chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7123183708123183709AG81GENICheterozygous115862224
7123183714123183715CT80GENICheterozygous115862226
7123183720123183721GA79GENICheterozygous115862228
7123183755123183756GA76GENICheterozygous115862230
7123183783123183784CT85GENICheterozygous115862232
7123183813123183814TC82GENICheterozygous115862234
7123183889123183890AG98GENICheterozygous115862236
7123183932123183933GA85GENICheterozygous115862238
7123183973123183974GA82GENICheterozygous115862240
7123183976123183977CA81GENICheterozygous115862242
7123184303123184304GA72GENICheterozygous115862244
7123184375123184376AG69GENICheterozygous115862246
7123184568123184569TC52GENIChomozygous115862248
7123185164123185165TC56GENICheterozygous115862250
7123187695123187696AG40GENICheterozygous116262981
7123188610123188611CG60GENICheterozygous115862252
7123190329123190330GA73GENICheterozygous115862254
7123190776123190777GA41GENIChomozygous115862256
7123191772123191773TC47GENIChomozygous115862260
7123193631123193632AG17GENIChomozygous115862262