chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2045782214578222CT19GENIChomozygous109233522
2045787094578710CA40GENIChomozygous109233523
2045798744579875AG19GENIChomozygous109074755
2045799994580000CT14GENIChomozygous109233524
2045814354581436CT18GENIChomozygous109233525
2045817894581790CT39GENIChomozygous109233526
2045826244582625CT22GENIChomozygous109233527
2045828304582831GA31GENIChomozygous109074767
2045829094582910TA33GENIChomozygous109233528
2045829564582957GT28GENIChomozygous109074769
2045829954582996GA31GENIChomozygous109074771
2045830484583049CT33GENIChomozygous109233529
2045832604583261TC36GENIChomozygous109233530
2045835624583563GT26GENIChomozygous109074777
2045846804584681CT26GENIChomozygous109233531
2045851984585199CT10GENIChomozygous109074779
2045854774585478GC35GENIChomozygous109233532
2045857044585705CT35GENIChomozygous109233533
2045863384586339GA10GENIChomozygous109074781
2045865354586536TA29GENIChomozygous109074783
2045867244586725AG20GENIChomozygous109074789
2045870634587064CT21GENIChomozygous109074791
2045875154587516GA34GENIChomozygous109233534
2045890254589026GA26GENIChomozygous109074793
2045891694589170CT30GENIChomozygous109074795
2045894224589423TC12GENIChomozygous109074797
2045904334590434GA19GENIChomozygous109233535
2045906954590696CT27GENIChomozygous109074799
2045908724590873GA40GENIChomozygous109074801
2045912304591231CT19GENIChomozygous109074803
2045913764591377AG28GENIChomozygous109074805
2045915054591506TC18GENIChomozygous109074807
2045915364591537GA24GENIChomozygous109233536
2045917554591756GA37GENIChomozygous109233537