | GA | G | 44 | a0001c0001t0001g0007 a0001c0001t0001g0106 a0001c0001t0001g0107 others(41): Show |
61 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.119-1256delA | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 75542535 | ||||||
| chr8:75542535 | GAA | G | 11 | a0001c0001t0005g0035 a0001c0001t0005g0039 a0001c0001t0005g0139 others(8): Show |
17 | HG00140.hp1 HG01070.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.119-1257_119-1256d others(4): Show |
HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 75542535 | ||||||
| chr8:75542535 | GAAA | G | 6 | a0001c0001t0005g0140 a0001c0001t0006g0022 a0001c0001t0006g0023 others(3): Show |
10 | HG01074.hp2 HG02257.hp2 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.119-1258_119-1256d others(5): Show |
HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 75542535 | ||||||
| chr8:75542700 | C | T | 2 | a0001c0001t0007g0029 a0001c0001t0007g0067 |
3 | HG00733.hp1 HG02735.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.119-1111C>T | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 1/9 | chr8 | 75542700 | |||||||
| chr8:75542739 | C | CT | 6 | a0002c0002t0001g0047 a0002c0002t0001g0147 a0002c0002t0001g0184 others(3): Show |
7 | HG00639.hp2 HG02622.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.119-1071dupT | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 75542739 | ||||||
| chr8:75542922 | C | T | 2 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
2 | HG03130.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.119-889C>T | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 1/9 | chr8 | 75542922 | |||||||
| chr8:75542950 | T | A | 2 | a0001c0003t0003g0191 a0001c0003t0003g0192 |
2 | HG00597.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.119-861T>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 1/9 | chr8 | 75542950 | |||||||
| chr8:75543018 | C | T | 1 | a0001c0001t0004g0120 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.119-793C>T | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 1/9 | chr8 | 75543018 | |||||||
| chr8:75543103 | A | C | 21 | a0001c0003t0001g0190 a0001c0003t0002g0122 a0001c0003t0003g0006 others(18): Show |
43 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.119-708A>C | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 1/9 | chr8 | 75543103 | |||||||
| chr8:75543110 | G | A | 1 | a0001c0001t0007g0029 | 2 | HG02735.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.119-701G>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 1/9 | chr8 | 75543110 | |||||||
| chr8:75543172 | T | A | 154 | a0001c0001t0001g0007 a0001c0001t0001g0028 a0001c0001t0001g0055 others(151): Show |
243 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.119-639T>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 1/9 | chr8 | 75543172 | |||||||
| chr8:75543187 | A | G | 1 | a0001c0001t0025g0145 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.119-624A>G | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 1/9 | chr8 | 75543187 | |||||||
| chr8:75543196 | A | T | 1 | a0002c0002t0001g0183 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.119-615A>T | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 1/9 | chr8 | 75543196 | |||||||
| chr8:75543291 | C | T | 1 | a0002c0002t0001g0182 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.119-520C>T | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 1/9 | chr8 | 75543291 | |||||||
| chr8:75543376 | G | A | 1 | a0001c0007t0006g0059 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.119-435G>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 1/9 | chr8 | 75543376 | |||||||
| chr8:75543437 | T | C | 1 | a0001c0001t0002g0069 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.119-374T>C | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 1/9 | chr8 | 75543437 | |||||||
| chr8:75543499 | C | T | 1 | a0001c0001t0004g0119 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.119-312C>T | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 1/9 | chr8 | 75543499 | |||||||
| chr8:75543609 | G | T | 1 | a0002c0002t0001g0181 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.119-202G>T | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 1/9 | chr8 | 75543609 | |||||||
| chr8:75543672 | G | A | 5 | a0002c0002t0001g0004 a0002c0002t0001g0024 a0002c0002t0001g0158 others(2): Show |
16 | HG00609.hp2 HG02129.hp1 NA18747.hp1 others(13): Show |
intron_variant | MODIFIER | c.119-139G>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 1/9 | chr8 | 75543672 | |||||||
| chr8:75543730 | T | C | 1 | a0001c0003t0021g0201 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.119-81T>C | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 1/9 | chr8 | 75543730 | |||||||
| chr8:75544000 | G | C | 1 | a0001c0003t0003g0193 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.287+21G>C | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 2/9 | chr8 | 75544000 | |||||||
| chr8:75544222 | G | A | 1 | a0002c0002t0001g0154 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.287+243G>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 2/9 | chr8 | 75544222 | |||||||
| chr8:75544282 | G | A | 1 | a0001c0001t0004g0108 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.287+303G>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 2/9 | chr8 | 75544282 | |||||||
| chr8:75544406 | A | T | 153 | a0001c0001t0001g0007 a0001c0001t0001g0028 a0001c0001t0001g0055 others(150): Show |
242 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.287+427A>T | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 2/9 | chr8 | 75544406 | |||||||
| chr8:75544620 | T | C | 1 | a0001c0007t0006g0059 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.287+641T>C | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 2/9 | chr8 | 75544620 | |||||||
| chr8:75544650 | GT | G | 134 | a0001c0001t0001g0007 a0001c0001t0001g0028 a0001c0001t0001g0055 others(131): Show |
218 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.287+683delT | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr8 | 75544650 | ||||||
| chr8:75544651 | T | A | 2 | a0001c0001t0006g0009 a0001c0001t0006g0141 |
3 | HG00140.hp1 HG01258.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.287+672T>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 2/9 | chr8 | 75544651 | |||||||
| chr8:75544651 | T | G | 1 | a0002c0002t0001g0046 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.287+672T>G | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 2/9 | chr8 | 75544651 | |||||||
| chr8:75544702 | A | G | 1 | a0001c0001t0002g0095 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.287+723A>G | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 2/9 | chr8 | 75544702 | |||||||
| chr8:75544703 | C | T | 9 | a0001c0001t0005g0035 a0001c0001t0006g0009 a0001c0001t0006g0036 others(6): Show |
14 | HG00140.hp1 HG01070.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.287+724C>T | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 2/9 | chr8 | 75544703 | |||||||
| chr8:75544755 | T | C | 1 | a0001c0001t0002g0076 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.287+776T>C | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 2/9 | chr8 | 75544755 | |||||||
| chr8:75544803 | A | G | 9 | a0001c0001t0005g0035 a0001c0001t0006g0009 a0001c0001t0006g0036 others(6): Show |
14 | HG00140.hp1 HG01070.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.287+824A>G | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 2/9 | chr8 | 75544803 | |||||||
| chr8:75544835 | G | A | 4 | a0001c0001t0001g0028 a0001c0001t0001g0055 a0001c0001t0001g0056 others(1): Show |
5 | HG02109.hp2 HG02258.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.287+856G>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 2/9 | chr8 | 75544835 | |||||||
| chr8:75544883 | T | A | 5 | a0001c0001t0003g0051 a0001c0001t0010g0049 a0001c0001t0011g0027 others(2): Show |
6 | HG01167.hp1 HG01891.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.287+904T>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 2/9 | chr8 | 75544883 | |||||||
| chr8:75545005 | G | A | 1 | a0001c0001t0002g0096 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.287+1026G>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 2/9 | chr8 | 75545005 | |||||||
| chr8:75545031 | C | T | 13 | a0001c0003t0002g0122 a0001c0003t0003g0006 a0001c0003t0003g0013 others(10): Show |
29 | HG00423.hp1 HG00597.hp2 HG02071.hp2 others(26): Show |
intron_variant | MODIFIER | c.287+1052C>T | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 2/9 | chr8 | 75545031 | |||||||
| chr8:75545056 | A | C | 6 | a0001c0001t0007g0014 a0001c0001t0007g0030 a0001c0001t0007g0057 others(3): Show |
10 | HG02004.hp1 HG02135.hp1 NA18948.hp1 others(7): Show |
intron_variant | MODIFIER | c.287+1077A>C | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 2/9 | chr8 | 75545056 | |||||||
| chr8:75545239 | A | ATG | 8 | a0001c0001t0007g0062 a0001c0001t0016g0099 a0001c0001t0025g0145 others(5): Show |
