chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7123183697123183698GA9GENICheterozygous115862222
7123183708123183709AG10GENICheterozygous115862224
7123183714123183715CT11GENICheterozygous115862226
7123183720123183721GA11GENICheterozygous115862228
7123183755123183756GA9GENICheterozygous115862230
7123183783123183784CT11GENICheterozygous115862232
7123183813123183814TC8GENICheterozygous115862234
7123183889123183890AG11GENICheterozygous115862236
7123183932123183933GA16GENICheterozygous115862238
7123183973123183974GA17GENICheterozygous115862240
7123183976123183977CA17GENICheterozygous115862242
7123184101123184102CT3GENIChomozygous118418566
7123184427123184428GA8GENIChomozygous118418567
7123184565123184566AT4GENIChomozygous118418568
7123184568123184569TC4GENIChomozygous115862248
7123185164123185165TC11GENICheterozygous115862250
7123187695123187696AG14GENICheterozygous116262981
7123188610123188611CG7GENICheterozygous115862252
7123189783123189784CT5GENIChomozygous118418569
7123190329123190330GA15GENICheterozygous115862254
7123191154123191155AG7GENIChomozygous115862258
7123193631123193632AG3GENIChomozygous115862262
7123193672123193673GA8GENICheterozygous115862264
7123193689123193690TC8GENICheterozygous115862266