chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5160123496160123497TC45GENIChomozygous114073873
5160126878160126879TC20GENIChomozygous114073890
5160127108160127109CT30GENIChomozygous114073891
5160127865160127866TA46GENIChomozygous114073892
5160130094160130095CA28GENIChomozygous114160513
5160131219160131220AG29GENICheterozygous114160514
5160131227160131228AG26GENICheterozygous114160515
5160131405160131406GA40GENIChomozygous114073895
5160132176160132177CT21GENIChomozygous114160516
5160133516160133517AG42GENIChomozygous114073897
5160135065160135066TA29GENIChomozygous114073898
5160136568160136569AG22GENIChomozygous114073906
5160137298160137299GA44GENIChomozygous114160517
5160137339160137340GA55GENICpossibly homozygous114160518
5160140920160140921AT26GENIChomozygous114073911
5160141398160141399GA34GENIChomozygous114160519
5160143389160143390GT45GENIChomozygous114160520
5160143850160143851AC15GENICpossibly homozygous114073914
5160143872160143873TC18GENICpossibly homozygous114073915
5160144527160144528CT39GENIChomozygous114160521
5160144560160144561CT40GENIChomozygous114160522
5160145654160145655TC37GENIChomozygous114073917
5160146547160146548GA43GENICpossibly homozygous114160523
5160146613160146614GT59GENICheterozygous114259302
5160147029160147030CA60GENICheterozygous114073918
5160147051160147052AG55GENICheterozygous114160524
5160153925160153926CA25GENICheterozygous114160526
5160155879160155880CT35GENIChomozygous114073921
5160155931160155932GC17GENIChomozygous114160528
5160155993160155994AC21GENIChomozygous114073922
5160156023160156024GA19GENIChomozygous114073923
5160156060160156061TG9GENIChomozygous114160529
5160156894160156895CG14GENIChomozygous114073924
5160157062160157063GT33GENIChomozygous114160530
5160157605160157606CT20GENIChomozygous114160531
5160157765160157766GC45GENIChomozygous114160532
5160158284160158285GA45GENIChomozygous114160533