10 | HG01074.hp2 HG02055.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.287+1292_287+1293d others(4): Show |
HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr8 | 75545239 | ||||||
| chr8:75545239 | A | ATGTG | 23 | a0001c0001t0002g0097 a0001c0001t0004g0109 a0001c0001t0006g0036 others(20): Show |
46 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.287+1290_287+1293d others(6): Show |
HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr8 | 75545239 | ||||||
| chr8:75545239 | A | ATGTGTG | 16 | a0001c0001t0001g0007 a0001c0001t0001g0106 a0001c0001t0001g0107 others(13): Show |
25 | HG00323.hp1 HG01192.hp2 HG01934.hp2 others(22): Show |
intron_variant | MODIFIER | c.287+1288_287+1293d others(8): Show |
HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr8 | 75545239 | ||||||
| chr8:75545239 | A | ATGTGTGT others(1): Show |
43 | a0001c0001t0001g0126 a0001c0001t0001g0129 a0001c0001t0001g0130 others(40): Show |
63 | HG00099.hp2 HG00438.hp1 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.287+1286_287+1293d others(10): Show |
HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr8 | 75545239 | ||||||
| chr8:75545239 | A | ATGTGTGT others(3): Show |
19 | a0001c0001t0001g0055 a0001c0001t0001g0061 a0001c0001t0001g0136 others(16): Show |
37 | HG01168.hp1 HG01169.hp2 HG01952.hp1 others(34): Show |
intron_variant | MODIFIER | c.287+1284_287+1293d others(12): Show |
HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr8 | 75545239 | ||||||
| chr8:75545239 | A | ATGTGTGT others(5): Show |
9 | a0001c0001t0001g0056 a0001c0001t0002g0033 a0001c0001t0002g0076 others(6): Show |
10 | HG00280.hp1 HG01433.hp2 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.287+1282_287+1293d others(14): Show |
HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr8 | 75545239 | ||||||
| chr8:75545239 | A | ATGTGTGT others(7): Show |
5 | a0001c0001t0001g0028 a0001c0001t0002g0064 a0001c0001t0002g0069 others(2): Show |
6 | HG02109.hp2 HG02129.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.287+1280_287+1293d others(16): Show |
HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr8 | 75545239 | ||||||
| chr8:75545239 | A | ATGTGTGT others(11): Show |
1 | a0005c0006t0010g0068 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.287+1276_287+1293d others(20): Show |
HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr8 | 75545239 | ||||||
| chr8:75545239 | ATG | A | 15 | a0001c0001t0003g0051 a0001c0001t0006g0144 a0001c0001t0010g0049 others(12): Show |
17 | HG00639.hp2 HG01891.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.287+1292_287+1293d others(4): Show |
HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr8 | 75545239 | ||||||
| chr8:75545239 | ATGTG | A | 4 | a0001c0001t0006g0022 a0001c0001t0006g0023 a0001c0001t0011g0027 others(1): Show |
9 | HG01167.hp1 HG02257.hp2 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.287+1290_287+1293d others(6): Show |
HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr8 | 75545239 | ||||||
| chr8:75545239 | ATGTGTGT others(3): Show |
A | 5 | a0001c0001t0005g0035 a0001c0001t0006g0009 a0001c0001t0006g0101 others(2): Show |
9 | HG00140.hp1 HG01071.hp1 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.287+1284_287+1293d others(12): Show |
HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr8 | 75545239 | ||||||
| chr8:75545265 | G | GTGTGTGT others(3): Show |
1 | a0001c0001t0009g0072 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.287+1293_287+1294i others(12): Show |
HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr8 | 75545265 | ||||||
| chr8:75545279 | A | C | 1 | a0001c0001t0001g0135 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.287+1300A>C | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 2/9 | chr8 | 75545279 | |||||||
| chr8:75545308 | G | A | 1 | a0002c0002t0001g0184 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.287+1329G>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 2/9 | chr8 | 75545308 | |||||||
| chr8:75545428 | G | C | 1 | a0001c0001t0002g0097 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.287+1449G>C | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 2/9 | chr8 | 75545428 | |||||||
| chr8:75545441 | G | T | 4 | a0001c0001t0001g0028 a0001c0001t0001g0055 a0001c0001t0001g0056 others(1): Show |
5 | HG02109.hp2 HG02258.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.287+1462G>T | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 2/9 | chr8 | 75545441 | |||||||
| chr8:75545559 | C | T | 9 | a0001c0001t0005g0035 a0001c0001t0006g0009 a0001c0001t0006g0036 others(6): Show |
14 | HG00140.hp1 HG01070.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.287+1580C>T | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 2/9 | chr8 | 75545559 | |||||||
| chr8:75545656 | T | G | 1 | a0001c0001t0006g0141 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.287+1677T>G | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 2/9 | chr8 | 75545656 | |||||||
| chr8:75545741 | A | G | 1 | a0001c0001t0014g0032 | 2 | NA18941.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.287+1762A>G | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 2/9 | chr8 | 75545741 | |||||||
| chr8:75545755 | AGATTATA others(14): Show |
A | 1 | a0001c0001t0008g0138 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.287+1777_287+1797d others(23): Show |
HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 2/9 | chr8 | 75545755 | |||||||
| chr8:75545843 | A | T | 3 | a0001c0001t0010g0074 a0001c0001t0010g0094 a0005c0006t0010g0068 |
3 | HG02109.hp1 HG02572.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.288-1744A>T | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 2/9 | chr8 | 75545843 | |||||||
| chr8:75546190 | C | T | 3 | a0001c0001t0010g0074 a0001c0001t0010g0094 a0005c0006t0010g0068 |
3 | HG02109.hp1 HG02572.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.288-1397C>T | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 2/9 | chr8 | 75546190 | |||||||
| chr8:75546712 | A | C | 22 | a0001c0003t0001g0190 a0001c0003t0002g0122 a0001c0003t0003g0006 others(19): Show |
44 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.288-875A>C | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 2/9 | chr8 | 75546712 | |||||||
| chr8:75546727 | A | T | 153 | a0001c0001t0001g0007 a0001c0001t0001g0028 a0001c0001t0001g0055 others(150): Show |
242 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.288-860A>T | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 2/9 | chr8 | 75546727 | |||||||
| chr8:75546863 | T | C | 1 | a0002c0002t0004g0146 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.288-724T>C | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 2/9 | chr8 | 75546863 | |||||||
| chr8:75546898 | G | A | 9 | a0001c0001t0007g0017 a0001c0001t0007g0029 a0001c0001t0007g0054 others(6): Show |
12 | HG00323.hp2 HG00733.hp1 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.288-689G>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 2/9 | chr8 | 75546898 | |||||||
| chr8:75546971 | T | C | 1 | a0001c0001t0004g0116 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.288-616T>C | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 2/9 | chr8 | 75546971 | |||||||
| chr8:75547014 | A | G | 2 | a0002c0002t0001g0046 a0002c0002t0001g0177 |
3 | HG00099.hp1 HG00741.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.288-573A>G | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 2/9 | chr8 | 75547014 | |||||||
| chr8:75547022 | A | C | 4 | a0001c0001t0025g0145 a0001c0004t0009g0031 a0001c0004t0009g0077 others(1): Show |
5 | HG01074.hp2 HG02145.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.288-565A>C | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 2/9 | chr8 | 75547022 | |||||||
| chr8:75547192 | A | C | 4 | a0001c0001t0025g0145 a0001c0004t0009g0031 a0001c0004t0009g0077 others(1): Show |
5 | HG01074.hp2 HG02145.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.288-395A>C | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 2/9 | chr8 | 75547192 | |||||||
| chr8:75547213 | A | C | 4 | a0001c0001t0001g0028 a0001c0001t0001g0055 a0001c0001t0001g0056 others(1): Show |
5 | HG02109.hp2 HG02258.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.288-374A>C | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 2/9 | chr8 | 75547213 | |||||||
| chr8:75547314 | C | T | 5 | a0001c0001t0003g0051 a0001c0001t0010g0049 a0001c0001t0011g0027 others(2): Show |
6 | HG01167.hp1 HG01891.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.288-273C>T | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 2/9 | chr8 | 75547314 | |||||||
| chr8:75547354 | A | G | 3 | a0001c0001t0002g0079 a0001c0001t0002g0096 a0001c0001t0002g0098 |
3 | HG02280.hp1 HG02486.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.288-233A>G | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 2/9 | chr8 | 75547354 | |||||||
