chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
41550578415505785AG26GENIChomozygous113083221
41550660415506605GA21GENIChomozygous113083222
41550864915508650AG25GENIChomozygous113083224
41550904815509049GA33GENIChomozygous113083225
41551010515510106GT35GENIChomozygous113083226
41551060015510601TG41GENIChomozygous113083227
41551288815512889CA17GENICheterozygous113251714
41551291715512918CA12GENIChomozygous119334645
41551294215512943AG19GENIChomozygous113083228
41551336315513364AG34GENIChomozygous113083229
41551390415513905GT27GENIChomozygous113083230
41551412015514121TC27GENIChomozygous112519793
41551507215515073TA30GENIChomozygous113083231
41551545015515451GC31GENIChomozygous112519795
41551707715517078GA30GENIChomozygous113083232
41551723615517237AG31GENIChomozygous112519797
41551752215517523GA34GENIChomozygous113083233
41551833315518334AG24GENIChomozygous113083234
41551844815518449CT28GENIChomozygous113083235
41551906615519067AG38GENIChomozygous113083236