chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104602098346020984TC19GENIChomozygous116772256
104602238846022389GA37GENIChomozygous116772258
104602405746024058GA48GENIChomozygous117252559
104602725246027253TC44GENIChomozygous116584986
104602776946027770AG21GENIChomozygous116584988
104602812546028126TA30GENIChomozygous116584990
104602832446028325GA34GENIChomozygous117252561
104603137046031371CT37GENIChomozygous117171880
104603524646035247CA34GENIChomozygous116772262
104603677246036773TA15GENIChomozygous117252563
104603746946037470TG8GENIChomozygous117171882
104604308446043085GC27GENIChomozygous116585003
104604534346045344GA63GENIChomozygous116772264
104604916246049163TC8GENIChomozygous116772266
104605082346050824GA42GENIChomozygous116772268
104605331446053315GA42GENIChomozygous116585013
104606092646060927CG46GENIChomozygous116585021
104607198446071985AG43GENIChomozygous116585043
104607341846073419TA19GENIChomozygous116585045
104607398046073981AG12GENIChomozygous116585049
104607637946076380TG21GENIChomozygous116772278
104605107046051071CT12GENIChomozygous116772270
104605305046053051CT51GENIChomozygous116772272
104606076946060770AG35GENIChomozygous116772274
104606615446066155CG25GENIChomozygous116772276
104607857646078577GA64GENIChomozygous116772280
104608073746080738AG44GENIChomozygous116585059
104608144346081444GA14GENIChomozygous116772282
104608152946081530GC25GENIChomozygous117252565
104608301346083014GA40GENIChomozygous116772284
104608814546088146AG38GENIChomozygous116585067
104609530046095301AG37GENIChomozygous116772286
104609853546098536GT37GENIChomozygous117171884
104610326846103269GT17GENICpossibly homozygous117171886
104611402846114029CT46GENIChomozygous116772290
104611675146116752AG51GENIChomozygous116585094
104611924246119243CG50GENIChomozygous116772292
104612220746122208CT42GENIChomozygous116772296
104612359146123592TC40GENIChomozygous116585098
104612359246123593GC40GENIChomozygous116585100
104612705846127059TC38GENIChomozygous116585104