| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:7787953-7788213 | Common:1; Rare:107 | ||||
| chr10:12195797-12196241 | Rare:120 | ||||
| chr10:14837974-14838338 | Common:2; Rare:104 | ||||
| chr10:14878617-14878884 | Common:2; Rare:83 | ||||
| chr10:14954023-14954172 | Rare:48 | ||||
| chr10:17228419-17228675 | Common:2; Rare:68 | ||||
| chr10:17643875-17644188 | Common:1; Rare:94 | ||||
| chr10:18651576-18651670 | Common:1; Rare:33 | ||||
| chr10:27154343-27154508 | Rare:48 | ||||
| chr10:27155264-27155391 | Common:3; Rare:44; Clinvar:1; Clinvar (benign):3 | ||||
| chr10:31319022-31319237 | Common:2; Rare:67 | ||||
| chr10:31928792-31928926 | Common:2; Rare:50 | ||||
| chr10:32056379-32056557 | Common:1; Rare:72 | ||||
| chr10:32958160-32958537 | Common:3; Rare:144 | ||||
| chr10:42782581-42782811 | Rare:66 |