Item | Value |
---|---|
geneid | 6927 |
ensemblid | ENSG00000135100.19 |
hgncid | 11621 |
symbol | HNF1A |
name | HNF1 homeobox A |
refseq_nuc | NM_000545.8 |
refseq_prot | NP_000536.6 |
ensembl_nuc | ENST00000257555.11 |
ensembl_prot | ENSP00000257555.5 |
mane_status | MANE Select |
chr | chr12 |
start | 120978543 |
end | 121002512 |
strand | + |
ver | v1.2 |
region | chr12:120978543-121002512 |
region5000 | chr12:120973543-121007512 |
regionname0 | HNF1A_chr12_120978543_121002512 |
regionname5000 | HNF1A_chr12_120973543_121007512 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 631 | 228 | 76 | 39 | 80 | 11 | 22 | 57 | HNF1A_chr12_120973543_121007512 | HNF1A | MVSKL others(626): Show |
chr12 | 120973543 | 121007512 |
a0002 | 0/1 | 631 | 117 | 4 | 21 | 78 | 4 | 9 | 64 | HNF1A_chr12_120973543_121007512 | HNF1A | MVSKL others(626): Show |
chr12 | 120973543 | 121007512 |
a0003 | 0/0 | 631 | 26 | 0 | 1 | 24 | 0 | 1 | 17 | HNF1A_chr12_120973543_121007512 | HNF1A | MVSKL others(626): Show |
chr12 | 120973543 | 121007512 |
a0004 | 0/0 | 631 | 17 | 5 | 2 | 7 | 1 | 2 | 5 | HNF1A_chr12_120973543_121007512 | HNF1A | MVSKL others(626): Show |
chr12 | 120973543 | 121007512 |
a0005 | 1/0 | 631 | 9 | 8 | 0 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | MVSKL others(626): Show |
chr12 | 120973543 | 121007512 |
a0006 | 0/0 | 315 | 7 | 2 | 5 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | MVSKL others(310): Show |
chr12 | 120973543 | 121007512 |
a0007 | 0/0 | 622 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | MVSKL others(617): Show |
chr12 | 120973543 | 121007512 |
a0008 | 0/0 | 631 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | MVSKL others(626): Show |
chr12 | 120973543 | 121007512 |
a0009 | 0/0 | 631 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | MVSKL others(626): Show |
chr12 | 120973543 | 121007512 |
a0010 | 0/0 | 631 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | MVSKL others(626): Show |
chr12 | 120973543 | 121007512 |
a0011 | 0/0 | 627 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HNF1A_chr12_120973543_121007512 | HNF1A | MVSKL others(622): Show |
chr12 | 120973543 | 121007512 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 1893 | 152 | 43 | 11 | 79 | 4 | 15 | HNF1A_chr12_120973543_121007512 | HNF1A | ATGGT others(1888): Show |
chr12 | 120973543 | 121007512 | ||
a0001c0003 | 0/0 | 1893 | 35 | 19 | 7 | 1 | 2 | 6 | HNF1A_chr12_120973543_121007512 | HNF1A | ATGGT others(1888): Show |
chr12 | 120973543 | 121007512 | ||
a0001c0004 | 0/0 | 1893 | 27 | 13 | 10 | 0 | 3 | 1 | HNF1A_chr12_120973543_121007512 | HNF1A | ATGGT others(1888): Show |
chr12 | 120973543 | 121007512 | ||
a0001c0006 | 0/0 | 1893 | 9 | 0 | 8 | 0 | 1 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | ATGGT others(1888): Show |
chr12 | 120973543 | 121007512 | ||
a0001c0015 | 0/0 | 1893 | 2 | 0 | 2 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | ATGGT others(1888): Show |
chr12 | 120973543 | 121007512 | ||
a0001c0017 | 0/0 | 1893 | 1 | 0 | 0 | 0 | 1 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | ATGGT others(1888): Show |
chr12 | 120973543 | 121007512 | ||
a0001c0018 | 0/0 | 1893 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | ATGGT others(1888): Show |
chr12 | 120973543 | 121007512 | ||
a0001c0019 | 0/0 | 1893 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | ATGGT others(1888): Show |
chr12 | 120973543 | 121007512 | ||
a0002c0002 | 0/0 | 1893 | 112 | 4 | 21 | 74 | 4 | 9 | HNF1A_chr12_120973543_121007512 | HNF1A | ATGGT others(1888): Show |
chr12 | 120973543 | 121007512 | ||
a0002c0011 | 0/0 | 1893 | 3 | 0 | 0 | 3 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | ATGGT others(1888): Show |
chr12 | 120973543 | 121007512 | ||
a0002c0025 | 0/0 | 1893 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | ATGGT others(1888): Show |
chr12 | 120973543 | 121007512 | ||
a0002c0026 | 0/1 | 1893 | 1 | 0 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | ATGGT others(1888): Show |
chr12 | 120973543 | 121007512 | ||
a0003c0005 | 0/0 | 1893 | 23 | 0 | 1 | 21 | 0 | 1 | HNF1A_chr12_120973543_121007512 | HNF1A | ATGGT others(1888): Show |
chr12 | 120973543 | 121007512 | ||
a0003c0012 | 0/0 | 1893 | 3 | 0 | 0 | 3 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | ATGGT others(1888): Show |
chr12 | 120973543 | 121007512 | ||
a0004c0008 | 0/0 | 1893 | 8 | 2 | 2 | 2 | 1 | 1 | HNF1A_chr12_120973543_121007512 | HNF1A | ATGGT others(1888): Show |
chr12 | 120973543 | 121007512 | ||
a0004c0010 | 0/0 | 1893 | 5 | 0 | 0 | 5 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | ATGGT others(1888): Show |
chr12 | 120973543 | 121007512 | ||
a0004c0013 | 0/0 | 1893 | 3 | 3 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | ATGGT others(1888): Show |
chr12 | 120973543 | 121007512 | ||
a0004c0024 | 0/0 | 1893 | 1 | 0 | 0 | 0 | 0 | 1 | HNF1A_chr12_120973543_121007512 | HNF1A | ATGGT others(1888): Show |
chr12 | 120973543 | 121007512 | ||
a0005c0007 | 1/0 | 1893 | 8 | 7 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | ATGGT others(1888): Show |
chr12 | 120973543 | 121007512 | ||
a0005c0021 | 0/0 | 1893 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | ATGGT others(1888): Show |
chr12 | 120973543 | 121007512 | ||
a0006c0009 | 0/0 | 1894 | 5 | 2 | 3 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | ATGGT others(1889): Show |
chr12 | 120973543 | 121007512 | ||
a0006c0014 | 0/0 | 1894 | 2 | 0 | 2 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | ATGGT others(1889): Show |
chr12 | 120973543 | 121007512 | ||
a0007c0016 | 0/0 | 1866 | 2 | 0 | 2 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | ATGGT others(1861): Show |
chr12 | 120973543 | 121007512 | ||
a0008c0027 | 0/0 | 1893 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | ATGGT others(1888): Show |
chr12 | 120973543 | 121007512 | ||
a0009c0023 | 0/0 | 1893 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | ATGGT others(1888): Show |
chr12 | 120973543 | 121007512 | ||
a0010c0022 | 0/0 | 1893 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | ATGGT others(1888): Show |
chr12 | 120973543 | 121007512 | ||
a0011c0020 | 0/0 | 1883 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | ATGGT others(1878): Show |
chr12 | 120973543 | 121007512 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3442 | 91 | 31 | 7 | 36 | 4 | 13 | HNF1A_chr12_120973543_121007512 | HNF1A | AGCTC others(3437): Show |
chr12 | 120973543 | 121007512 |
a0001c0001t0002 | 0/0 | 3442 | 2 | 0 | 0 | 1 | 0 | 1 | HNF1A_chr12_120973543_121007512 | HNF1A | AGCTC others(3437): Show |
chr12 | 120973543 | 121007512 |
a0001c0001t0003 | 0/0 | 3442 | 53 | 9 | 4 | 39 | 0 | 1 | HNF1A_chr12_120973543_121007512 | HNF1A | AGCTC others(3437): Show |
chr12 | 120973543 | 121007512 |
a0001c0001t0006 | 0/0 | 3442 | 3 | 0 | 0 | 3 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | AGCTC others(3437): Show |
chr12 | 120973543 | 121007512 |
a0001c0001t0008 | 0/0 | 3442 | 2 | 2 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | AGCTC others(3437): Show |
chr12 | 120973543 | 121007512 |
a0001c0001t0010 | 0/0 | 3442 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | AGCTC others(3437): Show |
chr12 | 120973543 | 121007512 |
a0001c0003t0001 | 0/0 | 3442 | 21 | 15 | 5 | 0 | 1 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | AGCTC others(3437): Show |
chr12 | 120973543 | 121007512 |
a0001c0003t0002 | 0/0 | 3442 | 7 | 0 | 2 | 1 | 0 | 4 | HNF1A_chr12_120973543_121007512 | HNF1A | AGCTC others(3437): Show |
chr12 | 120973543 | 121007512 |
a0001c0003t0003 | 0/0 | 3442 | 3 | 3 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | AGCTC others(3437): Show |
chr12 | 120973543 | 121007512 |
a0001c0003t0004 | 0/0 | 3442 | 3 | 1 | 0 | 0 | 0 | 2 | HNF1A_chr12_120973543_121007512 | HNF1A | AGCTC others(3437): Show |
chr12 | 120973543 | 121007512 |
a0001c0003t0014 | 0/0 | 3442 | 1 | 0 | 0 | 0 | 1 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | AGCTC others(3437): Show |
chr12 | 120973543 | 121007512 |
a0001c0004t0001 | 0/0 | 3442 | 3 | 3 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | AGCTC others(3437): Show |
chr12 | 120973543 | 121007512 |
a0001c0004t0004 | 0/0 | 3442 | 20 | 6 | 10 | 0 | 3 | 1 | HNF1A_chr12_120973543_121007512 | HNF1A | AGCTC others(3437): Show |
chr12 | 120973543 | 121007512 |
a0001c0004t0007 | 0/0 | 3441 | 3 | 3 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | AGCTC others(3436): Show |
chr12 | 120973543 | 121007512 |
a0001c0004t0015 | 0/0 | 3442 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | AGCTC others(3437): Show |
chr12 | 120973543 | 121007512 |
a0001c0006t0001 | 0/0 | 3442 | 8 | 0 | 7 | 0 | 1 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | AGCTC others(3437): Show |
chr12 | 120973543 | 121007512 |
a0001c0006t0013 | 0/0 | 3442 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | AGCTC others(3437): Show |
chr12 | 120973543 | 121007512 |
a0001c0015t0001 | 0/0 | 3442 | 2 | 0 | 2 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | AGCTC others(3437): Show |
chr12 | 120973543 | 121007512 |
a0001c0017t0001 | 0/0 | 3442 | 1 | 0 | 0 | 0 | 1 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | AGCTC others(3437): Show |
chr12 | 120973543 | 121007512 |
a0001c0018t0001 | 0/0 | 3442 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | AGCTC others(3437): Show |
chr12 | 120973543 | 121007512 |
a0001c0019t0011 | 0/0 | 3442 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | AGCTC others(3437): Show |
chr12 | 120973543 | 121007512 |
a0002c0002t0002 | 0/0 | 3442 | 104 | 4 | 21 | 68 | 3 | 8 | HNF1A_chr12_120973543_121007512 | HNF1A | AGCTC others(3437): Show |
chr12 | 120973543 | 121007512 |
a0002c0002t0005 | 0/0 | 3442 | 4 | 0 | 0 | 4 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | AGCTC others(3437): Show |
chr12 | 120973543 | 121007512 |
a0002c0002t0009 | 0/0 | 3442 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | AGCTC others(3437): Show |
chr12 | 120973543 | 121007512 |
a0002c0002t0012 | 0/0 | 3442 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | AGCTC others(3437): Show |
chr12 | 120973543 | 121007512 |
a0002c0002t0016 | 0/0 | 3442 | 1 | 0 | 0 | 0 | 1 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | AGCTC others(3437): Show |
chr12 | 120973543 | 121007512 |
a0002c0002t0017 | 0/0 | 3442 | 1 | 0 | 0 | 0 | 0 | 1 | HNF1A_chr12_120973543_121007512 | HNF1A | AGCTC others(3437): Show |
chr12 | 120973543 | 121007512 |
a0002c0011t0002 | 0/0 | 3442 | 3 | 0 | 0 | 3 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | AGCTC others(3437): Show |
chr12 | 120973543 | 121007512 |
a0002c0025t0002 | 0/0 | 3442 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | AGCTC others(3437): Show |
chr12 | 120973543 | 121007512 |
a0002c0026t0002 | 0/1 | 3442 | 1 | 0 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | AGCTC others(3437): Show |
chr12 | 120973543 | 121007512 |
a0003c0005t0002 | 0/0 | 3442 | 22 | 0 | 1 | 20 | 0 | 1 | HNF1A_chr12_120973543_121007512 | HNF1A | AGCTC others(3437): Show |
chr12 | 120973543 | 121007512 |
a0003c0005t0018 | 0/0 | 3442 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | AGCTC others(3437): Show |
chr12 | 120973543 | 121007512 |
a0003c0012t0002 | 0/0 | 3442 | 3 | 0 | 0 | 3 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | AGCTC others(3437): Show |
chr12 | 120973543 | 121007512 |
a0004c0008t0001 | 0/0 | 3442 | 6 | 2 | 1 | 2 | 1 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | AGCTC others(3437): Show |
chr12 | 120973543 | 121007512 |
a0004c0008t0002 | 0/0 | 3442 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | AGCTC others(3437): Show |
chr12 | 120973543 | 121007512 |
a0004c0008t0003 | 0/0 | 3442 | 1 | 0 | 0 | 0 | 0 | 1 | HNF1A_chr12_120973543_121007512 | HNF1A | AGCTC others(3437): Show |
chr12 | 120973543 | 121007512 |
a0004c0010t0001 | 0/0 | 3442 | 5 | 0 | 0 | 5 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | AGCTC others(3437): Show |
chr12 | 120973543 | 121007512 |
a0004c0013t0001 | 0/0 | 3442 | 3 | 3 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | AGCTC others(3437): Show |
chr12 | 120973543 | 121007512 |
a0004c0024t0004 | 0/0 | 3442 | 1 | 0 | 0 | 0 | 0 | 1 | HNF1A_chr12_120973543_121007512 | HNF1A | AGCTC others(3437): Show |
chr12 | 120973543 | 121007512 |
a0005c0007t0001 | 1/0 | 3442 | 8 | 7 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | AGCTC others(3437): Show |
chr12 | 120973543 | 121007512 |
a0005c0021t0001 | 0/0 | 3442 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | AGCTC others(3437): Show |
chr12 | 120973543 | 121007512 |
a0006c0009t0001 | 0/0 | 3443 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | AGCTC others(3438): Show |
chr12 | 120973543 | 121007512 |
a0006c0009t0004 | 0/0 | 3443 | 4 | 1 | 3 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | AGCTC others(3438): Show |
chr12 | 120973543 | 121007512 |
a0006c0014t0001 | 0/0 | 3443 | 2 | 0 | 2 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | AGCTC others(3438): Show |
chr12 | 120973543 | 121007512 |
a0007c0016t0002 | 0/0 | 3415 | 2 | 0 | 2 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | AGCTC others(3410): Show |
chr12 | 120973543 | 121007512 |
a0008c0027t0002 | 0/0 | 3442 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | AGCTC others(3437): Show |
chr12 | 120973543 | 121007512 |
a0009c0023t0001 | 0/0 | 3442 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | AGCTC others(3437): Show |
chr12 | 120973543 | 121007512 |
a0010c0022t0002 | 0/0 | 3442 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | AGCTC others(3437): Show |
chr12 | 120973543 | 121007512 |
a0011c0020t0001 | 0/0 | 3432 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | AGCTC others(3427): Show |
chr12 | 120973543 | 121007512 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0003g0012 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0003g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0003g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0003g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0003g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0003g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0003g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0003g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0003g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0003g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0003g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0006g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0006g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0008g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0008g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0001t0010g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0003t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0003t0001g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0003t0001g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0003t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0003t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0003t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0003t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0003t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0003t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0003t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0003t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0003t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0003t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0003t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0003t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0003t0002g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0003t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0003t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0003t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0003t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0003t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0003t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0003t0003g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0003t0003g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0003t0004g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0003t0004g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0003t0004g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0003t0014g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0004t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0004t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0004t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0004t0004g0017 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0004t0004g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0004t0004g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0004t0004g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0004t0004g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0004t0004g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0004t0004g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0004t0004g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0004t0004g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0004t0004g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0004t0004g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0004t0004g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0004t0004g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0004t0004g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0004t0004g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0004t0004g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0004t0004g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0004t0007g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0004t0007g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0004t0007g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0004t0015g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0006t0001g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0006t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0006t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0006t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0006t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0006t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0006t0013g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0015t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0017t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0018t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0001c0019t0011g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0002c0002t0002g0001 | 0/0 | 20 | 3 | 7 | 8 | 0 | 2 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0002c0002t0002g0003 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0002c0002t0002g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0002c0002t0002g0007 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0002c0002t0002g0008 