chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
166469790664697907AG18GENIChomozygous139963567
166469845964698463GCAC10GENIChomozygous145881554
166469869764698698AG20GENIChomozygous139963568
166469879464698818CTCTCTCTCTCTCTCTCCCTCTCC3GENIChomozygous147115698
166470099464700995GT30GENIChomozygous139963569
166470133564701336TA26GENIChomozygous139963570
166470159864701599AG22GENIChomozygous139963571
166470181964701820CA18GENIChomozygous139963572
166470205864702059AG22GENIChomozygous139963573
166470274464702745GA10GENIChomozygous139963574
166470291264702913GA18GENIChomozygous139963575
166470305764703058AG14GENIChomozygous139963576
166470323564703236CT10GENIChomozygous139963577
166470337464703375AG10GENIChomozygous139963578
166470374764703748CT14GENIChomozygous142566019
166469914464699153CACAGGCAG5GENIChomozygous139841796
166470343064703431A8GENIChomozygous139841797
166470181664701817CA18GENIChomozygous142566016
166470311564703116CA17GENIChomozygous142566017
166470348964703490CT5GENIChomozygous142566018
166470394764703948GA16GENIChomozygous142566020
166470403364704034TC23GENIChomozygous142566021
166470415764704158CA13GENIChomozygous142566022
166470430464704305GA13GENIChomozygous142566023
166470436064704361TC15GENIChomozygous139963583
166470438264704382TGTTG13GENIChomozygous139841799
166470403064704030T22GENIChomozygous142515789
166470409664704096T17GENIChomozygous142515790