chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5109335870109335871AC9GENIChomozygous55891369
5109335871109335872CA9GENIChomozygous56351200
5109335875109335876T-10GENIChomozygous55634234
5109335936109335937T-4GENIChomozygous55634235
5109335965109335966TC3GENIChomozygous55634238
5109381114109381116AC--4GENICheterozygous56444135
5109391085109391089GTGT----14GENICheterozygous56444141
5109391087109391089GT--14GENICheterozygous56444143
5109392252109392264ATCTATCTATCT------------10GENICheterozygous55634515
5109392260109392264ATCT----10GENICpossibly homozygous56222962
5109395083109395084T-14GENICheterozygous55634523
5109395240109395241T-11GENICheterozygous56222968
5109411356109411357AC20GENIChomozygous55634567
5109411358109411359GA18GENIChomozygous55634568
5109411392109411393TG19GENIChomozygous55634569
5109411407109411408GA19GENIChomozygous55634570
5109411730109411732AC--2GENIChomozygous56550192
5109411797109411799CT--6GENIChomozygous56550193
5109417141109417142C-16GENICheterozygous56332242
5109429284109429285TA16GENIChomozygous55634612
5109440426109440427GGATCT6GENIChomozygous56492114
5109453711109453712A-16GENICheterozygous55891382
5109456838109456839GGT10GENICheterozygous56444167
5109456839109456840T-10GENICheterozygous56492119
5109459288109459289TTTTTC18GENIChomozygous55634697
5109477352109477353AATGAAAGGTTTAATATACAGAAAACCATCAACATAATTCATTATAC22GENICheterozygous56444173
5109480627109480629AC--6GENICheterozygous56550196
5109485235109485237GT--8GENICheterozygous56223056
5109494474109494475AAAAGTAC3GENIChomozygous56492126
5109507075109507076TTAGTGAAACTTCCTTTCCTCCCTCCCTCCCTCCCTCCCTTCCTCCTCCCCTCCC10GENIChomozygous56444189
5109507645109507646AACCTCCTTTCCTCCCTCCCTCCCTC1GENIChomozygous56444191
5109518907109518908CCTCTA6GENIChomozygous56492134