chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
185642336756423368TG39GENICheterozygous46470054
185642429256424293AAGT8GENIChomozygous46470062
185642864256428643TTATCC19GENIChomozygous46608556
185642975456429757TAG---28GENICheterozygous46470115
185643588056435881CCAT26GENIChomozygous46470167
185644896056448961A-8GENICheterozygous46470230
185645238756452388GA52GENICpossibly homozygous46470260
185645240056452401CA52GENICpossibly homozygous46470262
185645240256452403GA51GENIChomozygous46470264
185645243656452437GC47GENIChomozygous46470266
185645244756452448AC50GENIChomozygous46470268