Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 3172 |
| ensemblid | ENSG00000101076.20 |
| hgncid | 5024 |
| symbol | HNF4A |
| name | hepatocyte nuclear factor 4 alpha |
| refseq_nuc | NM_175914.5 |
| refseq_prot | NP_787110.2 |
| ensembl_nuc | ENST00000316673.9 |
| ensembl_prot | ENSP00000315180.4 |
| mane_status | MANE Select |
| chr | chr20 |
| start | 44355699 |
| end | 44432845 |
| strand | + |
| ver | v1.2 |
| region | chr20:44355699-44432845 |
| region5000 | chr20:44350699-44437845 |
| regionname0 | HNF4A_chr20_44355699_44432845 |
| regionname5000 | HNF4A_chr20_44350699_44437845 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 452 | 309 | 87 | 51 | 114 | 18 | 37 | 80 | HNF4A_chr20_44350699_44437845 | HNF4A | MVSVN others(447): Show |
chr20 | 44350699 | 44437845 |
| a0002 | 0/0 | 452 | 7 | 0 | 3 | 2 | 0 | 2 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | MVSVN others(447): Show |
chr20 | 44350699 | 44437845 |
| a0003 | 0/0 | 452 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | MVSVN others(447): Show |
chr20 | 44350699 | 44437845 |
| a0004 | 0/0 | 452 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | MVSVN others(447): Show |
chr20 | 44350699 | 44437845 |
| a0005 | 0/0 | 452 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | MVSVN others(447): Show |
chr20 | 44350699 | 44437845 |
| a0006 | 0/0 | 452 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | MVSVN others(447): Show |
chr20 | 44350699 | 44437845 |
| a0007 | 0/0 | 452 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | MVSVN others(447): Show |
chr20 | 44350699 | 44437845 |
| a0008 | 0/0 | 452 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | MVSVN others(447): Show |
chr20 | 44350699 | 44437845 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1356 | 302 | 83 | 49 | 113 | 18 | 37 | HNF4A_chr20_44350699_44437845 | HNF4A | ATGGT others(1351): Show |
chr20 | 44350699 | 44437845 | ||
| a0001c0003 | 0/0 | 1356 | 2 | 2 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | ATGGT others(1351): Show |
chr20 | 44350699 | 44437845 | ||
| a0001c0009 | 0/0 | 1356 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | ATGGT others(1351): Show |
chr20 | 44350699 | 44437845 | ||
| a0001c0011 | 0/0 | 1356 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | ATGGT others(1351): Show |
chr20 | 44350699 | 44437845 | ||
| a0001c0012 | 0/0 | 1356 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | ATGGT others(1351): Show |
chr20 | 44350699 | 44437845 | ||
| a0001c0013 | 0/0 | 1356 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | ATGGT others(1351): Show |
chr20 | 44350699 | 44437845 | ||
| a0001c0014 | 0/0 | 1356 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | ATGGT others(1351): Show |
chr20 | 44350699 | 44437845 | ||
| a0002c0002 | 0/0 | 1356 | 7 | 0 | 3 | 2 | 0 | 2 | HNF4A_chr20_44350699_44437845 | HNF4A | ATGGT others(1351): Show |
chr20 | 44350699 | 44437845 | ||
| a0003c0010 | 0/0 | 1356 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | ATGGT others(1351): Show |
chr20 | 44350699 | 44437845 | ||
| a0004c0006 | 0/0 | 1356 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | ATGGT others(1351): Show |
chr20 | 44350699 | 44437845 | ||
| a0005c0007 | 0/0 | 1356 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | ATGGT others(1351): Show |
chr20 | 44350699 | 44437845 | ||
| a0006c0004 | 0/0 | 1356 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | ATGGT others(1351): Show |
chr20 | 44350699 | 44437845 | ||
| a0007c0005 | 0/0 | 1356 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | ATGGT others(1351): Show |
chr20 | 44350699 | 44437845 | ||
| a0008c0008 | 0/0 | 1356 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | ATGGT others(1351): Show |
chr20 | 44350699 | 44437845 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4646 | 46 | 12 | 14 | 6 | 6 | 8 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4641): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0002 | 0/0 | 4646 | 33 | 2 | 2 | 21 | 1 | 7 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4641): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0003 | 0/0 | 4627 | 28 | 1 | 2 | 19 | 3 | 3 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4622): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0004 | 0/0 | 4646 | 21 | 2 | 1 | 18 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4641): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0005 | 0/0 | 4646 | 12 | 1 | 3 | 4 | 2 | 2 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4641): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0006 | 0/0 | 4646 | 9 | 0 | 6 | 1 | 1 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4641): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0007 | 0/0 | 4646 | 7 | 1 | 3 | 3 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4641): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0008 | 0/0 | 4645 | 7 | 4 | 3 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4640): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0009 | 0/0 | 4625 | 5 | 0 | 0 | 0 | 0 | 5 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4620): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0010 | 0/0 | 4645 | 4 | 4 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4640): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0011 | 0/0 | 4645 | 5 | 3 | 1 | 0 | 1 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4640): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0012 | 0/0 | 4647 | 5 | 3 | 1 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4642): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0013 | 0/0 | 4646 | 4 | 3 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4641): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0014 | 0/0 | 4646 | 4 | 4 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4641): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0015 | 0/0 | 4627 | 4 | 0 | 0 | 4 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4622): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0016 | 0/0 | 4638 | 4 | 0 | 0 | 4 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4633): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0017 | 0/0 | 4626 | 2 | 0 | 0 | 2 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4621): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0018 | 0/0 | 4637 | 3 | 3 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4632): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0019 | 0/0 | 4644 | 3 | 3 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4639): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0020 | 0/0 | 4638 | 3 | 0 | 0 | 2 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4633): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0021 | 0/0 | 4646 | 3 | 0 | 0 | 3 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4641): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0022 | 0/0 | 4645 | 3 | 0 | 0 | 3 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4640): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0023 | 0/0 | 4626 | 2 | 1 | 0 | 0 | 1 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4621): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0024 | 0/0 | 4628 | 3 | 0 | 1 | 1 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4623): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0025 | 0/0 | 4646 | 2 | 0 | 0 | 2 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4641): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0026 | 0/0 | 4617 | 2 | 0 | 0 | 0 | 1 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4612): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0027 | 0/0 | 4626 | 2 | 2 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4621): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0028 | 0/0 | 4638 | 2 | 0 | 0 | 2 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4633): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0029 | 0/0 | 4644 | 2 | 0 | 0 | 0 | 2 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4639): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0030 | 0/0 | 4630 | 2 | 0 | 0 | 0 | 0 | 2 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4625): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0031 | 0/0 | 4645 | 2 | 2 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4640): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0032 | 0/0 | 4638 | 2 | 2 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4633): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0033 | 0/0 | 4645 | 2 | 1 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4640): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0034 | 0/0 | 4647 | 2 | 1 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4642): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0035 | 0/0 | 4647 | 2 | 0 | 0 | 2 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4642): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0036 | 0/0 | 4626 | 2 | 0 | 0 | 2 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4621): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0037 | 0/0 | 4645 | 2 | 2 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4640): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0038 | 0/0 | 4646 | 2 | 1 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4641): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0039 | 0/0 | 4638 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4633): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0040 | 0/0 | 4646 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4641): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0041 | 0/0 | 4626 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4621): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0042 | 0/0 | 4627 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4622): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0043 | 0/0 | 4646 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4641): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0044 | 0/0 | 4645 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4640): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0045 | 0/0 | 4646 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4641): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0046 | 0/0 | 4646 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4641): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0047 | 0/0 | 4619 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4614): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0048 | 0/0 | 4625 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4620): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0049 | 0/0 | 4646 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4641): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0050 | 0/0 | 4646 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4641): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0051 | 0/0 | 4636 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4631): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0052 | 0/0 | 4637 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4632): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0053 | 0/0 | 4646 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4641): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0054 | 0/0 | 4638 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4633): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0055 | 0/0 | 4647 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4642): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0057 | 0/0 | 4627 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4622): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0058 | 0/0 | 4638 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4633): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0059 | 0/0 | 4647 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4642): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0060 | 0/0 | 4646 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4641): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0061 | 0/0 | 4627 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4622): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0063 | 0/0 | 4626 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4621): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0064 | 0/0 | 4627 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4622): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0066 | 0/0 | 4645 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4640): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0067 | 0/0 | 4646 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4641): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0068 | 0/1 | 4636 | 1 | 0 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4631): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0070 | 0/0 | 4639 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4634): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0071 | 0/0 | 4646 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4641): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0072 | 0/0 | 4638 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4633): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0073 | 1/0 | 4645 | 1 | 0 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4640): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0074 | 0/0 | 4645 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4640): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0075 | 0/0 | 4644 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4639): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0076 | 0/0 | 4644 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4639): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0077 | 0/0 | 4645 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4640): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0078 | 0/0 | 4646 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4641): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0080 | 0/0 | 4637 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4632): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0082 | 0/0 | 4534 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4529): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0083 | 0/0 | 4638 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4633): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0084 | 0/0 | 4645 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4640): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0085 | 0/0 | 4637 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4632): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0086 | 0/0 | 4644 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4639): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0087 | 0/0 | 4645 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4640): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0088 | 0/0 | 4638 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4633): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0089 | 0/0 | 4646 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4641): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0091 | 0/0 | 4619 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4614): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0092 | 0/0 | 4627 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4622): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0093 | 0/0 | 4625 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4620): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0094 | 0/0 | 4789 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4784): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0095 | 0/0 | 4627 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4622): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0096 | 0/0 | 4626 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4621): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0097 | 0/0 | 4647 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4642): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0098 | 0/0 | 4637 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4632): Show |
chr20 | 44350699 | 44437845 |
| a0001c0001t0099 | 0/0 | 4646 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4641): Show |
chr20 | 44350699 | 44437845 |
| a0001c0003t0062 | 0/0 | 4626 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4621): Show |
chr20 | 44350699 | 44437845 |
| a0001c0003t0065 | 0/0 | 4645 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4640): Show |
chr20 | 44350699 | 44437845 |
| a0001c0009t0081 | 0/0 | 4627 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4622): Show |
chr20 | 44350699 | 44437845 |
| a0001c0011t0079 | 0/0 | 4637 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4632): Show |
chr20 | 44350699 | 44437845 |
| a0001c0012t0008 | 0/0 | 4645 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4640): Show |
chr20 | 44350699 | 44437845 |
| a0001c0013t0010 | 0/0 | 4645 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4640): Show |
chr20 | 44350699 | 44437845 |
| a0001c0014t0069 | 0/0 | 4638 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4633): Show |
chr20 | 44350699 | 44437845 |
| a0002c0002t0001 | 0/0 | 4646 | 4 | 0 | 2 | 1 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4641): Show |
chr20 | 44350699 | 44437845 |
| a0002c0002t0002 | 0/0 | 4646 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4641): Show |
chr20 | 44350699 | 44437845 |
| a0002c0002t0004 | 0/0 | 4646 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4641): Show |
chr20 | 44350699 | 44437845 |
| a0002c0002t0007 | 0/0 | 4646 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4641): Show |
chr20 | 44350699 | 44437845 |
| a0003c0010t0090 | 0/0 | 4646 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4641): Show |
chr20 | 44350699 | 44437845 |
| a0004c0006t0023 | 0/0 | 4626 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4621): Show |
chr20 | 44350699 | 44437845 |
| a0005c0007t0017 | 0/0 | 4626 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4621): Show |
chr20 | 44350699 | 44437845 |
| a0006c0004t0056 | 0/0 | 4627 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4622): Show |
chr20 | 44350699 | 44437845 |
| a0007c0005t0025 | 0/0 | 4646 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4641): Show |
chr20 | 44350699 | 44437845 |
| a0008c0008t0005 | 0/0 | 4646 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | GCACT others(4641): Show |
chr20 | 44350699 | 44437845 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0002g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0003g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0003g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0003g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0003g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0003g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0003g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0003g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0003g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0004g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0004g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0004g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0004g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0004g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0004g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0004g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0004g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0004g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0004g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0004g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0004g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0004g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0004g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0004g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0004g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0004g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0004g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0004g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0004g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0004g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0005g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0005g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0005g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0005g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0005g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0005g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0005g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0005g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0005g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0005g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0005g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0005g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0006g0001 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0006g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0006g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0006g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0006g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0006g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0006g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0006g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0007g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0007g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0007g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0007g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0007g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0007g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0007g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0008g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0008g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0008g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0008g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0008g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0008g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0009g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0009g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0009g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0009g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0009g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0010g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0010g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0010g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0010g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0011g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0011g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0011g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0011g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0011g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0012g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0012g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0012g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0012g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0012g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0013g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0013g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0013g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0013g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0014g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0014g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0014g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0014g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0015g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0015g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0015g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0015g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0016g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0016g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0016g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0016g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0017g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0017g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0018g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0018g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0018g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0019g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0019g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0019g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0020g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0020g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0020g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0021g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0021g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0021g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0022g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0022g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0022g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0023g0002 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0023g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0024g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0024g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0024g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0025g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0025g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0026g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0026g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0027g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0027g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0028g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0028g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0029g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0029g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0030g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0030g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0031g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0031g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0032g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0032g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0033g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0033g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0034g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0034g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0035g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0035g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0036g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0036g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0037g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0037g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0038g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0038g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0039g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0040g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0041g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0042g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0043g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0044g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0045g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0046g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0047g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0048g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0049g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0050g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0051g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0052g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0053g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0054g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0055g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0057g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0058g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0059g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0060g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0061g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0063g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0064g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0066g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0067g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0068g0197 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0070g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0071g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0072g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0073g0217 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0074g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0075g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0076g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0077g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0078g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0080g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0082g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0083g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0084g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0085g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0086g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0087g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0088g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0089g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0091g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0092g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0093g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0094g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0095g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0096g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0097g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0098g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0001t0099g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0003t0062g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0003t0065g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0009t0081g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0011t0079g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0012t0008g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0013t0010g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0001c0014t0069g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0002c0002t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0002c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0002c0002t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0002c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0002c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0002c0002t0004g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0002c0002t0007g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0003c0010t0090g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0004c0006t0023g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0005c0007t0017g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0006c0004t0056g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0007c0005t0025g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| a0008c0008t0005g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0011 | g0185 | EUR | GBR | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0097 | EUR | GBR | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0035 | EUR | GBR | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0265 | EUR | GBR | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG00280 | hp1 | a0001 | c0001 | t0026 | g0214 | EUR | FIN | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0110 | EUR | FIN | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0216 | EUR | FIN | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0095 | EUR | FIN | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG00423 | hp1 | a0003 | c0010 | t0090 | g0139 | EAS | CHS | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | CHS | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG00438 | hp1 | a0001 | c0001 | t0005 | g0144 | EAS | CHS | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG00438 | hp2 | a0001 | c0001 | t0083 | g0027 | EAS | CHS | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG00544 | hp1 | a0001 | c0001 | t0088 | g0137 | EAS | CHS | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG00544 | hp2 | a0001 | c0001 | t0049 | g0127 | EAS | CHS | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0091 | EAS | CHS | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG00597 | hp2 | a0001 | c0001 | t0039 | g0120 | EAS | CHS | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG00621 | hp1 | a0001 | c0001 | t0015 | g0121 | EAS | CHS | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0294 | EAS | CHS | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG00639 | hp1 | a0001 | c0001 | t0006 | g0109 | AMR | PUR | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0113 | AMR | PUR | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | CHS | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG00673 | hp2 | a0001 | c0001 | t0004 | g0045 | EAS | CHS | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG00735 | hp1 | a0001 | c0001 | t0024 | g0002 | AMR | PUR | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0263 | AMR | PUR | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG00738 | hp1 | a0001 | c0001 | t0006 | g0001 | AMR | PUR | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG00738 | hp2 | a0001 | c0001 | t0005 | g0262 | AMR | PUR | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0259 | AMR | PUR | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG00741 | hp2 | a0001 | c0001 | t0013 | g0211 | AMR | PUR | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG01069 | hp1 | a0001 | c0011 | t0079 | g0226 | AMR | PUR | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG01074 | hp1 | a0001 | c0001 | t0082 | g0169 | AMR | PUR | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG01074 | hp2 | a0001 | c0001 | t0038 | g0146 | AMR | PUR | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0267 | AMR | PUR | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG01109 | hp1 | a0001 | c0001 | t0006 | g0081 | AMR | PUR | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG01109 | hp2 | a0001 | c0001 | t0076 | g0094 | AMR | PUR | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0289 | AMR | PUR | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG01167 | hp2 | a0001 | c0001 | t0041 | g0221 | AMR | PUR | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0288 | AMR | PUR | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG01169 | hp2 | a0001 | c0001 | t0057 | g0130 | AMR | PUR | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG01175 | hp1 | a0001 | c0001 | t0078 | g0258 | AMR | PUR | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG01175 | hp2 | a0002 | c0002 | t0001 | g0132 | AMR | PUR | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG01255 | hp1 | a0001 | c0001 | t0006 | g0219 | AMR | CLM | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG01255 | hp2 | a0001 | c0001 | t0074 | g0033 | AMR | CLM | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG01256 | hp1 | a0001 | c0001 | t0011 | g0100 | AMR | CLM | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG01256 | hp2 | a0001 | c0001 | t0008 | g0003 | AMR | CLM | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG01258 | hp1 | a0001 | c0001 | t0008 | g0003 | AMR | CLM | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG01258 | hp2 | a0002 | c0002 | t0007 | g0028 | AMR | CLM | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG01261 | hp1 | a0001 | c0001 | t0012 | g0256 | AMR | CLM | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0281 | AMR | CLM | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG01346 | hp1 | a0001 | c0001 | t0006 | g0051 | AMR | CLM | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG01346 | hp2 | a0002 | c0002 | t0001 | g0175 | AMR | CLM | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | CLM | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG01361 | hp1 | a0001 | c0001 | t0004 | g0106 | AMR | CLM | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG01433 | hp1 | a0001 | c0014 | t0069 | g0192 | AMR | CLM | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG01433 | hp2 | a0001 | c0001 | t0008 | g0261 | AMR | CLM | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG01496 | hp1 | a0001 | c0001 | t0053 | g0057 | AMR | CLM | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG01496 | hp2 | a0001 | c0001 | t0093 | g0140 | AMR | CLM | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG01515 | hp1 | a0001 | c0001 | t0029 | g0266 | EUR | IBS | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0196 | EUR | IBS | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG01516 | hp1 | a0001 | c0001 | t0005 | g0083 | EUR | IBS | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG01516 | hp2 | a0001 | c0001 | t0023 | g0002 | EUR | IBS | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG01517 | hp1 | a0001 | c0001 | t0029 | g0268 | EUR | IBS | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG01517 | hp2 | a0001 | c0001 | t0005 | g0082 | EUR | IBS | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG01884 | hp1 | a0001 | c0001 | t0008 | g0008 | AFR | ACB | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG01884 | hp2 | a0001 | c0001 | t0008 | g0136 | AFR | ACB | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG01891 | hp1 | a0001 | c0001 | t0089 | g0107 | AFR | ACB | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG01891 | hp2 | a0001 | c0001 | t0027 | g0016 | AFR | ACB | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG01975 | hp1 | a0001 | c0001 | t0072 | g0142 | AMR | PEL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0039 | AMR | PEL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG02015 | hp1 | a0001 | c0001 | t0003 | g0042 | EAS | KHV | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG02015 | hp2 | a0001 | c0001 | t0033 | g0285 | EAS | KHV | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG02027 | hp1 | a0001 | c0001 | t0003 | g0055 | EAS | KHV | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG02027 | hp2 | a0001 | c0001 | t0024 | g0194 | EAS | KHV | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG02055 | hp1 | a0001 | c0001 | t0046 | g0317 | AFR | ACB | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG02055 | hp2 | a0001 | c0001 | t0087 | g0108 | AFR | ACB | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | KHV | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG02056 | hp2 | a0001 | c0001 | t0003 | g0093 | EAS | KHV | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG02071 | hp1 | a0001 | c0001 | t0017 | g0180 | EAS | KHV | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG02071 | hp2 | a0002 | c0002 | t0001 | g0243 | EAS | KHV | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG02074 | hp1 | a0001 | c0001 | t0004 | g0138 | EAS | KHV | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG02074 | hp2 | a0001 | c0001 | t0012 | g0092 | EAS | KHV | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | KHV | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG02083 | hp2 | a0001 | c0001 | t0040 | g0165 | EAS | KHV | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0284 | EAS | KHV | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0029 | EAS | KHV | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0283 | EAS | KHV | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG02145 | hp1 | a0001 | c0001 | t0010 | g0017 | AFR | ACB | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG02145 | hp2 | a0001 | c0001 | t0037 | g0009 | AFR | ACB | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG02148 | hp1 | a0001 | c0001 | t0007 | g0034 | AMR | PEL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0160 | EAS | CDX | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG02155 | hp2 | a0001 | c0001 | t0005 | g0073 | EAS | CDX | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | CDX | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | CDX | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG02257 | hp1 | a0001 | c0001 | t0033 | g0269 | AFR | ACB | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG02257 | hp2 | a0001 | c0001 | t0012 | g0061 | AFR | ACB | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG02280 | hp1 | a0001 | c0001 | t0014 | g0188 | AFR | ACB | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG02280 | hp2 | a0001 | c0001 | t0070 | g0264 | AFR | ACB | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG02293 | hp1 | a0001 | c0001 | t0005 | g0200 | AMR | PEL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG02293 | hp2 | a0001 | c0001 | t0007 | g0319 | AMR | PEL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG02300 | hp1 | a0001 | c0001 | t0005 | g0198 | AMR | PEL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG02300 | hp2 | a0001 | c0001 | t0007 | g0040 | AMR | PEL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG02451 | hp1 | a0001 | c0001 | t0018 | g0307 | AFR | ACB | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG02451 | hp2 | a0001 | c0001 | t0064 | g0207 | AFR | ACB | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0299 | AFR | GWD | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG02602 | hp1 | a0001 | c0001 | t0006 | g0271 | SAS | PJL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG02602 | hp2 | a0001 | c0001 | t0005 | g0234 | SAS | PJL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG02615 | hp1 | a0001 | c0001 | t0019 | g0161 | AFR | GWD | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0023 | AFR | GWD | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG02622 | hp2 | a0001 | c0001 | t0032 | g0314 | AFR | GWD | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG02630 | hp1 | a0001 | c0003 | t0065 | g0308 | AFR | GWD | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG02630 | hp2 | a0001 | c0001 | t0085 | g0310 | AFR | GWD | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG02647 | hp1 | a0001 | c0001 | t0010 | g0208 | AFR | GWD | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | GWD | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG02683 | hp2 | a0001 | c0001 | t0003 | g0148 | SAS | PJL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG02698 | hp1 | a0001 | c0001 | t0024 | g0291 | SAS | PJL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG02698 | hp2 | a0001 | c0001 | t0058 | g0287 | SAS | PJL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG02717 | hp2 | a0001 | c0001 | t0011 | g0115 | AFR | GWD | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG02723 | hp1 | a0001 | c0001 | t0054 | g0253 | AFR | GWD | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG02723 | hp2 | a0004 | c0006 | t0023 | g0105 | AFR | GWD | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0195 | SAS | PJL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG02738 | hp2 | a0001 | c0001 | t0009 | g0058 | SAS | PJL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG02809 | hp1 | a0001 | c0001 | t0031 | g0153 | AFR | GWD | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG02809 | hp2 | a0001 | c0001 | t0045 | g0022 | AFR | GWD | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0301 | AFR | GWD | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG02818 | hp2 | a0001 | c0001 | t0097 | g0123 | AFR | GWD | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG02886 | hp1 | a0001 | c0001 | t0013 | g0010 | AFR | GWD | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG02886 | hp2 | a0001 | c0001 | t0067 | g0171 | AFR | GWD | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG02896 | hp1 | a0001 | c0001 | t0011 | g0020 | AFR | GWD | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG02896 | hp2 | a0001 | c0001 | t0014 | g0229 | AFR | GWD | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG02897 | hp1 | a0001 | c0001 | t0014 | g0227 | AFR | GWD | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG02897 | hp2 | a0001 | c0001 | t0092 | g0212 | AFR | GWD | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | ESN | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG02922 | hp2 | a0001 | c0001 | t0043 | g0309 | AFR | ESN | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG02965 | hp1 | a0001 | c0001 | t0048 | g0013 | AFR | ESN | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG02965 | hp2 | a0001 | c0001 | t0047 | g0298 | AFR | ESN | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG02970 | hp1 | a0001 | c0001 | t0018 | g0209 | AFR | ESN | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG02970 | hp2 | a0001 | c0001 | t0010 | g0011 | AFR | ESN | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG02976 | hp1 | a0001 | c0001 | t0080 | g0304 | AFR | ESN | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG02976 | hp2 | a0001 | c0001 | t0066 | g0315 | AFR | ESN | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0114 | SAS | PJL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG03017 | hp2 | a0001 | c0001 | t0005 | g0048 | SAS | PJL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG03041 | hp1 | a0001 | c0001 | t0011 | g0117 | AFR | GWD | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG03041 | hp2 | a0001 | c0001 | t0086 | g0019 | AFR | GWD | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0302 | AFR | MSL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG03098 | hp2 | a0001 | c0001 | t0037 | g0224 | AFR | MSL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG03139 | hp1 | a0001 | c0001 | t0010 | g0015 | AFR | ESN | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG03139 | hp2 | a0001 | c0001 | t0018 | g0210 | AFR | ESN | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | ESN | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG03195 | hp2 | a0001 | c0001 | t0019 | g0151 | AFR | ESN | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG03209 | hp1 | a0001 | c0001 | t0008 | g0059 | AFR | MSL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG03209 | hp2 | a0001 | c0001 | t0094 | g0313 | AFR | MSL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG03225 | hp1 | a0001 | c0001 | t0038 | g0318 | AFR | MSL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | MSL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0280 | SAS | PJL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | MSL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG03453 | hp2 | a0001 | c0001 | t0052 | g0005 | AFR | MSL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG03486 | hp1 | a0001 | c0001 | t0055 | g0118 | AFR | MSL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG03486 | hp2 | a0001 | c0001 | t0034 | g0312 | AFR | MSL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0286 | SAS | PJL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG03491 | hp2 | a0001 | c0001 | t0030 | g0205 | SAS | PJL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG03492 | hp2 | a0001 | c0001 | t0030 | g0206 | SAS | PJL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG03516 | hp1 | a0001 | c0001 | t0012 | g0311 | AFR | ESN | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG03516 | hp2 | a0001 | c0001 | t0027 | g0014 | AFR | ESN | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG03540 | hp1 | a0001 | c0001 | t0019 | g0170 | AFR | GWD | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG03540 | hp2 | a0001 | c0001 | t0031 | g0145 | AFR | GWD | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | MSL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG03579 | hp2 | a0001 | c0001 | t0063 | g0173 | AFR | MSL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0074 | SAS | PJL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG03654 | hp2 | a0001 | c0001 | t0026 | g0075 | SAS | PJL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG03669 | hp1 | a0001 | c0001 | t0099 | g0147 | SAS | PJL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG03669 | hp2 | a0001 | c0001 | t0059 | g0096 | SAS | PJL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG03704 | hp1 | a0002 | c0002 | t0002 | g0079 | SAS | PJL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG03704 | hp2 | a0002 | c0002 | t0001 | g0174 | SAS | PJL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0240 | SAS | PJL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG03834 | hp1 | a0001 | c0001 | t0009 | g0179 | SAS | BEB | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | BEB | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | BEB | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG03927 | hp2 | a0001 | c0001 | t0077 | g0162 | SAS | BEB | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG03942 | hp1 | a0001 | c0001 | t0051 | g0157 | SAS | BEB | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG03942 | hp2 | a0001 | c0001 | t0050 | g0031 | SAS | BEB | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0201 | SAS | STU | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0202 | SAS | STU | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG04199 | hp1 | a0001 | c0001 | t0020 | g0049 | SAS | STU | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG04199 | hp2 | a0001 | c0001 | t0009 | g0190 | SAS | STU | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0236 | SAS | STU | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG04204 | hp2 | a0005 | c0007 | t0017 | g0124 | SAS | STU | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG04228 | hp1 | a0001 | c0001 | t0009 | g0149 | SAS | STU | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0065 | SAS | STU | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | CHB | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | CHB | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA18747 | hp1 | a0001 | c0001 | t0004 | g0068 | EAS | CHB | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA18747 | hp2 | a0001 | c0001 | t0007 | g0143 | EAS | CHB | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA18906 | hp1 | a0001 | c0001 | t0084 | g0306 | AFR | YRI | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA18906 | hp2 | a0001 | c0012 | t0008 | g0007 | AFR | YRI | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA18941 | hp1 | a0001 | c0001 | t0003 | g0248 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0245 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA18942 | hp2 | a0001 | c0001 | t0022 | g0078 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA18946 | hp1 | a0001 | c0001 | t0004 | g0297 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA18946 | hp2 | a0001 | c0001 | t0016 | g0237 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA18947 | hp1 | a0001 | c0001 | t0004 | g0087 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA18947 | hp2 | a0001 | c0001 | t0004 | g0276 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA18948 | hp1 | a0001 | c0001 | t0003 | g0257 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA18951 | hp1 | a0001 | c0001 | t0020 | g0244 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA18951 | hp2 | a0001 | c0001 | t0004 | g0072 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA18952 | hp1 | a0001 | c0001 | t0028 | g0235 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA18952 | hp2 | a0001 | c0001 | t0004 | g0030 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA18954 | hp1 | a0002 | c0002 | t0004 | g0182 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA18954 | hp2 | a0001 | c0001 | t0098 | g0080 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA18959 | hp1 | a0001 | c0001 | t0022 | g0089 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA18959 | hp2 | a0001 | c0001 | t0006 | g0249 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA18960 | hp1 | a0001 | c0001 | t0003 | g0101 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA18960 | hp2 | a0001 | c0001 | t0016 | g0273 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA18961 | hp1 | a0006 | c0004 | t0056 | g0077 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA18964 | hp1 | a0001 | c0001 | t0021 | g0278 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA18966 | hp1 | a0001 | c0001 | t0004 | g0250 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA18967 | hp1 | a0001 | c0001 | t0004 | g0270 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA18973 | hp1 | a0001 | c0001 | t0004 | g0296 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA18973 | hp2 | a0001 | c0001 | t0015 | g0086 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA18977 | hp2 | a0001 | c0001 | t0091 | g0103 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA18979 | hp1 | a0001 | c0001 | t0035 | g0043 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA18979 | hp2 | a0001 | c0001 | t0004 | g0172 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0305 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0233 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA18981 | hp1 | a0001 | c0001 | t0034 | g0199 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA18981 | hp2 | a0001 | c0001 | t0004 | g0047 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA18986 | hp2 | a0001 | c0001 | t0004 | g0088 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA18988 | hp2 | a0001 | c0001 | t0036 | g0129 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA18990 | hp1 | a0001 | c0009 | t0081 | g0275 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA18990 | hp2 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA18994 | hp1 | a0001 | c0001 | t0017 | g0292 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0084 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA18998 | hp1 | a0001 | c0001 | t0015 | g0247 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA19002 | hp1 | a0001 | c0001 | t0015 | g0274 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA19002 | hp2 | a0001 | c0001 | t0003 | g0231 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA19005 | hp1 | a0001 | c0001 | t0095 | g0069 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA19005 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA19007 | hp1 | a0001 | c0001 | t0036 | g0279 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA19007 | hp2 | a0001 | c0001 | t0007 | g0041 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA19009 | hp1 | a0001 | c0001 | t0007 | g0090 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA19009 | hp2 | a0001 | c0001 | t0004 | g0303 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA19011 | hp1 | a0001 | c0001 | t0028 | g0099 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA19011 | hp2 | a0001 | c0001 | t0021 | g0277 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA19043 | hp1 | a0001 | c0001 | t0075 | g0012 | AFR | LWK | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA19043 | hp2 | a0001 | c0001 | t0060 | g0255 | AFR | LWK | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA19056 | hp2 | a0001 | c0001 | t0042 | g0085 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA19057 | hp1 | a0001 | c0001 | t0004 | g0166 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA19057 | hp2 | a0001 | c0001 | t0022 | g0076 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA19058 | hp1 | a0001 | c0001 | t0005 | g0293 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA19058 | hp2 | a0001 | c0001 | t0071 | g0150 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA19062 | hp1 | a0001 | c0001 | t0096 | g0252 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA19064 | hp1 | a0007 | c0005 | t0025 | g0038 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA19064 | hp2 | a0001 | c0001 | t0004 | g0222 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA19065 | hp1 | a0001 | c0001 | t0025 | g0046 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA19065 | hp2 | a0001 | c0001 | t0004 | g0158 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA19068 | hp1 | a0001 | c0001 | t0005 | g0036 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA19068 | hp2 | a0001 | c0001 | t0021 | g0290 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA19077 | hp1 | a0001 | c0001 | t0025 | g0238 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA19077 | hp2 | a0001 | c0001 | t0020 | g0159 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0295 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA19079 | hp2 | a0001 | c0001 | t0003 | g0223 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA19080 | hp2 | a0008 | c0008 | t0005 | g0282 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA19083 | hp1 | a0001 | c0001 | t0035 | g0168 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA19083 | hp2 | a0001 | c0001 | t0016 | g0239 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA19088 | hp1 | a0001 | c0001 | t0016 | g0242 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA19240 | hp1 | a0001 | c0001 | t0032 | g0024 | AFR | YRI | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | YRI | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA20129 | hp1 | a0001 | c0001 | t0005 | g0063 | AFR | ASW | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA20129 | hp2 | a0001 | c0001 | t0014 | g0189 | AFR | ASW | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0213 | EUR | TSI | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA20752 | hp2 | a0001 | c0001 | t0006 | g0001 | EUR | TSI | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0218 | EUR | TSI | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0316 | EUR | TSI | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA20905 | hp1 | a0001 | c0001 | t0009 | g0125 | SAS | GIH | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0184 | SAS | GIH | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG01123 | hp1 | a0001 | c0001 | t0006 | g0176 | AMR | CLM | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG01123 | hp2 | a0001 | c0001 | t0061 | g0060 | AMR | CLM | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG02109 | hp2 | a0001 | c0001 | t0004 | g0181 | AFR | ACB | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG02486 | hp1 | a0001 | c0001 | t0013 | g0225 | AFR | ACB | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG02486 | hp2 | a0001 | c0003 | t0062 | g0062 | AFR | ACB | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG02559 | hp1 | a0001 | c0001 | t0013 | g0021 | AFR | ACB | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG02559 | hp2 | a0001 | c0001 | t0008 | g0135 | AFR | ACB | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG03471 | hp1 | a0001 | c0001 | t0023 | g0004 | AFR | MSL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG03471 | hp2 | a0001 | c0001 | t0004 | g0300 | AFR | MSL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG06807 | hp1 | a0001 | c0013 | t0010 | g0050 | AFR | USA | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| HG06807 | hp2 | a0001 | c0001 | t0012 | g0187 | AFR | USA | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA20300 | hp1 | a0001 | c0001 | t0007 | g0131 | AFR | USA | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| NA20300 | hp2 | a0001 | c0001 | t0044 | g0116 | AFR | USA | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0068 | g0197 | REF | REF | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0073 | g0217 | REF | REF | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:44413724 | C | T | 1 | a0002 | 7 | HG01175.hp2 HG01258.hp2 HG01346.hp2 others(4): Show |
missense_variant | MODERATE | c.350C>T | p.Thr117Ile | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 4/10 | 456/4645 | 350/1359 | 117/452 | chr20 | 44413724 | |||
| chr20:44413769 | C | A | 1 | a0007 | 1 | NA19064.hp1 | missense_variant | MODERATE | c.395C>A | p.Ala132Glu | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 4/10 | 501/4645 | 395/1359 | 132/452 | chr20 | 44413769 | |||
| chr20:44414519 | G | A | 1 | a0006 | 1 | NA18961.hp1 | missense_variant | MODERATE | c.439G>A | p.Val147Ile | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 5/10 | 545/4645 | 439/1359 | 147/452 | chr20 | 44414519 | |||
| chr20:44424032 | A | G | 1 | a0003 | 1 | HG00423.hp1 | missense_variant | MODERATE | c.841A>G | p.Ser281Gly | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 8/10 | 947/4645 | 841/1359 | 281/452 | chr20 | 44424032 | |||
| chr20:44428359 | C | T | 1 | a0008 | 1 | NA19080.hp2 | missense_variant | MODERATE | c.1088C>T | p.Ala363Val | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 9/10 | 1194/4645 | 1088/1359 | 363/452 | chr20 | 44428359 | |||
| chr20:44428398 | T | C | 1 | a0008 | 1 | NA19080.hp2 | missense_variant | MODERATE | c.1127T>C | p.Met376Thr | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 9/10 | 1233/4645 | 1127/1359 | 376/452 | chr20 | 44428398 | |||
| chr20:44428456 | G | A | 1 | a0004 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1185G>A | p.Met395Ile | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 9/10 | 1291/4645 | 1185/1359 | 395/452 | chr20 | 44428456 | |||
| chr20:44429549 | C | T | 1 | a0005 | 1 | HG04204.hp2 | missense_variant | MODERATE | c.1243C>T | p.Pro415Ser | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 1349/4645 | 1243/1359 | 415/452 | chr20 | 44429549 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:44406143 | C | T | 1 | a0001c0014 | 1 | HG01433.hp1 | synonymous_variant | LOW | c.135C>T | p.Ala45Ala | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 2/10 | 241/4645 | 135/1359 | 45/452 | chr20 | 44406143 | |||
| chr20:44413767 | T | C | 2 | a0001c0003 a0006c0004 |
3 | HG02486.hp2 HG02630.hp1 NA18961.hp1 |
synonymous_variant | LOW | c.393T>C | p.Asn131Asn | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 4/10 | 499/4645 | 393/1359 | 131/452 | chr20 | 44413767 | |||
| chr20:44414656 | C | T | 1 | a0001c0013 | 1 | HG06807.hp1 | synonymous_variant | LOW | c.576C>T | p.Asp192Asp | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 5/10 | 682/4645 | 576/1359 | 192/452 | chr20 | 44414656 | |||
| chr20:44418511 | A | G | 1 | a0001c0012 | 1 | NA18906.hp2 | splice_region_variant&synonymous_variant | LOW | c.669A>G | p.Leu223Leu | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 6/10 | 775/4645 | 669/1359 | 223/452 | chr20 | 44418511 | |||
| chr20:44419794 | C | T | 1 | a0001c0011 | 1 | HG01069.hp1 | synonymous_variant | LOW | c.744C>T | p.Asp248Asp | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/10 | 850/4645 | 744/1359 | 248/452 | chr20 | 44419794 | |||
| chr20:44424097 | C | T | 1 | a0001c0009 | 1 | NA18990.hp1 | synonymous_variant | LOW | c.906C>T | p.Asn302Asn | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 8/10 | 1012/4645 | 906/1359 | 302/452 | chr20 | 44424097 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:44355723 | G | C | 2 | a0001c0001t0039 a0001c0001t0040 |
2 | HG00597.hp2 HG02083.hp2 |
5_prime_UTR_variant | MODIFIER | c.-82G>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/10 | 82 | chr20 | 44355723 | ||||||
| chr20:44429741 | G | A | 1 | a0001c0001t0041 | 1 | HG01167.hp2 | 3_prime_UTR_variant | MODIFIER | c.*76G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 76 | chr20 | 44429741 | ||||||
| chr20:44429741 | G | T | 1 | a0001c0001t0099 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*76G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 76 | chr20 | 44429741 | ||||||
| chr20:44429820 | G | A | 5 | a0001c0001t0009 a0001c0001t0017 a0001c0001t0026 others(2): Show |
11 | HG00280.hp1 HG02071.hp1 HG02738.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*155G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 155 | chr20 | 44429820 | ||||||
| chr20:44429832 | T | A | 1 | a0001c0001t0043 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*167T>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 167 | chr20 | 44429832 | ||||||
| chr20:44429907 | T | C | 8 | a0001c0001t0013 a0001c0001t0018 a0001c0001t0027 others(5): Show |
14 | HG00741.hp2 HG01891.hp2 HG02055.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*242T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 242 | chr20 | 44429907 | ||||||
| chr20:44429942 | T | A | 1 | a0001c0001t0049 | 1 | HG00544.hp2 | 3_prime_UTR_variant | MODIFIER | c.*277T>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 277 | chr20 | 44429942 | ||||||
| chr20:44429942 | T | C | 1 | a0001c0001t0050 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*277T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 277 | chr20 | 44429942 | ||||||
| chr20:44429970 | A | G | 8 | a0001c0001t0013 a0001c0001t0018 a0001c0001t0027 others(5): Show |
14 | HG00741.hp2 HG01891.hp2 HG02055.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*305A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 305 | chr20 | 44429970 | ||||||
| chr20:44430057 | T | G | 22 | a0001c0001t0006 a0001c0001t0013 a0001c0001t0018 others(19): Show |
38 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*392T>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 392 | chr20 | 44430057 | ||||||
| chr20:44430058 | G | A | 1 | a0001c0001t0061 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*393G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 393 | chr20 | 44430058 | ||||||
| chr20:44430092 | G | T | 4 | a0001c0001t0016 a0001c0001t0025 a0001c0001t0098 others(1): Show |
8 | NA18946.hp2 NA18954.hp2 NA18960.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*427G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 427 | chr20 | 44430092 | ||||||
| chr20:44430111 | G | A | 1 | a0001c0001t0041 | 1 | HG01167.hp2 | 3_prime_UTR_variant | MODIFIER | c.*446G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 446 | chr20 | 44430111 | ||||||
| chr20:44430186 | G | A | 2 | a0001c0001t0063 a0001c0003t0062 |
2 | HG02486.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*521G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 521 | chr20 | 44430186 | ||||||
| chr20:44430233 | G | A | 1 | a0001c0001t0064 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*568G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 568 | chr20 | 44430233 | ||||||
| chr20:44430322 | G | A | 1 | a0001c0001t0019 | 3 | HG02615.hp1 HG03195.hp2 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*657G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 657 | chr20 | 44430322 | ||||||
| chr20:44430365 | T | C | 4 | a0001c0001t0014 a0001c0001t0066 a0001c0001t0067 others(1): Show |
7 | HG02280.hp1 HG02630.hp1 HG02886.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*700T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 700 | chr20 | 44430365 | ||||||
| chr20:44430450 | G | A | 1 | a0001c0003t0062 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*785G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 785 | chr20 | 44430450 | ||||||
| chr20:44430571 | A | C | 53 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(50): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
3_prime_UTR_variant | MODIFIER | c.*906A>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 906 | chr20 | 44430571 | ||||||
| chr20:44430571 | A | T | 9 | a0001c0001t0006 a0001c0001t0029 a0001c0001t0037 others(6): Show |
20 | HG00639.hp1 HG00738.hp1 HG01074.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*906A>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 906 | chr20 | 44430571 | ||||||
| chr20:44430572 | G | A | 1 | a0001c0001t0082 | 1 | HG01074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*907G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 907 | chr20 | 44430572 | ||||||
| chr20:44430597 | TGAGGAAG others(12): Show |
T | 28 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0015 others(25): Show |
69 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*937_*955delAAGAAT others(13): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 937 | INFO_REALIGN_3_PRIME | chr20 | 44430597 | |||||
| chr20:44430636 | GAGGGCCT others(104): Show |
G | 1 | a0001c0001t0082 | 1 | HG01074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*972_*1082del | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 972 | chr20 | 44430636 | ||||||
| chr20:44430642 | C | G | 1 | a0006c0004t0056 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*977C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 977 | chr20 | 44430642 | ||||||
| chr20:44430733 | C | T | 1 | a0001c0001t0013 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1068C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 1068 | chr20 | 44430733 | ||||||
| chr20:44430743 | G | A | 2 | a0001c0001t0001 a0001c0001t0011 |
2 | HG01256.hp1 NA20905.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1078G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 1078 | chr20 | 44430743 | ||||||
| chr20:44430797 | C | T | 52 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0007 others(49): Show |
142 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(139): Show |
3_prime_UTR_variant | MODIFIER | c.*1132C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 1132 | chr20 | 44430797 | ||||||
| chr20:44430955 | ATCCTCCC others(1): Show |
A | 15 | a0001c0001t0016 a0001c0001t0020 a0001c0001t0026 others(12): Show |
23 | HG00280.hp1 HG00438.hp2 HG00544.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1299_*1306delTCCT others(4): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 1299 | INFO_REALIGN_3_PRIME | chr20 | 44430955 | |||||
| chr20:44431029 | G | A | 1 | a0006c0004t0056 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1364G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 1364 | chr20 | 44431029 | ||||||
| chr20:44431445 | G | T | 1 | a0001c0001t0094 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1780G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 1780 | chr20 | 44431445 | ||||||
| chr20:44431446 | G | C | 1 | a0001c0001t0094 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1781G>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 1781 | chr20 | 44431446 | ||||||
| chr20:44431447 | G | A | 1 | a0001c0001t0094 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1782G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 1782 | chr20 | 44431447 | ||||||
| chr20:44431448 | G | T | 1 | a0001c0001t0094 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1783G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 1783 | chr20 | 44431448 | ||||||
| chr20:44431450 | C | CTCTGTCT others(155): Show |
1 | a0001c0001t0094 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1786_*1787insCTGT others(158): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 1787 | INFO_REALIGN_3_PRIME | chr20 | 44431450 | |||||
| chr20:44431497 | G | A | 7 | a0001c0001t0007 a0001c0001t0015 a0001c0001t0049 others(4): Show |
16 | HG00544.hp2 HG00621.hp1 HG01255.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1832G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 1832 | chr20 | 44431497 | ||||||
| chr20:44431640 | G | A | 3 | a0001c0001t0010 a0001c0001t0075 a0001c0013t0010 |
6 | HG02145.hp1 HG02647.hp1 HG02970.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1975G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 1975 | chr20 | 44431640 | ||||||
| chr20:44431847 | G | A | 1 | a0001c0001t0021 | 3 | NA18964.hp1 NA19011.hp2 NA19068.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2182G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 2182 | chr20 | 44431847 | ||||||
| chr20:44432027 | G | T | 1 | a0001c0001t0087 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2362G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 2362 | chr20 | 44432027 | ||||||
| chr20:44432031 | G | C | 17 | a0001c0001t0008 a0001c0001t0010 a0001c0001t0019 others(14): Show |
31 | HG01109.hp2 HG01175.hp1 HG01256.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*2366G>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 2366 | chr20 | 44432031 | ||||||
| chr20:44432107 | A | T | 1 | a0003c0010t0090 | 1 | HG00423.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2442A>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 2442 | chr20 | 44432107 | ||||||
| chr20:44432198 | G | A | 3 | a0001c0001t0018 a0001c0001t0085 a0001c0011t0079 |
5 | HG01069.hp1 HG02451.hp1 HG02630.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2533G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 2533 | chr20 | 44432198 | ||||||
| chr20:44432321 | G | A | 1 | a0001c0001t0092 | 1 | HG02897.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2656G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 2656 | chr20 | 44432321 | ||||||
| chr20:44432344 | C | CT | 53 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(50): Show |
225 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(222): Show |
3_prime_UTR_variant | MODIFIER | c.*2703dupT | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 2704 | INFO_REALIGN_3_PRIME | chr20 | 44432344 | |||||
| chr20:44432344 | C | CTT | 8 | a0001c0001t0012 a0001c0001t0024 a0001c0001t0034 others(5): Show |
16 | HG00735.hp1 HG01261.hp1 HG02027.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*2702_*2703dupTT | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 2704 | INFO_REALIGN_3_PRIME | chr20 | 44432344 | |||||
| chr20:44432344 | CT | C | 10 | a0001c0001t0009 a0001c0001t0019 a0001c0001t0026 others(7): Show |
18 | HG00280.hp1 HG01109.hp2 HG01496.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*2703delT | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 2703 | INFO_REALIGN_3_PRIME | chr20 | 44432344 | |||||
| chr20:44432344 | CTTTTTTT | C | 5 | a0001c0001t0030 a0001c0001t0032 a0001c0001t0047 others(2): Show |
7 | HG01975.hp1 HG02622.hp2 HG02723.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2697_*2703delTTTT others(3): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 2697 | INFO_REALIGN_3_PRIME | chr20 | 44432344 | |||||
| chr20:44432344 | CTTTTTTT others(1): Show |
C | 4 | a0001c0001t0018 a0001c0001t0080 a0001c0001t0085 others(1): Show |
6 | HG01069.hp1 HG02451.hp1 HG02630.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2696_*2703delTTTT others(4): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 2696 | INFO_REALIGN_3_PRIME | chr20 | 44432344 | |||||
| chr20:44432367 | T | G | 2 | a0001c0001t0063 a0001c0001t0066 |
2 | HG02976.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2702T>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 2702 | chr20 | 44432367 | ||||||
| chr20:44432751 | C | T | 1 | a0001c0001t0070 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3086C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 3086 | chr20 | 44432751 | ||||||
| chr20:44432803 | CA | C | 2 | a0001c0001t0036 a0001c0001t0096 |
3 | NA18988.hp2 NA19007.hp1 NA19062.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3142delA | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 3142 | INFO_REALIGN_3_PRIME | chr20 | 44432803 | |||||
| chr20:44432808 | G | T | 2 | a0001c0001t0036 a0001c0001t0096 |
3 | NA18988.hp2 NA19007.hp1 NA19062.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3143G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 3143 | chr20 | 44432808 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:44355908 | G | A | 2 | a0001c0001t0023g0004 a0001c0001t0052g0005 |
2 | HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.49+55G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44355908 | |||||||
| chr20:44355934 | T | C | 1 | a0001c0001t0003g0006 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.49+81T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44355934 | |||||||
| chr20:44356029 | C | G | 1 | a0001c0001t0007g0319 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.49+176C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44356029 | |||||||
| chr20:44356264 | C | A | 3 | a0001c0001t0008g0008 a0001c0001t0037g0009 a0001c0012t0008g0007 |
3 | HG01884.hp1 HG02145.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.49+411C>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44356264 | |||||||
| chr20:44356275 | G | A | 8 | a0001c0001t0010g0011 a0001c0001t0010g0015 a0001c0001t0010g0017 others(5): Show |
8 | HG01891.hp2 HG02145.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.49+422G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44356275 | |||||||
| chr20:44356475 | A | C | 2 | a0001c0001t0038g0318 a0001c0001t0046g0317 |
2 | HG02055.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.49+622A>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44356475 | |||||||
| chr20:44356615 | A | C | 1 | a0001c0001t0001g0316 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.49+762A>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44356615 | |||||||
| chr20:44356616 | C | T | 1 | a0001c0001t0066g0315 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.49+763C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44356616 | |||||||
| chr20:44356641 | T | G | 2 | a0001c0001t0001g0018 a0001c0001t0086g0019 |
2 | HG01361.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.49+788T>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44356641 | |||||||
| chr20:44356715 | A | G | 59 | a0001c0001t0001g0260 a0001c0001t0001g0263 a0001c0001t0001g0272 others(56): Show |
60 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.49+862A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44356715 | |||||||
| chr20:44356809 | G | T | 4 | a0001c0001t0001g0254 a0001c0001t0012g0256 a0001c0001t0054g0253 others(1): Show |
4 | HG01261.hp1 HG02723.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.49+956G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44356809 | |||||||
| chr20:44356834 | C | A | 5 | a0001c0001t0002g0023 a0001c0001t0011g0020 a0001c0001t0013g0021 others(2): Show |
5 | HG02559.hp1 HG02615.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.49+981C>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44356834 | |||||||
| chr20:44357077 | G | A | 82 | a0001c0001t0001g0026 a0001c0001t0001g0032 a0001c0001t0001g0035 others(79): Show |
82 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.49+1224G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44357077 | |||||||
| chr20:44357398 | A | G | 5 | a0001c0001t0002g0023 a0001c0001t0011g0020 a0001c0001t0013g0021 others(2): Show |
5 | HG02559.hp1 HG02615.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.49+1545A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44357398 | |||||||
| chr20:44357852 | CACAA | C | 49 | a0001c0001t0001g0260 a0001c0001t0001g0263 a0001c0001t0001g0272 others(46): Show |
50 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.49+2009_49+2012del others(4): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44357852 | ||||||
| chr20:44358137 | A | C | 1 | a0001c0001t0096g0252 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.49+2284A>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44358137 | |||||||
| chr20:44358143 | C | A | 4 | a0001c0001t0004g0106 a0001c0001t0087g0108 a0001c0001t0089g0107 others(1): Show |
4 | HG01361.hp1 HG01891.hp1 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.49+2290C>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44358143 | |||||||
| chr20:44358144 | A | T | 58 | a0001c0001t0001g0260 a0001c0001t0001g0263 a0001c0001t0001g0272 others(55): Show |
59 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.49+2291A>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44358144 | |||||||
| chr20:44358248 | GAA | G | 82 | a0001c0001t0001g0026 a0001c0001t0001g0032 a0001c0001t0001g0035 others(79): Show |
82 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.49+2408_49+2409del others(2): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44358248 | ||||||
| chr20:44358259 | A | AAAAAG | 47 | a0001c0001t0001g0260 a0001c0001t0001g0263 a0001c0001t0001g0272 others(44): Show |
48 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.49+2409_49+2410ins others(5): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44358259 | ||||||
| chr20:44358259 | A | AAAAG | 10 | a0001c0001t0012g0311 a0001c0001t0018g0307 a0001c0001t0032g0314 others(7): Show |
10 | HG02451.hp1 HG02622.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.49+2410_49+2413dup others(4): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44358259 | ||||||
| chr20:44358408 | G | A | 2 | a0001c0001t0011g0020 a0001c0001t0013g0021 |
2 | HG02559.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.49+2555G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44358408 | |||||||
| chr20:44358470 | T | C | 58 | a0001c0001t0001g0260 a0001c0001t0001g0263 a0001c0001t0001g0272 others(55): Show |
59 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.49+2617T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44358470 | |||||||
| chr20:44358490 | A | G | 5 | a0001c0001t0002g0251 a0001c0001t0003g0248 a0001c0001t0004g0250 others(2): Show |
5 | NA18941.hp1 NA18959.hp2 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.49+2637A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44358490 | |||||||
| chr20:44358496 | G | C | 3 | a0001c0001t0001g0110 a0001c0001t0006g0001 a0001c0001t0006g0109 |
4 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(1): Show |
intron_variant | MODIFIER | c.49+2643G>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44358496 | |||||||
| chr20:44358619 | CAAAA | C | 43 | a0001c0001t0001g0260 a0001c0001t0001g0263 a0001c0001t0001g0272 others(40): Show |
44 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.49+2767_49+2770del others(4): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44358619 | |||||||
| chr20:44358620 | A | C | 5 | a0001c0001t0001g0301 a0001c0001t0002g0302 a0001c0001t0003g0299 others(2): Show |
5 | HG02572.hp2 HG02818.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.49+2767A>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44358620 | |||||||
| chr20:44358620 | A | G | 3 | a0001c0001t0001g0246 a0001c0001t0038g0318 a0001c0001t0046g0317 |
3 | HG02055.hp1 HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.49+2767A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44358620 | |||||||
| chr20:44358622 | AACAAAAC | A | 5 | a0001c0001t0001g0301 a0001c0001t0002g0302 a0001c0001t0003g0299 others(2): Show |
5 | HG02572.hp2 HG02818.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.49+2771_49+2777del others(7): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44358622 | ||||||
| chr20:44358623 | A | C | 1 | a0001c0001t0004g0270 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.49+2770A>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44358623 | |||||||
| chr20:44358629 | CAAA | C | 44 | a0001c0001t0001g0260 a0001c0001t0001g0263 a0001c0001t0001g0272 others(41): Show |
45 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.49+2781_49+2783del others(3): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44358629 | ||||||
| chr20:44358632 | A | T | 5 | a0001c0001t0001g0301 a0001c0001t0002g0302 a0001c0001t0003g0299 others(2): Show |
5 | HG02572.hp2 HG02818.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.49+2779A>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44358632 | |||||||
| chr20:44358644 | C | A | 1 | a0001c0001t0002g0025 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.49+2791C>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44358644 | |||||||
| chr20:44358672 | C | G | 9 | a0001c0001t0012g0311 a0001c0001t0018g0307 a0001c0001t0032g0314 others(6): Show |
9 | HG02451.hp1 HG02622.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.49+2819C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44358672 | |||||||
| chr20:44358755 | C | T | 1 | a0001c0001t0032g0024 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.49+2902C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44358755 | |||||||
| chr20:44358869 | T | C | 1 | a0001c0001t0001g0026 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.49+3016T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44358869 | |||||||
| chr20:44358895 | T | C | 63 | a0001c0001t0001g0260 a0001c0001t0001g0263 a0001c0001t0001g0272 others(60): Show |
64 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.49+3042T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44358895 | |||||||
| chr20:44358916 | T | C | 49 | a0001c0001t0001g0260 a0001c0001t0001g0263 a0001c0001t0001g0272 others(46): Show |
50 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.49+3063T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44358916 | |||||||
| chr20:44358929 | G | C | 1 | a0001c0001t0001g0111 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.49+3076G>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44358929 | |||||||
| chr20:44358967 | G | A | 1 | a0001c0001t0002g0112 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.49+3114G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44358967 | |||||||
| chr20:44359113 | T | A | 49 | a0001c0001t0001g0260 a0001c0001t0001g0263 a0001c0001t0001g0272 others(46): Show |
50 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.49+3260T>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44359113 | |||||||
| chr20:44359197 | A | G | 1 | a0001c0001t0003g0245 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.49+3344A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44359197 | |||||||
| chr20:44359201 | T | C | 49 | a0001c0001t0001g0260 a0001c0001t0001g0263 a0001c0001t0001g0272 others(46): Show |
50 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.49+3348T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44359201 | |||||||
| chr20:44359237 | G | C | 146 | a0001c0001t0001g0026 a0001c0001t0001g0032 a0001c0001t0001g0035 others(143): Show |
147 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.49+3384G>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44359237 | |||||||
| chr20:44359398 | CT | C | 9 | a0001c0001t0012g0311 a0001c0001t0018g0307 a0001c0001t0032g0314 others(6): Show |
9 | HG02451.hp1 HG02622.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.49+3549delT | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44359398 | ||||||
| chr20:44359432 | C | T | 30 | a0001c0001t0001g0230 a0001c0001t0001g0241 a0001c0001t0002g0228 others(27): Show |
30 | HG01069.hp1 HG02071.hp2 HG02145.hp2 others(27): Show |
intron_variant | MODIFIER | c.49+3579C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44359432 | |||||||
| chr20:44359601 | C | A | 1 | a0001c0001t0002g0114 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.49+3748C>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44359601 | |||||||
| chr20:44359663 | G | A | 5 | a0001c0001t0002g0023 a0001c0001t0011g0020 a0001c0001t0013g0021 others(2): Show |
5 | HG02559.hp1 HG02615.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.49+3810G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44359663 | |||||||
| chr20:44359677 | C | T | 49 | a0001c0001t0001g0260 a0001c0001t0001g0263 a0001c0001t0001g0272 others(46): Show |
50 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.49+3824C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44359677 | |||||||
| chr20:44359809 | TG | T | 82 | a0001c0001t0001g0026 a0001c0001t0001g0032 a0001c0001t0001g0035 others(79): Show |
82 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.49+3960delG | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44359809 | ||||||
| chr20:44360062 | C | T | 49 | a0001c0001t0001g0260 a0001c0001t0001g0263 a0001c0001t0001g0272 others(46): Show |
50 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.49+4209C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44360062 | |||||||
| chr20:44360183 | G | A | 49 | a0001c0001t0001g0260 a0001c0001t0001g0263 a0001c0001t0001g0272 others(46): Show |
50 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.49+4330G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44360183 | |||||||
| chr20:44360201 | A | G | 49 | a0001c0001t0001g0260 a0001c0001t0001g0263 a0001c0001t0001g0272 others(46): Show |
50 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.49+4348A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44360201 | |||||||
| chr20:44360391 | G | A | 1 | a0001c0001t0011g0115 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.49+4538G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44360391 | |||||||
| chr20:44360549 | G | A | 3 | a0001c0001t0003g0113 a0001c0001t0023g0004 a0001c0001t0052g0005 |
3 | HG00639.hp2 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.49+4696G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44360549 | |||||||
| chr20:44360578 | T | A | 4 | a0001c0001t0011g0117 a0001c0001t0044g0116 a0001c0001t0055g0118 others(1): Show |
4 | HG02976.hp2 HG03041.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.49+4725T>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44360578 | |||||||
| chr20:44360627 | G | A | 82 | a0001c0001t0001g0026 a0001c0001t0001g0032 a0001c0001t0001g0035 others(79): Show |
82 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.49+4774G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44360627 | |||||||
| chr20:44360635 | A | G | 49 | a0001c0001t0001g0260 a0001c0001t0001g0263 a0001c0001t0001g0272 others(46): Show |
50 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.49+4782A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44360635 | |||||||
| chr20:44360722 | A | T | 2 | a0001c0001t0002g0023 a0001c0001t0032g0024 |
2 | HG02615.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.49+4869A>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44360722 | |||||||
| chr20:44360736 | T | C | 1 | a0001c0001t0001g0246 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.49+4883T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44360736 | |||||||
| chr20:44360841 | G | C | 49 | a0001c0001t0001g0260 a0001c0001t0001g0263 a0001c0001t0001g0272 others(46): Show |
50 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.49+4988G>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44360841 | |||||||