| chr8:75547388 | T | C | 1 | a0002c0002t0001g0161 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.288-199T>C | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 2/9 | chr8 | 75547388 | |||||||
| chr8:75547392 | G | T | 1 | a0001c0001t0002g0086 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.288-195G>T | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 2/9 | chr8 | 75547392 | |||||||
| chr8:75547409 | G | A | 7 | a0001c0001t0007g0017 a0001c0001t0007g0029 a0001c0001t0007g0054 others(4): Show |
10 | HG00323.hp2 HG00733.hp1 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.288-178G>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 2/9 | chr8 | 75547409 | |||||||
| chr8:75547491 | G | A | 153 | a0001c0001t0001g0007 a0001c0001t0001g0028 a0001c0001t0001g0055 others(150): Show |
242 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.288-96G>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 2/9 | chr8 | 75547491 | |||||||
| chr8:75547740 | A | G | 1 | a0001c0001t0002g0082 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.382+59A>G | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 3/9 | chr8 | 75547740 | |||||||
| chr8:75547985 | A | G | 15 | a0001c0001t0005g0020 a0001c0001t0005g0021 a0001c0001t0005g0039 others(12): Show |
19 | HG01884.hp2 HG02145.hp1 HG02523.hp2 others(16): Show |
intron_variant | MODIFIER | c.382+304A>G | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 3/9 | chr8 | 75547985 | |||||||
| chr8:75547989 | A | AT | 10 | a0001c0001t0002g0064 a0001c0001t0003g0051 a0001c0001t0006g0144 others(7): Show |
11 | HG01167.hp1 HG01891.hp1 HG03041.hp1 others(8): Show |
intron_variant | MODIFIER | c.382+325dupT | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 75547989 | ||||||
| chr8:75547989 | AT | A | 62 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0123 others(59): Show |
97 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.382+325delT | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 75547989 | ||||||
| chr8:75547989 | ATT | A | 8 | a0001c0001t0001g0007 a0001c0001t0001g0126 a0001c0001t0008g0007 others(5): Show |
16 | HG01192.hp2 HG01934.hp2 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.382+324_382+325del others(2): Show |
HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 75547989 | ||||||
| chr8:75548132 | G | T | 33 | a0001c0001t0001g0007 a0001c0001t0001g0106 a0001c0001t0001g0107 others(30): Show |
47 | HG00099.hp2 HG00639.hp1 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.382+451G>T | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 3/9 | chr8 | 75548132 | |||||||
| chr8:75548186 | T | C | 91 | a0001c0001t0001g0007 a0001c0001t0001g0028 a0001c0001t0001g0055 others(88): Show |
131 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.382+505T>C | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 3/9 | chr8 | 75548186 | |||||||
| chr8:75548354 | A | C | 153 | a0001c0001t0001g0007 a0001c0001t0001g0028 a0001c0001t0001g0055 others(150): Show |
242 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.382+673A>C | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 3/9 | chr8 | 75548354 | |||||||
| chr8:75548418 | A | G | 5 | a0001c0001t0003g0051 a0001c0001t0010g0049 a0001c0001t0011g0027 others(2): Show |
6 | HG01167.hp1 HG01891.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.382+737A>G | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 3/9 | chr8 | 75548418 | |||||||
| chr8:75548500 | C | A | 4 | a0001c0001t0001g0028 a0001c0001t0001g0055 a0001c0001t0001g0056 others(1): Show |
5 | HG02109.hp2 HG02258.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.382+819C>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 3/9 | chr8 | 75548500 | |||||||
| chr8:75548601 | T | A | 1 | a0002c0002t0012g0178 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.382+920T>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 3/9 | chr8 | 75548601 | |||||||
| chr8:75548642 | T | C | 5 | a0001c0001t0003g0051 a0001c0001t0010g0049 a0001c0001t0011g0027 others(2): Show |
6 | HG01167.hp1 HG01891.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.382+961T>C | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 3/9 | chr8 | 75548642 | |||||||
| chr8:75548656 | A | C | 4 | a0001c0001t0006g0022 a0001c0001t0006g0023 a0001c0001t0006g0144 others(1): Show |
8 | HG02257.hp2 HG02976.hp2 HG03139.hp2 others(5): Show |
intron_variant | MODIFIER | c.382+975A>C | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 3/9 | chr8 | 75548656 | |||||||
| chr8:75548660 | C | T | 1 | a0001c0001t0004g0115 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.382+979C>T | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 3/9 | chr8 | 75548660 | |||||||
| chr8:75548769 | T | C | 1 | a0002c0002t0001g0184 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.382+1088T>C | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 3/9 | chr8 | 75548769 | |||||||
| chr8:75548856 | C | G | 1 | a0002c0002t0012g0178 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.382+1175C>G | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 3/9 | chr8 | 75548856 | |||||||
| chr8:75548991 | A | G | 154 | a0001c0001t0001g0007 a0001c0001t0001g0028 a0001c0001t0001g0055 others(151): Show |
243 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.382+1310A>G | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 3/9 | chr8 | 75548991 | |||||||
| chr8:75549062 | G | C | 4 | a0001c0001t0006g0022 a0001c0001t0006g0023 a0001c0001t0006g0144 others(1): Show |
8 | HG02257.hp2 HG02976.hp2 HG03139.hp2 others(5): Show |
intron_variant | MODIFIER | c.382+1381G>C | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 3/9 | chr8 | 75549062 | |||||||
| chr8:75549079 | C | T | 3 | a0001c0001t0001g0028 a0001c0001t0001g0055 a0001c0001t0001g0056 |
4 | HG02109.hp2 HG02258.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.382+1398C>T | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 3/9 | chr8 | 75549079 | |||||||
| chr8:75549289 | T | C | 39 | a0001c0001t0001g0007 a0001c0001t0001g0106 a0001c0001t0001g0107 others(36): Show |
57 | HG00099.hp2 HG00639.hp1 HG00735.hp2 others(54): Show |
intron_variant | MODIFIER | c.382+1608T>C | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 3/9 | chr8 | 75549289 | |||||||
| chr8:75549379 | G | A | 1 | a0001c0001t0002g0098 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.382+1698G>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 3/9 | chr8 | 75549379 | |||||||
| chr8:75549496 | A | AT | 16 | a0001c0003t0002g0122 a0001c0003t0003g0006 a0001c0003t0003g0012 others(13): Show |
36 | HG00423.hp1 HG00597.hp2 HG02071.hp2 others(33): Show |
intron_variant | MODIFIER | c.382+1819dupT | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 75549496 | ||||||
| chr8:75549533 | C | T | 33 | a0001c0001t0001g0007 a0001c0001t0001g0106 a0001c0001t0001g0107 others(30): Show |
47 | HG00099.hp2 HG00639.hp1 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.382+1852C>T | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 3/9 | chr8 | 75549533 | |||||||
| chr8:75549549 | C | CT | 7 | a0001c0001t0002g0081 a0001c0001t0008g0138 a0001c0001t0010g0074 others(4): Show |
11 | HG02109.hp1 HG02572.hp2 HG03139.hp1 others(8): Show |
intron_variant | MODIFIER | c.383-1825dupT | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 75549549 | ||||||
| chr8:75549563 | T | C | 1 | a0002c0002t0001g0042 | 2 | HG03491.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.383-1825T>C | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 3/9 | chr8 | 75549563 | |||||||
| chr8:75549596 | G | A | 1 | a0001c0001t0005g0131 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.383-1792G>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 3/9 | chr8 | 75549596 | |||||||
| chr8:75549659 | G | A | 1 | a0001c0001t0005g0105 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.383-1729G>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 3/9 | chr8 | 75549659 | |||||||
| chr8:75549853 | T | A | 4 | a0001c0001t0001g0028 a0001c0001t0001g0055 a0001c0001t0001g0056 others(1): Show |
5 | HG02109.hp2 HG02258.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.383-1535T>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 3/9 | chr8 | 75549853 | |||||||
| chr8:75549882 | A | G | 1 | a0002c0002t0001g0175 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.383-1506A>G | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 3/9 | chr8 | 75549882 | |||||||
| chr8:75550148 | T | C | 33 | a0001c0001t0001g0007 a0001c0001t0001g0106 a0001c0001t0001g0107 others(30): Show |
47 | HG00099.hp2 HG00639.hp1 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.383-1240T>C | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 3/9 | chr8 | 75550148 | |||||||
| chr8:75550162 | G | A | 153 | a0001c0001t0001g0007 a0001c0001t0001g0028 a0001c0001t0001g0055 others(150): Show |
242 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.383-1226G>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 3/9 | chr8 | 75550162 | |||||||
