chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106749733767497338CCT3GENICheterozygous51682246
106749733867497339T-3GENICheterozygous51682248
106749778567497787TT--8GENICheterozygous53227548
106750109167501111ACACACACACACACACACAC--------------------19GENIChomozygous53227550
106750134767501348AATT25GENIChomozygous51682251
106750369767503699AA--9GENICheterozygous52724675
106750369867503699A-9GENICpossibly homozygous52383316
106750374867503749CCA9GENICheterozygous51682255
106750376967503770CT12GENICpossibly homozygous51682257
106750599567505996CT30GENIChomozygous51682259
106750619767506198GT27GENIChomozygous51682262
106750651567506516A-8GENICheterozygous51682266
106750863067508631TA33GENIChomozygous51682268
106750997367509974GGA10GENIChomozygous51682270
106751054867510549AG19GENIChomozygous51682272
106751067667510677T-15GENIChomozygous51480660
106751405267514053CT26INTERGENIChomozygous51682274
106751732867517329CT22INTERGENIChomozygous51682276
106751855367518555CG--11INTERGENICheterozygous51682280
106751895167518953AA--25INTERGENICheterozygous51682282
106751895267518953A-25INTERGENICpossibly homozygous51682284
106751933567519338TTT---22INTERGENIChomozygous51682286
106751934267519343TG22INTERGENIChomozygous53227552
106752053267520538CCCTCC------4INTERGENIChomozygous51682290
106752362067523621CCGT3GENIChomozygous52602314
106752365667523657CT7GENIChomozygous51682294
106752366267523663CT17GENIChomozygous51682296
106752446767524468TC31GENIChomozygous51682298
106752639967526400CT27GENIChomozygous51682300
106752711767527118TTGGAATGGAGGAGTCCCA34GENIChomozygous51682302
106752740967527410TC26GENIChomozygous51682303