Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 6928 |
| ensemblid | ENSG00000275410.6 |
| hgncid | 11630 |
| symbol | HNF1B |
| name | HNF1 homeobox B |
| refseq_nuc | NM_000458.4 |
| refseq_prot | NP_000449.1 |
| ensembl_nuc | ENST00000617811.5 |
| ensembl_prot | ENSP00000480291.1 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 37686431 |
| end | 37745059 |
| strand | - |
| ver | v1.2 |
| region | chr17:37686431-37745059 |
| region5000 | chr17:37681431-37750059 |
| regionname0 | HNF1B_chr17_37686431_37745059 |
| regionname5000 | HNF1B_chr17_37681431_37750059 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 557 | 405 | 92 | 68 | 182 | 18 | 44 | 137 | HNF1B_chr17_37681431_37750059 | HNF1B | MVSKL others(552): Show |
chr17 | 37681431 | 37750059 |
| a0002 | 0/0 | 557 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | MVSKL others(552): Show |
chr17 | 37681431 | 37750059 |
| a0003 | 0/0 | 557 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | MVSKL others(552): Show |
chr17 | 37681431 | 37750059 |
| a0004 | 0/0 | 557 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HNF1B_chr17_37681431_37750059 | HNF1B | MVSKL others(552): Show |
chr17 | 37681431 | 37750059 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1671 | 400 | 89 | 67 | 181 | 18 | 44 | HNF1B_chr17_37681431_37750059 | HNF1B | ATGGT others(1666): Show |
chr17 | 37681431 | 37750059 | ||
| a0001c0002 | 0/0 | 1671 | 2 | 2 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | ATGGT others(1666): Show |
chr17 | 37681431 | 37750059 | ||
| a0001c0003 | 0/0 | 1671 | 2 | 1 | 1 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | ATGGT others(1666): Show |
chr17 | 37681431 | 37750059 | ||
| a0001c0006 | 0/0 | 1671 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | ATGGT others(1666): Show |
chr17 | 37681431 | 37750059 | ||
| a0002c0004 | 0/0 | 1671 | 2 | 0 | 0 | 0 | 0 | 2 | HNF1B_chr17_37681431_37750059 | HNF1B | ATGGT others(1666): Show |
chr17 | 37681431 | 37750059 | ||
| a0003c0005 | 0/0 | 1671 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | ATGGT others(1666): Show |
chr17 | 37681431 | 37750059 | ||
| a0004c0007 | 0/0 | 1671 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | ATGGT others(1666): Show |
chr17 | 37681431 | 37750059 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2790 | 137 | 14 | 24 | 74 | 10 | 14 | HNF1B_chr17_37681431_37750059 | HNF1B | AGAAG others(2785): Show |
chr17 | 37681431 | 37750059 |
| a0001c0001t0002 | 0/0 | 2790 | 97 | 14 | 23 | 45 | 4 | 11 | HNF1B_chr17_37681431_37750059 | HNF1B | AGAAG others(2785): Show |
chr17 | 37681431 | 37750059 |
| a0001c0001t0003 | 0/0 | 2790 | 43 | 2 | 4 | 32 | 0 | 5 | HNF1B_chr17_37681431_37750059 | HNF1B | AGAAG others(2785): Show |
chr17 | 37681431 | 37750059 |
| a0001c0001t0004 | 0/0 | 2790 | 36 | 0 | 4 | 24 | 1 | 7 | HNF1B_chr17_37681431_37750059 | HNF1B | AGAAG others(2785): Show |
chr17 | 37681431 | 37750059 |
| a0001c0001t0005 | 0/0 | 2790 | 33 | 24 | 6 | 0 | 2 | 1 | HNF1B_chr17_37681431_37750059 | HNF1B | AGAAG others(2785): Show |
chr17 | 37681431 | 37750059 |
| a0001c0001t0006 | 0/0 | 2790 | 17 | 16 | 1 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | AGAAG others(2785): Show |
chr17 | 37681431 | 37750059 |
| a0001c0001t0007 | 0/0 | 2790 | 11 | 11 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | AGAAG others(2785): Show |
chr17 | 37681431 | 37750059 |
| a0001c0001t0008 | 0/0 | 2790 | 10 | 0 | 5 | 1 | 1 | 3 | HNF1B_chr17_37681431_37750059 | HNF1B | AGAAG others(2785): Show |
chr17 | 37681431 | 37750059 |
| a0001c0001t0009 | 0/0 | 2790 | 3 | 3 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | AGAAG others(2785): Show |
chr17 | 37681431 | 37750059 |
| a0001c0001t0010 | 0/0 | 2790 | 2 | 2 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | AGAAG others(2785): Show |
chr17 | 37681431 | 37750059 |
| a0001c0001t0011 | 0/0 | 2790 | 2 | 0 | 0 | 2 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | AGAAG others(2785): Show |
chr17 | 37681431 | 37750059 |
| a0001c0001t0012 | 0/0 | 2790 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | AGAAG others(2785): Show |
chr17 | 37681431 | 37750059 |
| a0001c0001t0013 | 0/0 | 2790 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | AGAAG others(2785): Show |
chr17 | 37681431 | 37750059 |
| a0001c0001t0014 | 0/0 | 2790 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | AGAAG others(2785): Show |
chr17 | 37681431 | 37750059 |
| a0001c0001t0015 | 0/0 | 2790 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | AGAAG others(2785): Show |
chr17 | 37681431 | 37750059 |
| a0001c0001t0016 | 0/0 | 2790 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | AGAAG others(2785): Show |
chr17 | 37681431 | 37750059 |
| a0001c0001t0017 | 0/0 | 2790 | 1 | 0 | 0 | 0 | 0 | 1 | HNF1B_chr17_37681431_37750059 | HNF1B | AGAAG others(2785): Show |
chr17 | 37681431 | 37750059 |
| a0001c0001t0018 | 0/0 | 2790 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | AGAAG others(2785): Show |
chr17 | 37681431 | 37750059 |
| a0001c0001t0019 | 0/0 | 2790 | 1 | 0 | 0 | 0 | 0 | 1 | HNF1B_chr17_37681431_37750059 | HNF1B | AGAAG others(2785): Show |
chr17 | 37681431 | 37750059 |
| a0001c0001t0020 | 0/0 | 2790 | 1 | 0 | 0 | 0 | 0 | 1 | HNF1B_chr17_37681431_37750059 | HNF1B | AGAAG others(2785): Show |
chr17 | 37681431 | 37750059 |
| a0001c0002t0009 | 0/0 | 2790 | 2 | 2 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | AGAAG others(2785): Show |
chr17 | 37681431 | 37750059 |
| a0001c0003t0005 | 0/0 | 2790 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | AGAAG others(2785): Show |
chr17 | 37681431 | 37750059 |
| a0001c0003t0006 | 0/0 | 2790 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | AGAAG others(2785): Show |
chr17 | 37681431 | 37750059 |
| a0001c0006t0001 | 0/0 | 2790 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | AGAAG others(2785): Show |
chr17 | 37681431 | 37750059 |
| a0002c0004t0001 | 0/0 | 2790 | 1 | 0 | 0 | 0 | 0 | 1 | HNF1B_chr17_37681431_37750059 | HNF1B | AGAAG others(2785): Show |
chr17 | 37681431 | 37750059 |
| a0002c0004t0003 | 0/0 | 2790 | 1 | 0 | 0 | 0 | 0 | 1 | HNF1B_chr17_37681431_37750059 | HNF1B | AGAAG others(2785): Show |
chr17 | 37681431 | 37750059 |
| a0003c0005t0002 | 0/0 | 2790 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | AGAAG others(2785): Show |
chr17 | 37681431 | 37750059 |
| a0004c0007t0001 | 0/0 | 2790 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | AGAAG others(2785): Show |
chr17 | 37681431 | 37750059 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0243 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0371 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0375 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0377 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0380 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0381 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0383 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0388 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0391 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0393 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0394 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0397 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0399 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0001g0400 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0382 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0390 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0398 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0002g0401 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0003g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0003g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0003g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0003g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0003g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0003g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0003g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0003g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0003g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0003g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0003g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0003g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0003g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0003g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0003g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0003g0402 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0003g0403 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0004g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0004g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0004g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0004g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0004g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0004g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0004g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0004g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0004g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0004g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0004g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0004g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0004g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0004g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0004g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0004g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0004g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0004g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0004g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0004g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0004g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0004g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0004g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0004g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0004g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0004g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0004g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0004g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0004g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0004g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0004g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0004g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0004g0376 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0004g0384 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0004g0386 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0005g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0005g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0005g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0005g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0005g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0005g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0005g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0005g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0005g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0005g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0005g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0005g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0005g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0005g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0005g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0005g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0005g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0005g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0005g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0005g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0005g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0005g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0005g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0005g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0005g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0005g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0005g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0005g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0005g0387 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0005g0389 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0005g0392 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0005g0395 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0005g0396 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0006g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0006g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0006g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0006g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0006g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0006g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0006g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0006g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0006g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0006g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0006g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0006g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0006g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0006g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0006g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0006g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0006g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0007g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0007g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0007g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0007g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0007g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0007g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0007g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0007g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0007g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0007g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0007g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0008g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0008g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0008g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0008g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0008g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0008g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0008g0369 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0008g0370 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0008g0378 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0008g0379 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0009g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0009g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0009g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0010g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0010g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0011g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0011g0385 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0012g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0013g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0014g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0015g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0016g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0017g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0018g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0019g0406 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0001t0020g0407 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0002t0009g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0002t0009g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0003t0005g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0003t0006g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0001c0006t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0002c0004t0001g0404 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0002c0004t0003g0405 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0003c0005t0002g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| a0004c0007t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0177 | EUR | GBR | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0158 | EUR | GBR | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG00140 | hp1 | a0001 | c0001 | t0005 | g0108 | EUR | GBR | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG00140 | hp2 | a0001 | c0001 | t0008 | g0017 | EUR | GBR | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG00280 | hp1 | a0001 | c0001 | t0005 | g0058 | EUR | FIN | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0318 | EUR | FIN | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0371 | EUR | FIN | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0128 | EUR | FIN | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | CHS | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | CHS | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | CHS | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG00423 | hp2 | a0001 | c0001 | t0003 | g0052 | EAS | CHS | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | CHS | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | CHS | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | CHS | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | CHS | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0356 | EAS | CHS | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | CHS | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | CHS | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG00597 | hp2 | a0001 | c0001 | t0004 | g0079 | EAS | CHS | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | CHS | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | CHS | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG00621 | hp1 | a0001 | c0001 | t0011 | g0385 | EAS | CHS | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0363 | EAS | CHS | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0383 | AMR | PUR | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0397 | AMR | PUR | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | CHS | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG00673 | hp2 | a0001 | c0001 | t0003 | g0122 | EAS | CHS | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG00733 | hp1 | a0001 | c0001 | t0003 | g0023 | AMR | PUR | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0297 | AMR | PUR | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0077 | AMR | PUR | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG00735 | hp2 | a0001 | c0001 | t0008 | g0025 | AMR | PUR | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0134 | AMR | PUR | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0300 | AMR | PUR | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG00741 | hp1 | a0001 | c0001 | t0008 | g0239 | AMR | PUR | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0381 | AMR | PUR | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0138 | AMR | PUR | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG01070 | hp1 | a0001 | c0001 | t0008 | g0378 | AMR | PUR | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG01071 | hp2 | a0001 | c0001 | t0008 | g0379 | AMR | PUR | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0298 | AMR | PUR | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0319 | AMR | PUR | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0273 | AMR | PUR | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0272 | AMR | PUR | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG01099 | hp2 | a0001 | c0001 | t0005 | g0109 | AMR | PUR | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG01109 | hp1 | a0001 | c0001 | t0004 | g0216 | AMR | PUR | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0342 | AMR | PUR | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0136 | AMR | PUR | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0401 | AMR | PUR | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG01168 | hp2 | a0001 | c0001 | t0005 | g0387 | AMR | PUR | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG01169 | hp1 | a0001 | c0001 | t0005 | g0389 | AMR | PUR | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0135 | AMR | PUR | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG01192 | hp2 | a0001 | c0001 | t0006 | g0038 | AMR | PUR | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG01243 | hp1 | a0001 | c0003 | t0006 | g0349 | AMR | PUR | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0172 | AMR | PUR | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG01255 | hp1 | a0001 | c0001 | t0008 | g0020 | AMR | CLM | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | CLM | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | CLM | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0326 | AMR | CLM | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG01257 | hp1 | a0001 | c0001 | t0005 | g0293 | AMR | CLM | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0329 | AMR | CLM | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0120 | AMR | CLM | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0324 | AMR | CLM | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0314 | AMR | CLM | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG01358 | hp2 | a0001 | c0001 | t0003 | g0125 | AMR | CLM | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | CLM | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG01361 | hp2 | a0001 | c0001 | t0004 | g0386 | AMR | CLM | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG01433 | hp1 | a0001 | c0001 | t0004 | g0376 | AMR | CLM | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG01433 | hp2 | a0001 | c0001 | t0005 | g0307 | AMR | CLM | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0312 | AMR | CLM | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0121 | AMR | CLM | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0133 | EUR | IBS | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0240 | EUR | IBS | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0377 | EUR | IBS | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0157 | EUR | IBS | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0236 | EUR | IBS | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0380 | EUR | IBS | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG01884 | hp1 | a0001 | c0001 | t0006 | g0005 | AFR | ACB | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG01884 | hp2 | a0001 | c0001 | t0007 | g0214 | AFR | ACB | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG01891 | hp1 | a0001 | c0001 | t0006 | g0270 | AFR | ACB | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG01891 | hp2 | a0001 | c0001 | t0006 | g0251 | AFR | ACB | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PEL | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0176 | AMR | PEL | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0306 | AMR | PEL | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0131 | AMR | PEL | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0110 | AMR | PEL | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0137 | AMR | PEL | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0132 | AMR | PEL | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0034 | AMR | PEL | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG01993 | hp1 | a0001 | c0001 | t0005 | g0208 | AMR | PEL | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02004 | hp1 | a0001 | c0001 | t0004 | g0215 | AMR | PEL | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0123 | AMR | PEL | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | KHV | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | KHV | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02055 | hp1 | a0001 | c0001 | t0007 | g0338 | AFR | ACB | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02055 | hp2 | a0001 | c0001 | t0005 | g0193 | AFR | ACB | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | KHV | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | KHV | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | KHV | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | KHV | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0054 | EAS | KHV | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | KHV | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | KHV | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | KHV | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | KHV | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02083 | hp2 | a0001 | c0001 | t0003 | g0402 | EAS | KHV | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0166 | EAS | KHV | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | KHV | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0126 | EAS | KHV | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0220 | AFR | ACB | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02145 | hp2 | a0001 | c0001 | t0010 | g0268 | AFR | ACB | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0388 | AMR | PEL | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0114 | AMR | PEL | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | CDX | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02155 | hp2 | a0001 | c0001 | t0004 | g0179 | EAS | CDX | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | CDX | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0391 | EAS | CDX | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02257 | hp2 | a0001 | c0001 | t0005 | g0012 | AFR | ACB | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0333 | AFR | ACB | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02258 | hp2 | a0001 | c0001 | t0007 | g0276 | AFR | ACB | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0219 | AFR | ACB | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02280 | hp2 | a0001 | c0001 | t0014 | g0280 | AFR | ACB | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0262 | AFR | ACB | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0351 | AFR | ACB | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02523 | hp1 | a0003 | c0005 | t0002 | g0003 | EAS | KHV | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0400 | EAS | KHV | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02572 | hp1 | a0001 | c0001 | t0005 | g0010 | AFR | GWD | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02572 | hp2 | a0001 | c0001 | t0006 | g0274 | AFR | GWD | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02602 | hp1 | a0001 | c0001 | t0004 | g0192 | SAS | PJL | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02602 | hp2 | a0001 | c0001 | t0004 | g0258 | SAS | PJL | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02615 | hp1 | a0001 | c0001 | t0005 | g0204 | AFR | GWD | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0226 | AFR | GWD | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02622 | hp1 | a0001 | c0001 | t0005 | g0290 | AFR | GWD | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0263 | AFR | GWD | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02630 | hp2 | a0001 | c0001 | t0006 | g0344 | AFR | GWD | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02647 | hp1 | a0001 | c0001 | t0005 | g0348 | AFR | GWD | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02647 | hp2 | a0001 | c0001 | t0007 | g0340 | AFR | GWD | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02683 | hp1 | a0001 | c0001 | t0003 | g0162 | SAS | PJL | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0147 | SAS | PJL | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02717 | hp1 | a0001 | c0001 | t0006 | g0275 | AFR | GWD | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02717 | hp2 | a0001 | c0001 | t0005 | g0352 | AFR | GWD | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02723 | hp1 | a0001 | c0001 | t0005 | g0353 | AFR | GWD | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0254 | SAS | PJL | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02738 | hp1 | a0001 | c0001 | t0004 | g0191 | SAS | PJL | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02738 | hp2 | a0001 | c0001 | t0004 | g0261 | SAS | PJL | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02809 | hp1 | a0001 | c0001 | t0006 | g0004 | AFR | GWD | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02809 | hp2 | a0001 | c0001 | t0005 | g0218 | AFR | GWD | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02818 | hp1 | a0001 | c0001 | t0006 | g0253 | AFR | GWD | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02818 | hp2 | a0001 | c0001 | t0006 | g0285 | AFR | GWD | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0308 | AFR | GWD | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02886 | hp2 | a0001 | c0001 | t0006 | g0246 | AFR | GWD | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0282 | AFR | GWD | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02895 | hp2 | a0001 | c0001 | t0009 | g0207 | AFR | GWD | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02896 | hp1 | a0001 | c0001 | t0009 | g0206 | AFR | GWD | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02896 | hp2 | a0001 | c0001 | t0005 | g0343 | AFR | GWD | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0289 | AFR | ESN | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02922 | hp2 | a0001 | c0001 | t0007 | g0201 | AFR | ESN | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02965 | hp1 | a0001 | c0001 | t0005 | g0196 | AFR | ESN | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0205 | AFR | ESN | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02970 | hp1 | a0001 | c0001 | t0005 | g0227 | AFR | ESN | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02970 | hp2 | a0001 | c0001 | t0006 | g0341 | AFR | ESN | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0375 | SAS | PJL | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG03017 | hp2 | a0002 | c0004 | t0001 | g0404 | SAS | PJL | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG03041 | hp1 | a0001 | c0001 | t0005 | g0266 | AFR | GWD | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG03041 | hp2 | a0001 | c0001 | t0005 | g0396 | AFR | GWD | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG03098 | hp1 | a0001 | c0002 | t0009 | g0265 | AFR | MSL | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG03098 | hp2 | a0001 | c0001 | t0012 | g0223 | AFR | MSL | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG03130 | hp1 | a0001 | c0001 | t0009 | g0008 | AFR | ESN | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG03130 | hp2 | a0001 | c0001 | t0005 | g0203 | AFR | ESN | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG03139 | hp2 | a0001 | c0001 | t0005 | g0337 | AFR | ESN | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG03195 | hp1 | a0001 | c0001 | t0010 | g0269 | AFR | ESN | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0222 | AFR | ESN | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG03209 | hp1 | a0001 | c0001 | t0007 | g0339 | AFR | MSL | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0283 | AFR | MSL | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | MSL | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG03225 | hp2 | a0001 | c0003 | t0005 | g0350 | AFR | MSL | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0018 | SAS | PJL | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0399 | SAS | PJL | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG03453 | hp1 | a0001 | c0001 | t0006 | g0264 | AFR | MSL | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG03453 | hp2 | a0001 | c0002 | t0009 | g0221 | AFR | MSL | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG03486 | hp1 | a0001 | c0001 | t0006 | g0014 | AFR | MSL | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG03486 | hp2 | a0001 | c0001 | t0006 | g0345 | AFR | MSL | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG03490 | hp1 | a0001 | c0001 | t0008 | g0369 | SAS | PJL | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0142 | SAS | PJL | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0124 | SAS | PJL | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG03492 | hp1 | a0001 | c0001 | t0008 | g0370 | SAS | PJL | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0347 | AFR | ESN | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | ESN | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0288 | AFR | GWD | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG03540 | hp2 | a0001 | c0001 | t0005 | g0194 | AFR | GWD | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | MSL | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG03579 | hp2 | a0001 | c0001 | t0005 | g0195 | AFR | MSL | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0393 | SAS | PJL | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG03669 | hp1 | a0001 | c0001 | t0004 | g0233 | SAS | PJL | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG03669 | hp2 | a0001 | c0001 | t0020 | g0407 | SAS | PJL | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0382 | SAS | STU | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0190 | SAS | STU | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG03704 | hp2 | a0001 | c0001 | t0017 | g0257 | SAS | PJL | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0260 | SAS | PJL | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0161 | SAS | PJL | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0097 | SAS | BEB | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0066 | SAS | BEB | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0325 | SAS | BEB | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | BEB | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG03942 | hp1 | a0001 | c0001 | t0004 | g0332 | SAS | BEB | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG03942 | hp2 | a0001 | c0001 | t0019 | g0406 | SAS | BEB | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0403 | SAS | STU | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0301 | SAS | STU | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG04184 | hp1 | a0001 | c0001 | t0005 | g0392 | SAS | BEB | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0118 | SAS | BEB | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0299 | SAS | STU | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0065 | SAS | STU | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | STU | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG04204 | hp2 | a0001 | c0001 | t0008 | g0305 | SAS | STU | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0259 | SAS | STU | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG04228 | hp2 | a0002 | c0004 | t0003 | g0405 | SAS | STU | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18522 | hp1 | a0001 | c0001 | t0005 | g0395 | AFR | YRI | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18522 | hp2 | a0001 | c0001 | t0007 | g0277 | AFR | YRI | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18612 | hp1 | a0001 | c0001 | t0003 | g0032 | EAS | CHB | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18612 | hp2 | a0001 | c0001 | t0016 | g0178 | EAS | CHB | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0141 | EAS | CHB | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18747 | hp2 | a0001 | c0001 | t0004 | g0088 | EAS | CHB | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0398 | AFR | YRI | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18906 | hp2 | a0001 | c0001 | t0006 | g0287 | AFR | YRI | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18939 | hp2 | a0001 | c0001 | t0004 | g0093 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18941 | hp1 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18941 | hp2 | a0001 | c0001 | t0018 | g0085 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18942 | hp1 | a0001 | c0001 | t0004 | g0165 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18943 | hp2 | a0001 | c0001 | t0004 | g0384 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18944 | hp2 | a0001 | c0001 | t0004 | g0042 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0327 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18945 | hp2 | a0001 | c0006 | t0001 | g0050 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18946 | hp2 | a0001 | c0001 | t0004 | g0068 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18949 | hp1 | a0001 | c0001 | t0003 | g0231 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18951 | hp2 | a0001 | c0001 | t0004 | g0035 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18952 | hp1 | a0001 | c0001 | t0004 | g0186 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18952 | hp2 | a0001 | c0001 | t0004 | g0094 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18953 | hp1 | a0001 | c0001 | t0003 | g0086 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18957 | hp1 | a0001 | c0001 | t0004 | g0167 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0217 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0373 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18964 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18968 | hp1 | a0001 | c0001 | t0004 | g0244 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0358 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18970 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18971 | hp1 | a0001 | c0001 | t0015 | g0175 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0102 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18973 | hp2 | a0001 | c0001 | t0003 | g0197 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0317 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18978 | hp1 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18981 | hp2 | a0001 | c0001 | t0003 | g0213 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18983 | hp2 | a0001 | c0001 | t0011 | g0374 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0368 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18986 | hp2 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18987 | hp2 | a0001 | c0001 | t0003 | g0323 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18989 | hp2 | a0001 | c0001 | t0003 | g0364 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18992 | hp2 | a0001 | c0001 | t0003 | g0367 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0390 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA18999 | hp2 | a0001 | c0001 | t0004 | g0036 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA19000 | hp2 | a0001 | c0001 | t0003 | g0211 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA19001 | hp1 | a0001 | c0001 | t0004 | g0089 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA19002 | hp1 | a0001 | c0001 | t0003 | g0087 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0328 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0372 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | LWK | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA19030 | hp2 | a0001 | c0001 | t0006 | g0286 | AFR | LWK | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA19043 | hp1 | a0001 | c0001 | t0007 | g0200 | AFR | LWK | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA19043 | hp2 | a0001 | c0001 | t0007 | g0284 | AFR | LWK | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0365 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA19058 | hp2 | a0001 | c0001 | t0004 | g0330 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA19060 | hp1 | a0004 | c0007 | t0001 | g0235 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0321 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0248 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0361 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA19068 | hp1 | a0001 | c0001 | t0004 | g0090 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0355 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA19078 | hp1 | a0001 | c0001 | t0003 | g0044 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0359 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0336 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0360 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA19081 | hp2 | a0001 | c0001 | t0004 | g0078 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0362 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA19083 | hp1 | a0001 | c0001 | t0004 | g0091 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0357 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA19084 | hp2 | a0001 | c0001 | t0003 | g0116 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA19085 | hp1 | a0001 | c0001 | t0008 | g0168 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA19086 | hp1 | a0001 | c0001 | t0004 | g0151 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0366 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA19087 | hp2 | a0001 | c0001 | t0004 | g0174 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA19090 | hp1 | a0001 | c0001 | t0004 | g0335 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0334 | AFR | ASW | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0316 | AFR | ASW | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0143 | EUR | TSI | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA20752 | hp2 | a0001 | c0001 | t0004 | g0021 | EUR | TSI | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0156 | EUR | TSI | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0247 | EUR | TSI | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA20905 | hp1 | a0001 | c0001 | t0004 | g0119 | SAS | GIH | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0331 | SAS | GIH | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0304 | AMR | CLM | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0171 | AMR | CLM | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02109 | hp1 | a0001 | c0001 | t0005 | g0295 | AFR | ACB | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0113 | AFR | ACB | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0394 | AFR | ACB | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02486 | hp2 | a0001 | c0001 | t0005 | g0346 | AFR | ACB | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0354 | AFR | ACB | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG02559 | hp2 | a0001 | c0001 | t0005 | g0279 | AFR | ACB | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG03471 | hp1 | a0001 | c0001 | t0005 | g0281 | AFR | MSL | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG03471 | hp2 | a0001 | c0001 | t0007 | g0267 | AFR | MSL | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG06807 | hp1 | a0001 | c0001 | t0007 | g0250 | AFR | USA | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| HG06807 | hp2 | a0001 | c0001 | t0013 | g0294 | AFR | USA | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0067 | AFR | USA | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | USA | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0243 | REF | REF | HNF1B_chr17_37681431_37750059 | HNF1B | chr17 | 37681431 | 37750059 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:37704959 | G | C | 1 | a0004 | 1 | NA19060.hp1 | missense_variant | MODERATE | c.1297C>G | p.Leu433Val | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 6/9 | 1472/2790 | 1297/1674 | 433/557 | chr17 | 37704959 | |||
| chr17:37744572 | C | T | 1 | a0003 | 1 | HG02523.hp1 | missense_variant | MODERATE | c.313G>A | p.Glu105Lys | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 1/9 | 488/2790 | 313/1674 | 105/557 | chr17 | 37744572 | |||
| chr17:37744812 | C | A | 1 | a0002 | 2 | HG03017.hp2 HG04228.hp2 |
missense_variant | MODERATE | c.73G>T | p.Val25Leu | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 1/9 | 248/2790 | 73/1674 | 25/557 | chr17 | 37744812 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:37701104 | G | A | 1 | a0001c0002 | 2 | HG03098.hp1 HG03453.hp2 |
synonymous_variant | LOW | c.1413C>T | p.Pro471Pro | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 7/9 | 1588/2790 | 1413/1674 | 471/557 | chr17 | 37701104 | |||
| chr17:37731689 | G | C | 1 | a0001c0003 | 2 | HG01243.hp1 HG03225.hp2 |
synonymous_variant | LOW | c.951C>G | p.Ala317Ala | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/9 | 1126/2790 | 951/1674 | 317/557 | chr17 | 37731689 | |||
| chr17:37731809 | C | T | 1 | a0001c0006 | 1 | NA18945.hp2 | synonymous_variant | LOW | c.831G>A | p.Gly277Gly | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/9 | 1006/2790 | 831/1674 | 277/557 | chr17 | 37731809 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:37686448 | G | C | 4 | a0001c0001t0002 a0001c0001t0011 a0001c0001t0014 others(1): Show |
101 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*924C>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 9/9 | 924 | chr17 | 37686448 | ||||||
| chr17:37686568 | A | G | 1 | a0001c0001t0010 | 2 | HG02145.hp2 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*804T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 9/9 | 804 | chr17 | 37686568 | ||||||
| chr17:37686595 | C | T | 1 | a0001c0001t0007 | 11 | HG01884.hp2 HG02055.hp1 HG02258.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*777G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 9/9 | 777 | chr17 | 37686595 | ||||||
| chr17:37686928 | T | G | 11 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(8): Show |
192 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(189): Show |
3_prime_UTR_variant | MODIFIER | c.*444A>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 9/9 | 444 | chr17 | 37686928 | ||||||
| chr17:37686969 | T | C | 1 | a0001c0001t0016 | 1 | NA18612.hp2 | 3_prime_UTR_variant | MODIFIER | c.*403A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 9/9 | 403 | chr17 | 37686969 | ||||||
| chr17:37686988 | T | C | 6 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0007 others(3): Show |
64 | HG00140.hp1 HG00280.hp1 HG01099.hp2 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*384A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 9/9 | 384 | chr17 | 37686988 | ||||||
| chr17:37687098 | A | T | 20 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(17): Show |
265 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(262): Show |
3_prime_UTR_variant | MODIFIER | c.*274T>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 9/9 | 274 | chr17 | 37687098 | ||||||
| chr17:37687253 | A | C | 1 | a0001c0001t0019 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*119T>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 9/9 | 119 | chr17 | 37687253 | ||||||
| chr17:37687264 | G | A | 1 | a0001c0001t0015 | 1 | NA18971.hp1 | 3_prime_UTR_variant | MODIFIER | c.*108C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 9/9 | 108 | chr17 | 37687264 | ||||||
| chr17:37687272 | T | C | 12 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0007 others(9): Show |
98 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*100A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 9/9 | 100 | chr17 | 37687272 | ||||||
| chr17:37687273 | G | T | 8 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0006 others(5): Show |
101 | HG00140.hp1 HG00280.hp1 HG00597.hp2 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*99C>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 9/9 | 99 | chr17 | 37687273 | ||||||
| chr17:37687325 | A | C | 2 | a0001c0001t0007 a0001c0001t0013 |
11 | HG01884.hp2 HG02055.hp1 HG02258.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*47T>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 9/9 | 47 | chr17 | 37687325 | ||||||
| chr17:37687347 | G | A | 1 | a0001c0001t0018 | 1 | NA18941.hp2 | 3_prime_UTR_variant | MODIFIER | c.*25C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 9/9 | 25 | chr17 | 37687347 | ||||||
| chr17:37744951 | G | A | 2 | a0001c0001t0019 a0001c0001t0020 |
2 | HG03669.hp2 HG03942.hp2 |
5_prime_UTR_variant | MODIFIER | c.-67C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 1/9 | 67 | chr17 | 37744951 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:37687414 | G | A | 144 | a0001c0001t0003g0011 a0001c0001t0003g0023 a0001c0001t0003g0030 others(141): Show |
145 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.1654-22C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37687414 | |||||||
| chr17:37687430 | A | G | 1 | a0001c0001t0002g0156 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1654-38T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37687430 | |||||||
| chr17:37687498 | G | A | 34 | a0001c0001t0005g0010 a0001c0001t0005g0012 a0001c0001t0005g0058 others(31): Show |
34 | HG00140.hp1 HG00280.hp1 HG01099.hp2 others(31): Show |
intron_variant | MODIFIER | c.1654-106C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37687498 | |||||||
| chr17:37687542 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1654-150C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37687542 | |||||||
| chr17:37687615 | G | A | 1 | a0001c0001t0001g0311 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1654-223C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37687615 | |||||||
| chr17:37687669 | A | T | 1 | a0001c0001t0001g0292 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1654-277T>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37687669 | |||||||
| chr17:37688045 | C | T | 1 | a0001c0001t0002g0083 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1654-653G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37688045 | |||||||
| chr17:37688173 | G | A | 1 | a0001c0001t0014g0280 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1654-781C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37688173 | |||||||
| chr17:37688234 | T | G | 1 | a0001c0001t0003g0333 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1654-842A>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37688234 | |||||||
| chr17:37688380 | A | AAC | 28 | a0001c0001t0001g0013 a0001c0001t0001g0146 a0001c0001t0001g0169 others(25): Show |
28 | HG00323.hp2 HG00438.hp1 HG00621.hp1 others(25): Show |
intron_variant | MODIFIER | c.1654-990_1654-989d others(4): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37688380 | |||||||
| chr17:37688380 | A | AACAC | 32 | a0001c0001t0001g0170 a0001c0001t0001g0225 a0001c0001t0001g0271 others(29): Show |
32 | HG01168.hp1 HG01192.hp2 HG01255.hp2 others(29): Show |
intron_variant | MODIFIER | c.1654-992_1654-989d others(6): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37688380 | |||||||
| chr17:37688380 | A | AACACAC | 64 | a0001c0001t0001g0371 a0001c0001t0002g0037 a0001c0001t0002g0048 others(61): Show |
64 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.1654-994_1654-989d others(8): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37688380 | |||||||
| chr17:37688380 | A | AACACACA others(1): Show |
56 | a0001c0001t0001g0009 a0001c0001t0001g0150 a0001c0001t0001g0202 others(53): Show |
56 | HG00408.hp1 HG00609.hp1 HG00735.hp1 others(53): Show |
intron_variant | MODIFIER | c.1654-996_1654-989d others(10): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37688380 | |||||||
| chr17:37688380 | A | AACACACA others(3): Show |
21 | a0001c0001t0001g0347 a0001c0001t0001g0351 a0001c0001t0001g0394 others(18): Show |
21 | HG01515.hp1 HG01928.hp2 HG01981.hp2 others(18): Show |
intron_variant | MODIFIER | c.1654-998_1654-989d others(12): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37688380 | |||||||
| chr17:37688380 | A | AACACACA others(5): Show |
5 | a0001c0001t0001g0283 a0001c0001t0002g0059 a0001c0001t0002g0219 others(2): Show |
5 | HG02074.hp2 HG02145.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.1654-1000_1654-989 others(15): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37688380 | |||||||
| chr17:37688380 | A | ACACACAC | 3 | a0001c0001t0002g0135 a0001c0001t0002g0325 a0001c0001t0003g0126 |
3 | HG01169.hp2 HG02135.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1654-989_1654-988i others(9): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37688380 | |||||||
| chr17:37688380 | A | C | 1 | a0001c0001t0009g0206 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1654-988T>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37688380 | |||||||
| chr17:37688380 | AAC | A | 49 | a0001c0001t0001g0185 a0001c0001t0001g0282 a0001c0001t0001g0288 others(46): Show |
50 | HG00597.hp2 HG01109.hp1 HG01109.hp2 others(47): Show |
intron_variant | MODIFIER | c.1654-990_1654-989d others(4): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37688380 | |||||||
| chr17:37688380 | AACAC | A | 17 | a0001c0001t0001g0040 a0001c0001t0001g0049 a0001c0001t0001g0104 others(14): Show |
17 | HG00099.hp2 HG00642.hp1 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.1654-992_1654-989d others(6): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37688380 | |||||||
| chr17:37688380 | AACACACA others(1): Show |
A | 3 | a0001c0001t0002g0359 a0001c0001t0006g0253 a0001c0003t0006g0349 |
3 | HG01243.hp1 HG02818.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.1654-996_1654-989d others(10): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37688380 | |||||||
| chr17:37688421 | A | T | 1 | a0001c0001t0001g0117 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1654-1029T>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37688421 | |||||||
| chr17:37688429 | C | T | 5 | a0001c0001t0002g0110 a0001c0001t0002g0120 a0001c0001t0002g0121 others(2): Show |
5 | HG00323.hp2 HG00738.hp1 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.1654-1037G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37688429 | |||||||
| chr17:37688518 | A | G | 261 | a0001c0001t0001g0150 a0001c0001t0001g0371 a0001c0001t0002g0006 others(258): Show |
262 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.1654-1126T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37688518 | |||||||
| chr17:37688818 | G | A | 245 | a0001c0001t0001g0150 a0001c0001t0001g0371 a0001c0001t0002g0006 others(242): Show |
246 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.1654-1426C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37688818 | |||||||
| chr17:37688834 | G | A | 1 | a0001c0001t0004g0167 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1654-1442C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37688834 | |||||||
| chr17:37688846 | T | A | 1 | a0001c0001t0001g0170 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1654-1454A>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37688846 | |||||||
| chr17:37688935 | A | G | 166 | a0001c0001t0001g0371 a0001c0001t0002g0006 a0001c0001t0002g0007 others(163): Show |
166 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.1654-1543T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37688935 | |||||||
| chr17:37689112 | T | C | 2 | a0001c0001t0001g0377 a0001c0001t0001g0380 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1654-1720A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37689112 | |||||||
| chr17:37689145 | A | AC | 14 | a0001c0001t0001g0019 a0001c0001t0001g0024 a0001c0001t0001g0143 others(11): Show |
14 | HG00733.hp2 HG01069.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.1654-1754dupG | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37689145 | |||||||
| chr17:37689146 | C | CA | 79 | a0001c0001t0001g0015 a0001c0001t0001g0063 a0001c0001t0001g0104 others(76): Show |
79 | HG00140.hp1 HG00280.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.1654-1755dupT | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37689146 | |||||||
| chr17:37689146 | C | CAA | 7 | a0001c0001t0005g0012 a0001c0001t0005g0195 a0001c0001t0005g0227 others(4): Show |
7 | HG02257.hp2 HG02486.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1654-1756_1654-175 others(6): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37689146 | |||||||
| chr17:37689146 | CA | C | 9 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0322 others(6): Show |
9 | HG02145.hp1 HG02280.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1654-1755delT | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37689146 | |||||||
| chr17:37689147 | A | C | 85 | a0001c0001t0001g0150 a0001c0001t0003g0011 a0001c0001t0003g0018 others(82): Show |
86 | HG00423.hp2 HG00597.hp2 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.1654-1755T>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37689147 | |||||||
| chr17:37689148 | A | C | 1 | a0001c0001t0004g0088 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1654-1756T>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37689148 | |||||||
| chr17:37689239 | G | A | 1 | a0001c0001t0001g0304 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1654-1847C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37689239 | |||||||
| chr17:37689547 | T | C | 124 | a0001c0001t0001g0371 a0001c0001t0002g0006 a0001c0001t0002g0007 others(121): Show |
