Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:21918288-21918364 | Rare:6 | ||||
chr10:21973768-21973967 | Common:1; Rare:36 | ||||
chr10:22002486-22002711 | Rare:41 | ||||
chr10:22251802-22252099 | Common:1; Rare:64 | ||||
chr10:22436935-22437086 | Common:6; Rare:71 | ||||
chr10:22437588-22438242 | Common:10; Rare:131 | ||||
chr10:22509238-22509240 | |||||
chr10:23118359-23118564 | Rare:20 | ||||
chr10:24497745-24497844 | Rare:13 | ||||
chr10:24606599-24606613 | Rare:2 | ||||
chr10:24624999-24625295 | Common:6; Rare:39 | ||||
chr10:24880976-24881014 | Common:1; Rare:7 | ||||
chr10:24928879-24929016 | Common:3; Rare:24 | ||||
chr10:25638320-25638529 | Common:5; Rare:55 | ||||
chr10:26742358-26742528 | Common:1; Rare:38; Clinvar:1; Clinvar (benign):2 |