chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7138947446138947447AACTCTGCCTGAGCCAGGTTGACTCTCCCAAGAGCCCTCCCCATGGCCCCCTTCATTTCCTTGTTGCGGAAGCT29GENICheterozygous735671255
7138947534138947535GA51GENIChomozygous610943850
7138947567138947568A-57GENICheterozygous735671256
7138947570138947571AAC55GENICheterozygous735671257
7138947582138947583TC65GENIChomozygous610943851
7138947619138947620GT66GENIChomozygous610943852
7138948227138948228AAG4GENIChomozygous735671258
7138948229138948230TTTGAG4GENIChomozygous735671259
7138948233138948234GGT5GENIChomozygous735671260
7138948245138948246T-5GENIChomozygous735671261
7138948642138948643AG6GENIChomozygous610943853
7138948653138948654AG8GENIChomozygous610943854
7138948877138948878TA30GENIChomozygous610943855
7138948908138948909GC31GENIChomozygous610943856
7138948930138948931TC33GENIChomozygous610943857
7138948935138948936CG32GENIChomozygous610943858
7138949108138949109CA25GENIChomozygous610943859
7138949121138949122TC31GENIChomozygous610943860
7138949149138949150CT32GENIChomozygous610943861
7138949181138949182AG28GENIChomozygous610943862
7138949491138949492GT32GENIChomozygous610943863