chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
102640255926402560GC19GENICpossibly homozygous629014022
102640292126402922AAT16GENIChomozygous744863521
102640309326403094TG18GENICheterozygous629014023
102640313226403133TC18GENICpossibly homozygous629014024
102640317126403172TTCAGCTACTGCTCATTG5GENICheterozygous744863522
102640334626403347A-6GENIChomozygous744863523
102640471626404717AT26GENICpossibly homozygous629014025
102640495526404956CA27GENIChomozygous629014026
102640620426406205TC20GENIChomozygous629014027
102640654126406542GA22GENIChomozygous629014028
102640705526407056GT19GENICpossibly homozygous629014029
102640806226408063AG7GENIChomozygous629014030
102640844526408446CT20GENIChomozygous629014031
102640920926409210TC29GENIChomozygous629014032
102641059026410591TC10GENIChomozygous629014033
102641178826411789GT26GENICpossibly homozygous629014034
102641237926412380AG16GENICheterozygous629014035
102641254626412547TC21GENICpossibly homozygous629014036
102641295026412951TC2GENICheterozygous629014037
102641305826413059TC21GENICpossibly homozygous629014038
102641446826414469TG27GENIChomozygous629014039
102641456126414562CCT12GENICpossibly homozygous744863525
102641526526415266CT24GENICpossibly homozygous629014040
102641543426415435AG20GENIChomozygous629014041
102641558826415589CT3GENIChomozygous629014042
102641561826415619CA2GENIChomozygous629014043
102641561926415620GA2GENIChomozygous629014044
102641564926415650AACAAGCT1GENIChomozygous744863526
102641608926416090AATCTTT7GENIChomozygous744863527
102641661126416612TC16GENIChomozygous629014045
102641847526418476GC20GENICpossibly homozygous629014046
102641859826418604AGTAAA------7GENIChomozygous744863528
102641860426418605AC7GENIChomozygous629014047
102641873326418734TG22GENICpossibly homozygous629014048
102641894626418947CT12GENIChomozygous629014049
102641934326419376CAAGGGAAAGGCCAGGCTGGAGTGCCTGGTCCA---------------------------------2GENIChomozygous744863529