chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1200606295200606296TA10GENIChomozygous108504552
1200621425200621426AG9GENIChomozygous108504554
1200635901200635902CG7GENIChomozygous108504556
1200650666200650667CT14GENIChomozygous108504558
1200654395200654396GA16GENIChomozygous108504560
1200655352200655353TC6GENIChomozygous108504562
1200655502200655503GA16GENIChomozygous108504566
1200655886200655887AG10GENIChomozygous108504568
1200656621200656622GA15GENIChomozygous108504570
1200657579200657580CT14GENIChomozygous108504572
1200658592200658593GC16GENIChomozygous108504574
1200658868200658869CT13GENIChomozygous108504576
1200664016200664017AC21GENIChomozygous108504578
1200665774200665775AG16GENIChomozygous108504580
1200670762200670763AG25GENIChomozygous108504582
1200672370200672371CT25GENIChomozygous108504584
1200674117200674118TC5GENIChomozygous120874781
1200675055200675056TC5GENIChomozygous108504588
1200675070200675071CG11GENIChomozygous108504590
1200675140200675141CT13GENIChomozygous108504592
1200675185200675186AG14GENIChomozygous108504594
1200675802200675803CT20GENIChomozygous108504596
1200675858200675859AG9GENIChomozygous108504598
1200676145200676146AT20GENIChomozygous108504600
1200676363200676364GA13GENIChomozygous108504602
1200676451200676452CT16GENIChomozygous108504604
1200676828200676829GA20GENIChomozygous108504606
1200679144200679145AC19GENIChomozygous108504612
1200682651200682652AT19GENIChomozygous108504616
1200685365200685366AT15GENIChomozygous108504618
1200686940200686941CT7GENIChomozygous108504620
1200687839200687840TC6GENIChomozygous108504622
1200689471200689472AG21GENIChomozygous108504627
1200690617200690618TC14GENIChomozygous108504629
1200690800200690801GT14GENIChomozygous108504635
1200692660200692661GT11GENICheterozygous108504637
1200694031200694032CA17GENIChomozygous108504639
1200694281200694282GA16GENIChomozygous108504641
1200695619200695620GA6GENIChomozygous120475454