chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
25688421156884212CT10GENIChomozygous109767725
25688422956884230AG10GENIChomozygous109767727
25688607556886076TG16GENICpossibly homozygous109767729
25688645456886455GC21GENIChomozygous109767731
25688651656886517GA25GENIChomozygous109767733
25688661456886615TC27GENIChomozygous109767735
25688665356886654CG26GENIChomozygous109767737
25688741256887413TC16GENIChomozygous109767739
25688805856888059GC15GENIChomozygous109767741
25688806956888070AT17GENIChomozygous109767743
25688890556888906AG22GENIChomozygous109767745
25688955156889552AC19GENIChomozygous109767747
25689002256890023TC27GENIChomozygous109767749
25689086056890861GC17GENIChomozygous109767750
25689257956892580CG14GENIChomozygous109767752
25689314056893141AC27GENIChomozygous109767754
25689314556893146CT28GENIChomozygous109767756
25689386056893861AG15GENIChomozygous109767758
25689596756895968AG14GENIChomozygous109767760
25690269456902695GA24GENIChomozygous109767762
25690357756903578GC25GENIChomozygous109767764
25689961856899619T10GENIChomozygous127625624
25689015456890154A23GENIChomozygous127625623
25690567056905675TAAAT20GENIChomozygous127625625
25689015556890156TA23GENIChomozygous120124156
25689015756890158TA23GENIChomozygous120124157