chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
107623351576233515G37GENIChomozygous128832203
107623351976233519G37GENIChomozygous128832204
107623354876233548C31GENIChomozygous128832205
107623358376233584GA38GENIChomozygous116640839
107623358576233586GT39GENIChomozygous116640841
107623359776233598CG42GENIChomozygous116640843
107623361576233616G39GENIChomozygous128832206
107623364076233640C47GENIChomozygous128832207
107623366176233661T47GENIChomozygous128832208
107623366276233663CT48GENIChomozygous116640845
107623369276233693C48GENIChomozygous128832209
107623370676233706T47GENIChomozygous128832210
107623371676233716A44GENIChomozygous128832211
107623375676233757C41GENIChomozygous128832212
107623376576233766TG39GENIChomozygous116801168
107623377276233773C36GENIChomozygous128832213
107623380076233800G29GENIChomozygous128832214
107623384976233849G18GENIChomozygous128832215
107623385376233854CT16GENIChomozygous118044231
107623385676233857TG14GENIChomozygous128871579
107623385876233859CT14GENIChomozygous128871580
107623387776233878C9GENIChomozygous128832216
107623388376233884CG6GENIChomozygous128871581
107623391376233913T2GENIChomozygous130682086
107625188476251884CCC25GENICheterozygous130682087
107623389776233898T3GENIChomozygous130393415