chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
41097625610976257TC18GENIChomozygous112497368
41097650210976503GA13GENIChomozygous112497370
41097883610978837AG29GENIChomozygous112497386
41097899410978995CT20GENIChomozygous112497388
41097911910979120GA21GENIChomozygous112497390
41097961110979612CT13GENIChomozygous112497394
41098087110980872AG21GENIChomozygous112497396
41098102210981023TC26GENIChomozygous112497398
41098133310981334CT29GENIChomozygous112497400
41098150410981505CT18GENIChomozygous112497402
41098176310981764CT17GENIChomozygous112497404
41098232910982330CA8GENIChomozygous112497408
41098233910982340TC7GENIChomozygous112497410
41098269410982695AG9GENIChomozygous112497412
41098276210982763CT17GENIChomozygous112497414
41098299710982998TA5GENIChomozygous113229379
41098305110983052CA5GENICheterozygous112497416
41098330410983305GT14GENIChomozygous112497422
41098343510983436CT19GENIChomozygous112497424
41098408410984085TG17GENIChomozygous112497426
41098412510984126TC4GENIChomozygous112497428
41098447710984478CT20GENIChomozygous112497430
41098465910984660TC19GENIChomozygous112497432
41098522610985227TA28GENIChomozygous112497434
41098531010985311CG10GENIChomozygous112497436