chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4176702934176702935TC10GENIChomozygous112964411
4176702953176702954GA11GENIChomozygous112964413
4176704300176704301GT19GENIChomozygous112964417
4176704378176704379AG13GENIChomozygous112964419
4176704473176704474CT22GENIChomozygous112964421
4176705377176705378TC18GENIChomozygous112964425
4176706798176706799CA20GENIChomozygous112964427
4176706952176706953GA16GENIChomozygous112964429
4176707312176707313CT20GENIChomozygous112964431
4176707421176707422TA24GENIChomozygous112964433
4176707454176707455TA30GENIChomozygous112964435
4176707678176707679AG22GENIChomozygous112964437
4176708655176708656CT20GENIChomozygous112964439
4176708880176708881GA19GENIChomozygous112964441
4176709106176709107TG15GENIChomozygous112964443
4176709804176709805GT11GENIChomozygous112964446
4176710004176710005GA21GENIChomozygous112964448
4176710678176710679GA23GENIChomozygous112964450
4176710979176710980AG29GENIChomozygous112964452
4176711582176711583AT16GENIChomozygous112964456
4176711888176711889GC7GENIChomozygous112964458
4176711905176711906TC12GENIChomozygous112964462
4176712929176712930CT32GENIChomozygous112964464
4176714397176714398TC19GENIChomozygous112964468
4176714471176714472GA19GENIChomozygous112964470
4176714943176714944CA12GENIChomozygous112964472
4176715920176715921CG17GENIChomozygous112964474
4176716509176716510CA4GENIChomozygous113248668
4176716760176716761TC6GENICheterozygous112964482
4176717067176717068AG28GENIChomozygous112964485
4176718481176718482TA21GENIChomozygous112964490
4176718725176718726TA15GENIChomozygous112964492
4176719087176719088TC25GENIChomozygous112964494
4176719466176719467CG11GENIChomozygous112964496
4176719647176719648CA5GENIChomozygous112964498
4176719886176719887GT19GENIChomozygous112964500