chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
125133829251338293AG8GENIChomozygous50244417
125133850651338507GA11GENICpossibly homozygous50625242
125133907351339074GC7GENICheterozygous50244427
125133943651339437CG8GENIChomozygous50625243
125133980251339803GT6GENIChomozygous50625244
125133990451339905AT11GENIChomozygous50244431
125133991251339913TA10GENIChomozygous50244433
125134015251340153TC10GENIChomozygous50244435
125134026151340262AG9GENIChomozygous50244437
125134029051340291TC11GENIChomozygous50244439
125134030951340310GA12GENIChomozygous50244441
125134035151340352AG13GENIChomozygous50244443
125134088151340882TC5GENICheterozygous50423291
125134113251341133AAAAACAAACAAAC9GENIChomozygous50625245
125134244851342449GGTCTCTCTGTC1GENIChomozygous50625246
125134247851342479GGTC1GENIChomozygous50244451
125134261251342613A-5GENIChomozygous50244453
125134261651342617A-6GENIChomozygous50244455
125134262351342624G-7GENIChomozygous50244457