chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X114928688114928689GA20GENICpossibly homozygous631843224
X114929263114929264TA1GENIChomozygous631843225
X114929559114929560GA15GENIChomozygous631843226
X114934944114934945AC5GENIChomozygous631843227
X114935007114935008TA1GENIChomozygous631843228
X114935946114935947CT13GENICpossibly homozygous631843229
X114937245114937246GC31GENICpossibly homozygous631843230
X114937462114937463TC9GENICpossibly homozygous631843231
X114938934114938941TGTCCAA-------5GENIChomozygous745799751
X114939476114939477GA15GENICpossibly homozygous631843232
X114939824114939825AG6GENIChomozygous631843233
X114940124114940125GT17GENIChomozygous631843234
X114940232114940233GA15GENIChomozygous631843235
X114941790114941791GA14GENICpossibly homozygous631843236
X114942746114942747GC2GENIChomozygous631843237
X114943654114943655CT20GENICpossibly homozygous631843238
X114945819114945820G-19GENIChomozygous745799752
X114946263114946264CCTACA5GENIChomozygous745799753
X114946536114946537CT12GENICpossibly homozygous631843239
X114946573114946574TC13GENIChomozygous631843240
X114946839114946840GT11GENICheterozygous631843241