chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1175574661175574663TT--26GENIChomozygous61560017
1175575045175575046GGA23GENICpossibly homozygous61560018
1175575391175575392CG12GENIChomozygous60959364
1175575401175575402CCG8GENICheterozygous60959366
1175575401175575402CCGG8GENICheterozygous62177848
1175577736175577737TC31GENIChomozygous60959376
1175578339175578340GA22GENIChomozygous61560020
1175578492175578493TTA17GENIChomozygous60959378
1175581243175581244TTAAAA8GENICheterozygous62234243
1175581243175581244TTAAAAAAAAAA8GENICpossibly homozygous62177850
1175581413175581414AC20GENIChomozygous60959395
1175581845175581846AAACACACACACAC2GENICheterozygous62177852
1175582243175582244CA41GENICpossibly homozygous61560021
1175582296175582297CT32GENIChomozygous60959399
1175582623175582624GC15GENIChomozygous60959401
1175582756175582757CT15GENIChomozygous60959403
1175582786175582787A-14GENIChomozygous61560022
1175583599175583600CT35GENICpossibly homozygous61560023
1175584395175584396CA38GENICpossibly homozygous61560024
1175584622175584623GA20GENIChomozygous61560025
1175584673175584674AC24GENIChomozygous61560026