chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1169435350169435351CG10GENIChomozygous108365457
1169437695169437696TC22GENIChomozygous108365467
1169437842169437843TC27GENIChomozygous108753325
1169437843169437844CT27GENIChomozygous109523706
1169437929169437930AC25GENIChomozygous108365469
1169438299169438300GA28GENIChomozygous108957449
1169441373169441374AC13GENIChomozygous108365477
1169442203169442204CA19GENICpossibly homozygous108957450
1169442256169442257CT20GENIChomozygous108365479
1169442583169442584GC14GENIChomozygous108365481
1169443559169443560CT36GENIChomozygous108957451
1169444355169444356CA32GENIChomozygous108957452
1169444582169444583GA25GENIChomozygous108957453
1169444633169444634AC24GENIChomozygous108957454
1169441224169441225CA4GENICheterozygous120811414
1169441219169441220GA5GENICheterozygous120811410
1169441223169441224GA4GENICheterozygous120811412