chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3128189952128189953CT28GENIChomozygous627552292
3128190049128190050CT22GENIChomozygous627552293
3128190236128190237TC24GENIChomozygous627552294
3128190243128190244AC20GENIChomozygous627552295
3128191392128191393AG29GENIChomozygous627552296
3128192195128192196AAT22GENIChomozygous743997655
3128192274128192275T-18GENICpossibly homozygous743997656
3128192648128192649GA21GENIChomozygous627552297
3128192691128192692AG24GENIChomozygous627552298
3128193115128193116CG17GENIChomozygous627552299
3128193221128193222TA10GENIChomozygous627552300