chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1261338174261338175AC14GENIChomozygous108629357
1261339472261339473AT14GENIChomozygous108629358
1261340002261340003CT9GENIChomozygous108629359
1261340112261340113GA12GENIChomozygous108629360
1261341260261341261AG34GENIChomozygous108629361
1261341870261341871AG28GENIChomozygous108629362
1261342554261342555AG31GENIChomozygous108629363
1261344363261344364AC25GENIChomozygous108629365
1261344933261344934AG29GENIChomozygous108629366
1261345751261345752GA29GENIChomozygous108629368
1261345902261345903CT19GENIChomozygous108629369
1261348114261348115AG23GENIChomozygous108629371
1261348418261348419GA23GENIChomozygous108629374
1261349886261349887CT28GENIChomozygous108629375
1261351067261351068AG19GENIChomozygous108629376
1261354375261354376CT24GENIChomozygous108629378
1261354381261354382CT21GENIChomozygous108629379
1261355899261355900TC27GENIChomozygous108629382
1261356565261356566TC22GENIChomozygous108629385
1261356892261356893AG23GENIChomozygous108629386
1261357931261357932TC25GENIChomozygous108629387
1261358048261358049AC25GENIChomozygous108629388
1261361693261361694CT29GENIChomozygous108629394
1261358218261358219GT14GENIChomozygous108629389
1261359684261359685GA22GENIChomozygous108629390
1261359926261359927TC21GENIChomozygous108629391
1261361483261361484TC25GENIChomozygous108629393
1261362469261362470CT19GENIChomozygous108629395