chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
18619636086196361A-12GENICpossibly homozygous62262158
18619669686196697CT15GENIChomozygous62262160
18619777786197778CT7GENICpossibly homozygous62262161
18619778186197782GA7GENIChomozygous62262162
18619844486198445TTA30GENIChomozygous62262163
18619863586198636AG14GENIChomozygous61456389
18619658786196588TTAGA2GENICheterozygous62139111
18619919186199192CT16GENICpossibly homozygous61456391
18619965386199654AG26GENIChomozygous61456392
18620000186200002GA17GENICheterozygous62262164
18620047286200473GA12GENICheterozygous61456393
18620122386201224TC20GENICpossibly homozygous61456395
18620126586201266TC8GENIChomozygous61456396
18620126886201269TC5GENIChomozygous61456397
18620140286201403TC5GENICheterozygous61456398
18620147286201473AG7GENIChomozygous61456399
18620167186201672AT22GENICpossibly homozygous62262165
18620220086202201AG15GENICpossibly homozygous61456401
18620227786202278CT18GENIChomozygous62262167
18620234886202349CT10GENICheterozygous61456402
18620246186202462CT7GENICpossibly homozygous61456403
18620268086202681AG20GENICpossibly homozygous61456404