| chr20:44361032 | C | T | 49 | a0001c0001t0001g0260 a0001c0001t0001g0263 a0001c0001t0001g0272 others(46): Show |
50 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.49+5179C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44361032 | |||||||
| chr20:44361050 | A | G | 49 | a0001c0001t0001g0260 a0001c0001t0001g0263 a0001c0001t0001g0272 others(46): Show |
50 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.49+5197A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44361050 | |||||||
| chr20:44361074 | T | C | 61 | a0001c0001t0001g0246 a0001c0001t0001g0260 a0001c0001t0001g0263 others(58): Show |
62 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.49+5221T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44361074 | |||||||
| chr20:44361078 | A | C | 1 | a0001c0001t0001g0104 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.49+5225A>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44361078 | |||||||
| chr20:44361137 | G | A | 82 | a0001c0001t0001g0026 a0001c0001t0001g0032 a0001c0001t0001g0035 others(79): Show |
82 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.49+5284G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44361137 | |||||||
| chr20:44361154 | C | A | 49 | a0001c0001t0001g0260 a0001c0001t0001g0263 a0001c0001t0001g0272 others(46): Show |
50 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.49+5301C>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44361154 | |||||||
| chr20:44361329 | T | A | 49 | a0001c0001t0001g0260 a0001c0001t0001g0263 a0001c0001t0001g0272 others(46): Show |
50 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.49+5476T>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44361329 | |||||||
| chr20:44361576 | A | C | 9 | a0001c0001t0012g0311 a0001c0001t0018g0307 a0001c0001t0032g0314 others(6): Show |
9 | HG02451.hp1 HG02622.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.49+5723A>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44361576 | |||||||
| chr20:44361655 | C | T | 9 | a0001c0001t0012g0311 a0001c0001t0018g0307 a0001c0001t0032g0314 others(6): Show |
9 | HG02451.hp1 HG02622.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.49+5802C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44361655 | |||||||
| chr20:44361671 | A | C | 49 | a0001c0001t0001g0260 a0001c0001t0001g0263 a0001c0001t0001g0272 others(46): Show |
50 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.49+5818A>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44361671 | |||||||
| chr20:44361692 | A | C | 6 | a0001c0001t0003g0294 a0001c0001t0003g0295 a0001c0001t0004g0296 others(3): Show |
6 | HG00621.hp2 NA18946.hp1 NA18973.hp1 others(3): Show |
intron_variant | MODIFIER | c.49+5839A>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44361692 | |||||||
| chr20:44361703 | C | CAAAA | 6 | a0001c0001t0003g0294 a0001c0001t0003g0295 a0001c0001t0004g0296 others(3): Show |
6 | HG00621.hp2 NA18946.hp1 NA18973.hp1 others(3): Show |
intron_variant | MODIFIER | c.49+5850_49+5851ins others(4): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44361703 | |||||||
| chr20:44361704 | CA | C | 51 | a0001c0001t0001g0260 a0001c0001t0001g0263 a0001c0001t0001g0272 others(48): Show |
52 | HG00140.hp2 HG00642.hp1 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.49+5860delA | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44361704 | ||||||
| chr20:44361705 | A | C | 6 | a0001c0001t0003g0294 a0001c0001t0003g0295 a0001c0001t0004g0296 others(3): Show |
6 | HG00621.hp2 NA18946.hp1 NA18973.hp1 others(3): Show |
intron_variant | MODIFIER | c.49+5852A>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44361705 | |||||||
| chr20:44361717 | C | CA | 51 | a0001c0001t0001g0246 a0001c0001t0001g0260 a0001c0001t0001g0263 others(48): Show |
52 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.49+5872dupA | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44361717 | ||||||
| chr20:44362000 | C | G | 49 | a0001c0001t0001g0260 a0001c0001t0001g0263 a0001c0001t0001g0272 others(46): Show |
50 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.49+6147C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44362000 | |||||||
| chr20:44362065 | T | C | 49 | a0001c0001t0001g0260 a0001c0001t0001g0263 a0001c0001t0001g0272 others(46): Show |
50 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.49+6212T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44362065 | |||||||
| chr20:44362075 | C | G | 1 | a0001c0001t0024g0291 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.49+6222C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44362075 | |||||||
| chr20:44362157 | C | A | 49 | a0001c0001t0001g0260 a0001c0001t0001g0263 a0001c0001t0001g0272 others(46): Show |
50 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.49+6304C>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44362157 | |||||||
| chr20:44362190 | C | T | 38 | a0001c0001t0001g0230 a0001c0001t0001g0241 a0001c0001t0002g0228 others(35): Show |
38 | HG01069.hp1 HG01891.hp2 HG02071.hp2 others(35): Show |
intron_variant | MODIFIER | c.49+6337C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44362190 | |||||||
| chr20:44362262 | A | T | 2 | a0001c0001t0002g0023 a0001c0001t0032g0024 |
2 | HG02615.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.49+6409A>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44362262 | |||||||
| chr20:44362312 | CG | C | 3 | a0001c0001t0003g0113 a0001c0001t0023g0004 a0001c0001t0052g0005 |
3 | HG00639.hp2 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.49+6462delG | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44362312 | ||||||
| chr20:44362313 | G | A | 94 | a0001c0001t0001g0026 a0001c0001t0001g0032 a0001c0001t0001g0035 others(91): Show |
94 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.49+6460G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44362313 | |||||||
| chr20:44362369 | G | A | 121 | a0001c0001t0001g0018 a0001c0001t0001g0110 a0001c0001t0001g0111 others(118): Show |
123 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.49+6516G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44362369 | |||||||
| chr20:44362371 | G | C | 3 | a0001c0001t0018g0307 a0001c0001t0084g0306 a0001c0003t0065g0308 |
3 | HG02451.hp1 HG02630.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.49+6518G>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44362371 | |||||||
| chr20:44362417 | T | C | 3 | a0001c0001t0003g0113 a0001c0001t0023g0004 a0001c0001t0052g0005 |
3 | HG00639.hp2 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.49+6564T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44362417 | |||||||
| chr20:44362418 | T | TA | 11 | a0001c0001t0001g0119 a0001c0001t0001g0122 a0001c0001t0001g0203 others(8): Show |
11 | HG00597.hp2 HG00621.hp1 HG02135.hp2 others(8): Show |
intron_variant | MODIFIER | c.49+6588dupA | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44362418 | ||||||
| chr20:44362418 | TA | T | 49 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0230 others(46): Show |
49 | HG00140.hp1 HG00438.hp2 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.49+6588delA | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44362418 | ||||||
| chr20:44362418 | TAA | T | 117 | a0001c0001t0001g0026 a0001c0001t0001g0052 a0001c0001t0001g0054 others(114): Show |
118 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.49+6587_49+6588del others(2): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44362418 | ||||||
| chr20:44362418 | TAAA | T | 6 | a0001c0001t0001g0289 a0001c0001t0003g0113 a0001c0001t0003g0257 others(3): Show |
6 | HG00639.hp2 HG01167.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.49+6586_49+6588del others(3): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44362418 | ||||||
| chr20:44362634 | G | C | 2 | a0001c0001t0004g0045 a0001c0001t0025g0046 |
2 | HG00673.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.49+6781G>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44362634 | |||||||
| chr20:44362646 | C | CCATTTTA others(9): Show |
1 | a0001c0001t0034g0199 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.49+6794_49+6809dup others(16): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44362646 | ||||||
| chr20:44362716 | G | T | 1 | a0001c0001t0002g0251 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.49+6863G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44362716 | |||||||
| chr20:44362787 | T | G | 52 | a0001c0001t0001g0260 a0001c0001t0001g0263 a0001c0001t0001g0272 others(49): Show |
53 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.49+6934T>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44362787 | |||||||
| chr20:44362843 | C | CT | 12 | a0001c0001t0001g0196 a0001c0001t0001g0220 a0001c0001t0002g0044 others(9): Show |
12 | HG01256.hp1 HG01515.hp2 HG02300.hp1 others(9): Show |
intron_variant | MODIFIER | c.49+7006dupT | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44362843 | ||||||
| chr20:44362848 | T | TC | 49 | a0001c0001t0001g0260 a0001c0001t0001g0263 a0001c0001t0001g0272 others(46): Show |
50 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.49+6995_49+6996ins others(1): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44362848 | |||||||
| chr20:44362864 | C | T | 145 | a0001c0001t0001g0026 a0001c0001t0001g0032 a0001c0001t0001g0035 others(142): Show |
146 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.49+7011C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44362864 | |||||||
| chr20:44362867 | A | G | 3 | a0001c0001t0018g0307 a0001c0001t0084g0306 a0001c0003t0065g0308 |
3 | HG02451.hp1 HG02630.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.49+7014A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44362867 | |||||||
| chr20:44362950 | T | C | 3 | a0001c0001t0001g0126 a0001c0001t0009g0125 a0005c0007t0017g0124 |
3 | HG03239.hp2 HG04204.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.49+7097T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44362950 | |||||||
| chr20:44362951 | C | T | 3 | a0001c0001t0001g0126 a0001c0001t0009g0125 a0005c0007t0017g0124 |
3 | HG03239.hp2 HG04204.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.49+7098C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44362951 | |||||||
| chr20:44363020 | AT | A | 49 | a0001c0001t0001g0260 a0001c0001t0001g0263 a0001c0001t0001g0272 others(46): Show |
50 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.49+7176delT | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44363020 | ||||||
| chr20:44363027 | T | G | 3 | a0001c0001t0018g0307 a0001c0001t0084g0306 a0001c0003t0065g0308 |
3 | HG02451.hp1 HG02630.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.49+7174T>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44363027 | |||||||
| chr20:44363119 | G | A | 3 | a0001c0001t0001g0246 a0001c0001t0038g0318 a0001c0001t0046g0317 |
3 | HG02055.hp1 HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.49+7266G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44363119 | |||||||
| chr20:44363159 | C | T | 49 | a0001c0001t0001g0260 a0001c0001t0001g0263 a0001c0001t0001g0272 others(46): Show |
50 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.49+7306C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44363159 | |||||||
| chr20:44363305 | G | A | 1 | a0001c0001t0049g0127 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.49+7452G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44363305 | |||||||
| chr20:44363706 | C | CT | 14 | a0001c0001t0001g0220 a0001c0001t0002g0193 a0001c0001t0002g0195 others(11): Show |
14 | HG01167.hp2 HG01433.hp1 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.49+7875dupT | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44363706 | ||||||
| chr20:44363706 | CT | C | 128 | a0001c0001t0001g0026 a0001c0001t0001g0032 a0001c0001t0001g0035 others(125): Show |
129 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.49+7875delT | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44363706 | ||||||
| chr20:44363706 | CTT | C | 12 | a0001c0001t0001g0289 a0001c0001t0004g0047 a0001c0001t0004g0270 others(9): Show |
12 | HG01167.hp1 HG01256.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.49+7874_49+7875del others(2): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44363706 | ||||||
| chr20:44363719 | T | C | 1 | a0001c0001t0054g0253 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.49+7866T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44363719 | |||||||
| chr20:44363839 | C | T | 3 | a0001c0001t0003g0113 a0001c0001t0023g0004 a0001c0001t0052g0005 |
3 | HG00639.hp2 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.49+7986C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44363839 | |||||||
| chr20:44363991 | C | T | 1 | a0001c0001t0001g0191 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.49+8138C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44363991 | |||||||
| chr20:44364113 | G | T | 1 | a0001c0001t0034g0199 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.49+8260G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44364113 | |||||||
| chr20:44364253 | G | T | 50 | a0001c0001t0001g0260 a0001c0001t0001g0263 a0001c0001t0001g0272 others(47): Show |
51 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.49+8400G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44364253 | |||||||
| chr20:44364289 | G | C | 1 | a0001c0001t0078g0258 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.49+8436G>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44364289 | |||||||
| chr20:44364307 | C | T | 2 | a0001c0001t0001g0288 a0001c0001t0001g0289 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.49+8454C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44364307 | |||||||
| chr20:44364412 | A | G | 1 | a0001c0001t0005g0048 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.49+8559A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44364412 | |||||||
| chr20:44364466 | AT | A | 53 | a0001c0001t0001g0260 a0001c0001t0001g0263 a0001c0001t0001g0272 others(50): Show |
54 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.49+8623delT | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44364466 | ||||||
| chr20:44364470 | T | A | 1 | a0001c0001t0045g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.49+8617T>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44364470 | |||||||
| chr20:44364474 | T | C | 86 | a0001c0001t0001g0026 a0001c0001t0001g0032 a0001c0001t0001g0035 others(83): Show |
86 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.49+8621T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44364474 | |||||||
| chr20:44364507 | G | C | 3 | a0001c0001t0018g0307 a0001c0001t0084g0306 a0001c0003t0065g0308 |
3 | HG02451.hp1 HG02630.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.49+8654G>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44364507 | |||||||
| chr20:44364517 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.49+8664C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44364517 | |||||||
| chr20:44364533 | C | T | 53 | a0001c0001t0001g0260 a0001c0001t0001g0263 a0001c0001t0001g0272 others(50): Show |
54 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.49+8680C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44364533 | |||||||
| chr20:44364557 | G | A | 4 | a0001c0001t0007g0131 a0001c0001t0057g0130 a0001c0014t0069g0192 others(1): Show |
4 | HG01169.hp2 HG01175.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.49+8704G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44364557 | |||||||
| chr20:44364641 | T | C | 1 | a0001c0001t0006g0271 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.49+8788T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44364641 | |||||||
| chr20:44364688 | T | C | 50 | a0001c0001t0001g0260 a0001c0001t0001g0263 a0001c0001t0001g0272 others(47): Show |
51 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.49+8835T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44364688 | |||||||
| chr20:44364718 | C | T | 53 | a0001c0001t0001g0260 a0001c0001t0001g0263 a0001c0001t0001g0272 others(50): Show |
54 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.49+8865C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44364718 | |||||||
| chr20:44364944 | C | A | 1 | a0001c0001t0034g0199 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.49+9091C>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44364944 | |||||||
| chr20:44365035 | G | A | 1 | a0001c0001t0011g0020 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.49+9182G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44365035 | |||||||
| chr20:44365173 | G | T | 4 | a0001c0001t0010g0208 a0001c0001t0013g0211 a0001c0001t0018g0209 others(1): Show |
4 | HG00741.hp2 HG02647.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.49+9320G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44365173 | |||||||
| chr20:44365314 | G | T | 5 | a0001c0001t0001g0301 a0001c0001t0002g0302 a0001c0001t0003g0299 others(2): Show |
5 | HG02572.hp2 HG02818.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.49+9461G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44365314 | |||||||
| chr20:44365476 | A | AT | 53 | a0001c0001t0001g0260 a0001c0001t0001g0263 a0001c0001t0001g0272 others(50): Show |
54 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.49+9629dupT | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44365476 | ||||||
| chr20:44365585 | C | T | 3 | a0001c0001t0003g0113 a0001c0001t0023g0004 a0001c0001t0052g0005 |
3 | HG00639.hp2 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.49+9732C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44365585 | |||||||
| chr20:44365692 | C | T | 1 | a0001c0001t0009g0190 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.49+9839C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44365692 | |||||||
| chr20:44365704 | G | A | 1 | a0001c0001t0002g0133 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.49+9851G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44365704 | |||||||
| chr20:44365728 | C | T | 3 | a0001c0001t0018g0307 a0001c0001t0084g0306 a0001c0003t0065g0308 |
3 | HG02451.hp1 HG02630.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.49+9875C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44365728 | |||||||
| chr20:44365729 | G | A | 3 | a0001c0001t0010g0208 a0001c0001t0018g0209 a0001c0001t0018g0210 |
3 | HG02647.hp1 HG02970.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.49+9876G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44365729 | |||||||
| chr20:44365733 | G | A | 3 | a0001c0001t0001g0246 a0001c0001t0038g0318 a0001c0001t0046g0317 |
3 | HG02055.hp1 HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.49+9880G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44365733 | |||||||
| chr20:44365749 | G | A | 53 | a0001c0001t0001g0260 a0001c0001t0001g0263 a0001c0001t0001g0272 others(50): Show |
54 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.49+9896G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44365749 | |||||||
| chr20:44365905 | G | A | 53 | a0001c0001t0001g0260 a0001c0001t0001g0263 a0001c0001t0001g0272 others(50): Show |
54 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.49+10052G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44365905 | |||||||
| chr20:44365956 | G | A | 2 | a0001c0001t0001g0272 a0001c0001t0016g0273 |
2 | NA18941.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.49+10103G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44365956 | |||||||
| chr20:44365990 | C | G | 47 | a0001c0001t0001g0260 a0001c0001t0001g0263 a0001c0001t0001g0272 others(44): Show |
48 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.49+10137C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44365990 | |||||||
| chr20:44366022 | C | T | 1 | a0001c0001t0016g0242 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.49+10169C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44366022 | |||||||
| chr20:44366086 | GA | G | 3 | a0001c0001t0012g0187 a0001c0001t0014g0188 a0001c0001t0014g0189 |
3 | HG02280.hp1 HG06807.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.49+10238delA | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44366086 | ||||||
| chr20:44366172 | T | C | 76 | a0001c0001t0001g0026 a0001c0001t0001g0032 a0001c0001t0001g0035 others(73): Show |
76 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.49+10319T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44366172 | |||||||
| chr20:44366280 | A | G | 1 | a0001c0001t0003g0091 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.49+10427A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44366280 | |||||||
| chr20:44366343 | G | A | 5 | a0001c0001t0012g0311 a0001c0001t0032g0314 a0001c0001t0034g0312 others(2): Show |
5 | HG02622.hp2 HG02630.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.49+10490G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44366343 | |||||||
| chr20:44366364 | TA | T | 6 | a0001c0001t0001g0301 a0001c0001t0002g0302 a0001c0001t0003g0299 others(3): Show |
6 | HG02572.hp2 HG02630.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.49+10513delA | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44366364 | ||||||
| chr20:44366387 | A | G | 6 | a0001c0001t0001g0301 a0001c0001t0002g0302 a0001c0001t0003g0299 others(3): Show |
6 | HG02572.hp2 HG02630.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.49+10534A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44366387 | |||||||
| chr20:44366490 | A | G | 120 | a0001c0001t0001g0110 a0001c0001t0001g0186 a0001c0001t0001g0220 others(117): Show |
122 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(119): Show |
intron_variant | MODIFIER | c.49+10637A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44366490 | |||||||
| chr20:44366493 | C | T | 5 | a0001c0001t0001g0301 a0001c0001t0002g0302 a0001c0001t0003g0299 others(2): Show |
5 | HG02572.hp2 HG02818.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.49+10640C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44366493 | |||||||
| chr20:44366552 | T | G | 5 | a0001c0001t0001g0301 a0001c0001t0002g0302 a0001c0001t0003g0299 others(2): Show |
5 | HG02572.hp2 HG02818.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.49+10699T>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44366552 | |||||||
| chr20:44366558 | T | C | 1 | a0001c0001t0096g0252 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.49+10705T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44366558 | |||||||
| chr20:44366563 | G | A | 1 | a0001c0001t0002g0134 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.49+10710G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44366563 | |||||||
| chr20:44366730 | T | C | 1 | a0001c0003t0065g0308 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.49+10877T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44366730 | |||||||
| chr20:44366919 | A | G | 1 | a0001c0001t0001g0184 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.49+11066A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44366919 | |||||||
| chr20:44366960 | G | A | 73 | a0001c0001t0001g0026 a0001c0001t0001g0032 a0001c0001t0001g0035 others(70): Show |
73 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.49+11107G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44366960 | |||||||
| chr20:44366994 | A | C | 1 | a0001c0001t0001g0183 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.49+11141A>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44366994 | |||||||
| chr20:44367019 | G | T | 1 | a0001c0001t0007g0319 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.49+11166G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44367019 | |||||||
| chr20:44367025 | C | T | 9 | a0001c0001t0001g0301 a0001c0001t0002g0302 a0001c0001t0003g0299 others(6): Show |
9 | HG02572.hp2 HG02630.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.49+11172C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44367025 | |||||||
| chr20:44367304 | C | T | 5 | a0001c0001t0012g0311 a0001c0001t0032g0314 a0001c0001t0034g0312 others(2): Show |
5 | HG02622.hp2 HG02630.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.49+11451C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44367304 | |||||||
| chr20:44367335 | CA | C | 14 | a0001c0001t0001g0289 a0001c0001t0003g0113 a0001c0001t0003g0257 others(11): Show |
14 | HG00639.hp2 HG01167.hp1 HG02602.hp1 others(11): Show |
intron_variant | MODIFIER | c.49+11500delA | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44367335 | ||||||
| chr20:44367419 | A | G | 123 | a0001c0001t0001g0110 a0001c0001t0001g0186 a0001c0001t0001g0220 others(120): Show |
125 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.49+11566A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44367419 | |||||||
| chr20:44367447 | C | T | 111 | a0001c0001t0001g0110 a0001c0001t0001g0186 a0001c0001t0001g0220 others(108): Show |
113 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(110): Show |
intron_variant | MODIFIER | c.49+11594C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44367447 | |||||||
| chr20:44367470 | G | C | 73 | a0001c0001t0001g0026 a0001c0001t0001g0032 a0001c0001t0001g0035 others(70): Show |
73 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.49+11617G>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44367470 | |||||||
| chr20:44367544 | G | C | 73 | a0001c0001t0001g0026 a0001c0001t0001g0032 a0001c0001t0001g0035 others(70): Show |
73 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.49+11691G>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44367544 | |||||||
| chr20:44367639 | C | CA | 110 | a0001c0001t0001g0110 a0001c0001t0001g0186 a0001c0001t0001g0220 others(107): Show |
112 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.49+11802dupA | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44367639 | ||||||
| chr20:44367639 | C | CAA | 9 | a0001c0001t0002g0023 a0001c0001t0002g0228 a0001c0001t0003g0113 others(6): Show |
9 | HG00639.hp2 HG02615.hp2 HG03098.hp2 others(6): Show |
intron_variant | MODIFIER | c.49+11801_49+11802d others(4): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44367639 | ||||||
| chr20:44367681 | C | T | 9 | a0001c0001t0001g0301 a0001c0001t0002g0302 a0001c0001t0003g0299 others(6): Show |
9 | HG02572.hp2 HG02630.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.49+11828C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44367681 | |||||||
| chr20:44367797 | C | A | 3 | a0001c0001t0001g0220 a0001c0001t0018g0307 a0001c0001t0084g0306 |
3 | HG02451.hp1 HG02922.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.49+11944C>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44367797 | |||||||
| chr20:44368053 | CT | C | 8 | a0001c0001t0001g0254 a0001c0001t0001g0301 a0001c0001t0002g0302 others(5): Show |
8 | HG02572.hp2 HG02818.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.49+12211delT | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368053 | ||||||
| chr20:44368073 | A | AAT | 4 | a0001c0001t0001g0301 a0001c0001t0003g0299 a0001c0001t0004g0300 others(1): Show |
4 | HG02572.hp2 HG02818.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.49+12233_49+12234d others(4): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368073 | ||||||
| chr20:44368084 | ATATG | A | 4 | a0001c0001t0010g0208 a0001c0001t0018g0209 a0001c0001t0018g0210 others(1): Show |
4 | HG02630.hp1 HG02647.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.49+12233_49+12236d others(6): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368084 | ||||||
| chr20:44368086 | A | ATG | 60 | a0001c0001t0001g0104 a0001c0001t0001g0110 a0001c0001t0001g0186 others(57): Show |
61 | HG00280.hp2 HG00423.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.49+12257_49+12258d others(4): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368086 | ||||||
| chr20:44368086 | A | ATGTG | 42 | a0001c0001t0001g0263 a0001c0001t0001g0272 a0001c0001t0001g0281 others(39): Show |
43 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(40): Show |
intron_variant | MODIFIER | c.49+12255_49+12258d others(6): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368086 | ||||||
| chr20:44368086 | A | ATGTGTG | 3 | a0001c0001t0003g0283 a0001c0001t0004g0276 a0001c0001t0058g0287 |
3 | HG02135.hp1 HG02698.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.49+12253_49+12258d others(8): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368086 | ||||||
| chr20:44368086 | A | G | 5 | a0001c0001t0003g0218 a0001c0001t0006g0219 a0001c0001t0023g0002 others(2): Show |
5 | HG00735.hp1 HG01255.hp1 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.49+12233A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44368086 | |||||||
| chr20:44368086 | ATG | A | 12 | a0001c0001t0001g0220 a0001c0001t0001g0246 a0001c0001t0003g0006 others(9): Show |
12 | HG00099.hp1 HG01261.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.49+12257_49+12258d others(4): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368086 | ||||||
| chr20:44368086 | ATGTG | A | 3 | a0001c0001t0011g0020 a0001c0001t0013g0021 a0001c0001t0045g0022 |
3 | HG02559.hp1 HG02809.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.49+12255_49+12258d others(6): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368086 | ||||||
| chr20:44368134 | G | GTATACAT others(9): Show |
2 | a0001c0001t0002g0302 a0001c0001t0003g0299 |
2 | HG02572.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.49+12285_49+12286i others(18): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368134 | ||||||
| chr20:44368134 | G | GTATACAT others(11): Show |
1 | a0001c0001t0047g0298 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.49+12285_49+12286i others(20): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368134 | ||||||
| chr20:44368139 | T | C | 6 | a0001c0001t0001g0301 a0001c0001t0004g0300 a0001c0001t0010g0208 others(3): Show |
6 | HG02630.hp1 HG02647.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.49+12286T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44368139 | |||||||
| chr20:44368141 | C | CAT | 10 | a0001c0001t0001g0119 a0001c0001t0001g0141 a0001c0001t0001g0183 others(7): Show |
10 | HG00544.hp1 HG01074.hp2 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.49+12307_49+12308d others(4): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368141 | ||||||
| chr20:44368141 | C | CATAT | 14 | a0001c0001t0001g0178 a0001c0001t0001g0196 a0001c0001t0002g0177 others(11): Show |
14 | HG01074.hp1 HG01123.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.49+12305_49+12308d others(6): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368141 | ||||||
| chr20:44368141 | C | T | 10 | a0001c0001t0001g0301 a0001c0001t0002g0302 a0001c0001t0003g0299 others(7): Show |
10 | HG02572.hp2 HG02630.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.49+12288C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44368141 | |||||||
| chr20:44368158 | A | ATTTTTTT others(3): Show |
1 | a0006c0004t0056g0077 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.49+12306_49+12307i others(12): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368158 | ||||||
| chr20:44368158 | A | ATTTTTTT others(4): Show |
3 | a0001c0001t0004g0047 a0001c0001t0004g0087 a0001c0001t0004g0088 |
3 | NA18947.hp1 NA18981.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.49+12306_49+12307i others(13): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368158 | ||||||
| chr20:44368158 | A | ATTTTTTT others(5): Show |
2 | a0001c0001t0015g0086 a0001c0001t0074g0033 |
2 | HG01255.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.49+12306_49+12307i others(14): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368158 | ||||||
| chr20:44368160 | A | ATATATAT others(11): Show |
1 | a0001c0001t0025g0238 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.49+12308_49+12309i others(20): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | ||||||
| chr20:44368160 | A | ATATATAT others(4): Show |
1 | a0001c0001t0003g0113 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.49+12308_49+12309i others(13): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | ||||||
| chr20:44368160 | A | ATATATAT others(12): Show |
1 | a0001c0001t0001g0301 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.49+12308_49+12309i others(21): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | ||||||
| chr20:44368160 | A | ATATATAT others(16): Show |
1 | a0001c0001t0004g0300 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.49+12308_49+12309i others(25): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | ||||||
| chr20:44368160 | A | ATATATAT others(21): Show |
1 | a0001c0001t0003g0233 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.49+12308_49+12309i others(30): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | ||||||
| chr20:44368160 | A | ATATATAT others(22): Show |
1 | a0001c0001t0003g0231 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.49+12308_49+12309i others(31): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | ||||||
| chr20:44368160 | A | ATATATAT others(21): Show |
1 | a0001c0001t0003g0245 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.49+12308_49+12309i others(30): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | ||||||
| chr20:44368160 | A | ATATATAT others(17): Show |
1 | a0001c0011t0079g0226 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.49+12308_49+12309i others(26): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | ||||||
| chr20:44368160 | A | ATATATAT others(14): Show |
1 | a0001c0001t0013g0225 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.49+12308_49+12309i others(23): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | ||||||
| chr20:44368160 | A | ATATATAT others(16): Show |
2 | a0001c0001t0012g0311 a0001c0001t0094g0313 |
2 | HG03209.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.49+12308_49+12309i others(25): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | ||||||
| chr20:44368160 | A | ATATATAT others(19): Show |
1 | a0001c0001t0002g0251 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.49+12308_49+12309i others(28): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | ||||||
| chr20:44368160 | A | ATATATAT others(13): Show |
2 | a0001c0001t0037g0009 a0001c0001t0037g0224 |
2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.49+12308_49+12309i others(22): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | ||||||
| chr20:44368160 | A | ATATATAT others(14): Show |
2 | a0001c0001t0034g0312 a0001c0001t0085g0310 |
2 | HG02630.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.49+12308_49+12309i others(23): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | ||||||
| chr20:44368160 | A | ATATATAT others(15): Show |
3 | a0001c0001t0006g0249 a0001c0001t0015g0247 a0001c0001t0016g0242 |
3 | NA18959.hp2 NA18998.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.49+12308_49+12309i others(24): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | ||||||
| chr20:44368160 | A | ATATATAT others(16): Show |
4 | a0001c0001t0002g0098 a0001c0001t0002g0232 a0001c0001t0028g0235 others(1): Show |
4 | HG02165.hp1 HG02622.hp2 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.49+12308_49+12309i others(25): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | ||||||
| chr20:44368160 | A | ATATATAT others(18): Show |
2 | a0001c0001t0003g0223 a0001c0001t0003g0236 |
2 | HG04204.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.49+12308_49+12309i others(27): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | ||||||
| chr20:44368160 | A | ATATATAT others(11): Show |
1 | a0001c0001t0097g0123 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.49+12308_49+12309i others(20): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | ||||||
| chr20:44368160 | A | ATATATAT others(12): Show |
3 | a0001c0001t0002g0228 a0001c0001t0003g0248 a0001c0001t0005g0234 |
3 | HG02602.hp2 NA18941.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.49+12308_49+12309i others(21): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | ||||||
| chr20:44368160 | A | ATATATAT others(13): Show |
2 | a0001c0001t0016g0237 a0001c0001t0016g0239 |
2 | NA18946.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.49+12308_49+12309i others(22): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | ||||||
| chr20:44368160 | A | ATATATAT others(15): Show |
2 | a0001c0001t0001g0241 a0001c0001t0004g0250 |
2 | NA18961.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.49+12308_49+12309i others(24): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | ||||||
| chr20:44368160 | A | ATATATAT others(10): Show |
3 | a0001c0001t0001g0230 a0001c0001t0014g0227 a0001c0001t0014g0229 |
3 | HG02647.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.49+12308_49+12309i others(19): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | ||||||
| chr20:44368160 | A | ATATATAT others(13): Show |
1 | a0001c0001t0020g0244 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.49+12308_49+12309i others(22): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | ||||||
| chr20:44368160 | A | ATATATAT others(15): Show |
1 | a0001c0001t0002g0240 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.49+12308_49+12309i others(24): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | ||||||
| chr20:44368160 | A | ATATATAT others(16): Show |
1 | a0002c0002t0001g0243 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.49+12308_49+12309i others(25): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | ||||||
| chr20:44368160 | A | ATATATAT others(5): Show |
1 | a0001c0001t0001g0220 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.49+12308_49+12309i others(14): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | ||||||
| chr20:44368160 | A | ATATATAT others(7): Show |
1 | a0001c0012t0008g0007 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.49+12308_49+12309i others(16): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | ||||||
| chr20:44368160 | A | ATATATAT others(8): Show |
1 | a0001c0001t0001g0110 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.49+12308_49+12309i others(17): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | ||||||
| chr20:44368160 | A | ATATATAT others(9): Show |
2 | a0001c0001t0001g0186 a0001c0001t0006g0109 |
2 | HG00639.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.49+12308_49+12309i others(18): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | ||||||
| chr20:44368160 | A | ATATATAT others(10): Show |
1 | a0001c0001t0005g0262 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.49+12308_49+12309i others(19): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | ||||||
| chr20:44368160 | A | ATATATAT others(12): Show |
1 | a0001c0001t0002g0265 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.49+12308_49+12309i others(21): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | ||||||
| chr20:44368160 | A | ATATATAT others(4): Show |
1 | a0001c0001t0018g0209 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.49+12308_49+12309i others(13): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | ||||||
| chr20:44368160 | A | ATATATAT others(7): Show |
3 | a0001c0001t0006g0271 a0001c0001t0038g0318 a0001c0001t0080g0304 |
3 | HG02602.hp1 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.49+12308_49+12309i others(16): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | ||||||
| chr20:44368160 | A | ATATATAT others(8): Show |
2 | a0001c0001t0011g0185 a0001c0001t0054g0253 |
2 | HG00099.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.49+12308_49+12309i others(17): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | ||||||
| chr20:44368160 | A | ATATATAT others(9): Show |
4 | a0001c0001t0006g0001 a0001c0001t0008g0008 a0001c0001t0012g0256 others(1): Show |
5 | HG00738.hp1 HG01109.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.49+12308_49+12309i others(18): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | ||||||
| chr20:44368160 | A | ATATATAT others(11): Show |
2 | a0001c0001t0001g0260 a0001c0001t0008g0261 |
2 | HG00642.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.49+12308_49+12309i others(20): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | ||||||
| chr20:44368160 | A | ATATATAT others(3): Show |
5 | a0001c0001t0018g0307 a0001c0001t0027g0014 a0001c0001t0027g0016 others(2): Show |
5 | HG01891.hp2 HG02451.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.49+12308_49+12309i others(12): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | ||||||
| chr20:44368160 | A | ATATATAT others(4): Show |
5 | a0001c0001t0005g0048 a0001c0001t0010g0208 a0001c0001t0013g0010 others(2): Show |
5 | HG02647.hp1 HG02886.hp1 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.49+12308_49+12309i others(13): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | ||||||
| chr20:44368160 | A | ATATATAT others(5): Show |
3 | a0001c0001t0004g0270 a0001c0001t0010g0011 a0001c0001t0010g0017 |
3 | HG02145.hp1 HG02970.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.49+12308_49+12309i others(14): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | ||||||
| chr20:44368160 | A | ATATATAT others(6): Show |
1 | a0001c0001t0033g0269 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.49+12308_49+12309i others(15): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | ||||||
| chr20:44368160 | A | ATATATAT others(7): Show |
1 | a0001c0001t0058g0287 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.49+12308_49+12309i others(16): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | ||||||
| chr20:44368160 | A | ATATATAT others(8): Show |
3 | a0001c0001t0004g0303 a0001c0001t0046g0317 a0001c0009t0081g0275 |
3 | HG02055.hp1 NA18990.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.49+12308_49+12309i others(17): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | ||||||
| chr20:44368160 | A | ATATATAT others(10): Show |
1 | a0001c0001t0008g0003 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.49+12308_49+12309i others(19): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | ||||||
| chr20:44368160 | A | ATATATAT others(11): Show |
4 | a0001c0001t0001g0263 a0001c0001t0001g0281 a0001c0001t0002g0259 others(1): Show |
4 | HG00735.hp2 HG00741.hp1 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.49+12308_49+12309i others(20): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | ||||||
| chr20:44368160 | A | ATATATAT others(13): Show |
1 | a0001c0001t0024g0291 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.49+12308_49+12309i others(22): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | ||||||
| chr20:44368160 | A | ATATATTT others(3): Show |
3 | a0001c0001t0002g0023 a0001c0001t0023g0004 a0001c0001t0052g0005 |
3 | HG02615.hp2 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.49+12308_49+12309i others(12): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | ||||||
| chr20:44368160 | A | ATATATTT others(4): Show |
3 | a0001c0001t0005g0036 a0001c0001t0010g0015 a0001c0003t0065g0308 |
3 | HG02630.hp1 HG03139.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.49+12308_49+12309i others(13): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | ||||||
| chr20:44368160 | A | ATATATTT others(5): Show |
5 | a0001c0001t0003g0029 a0001c0001t0005g0063 a0001c0001t0005g0073 others(2): Show |
5 | HG02132.hp2 HG02155.hp2 NA19007.hp1 others(2): Show |
intron_variant | MODIFIER | c.49+12308_49+12309i others(14): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | ||||||
| chr20:44368160 | A | ATATATTT others(6): Show |
2 | a0001c0001t0021g0277 a0001c0001t0042g0085 |
2 | NA19011.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.49+12308_49+12309i others(15): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | ||||||
| chr20:44368160 | A | ATATATTT others(7): Show |
10 | a0001c0001t0001g0272 a0001c0001t0003g0095 a0001c0001t0003g0097 others(7): Show |
10 | HG00099.hp2 HG00323.hp2 HG02015.hp2 others(7): Show |
intron_variant | MODIFIER | c.49+12308_49+12309i others(16): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | ||||||
| chr20:44368160 | A | ATATATTT others(8): Show |
3 | a0001c0001t0001g0246 a0001c0001t0003g0283 a0001c0001t0015g0274 |
3 | HG02135.hp1 HG03579.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.49+12308_49+12309i others(17): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | ||||||
| chr20:44368160 | A | ATATATTT others(9): Show |
1 | a0001c0001t0003g0257 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.49+12308_49+12309i others(18): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | ||||||
| chr20:44368160 | A | ATATATTT others(11): Show |
2 | a0001c0001t0003g0267 a0001c0001t0029g0266 |
2 | HG01081.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.49+12308_49+12309i others(20): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | ||||||
| chr20:44368160 | A | ATATATTT others(12): Show |
2 | a0001c0001t0029g0268 a0001c0001t0078g0258 |
2 | HG01175.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.49+12308_49+12309i others(21): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | ||||||
| chr20:44368160 | A | ATATTTTT others(3): Show |
3 | a0001c0001t0003g0042 a0001c0001t0004g0068 a0001c0001t0009g0058 |
3 | HG02015.hp1 HG02738.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.49+12308_49+12309i others(12): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | ||||||
