chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
153715670037156701CT28GENICheterozygous48501538
153715747137157472GC23GENICheterozygous48501548
153715812737158128CT37GENICheterozygous48501551
153716260537162606CG27INTERGENICheterozygous48501583
153716501237165013GA24GENICheterozygous48501588
153716910437169105AG23GENICheterozygous48501608
153716999237169993TC20GENICheterozygous48501610
153717322337173224AAAAAAAT30GENICheterozygous49119030
153718078837180789TC22GENICheterozygous48501669
153718195137181952TC21GENICheterozygous48501675
153718196137181962GA21GENICheterozygous48501677
153721750437217505TC11GENICheterozygous48501842
153722158437221585TC33GENICheterozygous48501866
153722197037221971TC18GENICheterozygous49498190
153722197937221980CCAAA19GENICheterozygous49048601
153722198337221984CA18GENICheterozygous49498192
153722198737221988TC19GENICheterozygous49498194
153722199037221991CT19GENICheterozygous48501868
153722199037221991CCAT19GENICheterozygous49560877
153722199837221999CA22GENICheterozygous49498196
153722200237222003AC21GENICheterozygous49498198
153722203437222035CG31GENICheterozygous49498200
153722205037222051AG29GENICheterozygous49498201
153722206937222070TA23GENICheterozygous49566377
153722207037222071AG23GENICheterozygous49566379
153722207237222073TG23GENICheterozygous49498203
153722207437222075GA18GENICheterozygous49566382
153722207837222079AG18GENICheterozygous49498204
153722208137222082GT19GENICheterozygous49498206
153722510437225105TC40GENICheterozygous48501894
153722596837225969GA23GENICheterozygous48501900
153722600437226005TTTCTTA24GENICheterozygous48501902
153722623937226240TC33GENICheterozygous48501904
153722685937226860GA16GENICheterozygous48501906
153722690737226908AG6GENICheterozygous48501908
153722718037227181CT23GENICheterozygous48501910