chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1458488915848892GA19GENIChomozygous800203591
1458493045849305AG25GENIChomozygous800203592
1458494455849446AC25GENIChomozygous800203593
1458494765849477GC19GENIChomozygous800203594
1458496305849631CA18GENIChomozygous800203595
1458497515849752CT29GENIChomozygous800203596
1458498535849854CG37GENIChomozygous800203597
1458498725849873CT40GENIChomozygous800203598
1458498855849886AG44GENIChomozygous800203599
1458499095849910TC50GENIChomozygous800203600
1458500305850031CT27GENIChomozygous800203601
1458502395850240GC38GENIChomozygous800203602
1458505225850523GC14GENIChomozygous800203603
1458516115851612GA19GENIChomozygous800203604
1458516165851617CT18GENIChomozygous800203605
1458516825851683AT34GENICheterozygous800203606
1458516905851691CT40GENICheterozygous800203607
1458517545851755CG75GENIChomozygous800203608