chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2045782214578222CT30GENIChomozygous109233522
2045787094578710CA26GENIChomozygous109233523
2045799994580000CT25GENIChomozygous109233524
2045814354581436CT25GENICpossibly homozygous109233525
2045817894581790CT20GENIChomozygous109233526
2045798744579875AG17GENIChomozygous109074755
2045826244582625CT30GENIChomozygous109233527
2045828304582831GA23GENIChomozygous109074767
2045829094582910TA21GENIChomozygous109233528
2045829564582957GT27GENIChomozygous109074769
2045829954582996GA26GENIChomozygous109074771
2045830484583049CT20GENIChomozygous109233529
2045832574583258CT37GENIChomozygous109074773
2045832604583261TC38GENIChomozygous109233530
2045835624583563GT30GENIChomozygous109074777
2045846804584681CT30GENIChomozygous109233531
2045851984585199CT18GENIChomozygous109074779
2045854774585478GC33GENICpossibly homozygous109233532
2045857044585705CT28GENIChomozygous109233533
2045863384586339GA15GENIChomozygous109074781
2045865354586536TA22GENIChomozygous109074783
2045867244586725AG17GENIChomozygous109074789
2045870634587064CT22GENIChomozygous109074791
2045875154587516GA40GENIChomozygous109233534
2045890254589026GA18GENIChomozygous109074793
2045891694589170CT30GENIChomozygous109074795
2045894224589423TC15GENIChomozygous109074797
2045906954590696CT18GENIChomozygous109074799
2045908724590873GA34GENIChomozygous109074801
2045912304591231CT25GENIChomozygous109074803
2045913764591377AG23GENIChomozygous109074805
2045915054591506TC10GENICpossibly homozygous109074807
2045915364591537GA17GENICpossibly homozygous109233536
2045917554591756GA41GENIChomozygous109233537
2045880084588009AT8GENICheterozygous109371131