| chr8:75550263 | A | C | 21 | a0001c0003t0001g0190 a0001c0003t0002g0122 a0001c0003t0003g0006 others(18): Show |
43 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.383-1125A>C | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 3/9 | chr8 | 75550263 | |||||||
| chr8:75550312 | T | C | 96 | a0001c0001t0001g0028 a0001c0001t0001g0055 a0001c0001t0001g0056 others(93): Show |
163 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.383-1076T>C | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 3/9 | chr8 | 75550312 | |||||||
| chr8:75550319 | T | A | 2 | a0002c0002t0001g0043 a0002c0002t0001g0155 |
3 | NA18951.hp2 NA18957.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.383-1069T>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 3/9 | chr8 | 75550319 | |||||||
| chr8:75550330 | T | C | 1 | a0002c0002t0001g0163 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.383-1058T>C | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 3/9 | chr8 | 75550330 | |||||||
| chr8:75550399 | G | T | 1 | a0002c0002t0004g0146 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.383-989G>T | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 3/9 | chr8 | 75550399 | |||||||
| chr8:75550469 | C | T | 1 | a0001c0001t0025g0145 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.383-919C>T | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 3/9 | chr8 | 75550469 | |||||||
| chr8:75550494 | G | A | 19 | a0001c0001t0004g0005 a0001c0001t0004g0010 a0001c0001t0004g0037 others(16): Show |
31 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.383-894G>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 3/9 | chr8 | 75550494 | |||||||
| chr8:75550502 | G | A | 5 | a0001c0001t0003g0051 a0001c0001t0010g0049 a0001c0001t0011g0027 others(2): Show |
6 | HG01167.hp1 HG01891.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.383-886G>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 3/9 | chr8 | 75550502 | |||||||
| chr8:75550566 | A | T | 1 | a0001c0001t0023g0133 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.383-822A>T | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 3/9 | chr8 | 75550566 | |||||||
| chr8:75550661 | A | T | 3 | a0001c0001t0010g0074 a0001c0001t0010g0094 a0005c0006t0010g0068 |
3 | HG02109.hp1 HG02572.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.383-727A>T | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 3/9 | chr8 | 75550661 | |||||||
| chr8:75550700 | CT | C | 150 | a0001c0001t0001g0007 a0001c0001t0001g0028 a0001c0001t0001g0055 others(147): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.383-675delT | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr8 | 75550700 | ||||||
| chr8:75550747 | C | T | 21 | a0001c0001t0004g0005 a0001c0001t0004g0010 a0001c0001t0004g0037 others(18): Show |
33 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.383-641C>T | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 3/9 | chr8 | 75550747 | |||||||
| chr8:75551038 | G | A | 1 | a0001c0001t0002g0087 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.383-350G>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 3/9 | chr8 | 75551038 | |||||||
| chr8:75551162 | T | C | 153 | a0001c0001t0001g0007 a0001c0001t0001g0028 a0001c0001t0001g0055 others(150): Show |
242 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.383-226T>C | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 3/9 | chr8 | 75551162 | |||||||
| chr8:75551316 | A | C | 1 | a0001c0001t0002g0069 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.383-72A>C | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 3/9 | chr8 | 75551316 | |||||||
| chr8:75551336 | T | C | 39 | a0001c0001t0001g0007 a0001c0001t0001g0106 a0001c0001t0001g0107 others(36): Show |
57 | HG00099.hp2 HG00639.hp1 HG00735.hp2 others(54): Show |
intron_variant | MODIFIER | c.383-52T>C | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 3/9 | chr8 | 75551336 | |||||||
| chr8:75551378 | T | C | 5 | a0001c0001t0002g0083 a0001c0001t0025g0145 a0001c0004t0009g0031 others(2): Show |
6 | HG01074.hp2 HG02145.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.383-10T>C | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 3/9 | chr8 | 75551378 | |||||||
| chr8:75551520 | C | A | 1 | a0002c0002t0001g0040 | 2 | HG02004.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.489+26C>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 4/9 | chr8 | 75551520 | |||||||
| chr8:75551681 | A | G | 3 | a0002c0002t0001g0011 a0002c0002t0001g0162 a0002c0002t0001g0163 |
7 | HG01109.hp1 HG01975.hp1 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.489+187A>G | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 4/9 | chr8 | 75551681 | |||||||
| chr8:75551788 | G | A | 3 | a0001c0001t0010g0074 a0001c0001t0010g0094 a0005c0006t0010g0068 |
3 | HG02109.hp1 HG02572.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.489+294G>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 4/9 | chr8 | 75551788 | |||||||
| chr8:75551823 | C | T | 1 | a0002c0002t0001g0173 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.489+329C>T | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 4/9 | chr8 | 75551823 | |||||||
| chr8:75551828 | A | G | 13 | a0001c0001t0005g0035 a0001c0001t0006g0009 a0001c0001t0006g0022 others(10): Show |
22 | HG00140.hp1 HG01070.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.489+334A>G | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 4/9 | chr8 | 75551828 | |||||||
| chr8:75551849 | G | T | 3 | a0002c0002t0001g0047 a0002c0002t0001g0185 a0002c0002t0001g0187 |
4 | HG00639.hp2 HG03017.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.489+355G>T | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 4/9 | chr8 | 75551849 | |||||||
| chr8:75551941 | G | A | 1 | a0001c0001t0007g0057 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.489+447G>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 4/9 | chr8 | 75551941 | |||||||
| chr8:75552019 | A | G | 1 | a0002c0002t0001g0172 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.489+525A>G | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 4/9 | chr8 | 75552019 | |||||||
| chr8:75552152 | A | G | 1 | a0001c0003t0003g0196 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.489+658A>G | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 4/9 | chr8 | 75552152 | |||||||
| chr8:75552175 | C | T | 1 | a0002c0002t0004g0146 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.489+681C>T | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 4/9 | chr8 | 75552175 | |||||||
| chr8:75552299 | A | G | 9 | a0001c0001t0005g0035 a0001c0001t0006g0009 a0001c0001t0006g0036 others(6): Show |
14 | HG00140.hp1 HG01070.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.490-743A>G | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 4/9 | chr8 | 75552299 | |||||||
| chr8:75552428 | T | G | 25 | a0001c0001t0001g0028 a0001c0001t0001g0055 a0001c0001t0001g0056 others(22): Show |
38 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.490-614T>G | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 4/9 | chr8 | 75552428 | |||||||
| chr8:75552561 | C | T | 1 | a0004c0008t0001g0071 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.490-481C>T | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 4/9 | chr8 | 75552561 | |||||||
| chr8:75552605 | G | T | 157 | a0001c0001t0001g0007 a0001c0001t0001g0028 a0001c0001t0001g0055 others(154): Show |
247 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.490-437G>T | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 4/9 | chr8 | 75552605 | |||||||
| chr8:75552937 | A | G | 1 | a0001c0001t0002g0069 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.490-105A>G | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 4/9 | chr8 | 75552937 | |||||||
| chr8:75553282 | C | T | 1 | a0002c0002t0004g0146 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.645+85C>T | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 5/9 | chr8 | 75553282 | |||||||
| chr8:75553287 | T | G | 159 | a0001c0001t0001g0007 a0001c0001t0001g0028 a0001c0001t0001g0055 others(156): Show |
249 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.645+90T>G | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 5/9 | chr8 | 75553287 | |||||||
| chr8:75553335 | T | C | 34 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0033 others(31): Show |
56 | HG00280.hp1 HG00738.hp1 HG01168.hp1 others(53): Show |
intron_variant | MODIFIER | c.645+138T>C | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 5/9 | chr8 | 75553335 | |||||||
| chr8:75553410 | T | C | 1 | a0001c0003t0003g0199 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.645+213T>C | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 5/9 | chr8 | 75553410 | |||||||
| chr8:75553578 | A | G | 4 | a0001c0001t0025g0145 a0001c0004t0009g0031 a0001c0004t0009g0077 others(1): Show |
5 | HG01074.hp2 HG02145.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.645+381A>G | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 5/9 | chr8 | 75553578 | |||||||
