chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
102640255926402560GC22GENIChomozygous638898628
102640261126402612CT22GENIChomozygous638898629
102640292126402922AAT19GENIChomozygous750325962
102640297526402976TTTTATTTTATAGCACTACTAGGTCATCCTGTAAAGGACTTTGCATGTTGC18GENIChomozygous750325963
102640309326403094TG6GENIChomozygous638898630
102640313226403133TC10GENIChomozygous638898631
102640317126403172TTCAGCTACTGCTCATTG10GENIChomozygous750325964
102640334626403347A-7GENICpossibly homozygous750325965
102640385526403859ACTT----6GENICheterozygous750325966
102640489226404893GA15GENIChomozygous638898632
102640495526404956CA12GENIChomozygous638898633
102640597626405977AC6GENIChomozygous638898634
102640742226407423AG14GENIChomozygous638898635
102640806226408063AG17GENIChomozygous638898636
102640920926409210TC8GENIChomozygous638898637
102641095726410959CA--1GENIChomozygous750325968
102641504726415048CA4GENIChomozygous638898638
102641564926415650AACAAGCT1GENIChomozygous750325970
102641577026415771CG3GENIChomozygous638898639
102641580026415801TC3GENIChomozygous638898640
102641581026415811CCTCTCTCTTTCTTTCTTTCTT2GENIChomozygous750325973
102641608926416090AATCTTT5GENIChomozygous750325975
102641647326416474CT9GENIChomozygous638898641
102641661126416612TC10GENIChomozygous638898642
102641798026417981GA19GENIChomozygous638898643
102641817926418180AG19GENIChomozygous638898644
102641847526418476GC17GENIChomozygous638898645
102641859826418604AGTAAA------13GENIChomozygous750325976
102641860426418605AC13GENIChomozygous638898646
102641934326419376CAAGGGAAAGGCCAGGCTGGAGTGCCTGGTCCA---------------------------------20GENIChomozygous750325977