chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71129700211297003AT27GENIChomozygous116273681
71129779811297799CT31GENIChomozygous116273683
71129782311297824CT36GENIChomozygous116273685
71129799611297997GA58GENICpossibly homozygous116273687
71129811911298120GA34GENIChomozygous115568186
71129902411299025AC34GENICpossibly homozygous115568187
71129907511299076TC32GENIChomozygous115568188
71129989111299892AG53GENIChomozygous115568189
71130021711300218TC24GENIChomozygous115568190
71130023311300234GA27GENIChomozygous115568191
71130031511300316GC37GENIChomozygous116273689
71130146911301470AG34GENIChomozygous115568193
71130250811302509GA54GENIChomozygous115568195
71130266611302667TC32GENIChomozygous115568196
71130293611302937CT47GENIChomozygous115568198
71130406711304068AC28GENIChomozygous115568200
71130460911304610TC31GENIChomozygous115568201
71130524411305245CT32GENIChomozygous116273691
71130535911305360CT9GENIChomozygous115568202
71130536811305369AG8GENIChomozygous115568203
71130563411305635GC18GENIChomozygous115568204
71130688211306883AG17GENIChomozygous115568205
71130874011308741GA34GENIChomozygous115568206
71131000911310010TC23GENIChomozygous115568207
71131184411311845TC42GENIChomozygous115568208
71131187111311872GA33GENIChomozygous115568209
71131237711312378GA37GENIChomozygous115568210
71131361011313611GT20GENIChomozygous116273693
71131431411314315AC34GENIChomozygous115568211
71131435811314359AG31GENIChomozygous115568212
71131438811314389AC34GENIChomozygous116273694