chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
102640255926402560GC22GENIChomozygous599697968
102640261126402612CT27GENIChomozygous599697969
102640292126402922AAT26GENICpossibly homozygous727547138
102640297526402976TTTTATTTTATAGCACTACTAGGTCATCCTGTAAAGGACTTTGCATGTTGC51GENIChomozygous727547139
102640309326403094TG27GENIChomozygous599697970
102640313226403133TC36GENIChomozygous599697971
102640317126403172TTCAGCTACTGCTCATTG37GENIChomozygous727547140
102640334626403347A-21GENICpossibly homozygous727547141
102640385526403859ACTT----23GENIChomozygous727547142
102640489226404893GA33GENIChomozygous599697972
102640495526404956CA41GENIChomozygous599697973
102640597626405977AC30GENIChomozygous599697974
102640742226407423AG28GENIChomozygous599697975
102640806226408063AG19GENIChomozygous599697976
102640920926409210TC36GENIChomozygous599697977
102641504726415048CA34GENIChomozygous599697978
102641564926415650AACAAGCT11GENIChomozygous727547143
102641577026415771CG8GENIChomozygous599697979
102641580026415801TC11GENIChomozygous605514768
102641581026415811CCTCTCTCTTTCTTTCTTTCTT8GENIChomozygous727547146
102641608926416090AATCTTT33GENIChomozygous727547148
102641647326416474CT32GENIChomozygous599697980
102641661126416612TC25GENIChomozygous599697981
102641739226417393TTACACACAC1GENIChomozygous727547150
102641798026417981GA23GENIChomozygous599697982
102641817926418180AG27GENIChomozygous605514769
102641847526418476GC28GENIChomozygous605514770
102641859826418604AGTAAA------27GENIChomozygous727547151
102641860426418605AC28GENIChomozygous605514771
102641934326419376CAAGGGAAAGGCCAGGCTGGAGTGCCTGGTCCA---------------------------------28GENIChomozygous727547152