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0002c0002t0002g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0002c0002t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0002c0002t0002g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0002c0002t0002g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0002c0002t0002g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0002c0002t0002g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0002c0002t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0002c0002t0002g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0002c0002t0002g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0002c0002t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0002c0002t0002g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0002c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0002c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0002c0002t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0002c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0002c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0002c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0002c0002t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0002c0002t0002g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0002c0002t0002g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0002c0002t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0002c0002t0002g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0002c0002t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0002c0002t0002g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0002c0002t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0002c0002t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0002c0002t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0002c0002t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0002c0002t0002g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0002c0002t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0002c0002t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0002c0002t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0002c0002t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0002c0002t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0002c0002t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0002c0002t0002g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0002c0002t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0002c0002t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0002c0002t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0002c0002t0002g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0002c0002t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0002c0002t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0002c0002t0002g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0002c0002t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0002c0002t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0002c0002t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0002c0002t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0002c0002t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0002c0002t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0002c0002t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0002c0002t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0002c0002t0002g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0002c0002t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0002c0002t0002g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0002c0002t0002g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0002c0002t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0002c0002t0005g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0002c0002t0005g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0002c0002t0005g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0002c0002t0009g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0002c0002t0012g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0002c0002t0016g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0002c0002t0017g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0002c0011t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0002c0011t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0002c0011t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0002c0025t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0002c0026t0002g0301 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0003c0005t0002g0002 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0003c0005t0002g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0003c0005t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0003c0005t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0003c0005t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0003c0005t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0003c0005t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0003c0005t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0003c0005t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0003c0005t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0003c0005t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0003c0005t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0003c0005t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0003c0005t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0003c0005t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0003c0005t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0003c0005t0018g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0003c0012t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0003c0012t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0003c0012t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0004c0008t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0004c0008t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0004c0008t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0004c0008t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0004c0008t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0004c0008t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0004c0008t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0004c0008t0003g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0004c0010t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0004c0010t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0004c0010t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0004c0010t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0004c0013t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0004c0013t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0004c0013t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0004c0024t0004g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0005c0007t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0005c0007t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0005c0007t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0005c0007t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0005c0007t0001g0240 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0005c0021t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0006c0009t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0006c0009t0004g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0006c0009t0004g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0006c0009t0004g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0006c0009t0004g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0006c0014t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0006c0014t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0007c0016t0002g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0008c0027t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0009c0023t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0010c0022t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
a0011c0020t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0120 | EUR | GBR | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG00099 | hp2 | a0002 | c0002 | t0016 | g0007 | EUR | GBR | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG00140 | hp1 | a0001 | c0004 | t0004 | g0085 | EUR | GBR | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0028 | EUR | GBR | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG00280 | hp1 | a0002 | c0002 | t0002 | g0300 | EUR | FIN | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0113 | EUR | FIN | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG00323 | hp1 | a0002 | c0002 | t0002 | g0262 | EUR | FIN | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0116 | EUR | FIN | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG00408 | hp1 | a0001 | c0001 | t0003 | g0094 | EAS | CHS | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG00408 | hp2 | a0003 | c0005 | t0002 | g0102 | EAS | CHS | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG00423 | hp1 | a0003 | c0012 | t0002 | g0254 | EAS | CHS | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG00423 | hp2 | a0003 | c0005 | t0002 | g0276 | EAS | CHS | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | CHS | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG00438 | hp2 | a0002 | c0002 | t0002 | g0277 | EAS | CHS | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG00558 | hp1 | a0001 | c0001 | t0003 | g0167 | EAS | CHS | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG00558 | hp2 | a0003 | c0005 | t0002 | g0096 | EAS | CHS | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG00597 | hp1 | a0003 | c0005 | t0002 | g0179 | EAS | CHS | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG00597 | hp2 | a0002 | c0002 | t0002 | g0267 | EAS | CHS | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG00609 | hp1 | a0004 | c0008 | t0001 | g0302 | EAS | CHS | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG00609 | hp2 | a0002 | c0002 | t0002 | g0043 | EAS | CHS | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | CHS | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG00621 | hp2 | a0002 | c0002 | t0002 | g0043 | EAS | CHS | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG00639 | hp1 | a0007 | c0016 | t0002 | g0021 | AMR | PUR | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG00639 | hp2 | a0002 | c0002 | t0002 | g0007 | AMR | PUR | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG00642 | hp1 | a0001 | c0006 | t0001 | g0225 | AMR | PUR | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG00673 | hp1 | a0002 | c0011 | t0002 | g0196 | EAS | CHS | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | CHS | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG00735 | hp1 | a0006 | c0014 | t0001 | g0222 | AMR | PUR | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG00738 | hp1 | a0001 | c0006 | t0001 | g0004 | AMR | PUR | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG00741 | hp1 | a0002 | c0002 | t0002 | g0246 | AMR | PUR | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG01069 | hp1 | a0008 | c0027 | t0002 | g0045 | AMR | PUR | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG01069 | hp2 | a0001 | c0006 | t0001 | g0004 | AMR | PUR | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG01071 | hp1 | a0001 | c0006 | t0001 | g0004 | AMR | PUR | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG01071 | hp2 | a0006 | c0009 | t0004 | g0082 | AMR | PUR | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG01074 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | PUR | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG01074 | hp2 | a0007 | c0016 | t0002 | g0021 | AMR | PUR | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG01081 | hp1 | a0006 | c0014 | t0001 | g0243 | AMR | PUR | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG01081 | hp2 | a0002 | c0002 | t0002 | g0288 | AMR | PUR | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG01099 | hp1 | a0002 | c0002 | t0002 | g0258 | AMR | PUR | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG01099 | hp2 | a0001 | c0003 | t0001 | g0128 | AMR | PUR | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG01106 | hp1 | a0001 | c0003 | t0001 | g0016 | AMR | PUR | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG01106 | hp2 | a0001 | c0006 | t0001 | g0218 | AMR | PUR | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG01109 | hp1 | a0001 | c0003 | t0001 | g0053 | AMR | PUR | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG01109 | hp2 | a0001 | c0003 | t0001 | g0105 | AMR | PUR | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG01167 | hp1 | a0001 | c0001 | t0003 | g0163 | AMR | PUR | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG01167 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | PUR | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG01168 | hp1 | a0001 | c0001 | t0003 | g0023 | AMR | PUR | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG01168 | hp2 | a0002 | c0002 | t0002 | g0007 | AMR | PUR | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG01169 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | PUR | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG01169 | hp2 | a0001 | c0001 | t0003 | g0023 | AMR | PUR | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG01175 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | PUR | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG01192 | hp1 | a0002 | c0002 | t0002 | g0260 | AMR | PUR | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG01192 | hp2 | a0002 | c0002 | t0002 | g0008 | AMR | PUR | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG01243 | hp1 | a0001 | c0019 | t0011 | g0245 | AMR | PUR | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG01243 | hp2 | a0001 | c0003 | t0001 | g0227 | AMR | PUR | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG01255 | hp1 | a0003 | c0005 | t0002 | g0210 | AMR | CLM | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG01255 | hp2 | a0004 | c0008 | t0002 | g0100 | AMR | CLM | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG01256 | hp1 | a0001 | c0015 | t0001 | g0004 | AMR | CLM | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG01256 | hp2 | a0001 | c0006 | t0001 | g0224 | AMR | CLM | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG01257 | hp1 | a0001 | c0001 | t0003 | g0166 | AMR | CLM | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG01257 | hp2 | a0001 | c0003 | t0002 | g0020 | AMR | CLM | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG01258 | hp1 | a0001 | c0003 | t0002 | g0020 | AMR | CLM | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG01258 | hp2 | a0001 | c0015 | t0001 | g0004 | AMR | CLM | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG01358 | hp1 | a0004 | c0008 | t0001 | g0280 | AMR | CLM | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG01358 | hp2 | a0001 | c0004 | t0004 | g0088 | AMR | CLM | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG01361 | hp1 | a0001 | c0006 | t0001 | g0219 | AMR | CLM | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG01361 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | CLM | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG01433 | hp1 | a0002 | c0002 | t0002 | g0044 | AMR | CLM | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG01433 | hp2 | a0001 | c0004 | t0004 | g0087 | AMR | CLM | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG01515 | hp1 | a0001 | c0004 | t0004 | g0079 | EUR | IBS | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG01515 | hp2 | a0001 | c0003 | t0014 | g0016 | EUR | IBS | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG01516 | hp1 | a0001 | c0006 | t0001 | g0221 | EUR | IBS | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG01516 | hp2 | a0001 | c0004 | t0004 | g0017 | EUR | IBS | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG01884 | hp1 | a0001 | c0001 | t0010 | g0216 | AFR | ACB | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG01884 | hp2 | a0009 | c0023 | t0001 | g0135 | AFR | ACB | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | ACB | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG01891 | hp2 | a0005 | c0021 | t0001 | g0038 | AFR | ACB | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG01934 | hp1 | a0002 | c0002 | t0002 | g0271 | AMR | PEL | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG01934 | hp2 | a0006 | c0009 | t0004 | g0084 | AMR | PEL | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG01943 | hp1 | a0001 | c0004 | t0004 | g0075 | AMR | PEL | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG01943 | hp2 | a0010 | c0022 | t0002 | g0244 | AMR | PEL | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG01952 | hp1 | a0002 | c0002 | t0002 | g0263 | AMR | PEL | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG01952 | hp2 | a0001 | c0004 | t0004 | g0080 | AMR | PEL | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG01978 | hp1 | a0001 | c0004 | t0004 | g0018 | AMR | PEL | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG01978 | hp2 | a0002 | c0002 | t0002 | g0007 | AMR | PEL | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG01981 | hp1 | a0002 | c0002 | t0002 | g0045 | AMR | PEL | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG01981 | hp2 | a0001 | c0004 | t0004 | g0019 | AMR | PEL | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG01993 | hp1 | a0001 | c0006 | t0013 | g0220 | AMR | PEL | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG01993 | hp2 | a0001 | c0004 | t0004 | g0018 | AMR | PEL | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02004 | hp1 | a0002 | c0002 | t0002 | g0044 | AMR | PEL | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | PEL | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02027 | hp1 | a0001 | c0001 | t0003 | g0142 | EAS | KHV | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02027 | hp2 | a0002 | c0002 | t0002 | g0042 | EAS | KHV | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02040 | hp1 | a0002 | c0002 | t0002 | g0290 | EAS | KHV | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02040 | hp2 | a0001 | c0001 | t0003 | g0175 | EAS | KHV | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | ACB | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02055 | hp2 | a0001 | c0003 | t0003 | g0178 | AFR | ACB | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02056 | hp1 | a0004 | c0008 | t0001 | g0303 | EAS | KHV | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02071 | hp1 | a0001 | c0001 | t0003 | g0148 | EAS | KHV | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02071 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | KHV | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02074 | hp1 | a0003 | c0005 | t0002 | g0098 | EAS | KHV | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02074 | hp2 | a0002 | c0002 | t0002 | g0295 | EAS | KHV | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | KHV | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | KHV | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02083 | hp1 | a0001 | c0001 | t0003 | g0140 | EAS | KHV | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02129 | hp1 | a0002 | c0002 | t0002 | g0256 | EAS | KHV | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02129 | hp2 | a0001 | c0001 | t0003 | g0195 | EAS | KHV | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | KHV | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02132 | hp2 | a0001 | c0001 | t0003 | g0159 | EAS | KHV | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02135 | hp1 | a0001 | c0001 | t0003 | g0095 | EAS | KHV | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02135 | hp2 | a0002 | c0002 | t0002 | g0042 | EAS | KHV | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02145 | hp1 | a0001 | c0001 | t0003 | g0171 | AFR | ACB | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02145 | hp2 | a0001 | c0004 | t0004 | g0060 | AFR | ACB | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02148 | hp1 | a0006 | c0009 | t0004 | g0077 | AMR | PEL | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PEL | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02155 | hp1 | a0002 | c0002 | t0002 | g0011 | EAS | CDX | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | CDX | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02165 | hp1 | a0001 | c0001 | t0003 | g0068 | EAS | CDX | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02165 | hp2 | a0002 | c0002 | t0002 | g0283 | EAS | CDX | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02257 | hp2 | a0001 | c0003 | t0001 | g0037 | AFR | ACB | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02258 | hp1 | a0005 | c0007 | t0001 | g0039 | AFR | ACB | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | ACB | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | ACB | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02280 | hp2 | a0001 | c0003 | t0001 | g0005 | AFR | ACB | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02293 | hp1 | a0002 | c0002 | t0002 | g0285 | AMR | PEL | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02293 | hp2 | a0001 | c0004 | t0004 | g0019 | AMR | PEL | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02300 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | PEL | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02300 | hp2 | a0001 | c0004 | t0004 | g0081 | AMR | PEL | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | ACB | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02523 | hp1 | a0001 | c0001 | t0003 | g0176 | EAS | KHV | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02523 | hp2 | a0001 | c0001 | t0003 | g0180 | EAS | KHV | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02572 | hp1 | a0001 | c0004 | t0015 | g0089 | AFR | GWD | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02572 | hp2 | a0001 | c0003 | t0001 | g0108 | AFR | GWD | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02602 | hp1 | a0002 | c0002 | t0017 | g0008 | SAS | PJL | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02615 | hp1 | a0001 | c0001 | t0003 | g0161 | AFR | GWD | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02615 | hp2 | a0006 | c0009 | t0004 | g0059 | AFR | GWD | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | GWD | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02630 | hp2 | a0001 | c0003 | t0003 | g0147 | AFR | GWD | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02683 | hp1 | a0004 | c0024 | t0004 | g0078 | SAS | PJL | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02683 | hp2 | a0003 | c0005 | t0002 | g0192 | SAS | PJL | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02717 | hp1 | a0001 | c0004 | t0001 | g0237 | AFR | GWD | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02723 | hp1 | a0001 | c0004 | t0004 | g0050 | AFR | GWD | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02723 | hp2 | a0001 | c0004 | t0004 | g0074 | AFR | GWD | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02735 | hp1 | a0002 | c0002 | t0002 | g0259 | SAS | PJL | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02738 | hp1 | a0002 | c0002 | t0002 | g0279 | SAS | PJL | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02738 | hp2 | a0001 | c0003 | t0004 | g0138 | SAS | PJL | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02809 | hp1 | a0005 | c0007 | t0001 | g0010 | AFR | GWD | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02809 | hp2 | a0001 | c0018 | t0001 | g0234 | AFR | GWD | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02818 | hp1 | a0004 | c0013 | t0001 | g0064 | AFR | GWD | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02818 | hp2 | a0005 | c0007 | t0001 | g0040 | AFR | GWD | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02886 | hp1 | a0001 | c0003 | t0003 | g0157 | AFR | GWD | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02895 | hp1 | a0001 | c0003 | t0001 | g0014 | AFR | GWD | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | GWD | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02897 | hp2 | a0001 | c0001 | t0003 | g0182 | AFR | GWD | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02922 | hp1 | a0001 | c0004 | t0001 | g0061 | AFR | ESN | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | ESN | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02965 | hp1 | a0001 | c0004 | t0007 | g0049 | AFR | ESN | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02965 | hp2 | a0001 | c0004 | t0007 | g0055 | AFR | ESN | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | ESN | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02976 | hp1 | a0001 | c0001 | t0003 | g0153 | AFR | ESN | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02976 | hp2 | a0001 | c0003 | t0001 | g0013 | AFR | ESN | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG03017 | hp1 | a0001 | c0004 | t0004 | g0086 | SAS | PJL | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | GWD | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG03041 | hp2 | a0001 | c0001 | t0003 | g0226 | AFR | GWD | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG03098 | hp1 | a0001 | c0001 | t0003 | g0012 | AFR | MSL | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG03098 | hp2 | a0002 | c0002 | t0002 | g0001 | AFR | MSL | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG03130 | hp1 | a0004 | c0008 | t0001 | g0090 | AFR | ESN | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | ESN | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG03139 | hp1 | a0005 | c0007 | t0001 | g0038 | AFR | ESN | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG03139 | hp2 | a0001 | c0004 | t0004 | g0057 | AFR | ESN | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG03195 | hp2 | a0001 | c0003 | t0001 | g0032 | AFR | ESN | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG03209 | hp1 | a0001 | c0001 | t0003 | g0062 | AFR | MSL | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG03209 | hp2 | a0001 | c0004 | t0004 | g0076 | AFR | MSL | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG03225 | hp2 | a0001 | c0004 | t0007 | g0051 | AFR | MSL | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0198 | SAS | PJL | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG03239 | hp2 | a0001 | c0003 | t0004 | g0126 | SAS | PJL | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG03453 | hp1 | a0005 | c0007 | t0001 | g0010 | AFR | MSL | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG03453 | hp2 | a0004 | c0013 | t0001 | g0063 | AFR | MSL | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG03486 | hp1 | a0001 | c0003 | t0001 | g0013 | AFR | MSL | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG03486 | hp2 | a0004 | c0013 | t0001 | g0065 | AFR | MSL | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG03490 | hp2 | a0001 | c0003 | t0002 | g0071 | SAS | PJL | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG03492 | hp1 | a0001 | c0003 | t0002 | g0073 | SAS | PJL | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG03516 | hp2 | a0001 | c0003 | t0001 | g0014 | AFR | ESN | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG03540 | hp1 | a0001 | c0001 | t0008 | g0241 | AFR | GWD | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | GWD | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG03579 | hp1 | a0001 | c0003 | t0001 | g0013 | AFR | MSL | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | MSL | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG03669 | hp1 | a0004 | c0008 | t0003 | g0306 | SAS | PJL | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG03669 | hp2 | a0002 | c0002 | t0002 | g0305 | SAS | PJL | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | STU | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG03688 | hp2 | a0001 | c0003 | t0002 | g0070 | SAS | STU | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG03834 | hp1 | a0001 | c0003 | t0002 | g0072 | SAS | BEB | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG03834 | hp2 | a0002 | c0002 | t0002 | g0001 | SAS | BEB | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG03927 | hp1 | a0002 | c0002 | t0002 | g0001 | SAS | BEB | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG03927 | hp2 | a0001 | c0001 | t0003 | g0099 | SAS | BEB | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG03942 | hp1 | a0002 | c0002 | t0002 | g0247 | SAS | BEB | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0200 | SAS | BEB | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0207 | SAS | BEB | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG04184 | hp2 | a0002 | c0002 | t0002 | g0308 | SAS | BEB | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0211 | SAS | STU | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG04228 | hp2 | a0002 | c0002 | t0002 | g0264 | SAS | STU | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18522 | hp1 | a0001 | c0001 | t0003 | g0150 | AFR | YRI | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | YRI | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18612 | hp1 | a0001 | c0001 | t0003 | g0164 | EAS | CHB | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18612 | hp2 | a0002 | c0002 | t0012 | g0255 | EAS | CHB | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18747 | hp1 | a0003 | c0005 | t0002 | g0155 | EAS | CHB | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18747 | hp2 | a0001 | c0001 | t0003 | g0121 | EAS | CHB | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18906 | hp1 | a0002 | c0002 | t0002 | g0001 | AFR | YRI | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18939 | hp1 | a0004 | c0010 | t0001 | g0127 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18939 | hp2 | a0002 | c0002 | t0002 | g0251 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18940 | hp1 | a0003 | c0005 | t0002 | g0008 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18940 | hp2 | a0001 | c0001 | t0003 | g0173 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18941 | hp2 | a0002 | c0002 | t0002 | g0266 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18942 | hp1 | a0002 | c0002 | t0002 | g0270 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18942 | hp2 | a0002 | c0002 | t0002 | g0274 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18945 | hp1 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18945 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18946 | hp1 | a0002 | c0002 | t0005 | g0047 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18946 | hp2 | a0002 | c0002 | t0002 | g0268 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18949 | hp1 | a0001 | c0001 | t0003 | g0168 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18949 | hp2 | a0002 | c0002 | t0002 | g0289 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18950 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18951 | hp1 | a0001 | c0001 | t0003 | g0174 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18951 | hp2 | a0002 | c0002 | t0002 | g0248 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18952 | hp1 | a0001 | c0001 | t0003 | g0154 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18954 | hp1 | a0003 | c0005 | t0002 | g0002 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18954 | hp2 | a0002 | c0002 | t0002 | g0048 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18957 | hp1 | a0003 | c0005 | t0002 | g0002 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18957 | hp2 | a0002 | c0002 | t0002 | g0250 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18959 | hp1 | a0001 | c0001 | t0003 | g0181 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18959 | hp2 | a0002 | c0002 | t0002 | g0273 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18960 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18960 | hp2 | a0003 | c0005 | t0002 | g0002 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18962 | hp1 | a0003 | c0005 | t0002 | g0002 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18962 | hp2 | a0002 | c0002 | t0002 | g0275 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18963 | hp2 | a0002 | c0002 | t0002 | g0257 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18964 | hp1 | a0002 | c0002 | t0005 | g0292 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18964 | hp2 | a0002 | c0002 | t0009 | g0249 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18965 | hp1 | a0002 | c0002 | t0002 | g0008 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18966 | hp1 | a0002 | c0002 | t0002 | g0297 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18966 | hp2 | a0003 | c0005 | t0002 | g0214 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18968 | hp1 | a0002 | c0002 | t0002 | g0299 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18969 | hp2 | a0002 | c0002 | t0002 | g0041 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18970 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18970 | hp2 | a0002 | c0011 | t0002 | g0054 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18972 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18972 | hp2 | a0011 | c0020 | t0001 | g0123 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18973 | hp1 | a0002 | c0002 | t0002 | g0048 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18973 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18975 | hp1 | a0004 | c0010 | t0001 | g0029 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18975 | hp2 | a0002 | c0002 | t0002 | g0287 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18977 | hp1 | a0002 | c0002 | t0002 | g0041 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18977 | hp2 | a0002 | c0002 | t0002 | g0011 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18979 | hp1 | a0001 | c0001 | t0003 | g0033 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18979 | hp2 | a0002 | c0002 | t0002 | g0008 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18980 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18980 | hp2 | a0001 | c0001 | t0006 | g0009 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18981 | hp1 | a0003 | c0005 | t0002 | g0091 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18981 | hp2 | a0001 | c0001 | t0003 | g0152 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18982 | hp1 | a0001 | c0001 | t0003 | g0172 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18982 | hp2 | a0002 | c0002 | t0002 | g0278 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18983 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18984 | hp1 | a0001 | c0001 | t0003 | g0177 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18984 | hp2 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18985 | hp1 | a0001 | c0001 | t0003 | g0151 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18985 | hp2 | a0002 | c0002 | t0005 | g0047 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18987 | hp2 | a0001 | c0001 | t0003 | g0144 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18990 | hp1 | a0001 | c0001 | t0003 | g0143 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18990 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18991 | hp1 | a0002 | c0002 | t0002 | g0261 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18994 | hp1 | a0002 | c0002 | t0002 | g0294 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18994 | hp2 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18995 | hp1 | a0002 | c0002 | t0005 | g0291 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18997 | hp2 | a0002 | c0002 | t0002 | g0298 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18998 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA18998 | hp2 | a0003 | c0005 | t0002 | g0146 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA19000 | hp1 | a0002 | c0002 | t0002 | g0011 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA19000 | hp2 | a0001 | c0001 | t0003 | g0170 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA19002 | hp1 | a0001 | c0003 | t0002 | g0101 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA19002 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA19003 | hp1 | a0002 | c0002 | t0002 | g0015 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA19004 | hp1 | a0002 | c0025 | t0002 | g0015 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA19007 | hp1 | a0004 | c0010 | t0001 | g0112 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA19007 | hp2 | a0003 | c0005 | t0018 | g0002 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA19009 | hp1 | a0001 | c0001 | t0003 | g0156 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA19009 | hp2 | a0004 | c0010 | t0001 | g0029 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA19010 | hp1 | a0002 | c0002 | t0002 | g0253 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA19010 | hp2 | a0001 | c0001 | t0003 | g0160 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA19011 | hp1 | a0003 | c0005 | t0002 | g0002 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA19030 | hp1 | a0002 | c0002 | t0002 | g0001 | AFR | LWK | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA19030 | hp2 | a0006 | c0009 | t0001 | g0129 | AFR | LWK | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA19043 | hp1 | a0004 | c0008 | t0001 | g0269 | AFR | LWK | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA19043 | hp2 | a0001 | c0003 | t0001 | g0014 | AFR | LWK | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA19055 | hp2 | a0003 | c0012 | t0002 | g0281 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA19056 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA19057 | hp1 | a0003 | c0012 | t0002 | g0265 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA19057 | hp2 | a0002 | c0002 | t0002 | g0046 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA19060 | hp1 | a0001 | c0001 | t0006 | g0036 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA19060 | hp2 | a0001 | c0001 | t0003 | g0141 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA19062 | hp1 | a0002 | c0011 | t0002 | g0252 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA19062 | hp2 | a0002 | c0002 | t0002 | g0286 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA19064 | hp2 | a0002 | c0002 | t0002 | g0293 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA19065 | hp1 | a0002 | c0002 | t0002 | g0015 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA19067 | hp1 | a0001 | c0001 | t0003 | g0149 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA19067 | hp2 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA19068 | hp2 | a0002 | c0002 | t0002 | g0284 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA19070 | hp1 | a0002 | c0002 | t0002 | g0304 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA19070 | hp2 | a0003 | c0005 | t0002 | g0002 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA19072 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA19074 | hp1 | a0003 | c0005 | t0002 | g0002 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA19074 | hp2 | a0003 | c0005 | t0002 | g0052 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA19078 | hp1 | a0003 | c0005 | t0002 | g0092 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA19078 | hp2 | a0002 | c0002 | t0002 | g0272 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA19080 | hp1 | a0001 | c0001 | t0003 | g0145 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA19080 | hp2 | a0002 | c0002 | t0002 | g0309 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA19081 | hp1 | a0001 | c0001 | t0003 | g0169 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA19084 | hp2 | a0002 | c0002 | t0002 | g0046 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA19085 | hp2 | a0001 | c0001 | t0006 | g0009 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA19086 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA19086 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA19087 | hp1 | a0003 | c0005 | t0002 | g0097 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA19087 | hp2 | a0001 | c0001 | t0003 | g0033 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA19088 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA19088 | hp2 | a0001 | c0001 | t0003 | g0066 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA19090 | hp1 | a0004 | c0010 | t0001 | g0122 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA19090 | hp2 | a0002 | c0002 | t0002 | g0011 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA19091 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA19091 | hp2 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA19240 | hp1 | a0001 | c0003 | t0004 | g0107 | AFR | YRI | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA19240 | hp2 | a0001 | c0003 | t0001 | g0228 | AFR | YRI | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA20129 | hp1 | a0001 | c0004 | t0004 | g0017 | AFR | ASW | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA20129 | hp2 | a0001 | c0001 | t0003 | g0158 | AFR | ASW | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA20752 | hp1 | a0001 | c0003 | t0001 | g0217 | EUR | TSI | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA20752 | hp2 | a0004 | c0008 | t0001 | g0296 | EUR | TSI | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA20805 | hp1 | a0001 | c0017 | t0001 | g0223 | EUR | TSI | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA20805 | hp2 | a0002 | c0002 | t0002 | g0007 | EUR | TSI | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG01123 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | CLM | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG01123 | hp2 | a0001 | c0004 | t0004 | g0056 | AMR | CLM | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02109 | hp1 | a0005 | c0007 | t0001 | g0039 | AFR | ACB | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02486 | hp2 | a0001 | c0003 | t0001 | g0032 | AFR | ACB | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02559 | hp1 | a0005 | c0007 | t0001 | g0040 | AFR | ACB | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG02559 | hp2 | a0001 | c0001 | t0008 | g0242 | AFR | ACB | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG03471 | hp1 | a0001 | c0003 | t0001 | g0229 | AFR | MSL | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | MSL | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG06807 | hp1 | a0001 | c0004 | t0001 | g0187 | AFR | USA | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
