chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122634676826346769GA22GENIChomozygous50405104
122634685626346857AG40GENIChomozygous50147602
122634765626347657CCAAAAA4GENIChomozygous50539336
122634875726348759AA--20GENICheterozygous50539337
122634875826348759A-20GENICheterozygous50539338
122634969226349693TC25GENIChomozygous50405106
122635017726350178CG23GENIChomozygous50485102
122635071726350718AG24GENIChomozygous50147612
122635314526353146A-14GENIChomozygous50485104
122635563426355635CA11GENIChomozygous50147620
122635563626355637CCAAA6GENIChomozygous50539339
122635596426355965TC25GENIChomozygous50147624
122635608526356086AG31GENIChomozygous50147626
122635671826356719CG33GENIChomozygous50147628
122635723726357238TTTTTATTTA7GENIChomozygous50557817
122635730326357309GTGTGT------2GENIChomozygous50147636
122635795126357952CT24GENIChomozygous50485108
122635826826358269GC32GENIChomozygous50485110
122635876426358765TC20GENIChomozygous50147648
122635914526359167TTATATATATATATATATATAT----------------------26GENICpossibly homozygous50539340
122635914526359169TTATATATATATATATATATATAT------------------------26GENICheterozygous50692772
122635999726359998AAT26GENIChomozygous50147664
122636002926360030AG28GENIChomozygous50147666
122636128026361281GGTT17GENICheterozygous50298927
122636128026361281GGT17GENICheterozygous50147682