chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4155363259155363260GT14GENIChomozygous112895390
4155363323155363324AT11GENIChomozygous119282325
4155363370155363371GA12GENIChomozygous112895392
4155363512155363513GA24GENIChomozygous112895394
4155363976155363977CT17GENIChomozygous112895398
4155364036155364037GA18GENIChomozygous112895400
4155364067155364068AT19GENIChomozygous112895402
4155364248155364249CT15GENIChomozygous112895404
4155364363155364364GT17GENIChomozygous112895406
4155364606155364607CA28GENIChomozygous112895414
4155364628155364629GA29GENIChomozygous112895416
4155364637155364638AG29GENIChomozygous112895418
4155364684155364685GA35GENIChomozygous112895420
4155364687155364688GA38GENIChomozygous112895422
4155364704155364705CT37GENIChomozygous112895424
4155364715155364716TC36GENIChomozygous112895426
4155364805155364806AG34GENIChomozygous112895428
4155364835155364836CT29GENIChomozygous112895430
4155364952155364953AG24GENIChomozygous112895432
4155365104155365105AG28GENIChomozygous112895434
4155365451155365452TA18GENIChomozygous113307909
4155366099155366100GA28GENIChomozygous112895444
4155366315155366316CG18GENIChomozygous112895446
4155366428155366429TC17GENIChomozygous112895448
4155366436155366437CA17GENIChomozygous112895450
4155366604155366605CT21GENIChomozygous112895452
4155366728155366729GA27GENIChomozygous112895454
4155366745155366746AG25GENIChomozygous112895456
4155367091155367092CT18GENIChomozygous112895462
4155367139155367140AC21GENIChomozygous112895464
4155367185155367186AG16GENIChomozygous112895466
4155367199155367200TA14GENICpossibly homozygous112895468
4155367863155367864TC24GENIChomozygous112895470
4155368139155368140TC19GENIChomozygous112895474
4155368232155368233AG21GENIChomozygous112895476
4155368259155368260CT24GENIChomozygous112895478
4155368880155368881TG24GENIChomozygous112895480
4155369725155369726AG23GENIChomozygous112895482
4155370576155370577AG24GENIChomozygous112895484