chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
107623351576233515G33GENIChomozygous128832203
107623351976233519G34GENIChomozygous128832204
107623354876233548C32GENIChomozygous128832205
107623358376233584GA31GENIChomozygous116640839
107623358576233586GT31GENIChomozygous116640841
107623359776233598CG28GENIChomozygous116640843
107623361576233616G29GENIChomozygous128832206
107623364076233640C37GENIChomozygous128832207
107623366176233661T39GENIChomozygous128832208
107623366276233663CT41GENIChomozygous116640845
107623369276233693C39GENIChomozygous128832209
107623376576233766TG30GENIChomozygous116801168
107623377276233773C28GENIChomozygous128832213
107623370676233706T38GENIChomozygous128832210
107623371676233716A35GENIChomozygous128832211
107623375676233757C31GENIChomozygous128832212
107623380076233800G16GENIChomozygous128832214
107623384976233849G7GENIChomozygous128832215
107623385376233854CT6GENIChomozygous118044231
107623385676233857TG6GENIChomozygous128871579
107623385876233859CT6GENIChomozygous128871580
107623387776233878C3GENIChomozygous128832216
107623388376233884CG2GENIChomozygous128871581
107625188476251884CCC11GENICheterozygous130682087