chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1171006637171006638AAG22GENIChomozygous60941889
1171006648171006650AA--24GENICheterozygous60941890
1171006649171006650AAG21GENIChomozygous60941891
1171006678171006679AAG15GENICheterozygous60941893
1171006679171006680AAG11GENIChomozygous60941894
1171006737171006738GGA16GENIChomozygous60941895
1171008278171008279CCAA7GENICpossibly homozygous61555235
1171009510171009511TTAA14GENIChomozygous61555236
1171009879171009880GA16GENICheterozygous61555238
1171009885171009886CT17GENICheterozygous61555239
1171009908171009909GGA7GENIChomozygous60941899
1171010472171010474AA--5GENIChomozygous60941904
1171010794171010795CT29GENIChomozygous61555240
1171011120171011121CT22GENIChomozygous61555241
1171011885171011886CT21GENIChomozygous61555242
1171012238171012239AG21GENIChomozygous61555243
1171013099171013100AAG21GENIChomozygous61555244
1171013457171013458TTA13GENICpossibly homozygous61555245
1171013457171013458TTAAAAA13GENICheterozygous61555246
1171013701171013702GA30GENIChomozygous61555247
1171014231171014232AG21GENIChomozygous61555248
1171014391171014392TC26GENIChomozygous61555249
1171014858171014859CT26GENIChomozygous61555250
1171015885171015886CT22GENIChomozygous61555251
1171015996171015997CCTAAA25GENIChomozygous61555252
1171016250171016251TC21GENIChomozygous61555253
1171016464171016465CT14GENIChomozygous61555254