chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
177916966779169668GC34GENICheterozygous403423824
177916966779169668G34GENICheterozygous403423825
177922322779223228A16GENICpossibly homozygous403423832
177922322779223228AT16GENICheterozygous403423833
177922322979223230A24GENICheterozygous403423834
177922322979223230AT24GENICheterozygous403423835
177925809379258094GT33GENICheterozygous140188317
177932779179327792AG18GENICheterozygous155049714
177932779179327792A18GENICheterozygous403423874
177934995379349954CA5GENIChomozygous403779858
177934995379349954CT5GENICheterozygous403779859
177934990779349908TC15GENIChomozygous141054032
177934990979349910AT13GENIChomozygous141054033
177954600579546006TG20GENICheterozygous155047001
177954600579546006T20GENICheterozygous403423912
177953440679534408GT23GENICheterozygous141052433
177931987579319877GT28GENICheterozygous141099006
177938172879381730AG34GENICheterozygous141052431