chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1205270043205270044TA13GENICpossibly homozygous61064510
1205271430205271431AG21GENICpossibly homozygous61064511
1205272361205272362G-3GENICheterozygous61064513
1205273095205273096CA9GENIChomozygous61585539
1205275621205275622T-2GENIChomozygous61064516
1205275986205275987GA19GENICpossibly homozygous61064518
1205277190205277192TT--2GENIChomozygous61585543
1205277421205277422A-15GENICpossibly homozygous61064522
1205278167205278168GC8GENICpossibly homozygous61585544
1205278201205278202TA2GENICheterozygous61585547