chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3168690606168690606AAACAA49GENIChomozygous136601588
3168690629168690630TA60GENIChomozygous136860710
3168690798168690799G16GENICheterozygous403086133
3168690797168690798GT16GENIChomozygous403086130
3168690797168690798G16GENICheterozygous403086131
3168690798168690799GT16GENIChomozygous403086132
3168690799168690800GT16GENICpossibly homozygous403086134
3168690799168690800G16GENICheterozygous403086135
3168690909168690910T50GENICheterozygous136601589
3168691283168691284TC58GENIChomozygous136860711
3168691716168691717C54GENIChomozygous136601590
3168694968168694969TC75GENIChomozygous136860712
3168696885168696886CT65GENIChomozygous136860713