chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1197033815197033816GA30GENIChomozygous108981385
1197036683197036684TC20GENIChomozygous108981386
1197037967197037968CT21GENIChomozygous108981387
1197043356197043357GA20GENIChomozygous108493166
1197049011197049012AG31GENIChomozygous108493194
1197049535197049536CT22GENIChomozygous108981388
1197052358197052359TC29GENIChomozygous108981389
1197052820197052821CG37GENIChomozygous108981390
1197053377197053378AG39GENIChomozygous108493200
1197054665197054666CT17GENIChomozygous108493202
1197054846197054847AG25GENIChomozygous108493204
1197058586197058587TC28GENIChomozygous108981391
1197059035197059036CT23GENIChomozygous108981392
1197061095197061096TC34GENIChomozygous108493208
1197061155197061156GC30GENIChomozygous108981393
1197068403197068404GC36GENIChomozygous108493230
1197068998197068999TC23GENIChomozygous108981395
1197069225197069226AG29GENIChomozygous108493234
1197069237197069238GA28GENIChomozygous108981396
1197069830197069831CT20GENIChomozygous108981397
1197072130197072131GA23GENIChomozygous108981398
1197073359197073360TC28GENIChomozygous108493250
1197073513197073514AG26GENIChomozygous108493254
1197074556197074557AC28GENIChomozygous108981400
1197075251197075252CT25GENIChomozygous108981401
1197075333197075334TC28GENIChomozygous108981402
1197075334197075335AC29GENIChomozygous108981403
1197076676197076677GA34GENIChomozygous108981404
1197077948197077949AG32GENIChomozygous108493278
1197079214197079215AG21GENIChomozygous108493286
1197080710197080711TC37GENIChomozygous108493292
1197082265197082266TC36GENIChomozygous108493303
1197085371197085372AG24GENIChomozygous108493325
1197085698197085699TC38GENIChomozygous108493329