chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2045782214578222CT27GENIChomozygous109233522
2045787094578710CA22GENIChomozygous109233523
2045793804579381TC24GENICpossibly homozygous119844817
2045799994580000CT20GENIChomozygous109233524
2045814354581436CT35GENIChomozygous109233525
2045798744579875AG35GENICpossibly homozygous109074755
2045802554580256TC15GENICpossibly homozygous109477643
2045802594580260TC15GENICpossibly homozygous109477646
2045817894581790CT22GENIChomozygous109233526
2045826244582625CT38GENIChomozygous109233527
2045828304582831GA40GENIChomozygous109074767
2045829094582910TA37GENIChomozygous109233528
2045829564582957GT25GENIChomozygous109074769
2045829954582996GA44GENIChomozygous109074771
2045830484583049CT29GENIChomozygous109233529
2045832574583258CT27GENIChomozygous109074773
2045832604583261TC28GENIChomozygous109233530
2045835624583563GT34GENIChomozygous109074777
2045846804584681CT28GENIChomozygous109233531
2045851984585199CT36GENIChomozygous109074779
2045854774585478GC27GENIChomozygous109233532
2045857044585705CT39GENIChomozygous109233533
2045863384586339GA46GENIChomozygous109074781
2045865354586536TA41GENIChomozygous109074783
2045867244586725AG34GENIChomozygous109074789
2045870634587064CT40GENIChomozygous109074791
2045875154587516GA23GENIChomozygous109233534
2045890254589026GA22GENIChomozygous109074793
2045891694589170CT26GENIChomozygous109074795
2045894224589423TC20GENIChomozygous109074797
2045904334590434GA19GENIChomozygous109233535
2045906954590696CT43GENIChomozygous109074799
2045908724590873GA63GENIChomozygous109074801
2045912304591231CT29GENIChomozygous109074803
2045913764591377AG40GENIChomozygous109074805
2045915054591506TC30GENIChomozygous109074807
2045915364591537GA30GENIChomozygous109233536
2045917554591756GA38GENIChomozygous109233537