chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5158306118158306119AT30GENIChomozygous145560323
5158307800158307800TGTT18GENICpossibly homozygous149563882
5158308009158308010CT17GENIChomozygous145560327
5158308486158308487TC21GENIChomozygous137661127
5158308490158308491TC22GENIChomozygous137661128
5158316070158316071CA26GENIChomozygous149579416
5158316715158316716AG26GENIChomozygous145560334
5158319365158319366TA29GENIChomozygous149579417
5158319553158319554TC17GENIChomozygous145560336
5158319712158319712AGAT13GENIChomozygous149563883
5158322723158322724GA17GENIChomozygous149579418
5158324539158324540GA18GENIChomozygous145560346
5158325219158325219AAAC15GENIChomozygous145536615
5158326868158326869GT9GENIChomozygous145560352
5158328194158328195GA18GENIChomozygous149579419
5158330383158330384CT20GENIChomozygous149579420
5158331445158331446AG15GENIChomozygous145560358