HG06807 | hp2 | a0001 | c0003 | t0001 | g0037 | AFR | USA | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA20300 | hp1 | a0002 | c0002 | t0002 | g0282 | AFR | USA | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | USA | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA21309 | hp1 | a0001 | c0003 | t0001 | g0230 | AFR | LWK | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | LWK | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
homoSapiens | chm13v2 | a0002 | c0026 | t0002 | g0301 | REF | REF | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
homoSapiens | grch38p0 | a0005 | c0007 | t0001 | g0240 | REF | REF | HNF1A_chr12_120973543_121007512 | HNF1A | chr12 | 120973543 | 121007512 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:120978847 | A | C | 3 | a0002 a0004 a0008 |
134 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(131): Show |
missense_variant | MODERATE | c.79A>C | p.Ile27Leu | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/10 | 305/3442 | 79/1896 | 27/631 | chr12 | 120978847 | |||
chr12:120979061 | C | T | 1 | a0010 | 1 | HG01943.hp2 | missense_variant | MODERATE | c.293C>T | p.Ala98Val | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/10 | 519/3442 | 293/1896 | 98/631 | chr12 | 120979061 | |||
chr12:120988970 | A | G | 1 | a0008 | 1 | HG01069.hp1 | missense_variant | MODERATE | c.464A>G | p.Lys155Arg | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 2/10 | 690/3442 | 464/1896 | 155/631 | chr12 | 120988970 | |||
chr12:120994313 | G | GC | 1 | a0006 | 7 | HG00735.hp1 HG01071.hp2 HG01081.hp1 others(4): Show |
frameshift_variant | HIGH | c.863_864insC | p.Pro289fs | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 4/10 | 1090/3442 | 864/1896 | 288/631 | chr12 | 120994313 | |||
chr12:120996271 | A | G | 1 | a0009 | 1 | HG01884.hp2 | missense_variant | MODERATE | c.965A>G | p.Tyr322Cys | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 5/10 | 1191/3442 | 965/1896 | 322/631 | chr12 | 120996271 | |||
chr12:120996598 | T | G | 1 | a0009 | 1 | HG01884.hp2 | missense_variant | MODERATE | c.1165T>G | p.Leu389Val | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 6/10 | 1391/3442 | 1165/1896 | 389/631 | chr12 | 120996598 | |||
chr12:120997538 | CCTGCAGC others(20): Show |
C | 1 | a0007 | 2 | HG00639.hp1 HG01074.hp2 |
disruptive_inframe_deletion | MODERATE | c.1380_1406delGCCCGT others(21): Show |
p.Gln460_Leu468del | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 7/10 | 1606/3442 | 1380/1896 | 460/631 | INFO_REALIGN_3_PRIME | chr12 | 120997538 | ||
chr12:120997624 | G | A | 3 | a0002 a0003 a0008 |
143 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(140): Show |
missense_variant | MODERATE | c.1460G>A | p.Ser487Asn | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 7/10 | 1686/3442 | 1460/1896 | 487/631 | chr12 | 120997624 | |||
chr12:120999566 | CCAGGACC others(3): Show |
C | 1 | a0011 | 1 | NA18972.hp2 | frameshift_variant | HIGH | c.1709_1718delAGGACC others(4): Show |
p.Gln570fs | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 9/10 | 1935/3442 | 1709/1896 | 570/631 | INFO_REALIGN_3_PRIME | chr12 | 120999566 | ||
chr12:120999579 | A | G | 10 | a0001 a0002 a0003 others(7): Show |
400 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(397): Show |
missense_variant | MODERATE | c.1720A>G | p.Ser574Gly | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 9/10 | 1946/3442 | 1720/1896 | 574/631 | chr12 | 120999579 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:120978819 | C | G | 12 | a0001c0003 a0001c0015 a0002c0002 others(9): Show |
170 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(167): Show |
synonymous_variant | LOW | c.51C>G | p.Leu17Leu | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/10 | 277/3442 | 51/1896 | 17/631 | chr12 | 120978819 | |||
chr12:120979020 | C | T | 1 | a0009c0023 | 1 | HG01884.hp2 | synonymous_variant | LOW | c.252C>T | p.Pro84Pro | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/10 | 478/3442 | 252/1896 | 84/631 | chr12 | 120979020 | |||
chr12:120979044 | C | T | 1 | a0004c0013 | 3 | HG02818.hp1 HG03453.hp2 HG03486.hp2 |
synonymous_variant | LOW | c.276C>T | p.Leu92Leu | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/10 | 502/3442 | 276/1896 | 92/631 | chr12 | 120979044 | |||
chr12:120993581 | C | A | 1 | a0001c0017 | 1 | NA20805.hp1 | synonymous_variant | LOW | c.588C>A | p.Thr196Thr | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 3/10 | 814/3442 | 588/1896 | 196/631 | chr12 | 120993581 | |||
chr12:120994314 | G | C | 9 | a0001c0004 a0001c0006 a0001c0015 others(6): Show |
51 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(48): Show |
synonymous_variant | LOW | c.864G>C | p.Gly288Gly | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 4/10 | 1090/3442 | 864/1896 | 288/631 | chr12 | 120994314 | |||
chr12:120996317 | C | T | 1 | a0005c0021 | 1 | HG01891.hp2 | synonymous_variant | LOW | c.1011C>T | p.Ser337Ser | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 5/10 | 1237/3442 | 1011/1896 | 337/631 | chr12 | 120996317 | |||
chr12:120996705 | T | C | 1 | a0001c0018 | 1 | HG02809.hp2 | synonymous_variant | LOW | c.1272T>C | p.Pro424Pro | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 6/10 | 1498/3442 | 1272/1896 | 424/631 | chr12 | 120996705 | |||
chr12:120997539 | C | T | 6 | a0002c0002 a0002c0011 a0002c0025 others(3): Show |
143 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(140): Show |
synonymous_variant | LOW | c.1375C>T | p.Leu459Leu | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 7/10 | 1601/3442 | 1375/1896 | 459/631 | chr12 | 120997539 | |||
chr12:120997589 | G | A | 1 | a0001c0019 | 1 | HG01243.hp1 | synonymous_variant | LOW | c.1425G>A | p.Pro475Pro | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 7/10 | 1651/3442 | 1425/1896 | 475/631 | chr12 | 120997589 | |||
chr12:120997658 | C | T | 1 | a0002c0025 | 1 | NA19004.hp1 | synonymous_variant | LOW | c.1494C>T | p.Ser498Ser | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 7/10 | 1720/3442 | 1494/1896 | 498/631 | chr12 | 120997658 | |||
chr12:120999311 | G | A | 4 | a0001c0006 a0001c0015 a0001c0017 others(1): Show |
14 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(11): Show |
synonymous_variant | LOW | c.1545G>A | p.Thr515Thr | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 8/10 | 1771/3442 | 1545/1896 | 515/631 | chr12 | 120999311 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:120978645 | G | A | 1 | a0002c0002t0009 | 1 | NA18964.hp2 | 5_prime_UTR_variant | MODIFIER | c.-124G>A | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/10 | 124 | chr12 | 120978645 | ||||||
chr12:120978645 | G | C | 1 | a0002c0002t0005 | 4 | NA18946.hp1 NA18964.hp1 NA18985.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-124G>C | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/10 | 124 | chr12 | 120978645 | ||||||
chr12:120978740 | G | A | 1 | a0001c0001t0010 | 1 | HG01884.hp1 | 5_prime_UTR_variant | MODIFIER | c.-29G>A | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/10 | 29 | chr12 | 120978740 | ||||||
chr12:120978746 | C | G | 1 | a0003c0005t0018 | 1 | NA19007.hp2 | 5_prime_UTR_variant | MODIFIER | c.-23C>G | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/10 | 23 | chr12 | 120978746 | ||||||
chr12:120978765 | A | G | 1 | a0002c0002t0017 | 1 | HG02602.hp1 | 5_prime_UTR_variant | MODIFIER | c.-4A>G | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/10 | 4 | chr12 | 120978765 | ||||||
chr12:121001197 | G | A | 1 | a0001c0019t0011 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5G>A | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 10/10 | 5 | chr12 | 121001197 | ||||||
chr12:121001281 | C | A | 1 | a0002c0002t0012 | 1 | NA18612.hp2 | 3_prime_UTR_variant | MODIFIER | c.*89C>A | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 10/10 | 89 | chr12 | 121001281 | ||||||
chr12:121001389 | G | T | 17 | a0001c0001t0002 a0001c0003t0002 a0002c0002t0002 others(14): Show |
156 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(153): Show |
3_prime_UTR_variant | MODIFIER | c.*197G>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 10/10 | 197 | chr12 | 121001389 | ||||||
chr12:121001406 | G | A | 1 | a0002c0002t0016 | 1 | HG00099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*214G>A | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 10/10 | 214 | chr12 | 121001406 | ||||||
chr12:121001515 | G | C | 1 | a0001c0006t0013 | 1 | HG01993.hp1 | 3_prime_UTR_variant | MODIFIER | c.*323G>C | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 10/10 | 323 | chr12 | 121001515 | ||||||
chr12:121001630 | G | A | 17 | a0001c0001t0002 a0001c0003t0002 a0002c0002t0002 others(14): Show |
156 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(153): Show |
3_prime_UTR_variant | MODIFIER | c.*438G>A | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 10/10 | 438 | chr12 | 121001630 | ||||||
chr12:121001639 | T | A | 1 | a0001c0001t0006 | 3 | NA18980.hp2 NA19060.hp1 NA19085.hp2 |
3_prime_UTR_variant | MODIFIER | c.*447T>A | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 10/10 | 447 | chr12 | 121001639 | ||||||
chr12:121001781 | C | T | 1 | a0001c0004t0015 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*589C>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 10/10 | 589 | chr12 | 121001781 | ||||||
chr12:121001795 | G | A | 4 | a0001c0001t0003 a0001c0001t0010 a0001c0003t0003 others(1): Show |
58 | HG00408.hp1 HG00558.hp1 HG01167.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*603G>A | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 10/10 | 603 | chr12 | 121001795 | ||||||
chr12:121002013 | AC | A | 1 | a0001c0004t0007 | 3 | HG02965.hp1 HG02965.hp2 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*824delC | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 10/10 | 824 | INFO_REALIGN_3_PRIME | chr12 | 121002013 | |||||
chr12:121002100 | G | A | 1 | a0001c0003t0014 | 1 | HG01515.hp2 | 3_prime_UTR_variant | MODIFIER | c.*908G>A | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 10/10 | 908 | chr12 | 121002100 | ||||||
chr12:121002141 | G | A | 1 | a0001c0001t0008 | 2 | HG02559.hp2 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*949G>A | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 10/10 | 949 | chr12 | 121002141 | ||||||
chr12:121002460 | G | A | 5 | a0001c0003t0004 a0001c0004t0004 a0001c0004t0007 others(2): Show |
31 | HG00140.hp1 HG01071.hp2 HG01123.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*1268G>A | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 10/10 | 1268 | chr12 | 121002460 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:120979114 | C | A | 3 | a0001c0004t0004g0050 a0001c0004t0007g0049 a0001c0004t0007g0051 |
3 | HG02723.hp1 HG02965.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.326+20C>A | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120979114 | |||||||
chr12:120979185 | A | G | 83 | a0001c0001t0001g0307 a0002c0002t0002g0001 a0002c0002t0002g0003 others(80): Show |
127 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.326+91A>G | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120979185 | |||||||
chr12:120979219 | G | C | 1 | a0003c0005t0002g0052 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.326+125G>C | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120979219 | |||||||
chr12:120979335 | T | C | 1 | a0002c0002t0002g0246 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.326+241T>C | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120979335 | |||||||
chr12:120979415 | C | T | 1 | a0002c0002t0002g0309 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.326+321C>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120979415 | |||||||
chr12:120979471 | A | T | 1 | a0001c0019t0011g0245 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.326+377A>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120979471 | |||||||
chr12:120979503 | C | T | 1 | a0010c0022t0002g0244 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.326+409C>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120979503 | |||||||
chr12:120979555 | G | T | 1 | a0002c0002t0002g0308 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.326+461G>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120979555 | |||||||
chr12:120979583 | G | A | 4 | a0001c0003t0001g0016 a0001c0003t0001g0053 a0001c0003t0014g0016 others(1): Show |
4 | HG01106.hp1 HG01109.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.326+489G>A | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120979583 | |||||||
chr12:120979715 | C | T | 4 | a0001c0003t0001g0016 a0001c0003t0001g0053 a0001c0003t0014g0016 others(1): Show |
4 | HG01106.hp1 HG01109.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.326+621C>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120979715 | |||||||
chr12:120979733 | G | GACTC | 92 | a0001c0001t0001g0058 a0001c0001t0001g0067 a0001c0001t0003g0062 others(89): Show |
136 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.326+640_326+643dup others(4): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 120979733 | ||||||
chr12:120980184 | G | A | 3 | a0001c0003t0001g0105 a0001c0003t0001g0108 a0001c0003t0001g0128 |
3 | HG01099.hp2 HG01109.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.326+1090G>A | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120980184 | |||||||
chr12:120980236 | C | A | 1 | a0001c0001t0003g0068 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.326+1142C>A | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120980236 | |||||||
chr12:120980354 | C | T | 1 | a0006c0014t0001g0243 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.326+1260C>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120980354 | |||||||
chr12:120980437 | G | C | 1 | a0001c0001t0001g0069 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.326+1343G>C | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120980437 | |||||||
chr12:120980553 | T | C | 299 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0024 others(296): Show |
380 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(377): Show |
intron_variant | MODIFIER | c.326+1459T>C | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120980553 | |||||||
chr12:120980583 | A | C | 1 | a0001c0001t0001g0232 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.326+1489A>C | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120980583 | |||||||
chr12:120980656 | G | T | 8 | a0001c0001t0001g0231 a0001c0003t0001g0013 a0001c0003t0001g0014 others(5): Show |
13 | HG01243.hp2 HG02257.hp2 HG02895.hp1 others(10): Show |
intron_variant | MODIFIER | c.326+1562G>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120980656 | |||||||
chr12:120980657 | C | T | 8 | a0001c0001t0001g0231 a0001c0003t0001g0013 a0001c0003t0001g0014 others(5): Show |
13 | HG01243.hp2 HG02257.hp2 HG02895.hp1 others(10): Show |
intron_variant | MODIFIER | c.326+1563C>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120980657 | |||||||
chr12:120980864 | T | G | 4 | a0001c0003t0002g0070 a0001c0003t0002g0071 a0001c0003t0002g0072 others(1): Show |
4 | HG03490.hp2 HG03492.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.326+1770T>G | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120980864 | |||||||
chr12:120981095 | C | G | 1 | a0001c0001t0003g0226 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.326+2001C>G | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120981095 | |||||||
chr12:120981188 | C | CT | 12 | a0001c0003t0001g0217 a0001c0006t0001g0004 a0001c0006t0001g0218 others(9): Show |
15 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.326+2095dupT | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 120981188 | ||||||
chr12:120981253 | T | C | 120 | a0001c0001t0001g0058 a0001c0001t0001g0083 a0001c0001t0002g0093 others(117): Show |
173 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.326+2159T>C | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120981253 | |||||||
chr12:120981286 | G | A | 9 | a0001c0003t0002g0020 a0001c0003t0002g0070 a0001c0003t0002g0071 others(6): Show |
11 | HG00639.hp1 HG01074.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.326+2192G>A | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120981286 | |||||||
chr12:120981410 | C | T | 1 | a0001c0001t0001g0232 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.326+2316C>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120981410 | |||||||
chr12:120981737 | C | T | 298 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0024 others(295): Show |
379 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(376): Show |
intron_variant | MODIFIER | c.326+2643C>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120981737 | |||||||
chr12:120981973 | C | T | 1 | a0001c0001t0010g0216 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.326+2879C>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120981973 | |||||||
chr12:120982019 | G | A | 9 | a0001c0003t0002g0020 a0001c0003t0002g0070 a0001c0003t0002g0071 others(6): Show |
11 | HG00639.hp1 HG01074.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.326+2925G>A | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120982019 | |||||||
chr12:120982059 | T | C | 1 | a0002c0002t0002g0248 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.326+2965T>C | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120982059 | |||||||
chr12:120982068 | G | T | 53 | a0001c0001t0001g0009 a0001c0001t0001g0034 a0001c0001t0001g0035 others(50): Show |
63 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.326+2974G>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120982068 | |||||||
chr12:120982083 | A | AT | 9 | a0001c0003t0002g0020 a0001c0003t0002g0070 a0001c0003t0002g0071 others(6): Show |
11 | HG00639.hp1 HG01074.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.326+2994dupT | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 120982083 | ||||||
chr12:120982114 | C | CA | 9 | a0001c0003t0002g0020 a0001c0003t0002g0070 a0001c0003t0002g0071 others(6): Show |
11 | HG00639.hp1 HG01074.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.326+3020_326+3021i others(3): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120982114 | |||||||
chr12:120982114 | C | T | 50 | a0001c0001t0001g0162 a0001c0001t0001g0165 a0001c0001t0003g0012 others(47): Show |
55 | HG00558.hp1 HG00597.hp1 HG01167.hp1 others(52): Show |
intron_variant | MODIFIER | c.326+3020C>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120982114 | |||||||
