chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1142575581142575582GA8GENICpossibly homozygous61902435
1142576052142576053TC2GENICheterozygous61531037
1142576697142576698CT20GENICpossibly homozygous61902439
1142576902142576903CA12GENICpossibly homozygous61902440
1142577646142577647TA11GENICpossibly homozygous61902441
1142578205142578206CT14GENIChomozygous61531048
1142579734142579735GA10GENIChomozygous61902442
1142582435142582436GA11GENIChomozygous61902443
1142583394142583395TA11GENIChomozygous61902444
1142584110142584111GA13GENIChomozygous61902445
1142584811142584812GA13GENIChomozygous61902446
1142585462142585463TC10GENICheterozygous61531070
1142591967142591968CT8GENIChomozygous60876195
1142594258142594259AG11GENIChomozygous61902447
1142614102142614103CA6GENIChomozygous60876204
1142614225142614226G-2GENIChomozygous60876205