chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8118776728118776729AC56GENIChomozygous138433308
8118778201118778202TC53GENIChomozygous138433310
8118779704118779705AG52GENIChomozygous138433312
8118780490118780491AC26GENIChomozygous138433315
8118781077118781078C45GENIChomozygous138268802
8118778149118778150CT47GENIChomozygous146891895
8118778610118778611GA48GENIChomozygous146891896
8118778616118778617GA50GENIChomozygous146891897
8118780116118780117CT67GENIChomozygous146891898
8118780436118780437TG30GENIChomozygous146891899
8118780442118780443TG23GENIChomozygous146891900
8118780434118780434G31GENIChomozygous146849941
8118780520118780520GCCTCCTAGGCAAGCGCTCT24GENIChomozygous138268801
8118782200118782200TTCTTGTACGCACATACA44GENIChomozygous138268803
8118782697118782698TC16GENIChomozygous138433316
8118783055118783056GC54GENIChomozygous138433319
8118785184118785185TC45GENIChomozygous138433320
8118785696118785697AG53GENIChomozygous138433321
8118786284118786285AG51GENIChomozygous138433322
8118787115118787116TC49GENIChomozygous138433324
8118787935118787936GA48GENIChomozygous146891901
8118788509118788510GA48GENIChomozygous146891902
8118788922118788923AC60GENIChomozygous138433325
8118789120118789121AC59GENIChomozygous138433326
8118789177118789178AC65GENIChomozygous138433327
8118789612118789621TCCTGGGTC50GENIChomozygous146849942
8118789969118789970CT66GENIChomozygous146891903
8118790747118790748TA52GENIChomozygous138433328
8118790836118790836GGACT37GENIChomozygous138268804
8118791191118791192TC52GENIChomozygous138433329
8118791594118791595CA53GENIChomozygous146891904
8118793308118793309GA54GENIChomozygous146891905
8118793912118793913TA51GENIChomozygous146891906
8118794615118794616C17GENIChomozygous142031654
8118794826118794827CT25GENIChomozygous146891907
8118794639118794640TC17GENICheterozygous403251789
8118780446118780447G24GENICheterozygous404009449
8118780446118780447GT24GENICpossibly homozygous404009450
8118794639118794640T17GENIChomozygous403251788