chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
181531312215313123CT27GENIChomozygous110281732
181531526415315265AG24GENIChomozygous110281734
181531647215316473AG28GENIChomozygous110281736
181531832615318327AG23GENIChomozygous110281738
181531869015318691AT24GENIChomozygous110281740
181531879615318797AT33GENIChomozygous110281742
181531905115319052AC24GENIChomozygous110281744
181532138515321386GC19GENIChomozygous110281746
181532165615321657GC25GENIChomozygous110281748
181532333715323338TG22GENIChomozygous110281750
181532462015324621AT14GENIChomozygous110281752
181532758115327582TA43GENIChomozygous110281754
181533031815330319GT17GENIChomozygous110281756
181533219315332194AC11GENIChomozygous110281758
181533510915335110CG16GENIChomozygous110281760
181533757915337580AG14GENIChomozygous110281762
181534017415340175AT20GENIChomozygous110281764
181534028115340282AG25GENIChomozygous110281766
181534203315342034TC25GENIChomozygous110281768
181534770315347704CT35GENIChomozygous110281770
181535200915352010CT27GENIChomozygous110281772
181535477415354775TC34GENIChomozygous110281774
181535559115355592GA17GENIChomozygous110281776
181535673715356738TA32GENIChomozygous110281778
181535689615356897GA27GENIChomozygous110281780
181536047815360479AG29GENIChomozygous110281782
181536160015361601AG29GENIChomozygous110281784
181536176815361769CT29GENIChomozygous110281786
181536360915363610AT26GENIChomozygous110281790
181536454115364542CT28GENIChomozygous110281792
181536530115365302CT14GENIChomozygous110281794
181536659815366599AT28GENIChomozygous110281796
181537114215371143AG28GENIChomozygous110281798
181537201215372013TC28GENIChomozygous110281800
181537444015374441TG24GENIChomozygous110281803
181537484915374850AT30GENIChomozygous110281805