chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3113133051113133052AG17GENIChomozygous111676675
3113133638113133639GA16GENIChomozygous111676676
3113134396113134397AG12GENIChomozygous111676677
3113136143113136144G15GENIChomozygous127919530
3113136202113136203TA15GENIChomozygous112139733
3113136891113136892TC17GENIChomozygous111676679
3113137175113137176TC19GENIChomozygous111676680
3113141004113141005CT11GENIChomozygous112139734
3113142016113142017GT20GENICpossibly homozygous111676688
3113142314113142315AG25GENIChomozygous112139735
3113142404113142405TA17GENIChomozygous112139736
3113143815113143816AG20GENIChomozygous111676689
3113144465113144466TC9GENIChomozygous112007839
3113146782113146783AC25GENIChomozygous111676696
3113147001113147002TG13GENIChomozygous120111119
3113147003113147004GT13GENIChomozygous119938593
3113147222113147223TG12GENIChomozygous112139741
3113148127113148135AAATAAAT8GENIChomozygous130908273
3113148155113148156AG10GENIChomozygous112007853
3113148211113148214GGG8GENIChomozygous130908274
3113148215113148216G8GENIChomozygous130908275
3113148300113148301GA11GENICheterozygous119714318
3113149289113149290AG18GENIChomozygous111676703
3113150258113150258G21GENIChomozygous127919534
3113151248113151248CC10GENIChomozygous127919535
3113151380113151380CTTTATTGCCTCCCAGTGCTG13GENIChomozygous127919536
3113151871113151882CCTATGAAGAT17GENIChomozygous127919537
3113152067113152068AT22GENIChomozygous112139746
3113153479113153480TC26GENIChomozygous112007859
3113154094113154095CG23GENIChomozygous111676707
3113154819113154820CT20GENIChomozygous112139747
3113155245113155246AG20GENIChomozygous111676708
3113155310113155311AG16GENIChomozygous111676709
3113156379113156380TC15GENIChomozygous111676712
3113156535113156535G9GENICpossibly homozygous130908276
3113158865113158866GA24GENIChomozygous112139748
3113159175113159176GT13GENIChomozygous112139749
3113159338113159339CT17GENIChomozygous112139750
3113159761113159762CT19GENIChomozygous112139751
3113148302113148303GA11GENICheterozygous132394869