chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
178495811684958117CG42GENICheterozygous47213766
178505706385057064CT10GENICheterozygous47214006
178506438185064382CT18GENICheterozygous47214031
178506449985064500AG20GENICheterozygous47214032
178508317685083177CG23GENICheterozygous47214163
178508318585083186GA22GENICheterozygous47214164
178512691885126919GA14GENICheterozygous47214269
178512711285127113TA5GENICheterozygous47214270
178515179785151798TC14GENICheterozygous47214366
178517397385173975TC--41GENICheterozygous47214472
178517409085174091AG29GENICheterozygous47214473
178520278485202785TC41GENICheterozygous47214603
178520295985202960TC18GENICheterozygous47214604
178524374585243746TG46GENICheterozygous47214730
178524385485243874TGATTGATTGATTGATTGAT--------------------18GENICheterozygous47214731
178528239185282392TG9GENICheterozygous47214897
178528549485285495GA28GENICheterozygous47214915
178528559385285594AG19GENICheterozygous48166022
178530767685307677TC19GENICheterozygous47215063
178530778685307787TC19GENICheterozygous47215064
178530898785308988TC18GENICheterozygous47215076
178530902085309021AG16GENICheterozygous47215077
178532245885322459TC11GENICheterozygous47215168
178534442285344423TA9GENICheterozygous47215212
178534543285345433CA20GENICheterozygous47215213