chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
185642429256424293AAGT16GENICpossibly homozygous46470062
185642469756424698T-59GENICheterozygous46470066
185642864256428643TTATCC13GENIChomozygous46608556
185643588056435881CCAT20GENIChomozygous46470167
185644894456448946AG--11GENICheterozygous46470228
185644896056448961A-13GENICheterozygous46470230
185645238756452388GA40GENIChomozygous46470260
185645240056452401CA39GENIChomozygous46470262
185645240256452403GA41GENIChomozygous46470264
185645243656452437GC43GENIChomozygous46470266
185645244756452448AC40GENIChomozygous46470268