chr12:120982123 | T | C | 86 | a0001c0003t0001g0013 a0001c0003t0001g0014 a0001c0003t0001g0037 others(83): Show |
135 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.326+3029T>C | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120982123 | |||||||
chr12:120982170 | C | T | 1 | a0001c0001t0003g0182 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.326+3076C>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120982170 | |||||||
chr12:120982207 | T | C | 1 | a0003c0005t0002g0102 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.326+3113T>C | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120982207 | |||||||
chr12:120982224 | C | G | 1 | a0001c0001t0001g0215 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.326+3130C>G | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120982224 | |||||||
chr12:120982329 | C | T | 1 | a0001c0001t0001g0139 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.326+3235C>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120982329 | |||||||
chr12:120982456 | CA | C | 3 | a0004c0013t0001g0063 a0004c0013t0001g0064 a0004c0013t0001g0065 |
3 | HG02818.hp1 HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.326+3363delA | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120982456 | |||||||
chr12:120982457 | A | G | 200 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0024 others(197): Show |
230 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.326+3363A>G | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120982457 | |||||||
chr12:120982460 | A | G | 203 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0024 others(200): Show |
233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.326+3366A>G | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120982460 | |||||||
chr12:120982466 | G | C | 228 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0024 others(225): Show |
299 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.326+3372G>C | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120982466 | |||||||
chr12:120982466 | G | GC | 56 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0083 others(53): Show |
60 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.326+3372_326+3373i others(3): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120982466 | |||||||
chr12:120982485 | G | A | 7 | a0001c0003t0001g0013 a0001c0003t0001g0014 a0001c0003t0001g0037 others(4): Show |
12 | HG01243.hp2 HG02257.hp2 HG02895.hp1 others(9): Show |
intron_variant | MODIFIER | c.326+3391G>A | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120982485 | |||||||
chr12:120982610 | T | C | 1 | a0001c0001t0001g0103 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.326+3516T>C | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120982610 | |||||||
chr12:120982627 | C | T | 1 | a0002c0002t0002g0300 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.326+3533C>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120982627 | |||||||
chr12:120982739 | C | T | 1 | a0001c0001t0008g0242 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.326+3645C>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120982739 | |||||||
chr12:120982797 | C | T | 1 | a0001c0001t0001g0206 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.326+3703C>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120982797 | |||||||
chr12:120982934 | T | C | 2 | a0001c0001t0001g0104 a0001c0001t0001g0124 |
2 | HG00673.hp2 NA18997.hp1 |
intron_variant | MODIFIER | c.326+3840T>C | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120982934 | |||||||
chr12:120983004 | G | A | 79 | a0002c0002t0002g0001 a0002c0002t0002g0003 a0002c0002t0002g0006 others(76): Show |
123 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.326+3910G>A | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120983004 | |||||||
chr12:120983374 | G | A | 1 | a0001c0001t0001g0207 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.326+4280G>A | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120983374 | |||||||
chr12:120983396 | G | A | 1 | a0002c0002t0009g0249 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.326+4302G>A | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120983396 | |||||||
chr12:120983410 | G | T | 4 | a0002c0002t0002g0048 a0002c0002t0002g0297 a0002c0002t0002g0298 others(1): Show |
5 | NA18954.hp2 NA18966.hp1 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.326+4316G>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120983410 | |||||||
chr12:120983550 | C | CTT | 7 | a0001c0003t0001g0013 a0001c0003t0001g0014 a0001c0003t0001g0037 others(4): Show |
12 | HG01243.hp2 HG02257.hp2 HG02895.hp1 others(9): Show |
intron_variant | MODIFIER | c.326+4468_326+4469d others(4): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 120983550 | ||||||
chr12:120983638 | C | T | 1 | a0009c0023t0001g0135 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.326+4544C>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120983638 | |||||||
chr12:120983694 | C | G | 3 | a0001c0006t0001g0221 a0001c0006t0001g0225 a0006c0014t0001g0222 |
3 | HG00642.hp1 HG00735.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.326+4600C>G | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120983694 | |||||||
chr12:120983908 | T | G | 9 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0003c0005t0002g0002 others(6): Show |
15 | HG00558.hp2 HG02074.hp1 NA18954.hp1 others(12): Show |
intron_variant | MODIFIER | c.326+4814T>G | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120983908 | |||||||
chr12:120983916 | C | CTG | 4 | a0001c0003t0002g0101 a0003c0005t0002g0179 a0005c0007t0001g0038 others(1): Show |
4 | HG00597.hp1 HG01891.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.326+4854_326+4855d others(4): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 120983916 | ||||||
chr12:120983916 | C | CTGTGTG | 4 | a0001c0003t0002g0070 a0001c0003t0002g0071 a0001c0003t0002g0072 others(1): Show |
4 | HG03490.hp2 HG03492.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.326+4850_326+4855d others(8): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 120983916 | ||||||
chr12:120983916 | C | CTGTGTGT others(1): Show |
8 | a0001c0001t0001g0204 a0001c0001t0003g0141 a0001c0003t0001g0013 others(5): Show |
13 | HG02257.hp2 HG02895.hp1 HG02976.hp2 others(10): Show |
intron_variant | MODIFIER | c.326+4848_326+4855d others(10): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 120983916 | ||||||
chr12:120983916 | C | CTGTGTGT others(3): Show |
18 | a0001c0001t0001g0058 a0001c0001t0001g0199 a0001c0001t0001g0200 others(15): Show |
18 | HG00558.hp1 HG00735.hp1 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.326+4846_326+4855d others(12): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 120983916 | ||||||
chr12:120983916 | C | CTGTGTGT others(5): Show |
15 | a0001c0001t0001g0134 a0001c0001t0001g0183 a0001c0001t0001g0184 others(12): Show |
17 | HG00639.hp1 HG01074.hp2 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.326+4844_326+4855d others(14): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 120983916 | ||||||
chr12:120983916 | C | CTGTGTGT others(7): Show |
53 | a0001c0001t0001g0009 a0001c0001t0001g0035 a0001c0001t0001g0036 others(50): Show |
67 | HG00438.hp1 HG00558.hp2 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.326+4842_326+4855d others(16): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 120983916 | ||||||
chr12:120983916 | C | CTGTGTGT others(9): Show |
62 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0028 others(59): Show |
71 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(68): Show |
intron_variant | MODIFIER | c.326+4840_326+4855d others(18): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 120983916 | ||||||
chr12:120983916 | C | CTGTGTGT others(11): Show |
33 | a0001c0001t0001g0024 a0001c0001t0001g0030 a0001c0001t0001g0034 others(30): Show |
37 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(34): Show |
intron_variant | MODIFIER | c.326+4838_326+4855d others(20): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 120983916 | ||||||
chr12:120983916 | C | CTGTGTGT others(13): Show |
11 | a0001c0001t0001g0208 a0001c0001t0002g0093 a0001c0001t0003g0062 others(8): Show |
11 | HG01884.hp2 HG01934.hp2 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.326+4836_326+4855d others(22): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 120983916 | ||||||
chr12:120983916 | C | CTGTGTGT others(15): Show |
7 | a0001c0001t0001g0022 a0001c0001t0001g0027 a0001c0001t0001g0083 others(4): Show |
10 | HG01109.hp2 HG01168.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.326+4834_326+4855d others(24): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 120983916 | ||||||
chr12:120983916 | C | CTGTGTGT others(17): Show |
1 | a0001c0001t0001g0125 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.326+4832_326+4855d others(26): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 120983916 | ||||||
chr12:120983916 | C | CTGTGTGT others(21): Show |
1 | a0001c0001t0001g0069 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.326+4828_326+4855d others(30): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 120983916 | ||||||
chr12:120983916 | CTGTG | C | 6 | a0001c0001t0008g0241 a0002c0002t0002g0006 a0002c0002t0002g0250 others(3): Show |
10 | HG03540.hp1 NA18939.hp2 NA18957.hp2 others(7): Show |
intron_variant | MODIFIER | c.326+4852_326+4855d others(6): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 120983916 | ||||||
chr12:120983916 | CTGTGTG | C | 72 | a0002c0002t0002g0001 a0002c0002t0002g0003 a0002c0002t0002g0007 others(69): Show |
111 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.326+4850_326+4855d others(8): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 120983916 | ||||||
chr12:120983916 | CTGTGTGT others(3): Show |
C | 1 | a0004c0008t0001g0296 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.326+4846_326+4855d others(12): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 120983916 | ||||||
chr12:120983949 | T | TGTGTGTG others(4): Show |
1 | a0001c0001t0001g0205 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.326+4855_326+4856i others(13): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120983949 | |||||||
chr12:120983949 | T | TGTGTGTG others(10): Show |
1 | a0001c0001t0003g0180 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.326+4855_326+4856i others(19): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120983949 | |||||||
chr12:120983950 | T | G | 7 | a0001c0001t0003g0031 a0001c0001t0003g0140 a0001c0001t0003g0141 others(4): Show |
8 | HG02027.hp1 HG02083.hp1 NA18945.hp1 others(5): Show |
intron_variant | MODIFIER | c.326+4856T>G | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120983950 | |||||||
chr12:120983977 | AAGAG | A | 3 | a0001c0003t0001g0014 a0001c0003t0001g0227 a0001c0003t0001g0230 |
5 | HG01243.hp2 HG02895.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.327-4849_327-4846d others(6): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 120983977 | ||||||
chr12:120984003 | G | A | 3 | a0004c0013t0001g0063 a0004c0013t0001g0064 a0004c0013t0001g0065 |
3 | HG02818.hp1 HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.327-4830G>A | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120984003 | |||||||
chr12:120984189 | C | T | 3 | a0001c0006t0001g0219 a0001c0006t0001g0224 a0001c0006t0013g0220 |
3 | HG01256.hp2 HG01361.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.327-4644C>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120984189 | |||||||
chr12:120984331 | A | AGAGAAT | 288 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0024 others(285): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.327-4491_327-4486d others(8): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 120984331 | ||||||
chr12:120984367 | A | G | 57 | a0001c0001t0001g0162 a0001c0001t0001g0165 a0001c0001t0002g0093 others(54): Show |
63 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.327-4466A>G | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120984367 | |||||||
chr12:120984431 | G | A | 1 | a0001c0001t0001g0204 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.327-4402G>A | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120984431 | |||||||
chr12:120984440 | G | A | 8 | a0001c0003t0002g0020 a0001c0003t0002g0070 a0001c0003t0002g0071 others(5): Show |
10 | HG00639.hp1 HG01074.hp2 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.327-4393G>A | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120984440 | |||||||
chr12:120984469 | T | G | 2 | a0001c0003t0001g0037 a0001c0003t0001g0228 |
3 | HG02257.hp2 HG06807.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.327-4364T>G | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120984469 | |||||||
chr12:120984491 | GAGGGAGG others(1): Show |
G | 2 | a0001c0003t0001g0013 a0001c0003t0001g0229 |
4 | HG02976.hp2 HG03471.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.327-4333_327-4326d others(10): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 120984491 | ||||||
chr12:120984645 | TCTGACTG others(9): Show |
T | 213 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0024 others(210): Show |
245 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.327-4187_327-4172d others(18): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120984645 | |||||||
chr12:120984662 | A | T | 213 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0024 others(210): Show |
245 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.327-4171A>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120984662 | |||||||
chr12:120984739 | G | A | 1 | a0004c0008t0001g0302 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.327-4094G>A | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120984739 | |||||||
chr12:120984859 | C | A | 1 | a0001c0018t0001g0234 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.327-3974C>A | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120984859 | |||||||
chr12:120984945 | C | CT | 196 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0024 others(193): Show |
230 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.327-3870dupT | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 120984945 | ||||||
chr12:120984945 | C | CTT | 8 | a0001c0001t0003g0141 a0001c0001t0003g0142 a0001c0001t0003g0144 others(5): Show |
8 | HG02027.hp1 HG02055.hp2 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.327-3871_327-3870d others(4): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 120984945 | ||||||
chr12:120985006 | C | T | 10 | a0001c0001t0002g0093 a0001c0003t0002g0020 a0001c0003t0002g0070 others(7): Show |
12 | HG00639.hp1 HG01074.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.327-3827C>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120985006 | |||||||
chr12:120985237 | T | C | 1 | a0001c0001t0001g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.327-3596T>C | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120985237 | |||||||
chr12:120985255 | T | A | 3 | a0001c0003t0004g0107 a0001c0003t0004g0126 a0001c0003t0004g0138 |
3 | HG02738.hp2 HG03239.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.327-3578T>A | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120985255 | |||||||
chr12:120985364 | G | A | 22 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0235 others(19): Show |
29 | HG01106.hp1 HG01109.hp1 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.327-3469G>A | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120985364 | |||||||
chr12:120985446 | G | A | 1 | a0001c0001t0001g0204 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.327-3387G>A | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120985446 | |||||||
chr12:120985482 | T | C | 240 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(237): Show |
284 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(281): Show |
intron_variant | MODIFIER | c.327-3351T>C | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120985482 | |||||||
chr12:120985483 | G | GA | 7 | a0001c0001t0001g0199 a0001c0001t0002g0093 a0001c0001t0003g0151 others(4): Show |
7 | HG00423.hp1 HG02074.hp2 HG02080.hp2 others(4): Show |
intron_variant | MODIFIER | c.327-3338dupA | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 120985483 | ||||||
chr12:120985573 | G | A | 208 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0024 others(205): Show |
243 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.327-3260G>A | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120985573 | |||||||
chr12:120985583 | A | G | 240 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(237): Show |
284 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(281): Show |
intron_variant | MODIFIER | c.327-3250A>G | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120985583 | |||||||
chr12:120985716 | G | A | 8 | a0001c0003t0002g0020 a0001c0003t0002g0070 a0001c0003t0002g0071 others(5): Show |
10 | HG00639.hp1 HG01074.hp2 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.327-3117G>A | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120985716 | |||||||
chr12:120985810 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.327-3023C>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120985810 | |||||||
chr12:120985846 | G | A | 10 | a0001c0001t0002g0093 a0001c0003t0002g0020 a0001c0003t0002g0070 others(7): Show |
12 | HG00639.hp1 HG01074.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.327-2987G>A | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120985846 | |||||||
chr12:120985856 | A | G | 208 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0024 others(205): Show |
243 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.327-2977A>G | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120985856 | |||||||
chr12:120985939 | C | T | 10 | a0001c0001t0002g0093 a0001c0003t0002g0020 a0001c0003t0002g0070 others(7): Show |
12 | HG00639.hp1 HG01074.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.327-2894C>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120985939 | |||||||
chr12:120985983 | C | CA | 33 | a0001c0001t0001g0058 a0001c0001t0001g0183 a0001c0003t0002g0070 others(30): Show |
36 | HG00140.hp1 HG01071.hp2 HG01123.hp2 others(33): Show |
intron_variant | MODIFIER | c.327-2839dupA | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 120985983 | ||||||
chr12:120986012 | T | C | 2 | a0001c0001t0002g0093 a0001c0003t0002g0101 |
2 | HG02080.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.327-2821T>C | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120986012 | |||||||
chr12:120986106 | G | A | 1 | a0001c0001t0003g0121 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.327-2727G>A | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120986106 | |||||||
chr12:120986153 | C | T | 208 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0024 others(205): Show |
243 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.327-2680C>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120986153 | |||||||
chr12:120986164 | A | C | 1 | a0001c0001t0001g0206 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.327-2669A>C | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120986164 | |||||||
chr12:120986195 | C | A | 32 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0235 others(29): Show |
41 | HG00639.hp1 HG01074.hp2 HG01106.hp1 others(38): Show |
intron_variant | MODIFIER | c.327-2638C>A | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120986195 | |||||||
chr12:120986215 | A | C | 2 | a0001c0001t0002g0093 a0001c0003t0002g0101 |
2 | HG02080.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.327-2618A>C | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120986215 | |||||||
chr12:120986269 | A | C | 3 | a0001c0003t0004g0107 a0001c0003t0004g0126 a0001c0003t0004g0138 |
3 | HG02738.hp2 HG03239.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.327-2564A>C | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120986269 | |||||||
