chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
107363377273633773GA29GENIChomozygous116635355
107363379073633791AG24GENIChomozygous116635357
107363452973634530TA23GENIChomozygous116635359
107363613073636131AT3GENIChomozygous118001213
107363633573636336AT35GENIChomozygous118001214
107363655373636554CT36GENIChomozygous116635361
107363711573637116GA51GENIChomozygous116635363
107363868273638683GA44GENIChomozygous116635365
107363874573638746GT50GENIChomozygous116635367
107363984173639842AC33GENIChomozygous116635369
107364015373640154GA54GENIChomozygous116635371
107364097173640972TA22GENICpossibly homozygous116635373
107364218473642185TG39GENIChomozygous116635375
107364225473642255CT41GENIChomozygous116635377
107364240873642409AC16GENIChomozygous116635379
107364621873646219CT47GENICpossibly homozygous118001215
107364923573649236GC30GENIChomozygous116635381
107364949773649498GA27GENIChomozygous116635383
107365002773650028GA54GENIChomozygous116635385
107365025273650253CT45GENIChomozygous116635387
107365277373652774CA25GENIChomozygous116635389
107365661873656619AG51GENIChomozygous116635391
107365673073656731AG28GENIChomozygous118001216
107365769873657699AG49GENIChomozygous116635393
107366285673662857AG21GENIChomozygous118001217
107366298473662985TC21GENIChomozygous117016644
107366379773663798AG30GENIChomozygous116635395
107366454873664549AG42GENIChomozygous116635397
107367122373671224TA41GENIChomozygous116635399
107367164573671646CT32GENIChomozygous116635401
107367244973672450CT36GENIChomozygous118001218
107367390173673902AG29GENIChomozygous116635403
107367550473675505AG22GENIChomozygous116635405
107367875273678753TC39GENIChomozygous116942741
107367878273678783AC37GENIChomozygous116978928
107368222773682228AG46GENIChomozygous116635413
107368351473683515AC36GENIChomozygous116635415
107368459973684600AG53GENIChomozygous116635417
107368550373685504AG48GENIChomozygous116635419
107368562773685628CT60GENICheterozygous118001219
107368675873686759CA40GENIChomozygous116635421