chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1151919155151919156AG12GENIChomozygous109148337
1151920107151920108AG21GENIChomozygous108306970
1151920703151920704TC20GENICheterozygous120872662
1151920706151920707AC23GENICheterozygous120872663
1151923213151923214GA28GENIChomozygous108306972
1151923722151923723TC29GENIChomozygous108306974
1151923723151923724TC28GENIChomozygous108306976
1151924847151924848GA25GENIChomozygous109148339
1151925121151925122AG15GENIChomozygous109148341
1151925674151925675GT33GENIChomozygous109148343
1151925837151925838TC19GENIChomozygous108306982
1151928587151928588GA32GENIChomozygous109148345
1151929317151929318AG29GENIChomozygous108306998
1151930170151930171TC26GENIChomozygous108307006
1151931294151931295GC28GENIChomozygous108307017
1151933337151933338TA39GENIChomozygous120474106
1151933548151933549AC30GENIChomozygous108307037
1151933612151933613GA28GENIChomozygous109148348
1151933742151933743AT33GENIChomozygous109148350
1151933829151933830GT26GENIChomozygous109148352
1151934817151934818GA31GENIChomozygous109148354
1151938096151938097CT27GENIChomozygous109148356
1151939432151939433CT11GENIChomozygous109148358
1151946736151946737CT22GENIChomozygous108307048
1151946895151946896GT21GENIChomozygous108307050