chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108670808786708088GA19GENIChomozygous143464393
108670915986709160AT15GENIChomozygous143464394
108670922386709224AG18GENIChomozygous143464395
108670984586709846AG14GENIChomozygous143464396
108671032686710327TC17GENIChomozygous143464397
108671041886710419A22GENICpossibly homozygous141037429
108671102886711029TC22GENIChomozygous143464398
108671113386711134TC19GENIChomozygous143464399
108671123286711233GA21GENIChomozygous143464400
108671200886712009AG28GENIChomozygous143464401
108671235886712359T17GENICpossibly homozygous141037430
108671245786712458C18GENIChomozygous143435302
108671291886712919CT23GENIChomozygous143464402
108671379686713796C9GENIChomozygous143435303
108671413786714138AC24GENIChomozygous143464403
108671433586714336GA14GENIChomozygous143464404
108671465886714659AT14GENICheterozygous154657499
108671465886714659A14GENIChomozygous403293871
108671598386715984AG17GENIChomozygous143464405
108671599686715996AAAT15GENIChomozygous143435304
108671605186716052AT20GENIChomozygous143464406
108671605186716052A20GENICheterozygous403293872
108671627286716273TC20GENIChomozygous143464407
108671661886716619GA18GENIChomozygous143464408
108671712686717127AT26GENIChomozygous143464409
108671716686717167CG21GENIChomozygous143464410
108671741786717418CT27GENICpossibly homozygous143464411
108671753286717533AG9GENIChomozygous143464412
108671754786717548TC11GENIChomozygous143464413
108671802586718026AG13GENIChomozygous143464414
108671810386718104AG14GENIChomozygous143464415
108671873686718737CT11GENIChomozygous143464416
108671894886718949GA9GENIChomozygous143464417
108671902686719026TA15GENIChomozygous143435306
108671917586719176TC15GENIChomozygous143464418
108672036986720369AAAG15GENIChomozygous143435307
108672152786721531GTGT9GENIChomozygous143435308