chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4136110536136110537GC9GENIChomozygous56940017
4136110720136110721GA8GENIChomozygous56940018
4136110835136110836AC15GENIChomozygous56940019
4136110909136110910AG8GENICpossibly homozygous56940020
4136110954136110955CT9GENIChomozygous56940021
4136110960136110961CG9GENIChomozygous56940022
4136111031136111032TC12GENIChomozygous56940023
4136111098136111099CT15GENIChomozygous56940024
4136111170136111171GA6GENIChomozygous56940025
4136111227136111228TA9GENIChomozygous56940026
4136111299136111300AC9GENIChomozygous56940027
4136111384136111385CG6GENIChomozygous56940028
4136111468136111469AC7GENIChomozygous56940029
4136111652136111653AG5GENIChomozygous56940030
4136111961136111962CT13GENIChomozygous56940031
4136112158136112159TTGAAAGGG2GENIChomozygous56940032
4136112159136112160TTCACCTGA3GENIChomozygous56940033
4136112220136112221CG5GENIChomozygous56940034
4136112376136112377TTCC9GENIChomozygous56940035
4136112628136112629GA2GENIChomozygous56940036
4136112694136112695AG5GENIChomozygous56940037
4136112778136112779AG8GENIChomozygous56940038
4136113093136113094GA5GENIChomozygous56940039
4136113250136113251AG9GENIChomozygous56940040
4136113414136113416GG--5GENIChomozygous56940041
4136113431136113432G-5GENICheterozygous56940042
4136113433136113434G-5GENICheterozygous56940043
4136113453136113454GGTA4GENIChomozygous56940044
4136113461136113462AATG2GENIChomozygous56940045
4136113541136113542AC1GENIChomozygous56940046
4136113579136113580AC2GENIChomozygous56940047
4136113625136113626CT8GENIChomozygous56940048
4136113750136113751TG6GENIChomozygous56940049
4136113770136113771CG7GENIChomozygous56940050
4136113933136113934TG6GENIChomozygous56940051
4136113975136113976AC8GENIChomozygous56940052
4136114069136114070GA11GENIChomozygous56940053
4136114208136114209GA6GENIChomozygous56940054
4136114614136114615GA11GENIChomozygous56940055