| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:28138010-28138263 | Common:8; Rare:327 | ||||
| chr13:28138281-28138691 | Common:12; Rare:332 | ||||
| chr13:28139139-28139617 | Common:3; Rare:466 | ||||
| chr13:28658917-28659220 | Common:1; Rare:525; Clinvar (pathogenic):7 | ||||
| chr13:28659408-28659808 | Common:2; Rare:105 | ||||
| chr13:28718710-28719240 | Common:9; Rare:512 | ||||
| chr13:29428250-29428700 | Common:5; Rare:139 | ||||
| chr13:29595090-29595505 | Common:1; Rare:104 | ||||
| chr13:29595600-29596170 | Common:10; Rare:447 | ||||
| chr13:29850179-29850579 | Common:8; Rare:186 | ||||
| chr13:29850542-29850669 | Common:1; Rare:63 | ||||
| chr13:30306641-30307333 | Common:43; Rare:872 | ||||
| chr13:30307324-30308180 | Common:22; Rare:700 | ||||
| chr13:30464310-30465150 | Common:20; Rare:820 | ||||
| chr13:30465817-30466165 | Common:2; Rare:398 |