chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
174013277340132774AC37GENIChomozygous140114862
174013338840133389GA37GENIChomozygous140114863
174013384040133841AG41GENIChomozygous140114864
174013390340134016ATTGGACTACAGGGAGGGGCTGGGGATTTAGCTCAGTGGTAGAGCGCTTACCTAGGAAGCACAAGGCCCTGGGTTCGGTCCCCAGCTCCGAAAAAAAAAAAGAACCAAAAAAA33GENIChomozygous140022386
174013477540134776AC37GENIChomozygous140114865
174013782140137822AG33GENIChomozygous140114870
174013583140135832AG50GENIChomozygous140114866
174013630240136303GA38GENIChomozygous140114867
174013647240136473AG30GENIChomozygous140114868
174013724740137248TC44GENIChomozygous140114869
174013843540138436CT20GENICpossibly homozygous140114871
174013913340139134AG47GENIChomozygous140114872
174013921840139218C40GENIChomozygous140022387
174014078040140781GT34GENIChomozygous140114873
174014246240142463CT41GENIChomozygous140114874
174014287740142878TC49GENIChomozygous140114875
174014500240145003AG42GENIChomozygous140114876
174014525040145251GA43GENIChomozygous140114877
174014534940145350GA36GENIChomozygous140114878
174013914440139145CT44GENIChomozygous145031395
174014869940148700TC57GENIChomozygous140114879
174015021040150211GA28GENIChomozygous140114880
174015143340151434TC49GENIChomozygous140114881
174015475240154753CG35GENIChomozygous140114882
174015568740155688CT34GENIChomozygous140114883
174015677740156778AG35GENIChomozygous140114884
174015703840157038TCTGAAAATAAGCATTTT15GENIChomozygous140022388
174015715140157151T33GENICpossibly homozygous140022389
174015858940158590TG40GENIChomozygous140114885