chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1100594235100594236GA26INTERGENIChomozygous61483181
1100594971100594972AG21INTERGENIChomozygous61483182
1100595780100595781A-13GENIChomozygous61483183
1100595896100595897TC24GENICpossibly homozygous61483184
1100595921100595922GA21GENICpossibly homozygous61483185
1100596215100596216CCTTTTT10GENIChomozygous61483186
1100596863100596864AG20GENIChomozygous61483187
1100596900100596901GC20GENIChomozygous61483188
1100597622100597623AC15GENIChomozygous61483189
1100600166100600167AG9GENIChomozygous61483190
1100600642100600643TC30GENIChomozygous61483191
1100600972100600973TTACAC11GENICheterozygous60779560
1100600973100600979ACACAC------11GENICpossibly homozygous61483192
1100601209100601210GA20GENIChomozygous61483193
1100601288100601289AG21GENIChomozygous61483194
1100601438100601439CT14GENIChomozygous61483195
1100601502100601503GA19GENIChomozygous61483196
1100601512100601515AAA---16GENIChomozygous61483197
1100601761100601762GA26GENIChomozygous61483198
1100601830100601831CT26GENIChomozygous61483199
1100602150100602151GA20GENIChomozygous61483200
1100602442100602443AATC13GENIChomozygous61483201
1100602509100602510TC20GENIChomozygous61483202
1100602689100602690GA18GENIChomozygous61483203
1100603588100603589T-14GENICpossibly homozygous61483204
1100604705100604706AC27GENIChomozygous61483205
1100605232100605233CT19GENIChomozygous61483206
1100606549100606550AG19GENIChomozygous61483207
1100607037100607038TG23GENIChomozygous61483208