chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
109039804990398050GA28GENIChomozygous116904589
109039806890398069CT22GENIChomozygous116904591
109039810490398105CA26GENIChomozygous116904593
109039874090398741TC21GENIChomozygous116904595
109039896290398963GA15GENIChomozygous116904597
109039935490399355TC24GENIChomozygous116904599
109039937390399374CT20GENIChomozygous116904601
109039940590399406CT20GENIChomozygous116904603
109040050090400501GT18GENIChomozygous116904605
109040050190400502GC18GENIChomozygous116676210
109040051090400511TC17GENIChomozygous116676212
109040507890405079CT11GENIChomozygous116904611
109040525290405253AC19GENIChomozygous116904613
109040530590405306AT17GENIChomozygous116904615
109040652890406529GA20GENIChomozygous116904617
109040709390407094GC26GENIChomozygous116676216
109040721390407214AG28GENIChomozygous116904619
109040748590407486GA9GENIChomozygous116676218
109040857690408577TC24GENIChomozygous116904621
109040947890409479CT22GENIChomozygous116904623
109040990290409903GT22GENIChomozygous116676222
109041002490410025GA24GENIChomozygous116904625
109041420490414205CT30GENIChomozygous116904627
109041465090414651GA33GENIChomozygous116904629
109041491290414913TC24GENIChomozygous116904631
109041516390415164GA28GENIChomozygous116676236
109041539090415391AT23GENIChomozygous116676238