| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:29735373-29735527 | Rare:41 | ||||
| chr10:30348809-30348936 | Rare:25 | ||||
| chr10:30349017-30349151 | Common:1; Rare:39; Clinvar (benign):1 | ||||
| chr10:30349206-30349451 | Common:12; Rare:106 | ||||
| chr10:30433198-30433659 | Common:1; Rare:118 | ||||
| chr10:30433714-30434255 | Common:4; Rare:157 | ||||
| chr10:30434510-30434842 | Common:3; Rare:88 | ||||
| chr10:31031557-31031735 | Common:2; Rare:40 | ||||
| chr10:31031782-31032081 | Common:2; Rare:120 | ||||
| chr10:31032313-31032622 | Common:13; Rare:98 | ||||
| chr10:31318247-31318591 | Common:5; Rare:78 | ||||
| chr10:31318701-31318863 | Common:1; Rare:50 | ||||
| chr10:31318879-31319293 | Common:2; Rare:108 | ||||
| chr10:31319414-31319631 | Common:4; Rare:75 | ||||
| chr10:31320236-31320458 | Common:2; Rare:57 |