chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7121662929121662931GT--15GENICpossibly homozygous54086824
7121674372121674373CCT12GENICheterozygous55361891
7121674979121674989TGTGTGTGTG----------7GENIChomozygous55059704
7121684217121684218TA34GENIChomozygous54086846
7121686876121686878AC--9GENIChomozygous55632014
7121697045121697046CCTGTGTG7GENIChomozygous55632016
7121709817121709820AAA---19GENICheterozygous54086900
7121709818121709820AA--19GENICpossibly homozygous55096478
7121711614121711615TTACAC12GENIChomozygous55002527
7121713466121713467AAGT20GENICheterozygous55632018
7121715956121715957GGT17GENIChomozygous54086915
7121721347121721348GGTT5GENICheterozygous55096486
7121721799121721800CA32GENIChomozygous54086922
7121740335121740336TTCACA5GENICheterozygous55059705
7121743058121743059TTAA18GENICheterozygous54509850
7121743059121743060A-18GENICheterozygous54087012
7121744727121744728G-28GENIChomozygous54087015
7121748520121748521A-17GENICpossibly homozygous54087022
7121755582121755584AC--11GENICheterozygous55632020
7121770296121770297T-28GENIChomozygous55470084
7121713497121713498GA29GENICpossibly homozygous55586047
7121749590121749591TTA10GENIChomozygous55586050