| chr8:75553588 | T | G | 21 | a0001c0003t0001g0190 a0001c0003t0002g0122 a0001c0003t0003g0006 others(18): Show |
43 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.645+391T>G | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 5/9 | chr8 | 75553588 | |||||||
| chr8:75553652 | G | T | 1 | a0002c0002t0001g0171 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.645+455G>T | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 5/9 | chr8 | 75553652 | |||||||
| chr8:75553656 | G | A | 1 | a0002c0002t0005g0165 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.645+459G>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 5/9 | chr8 | 75553656 | |||||||
| chr8:75553674 | C | T | 92 | a0001c0001t0001g0007 a0001c0001t0001g0106 a0001c0001t0001g0107 others(89): Show |
154 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.645+477C>T | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 5/9 | chr8 | 75553674 | |||||||
| chr8:75553675 | A | G | 153 | a0001c0001t0001g0007 a0001c0001t0001g0028 a0001c0001t0001g0055 others(150): Show |
242 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.645+478A>G | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 5/9 | chr8 | 75553675 | |||||||
| chr8:75553860 | C | T | 2 | a0002c0002t0001g0045 a0002c0002t0005g0165 |
3 | HG01074.hp1 HG01099.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.645+663C>T | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 5/9 | chr8 | 75553860 | |||||||
| chr8:75553967 | T | C | 1 | a0002c0002t0001g0166 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.645+770T>C | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 5/9 | chr8 | 75553967 | |||||||
| chr8:75554028 | A | G | 9 | a0001c0001t0007g0017 a0001c0001t0007g0029 a0001c0001t0007g0054 others(6): Show |
12 | HG00323.hp2 HG00733.hp1 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.645+831A>G | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 5/9 | chr8 | 75554028 | |||||||
| chr8:75554030 | GGTAA | G | 5 | a0001c0001t0003g0051 a0001c0001t0010g0049 a0001c0001t0011g0027 others(2): Show |
6 | HG01167.hp1 HG01891.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.645+836_645+839del others(4): Show |
HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr8 | 75554030 | ||||||
| chr8:75554048 | T | C | 1 | a0001c0001t0002g0098 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.645+851T>C | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 5/9 | chr8 | 75554048 | |||||||
| chr8:75554069 | G | C | 7 | a0001c0001t0007g0017 a0001c0001t0007g0029 a0001c0001t0007g0054 others(4): Show |
10 | HG00323.hp2 HG00733.hp1 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.645+872G>C | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 5/9 | chr8 | 75554069 | |||||||
| chr8:75554206 | G | A | 3 | a0001c0001t0006g0102 a0001c0001t0006g0103 a0001c0001t0006g0104 |
3 | HG01109.hp2 HG02717.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.645+1009G>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 5/9 | chr8 | 75554206 | |||||||
| chr8:75554321 | T | C | 4 | a0001c0001t0025g0145 a0001c0004t0009g0031 a0001c0004t0009g0077 others(1): Show |
5 | HG01074.hp2 HG02145.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.645+1124T>C | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 5/9 | chr8 | 75554321 | |||||||
| chr8:75554502 | C | T | 4 | a0001c0001t0001g0028 a0001c0001t0001g0055 a0001c0001t0001g0056 others(1): Show |
5 | HG02109.hp2 HG02258.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.645+1305C>T | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 5/9 | chr8 | 75554502 | |||||||
| chr8:75554532 | G | A | 3 | a0001c0001t0002g0088 a0001c0001t0005g0019 a0001c0001t0005g0148 |
5 | HG00099.hp2 HG00280.hp1 HG00735.hp2 others(2): Show |
intron_variant | MODIFIER | c.645+1335G>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 5/9 | chr8 | 75554532 | |||||||
| chr8:75554539 | G | A | 4 | a0001c0001t0001g0028 a0001c0001t0001g0055 a0001c0001t0001g0056 others(1): Show |
5 | HG02109.hp2 HG02258.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.645+1342G>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 5/9 | chr8 | 75554539 | |||||||
| chr8:75554566 | C | T | 1 | a0004c0008t0001g0071 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.645+1369C>T | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 5/9 | chr8 | 75554566 | |||||||
| chr8:75554674 | A | T | 3 | a0001c0001t0006g0022 a0001c0001t0006g0023 a0001c0001t0006g0144 |
7 | HG02257.hp2 HG02976.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.646-1308A>T | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 5/9 | chr8 | 75554674 | |||||||
| chr8:75554697 | C | T | 1 | a0001c0003t0003g0195 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.646-1285C>T | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 5/9 | chr8 | 75554697 | |||||||
| chr8:75554808 | G | A | 1 | a0005c0006t0010g0068 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.646-1174G>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 5/9 | chr8 | 75554808 | |||||||
| chr8:75554866 | G | C | 2 | a0002c0002t0001g0179 a0002c0002t0001g0180 |
2 | HG03704.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.646-1116G>C | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 5/9 | chr8 | 75554866 | |||||||
| chr8:75555000 | C | G | 1 | a0001c0001t0005g0139 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.646-982C>G | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 5/9 | chr8 | 75555000 | |||||||
| chr8:75555104 | G | C | 1 | a0001c0001t0006g0144 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.646-878G>C | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 5/9 | chr8 | 75555104 | |||||||
| chr8:75555358 | C | T | 1 | a0001c0007t0006g0059 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.646-624C>T | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 5/9 | chr8 | 75555358 | |||||||
| chr8:75555440 | G | A | 4 | a0001c0001t0001g0028 a0001c0001t0001g0055 a0001c0001t0001g0056 others(1): Show |
5 | HG02109.hp2 HG02258.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.646-542G>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 5/9 | chr8 | 75555440 | |||||||
| chr8:75555580 | T | TA | 153 | a0001c0001t0001g0007 a0001c0001t0001g0028 a0001c0001t0001g0055 others(150): Show |
242 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.646-401dupA | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr8 | 75555580 | ||||||
| chr8:75555613 | T | G | 7 | a0001c0001t0007g0017 a0001c0001t0007g0029 a0001c0001t0007g0054 others(4): Show |
10 | HG00323.hp2 HG00733.hp1 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.646-369T>G | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 5/9 | chr8 | 75555613 | |||||||
| chr8:75555644 | A | G | 1 | a0001c0001t0006g0101 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.646-338A>G | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 5/9 | chr8 | 75555644 | |||||||
| chr8:75555730 | C | CT | 10 | a0001c0001t0007g0017 a0001c0001t0007g0029 a0001c0001t0007g0054 others(7): Show |
13 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.646-239dupT | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr8 | 75555730 | ||||||
| chr8:75555730 | CT | C | 12 | a0001c0001t0001g0028 a0001c0001t0001g0055 a0001c0001t0001g0056 others(9): Show |
15 | HG00639.hp2 HG01070.hp2 HG02015.hp1 others(12): Show |
intron_variant | MODIFIER | c.646-239delT | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr8 | 75555730 | ||||||
| chr8:75555779 | T | G | 21 | a0001c0003t0001g0190 a0001c0003t0002g0122 a0001c0003t0003g0006 others(18): Show |
43 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.646-203T>G | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 5/9 | chr8 | 75555779 | |||||||
| chr8:75555842 | A | G | 49 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0033 others(46): Show |
81 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.646-140A>G | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 5/9 | chr8 | 75555842 | |||||||
| chr8:75555904 | C | G | 153 | a0001c0001t0001g0007 a0001c0001t0001g0028 a0001c0001t0001g0055 others(150): Show |
242 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.646-78C>G | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 5/9 | chr8 | 75555904 | |||||||
| chr8:75556074 | GTT | G | 149 | a0001c0001t0001g0007 a0001c0001t0001g0028 a0001c0001t0001g0055 others(146): Show |
238 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.733+16_733+17delTT | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr8 | 75556074 | ||||||
| chr8:75556148 | G | C | 7 | a0001c0001t0004g0010 a0001c0001t0004g0108 a0001c0001t0004g0110 others(4): Show |
10 | HG00597.hp1 NA18941.hp1 NA18947.hp1 others(7): Show |
intron_variant | MODIFIER | c.733+79G>C | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 6/9 | chr8 | 75556148 | |||||||
