chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1154139811154139812GA17GENIChomozygous147646012
1154139862154139862T16GENIChomozygous147635648
1154141057154141058GA34GENIChomozygous135713169
1154141632154141633AG22GENIChomozygous135713171
1154141664154141665TC20GENIChomozygous147646013
1154141809154141810GA14GENIChomozygous135713172
1154142179154142180GA21GENIChomozygous135713174
1154142774154142775GT28GENIChomozygous147646014
1154145589154145590TC27GENIChomozygous147646015
1154145600154145601CA29GENICpossibly homozygous147646016
1154145789154145790AG20GENIChomozygous145310409
1154145949154145950TC19GENIChomozygous145310410
1154146928154146929AC25GENIChomozygous147646017
1154147443154147444CT23GENIChomozygous145310412
1154142709154142710CT26GENIChomozygous144564567
1154142352154142353CT19GENIChomozygous141264396