124 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.1654-2155A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37689547 | |||||||
| chr17:37689657 | C | T | 2 | a0001c0001t0003g0102 a0001c0001t0003g0116 |
2 | NA18971.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.1654-2265G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37689657 | |||||||
| chr17:37689758 | C | T | 1 | a0001c0001t0007g0277 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1654-2366G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37689758 | |||||||
| chr17:37689781 | A | G | 69 | a0001c0001t0001g0019 a0001c0001t0001g0024 a0001c0001t0001g0027 others(66): Show |
70 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.1654-2389T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37689781 | |||||||
| chr17:37689815 | G | A | 48 | a0001c0001t0005g0010 a0001c0001t0005g0012 a0001c0001t0005g0058 others(45): Show |
48 | HG00140.hp1 HG00280.hp1 HG01099.hp2 others(45): Show |
intron_variant | MODIFIER | c.1654-2423C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37689815 | |||||||
| chr17:37689825 | G | A | 2 | a0001c0001t0006g0274 a0001c0001t0006g0275 |
2 | HG02572.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1654-2433C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37689825 | |||||||
| chr17:37689911 | G | A | 3 | a0001c0001t0003g0161 a0001c0001t0003g0403 a0002c0004t0003g0405 |
3 | HG03710.hp2 HG04115.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1654-2519C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37689911 | |||||||
| chr17:37689930 | C | G | 5 | a0001c0001t0007g0277 a0001c0001t0010g0268 a0001c0001t0010g0269 others(2): Show |
5 | HG02145.hp2 HG03098.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1654-2538G>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37689930 | |||||||
| chr17:37689934 | C | T | 1 | a0001c0001t0005g0208 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1654-2542G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37689934 | |||||||
| chr17:37690000 | C | T | 1 | a0001c0001t0004g0261 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1654-2608G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37690000 | |||||||
| chr17:37690003 | GCA | G | 36 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0049 others(33): Show |
36 | HG00438.hp1 HG00597.hp2 HG00733.hp2 others(33): Show |
intron_variant | MODIFIER | c.1654-2613_1654-261 others(6): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37690003 | |||||||
| chr17:37690003 | GCACA | G | 120 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0016 others(117): Show |
121 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.1654-2615_1654-261 others(8): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37690003 | |||||||
| chr17:37690003 | GCACACA | G | 80 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0225 others(77): Show |
80 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.1654-2617_1654-261 others(10): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37690003 | |||||||
| chr17:37690003 | GCACACAC others(1): Show |
G | 155 | a0001c0001t0001g0022 a0001c0001t0001g0095 a0001c0001t0001g0150 others(152): Show |
155 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.1654-2619_1654-261 others(12): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37690003 | |||||||
| chr17:37690003 | GCACACAC others(3): Show |
G | 4 | a0001c0001t0002g0138 a0001c0001t0002g0156 a0001c0001t0002g0260 others(1): Show |
4 | HG01069.hp1 HG03710.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.1654-2621_1654-261 others(14): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37690003 | |||||||
| chr17:37690003 | GCACACAC others(7): Show |
G | 1 | a0001c0001t0002g0123 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1654-2625_1654-261 others(18): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37690003 | |||||||
| chr17:37690089 | G | A | 1 | a0001c0001t0017g0257 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1654-2697C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37690089 | |||||||
| chr17:37690200 | T | A | 1 | a0001c0001t0001g0245 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1654-2808A>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37690200 | |||||||
| chr17:37690206 | G | T | 1 | a0001c0001t0001g0245 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1654-2814C>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37690206 | |||||||
| chr17:37690253 | T | C | 3 | a0001c0001t0010g0268 a0001c0001t0010g0269 a0001c0001t0014g0280 |
3 | HG02145.hp2 HG02280.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1654-2861A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37690253 | |||||||
| chr17:37690302 | G | GAGGA | 3 | a0001c0001t0006g0274 a0001c0001t0006g0275 a0001c0001t0009g0008 |
3 | HG02572.hp2 HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1654-2914_1654-291 others(8): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37690302 | |||||||
| chr17:37690326 | A | G | 49 | a0001c0001t0001g0150 a0001c0001t0003g0011 a0001c0001t0003g0018 others(46): Show |
49 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.1654-2934T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37690326 | |||||||
| chr17:37690346 | A | G | 35 | a0001c0001t0005g0010 a0001c0001t0005g0012 a0001c0001t0005g0058 others(32): Show |
35 | HG00140.hp1 HG00280.hp1 HG01099.hp2 others(32): Show |
intron_variant | MODIFIER | c.1654-2954T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37690346 | |||||||
| chr17:37690529 | G | C | 2 | a0001c0001t0002g0006 a0001c0001t0005g0193 |
2 | HG02055.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1654-3137C>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37690529 | |||||||
| chr17:37690579 | T | C | 1 | a0001c0001t0014g0280 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1654-3187A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37690579 | |||||||
| chr17:37690604 | T | C | 1 | a0001c0001t0001g0238 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1654-3212A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37690604 | |||||||
| chr17:37690710 | A | G | 1 | a0001c0001t0006g0014 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1654-3318T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37690710 | |||||||
| chr17:37690777 | G | A | 3 | a0001c0001t0001g0019 a0001c0001t0001g0024 a0001c0001t0005g0307 |
3 | HG01069.hp2 HG01071.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.1654-3385C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37690777 | |||||||
| chr17:37690812 | T | G | 3 | a0001c0001t0002g0073 a0001c0001t0002g0148 a0001c0001t0002g0336 |
3 | NA18999.hp1 NA19074.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.1654-3420A>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37690812 | |||||||
| chr17:37690827 | C | T | 2 | a0001c0002t0009g0221 a0001c0002t0009g0265 |
2 | HG03098.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1654-3435G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37690827 | |||||||
| chr17:37690858 | C | T | 15 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0092 others(12): Show |
15 | HG02129.hp1 HG02132.hp2 NA18948.hp1 others(12): Show |
intron_variant | MODIFIER | c.1654-3466G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37690858 | |||||||
| chr17:37690881 | A | C | 1 | a0001c0001t0002g0137 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1654-3489T>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37690881 | |||||||
| chr17:37691234 | G | C | 1 | a0001c0001t0003g0333 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1654-3842C>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37691234 | |||||||
| chr17:37691354 | C | T | 6 | a0001c0001t0005g0010 a0001c0001t0005g0218 a0001c0001t0005g0227 others(3): Show |
6 | HG02572.hp1 HG02809.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1654-3962G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37691354 | |||||||
| chr17:37691367 | T | C | 68 | a0001c0001t0001g0177 a0001c0001t0001g0282 a0001c0001t0001g0288 others(65): Show |
69 | HG00099.hp1 HG00597.hp2 HG01109.hp1 others(66): Show |
intron_variant | MODIFIER | c.1654-3975A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37691367 | |||||||
| chr17:37691386 | A | C | 1 | a0001c0001t0001g0334 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1654-3994T>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37691386 | |||||||
| chr17:37691435 | C | G | 3 | a0001c0001t0001g0009 a0001c0001t0001g0283 a0001c0001t0001g0351 |
3 | HG02451.hp2 HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1654-4043G>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37691435 | |||||||
| chr17:37691522 | G | A | 4 | a0001c0001t0003g0333 a0001c0001t0006g0253 a0001c0001t0006g0270 others(1): Show |
4 | HG01243.hp1 HG01891.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.1654-4130C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37691522 | |||||||
| chr17:37691552 | G | A | 13 | a0001c0001t0006g0004 a0001c0001t0006g0014 a0001c0001t0006g0246 others(10): Show |
13 | HG01891.hp2 HG02630.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.1654-4160C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37691552 | |||||||
| chr17:37691738 | A | G | 2 | a0001c0001t0001g0099 a0001c0001t0001g0100 |
2 | HG01978.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.1654-4346T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37691738 | |||||||
| chr17:37691774 | C | T | 20 | a0001c0001t0001g0282 a0001c0001t0001g0288 a0001c0001t0001g0342 others(17): Show |
20 | HG01109.hp2 HG01891.hp2 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.1654-4382G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37691774 | |||||||
| chr17:37691815 | C | T | 3 | a0001c0001t0006g0253 a0001c0001t0006g0270 a0001c0003t0006g0349 |
3 | HG01243.hp1 HG01891.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1654-4423G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37691815 | |||||||
| chr17:37691818 | A | G | 1 | a0001c0001t0002g0180 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1654-4426T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37691818 | |||||||
| chr17:37691844 | C | G | 1 | a0001c0001t0007g0200 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1654-4452G>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37691844 | |||||||
| chr17:37692052 | C | A | 7 | a0001c0001t0001g0282 a0001c0001t0001g0288 a0001c0001t0001g0342 others(4): Show |
7 | HG01109.hp2 HG02145.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1654-4660G>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37692052 | |||||||
| chr17:37692071 | G | T | 7 | a0001c0001t0001g0282 a0001c0001t0001g0288 a0001c0001t0001g0342 others(4): Show |
7 | HG01109.hp2 HG02145.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1654-4679C>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37692071 | |||||||
| chr17:37692090 | A | T | 5 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0002g0226 others(2): Show |
5 | HG02145.hp1 HG02280.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1654-4698T>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37692090 | |||||||
| chr17:37692169 | G | A | 1 | a0001c0001t0003g0333 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1654-4777C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37692169 | |||||||
| chr17:37692179 | C | CA | 7 | a0001c0001t0001g0282 a0001c0001t0001g0288 a0001c0001t0001g0342 others(4): Show |
7 | HG01109.hp2 HG02145.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1654-4788_1654-478 others(5): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37692179 | |||||||
| chr17:37692197 | G | C | 1 | a0001c0001t0005g0194 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1654-4805C>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37692197 | |||||||
| chr17:37692339 | A | G | 4 | a0001c0001t0006g0253 a0001c0001t0006g0270 a0001c0001t0007g0277 others(1): Show |
4 | HG01243.hp1 HG01891.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1654-4947T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37692339 | |||||||
| chr17:37692487 | G | A | 3 | a0001c0001t0001g0282 a0001c0001t0001g0288 a0001c0001t0001g0342 |
3 | HG01109.hp2 HG02895.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1654-5095C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37692487 | |||||||
| chr17:37692522 | G | A | 1 | a0001c0001t0002g0006 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1654-5130C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37692522 | |||||||
| chr17:37692610 | G | A | 61 | a0001c0001t0001g0033 a0001c0001t0001g0282 a0001c0001t0001g0288 others(58): Show |
62 | HG00597.hp2 HG01109.hp1 HG01109.hp2 others(59): Show |
intron_variant | MODIFIER | c.1654-5218C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37692610 | |||||||
| chr17:37692613 | C | CATTT | 61 | a0001c0001t0001g0033 a0001c0001t0001g0282 a0001c0001t0001g0288 others(58): Show |
62 | HG00597.hp2 HG01109.hp1 HG01109.hp2 others(59): Show |
intron_variant | MODIFIER | c.1654-5222_1654-522 others(8): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37692613 | |||||||
| chr17:37692682 | G | A | 72 | a0001c0001t0001g0039 a0001c0001t0001g0060 a0001c0001t0001g0070 others(69): Show |
72 | HG00099.hp2 HG00544.hp2 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.1654-5290C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37692682 | |||||||
| chr17:37692718 | T | C | 1 | a0001c0001t0007g0277 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1654-5326A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37692718 | |||||||
| chr17:37692771 | G | C | 72 | a0001c0001t0001g0039 a0001c0001t0001g0060 a0001c0001t0001g0070 others(69): Show |
72 | HG00099.hp2 HG00544.hp2 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.1654-5379C>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37692771 | |||||||
| chr17:37692784 | G | A | 2 | a0001c0001t0001g0092 a0001c0001t0001g0366 |
2 | NA19077.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.1654-5392C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37692784 | |||||||
| chr17:37692787 | G | A | 2 | a0001c0001t0012g0223 a0001c0003t0005g0350 |
2 | HG03098.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1654-5395C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37692787 | |||||||
| chr17:37693059 | C | A | 14 | a0001c0001t0006g0004 a0001c0001t0006g0251 a0001c0001t0006g0274 others(11): Show |
14 | HG01891.hp2 HG02145.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.1654-5667G>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37693059 | |||||||
| chr17:37693059 | C | G | 120 | a0001c0001t0001g0033 a0001c0001t0001g0039 a0001c0001t0001g0056 others(117): Show |
121 | HG00099.hp2 HG00544.hp2 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.1654-5667G>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37693059 | |||||||
| chr17:37693095 | C | T | 6 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0026 others(3): Show |
6 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.1654-5703G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37693095 | |||||||
| chr17:37693189 | C | CA | 30 | a0001c0001t0001g0080 a0001c0001t0001g0153 a0001c0001t0001g0164 others(27): Show |
30 | HG00408.hp1 HG00609.hp1 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.1654-5798dupT | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37693189 | |||||||
| chr17:37693189 | CA | C | 92 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0039 others(89): Show |
92 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.1654-5798delT | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37693189 | |||||||
| chr17:37693189 | CAA | C | 9 | a0001c0001t0001g0377 a0001c0001t0003g0116 a0001c0001t0003g0323 others(6): Show |
9 | HG01516.hp1 HG02258.hp1 HG03098.hp2 others(6): Show |
intron_variant | MODIFIER | c.1654-5799_1654-579 others(6): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37693189 | |||||||
| chr17:37693189 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0002g0355 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1654-5808_1654-579 others(15): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37693189 | |||||||
| chr17:37693430 | G | T | 2 | a0001c0001t0001g0225 a0001c0001t0005g0227 |
2 | HG02970.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1653+5646C>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37693430 | |||||||
| chr17:37693494 | T | C | 1 | a0001c0001t0006g0005 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1653+5582A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37693494 | |||||||
| chr17:37693570 | A | G | 6 | a0001c0001t0002g0073 a0001c0001t0002g0096 a0001c0001t0002g0148 others(3): Show |
6 | NA18981.hp1 NA18988.hp1 NA18999.hp1 others(3): Show |
intron_variant | MODIFIER | c.1653+5506T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37693570 | |||||||
| chr17:37693738 | G | A | 1 | a0001c0001t0001g0155 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1653+5338C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37693738 | |||||||
| chr17:37693760 | G | A | 6 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0026 others(3): Show |
6 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.1653+5316C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37693760 | |||||||
| chr17:37693769 | G | A | 5 | a0001c0001t0005g0395 a0001c0001t0005g0396 a0001c0001t0006g0038 others(2): Show |
5 | HG01192.hp2 HG03041.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1653+5307C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37693769 | |||||||
| chr17:37693782 | A | C | 45 | a0001c0001t0001g0202 a0001c0001t0002g0219 a0001c0001t0002g0220 others(42): Show |
45 | HG00140.hp1 HG00280.hp1 HG01099.hp2 others(42): Show |
intron_variant | MODIFIER | c.1653+5294T>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37693782 | |||||||
| chr17:37693881 | C | G | 10 | a0001c0001t0003g0333 a0001c0001t0005g0196 a0001c0001t0005g0204 others(7): Show |
10 | HG01192.hp2 HG02258.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1653+5195G>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37693881 | |||||||
| chr17:37693987 | T | A | 45 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0026 others(42): Show |
46 | HG00597.hp2 HG01081.hp2 HG01109.hp1 others(43): Show |
intron_variant | MODIFIER | c.1653+5089A>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37693987 | |||||||
| chr17:37694234 | C | G | 45 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0026 others(42): Show |
46 | HG00597.hp2 HG01081.hp2 HG01109.hp1 others(43): Show |
intron_variant | MODIFIER | c.1653+4842G>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37694234 | |||||||
| chr17:37694422 | A | G | 45 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0026 others(42): Show |
46 | HG00597.hp2 HG01081.hp2 HG01109.hp1 others(43): Show |
intron_variant | MODIFIER | c.1653+4654T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37694422 | |||||||
| chr17:37694438 | G | C | 1 | a0001c0001t0003g0044 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1653+4638C>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37694438 | |||||||
| chr17:37694438 | G | GC | 26 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0046 others(23): Show |
26 | HG00408.hp2 HG00673.hp2 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.1653+4637dupG | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37694438 | |||||||
| chr17:37694438 | G | GCC | 60 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0027 others(57): Show |
61 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.1653+4636_1653+463 others(6): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37694438 | |||||||
| chr17:37694438 | G | GCCC | 80 | a0001c0001t0001g0040 a0001c0001t0001g0069 a0001c0001t0001g0071 others(77): Show |
80 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.1653+4635_1653+463 others(7): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37694438 | |||||||
| chr17:37694438 | G | GCCCC | 39 | a0001c0001t0001g0039 a0001c0001t0001g0056 a0001c0001t0001g0066 others(36): Show |
39 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(36): Show |
intron_variant | MODIFIER | c.1653+4634_1653+463 others(8): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37694438 | |||||||
| chr17:37694438 | G | GCCCCC | 39 | a0001c0001t0001g0101 a0001c0001t0001g0104 a0001c0001t0001g0146 others(36): Show |
39 | HG00438.hp2 HG00544.hp1 HG00733.hp1 others(36): Show |
intron_variant | MODIFIER | c.1653+4633_1653+463 others(9): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37694438 | |||||||
| chr17:37694438 | G | GCCCCCC | 26 | a0001c0001t0001g0063 a0001c0001t0001g0129 a0001c0001t0001g0130 others(23): Show |
26 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.1653+4632_1653+463 others(10): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37694438 | |||||||
| chr17:37694438 | G | GCCCCCCC | 20 | a0001c0001t0001g0150 a0001c0001t0001g0155 a0001c0001t0001g0371 others(17): Show |
20 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(17): Show |
intron_variant | MODIFIER | c.1653+4631_1653+463 others(11): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37694438 | |||||||
| chr17:37694438 | G | GCCCCCCC others(3): Show |
1 | a0001c0001t0005g0010 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1653+4628_1653+463 others(14): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37694438 | |||||||
| chr17:37694438 | G | GCCCCCCC others(4): Show |
1 | a0001c0001t0002g0136 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1653+4627_1653+463 others(15): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37694438 | |||||||
| chr17:37694438 | G | GCCCCCCC others(6): Show |
1 | a0001c0001t0002g0059 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1653+4625_1653+463 others(17): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37694438 | |||||||
| chr17:37694438 | GCCC | G | 41 | a0001c0001t0002g0263 a0001c0001t0003g0161 a0001c0001t0003g0403 others(38): Show |
42 | HG00597.hp2 HG01109.hp1 HG01192.hp2 others(39): Show |
intron_variant | MODIFIER | c.1653+4635_1653+463 others(7): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37694438 | |||||||
| chr17:37694448 | C | CG | 5 | a0001c0001t0006g0004 a0001c0001t0006g0251 a0001c0001t0006g0286 others(2): Show |
5 | HG01891.hp2 HG02809.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1653+4627_1653+462 others(5): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37694448 | |||||||
| chr17:37694448 | C | G | 4 | a0001c0001t0006g0285 a0001c0001t0006g0344 a0001c0001t0007g0250 others(1): Show |
4 | HG02630.hp2 HG02818.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1653+4628G>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37694448 | |||||||
| chr17:37694449 | C | T | 46 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0026 others(43): Show |
47 | HG00597.hp2 HG01081.hp2 HG01109.hp1 others(44): Show |
intron_variant | MODIFIER | c.1653+4627G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37694449 | |||||||
| chr17:37694461 | A | G | 1 | a0001c0001t0001g0209 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1653+4615T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37694461 | |||||||
| chr17:37694467 | A | G | 39 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0026 others(36): Show |
40 | HG00597.hp2 HG01081.hp2 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.1653+4609T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37694467 | |||||||
| chr17:37694498 | TG | T | 29 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0002g0226 others(26): Show |
29 | HG00140.hp1 HG00280.hp1 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.1653+4577delC | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37694498 | |||||||
| chr17:37694647 | A | G | 2 | a0001c0001t0001g0158 a0001c0001t0001g0383 |
2 | HG00099.hp2 HG00642.hp1 |
intron_variant | MODIFIER | c.1653+4429T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37694647 | |||||||
| chr17:37694844 | C | A | 21 | a0001c0001t0001g0028 a0001c0001t0001g0056 a0001c0001t0001g0057 others(18): Show |
21 | HG02129.hp1 HG02132.hp2 NA18944.hp2 others(18): Show |
intron_variant | MODIFIER | c.1653+4232G>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37694844 | |||||||
| chr17:37695034 | T | C | 2 | a0001c0001t0007g0250 a0001c0001t0007g0284 |
2 | HG06807.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1653+4042A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37695034 | |||||||
| chr17:37695225 | A | G | 224 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0015 others(221): Show |
225 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.1653+3851T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37695225 | |||||||
| chr17:37695227 | C | A | 46 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0026 others(43): Show |
47 | HG00597.hp2 HG01081.hp2 HG01109.hp1 others(44): Show |
intron_variant | MODIFIER | c.1653+3849G>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37695227 | |||||||
| chr17:37695366 | T | G | 305 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0015 others(302): Show |
306 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(303): Show |
intron_variant | MODIFIER | c.1653+3710A>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37695366 | |||||||
| chr17:37695552 | A | G | 178 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0033 others(175): Show |
178 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.1653+3524T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37695552 | |||||||
| chr17:37695576 | T | G | 10 | a0001c0001t0006g0004 a0001c0001t0006g0251 a0001c0001t0006g0285 others(7): Show |
10 | HG01891.hp2 HG02630.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.1653+3500A>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37695576 | |||||||
| chr17:37695608 | G | C | 47 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0026 others(44): Show |
48 | HG00597.hp2 HG01081.hp2 HG01109.hp1 others(45): Show |
intron_variant | MODIFIER | c.1653+3468C>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37695608 | |||||||
| chr17:37695646 | A | G | 1 | a0001c0001t0002g0296 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1653+3430T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37695646 | |||||||
| chr17:37695694 | A | G | 2 | a0001c0001t0006g0274 a0001c0001t0006g0275 |
2 | HG02572.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1653+3382T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37695694 | |||||||
| chr17:37695748 | T | C | 11 | a0001c0001t0005g0279 a0001c0001t0006g0270 a0001c0001t0007g0200 others(8): Show |
11 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1653+3328A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37695748 | |||||||
| chr17:37695973 | G | A | 1 | a0001c0001t0014g0280 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1653+3103C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37695973 | |||||||
| chr17:37696061 | G | C | 47 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0026 others(44): Show |
48 | HG00597.hp2 HG01081.hp2 HG01109.hp1 others(45): Show |
intron_variant | MODIFIER | c.1653+3015C>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37696061 | |||||||
| chr17:37696070 | G | C | 112 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0033 others(109): Show |
112 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.1653+3006C>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37696070 | |||||||
| chr17:37696186 | T | G | 112 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0033 others(109): Show |
112 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.1653+2890A>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37696186 | |||||||
| chr17:37696270 | C | CA | 15 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0033 others(12): Show |
15 | HG02451.hp1 HG02451.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.1653+2805dupT | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37696270 | |||||||
| chr17:37696393 | C | T | 3 | a0001c0001t0001g0313 a0001c0001t0002g0189 a0001c0001t0002g0321 |
3 | HG02071.hp1 HG02080.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.1653+2683G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37696393 | |||||||
| chr17:37696468 | G | A | 47 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0026 others(44): Show |