| chr20:44368160 | A | ATATTTTT others(4): Show |
9 | a0001c0001t0001g0056 a0001c0001t0002g0064 a0001c0001t0002g0074 others(6): Show |
9 | HG00423.hp2 HG00642.hp2 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.49+12308_49+12309i others(13): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | ||||||
| chr20:44368160 | A | ATATTTTT others(5): Show |
6 | a0001c0001t0001g0026 a0001c0001t0003g0071 a0001c0001t0003g0084 others(3): Show |
6 | HG02148.hp2 HG03669.hp2 HG03942.hp2 others(3): Show |
intron_variant | MODIFIER | c.49+12308_49+12309i others(14): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | ||||||
| chr20:44368160 | A | ATATTTTT others(6): Show |
1 | a0001c0001t0022g0076 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.49+12308_49+12309i others(15): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | ||||||
| chr20:44368160 | A | ATATTTTT others(7): Show |
3 | a0001c0001t0001g0286 a0001c0001t0083g0027 a0001c0001t0095g0069 |
3 | HG00438.hp2 HG03491.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.49+12308_49+12309i others(16): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | ||||||
| chr20:44368160 | A | ATTTTTTT others(3): Show |
2 | a0001c0001t0002g0037 a0001c0013t0010g0050 |
2 | HG06807.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.49+12322_49+12331d others(12): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | ||||||
| chr20:44368160 | A | ATTTTTTT others(4): Show |
16 | a0001c0001t0001g0035 a0001c0001t0001g0054 a0001c0001t0001g0067 others(13): Show |
16 | HG00140.hp1 HG01081.hp2 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.49+12321_49+12331d others(13): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | ||||||
| chr20:44368160 | A | ATTTTTTT others(5): Show |
18 | a0001c0001t0001g0032 a0001c0001t0001g0052 a0001c0001t0001g0104 others(15): Show |
18 | HG00597.hp1 HG00673.hp2 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.49+12320_49+12331d others(14): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | ||||||
| chr20:44368160 | A | ATTTTTTT others(6): Show |
3 | a0001c0001t0002g0039 a0001c0001t0020g0049 a0002c0002t0007g0028 |
3 | HG01258.hp2 HG01975.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.49+12319_49+12331d others(15): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | ||||||
| chr20:44368160 | A | ATTTTTTT others(7): Show |
1 | a0001c0003t0062g0062 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.49+12318_49+12331d others(16): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | ||||||
| chr20:44368160 | A | T | 6 | a0001c0001t0004g0047 a0001c0001t0004g0087 a0001c0001t0004g0088 others(3): Show |
6 | HG01255.hp2 NA18947.hp1 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.49+12307A>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44368160 | |||||||
| chr20:44368161 | T | TA | 56 | a0001c0001t0001g0155 a0001c0001t0001g0163 a0001c0001t0001g0164 others(53): Show |
56 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.49+12308_49+12309i others(3): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44368161 | |||||||
| chr20:44368161 | T | TATA | 10 | a0001c0001t0002g0152 a0001c0001t0002g0156 a0001c0001t0002g0160 others(7): Show |
10 | HG00597.hp2 HG00621.hp1 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.49+12308_49+12309i others(5): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44368161 | |||||||
| chr20:44368162 | T | A | 27 | a0001c0001t0001g0018 a0001c0001t0001g0111 a0001c0001t0001g0119 others(24): Show |
27 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(24): Show |
intron_variant | MODIFIER | c.49+12309T>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44368162 | |||||||
| chr20:44368163 | T | A | 51 | a0001c0001t0001g0155 a0001c0001t0001g0163 a0001c0001t0001g0164 others(48): Show |
51 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.49+12310T>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44368163 | |||||||
| chr20:44368164 | T | A | 16 | a0001c0001t0001g0018 a0001c0001t0001g0111 a0001c0001t0001g0141 others(13): Show |
16 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(13): Show |
intron_variant | MODIFIER | c.49+12311T>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44368164 | |||||||
| chr20:44368165 | T | A | 2 | a0001c0001t0066g0315 a0001c0001t0099g0147 |
2 | HG02976.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.49+12312T>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44368165 | |||||||
| chr20:44368167 | T | A | 1 | a0001c0001t0066g0315 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.49+12314T>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44368167 | |||||||
| chr20:44368168 | T | A | 2 | a0001c0001t0001g0254 a0001c0001t0060g0255 |
2 | HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.49+12315T>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44368168 | |||||||
| chr20:44368170 | T | A | 1 | a0001c0001t0001g0254 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.49+12317T>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44368170 | |||||||
| chr20:44368334 | T | C | 1 | a0001c0001t0046g0317 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.49+12481T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44368334 | |||||||
| chr20:44368457 | A | C | 5 | a0001c0001t0001g0301 a0001c0001t0002g0302 a0001c0001t0003g0299 others(2): Show |
5 | HG02572.hp2 HG02818.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.49+12604A>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44368457 | |||||||
| chr20:44368457 | A | G | 4 | a0001c0001t0010g0208 a0001c0001t0018g0209 a0001c0001t0018g0210 others(1): Show |
4 | HG02630.hp1 HG02647.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.49+12604A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44368457 | |||||||
| chr20:44368464 | G | A | 1 | a0001c0001t0003g0148 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.49+12611G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44368464 | |||||||
| chr20:44368593 | G | T | 4 | a0001c0001t0010g0208 a0001c0001t0018g0209 a0001c0001t0018g0210 others(1): Show |
4 | HG02630.hp1 HG02647.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.49+12740G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44368593 | |||||||
| chr20:44368709 | T | A | 1 | a0001c0001t0044g0116 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.49+12856T>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44368709 | |||||||
| chr20:44368739 | A | G | 2 | a0001c0001t0003g0006 a0001c0001t0003g0084 |
2 | NA18995.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.49+12886A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44368739 | |||||||
| chr20:44368800 | T | C | 1 | a0001c0001t0001g0220 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.49+12947T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44368800 | |||||||
| chr20:44368863 | T | C | 4 | a0001c0001t0010g0208 a0001c0001t0018g0209 a0001c0001t0018g0210 others(1): Show |
4 | HG02630.hp1 HG02647.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.49+13010T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44368863 | |||||||
| chr20:44368888 | G | A | 1 | a0001c0001t0001g0220 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.49+13035G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44368888 | |||||||
| chr20:44368949 | T | G | 4 | a0001c0001t0001g0301 a0001c0001t0002g0302 a0001c0001t0003g0299 others(1): Show |
4 | HG02572.hp2 HG02818.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.49+13096T>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44368949 | |||||||
| chr20:44368955 | T | A | 9 | a0001c0001t0001g0301 a0001c0001t0002g0302 a0001c0001t0003g0299 others(6): Show |
9 | HG02572.hp2 HG02630.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.49+13102T>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44368955 | |||||||
| chr20:44368985 | C | T | 2 | a0001c0001t0005g0082 a0001c0001t0005g0083 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.49+13132C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44368985 | |||||||
| chr20:44369072 | CCT | C | 109 | a0001c0001t0001g0110 a0001c0001t0001g0186 a0001c0001t0001g0220 others(106): Show |
111 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.49+13220_49+13221d others(4): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44369072 | |||||||
| chr20:44369147 | G | T | 1 | a0001c0001t0052g0005 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.49+13294G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44369147 | |||||||
| chr20:44369188 | T | G | 9 | a0001c0001t0001g0301 a0001c0001t0002g0302 a0001c0001t0003g0299 others(6): Show |
9 | HG02572.hp2 HG02630.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.49+13335T>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44369188 | |||||||
| chr20:44369249 | C | CA | 92 | a0001c0001t0001g0018 a0001c0001t0001g0104 a0001c0001t0001g0119 others(89): Show |
93 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.49+13425dupA | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44369249 | ||||||
| chr20:44369249 | C | CAA | 58 | a0001c0001t0001g0026 a0001c0001t0001g0032 a0001c0001t0001g0035 others(55): Show |
59 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.49+13424_49+13425d others(4): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44369249 | ||||||
| chr20:44369249 | C | CAAA | 27 | a0001c0001t0001g0052 a0001c0001t0001g0054 a0001c0001t0001g0056 others(24): Show |
27 | HG00099.hp1 HG00597.hp1 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.49+13423_49+13425d others(5): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44369249 | ||||||
| chr20:44369249 | C | CAAAA | 9 | a0001c0001t0004g0047 a0001c0001t0004g0106 a0001c0001t0006g0051 others(6): Show |
9 | HG01069.hp1 HG01169.hp2 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.49+13422_49+13425d others(6): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44369249 | ||||||
| chr20:44369249 | C | CAAAAAAA others(3): Show |
1 | a0001c0001t0054g0253 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.49+13416_49+13425d others(12): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44369249 | ||||||
| chr20:44369249 | CA | C | 18 | a0001c0001t0001g0122 a0001c0001t0001g0126 a0001c0001t0001g0178 others(15): Show |
18 | HG00735.hp1 HG01074.hp2 HG01123.hp1 others(15): Show |
intron_variant | MODIFIER | c.49+13425delA | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44369249 | ||||||
| chr20:44369279 | C | T | 2 | a0001c0001t0011g0020 a0001c0001t0013g0021 |
2 | HG02559.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.49+13426C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44369279 | |||||||
| chr20:44369286 | G | A | 1 | a0001c0001t0003g0294 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.49+13433G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44369286 | |||||||
| chr20:44369631 | G | A | 6 | a0001c0001t0004g0106 a0001c0001t0033g0269 a0001c0001t0080g0304 others(3): Show |
6 | HG01361.hp1 HG01891.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.49+13778G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44369631 | |||||||
| chr20:44369707 | T | C | 8 | a0001c0001t0001g0246 a0001c0001t0001g0301 a0001c0001t0002g0023 others(5): Show |
8 | HG02572.hp2 HG02615.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.49+13854T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44369707 | |||||||
| chr20:44369733 | C | G | 1 | a0001c0001t0003g0097 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.49+13880C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44369733 | |||||||
| chr20:44369782 | G | A | 3 | a0001c0001t0003g0006 a0001c0001t0003g0084 a0001c0001t0004g0072 |
3 | NA18951.hp2 NA18995.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.49+13929G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44369782 | |||||||
| chr20:44370028 | G | T | 1 | a0001c0001t0001g0246 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.49+14175G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44370028 | |||||||
| chr20:44370082 | G | A | 5 | a0001c0001t0001g0301 a0001c0001t0002g0302 a0001c0001t0003g0299 others(2): Show |
5 | HG02572.hp2 HG02818.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.49+14229G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44370082 | |||||||
| chr20:44370089 | C | G | 5 | a0001c0001t0001g0301 a0001c0001t0002g0302 a0001c0001t0003g0299 others(2): Show |
5 | HG02572.hp2 HG02818.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.49+14236C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44370089 | |||||||
| chr20:44370089 | C | T | 1 | a0001c0001t0003g0071 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.49+14236C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44370089 | |||||||
| chr20:44370090 | G | A | 1 | a0001c0001t0032g0024 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.49+14237G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44370090 | |||||||
| chr20:44370096 | G | C | 1 | a0001c0001t0006g0176 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.49+14243G>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44370096 | |||||||
| chr20:44370112 | C | T | 1 | a0001c0001t0058g0287 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.49+14259C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44370112 | |||||||
| chr20:44370119 | C | T | 6 | a0001c0001t0001g0246 a0001c0001t0001g0301 a0001c0001t0002g0302 others(3): Show |
6 | HG02572.hp2 HG02818.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.49+14266C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44370119 | |||||||
| chr20:44370121 | G | A | 2 | a0001c0001t0003g0093 a0001c0001t0024g0194 |
2 | HG02027.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.49+14268G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44370121 | |||||||
| chr20:44370147 | C | A | 1 | a0001c0001t0002g0177 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.49+14294C>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44370147 | |||||||
| chr20:44370646 | T | C | 3 | a0001c0001t0001g0141 a0001c0001t0072g0142 a0001c0001t0093g0140 |
3 | HG01496.hp2 HG01975.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.49+14793T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44370646 | |||||||
| chr20:44370691 | A | G | 5 | a0001c0001t0001g0301 a0001c0001t0002g0302 a0001c0001t0003g0299 others(2): Show |
5 | HG02572.hp2 HG02818.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.49+14838A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44370691 | |||||||
| chr20:44370697 | C | T | 1 | a0001c0001t0007g0090 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.49+14844C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44370697 | |||||||
| chr20:44370714 | C | T | 2 | a0001c0001t0001g0241 a0002c0002t0001g0243 |
2 | HG02071.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.49+14861C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44370714 | |||||||
| chr20:44370715 | G | A | 5 | a0001c0001t0001g0301 a0001c0001t0002g0302 a0001c0001t0003g0299 others(2): Show |
5 | HG02572.hp2 HG02818.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.49+14862G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44370715 | |||||||
| chr20:44370793 | G | A | 5 | a0001c0001t0001g0301 a0001c0001t0002g0302 a0001c0001t0003g0299 others(2): Show |
5 | HG02572.hp2 HG02818.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.49+14940G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44370793 | |||||||
| chr20:44370806 | T | C | 3 | a0001c0001t0011g0020 a0001c0001t0013g0021 a0001c0001t0045g0022 |
3 | HG02559.hp1 HG02809.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.49+14953T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44370806 | |||||||
| chr20:44370867 | C | G | 1 | a0001c0001t0004g0250 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.49+15014C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44370867 | |||||||
| chr20:44370893 | C | A | 2 | a0001c0001t0018g0307 a0001c0001t0084g0306 |
2 | HG02451.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.49+15040C>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44370893 | |||||||
| chr20:44370990 | A | C | 138 | a0001c0001t0001g0026 a0001c0001t0001g0032 a0001c0001t0001g0035 others(135): Show |
139 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.49+15137A>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44370990 | |||||||
| chr20:44371003 | C | G | 258 | a0001c0001t0001g0018 a0001c0001t0001g0026 a0001c0001t0001g0032 others(255): Show |
259 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.49+15150C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44371003 | |||||||
| chr20:44371048 | T | G | 1 | a0001c0001t0001g0254 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.49+15195T>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44371048 | |||||||
| chr20:44371199 | A | C | 13 | a0001c0001t0001g0111 a0001c0001t0001g0246 a0001c0001t0001g0254 others(10): Show |
13 | HG02572.hp1 HG02572.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.49+15346A>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44371199 | |||||||
| chr20:44371224 | C | A | 7 | a0001c0001t0001g0111 a0001c0001t0001g0254 a0001c0001t0002g0023 others(4): Show |
7 | HG02572.hp1 HG02615.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.49+15371C>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44371224 | |||||||
| chr20:44371267 | A | AT | 8 | a0001c0001t0001g0111 a0001c0001t0001g0246 a0001c0001t0001g0254 others(5): Show |
8 | HG02572.hp1 HG02615.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.49+15422dupT | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44371267 | ||||||
| chr20:44371363 | C | T | 1 | a0001c0001t0001g0254 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.49+15510C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44371363 | |||||||
| chr20:44371475 | C | T | 1 | a0001c0001t0002g0156 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.49+15622C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44371475 | |||||||
| chr20:44371553 | G | A | 1 | a0001c0001t0001g0254 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.49+15700G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44371553 | |||||||
| chr20:44371698 | G | A | 8 | a0001c0001t0010g0011 a0001c0001t0010g0015 a0001c0001t0010g0017 others(5): Show |
8 | HG01891.hp2 HG02145.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.49+15845G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44371698 | |||||||
| chr20:44371814 | C | T | 8 | a0001c0001t0001g0155 a0001c0001t0001g0163 a0001c0001t0001g0164 others(5): Show |
8 | HG01358.hp1 HG02280.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.49+15961C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44371814 | |||||||
| chr20:44371817 | T | A | 5 | a0001c0001t0001g0301 a0001c0001t0002g0302 a0001c0001t0003g0299 others(2): Show |
5 | HG02572.hp2 HG02818.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.49+15964T>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44371817 | |||||||
| chr20:44371903 | A | G | 1 | a0001c0001t0060g0255 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.49+16050A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44371903 | |||||||
| chr20:44371950 | C | T | 110 | a0001c0001t0001g0018 a0001c0001t0001g0122 a0001c0001t0001g0126 others(107): Show |
110 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.49+16097C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44371950 | |||||||
| chr20:44371982 | C | T | 1 | a0001c0001t0002g0154 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.49+16129C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44371982 | |||||||
| chr20:44372123 | C | A | 6 | a0001c0001t0001g0301 a0001c0001t0002g0302 a0001c0001t0003g0299 others(3): Show |
6 | HG02572.hp2 HG02809.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.49+16270C>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44372123 | |||||||
| chr20:44372340 | C | T | 3 | a0001c0001t0007g0131 a0001c0014t0069g0192 a0002c0002t0001g0132 |
3 | HG01175.hp2 HG01433.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.49+16487C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44372340 | |||||||
| chr20:44372565 | T | C | 2 | a0001c0001t0011g0020 a0001c0001t0013g0021 |
2 | HG02559.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.49+16712T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44372565 | |||||||
| chr20:44372661 | GT | G | 9 | a0001c0001t0001g0301 a0001c0001t0002g0302 a0001c0001t0003g0299 others(6): Show |
9 | HG02451.hp2 HG02559.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.49+16817delT | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44372661 | ||||||
| chr20:44372666 | T | C | 1 | a0001c0001t0001g0111 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.49+16813T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44372666 | |||||||
| chr20:44372812 | G | A | 1 | a0001c0001t0001g0254 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.49+16959G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44372812 | |||||||
| chr20:44372814 | G | A | 1 | a0001c0001t0032g0024 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.49+16961G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44372814 | |||||||
| chr20:44372830 | A | G | 2 | a0001c0001t0001g0184 a0001c0001t0077g0162 |
2 | HG03927.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.49+16977A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44372830 | |||||||
| chr20:44372843 | C | T | 1 | a0001c0001t0001g0246 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.49+16990C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44372843 | |||||||
| chr20:44373081 | C | T | 75 | a0001c0001t0001g0026 a0001c0001t0001g0032 a0001c0001t0001g0035 others(72): Show |
75 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.49+17228C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44373081 | |||||||
| chr20:44373192 | C | T | 4 | a0001c0001t0018g0307 a0001c0001t0031g0145 a0001c0001t0031g0153 others(1): Show |
4 | HG02451.hp1 HG02809.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.49+17339C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44373192 | |||||||
| chr20:44373503 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.49+17650C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44373503 | |||||||
| chr20:44373909 | C | T | 3 | a0001c0001t0001g0126 a0001c0001t0009g0125 a0005c0007t0017g0124 |
3 | HG03239.hp2 HG04204.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.49+18056C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44373909 | |||||||
| chr20:44373988 | C | T | 1 | a0001c0001t0046g0317 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.49+18135C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44373988 | |||||||
| chr20:44374144 | C | G | 1 | a0001c0001t0095g0069 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.49+18291C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44374144 | |||||||
| chr20:44374183 | A | C | 14 | a0001c0001t0001g0111 a0001c0001t0001g0254 a0001c0001t0001g0301 others(11): Show |
14 | HG02572.hp1 HG02572.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.49+18330A>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44374183 | |||||||
| chr20:44374185 | C | T | 1 | a0001c0001t0001g0254 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.49+18332C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44374185 | |||||||
| chr20:44374270 | G | T | 258 | a0001c0001t0001g0018 a0001c0001t0001g0026 a0001c0001t0001g0032 others(255): Show |
259 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.49+18417G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44374270 | |||||||
| chr20:44374317 | C | T | 8 | a0001c0001t0001g0254 a0001c0001t0001g0301 a0001c0001t0002g0302 others(5): Show |
8 | HG02572.hp2 HG02809.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.49+18464C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44374317 | |||||||
| chr20:44374344 | TGAACTTG others(99): Show |
T | 1 | a0001c0001t0002g0154 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.49+18492_49+18597d others(2): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44374344 | |||||||
| chr20:44374455 | A | T | 1 | a0001c0001t0002g0154 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.49+18602A>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44374455 | |||||||
| chr20:44374457 | G | T | 1 | a0001c0001t0002g0154 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.49+18604G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44374457 | |||||||
| chr20:44374459 | C | T | 1 | a0001c0001t0002g0154 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.49+18606C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44374459 | |||||||
| chr20:44374463 | C | T | 1 | a0001c0001t0002g0154 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.49+18610C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44374463 | |||||||
| chr20:44374465 | A | T | 1 | a0001c0001t0002g0154 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.49+18612A>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44374465 | |||||||
| chr20:44374466 | C | T | 10 | a0001c0001t0001g0246 a0001c0001t0001g0254 a0001c0001t0001g0301 others(7): Show |
10 | HG02572.hp2 HG02809.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.49+18613C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44374466 | |||||||
| chr20:44374468 | G | T | 1 | a0001c0001t0002g0154 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.49+18615G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44374468 | |||||||
| chr20:44374473 | G | T | 1 | a0001c0001t0002g0154 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.49+18620G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44374473 | |||||||
| chr20:44374478 | G | T | 1 | a0001c0001t0002g0154 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.49+18625G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44374478 | |||||||
| chr20:44374482 | G | A | 73 | a0001c0001t0001g0026 a0001c0001t0001g0032 a0001c0001t0001g0035 others(70): Show |
73 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.49+18629G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44374482 | |||||||
| chr20:44374486 | T | C | 1 | a0001c0001t0002g0154 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.49+18633T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44374486 | |||||||
| chr20:44374495 | A | G | 1 | a0001c0001t0002g0154 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.49+18642A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44374495 | |||||||
| chr20:44374503 | A | G | 1 | a0001c0001t0002g0154 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.49+18650A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44374503 | |||||||
| chr20:44374527 | A | G | 1 | a0001c0001t0002g0154 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.49+18674A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44374527 | |||||||
| chr20:44374533 | A | G | 1 | a0001c0001t0002g0154 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.49+18680A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44374533 | |||||||
| chr20:44374545 | C | G | 1 | a0001c0001t0002g0154 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.49+18692C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44374545 | |||||||
| chr20:44374549 | T | C | 1 | a0001c0001t0002g0154 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.49+18696T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44374549 | |||||||
| chr20:44374557 | A | G | 1 | a0001c0001t0002g0154 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.49+18704A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44374557 | |||||||
| chr20:44374564 | A | C | 1 | a0001c0001t0002g0154 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.49+18711A>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44374564 | |||||||
| chr20:44374577 | T | C | 1 | a0001c0001t0002g0154 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.49+18724T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44374577 | |||||||
| chr20:44374589 | A | G | 1 | a0001c0001t0002g0154 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.49+18736A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44374589 | |||||||
| chr20:44374601 | T | C | 1 | a0001c0001t0002g0154 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.49+18748T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44374601 | |||||||
| chr20:44374603 | A | G | 7 | a0001c0001t0001g0111 a0001c0001t0001g0254 a0001c0001t0002g0023 others(4): Show |
7 | HG02572.hp1 HG02615.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.49+18750A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44374603 | |||||||
| chr20:44374609 | A | G | 1 | a0001c0001t0002g0154 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.49+18756A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44374609 | |||||||
| chr20:44374610 | T | C | 1 | a0001c0001t0002g0154 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.49+18757T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44374610 | |||||||
| chr20:44374611 | G | C | 1 | a0001c0001t0002g0154 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.49+18758G>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44374611 | |||||||
| chr20:44374612 | T | C | 1 | a0001c0001t0002g0154 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.49+18759T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44374612 | |||||||
| chr20:44374615 | C | T | 1 | a0001c0001t0002g0154 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.49+18762C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44374615 | |||||||
| chr20:44374620 | T | C | 1 | a0001c0001t0002g0154 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.49+18767T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44374620 | |||||||
| chr20:44374624 | T | C | 1 | a0001c0001t0002g0154 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.49+18771T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44374624 | |||||||
| chr20:44374711 | G | A | 1 | a0001c0001t0013g0010 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.49+18858G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44374711 | |||||||
| chr20:44374744 | G | A | 3 | a0001c0001t0010g0208 a0001c0001t0018g0209 a0001c0001t0018g0210 |
3 | HG02647.hp1 HG02970.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.49+18891G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44374744 | |||||||
| chr20:44375168 | G | A | 3 | a0001c0001t0003g0113 a0001c0001t0023g0004 a0001c0001t0052g0005 |
3 | HG00639.hp2 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.49+19315G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44375168 | |||||||
| chr20:44375178 | C | A | 3 | a0001c0001t0003g0113 a0001c0001t0023g0004 a0001c0001t0052g0005 |
3 | HG00639.hp2 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.49+19325C>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44375178 | |||||||
| chr20:44375255 | TTAAGTTC others(30): Show |
T | 1 | a0001c0001t0001g0111 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.49+19417_49+19453d others(39): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44375255 | ||||||
| chr20:44375396 | G | A | 2 | a0001c0001t0051g0157 a0001c0001t0099g0147 |
2 | HG03669.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.49+19543G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44375396 | |||||||
| chr20:44375495 | G | GT | 12 | a0001c0001t0001g0110 a0001c0001t0001g0215 a0001c0001t0001g0216 others(9): Show |
12 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(9): Show |
intron_variant | MODIFIER | c.49+19654dupT | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44375495 | ||||||
| chr20:44375495 | GT | G | 8 | a0001c0001t0001g0254 a0001c0001t0001g0301 a0001c0001t0002g0302 others(5): Show |
8 | HG02572.hp2 HG02809.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.49+19654delT | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44375495 | ||||||
| chr20:44375598 | T | C | 1 | a0001c0001t0002g0202 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.49+19745T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44375598 | |||||||
| chr20:44375986 | C | A | 1 | a0001c0001t0001g0246 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.49+20133C>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44375986 | |||||||
| chr20:44376084 | A | G | 6 | a0001c0001t0011g0020 a0001c0001t0012g0256 a0001c0001t0013g0021 others(3): Show |
6 | HG01261.hp1 HG02451.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.49+20231A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44376084 | |||||||
| chr20:44376121 | C | T | 1 | a0001c0001t0002g0240 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.49+20268C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44376121 | |||||||
| chr20:44376126 | A | G | 14 | a0001c0001t0001g0111 a0001c0001t0001g0254 a0001c0001t0001g0301 others(11): Show |
14 | HG02572.hp1 HG02572.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.49+20273A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44376126 | |||||||
| chr20:44376147 | C | T | 6 | a0001c0001t0001g0111 a0001c0001t0002g0023 a0001c0001t0010g0208 others(3): Show |
6 | HG02572.hp1 HG02615.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.49+20294C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44376147 | |||||||
| chr20:44376213 | C | T | 1 | a0001c0001t0003g0236 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.49+20360C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44376213 | |||||||
| chr20:44376276 | T | A | 1 | a0001c0001t0038g0146 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.49+20423T>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44376276 | |||||||
| chr20:44376284 | T | G | 1 | a0001c0001t0012g0061 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.49+20431T>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44376284 | |||||||
| chr20:44376375 | A | G | 240 | a0001c0001t0001g0018 a0001c0001t0001g0026 a0001c0001t0001g0032 others(237): Show |
241 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.49+20522A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44376375 | |||||||
| chr20:44376385 | G | A | 2 | a0001c0001t0001g0254 a0001c0001t0002g0177 |
2 | HG03453.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.49+20532G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44376385 | |||||||
| chr20:44376489 | A | G | 5 | a0001c0001t0012g0311 a0001c0001t0032g0314 a0001c0001t0034g0312 others(2): Show |
5 | HG02622.hp2 HG02630.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.49+20636A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44376489 | |||||||
| chr20:44376806 | G | T | 1 | a0007c0005t0025g0038 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.49+20953G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44376806 | |||||||
| chr20:44376965 | C | T | 2 | a0001c0001t0011g0020 a0001c0001t0013g0021 |
2 | HG02559.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.49+21112C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44376965 | |||||||
| chr20:44377194 | C | G | 1 | a0001c0001t0038g0146 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.49+21341C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44377194 | |||||||
| chr20:44377205 | T | C | 1 | a0001c0001t0009g0149 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.49+21352T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44377205 | |||||||
| chr20:44377292 | A | G | 2 | a0002c0002t0001g0174 a0002c0002t0001g0175 |
2 | HG01346.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.49+21439A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44377292 | |||||||
| chr20:44377335 | C | T | 1 | a0001c0001t0004g0181 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.49+21482C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44377335 | |||||||
| chr20:44377613 | A | G | 1 | a0001c0001t0001g0246 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.49+21760A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44377613 | |||||||
| chr20:44377681 | T | TAAACCTG others(4): Show |
1 | a0001c0001t0009g0190 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.49+21829_49+21839d others(13): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44377681 | ||||||
| chr20:44377698 | TAA | T | 7 | a0001c0001t0001g0301 a0001c0001t0002g0302 a0001c0001t0003g0299 others(4): Show |
7 | HG02572.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.49+21852_49+21853d others(4): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44377698 | ||||||
| chr20:44377895 | G | T | 1 | a0001c0001t0063g0173 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.49+22042G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44377895 | |||||||
| chr20:44378139 | T | A | 1 | a0001c0001t0001g0246 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.49+22286T>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44378139 | |||||||
| chr20:44378198 | A | G | 3 | a0001c0001t0001g0111 a0001c0001t0002g0023 a0001c0001t0032g0024 |
3 | HG02572.hp1 HG02615.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.49+22345A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44378198 | |||||||
| chr20:44378226 | T | C | 1 | a0001c0001t0045g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.49+22373T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44378226 | |||||||
| chr20:44378271 | A | AT | 76 | a0001c0001t0001g0026 a0001c0001t0001g0032 a0001c0001t0001g0035 others(73): Show |
76 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.49+22433dupT | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44378271 | ||||||
| chr20:44378271 | AT | A | 9 | a0001c0001t0001g0111 a0001c0001t0001g0254 a0001c0001t0001g0272 others(6): Show |
9 | HG02451.hp2 HG02572.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.49+22433delT | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44378271 | ||||||
| chr20:44378512 | T | C | 7 | a0001c0001t0001g0301 a0001c0001t0002g0302 a0001c0001t0003g0299 others(4): Show |
7 | HG02572.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.49+22659T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44378512 | |||||||
| chr20:44378627 | T | G | 3 | a0001c0001t0003g0113 a0001c0001t0023g0004 a0001c0001t0052g0005 |
3 | HG00639.hp2 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.49+22774T>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44378627 | |||||||
| chr20:44378780 | G | A | 1 | a0001c0001t0001g0246 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.49+22927G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44378780 | |||||||
| chr20:44378789 | C | T | 8 | a0001c0001t0001g0254 a0001c0001t0001g0301 a0001c0001t0002g0302 others(5): Show |
8 | HG02572.hp2 HG02809.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.49+22936C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44378789 | |||||||
| chr20:44378792 | G | C | 49 | a0001c0001t0001g0110 a0001c0001t0001g0167 a0001c0001t0001g0186 others(46): Show |
50 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.49+22939G>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44378792 | |||||||
| chr20:44378848 | A | G | 7 | a0001c0001t0001g0301 a0001c0001t0002g0302 a0001c0001t0003g0299 others(4): Show |
7 | HG02572.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.49+22995A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44378848 | |||||||
| chr20:44378918 | C | CA | 6 | a0001c0001t0003g0284 a0001c0001t0004g0106 a0001c0001t0004g0303 others(3): Show |
6 | HG01361.hp1 HG02055.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.49+23081dupA | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44378918 | ||||||
| chr20:44378918 | CA | C | 81 | a0001c0001t0001g0026 a0001c0001t0001g0032 a0001c0001t0001g0035 others(78): Show |
82 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.49+23081delA | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44378918 | ||||||
| chr20:44378918 | CAA | C | 170 | a0001c0001t0001g0018 a0001c0001t0001g0111 a0001c0001t0001g0122 others(167): Show |
170 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(167): Show |
intron_variant | MODIFIER | c.49+23080_49+23081d others(4): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44378918 | ||||||
| chr20:44378918 | CAAA | C | 7 | a0001c0001t0001g0301 a0001c0001t0002g0302 a0001c0001t0003g0299 others(4): Show |
7 | HG02572.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.49+23079_49+23081d others(5): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44378918 | ||||||
| chr20:44378928 | A | G | 7 | a0001c0001t0001g0301 a0001c0001t0002g0302 a0001c0001t0003g0299 others(4): Show |
7 | HG02572.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.49+23075A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44378928 | |||||||
| chr20:44378950 | G | T | 3 | a0001c0001t0003g0113 a0001c0001t0023g0004 a0001c0001t0052g0005 |
3 | HG00639.hp2 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.49+23097G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44378950 | |||||||
| chr20:44379105 | T | A | 44 | a0001c0001t0001g0018 a0001c0001t0001g0141 a0001c0001t0001g0155 others(41): Show |
44 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.49+23252T>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44379105 | |||||||
| chr20:44379105 | T | C | 1 | a0001c0001t0058g0287 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.49+23252T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44379105 | |||||||
| chr20:44379179 | T | G | 1 | a0001c0001t0001g0254 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.49+23326T>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44379179 | |||||||
| chr20:44379219 | G | C | 7 | a0001c0001t0001g0301 a0001c0001t0002g0302 a0001c0001t0003g0299 others(4): Show |
7 | HG02572.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.49+23366G>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44379219 | |||||||
| chr20:44379251 | T | C | 1 | a0001c0001t0003g0006 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.49+23398T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44379251 | |||||||
| chr20:44379367 | C | T | 1 | a0001c0001t0033g0269 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.49+23514C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44379367 | |||||||
| chr20:44379428 | G | A | 1 | a0001c0001t0001g0254 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.49+23575G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44379428 | |||||||
| chr20:44379508 | A | C | 1 | a0001c0001t0005g0144 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.49+23655A>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44379508 | |||||||
| chr20:44379545 | T | C | 1 | a0001c0001t0010g0011 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.49+23692T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44379545 | |||||||
| chr20:44379591 | G | A | 1 | a0001c0001t0001g0254 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.49+23738G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44379591 | |||||||
| chr20:44379698 | T | G | 1 | a0001c0001t0001g0254 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.49+23845T>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44379698 | |||||||
| chr20:44379720 | T | TTC | 9 | a0001c0001t0001g0246 a0001c0001t0001g0254 a0001c0001t0001g0301 others(6): Show |
9 | HG02572.hp2 HG02809.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.49+23868_49+23869i others(4): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44379720 | ||||||
| chr20:44379728 | TC | T | 7 | a0001c0001t0001g0301 a0001c0001t0002g0302 a0001c0001t0003g0299 others(4): Show |
7 | HG02572.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.49+23877delC | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44379728 | ||||||
| chr20:44379730 | CT | C | 82 | a0001c0001t0001g0026 a0001c0001t0001g0032 a0001c0001t0001g0035 others(79): Show |
82 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.49+23898delT | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44379730 | ||||||
| chr20:44379730 | CTT | C | 101 | a0001c0001t0001g0018 a0001c0001t0001g0122 a0001c0001t0001g0126 others(98): Show |
101 | HG00438.hp1 HG00544.hp1 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.49+23897_49+23898d others(4): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44379730 | ||||||
| chr20:44379734 | T | G | 7 | a0001c0001t0001g0301 a0001c0001t0002g0302 a0001c0001t0003g0299 others(4): Show |
7 | HG02572.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.49+23881T>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44379734 | |||||||
| chr20:44379838 | A | T | 1 | a0001c0001t0003g0113 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.49+23985A>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44379838 | |||||||
| chr20:44379918 | G | A | 7 | a0001c0001t0001g0301 a0001c0001t0002g0302 a0001c0001t0003g0299 others(4): Show |
7 | HG02572.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.49+24065G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44379918 | |||||||
