chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1175573774175573775AG21GENICpossibly homozygous60959361
1175574661175574663TT--29GENICheterozygous61560017
1175575391175575392CG10GENIChomozygous60959364
1175575413175575414GT9GENIChomozygous60959368
1175576268175576269GA28GENICpossibly homozygous60959370
1175576697175576698CT22GENIChomozygous60959372
1175576744175576745CA23GENIChomozygous60959374
1175577736175577737TC29GENIChomozygous60959376
1175578492175578493TTA20GENIChomozygous60959378
1175578538175578546AAACAAAC--------20GENIChomozygous60959380
1175578717175578718GA22GENIChomozygous60959382
1175579593175579594AT22GENICpossibly homozygous60959384
1175579617175579638TGTGTGTGTGTGGGGGGGGCG---------------------18GENIChomozygous60959386
1175579939175579940TC27GENICpossibly homozygous60959390
1175580197175580198T-26GENIChomozygous60959392
1175581243175581244TTAAAAAAAAAA11GENICheterozygous62177850
1175581413175581414AC20GENIChomozygous60959395
1175581846175581848AC--3GENIChomozygous60959397
1175582296175582297CT18GENIChomozygous60959399
1175582623175582624GC29GENIChomozygous60959401
1175582756175582757CT29GENIChomozygous60959403
1175583452175583453CT40GENICpossibly homozygous60959405
1175584302175584303GA21GENICpossibly homozygous60959407
1175584726175584727TC23GENIChomozygous60959409
1175581243175581244TTAAAA11GENICheterozygous62234243