chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2045782214578222CT13GENIChomozygous109233522
2045787094578710CA16GENIChomozygous109233523
2045793804579381TC34GENIChomozygous119844817
2045799994580000CT25GENIChomozygous109233524
2045814354581436CT19GENIChomozygous109233525
2045798744579875AG24GENIChomozygous109074755
2045802554580256TC30GENICheterozygous109477643
2045802594580260TC32GENICheterozygous109477646
2045817894581790CT24GENIChomozygous109233526
2045826244582625CT29GENICpossibly homozygous109233527
2045828304582831GA38GENIChomozygous109074767
2045829094582910TA31GENIChomozygous109233528
2045829564582957GT33GENIChomozygous109074769
2045829954582996GA34GENIChomozygous109074771
2045830484583049CT35GENIChomozygous109233529
2045832574583258CT24GENIChomozygous109074773
2045832604583261TC22GENIChomozygous109233530
2045835624583563GT32GENICpossibly homozygous109074777
2045846804584681CT42GENIChomozygous109233531
2045851984585199CT44GENIChomozygous109074779
2045854774585478GC32GENIChomozygous109233532
2045857044585705CT32GENIChomozygous109233533
2045863384586339GA35GENIChomozygous109074781
2045865354586536TA37GENIChomozygous109074783
2045867244586725AG42GENIChomozygous109074789
2045870634587064CT23GENIChomozygous109074791
2045875154587516GA24GENIChomozygous109233534
2045890254589026GA21GENIChomozygous109074793
2045891694589170CT27GENIChomozygous109074795
2045894224589423TC19GENIChomozygous109074797
2045904334590434GA31GENIChomozygous109233535
2045906954590696CT37GENIChomozygous109074799
2045908724590873GA35GENIChomozygous109074801
2045912304591231CT26GENIChomozygous109074803
2045913764591377AG32GENIChomozygous109074805
2045915054591506TC42GENIChomozygous109074807
2045915364591537GA34GENIChomozygous109233536
2045917554591756GA24GENIChomozygous109233537