chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3145115139145115140A-52GENIChomozygous57715258
3145115840145115841CT38GENIChomozygous57715259
3145116337145116338TC28GENIChomozygous57715260
3145116531145116534GGG---9GENICheterozygous57715261
3145116532145116534GG--9GENICheterozygous57715262
3145116532145116535GGT---1GENIChomozygous57715263
3145116974145116975AG8GENICpossibly homozygous57715264
3145120345145120346AAT13GENIChomozygous57715265
3145121107145121108TG20GENIChomozygous57715266
3145121169145121170TC18GENIChomozygous57715267
3145121296145121297AT60GENICpossibly homozygous57715268
3145121312145121313TG60GENICpossibly homozygous57715269
3145122811145122812TG36GENIChomozygous57715270
3145124304145124305AG37GENIChomozygous57715271
3145125064145125065TC30GENIChomozygous57715272
3145125639145125640AG32GENIChomozygous57715273
3145125952145125953GA43GENICheterozygous57715274
3145126580145126581TG52GENIChomozygous57715275
3145127440145127441GGT15GENICpossibly homozygous57715276
3145128009145128010TC40GENIChomozygous57715277
3145128262145128263TA32GENIChomozygous57715278
3145129481145129482AG50GENIChomozygous57715279
3145129493145129494CT53GENIChomozygous57715280
3145129660145129661GA44GENIChomozygous57715281
3145130261145130262CA68GENICheterozygous57715284
3145130080145130081C-43GENIChomozygous57715282
3145130215145130216TA62GENICheterozygous57715283
3145130268145130269GA72GENICheterozygous57715285
3145130652145130653TA37GENICheterozygous57715286
3145130663145130664G-35GENICheterozygous57715287
3145130693145130694CT38GENICheterozygous57715288
3145130707145130708GT38GENICheterozygous57715289