chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2045782214578222CT15GENIChomozygous109233522
2045787094578710CA15GENIChomozygous109233523
2045799994580000CT25GENIChomozygous109233524
2045814354581436CT19GENIChomozygous109233525
2045817894581790CT23GENIChomozygous109233526
2045826244582625CT27GENIChomozygous109233527
2045828304582831GA36GENIChomozygous109074767
2045829094582910TA32GENIChomozygous109233528
2045829564582957GT33GENIChomozygous109074769
2045829954582996GA33GENIChomozygous109074771
2045830484583049CT33GENIChomozygous109233529
2045832574583258CT24GENIChomozygous109074773
2045832604583261TC22GENIChomozygous109233530
2045835624583563GT32GENICpossibly homozygous109074777
2045846804584681CT38GENIChomozygous109233531
2045851984585199CT43GENIChomozygous109074779
2045854774585478GC31GENIChomozygous109233532
2045857044585705CT31GENIChomozygous109233533
2045863384586339GA35GENIChomozygous109074781
2045865354586536TA37GENIChomozygous109074783
2045867244586725AG41GENIChomozygous109074789
2045870634587064CT23GENIChomozygous109074791
2045875154587516GA22GENIChomozygous109233534
2045890254589026GA21GENIChomozygous109074793
2045891694589170CT27GENIChomozygous109074795
2045894224589423TC20GENIChomozygous109074797
2045904334590434GA27GENIChomozygous109233535
2045906954590696CT36GENIChomozygous109074799
2045908724590873GA36GENIChomozygous109074801
2045912304591231CT25GENIChomozygous109074803
2045913764591377AG32GENIChomozygous109074805
2045915054591506TC42GENIChomozygous109074807
2045915364591537GA34GENIChomozygous109233536
2045917554591756GA23GENIChomozygous109233537
2045880084588009AT11GENICheterozygous109371131