chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122634676826346769GA12GENIChomozygous50405104
122634685626346857AG4GENIChomozygous50147602
122634765626347657CCAAAAA4GENICheterozygous50539336
122634875726348759AA--8GENICheterozygous50539337
122634875826348759A-8GENICpossibly homozygous50539338
122634969226349693TC9GENIChomozygous50405106
122635017726350178CG13GENIChomozygous50485102
122635071726350718AG15GENIChomozygous50147612
122635314526353146A-15GENIChomozygous50485104
122635563426355635CA4GENIChomozygous50147620
122635563626355637CCAAA5GENICheterozygous50539339
122635563726355638A-5GENICheterozygous50147622
122635596426355965TC10GENIChomozygous50147624
122635608526356086AG12GENIChomozygous50147626
122635671826356719CG21GENIChomozygous50147628
122635723726357238TTTTTATTTA2GENIChomozygous50557817
122635730126357309GTGTGTGT--------4GENICheterozygous50405112
122635730326357309GTGTGT------4GENICheterozygous50147636
122635795126357952CT16GENIChomozygous50485108
122635826826358269GC9GENIChomozygous50485110
122635876426358765TC6GENIChomozygous50147648
122635914526359167TTATATATATATATATATATAT----------------------4GENICheterozygous50539340
122635914526359169TTATATATATATATATATATATAT------------------------4GENICheterozygous50692772
122635999726359998AAT15GENIChomozygous50147664
122636002926360030AG20GENICpossibly homozygous50147666
122636128026361281GGT10GENICheterozygous50147682