| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:11611543-11611914 | Common:5; Rare:317 | ||||
| chr10:11742160-11742515 | Common:5; Rare:199 | ||||
| chr10:11823242-11823468 | Common:6; Rare:196 | ||||
| chr10:11831192-11832020 | Common:16; Rare:391 | ||||
| chr10:12042748-12042959 | Rare:107 | ||||
| chr10:12043120-12043516 | Common:5; Rare:308 | ||||
| chr10:12068586-12069120 | Common:7; Rare:470 | ||||
| chr10:12129346-12129759 | Common:1; Rare:420 | ||||
| chr10:12194640-12195656 | Common:6; Rare:221 | ||||
| chr10:12195761-12196370 | Common:1; Rare:335 | ||||
| chr10:12348610-12349280 | Common:8; Rare:212 | ||||
| chr10:12349270-12349720 | Common:5; Rare:219 | ||||
| chr10:13099571-13100213 | Common:8; Rare:259; Clinvar:4; Clinvar (benign):9 | ||||
| chr10:13161271-13161646 | Common:3; Rare:277 | ||||
| chr10:13299450-13299730 | Common:4; Rare:107 |