| chr8:75556262 | C | T | 1 | a0001c0001t0007g0057 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.733+193C>T | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 6/9 | chr8 | 75556262 | |||||||
| chr8:75556268 | G | A | 1 | a0002c0002t0001g0168 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.733+199G>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 6/9 | chr8 | 75556268 | |||||||
| chr8:75556271 | A | T | 1 | a0001c0001t0005g0132 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.733+202A>T | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 6/9 | chr8 | 75556271 | |||||||
| chr8:75556316 | A | G | 13 | a0001c0003t0002g0122 a0001c0003t0003g0006 a0001c0003t0003g0013 others(10): Show |
29 | HG00423.hp1 HG00597.hp2 HG02071.hp2 others(26): Show |
intron_variant | MODIFIER | c.733+247A>G | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 6/9 | chr8 | 75556316 | |||||||
| chr8:75556329 | T | C | 4 | a0001c0001t0009g0072 a0001c0004t0009g0031 a0001c0004t0009g0077 others(1): Show |
5 | HG02055.hp2 HG02145.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.733+260T>C | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 6/9 | chr8 | 75556329 | |||||||
| chr8:75556339 | T | A | 8 | a0001c0001t0005g0035 a0001c0001t0006g0009 a0001c0001t0006g0101 others(5): Show |
12 | HG00140.hp1 HG01071.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.733+270T>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 6/9 | chr8 | 75556339 | |||||||
| chr8:75556348 | T | C | 1 | a0001c0001t0005g0132 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.733+279T>C | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 6/9 | chr8 | 75556348 | |||||||
| chr8:75556522 | G | A | 1 | a0001c0001t0002g0082 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.733+453G>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 6/9 | chr8 | 75556522 | |||||||
| chr8:75556559 | G | C | 7 | a0001c0001t0005g0035 a0001c0001t0006g0009 a0001c0001t0006g0101 others(4): Show |
11 | HG00140.hp1 HG01071.hp1 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.733+490G>C | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 6/9 | chr8 | 75556559 | |||||||
| chr8:75556562 | T | A | 7 | a0001c0001t0007g0017 a0001c0001t0007g0029 a0001c0001t0007g0054 others(4): Show |
10 | HG00323.hp2 HG00733.hp1 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.733+493T>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 6/9 | chr8 | 75556562 | |||||||
| chr8:75556570 | G | A | 1 | a0001c0001t0002g0084 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.733+501G>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 6/9 | chr8 | 75556570 | |||||||
| chr8:75556634 | G | T | 6 | a0001c0001t0007g0014 a0001c0001t0007g0030 a0001c0001t0007g0057 others(3): Show |
10 | HG02004.hp1 HG02135.hp1 NA18948.hp1 others(7): Show |
intron_variant | MODIFIER | c.733+565G>T | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 6/9 | chr8 | 75556634 | |||||||
| chr8:75556713 | T | A | 7 | a0001c0001t0007g0017 a0001c0001t0007g0029 a0001c0001t0007g0054 others(4): Show |
10 | HG00323.hp2 HG00733.hp1 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.733+644T>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 6/9 | chr8 | 75556713 | |||||||
| chr8:75556725 | C | G | 1 | a0001c0003t0003g0194 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.733+656C>G | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 6/9 | chr8 | 75556725 | |||||||
| chr8:75556758 | T | A | 4 | a0001c0001t0010g0049 a0001c0001t0010g0074 a0001c0001t0010g0094 others(1): Show |
4 | HG02109.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.733+689T>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 6/9 | chr8 | 75556758 | |||||||
| chr8:75556796 | T | C | 139 | a0001c0001t0001g0028 a0001c0001t0001g0055 a0001c0001t0001g0056 others(136): Show |
220 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.733+727T>C | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 6/9 | chr8 | 75556796 | |||||||
| chr8:75556925 | G | A | 2 | a0001c0003t0003g0191 a0001c0003t0003g0192 |
2 | HG00597.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.733+856G>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 6/9 | chr8 | 75556925 | |||||||
| chr8:75556950 | A | G | 3 | a0001c0001t0010g0049 a0001c0001t0016g0070 a0001c0001t0016g0099 |
3 | HG02055.hp1 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.733+881A>G | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 6/9 | chr8 | 75556950 | |||||||
| chr8:75557273 | T | C | 4 | a0001c0001t0010g0049 a0001c0001t0010g0074 a0001c0001t0010g0094 others(1): Show |
4 | HG02109.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.733+1204T>C | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 6/9 | chr8 | 75557273 | |||||||
| chr8:75557418 | G | A | 1 | a0001c0001t0002g0091 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.734-1100G>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 6/9 | chr8 | 75557418 | |||||||
| chr8:75557511 | C | G | 1 | a0001c0001t0002g0083 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.734-1007C>G | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 6/9 | chr8 | 75557511 | |||||||
| chr8:75557785 | G | A | 139 | a0001c0001t0001g0028 a0001c0001t0001g0055 a0001c0001t0001g0056 others(136): Show |
220 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.734-733G>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 6/9 | chr8 | 75557785 | |||||||
| chr8:75558036 | TA | T | 47 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0033 others(44): Show |
73 | HG00280.hp1 HG00323.hp2 HG00733.hp1 others(70): Show |
intron_variant | MODIFIER | c.734-471delA | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr8 | 75558036 | ||||||
| chr8:75558133 | C | T | 1 | a0001c0001t0002g0080 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.734-385C>T | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 6/9 | chr8 | 75558133 | |||||||
| chr8:75558169 | G | A | 139 | a0001c0001t0001g0028 a0001c0001t0001g0055 a0001c0001t0001g0056 others(136): Show |
220 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.734-349G>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 6/9 | chr8 | 75558169 | |||||||
| chr8:75558190 | G | A | 1 | a0001c0001t0002g0080 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.734-328G>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 6/9 | chr8 | 75558190 | |||||||
| chr8:75558244 | A | C | 1 | a0002c0002t0001g0044 | 2 | HG00733.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.734-274A>C | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 6/9 | chr8 | 75558244 | |||||||
| chr8:75558797 | T | C | 1 | a0001c0001t0007g0073 | 1 | NA19084.hp1 | splice_region_variant&intron_variant | LOW | c.887-4T>C | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 7/9 | chr8 | 75558797 | |||||||
| chr8:75559175 | G | T | 1 | a0001c0003t0003g0197 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1123+138G>T | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 8/9 | chr8 | 75559175 | |||||||
| chr8:75559272 | TG | T | 129 | a0001c0001t0001g0028 a0001c0001t0001g0055 a0001c0001t0001g0056 others(126): Show |
207 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.1123+236delG | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 8/9 | chr8 | 75559272 | |||||||
| chr8:75559273 | G | T | 3 | a0001c0001t0002g0098 a0001c0001t0007g0060 a0002c0002t0001g0025 |
3 | HG02486.hp2 HG02738.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.1123+236G>T | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 8/9 | chr8 | 75559273 | |||||||
| chr8:75559275 | T | TG | 9 | a0001c0001t0002g0092 a0001c0001t0004g0010 a0001c0001t0004g0108 others(6): Show |
12 | HG00597.hp1 NA18941.hp1 NA18947.hp1 others(9): Show |
intron_variant | MODIFIER | c.1123+238_1123+239i others(3): Show |
HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 8/9 | chr8 | 75559275 | |||||||
| chr8:75559277 | G | T | 9 | a0001c0001t0002g0092 a0001c0001t0004g0010 a0001c0001t0004g0108 others(6): Show |
12 | HG00597.hp1 NA18941.hp1 NA18947.hp1 others(9): Show |
intron_variant | MODIFIER | c.1123+240G>T | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 8/9 | chr8 | 75559277 | |||||||
| chr8:75559278 | T | G | 9 | a0001c0001t0002g0092 a0001c0001t0004g0010 a0001c0001t0004g0108 others(6): Show |
12 | HG00597.hp1 NA18941.hp1 NA18947.hp1 others(9): Show |
intron_variant | MODIFIER | c.1123+241T>G | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 8/9 | chr8 | 75559278 | |||||||
| chr8:75559278 | T | TTG | 131 | a0001c0001t0001g0028 a0001c0001t0001g0055 a0001c0001t0001g0056 others(128): Show |
209 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.1123+242_1123+243i others(4): Show |
HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr8 | 75559278 | ||||||
| chr8:75559281 | T | G | 140 | a0001c0001t0001g0028 a0001c0001t0001g0055 a0001c0001t0001g0056 others(137): Show |
221 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.1123+244T>G | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 8/9 | chr8 | 75559281 | |||||||