| chr20:44379953 | T | C | 8 | a0001c0001t0001g0254 a0001c0001t0001g0301 a0001c0001t0002g0302 others(5): Show |
8 | HG00639.hp2 HG02572.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.49+24100T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44379953 | |||||||
| chr20:44379979 | G | A | 1 | a0001c0001t0041g0221 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.49+24126G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44379979 | |||||||
| chr20:44379989 | C | T | 2 | a0001c0001t0002g0265 a0001c0001t0005g0262 |
2 | HG00140.hp2 HG00738.hp2 |
intron_variant | MODIFIER | c.49+24136C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44379989 | |||||||
| chr20:44380269 | G | A | 3 | a0001c0001t0003g0113 a0001c0001t0023g0004 a0001c0001t0052g0005 |
3 | HG00639.hp2 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.49+24416G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44380269 | |||||||
| chr20:44380317 | A | G | 1 | a0001c0001t0071g0150 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.49+24464A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44380317 | |||||||
| chr20:44380341 | C | T | 2 | a0002c0002t0001g0174 a0002c0002t0001g0175 |
2 | HG01346.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.49+24488C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44380341 | |||||||
| chr20:44380361 | C | T | 1 | a0001c0001t0028g0099 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.49+24508C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44380361 | |||||||
| chr20:44380500 | C | T | 56 | a0001c0001t0001g0110 a0001c0001t0001g0167 a0001c0001t0001g0186 others(53): Show |
57 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.49+24647C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44380500 | |||||||
| chr20:44380515 | A | T | 4 | a0001c0001t0001g0301 a0001c0001t0002g0302 a0001c0001t0003g0299 others(1): Show |
4 | HG02572.hp2 HG02818.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.49+24662A>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44380515 | |||||||
| chr20:44380519 | C | T | 106 | a0001c0001t0001g0018 a0001c0001t0001g0122 a0001c0001t0001g0126 others(103): Show |
106 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.49+24666C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44380519 | |||||||
| chr20:44380625 | G | C | 1 | a0001c0001t0024g0291 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.49+24772G>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44380625 | |||||||
| chr20:44381044 | C | CTTTGA | 253 | a0001c0001t0001g0018 a0001c0001t0001g0026 a0001c0001t0001g0032 others(250): Show |
254 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.50-25013_50-25009d others(7): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44381044 | ||||||
| chr20:44381060 | A | G | 11 | a0001c0001t0001g0111 a0001c0001t0001g0254 a0001c0001t0001g0301 others(8): Show |
11 | HG02572.hp1 HG02572.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.50-24998A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44381060 | |||||||
| chr20:44381277 | A | AG | 3 | a0001c0001t0001g0111 a0001c0001t0001g0254 a0001c0001t0032g0024 |
3 | HG02572.hp1 HG03453.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.50-24780dupG | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44381277 | ||||||
| chr20:44381279 | C | G | 1 | a0001c0001t0002g0023 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.50-24779C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44381279 | |||||||
| chr20:44381279 | C | T | 3 | a0001c0001t0001g0111 a0001c0001t0001g0254 a0001c0001t0032g0024 |
3 | HG02572.hp1 HG03453.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.50-24779C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44381279 | |||||||
| chr20:44381279 | CT | C | 232 | a0001c0001t0001g0018 a0001c0001t0001g0026 a0001c0001t0001g0032 others(229): Show |
233 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.50-24760delT | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44381279 | ||||||
| chr20:44381279 | CTT | C | 9 | a0001c0001t0001g0246 a0001c0001t0002g0039 a0001c0001t0011g0115 others(6): Show |
9 | HG01496.hp2 HG01975.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.50-24761_50-24760d others(4): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44381279 | ||||||
| chr20:44381424 | G | T | 1 | a0001c0001t0009g0149 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.50-24634G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44381424 | |||||||
| chr20:44381490 | G | A | 242 | a0001c0001t0001g0018 a0001c0001t0001g0026 a0001c0001t0001g0032 others(239): Show |
243 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.50-24568G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44381490 | |||||||
| chr20:44381661 | C | G | 1 | a0001c0001t0046g0317 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.50-24397C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44381661 | |||||||
| chr20:44381723 | G | A | 1 | a0001c0001t0002g0025 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.50-24335G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44381723 | |||||||
| chr20:44381907 | G | A | 5 | a0001c0001t0002g0064 a0001c0001t0003g0006 a0001c0001t0003g0084 others(2): Show |
5 | HG00423.hp2 HG02155.hp2 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.50-24151G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44381907 | |||||||
| chr20:44381994 | C | T | 3 | a0001c0001t0010g0208 a0001c0001t0018g0209 a0001c0001t0018g0210 |
3 | HG02647.hp1 HG02970.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.50-24064C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44381994 | |||||||
| chr20:44382063 | A | G | 1 | a0001c0001t0034g0199 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.50-23995A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44382063 | |||||||
| chr20:44382177 | C | G | 1 | a0001c0001t0001g0254 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.50-23881C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44382177 | |||||||
| chr20:44382181 | C | T | 1 | a0001c0001t0055g0118 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.50-23877C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44382181 | |||||||
| chr20:44382185 | A | G | 179 | a0001c0001t0001g0018 a0001c0001t0001g0110 a0001c0001t0001g0111 others(176): Show |
180 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.50-23873A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44382185 | |||||||
| chr20:44382215 | A | G | 1 | a0001c0001t0001g0254 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.50-23843A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44382215 | |||||||
| chr20:44382245 | C | CT | 121 | a0001c0001t0001g0018 a0001c0001t0001g0110 a0001c0001t0001g0111 others(118): Show |
122 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.50-23801dupT | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44382245 | ||||||
| chr20:44382245 | CTTTT | C | 7 | a0001c0001t0002g0228 a0001c0001t0016g0237 a0001c0001t0016g0239 others(4): Show |
7 | NA18946.hp2 NA18952.hp1 NA18994.hp2 others(4): Show |
intron_variant | MODIFIER | c.50-23804_50-23801d others(6): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44382245 | ||||||
| chr20:44382249 | T | C | 77 | a0001c0001t0001g0026 a0001c0001t0001g0032 a0001c0001t0001g0035 others(74): Show |
77 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.50-23809T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44382249 | |||||||
| chr20:44382281 | C | T | 1 | a0001c0001t0004g0270 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.50-23777C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44382281 | |||||||
| chr20:44382324 | C | T | 3 | a0001c0001t0001g0111 a0001c0001t0002g0023 a0001c0001t0032g0024 |
3 | HG02572.hp1 HG02615.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.50-23734C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44382324 | |||||||
| chr20:44382385 | C | T | 1 | a0001c0001t0002g0098 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.50-23673C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44382385 | |||||||
| chr20:44382396 | G | A | 1 | a0001c0001t0001g0246 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.50-23662G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44382396 | |||||||
| chr20:44382435 | C | A | 1 | a0001c0001t0002g0154 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.50-23623C>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44382435 | |||||||
| chr20:44382450 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.50-23608C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44382450 | |||||||
| chr20:44382529 | G | A | 16 | a0001c0001t0001g0110 a0001c0001t0001g0167 a0001c0001t0001g0186 others(13): Show |
17 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(14): Show |
intron_variant | MODIFIER | c.50-23529G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44382529 | |||||||
| chr20:44382705 | T | G | 3 | a0001c0001t0037g0009 a0001c0001t0037g0224 a0001c0001t0097g0123 |
3 | HG02145.hp2 HG02818.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.50-23353T>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44382705 | |||||||
| chr20:44382906 | C | T | 2 | a0001c0001t0001g0272 a0001c0001t0016g0273 |
2 | NA18941.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.50-23152C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44382906 | |||||||
| chr20:44382923 | C | T | 75 | a0001c0001t0001g0026 a0001c0001t0001g0032 a0001c0001t0001g0035 others(72): Show |
75 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.50-23135C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44382923 | |||||||
| chr20:44383051 | C | T | 8 | a0001c0001t0001g0026 a0001c0001t0006g0051 a0001c0001t0006g0081 others(5): Show |
8 | HG01109.hp1 HG01123.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.50-23007C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44383051 | |||||||
| chr20:44383378 | T | C | 6 | a0001c0001t0001g0110 a0001c0001t0001g0167 a0001c0001t0006g0001 others(3): Show |
7 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(4): Show |
intron_variant | MODIFIER | c.50-22680T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44383378 | |||||||
| chr20:44383451 | T | C | 2 | a0001c0001t0023g0004 a0001c0001t0052g0005 |
2 | HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.50-22607T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44383451 | |||||||
| chr20:44383489 | T | C | 6 | a0001c0001t0001g0301 a0001c0001t0002g0302 a0001c0001t0003g0299 others(3): Show |
6 | HG02572.hp2 HG02809.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.50-22569T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44383489 | |||||||
| chr20:44383549 | C | CT | 84 | a0001c0001t0001g0026 a0001c0001t0001g0032 a0001c0001t0001g0035 others(81): Show |
84 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.50-22491dupT | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44383549 | ||||||
| chr20:44383549 | CT | C | 10 | a0001c0001t0001g0183 a0001c0001t0001g0196 a0001c0001t0001g0216 others(7): Show |
10 | HG00323.hp1 HG01433.hp1 HG01515.hp2 others(7): Show |
intron_variant | MODIFIER | c.50-22491delT | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44383549 | ||||||
| chr20:44383566 | T | A | 1 | a0001c0001t0002g0232 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.50-22492T>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44383566 | |||||||
| chr20:44383567 | TA | T | 12 | a0001c0001t0001g0111 a0001c0001t0001g0301 a0001c0001t0002g0023 others(9): Show |
12 | HG02572.hp1 HG02615.hp2 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.50-22488delA | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44383567 | ||||||
| chr20:44383568 | A | T | 129 | a0001c0001t0001g0026 a0001c0001t0001g0032 a0001c0001t0001g0035 others(126): Show |
130 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.50-22490A>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44383568 | |||||||
| chr20:44383588 | C | T | 1 | a0001c0001t0071g0150 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.50-22470C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44383588 | |||||||
| chr20:44383589 | T | C | 1 | a0001c0001t0071g0150 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.50-22469T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44383589 | |||||||
| chr20:44383638 | G | A | 75 | a0001c0001t0001g0026 a0001c0001t0001g0032 a0001c0001t0001g0035 others(72): Show |
75 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.50-22420G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44383638 | |||||||
| chr20:44383638 | G | T | 6 | a0001c0001t0002g0228 a0001c0001t0016g0237 a0001c0001t0016g0239 others(3): Show |
6 | NA18946.hp2 NA18952.hp1 NA18994.hp2 others(3): Show |
intron_variant | MODIFIER | c.50-22420G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44383638 | |||||||
| chr20:44383680 | A | T | 257 | a0001c0001t0001g0018 a0001c0001t0001g0026 a0001c0001t0001g0032 others(254): Show |
258 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.50-22378A>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44383680 | |||||||
| chr20:44383857 | AT | A | 104 | a0001c0001t0001g0026 a0001c0001t0001g0032 a0001c0001t0001g0035 others(101): Show |
105 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.50-22191delT | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44383857 | ||||||
| chr20:44383862 | TTTTTTAA others(5): Show |
T | 1 | a0001c0001t0017g0292 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.50-22195_50-22184d others(14): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44383862 | |||||||
| chr20:44383914 | G | A | 2 | a0001c0001t0001g0254 a0001c0001t0038g0318 |
2 | HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.50-22144G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44383914 | |||||||
| chr20:44383918 | T | C | 1 | a0001c0001t0038g0318 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.50-22140T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44383918 | |||||||
| chr20:44384011 | C | T | 1 | a0001c0001t0017g0180 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.50-22047C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44384011 | |||||||
| chr20:44384103 | G | A | 1 | a0001c0001t0003g0295 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.50-21955G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44384103 | |||||||
| chr20:44384133 | G | A | 1 | a0001c0001t0001g0254 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.50-21925G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44384133 | |||||||
| chr20:44384152 | CT | C | 15 | a0001c0001t0001g0110 a0001c0001t0001g0167 a0001c0001t0001g0186 others(12): Show |
16 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(13): Show |
intron_variant | MODIFIER | c.50-21905delT | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44384152 | |||||||
| chr20:44384153 | T | C | 36 | a0001c0001t0001g0241 a0001c0001t0002g0098 a0001c0001t0002g0228 others(33): Show |
36 | HG00639.hp2 HG02055.hp1 HG02071.hp2 others(33): Show |
intron_variant | MODIFIER | c.50-21905T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44384153 | |||||||
| chr20:44384159 | CT | C | 83 | a0001c0001t0001g0026 a0001c0001t0001g0032 a0001c0001t0001g0035 others(80): Show |
84 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.50-21873delT | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44384159 | ||||||
| chr20:44384159 | CTT | C | 44 | a0001c0001t0001g0220 a0001c0001t0001g0241 a0001c0001t0002g0228 others(41): Show |
44 | HG00639.hp2 HG01169.hp2 HG02055.hp1 others(41): Show |
intron_variant | MODIFIER | c.50-21874_50-21873d others(4): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44384159 | ||||||
| chr20:44384159 | CTTT | C | 7 | a0001c0001t0001g0254 a0001c0001t0002g0098 a0001c0001t0012g0256 others(4): Show |
7 | HG01261.hp1 HG02165.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.50-21875_50-21873d others(5): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44384159 | ||||||
| chr20:44384159 | CTTTTTTT | C | 6 | a0001c0001t0004g0172 a0001c0001t0024g0194 a0001c0001t0035g0168 others(3): Show |
6 | HG02027.hp2 HG02630.hp1 HG03669.hp1 others(3): Show |
intron_variant | MODIFIER | c.50-21879_50-21873d others(9): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44384159 | ||||||
| chr20:44384159 | CTTTTTTT others(1): Show |
C | 98 | a0001c0001t0001g0018 a0001c0001t0001g0122 a0001c0001t0001g0126 others(95): Show |
98 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.50-21880_50-21873d others(10): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44384159 | ||||||
| chr20:44384159 | CTTTTTTT others(2): Show |
C | 6 | a0001c0001t0001g0178 a0001c0001t0004g0181 a0001c0001t0014g0188 others(3): Show |
6 | HG02109.hp2 HG02280.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.50-21881_50-21873d others(11): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44384159 | ||||||
| chr20:44384185 | T | A | 4 | a0001c0001t0002g0025 a0001c0001t0007g0090 a0001c0001t0022g0089 others(1): Show |
4 | NA18612.hp2 NA18959.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.50-21873T>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44384185 | |||||||
| chr20:44384298 | CTGTTTCA others(11): Show |
C | 1 | a0001c0001t0002g0228 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.50-21758_50-21741d others(20): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44384298 | ||||||
| chr20:44384472 | C | CA | 7 | a0001c0001t0002g0154 a0001c0001t0004g0138 a0001c0001t0006g0249 others(4): Show |
7 | HG02074.hp1 HG03516.hp2 HG03942.hp1 others(4): Show |
intron_variant | MODIFIER | c.50-21579dupA | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44384472 | ||||||
| chr20:44384574 | C | T | 1 | a0001c0001t0020g0049 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.50-21484C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44384574 | |||||||
| chr20:44384668 | G | A | 5 | a0001c0001t0002g0114 a0001c0001t0003g0148 a0001c0001t0005g0200 others(2): Show |
5 | HG02083.hp2 HG02293.hp1 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.50-21390G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44384668 | |||||||
| chr20:44384698 | T | A | 1 | a0001c0001t0004g0270 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.50-21360T>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44384698 | |||||||
| chr20:44384701 | T | C | 1 | a0001c0001t0004g0270 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.50-21357T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44384701 | |||||||
| chr20:44384709 | G | A | 1 | a0001c0001t0004g0270 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.50-21349G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44384709 | |||||||
| chr20:44384710 | A | T | 1 | a0001c0001t0004g0270 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.50-21348A>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44384710 | |||||||
| chr20:44384711 | A | C | 1 | a0001c0001t0004g0270 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.50-21347A>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44384711 | |||||||
| chr20:44384714 | A | G | 1 | a0001c0001t0004g0270 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.50-21344A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44384714 | |||||||
| chr20:44384715 | A | T | 1 | a0001c0001t0004g0270 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.50-21343A>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44384715 | |||||||
| chr20:44384766 | A | G | 2 | a0001c0001t0011g0020 a0001c0001t0013g0021 |
2 | HG02559.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.50-21292A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44384766 | |||||||
| chr20:44384987 | C | G | 1 | a0001c0001t0002g0037 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.50-21071C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44384987 | |||||||
| chr20:44385004 | G | T | 1 | a0001c0001t0004g0270 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.50-21054G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44385004 | |||||||
| chr20:44385005 | T | G | 1 | a0001c0001t0004g0270 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.50-21053T>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44385005 | |||||||
| chr20:44385057 | A | ATTTTTTT others(6): Show |
1 | a0001c0001t0023g0004 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.50-21000_50-20999i others(15): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44385057 | ||||||
| chr20:44385057 | A | ATTTTTTT others(9): Show |
1 | a0001c0001t0064g0207 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.50-21000_50-20999i others(18): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44385057 | ||||||
| chr20:44385057 | A | ATTTTTTT others(10): Show |
1 | a0001c0001t0051g0157 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.50-21000_50-20999i others(19): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44385057 | ||||||
| chr20:44385059 | C | CT | 12 | a0001c0001t0001g0230 a0001c0001t0001g0272 a0001c0001t0007g0131 others(9): Show |
12 | HG00735.hp1 HG01069.hp1 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.50-20971dupT | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44385059 | ||||||
| chr20:44385059 | C | CTTTT | 6 | a0001c0001t0012g0187 a0001c0001t0012g0311 a0001c0001t0032g0314 others(3): Show |
6 | HG02622.hp2 HG02630.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.50-20974_50-20971d others(6): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44385059 | ||||||
| chr20:44385059 | C | CTTTTTT | 11 | a0001c0001t0001g0204 a0001c0001t0001g0241 a0001c0001t0003g0223 others(8): Show |
11 | HG02818.hp2 HG02896.hp1 HG03209.hp1 others(8): Show |
intron_variant | MODIFIER | c.50-20976_50-20971d others(8): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44385059 | ||||||
| chr20:44385059 | C | CTTTTTTT | 14 | a0001c0001t0002g0098 a0001c0001t0002g0240 a0001c0001t0003g0236 others(11): Show |
14 | HG02071.hp2 HG02145.hp2 HG02165.hp1 others(11): Show |
intron_variant | MODIFIER | c.50-20977_50-20971d others(9): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44385059 | ||||||
| chr20:44385059 | C | CTTTTTTT others(3): Show |
2 | a0001c0001t0002g0065 a0001c0001t0005g0036 |
2 | HG04228.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.50-20980_50-20971d others(12): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44385059 | ||||||
| chr20:44385059 | C | CTTTTTTT others(4): Show |
2 | a0001c0001t0001g0246 a0001c0001t0007g0040 |
2 | HG02300.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.50-20981_50-20971d others(13): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44385059 | ||||||
| chr20:44385059 | C | CTTTTTTT others(5): Show |
28 | a0001c0001t0001g0035 a0001c0001t0001g0111 a0001c0001t0002g0037 others(25): Show |
28 | HG00140.hp1 HG01169.hp2 HG01255.hp2 others(25): Show |
intron_variant | MODIFIER | c.50-20982_50-20971d others(14): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44385059 | ||||||
| chr20:44385059 | C | CTTTTTTT others(6): Show |
27 | a0001c0001t0001g0032 a0001c0001t0001g0052 a0001c0001t0001g0054 others(24): Show |
27 | HG00423.hp2 HG00438.hp2 HG00673.hp2 others(24): Show |
intron_variant | MODIFIER | c.50-20983_50-20971d others(15): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44385059 | ||||||
| chr20:44385059 | C | CTTTTTTT others(7): Show |
8 | a0001c0001t0001g0067 a0001c0001t0001g0128 a0001c0001t0002g0044 others(5): Show |
8 | HG00597.hp1 HG01081.hp2 HG02083.hp2 others(5): Show |
intron_variant | MODIFIER | c.50-20984_50-20971d others(16): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44385059 | ||||||
| chr20:44385059 | C | CTTTTTTT others(8): Show |
11 | a0001c0001t0001g0018 a0001c0001t0001g0056 a0001c0001t0001g0155 others(8): Show |
11 | HG00642.hp2 HG01361.hp2 HG02132.hp2 others(8): Show |
intron_variant | MODIFIER | c.50-20985_50-20971d others(17): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44385059 | ||||||
| chr20:44385059 | C | CTTTTTTT others(9): Show |
19 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0183 others(16): Show |
19 | HG00741.hp2 HG01358.hp1 HG01496.hp2 others(16): Show |
intron_variant | MODIFIER | c.50-20986_50-20971d others(18): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44385059 | ||||||
| chr20:44385059 | C | CTTTTTTT others(10): Show |
15 | a0001c0001t0001g0141 a0001c0001t0002g0023 a0001c0001t0002g0305 others(12): Show |
15 | HG00423.hp1 HG01891.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.50-20987_50-20971d others(19): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44385059 | ||||||
| chr20:44385059 | C | CTTTTTTT others(11): Show |
13 | a0001c0001t0002g0156 a0001c0001t0002g0160 a0001c0001t0002g0193 others(10): Show |
13 | HG00438.hp1 HG00544.hp2 HG00621.hp1 others(10): Show |
intron_variant | MODIFIER | c.50-20988_50-20971d others(20): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44385059 | ||||||
| chr20:44385059 | C | CTTTTTTT others(12): Show |
7 | a0001c0001t0001g0254 a0001c0001t0002g0134 a0001c0001t0002g0152 others(4): Show |
7 | HG00597.hp2 HG02056.hp1 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.50-20989_50-20971d others(21): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44385059 | ||||||
| chr20:44385059 | C | CTTTTTTT others(13): Show |
8 | a0001c0001t0001g0126 a0001c0001t0002g0025 a0001c0001t0002g0195 others(5): Show |
8 | HG02027.hp2 HG02280.hp1 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.50-20990_50-20971d others(22): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44385059 | ||||||
| chr20:44385059 | C | CTTTTTTT others(14): Show |
9 | a0001c0001t0001g0122 a0001c0001t0001g0196 a0001c0001t0004g0172 others(6): Show |
9 | HG01074.hp1 HG01515.hp2 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.50-20991_50-20971d others(23): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44385059 | ||||||
| chr20:44385059 | C | CTTTTTTT others(15): Show |
5 | a0001c0001t0001g0178 a0001c0001t0001g0184 a0001c0001t0009g0125 others(2): Show |
5 | HG03491.hp2 HG03492.hp1 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.50-20992_50-20971d others(24): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44385059 | ||||||
| chr20:44385059 | C | CTTTTTTT others(16): Show |
4 | a0001c0001t0002g0201 a0001c0001t0030g0206 a0001c0001t0096g0252 others(1): Show |
4 | HG01346.hp2 HG03492.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.50-20993_50-20971d others(25): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44385059 | ||||||
| chr20:44385059 | C | CTTTTTTT others(17): Show |
3 | a0001c0001t0001g0203 a0001c0001t0001g0263 a0001c0001t0035g0168 |
3 | HG00735.hp2 NA19062.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.50-20994_50-20971d others(26): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44385059 | ||||||
| chr20:44385059 | C | CTTTTTTT others(18): Show |
1 | a0001c0001t0004g0166 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.50-20995_50-20971d others(27): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44385059 | ||||||
| chr20:44385059 | C | CTTTTTTT others(20): Show |
1 | a0001c0001t0001g0215 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.50-20997_50-20971d others(29): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44385059 | ||||||
| chr20:44385059 | C | CTTTTTTT others(27): Show |
1 | a0001c0001t0001g0216 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.50-20971_50-20970i others(36): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44385059 | ||||||
| chr20:44385059 | C | CTTTTTTT others(28): Show |
1 | a0001c0001t0026g0214 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.50-20971_50-20970i others(37): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44385059 | ||||||
| chr20:44385059 | C | T | 5 | a0001c0001t0011g0115 a0001c0001t0023g0004 a0001c0001t0051g0157 others(2): Show |
5 | HG02451.hp2 HG02717.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.50-20999C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44385059 | |||||||
| chr20:44385059 | CTTTTTT | C | 22 | a0001c0001t0001g0110 a0001c0001t0001g0167 a0001c0001t0001g0186 others(19): Show |
24 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(21): Show |
intron_variant | MODIFIER | c.50-20976_50-20971d others(8): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44385059 | ||||||
| chr20:44385059 | CTTTTTTT others(2): Show |
C | 9 | a0001c0001t0001g0301 a0001c0001t0002g0302 a0001c0001t0003g0299 others(6): Show |
9 | HG01167.hp2 HG02572.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.50-20979_50-20971d others(11): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44385059 | ||||||
| chr20:44385059 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0002g0114 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.50-20981_50-20971d others(13): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44385059 | ||||||
| chr20:44385168 | G | A | 1 | a0001c0001t0004g0270 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.50-20890G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44385168 | |||||||
| chr20:44385228 | T | G | 1 | a0001c0001t0004g0270 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.50-20830T>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44385228 | |||||||
| chr20:44385286 | C | T | 28 | a0001c0001t0001g0110 a0001c0001t0001g0167 a0001c0001t0001g0186 others(25): Show |
30 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(27): Show |
intron_variant | MODIFIER | c.50-20772C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44385286 | |||||||
| chr20:44385326 | A | G | 111 | a0001c0001t0001g0018 a0001c0001t0001g0122 a0001c0001t0001g0126 others(108): Show |
111 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.50-20732A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44385326 | |||||||
| chr20:44385511 | C | A | 1 | a0001c0001t0034g0199 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.50-20547C>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44385511 | |||||||
| chr20:44385573 | A | C | 1 | a0001c0001t0038g0318 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.50-20485A>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44385573 | |||||||
| chr20:44385586 | A | G | 73 | a0001c0001t0001g0110 a0001c0001t0001g0167 a0001c0001t0001g0186 others(70): Show |
75 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.50-20472A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44385586 | |||||||
| chr20:44385712 | A | G | 73 | a0001c0001t0001g0110 a0001c0001t0001g0167 a0001c0001t0001g0186 others(70): Show |
75 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.50-20346A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44385712 | |||||||
| chr20:44385720 | T | C | 1 | a0001c0001t0046g0317 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.50-20338T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44385720 | |||||||
| chr20:44385721 | G | A | 1 | a0001c0001t0046g0317 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.50-20337G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44385721 | |||||||
| chr20:44385729 | A | G | 1 | a0001c0001t0046g0317 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.50-20329A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44385729 | |||||||
| chr20:44385899 | G | A | 4 | a0001c0001t0001g0246 a0001c0001t0001g0254 a0001c0001t0011g0020 others(1): Show |
4 | HG02559.hp1 HG02896.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.50-20159G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44385899 | |||||||
| chr20:44385912 | T | G | 1 | a0001c0001t0004g0270 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.50-20146T>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44385912 | |||||||
| chr20:44385920 | C | T | 1 | a0001c0001t0001g0254 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.50-20138C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44385920 | |||||||
| chr20:44385985 | G | A | 2 | a0001c0001t0001g0272 a0001c0001t0016g0273 |
2 | NA18941.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.50-20073G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44385985 | |||||||
| chr20:44386016 | C | G | 1 | a0001c0001t0004g0270 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.50-20042C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44386016 | |||||||
| chr20:44386031 | T | TGTA | 110 | a0001c0001t0001g0018 a0001c0001t0001g0122 a0001c0001t0001g0126 others(107): Show |
110 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.50-20027_50-20026i others(5): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44386031 | |||||||
| chr20:44386085 | G | T | 28 | a0001c0001t0001g0110 a0001c0001t0001g0167 a0001c0001t0001g0186 others(25): Show |
30 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(27): Show |
intron_variant | MODIFIER | c.50-19973G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44386085 | |||||||
| chr20:44386086 | A | T | 28 | a0001c0001t0001g0110 a0001c0001t0001g0167 a0001c0001t0001g0186 others(25): Show |
30 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(27): Show |
intron_variant | MODIFIER | c.50-19972A>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44386086 | |||||||
| chr20:44386127 | A | C | 1 | a0001c0001t0002g0232 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.50-19931A>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44386127 | |||||||
| chr20:44386128 | G | A | 1 | a0001c0001t0002g0232 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.50-19930G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44386128 | |||||||
| chr20:44386130 | C | G | 4 | a0001c0001t0002g0044 a0001c0001t0002g0066 a0001c0001t0002g0102 others(1): Show |
4 | NA18948.hp2 NA18960.hp1 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.50-19928C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44386130 | |||||||
| chr20:44386152 | C | T | 1 | a0001c0001t0003g0071 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.50-19906C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44386152 | |||||||
| chr20:44386159 | A | AT | 22 | a0001c0001t0001g0122 a0001c0001t0001g0204 a0001c0001t0002g0025 others(19): Show |
22 | HG00438.hp1 HG01255.hp1 HG02027.hp2 others(19): Show |
intron_variant | MODIFIER | c.50-19874dupT | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44386159 | ||||||
| chr20:44386159 | AT | A | 112 | a0001c0001t0001g0018 a0001c0001t0001g0032 a0001c0001t0001g0035 others(109): Show |
112 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.50-19874delT | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44386159 | ||||||
| chr20:44386159 | ATT | A | 41 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0167 others(38): Show |
43 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(40): Show |
intron_variant | MODIFIER | c.50-19875_50-19874d others(4): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44386159 | ||||||
| chr20:44386220 | T | G | 2 | a0001c0001t0012g0256 a0001c0001t0054g0253 |
2 | HG01261.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.50-19838T>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44386220 | |||||||
| chr20:44386282 | C | T | 73 | a0001c0001t0001g0110 a0001c0001t0001g0167 a0001c0001t0001g0186 others(70): Show |
75 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.50-19776C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44386282 | |||||||
| chr20:44386325 | G | A | 28 | a0001c0001t0001g0110 a0001c0001t0001g0167 a0001c0001t0001g0186 others(25): Show |
30 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(27): Show |
intron_variant | MODIFIER | c.50-19733G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44386325 | |||||||
| chr20:44386326 | C | G | 1 | a0001c0001t0003g0042 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.50-19732C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44386326 | |||||||
| chr20:44386355 | C | A | 2 | a0001c0001t0011g0020 a0001c0001t0013g0021 |
2 | HG02559.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.50-19703C>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44386355 | |||||||
| chr20:44386400 | C | T | 1 | a0001c0001t0071g0150 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.50-19658C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44386400 | |||||||
| chr20:44386468 | C | G | 73 | a0001c0001t0001g0110 a0001c0001t0001g0167 a0001c0001t0001g0186 others(70): Show |
75 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.50-19590C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44386468 | |||||||
| chr20:44386478 | T | G | 1 | a0001c0001t0071g0150 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.50-19580T>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44386478 | |||||||
| chr20:44386641 | A | G | 268 | a0001c0001t0001g0018 a0001c0001t0001g0032 a0001c0001t0001g0035 others(265): Show |
270 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.50-19417A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44386641 | |||||||
| chr20:44386641 | A | T | 1 | a0001c0001t0002g0177 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.50-19417A>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44386641 | |||||||
| chr20:44386916 | C | T | 1 | a0001c0001t0001g0254 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.50-19142C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44386916 | |||||||
| chr20:44387012 | T | G | 4 | a0001c0001t0001g0128 a0001c0001t0001g0220 a0001c0001t0012g0256 others(1): Show |
4 | HG01261.hp1 HG02109.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.50-19046T>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44387012 | |||||||
| chr20:44387023 | C | G | 1 | a0001c0001t0038g0318 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.50-19035C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44387023 | |||||||
| chr20:44387025 | A | G | 47 | a0001c0001t0001g0128 a0001c0001t0001g0220 a0001c0001t0001g0241 others(44): Show |
47 | HG00639.hp2 HG01261.hp1 HG02055.hp1 others(44): Show |
intron_variant | MODIFIER | c.50-19033A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44387025 | |||||||
| chr20:44387073 | T | G | 1 | a0001c0001t0004g0270 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.50-18985T>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44387073 | |||||||
| chr20:44387114 | C | A | 1 | a0001c0001t0003g0257 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.50-18944C>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44387114 | |||||||
| chr20:44387231 | C | T | 3 | a0001c0001t0001g0111 a0001c0001t0002g0023 a0001c0001t0032g0024 |
3 | HG02572.hp1 HG02615.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.50-18827C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44387231 | |||||||
| chr20:44387237 | G | A | 7 | a0001c0001t0001g0301 a0001c0001t0002g0302 a0001c0001t0003g0299 others(4): Show |
7 | HG02572.hp2 HG02717.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.50-18821G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44387237 | |||||||
| chr20:44387242 | C | T | 3 | a0001c0001t0013g0021 a0001c0001t0063g0173 a0001c0001t0067g0171 |
3 | HG02559.hp1 HG02886.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.50-18816C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44387242 | |||||||
| chr20:44387288 | T | TA | 39 | a0001c0001t0001g0032 a0001c0001t0001g0104 a0001c0001t0001g0111 others(36): Show |
39 | HG00597.hp1 HG00621.hp2 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.50-18745dupA | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44387288 | ||||||
| chr20:44387288 | TA | T | 27 | a0001c0001t0001g0035 a0001c0001t0001g0204 a0001c0001t0001g0289 others(24): Show |
27 | HG00140.hp1 HG00597.hp2 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.50-18745delA | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44387288 | ||||||
| chr20:44387288 | TAAA | T | 23 | a0001c0001t0001g0110 a0001c0001t0001g0167 a0001c0001t0001g0186 others(20): Show |
25 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.50-18747_50-18745d others(5): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44387288 | ||||||
| chr20:44387288 | TAAAAAAA others(3): Show |
T | 35 | a0001c0001t0001g0241 a0001c0001t0001g0246 a0001c0001t0002g0098 others(32): Show |
35 | HG00639.hp2 HG01433.hp1 HG02055.hp1 others(32): Show |
intron_variant | MODIFIER | c.50-18754_50-18745d others(12): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44387288 | ||||||
| chr20:44387288 | TAAAAAAA others(4): Show |
T | 2 | a0001c0001t0002g0228 a0001c0001t0097g0123 |
2 | HG02818.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.50-18755_50-18745d others(13): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44387288 | ||||||
| chr20:44387344 | G | A | 2 | a0001c0001t0018g0307 a0001c0001t0084g0306 |
2 | HG02451.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.50-18714G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44387344 | |||||||
| chr20:44387395 | G | A | 1 | a0001c0001t0045g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.50-18663G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44387395 | |||||||
| chr20:44387406 | G | A | 1 | a0001c0001t0038g0318 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.50-18652G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44387406 | |||||||
| chr20:44387645 | T | C | 1 | a0001c0001t0001g0246 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.50-18413T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44387645 | |||||||
| chr20:44387655 | C | CG | 100 | a0001c0001t0001g0018 a0001c0001t0001g0026 a0001c0001t0001g0054 others(97): Show |
100 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.50-18391dupG | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44387655 | ||||||
| chr20:44387655 | C | CGG | 51 | a0001c0001t0001g0122 a0001c0001t0001g0126 a0001c0001t0001g0141 others(48): Show |
51 | HG00621.hp2 HG00642.hp1 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.50-18392_50-18391d others(4): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44387655 | ||||||
| chr20:44387655 | C | CGGG | 26 | a0001c0001t0001g0110 a0001c0001t0001g0155 a0001c0001t0001g0167 others(23): Show |
27 | HG00280.hp2 HG00738.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.50-18393_50-18391d others(5): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44387655 | ||||||
| chr20:44387655 | CG | C | 18 | a0001c0001t0001g0220 a0001c0001t0002g0102 a0001c0001t0002g0112 others(15): Show |
18 | HG01258.hp2 HG02015.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.50-18391delG | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44387655 | ||||||
| chr20:44387658 | G | C | 2 | a0001c0001t0001g0104 a0001c0001t0013g0021 |
2 | HG02559.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.50-18400G>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44387658 | |||||||
| chr20:44387658 | G | GC | 6 | a0001c0001t0002g0133 a0001c0001t0002g0156 a0001c0001t0002g0160 others(3): Show |
6 | HG00621.hp1 HG00673.hp1 HG02083.hp1 others(3): Show |
intron_variant | MODIFIER | c.50-18400_50-18399i others(3): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44387658 | |||||||
| chr20:44387660 | G | C | 1 | a0001c0001t0096g0252 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.50-18398G>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44387660 | |||||||
| chr20:44387661 | G | T | 2 | a0001c0001t0003g0042 a0001c0001t0005g0198 |
2 | HG02015.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.50-18397G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44387661 | |||||||
| chr20:44387662 | G | T | 1 | a0001c0001t0012g0061 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.50-18396G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44387662 | |||||||
| chr20:44387665 | G | A | 2 | a0001c0001t0002g0228 a0001c0001t0097g0123 |
2 | HG02818.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.50-18393G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44387665 | |||||||
| chr20:44387668 | A | C | 1 | a0001c0001t0097g0123 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.50-18390A>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44387668 | |||||||
| chr20:44387668 | A | G | 5 | a0001c0001t0009g0179 a0001c0001t0017g0292 a0001c0001t0021g0278 others(2): Show |
5 | HG03834.hp1 NA18964.hp1 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.50-18390A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44387668 | |||||||
| chr20:44387670 | G | C | 1 | a0001c0001t0002g0228 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.50-18388G>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44387670 | |||||||
| chr20:44387670 | G | GGC | 3 | a0001c0001t0035g0043 a0001c0001t0071g0150 a0008c0008t0005g0282 |
3 | NA18979.hp1 NA19058.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.50-18388_50-18387i others(4): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44387670 | |||||||
| chr20:44387671 | C | CG | 44 | a0001c0001t0001g0032 a0001c0001t0001g0128 a0001c0001t0001g0178 others(41): Show |
44 | HG00597.hp1 HG01069.hp2 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.50-18379dupG | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44387671 | ||||||
