chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
102640255926402560GC14GENICpossibly homozygous668506401
102640261126402612CT19GENIChomozygous668506402
102640292126402922AAT14GENICpossibly homozygous768164080
102640309326403094TG12GENICpossibly homozygous668506403
102640313226403133TC14GENIChomozygous668506404
102640334626403347A-2GENIChomozygous768164081
102640489226404893GA17GENIChomozygous668506405
102640495526404956CA19GENIChomozygous668506406
102640597626405977AC9GENIChomozygous668506407
102640742226407423AG14GENICpossibly homozygous668506408
102640806226408063AG10GENIChomozygous668506409
102640920926409210TC27GENIChomozygous668506410
102641504726415048CA14GENICpossibly homozygous668506411
102641577026415771CG6GENIChomozygous668506412
102641608926416090AATCTTT5GENIChomozygous768164082
102641647326416474CT7GENIChomozygous668506413
102641661126416612TC13GENIChomozygous668506414
102641798026417981GA19GENICpossibly homozygous668506415
102641817926418180AG14GENICpossibly homozygous668506416
102641847526418476GC10GENICpossibly homozygous668506417
102641859826418604AGTAAA------5GENIChomozygous768164083
102641860426418605AC5GENIChomozygous668506418
102641934326419376CAAGGGAAAGGCCAGGCTGGAGTGCCTGGTCCA---------------------------------1GENIChomozygous768164084