chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
107623351576233515G15GENIChomozygous128832203
107623351976233519G15GENIChomozygous128832204
107623354876233548C14GENIChomozygous128832205
107623358376233584GA17GENIChomozygous116640839
107623358576233586GT17GENIChomozygous116640841
107623359776233598CG19GENIChomozygous116640843
107623361576233616G18GENIChomozygous128832206
107623366276233663CT18GENIChomozygous116640845
107623370676233706T15GENIChomozygous128832210
107623364076233640C19GENIChomozygous128832207
107623366176233661T18GENIChomozygous128832208
107623369276233693C16GENIChomozygous128832209
107623371676233716A14GENIChomozygous128832211
107623375676233757C11GENIChomozygous128832212
107623376576233766TG11GENIChomozygous116801168
107623377276233773C10GENIChomozygous128832213
107623380076233800G8GENIChomozygous128832214
107623384976233849G6GENIChomozygous128832215
107623385376233854CT6GENIChomozygous118044231
107623385676233857TG6GENIChomozygous128871579
107623385876233859CT6GENIChomozygous128871580
107623387776233878C4GENIChomozygous128832216
107623388376233884CG4GENIChomozygous128871581
107623389776233898T2GENIChomozygous130393415