| chr20:44387671 | C | G | 4 | a0001c0001t0017g0292 a0001c0001t0035g0043 a0001c0001t0071g0150 others(1): Show |
4 | NA18979.hp1 NA18994.hp1 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.50-18387C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44387671 | |||||||
| chr20:44387680 | C | G | 1 | a0001c0001t0001g0196 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.50-18378C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44387680 | |||||||
| chr20:44387680 | C | T | 1 | a0004c0006t0023g0105 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.50-18378C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44387680 | |||||||
| chr20:44387683 | T | C | 75 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0052 others(72): Show |
75 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.50-18375T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44387683 | |||||||
| chr20:44387689 | G | C | 1 | a0001c0001t0058g0287 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.50-18369G>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44387689 | |||||||
| chr20:44387721 | T | TA | 17 | a0001c0001t0001g0128 a0001c0001t0001g0196 a0001c0001t0001g0246 others(14): Show |
17 | HG01256.hp1 HG01261.hp1 HG01515.hp2 others(14): Show |
intron_variant | MODIFIER | c.50-18324dupA | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44387721 | ||||||
| chr20:44387721 | T | TAA | 92 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0052 others(89): Show |
94 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(91): Show |
intron_variant | MODIFIER | c.50-18325_50-18324d others(4): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44387721 | ||||||
| chr20:44387735 | G | A | 1 | a0001c0001t0098g0080 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.50-18323G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44387735 | |||||||
| chr20:44388090 | AT | A | 12 | a0001c0001t0001g0128 a0001c0001t0001g0220 a0001c0001t0001g0246 others(9): Show |
12 | HG01261.hp1 HG02109.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.50-17957delT | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44388090 | ||||||
| chr20:44388102 | A | T | 1 | a0001c0001t0005g0293 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.50-17956A>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44388102 | |||||||
| chr20:44388111 | C | CA | 168 | a0001c0001t0001g0018 a0001c0001t0001g0111 a0001c0001t0001g0122 others(165): Show |
168 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.50-17946dupA | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44388111 | ||||||
| chr20:44388269 | T | A | 1 | a0001c0001t0004g0270 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.50-17789T>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44388269 | |||||||
| chr20:44388273 | T | G | 203 | a0001c0001t0001g0018 a0001c0001t0001g0111 a0001c0001t0001g0122 others(200): Show |
203 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(200): Show |
intron_variant | MODIFIER | c.50-17785T>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44388273 | |||||||
| chr20:44388278 | C | T | 202 | a0001c0001t0001g0018 a0001c0001t0001g0111 a0001c0001t0001g0122 others(199): Show |
202 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.50-17780C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44388278 | |||||||
| chr20:44388360 | C | T | 2 | a0001c0001t0003g0299 a0004c0006t0023g0105 |
2 | HG02572.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.50-17698C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44388360 | |||||||
| chr20:44388371 | G | GCACCCCC others(9): Show |
1 | a0001c0001t0044g0116 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.50-17687_50-17686i others(18): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44388371 | |||||||
| chr20:44388372 | A | AC | 24 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0128 others(21): Show |
24 | HG00140.hp1 HG00438.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.50-17678dupC | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44388372 | ||||||
| chr20:44388372 | A | ACCCCCCC others(2): Show |
20 | a0001c0001t0001g0111 a0001c0001t0001g0163 a0001c0001t0001g0216 others(17): Show |
20 | HG00323.hp1 HG00735.hp2 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.50-17678_50-17677i others(11): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44388372 | ||||||
| chr20:44388372 | A | ACCCCCCC others(3): Show |
20 | a0001c0001t0001g0164 a0001c0001t0001g0215 a0001c0001t0002g0074 others(17): Show |
20 | HG00280.hp1 HG01358.hp1 HG01358.hp2 others(17): Show |
intron_variant | MODIFIER | c.50-17678_50-17677i others(12): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44388372 | ||||||
| chr20:44388372 | A | ACCCCCCC others(4): Show |
16 | a0001c0001t0001g0241 a0001c0001t0002g0195 a0001c0001t0008g0135 others(13): Show |
16 | HG02071.hp2 HG02280.hp1 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.50-17678_50-17677i others(13): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44388372 | ||||||
| chr20:44388372 | A | ACCCCCCC others(5): Show |
21 | a0001c0001t0001g0183 a0001c0001t0002g0025 a0001c0001t0002g0134 others(18): Show |
21 | HG00544.hp2 HG00621.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.50-17678_50-17677i others(14): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44388372 | ||||||
| chr20:44388372 | A | ACCCCCCC others(6): Show |
23 | a0001c0001t0001g0204 a0001c0001t0001g0260 a0001c0001t0002g0305 others(20): Show |
23 | HG00438.hp1 HG00544.hp1 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.50-17678_50-17677i others(15): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44388372 | ||||||
| chr20:44388372 | A | ACCCCCCC others(7): Show |
31 | a0001c0001t0001g0155 a0001c0001t0001g0178 a0001c0001t0001g0272 others(28): Show |
31 | HG00597.hp1 HG00741.hp2 HG01346.hp2 others(28): Show |
intron_variant | MODIFIER | c.50-17678_50-17677i others(16): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44388372 | ||||||
| chr20:44388372 | A | ACCCCCCC others(8): Show |
16 | a0001c0001t0001g0122 a0001c0001t0001g0316 a0001c0001t0003g0055 others(13): Show |
16 | HG00423.hp1 HG00597.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.50-17678_50-17677i others(17): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44388372 | ||||||
| chr20:44388372 | A | ACCCCCCC others(9): Show |
8 | a0001c0001t0001g0126 a0001c0001t0001g0141 a0001c0001t0002g0232 others(5): Show |
8 | HG02074.hp1 HG02074.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.50-17678_50-17677i others(18): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44388372 | ||||||
| chr20:44388372 | A | ACCCCCCC others(10): Show |
5 | a0001c0001t0001g0203 a0001c0001t0002g0023 a0001c0001t0004g0158 others(2): Show |
5 | HG02300.hp1 HG02615.hp2 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.50-17678_50-17677i others(19): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44388372 | ||||||
| chr20:44388372 | A | ACCCCCCC others(11): Show |
2 | a0001c0001t0005g0200 a0001c0001t0035g0168 |
2 | HG02293.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.50-17678_50-17677i others(20): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44388372 | ||||||
| chr20:44388372 | A | ACCCCCCC others(12): Show |
2 | a0001c0001t0001g0184 a0001c0012t0008g0007 |
2 | NA18906.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.50-17678_50-17677i others(21): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44388372 | ||||||
| chr20:44388372 | A | ACCCCCCC others(13): Show |
4 | a0001c0001t0001g0018 a0001c0001t0002g0177 a0001c0001t0004g0106 others(1): Show |
4 | HG01361.hp1 HG01361.hp2 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.50-17678_50-17677i others(22): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44388372 | ||||||
| chr20:44388372 | A | ACCCCCCC others(9): Show |
1 | a0001c0001t0002g0154 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.50-17678_50-17677i others(18): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44388372 | ||||||
| chr20:44388372 | A | C | 1 | a0001c0001t0044g0116 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.50-17686A>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44388372 | |||||||
| chr20:44388374 | C | CCCCCCCC others(23): Show |
1 | a0001c0001t0036g0129 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.50-17678_50-17677i others(32): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44388374 | ||||||
| chr20:44388380 | C | CCCCCCCC others(10): Show |
1 | a0001c0001t0001g0196 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.50-17678_50-17677i others(19): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44388380 | |||||||
| chr20:44388381 | A | C | 216 | a0001c0001t0001g0018 a0001c0001t0001g0032 a0001c0001t0001g0035 others(213): Show |
216 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.50-17677A>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44388381 | |||||||
| chr20:44388381 | A | G | 2 | a0001c0001t0001g0246 a0001c0001t0011g0020 |
2 | HG02896.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.50-17677A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44388381 | |||||||
| chr20:44388382 | C | A | 1 | a0001c0001t0002g0240 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.50-17676C>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44388382 | |||||||
| chr20:44388383 | C | CCCCCCCC others(18): Show |
1 | a0001c0001t0002g0228 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.50-17672_50-17671i others(27): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44388383 | ||||||
| chr20:44388430 | T | G | 1 | a0001c0001t0004g0270 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.50-17628T>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44388430 | |||||||
| chr20:44388431 | G | T | 1 | a0001c0001t0004g0270 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.50-17627G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44388431 | |||||||
| chr20:44388476 | C | T | 26 | a0001c0001t0001g0241 a0001c0001t0002g0098 a0001c0001t0002g0195 others(23): Show |
26 | HG02071.hp2 HG02145.hp2 HG02165.hp1 others(23): Show |
intron_variant | MODIFIER | c.50-17582C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44388476 | |||||||
| chr20:44388644 | G | T | 5 | a0001c0001t0001g0301 a0001c0001t0002g0302 a0001c0001t0004g0300 others(2): Show |
5 | HG02717.hp2 HG02818.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.50-17414G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44388644 | |||||||
| chr20:44388899 | C | A | 1 | a0001c0001t0038g0146 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.50-17159C>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44388899 | |||||||
| chr20:44388908 | C | T | 3 | a0001c0001t0001g0220 a0001c0001t0023g0004 a0001c0001t0052g0005 |
3 | HG02922.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.50-17150C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44388908 | |||||||
| chr20:44389018 | C | A | 1 | a0001c0001t0009g0125 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.50-17040C>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44389018 | |||||||
| chr20:44389133 | T | G | 1 | a0001c0001t0006g0249 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.50-16925T>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44389133 | |||||||
| chr20:44389186 | C | G | 1 | a0001c0001t0011g0020 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.50-16872C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44389186 | |||||||
| chr20:44389439 | C | T | 3 | a0001c0001t0003g0095 a0001c0001t0003g0097 a0001c0001t0059g0096 |
3 | HG00099.hp2 HG00323.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.50-16619C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44389439 | |||||||
| chr20:44389616 | T | C | 1 | a0001c0001t0002g0201 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.50-16442T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44389616 | |||||||
| chr20:44389620 | G | A | 62 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0052 others(59): Show |
62 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.50-16438G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44389620 | |||||||
| chr20:44389737 | G | T | 1 | a0001c0001t0004g0270 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.50-16321G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44389737 | |||||||
| chr20:44389738 | T | C | 1 | a0001c0001t0004g0270 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.50-16320T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44389738 | |||||||
| chr20:44389904 | G | C | 1 | a0001c0001t0028g0099 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.50-16154G>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44389904 | |||||||
| chr20:44390107 | A | G | 1 | a0001c0001t0005g0036 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.50-15951A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44390107 | |||||||
| chr20:44390112 | C | G | 1 | a0001c0001t0004g0270 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.50-15946C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44390112 | |||||||
| chr20:44390210 | G | A | 1 | a0001c0001t0011g0020 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.50-15848G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44390210 | |||||||
| chr20:44390299 | A | T | 1 | a0001c0001t0004g0270 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.50-15759A>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44390299 | |||||||
| chr20:44390517 | T | A | 1 | a0001c0001t0004g0270 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.50-15541T>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44390517 | |||||||
| chr20:44390518 | T | C | 1 | a0001c0001t0004g0270 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.50-15540T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44390518 | |||||||
| chr20:44390520 | A | C | 1 | a0001c0001t0004g0270 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.50-15538A>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44390520 | |||||||
| chr20:44390521 | G | T | 1 | a0001c0001t0004g0270 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.50-15537G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44390521 | |||||||
| chr20:44390522 | G | A | 1 | a0001c0001t0004g0270 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.50-15536G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44390522 | |||||||
| chr20:44390526 | T | C | 1 | a0001c0001t0004g0270 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.50-15532T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44390526 | |||||||
| chr20:44390527 | A | G | 1 | a0001c0001t0004g0270 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.50-15531A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44390527 | |||||||
| chr20:44390528 | A | C | 1 | a0001c0001t0004g0270 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.50-15530A>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44390528 | |||||||
| chr20:44390529 | C | G | 1 | a0001c0001t0004g0270 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.50-15529C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44390529 | |||||||
| chr20:44390531 | C | G | 1 | a0001c0001t0004g0270 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.50-15527C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44390531 | |||||||
| chr20:44390538 | G | T | 1 | a0001c0001t0004g0270 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.50-15520G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44390538 | |||||||
| chr20:44390634 | A | G | 1 | a0001c0001t0004g0270 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.50-15424A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44390634 | |||||||
| chr20:44391065 | A | T | 1 | a0001c0001t0001g0246 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.50-14993A>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44391065 | |||||||
| chr20:44391066 | A | G | 1 | a0001c0001t0003g0223 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.50-14992A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44391066 | |||||||
| chr20:44391069 | A | G | 21 | a0001c0001t0001g0052 a0001c0001t0001g0054 a0001c0001t0001g0056 others(18): Show |
21 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(18): Show |
intron_variant | MODIFIER | c.50-14989A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44391069 | |||||||
| chr20:44391072 | C | T | 1 | a0001c0001t0078g0258 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.50-14986C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44391072 | |||||||
| chr20:44391095 | C | T | 1 | a0001c0001t0052g0005 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.50-14963C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44391095 | |||||||
| chr20:44391167 | G | T | 1 | a0001c0001t0002g0023 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.50-14891G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44391167 | |||||||
| chr20:44391183 | T | C | 6 | a0001c0001t0004g0181 a0001c0001t0008g0135 a0001c0001t0008g0136 others(3): Show |
6 | HG01884.hp2 HG02109.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.50-14875T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44391183 | |||||||
| chr20:44391231 | C | G | 1 | a0001c0001t0038g0146 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.50-14827C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44391231 | |||||||
| chr20:44391407 | G | T | 1 | a0001c0001t0001g0263 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.50-14651G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44391407 | |||||||
| chr20:44391463 | A | G | 122 | a0001c0001t0001g0054 a0001c0001t0001g0056 a0001c0001t0001g0067 others(119): Show |
124 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.50-14595A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44391463 | |||||||
| chr20:44391510 | T | C | 10 | a0001c0001t0001g0128 a0001c0001t0001g0178 a0001c0001t0001g0246 others(7): Show |
10 | HG00639.hp2 HG01074.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.50-14548T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44391510 | |||||||
| chr20:44391519 | G | A | 1 | a0001c0001t0001g0246 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.50-14539G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44391519 | |||||||
| chr20:44391523 | C | T | 1 | a0001c0001t0002g0039 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.50-14535C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44391523 | |||||||
| chr20:44391837 | A | G | 1 | a0001c0001t0011g0020 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.50-14221A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44391837 | |||||||
| chr20:44391928 | C | T | 13 | a0001c0001t0001g0301 a0001c0001t0002g0302 a0001c0001t0004g0300 others(10): Show |
13 | HG02055.hp1 HG02451.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.50-14130C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44391928 | |||||||
| chr20:44392029 | G | A | 1 | a0001c0001t0052g0005 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.50-14029G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44392029 | |||||||
| chr20:44392061 | T | G | 1 | a0001c0001t0006g0109 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.50-13997T>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44392061 | |||||||
| chr20:44392196 | T | G | 2 | a0001c0001t0001g0128 a0001c0001t0038g0318 |
2 | HG02109.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.50-13862T>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44392196 | |||||||
| chr20:44392215 | C | G | 1 | a0001c0001t0007g0034 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.50-13843C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44392215 | |||||||
| chr20:44392229 | T | C | 12 | a0001c0001t0001g0301 a0001c0001t0002g0302 a0001c0001t0004g0300 others(9): Show |
12 | HG02055.hp1 HG02451.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.50-13829T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44392229 | |||||||
| chr20:44392244 | G | A | 1 | a0001c0001t0049g0127 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.50-13814G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44392244 | |||||||
| chr20:44392257 | G | GT | 12 | a0001c0001t0001g0301 a0001c0001t0002g0302 a0001c0001t0004g0300 others(9): Show |
12 | HG02055.hp1 HG02451.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.50-13800dupT | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44392257 | ||||||
| chr20:44392266 | C | T | 1 | a0001c0001t0011g0100 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.50-13792C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44392266 | |||||||
| chr20:44392284 | T | C | 4 | a0001c0001t0002g0044 a0001c0001t0002g0066 a0001c0001t0002g0102 others(1): Show |
4 | NA18948.hp2 NA18960.hp1 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.50-13774T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44392284 | |||||||
| chr20:44392302 | G | A | 2 | a0001c0001t0001g0128 a0001c0001t0038g0318 |
2 | HG02109.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.50-13756G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44392302 | |||||||
| chr20:44392417 | C | T | 4 | a0001c0001t0002g0044 a0001c0001t0002g0066 a0001c0001t0002g0102 others(1): Show |
4 | NA18948.hp2 NA18960.hp1 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.50-13641C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44392417 | |||||||
| chr20:44392574 | G | A | 24 | a0001c0001t0001g0167 a0001c0001t0001g0186 a0001c0001t0001g0246 others(21): Show |
25 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(22): Show |
intron_variant | MODIFIER | c.50-13484G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44392574 | |||||||
| chr20:44392583 | A | G | 24 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0003g0280 others(21): Show |
24 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.50-13475A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44392583 | |||||||
| chr20:44392816 | T | C | 276 | a0001c0001t0001g0018 a0001c0001t0001g0032 a0001c0001t0001g0035 others(273): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.50-13242T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44392816 | |||||||
| chr20:44392885 | C | T | 2 | a0001c0001t0008g0003 a0001c0001t0008g0261 |
3 | HG01256.hp2 HG01258.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.50-13173C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44392885 | |||||||
| chr20:44393184 | G | A | 1 | a0001c0001t0038g0318 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.50-12874G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44393184 | |||||||
| chr20:44393188 | C | G | 1 | a0001c0001t0080g0304 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.50-12870C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44393188 | |||||||
| chr20:44393395 | G | A | 4 | a0001c0001t0002g0134 a0001c0001t0003g0006 a0001c0001t0005g0144 others(1): Show |
4 | HG00438.hp1 NA18988.hp2 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.50-12663G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44393395 | |||||||
| chr20:44393469 | T | G | 5 | a0001c0001t0004g0181 a0001c0001t0008g0135 a0001c0001t0008g0136 others(2): Show |
5 | HG01261.hp1 HG01884.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.50-12589T>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44393469 | |||||||
| chr20:44393482 | T | C | 2 | a0001c0001t0001g0184 a0001c0001t0011g0100 |
2 | HG01256.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.50-12576T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44393482 | |||||||
| chr20:44393503 | A | G | 2 | a0001c0001t0002g0023 a0001c0001t0032g0024 |
2 | HG02615.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.50-12555A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44393503 | |||||||
| chr20:44393570 | G | C | 4 | a0001c0001t0006g0271 a0001c0001t0011g0117 a0001c0001t0044g0116 others(1): Show |
4 | HG02602.hp1 HG02630.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.50-12488G>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44393570 | |||||||
| chr20:44393676 | C | T | 1 | a0001c0001t0077g0162 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.50-12382C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44393676 | |||||||
| chr20:44393807 | A | G | 2 | a0001c0001t0002g0023 a0001c0001t0032g0024 |
2 | HG02615.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.50-12251A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44393807 | |||||||
| chr20:44393818 | G | C | 1 | a0001c0001t0001g0196 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.50-12240G>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44393818 | |||||||
| chr20:44393892 | T | A | 1 | a0001c0001t0050g0031 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.50-12166T>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44393892 | |||||||
| chr20:44394227 | A | G | 3 | a0001c0001t0008g0008 a0001c0001t0008g0059 a0001c0012t0008g0007 |
3 | HG01884.hp1 HG03209.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.50-11831A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44394227 | |||||||
| chr20:44394233 | C | T | 12 | a0001c0001t0001g0301 a0001c0001t0002g0302 a0001c0001t0004g0300 others(9): Show |
12 | HG02055.hp1 HG02451.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.50-11825C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44394233 | |||||||
| chr20:44394280 | C | A | 12 | a0001c0001t0001g0301 a0001c0001t0002g0302 a0001c0001t0004g0300 others(9): Show |
12 | HG02055.hp1 HG02451.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.50-11778C>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44394280 | |||||||
| chr20:44394289 | C | T | 12 | a0001c0001t0001g0301 a0001c0001t0002g0302 a0001c0001t0004g0300 others(9): Show |
12 | HG02055.hp1 HG02451.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.50-11769C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44394289 | |||||||
| chr20:44394355 | T | C | 4 | a0001c0001t0006g0271 a0001c0001t0011g0117 a0001c0001t0044g0116 others(1): Show |
4 | HG02602.hp1 HG02630.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.50-11703T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44394355 | |||||||
| chr20:44394749 | G | A | 1 | a0001c0001t0001g0220 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.50-11309G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44394749 | |||||||
| chr20:44394784 | C | A | 1 | a0001c0001t0001g0230 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.50-11274C>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44394784 | |||||||
| chr20:44394788 | G | A | 1 | a0001c0001t0019g0170 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.50-11270G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44394788 | |||||||
| chr20:44394941 | G | C | 1 | a0001c0001t0001g0203 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.50-11117G>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44394941 | |||||||
| chr20:44394943 | C | G | 6 | a0001c0001t0001g0155 a0001c0001t0001g0163 a0001c0001t0001g0164 others(3): Show |
6 | HG01358.hp1 HG02280.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.50-11115C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44394943 | |||||||
| chr20:44395072 | A | G | 2 | a0001c0001t0002g0023 a0001c0001t0032g0024 |
2 | HG02615.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.50-10986A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44395072 | |||||||
| chr20:44395201 | A | G | 122 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0052 others(119): Show |
123 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(120): Show |
intron_variant | MODIFIER | c.50-10857A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44395201 | |||||||
| chr20:44395229 | G | T | 2 | a0001c0001t0001g0220 a0001c0001t0003g0113 |
2 | HG00639.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.50-10829G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44395229 | |||||||
| chr20:44395267 | C | T | 3 | a0001c0001t0055g0118 a0001c0001t0087g0108 a0001c0001t0089g0107 |
3 | HG01891.hp1 HG02055.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.50-10791C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44395267 | |||||||
| chr20:44395353 | G | T | 1 | a0001c0001t0001g0203 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.50-10705G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44395353 | |||||||
| chr20:44395368 | T | C | 123 | a0001c0001t0001g0018 a0001c0001t0001g0104 a0001c0001t0001g0122 others(120): Show |
124 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.50-10690T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44395368 | |||||||
| chr20:44395403 | G | T | 1 | a0001c0001t0038g0318 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.50-10655G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44395403 | |||||||
| chr20:44395409 | G | T | 115 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0052 others(112): Show |
116 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(113): Show |
intron_variant | MODIFIER | c.50-10649G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44395409 | |||||||
| chr20:44395565 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.50-10493C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44395565 | |||||||
| chr20:44395622 | A | G | 1 | a0001c0001t0001g0203 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.50-10436A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44395622 | |||||||
| chr20:44395624 | G | A | 1 | a0001c0001t0001g0203 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.50-10434G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44395624 | |||||||
| chr20:44395626 | A | G | 1 | a0001c0001t0001g0203 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.50-10432A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44395626 | |||||||
| chr20:44396117 | G | C | 2 | a0001c0001t0014g0227 a0001c0001t0014g0229 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.50-9941G>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44396117 | |||||||
| chr20:44396147 | G | A | 2 | a0001c0001t0031g0145 a0001c0001t0031g0153 |
2 | HG02809.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.50-9911G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44396147 | |||||||
| chr20:44396148 | G | A | 1 | a0001c0001t0003g0113 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.50-9910G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44396148 | |||||||
| chr20:44396174 | G | A | 3 | a0001c0001t0001g0122 a0001c0001t0001g0178 a0001c0001t0082g0169 |
3 | HG01074.hp1 HG03492.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.50-9884G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44396174 | |||||||
| chr20:44396239 | G | A | 1 | a0001c0001t0071g0150 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.50-9819G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44396239 | |||||||
| chr20:44396436 | A | G | 2 | a0001c0001t0001g0220 a0001c0001t0003g0113 |
2 | HG00639.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.50-9622A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44396436 | |||||||
| chr20:44396467 | G | A | 2 | a0001c0001t0001g0220 a0001c0001t0003g0113 |
2 | HG00639.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.50-9591G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44396467 | |||||||
| chr20:44396475 | T | C | 1 | a0001c0001t0076g0094 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.50-9583T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44396475 | |||||||
| chr20:44396708 | G | A | 2 | a0001c0001t0001g0220 a0001c0001t0003g0113 |
2 | HG00639.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.50-9350G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44396708 | |||||||
| chr20:44396910 | C | T | 2 | a0001c0001t0001g0220 a0001c0001t0003g0113 |
2 | HG00639.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.50-9148C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44396910 | |||||||
| chr20:44396933 | A | C | 4 | a0001c0001t0001g0301 a0001c0001t0002g0302 a0001c0001t0004g0300 others(1): Show |
4 | HG02717.hp2 HG02818.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.50-9125A>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44396933 | |||||||
| chr20:44396955 | T | C | 2 | a0001c0001t0001g0220 a0001c0001t0003g0113 |
2 | HG00639.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.50-9103T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44396955 | |||||||
| chr20:44396965 | T | C | 24 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0003g0280 others(21): Show |
24 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.50-9093T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44396965 | |||||||
| chr20:44397025 | T | A | 1 | a0001c0001t0022g0089 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.50-9033T>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44397025 | |||||||
| chr20:44397026 | A | T | 1 | a0001c0001t0022g0089 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.50-9032A>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44397026 | |||||||
| chr20:44397144 | T | C | 134 | a0001c0001t0001g0018 a0001c0001t0001g0104 a0001c0001t0001g0122 others(131): Show |
135 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(132): Show |
intron_variant | MODIFIER | c.50-8914T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44397144 | |||||||
| chr20:44397272 | C | T | 2 | a0001c0001t0001g0220 a0001c0001t0003g0113 |
2 | HG00639.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.50-8786C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44397272 | |||||||
| chr20:44397338 | G | A | 4 | a0001c0001t0001g0119 a0001c0001t0002g0037 a0001c0001t0022g0076 others(1): Show |
4 | HG02135.hp2 NA18612.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.50-8720G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44397338 | |||||||
| chr20:44397347 | T | A | 2 | a0001c0001t0033g0269 a0001c0001t0080g0304 |
2 | HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.50-8711T>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44397347 | |||||||
| chr20:44397473 | C | G | 1 | a0001c0001t0037g0009 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.50-8585C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44397473 | |||||||
| chr20:44397973 | T | A | 1 | a0001c0001t0018g0307 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.50-8085T>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44397973 | |||||||
| chr20:44397976 | T | C | 136 | a0001c0001t0001g0018 a0001c0001t0001g0104 a0001c0001t0001g0122 others(133): Show |
137 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(134): Show |
intron_variant | MODIFIER | c.50-8082T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44397976 | |||||||
| chr20:44397989 | C | T | 271 | a0001c0001t0001g0018 a0001c0001t0001g0032 a0001c0001t0001g0035 others(268): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.50-8069C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44397989 | |||||||
| chr20:44398035 | C | T | 2 | a0001c0001t0030g0205 a0001c0001t0030g0206 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.50-8023C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44398035 | |||||||
| chr20:44398148 | G | A | 2 | a0001c0001t0001g0220 a0001c0001t0003g0113 |
2 | HG00639.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.50-7910G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44398148 | |||||||
| chr20:44398500 | A | T | 1 | a0001c0001t0007g0041 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.50-7558A>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44398500 | |||||||
| chr20:44398562 | T | C | 2 | a0001c0001t0052g0005 a0001c0001t0063g0173 |
2 | HG03453.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.50-7496T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44398562 | |||||||
| chr20:44398803 | C | T | 1 | a0001c0001t0020g0159 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.50-7255C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44398803 | |||||||
| chr20:44398870 | A | G | 116 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0052 others(113): Show |
117 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(114): Show |
intron_variant | MODIFIER | c.50-7188A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44398870 | |||||||
| chr20:44399114 | T | C | 5 | a0001c0001t0001g0220 a0001c0001t0006g0271 a0001c0001t0011g0117 others(2): Show |
5 | HG02602.hp1 HG02630.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.50-6944T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44399114 | |||||||
| chr20:44399210 | CAT | C | 29 | a0001c0001t0001g0104 a0001c0001t0001g0122 a0001c0001t0001g0178 others(26): Show |
29 | HG00741.hp2 HG01074.hp1 HG01074.hp2 others(26): Show |
intron_variant | MODIFIER | c.50-6846_50-6845del others(2): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44399210 | ||||||
| chr20:44399397 | A | G | 225 | a0001c0001t0001g0018 a0001c0001t0001g0032 a0001c0001t0001g0035 others(222): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.50-6661A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44399397 | |||||||
| chr20:44399398 | T | C | 34 | a0001c0001t0001g0104 a0001c0001t0001g0122 a0001c0001t0001g0178 others(31): Show |
34 | HG00639.hp2 HG00741.hp2 HG01074.hp1 others(31): Show |
intron_variant | MODIFIER | c.50-6660T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44399398 | |||||||
| chr20:44399438 | T | C | 1 | a0001c0001t0038g0318 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.50-6620T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44399438 | |||||||
| chr20:44399531 | A | G | 1 | a0001c0001t0001g0104 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.50-6527A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44399531 | |||||||
| chr20:44399565 | C | T | 1 | a0001c0001t0011g0185 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.50-6493C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44399565 | |||||||
| chr20:44399603 | G | A | 1 | a0001c0001t0055g0118 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.50-6455G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44399603 | |||||||
| chr20:44399666 | C | A | 47 | a0001c0001t0001g0026 a0001c0001t0001g0126 a0001c0001t0001g0183 others(44): Show |
47 | HG00438.hp1 HG00621.hp2 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.50-6392C>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44399666 | |||||||
| chr20:44399701 | C | G | 1 | a0001c0001t0003g0267 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.50-6357C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44399701 | |||||||
| chr20:44399718 | C | T | 1 | a0001c0001t0020g0049 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.50-6340C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44399718 | |||||||
| chr20:44399750 | A | G | 100 | a0001c0001t0001g0018 a0001c0001t0001g0119 a0001c0001t0001g0155 others(97): Show |
101 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(98): Show |
intron_variant | MODIFIER | c.50-6308A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44399750 | |||||||
| chr20:44399939 | C | T | 6 | a0001c0001t0001g0254 a0001c0001t0027g0014 a0001c0001t0027g0016 others(3): Show |
6 | HG00544.hp2 HG01891.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.50-6119C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44399939 | |||||||
| chr20:44400231 | G | A | 1 | a0001c0001t0012g0092 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.50-5827G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44400231 | |||||||
| chr20:44400321 | G | T | 1 | a0001c0003t0062g0062 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.50-5737G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44400321 | |||||||
| chr20:44400328 | C | T | 4 | a0001c0001t0006g0051 a0001c0001t0006g0081 a0001c0001t0053g0057 others(1): Show |
4 | HG01109.hp1 HG01169.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.50-5730C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44400328 | |||||||
| chr20:44400347 | AGGG | A | 65 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0070 others(62): Show |
65 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.50-5708_50-5706del others(3): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44400347 | ||||||
| chr20:44400350 | G | A | 1 | a0001c0001t0047g0298 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.50-5708G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44400350 | |||||||
| chr20:44400364 | C | T | 1 | a0001c0001t0003g0071 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.50-5694C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44400364 | |||||||
| chr20:44400468 | C | T | 1 | a0002c0002t0001g0174 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.50-5590C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44400468 | |||||||
| chr20:44400645 | A | C | 174 | a0001c0001t0001g0018 a0001c0001t0001g0032 a0001c0001t0001g0035 others(171): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.50-5413A>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44400645 | |||||||
| chr20:44400675 | G | A | 1 | a0001c0001t0023g0004 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.50-5383G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44400675 | |||||||
| chr20:44400741 | G | A | 1 | a0001c0009t0081g0275 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.50-5317G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44400741 | |||||||
| chr20:44401013 | G | A | 1 | a0001c0001t0004g0172 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.50-5045G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44401013 | |||||||
| chr20:44401024 | T | C | 13 | a0001c0001t0002g0023 a0001c0001t0010g0011 a0001c0001t0010g0015 others(10): Show |
13 | HG02145.hp1 HG02615.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.50-5034T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44401024 | |||||||
| chr20:44401353 | G | A | 1 | a0001c0001t0004g0300 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.50-4705G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44401353 | |||||||
| chr20:44401520 | G | A | 1 | a0001c0014t0069g0192 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.50-4538G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44401520 | |||||||
| chr20:44401671 | A | C | 7 | a0001c0001t0002g0302 a0001c0001t0018g0209 a0001c0001t0018g0210 others(4): Show |
7 | HG02055.hp1 HG02451.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.50-4387A>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44401671 | |||||||
| chr20:44401718 | G | A | 1 | a0001c0001t0025g0046 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.50-4340G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44401718 | |||||||
| chr20:44401795 | G | A | 63 | a0001c0001t0001g0070 a0001c0001t0002g0039 a0001c0001t0002g0044 others(60): Show |
63 | HG00423.hp2 HG00438.hp2 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.50-4263G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44401795 | |||||||
| chr20:44401831 | G | A | 2 | a0001c0001t0037g0224 a0001c0001t0097g0123 |
2 | HG02818.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.50-4227G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44401831 | |||||||
| chr20:44401844 | A | T | 3 | a0001c0001t0028g0099 a0001c0001t0049g0127 a0001c0001t0063g0173 |
3 | HG00544.hp2 HG03579.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.50-4214A>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44401844 | |||||||
| chr20:44402073 | T | C | 3 | a0001c0001t0028g0099 a0001c0001t0049g0127 a0001c0001t0063g0173 |
3 | HG00544.hp2 HG03579.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.50-3985T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44402073 | |||||||
| chr20:44402114 | C | G | 3 | a0001c0001t0028g0099 a0001c0001t0049g0127 a0001c0001t0063g0173 |
3 | HG00544.hp2 HG03579.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.50-3944C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44402114 | |||||||
| chr20:44402114 | C | T | 3 | a0001c0001t0003g0113 a0001c0001t0003g0299 a0004c0006t0023g0105 |
3 | HG00639.hp2 HG02572.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.50-3944C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44402114 | |||||||
| chr20:44402131 | G | A | 2 | a0001c0001t0050g0031 a0006c0004t0056g0077 |
2 | HG03942.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.50-3927G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44402131 | |||||||
| chr20:44402143 | CTG | C | 8 | a0001c0001t0002g0302 a0001c0001t0012g0256 a0001c0001t0018g0209 others(5): Show |
8 | HG01261.hp1 HG02055.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.50-3908_50-3907del others(2): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44402143 | ||||||
| chr20:44402169 | C | A | 40 | a0001c0001t0001g0026 a0001c0001t0001g0054 a0001c0001t0001g0056 others(37): Show |
40 | HG00438.hp1 HG00621.hp2 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.50-3889C>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44402169 | |||||||
| chr20:44402211 | T | G | 3 | a0001c0001t0028g0099 a0001c0001t0049g0127 a0001c0001t0063g0173 |
