chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1140845519140845520GA48GENIChomozygous108259022
1140847799140847800GA31GENIChomozygous108259024
1140848283140848284GA48GENIChomozygous108259026
1140849398140849399TC45GENIChomozygous108259032
1140849499140849500GA39GENIChomozygous108259034
1140850550140850551GT46GENIChomozygous108259035
1140850659140850660GA56GENIChomozygous108259037
1140851129140851130CT44GENIChomozygous108259039
1140851141140851142AT43GENIChomozygous108259041
1140851469140851470TC28GENIChomozygous108259043
1140851904140851905CT32GENIChomozygous108259045
1140855002140855003AG57GENIChomozygous108259049
1140855711140855712CT55GENIChomozygous108259051
1140848084140848084TG35GENIChomozygous127438686
1140854126140854126T48GENIChomozygous127438687
1140849291140849297TCTCTT8GENIChomozygous131779952
1140857565140857566TC65GENIChomozygous108259053
1140858263140858264GC48GENIChomozygous108259055
1140858312140858313AC47GENICpossibly homozygous108259057
1140858624140858628TGTC42GENIChomozygous127438688