| chr8:75559286 | T | G | 140 | a0001c0001t0001g0028 a0001c0001t0001g0055 a0001c0001t0001g0056 others(137): Show |
221 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.1123+249T>G | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 8/9 | chr8 | 75559286 | |||||||
| chr8:75559398 | G | A | 140 | a0001c0001t0001g0028 a0001c0001t0001g0055 a0001c0001t0001g0056 others(137): Show |
221 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.1123+361G>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 8/9 | chr8 | 75559398 | |||||||
| chr8:75559400 | A | C | 1 | a0001c0001t0007g0054 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1123+363A>C | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 8/9 | chr8 | 75559400 | |||||||
| chr8:75559484 | G | A | 1 | a0002c0002t0001g0151 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1123+447G>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 8/9 | chr8 | 75559484 | |||||||
| chr8:75559512 | T | A | 1 | a0002c0002t0001g0169 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1123+475T>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 8/9 | chr8 | 75559512 | |||||||
| chr8:75559544 | A | G | 1 | a0002c0002t0001g0183 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1123+507A>G | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 8/9 | chr8 | 75559544 | |||||||
| chr8:75559589 | T | A | 1 | a0001c0001t0004g0112 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1123+552T>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 8/9 | chr8 | 75559589 | |||||||
| chr8:75559612 | A | T | 1 | a0001c0001t0004g0114 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1123+575A>T | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 8/9 | chr8 | 75559612 | |||||||
| chr8:75559637 | G | C | 1 | a0002c0002t0001g0149 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1123+600G>C | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 8/9 | chr8 | 75559637 | |||||||
| chr8:75559643 | T | A | 1 | a0002c0002t0001g0156 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1123+606T>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 8/9 | chr8 | 75559643 | |||||||
| chr8:75559765 | C | CAT | 6 | a0001c0001t0005g0021 a0001c0001t0005g0125 a0001c0001t0005g0131 others(3): Show |
8 | HG02145.hp1 HG02717.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1124-567_1124-566d others(4): Show |
HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr8 | 75559765 | ||||||
| chr8:75559816 | A | G | 4 | a0001c0001t0010g0049 a0001c0001t0010g0074 a0001c0001t0010g0094 others(1): Show |
4 | HG02109.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1124-528A>G | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 8/9 | chr8 | 75559816 | |||||||
| chr8:75559904 | T | G | 7 | a0001c0001t0005g0020 a0001c0001t0005g0035 a0001c0001t0005g0105 others(4): Show |
9 | HG01884.hp2 HG02630.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1124-440T>G | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 8/9 | chr8 | 75559904 | |||||||
| chr8:75559934 | C | A | 1 | a0001c0001t0004g0110 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1124-410C>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 8/9 | chr8 | 75559934 | |||||||
| chr8:75560024 | C | T | 7 | a0001c0001t0006g0009 a0001c0001t0006g0036 a0001c0001t0006g0101 others(4): Show |
11 | HG00140.hp1 HG01070.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.1124-320C>T | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 8/9 | chr8 | 75560024 | |||||||
| chr8:75560073 | A | C | 1 | a0001c0001t0006g0022 | 3 | HG02257.hp2 HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1124-271A>C | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 8/9 | chr8 | 75560073 | |||||||
| chr8:75560080 | G | A | 9 | a0001c0001t0007g0017 a0001c0001t0007g0029 a0001c0001t0007g0054 others(6): Show |
12 | HG00323.hp2 HG00733.hp1 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.1124-264G>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 8/9 | chr8 | 75560080 | |||||||
| chr8:75560101 | C | T | 1 | a0002c0002t0001g0155 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1124-243C>T | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 8/9 | chr8 | 75560101 | |||||||
| chr8:75560250 | G | A | 157 | a0001c0001t0001g0007 a0001c0001t0001g0028 a0001c0001t0001g0055 others(154): Show |
247 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.1124-94G>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 8/9 | chr8 | 75560250 | |||||||
| chr8:75560325 | A | G | 5 | a0001c0001t0009g0072 a0001c0001t0025g0145 a0001c0004t0009g0031 others(2): Show |
6 | HG01074.hp2 HG02055.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1124-19A>G | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 8/9 | chr8 | 75560325 | |||||||
| chr8:75560325 | A | T | 112 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0033 others(109): Show |
184 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.1124-19A>T | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 8/9 | chr8 | 75560325 | |||||||
| chr8:75560500 | T | A | 22 | a0001c0001t0003g0051 a0001c0003t0001g0190 a0001c0003t0002g0122 others(19): Show |
44 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.1246+34T>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 9/9 | chr8 | 75560500 | |||||||
| chr8:75560640 | A | C | 1 | a0002c0002t0001g0180 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1246+174A>C | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 9/9 | chr8 | 75560640 | |||||||
| chr8:75560699 | G | A | 1 | a0001c0001t0005g0143 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1246+233G>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 9/9 | chr8 | 75560699 | |||||||
| chr8:75560758 | C | T | 1 | a0001c0001t0002g0085 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1246+292C>T | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 9/9 | chr8 | 75560758 | |||||||
| chr8:75560795 | T | A | 2 | a0001c0001t0016g0070 a0001c0001t0016g0099 |
2 | HG02055.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1246+329T>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 9/9 | chr8 | 75560795 | |||||||
| chr8:75560837 | C | T | 15 | a0001c0001t0007g0014 a0001c0001t0007g0017 a0001c0001t0007g0029 others(12): Show |
22 | HG00323.hp2 HG00733.hp1 HG01168.hp2 others(19): Show |
intron_variant | MODIFIER | c.1246+371C>T | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 9/9 | chr8 | 75560837 | |||||||
| chr8:75560912 | G | T | 1 | a0001c0003t0003g0192 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1246+446G>T | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 9/9 | chr8 | 75560912 | |||||||
| chr8:75560937 | G | A | 1 | a0002c0002t0001g0024 | 3 | NA18966.hp2 NA19055.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.1246+471G>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 9/9 | chr8 | 75560937 | |||||||
| chr8:75560943 | C | T | 15 | a0001c0001t0007g0014 a0001c0001t0007g0017 a0001c0001t0007g0029 others(12): Show |
22 | HG00323.hp2 HG00733.hp1 HG01168.hp2 others(19): Show |
intron_variant | MODIFIER | c.1246+477C>T | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 9/9 | chr8 | 75560943 | |||||||
| chr8:75561064 | A | AT | 7 | a0001c0001t0007g0017 a0001c0001t0007g0029 a0001c0001t0007g0054 others(4): Show |
10 | HG00323.hp2 HG00733.hp1 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.1246+604dupT | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 75561064 | ||||||
| chr8:75561074 | T | C | 15 | a0001c0001t0007g0014 a0001c0001t0007g0017 a0001c0001t0007g0029 others(12): Show |
22 | HG00323.hp2 HG00733.hp1 HG01168.hp2 others(19): Show |
intron_variant | MODIFIER | c.1246+608T>C | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 9/9 | chr8 | 75561074 | |||||||
| chr8:75561163 | A | G | 15 | a0001c0001t0007g0014 a0001c0001t0007g0017 a0001c0001t0007g0029 others(12): Show |
22 | HG00323.hp2 HG00733.hp1 HG01168.hp2 others(19): Show |
intron_variant | MODIFIER | c.1246+697A>G | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 9/9 | chr8 | 75561163 | |||||||
| chr8:75561191 | G | T | 1 | a0002c0002t0004g0146 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1246+725G>T | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 9/9 | chr8 | 75561191 | |||||||
| chr8:75561210 | C | G | 1 | a0001c0001t0002g0089 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1246+744C>G | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 9/9 | chr8 | 75561210 | |||||||
| chr8:75561226 | G | A | 4 | a0001c0001t0001g0123 a0001c0001t0001g0129 a0001c0001t0001g0135 others(1): Show |
4 | HG03195.hp1 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1246+760G>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 9/9 | chr8 | 75561226 | |||||||
| chr8:75561287 | A | G | 2 | a0001c0001t0006g0102 a0001c0001t0006g0103 |
2 | HG02717.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1246+821A>G | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 9/9 | chr8 | 75561287 | |||||||
