chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1197033815197033816GA10GENIChomozygous108981385
1197036683197036684TC12GENIChomozygous108981386
1197037967197037968CT13GENICpossibly homozygous108981387
1197049011197049012AG9GENIChomozygous108493194
1197049535197049536CT9GENIChomozygous108981388
1197052358197052359TC14GENIChomozygous108981389
1197052820197052821CG19GENIChomozygous108981390
1197053377197053378AG8GENIChomozygous108493200
1197054665197054666CT15GENIChomozygous108493202
1197054846197054847AG16GENIChomozygous108493204
1197058586197058587TC7GENIChomozygous108981391
1197059035197059036CT13GENIChomozygous108981392
1197061095197061096TC6GENIChomozygous108493208
1197061155197061156GC10GENIChomozygous108981393
1197065361197065362AG9GENIChomozygous108981394
1197068403197068404GC10GENIChomozygous108493230
1197068998197068999TC13GENIChomozygous108981395
1197069225197069226AG13GENIChomozygous108493234
1197069237197069238GA12GENIChomozygous108981396
1197069830197069831CT15GENIChomozygous108981397
1197072130197072131GA9GENIChomozygous108981398
1197073359197073360TC6GENIChomozygous108493250
1197073513197073514AG9GENIChomozygous108493254
1197074556197074557AC11GENIChomozygous108981400
1197075251197075252CT11GENIChomozygous108981401
1197075333197075334TC13GENIChomozygous108981402
1197075334197075335AC13GENIChomozygous108981403
1197076676197076677GA5GENIChomozygous108981404
1197077948197077949AG8GENIChomozygous108493278
1197079214197079215AG9GENIChomozygous108493286
1197080710197080711TC13GENIChomozygous108493292
1197082265197082266TC5GENIChomozygous108493303
1197085371197085372AG13GENIChomozygous108493325
1197085698197085699TC15GENIChomozygous108493329