chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
31541025215410253AG37GENICpossibly homozygous111454662
31541051115410512CG38GENIChomozygous112437316
31541051615410517AC40GENICpossibly homozygous112264261
31541239515412396AG59GENIChomozygous111454664
31541559215415593AC26GENIChomozygous111454665
31541565015415651CT47GENIChomozygous111454666
31541566415415665CT44GENIChomozygous111454667
31541594815415949GA28GENIChomozygous111454668
31541670915416710GA30GENIChomozygous111454669
31541704415417045TG19GENIChomozygous111454670
31541745315417454AG30GENIChomozygous111454671
31541810615418107AG21GENIChomozygous111454672
31541823715418238AG32GENIChomozygous111454673
31541851515418516CA28GENIChomozygous111454674
31541880815418809TC21GENIChomozygous111454675
31541900115419002TC33GENIChomozygous111454676
31541929715419298TC24GENIChomozygous111454677
31541969415419695CG47GENIChomozygous111454678
31542009015420091TC37GENIChomozygous111454679
31542138415421385TG33GENIChomozygous111454680
31542208815422089GC50GENIChomozygous111454681
31542404815424049GA31GENIChomozygous111454682
31542546915425470TC33GENIChomozygous111454684
31542651715426518AT48GENIChomozygous111454685
31542762415427625TC26GENIChomozygous111454687
31542770715427708TC24GENIChomozygous111454688
31542825615428257CT17GENIChomozygous111454689
31542855615428557TC34GENIChomozygous111454690
31542864915428650GA35GENIChomozygous111454691
31542905915429060GA23GENIChomozygous111454692
31542908815429089CG26GENIChomozygous111454693
31542922415429225CG37GENIChomozygous111454694
31542947015429471TA45GENIChomozygous111454695
31542952115429522TC36GENIChomozygous111454696
31542962415429625GA28GENIChomozygous111454697
31542968415429685AG25GENICpossibly homozygous111454698
31542969815429699GA25GENIChomozygous111454699
31543043115430432AG58GENIChomozygous111454700
31543059115430592GA32GENIChomozygous111454701
31543072415430725GT36GENIChomozygous111454702
31543106215431063CT16GENICpossibly homozygous111454703
31543171815431719TC45GENIChomozygous111454704