chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105983098759830988AG28INTERGENIChomozygous51466334
105983444859834449GGA13INTERGENIChomozygous51466335
105983521059835211GGT18INTERGENIChomozygous51466336
105983527159835275ATTT----4INTERGENIChomozygous51466337
105983600759836008GA54INTERGENICpossibly homozygous51466338
105983702459837025TC2INTERGENIChomozygous51466339
105983722059837221CT59INTERGENICheterozygous51466340
105983733859837339CT64INTERGENICheterozygous51466341
105983735559837356GT58INTERGENICheterozygous51466342
105983736859837369GA55INTERGENICheterozygous51466343
105983736959837370TA55INTERGENICheterozygous51466344
105983737659837377GC58INTERGENICheterozygous51466345
105983844359838444CA58INTERGENICpossibly homozygous51466346
105983920159839202AG28INTERGENIChomozygous51466347
105983963559839636TC35INTERGENICpossibly homozygous51466348
105983985559839856AG39INTERGENIChomozygous51466349
105984095759840958GC37INTERGENIChomozygous51466350
105984462759844628TC14INTERGENIChomozygous51466351
105984567859845679CT26INTERGENIChomozygous51466352
105984608159846082T-26INTERGENIChomozygous51466353
105984611359846114AG25INTERGENIChomozygous51466354
105984616559846166GA25INTERGENIChomozygous51466355
105984660459846605CT94INTERGENICheterozygous51466356
105984670959846710CT61INTERGENICpossibly homozygous51466357
105984736459847365AATTT18INTERGENIChomozygous51466358
105984767859847679TTA31INTERGENIChomozygous51466359
105984844259848443AC26INTERGENIChomozygous51466360
105985206259852063AG31INTERGENICheterozygous51466361
105985272659852727GA11INTERGENIChomozygous51466362
105985315459853155CT19INTERGENIChomozygous51466363
105985491659854917CT18INTERGENIChomozygous51466364
105985572659855727TG35INTERGENICheterozygous51466365
105986254559862548AGA---26INTERGENIChomozygous51466366