chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10104726060104726063TCC---42INTERGENICheterozygous52404460
10104726064104726073GTGGCACCG---------50INTERGENICheterozygous52404462
10104726211104726212AAGG42INTERGENICheterozygous52404464
10104727548104727555CAAAGTC-------47INTERGENIChomozygous51589476
10104728091104728092TTTATTGGC17INTERGENIChomozygous51589478
10104743138104743139CG17GENIChomozygous51589486
10104743140104743141AG19GENIChomozygous51589488
10104743326104743327AG27GENIChomozygous51589490
10104743330104743331AG26GENIChomozygous51589492
10104743332104743333AT26GENIChomozygous51589494
10104743344104743345AG25GENIChomozygous51589496
10104743347104743348CG24GENIChomozygous51589498
10104743356104743357AG24GENIChomozygous51589500
10104743360104743361AG24GENIChomozygous51589502
10104743362104743363GT24GENIChomozygous51589504
10104743390104743391G-17GENIChomozygous51589506
10104743406104743407AG18GENIChomozygous51589509
10104743503104743504A-29GENIChomozygous51589511
10104743600104743601G-42GENIChomozygous51589513
10104743612104743613T-40GENIChomozygous51589515
10104743652104743653G-33GENIChomozygous51589517
10104743661104743662G-33GENIChomozygous51589519
10104743856104743857GGC9GENIChomozygous51589521
10104743871104743872GGC9GENIChomozygous51589523
10104728472104728474CA--6INTERGENICheterozygous52651792
10104747399104747402CCC---1GENIChomozygous52447535