chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1255382876255382877TC5GENIChomozygous675761928
1255382893255382894AG5GENIChomozygous675761929
1255383393255383406ATATGGGTACCTA-------------5GENIChomozygous771589555
1255383559255383560CCCGTTA13GENIChomozygous771589556
1255383787255383788TC7GENIChomozygous675761930
1255384349255384350CCCTT5GENIChomozygous771589557
1255384674255384675TTA5GENIChomozygous771589558
1255385730255385731TTGG6GENIChomozygous771589559
1255385744255385745AG6GENIChomozygous675761931
1255386260255386262TT--2GENIChomozygous771589561
1255386723255386724TC7GENIChomozygous675761932
1255387328255387329CT8GENIChomozygous675761933
1255387576255387577AG6GENIChomozygous675761934
1255387694255387695AG6GENIChomozygous675761935
1255388344255388345AG7GENIChomozygous675761936
1255388668255388672AAAC----6GENIChomozygous771589562
1255389434255389435GA7GENICpossibly homozygous675761937
1255389453255389454TA3GENIChomozygous675761938
1255391173255391174GA10GENIChomozygous675761939
1255391571255391572AG8GENICpossibly homozygous675761940
1255391695255391696TC9GENIChomozygous675761941
1255393301255393302AG4GENIChomozygous675761942
1255393392255393393TA7GENIChomozygous675761943
1255393493255393494AAT3GENIChomozygous771589563
1255393562255393563TTGTAA4GENIChomozygous771589564
1255393574255393575TG5GENIChomozygous675761944
1255393970255393971TA5GENIChomozygous675761945
1255394369255394370AC6GENIChomozygous675761946
1255395592255395593GA2GENIChomozygous675761947
1255397033255397034CA12GENIChomozygous675761948
1255397392255397393AG13GENIChomozygous675761949
1255397632255397633CT11GENIChomozygous675761950