48 | HG00597.hp2 HG01081.hp2 HG01109.hp1 others(45): Show |
intron_variant | MODIFIER | c.1653+2608C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37696468 | |||||||
| chr17:37696550 | T | C | 48 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0026 others(45): Show |
49 | HG00597.hp2 HG01081.hp2 HG01109.hp1 others(46): Show |
intron_variant | MODIFIER | c.1653+2526A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37696550 | |||||||
| chr17:37696570 | T | C | 304 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0015 others(301): Show |
305 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(302): Show |
intron_variant | MODIFIER | c.1653+2506A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37696570 | |||||||
| chr17:37696576 | G | A | 2 | a0001c0001t0003g0054 a0001c0001t0003g0166 |
2 | HG02074.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.1653+2500C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37696576 | |||||||
| chr17:37696623 | A | G | 1 | a0001c0001t0003g0162 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1653+2453T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37696623 | |||||||
| chr17:37696679 | C | G | 2 | a0001c0001t0005g0395 a0001c0001t0005g0396 |
2 | HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1653+2397G>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37696679 | |||||||
| chr17:37696695 | C | T | 1 | a0001c0001t0012g0223 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1653+2381G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37696695 | |||||||
| chr17:37696710 | C | T | 14 | a0001c0001t0001g0202 a0001c0001t0001g0324 a0001c0001t0005g0279 others(11): Show |
14 | HG01261.hp2 HG01884.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.1653+2366G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37696710 | |||||||
| chr17:37696841 | C | T | 1 | a0001c0001t0005g0204 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1653+2235G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37696841 | |||||||
| chr17:37696893 | A | G | 33 | a0001c0001t0003g0161 a0001c0001t0003g0403 a0001c0001t0004g0001 others(30): Show |
34 | HG00597.hp2 HG01109.hp1 HG01361.hp2 others(31): Show |
intron_variant | MODIFIER | c.1653+2183T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37696893 | |||||||
| chr17:37697558 | T | C | 3 | a0001c0001t0003g0011 a0001c0001t0003g0141 a0001c0001t0003g0328 |
3 | HG00673.hp1 NA18747.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.1653+1518A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37697558 | |||||||
| chr17:37697638 | C | T | 1 | a0001c0001t0001g0254 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1653+1438G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37697638 | |||||||
| chr17:37697686 | C | T | 1 | a0001c0001t0001g0169 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1653+1390G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37697686 | |||||||
| chr17:37697713 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1653+1363C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37697713 | |||||||
| chr17:37697828 | C | A | 2 | a0001c0001t0006g0274 a0001c0001t0006g0275 |
2 | HG02572.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1653+1248G>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37697828 | |||||||
| chr17:37697872 | G | C | 1 | a0001c0001t0001g0040 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1653+1204C>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37697872 | |||||||
| chr17:37697968 | G | A | 1 | a0001c0001t0014g0280 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1653+1108C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37697968 | |||||||
| chr17:37698040 | C | T | 11 | a0001c0001t0005g0279 a0001c0001t0006g0270 a0001c0001t0007g0200 others(8): Show |
11 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1653+1036G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37698040 | |||||||
| chr17:37698042 | GGGCAAA | G | 99 | a0001c0001t0001g0129 a0001c0001t0001g0146 a0001c0001t0001g0212 others(96): Show |
99 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.1653+1028_1653+103 others(10): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37698042 | |||||||
| chr17:37698050 | G | A | 99 | a0001c0001t0001g0129 a0001c0001t0001g0146 a0001c0001t0001g0212 others(96): Show |
99 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.1653+1026C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37698050 | |||||||
| chr17:37698051 | A | T | 99 | a0001c0001t0001g0129 a0001c0001t0001g0146 a0001c0001t0001g0212 others(96): Show |
99 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.1653+1025T>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37698051 | |||||||
| chr17:37698052 | A | C | 99 | a0001c0001t0001g0129 a0001c0001t0001g0146 a0001c0001t0001g0212 others(96): Show |
99 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.1653+1024T>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37698052 | |||||||
| chr17:37698100 | G | A | 1 | a0001c0001t0002g0260 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1653+976C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37698100 | |||||||
| chr17:37698147 | A | T | 57 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0015 others(54): Show |
58 | HG00597.hp2 HG01081.hp2 HG01123.hp1 others(55): Show |
intron_variant | MODIFIER | c.1653+929T>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37698147 | |||||||
| chr17:37698195 | T | C | 13 | a0001c0001t0001g0202 a0001c0001t0005g0279 a0001c0001t0006g0005 others(10): Show |
13 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.1653+881A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37698195 | |||||||
| chr17:37698309 | T | C | 2 | a0001c0001t0007g0277 a0001c0001t0009g0008 |
2 | HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1653+767A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37698309 | |||||||
| chr17:37698719 | G | A | 56 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0015 others(53): Show |
57 | HG00597.hp2 HG01081.hp2 HG01123.hp1 others(54): Show |
intron_variant | MODIFIER | c.1653+357C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37698719 | |||||||
| chr17:37698808 | G | A | 44 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0026 others(41): Show |
45 | HG00597.hp2 HG01081.hp2 HG01123.hp1 others(42): Show |
intron_variant | MODIFIER | c.1653+268C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37698808 | |||||||
| chr17:37698862 | C | T | 1 | a0001c0001t0003g0273 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1653+214G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37698862 | |||||||
| chr17:37698911 | CT | C | 302 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0015 others(299): Show |
303 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(300): Show |
intron_variant | MODIFIER | c.1653+164delA | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37698911 | |||||||
| chr17:37698974 | C | T | 284 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0015 others(281): Show |
285 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(282): Show |
intron_variant | MODIFIER | c.1653+102G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37698974 | |||||||
| chr17:37698987 | C | T | 10 | a0001c0001t0006g0004 a0001c0001t0006g0251 a0001c0001t0006g0285 others(7): Show |
10 | HG01891.hp2 HG02630.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.1653+89G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37698987 | |||||||
| chr17:37699020 | A | G | 1 | a0001c0001t0001g0202 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1653+56T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37699020 | |||||||
| chr17:37699028 | A | AG | 57 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0015 others(54): Show |
58 | HG00597.hp2 HG01081.hp2 HG01123.hp1 others(55): Show |
intron_variant | MODIFIER | c.1653+47_1653+48ins others(1): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 8/8 | chr17 | 37699028 | |||||||
| chr17:37699238 | C | G | 1 | a0001c0001t0014g0280 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1535-44G>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 7/8 | chr17 | 37699238 | |||||||
| chr17:37699240 | A | C | 130 | a0001c0001t0001g0039 a0001c0001t0001g0060 a0001c0001t0001g0063 others(127): Show |
130 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.1535-46T>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 7/8 | chr17 | 37699240 | |||||||
| chr17:37699296 | T | C | 28 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0002g0226 others(25): Show |
28 | HG00140.hp1 HG00280.hp1 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.1535-102A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 7/8 | chr17 | 37699296 | |||||||
| chr17:37699371 | A | G | 130 | a0001c0001t0001g0039 a0001c0001t0001g0060 a0001c0001t0001g0063 others(127): Show |
130 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.1535-177T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 7/8 | chr17 | 37699371 | |||||||
| chr17:37699379 | C | G | 116 | a0001c0001t0001g0129 a0001c0001t0001g0146 a0001c0001t0001g0202 others(113): Show |
116 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.1535-185G>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 7/8 | chr17 | 37699379 | |||||||
| chr17:37699382 | G | A | 8 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0002g0226 others(5): Show |
8 | HG02145.hp1 HG02280.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1535-188C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 7/8 | chr17 | 37699382 | |||||||
| chr17:37699418 | A | AG | 130 | a0001c0001t0001g0039 a0001c0001t0001g0060 a0001c0001t0001g0063 others(127): Show |
130 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.1535-225_1535-224i others(3): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 7/8 | chr17 | 37699418 | |||||||
| chr17:37699466 | C | T | 8 | a0001c0001t0003g0030 a0001c0001t0003g0031 a0001c0001t0003g0032 others(5): Show |
8 | NA18612.hp1 NA18941.hp1 NA18941.hp2 others(5): Show |
intron_variant | MODIFIER | c.1535-272G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 7/8 | chr17 | 37699466 | |||||||
| chr17:37699523 | G | A | 2 | a0001c0001t0001g0070 a0001c0001t0001g0071 |
2 | NA19011.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1535-329C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 7/8 | chr17 | 37699523 | |||||||
| chr17:37699567 | G | A | 2 | a0001c0001t0003g0052 a0001c0001t0015g0175 |
2 | HG00423.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.1535-373C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 7/8 | chr17 | 37699567 | |||||||
| chr17:37699689 | A | G | 2 | a0001c0001t0005g0227 a0001c0001t0005g0281 |
2 | HG02970.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1535-495T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 7/8 | chr17 | 37699689 | |||||||
| chr17:37699741 | G | C | 93 | a0001c0001t0001g0129 a0001c0001t0001g0146 a0001c0001t0001g0212 others(90): Show |
93 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.1535-547C>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 7/8 | chr17 | 37699741 | |||||||
| chr17:37699872 | C | A | 2 | a0001c0001t0001g0375 a0001c0001t0002g0147 |
2 | HG02683.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.1535-678G>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 7/8 | chr17 | 37699872 | |||||||
| chr17:37699875 | C | T | 2 | a0001c0001t0006g0253 a0001c0003t0006g0349 |
2 | HG01243.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1535-681G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 7/8 | chr17 | 37699875 | |||||||
| chr17:37699917 | A | G | 1 | a0001c0001t0002g0064 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1535-723T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 7/8 | chr17 | 37699917 | |||||||
| chr17:37700044 | T | C | 2 | a0001c0001t0001g0080 a0001c0001t0001g0360 |
2 | NA18975.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.1535-850A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 7/8 | chr17 | 37700044 | |||||||
| chr17:37700099 | G | A | 103 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0019 others(100): Show |
104 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.1534+884C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 7/8 | chr17 | 37700099 | |||||||
| chr17:37700112 | G | GT | 160 | a0001c0001t0001g0111 a0001c0001t0001g0129 a0001c0001t0001g0146 others(157): Show |
160 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.1534+870dupA | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 7/8 | chr17 | 37700112 | |||||||
| chr17:37700210 | C | T | 142 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0016 others(139): Show |
143 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.1534+773G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 7/8 | chr17 | 37700210 | |||||||
| chr17:37700217 | TC | T | 100 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0019 others(97): Show |
101 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.1534+765delG | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 7/8 | chr17 | 37700217 | |||||||
| chr17:37700255 | G | A | 1 | a0001c0001t0004g0094 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1534+728C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 7/8 | chr17 | 37700255 | |||||||
| chr17:37700469 | T | C | 1 | a0001c0001t0001g0388 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1534+514A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 7/8 | chr17 | 37700469 | |||||||
| chr17:37700510 | C | T | 103 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0016 others(100): Show |
104 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.1534+473G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 7/8 | chr17 | 37700510 | |||||||
| chr17:37700579 | A | G | 3 | a0001c0001t0001g0282 a0001c0001t0001g0288 a0001c0001t0001g0342 |
3 | HG01109.hp2 HG02895.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1534+404T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 7/8 | chr17 | 37700579 | |||||||
| chr17:37700697 | C | A | 1 | a0001c0001t0001g0046 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1534+286G>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 7/8 | chr17 | 37700697 | |||||||
| chr17:37700731 | C | G | 11 | a0001c0001t0001g0371 a0001c0001t0002g0172 a0001c0001t0002g0301 others(8): Show |
11 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.1534+252G>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 7/8 | chr17 | 37700731 | |||||||
| chr17:37700878 | T | C | 10 | a0001c0001t0006g0004 a0001c0001t0006g0251 a0001c0001t0006g0285 others(7): Show |
10 | HG01891.hp2 HG02630.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.1534+105A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 7/8 | chr17 | 37700878 | |||||||
| chr17:37701274 | C | T | 13 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0033 others(10): Show |
13 | HG02451.hp2 HG02602.hp2 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.1340-97G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 6/8 | chr17 | 37701274 | |||||||
| chr17:37701277 | G | A | 33 | a0001c0001t0001g0297 a0001c0001t0002g0097 a0001c0001t0002g0114 others(30): Show |
33 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(30): Show |
intron_variant | MODIFIER | c.1340-100C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 6/8 | chr17 | 37701277 | |||||||
| chr17:37701292 | T | C | 98 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0019 others(95): Show |
99 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.1340-115A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 6/8 | chr17 | 37701292 | |||||||
| chr17:37701480 | A | T | 3 | a0001c0001t0009g0008 a0001c0001t0010g0268 a0001c0001t0010g0269 |
3 | HG02145.hp2 HG03130.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1340-303T>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 6/8 | chr17 | 37701480 | |||||||
| chr17:37701537 | T | C | 6 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0398 others(3): Show |
6 | HG02145.hp2 HG03130.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.1340-360A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 6/8 | chr17 | 37701537 | |||||||
| chr17:37701545 | G | A | 1 | a0001c0001t0001g0311 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1340-368C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 6/8 | chr17 | 37701545 | |||||||
| chr17:37701604 | C | A | 1 | a0001c0001t0001g0049 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1340-427G>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 6/8 | chr17 | 37701604 | |||||||
| chr17:37701654 | T | G | 205 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0019 others(202): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.1340-477A>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 6/8 | chr17 | 37701654 | |||||||
| chr17:37701938 | A | G | 14 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0033 others(11): Show |
14 | HG02451.hp2 HG02602.hp2 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.1340-761T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 6/8 | chr17 | 37701938 | |||||||
| chr17:37702238 | G | A | 1 | a0001c0001t0003g0023 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1340-1061C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 6/8 | chr17 | 37702238 | |||||||
| chr17:37702294 | G | A | 219 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0013 others(216): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.1340-1117C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 6/8 | chr17 | 37702294 | |||||||
| chr17:37702336 | G | A | 3 | a0001c0001t0002g0262 a0001c0001t0002g0354 a0001c0001t0005g0194 |
3 | HG02451.hp1 HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1340-1159C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 6/8 | chr17 | 37702336 | |||||||
| chr17:37702382 | G | T | 1 | a0001c0001t0001g0117 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1340-1205C>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 6/8 | chr17 | 37702382 | |||||||
| chr17:37702423 | G | C | 44 | a0001c0001t0001g0297 a0001c0001t0002g0097 a0001c0001t0002g0114 others(41): Show |
44 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.1340-1246C>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 6/8 | chr17 | 37702423 | |||||||
| chr17:37702453 | A | G | 315 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0013 others(312): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.1340-1276T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 6/8 | chr17 | 37702453 | |||||||
| chr17:37702472 | G | A | 5 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(2): Show |
5 | HG00558.hp1 NA18953.hp2 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.1340-1295C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 6/8 | chr17 | 37702472 | |||||||
| chr17:37702768 | C | A | 2 | a0001c0001t0002g0007 a0001c0001t0002g0398 |
2 | NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1340-1591G>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 6/8 | chr17 | 37702768 | |||||||
| chr17:37702930 | T | C | 99 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0026 others(96): Show |
99 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.1340-1753A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 6/8 | chr17 | 37702930 | |||||||
| chr17:37703047 | T | A | 5 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(2): Show |
5 | HG00558.hp1 NA18953.hp2 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.1339+1870A>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 6/8 | chr17 | 37703047 | |||||||
| chr17:37703085 | G | GC | 3 | a0001c0001t0005g0295 a0001c0001t0005g0348 a0001c0001t0006g0264 |
3 | HG02109.hp1 HG02647.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1339+1831dupG | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 6/8 | chr17 | 37703085 | |||||||
| chr17:37703295 | C | T | 3 | a0001c0001t0001g0282 a0001c0001t0001g0288 a0001c0001t0001g0342 |
3 | HG01109.hp2 HG02895.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1339+1622G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 6/8 | chr17 | 37703295 | |||||||
| chr17:37703413 | G | GTA | 184 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0013 others(181): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.1339+1502_1339+150 others(6): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 6/8 | chr17 | 37703413 | |||||||
| chr17:37703413 | G | GTATA | 4 | a0001c0001t0005g0346 a0001c0001t0006g0274 a0001c0001t0006g0275 others(1): Show |
4 | HG02486.hp2 HG02572.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1339+1500_1339+150 others(8): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 6/8 | chr17 | 37703413 | |||||||
| chr17:37703507 | A | G | 1 | a0001c0001t0006g0005 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1339+1410T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 6/8 | chr17 | 37703507 | |||||||
| chr17:37703638 | C | T | 3 | a0001c0001t0001g0282 a0001c0001t0001g0288 a0001c0001t0001g0342 |
3 | HG01109.hp2 HG02895.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1339+1279G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 6/8 | chr17 | 37703638 | |||||||
| chr17:37703678 | G | A | 8 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0026 others(5): Show |
8 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.1339+1239C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 6/8 | chr17 | 37703678 | |||||||
| chr17:37703820 | T | C | 6 | a0001c0001t0001g0297 a0001c0001t0005g0058 a0001c0001t0005g0108 others(3): Show |
6 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(3): Show |
intron_variant | MODIFIER | c.1339+1097A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 6/8 | chr17 | 37703820 | |||||||
| chr17:37703909 | G | A | 15 | a0001c0001t0002g0029 a0001c0001t0002g0047 a0001c0001t0002g0051 others(12): Show |
15 | HG00408.hp1 HG00423.hp1 HG00609.hp1 others(12): Show |
intron_variant | MODIFIER | c.1339+1008C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 6/8 | chr17 | 37703909 | |||||||
| chr17:37704081 | G | C | 34 | a0001c0001t0001g0297 a0001c0001t0002g0097 a0001c0001t0002g0114 others(31): Show |
34 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(31): Show |
intron_variant | MODIFIER | c.1339+836C>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 6/8 | chr17 | 37704081 | |||||||
| chr17:37704710 | A | G | 3 | a0001c0001t0001g0002 a0001c0001t0001g0160 a0001c0001t0001g0299 |
4 | HG03491.hp1 HG03492.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.1339+207T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 6/8 | chr17 | 37704710 | |||||||
| chr17:37704851 | A | G | 1 | a0001c0001t0002g0006 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1339+66T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 6/8 | chr17 | 37704851 | |||||||
| chr17:37704890 | A | G | 8 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0026 others(5): Show |
8 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.1339+27T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 6/8 | chr17 | 37704890 | |||||||
| chr17:37705103 | C | T | 11 | a0001c0001t0001g0013 a0001c0001t0001g0033 a0001c0001t0001g0225 others(8): Show |
11 | HG02602.hp2 HG02723.hp2 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.1207-54G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 5/8 | chr17 | 37705103 | |||||||
| chr17:37705115 | C | T | 1 | a0001c0001t0006g0005 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1207-66G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 5/8 | chr17 | 37705115 | |||||||
| chr17:37705135 | T | C | 3 | a0001c0001t0005g0343 a0001c0001t0005g0387 a0001c0001t0005g0389 |
3 | HG01168.hp2 HG01169.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.1207-86A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 5/8 | chr17 | 37705135 | |||||||
| chr17:37705263 | A | G | 1 | a0001c0001t0005g0208 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1207-214T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 5/8 | chr17 | 37705263 | |||||||
| chr17:37705295 | T | TCC | 130 | a0001c0001t0001g0009 a0001c0001t0001g0069 a0001c0001t0001g0111 others(127): Show |
130 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.1207-247_1207-246i others(4): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 5/8 | chr17 | 37705295 | |||||||
| chr17:37705306 | A | C | 1 | a0001c0001t0001g0101 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1207-257T>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 5/8 | chr17 | 37705306 | |||||||
| chr17:37705488 | C | T | 182 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0015 others(179): Show |
182 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.1207-439G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 5/8 | chr17 | 37705488 | |||||||
| chr17:37705532 | A | T | 2 | a0001c0001t0001g0299 a0001c0001t0001g0394 |
2 | HG02486.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1207-483T>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 5/8 | chr17 | 37705532 | |||||||
| chr17:37705615 | T | A | 6 | a0001c0001t0001g0074 a0001c0001t0001g0115 a0001c0001t0001g0199 others(3): Show |
6 | NA18944.hp1 NA18962.hp2 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.1207-566A>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 5/8 | chr17 | 37705615 | |||||||
| chr17:37705626 | T | G | 16 | a0001c0001t0001g0347 a0001c0001t0001g0394 a0001c0001t0002g0006 others(13): Show |
16 | HG01243.hp1 HG02257.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.1207-577A>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 5/8 | chr17 | 37705626 | |||||||
| chr17:37705674 | C | T | 1 | a0001c0001t0002g0075 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1207-625G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 5/8 | chr17 | 37705674 | |||||||
| chr17:37705707 | C | T | 1 | a0001c0001t0002g0123 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1207-658G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 5/8 | chr17 | 37705707 | |||||||
| chr17:37705724 | C | A | 3 | a0001c0001t0001g0282 a0001c0001t0001g0288 a0001c0001t0001g0342 |
3 | HG01109.hp2 HG02895.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1207-675G>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 5/8 | chr17 | 37705724 | |||||||
| chr17:37705891 | C | A | 2 | a0001c0001t0001g0039 a0001c0001t0003g0231 |
2 | HG00597.hp1 NA18949.hp1 |
intron_variant | MODIFIER | c.1207-842G>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 5/8 | chr17 | 37705891 | |||||||
| chr17:37706107 | T | C | 1 | a0001c0001t0004g0233 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1207-1058A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 5/8 | chr17 | 37706107 | |||||||
| chr17:37706283 | T | G | 1 | a0001c0001t0006g0286 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1207-1234A>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 5/8 | chr17 | 37706283 | |||||||
| chr17:37706328 | A | C | 1 | a0001c0001t0001g0127 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1207-1279T>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 5/8 | chr17 | 37706328 | |||||||
| chr17:37706338 | G | A | 1 | a0001c0001t0002g0006 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1207-1289C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 5/8 | chr17 | 37706338 | |||||||
| chr17:37706499 | A | G | 1 | a0001c0001t0001g0170 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1207-1450T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 5/8 | chr17 | 37706499 | |||||||
| chr17:37706676 | T | TA | 136 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0026 others(133): Show |
136 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.1207-1628dupT | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 5/8 | chr17 | 37706676 | |||||||
| chr17:37706676 | T | TAA | 121 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0016 others(118): Show |
122 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(119): Show |
intron_variant | MODIFIER | c.1207-1629_1207-162 others(6): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 5/8 | chr17 | 37706676 | |||||||
| chr17:37706958 | C | A | 1 | a0001c0001t0005g0218 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1207-1909G>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 5/8 | chr17 | 37706958 | |||||||
