chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7124460787124460788CT8GENIChomozygous115865936
7124461914124461915AG13GENIChomozygous115865938
7124462214124462215CT8GENIChomozygous115865940
7124463086124463087GA12GENIChomozygous115865942
7124463601124463602AG10GENIChomozygous115865944
7124465205124465206AG3GENIChomozygous115865954
7124465578124465579CG7GENIChomozygous115865958
7124466129124466130CG6GENIChomozygous115865964
7124466643124466644CG4GENIChomozygous118286505
7124466660124466661CG4GENIChomozygous118286507
7124467422124467423TG18GENIChomozygous118259352
7124467431124467432TG18GENIChomozygous118259354
7124467437124467438TG15GENIChomozygous118259356
7124467691124467692GC5GENICheterozygous118286509
7124467692124467693TC5GENICheterozygous118286511
7124469887124469888AT11GENIChomozygous115865976