| chr8:75561302 | C | A | 1 | a0001c0001t0004g0113 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1246+836C>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 9/9 | chr8 | 75561302 | |||||||
| chr8:75561391 | T | A | 1 | a0001c0001t0005g0137 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1246+925T>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 9/9 | chr8 | 75561391 | |||||||
| chr8:75561486 | G | A | 1 | a0002c0002t0001g0158 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1246+1020G>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 9/9 | chr8 | 75561486 | |||||||
| chr8:75561634 | G | C | 1 | a0001c0001t0007g0029 | 2 | HG02735.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1246+1168G>C | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 9/9 | chr8 | 75561634 | |||||||
| chr8:75561697 | G | A | 5 | a0001c0001t0010g0049 a0001c0001t0010g0074 a0001c0001t0010g0094 others(2): Show |
5 | HG01074.hp2 HG02109.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1246+1231G>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 9/9 | chr8 | 75561697 | |||||||
| chr8:75561704 | T | C | 177 | a0001c0001t0001g0007 a0001c0001t0001g0028 a0001c0001t0001g0055 others(174): Show |
291 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.1246+1238T>C | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 9/9 | chr8 | 75561704 | |||||||
| chr8:75561823 | A | G | 21 | a0001c0001t0005g0019 a0001c0001t0005g0020 a0001c0001t0005g0021 others(18): Show |
28 | HG00099.hp2 HG00639.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.1246+1357A>G | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 9/9 | chr8 | 75561823 | |||||||
| chr8:75561839 | C | T | 7 | a0001c0001t0006g0009 a0001c0001t0006g0036 a0001c0001t0006g0101 others(4): Show |
11 | HG00140.hp1 HG01070.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.1246+1373C>T | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 9/9 | chr8 | 75561839 | |||||||
| chr8:75562027 | C | T | 1 | a0001c0003t0003g0195 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1246+1561C>T | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 9/9 | chr8 | 75562027 | |||||||
| chr8:75562136 | AT | A | 136 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0033 others(133): Show |
216 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1246+1680delT | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 75562136 | ||||||
| chr8:75562151 | C | T | 1 | a0001c0004t0009g0031 | 2 | HG02145.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.1246+1685C>T | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 9/9 | chr8 | 75562151 | |||||||
| chr8:75562169 | T | C | 127 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0033 others(124): Show |
206 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.1246+1703T>C | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 9/9 | chr8 | 75562169 | |||||||
| chr8:75562178 | T | C | 1 | a0001c0001t0010g0049 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1246+1712T>C | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 9/9 | chr8 | 75562178 | |||||||
| chr8:75562236 | C | T | 3 | a0001c0001t0010g0074 a0001c0001t0010g0094 a0005c0006t0010g0068 |
3 | HG02109.hp1 HG02572.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1247-1739C>T | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 9/9 | chr8 | 75562236 | |||||||
| chr8:75562244 | C | A | 3 | a0001c0001t0011g0027 a0001c0001t0011g0052 a0001c0001t0018g0050 |
4 | HG01167.hp1 HG01891.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1247-1731C>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 9/9 | chr8 | 75562244 | |||||||
| chr8:75562324 | A | G | 136 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0033 others(133): Show |
216 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1247-1651A>G | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 9/9 | chr8 | 75562324 | |||||||
| chr8:75562329 | A | G | 3 | a0001c0001t0002g0082 a0001c0001t0002g0095 a0001c0001t0002g0097 |
3 | HG02717.hp2 HG02723.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1247-1646A>G | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 9/9 | chr8 | 75562329 | |||||||
| chr8:75562423 | A | G | 1 | a0002c0002t0004g0146 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1247-1552A>G | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 9/9 | chr8 | 75562423 | |||||||
| chr8:75562468 | A | C | 1 | a0001c0003t0003g0200 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1247-1507A>C | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 9/9 | chr8 | 75562468 | |||||||
| chr8:75562472 | CAGAA | C | 6 | a0001c0001t0007g0014 a0001c0001t0007g0030 a0001c0001t0007g0057 others(3): Show |
10 | HG02004.hp1 HG02135.hp1 NA18948.hp1 others(7): Show |
intron_variant | MODIFIER | c.1247-1499_1247-149 others(8): Show |
HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 75562472 | ||||||
| chr8:75562484 | G | A | 112 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0033 others(109): Show |
184 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.1247-1491G>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 9/9 | chr8 | 75562484 | |||||||
| chr8:75562557 | A | G | 21 | a0001c0001t0003g0051 a0001c0003t0001g0190 a0001c0003t0002g0122 others(18): Show |
43 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.1247-1418A>G | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 9/9 | chr8 | 75562557 | |||||||
| chr8:75562658 | T | C | 1 | a0001c0001t0014g0032 | 2 | NA18941.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.1247-1317T>C | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 9/9 | chr8 | 75562658 | |||||||
| chr8:75562702 | C | T | 7 | a0001c0001t0004g0010 a0001c0001t0004g0108 a0001c0001t0004g0110 others(4): Show |
10 | HG00597.hp1 NA18941.hp1 NA18947.hp1 others(7): Show |
intron_variant | MODIFIER | c.1247-1273C>T | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 9/9 | chr8 | 75562702 | |||||||
| chr8:75562818 | A | G | 1 | a0001c0003t0003g0200 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1247-1157A>G | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 9/9 | chr8 | 75562818 | |||||||
| chr8:75562890 | G | A | 112 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0033 others(109): Show |
184 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.1247-1085G>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 9/9 | chr8 | 75562890 | |||||||
| chr8:75563069 | T | C | 5 | a0001c0001t0005g0019 a0001c0001t0005g0127 a0001c0001t0005g0148 others(2): Show |
7 | HG00099.hp2 HG00639.hp1 HG00735.hp2 others(4): Show |
intron_variant | MODIFIER | c.1247-906T>C | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 9/9 | chr8 | 75563069 | |||||||
| chr8:75563186 | G | A | 2 | a0001c0001t0002g0064 a0002c0002t0004g0146 |
2 | HG02622.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1247-789G>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 9/9 | chr8 | 75563186 | |||||||
| chr8:75563260 | T | C | 1 | a0001c0003t0003g0200 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1247-715T>C | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 9/9 | chr8 | 75563260 | |||||||
| chr8:75563386 | G | A | 2 | a0001c0001t0016g0070 a0001c0001t0016g0099 |
2 | HG02055.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1247-589G>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 9/9 | chr8 | 75563386 | |||||||
| chr8:75563430 | CA | C | 127 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0033 others(124): Show |
206 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.1247-533delA | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 75563430 | ||||||
| chr8:75563540 | T | A | 1 | a0001c0003t0003g0200 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1247-435T>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 9/9 | chr8 | 75563540 | |||||||
| chr8:75563661 | T | C | 6 | a0001c0001t0007g0014 a0001c0001t0007g0030 a0001c0001t0007g0057 others(3): Show |
10 | HG02004.hp1 HG02135.hp1 NA18948.hp1 others(7): Show |
intron_variant | MODIFIER | c.1247-314T>C | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 9/9 | chr8 | 75563661 | |||||||
| chr8:75563678 | T | C | 1 | a0002c0002t0004g0146 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1247-297T>C | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 9/9 | chr8 | 75563678 | |||||||
| chr8:75563739 | GA | G | 15 | a0001c0001t0007g0014 a0001c0001t0007g0017 a0001c0001t0007g0029 others(12): Show |
22 | HG00323.hp2 HG00733.hp1 HG01168.hp2 others(19): Show |
intron_variant | MODIFIER | c.1247-229delA | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 75563739 | ||||||
| chr8:75563958 | C | A | 7 | a0001c0001t0006g0009 a0001c0001t0006g0036 a0001c0001t0006g0101 others(4): Show |
11 | HG00140.hp1 HG01070.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.1247-17C>A | HNF4G | ENSG00000164749.13 | transcript | ENST00000396423.4 | protein_coding | 9/9 | chr8 | 75563958 |