| chr17:37707117 | A | AT | 85 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0026 others(82): Show |
85 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.1207-2069dupA | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 5/8 | chr17 | 37707117 | |||||||
| chr17:37707117 | AT | A | 133 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0019 others(130): Show |
134 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.1207-2069delA | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 5/8 | chr17 | 37707117 | |||||||
| chr17:37707161 | G | A | 74 | a0001c0001t0001g0129 a0001c0001t0001g0146 a0001c0001t0001g0153 others(71): Show |
74 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.1207-2112C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 5/8 | chr17 | 37707161 | |||||||
| chr17:37707218 | C | T | 1 | a0001c0001t0002g0134 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1207-2169G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 5/8 | chr17 | 37707218 | |||||||
| chr17:37707301 | G | A | 37 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0033 others(34): Show |
37 | HG01109.hp2 HG01884.hp1 HG02258.hp1 others(34): Show |
intron_variant | MODIFIER | c.1207-2252C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 5/8 | chr17 | 37707301 | |||||||
| chr17:37707421 | A | G | 1 | a0001c0001t0010g0268 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1207-2372T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 5/8 | chr17 | 37707421 | |||||||
| chr17:37707597 | C | A | 1 | a0001c0001t0006g0274 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1207-2548G>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 5/8 | chr17 | 37707597 | |||||||
| chr17:37707769 | C | CT | 7 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0255 others(4): Show |
7 | HG01978.hp1 HG01993.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1207-2721dupA | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 5/8 | chr17 | 37707769 | |||||||
| chr17:37707769 | CT | C | 20 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0026 others(17): Show |
20 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.1207-2721delA | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 5/8 | chr17 | 37707769 | |||||||
| chr17:37707771 | T | C | 5 | a0001c0001t0006g0038 a0001c0001t0009g0008 a0001c0001t0010g0268 others(2): Show |
5 | HG01192.hp2 HG02145.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.1207-2722A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 5/8 | chr17 | 37707771 | |||||||
| chr17:37707822 | C | T | 1 | a0001c0001t0003g0118 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1206+2681G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 5/8 | chr17 | 37707822 | |||||||
| chr17:37707860 | C | T | 280 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0013 others(277): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.1206+2643G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 5/8 | chr17 | 37707860 | |||||||
| chr17:37707922 | C | T | 1 | a0001c0001t0002g0034 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1206+2581G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 5/8 | chr17 | 37707922 | |||||||
| chr17:37707951 | A | G | 106 | a0001c0001t0001g0129 a0001c0001t0001g0146 a0001c0001t0001g0153 others(103): Show |
106 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.1206+2552T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 5/8 | chr17 | 37707951 | |||||||
| chr17:37708482 | G | C | 1 | a0001c0001t0005g0208 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1206+2021C>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 5/8 | chr17 | 37708482 | |||||||
| chr17:37708720 | C | T | 256 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0013 others(253): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.1206+1783G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 5/8 | chr17 | 37708720 | |||||||
| chr17:37708821 | C | T | 6 | a0001c0001t0001g0009 a0001c0001t0001g0283 a0001c0001t0001g0351 others(3): Show |
6 | HG02451.hp2 HG02622.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1206+1682G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 5/8 | chr17 | 37708821 | |||||||
| chr17:37708856 | G | T | 2 | a0001c0001t0001g0236 a0001c0001t0001g0240 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1206+1647C>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 5/8 | chr17 | 37708856 | |||||||
| chr17:37709072 | C | A | 2 | a0001c0001t0001g0282 a0001c0001t0001g0342 |
2 | HG01109.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1206+1431G>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 5/8 | chr17 | 37709072 | |||||||
| chr17:37709073 | G | A | 1 | a0001c0001t0011g0374 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1206+1430C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 5/8 | chr17 | 37709073 | |||||||
| chr17:37709305 | A | G | 5 | a0001c0001t0001g0146 a0001c0001t0001g0291 a0001c0001t0002g0081 others(2): Show |
5 | HG02083.hp1 NA18966.hp2 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.1206+1198T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 5/8 | chr17 | 37709305 | |||||||
| chr17:37709313 | G | A | 1 | a0001c0001t0002g0156 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1206+1190C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 5/8 | chr17 | 37709313 | |||||||
| chr17:37709398 | T | A | 1 | a0001c0001t0005g0281 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1206+1105A>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 5/8 | chr17 | 37709398 | |||||||
| chr17:37709409 | C | A | 1 | a0001c0001t0005g0281 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1206+1094G>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 5/8 | chr17 | 37709409 | |||||||
| chr17:37709424 | A | AT | 26 | a0001c0001t0001g0013 a0001c0001t0001g0033 a0001c0001t0001g0225 others(23): Show |
26 | HG01256.hp2 HG01257.hp2 HG02148.hp2 others(23): Show |
intron_variant | MODIFIER | c.1206+1078dupA | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 5/8 | chr17 | 37709424 | |||||||
| chr17:37709772 | G | A | 2 | a0001c0001t0003g0023 a0001c0001t0003g0273 |
2 | HG00733.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.1206+731C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 5/8 | chr17 | 37709772 | |||||||
| chr17:37709799 | A | AC | 3 | a0001c0001t0001g0187 a0001c0001t0004g0091 a0001c0001t0004g0151 |
3 | NA18978.hp2 NA19083.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.1206+703dupG | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 5/8 | chr17 | 37709799 | |||||||
| chr17:37709801 | C | T | 3 | a0001c0001t0001g0288 a0001c0001t0002g0007 a0001c0001t0002g0398 |
3 | HG03540.hp1 NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1206+702G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 5/8 | chr17 | 37709801 | |||||||
| chr17:37709830 | C | T | 1 | a0001c0001t0005g0193 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1206+673G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 5/8 | chr17 | 37709830 | |||||||
| chr17:37709853 | C | T | 2 | a0001c0001t0001g0027 a0001c0001t0001g0169 |
2 | HG00438.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.1206+650G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 5/8 | chr17 | 37709853 | |||||||
| chr17:37710016 | A | G | 1 | a0001c0001t0001g0159 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1206+487T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 5/8 | chr17 | 37710016 | |||||||
| chr17:37710041 | T | C | 2 | a0001c0001t0002g0262 a0001c0001t0002g0354 |
2 | HG02451.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1206+462A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 5/8 | chr17 | 37710041 | |||||||
| chr17:37710172 | G | A | 18 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0026 others(15): Show |
18 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(15): Show |
intron_variant | MODIFIER | c.1206+331C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 5/8 | chr17 | 37710172 | |||||||
| chr17:37710172 | GGAT | G | 38 | a0001c0001t0001g0016 a0001c0001t0001g0046 a0001c0001t0001g0069 others(35): Show |
38 | HG00280.hp2 HG00544.hp2 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.1206+328_1206+330d others(5): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 5/8 | chr17 | 37710172 | |||||||
| chr17:37710942 | C | T | 13 | a0001c0001t0001g0009 a0001c0001t0001g0225 a0001c0001t0001g0283 others(10): Show |
13 | HG01884.hp2 HG02451.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.1046-279G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37710942 | |||||||
| chr17:37711000 | G | A | 3 | a0001c0001t0006g0253 a0001c0001t0006g0264 a0001c0003t0006g0349 |
3 | HG01243.hp1 HG02818.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1046-337C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37711000 | |||||||
| chr17:37711026 | T | G | 17 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0022 others(14): Show |
17 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.1046-363A>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37711026 | |||||||
| chr17:37711139 | C | T | 10 | a0001c0001t0001g0202 a0001c0001t0003g0333 a0001c0001t0006g0285 others(7): Show |
10 | HG02258.hp1 HG02630.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.1046-476G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37711139 | |||||||
| chr17:37711276 | C | G | 1 | a0001c0001t0001g0022 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1046-613G>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37711276 | |||||||
| chr17:37711467 | C | T | 1 | a0001c0001t0001g0022 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1046-804G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37711467 | |||||||
| chr17:37711478 | C | T | 1 | a0001c0001t0001g0381 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1046-815G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37711478 | |||||||
| chr17:37711642 | G | A | 1 | a0001c0001t0003g0118 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1046-979C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37711642 | |||||||
| chr17:37711644 | A | G | 16 | a0001c0001t0001g0158 a0001c0001t0001g0254 a0001c0001t0001g0297 others(13): Show |
16 | HG00099.hp2 HG00642.hp1 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.1046-981T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37711644 | |||||||
| chr17:37711817 | A | G | 1 | a0001c0001t0005g0343 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1046-1154T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37711817 | |||||||
| chr17:37711901 | C | T | 9 | a0001c0001t0002g0144 a0001c0001t0002g0145 a0001c0001t0003g0030 others(6): Show |
9 | HG02602.hp2 HG02647.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1046-1238G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37711901 | |||||||
| chr17:37711911 | G | A | 10 | a0001c0001t0001g0394 a0001c0001t0005g0193 a0001c0001t0006g0014 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1046-1248C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37711911 | |||||||
| chr17:37712033 | G | A | 1 | a0001c0001t0002g0188 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1046-1370C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37712033 | |||||||
| chr17:37712267 | T | C | 1 | a0001c0001t0001g0311 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1046-1604A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37712267 | |||||||
| chr17:37712436 | T | TTAAATGA others(311): Show |
4 | a0001c0001t0002g0263 a0001c0001t0005g0395 a0001c0001t0005g0396 others(1): Show |
4 | HG02622.hp2 HG03041.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1046-1774_1046-177 others(322): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37712436 | |||||||
| chr17:37712444 | G | A | 4 | a0001c0001t0002g0263 a0001c0001t0005g0395 a0001c0001t0005g0396 others(1): Show |
4 | HG02622.hp2 HG03041.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1046-1781C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37712444 | |||||||
| chr17:37712460 | G | A | 10 | a0001c0001t0001g0394 a0001c0001t0005g0193 a0001c0001t0006g0014 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1046-1797C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37712460 | |||||||
| chr17:37712725 | C | T | 7 | a0001c0001t0001g0158 a0001c0001t0001g0254 a0001c0001t0001g0297 others(4): Show |
7 | HG00099.hp2 HG00642.hp1 HG00733.hp2 others(4): Show |
intron_variant | MODIFIER | c.1046-2062G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37712725 | |||||||
| chr17:37712966 | G | A | 3 | a0001c0001t0002g0097 a0001c0001t0002g0114 a0001c0001t0005g0108 |
3 | HG00140.hp1 HG02148.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1046-2303C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37712966 | |||||||
| chr17:37713015 | T | G | 1 | a0001c0001t0001g0303 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1046-2352A>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37713015 | |||||||
| chr17:37713168 | T | G | 20 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0026 others(17): Show |
20 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(17): Show |
intron_variant | MODIFIER | c.1046-2505A>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37713168 | |||||||
| chr17:37713188 | T | G | 20 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0026 others(17): Show |
20 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(17): Show |
intron_variant | MODIFIER | c.1046-2525A>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37713188 | |||||||
| chr17:37713312 | C | A | 63 | a0001c0001t0001g0027 a0001c0001t0001g0033 a0001c0001t0001g0040 others(60): Show |
63 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.1046-2649G>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37713312 | |||||||
| chr17:37713469 | C | T | 1 | a0001c0001t0002g0401 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1046-2806G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37713469 | |||||||
| chr17:37713484 | T | C | 28 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0026 others(25): Show |
28 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.1046-2821A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37713484 | |||||||
| chr17:37713612 | T | C | 28 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0026 others(25): Show |
28 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.1046-2949A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37713612 | |||||||
| chr17:37713631 | T | A | 9 | a0001c0001t0001g0040 a0001c0001t0001g0066 a0001c0001t0001g0105 others(6): Show |
9 | HG00558.hp1 HG00558.hp2 HG00621.hp2 others(6): Show |
intron_variant | MODIFIER | c.1046-2968A>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37713631 | |||||||
| chr17:37713674 | C | G | 1 | a0001c0001t0006g0270 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1046-3011G>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37713674 | |||||||
| chr17:37713788 | G | A | 1 | a0001c0001t0004g0261 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1046-3125C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37713788 | |||||||
| chr17:37713802 | G | A | 4 | a0001c0001t0001g0303 a0001c0001t0003g0323 a0001c0001t0003g0327 others(1): Show |
4 | NA18945.hp1 NA18987.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.1046-3139C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37713802 | |||||||
| chr17:37713821 | A | T | 2 | a0001c0001t0002g0301 a0001c0001t0006g0038 |
2 | HG01192.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1046-3158T>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37713821 | |||||||
| chr17:37713882 | C | T | 2 | a0001c0001t0003g0018 a0001c0001t0020g0407 |
2 | HG03239.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.1046-3219G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37713882 | |||||||
| chr17:37713957 | A | G | 2 | a0001c0001t0002g0037 a0001c0001t0002g0048 |
2 | HG02027.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.1046-3294T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37713957 | |||||||
| chr17:37714146 | T | C | 1 | a0001c0001t0001g0245 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1046-3483A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37714146 | |||||||
| chr17:37714152 | A | C | 1 | a0001c0001t0001g0056 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1046-3489T>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37714152 | |||||||
| chr17:37714224 | G | A | 1 | a0001c0001t0002g0210 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1046-3561C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37714224 | |||||||
| chr17:37714382 | G | T | 1 | a0001c0001t0020g0407 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1046-3719C>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37714382 | |||||||
| chr17:37714505 | T | C | 17 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0026 others(14): Show |
17 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.1046-3842A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37714505 | |||||||
| chr17:37714525 | C | A | 2 | a0001c0001t0004g0215 a0001c0001t0004g0216 |
2 | HG01109.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.1046-3862G>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37714525 | |||||||
| chr17:37714689 | C | T | 17 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0026 others(14): Show |
17 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.1046-4026G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37714689 | |||||||
| chr17:37714839 | G | T | 9 | a0001c0001t0001g0394 a0001c0001t0002g0222 a0001c0001t0005g0012 others(6): Show |
9 | HG01884.hp1 HG02145.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1046-4176C>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37714839 | |||||||
| chr17:37714897 | C | T | 17 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0026 others(14): Show |
17 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.1046-4234G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37714897 | |||||||
| chr17:37714971 | A | G | 334 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0013 others(331): Show |
336 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(333): Show |
intron_variant | MODIFIER | c.1046-4308T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37714971 | |||||||
| chr17:37715161 | A | G | 1 | a0001c0001t0002g0205 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1046-4498T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37715161 | |||||||
| chr17:37715188 | A | G | 12 | a0001c0001t0001g0013 a0001c0001t0002g0007 a0001c0001t0002g0398 others(9): Show |
12 | HG01891.hp2 HG02055.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1046-4525T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37715188 | |||||||
| chr17:37715258 | C | T | 1 | a0001c0001t0001g0303 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1046-4595G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37715258 | |||||||
| chr17:37715322 | G | A | 8 | a0001c0001t0001g0368 a0001c0001t0003g0030 a0001c0001t0003g0031 others(5): Show |
8 | HG02602.hp2 HG02647.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1046-4659C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37715322 | |||||||
| chr17:37715466 | T | C | 5 | a0001c0001t0002g0113 a0001c0001t0002g0318 a0001c0001t0002g0401 others(2): Show |
5 | HG00280.hp2 HG01168.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.1046-4803A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37715466 | |||||||
| chr17:37715597 | C | T | 87 | a0001c0001t0001g0027 a0001c0001t0001g0033 a0001c0001t0001g0040 others(84): Show |
87 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.1046-4934G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37715597 | |||||||
| chr17:37715643 | G | A | 1 | a0001c0001t0005g0203 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1046-4980C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37715643 | |||||||
| chr17:37715645 | A | G | 1 | a0001c0001t0007g0214 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1046-4982T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37715645 | |||||||
| chr17:37715665 | A | G | 12 | a0001c0001t0001g0009 a0001c0001t0001g0225 a0001c0001t0001g0283 others(9): Show |
12 | HG02451.hp2 HG02486.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.1046-5002T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37715665 | |||||||
| chr17:37715687 | C | T | 1 | a0001c0001t0004g0091 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1046-5024G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37715687 | |||||||
| chr17:37715711 | G | A | 11 | a0001c0001t0001g0394 a0001c0001t0002g0222 a0001c0001t0005g0012 others(8): Show |
11 | HG01884.hp1 HG02145.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.1046-5048C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37715711 | |||||||
| chr17:37715776 | T | C | 1 | a0001c0001t0012g0223 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1046-5113A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37715776 | |||||||
| chr17:37715794 | C | T | 1 | a0001c0001t0006g0286 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1046-5131G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37715794 | |||||||
| chr17:37715807 | C | G | 206 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0028 others(203): Show |
208 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.1046-5144G>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37715807 | |||||||
| chr17:37715810 | G | T | 11 | a0001c0001t0001g0055 a0001c0001t0001g0107 a0001c0001t0003g0011 others(8): Show |
11 | HG00673.hp1 NA18747.hp1 NA18942.hp2 others(8): Show |
intron_variant | MODIFIER | c.1046-5147C>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37715810 | |||||||
| chr17:37715860 | G | C | 17 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0026 others(14): Show |
17 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.1046-5197C>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37715860 | |||||||
| chr17:37715897 | C | T | 2 | a0001c0001t0007g0277 a0001c0003t0005g0350 |
2 | HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1046-5234G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37715897 | |||||||
| chr17:37716003 | G | A | 27 | a0001c0001t0001g0022 a0001c0001t0001g0026 a0001c0001t0001g0157 others(24): Show |
27 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.1046-5340C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37716003 | |||||||
| chr17:37716005 | G | A | 1 | a0001c0001t0002g0205 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1046-5342C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37716005 | |||||||
| chr17:37716084 | G | A | 4 | a0001c0001t0001g0146 a0001c0001t0002g0075 a0001c0001t0002g0076 others(1): Show |
4 | HG00544.hp1 HG02027.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.1046-5421C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37716084 | |||||||
| chr17:37716148 | T | C | 1 | a0001c0001t0012g0223 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1046-5485A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37716148 | |||||||
| chr17:37716221 | A | G | 5 | a0001c0001t0002g0222 a0001c0001t0005g0012 a0001c0001t0006g0005 others(2): Show |
5 | HG01884.hp1 HG02145.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.1046-5558T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37716221 | |||||||
| chr17:37716773 | G | A | 1 | a0001c0001t0004g0332 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1046-6110C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37716773 | |||||||
| chr17:37716842 | A | ATC | 22 | a0001c0001t0001g0027 a0001c0001t0001g0049 a0001c0001t0001g0160 others(19): Show |
22 | HG00735.hp1 HG00738.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.1046-6181_1046-618 others(6): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37716842 | |||||||
| chr17:37716842 | A | ATCTC | 20 | a0001c0001t0001g0055 a0001c0001t0001g0070 a0001c0001t0001g0071 others(17): Show |
20 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(17): Show |
intron_variant | MODIFIER | c.1046-6183_1046-618 others(8): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37716842 | |||||||
| chr17:37716842 | A | ATCTCTC | 8 | a0001c0001t0001g0107 a0001c0001t0002g0097 a0001c0001t0003g0011 others(5): Show |
8 | HG00673.hp1 HG02055.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1046-6185_1046-618 others(10): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37716842 | |||||||
| chr17:37716842 | A | ATCTCTCT others(1): Show |
5 | a0001c0001t0001g0393 a0001c0001t0002g0114 a0001c0001t0003g0043 others(2): Show |
5 | HG01891.hp1 HG02148.hp2 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.1046-6187_1046-618 others(12): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37716842 | |||||||
| chr17:37716842 | A | ATCTCTCT others(3): Show |
2 | a0001c0001t0001g0033 a0001c0001t0006g0246 |
2 | HG02886.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.1046-6189_1046-618 others(14): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37716842 | |||||||
| chr17:37716842 | A | ATCTCTCT others(5): Show |
3 | a0001c0001t0003g0045 a0001c0001t0017g0257 a0001c0002t0009g0221 |
3 | HG03453.hp2 HG03704.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.1046-6191_1046-618 others(16): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37716842 | |||||||
| chr17:37716842 | A | ATCTCTCT others(7): Show |
1 | a0001c0001t0001g0394 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1046-6193_1046-618 others(18): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37716842 | |||||||
| chr17:37716842 | A | ATCTCTCT others(9): Show |
2 | a0001c0001t0006g0014 a0001c0002t0009g0265 |
2 | HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1046-6195_1046-618 others(20): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37716842 | |||||||
| chr17:37716842 | ATC | A | 23 | a0001c0001t0001g0056 a0001c0001t0001g0209 a0001c0001t0002g0037 others(20): Show |
23 | HG00597.hp2 HG00673.hp2 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.1046-6181_1046-618 others(6): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37716842 | |||||||
| chr17:37716842 | ATCTC | A | 35 | a0001c0001t0001g0060 a0001c0001t0001g0080 a0001c0001t0001g0153 others(32): Show |
35 | HG00423.hp1 HG00609.hp1 HG01192.hp2 others(32): Show |
intron_variant | MODIFIER | c.1046-6183_1046-618 others(8): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37716842 | |||||||
| chr17:37716842 | ATCTCTC | A | 13 | a0001c0001t0001g0013 a0001c0001t0001g0040 a0001c0001t0001g0100 others(10): Show |
13 | HG01074.hp1 HG01261.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.1046-6185_1046-618 others(10): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37716842 | |||||||
| chr17:37716842 | ATCTCTCT others(1): Show |
A | 14 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0159 others(11): Show |
15 | HG01167.hp1 HG02129.hp2 HG02155.hp2 others(12): Show |
intron_variant | MODIFIER | c.1046-6187_1046-618 others(12): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37716842 | |||||||
| chr17:37716842 | ATCTCTCT others(3): Show |
A | 82 | a0001c0001t0001g0002 a0001c0001t0001g0028 a0001c0001t0001g0039 others(79): Show |
83 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.1046-6189_1046-618 others(14): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37716842 | |||||||
| chr17:37716842 | ATCTCTCT others(5): Show |
A | 29 | a0001c0001t0001g0282 a0001c0001t0001g0311 a0001c0001t0001g0342 others(26): Show |
29 | HG00544.hp2 HG01109.hp2 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.1046-6191_1046-618 others(16): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37716842 | |||||||
| chr17:37716842 | ATCTCTCT others(7): Show |
A | 60 | a0001c0001t0001g0009 a0001c0001t0001g0069 a0001c0001t0001g0202 others(57): Show |
60 | HG00280.hp1 HG00280.hp2 HG01099.hp2 others(57): Show |
intron_variant | MODIFIER | c.1046-6193_1046-618 others(18): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37716842 | |||||||
| chr17:37716842 | ATCTCTCT others(9): Show |
A | 1 | a0001c0001t0001g0245 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1046-6195_1046-618 others(20): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37716842 | |||||||
| chr17:37716846 | C | CTA | 5 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0157 others(2): Show |