chr12:120986280 | C | T | 1 | a0001c0019t0011g0245 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.327-2553C>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120986280 | |||||||
chr12:120986337 | C | T | 3 | a0001c0003t0004g0107 a0001c0003t0004g0126 a0001c0003t0004g0138 |
3 | HG02738.hp2 HG03239.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.327-2496C>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120986337 | |||||||
chr12:120986473 | G | A | 1 | a0003c0005t0002g0192 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.327-2360G>A | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120986473 | |||||||
chr12:120986538 | T | G | 3 | a0001c0004t0004g0050 a0001c0004t0007g0049 a0001c0004t0007g0051 |
3 | HG02723.hp1 HG02965.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.327-2295T>G | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120986538 | |||||||
chr12:120986596 | T | C | 1 | a0001c0001t0001g0110 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.327-2237T>C | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120986596 | |||||||
chr12:120986597 | T | C | 23 | a0001c0001t0001g0058 a0001c0004t0004g0017 a0001c0004t0004g0018 others(20): Show |
26 | HG00140.hp1 HG01071.hp2 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.327-2236T>C | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120986597 | |||||||
chr12:120986603 | G | A | 208 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0024 others(205): Show |
243 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.327-2230G>A | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120986603 | |||||||
chr12:120986648 | C | T | 4 | a0001c0006t0001g0218 a0001c0006t0001g0221 a0001c0006t0001g0225 others(1): Show |
4 | HG00642.hp1 HG00735.hp1 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.327-2185C>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120986648 | |||||||
chr12:120986687 | C | T | 80 | a0002c0002t0002g0001 a0002c0002t0002g0003 a0002c0002t0002g0006 others(77): Show |
124 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.327-2146C>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120986687 | |||||||
chr12:120986771 | G | A | 208 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0024 others(205): Show |
243 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.327-2062G>A | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120986771 | |||||||
chr12:120986948 | G | C | 6 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(3): Show |
6 | HG00738.hp2 HG02698.hp1 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.327-1885G>C | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120986948 | |||||||
chr12:120987058 | A | G | 208 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0024 others(205): Show |
243 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.327-1775A>G | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120987058 | |||||||
chr12:120987197 | G | A | 1 | a0002c0002t0012g0255 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.327-1636G>A | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120987197 | |||||||
chr12:120987200 | C | T | 1 | a0002c0002t0002g0299 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.327-1633C>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120987200 | |||||||
chr12:120987231 | T | C | 1 | a0001c0001t0001g0111 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.327-1602T>C | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120987231 | |||||||
chr12:120987300 | C | T | 1 | a0006c0009t0001g0129 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.327-1533C>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120987300 | |||||||
chr12:120987302 | G | A | 17 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0235 others(14): Show |
24 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.327-1531G>A | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120987302 | |||||||
chr12:120987452 | G | A | 2 | a0001c0001t0001g0162 a0001c0001t0003g0182 |
2 | HG01891.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.327-1381G>A | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120987452 | |||||||
chr12:120987473 | T | C | 1 | a0002c0002t0002g0256 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.327-1360T>C | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120987473 | |||||||
chr12:120987474 | C | CA | 13 | a0001c0001t0001g0162 a0001c0001t0001g0183 a0001c0001t0001g0200 others(10): Show |
13 | HG01081.hp1 HG01099.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.327-1341dupA | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 120987474 | ||||||
chr12:120987474 | CA | C | 38 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0069 others(35): Show |
47 | HG00639.hp1 HG01074.hp2 HG01106.hp1 others(44): Show |
intron_variant | MODIFIER | c.327-1341delA | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 120987474 | ||||||
chr12:120987487 | A | G | 1 | a0001c0001t0003g0140 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.327-1346A>G | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120987487 | |||||||
chr12:120987516 | T | A | 8 | a0001c0003t0001g0013 a0001c0003t0001g0014 a0001c0003t0001g0037 others(5): Show |
13 | HG00280.hp1 HG01243.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.327-1317T>A | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120987516 | |||||||
chr12:120987516 | T | G | 280 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0024 others(277): Show |
354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.327-1317T>G | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120987516 | |||||||
chr12:120987586 | A | T | 65 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0030 others(62): Show |
82 | HG00438.hp1 HG00558.hp2 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.327-1247A>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120987586 | |||||||
chr12:120987589 | A | AAT | 3 | a0004c0008t0002g0100 a0005c0007t0001g0038 a0005c0021t0001g0038 |
3 | HG01255.hp2 HG01891.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.327-1226_327-1225d others(4): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 120987589 | ||||||
chr12:120987589 | AAT | A | 287 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0024 others(284): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.327-1226_327-1225d others(4): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 120987589 | ||||||
chr12:120987591 | T | A | 1 | a0002c0011t0002g0252 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.327-1242T>A | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120987591 | |||||||
chr12:120987593 | T | A | 283 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0024 others(280): Show |
362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.327-1240T>A | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120987593 | |||||||
chr12:120987595 | T | A | 5 | a0001c0003t0004g0107 a0001c0003t0004g0126 a0001c0003t0004g0138 others(2): Show |
5 | HG02572.hp1 HG02735.hp1 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.327-1238T>A | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120987595 | |||||||
chr12:120987601 | T | C | 1 | a0002c0002t0002g0260 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.327-1232T>C | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120987601 | |||||||
chr12:120987605 | T | C | 1 | a0002c0011t0002g0252 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.327-1228T>C | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120987605 | |||||||
chr12:120987607 | T | C | 288 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0024 others(285): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.327-1226T>C | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120987607 | |||||||
chr12:120987607 | T | TATAC | 7 | a0001c0003t0002g0020 a0001c0003t0002g0070 a0001c0003t0002g0071 others(4): Show |
9 | HG00639.hp1 HG01074.hp2 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.327-1225_327-1224i others(6): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 120987607 | ||||||
chr12:120987611 | C | T | 10 | a0001c0001t0002g0093 a0001c0003t0002g0020 a0001c0003t0002g0070 others(7): Show |
12 | HG00639.hp1 HG01074.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.327-1222C>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120987611 | |||||||
chr12:120987613 | T | C | 1 | a0001c0001t0003g0166 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.327-1220T>C | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120987613 | |||||||
chr12:120987649 | C | T | 1 | a0010c0022t0002g0244 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.327-1184C>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120987649 | |||||||
chr12:120987711 | C | T | 1 | a0001c0001t0001g0199 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.327-1122C>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120987711 | |||||||
chr12:120987763 | G | GATCT | 11 | a0001c0001t0001g0115 a0001c0001t0001g0120 a0001c0001t0003g0161 others(8): Show |
12 | HG00099.hp1 HG01358.hp2 HG02129.hp2 others(9): Show |
intron_variant | MODIFIER | c.327-1024_327-1021d others(6): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 120987763 | ||||||
chr12:120987763 | G | GATCTATC others(1): Show |
3 | a0001c0001t0003g0068 a0002c0011t0002g0196 a0006c0009t0004g0082 |
3 | HG00673.hp1 HG01071.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.327-1028_327-1021d others(10): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 120987763 | ||||||
chr12:120987763 | GATCT | G | 142 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0022 others(139): Show |
207 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.327-1024_327-1021d others(6): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 120987763 | ||||||
chr12:120987763 | GATCTATC others(1): Show |
G | 79 | a0001c0001t0001g0005 a0001c0001t0001g0058 a0001c0001t0001g0111 others(76): Show |
90 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.327-1028_327-1021d others(10): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 120987763 | ||||||
chr12:120987763 | GATCTATC others(5): Show |
G | 6 | a0001c0001t0003g0153 a0001c0001t0003g0163 a0001c0003t0001g0037 others(3): Show |
7 | HG01167.hp1 HG02165.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.327-1032_327-1021d others(14): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 120987763 | ||||||
chr12:120987987 | G | GTCCATCC others(56): Show |
15 | a0001c0001t0001g0106 a0001c0001t0002g0093 a0001c0001t0003g0031 others(12): Show |
21 | HG00140.hp1 HG01257.hp1 HG02080.hp2 others(18): Show |
intron_variant | MODIFIER | c.327-824_327-762dup others(63): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 120987987 | ||||||
chr12:120987987 | G | GTCCATCC others(119): Show |
17 | a0001c0001t0001g0109 a0001c0001t0001g0189 a0001c0001t0003g0099 others(14): Show |
19 | HG01433.hp2 HG01515.hp1 HG01516.hp2 others(16): Show |
intron_variant | MODIFIER | c.327-762_327-761ins others(126): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 120987987 | ||||||
chr12:120987987 | G | GTCCATCC others(182): Show |
9 | a0001c0001t0003g0023 a0001c0001t0003g0154 a0001c0001t0003g0175 others(6): Show |
10 | HG00597.hp1 HG00642.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.327-762_327-761ins others(189): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 120987987 | ||||||
chr12:120987987 | G | GTCCATCC others(245): Show |
43 | a0001c0001t0001g0165 a0001c0001t0001g0208 a0001c0001t0003g0012 others(40): Show |
53 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.327-762_327-761ins others(252): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 120987987 | ||||||
chr12:120987987 | G | GTCCATCC others(556): Show |
1 | a0001c0001t0003g0153 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.327-762_327-761ins others(563): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 120987987 | ||||||
chr12:120987987 | G | GTCCATCC others(434): Show |
1 | a0001c0001t0001g0162 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.327-762_327-761ins others(441): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 120987987 | ||||||
chr12:120987987 | G | GTCCATCC others(560): Show |
3 | a0001c0001t0003g0158 a0001c0003t0003g0157 a0001c0003t0003g0178 |
3 | HG02055.hp2 HG02886.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.327-762_327-761ins others(567): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 120987987 | ||||||
chr12:120987987 | GTCCATCC others(182): Show |
G | 3 | a0002c0002t0002g0253 a0002c0002t0002g0258 a0002c0002t0002g0279 |
3 | HG01099.hp1 HG02738.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.327-692_327-504del | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 120987987 | ||||||
chr12:120988009 | T | TACCCACC others(245): Show |
2 | a0001c0001t0008g0241 a0001c0001t0008g0242 |
2 | HG02559.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.327-755_327-504dup others(252): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 120988009 | ||||||
chr12:120988009 | TACCCACC others(56): Show |
T | 8 | a0001c0001t0001g0083 a0001c0001t0001g0132 a0001c0001t0001g0133 others(5): Show |
8 | HG00621.hp1 HG01175.hp1 HG02083.hp2 others(5): Show |
intron_variant | MODIFIER | c.327-698_327-636del others(63): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 120988009 | ||||||
chr12:120988009 | TACCCACC others(119): Show |
T | 25 | a0001c0001t0001g0124 a0001c0003t0002g0020 a0001c0003t0002g0070 others(22): Show |
30 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.327-761_327-636del | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 120988009 | ||||||
chr12:120988047 | A | ACCATCCA others(60): Show |
4 | a0001c0003t0001g0016 a0001c0003t0001g0053 a0001c0003t0014g0016 others(1): Show |
4 | HG01106.hp1 HG01109.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.327-762_327-761ins others(67): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 120988047 | ||||||
chr12:120988059 | T | G | 1 | a0002c0011t0002g0252 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.327-774T>G | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120988059 | |||||||
chr12:120988072 | C | T | 263 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0024 others(260): Show |
339 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(336): Show |
intron_variant | MODIFIER | c.327-761C>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120988072 | |||||||
chr12:120988135 | C | T | 271 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0024 others(268): Show |
347 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(344): Show |
intron_variant | MODIFIER | c.327-698C>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120988135 | |||||||
chr12:120988173 | A | ACCATCCA others(119): Show |
7 | a0001c0004t0004g0019 a0001c0004t0004g0081 a0001c0004t0004g0086 others(4): Show |
8 | HG01071.hp2 HG01358.hp2 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.327-573_327-572ins others(126): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 120988173 | ||||||
chr12:120988173 | A | ACCATCCA others(56): Show |
1 | a0001c0004t0004g0056 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.327-598_327-597ins others(63): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 120988173 | ||||||
chr12:120988198 | TACCCACC others(56): Show |
T | 57 | a0001c0006t0001g0219 a0001c0006t0001g0224 a0002c0002t0002g0001 others(54): Show |
92 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.327-566_327-504del others(63): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 120988198 | ||||||
chr12:120988241 | CCATCCAT others(4): Show |
C | 1 | a0001c0001t0003g0226 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.327-581_327-571del others(11): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 120988241 | ||||||
chr12:120988261 | C | T | 30 | a0001c0001t0003g0226 a0001c0006t0013g0220 a0002c0002t0002g0003 others(27): Show |
39 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.327-572C>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120988261 | |||||||
chr12:120988362 | A | G | 3 | a0001c0004t0004g0050 a0001c0004t0007g0049 a0001c0004t0007g0051 |
3 | HG02723.hp1 HG02965.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.327-471A>G | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120988362 | |||||||
chr12:120988525 | G | C | 1 | a0002c0002t0002g0042 | 2 | HG02027.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.327-308G>C | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120988525 | |||||||
chr12:120988527 | G | T | 1 | a0002c0002t0002g0042 | 2 | HG02027.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.327-306G>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120988527 | |||||||
chr12:120988587 | G | A | 1 | a0003c0012t0002g0265 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.327-246G>A | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120988587 | |||||||
chr12:120988675 | C | T | 83 | a0002c0002t0002g0001 a0002c0002t0002g0003 a0002c0002t0002g0006 others(80): Show |
127 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.327-158C>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120988675 | |||||||
chr12:120988742 | G | A | 288 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0024 others(285): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.327-91G>A | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120988742 | |||||||
chr12:120988791 | G | A | 88 | a0001c0004t0015g0089 a0002c0002t0002g0001 a0002c0002t0002g0003 others(85): Show |
132 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.327-42G>A | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120988791 | |||||||
chr12:120988800 | T | G | 1 | a0001c0001t0003g0166 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.327-33T>G | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 1/9 | chr12 | 120988800 | |||||||
chr12:120989085 | C | G | 3 | a0001c0001t0001g0005 a0001c0003t0001g0005 a0001c0018t0001g0234 |
6 | HG02257.hp1 HG02280.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.526+53C>G | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 2/9 | chr12 | 120989085 | |||||||
chr12:120989098 | G | C | 12 | a0001c0003t0001g0217 a0001c0006t0001g0004 a0001c0006t0001g0218 others(9): Show |
15 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.526+66G>C | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 2/9 | chr12 | 120989098 | |||||||
chr12:120989405 | C | T | 3 | a0001c0004t0004g0050 a0001c0004t0007g0049 a0001c0004t0007g0051 |
3 | HG02723.hp1 HG02965.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.526+373C>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 2/9 | chr12 | 120989405 | |||||||
chr12:120989507 | A | G | 298 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0024 others(295): Show |
379 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(376): Show |
intron_variant | MODIFIER | c.526+475A>G | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 2/9 | chr12 | 120989507 | |||||||
chr12:120989627 | C | T | 1 | a0009c0023t0001g0135 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.526+595C>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 2/9 | chr12 | 120989627 | |||||||
chr12:120989670 | C | T | 4 | a0002c0002t0002g0003 a0002c0002t0002g0268 a0002c0002t0002g0273 others(1): Show |
9 | NA18945.hp2 NA18946.hp2 NA18950.hp2 others(6): Show |
intron_variant | MODIFIER | c.526+638C>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 2/9 | chr12 | 120989670 | |||||||
chr12:120989687 | T | C | 54 | a0001c0001t0001g0162 a0001c0001t0002g0093 a0001c0001t0003g0012 others(51): Show |
59 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.526+655T>C | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 2/9 | chr12 | 120989687 | |||||||
chr12:120989850 | G | C | 2 | a0002c0002t0002g0045 a0008c0027t0002g0045 |
2 | HG01069.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.526+818G>C | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 2/9 | chr12 | 120989850 | |||||||
