chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1171006637171006638AAG10GENIChomozygous60941889
1171006648171006650AA--18GENICheterozygous60941890
1171006649171006650AAG19GENIChomozygous60941891
1171006678171006679AAG14GENICheterozygous60941893
1171006679171006680AAG12GENIChomozygous60941894
1171006737171006738GGA13GENIChomozygous60941895
1171008278171008279CCA6GENICheterozygous60941896
1171008278171008279CCAA6GENICheterozygous61555235
1171009510171009511TTAA25GENICpossibly homozygous61555236
1171009510171009511TTA25GENICheterozygous61555237
1171009879171009880GA24GENIChomozygous61555238
1171009885171009886CT22GENIChomozygous61555239
1171009908171009909GGA12GENICheterozygous60941899
1171010472171010474AA--2GENIChomozygous60941904
1171010794171010795CT21GENIChomozygous61555240
1171011120171011121CT20GENIChomozygous61555241
1171011885171011886CT30GENIChomozygous61555242
1171012238171012239AG25GENIChomozygous61555243
1171013099171013100AAG19GENIChomozygous61555244
1171013457171013458TTA19GENICpossibly homozygous61555245
1171013457171013458TTAAAAA19GENICheterozygous61555246
1171013701171013702GA29GENIChomozygous61555247
1171014231171014232AG16GENIChomozygous61555248
1171014391171014392TC12GENIChomozygous61555249
1171014858171014859CT25GENIChomozygous61555250
1171015885171015886CT47GENIChomozygous61555251
1171015996171015997CCTAAA24GENIChomozygous61555252
1171016250171016251TC29GENIChomozygous61555253
1171016464171016465CT19GENIChomozygous61555254