5 | HG01192.hp1 HG01516.hp1 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1046-6184_1046-618 others(6): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37716846 | |||||||
| chr17:37716848 | C | A | 12 | a0001c0001t0001g0026 a0001c0001t0001g0371 a0001c0001t0001g0380 others(9): Show |
12 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.1046-6185G>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37716848 | |||||||
| chr17:37716853 | T | C | 1 | a0001c0001t0003g0272 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1046-6190A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37716853 | |||||||
| chr17:37716956 | C | T | 1 | a0001c0001t0003g0231 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1046-6293G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37716956 | |||||||
| chr17:37717101 | A | G | 333 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0013 others(330): Show |
335 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.1046-6438T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37717101 | |||||||
| chr17:37717109 | G | A | 1 | a0001c0001t0002g0006 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1046-6446C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37717109 | |||||||
| chr17:37717189 | C | G | 1 | a0001c0001t0007g0200 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1046-6526G>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37717189 | |||||||
| chr17:37717222 | T | G | 4 | a0001c0001t0001g0146 a0001c0001t0002g0075 a0001c0001t0002g0076 others(1): Show |
4 | HG00544.hp1 HG02027.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.1046-6559A>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37717222 | |||||||
| chr17:37717281 | T | C | 333 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0013 others(330): Show |
335 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.1046-6618A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37717281 | |||||||
| chr17:37717463 | C | T | 1 | a0001c0001t0002g0034 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1046-6800G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37717463 | |||||||
| chr17:37717464 | G | A | 2 | a0001c0001t0007g0277 a0001c0003t0005g0350 |
2 | HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1046-6801C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37717464 | |||||||
| chr17:37717568 | A | G | 9 | a0001c0001t0001g0202 a0001c0001t0001g0271 a0001c0001t0001g0288 others(6): Show |
9 | HG01243.hp1 HG02109.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1046-6905T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37717568 | |||||||
| chr17:37717746 | A | T | 1 | a0001c0001t0002g0172 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1046-7083T>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37717746 | |||||||
| chr17:37717776 | G | A | 1 | a0001c0001t0002g0006 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1046-7113C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37717776 | |||||||
| chr17:37717865 | C | A | 321 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0013 others(318): Show |
323 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.1046-7202G>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37717865 | |||||||
| chr17:37718406 | T | C | 4 | a0001c0001t0001g0394 a0001c0001t0006g0014 a0001c0001t0006g0274 others(1): Show |
4 | HG02486.hp1 HG02572.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1046-7743A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37718406 | |||||||
| chr17:37718425 | C | A | 10 | a0001c0001t0001g0394 a0001c0001t0002g0222 a0001c0001t0005g0012 others(7): Show |
10 | HG01884.hp1 HG02145.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1046-7762G>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37718425 | |||||||
| chr17:37718503 | CTG | C | 9 | a0001c0001t0001g0368 a0001c0001t0003g0030 a0001c0001t0003g0031 others(6): Show |
9 | HG02602.hp2 HG02647.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1046-7842_1046-784 others(6): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37718503 | |||||||
| chr17:37718504 | T | C | 17 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0026 others(14): Show |
17 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.1046-7841A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37718504 | |||||||
| chr17:37718512 | A | G | 332 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0013 others(329): Show |
334 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(331): Show |
intron_variant | MODIFIER | c.1046-7849T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37718512 | |||||||
| chr17:37718601 | T | G | 2 | a0001c0001t0002g0007 a0001c0001t0002g0398 |
2 | NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1046-7938A>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37718601 | |||||||
| chr17:37718766 | T | C | 1 | a0001c0001t0003g0023 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1046-8103A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37718766 | |||||||
| chr17:37718880 | T | C | 1 | a0001c0001t0006g0286 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1046-8217A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37718880 | |||||||
| chr17:37719113 | ATAT | A | 330 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0015 others(327): Show |
331 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(328): Show |
intron_variant | MODIFIER | c.1046-8453_1046-845 others(7): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37719113 | |||||||
| chr17:37719306 | G | A | 1 | a0001c0001t0002g0355 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1046-8643C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37719306 | |||||||
| chr17:37719458 | A | C | 17 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0026 others(14): Show |
17 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.1046-8795T>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37719458 | |||||||
| chr17:37719570 | A | G | 336 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0013 others(333): Show |
338 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(335): Show |
intron_variant | MODIFIER | c.1046-8907T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37719570 | |||||||
| chr17:37719723 | A | G | 1 | a0001c0001t0002g0064 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1046-9060T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37719723 | |||||||
| chr17:37719911 | AG | A | 5 | a0001c0001t0002g0222 a0001c0001t0005g0012 a0001c0001t0006g0005 others(2): Show |
5 | HG01884.hp1 HG02145.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.1046-9249delC | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37719911 | |||||||
| chr17:37720025 | C | A | 1 | a0002c0004t0003g0405 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1046-9362G>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37720025 | |||||||
| chr17:37720154 | G | C | 1 | a0001c0001t0002g0083 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1046-9491C>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37720154 | |||||||
| chr17:37720170 | G | C | 68 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0024 others(65): Show |
68 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.1046-9507C>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37720170 | |||||||
| chr17:37720378 | G | A | 1 | a0001c0001t0001g0255 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1046-9715C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37720378 | |||||||
| chr17:37720433 | T | C | 280 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0022 others(277): Show |
282 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.1046-9770A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37720433 | |||||||
| chr17:37720480 | G | A | 13 | a0001c0001t0001g0009 a0001c0001t0001g0225 a0001c0001t0001g0283 others(10): Show |
13 | HG02451.hp2 HG02486.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.1046-9817C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37720480 | |||||||
| chr17:37720547 | A | G | 2 | a0001c0001t0002g0262 a0001c0001t0002g0354 |
2 | HG02451.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1046-9884T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37720547 | |||||||
| chr17:37720815 | A | G | 108 | a0001c0001t0001g0027 a0001c0001t0001g0033 a0001c0001t0001g0040 others(105): Show |
108 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.1046-10152T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37720815 | |||||||
| chr17:37721040 | G | C | 1 | a0001c0001t0001g0015 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1046-10377C>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37721040 | |||||||
| chr17:37721074 | A | G | 1 | a0001c0001t0002g0189 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1046-10411T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37721074 | |||||||
| chr17:37721098 | C | G | 2 | a0001c0001t0003g0372 a0001c0001t0003g0373 |
2 | NA18964.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.1046-10435G>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37721098 | |||||||
| chr17:37721213 | T | C | 1 | a0001c0001t0005g0295 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1045+10382A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37721213 | |||||||
| chr17:37721584 | G | T | 1 | a0001c0001t0004g0332 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1045+10011C>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37721584 | |||||||
| chr17:37721585 | G | C | 1 | a0001c0001t0004g0332 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1045+10010C>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37721585 | |||||||
| chr17:37721587 | C | T | 1 | a0001c0001t0004g0332 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1045+10008G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37721587 | |||||||
| chr17:37721631 | A | G | 2 | a0001c0001t0005g0395 a0001c0001t0005g0396 |
2 | HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1045+9964T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37721631 | |||||||
| chr17:37721719 | C | CT | 21 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0026 others(18): Show |
21 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.1045+9875dupA | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37721719 | |||||||
| chr17:37721719 | CT | C | 154 | a0001c0001t0001g0019 a0001c0001t0001g0028 a0001c0001t0001g0039 others(151): Show |
155 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.1045+9875delA | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37721719 | |||||||
| chr17:37721719 | CTTT | C | 16 | a0001c0001t0001g0158 a0001c0001t0001g0254 a0001c0001t0001g0383 others(13): Show |
16 | HG00099.hp2 HG00642.hp1 HG01256.hp2 others(13): Show |
intron_variant | MODIFIER | c.1045+9873_1045+987 others(7): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37721719 | |||||||
| chr17:37721721 | T | C | 5 | a0001c0001t0001g0024 a0001c0001t0001g0319 a0001c0001t0001g0397 others(2): Show |
5 | HG00642.hp2 HG01071.hp1 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.1045+9874A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37721721 | |||||||
| chr17:37721722 | T | C | 1 | a0001c0001t0001g0019 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1045+9873A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37721722 | |||||||
| chr17:37721724 | T | C | 16 | a0001c0001t0001g0158 a0001c0001t0001g0254 a0001c0001t0001g0383 others(13): Show |
16 | HG00099.hp2 HG00642.hp1 HG01256.hp2 others(13): Show |
intron_variant | MODIFIER | c.1045+9871A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37721724 | |||||||
| chr17:37722187 | T | C | 1 | a0001c0001t0012g0223 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1045+9408A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37722187 | |||||||
| chr17:37722217 | T | C | 3 | a0001c0001t0006g0246 a0001c0002t0009g0221 a0001c0002t0009g0265 |
3 | HG02886.hp2 HG03098.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1045+9378A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37722217 | |||||||
| chr17:37722426 | C | T | 144 | a0001c0001t0001g0028 a0001c0001t0001g0039 a0001c0001t0001g0056 others(141): Show |
145 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.1045+9169G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37722426 | |||||||
| chr17:37722478 | G | T | 289 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0022 others(286): Show |
290 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.1045+9117C>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37722478 | |||||||
| chr17:37722776 | G | A | 41 | a0001c0001t0001g0013 a0001c0001t0001g0368 a0001c0001t0001g0394 others(38): Show |
41 | HG00140.hp1 HG01884.hp1 HG01891.hp2 others(38): Show |
intron_variant | MODIFIER | c.1045+8819C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37722776 | |||||||
| chr17:37722812 | A | C | 11 | a0001c0001t0001g0013 a0001c0001t0005g0279 a0001c0001t0006g0251 others(8): Show |
11 | HG01891.hp2 HG02055.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1045+8783T>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37722812 | |||||||
| chr17:37722912 | C | A | 335 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0015 others(332): Show |
336 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(333): Show |
intron_variant | MODIFIER | c.1045+8683G>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37722912 | |||||||
| chr17:37722916 | T | C | 1 | a0001c0001t0001g0302 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1045+8679A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37722916 | |||||||
| chr17:37722971 | C | G | 18 | a0001c0001t0001g0368 a0001c0001t0001g0394 a0001c0001t0002g0097 others(15): Show |
18 | HG00140.hp1 HG01993.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1045+8624G>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37722971 | |||||||
| chr17:37723079 | G | C | 1 | a0001c0001t0001g0334 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1045+8516C>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37723079 | |||||||
| chr17:37723091 | G | A | 1 | a0001c0001t0001g0074 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1045+8504C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37723091 | |||||||
| chr17:37723113 | G | A | 6 | a0001c0001t0001g0288 a0001c0001t0005g0012 a0001c0001t0005g0295 others(3): Show |
6 | HG01243.hp1 HG02109.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1045+8482C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37723113 | |||||||
| chr17:37723163 | C | T | 1 | a0001c0002t0009g0221 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1045+8432G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37723163 | |||||||
| chr17:37723167 | G | A | 2 | a0001c0001t0002g0234 a0001c0001t0002g0317 |
2 | NA18967.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.1045+8428C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37723167 | |||||||
| chr17:37723175 | T | TA | 22 | a0001c0001t0001g0013 a0001c0001t0001g0202 a0001c0001t0001g0271 others(19): Show |
22 | HG01891.hp2 HG02055.hp1 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.1045+8419dupT | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37723175 | |||||||
| chr17:37723175 | TA | T | 13 | a0001c0001t0001g0368 a0001c0001t0002g0097 a0001c0001t0002g0114 others(10): Show |
13 | HG00140.hp1 HG02148.hp2 HG02602.hp2 others(10): Show |
intron_variant | MODIFIER | c.1045+8419delT | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37723175 | |||||||
| chr17:37723215 | T | C | 2 | a0001c0001t0007g0200 a0001c0001t0007g0250 |
2 | HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1045+8380A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37723215 | |||||||
| chr17:37723218 | A | G | 2 | a0001c0001t0007g0200 a0001c0001t0007g0250 |
2 | HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1045+8377T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37723218 | |||||||
| chr17:37723229 | C | T | 1 | a0001c0001t0008g0168 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1045+8366G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37723229 | |||||||
| chr17:37723309 | T | C | 170 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0013 others(167): Show |
171 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.1045+8286A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37723309 | |||||||
| chr17:37723433 | G | C | 1 | a0001c0001t0001g0311 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1045+8162C>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37723433 | |||||||
| chr17:37723607 | C | G | 1 | a0001c0001t0005g0208 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1045+7988G>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37723607 | |||||||
| chr17:37723715 | A | C | 32 | a0001c0001t0001g0069 a0001c0001t0001g0150 a0001c0001t0001g0297 others(29): Show |
32 | HG00280.hp2 HG00544.hp2 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.1045+7880T>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37723715 | |||||||
| chr17:37723718 | A | T | 145 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0015 others(142): Show |
146 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.1045+7877T>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37723718 | |||||||
| chr17:37723787 | T | C | 4 | a0001c0001t0002g0222 a0001c0001t0006g0005 a0001c0001t0010g0268 others(1): Show |
4 | HG01884.hp1 HG02145.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1045+7808A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37723787 | |||||||
| chr17:37724008 | T | C | 265 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0013 others(262): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.1045+7587A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37724008 | |||||||
| chr17:37724053 | G | A | 6 | a0001c0001t0002g0222 a0001c0001t0006g0005 a0001c0001t0006g0274 others(3): Show |
6 | HG01884.hp1 HG02145.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1045+7542C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37724053 | |||||||
| chr17:37724091 | G | T | 1 | a0001c0001t0001g0046 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1045+7504C>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37724091 | |||||||
| chr17:37724112 | A | T | 1 | a0001c0001t0001g0202 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1045+7483T>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37724112 | |||||||
| chr17:37724170 | T | G | 1 | a0001c0003t0005g0350 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1045+7425A>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37724170 | |||||||
| chr17:37724207 | T | C | 181 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0013 others(178): Show |
182 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.1045+7388A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37724207 | |||||||
| chr17:37724232 | C | T | 53 | a0001c0001t0001g0009 a0001c0001t0001g0158 a0001c0001t0001g0225 others(50): Show |
53 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.1045+7363G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37724232 | |||||||
| chr17:37724249 | C | T | 374 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0013 others(371): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.1045+7346G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37724249 | |||||||
| chr17:37724266 | A | G | 22 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0022 others(19): Show |
22 | HG00140.hp2 HG00323.hp1 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.1045+7329T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37724266 | |||||||
| chr17:37724297 | CTGGTTCT others(17): Show |
C | 22 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0022 others(19): Show |
22 | HG00140.hp2 HG00323.hp1 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.1045+7274_1045+729 others(28): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37724297 | |||||||
| chr17:37724428 | G | A | 5 | a0001c0001t0001g0159 a0001c0001t0001g0177 a0001c0001t0001g0249 others(2): Show |
5 | HG00099.hp1 HG01109.hp1 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.1045+7167C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37724428 | |||||||
| chr17:37724830 | C | T | 4 | a0001c0001t0002g0222 a0001c0001t0006g0005 a0001c0001t0010g0268 others(1): Show |
4 | HG01884.hp1 HG02145.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1045+6765G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37724830 | |||||||
| chr17:37724903 | C | CGTGT | 4 | a0001c0001t0002g0113 a0001c0001t0002g0401 a0001c0001t0008g0369 others(1): Show |
4 | HG01168.hp1 HG02109.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.1045+6688_1045+669 others(8): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37724903 | |||||||
| chr17:37724903 | CGT | C | 85 | a0001c0001t0001g0039 a0001c0001t0001g0056 a0001c0001t0001g0057 others(82): Show |
86 | HG00597.hp1 HG00673.hp1 HG01070.hp2 others(83): Show |
intron_variant | MODIFIER | c.1045+6690_1045+669 others(6): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37724903 | |||||||
| chr17:37724903 | CGTGT | C | 94 | a0001c0001t0001g0027 a0001c0001t0001g0033 a0001c0001t0001g0049 others(91): Show |
94 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.1045+6688_1045+669 others(8): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37724903 | |||||||
| chr17:37724903 | CGTGTGT | C | 36 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0022 others(33): Show |
36 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(33): Show |
intron_variant | MODIFIER | c.1045+6686_1045+669 others(10): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37724903 | |||||||
| chr17:37724903 | CGTGTGTG others(1): Show |
C | 26 | a0001c0001t0001g0013 a0001c0001t0001g0202 a0001c0001t0002g0006 others(23): Show |
26 | HG01891.hp1 HG01891.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1045+6684_1045+669 others(12): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37724903 | |||||||
| chr17:37724903 | CGTGTGTG others(9): Show |
C | 1 | a0001c0001t0004g0332 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1045+6676_1045+669 others(20): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37724903 | |||||||
| chr17:37724908 | G | A | 1 | a0001c0001t0006g0005 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1045+6687C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37724908 | |||||||
| chr17:37724910 | G | A | 5 | a0001c0001t0002g0222 a0001c0001t0006g0274 a0001c0001t0006g0275 others(2): Show |
5 | HG02145.hp2 HG02572.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1045+6685C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37724910 | |||||||
| chr17:37724921 | T | C | 2 | a0001c0001t0002g0262 a0001c0001t0002g0354 |
2 | HG02451.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1045+6674A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37724921 | |||||||
| chr17:37724923 | T | C | 34 | a0001c0001t0001g0009 a0001c0001t0001g0158 a0001c0001t0001g0225 others(31): Show |
34 | HG00099.hp2 HG00642.hp1 HG01256.hp2 others(31): Show |
intron_variant | MODIFIER | c.1045+6672A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37724923 | |||||||
| chr17:37724926 | GTGTGTGT others(5): Show |
G | 2 | a0001c0001t0002g0262 a0001c0001t0002g0354 |
2 | HG02451.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1045+6657_1045+666 others(16): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37724926 | |||||||
| chr17:37724928 | G | C | 3 | a0001c0001t0001g0271 a0001c0001t0001g0334 a0001c0001t0006g0004 |
3 | HG02809.hp1 HG03579.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1045+6667C>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37724928 | |||||||
| chr17:37724928 | GTGTGTGT others(3): Show |
G | 35 | a0001c0001t0001g0009 a0001c0001t0001g0028 a0001c0001t0001g0158 others(32): Show |
35 | HG00099.hp2 HG00642.hp1 HG01256.hp2 others(32): Show |
intron_variant | MODIFIER | c.1045+6657_1045+666 others(14): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37724928 | |||||||
| chr17:37724930 | G | C | 17 | a0001c0001t0001g0013 a0001c0001t0001g0202 a0001c0001t0002g0007 others(14): Show |
17 | HG01891.hp2 HG02055.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.1045+6665C>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37724930 | |||||||
| chr17:37724930 | GTGTGTGT others(1): Show |
G | 66 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0024 others(63): Show |
67 | HG00140.hp1 HG00597.hp2 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.1045+6657_1045+666 others(12): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37724930 | |||||||
| chr17:37724932 | GTGTGTAT others(1): Show |
G | 12 | a0001c0001t0001g0368 a0001c0001t0002g0073 a0001c0001t0002g0300 others(9): Show |
12 | HG00621.hp1 HG00738.hp2 HG01993.hp1 others(9): Show |
intron_variant | MODIFIER | c.1045+6655_1045+666 others(12): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37724932 | |||||||
| chr17:37724934 | G | A | 9 | a0001c0001t0001g0271 a0001c0001t0001g0334 a0001c0001t0002g0222 others(6): Show |
9 | HG01884.hp1 HG02145.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1045+6661C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37724934 | |||||||
| chr17:37724936 | G | A | 32 | a0001c0001t0001g0013 a0001c0001t0001g0202 a0001c0001t0001g0271 others(29): Show |
32 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.1045+6659C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37724936 | |||||||
| chr17:37724938 | A | G | 1 | a0001c0001t0004g0036 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1045+6657T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37724938 | |||||||
| chr17:37725150 | C | T | 3 | a0001c0001t0002g0006 a0001c0001t0005g0193 a0001c0001t0007g0277 |
3 | HG02055.hp2 HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1045+6445G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37725150 | |||||||
| chr17:37725359 | A | G | 3 | a0001c0001t0005g0281 a0001c0001t0007g0201 a0001c0001t0014g0280 |
3 | HG02280.hp2 HG02922.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1045+6236T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37725359 | |||||||
| chr17:37725484 | C | A | 1 | a0001c0001t0001g0380 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1045+6111G>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37725484 | |||||||
| chr17:37725600 | G | A | 21 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0002g0034 others(18): Show |
21 | HG00323.hp2 HG00735.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.1045+5995C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37725600 | |||||||
| chr17:37725604 | C | CT | 3 | a0001c0001t0001g0154 a0001c0001t0001g0182 a0001c0001t0001g0361 |
3 | NA18949.hp2 NA19066.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.1045+5990dupA | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37725604 | |||||||
| chr17:37725779 | G | A | 2 | a0001c0001t0001g0160 a0002c0004t0003g0405 |
2 | HG03704.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1045+5816C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37725779 | |||||||
| chr17:37725803 | C | T | 1 | a0001c0001t0004g0376 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1045+5792G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37725803 | |||||||
| chr17:37725819 | G | A | 1 | a0001c0001t0001g0303 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1045+5776C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37725819 | |||||||
| chr17:37725856 | A | G | 2 | a0001c0001t0002g0007 a0001c0001t0002g0398 |
2 | NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1045+5739T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37725856 | |||||||
| chr17:37725943 | G | T | 32 | a0001c0001t0001g0009 a0001c0001t0001g0225 a0001c0001t0001g0271 others(29): Show |
32 | HG01884.hp2 HG02145.hp1 HG02258.hp1 others(29): Show |
intron_variant | MODIFIER | c.1045+5652C>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37725943 | |||||||
| chr17:37725970 | G | C | 35 | a0001c0001t0001g0028 a0001c0001t0001g0063 a0001c0001t0001g0153 others(32): Show |
35 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.1045+5625C>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37725970 | |||||||
| chr17:37725970 | G | T | 1 | a0001c0001t0005g0343 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1045+5625C>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37725970 | |||||||
