chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
144563885845638859GC22GENIChomozygous48696399
144563889745638898AG15GENIChomozygous48696401
144563893445638935CG13GENIChomozygous48696403
144564153345641534AC1GENIChomozygous48696415
144564767745647678AC8GENIChomozygous48696467
144565078445650785GA16GENICpossibly homozygous48696474
144565151245651517AAAAG-----1GENIChomozygous48696476
144565296345652964AG25GENICpossibly homozygous48696478
144565319445653195GA8GENICpossibly homozygous48696480
144565363445653635TC16GENICpossibly homozygous48696482
144565506245655063AAGCCACGCCTACTT4GENIChomozygous48696484
144565592145655922GGT5GENIChomozygous48696486
144565592645655928TC--5GENIChomozygous48696488
144565768745657688GA16GENICheterozygous48696492
144565877445658775CT18GENICpossibly homozygous48696494
144566044745660448TG4GENIChomozygous48696502
144566100145661002A-2GENIChomozygous49308265
144566105345661054AG16GENIChomozygous48696504
144566217945662180GA21GENICpossibly homozygous48696506
144566304945663050TC19GENIChomozygous48696510
144566400145664002T-2GENICheterozygous48696512
144566446145664462CT11GENICpossibly homozygous48696514
144566804145668042CT9GENICpossibly homozygous48696516
144566903245669033GA16GENIChomozygous48696518
144566924545669246GA13GENIChomozygous48696520