chr12:120990019 | G | A | 25 | a0001c0003t0004g0107 a0001c0003t0004g0126 a0001c0003t0004g0138 others(22): Show |
28 | HG00140.hp1 HG01071.hp2 HG01123.hp2 others(25): Show |
intron_variant | MODIFIER | c.526+987G>A | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 2/9 | chr12 | 120990019 | |||||||
chr12:120990044 | C | T | 1 | a0001c0001t0003g0156 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.526+1012C>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 2/9 | chr12 | 120990044 | |||||||
chr12:120990131 | AT | A | 6 | a0001c0003t0002g0071 a0001c0004t0001g0187 a0002c0002t0002g0261 others(3): Show |
6 | HG03490.hp2 HG06807.hp1 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.526+1108delT | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 120990131 | ||||||
chr12:120990202 | C | G | 3 | a0001c0003t0004g0107 a0001c0003t0004g0126 a0001c0003t0004g0138 |
3 | HG02738.hp2 HG03239.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.526+1170C>G | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 2/9 | chr12 | 120990202 | |||||||
chr12:120990202 | C | T | 1 | a0001c0003t0002g0070 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.526+1170C>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 2/9 | chr12 | 120990202 | |||||||
chr12:120990210 | C | T | 1 | a0001c0006t0001g0224 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.526+1178C>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 2/9 | chr12 | 120990210 | |||||||
chr12:120990224 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.526+1192C>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 2/9 | chr12 | 120990224 | |||||||
chr12:120990242 | T | C | 2 | a0001c0001t0002g0093 a0002c0002t0002g0266 |
2 | HG02080.hp2 NA18941.hp2 |
intron_variant | MODIFIER | c.526+1210T>C | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 2/9 | chr12 | 120990242 | |||||||
chr12:120990299 | G | A | 3 | a0005c0007t0001g0038 a0005c0007t0001g0039 a0005c0021t0001g0038 |
4 | HG01891.hp2 HG02109.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.526+1267G>A | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 2/9 | chr12 | 120990299 | |||||||
chr12:120990342 | C | CGTGTTAG others(5): Show |
1 | a0001c0003t0001g0228 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.526+1310_526+1311i others(14): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 2/9 | chr12 | 120990342 | |||||||
chr12:120990343 | A | G | 4 | a0001c0001t0001g0239 a0004c0013t0001g0063 a0004c0013t0001g0064 others(1): Show |
4 | HG02622.hp2 HG02818.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.526+1311A>G | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 2/9 | chr12 | 120990343 | |||||||
chr12:120990376 | G | A | 3 | a0001c0003t0001g0014 a0001c0003t0001g0227 a0001c0003t0001g0230 |
5 | HG01243.hp2 HG02895.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.526+1344G>A | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 2/9 | chr12 | 120990376 | |||||||
chr12:120990393 | C | T | 1 | a0006c0009t0001g0129 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.526+1361C>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 2/9 | chr12 | 120990393 | |||||||
chr12:120990459 | AGCCAGGC others(2): Show |
A | 45 | a0001c0001t0001g0162 a0001c0001t0003g0012 a0001c0001t0003g0023 others(42): Show |
50 | HG00597.hp1 HG01167.hp1 HG01168.hp1 others(47): Show |
intron_variant | MODIFIER | c.526+1429_526+1437d others(11): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 120990459 | ||||||
chr12:120990465 | G | A | 1 | a0004c0008t0001g0269 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.526+1433G>A | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 2/9 | chr12 | 120990465 | |||||||
chr12:120990596 | T | TGATAGGA others(11): Show |
6 | a0001c0001t0001g0035 a0001c0001t0001g0188 a0001c0001t0001g0193 others(3): Show |
7 | HG01358.hp1 HG02004.hp2 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.526+1602_526+1619d others(20): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 120990596 | ||||||
chr12:120990596 | T | TGATAGGA others(11): Show |
2 | a0002c0002t0002g0250 a0002c0002t0002g0278 |
2 | NA18957.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.526+1571_526+1572i others(20): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 120990596 | ||||||
chr12:120990596 | T | TGATAGGA others(29): Show |
1 | a0002c0002t0002g0044 | 2 | HG01433.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.526+1571_526+1572i others(38): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 120990596 | ||||||
chr12:120990596 | TGATAGGA others(11): Show |
T | 49 | a0001c0001t0001g0109 a0001c0001t0001g0162 a0001c0001t0003g0012 others(46): Show |
54 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.526+1602_526+1619d others(20): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 120990596 | ||||||
chr12:120990604 | A | G | 97 | a0001c0001t0001g0022 a0001c0001t0001g0028 a0001c0001t0001g0120 others(94): Show |
147 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.526+1572A>G | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 2/9 | chr12 | 120990604 | |||||||
chr12:120990616 | ATAGGAAA others(29): Show |
A | 8 | a0001c0001t0003g0141 a0001c0001t0003g0142 a0001c0001t0003g0143 others(5): Show |
8 | HG02027.hp1 HG02738.hp2 HG03239.hp2 others(5): Show |
intron_variant | MODIFIER | c.526+1602_526+1637d others(38): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 120990616 | ||||||
chr12:120990616 | ATAGGAAA others(47): Show |
A | 3 | a0004c0013t0001g0063 a0004c0013t0001g0064 a0004c0013t0001g0065 |
3 | HG02818.hp1 HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.526+1600_526+1653d others(56): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 120990616 | ||||||
chr12:120990626 | GAGGAAAG others(2): Show |
G | 7 | a0001c0001t0002g0093 a0001c0003t0002g0020 a0001c0003t0002g0072 others(4): Show |
9 | HG00639.hp1 HG01074.hp2 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.526+1602_526+1610d others(11): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 120990626 | ||||||
chr12:120990626 | GAGGAAAG others(20): Show |
G | 22 | a0001c0001t0002g0198 a0001c0004t0004g0017 a0001c0004t0004g0018 others(19): Show |
25 | HG00140.hp1 HG01071.hp2 HG01123.hp2 others(22): Show |
intron_variant | MODIFIER | c.526+1602_526+1628d others(29): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 120990626 | ||||||
chr12:120990634 | A | ATAGGAAA others(11): Show |
1 | a0001c0001t0001g0028 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.526+1636_526+1653d others(20): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 120990634 | ||||||
chr12:120990634 | A | G | 3 | a0001c0001t0003g0154 a0001c0001t0003g0158 a0006c0009t0001g0129 |
3 | NA18952.hp1 NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.526+1602A>G | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 2/9 | chr12 | 120990634 | |||||||
chr12:120990634 | ATAGGAAA others(11): Show |
A | 26 | a0001c0001t0001g0010 a0001c0001t0001g0083 a0001c0001t0001g0231 others(23): Show |
40 | HG00558.hp2 HG01074.hp1 HG01099.hp1 others(37): Show |
intron_variant | MODIFIER | c.526+1636_526+1653d others(20): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 120990634 | ||||||
chr12:120990634 | ATAGGAAA others(29): Show |
A | 1 | a0001c0004t0015g0089 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.526+1618_526+1653d others(38): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 120990634 | ||||||
chr12:120990652 | G | A | 92 | a0001c0001t0001g0022 a0001c0001t0001g0120 a0001c0001t0001g0130 others(89): Show |
130 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.526+1620G>A | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 2/9 | chr12 | 120990652 | |||||||
chr12:120990652 | G | GTAGGAAA others(29): Show |
1 | a0005c0007t0001g0039 | 2 | HG02109.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.526+1637_526+1638i others(38): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 120990652 | ||||||
chr12:120990652 | G | GTAGGAAA others(83): Show |
1 | a0005c0021t0001g0038 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.526+1637_526+1638i others(92): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 120990652 | ||||||
chr12:120990652 | G | GTAGGAAA others(101): Show |
1 | a0005c0007t0001g0038 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.526+1637_526+1638i others(110): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 120990652 | ||||||
chr12:120990653 | T | G | 1 | a0009c0023t0001g0135 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.526+1621T>G | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 2/9 | chr12 | 120990653 | |||||||
chr12:120990670 | G | A | 2 | a0001c0001t0002g0198 a0002c0002t0002g0258 |
2 | HG01099.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.526+1638G>A | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 2/9 | chr12 | 120990670 | |||||||
chr12:120990671 | T | G | 6 | a0001c0001t0001g0239 a0001c0001t0008g0241 a0001c0001t0008g0242 others(3): Show |
6 | HG01243.hp1 HG01884.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.526+1639T>G | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 2/9 | chr12 | 120990671 | |||||||
chr12:120990680 | G | T | 4 | a0001c0001t0001g0239 a0001c0001t0008g0241 a0001c0001t0008g0242 others(1): Show |
4 | HG01243.hp1 HG02559.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.526+1648G>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 2/9 | chr12 | 120990680 | |||||||
chr12:120990680 | GAGGA | G | 6 | a0001c0001t0001g0120 a0002c0002t0002g0271 a0002c0002t0005g0047 others(3): Show |
7 | HG00099.hp1 HG01934.hp1 NA18946.hp1 others(4): Show |
intron_variant | MODIFIER | c.526+1666_526+1669d others(6): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 120990680 | ||||||
chr12:120990684 | A | AAAGGG | 4 | a0001c0001t0001g0239 a0001c0001t0008g0241 a0001c0001t0008g0242 others(1): Show |
4 | HG01243.hp1 HG02559.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.526+1653_526+1654i others(7): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 120990684 | ||||||
chr12:120990800 | C | A | 47 | a0001c0001t0001g0162 a0001c0001t0003g0012 a0001c0001t0003g0023 others(44): Show |
52 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.526+1768C>A | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 2/9 | chr12 | 120990800 | |||||||
chr12:120990831 | A | G | 1 | a0001c0001t0001g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.526+1799A>G | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 2/9 | chr12 | 120990831 | |||||||
chr12:120990866 | A | G | 1 | a0002c0002t0002g0300 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.526+1834A>G | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 2/9 | chr12 | 120990866 | |||||||
chr12:120990970 | C | T | 1 | a0001c0001t0003g0151 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.526+1938C>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 2/9 | chr12 | 120990970 | |||||||
chr12:120991011 | C | T | 3 | a0001c0001t0001g0005 a0001c0003t0001g0005 a0001c0018t0001g0234 |
6 | HG02257.hp1 HG02280.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.526+1979C>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 2/9 | chr12 | 120991011 | |||||||
chr12:120991084 | C | T | 1 | a0001c0001t0001g0232 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.526+2052C>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 2/9 | chr12 | 120991084 | |||||||
chr12:120991235 | G | T | 1 | a0005c0007t0001g0039 | 2 | HG02109.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.526+2203G>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 2/9 | chr12 | 120991235 | |||||||
chr12:120991391 | T | C | 158 | a0001c0001t0001g0025 a0001c0001t0001g0028 a0001c0001t0001g0113 others(155): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.527-2129T>C | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 2/9 | chr12 | 120991391 | |||||||
chr12:120991593 | AATAAATG others(5): Show |
A | 34 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0025 others(31): Show |
40 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.527-1924_527-1913d others(14): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 120991593 | ||||||
chr12:120991613 | TATGTATG others(8): Show |
T | 147 | a0001c0001t0001g0120 a0001c0001t0001g0162 a0001c0001t0003g0012 others(144): Show |
200 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.527-1891_527-1877d others(17): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 120991613 | ||||||
chr12:120991617 | TATGTATG others(4): Show |
T | 77 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(74): Show |
97 | HG00438.hp1 HG00609.hp2 HG00621.hp1 others(94): Show |
intron_variant | MODIFIER | c.527-1891_527-1881d others(13): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 120991617 | ||||||
chr12:120991621 | TATGTATG | T | 11 | a0001c0001t0001g0193 a0001c0001t0002g0093 a0001c0003t0002g0101 others(8): Show |
12 | HG01071.hp2 HG01123.hp2 HG01358.hp2 others(9): Show |
intron_variant | MODIFIER | c.527-1891_527-1885d others(9): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 120991621 | ||||||
chr12:120991625 | TATG | T | 58 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0025 others(55): Show |
66 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.527-1891_527-1889d others(5): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 120991625 | ||||||
chr12:120991628 | G | GT | 21 | a0001c0003t0001g0217 a0001c0003t0002g0070 a0001c0003t0002g0071 others(18): Show |
23 | HG00639.hp1 HG00642.hp1 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.527-1892_527-1891i others(3): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 2/9 | chr12 | 120991628 | |||||||
chr12:120991628 | G | GTATGT | 6 | a0001c0004t0001g0061 a0001c0006t0001g0004 a0006c0009t0001g0129 others(3): Show |
8 | HG00735.hp1 HG00738.hp1 HG01069.hp2 others(5): Show |
intron_variant | MODIFIER | c.527-1892_527-1891i others(7): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 2/9 | chr12 | 120991628 | |||||||
chr12:120991640 | T | C | 2 | a0002c0002t0002g0043 a0009c0023t0001g0135 |
3 | HG00609.hp2 HG00621.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.527-1880T>C | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 2/9 | chr12 | 120991640 | |||||||
chr12:120991644 | C | T | 3 | a0001c0003t0001g0037 a0001c0003t0001g0228 a0001c0019t0011g0245 |
4 | HG01243.hp1 HG02257.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.527-1876C>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 2/9 | chr12 | 120991644 | |||||||
chr12:120991817 | G | GTTAGAAC others(72): Show |
1 | a0004c0013t0001g0065 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.527-1702_527-1624d others(81): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 120991817 | ||||||
chr12:120991877 | A | T | 1 | a0002c0002t0002g0258 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.527-1643A>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 2/9 | chr12 | 120991877 | |||||||
chr12:120991965 | A | G | 1 | a0001c0001t0001g0106 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.527-1555A>G | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 2/9 | chr12 | 120991965 | |||||||
chr12:120991984 | T | C | 1 | a0001c0004t0015g0089 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.527-1536T>C | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 2/9 | chr12 | 120991984 | |||||||
chr12:120992098 | A | G | 14 | a0001c0003t0001g0217 a0001c0004t0001g0061 a0001c0006t0001g0004 others(11): Show |
17 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.527-1422A>G | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 2/9 | chr12 | 120992098 | |||||||
chr12:120992474 | C | T | 1 | a0001c0004t0001g0187 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.527-1046C>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 2/9 | chr12 | 120992474 | |||||||
chr12:120992526 | T | C | 7 | a0001c0001t0002g0093 a0001c0001t0002g0198 a0001c0003t0002g0020 others(4): Show |
9 | HG00639.hp1 HG01074.hp2 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.527-994T>C | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 2/9 | chr12 | 120992526 | |||||||
chr12:120992534 | A | ACTTTTAA others(109): Show |
1 | a0001c0003t0003g0178 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.527-983_527-868dup others(116): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 120992534 | ||||||
chr12:120992734 | C | A | 26 | a0001c0004t0001g0237 a0001c0004t0004g0017 a0001c0004t0004g0018 others(23): Show |
29 | HG00140.hp1 HG01071.hp2 HG01123.hp2 others(26): Show |
intron_variant | MODIFIER | c.527-786C>A | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 2/9 | chr12 | 120992734 | |||||||
chr12:120992815 | C | A | 11 | a0001c0001t0002g0093 a0001c0001t0002g0198 a0001c0003t0002g0020 others(8): Show |
13 | HG00639.hp1 HG01074.hp2 HG01255.hp2 others(10): Show |
intron_variant | MODIFIER | c.527-705C>A | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 2/9 | chr12 | 120992815 | |||||||
chr12:120992983 | A | G | 1 | a0001c0001t0001g0197 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.527-537A>G | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 2/9 | chr12 | 120992983 | |||||||
chr12:120992984 | C | A | 1 | a0001c0001t0001g0197 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.527-536C>A | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 2/9 | chr12 | 120992984 | |||||||
chr12:120993019 | C | T | 31 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0026 others(28): Show |
35 | HG00609.hp1 HG00673.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.527-501C>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 2/9 | chr12 | 120993019 | |||||||
chr12:120993059 | G | A | 1 | a0001c0001t0001g0118 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.527-461G>A | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 2/9 | chr12 | 120993059 | |||||||
chr12:120993205 | A | T | 1 | a0001c0001t0001g0197 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.527-315A>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 2/9 | chr12 | 120993205 | |||||||
chr12:120993393 | G | A | 2 | a0001c0001t0003g0031 a0001c0001t0003g0168 |
3 | NA18945.hp1 NA18949.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.527-127G>A | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 2/9 | chr12 | 120993393 | |||||||
chr12:120993422 | G | A | 92 | a0002c0002t0002g0001 a0002c0002t0002g0003 a0002c0002t0002g0006 others(89): Show |
142 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.527-98G>A | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 2/9 | chr12 | 120993422 | |||||||
chr12:120993469 | T | A | 87 | a0001c0001t0001g0025 a0001c0001t0001g0028 a0001c0001t0001g0113 others(84): Show |
97 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.527-51T>A | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 2/9 | chr12 | 120993469 | |||||||
chr12:120993497 | C | T | 92 | a0002c0002t0002g0001 a0002c0002t0002g0003 a0002c0002t0002g0006 others(89): Show |
142 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.527-23C>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 2/9 | chr12 | 120993497 | |||||||
chr12:120994496 | C | T | 33 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0026 others(30): Show |
37 | HG00438.hp2 HG00597.hp2 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.955+91C>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 4/9 | chr12 | 120994496 | |||||||
chr12:120994499 | T | G | 152 | a0001c0001t0001g0025 a0001c0001t0001g0028 a0001c0001t0001g0113 others(149): Show |
209 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.955+94T>G | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 4/9 | chr12 | 120994499 | |||||||
chr12:120994532 | TTATCACT others(4): Show |
T | 1 | a0001c0003t0003g0178 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.955+129_955+139del others(11): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | 120994532 | ||||||