| chr17:37726002 | T | A | 2 | a0001c0001t0006g0274 a0001c0001t0006g0275 |
2 | HG02572.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1045+5593A>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37726002 | |||||||
| chr17:37726136 | C | CTG | 34 | a0001c0001t0001g0009 a0001c0001t0001g0202 a0001c0001t0001g0225 others(31): Show |
34 | HG01081.hp1 HG01884.hp2 HG02145.hp1 others(31): Show |
intron_variant | MODIFIER | c.1045+5457_1045+545 others(6): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37726136 | |||||||
| chr17:37726136 | C | CTGTG | 19 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0022 others(16): Show |
19 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.1045+5455_1045+545 others(8): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37726136 | |||||||
| chr17:37726136 | C | CTGTGTG | 35 | a0001c0001t0001g0028 a0001c0001t0001g0063 a0001c0001t0001g0153 others(32): Show |
35 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.1045+5453_1045+545 others(10): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37726136 | |||||||
| chr17:37726136 | C | CTGTGTGT others(3): Show |
117 | a0001c0001t0001g0002 a0001c0001t0001g0057 a0001c0001t0001g0060 others(114): Show |
119 | HG00280.hp2 HG00544.hp2 HG00609.hp2 others(116): Show |
intron_variant | MODIFIER | c.1045+5449_1045+545 others(14): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37726136 | |||||||
| chr17:37726136 | C | CTGTGTGT others(5): Show |
9 | a0001c0001t0001g0095 a0001c0001t0001g0150 a0001c0001t0001g0342 others(6): Show |
9 | HG01109.hp2 HG01243.hp1 HG02129.hp1 others(6): Show |
intron_variant | MODIFIER | c.1045+5447_1045+545 others(16): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37726136 | |||||||
| chr17:37726136 | C | CTGTGTGT others(7): Show |
15 | a0001c0001t0001g0092 a0001c0001t0001g0115 a0001c0001t0002g0064 others(12): Show |
15 | HG02602.hp1 HG02922.hp1 NA18939.hp2 others(12): Show |
intron_variant | MODIFIER | c.1045+5445_1045+545 others(18): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37726136 | |||||||
| chr17:37726136 | C | G | 1 | a0001c0001t0001g0380 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1045+5459G>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37726136 | |||||||
| chr17:37726136 | CTG | C | 14 | a0001c0001t0001g0013 a0001c0001t0005g0279 a0001c0001t0006g0246 others(11): Show |
14 | HG01891.hp2 HG02055.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.1045+5457_1045+545 others(6): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37726136 | |||||||
| chr17:37726141 | T | C | 2 | a0001c0001t0002g0106 a0001c0001t0002g0210 |
2 | NA18963.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.1045+5454A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37726141 | |||||||
| chr17:37726160 | T | TTC | 3 | a0001c0001t0002g0007 a0001c0001t0002g0398 a0001c0001t0007g0277 |
3 | NA18522.hp2 NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1045+5433_1045+543 others(6): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37726160 | |||||||
| chr17:37726251 | C | T | 10 | a0001c0001t0001g0027 a0001c0001t0001g0169 a0001c0001t0001g0252 others(7): Show |
10 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(7): Show |
intron_variant | MODIFIER | c.1045+5344G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37726251 | |||||||
| chr17:37726360 | C | T | 1 | a0001c0003t0006g0349 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1045+5235G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37726360 | |||||||
| chr17:37726377 | T | G | 3 | a0001c0001t0002g0007 a0001c0001t0002g0398 a0001c0001t0007g0277 |
3 | NA18522.hp2 NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1045+5218A>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37726377 | |||||||
| chr17:37726476 | G | A | 1 | a0001c0001t0004g0332 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1045+5119C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37726476 | |||||||
| chr17:37726698 | G | A | 129 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0028 others(126): Show |
130 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.1045+4897C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37726698 | |||||||
| chr17:37726880 | A | G | 1 | a0001c0001t0003g0273 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1045+4715T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37726880 | |||||||
| chr17:37726986 | G | A | 1 | a0001c0001t0006g0251 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1045+4609C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37726986 | |||||||
| chr17:37727005 | G | A | 4 | a0001c0001t0002g0205 a0001c0001t0005g0204 a0001c0001t0005g0289 others(1): Show |
4 | HG02615.hp1 HG02622.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1045+4590C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37727005 | |||||||
| chr17:37727005 | G | C | 11 | a0001c0001t0001g0160 a0001c0001t0001g0225 a0001c0001t0002g0226 others(8): Show |
11 | HG02559.hp1 HG02602.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.1045+4590C>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37727005 | |||||||
| chr17:37727097 | G | A | 2 | a0001c0001t0002g0263 a0001c0001t0006g0270 |
2 | HG01891.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1045+4498C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37727097 | |||||||
| chr17:37727280 | A | G | 4 | a0001c0001t0003g0273 a0001c0001t0005g0218 a0001c0001t0006g0004 others(1): Show |
4 | HG01081.hp1 HG02809.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1045+4315T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37727280 | |||||||
| chr17:37727362 | A | G | 2 | a0001c0001t0003g0273 a0001c0001t0012g0223 |
2 | HG01081.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1045+4233T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37727362 | |||||||
| chr17:37727472 | G | T | 1 | a0001c0001t0008g0239 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1045+4123C>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37727472 | |||||||
| chr17:37727751 | A | G | 5 | a0001c0001t0001g0202 a0001c0001t0002g0006 a0001c0001t0002g0007 others(2): Show |
5 | HG01891.hp1 HG02622.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1045+3844T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37727751 | |||||||
| chr17:37727834 | T | C | 1 | a0001c0001t0005g0195 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1045+3761A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37727834 | |||||||
| chr17:37727850 | G | A | 2 | a0001c0001t0002g0006 a0001c0001t0002g0007 |
2 | HG03516.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1045+3745C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37727850 | |||||||
| chr17:37727850 | G | C | 6 | a0001c0001t0002g0262 a0001c0001t0005g0266 a0001c0001t0005g0337 others(3): Show |
6 | HG01884.hp2 HG02451.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1045+3745C>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37727850 | |||||||
| chr17:37727851 | G | A | 6 | a0001c0001t0002g0262 a0001c0001t0005g0266 a0001c0001t0005g0337 others(3): Show |
6 | HG01884.hp2 HG02451.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1045+3744C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37727851 | |||||||
| chr17:37727883 | G | C | 46 | a0001c0001t0001g0057 a0001c0001t0001g0066 a0001c0001t0001g0070 others(43): Show |
47 | HG00323.hp1 HG00741.hp1 HG01192.hp1 others(44): Show |
intron_variant | MODIFIER | c.1045+3712C>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37727883 | |||||||
| chr17:37727916 | T | C | 1 | a0001c0001t0002g0059 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1045+3679A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37727916 | |||||||
| chr17:37727962 | T | G | 2 | a0001c0001t0002g0398 a0001c0001t0005g0348 |
2 | HG02647.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1045+3633A>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37727962 | |||||||
| chr17:37728087 | C | T | 1 | a0001c0001t0002g0355 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1045+3508G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37728087 | |||||||
| chr17:37728158 | C | T | 2 | a0001c0001t0001g0334 a0001c0001t0007g0277 |
2 | NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1045+3437G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37728158 | |||||||
| chr17:37728202 | A | G | 1 | a0001c0001t0012g0223 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1045+3393T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37728202 | |||||||
| chr17:37728294 | A | C | 33 | a0001c0001t0001g0160 a0001c0001t0001g0259 a0001c0001t0001g0288 others(30): Show |
33 | HG01243.hp1 HG02145.hp1 HG02258.hp1 others(30): Show |
intron_variant | MODIFIER | c.1045+3301T>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37728294 | |||||||
| chr17:37728305 | A | C | 3 | a0001c0001t0005g0196 a0001c0001t0005g0208 a0001c0002t0009g0265 |
3 | HG01993.hp1 HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1045+3290T>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37728305 | |||||||
| chr17:37728310 | G | GT | 37 | a0001c0001t0001g0055 a0001c0001t0001g0183 a0001c0001t0001g0184 others(34): Show |
37 | HG00280.hp1 HG00408.hp1 HG01169.hp1 others(34): Show |
intron_variant | MODIFIER | c.1045+3284dupA | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37728310 | |||||||
| chr17:37728310 | GT | G | 14 | a0001c0001t0001g0009 a0001c0001t0002g0262 a0001c0001t0005g0010 others(11): Show |
14 | HG01884.hp2 HG01891.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1045+3284delA | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37728310 | |||||||
| chr17:37728320 | T | C | 1 | a0001c0001t0005g0203 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1045+3275A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37728320 | |||||||
| chr17:37728338 | G | A | 53 | a0001c0001t0001g0046 a0001c0001t0001g0066 a0001c0001t0001g0070 others(50): Show |
54 | HG00323.hp1 HG00741.hp1 HG01192.hp1 others(51): Show |
intron_variant | MODIFIER | c.1045+3257C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37728338 | |||||||
| chr17:37728467 | C | T | 5 | a0001c0001t0001g0202 a0001c0001t0002g0222 a0001c0001t0006g0005 others(2): Show |
5 | HG01884.hp1 HG02145.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1045+3128G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37728467 | |||||||
| chr17:37728488 | A | T | 1 | a0001c0001t0012g0223 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1045+3107T>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37728488 | |||||||
| chr17:37728538 | C | A | 1 | a0001c0001t0002g0354 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1045+3057G>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37728538 | |||||||
| chr17:37728539 | T | C | 263 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0015 others(260): Show |
264 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.1045+3056A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37728539 | |||||||
| chr17:37728605 | C | CT | 15 | a0001c0001t0001g0040 a0001c0001t0001g0182 a0001c0001t0001g0309 others(12): Show |
15 | HG00597.hp2 HG00735.hp2 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.1045+2989dupA | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37728605 | |||||||
| chr17:37728605 | CT | C | 96 | a0001c0001t0001g0046 a0001c0001t0001g0055 a0001c0001t0001g0066 others(93): Show |
97 | HG00323.hp1 HG00741.hp1 HG01109.hp2 others(94): Show |
intron_variant | MODIFIER | c.1045+2989delA | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37728605 | |||||||
| chr17:37728624 | T | C | 1 | a0001c0001t0002g0355 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1045+2971A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37728624 | |||||||
| chr17:37728924 | G | C | 102 | a0001c0001t0001g0039 a0001c0001t0001g0069 a0001c0001t0001g0080 others(99): Show |
102 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.1045+2671C>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37728924 | |||||||
| chr17:37728943 | T | G | 8 | a0001c0001t0001g0225 a0001c0001t0001g0351 a0001c0001t0002g0006 others(5): Show |
8 | HG02451.hp2 HG02559.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1045+2652A>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37728943 | |||||||
| chr17:37729021 | T | C | 57 | a0001c0001t0001g0046 a0001c0001t0001g0066 a0001c0001t0001g0070 others(54): Show |
58 | HG00323.hp1 HG00741.hp1 HG01192.hp1 others(55): Show |
intron_variant | MODIFIER | c.1045+2574A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37729021 | |||||||
| chr17:37729047 | G | A | 24 | a0001c0001t0001g0040 a0001c0001t0001g0060 a0001c0001t0001g0061 others(21): Show |
24 | HG00408.hp2 HG00558.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.1045+2548C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37729047 | |||||||
| chr17:37729193 | C | A | 1 | a0001c0001t0005g0193 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1045+2402G>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37729193 | |||||||
| chr17:37729264 | C | A | 1 | a0001c0001t0001g0391 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1045+2331G>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37729264 | |||||||
| chr17:37729291 | T | C | 67 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0019 others(64): Show |
67 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(64): Show |
intron_variant | MODIFIER | c.1045+2304A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37729291 | |||||||
| chr17:37729320 | C | A | 44 | a0001c0001t0001g0160 a0001c0001t0001g0202 a0001c0001t0001g0225 others(41): Show |
44 | HG01884.hp1 HG02145.hp1 HG02145.hp2 others(41): Show |
intron_variant | MODIFIER | c.1045+2275G>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37729320 | |||||||
| chr17:37729434 | C | CA | 23 | a0001c0001t0001g0056 a0001c0001t0001g0146 a0001c0001t0001g0169 others(20): Show |
23 | HG00423.hp1 HG00438.hp1 HG00609.hp2 others(20): Show |
intron_variant | MODIFIER | c.1045+2160dupT | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37729434 | |||||||
| chr17:37729434 | CA | C | 81 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0019 others(78): Show |
81 | HG00323.hp1 HG00741.hp1 HG01069.hp2 others(78): Show |
intron_variant | MODIFIER | c.1045+2160delT | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37729434 | |||||||
| chr17:37729597 | G | A | 2 | a0001c0001t0002g0398 a0001c0001t0005g0348 |
2 | HG02647.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1045+1998C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37729597 | |||||||
| chr17:37729608 | G | A | 1 | a0001c0001t0001g0209 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1045+1987C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37729608 | |||||||
| chr17:37729719 | A | T | 5 | a0001c0001t0001g0202 a0001c0001t0002g0222 a0001c0001t0006g0005 others(2): Show |
5 | HG01884.hp1 HG02145.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1045+1876T>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37729719 | |||||||
| chr17:37729958 | G | T | 1 | a0001c0001t0005g0108 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1045+1637C>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37729958 | |||||||
| chr17:37729966 | C | CCCTGCTC others(41): Show |
1 | a0001c0001t0001g0334 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1045+1581_1045+162 others(52): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37729966 | |||||||
| chr17:37729966 | C | CCCTGCTC others(88): Show |
61 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0019 others(58): Show |
61 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(58): Show |
intron_variant | MODIFIER | c.1045+1628_1045+162 others(99): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37729966 | |||||||
| chr17:37729966 | C | CCCTGCTC others(136): Show |
5 | a0001c0001t0001g0202 a0001c0001t0002g0222 a0001c0001t0006g0005 others(2): Show |
5 | HG01884.hp1 HG02145.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1045+1628_1045+162 others(147): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37729966 | |||||||
| chr17:37730058 | G | A | 2 | a0001c0001t0002g0398 a0001c0001t0005g0348 |
2 | HG02647.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1045+1537C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37730058 | |||||||
| chr17:37730196 | T | C | 1 | a0001c0001t0001g0040 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1045+1399A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37730196 | |||||||
| chr17:37730197 | C | T | 1 | a0001c0001t0001g0040 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1045+1398G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37730197 | |||||||
| chr17:37730405 | T | C | 10 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0057 others(7): Show |
10 | HG00423.hp2 HG02074.hp1 HG02132.hp2 others(7): Show |
intron_variant | MODIFIER | c.1045+1190A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37730405 | |||||||
| chr17:37730436 | C | G | 1 | a0001c0001t0001g0040 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1045+1159G>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37730436 | |||||||
| chr17:37730484 | C | A | 1 | a0001c0001t0002g0149 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1045+1111G>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37730484 | |||||||
| chr17:37730543 | C | G | 11 | a0001c0001t0001g0288 a0001c0001t0005g0266 a0001c0001t0006g0251 others(8): Show |
11 | HG01243.hp1 HG01891.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1045+1052G>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37730543 | |||||||
| chr17:37730554 | T | C | 2 | a0001c0001t0001g0306 a0001c0001t0008g0305 |
2 | HG01952.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1045+1041A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37730554 | |||||||
| chr17:37730555 | G | A | 1 | a0001c0001t0005g0208 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1045+1040C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37730555 | |||||||
| chr17:37730573 | G | C | 3 | a0001c0001t0001g0271 a0001c0001t0002g0205 a0001c0002t0009g0221 |
3 | HG02965.hp2 HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1045+1022C>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37730573 | |||||||
| chr17:37730711 | G | A | 9 | a0001c0001t0001g0015 a0001c0001t0001g0019 a0001c0001t0001g0022 others(6): Show |
9 | HG00733.hp1 HG00735.hp2 HG01069.hp2 others(6): Show |
intron_variant | MODIFIER | c.1045+884C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37730711 | |||||||
| chr17:37730828 | C | T | 1 | a0001c0001t0003g0213 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1045+767G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37730828 | |||||||
| chr17:37730894 | A | G | 145 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0033 others(142): Show |
145 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.1045+701T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37730894 | |||||||
| chr17:37731067 | C | G | 10 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0398 others(7): Show |
10 | HG01891.hp2 HG02055.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.1045+528G>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37731067 | |||||||
| chr17:37731255 | C | T | 12 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0292 others(9): Show |
12 | HG00408.hp2 HG00558.hp1 HG00621.hp2 others(9): Show |
intron_variant | MODIFIER | c.1045+340G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37731255 | |||||||
| chr17:37731265 | C | G | 68 | a0001c0001t0001g0009 a0001c0001t0001g0046 a0001c0001t0001g0164 others(65): Show |
69 | HG00741.hp1 HG01081.hp1 HG01192.hp1 others(66): Show |
intron_variant | MODIFIER | c.1045+330G>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37731265 | |||||||
| chr17:37731433 | C | T | 1 | a0001c0001t0004g0233 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1045+162G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 4/8 | chr17 | 37731433 | |||||||
| chr17:37732035 | C | T | 1 | a0001c0001t0002g0189 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.810-205G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 3/8 | chr17 | 37732035 | |||||||
| chr17:37732117 | G | A | 1 | a0001c0001t0002g0321 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.810-287C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 3/8 | chr17 | 37732117 | |||||||
| chr17:37732364 | T | A | 1 | a0001c0001t0002g0321 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.810-534A>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 3/8 | chr17 | 37732364 | |||||||
| chr17:37732447 | G | A | 3 | a0001c0001t0001g0225 a0001c0001t0002g0226 a0001c0001t0005g0227 |
3 | HG02615.hp2 HG02970.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.810-617C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 3/8 | chr17 | 37732447 | |||||||
| chr17:37732680 | T | TA | 116 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(113): Show |
116 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.810-851dupT | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 3/8 | chr17 | 37732680 | |||||||
| chr17:37732828 | G | A | 2 | a0001c0001t0005g0395 a0001c0001t0005g0396 |
2 | HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.809+729C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 3/8 | chr17 | 37732828 | |||||||
| chr17:37732849 | G | GT | 140 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(137): Show |
140 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.809+707dupA | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 3/8 | chr17 | 37732849 | |||||||
| chr17:37732971 | G | A | 3 | a0001c0001t0002g0152 a0001c0001t0004g0151 a0001c0001t0004g0186 |
3 | NA18952.hp1 NA18988.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.809+586C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 3/8 | chr17 | 37732971 | |||||||
| chr17:37733029 | G | A | 137 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(134): Show |
137 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.809+528C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 3/8 | chr17 | 37733029 | |||||||
| chr17:37733037 | C | T | 1 | a0001c0001t0005g0293 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.809+520G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 3/8 | chr17 | 37733037 | |||||||
| chr17:37733087 | C | A | 8 | a0001c0001t0005g0266 a0001c0001t0006g0014 a0001c0001t0006g0264 others(5): Show |
8 | HG01891.hp1 HG02145.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.809+470G>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 3/8 | chr17 | 37733087 | |||||||
| chr17:37733448 | T | C | 3 | a0001c0001t0005g0208 a0001c0001t0006g0275 a0001c0001t0007g0276 |
3 | HG01993.hp1 HG02258.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.809+109A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 3/8 | chr17 | 37733448 | |||||||
| chr17:37733479 | A | G | 3 | a0001c0001t0003g0403 a0001c0001t0004g0191 a0001c0001t0004g0192 |
3 | HG02602.hp1 HG02738.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.809+78T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 3/8 | chr17 | 37733479 | |||||||
| chr17:37733492 | C | T | 2 | a0001c0001t0006g0275 a0001c0001t0007g0276 |
2 | HG02258.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.809+65G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 3/8 | chr17 | 37733492 | |||||||
| chr17:37733494 | A | G | 3 | a0001c0001t0007g0200 a0001c0001t0007g0201 a0001c0001t0012g0223 |
3 | HG02922.hp2 HG03098.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.809+63T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 3/8 | chr17 | 37733494 | |||||||
| chr17:37733870 | GCAGA | G | 135 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(132): Show |
135 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.545-53_545-50delTC others(2): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 2/8 | chr17 | 37733870 | |||||||
| chr17:37734057 | C | A | 1 | a0001c0001t0009g0008 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.545-236G>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 2/8 | chr17 | 37734057 | |||||||
| chr17:37734295 | T | C | 1 | a0001c0001t0003g0248 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.545-474A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 2/8 | chr17 | 37734295 | |||||||
| chr17:37734419 | A | G | 1 | a0001c0001t0001g0009 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.545-598T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 2/8 | chr17 | 37734419 | |||||||
| chr17:37734476 | C | A | 1 | a0001c0001t0002g0390 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.545-655G>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 2/8 | chr17 | 37734476 | |||||||
| chr17:37734720 | T | C | 1 | a0001c0001t0004g0167 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.545-899A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 2/8 | chr17 | 37734720 | |||||||
| chr17:37734746 | T | C | 1 | a0001c0001t0002g0181 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.545-925A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 2/8 | chr17 | 37734746 | |||||||
| chr17:37734789 | C | CT | 154 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0015 others(151): Show |
154 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.545-969dupA | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 2/8 | chr17 | 37734789 | |||||||
| chr17:37734789 | C | CTT | 7 | a0001c0001t0001g0160 a0001c0001t0001g0259 a0001c0001t0001g0356 others(4): Show |
7 | HG00558.hp1 HG02602.hp2 HG03704.hp1 others(4): Show |
intron_variant | MODIFIER | c.545-970_545-969dup others(2): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 2/8 | chr17 | 37734789 | |||||||
| chr17:37734789 | CT | C | 7 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0155 others(4): Show |
7 | HG01168.hp1 HG01257.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.545-969delA | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 2/8 | chr17 | 37734789 | |||||||
| chr17:37734847 | G | A | 1 | a0001c0001t0003g0272 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.545-1026C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 2/8 | chr17 | 37734847 | |||||||
| chr17:37735074 | G | C | 1 | a0001c0001t0006g0270 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.545-1253C>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 2/8 | chr17 | 37735074 | |||||||
| chr17:37735085 | C | T | 3 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0045 |
3 | NA18978.hp1 NA19010.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.545-1264G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 2/8 | chr17 | 37735085 | |||||||
| chr17:37735191 | C | T | 9 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0057 others(6): Show |
9 | HG00423.hp2 HG02074.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.545-1370G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 2/8 | chr17 | 37735191 | |||||||
| chr17:37735256 | T | G | 12 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0019 others(9): Show |
12 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.545-1435A>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 2/8 | chr17 | 37735256 | |||||||
| chr17:37735307 | C | T | 1 | a0001c0001t0002g0190 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.545-1486G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 2/8 | chr17 | 37735307 | |||||||
| chr17:37735487 | T | C | 1 | a0001c0001t0005g0208 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.545-1666A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 2/8 | chr17 | 37735487 | |||||||
| chr17:37735501 | T | G | 1 | a0001c0001t0004g0174 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.545-1680A>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 2/8 | chr17 | 37735501 | |||||||
| chr17:37735564 | G | C | 1 | a0001c0001t0005g0012 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.545-1743C>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 2/8 | chr17 | 37735564 | |||||||
| chr17:37735600 | T | C | 1 | a0001c0001t0002g0156 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.545-1779A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 2/8 | chr17 | 37735600 | |||||||
