chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
61033280210332803TC25GENIChomozygous114721362
61033385710333858TC22GENIChomozygous114721364
61033420810334209AC20GENIChomozygous114721366
61033486810334869CT26GENIChomozygous114721370
61033662710336628GA40GENIChomozygous114721372
61033693410336935TC22GENIChomozygous114721374
61033736810337369TC24GENIChomozygous114721376
61033845410338455AG44GENIChomozygous114721378
61033901910339020AC34GENIChomozygous114721380
61034091010340911AG32GENIChomozygous114721382
61034225010342251TA23GENIChomozygous114721384
61034284610342847GA26GENIChomozygous114721386
61034296710342968CG17GENIChomozygous114721388
61034304110343042CT16GENIChomozygous114721390
61034306110343062AT14GENIChomozygous114721392
61034339310343394TC21GENIChomozygous114721394
61034340710343408TC18GENIChomozygous114721396
61034365110343652AT17GENIChomozygous114721398
61034416810344169TA21GENIChomozygous114721400
61034420710344208AG20GENIChomozygous114721402
61034426210344263GT25GENICheterozygous114721404
61034446710344468GC29GENICheterozygous114721406
61034446810344469TC29GENICheterozygous114721408
61034447310344474AG29GENICheterozygous114721410
61034451210344513GC16GENIChomozygous114721412
61034464810344649CA60GENICheterozygous114721414
61034475410344755CT28GENIChomozygous114721416
61034502210345023AG25GENIChomozygous114721418
61034510210345103GC26GENIChomozygous114721420
61034535310345354TC28GENIChomozygous114721422
61034535810345359GA34GENIChomozygous114721424
61034549810345499GA45GENIChomozygous114721426
61034570410345705CA34GENIChomozygous114721428
61034577010345771AG34GENIChomozygous114721430
61034577210345773TA34GENIChomozygous114721432
61034591710345918GA37GENIChomozygous114721434
61034613010346131GA32GENIChomozygous114721436
61034623710346238AG15GENIChomozygous114721437