chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
9100172198100172199TG16GENIChomozygous117618624
9100173003100173004GT23GENIChomozygous117618626
9100173696100173697AG15GENIChomozygous117618628
9100176108100176109GA17GENIChomozygous120421796
9100176845100176846CT12GENIChomozygous120421797
9100177992100177993TC29GENIChomozygous117618632
9100179373100179374TC22GENIChomozygous117618634
9100180316100180317GA22GENIChomozygous120421798
9100181757100181758AT30GENIChomozygous120421799
9100183248100183249CT14GENIChomozygous120421800
9100184631100184632AG23GENIChomozygous117618640
9100185931100185932GA23GENIChomozygous117618642
9100187531100187532AT22GENIChomozygous117618646
9100189318100189319TC20GENIChomozygous117618648
9100189618100189619CT19GENIChomozygous120421801
9100194772100194773TC27GENIChomozygous117618652
9100195266100195267TC24GENIChomozygous117618654
9100196300100196301CT20GENIChomozygous117763385
9100197523100197524AG15GENIChomozygous117618656
9100198926100198927TC33GENIChomozygous117618658
9100199038100199039GT27GENIChomozygous117618660
9100199691100199692GA22GENIChomozygous117618662
9100201852100201853GC21GENIChomozygous117618666
9100203850100203851CT17GENIChomozygous120421802
9100223137100223138TC24GENIChomozygous117618750
9100228662100228663CG21GENIChomozygous117618789
9100228829100228830CT20GENIChomozygous120421803
9100240390100240391GA33GENIChomozygous120421804
9100244436100244437TG26GENIChomozygous120421805
9100247334100247335CA20GENIChomozygous120421806
9100248444100248445TC15GENIChomozygous117618835
9100249442100249443CT21GENIChomozygous117618837
9100250240100250241AG20GENIChomozygous117618839
9100250258100250259TC21GENIChomozygous120421807
9100250813100250814GA16GENIChomozygous117618843
9100251564100251565AC16GENIChomozygous120421808
9100253182100253183AG20GENIChomozygous117618849
9100253451100253452GA8GENIChomozygous117618851