chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
13101699756101699757GC18GENIChomozygous114654738
13101700248101700249CT8GENICheterozygous114654739
13101700642101700643CT18GENIChomozygous114654740
13101700740101700741GA6GENIChomozygous114437832
13101700743101700744AT5GENIChomozygous114437834
13101701378101701379AG7GENICheterozygous126125957
13101701418101701419CG21GENIChomozygous114654741
13101704705101704706GC30GENIChomozygous123794899
13101705319101705320CT9GENIChomozygous123794900
13101706136101706137AC9GENIChomozygous126111914
13101706465101706466CT8GENIChomozygous123794904
13101707319101707320GA15GENIChomozygous123794905
13101707924101707925GA18GENICpossibly homozygous123794906
13101708094101708095CG11GENIChomozygous114654742
13101709006101709007GA16GENIChomozygous114654743
13101709027101709028TC15GENIChomozygous114654744
13101709524101709525CT18GENICheterozygous114654745
13101710531101710532TC6GENIChomozygous126111915
13101711118101711119TC15GENICheterozygous126111916
13101711973101711974GA32GENIChomozygous114654746
13101712012101712013AG35GENIChomozygous114654747
13101714708101714709TA24GENIChomozygous126072907