chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
182593188425931884GGTGC16GENIChomozygous140216857
182593201925932020TC22GENIChomozygous140291105
182593209725932098CG22GENIChomozygous140291107
182593321425933215GC16GENIChomozygous146300236
182593218725932188TA26GENIChomozygous146300233
182593245825932459CT13GENIChomozygous146300234
182593250425932505GA13GENIChomozygous146300235
182593363625933637CA13GENIChomozygous146300237
182593365725933658TC15GENIChomozygous146300238
182593379625933797AG14GENIChomozygous140291108
182593394925933950TC21GENIChomozygous140291109
182593408625934087CG20GENIChomozygous146300239
182593412025934121GA23GENIChomozygous146300240
182593426425934265AG13GENIChomozygous146300241
182593445925934460AC18GENIChomozygous146300242
182593446725934468CT17GENIChomozygous146300243
182593459325934594AG15GENIChomozygous140291111
182593492425934925GA18GENIChomozygous146300244
182593526425935265AG24GENIChomozygous146300245
182593530025935301GA23GENIChomozygous146300246
182593543325935434TC25GENIChomozygous146300247
182593548125935482GT23GENIChomozygous146300248
182593549625935497AG26GENIChomozygous146300249
182593551125935512AG24GENIChomozygous146300250
182593555725935558GA24GENIChomozygous146300251
182593584425935845AG21GENIChomozygous140291113
182593643125936432TC15GENIChomozygous146300252
182593660125936602AG23GENIChomozygous146300253
182593685025936851GA9GENIChomozygous146300254
182593720225937203TC21GENIChomozygous140291114
182593737125937372GA22GENIChomozygous146300255
182593770025937701GA15GENIChomozygous140291116