chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3168690606168690606AAACAA29GENIChomozygous136601588
3168690629168690630TA37GENIChomozygous136860710
3168690798168690799G14GENIChomozygous403086133
3168690797168690798GT14GENICheterozygous403086130
3168690797168690798G14GENIChomozygous403086131
3168690798168690799GT14GENICheterozygous403086132
3168690799168690800GT14GENIChomozygous403086134
3168690799168690800G14GENICheterozygous403086135
3168690909168690910T36GENICpossibly homozygous136601589
3168691283168691284TC50GENIChomozygous136860711
3168691716168691717C44GENIChomozygous136601590
3168694968168694969TC62GENIChomozygous136860712
3168697550168697551GA36GENIChomozygous141573104