chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1197033815197033816GA19GENIChomozygous108981385
1197036683197036684TC26GENIChomozygous108981386
1197037967197037968CT28GENIChomozygous108981387
1197043356197043357GA12GENICheterozygous108493166
1197048065197048066AG18GENIChomozygous108493190
1197048694197048695TC36GENIChomozygous108493192
1197049011197049012AG26GENIChomozygous108493194
1197049535197049536CT25GENICpossibly homozygous108981388
1197052358197052359TC34GENIChomozygous108981389
1197052820197052821CG27GENIChomozygous108981390
1197053377197053378AG20GENIChomozygous108493200
1197054665197054666CT26GENIChomozygous108493202
1197054846197054847AG23GENIChomozygous108493204
1197058586197058587TC35GENIChomozygous108981391
1197059035197059036CT22GENIChomozygous108981392
1197061095197061096TC23GENIChomozygous108493208
1197061155197061156GC19GENIChomozygous108981393
1197065361197065362AG36GENICpossibly homozygous108981394
1197066327197066328TC3GENIChomozygous108493220
1197068403197068404GC12GENIChomozygous108493230
1197068998197068999TC26GENIChomozygous108981395
1197069225197069226AG28GENIChomozygous108493234
1197069237197069238GA26GENIChomozygous108981396
1197069830197069831CT26GENIChomozygous108981397
1197072130197072131GA30GENIChomozygous108981398
1197072963197072964CT14GENIChomozygous108981399
1197073359197073360TC23GENIChomozygous108493250
1197073513197073514AG19GENICpossibly homozygous108493254
1197074556197074557AC30GENIChomozygous108981400
1197075251197075252CT14GENIChomozygous108981401
1197075333197075334TC16GENIChomozygous108981402
1197075334197075335AC16GENIChomozygous108981403
1197076676197076677GA25GENICpossibly homozygous108981404
1197077948197077949AG24GENIChomozygous108493278
1197079214197079215AG28GENIChomozygous108493286
1197080710197080711TC19GENIChomozygous108493292
1197082265197082266TC25GENIChomozygous108493303
1197085371197085372AG28GENIChomozygous108493325
1197085698197085699TC18GENIChomozygous108493329