chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
183089169130891692GT26GENIChomozygous110532700
183089180330891804CT28GENIChomozygous110321219
183089181630891817TC24GENIChomozygous110532702
183089186130891862TC19GENIChomozygous110532704
183089213530892136AT11GENIChomozygous110321225
183089215530892156AG18GENIChomozygous110532706
183089321130893212TC18GENIChomozygous110321227
183089327630893277CT19GENIChomozygous110321229
183089327830893279CT20GENIChomozygous110321231
183089335130893352CT31GENIChomozygous110321233
183089348630893487AT29GENIChomozygous110321237
183089348930893490TC29GENIChomozygous110321239
183089355230893553AG20GENIChomozygous110321241
183089358030893581AG19GENIChomozygous110321243
183089360830893609CT20GENIChomozygous110321245
183089361330893614AT21GENIChomozygous110321247
183089363830893639TA25GENIChomozygous110321249
183089303630893037CT8GENIChomozygous110457545