chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124120386841203869GT27GENIChomozygous115384703
124120407041204071TC40GENIChomozygous115329620
124120418841204189GA31GENIChomozygous115384705
124120422841204229GA30GENICpossibly homozygous115384707
124120424241204243GA29GENIChomozygous115329624
124120475341204754TC20GENIChomozygous115329626
124120478541204786TA26GENIChomozygous115329628
124120497841204979GA23GENIChomozygous115329630
124120593741205938TC31GENIChomozygous115384713
124120597441205975TC38GENIChomozygous115384715
124120641341206414GC24GENIChomozygous115329634
124120713641207137TC23GENIChomozygous115384717
124120717741207178AG28GENIChomozygous115384719
124120739441207395TC25GENIChomozygous115384721
124120750841207509GA25GENIChomozygous115384723
124120755841207559TC34GENIChomozygous115384725
124120759041207591AG33GENIChomozygous115384727
124120767641207677AG16GENIChomozygous115384729
124120770241207703AT17GENIChomozygous115384731
124120781941207820CG32GENIChomozygous115384735
124120788541207886TG26GENIChomozygous115384737
124120789941207900TC30GENIChomozygous115384739
124120837141208372AG22GENIChomozygous115477909
124120838041208381TC20GENIChomozygous115477911
124120852941208530TA20GENIChomozygous115384745
124120901841209019AG29GENIChomozygous115384747