chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
166469790664697907AG22GENIChomozygous139963567
166469869764698698AG17GENIChomozygous139963568
166469914464699153CACAGGCAG10GENIChomozygous139841796
166470099464700995GT20GENIChomozygous139963569
166470133564701336TA14GENIChomozygous139963570
166470159864701599AG19GENIChomozygous139963571
166470181664701817CA25GENIChomozygous142566016
166470181964701820CA24GENIChomozygous139963572
166470205864702059AG20GENIChomozygous139963573
166470274464702745GA16GENIChomozygous139963574
166470291264702913GA15GENIChomozygous139963575
166470305764703058AG16GENIChomozygous139963576
166470311564703116CA20GENIChomozygous142566017
166470323564703236CT11GENIChomozygous139963577
166470337464703375AG10GENIChomozygous139963578
166470343064703431A6GENIChomozygous139841797
166470348964703490CT4GENIChomozygous142566018
166470374764703748CT20GENIChomozygous142566019
166470394764703948GA14GENIChomozygous142566020
166470403364704034TC22GENIChomozygous142566021
166470415764704158CA27GENIChomozygous142566022
166470430464704305GA16GENIChomozygous142566023
166470436064704361TC10GENIChomozygous139963583
166470438264704382TGTTG12GENIChomozygous139841799
166470403064704030T20GENIChomozygous142515789
166470409664704096T22GENIChomozygous142515790