chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
102640255926402560GC20GENIChomozygous576606086
102640261126402612CT18GENIChomozygous576606087
102640292126402922AAT21GENIChomozygous715040902
102640297526402976TTTTATTTTATAGCACTACTAGGTCATCCTGTAAAGGACTTTGCATGTTGC33GENIChomozygous715040903
102640309326403094TG23GENIChomozygous576606088
102640313226403133TC18GENIChomozygous576606089
102640317126403172TTCAGCTACTGCTCATTG27GENIChomozygous715040904
102640334626403347A-17GENIChomozygous715040905
102640385526403859ACTT----17GENIChomozygous715040906
102640489226404893GA23GENIChomozygous576606090
102640495526404956CA28GENIChomozygous576606091
102640597626405977AC15GENIChomozygous576606092
102640742226407423AG30GENIChomozygous576606093
102640806226408063AG17GENIChomozygous576606094
102640920926409210TC29GENIChomozygous576606095
102641095026410951TTCA1GENIChomozygous715040909
102641504726415048CA26GENIChomozygous576606096
102641564926415650AACAAGCT17GENIChomozygous715040910
102641577026415771CG11GENIChomozygous576606097
102641580026415801TC9GENIChomozygous603972830
102641581026415811CCTCTCTCTTTCTTTCTTTCTT7GENICheterozygous715040913
102641581026415811CCTCTCTCTTTCTTTCTTTCTTTCTT7GENICpossibly homozygous715040914
102641608926416090AATCTTT20GENIChomozygous715040915
102641647326416474CT25GENIChomozygous576606098
102641661126416612TC24GENIChomozygous576606099
102641739226417393TTACACACAC3GENIChomozygous715040917
102641798026417981GA24GENIChomozygous576606100
102641817926418180AG26GENIChomozygous603972831
102641847526418476GC23GENIChomozygous603972832
102641859826418604AGTAAA------22GENIChomozygous715040918
102641860426418605AC21GENIChomozygous603972833
102641934326419376CAAGGGAAAGGCCAGGCTGGAGTGCCTGGTCCA---------------------------------18GENIChomozygous715040919