chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2205527492205527493CT22GENIChomozygous110214354
2205528302205528303CT7GENIChomozygous110214355
2205528309205528310CT7GENIChomozygous110214356
2205529864205529865TC10GENIChomozygous110214358
2205531787205531788GA16GENIChomozygous110214359
2205532348205532349TG5GENIChomozygous110214360
2205533114205533115CG12GENICheterozygous110214361
2205538433205538434AG11GENIChomozygous110214362
2205541971205541972CA9GENIChomozygous111008202
2205542317205542318CT7GENIChomozygous111008204
2205544752205544753AG12GENIChomozygous110214363
2205545812205545813TG20GENIChomozygous110214364
2205545975205545976TA12GENIChomozygous110214365
2205547131205547132AG10GENIChomozygous110214366
2205547862205547863TA14GENIChomozygous110214367
2205549042205549043GA12GENICheterozygous110214368