chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104615459046154591AG22GENIChomozygous51444202
104615490846154909AT27GENIChomozygous51874917
104615576046155761CT14GENIChomozygous51874919
104615694646156947CCTG12GENICheterozygous51444205
104615731346157314TC26GENIChomozygous51874922
104615774246157743TC17GENIChomozygous51874925
104615799946158000CT29GENIChomozygous51874928
104615827546158276GA23GENIChomozygous51444207
104615850246158503TC22GENIChomozygous51444208
104615851146158512TG22GENIChomozygous51444209
104615944546159446AG22GENIChomozygous51874931
104615950346159504CG15GENIChomozygous51636700
104616126446161265AAC10GENIChomozygous51636702
104616322446163227AAG---23INTERGENIChomozygous51444210
104616449246164493CT26INTERGENIChomozygous51444211
104616452646164527A-25INTERGENIChomozygous51444212
104616676746166768TC20INTERGENIChomozygous51444215
104616678246166783CG22INTERGENIChomozygous51874934
104616704846167049AAG15INTERGENIChomozygous51444216
104616720846167209GGGGGA15INTERGENIChomozygous51444217
104616729646167297TC22INTERGENIChomozygous51444218
104616832846168329AAGG1INTERGENIChomozygous51874936
104617008546170086GA23INTERGENIChomozygous51874939