chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1254751696254751697AAACACAC6GENIChomozygous61165513
1254752437254752439GT--12GENIChomozygous61165514
1254753805254753806AC60GENIChomozygous61165515
1254753917254753918CT61GENIChomozygous61165516
1254754437254754443TTTAGT------19GENIChomozygous61165517
1254754442254754443T-20GENIChomozygous61165518
1254754518254754519AAT26GENIChomozygous61165519
1254754611254754612TA31GENIChomozygous61165520
1254754808254754814CAGCAG------12GENIChomozygous61165521
1254754831254754832GA40GENICheterozygous61165522
1254755818254755819CA23GENIChomozygous61165523
1254755819254755820CG21GENIChomozygous61165524
1254755893254755903CGCGCGCGCG----------8GENICpossibly homozygous61165525
1254756636254756637AAAT1GENIChomozygous61165526
1254757075254757076GT52GENIChomozygous61165527
1254757592254757610CAGTGGATTCCCGACACT------------------20GENIChomozygous61165528
1254758636254758637T-44GENIChomozygous61165529
1254758749254758750CG36GENIChomozygous61165530
1254758780254758786ACACAC------18GENICpossibly homozygous61165531
1254758803254758804CT34GENICheterozygous61165532
1254758827254758828TTAC26GENIChomozygous61165533
1254758954254758955GT32GENIChomozygous61165534
1254759079254759080AG40GENIChomozygous61165535
1254759677254759678CCTTT34GENIChomozygous61165536
1254760067254760072GGTTC-----14GENIChomozygous61165537
1254760098254760099GGA19GENICpossibly homozygous61165538
1254760113254760114AG34GENICpossibly homozygous61165539
1254760216254760217AG35GENIChomozygous61165540
1254760793254760795AA--19GENIChomozygous61165541
1254760934254760935TC21GENIChomozygous61165542
1254760958254760959AAT25GENIChomozygous61165543
1254761476254761477GA63GENIChomozygous61165544
1254761867254761869CG--19GENIChomozygous61165545
1254761875254761877CA--16GENICheterozygous61165546
1254762700254762701GA59GENIChomozygous61165547
1254763023254763024GA43GENIChomozygous61165548