chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8127886115127886116AG9GENICheterozygous116989735
8127886216127886216T11GENICheterozygous130368020
8127886223127886224T10GENICheterozygous130368021
8127886225127886226GA10GENICheterozygous128668472
8127886257127886258TG11GENICheterozygous130375222
8127886262127886275GGCACTTTGGAAG13GENICheterozygous130368022
8127886429127886430CG8GENICheterozygous117127364
8127891519127891520T20GENICheterozygous130368023
8127891553127891555CG22GENICheterozygous130368024
8127893207127893207ATATG32GENICheterozygous130368025
8127893208127893208AAACCA33GENICheterozygous130368026
8127893210127893210GGGC32GENICheterozygous130368027
8127893211127893211TC32GENICheterozygous130368028
8127893824127893825TG53GENICheterozygous130375225
8127888097127888098AG40GENICheterozygous116719700
8127889206127889207TG44GENICheterozygous118151131
8127891789127891790AC30GENICheterozygous116719702
8127892629127892630CT46GENICheterozygous116901114
8127893229127893230GA31GENICheterozygous130375224
8127894275127894276CT52GENICheterozygous116719706
8127894384127894385CT44GENICheterozygous116719708
8127894494127894495CT33GENICheterozygous116719710
8127895647127895648GA47GENICheterozygous126679926
8127895758127895759GA41GENICheterozygous116719712
8127896466127896467AC35GENICheterozygous116901116
8127896731127896734CAG1GENIChomozygous128646806
8127899987127899987A12GENIChomozygous128646809