chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
97960381879603818TG22GENIChomozygous128726870
97960382279603822TATTTGTTTTGGTGTTGTTGGGTTTTTTGGGGGGTGTGGGG22GENIChomozygous128726871
97960473579604736G10GENIChomozygous128726872
97960474179604742T10GENIChomozygous128726873
97960475179604752G9GENIChomozygous128726874
97960475379604754G8GENIChomozygous128726875
97960475679604757C8GENIChomozygous128726876
97960476479604765G7GENIChomozygous128726877
97960476779604768AG5GENIChomozygous117380740
97960477679604777G3GENIChomozygous128726878
97960480679604807AG15GENIChomozygous117380741
97960481579604816G13GENIChomozygous128726879
97960483379604834C11GENIChomozygous128726880
97960484079604840C12GENIChomozygous128726881
97960484879604849G11GENIChomozygous128726882
97960485379604854A10GENIChomozygous128726883
97960487379604873G10GENIChomozygous128726884
97960495979604963ATAC11GENIChomozygous128726885
97960496579604965T11GENIChomozygous128726886
97960497179604972TC12GENIChomozygous117380742
97960498779604987C15GENIChomozygous128726887
97960498979604990T13GENIChomozygous128726888
97960499179604992G13GENIChomozygous128726889
97960500279605002C12GENIChomozygous128726890
97960500679605006C11GENIChomozygous128726891
97960501479605015C11GENIChomozygous128726892
97960502479605025A13GENIChomozygous128726893
97960502579605026CG13GENIChomozygous120463370
97960502979605030G13GENIChomozygous128726894
97960503679605036GCGTG13GENIChomozygous128726895
97960852679608527A13GENICheterozygous130677191
97961850779618508AC26GENICheterozygous133004440
97962130679621307TA27GENIChomozygous117380743
97962130779621308TG27GENIChomozygous117380744