chr12:120994544 | T | C | 1 | a0001c0003t0003g0178 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.955+139T>C | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 4/9 | chr12 | 120994544 | |||||||
chr12:120994595 | T | G | 1 | a0001c0003t0003g0178 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.955+190T>G | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 4/9 | chr12 | 120994595 | |||||||
chr12:120994601 | C | T | 1 | a0004c0013t0001g0065 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.955+196C>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 4/9 | chr12 | 120994601 | |||||||
chr12:120994622 | C | G | 1 | a0001c0003t0003g0178 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.955+217C>G | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 4/9 | chr12 | 120994622 | |||||||
chr12:120994624 | A | T | 1 | a0001c0003t0003g0178 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.955+219A>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 4/9 | chr12 | 120994624 | |||||||
chr12:120994631 | A | C | 1 | a0004c0013t0001g0065 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.955+226A>C | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 4/9 | chr12 | 120994631 | |||||||
chr12:120994634 | C | T | 1 | a0001c0003t0003g0178 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.955+229C>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 4/9 | chr12 | 120994634 | |||||||
chr12:120994682 | T | G | 1 | a0001c0003t0003g0178 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.955+277T>G | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 4/9 | chr12 | 120994682 | |||||||
chr12:120994725 | C | A | 1 | a0004c0013t0001g0065 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.955+320C>A | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 4/9 | chr12 | 120994725 | |||||||
chr12:120994726 | G | A | 1 | a0001c0003t0003g0178 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.955+321G>A | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 4/9 | chr12 | 120994726 | |||||||
chr12:120994726 | G | C | 1 | a0004c0013t0001g0065 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.955+321G>C | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 4/9 | chr12 | 120994726 | |||||||
chr12:120994733 | T | C | 1 | a0004c0013t0001g0065 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.955+328T>C | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 4/9 | chr12 | 120994733 | |||||||
chr12:120994742 | TCCACTAC others(67): Show |
T | 1 | a0001c0003t0003g0178 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.955+339_955+412del others(74): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | 120994742 | ||||||
chr12:120994800 | C | T | 104 | a0001c0001t0002g0093 a0001c0001t0002g0198 a0001c0003t0002g0020 others(101): Show |
156 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.955+395C>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 4/9 | chr12 | 120994800 | |||||||
chr12:120994802 | C | A | 1 | a0004c0013t0001g0065 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.955+397C>A | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 4/9 | chr12 | 120994802 | |||||||
chr12:120994803 | A | C | 1 | a0004c0013t0001g0065 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.955+398A>C | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 4/9 | chr12 | 120994803 | |||||||
chr12:120994849 | A | T | 1 | a0004c0013t0001g0065 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.955+444A>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 4/9 | chr12 | 120994849 | |||||||
chr12:120994851 | T | A | 1 | a0004c0013t0001g0065 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.955+446T>A | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 4/9 | chr12 | 120994851 | |||||||
chr12:120994855 | T | C | 1 | a0004c0013t0001g0065 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.955+450T>C | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 4/9 | chr12 | 120994855 | |||||||
chr12:120994863 | TACTCCAT others(7): Show |
T | 14 | a0001c0004t0001g0061 a0001c0004t0001g0187 a0001c0006t0001g0004 others(11): Show |
17 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.955+469_955+482del others(14): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | 120994863 | ||||||
chr12:120994885 | C | G | 1 | a0001c0003t0003g0178 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.955+480C>G | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 4/9 | chr12 | 120994885 | |||||||
chr12:120994917 | T | C | 1 | a0004c0013t0001g0065 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.955+512T>C | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 4/9 | chr12 | 120994917 | |||||||
chr12:120994937 | TCCACTCC others(3): Show |
T | 1 | a0004c0013t0001g0065 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.955+534_955+543del others(10): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | 120994937 | ||||||
chr12:120994959 | A | T | 1 | a0004c0013t0001g0065 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.955+554A>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 4/9 | chr12 | 120994959 | |||||||
chr12:120994962 | T | C | 1 | a0004c0013t0001g0065 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.955+557T>C | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 4/9 | chr12 | 120994962 | |||||||
chr12:120994967 | C | T | 1 | a0004c0013t0001g0065 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.955+562C>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 4/9 | chr12 | 120994967 | |||||||
chr12:120995037 | T | C | 1 | a0004c0013t0001g0065 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.955+632T>C | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 4/9 | chr12 | 120995037 | |||||||
chr12:120995039 | C | T | 1 | a0004c0013t0001g0065 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.955+634C>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 4/9 | chr12 | 120995039 | |||||||
chr12:120995090 | T | C | 2 | a0002c0002t0005g0291 a0002c0002t0005g0292 |
2 | NA18964.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.955+685T>C | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 4/9 | chr12 | 120995090 | |||||||
chr12:120995124 | T | C | 1 | a0004c0013t0001g0065 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.955+719T>C | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 4/9 | chr12 | 120995124 | |||||||
chr12:120995125 | C | T | 1 | a0004c0013t0001g0065 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.955+720C>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 4/9 | chr12 | 120995125 | |||||||
chr12:120995217 | C | T | 1 | a0001c0019t0011g0245 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.955+812C>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 4/9 | chr12 | 120995217 | |||||||
chr12:120995534 | C | G | 1 | a0003c0012t0002g0254 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.956-728C>G | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 4/9 | chr12 | 120995534 | |||||||
chr12:120995740 | A | C | 1 | a0001c0004t0015g0089 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.956-522A>C | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 4/9 | chr12 | 120995740 | |||||||
chr12:120996013 | C | T | 10 | a0002c0002t0002g0263 a0002c0002t0002g0272 a0002c0002t0002g0282 others(7): Show |
16 | HG01952.hp1 HG02074.hp1 NA18747.hp1 others(13): Show |
intron_variant | MODIFIER | c.956-249C>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 4/9 | chr12 | 120996013 | |||||||
chr12:120996041 | A | G | 244 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0025 others(241): Show |
313 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(310): Show |
intron_variant | MODIFIER | c.956-221A>G | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 4/9 | chr12 | 120996041 | |||||||
chr12:120996422 | C | G | 4 | a0002c0002t0002g0011 a0002c0002t0002g0043 a0002c0002t0002g0256 others(1): Show |
8 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(5): Show |
intron_variant | MODIFIER | c.1107+9C>G | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 5/9 | chr12 | 120996422 | |||||||
chr12:120996499 | G | T | 31 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0026 others(28): Show |
35 | HG00609.hp1 HG00673.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.1108-42G>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 5/9 | chr12 | 120996499 | |||||||
chr12:120996768 | C | T | 3 | a0001c0001t0001g0236 a0001c0001t0001g0238 a0004c0008t0001g0090 |
3 | HG02258.hp2 HG03130.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1309+26C>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 6/9 | chr12 | 120996768 | |||||||
chr12:120996794 | C | T | 1 | a0005c0007t0001g0039 | 2 | HG02109.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1309+52C>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 6/9 | chr12 | 120996794 | |||||||
chr12:120996797 | A | G | 1 | a0001c0001t0001g0193 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1309+55A>G | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 6/9 | chr12 | 120996797 | |||||||
chr12:120996827 | C | CTCATTCA others(1): Show |
244 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0025 others(241): Show |
313 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(310): Show |
intron_variant | MODIFIER | c.1309+94_1309+101du others(9): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr12 | 120996827 | ||||||
chr12:120996849 | A | G | 3 | a0001c0003t0004g0107 a0001c0003t0004g0126 a0001c0003t0004g0138 |
3 | HG02738.hp2 HG03239.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1309+107A>G | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 6/9 | chr12 | 120996849 | |||||||
chr12:120996929 | T | A | 1 | a0001c0001t0001g0106 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1309+187T>A | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 6/9 | chr12 | 120996929 | |||||||
chr12:120997030 | G | A | 104 | a0001c0001t0002g0093 a0001c0001t0002g0198 a0001c0003t0002g0020 others(101): Show |
156 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.1309+288G>A | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 6/9 | chr12 | 120997030 | |||||||
chr12:120997378 | G | A | 7 | a0001c0001t0002g0093 a0001c0001t0002g0198 a0001c0003t0002g0020 others(4): Show |
9 | HG00639.hp1 HG01074.hp2 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.1310-96G>A | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 6/9 | chr12 | 120997378 | |||||||
chr12:120997378 | G | T | 35 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0026 others(32): Show |
39 | HG00609.hp1 HG00673.hp2 HG01106.hp1 others(36): Show |
intron_variant | MODIFIER | c.1310-96G>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 6/9 | chr12 | 120997378 | |||||||
chr12:120997462 | C | T | 2 | a0001c0001t0001g0022 a0001c0001t0001g0131 |
3 | HG02602.hp2 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1310-12C>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 6/9 | chr12 | 120997462 | |||||||
chr12:120997672 | G | A | 104 | a0001c0001t0002g0093 a0001c0001t0002g0198 a0001c0003t0002g0020 others(101): Show |
156 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(153): Show |
splice_region_variant&intron_variant | LOW | c.1501+7G>A | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 7/9 | chr12 | 120997672 | |||||||
chr12:120997730 | G | C | 4 | a0001c0003t0002g0070 a0001c0003t0002g0071 a0001c0003t0002g0072 others(1): Show |
4 | HG03490.hp2 HG03492.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.1501+65G>C | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 7/9 | chr12 | 120997730 | |||||||
chr12:120997733 | A | G | 3 | a0001c0003t0002g0020 a0004c0008t0002g0100 a0007c0016t0002g0021 |
5 | HG00639.hp1 HG01074.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.1501+68A>G | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 7/9 | chr12 | 120997733 | |||||||
chr12:120997784 | G | T | 103 | a0001c0001t0002g0093 a0001c0001t0002g0198 a0001c0003t0002g0020 others(100): Show |
155 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.1501+119G>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 7/9 | chr12 | 120997784 | |||||||
chr12:120997968 | A | G | 1 | a0003c0005t0002g0091 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1501+303A>G | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 7/9 | chr12 | 120997968 | |||||||
chr12:120997975 | C | T | 61 | a0001c0001t0001g0025 a0001c0001t0001g0028 a0001c0001t0001g0113 others(58): Show |
68 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.1501+310C>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 7/9 | chr12 | 120997975 | |||||||
chr12:120998032 | C | A | 1 | a0001c0001t0002g0198 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1501+367C>A | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 7/9 | chr12 | 120998032 | |||||||
chr12:120998140 | C | G | 7 | a0001c0001t0003g0033 a0001c0001t0003g0173 a0001c0001t0003g0174 others(4): Show |
8 | HG02040.hp2 HG02523.hp1 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.1501+475C>G | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 7/9 | chr12 | 120998140 | |||||||
chr12:120998280 | C | CA | 60 | a0001c0001t0001g0025 a0001c0001t0001g0028 a0001c0001t0001g0113 others(57): Show |
67 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.1501+629dupA | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 120998280 | ||||||
chr12:120998280 | CA | C | 168 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0026 others(165): Show |
228 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.1501+629delA | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 120998280 | ||||||
chr12:120998521 | G | A | 1 | a0001c0001t0003g0159 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1502-747G>A | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 7/9 | chr12 | 120998521 | |||||||
chr12:120998573 | A | C | 167 | a0001c0001t0001g0025 a0001c0001t0001g0028 a0001c0001t0001g0113 others(164): Show |
226 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.1502-695A>C | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 7/9 | chr12 | 120998573 | |||||||
chr12:120998588 | T | C | 9 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0002c0002t0002g0048 others(6): Show |
10 | NA18942.hp1 NA18954.hp2 NA18964.hp2 others(7): Show |
intron_variant | MODIFIER | c.1502-680T>C | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 7/9 | chr12 | 120998588 | |||||||
chr12:120998699 | T | C | 1 | a0009c0023t0001g0135 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1502-569T>C | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 7/9 | chr12 | 120998699 | |||||||
chr12:120998825 | TTTAGTAC others(14): Show |
T | 1 | a0001c0019t0011g0245 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1502-434_1502-414d others(23): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 120998825 | ||||||
chr12:120998926 | CGCTTAGT others(13): Show |
C | 1 | a0001c0001t0001g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1502-332_1502-313d others(22): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 120998926 | ||||||
chr12:120998927 | G | A | 1 | a0002c0002t0002g0007 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1502-341G>A | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 7/9 | chr12 | 120998927 | |||||||
chr12:120999189 | C | G | 2 | a0002c0002t0002g0274 a0002c0002t0002g0275 |
2 | NA18942.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.1502-79C>G | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 7/9 | chr12 | 120999189 | |||||||
chr12:120999207 | G | A | 1 | a0001c0003t0002g0070 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1502-61G>A | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 7/9 | chr12 | 120999207 | |||||||
chr12:120999418 | T | C | 250 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0025 others(247): Show |
322 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(319): Show |
intron_variant | MODIFIER | c.1623+29T>C | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 8/9 | chr12 | 120999418 | |||||||
chr12:120999464 | G | A | 4 | a0001c0003t0002g0070 a0001c0003t0002g0071 a0001c0003t0002g0072 others(1): Show |
4 | HG03490.hp2 HG03492.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.1624-19G>A | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 8/9 | chr12 | 120999464 | |||||||
chr12:120999671 | C | T | 3 | a0001c0004t0004g0017 a0001c0004t0004g0075 a0001c0004t0004g0085 |
4 | HG00140.hp1 HG01516.hp2 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.1768+44C>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 9/9 | chr12 | 120999671 | |||||||
chr12:120999760 | G | T | 1 | a0001c0001t0002g0093 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1768+133G>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 9/9 | chr12 | 120999760 | |||||||
chr12:120999999 | A | G | 60 | a0001c0001t0001g0025 a0001c0001t0001g0028 a0001c0001t0001g0113 others(57): Show |
67 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.1768+372A>G | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 9/9 | chr12 | 120999999 | |||||||
chr12:121000075 | CAT | C | 31 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0026 others(28): Show |
35 | HG00609.hp1 HG00673.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.1768+452_1768+453d others(4): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr12 | 121000075 | ||||||
chr12:121000135 | G | A | 30 | a0001c0001t0001g0009 a0001c0001t0001g0035 a0001c0001t0001g0036 others(27): Show |
33 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.1768+508G>A | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 9/9 | chr12 | 121000135 | |||||||
chr12:121000161 | T | C | 2 | a0002c0002t0002g0045 a0008c0027t0002g0045 |
2 | HG01069.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.1768+534T>C | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 9/9 | chr12 | 121000161 | |||||||
chr12:121000339 | C | T | 26 | a0001c0004t0001g0237 a0001c0004t0004g0017 a0001c0004t0004g0018 others(23): Show |
29 | HG00140.hp1 HG01071.hp2 HG01123.hp2 others(26): Show |
intron_variant | MODIFIER | c.1768+712C>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 9/9 | chr12 | 121000339 | |||||||
chr12:121000508 | C | T | 104 | a0001c0001t0002g0093 a0001c0001t0002g0198 a0001c0003t0002g0020 others(101): Show |
156 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.1769-557C>T | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 9/9 | chr12 | 121000508 | |||||||
chr12:121000579 | T | C | 225 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0025 others(222): Show |
291 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(288): Show |
intron_variant | MODIFIER | c.1769-486T>C | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 9/9 | chr12 | 121000579 | |||||||
chr12:121000605 | G | A | 1 | a0002c0002t0002g0273 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1769-460G>A | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 9/9 | chr12 | 121000605 | |||||||
chr12:121000906 | G | GTT | 244 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0025 others(241): Show |
313 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(310): Show |
intron_variant | MODIFIER | c.1769-159_1769-158i others(4): Show |
HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 9/9 | chr12 | 121000906 | |||||||
chr12:121000944 | T | A | 4 | a0001c0003t0002g0070 a0001c0003t0002g0071 a0001c0003t0002g0072 others(1): Show |
4 | HG03490.hp2 HG03492.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.1769-121T>A | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 9/9 | chr12 | 121000944 | |||||||
chr12:121001041 | T | C | 104 | a0001c0001t0002g0093 a0001c0001t0002g0198 a0001c0003t0002g0020 others(101): Show |
156 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.1769-24T>C | HNF1A | ENSG00000135100.19 | transcript | ENST00000257555.11 | protein_coding | 9/9 | chr12 | 121001041 |