chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5166913889166913890GA31GENIChomozygous114454877
5166914027166914028AG23GENIChomozygous114281731
5166914028166914029AG22GENIChomozygous114281733
5166914082166914083GC27GENIChomozygous114281735
5166914115166914116CT24GENIChomozygous114281737
5166914157166914158TA16GENIChomozygous114281739
5166914380166914381CT23GENIChomozygous114281741
5166914512166914513TC26GENIChomozygous114281743
5166914525166914526AT25GENIChomozygous114281745
5166914550166914551GC31GENIChomozygous114281747
5166915276166915277TG22GENIChomozygous114281749
5166915776166915777CT33GENIChomozygous114281751
5166916106166916107GA44GENIChomozygous114281755
5166919035166919036GA24GENIChomozygous114454878
5166922325166922326CT54GENICheterozygous114082167
5166923041166923042GA48GENIChomozygous114454879
5166941539166941540CG41GENICheterozygous114281831
5166944093166944094TC43GENIChomozygous114454881
5166949498166949499GA30GENIChomozygous114454882
5166956963166956964AC29GENIChomozygous114082168
5166959139166959140CT19GENICpossibly homozygous114082169
5166959154166959155TG8GENICpossibly homozygous114082170
5166959241166959242GA83GENICheterozygous114082172
5166969179166969180GA38GENIChomozygous114454884
5166975387166975388GA45GENIChomozygous114684308