chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2152786467152786468T22GENIChomozygous127691718
2152786503152786503C22GENIChomozygous127691719
2152786934152786935GC16GENIChomozygous120374352
2152793105152793106CA11GENIChomozygous120374353
2152822049152822050GC21GENIChomozygous110058909
2152808288152808289GA26GENIChomozygous120374354
2152813113152813114CT24GENIChomozygous120374355
2152813281152813282GA12GENIChomozygous120374356
2152815849152815850GT15GENIChomozygous110058872
2152822305152822306CT13GENIChomozygous111268678
2152822328152822329CT13GENIChomozygous110058913
2152822560152822561CT20GENIChomozygous120374357
2152822870152822870A18GENIChomozygous127691744
2152822875152822876A18GENIChomozygous127691745
2152822901152822903CC17GENIChomozygous127691746
2152822918152822920GC16GENIChomozygous127691747
2152822927152822928G15GENIChomozygous127691748
2152822944152822945C13GENIChomozygous127691749
2152822968152822969G13GENIChomozygous127691750
2152823252152823253GA18GENIChomozygous120374358
2152823831152823832TG20GENIChomozygous111268684
2152824203152824204A22GENIChomozygous131293066