chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
177666900076669001GA17GENIChomozygous140182576
177666929376669294GC16GENIChomozygous140182577
177666971776669718TG15GENIChomozygous140182578
177667018876670189T13GENIChomozygous140037329
177667026776670268CT11GENIChomozygous140182579
177667032776670328A14GENIChomozygous140037330
177667091176670912CT16GENIChomozygous140182580
177667099476670995TA12GENIChomozygous140182581
177667105176671052AC13GENIChomozygous140182582
177667162276671623GA16GENIChomozygous140182583
177667194276671943CT16GENIChomozygous140182584
177667205776672058GA6GENIChomozygous140182585
177667210476672106CA8GENIChomozygous140037331
177667219776672198CT14GENIChomozygous140182586
177667237176672372TC17GENIChomozygous140182587
177667241076672411CT20GENIChomozygous140182588
177667379976673800CA15GENIChomozygous140182589
177667397176673972AT20GENIChomozygous140182590
177667407676674077CT27GENIChomozygous140182591
177667495776674958AG12GENIChomozygous140182592
177667496076674961GA12GENIChomozygous140182593
177667522876675229AC23GENIChomozygous140182594
177667528176675282TC21GENIChomozygous140182595
177667549976675500GA10GENIChomozygous140182596
177667575276675753AG17GENIChomozygous140182597
177667675676676757CT12GENIChomozygous140182598
177667126176671262CT13GENIChomozygous142616264
177667018876670189TC13GENICheterozygous403423208