chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5169574337169574338GA38GENICpossibly homozygous57594831
5169575448169575449TC15GENIChomozygous56085554
5169576662169576663CCT22GENICheterozygous56085556
5169579319169579320GA15GENIChomozygous56364794
5169579619169579620GA25GENICpossibly homozygous57594835
5169580035169580036GA15GENIChomozygous56085572
5169580561169580562TTCTTCCTTCCTTCCTTCCTTC13GENICheterozygous57594838
5169581128169581134GTGTGT------8GENIChomozygous56905257
5169581633169581634GGA22GENIChomozygous57594841
5169585100169585101TG22GENIChomozygous56085577
5169585691169585692TTGTGC18GENICpossibly homozygous57594844
5169578998169578999CCTG2GENICheterozygous55838216
5169578998169578999CCTGTG2GENICheterozygous56465223