chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
102640255926402560GC16GENIChomozygous601556069
102640261126402612CT31GENICpossibly homozygous601556070
102640292126402922AAT27GENIChomozygous729707406
102640297526402976TTTTATTTTATAGCACTACTAGGTCATCCTGTAAAGGACTTTGCATGTTGC45GENIChomozygous729707407
102640309326403094TG26GENIChomozygous601556071
102640313226403133TC27GENIChomozygous601556072
102640317126403172TTCAGCTACTGCTCATTG36GENIChomozygous729707408
102640334626403347A-27GENIChomozygous729707409
102640385526403859ACTT----28GENIChomozygous729707410
102640489226404893GA31GENIChomozygous601556073
102640495526404956CA36GENIChomozygous601556074
102640597626405977AC26GENIChomozygous601556075
102640742226407423AG41GENIChomozygous601556076
102640806226408063AG28GENIChomozygous601556077
102640920926409210TC27GENIChomozygous601556078
102641095726410959CA--4GENIChomozygous729707412
102641504726415048CA42GENIChomozygous601556079
102641564926415650AACAAGCT10GENIChomozygous729707414
102641577026415771CG11GENIChomozygous601556080
102641580026415801TC14GENIChomozygous603477533
102641581026415811CCTCTCTCTTTCTTTCTTTCTT5GENIChomozygous729707417
102641608926416090AATCTTT21GENIChomozygous729707419
102641647326416474CT35GENIChomozygous601556081
102641661126416612TC39GENIChomozygous601556082
102641739226417393TTACACAC1GENIChomozygous729707420
102641798026417981GA32GENIChomozygous601556083
102641817926418180AG29GENIChomozygous603477534
102641847526418476GC34GENIChomozygous603477535
102641859826418604AGTAAA------23GENIChomozygous729707422
102641860426418605AC20GENIChomozygous603477536
102641934326419376CAAGGGAAAGGCCAGGCTGGAGTGCCTGGTCCA---------------------------------31GENIChomozygous729707423