chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1795520339552034CT32GENICpossibly homozygous953539792
1795521559552156TC21GENIChomozygous953539793
1795531469553147AG20GENIChomozygous953539794
1795540759554076TG22GENIChomozygous953539795
1795550049555005GT24GENIChomozygous953539796
1795550849555085TA26GENIChomozygous953539797
1795562369556237AG26GENIChomozygous953539798
1795565539556554CT29GENIChomozygous953539799
1795573989557399GA30GENIChomozygous953539800
1795574379557438CA35GENIChomozygous953539801