chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
151401254314012544C-6GENICheterozygous48232683
151401254514012546GGT6GENICheterozygous48232684
151401409314014094CT27GENICpossibly homozygous49322719
151403634114036343TT--7GENICheterozygous48465435
151404844214048443TTA5GENIChomozygous48232689
151404846014048461TG3GENIChomozygous48232690
151404846314048464CA4GENIChomozygous48232691
151405399614053997CCGT2GENICheterozygous48465463
151406809014068091CT27GENIChomozygous49322720
151407180914071810GGT4GENICheterozygous48232696
151409410514094106C-6GENIChomozygous48232699
151410055814100559AG7GENICheterozygous48887496
151411249414112496TT--12GENIChomozygous48232703
151411261814112619GGT18GENIChomozygous48232704
151413551614135517T-8GENICheterozygous49164105
151414045014140451CCATAT1GENIChomozygous49117507
151414970414149790GCCGTGTTTCACAGCTGTACACTGCATTTCTACCTGGAGTGAGCAGTGTTTCACAGCTGGATAGGGTATTTCCGCCGACAGTGAGG--------------------------------------------------------------------------------------62GENICheterozygous49270319
151417066514170666GGT2GENICheterozygous48232712
151417204514172046GT3GENIChomozygous48232714
151417204714172048CT1GENIChomozygous48564964
151417204814172049TA1GENIChomozygous48232715
151417206014172061GT2GENIChomozygous49036032
151417206214172063TA2GENIChomozygous48232716
151417206714172068TG4GENIChomozygous48232717
151418818614188187AAG3GENIChomozygous48232718
151420224614202247C-3GENICheterozygous49185340
151420313614203137GT10GENICheterozygous48232720
151420486514204866T-4GENICheterozygous48665609
151420668714206688GC8GENICheterozygous48232723
151421667814216679A-9GENIChomozygous48232724
151421669514216696GT12GENICpossibly homozygous48232725
151421715414217155GA16GENICheterozygous49294645
151426394214263943A-2GENICheterozygous49185342
151426688514266886CCAAA5GENICheterozygous48944971
151427753614277537AT21GENICheterozygous49322721