| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:11742106-11742878 | Common:11; Rare:362 | ||||
| chr10:11823101-11823501 | Common:6; Rare:246 | ||||
| chr10:12042198-12043094 | Common:10; Rare:568 | ||||
| chr10:12043090-12043532 | Common:14; Rare:634 | ||||
| chr10:12068617-12069057 | Common:10; Rare:662 | ||||
| chr10:12128792-12129743 | Common:3; Rare:1048 | ||||
| chr10:12195139-12195796 | Rare:216 | ||||
| chr10:12195789-12196380 | Common:1; Rare:726 | ||||
| chr10:12196436-12196729 | Common:1; Rare:68 | ||||
| chr10:12348899-12349702 | Common:14; Rare:456 | ||||
| chr10:13099825-13100225 | Common:8; Rare:217; Clinvar:6; Clinvar (benign):12 | ||||
| chr10:13161239-13161677 | Common:4; Rare:368 | ||||
| chr10:13299420-13299760 | Common:6; Rare:128 | ||||
| chr10:13299980-13300340 | Rare:314; Clinvar:8 | ||||
| chr10:13301940-13302230 | Common:4; Rare:101 |