chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4143595239143595240TA23GENIChomozygous581838718
4143595754143595755AG35GENIChomozygous581838719
4143596309143596310GA24GENIChomozygous584599513
4143597231143597232AAATAT12GENIChomozygous719391649
4143597443143597444AT26GENIChomozygous584599514
4143598137143598138GGA26GENICpossibly homozygous719391650
4143598221143598222CA25GENIChomozygous581838720
4143598596143598597CT15GENIChomozygous584599515
4143599907143599908TC56GENIChomozygous581838721
4143600914143600916AA--12GENICheterozygous719391653
4143600915143600916A-12GENICheterozygous719391654
4143603066143603067A-15GENIChomozygous719391657
4143604389143604390TC23GENIChomozygous584599516
4143604440143604441C-17GENIChomozygous719391658
4143605245143605246AATT19GENIChomozygous719391660
4143605468143605469GT13GENIChomozygous581838722
4143606108143606109CCT13GENIChomozygous719391661
4143606224143606225AG29GENIChomozygous584599517
4143606248143606249TC32GENIChomozygous584599518
4143606935143606936TG22GENIChomozygous584599519
4143606958143606961CCC---13GENIChomozygous719391662
4143607052143607053T-14GENIChomozygous719391664
4143609308143609309AAT19GENICheterozygous719391665
4143609647143609650ACG---37GENIChomozygous719391668
4143610209143610210GGT5GENICheterozygous719391670
4143610355143610356AG36GENIChomozygous581838723
4143610545143610546CA26GENIChomozygous584599520
4143610766143610767GA21GENIChomozygous584599521
4143611152143611153AT16GENIChomozygous581838724
4143611578143611579A-25GENIChomozygous719391672
4143612108143612109A-17GENICpossibly homozygous719391673
4143612122143612129AAAAAAA-------9GENICheterozygous719391674
4143612124143612129AAAAA-----9GENICheterozygous719391675
4143613236143613237AT17GENIChomozygous584599522