chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
202802737928027380GA6GENIChomozygous125223320
202802743428027435TA16GENIChomozygous125214015
202802824228028243TC7GENIChomozygous125188521
202802923028029231CT17GENIChomozygous125204071
202803156028031561CT8GENIChomozygous125204072
202803244428032445GA5GENIChomozygous125204073
202803261128032612AG16GENIChomozygous125188524
202803690628036907GA7GENICheterozygous125223321
202803822628038227CT9GENIChomozygous125204074
202804421828044219GT10GENIChomozygous125204077
202804896228048963GA30GENIChomozygous125188537
202805066728050668TC10GENIChomozygous125188539
202805150728051508TC4GENIChomozygous125204078
202805403628054037TC21GENIChomozygous125188544
202805482328054824TC23GENIChomozygous125188546
202805523128055232TA6GENIChomozygous125188547
202805538328055384CT8GENIChomozygous125204079
202805757728057578GA13GENIChomozygous125204080
202805801728058018AG19GENIChomozygous125188551
202805827928058280GT20GENIChomozygous125188552
202806153228061533GC12GENIChomozygous125188553
202806638228066383AG13GENIChomozygous125188559
202806668628066687TC19GENIChomozygous125188560
202806842628068427GA11GENIChomozygous125204082
202806868728068688AC11GENIChomozygous125204083
202807060828070609GT6GENIChomozygous125188562
202807268228072683AG21GENIChomozygous125188565
202807295128072952TC18GENIChomozygous125188566
202807496428074965AG11GENIChomozygous125188571
202807619928076200TC11GENIChomozygous125188573
202807630628076307CT4GENIChomozygous125188574
202807654328076544CA7GENICheterozygous125188575