chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
177666900076669001GA22GENIChomozygous140182576
177666929376669294GC15GENIChomozygous140182577
177666971776669718TG6GENIChomozygous140182578
177667018876670189T17GENIChomozygous140037329
177667026776670268CT19GENIChomozygous140182579
177667032776670328A22GENIChomozygous140037330
177667091176670912CT17GENIChomozygous140182580
177667099476670995TA22GENIChomozygous140182581
177667105176671052AC26GENIChomozygous140182582
177667162276671623GA18GENIChomozygous140182583
177667194276671943CT19GENIChomozygous140182584
177667205776672058GA26GENIChomozygous140182585
177667210476672106CA37GENIChomozygous140037331
177667219776672198CT38GENIChomozygous140182586
177667237176672372TC30GENIChomozygous140182587
177667241076672411CT32GENIChomozygous140182588
177667379976673800CA23GENIChomozygous140182589
177667397176673972AT19GENIChomozygous140182590
177667407676674077CT26GENIChomozygous140182591
177667495776674958AG12GENIChomozygous140182592
177667496076674961GA12GENIChomozygous140182593
177667522876675229AC16GENIChomozygous140182594
177667528176675282TC14GENIChomozygous140182595
177667549976675500GA21GENIChomozygous140182596
177667575276675753AG15GENIChomozygous140182597
177667675676676757CT16GENIChomozygous140182598
177667018876670189TC17GENICheterozygous403423208