| chr17:37736240 | G | C | 1 | a0001c0001t0001g0399 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.545-2419C>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 2/8 | chr17 | 37736240 | |||||||
| chr17:37736297 | G | C | 1 | a0001c0001t0001g0002 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.545-2476C>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 2/8 | chr17 | 37736297 | |||||||
| chr17:37736310 | G | A | 148 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0016 others(145): Show |
148 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.545-2489C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 2/8 | chr17 | 37736310 | |||||||
| chr17:37736409 | C | T | 8 | a0001c0001t0005g0266 a0001c0001t0006g0014 a0001c0001t0006g0264 others(5): Show |
8 | HG01891.hp1 HG02145.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.545-2588G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 2/8 | chr17 | 37736409 | |||||||
| chr17:37736431 | C | T | 402 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0013 others(399): Show |
404 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(401): Show |
intron_variant | MODIFIER | c.545-2610G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 2/8 | chr17 | 37736431 | |||||||
| chr17:37736488 | T | C | 243 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0013 others(240): Show |
245 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(242): Show |
intron_variant | MODIFIER | c.545-2667A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 2/8 | chr17 | 37736488 | |||||||
| chr17:37736525 | C | G | 1 | a0001c0001t0001g0049 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.545-2704G>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 2/8 | chr17 | 37736525 | |||||||
| chr17:37736525 | C | T | 137 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(134): Show |
137 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.545-2704G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 2/8 | chr17 | 37736525 | |||||||
| chr17:37736610 | C | T | 1 | a0001c0001t0005g0208 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.545-2789G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 2/8 | chr17 | 37736610 | |||||||
| chr17:37736666 | T | G | 1 | a0001c0001t0001g0057 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.544+2774A>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 2/8 | chr17 | 37736666 | |||||||
| chr17:37736708 | T | A | 2 | a0001c0001t0001g0169 a0001c0001t0008g0168 |
2 | HG00438.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.544+2732A>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 2/8 | chr17 | 37736708 | |||||||
| chr17:37736878 | A | G | 2 | a0001c0001t0002g0229 a0001c0001t0002g0230 |
2 | NA18950.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.544+2562T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 2/8 | chr17 | 37736878 | |||||||
| chr17:37737171 | C | T | 1 | a0001c0001t0002g0059 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.544+2269G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 2/8 | chr17 | 37737171 | |||||||
| chr17:37737210 | A | G | 2 | a0001c0001t0007g0200 a0001c0001t0007g0201 |
2 | HG02922.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.544+2230T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 2/8 | chr17 | 37737210 | |||||||
| chr17:37737309 | T | A | 1 | a0001c0001t0001g0249 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.544+2131A>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 2/8 | chr17 | 37737309 | |||||||
| chr17:37737321 | C | T | 2 | a0001c0001t0006g0275 a0001c0001t0007g0276 |
2 | HG02258.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.544+2119G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 2/8 | chr17 | 37737321 | |||||||
| chr17:37737343 | G | C | 2 | a0001c0001t0001g0170 a0001c0001t0002g0171 |
2 | HG01123.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.544+2097C>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 2/8 | chr17 | 37737343 | |||||||
| chr17:37737522 | G | A | 3 | a0001c0001t0002g0398 a0001c0001t0006g0264 a0001c0002t0009g0265 |
3 | HG03098.hp1 HG03453.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.544+1918C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 2/8 | chr17 | 37737522 | |||||||
| chr17:37737602 | G | A | 2 | a0001c0001t0007g0200 a0001c0001t0007g0201 |
2 | HG02922.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.544+1838C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 2/8 | chr17 | 37737602 | |||||||
| chr17:37737639 | A | G | 12 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0019 others(9): Show |
12 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.544+1801T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 2/8 | chr17 | 37737639 | |||||||
| chr17:37737654 | G | T | 8 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0057 others(5): Show |
8 | HG00423.hp2 HG02074.hp1 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.544+1786C>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 2/8 | chr17 | 37737654 | |||||||
| chr17:37737671 | C | CA | 143 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(140): Show |
143 | HG00280.hp2 HG00323.hp1 HG00544.hp2 others(140): Show |
intron_variant | MODIFIER | c.544+1768dupT | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 2/8 | chr17 | 37737671 | |||||||
| chr17:37737678 | A | G | 4 | a0001c0001t0006g0004 a0001c0001t0006g0005 a0001c0001t0006g0275 others(1): Show |
4 | HG01884.hp1 HG02258.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.544+1762T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 2/8 | chr17 | 37737678 | |||||||
| chr17:37737699 | G | A | 1 | a0001c0001t0015g0175 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.544+1741C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 2/8 | chr17 | 37737699 | |||||||
| chr17:37737748 | T | C | 1 | a0001c0001t0007g0277 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.544+1692A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 2/8 | chr17 | 37737748 | |||||||
| chr17:37737766 | C | T | 2 | a0001c0001t0019g0406 a0001c0001t0020g0407 |
2 | HG03669.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.544+1674G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 2/8 | chr17 | 37737766 | |||||||
| chr17:37737784 | A | G | 158 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0019 others(155): Show |
158 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.544+1656T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 2/8 | chr17 | 37737784 | |||||||
| chr17:37737790 | G | A | 2 | a0001c0001t0006g0275 a0001c0001t0007g0276 |
2 | HG02258.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.544+1650C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 2/8 | chr17 | 37737790 | |||||||
| chr17:37737791 | C | T | 1 | a0001c0001t0001g0228 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.544+1649G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 2/8 | chr17 | 37737791 | |||||||
| chr17:37737841 | T | C | 1 | a0001c0001t0005g0392 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.544+1599A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 2/8 | chr17 | 37737841 | |||||||
| chr17:37737841 | T | TTAAA | 5 | a0001c0001t0001g0177 a0001c0001t0002g0176 a0001c0001t0003g0403 others(2): Show |
5 | HG00099.hp1 HG01928.hp2 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.544+1595_544+1598d others(6): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 2/8 | chr17 | 37737841 | |||||||
| chr17:37737866 | A | G | 6 | a0001c0001t0005g0266 a0001c0001t0006g0014 a0001c0001t0006g0270 others(3): Show |
6 | HG01891.hp1 HG02145.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.544+1574T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 2/8 | chr17 | 37737866 | |||||||
| chr17:37737875 | A | G | 1 | a0001c0001t0006g0038 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.544+1565T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 2/8 | chr17 | 37737875 | |||||||
| chr17:37737897 | G | A | 2 | a0001c0001t0005g0193 a0001c0001t0006g0251 |
2 | HG01891.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.544+1543C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 2/8 | chr17 | 37737897 | |||||||
| chr17:37737992 | C | T | 1 | a0001c0001t0001g0049 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.544+1448G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 2/8 | chr17 | 37737992 | |||||||
| chr17:37738049 | A | G | 171 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0015 others(168): Show |
171 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.544+1391T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 2/8 | chr17 | 37738049 | |||||||
| chr17:37738057 | A | ACC | 4 | a0001c0001t0001g0351 a0001c0001t0002g0354 a0001c0001t0005g0352 others(1): Show |
4 | HG02451.hp2 HG02559.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.544+1382_544+1383i others(4): Show |
HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 2/8 | chr17 | 37738057 | |||||||
| chr17:37738059 | A | T | 4 | a0001c0001t0001g0351 a0001c0001t0002g0354 a0001c0001t0005g0352 others(1): Show |
4 | HG02451.hp2 HG02559.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.544+1381T>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 2/8 | chr17 | 37738059 | |||||||
| chr17:37738519 | G | A | 2 | a0001c0001t0007g0200 a0001c0001t0007g0201 |
2 | HG02922.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.544+921C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 2/8 | chr17 | 37738519 | |||||||
| chr17:37738996 | A | G | 131 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0039 others(128): Show |
131 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.544+444T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 2/8 | chr17 | 37738996 | |||||||
| chr17:37739658 | G | A | 2 | a0001c0001t0007g0200 a0001c0001t0007g0201 |
2 | HG02922.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.345-19C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 1/8 | chr17 | 37739658 | |||||||
| chr17:37739849 | T | C | 176 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0015 others(173): Show |
176 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.345-210A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 1/8 | chr17 | 37739849 | |||||||
| chr17:37739867 | G | C | 12 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0019 others(9): Show |
12 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.345-228C>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 1/8 | chr17 | 37739867 | |||||||
| chr17:37739957 | A | T | 1 | a0001c0001t0005g0012 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.345-318T>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 1/8 | chr17 | 37739957 | |||||||
| chr17:37739961 | A | T | 126 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0019 others(123): Show |
126 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.345-322T>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 1/8 | chr17 | 37739961 | |||||||
| chr17:37739965 | T | A | 2 | a0001c0001t0002g0354 a0001c0001t0005g0203 |
2 | HG02559.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.345-326A>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 1/8 | chr17 | 37739965 | |||||||
| chr17:37739976 | A | AT | 18 | a0001c0001t0001g0009 a0001c0001t0001g0259 a0001c0001t0002g0260 others(15): Show |
18 | HG01891.hp1 HG02145.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.345-338dupA | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 1/8 | chr17 | 37739976 | |||||||
| chr17:37739976 | A | T | 2 | a0001c0001t0003g0273 a0001c0001t0006g0274 |
2 | HG01081.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.345-337T>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 1/8 | chr17 | 37739976 | |||||||
| chr17:37739979 | T | C | 40 | a0001c0001t0001g0278 a0001c0001t0001g0292 a0001c0001t0001g0356 others(37): Show |
40 | HG00323.hp1 HG00558.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.345-340A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 1/8 | chr17 | 37739979 | |||||||
| chr17:37739994 | T | C | 2 | a0001c0001t0003g0030 a0001c0001t0003g0031 |
2 | NA18941.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.345-355A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 1/8 | chr17 | 37739994 | |||||||
| chr17:37740096 | G | A | 1 | a0001c0001t0001g0026 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.345-457C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 1/8 | chr17 | 37740096 | |||||||
| chr17:37740105 | A | G | 22 | a0001c0001t0001g0199 a0001c0001t0001g0209 a0001c0001t0001g0212 others(19): Show |
22 | HG01099.hp1 HG01109.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.345-466T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 1/8 | chr17 | 37740105 | |||||||
| chr17:37740136 | A | T | 2 | a0001c0001t0009g0206 a0001c0001t0009g0207 |
2 | HG02895.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.345-497T>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 1/8 | chr17 | 37740136 | |||||||
| chr17:37740530 | T | C | 1 | a0001c0001t0001g0252 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.345-891A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 1/8 | chr17 | 37740530 | |||||||
| chr17:37740539 | A | G | 2 | a0001c0001t0006g0275 a0001c0001t0007g0276 |
2 | HG02258.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.345-900T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 1/8 | chr17 | 37740539 | |||||||
| chr17:37740636 | T | TA | 17 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0016 others(14): Show |
17 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.345-998dupT | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 1/8 | chr17 | 37740636 | |||||||
| chr17:37740655 | C | T | 1 | a0001c0001t0001g0013 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.345-1016G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 1/8 | chr17 | 37740655 | |||||||
| chr17:37740699 | A | G | 3 | a0001c0001t0005g0194 a0001c0001t0005g0195 a0001c0001t0005g0196 |
3 | HG02965.hp1 HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.345-1060T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 1/8 | chr17 | 37740699 | |||||||
| chr17:37740776 | G | A | 140 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0027 others(137): Show |
140 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.345-1137C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 1/8 | chr17 | 37740776 | |||||||
| chr17:37740860 | T | C | 1 | a0001c0001t0002g0205 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.345-1221A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 1/8 | chr17 | 37740860 | |||||||
| chr17:37740862 | G | A | 3 | a0001c0001t0005g0194 a0001c0001t0005g0195 a0001c0001t0005g0196 |
3 | HG02965.hp1 HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.345-1223C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 1/8 | chr17 | 37740862 | |||||||
| chr17:37741092 | A | G | 12 | a0001c0001t0001g0259 a0001c0001t0002g0260 a0001c0001t0002g0262 others(9): Show |
12 | HG02257.hp2 HG02451.hp1 HG02602.hp2 others(9): Show |
intron_variant | MODIFIER | c.345-1453T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 1/8 | chr17 | 37741092 | |||||||
| chr17:37741165 | C | T | 139 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0027 others(136): Show |
139 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(136): Show |
intron_variant | MODIFIER | c.345-1526G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 1/8 | chr17 | 37741165 | |||||||
| chr17:37741595 | C | A | 157 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0015 others(154): Show |
157 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.345-1956G>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 1/8 | chr17 | 37741595 | |||||||
| chr17:37741642 | T | G | 238 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0015 others(235): Show |
238 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(235): Show |
intron_variant | MODIFIER | c.345-2003A>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 1/8 | chr17 | 37741642 | |||||||
| chr17:37741700 | T | C | 2 | a0001c0001t0006g0275 a0001c0001t0007g0276 |
2 | HG02258.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.345-2061A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 1/8 | chr17 | 37741700 | |||||||
| chr17:37741743 | T | C | 1 | a0001c0001t0001g0254 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.345-2104A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 1/8 | chr17 | 37741743 | |||||||
| chr17:37741822 | A | C | 5 | a0001c0001t0001g0288 a0001c0001t0005g0289 a0001c0001t0005g0290 others(2): Show |
5 | HG02622.hp1 HG02922.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.345-2183T>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 1/8 | chr17 | 37741822 | |||||||
| chr17:37741835 | G | A | 3 | a0001c0001t0002g0180 a0001c0001t0004g0179 a0001c0001t0016g0178 |
3 | HG02155.hp2 NA18612.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.345-2196C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 1/8 | chr17 | 37741835 | |||||||
| chr17:37741855 | G | C | 1 | a0001c0001t0001g0394 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.345-2216C>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 1/8 | chr17 | 37741855 | |||||||
| chr17:37741866 | A | G | 4 | a0001c0001t0002g0205 a0001c0001t0003g0273 a0001c0001t0005g0204 others(1): Show |
4 | HG01081.hp1 HG02572.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.345-2227T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 1/8 | chr17 | 37741866 | |||||||
| chr17:37741935 | A | G | 238 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0015 others(235): Show |
238 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(235): Show |
intron_variant | MODIFIER | c.345-2296T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 1/8 | chr17 | 37741935 | |||||||
| chr17:37741956 | C | G | 1 | a0001c0001t0002g0037 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.345-2317G>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 1/8 | chr17 | 37741956 | |||||||
| chr17:37742044 | C | G | 236 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0016 others(233): Show |
236 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.345-2405G>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 1/8 | chr17 | 37742044 | |||||||
| chr17:37742062 | C | T | 1 | a0001c0001t0005g0203 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.345-2423G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 1/8 | chr17 | 37742062 | |||||||
| chr17:37742138 | C | T | 4 | a0001c0001t0001g0013 a0001c0001t0001g0283 a0001c0001t0006g0285 others(1): Show |
4 | HG02723.hp2 HG02818.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.344+2403G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 1/8 | chr17 | 37742138 | |||||||
| chr17:37742221 | G | C | 12 | a0001c0001t0001g0259 a0001c0001t0002g0260 a0001c0001t0002g0262 others(9): Show |
12 | HG02257.hp2 HG02451.hp1 HG02602.hp2 others(9): Show |
intron_variant | MODIFIER | c.344+2320C>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 1/8 | chr17 | 37742221 | |||||||
| chr17:37742368 | C | T | 1 | a0001c0001t0001g0202 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.344+2173G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 1/8 | chr17 | 37742368 | |||||||
| chr17:37742390 | G | A | 158 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0015 others(155): Show |
158 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.344+2151C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 1/8 | chr17 | 37742390 | |||||||
| chr17:37742480 | T | C | 1 | a0001c0001t0001g0182 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.344+2061A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 1/8 | chr17 | 37742480 | |||||||
| chr17:37742715 | G | A | 2 | a0001c0001t0006g0004 a0001c0001t0006g0005 |
2 | HG01884.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.344+1826C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 1/8 | chr17 | 37742715 | |||||||
| chr17:37742828 | A | C | 1 | a0001c0001t0002g0034 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.344+1713T>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 1/8 | chr17 | 37742828 | |||||||
| chr17:37742842 | A | G | 238 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0015 others(235): Show |
238 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(235): Show |
intron_variant | MODIFIER | c.344+1699T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 1/8 | chr17 | 37742842 | |||||||
| chr17:37742882 | G | A | 3 | a0001c0001t0005g0194 a0001c0001t0005g0195 a0001c0001t0005g0196 |
3 | HG02965.hp1 HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.344+1659C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 1/8 | chr17 | 37742882 | |||||||
| chr17:37742925 | T | C | 1 | a0001c0001t0003g0272 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.344+1616A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 1/8 | chr17 | 37742925 | |||||||
| chr17:37742980 | CA | C | 85 | a0001c0001t0001g0199 a0001c0001t0001g0202 a0001c0001t0001g0209 others(82): Show |
85 | HG00609.hp2 HG00741.hp1 HG01081.hp1 others(82): Show |
intron_variant | MODIFIER | c.344+1560delT | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 1/8 | chr17 | 37742980 | |||||||
| chr17:37743035 | C | T | 1 | a0001c0001t0001g0015 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.344+1506G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 1/8 | chr17 | 37743035 | |||||||
| chr17:37743084 | C | A | 1 | a0001c0001t0001g0013 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.344+1457G>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 1/8 | chr17 | 37743084 | |||||||
| chr17:37743117 | G | C | 2 | a0001c0001t0003g0273 a0001c0001t0006g0274 |
2 | HG01081.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.344+1424C>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 1/8 | chr17 | 37743117 | |||||||
| chr17:37743128 | G | T | 5 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(2): Show |
5 | NA18952.hp1 NA18953.hp2 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.344+1413C>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 1/8 | chr17 | 37743128 | |||||||
| chr17:37743158 | A | G | 237 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0015 others(234): Show |
237 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(234): Show |
intron_variant | MODIFIER | c.344+1383T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 1/8 | chr17 | 37743158 | |||||||
| chr17:37743176 | C | T | 2 | a0001c0001t0007g0200 a0001c0001t0007g0201 |
2 | HG02922.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.344+1365G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 1/8 | chr17 | 37743176 | |||||||
| chr17:37743269 | G | A | 6 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(3): Show |
6 | NA18948.hp2 NA18952.hp1 NA18953.hp2 others(3): Show |
intron_variant | MODIFIER | c.344+1272C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 1/8 | chr17 | 37743269 | |||||||
| chr17:37743331 | T | C | 3 | a0001c0001t0005g0194 a0001c0001t0005g0195 a0001c0001t0005g0196 |
3 | HG02965.hp1 HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.344+1210A>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 1/8 | chr17 | 37743331 | |||||||
| chr17:37743443 | A | C | 3 | a0001c0001t0001g0199 a0001c0001t0002g0198 a0001c0001t0003g0197 |
3 | NA18962.hp2 NA18973.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.344+1098T>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 1/8 | chr17 | 37743443 | |||||||
| chr17:37743574 | A | G | 142 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0016 others(139): Show |
142 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.344+967T>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 1/8 | chr17 | 37743574 | |||||||
| chr17:37743723 | G | T | 3 | a0001c0001t0005g0194 a0001c0001t0005g0195 a0001c0001t0005g0196 |
3 | HG02965.hp1 HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.344+818C>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 1/8 | chr17 | 37743723 | |||||||
| chr17:37743852 | G | A | 1 | a0001c0001t0001g0399 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.344+689C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 1/8 | chr17 | 37743852 | |||||||
| chr17:37743881 | G | C | 131 | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0001g0028 others(128): Show |
131 | HG00280.hp2 HG00323.hp1 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.344+660C>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 1/8 | chr17 | 37743881 | |||||||
| chr17:37743961 | C | G | 1 | a0001c0001t0003g0032 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.344+580G>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 1/8 | chr17 | 37743961 | |||||||
| chr17:37743977 | C | A | 1 | a0001c0001t0002g0189 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.344+564G>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 1/8 | chr17 | 37743977 | |||||||
| chr17:37744096 | G | A | 4 | a0001c0001t0002g0190 a0001c0001t0003g0403 a0001c0001t0004g0191 others(1): Show |
4 | HG02602.hp1 HG02738.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.344+445C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 1/8 | chr17 | 37744096 | |||||||
| chr17:37744124 | A | T | 1 | a0001c0001t0005g0193 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.344+417T>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 1/8 | chr17 | 37744124 | |||||||
| chr17:37744130 | G | C | 239 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0015 others(236): Show |
239 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.344+411C>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 1/8 | chr17 | 37744130 | |||||||
| chr17:37744163 | G | A | 1 | a0001c0001t0001g0400 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.344+378C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 1/8 | chr17 | 37744163 | |||||||
| chr17:37744256 | C | G | 5 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0002g0029 others(2): Show |
5 | HG00609.hp1 NA18941.hp1 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.344+285G>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 1/8 | chr17 | 37744256 | |||||||
| chr17:37744285 | C | G | 12 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0019 others(9): Show |
12 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.344+256G>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 1/8 | chr17 | 37744285 | |||||||
| chr17:37744313 | C | G | 12 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0019 others(9): Show |
12 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.344+228G>C | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 1/8 | chr17 | 37744313 | |||||||
| chr17:37744334 | G | T | 1 | a0001c0001t0006g0014 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.344+207C>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 1/8 | chr17 | 37744334 | |||||||
| chr17:37744343 | A | C | 1 | a0001c0001t0001g0013 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.344+198T>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 1/8 | chr17 | 37744343 | |||||||
| chr17:37744345 | G | T | 1 | a0001c0001t0005g0012 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.344+196C>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 1/8 | chr17 | 37744345 | |||||||
| chr17:37744382 | G | A | 1 | a0001c0001t0002g0401 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.344+159C>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 1/8 | chr17 | 37744382 | |||||||
| chr17:37744420 | C | T | 1 | a0001c0001t0003g0011 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.344+121G>A | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 1/8 | chr17 | 37744420 | |||||||
| chr17:37744476 | A | C | 7 | a0001c0001t0001g0009 a0001c0001t0002g0006 a0001c0001t0002g0007 others(4): Show |
7 | HG01884.hp1 HG02572.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.344+65T>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 1/8 | chr17 | 37744476 | |||||||
| chr17:37744493 | G | C | 1 | a0001c0001t0003g0402 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.344+48C>G | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 1/8 | chr17 | 37744493 | |||||||
| chr17:37744496 | C | A | 1 | a0001c0001t0003g0403 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.344+45G>T | HNF1B | ENSG00000275410.6 | transcript | ENST00000617811.5 | protein_coding | 1/8 | chr17 | 37744496 |