3 | HG00544.hp2 HG03579.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.50-3847T>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44402211 | |||||||
| chr20:44402226 | T | C | 41 | a0001c0001t0001g0026 a0001c0001t0001g0054 a0001c0001t0001g0056 others(38): Show |
41 | HG00438.hp1 HG00621.hp2 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.50-3832T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44402226 | |||||||
| chr20:44402271 | G | A | 1 | a0001c0001t0004g0166 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.50-3787G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44402271 | |||||||
| chr20:44402288 | G | A | 1 | a0001c0001t0063g0173 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.50-3770G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44402288 | |||||||
| chr20:44402316 | C | T | 137 | a0001c0001t0001g0026 a0001c0001t0001g0054 a0001c0001t0001g0056 others(134): Show |
137 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(134): Show |
intron_variant | MODIFIER | c.50-3742C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44402316 | |||||||
| chr20:44402453 | C | T | 1 | a0001c0001t0017g0180 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.50-3605C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44402453 | |||||||
| chr20:44402652 | A | G | 1 | a0001c0001t0025g0046 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.50-3406A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44402652 | |||||||
| chr20:44402897 | C | T | 3 | a0001c0001t0028g0099 a0001c0001t0049g0127 a0001c0001t0063g0173 |
3 | HG00544.hp2 HG03579.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.50-3161C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44402897 | |||||||
| chr20:44402917 | A | AC | 4 | a0001c0001t0028g0099 a0001c0001t0049g0127 a0001c0001t0054g0253 others(1): Show |
4 | HG00544.hp2 HG02723.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.50-3140dupC | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44402917 | ||||||
| chr20:44403004 | G | A | 10 | a0001c0001t0001g0163 a0001c0001t0001g0230 a0001c0001t0001g0301 others(7): Show |
10 | HG01069.hp1 HG02647.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.50-3054G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44403004 | |||||||
| chr20:44403042 | G | A | 1 | a0001c0001t0011g0117 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.50-3016G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44403042 | |||||||
| chr20:44403113 | G | A | 1 | a0001c0001t0052g0005 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.50-2945G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44403113 | |||||||
| chr20:44403118 | C | G | 1 | a0001c0001t0013g0010 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.50-2940C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44403118 | |||||||
| chr20:44403215 | G | T | 30 | a0001c0001t0001g0128 a0001c0001t0001g0155 a0001c0001t0001g0164 others(27): Show |
30 | HG01167.hp2 HG01358.hp1 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.50-2843G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44403215 | |||||||
| chr20:44403745 | G | A | 1 | a0001c0001t0050g0031 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.50-2313G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44403745 | |||||||
| chr20:44403745 | G | C | 42 | a0001c0001t0001g0026 a0001c0001t0001g0054 a0001c0001t0001g0056 others(39): Show |
42 | HG00438.hp1 HG00621.hp2 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.50-2313G>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44403745 | |||||||
| chr20:44403806 | T | A | 14 | a0001c0001t0001g0241 a0001c0001t0002g0053 a0001c0001t0003g0091 others(11): Show |
14 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(11): Show |
intron_variant | MODIFIER | c.50-2252T>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44403806 | |||||||
| chr20:44403926 | G | A | 1 | a0001c0001t0011g0185 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.50-2132G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44403926 | |||||||
| chr20:44404056 | C | T | 2 | a0001c0001t0050g0031 a0006c0004t0056g0077 |
2 | HG03942.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.50-2002C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44404056 | |||||||
| chr20:44404064 | T | C | 1 | a0001c0001t0045g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.50-1994T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44404064 | |||||||
| chr20:44404227 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.50-1831G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44404227 | |||||||
| chr20:44404301 | A | G | 2 | a0001c0001t0013g0010 a0001c0001t0054g0253 |
2 | HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.50-1757A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44404301 | |||||||
| chr20:44404365 | A | G | 1 | a0001c0001t0051g0157 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.50-1693A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44404365 | |||||||
| chr20:44404455 | G | C | 112 | a0001c0001t0001g0070 a0001c0001t0001g0122 a0001c0001t0001g0178 others(109): Show |
112 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.50-1603G>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44404455 | |||||||
| chr20:44404518 | G | A | 2 | a0001c0001t0012g0256 a0001c0001t0055g0118 |
2 | HG01261.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.50-1540G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44404518 | |||||||
| chr20:44404594 | G | A | 55 | a0001c0001t0001g0018 a0001c0001t0001g0104 a0001c0001t0001g0111 others(52): Show |
55 | HG00099.hp1 HG00544.hp1 HG01074.hp2 others(52): Show |
intron_variant | MODIFIER | c.50-1464G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44404594 | |||||||
| chr20:44404613 | T | G | 3 | a0001c0001t0019g0151 a0001c0001t0019g0161 a0001c0001t0019g0170 |
3 | HG02615.hp1 HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.50-1445T>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44404613 | |||||||
| chr20:44404672 | G | T | 1 | a0001c0001t0035g0168 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.50-1386G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44404672 | |||||||
| chr20:44404728 | CTG | C | 43 | a0001c0001t0001g0128 a0001c0001t0001g0155 a0001c0001t0001g0163 others(40): Show |
43 | HG01069.hp1 HG01167.hp2 HG01261.hp1 others(40): Show |
intron_variant | MODIFIER | c.50-1326_50-1325del others(2): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44404728 | ||||||
| chr20:44404776 | T | TGTGTTTG others(757): Show |
4 | a0001c0001t0001g0128 a0001c0001t0001g0155 a0001c0001t0001g0163 others(1): Show |
4 | HG01358.hp1 HG02109.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.50-1278_50-1277ins others(764): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44404776 | ||||||
| chr20:44404776 | T | TGTGTTTG others(771): Show |
1 | a0006c0004t0056g0077 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.50-1278_50-1277ins others(778): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44404776 | ||||||
| chr20:44404776 | T | TGTGTTTG others(772): Show |
1 | a0001c0001t0035g0168 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.50-1278_50-1277ins others(779): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44404776 | ||||||
| chr20:44404776 | T | TGTGTTTG others(769): Show |
1 | a0001c0001t0052g0005 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.50-1278_50-1277ins others(776): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44404776 | ||||||
| chr20:44404776 | T | TGTGTTTG others(925): Show |
2 | a0001c0001t0013g0010 a0001c0001t0054g0253 |
2 | HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.50-1278_50-1277ins others(932): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44404776 | ||||||
| chr20:44404776 | T | TGTGTTTG others(769): Show |
3 | a0001c0001t0038g0318 a0001c0001t0087g0108 a0001c0003t0062g0062 |
3 | HG02055.hp2 HG02486.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.50-1278_50-1277ins others(776): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44404776 | ||||||
| chr20:44404776 | T | TGTGTTTG others(771): Show |
46 | a0001c0001t0001g0018 a0001c0001t0001g0111 a0001c0001t0001g0126 others(43): Show |
46 | HG00099.hp1 HG00544.hp1 HG01074.hp2 others(43): Show |
intron_variant | MODIFIER | c.50-1278_50-1277ins others(778): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44404776 | ||||||
| chr20:44404776 | T | TGTGTTTG others(773): Show |
2 | a0001c0001t0001g0104 a0001c0001t0001g0119 |
2 | HG02135.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.50-1278_50-1277ins others(780): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44404776 | ||||||
| chr20:44404776 | T | TGTGTTTG others(739): Show |
2 | a0001c0001t0001g0184 a0001c0001t0011g0100 |
2 | HG01256.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.50-1278_50-1277ins others(746): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44404776 | ||||||
| chr20:44404776 | T | TGTGTTTG others(755): Show |
50 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0052 others(47): Show |
52 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(49): Show |
intron_variant | MODIFIER | c.50-1278_50-1277ins others(762): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44404776 | ||||||
| chr20:44404776 | T | TGTGTTTG others(757): Show |
32 | a0001c0001t0001g0191 a0001c0001t0002g0023 a0001c0001t0004g0181 others(29): Show |
32 | HG00544.hp2 HG01167.hp2 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.50-1278_50-1277ins others(764): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44404776 | ||||||
| chr20:44404776 | T | TGTGTTTG others(759): Show |
1 | a0001c0001t0050g0031 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.50-1278_50-1277ins others(766): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44404776 | ||||||
| chr20:44404776 | T | TGTGTTTG others(732): Show |
4 | a0001c0001t0001g0230 a0001c0001t0014g0227 a0001c0001t0014g0229 others(1): Show |
4 | HG01069.hp1 HG02647.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.50-1278_50-1277ins others(739): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44404776 | ||||||
| chr20:44404776 | T | TGTGTTTG others(722): Show |
5 | a0001c0001t0018g0209 a0001c0001t0018g0210 a0001c0001t0018g0307 others(2): Show |
5 | HG02055.hp1 HG02451.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.50-1278_50-1277ins others(729): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44404776 | ||||||
| chr20:44404776 | T | TGTGTTTG others(720): Show |
1 | a0001c0001t0002g0302 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.50-1278_50-1277ins others(727): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44404776 | ||||||
| chr20:44404776 | T | TGTGTTTG others(734): Show |
2 | a0001c0001t0012g0256 a0001c0001t0055g0118 |
2 | HG01261.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.50-1278_50-1277ins others(741): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44404776 | ||||||
| chr20:44404777 | G | GTGTTTGT others(765): Show |
1 | a0001c0001t0005g0198 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.50-1278_50-1277ins others(772): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44404777 | ||||||
| chr20:44404778 | T | TGTTTGTT others(765): Show |
1 | a0001c0001t0096g0252 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.50-1278_50-1277ins others(772): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44404778 | ||||||
| chr20:44404778 | T | TGTTTGTT others(731): Show |
2 | a0001c0001t0003g0084 a0001c0001t0042g0085 |
2 | NA18995.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.50-1278_50-1277ins others(738): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44404778 | ||||||
| chr20:44404778 | T | TGTTTGTT others(763): Show |
1 | a0001c0001t0002g0133 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.50-1278_50-1277ins others(770): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44404778 | ||||||
| chr20:44404778 | T | TGTTTGTT others(765): Show |
150 | a0001c0001t0001g0026 a0001c0001t0001g0054 a0001c0001t0001g0056 others(147): Show |
150 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.50-1278_50-1277ins others(772): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44404778 | ||||||
| chr20:44404778 | T | TGTTTGTT others(753): Show |
1 | a0001c0001t0017g0180 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.50-1278_50-1277ins others(760): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44404778 | ||||||
| chr20:44404778 | T | TGTTTGTT others(767): Show |
1 | a0001c0001t0015g0121 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.50-1278_50-1277ins others(774): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44404778 | ||||||
| chr20:44404778 | T | TGTTTGTT others(763): Show |
1 | a0001c0001t0045g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.50-1278_50-1277ins others(770): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44404778 | ||||||
| chr20:44404778 | T | TGTTTGTT others(769): Show |
1 | a0001c0001t0082g0169 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.50-1278_50-1277ins others(776): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44404778 | ||||||
| chr20:44404780 | T | TTTGTTGA others(763): Show |
1 | a0001c0001t0001g0220 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.50-1278_50-1277ins others(770): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44404780 | |||||||
| chr20:44404781 | G | T | 1 | a0001c0001t0023g0004 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.50-1277G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44404781 | |||||||
| chr20:44404786 | C | T | 161 | a0001c0001t0001g0026 a0001c0001t0001g0054 a0001c0001t0001g0056 others(158): Show |
161 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.50-1272C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44404786 | |||||||
| chr20:44404788 | T | C | 159 | a0001c0001t0001g0026 a0001c0001t0001g0054 a0001c0001t0001g0056 others(156): Show |
159 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(156): Show |
intron_variant | MODIFIER | c.50-1270T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44404788 | |||||||
| chr20:44404790 | T | C | 1 | a0001c0001t0001g0220 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.50-1268T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44404790 | |||||||
| chr20:44404793 | C | A | 1 | a0001c0001t0023g0004 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.50-1265C>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44404793 | |||||||
| chr20:44404793 | C | G | 1 | a0001c0001t0001g0220 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.50-1265C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44404793 | |||||||
| chr20:44404797 | G | C | 1 | a0001c0001t0001g0220 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.50-1261G>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44404797 | |||||||
| chr20:44404806 | G | GTGAATTG others(750): Show |
1 | a0001c0001t0023g0004 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.50-1252_50-1251ins others(757): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44404806 | |||||||
| chr20:44404808 | A | T | 1 | a0001c0001t0023g0004 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.50-1250A>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44404808 | |||||||
| chr20:44404854 | G | GGT | 168 | a0001c0001t0001g0026 a0001c0001t0001g0054 a0001c0001t0001g0056 others(165): Show |
168 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(165): Show |
intron_variant | MODIFIER | c.50-1196_50-1195dup others(2): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44404854 | ||||||
| chr20:44404864 | C | T | 1 | a0004c0006t0023g0105 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.50-1194C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44404864 | |||||||
| chr20:44404868 | T | C | 1 | a0004c0006t0023g0105 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.50-1190T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44404868 | |||||||
| chr20:44404929 | G | GGTGT | 157 | a0001c0001t0001g0026 a0001c0001t0001g0054 a0001c0001t0001g0056 others(154): Show |
157 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.50-1123_50-1120dup others(4): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44404929 | ||||||
| chr20:44404939 | C | G | 1 | a0001c0001t0023g0004 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.50-1119C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44404939 | |||||||
| chr20:44404985 | G | A | 1 | a0001c0001t0023g0004 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.50-1073G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44404985 | |||||||
| chr20:44404986 | TGTGTGTG others(10): Show |
T | 1 | a0001c0001t0054g0253 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.50-1063_50-1047del others(17): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44404986 | ||||||
| chr20:44404992 | T | C | 4 | a0001c0001t0001g0301 a0001c0001t0004g0300 a0001c0001t0011g0115 others(1): Show |
4 | HG02717.hp2 HG02818.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.50-1066T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44404992 | |||||||
| chr20:44404998 | T | A | 1 | a0001c0001t0096g0252 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.50-1060T>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44404998 | |||||||
| chr20:44405012 | G | A | 55 | a0001c0001t0001g0018 a0001c0001t0001g0104 a0001c0001t0001g0111 others(52): Show |
55 | HG00099.hp1 HG00544.hp1 HG01074.hp2 others(52): Show |
intron_variant | MODIFIER | c.50-1046G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44405012 | |||||||
| chr20:44405012 | G | T | 1 | a0001c0001t0023g0004 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.50-1046G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44405012 | |||||||
| chr20:44405033 | C | G | 1 | a0001c0001t0001g0220 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.50-1025C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44405033 | |||||||
| chr20:44405044 | T | TTGTGTGT others(15): Show |
152 | a0001c0001t0001g0026 a0001c0001t0001g0054 a0001c0001t0001g0056 others(149): Show |
152 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.50-983_50-962dupGA others(20): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44405044 | ||||||
| chr20:44405083 | GGTGCGTG others(22): Show |
G | 2 | a0001c0001t0013g0010 a0001c0001t0054g0253 |
2 | HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.50-961_50-933delCT others(27): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44405083 | ||||||
| chr20:44405170 | T | C | 2 | a0001c0001t0001g0281 a0001c0001t0070g0264 |
2 | HG01261.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.50-888T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44405170 | |||||||
| chr20:44405268 | C | CAAATTTT others(2): Show |
53 | a0001c0001t0001g0018 a0001c0001t0001g0104 a0001c0001t0001g0111 others(50): Show |
53 | HG00099.hp1 HG00544.hp1 HG01074.hp2 others(50): Show |
intron_variant | MODIFIER | c.50-765_50-757dupTT others(7): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44405268 | ||||||
| chr20:44405281 | T | A | 1 | a0001c0001t0003g0029 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.50-777T>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44405281 | |||||||
| chr20:44405290 | T | G | 4 | a0001c0001t0013g0010 a0001c0001t0050g0031 a0001c0001t0054g0253 others(1): Show |
4 | HG02723.hp1 HG02886.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.50-768T>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44405290 | |||||||
| chr20:44405376 | G | A | 102 | a0001c0001t0001g0018 a0001c0001t0001g0026 a0001c0001t0001g0054 others(99): Show |
102 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.50-682G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44405376 | |||||||
| chr20:44405439 | G | A | 41 | a0001c0001t0001g0026 a0001c0001t0001g0054 a0001c0001t0001g0056 others(38): Show |
41 | HG00438.hp1 HG00621.hp2 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.50-619G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44405439 | |||||||
| chr20:44405476 | C | A | 1 | a0001c0001t0060g0255 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.50-582C>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44405476 | |||||||
| chr20:44405484 | C | T | 1 | a0001c0001t0001g0254 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.50-574C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44405484 | |||||||
| chr20:44405531 | A | T | 51 | a0001c0001t0001g0018 a0001c0001t0001g0104 a0001c0001t0001g0111 others(48): Show |
51 | HG00099.hp1 HG00544.hp1 HG01074.hp2 others(48): Show |
intron_variant | MODIFIER | c.50-527A>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44405531 | |||||||
| chr20:44405700 | A | G | 2 | a0001c0001t0050g0031 a0006c0004t0056g0077 |
2 | HG03942.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.50-358A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44405700 | |||||||
| chr20:44405828 | A | G | 267 | a0001c0001t0001g0018 a0001c0001t0001g0026 a0001c0001t0001g0054 others(264): Show |
267 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(264): Show |
intron_variant | MODIFIER | c.50-230A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44405828 | |||||||
| chr20:44405832 | C | T | 42 | a0001c0001t0001g0026 a0001c0001t0001g0054 a0001c0001t0001g0056 others(39): Show |
42 | HG00438.hp1 HG00621.hp2 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.50-226C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44405832 | |||||||
| chr20:44405842 | C | T | 2 | a0001c0001t0013g0010 a0001c0001t0054g0253 |
2 | HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.50-216C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44405842 | |||||||
| chr20:44405873 | C | G | 48 | a0001c0001t0001g0026 a0001c0001t0001g0054 a0001c0001t0001g0056 others(45): Show |
48 | HG00438.hp1 HG00621.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.50-185C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44405873 | |||||||
| chr20:44406020 | T | C | 179 | a0001c0001t0001g0018 a0001c0001t0001g0070 a0001c0001t0001g0104 others(176): Show |
179 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.50-38T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44406020 | |||||||
| chr20:44406053 | C | T | 55 | a0001c0001t0001g0018 a0001c0001t0001g0104 a0001c0001t0001g0111 others(52): Show |
55 | HG00099.hp1 HG00544.hp1 HG01074.hp2 others(52): Show |
splice_region_variant&intron_variant | LOW | c.50-5C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44406053 | |||||||
| chr20:44406440 | C | T | 1 | a0001c0001t0051g0157 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.224+208C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 2/9 | chr20 | 44406440 | |||||||
| chr20:44406498 | C | T | 226 | a0001c0001t0001g0018 a0001c0001t0001g0026 a0001c0001t0001g0054 others(223): Show |
226 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(223): Show |
intron_variant | MODIFIER | c.224+266C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 2/9 | chr20 | 44406498 | |||||||
| chr20:44406520 | G | C | 269 | a0001c0001t0001g0018 a0001c0001t0001g0026 a0001c0001t0001g0054 others(266): Show |
269 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(266): Show |
intron_variant | MODIFIER | c.224+288G>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 2/9 | chr20 | 44406520 | |||||||
| chr20:44406650 | C | T | 1 | a0001c0012t0008g0007 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.224+418C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 2/9 | chr20 | 44406650 | |||||||
| chr20:44406688 | G | A | 1 | a0001c0001t0003g0148 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.224+456G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 2/9 | chr20 | 44406688 | |||||||
| chr20:44407103 | A | G | 56 | a0001c0001t0001g0018 a0001c0001t0001g0104 a0001c0001t0001g0111 others(53): Show |
56 | HG00099.hp1 HG00544.hp1 HG01074.hp2 others(53): Show |
intron_variant | MODIFIER | c.225-278A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 2/9 | chr20 | 44407103 | |||||||
| chr20:44407140 | C | T | 45 | a0001c0001t0001g0018 a0001c0001t0001g0104 a0001c0001t0001g0119 others(42): Show |
45 | HG00099.hp1 HG00544.hp1 HG01074.hp2 others(42): Show |
intron_variant | MODIFIER | c.225-241C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 2/9 | chr20 | 44407140 | |||||||
| chr20:44407154 | A | C | 1 | a0001c0001t0050g0031 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.225-227A>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 2/9 | chr20 | 44407154 | |||||||
| chr20:44407182 | C | T | 1 | a0001c0001t0002g0195 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.225-199C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 2/9 | chr20 | 44407182 | |||||||
| chr20:44407200 | A | T | 4 | a0001c0001t0001g0301 a0001c0001t0004g0300 a0001c0001t0011g0115 others(1): Show |
4 | HG02717.hp2 HG02818.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.225-181A>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 2/9 | chr20 | 44407200 | |||||||
| chr20:44407298 | C | T | 1 | a0001c0001t0004g0250 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.225-83C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 2/9 | chr20 | 44407298 | |||||||
| chr20:44407494 | C | T | 4 | a0001c0001t0001g0301 a0001c0001t0004g0300 a0001c0001t0011g0115 others(1): Show |
4 | HG02717.hp2 HG02818.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.319+19C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44407494 | |||||||
| chr20:44407711 | A | G | 1 | a0001c0001t0001g0111 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.319+236A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44407711 | |||||||
| chr20:44407757 | T | TTG | 92 | a0001c0001t0001g0070 a0001c0001t0001g0119 a0001c0001t0001g0122 others(89): Show |
92 | HG00438.hp2 HG00597.hp1 HG00597.hp2 others(89): Show |
intron_variant | MODIFIER | c.319+316_319+317dup others(2): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr20 | 44407757 | ||||||
| chr20:44407757 | T | TTGTG | 64 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0128 others(61): Show |
65 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.319+314_319+317dup others(4): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr20 | 44407757 | ||||||
| chr20:44407757 | T | TTGTGTG | 18 | a0001c0001t0001g0213 a0001c0001t0001g0230 a0001c0001t0010g0208 others(15): Show |
18 | HG00544.hp2 HG01261.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.319+312_319+317dup others(6): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr20 | 44407757 | ||||||
| chr20:44407757 | T | TTGTGTGT others(1): Show |
32 | a0001c0001t0001g0026 a0001c0001t0001g0054 a0001c0001t0001g0056 others(29): Show |
32 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.319+310_319+317dup others(8): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr20 | 44407757 | ||||||
| chr20:44407757 | T | TTGTGTGT others(3): Show |
14 | a0001c0001t0001g0141 a0001c0001t0001g0301 a0001c0001t0003g0071 others(11): Show |
14 | HG00639.hp2 HG01255.hp1 HG01515.hp1 others(11): Show |
intron_variant | MODIFIER | c.319+308_319+317dup others(10): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr20 | 44407757 | ||||||
| chr20:44407757 | T | TTGTGTGT others(5): Show |
5 | a0001c0001t0001g0220 a0001c0001t0003g0299 a0001c0001t0004g0300 others(2): Show |
5 | HG02486.hp2 HG02572.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.319+306_319+317dup others(12): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr20 | 44407757 | ||||||
| chr20:44407757 | T | TTGTGTGT others(7): Show |
1 | a0001c0001t0084g0306 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.319+304_319+317dup others(14): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr20 | 44407757 | ||||||
| chr20:44407757 | TTG | T | 7 | a0001c0001t0001g0067 a0001c0001t0001g0196 a0001c0001t0004g0172 others(4): Show |
7 | HG01081.hp2 HG01515.hp2 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.319+316_319+317del others(2): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr20 | 44407757 | ||||||
| chr20:44407757 | TTGTG | T | 7 | a0001c0001t0001g0178 a0001c0001t0002g0251 a0001c0001t0006g0051 others(4): Show |
7 | HG01109.hp1 HG01169.hp2 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.319+314_319+317del others(4): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr20 | 44407757 | ||||||
| chr20:44407757 | TTGTGTGT others(3): Show |
T | 1 | a0001c0001t0052g0005 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.319+308_319+317del others(10): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr20 | 44407757 | ||||||
| chr20:44407802 | T | G | 1 | a0006c0004t0056g0077 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.319+327T>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44407802 | |||||||
| chr20:44407812 | G | A | 164 | a0001c0001t0001g0018 a0001c0001t0001g0026 a0001c0001t0001g0054 others(161): Show |
164 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(161): Show |
intron_variant | MODIFIER | c.319+337G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44407812 | |||||||
| chr20:44407866 | A | G | 1 | a0001c0001t0067g0171 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.319+391A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44407866 | |||||||
| chr20:44408009 | A | G | 56 | a0001c0001t0001g0018 a0001c0001t0001g0104 a0001c0001t0001g0111 others(53): Show |
56 | HG00099.hp1 HG00544.hp1 HG01074.hp2 others(53): Show |
intron_variant | MODIFIER | c.319+534A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44408009 | |||||||
| chr20:44408037 | A | C | 1 | a0006c0004t0056g0077 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.319+562A>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44408037 | |||||||
| chr20:44408051 | T | G | 56 | a0001c0001t0001g0018 a0001c0001t0001g0104 a0001c0001t0001g0111 others(53): Show |
56 | HG00099.hp1 HG00544.hp1 HG01074.hp2 others(53): Show |
intron_variant | MODIFIER | c.319+576T>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44408051 | |||||||
| chr20:44408373 | G | A | 56 | a0001c0001t0001g0122 a0001c0001t0001g0178 a0001c0001t0001g0183 others(53): Show |
56 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(53): Show |
intron_variant | MODIFIER | c.319+898G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44408373 | |||||||
| chr20:44408512 | G | T | 2 | a0001c0001t0033g0269 a0001c0001t0080g0304 |
2 | HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.319+1037G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44408512 | |||||||
| chr20:44408720 | C | G | 1 | a0001c0001t0003g0294 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.319+1245C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44408720 | |||||||
| chr20:44408725 | A | T | 114 | a0001c0001t0001g0018 a0001c0001t0001g0056 a0001c0001t0001g0104 others(111): Show |
114 | HG00099.hp2 HG00323.hp2 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.319+1250A>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44408725 | |||||||
| chr20:44408726 | A | C | 114 | a0001c0001t0001g0018 a0001c0001t0001g0056 a0001c0001t0001g0104 others(111): Show |
114 | HG00099.hp2 HG00323.hp2 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.319+1251A>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44408726 | |||||||
| chr20:44408739 | A | T | 48 | a0001c0001t0001g0026 a0001c0001t0001g0054 a0001c0001t0001g0141 others(45): Show |
48 | HG00438.hp1 HG00621.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.319+1264A>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44408739 | |||||||
| chr20:44408740 | G | A | 57 | a0001c0001t0001g0122 a0001c0001t0001g0183 a0001c0001t0001g0191 others(54): Show |
57 | HG00673.hp2 HG00741.hp2 HG01069.hp1 others(54): Show |
intron_variant | MODIFIER | c.319+1265G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44408740 | |||||||
| chr20:44408782 | A | G | 50 | a0001c0001t0001g0026 a0001c0001t0001g0054 a0001c0001t0001g0141 others(47): Show |
50 | HG00438.hp1 HG00621.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.319+1307A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44408782 | |||||||
| chr20:44408786 | T | G | 1 | a0001c0001t0004g0300 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.319+1311T>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44408786 | |||||||
| chr20:44408880 | C | T | 1 | a0001c0001t0043g0309 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.319+1405C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44408880 | |||||||
| chr20:44408932 | C | T | 23 | a0001c0001t0001g0191 a0001c0001t0001g0241 a0001c0001t0002g0053 others(20): Show |
23 | HG01433.hp1 HG01496.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.319+1457C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44408932 | |||||||
| chr20:44408953 | G | C | 1 | a0001c0001t0006g0051 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.319+1478G>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44408953 | |||||||
| chr20:44409000 | C | G | 1 | a0001c0001t0052g0005 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.319+1525C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44409000 | |||||||
| chr20:44409344 | T | C | 8 | a0001c0001t0010g0208 a0001c0001t0013g0021 a0001c0001t0014g0188 others(5): Show |
8 | HG02280.hp1 HG02559.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.319+1869T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44409344 | |||||||
| chr20:44409351 | T | C | 1 | a0001c0001t0067g0171 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.319+1876T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44409351 | |||||||
| chr20:44409426 | A | G | 2 | a0001c0003t0062g0062 a0001c0003t0065g0308 |
2 | HG02486.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.319+1951A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44409426 | |||||||
| chr20:44409446 | T | C | 1 | a0001c0001t0001g0184 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.319+1971T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44409446 | |||||||
| chr20:44409492 | G | A | 1 | a0001c0001t0005g0200 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.319+2017G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44409492 | |||||||
| chr20:44409568 | T | C | 211 | a0001c0001t0001g0018 a0001c0001t0001g0052 a0001c0001t0001g0067 others(208): Show |
212 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.319+2093T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44409568 | |||||||
| chr20:44409609 | C | T | 73 | a0001c0001t0001g0220 a0001c0001t0002g0025 a0001c0001t0002g0039 others(70): Show |
73 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.319+2134C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44409609 | |||||||
| chr20:44409832 | G | A | 1 | a0001c0001t0043g0309 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.319+2357G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44409832 | |||||||
| chr20:44409839 | CT | C | 129 | a0001c0001t0001g0026 a0001c0001t0001g0032 a0001c0001t0001g0035 others(126): Show |
130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.319+2380delT | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr20 | 44409839 | ||||||
| chr20:44409839 | CTT | C | 173 | a0001c0001t0001g0018 a0001c0001t0001g0052 a0001c0001t0001g0067 others(170): Show |
173 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.319+2379_319+2380d others(4): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr20 | 44409839 | ||||||
| chr20:44409907 | G | A | 1 | a0001c0001t0003g0223 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.319+2432G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44409907 | |||||||
| chr20:44409919 | C | A | 174 | a0001c0001t0001g0018 a0001c0001t0001g0052 a0001c0001t0001g0067 others(171): Show |
174 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.319+2444C>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44409919 | |||||||
| chr20:44409988 | C | T | 71 | a0001c0001t0001g0220 a0001c0001t0002g0025 a0001c0001t0002g0039 others(68): Show |
71 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.319+2513C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44409988 | |||||||
| chr20:44410028 | G | T | 1 | a0001c0001t0055g0118 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.319+2553G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44410028 | |||||||
| chr20:44410051 | G | T | 11 | a0001c0001t0001g0301 a0001c0001t0004g0300 a0001c0001t0011g0115 others(8): Show |
11 | HG02055.hp1 HG02451.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.319+2576G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44410051 | |||||||
| chr20:44410064 | T | C | 191 | a0001c0001t0001g0018 a0001c0001t0001g0052 a0001c0001t0001g0067 others(188): Show |
191 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.319+2589T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44410064 | |||||||
| chr20:44410079 | C | T | 71 | a0001c0001t0001g0220 a0001c0001t0002g0025 a0001c0001t0002g0039 others(68): Show |
71 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.319+2604C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44410079 | |||||||
| chr20:44410080 | G | A | 46 | a0001c0001t0001g0026 a0001c0001t0001g0054 a0001c0001t0001g0056 others(43): Show |
46 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.319+2605G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44410080 | |||||||
| chr20:44410128 | C | T | 96 | a0001c0001t0001g0018 a0001c0001t0001g0052 a0001c0001t0001g0067 others(93): Show |
96 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.319+2653C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44410128 | |||||||
| chr20:44410142 | T | C | 101 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0167 others(98): Show |
102 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.319+2667T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44410142 | |||||||
| chr20:44410304 | C | A | 71 | a0001c0001t0001g0220 a0001c0001t0002g0025 a0001c0001t0002g0039 others(68): Show |
71 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.319+2829C>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44410304 | |||||||
| chr20:44410400 | G | A | 15 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0167 others(12): Show |
16 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(13): Show |
intron_variant | MODIFIER | c.319+2925G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44410400 | |||||||
| chr20:44410605 | A | G | 2 | a0001c0001t0001g0196 a0001c0001t0082g0169 |
2 | HG01074.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.320-3089A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44410605 | |||||||
| chr20:44410623 | C | T | 15 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0167 others(12): Show |
16 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(13): Show |
intron_variant | MODIFIER | c.320-3071C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44410623 | |||||||
| chr20:44410720 | C | A | 2 | a0001c0003t0062g0062 a0001c0003t0065g0308 |
2 | HG02486.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.320-2974C>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44410720 | |||||||
| chr20:44410735 | G | A | 26 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0167 others(23): Show |
27 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.320-2959G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44410735 | |||||||
| chr20:44410797 | C | G | 1 | a0001c0001t0043g0309 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.320-2897C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44410797 | |||||||
| chr20:44410842 | C | T | 1 | a0001c0001t0052g0005 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.320-2852C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44410842 | |||||||
| chr20:44410897 | G | C | 48 | a0001c0001t0001g0026 a0001c0001t0001g0054 a0001c0001t0001g0056 others(45): Show |
48 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.320-2797G>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44410897 | |||||||
| chr20:44411083 | G | T | 4 | a0001c0001t0023g0004 a0001c0001t0044g0116 a0001c0001t0045g0022 others(1): Show |
4 | HG01069.hp1 HG02809.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.320-2611G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44411083 | |||||||
| chr20:44411146 | C | T | 11 | a0001c0001t0001g0301 a0001c0001t0004g0300 a0001c0001t0011g0115 others(8): Show |
11 | HG02055.hp1 HG02451.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.320-2548C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44411146 | |||||||
| chr20:44411211 | C | T | 26 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0167 others(23): Show |
27 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.320-2483C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44411211 | |||||||
| chr20:44411387 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.320-2307G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44411387 | |||||||
| chr20:44411497 | C | T | 25 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0167 others(22): Show |
26 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.320-2197C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44411497 | |||||||
| chr20:44411540 | G | T | 10 | a0001c0001t0001g0301 a0001c0001t0004g0300 a0001c0001t0011g0115 others(7): Show |
10 | HG02055.hp1 HG02451.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.320-2154G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44411540 | |||||||
| chr20:44411553 | C | A | 26 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0167 others(23): Show |
27 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.320-2141C>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44411553 | |||||||
| chr20:44411566 | C | T | 1 | a0001c0001t0001g0163 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.320-2128C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44411566 | |||||||
| chr20:44411585 | G | A | 11 | a0001c0001t0001g0301 a0001c0001t0004g0300 a0001c0001t0011g0115 others(8): Show |
11 | HG02055.hp1 HG02451.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.320-2109G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44411585 | |||||||
| chr20:44411639 | A | G | 1 | a0001c0001t0054g0253 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.320-2055A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44411639 | |||||||
| chr20:44411648 | C | T | 98 | a0001c0001t0001g0018 a0001c0001t0001g0052 a0001c0001t0001g0067 others(95): Show |
98 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.320-2046C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44411648 | |||||||
| chr20:44411791 | T | C | 2 | a0001c0001t0002g0228 a0001c0001t0020g0244 |
2 | NA18951.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.320-1903T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44411791 | |||||||
| chr20:44411796 | C | T | 15 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0167 others(12): Show |
16 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(13): Show |
intron_variant | MODIFIER | c.320-1898C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44411796 | |||||||
| chr20:44411853 | C | T | 1 | a0006c0004t0056g0077 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.320-1841C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44411853 | |||||||
| chr20:44411891 | C | CA | 14 | a0001c0001t0001g0301 a0001c0001t0002g0302 a0001c0001t0004g0300 others(11): Show |
14 | HG01074.hp2 HG02055.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.320-1788dupA | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr20 | 44411891 | ||||||
| chr20:44411907 | T | A | 19 | a0001c0001t0001g0178 a0001c0001t0006g0271 a0001c0001t0009g0125 others(16): Show |
19 | HG00280.hp1 HG00741.hp2 HG02071.hp1 others(16): Show |
intron_variant | MODIFIER | c.320-1787T>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44411907 | |||||||
| chr20:44411908 | T | G | 1 | a0001c0001t0054g0253 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.320-1786T>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44411908 | |||||||
| chr20:44411929 | C | T | 130 | a0001c0001t0001g0018 a0001c0001t0001g0032 a0001c0001t0001g0035 others(127): Show |
131 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.320-1765C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44411929 | |||||||
| chr20:44411965 | G | C | 2 | a0001c0003t0062g0062 a0001c0003t0065g0308 |
2 | HG02486.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.320-1729G>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44411965 | |||||||
| chr20:44412057 | G | GA | 17 | a0001c0001t0001g0301 a0001c0001t0004g0300 a0001c0001t0005g0082 others(14): Show |
17 | HG01516.hp1 HG01517.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.320-1626dupA | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr20 | 44412057 | ||||||
| chr20:44412057 | G | GAA | 15 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0167 others(12): Show |
16 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(13): Show |
