chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8127144599127144600GA56GENICheterozygous116715787
8127144602127144603GA52GENICheterozygous116899191
8127144623127144624AG52GENICpossibly homozygous116715789
8127144636127144637AG56GENICheterozygous116715791
8127145526127145527GC20GENIChomozygous116715795
8127145662127145663CA49GENIChomozygous116899193
8127145877127145878TC4GENIChomozygous116899195
8127145920127145921CG28GENIChomozygous116715797
8127146408127146409GA12GENIChomozygous116715799
8127146767127146768GA31GENIChomozygous116715801
8127146828127146829AG21GENICpossibly homozygous116715803
8127146835127146836CT23GENICpossibly homozygous116899197
8127147912127147913AG49GENIChomozygous116715805
8127148382127148383GT30GENICpossibly homozygous116899199
8127148386127148387GT29GENICpossibly homozygous116899201
8127148644127148645TC76GENIChomozygous116715809
8127148787127148788CT48GENIChomozygous116715811
8127149179127149180GC78GENIChomozygous116715813
8127149406127149407CT52GENICheterozygous116899203
8127150167127150168AG38GENICpossibly homozygous116715815
8127152351127152352GA53GENICpossibly homozygous116715817
8127152598127152599CG75GENIChomozygous116715819