chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
51690580416905805TC67GENIChomozygous113675387
51690622016906221CT78GENIChomozygous113675389
51690702516907026GC47GENIChomozygous113675391
51690709316907094AG41GENICpossibly homozygous113675393
51690748216907483CT36GENICpossibly homozygous113675397
51690905616909057AG73GENIChomozygous113675399
51691035216910353CT46GENIChomozygous113675401
51691231716912318GA43GENIChomozygous113675403
51691665716916658GA46GENIChomozygous113675405
51691762116917622AG87GENICpossibly homozygous113675407
51691797416917975CA111GENICheterozygous114108818
51691252716912528CT46GENICheterozygous114108813
51691793316917934TC97GENICheterozygous114108814
51691793416917935GA98GENICheterozygous114108815
51691794716917948AC110GENICheterozygous114108816
51691796916917970CG112GENICheterozygous114108817
51691801216918013CA92GENICheterozygous114108819
51691803116918032GA80GENICheterozygous114108820
51691832416918325AT57GENIChomozygous113675411
51691955016919551CA152GENICheterozygous114108821
51691956616919567GA156GENICheterozygous114108822
51691963316919634GC98GENICheterozygous113675413
51691974416919745TC61GENIChomozygous113675415
51691978616919787AC62GENICpossibly homozygous113675417
51692257716922578GA60GENIChomozygous113675421
51692430316924304TC54GENIChomozygous113675423
51692457316924574TC56GENICpossibly homozygous113675425
51692562616925627AG56GENIChomozygous113675427
51692655916926560CT61GENICpossibly homozygous113675429