chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
42300499823004999AC17GENIChomozygous112547222
42300530723005308AT10GENIChomozygous112547224
42300548623005487CT17GENIChomozygous112547226
42300613923006140GC26GENIChomozygous112547228
42300855723008558GA38GENIChomozygous112547283
42300855823008559GT38GENIChomozygous112547285
42300858123008582GT38GENIChomozygous112999705
42300867623008677CA34GENIChomozygous112547287
42300868323008684TC34GENIChomozygous112999707
42300868623008687GC33GENIChomozygous119303406
42301220623012207CG19GENIChomozygous112547299
42301276423012765TC17GENIChomozygous112547305
42301492023014921GA26GENIChomozygous112547309
42301497923014980CT23GENICpossibly homozygous112547311
42301513423015135TC32GENIChomozygous112547313
42301597023015971CT29GENIChomozygous112547315
42301609323016094GA19GENIChomozygous112547317
42301612823016129CG22GENIChomozygous112547319
42301626223016263AG20GENIChomozygous112547321
42301651123016512AG15GENIChomozygous112547323
42301671723016718GA17GENIChomozygous112547325
42301673623016737CT21GENIChomozygous112547327
42301710423017105CT16GENIChomozygous112547329
42301753023017531CT25GENIChomozygous112547331
42301855423018555GC38GENIChomozygous112547333
42302107923021080CT14GENIChomozygous112547335
42302124723021248TG23GENIChomozygous112547337
42302193223021933TG18GENIChomozygous112547339
42302303423023035CT14GENIChomozygous112547343
42302310023023101CT23GENIChomozygous112547345
42302449723024498TC26GENIChomozygous112547349
42302739623027397AG30GENIChomozygous112547357