chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5142704483142704484CA24GENICpossibly homozygous775448585
5142706126142706127GA34GENIChomozygous775448586
5142706502142706503TC31GENIChomozygous775448587
5142708301142708302TC26GENIChomozygous775448588
5142710505142710506GC25GENIChomozygous775448589
5142710670142710671GA27GENIChomozygous775448590
5142713885142713886TC26GENIChomozygous775448591
5142715483142715484AG47GENIChomozygous775448592
5142716410142716411CT57GENICpossibly homozygous775448593
5142716668142716669AG43GENIChomozygous775448594
5142717464142717465AG48GENIChomozygous775448595
5142719742142719743CT24GENICpossibly homozygous775448596
5142720222142720223TC44GENICheterozygous775448597
5142721524142721525AG53GENIChomozygous775448598