chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
12300587123005872AG17GENICpossibly homozygous61273480
12300648123006482AG19GENICpossibly homozygous61273481
12300663923006640AC19GENICheterozygous62526746
12300664023006641GT19GENICheterozygous62526747
12300947923009481TT--4GENICheterozygous61273485
12300988023009881AT25GENIChomozygous62526748
12300995123009952GA24GENICpossibly homozygous62526749
12301010323010104GA22GENIChomozygous61273487
12301046723010468GT10GENIChomozygous61395140
12301081723010818AG27GENIChomozygous62526750
12301106923011070AG26GENIChomozygous61273489
12301122323011224TG15GENICpossibly homozygous61273490
12301125423011255GC13GENIChomozygous61273491
12301130323011304AG3GENIChomozygous61273492
12301136823011369AG1GENIChomozygous61273493
12301137923011380A-1GENIChomozygous62072643
12301138023011381AG1GENIChomozygous62072645
12301176223011763TC17GENIChomozygous61273495
12301178123011782CG7GENIChomozygous61273496
12301178523011786GA10GENIChomozygous61273497
12301202023012021TC13GENICheterozygous61273498
12301284823012849AG1GENIChomozygous62526751
12301293323012937AAAA----1GENIChomozygous61273502
12301306723013068T-7GENICheterozygous61273503
12301348323013484TC17GENICheterozygous62526752
12301349823013499TC12GENICpossibly homozygous61273504
12301619723016198GGTA8GENICpossibly homozygous61395155
12301624223016243AATAATGTT1GENIChomozygous61395157
12301635923016360GA9GENIChomozygous61981265