chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
153167449431674495G46GENIChomozygous139626328
153168101631681017T40GENIChomozygous139626329
153168394031683940A45GENIChomozygous139626330
153168550931685509G45GENIChomozygous139626331
153168766831687668A51GENIChomozygous139626332
153168770531687706T46GENIChomozygous139626333
153168773831687738T42GENIChomozygous139626334
153168798231687983C61GENIChomozygous139626335
153168800531688006TA60GENIChomozygous139709030
153168806431688064C54GENIChomozygous139626336
153168808431688085C54GENIChomozygous139626337
153168811931688119C54GENIChomozygous139626338
153168821731688217A55GENIChomozygous139626339
153168823231688233T48GENIChomozygous139626340
153168824031688241G51GENIChomozygous139626341
153168836831688370AC40GENIChomozygous139626342
153168838531688385C42GENIChomozygous139626343
153168848831688488G55GENIChomozygous139626344
153168851531688517AT54GENIChomozygous139626345
153168865531688655C55GENIChomozygous139626346
153168875631688757C50GENIChomozygous139626347
153168883931688840G52GENICpossibly homozygous139626348