chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2045782214578222CT9GENIChomozygous109233522
2045787094578710CA10GENIChomozygous109233523
2045798744579875AG11GENIChomozygous109074755
2045799994580000CT3GENIChomozygous109233524
2045814354581436CT26GENIChomozygous109233525
2045817894581790CT18GENIChomozygous109233526
2045826244582625CT27GENIChomozygous109233527
2045828304582831GA23GENIChomozygous109074767
2045829094582910TA24GENIChomozygous109233528
2045829564582957GT24GENIChomozygous109074769
2045829954582996GA17GENIChomozygous109074771
2045830484583049CT16GENIChomozygous109233529
2045832574583258CT23GENIChomozygous109074773
2045832604583261TC23GENIChomozygous109233530
2045835624583563GT11GENIChomozygous109074777
2045846804584681CT10GENIChomozygous109233531
2045851984585199CT9GENIChomozygous109074779
2045854774585478GC14GENIChomozygous109233532
2045857044585705CT16GENIChomozygous109233533
2045863384586339GA7GENIChomozygous109074781
2045865354586536TA15GENIChomozygous109074783
2045867244586725AG10GENIChomozygous109074789
2045870634587064CT7GENIChomozygous109074791
2045875154587516GA18GENIChomozygous109233534
2045890254589026GA6GENIChomozygous109074793
2045891694589170CT16GENIChomozygous109074795
2045894224589423TC9GENIChomozygous109074797
2045904334590434GA11GENIChomozygous109233535
2045906954590696CT14GENIChomozygous109074799
2045908724590873GA13GENIChomozygous109074801
2045912304591231CT16GENIChomozygous109074803
2045913764591377AG14GENIChomozygous109074805
2045915054591506TC10GENIChomozygous109074807
2045915364591537GA4GENIChomozygous109233536
2045917554591756GA16GENIChomozygous109233537