chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
177666900076669001GA52GENIChomozygous140182576
177666929376669294GC48GENIChomozygous140182577
177666971776669718TG47GENIChomozygous140182578
177667018876670189T43GENIChomozygous140037329
177667026776670268CT46GENIChomozygous140182579
177667032776670328A49GENIChomozygous140037330
177667091176670912CT46GENIChomozygous140182580
177667099476670995TA49GENIChomozygous140182581
177667105176671052AC40GENIChomozygous140182582
177667162276671623GA55GENIChomozygous140182583
177667194276671943CT53GENIChomozygous140182584
177667205776672058GA38GENIChomozygous140182585
177667210476672106CA38GENIChomozygous140037331
177667219776672198CT52GENIChomozygous140182586
177667237176672372TC33GENIChomozygous140182587
177667241076672411CT35GENIChomozygous140182588
177667379976673800CA39GENICpossibly homozygous140182589
177667397176673972AT46GENIChomozygous140182590
177667407676674077CT37GENIChomozygous140182591
177667495776674958AG49GENIChomozygous140182592
177667496076674961GA47GENIChomozygous140182593
177667522876675229AC47GENIChomozygous140182594
177667528176675282TC44GENIChomozygous140182595
177667549976675500GA47GENIChomozygous140182596
177667575276675753AG39GENIChomozygous140182597
177667675676676757CT51GENIChomozygous140182598
177667018876670189TC43GENICheterozygous403423208