intron_variant | MODIFIER | c.320-1627_320-1626d others(4): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr20 | 44412057 | ||||||
| chr20:44412087 | G | T | 1 | a0001c0001t0011g0185 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.320-1607G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44412087 | |||||||
| chr20:44412092 | T | C | 30 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0167 others(27): Show |
31 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.320-1602T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44412092 | |||||||
| chr20:44412153 | C | T | 1 | a0006c0004t0056g0077 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.320-1541C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44412153 | |||||||
| chr20:44412275 | A | C | 102 | a0001c0001t0001g0018 a0001c0001t0001g0052 a0001c0001t0001g0067 others(99): Show |
102 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.320-1419A>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44412275 | |||||||
| chr20:44412359 | A | G | 1 | a0001c0001t0002g0098 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.320-1335A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44412359 | |||||||
| chr20:44412362 | G | A | 2 | a0001c0001t0001g0246 a0001c0001t0002g0302 |
2 | HG03098.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.320-1332G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44412362 | |||||||
| chr20:44412455 | G | A | 1 | a0001c0001t0001g0272 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.320-1239G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44412455 | |||||||
| chr20:44412480 | C | T | 1 | a0001c0001t0015g0086 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.320-1214C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44412480 | |||||||
| chr20:44412491 | G | A | 178 | a0001c0001t0001g0026 a0001c0001t0001g0054 a0001c0001t0001g0056 others(175): Show |
178 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(175): Show |
intron_variant | MODIFIER | c.320-1203G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44412491 | |||||||
| chr20:44412491 | G | T | 15 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0167 others(12): Show |
16 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(13): Show |
intron_variant | MODIFIER | c.320-1203G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44412491 | |||||||
| chr20:44412498 | G | C | 5 | a0001c0001t0004g0106 a0001c0001t0004g0181 a0001c0001t0008g0135 others(2): Show |
5 | HG01361.hp1 HG01884.hp2 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.320-1196G>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44412498 | |||||||
| chr20:44412552 | G | A | 3 | a0001c0003t0062g0062 a0001c0003t0065g0308 a0006c0004t0056g0077 |
3 | HG02486.hp2 HG02630.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.320-1142G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44412552 | |||||||
| chr20:44412594 | C | G | 30 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0167 others(27): Show |
31 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.320-1100C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44412594 | |||||||
| chr20:44412700 | G | A | 26 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0167 others(23): Show |
27 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.320-994G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44412700 | |||||||
| chr20:44412747 | G | A | 1 | a0001c0001t0039g0120 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.320-947G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44412747 | |||||||
| chr20:44412755 | T | C | 4 | a0001c0001t0043g0309 a0001c0003t0062g0062 a0001c0003t0065g0308 others(1): Show |
4 | HG02486.hp2 HG02630.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.320-939T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44412755 | |||||||
| chr20:44412801 | T | C | 15 | a0001c0001t0001g0301 a0001c0001t0004g0300 a0001c0001t0011g0115 others(12): Show |
15 | HG02055.hp1 HG02451.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.320-893T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44412801 | |||||||
| chr20:44412811 | G | A | 1 | a0001c0001t0051g0157 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.320-883G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44412811 | |||||||
| chr20:44412846 | G | A | 1 | a0001c0001t0043g0309 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.320-848G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44412846 | |||||||
| chr20:44412906 | T | C | 3 | a0001c0001t0003g0042 a0001c0001t0028g0099 a0001c0001t0028g0235 |
3 | HG02015.hp1 NA18952.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.320-788T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44412906 | |||||||
| chr20:44412951 | C | T | 108 | a0001c0001t0001g0018 a0001c0001t0001g0052 a0001c0001t0001g0067 others(105): Show |
108 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.320-743C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44412951 | |||||||
| chr20:44412961 | T | C | 3 | a0001c0003t0062g0062 a0001c0003t0065g0308 a0006c0004t0056g0077 |
3 | HG02486.hp2 HG02630.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.320-733T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44412961 | |||||||
| chr20:44412977 | C | T | 1 | a0001c0001t0003g0101 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.320-717C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44412977 | |||||||
| chr20:44413018 | T | TC | 3 | a0001c0003t0062g0062 a0001c0003t0065g0308 a0006c0004t0056g0077 |
3 | HG02486.hp2 HG02630.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.320-674dupC | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr20 | 44413018 | ||||||
| chr20:44413092 | G | A | 100 | a0001c0001t0001g0018 a0001c0001t0001g0052 a0001c0001t0001g0067 others(97): Show |
100 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.320-602G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44413092 | |||||||
| chr20:44413103 | C | T | 5 | a0001c0001t0002g0044 a0001c0001t0002g0066 a0001c0001t0002g0102 others(2): Show |
5 | HG02027.hp2 HG02056.hp2 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.320-591C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44413103 | |||||||
| chr20:44413170 | G | A | 5 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0003t0062g0062 others(2): Show |
5 | HG02486.hp2 HG02630.hp1 NA18961.hp1 others(2): Show |
intron_variant | MODIFIER | c.320-524G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44413170 | |||||||
| chr20:44413261 | T | C | 3 | a0001c0003t0062g0062 a0001c0003t0065g0308 a0006c0004t0056g0077 |
3 | HG02486.hp2 HG02630.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.320-433T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44413261 | |||||||
| chr20:44413328 | C | T | 1 | a0001c0001t0035g0168 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.320-366C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44413328 | |||||||
| chr20:44413333 | A | G | 1 | a0001c0001t0002g0152 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.320-361A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44413333 | |||||||
| chr20:44413383 | G | T | 3 | a0001c0003t0062g0062 a0001c0003t0065g0308 a0006c0004t0056g0077 |
3 | HG02486.hp2 HG02630.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.320-311G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44413383 | |||||||
| chr20:44413424 | A | G | 3 | a0001c0003t0062g0062 a0001c0003t0065g0308 a0006c0004t0056g0077 |
3 | HG02486.hp2 HG02630.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.320-270A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44413424 | |||||||
| chr20:44413451 | C | T | 6 | a0001c0001t0023g0004 a0001c0001t0044g0116 a0001c0001t0045g0022 others(3): Show |
6 | HG02486.hp2 HG02630.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.320-243C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44413451 | |||||||
| chr20:44413490 | C | G | 27 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0167 others(24): Show |
28 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.320-204C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44413490 | |||||||
| chr20:44413594 | C | T | 4 | a0001c0001t0023g0004 a0001c0001t0044g0116 a0001c0001t0045g0022 others(1): Show |
4 | HG02809.hp2 HG03453.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.320-100C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44413594 | |||||||
| chr20:44413647 | T | C | 3 | a0001c0003t0062g0062 a0001c0003t0065g0308 a0006c0004t0056g0077 |
3 | HG02486.hp2 HG02630.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.320-47T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44413647 | |||||||
| chr20:44413660 | T | C | 3 | a0001c0003t0062g0062 a0001c0003t0065g0308 a0006c0004t0056g0077 |
3 | HG02486.hp2 HG02630.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.320-34T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44413660 | |||||||
| chr20:44413905 | G | C | 3 | a0001c0003t0062g0062 a0001c0003t0065g0308 a0006c0004t0056g0077 |
3 | HG02486.hp2 HG02630.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.426+105G>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 4/9 | chr20 | 44413905 | |||||||
| chr20:44413940 | C | G | 27 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0167 others(24): Show |
28 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.426+140C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 4/9 | chr20 | 44413940 | |||||||
| chr20:44413966 | C | A | 3 | a0001c0003t0062g0062 a0001c0003t0065g0308 a0006c0004t0056g0077 |
3 | HG02486.hp2 HG02630.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.426+166C>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 4/9 | chr20 | 44413966 | |||||||
| chr20:44413975 | G | A | 3 | a0001c0003t0062g0062 a0001c0003t0065g0308 a0006c0004t0056g0077 |
3 | HG02486.hp2 HG02630.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.426+175G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 4/9 | chr20 | 44413975 | |||||||
| chr20:44414221 | T | C | 1 | a0001c0001t0031g0153 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.427-286T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 4/9 | chr20 | 44414221 | |||||||
| chr20:44414284 | G | A | 1 | a0001c0001t0003g0283 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.427-223G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 4/9 | chr20 | 44414284 | |||||||
| chr20:44414310 | A | C | 31 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0167 others(28): Show |
32 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.427-197A>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 4/9 | chr20 | 44414310 | |||||||
| chr20:44414411 | C | G | 18 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0167 others(15): Show |
19 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.427-96C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 4/9 | chr20 | 44414411 | |||||||
| chr20:44414455 | G | A | 29 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0167 others(26): Show |
30 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.427-52G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 4/9 | chr20 | 44414455 | |||||||
| chr20:44414459 | G | A | 1 | a0006c0004t0056g0077 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.427-48G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 4/9 | chr20 | 44414459 | |||||||
| chr20:44414478 | C | T | 1 | a0006c0004t0056g0077 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.427-29C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 4/9 | chr20 | 44414478 | |||||||
| chr20:44414487 | C | T | 1 | a0006c0004t0056g0077 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.427-20C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 4/9 | chr20 | 44414487 | |||||||
| chr20:44414503 | G | A | 1 | a0006c0004t0056g0077 | 1 | NA18961.hp1 | splice_region_variant&intron_variant | LOW | c.427-4G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 4/9 | chr20 | 44414503 | |||||||
| chr20:44414666 | A | G | 1 | a0001c0001t0002g0074 | 1 | HG03654.hp1 | splice_region_variant&intron_variant | LOW | c.582+4A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 5/9 | chr20 | 44414666 | |||||||
| chr20:44415037 | G | T | 6 | a0001c0001t0023g0004 a0001c0001t0044g0116 a0001c0001t0045g0022 others(3): Show |
6 | HG01069.hp1 HG02723.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.582+375G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 5/9 | chr20 | 44415037 | |||||||
| chr20:44415088 | A | G | 1 | a0001c0001t0011g0100 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.582+426A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 5/9 | chr20 | 44415088 | |||||||
| chr20:44415208 | G | A | 2 | a0001c0001t0002g0065 a0001c0001t0002g0114 |
2 | HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.582+546G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 5/9 | chr20 | 44415208 | |||||||
| chr20:44415421 | G | A | 1 | a0001c0001t0043g0309 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.582+759G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 5/9 | chr20 | 44415421 | |||||||
| chr20:44415567 | T | C | 310 | a0001c0001t0001g0018 a0001c0001t0001g0026 a0001c0001t0001g0032 others(307): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.582+905T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 5/9 | chr20 | 44415567 | |||||||
| chr20:44415722 | C | T | 117 | a0001c0001t0001g0018 a0001c0001t0001g0032 a0001c0001t0001g0035 others(114): Show |
118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.582+1060C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 5/9 | chr20 | 44415722 | |||||||
| chr20:44416058 | G | A | 2 | a0001c0001t0002g0023 a0001c0001t0034g0312 |
2 | HG02615.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.582+1396G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 5/9 | chr20 | 44416058 | |||||||
| chr20:44416119 | C | T | 1 | a0001c0001t0002g0302 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.582+1457C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 5/9 | chr20 | 44416119 | |||||||
| chr20:44416153 | A | G | 1 | a0001c0001t0038g0318 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.582+1491A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 5/9 | chr20 | 44416153 | |||||||
| chr20:44416180 | G | A | 1 | a0001c0001t0002g0302 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.582+1518G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 5/9 | chr20 | 44416180 | |||||||
| chr20:44416290 | C | T | 2 | a0001c0001t0038g0318 a0006c0004t0056g0077 |
2 | HG03225.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.582+1628C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 5/9 | chr20 | 44416290 | |||||||
| chr20:44416423 | G | A | 2 | a0001c0003t0062g0062 a0001c0003t0065g0308 |
2 | HG02486.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.582+1761G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 5/9 | chr20 | 44416423 | |||||||
| chr20:44416443 | C | G | 1 | a0006c0004t0056g0077 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.582+1781C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 5/9 | chr20 | 44416443 | |||||||
| chr20:44416763 | T | C | 2 | a0001c0003t0062g0062 a0001c0003t0065g0308 |
2 | HG02486.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.583-1662T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 5/9 | chr20 | 44416763 | |||||||
| chr20:44416767 | G | A | 1 | a0001c0001t0003g0148 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.583-1658G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 5/9 | chr20 | 44416767 | |||||||
| chr20:44416810 | T | C | 14 | a0001c0001t0006g0001 a0001c0001t0006g0051 a0001c0001t0006g0081 others(11): Show |
15 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.583-1615T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 5/9 | chr20 | 44416810 | |||||||
| chr20:44416856 | C | T | 2 | a0001c0001t0001g0203 a0001c0001t0001g0204 |
2 | NA18966.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.583-1569C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 5/9 | chr20 | 44416856 | |||||||
| chr20:44417093 | A | G | 1 | a0006c0004t0056g0077 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.583-1332A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 5/9 | chr20 | 44417093 | |||||||
| chr20:44417158 | G | GC | 132 | a0001c0001t0001g0018 a0001c0001t0001g0032 a0001c0001t0001g0035 others(129): Show |
133 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.583-1267_583-1266i others(3): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 5/9 | chr20 | 44417158 | |||||||
| chr20:44417389 | T | C | 13 | a0001c0001t0013g0225 a0001c0001t0018g0209 a0001c0001t0018g0210 others(10): Show |
13 | HG01891.hp2 HG02055.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.583-1036T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 5/9 | chr20 | 44417389 | |||||||
| chr20:44417405 | T | G | 133 | a0001c0001t0001g0018 a0001c0001t0001g0032 a0001c0001t0001g0035 others(130): Show |
134 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.583-1020T>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 5/9 | chr20 | 44417405 | |||||||
| chr20:44417424 | C | T | 1 | a0001c0001t0094g0313 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.583-1001C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 5/9 | chr20 | 44417424 | |||||||
| chr20:44417448 | C | G | 1 | a0001c0001t0004g0297 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.583-977C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 5/9 | chr20 | 44417448 | |||||||
| chr20:44417538 | C | T | 4 | a0001c0001t0028g0099 a0001c0001t0028g0235 a0001c0001t0051g0157 others(1): Show |
4 | HG03453.hp2 HG03942.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.583-887C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 5/9 | chr20 | 44417538 | |||||||
| chr20:44417801 | G | A | 11 | a0001c0001t0013g0225 a0001c0001t0018g0209 a0001c0001t0018g0210 others(8): Show |
11 | HG01891.hp2 HG02055.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.583-624G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 5/9 | chr20 | 44417801 | |||||||
| chr20:44417838 | G | A | 4 | a0001c0001t0028g0099 a0001c0001t0028g0235 a0001c0001t0051g0157 others(1): Show |
4 | HG03453.hp2 HG03942.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.583-587G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 5/9 | chr20 | 44417838 | |||||||
| chr20:44417841 | C | T | 2 | a0001c0001t0001g0032 a0001c0001t0001g0035 |
2 | HG00140.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.583-584C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 5/9 | chr20 | 44417841 | |||||||
| chr20:44417968 | C | CA | 9 | a0001c0001t0003g0257 a0001c0001t0004g0047 a0001c0001t0004g0087 others(6): Show |
9 | HG00544.hp2 HG02055.hp2 NA18947.hp1 others(6): Show |
intron_variant | MODIFIER | c.583-440dupA | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr20 | 44417968 | ||||||
| chr20:44417992 | C | G | 2 | a0001c0001t0008g0008 a0001c0001t0008g0059 |
2 | HG01884.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.583-433C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 5/9 | chr20 | 44417992 | |||||||
| chr20:44417994 | G | T | 2 | a0001c0003t0062g0062 a0001c0003t0065g0308 |
2 | HG02486.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.583-431G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 5/9 | chr20 | 44417994 | |||||||
| chr20:44418033 | G | T | 1 | a0001c0001t0006g0051 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.583-392G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 5/9 | chr20 | 44418033 | |||||||
| chr20:44418044 | G | A | 1 | a0001c0001t0026g0075 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.583-381G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 5/9 | chr20 | 44418044 | |||||||
| chr20:44418220 | G | A | 1 | a0001c0001t0059g0096 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.583-205G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 5/9 | chr20 | 44418220 | |||||||
| chr20:44418289 | T | C | 36 | a0001c0001t0001g0070 a0001c0001t0001g0119 a0001c0001t0001g0203 others(33): Show |
36 | HG00544.hp1 HG02027.hp1 HG02074.hp1 others(33): Show |
intron_variant | MODIFIER | c.583-136T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 5/9 | chr20 | 44418289 | |||||||
| chr20:44418653 | A | G | 131 | a0001c0001t0001g0018 a0001c0001t0001g0032 a0001c0001t0001g0035 others(128): Show |
132 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.670+141A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 6/9 | chr20 | 44418653 | |||||||
| chr20:44418708 | G | A | 14 | a0001c0001t0006g0001 a0001c0001t0006g0051 a0001c0001t0006g0081 others(11): Show |
15 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.670+196G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 6/9 | chr20 | 44418708 | |||||||
| chr20:44418871 | G | A | 13 | a0001c0001t0006g0001 a0001c0001t0006g0051 a0001c0001t0006g0081 others(10): Show |
14 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.670+359G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 6/9 | chr20 | 44418871 | |||||||
| chr20:44418895 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.670+383C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 6/9 | chr20 | 44418895 | |||||||
| chr20:44418903 | G | C | 4 | a0001c0001t0028g0099 a0001c0001t0028g0235 a0001c0001t0051g0157 others(1): Show |
4 | HG03453.hp2 HG03942.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.670+391G>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 6/9 | chr20 | 44418903 | |||||||
| chr20:44419149 | C | T | 2 | a0001c0001t0002g0228 a0001c0001t0020g0244 |
2 | NA18951.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.671-572C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 6/9 | chr20 | 44419149 | |||||||
| chr20:44419194 | A | G | 1 | a0001c0001t0043g0309 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.671-527A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 6/9 | chr20 | 44419194 | |||||||
| chr20:44419495 | T | G | 3 | a0001c0001t0001g0286 a0001c0001t0001g0288 a0001c0001t0001g0289 |
3 | HG01167.hp1 HG01169.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.671-226T>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 6/9 | chr20 | 44419495 | |||||||
| chr20:44419506 | C | G | 1 | a0001c0011t0079g0226 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.671-215C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 6/9 | chr20 | 44419506 | |||||||
| chr20:44419633 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.671-88G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 6/9 | chr20 | 44419633 | |||||||
| chr20:44420003 | G | A | 1 | a0001c0001t0063g0173 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.826+127G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44420003 | |||||||
| chr20:44420045 | A | C | 1 | a0006c0004t0056g0077 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.826+169A>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44420045 | |||||||
| chr20:44420045 | A | G | 131 | a0001c0001t0001g0018 a0001c0001t0001g0032 a0001c0001t0001g0035 others(128): Show |
132 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.826+169A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44420045 | |||||||
| chr20:44420106 | C | A | 1 | a0001c0001t0002g0074 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.826+230C>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44420106 | |||||||
| chr20:44420204 | C | T | 1 | a0001c0001t0050g0031 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.826+328C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44420204 | |||||||
| chr20:44420205 | G | A | 11 | a0001c0001t0013g0225 a0001c0001t0018g0209 a0001c0001t0018g0210 others(8): Show |
11 | HG01891.hp2 HG02055.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.826+329G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44420205 | |||||||
| chr20:44420227 | G | A | 1 | a0001c0001t0052g0005 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.826+351G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44420227 | |||||||
| chr20:44420352 | T | C | 1 | a0001c0001t0011g0117 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.826+476T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44420352 | |||||||
| chr20:44420480 | T | A | 1 | a0001c0001t0001g0070 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.826+604T>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44420480 | |||||||
| chr20:44420518 | A | G | 1 | a0001c0001t0028g0099 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.826+642A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44420518 | |||||||
| chr20:44420536 | T | A | 95 | a0001c0001t0001g0018 a0001c0001t0001g0032 a0001c0001t0001g0035 others(92): Show |
95 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.826+660T>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44420536 | |||||||
| chr20:44420608 | C | T | 2 | a0001c0001t0014g0227 a0001c0001t0014g0229 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.826+732C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44420608 | |||||||
| chr20:44420678 | A | G | 178 | a0001c0001t0001g0018 a0001c0001t0001g0026 a0001c0001t0001g0032 others(175): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.826+802A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44420678 | |||||||
| chr20:44420771 | T | C | 1 | a0001c0001t0052g0005 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.826+895T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44420771 | |||||||
| chr20:44420873 | C | T | 1 | a0001c0001t0083g0027 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.826+997C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44420873 | |||||||
| chr20:44420936 | A | G | 2 | a0001c0001t0003g0095 a0001c0001t0003g0097 |
2 | HG00099.hp2 HG00323.hp2 |
intron_variant | MODIFIER | c.826+1060A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44420936 | |||||||
| chr20:44421132 | TTA | T | 11 | a0001c0001t0013g0225 a0001c0001t0018g0209 a0001c0001t0018g0210 others(8): Show |
11 | HG01891.hp2 HG02055.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.826+1258_826+1259d others(4): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr20 | 44421132 | ||||||
| chr20:44421147 | T | C | 1 | a0001c0001t0047g0298 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.826+1271T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44421147 | |||||||
| chr20:44421489 | C | G | 1 | a0001c0001t0008g0059 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.826+1613C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44421489 | |||||||
| chr20:44421728 | T | G | 132 | a0001c0001t0001g0018 a0001c0001t0001g0032 a0001c0001t0001g0035 others(129): Show |
133 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.826+1852T>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44421728 | |||||||
| chr20:44421767 | A | G | 3 | a0001c0001t0003g0113 a0001c0001t0003g0299 a0004c0006t0023g0105 |
3 | HG00639.hp2 HG02572.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.826+1891A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44421767 | |||||||
| chr20:44421773 | G | GTA | 6 | a0001c0001t0004g0300 a0001c0001t0028g0099 a0001c0001t0028g0235 others(3): Show |
6 | HG01515.hp1 HG01517.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.826+1908_826+1909d others(4): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr20 | 44421773 | ||||||
| chr20:44421773 | G | GTATATAT others(13): Show |
1 | a0001c0001t0001g0163 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.826+1917_826+1936d others(22): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr20 | 44421773 | ||||||
| chr20:44421773 | G | GTATATAT others(15): Show |
1 | a0001c0001t0051g0157 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.826+1909_826+1910i others(24): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr20 | 44421773 | ||||||
| chr20:44421785 | A | T | 1 | a0001c0001t0043g0309 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.826+1909A>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44421785 | |||||||
| chr20:44421843 | C | T | 3 | a0001c0001t0019g0151 a0001c0001t0019g0161 a0001c0001t0019g0170 |
3 | HG02615.hp1 HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.826+1967C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44421843 | |||||||
| chr20:44421940 | T | A | 1 | a0001c0001t0093g0140 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.826+2064T>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44421940 | |||||||
| chr20:44422036 | T | A | 1 | a0001c0001t0001g0260 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.827-1982T>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44422036 | |||||||
| chr20:44422092 | C | T | 8 | a0001c0001t0013g0225 a0001c0001t0018g0209 a0001c0001t0018g0210 others(5): Show |
8 | HG01891.hp2 HG02055.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.827-1926C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44422092 | |||||||
| chr20:44422121 | T | G | 131 | a0001c0001t0001g0018 a0001c0001t0001g0032 a0001c0001t0001g0035 others(128): Show |
132 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.827-1897T>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44422121 | |||||||
| chr20:44422130 | C | T | 2 | a0001c0001t0005g0073 a0008c0008t0005g0282 |
2 | HG02155.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.827-1888C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44422130 | |||||||
| chr20:44422142 | A | G | 4 | a0001c0001t0028g0099 a0001c0001t0028g0235 a0001c0001t0051g0157 others(1): Show |
4 | HG03453.hp2 HG03942.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.827-1876A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44422142 | |||||||
| chr20:44422202 | G | T | 1 | a0001c0001t0001g0184 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.827-1816G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44422202 | |||||||
| chr20:44422214 | G | A | 1 | a0001c0001t0006g0249 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.827-1804G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44422214 | |||||||
| chr20:44422341 | A | C | 135 | a0001c0001t0001g0018 a0001c0001t0001g0032 a0001c0001t0001g0035 others(132): Show |
136 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.827-1677A>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44422341 | |||||||
| chr20:44422343 | C | G | 1 | a0006c0004t0056g0077 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.827-1675C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44422343 | |||||||
| chr20:44422557 | C | T | 14 | a0001c0001t0006g0001 a0001c0001t0006g0051 a0001c0001t0006g0081 others(11): Show |
15 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.827-1461C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44422557 | |||||||
| chr20:44422573 | T | C | 135 | a0001c0001t0001g0018 a0001c0001t0001g0032 a0001c0001t0001g0035 others(132): Show |
136 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.827-1445T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44422573 | |||||||
| chr20:44422696 | A | AAT | 14 | a0001c0001t0001g0128 a0001c0001t0001g0155 a0001c0001t0001g0163 others(11): Show |
14 | HG01261.hp1 HG01358.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.827-1308_827-1307d others(4): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr20 | 44422696 | ||||||
| chr20:44422714 | C | A | 1 | a0001c0001t0002g0251 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.827-1304C>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44422714 | |||||||
| chr20:44422728 | G | A | 2 | a0001c0001t0001g0301 a0001c0001t0011g0115 |
2 | HG02717.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.827-1290G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44422728 | |||||||
| chr20:44422758 | C | T | 1 | a0006c0004t0056g0077 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.827-1260C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44422758 | |||||||
| chr20:44422767 | C | T | 1 | a0002c0002t0002g0079 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.827-1251C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44422767 | |||||||
| chr20:44422931 | G | A | 4 | a0001c0001t0028g0099 a0001c0001t0028g0235 a0001c0001t0051g0157 others(1): Show |
4 | HG03453.hp2 HG03942.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.827-1087G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44422931 | |||||||
| chr20:44423057 | C | A | 1 | a0001c0001t0049g0127 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.827-961C>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44423057 | |||||||
| chr20:44423146 | G | A | 1 | a0001c0001t0002g0259 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.827-872G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44423146 | |||||||
| chr20:44423230 | C | T | 2 | a0001c0001t0001g0203 a0001c0001t0001g0204 |
2 | NA18966.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.827-788C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44423230 | |||||||
| chr20:44423316 | A | C | 1 | a0001c0001t0001g0178 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.827-702A>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44423316 | |||||||
| chr20:44423472 | A | G | 2 | a0001c0003t0062g0062 a0001c0003t0065g0308 |
2 | HG02486.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.827-546A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44423472 | |||||||
| chr20:44423508 | A | C | 1 | a0006c0004t0056g0077 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.827-510A>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44423508 | |||||||
| chr20:44423930 | T | C | 148 | a0001c0001t0001g0018 a0001c0001t0001g0032 a0001c0001t0001g0035 others(145): Show |
149 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.827-88T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44423930 | |||||||
| chr20:44423974 | G | C | 1 | a0001c0001t0084g0306 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.827-44G>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44423974 | |||||||
| chr20:44424460 | C | T | 2 | a0001c0003t0062g0062 a0001c0003t0065g0308 |
2 | HG02486.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1063+206C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 8/9 | chr20 | 44424460 | |||||||
| chr20:44424500 | A | C | 3 | a0001c0001t0019g0151 a0001c0001t0019g0161 a0001c0001t0019g0170 |
3 | HG02615.hp1 HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1063+246A>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 8/9 | chr20 | 44424500 | |||||||
| chr20:44424671 | A | G | 4 | a0001c0001t0028g0099 a0001c0001t0028g0235 a0001c0001t0051g0157 others(1): Show |
4 | HG03453.hp2 HG03942.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.1063+417A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 8/9 | chr20 | 44424671 | |||||||
| chr20:44424691 | C | T | 1 | a0001c0001t0004g0166 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1063+437C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 8/9 | chr20 | 44424691 | |||||||
| chr20:44424948 | A | T | 129 | a0001c0001t0001g0018 a0001c0001t0001g0032 a0001c0001t0001g0035 others(126): Show |
130 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.1063+694A>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 8/9 | chr20 | 44424948 | |||||||
| chr20:44425020 | C | A | 1 | a0001c0001t0052g0005 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1063+766C>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 8/9 | chr20 | 44425020 | |||||||
| chr20:44425023 | C | G | 1 | a0001c0001t0004g0222 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1063+769C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 8/9 | chr20 | 44425023 | |||||||
| chr20:44425151 | T | C | 1 | a0001c0001t0020g0049 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1063+897T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 8/9 | chr20 | 44425151 | |||||||
| chr20:44425598 | G | T | 1 | a0001c0001t0002g0202 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1063+1344G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 8/9 | chr20 | 44425598 | |||||||
| chr20:44425633 | T | C | 4 | a0001c0001t0028g0099 a0001c0001t0028g0235 a0001c0001t0051g0157 others(1): Show |
4 | HG03453.hp2 HG03942.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.1063+1379T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 8/9 | chr20 | 44425633 | |||||||
| chr20:44425656 | C | CT | 45 | a0001c0001t0001g0026 a0001c0001t0002g0134 a0001c0001t0003g0042 others(42): Show |
45 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.1063+1418dupT | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr20 | 44425656 | ||||||
| chr20:44425656 | C | CTTT | 7 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0216 others(4): Show |
7 | HG00323.hp1 HG01081.hp2 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.1063+1416_1063+141 others(7): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr20 | 44425656 | ||||||
| chr20:44425656 | C | CTTTT | 90 | a0001c0001t0001g0018 a0001c0001t0001g0032 a0001c0001t0001g0035 others(87): Show |
90 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.1063+1415_1063+141 others(8): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr20 | 44425656 | ||||||
| chr20:44425656 | C | CTTTTT | 6 | a0001c0001t0001g0263 a0001c0001t0004g0047 a0001c0001t0054g0253 others(3): Show |
6 | HG00735.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1063+1414_1063+141 others(9): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr20 | 44425656 | ||||||
| chr20:44425801 | C | T | 73 | a0001c0001t0001g0018 a0001c0001t0001g0032 a0001c0001t0001g0035 others(70): Show |
73 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.1063+1547C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 8/9 | chr20 | 44425801 | |||||||
| chr20:44425841 | A | G | 103 | a0001c0001t0001g0018 a0001c0001t0001g0032 a0001c0001t0001g0035 others(100): Show |
103 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.1063+1587A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 8/9 | chr20 | 44425841 | |||||||
| chr20:44425843 | A | G | 86 | a0001c0001t0001g0018 a0001c0001t0001g0032 a0001c0001t0001g0035 others(83): Show |
86 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.1063+1589A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 8/9 | chr20 | 44425843 | |||||||
| chr20:44426018 | GCTGTTGA others(155): Show |
G | 1 | a0001c0001t0094g0313 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1063+1765_1063+192 others(4): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 8/9 | chr20 | 44426018 | |||||||
| chr20:44426020 | T | A | 96 | a0001c0001t0001g0018 a0001c0001t0001g0032 a0001c0001t0001g0035 others(93): Show |
96 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.1063+1766T>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 8/9 | chr20 | 44426020 | |||||||
| chr20:44426190 | A | G | 1 | a0001c0001t0003g0295 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1063+1936A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 8/9 | chr20 | 44426190 | |||||||
| chr20:44426231 | A | G | 96 | a0001c0001t0001g0018 a0001c0001t0001g0032 a0001c0001t0001g0035 others(93): Show |
96 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.1063+1977A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 8/9 | chr20 | 44426231 | |||||||
| chr20:44426239 | G | T | 1 | a0006c0004t0056g0077 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1063+1985G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 8/9 | chr20 | 44426239 | |||||||
| chr20:44426526 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1064-1809G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 8/9 | chr20 | 44426526 | |||||||
| chr20:44426785 | C | T | 1 | a0001c0001t0001g0246 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1064-1550C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 8/9 | chr20 | 44426785 | |||||||
| chr20:44427064 | G | A | 1 | a0001c0001t0004g0300 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1064-1271G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 8/9 | chr20 | 44427064 | |||||||
| chr20:44427177 | A | T | 1 | a0001c0001t0023g0004 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1064-1158A>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 8/9 | chr20 | 44427177 | |||||||
| chr20:44427204 | A | G | 1 | a0007c0005t0025g0038 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1064-1131A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 8/9 | chr20 | 44427204 | |||||||
| chr20:44427457 | T | C | 4 | a0001c0001t0028g0099 a0001c0001t0028g0235 a0001c0001t0051g0157 others(1): Show |
4 | HG03453.hp2 HG03942.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.1064-878T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 8/9 | chr20 | 44427457 | |||||||
| chr20:44427509 | G | T | 132 | a0001c0001t0001g0018 a0001c0001t0001g0026 a0001c0001t0001g0032 others(129): Show |
133 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.1064-826G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 8/9 | chr20 | 44427509 | |||||||
| chr20:44427767 | G | A | 1 | a0001c0011t0079g0226 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1064-568G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 8/9 | chr20 | 44427767 | |||||||
| chr20:44427845 | T | C | 2 | a0001c0003t0062g0062 a0001c0003t0065g0308 |
2 | HG02486.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1064-490T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 8/9 | chr20 | 44427845 | |||||||
| chr20:44427922 | T | C | 47 | a0001c0001t0001g0178 a0001c0001t0006g0001 a0001c0001t0006g0051 others(44): Show |
48 | HG00280.hp1 HG00639.hp1 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.1064-413T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 8/9 | chr20 | 44427922 | |||||||
| chr20:44427925 | G | A | 1 | a0001c0001t0052g0005 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1064-410G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 8/9 | chr20 | 44427925 | |||||||
| chr20:44428092 | A | G | 4 | a0001c0001t0028g0099 a0001c0001t0028g0235 a0001c0001t0051g0157 others(1): Show |
4 | HG03453.hp2 HG03942.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.1064-243A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 8/9 | chr20 | 44428092 | |||||||
| chr20:44428840 | G | T | 159 | a0001c0001t0001g0104 a0001c0001t0001g0191 a0001c0001t0001g0263 others(156): Show |
160 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.1216+353G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 9/9 | chr20 | 44428840 | |||||||
| chr20:44429074 | G | A | 1 | a0001c0001t0008g0003 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1217-449G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 9/9 | chr20 | 44429074 | |||||||
| chr20:44429154 | A | G | 1 | a0001c0001t0022g0076 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1217-369A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 9/9 | chr20 | 44429154 | |||||||
| chr20:44429180 | C | A | 150 | a0001c0001t0001g0018 a0001c0001t0001g0026 a0001c0001t0001g0032 others(147): Show |
151 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.1217-343C>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 9/9 | chr20 | 44429180 | |||||||
| chr20:44429191 | A | G | 1 | a0001c0001t0055g0118 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1217-332A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 9/9 | chr20 | 44429191 | |||||||
| chr20:44429206 | G | A | 3 | a0001c0001t0027g0014 a0001c0001t0027g0016 a0001c0001t0048g0013 |
3 | HG01891.hp2 HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1217-317G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 9/9 | chr20 | 44429206 | |||||||
| chr20:44429226 | G | A | 1 | a0001c0001t0023g0004 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1217-297G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 9/9 | chr20 | 44429226 | |||||||
| chr20:44429344 | G | A | 1 | a0006c0004t0056g0077 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1217-179G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 9/9 | chr20 | 44429344 | |||||||
| chr20:44429372 | A | C | 16 | a0001c0001t0006g0001 a0001c0001t0006g0051 a0001c0001t0006g0081 others(13): Show |
17 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1217-151A>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 9/9 | chr20 | 44429372 | |||||||
| chr20:44429378 | T | C | 119 | a0001c0001t0001g0018 a0001c0001t0001g0026 a0001c0001t0001g0032 others(116): Show |
119 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.1217-145T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 9/9 | chr20 | 44429378 | |||||||
| chr20:44429440 | G | A | 6 | a0001c0001t0013g0225 a0001c0001t0018g0209 a0001c0001t0018g0210 others(3): Show |
6 | HG02055.hp1 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1217-83G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 9/9 | chr20 | 44429440 | |||||||
| chr20:44429456 | C | G | 150 | a0001c0001t0001g0018 a0001c0001t0001g0026 a0001c0001t0001g0032 others(147): Show |
151 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.1217-67C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 9/9 | chr20 | 44429456 |