chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
176183345761833459AA--4GENICheterozygous47438541
176183345861833459A-4GENICheterozygous47158107
176183661661836617GT3GENICheterozygous47158117
176186100861861009CCGG11GENICheterozygous47158145
176187265161872653AC--4GENICheterozygous47335230
176187302661873027TC9GENIChomozygous47158192
176187352661873527TA2GENICheterozygous47158193
176187566361875664C-2GENICheterozygous47158201
176187566861875669G-1GENIChomozygous47158202
176187567261875673AAC2GENIChomozygous47158203
176188083661880837T-7GENICheterozygous47158229
176188169961881700GGC9GENICheterozygous47158237
176188410461884105CCA1GENIChomozygous47158250
176188887861888879C-4GENIChomozygous47158266
176188888361888884G-3GENIChomozygous47158267
176189301261893013T-9GENICheterozygous47497076
176189943661899437G-8GENIChomozygous47158283
176190293961902940T-6GENICheterozygous47158284
176192839161928394GTG---1GENIChomozygous47158358
176192843861928439TA2GENIChomozygous47747172
176192843961928440AT1GENIChomozygous47747174
176192846861928469C-1GENIChomozygous47158362
176192848261928483AG1GENIChomozygous47158363
176192848761928488AG1GENIChomozygous47158364
176192855061928551C-3GENIChomozygous47158371
176194752361947524GGATCTCTCCAAGACTTTTATCAT1GENIChomozygous47158411
176195388861953889CCT10GENIChomozygous47158428
176195390961953910GGT1GENIChomozygous47158429
176195397361953974CG2GENIChomozygous47158432
176195397861953979T-2GENIChomozygous47158433
176196205161962052CCT4GENIChomozygous47497205
176196327161963272AG14GENICheterozygous47158459
176197226361972264TG7GENICpossibly homozygous47158470
176198307861983079CA7GENICheterozygous47497239
176200234062002341TC3GENICheterozygous47158513
176202294762022948G-19GENIChomozygous47158581
176202924362029244TTC4GENIChomozygous47158590
176202924862029249TC4GENIChomozygous47747234
176202925662029257TTC2GENIChomozygous47747236
176203398662033988TC--2GENIChomozygous47158601