chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
41063183510631836CT16GENIChomozygous112496467
41063292510632926CG6GENIChomozygous112496469
41063446510634466GA12GENIChomozygous112496471
41063687710636878CT20GENIChomozygous112496473
41063815110638152AT10GENIChomozygous112496475
41063861010638611TA15GENIChomozygous112496477
41064028410640285AC22GENIChomozygous112496479
41064101710641018CT25GENIChomozygous112496481
41064334110643342AG10GENIChomozygous112496483
41064657610646577TC13GENIChomozygous112496485
41064762410647625GT23GENIChomozygous112496487
41064799410647995GC13GENIChomozygous112496489
41064819010648191TG17GENIChomozygous112496491
41064840610648407TC10GENIChomozygous112496493
41064853710648538AG6GENIChomozygous112496495
41064892710648928CT7GENIChomozygous112496497
41065109210651093GA17GENIChomozygous112496499
41065131810651319AG11GENIChomozygous112496501
41065136010651361AG7GENIChomozygous112496503
41065141210651413AG24GENIChomozygous112496505
41065436810654369AG20GENIChomozygous112496507
41065995310659954CT18GENIChomozygous112496511
41065999910660000CA12GENIChomozygous112496513
41066301010663011CT10GENIChomozygous112496517
41066464310664644TG7GENIChomozygous112496521
41067208810672089CT35GENIChomozygous112496523
41067250410672505GA14GENIChomozygous112496525
41067455610674557CT9GENIChomozygous112496529
41067498510674986AG20GENIChomozygous112496531
41067570410675705GA15GENIChomozygous112496535
41067648110676482GA8GENIChomozygous112496537
41068167610681677CT21GENIChomozygous112496539
41068301710683018TC22GENIChomozygous112496543
41068688510686886CT22GENIChomozygous112496547
41068724210687243AG17GENIChomozygous112496549
41068937810689379CT4GENIChomozygous112496551
41068954510689546AG16GENIChomozygous112496553
41068993310689934TC23GENIChomozygous112496555
41069008010690081AG20GENIChomozygous112496557
41069232610692327GA14GENIChomozygous112496559
41069647610696477AG11GENIChomozygous112496561
41070227610702277AC14GENIChomozygous112496565