chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
144417005544170056GC25GENIChomozygous139527738
144417009444170095AG23GENIChomozygous139527739
144417013144170132CG20GENIChomozygous139527740
144417031944170323AAAG12GENIChomozygous139396235
144417106644171067AG16GENIChomozygous139527741
144417150844171509TC15GENIChomozygous139527742
144417245444172455CT26GENICpossibly homozygous139527743
144417273044172731AC10GENIChomozygous139527744
144417281044172810G14GENIChomozygous139396236
144417196344171964CT20GENICheterozygous145189552
144417197944171980TC22GENICheterozygous145189553
144417452244174523CT9GENIChomozygous139527745
144417524144175241CAGCGAGTTAGA13GENIChomozygous139396237
144417557344175574TA15GENIChomozygous139527746
144417799644177997AC20GENIChomozygous139527747
144418086944180870GA12GENIChomozygous139527748
144418159744181602AAAAG20GENIChomozygous139396238
144418304844183049AG13GENIChomozygous139527749
144418327944183280GA14GENIChomozygous139527750
144418371944183720TC22GENIChomozygous139527751
144418514844185148GCCACGCCTACTT23GENIChomozygous139396239
144418671344186713CGTGACTGTGACAACATGAGGCCA12GENIChomozygous139396240
144418777144187772GA22GENIChomozygous139527752
144418885844188859CT14GENIChomozygous139527753
144418971244189713TA21GENIChomozygous139527754
144419053144190532TG16GENIChomozygous139527755
144419113744191138AG20GENIChomozygous139527756
144419226344192264GA23GENIChomozygous139527757
144419926344199264GA21GENIChomozygous139527762
144419313344193134TC18GENIChomozygous139527758
144419454544194546CT15GENIChomozygous139527759
144419806044198061CT19GENIChomozygous139527760
144419905044199051GA14GENIChomozygous139527761
144419041944190420A19GENICheterozygous141043425