chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10104727342104727343AAC12INTERGENICheterozygous52605350
10104727548104727555CAAAGTC-------6INTERGENIChomozygous51589476
10104728091104728092TTTATTGGC3INTERGENIChomozygous51589478
10104743138104743139CG2GENIChomozygous51589486
10104743140104743141AG2GENIChomozygous51589488
10104743326104743327AG18GENIChomozygous51589490
10104743330104743331AG19GENIChomozygous51589492
10104743332104743333AT18GENIChomozygous51589494
10104743344104743345AG18GENIChomozygous51589496
10104743347104743348CG18GENIChomozygous51589498
10104743356104743357AG15GENIChomozygous51589500
10104743360104743361AG15GENIChomozygous51589502
10104743362104743363GT14GENIChomozygous51589504
10104743390104743391G-12GENIChomozygous51589506
10104743406104743407AG12GENIChomozygous51589509
10104743503104743504A-3GENIChomozygous51589511
10104743600104743601G-12GENIChomozygous51589513
10104743612104743613T-12GENIChomozygous51589515
10104743652104743653G-8GENIChomozygous51589517
10104743661104743662G-7GENIChomozygous51589519
10104743856104743857GGC2GENIChomozygous51589521
10104743871104743872GGC1GENIChomozygous51589523
10104747399104747402CCC---3GENIChomozygous52447535