chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
162125752821257529AG29GENIChomozygous47330448
162125762321257624TC32GENICpossibly homozygous47741387
162125774121257742GA35GENIChomozygous47330450
162125809921258100AG19GENIChomozygous47330452
162125897521258976GC22GENIChomozygous47741391
162125913721259138CT33GENIChomozygous47741393
162125940521259406AG13GENIChomozygous47330458
162126114621261147C-27GENIChomozygous47330464
162126129821261299TC41GENIChomozygous47330466
162126132621261327AT36GENICpossibly homozygous47330468
162126200121262004CCC---36GENIChomozygous47330470
162126207521262076AG30GENIChomozygous47330472
162126286521262866C-6GENIChomozygous47330474
162126287321262874C-8GENIChomozygous47330476
162126288121262882CA8GENIChomozygous47330478
162126288521262886A-5GENIChomozygous47330480
162126290021262901G-7GENIChomozygous47330482