chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X1629097616290977AG28GENIChomozygous45098216
X1629184016291841GA6GENIChomozygous45098217
X1629286216292870TGAACTCA--------33GENICheterozygous45647167
X1629305316293055TG--4GENICheterozygous45501372
X1629539416295395TG12GENIChomozygous45098218
X1629590616295907CT11GENIChomozygous45098219
X1629591816295919TC10GENIChomozygous45098220
X1629688716296888CCT23GENICpossibly homozygous45098221
X1629859116298594AAA---4GENIChomozygous45274230