| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:17246589-17247109 | Common:5; Rare:209 | ||||
| chr8:17413304-17413506 | Common:3; Rare:106 | ||||
| chr8:17651761-17651996 | Common:1; Rare:57 | ||||
| chr8:17675195-17675481 | Common:4; Rare:86 | ||||
| chr8:17676315-17676424 | Common:1; Rare:35 | ||||
| chr8:17692188-17692405 | Common:2; Rare:65 | ||||
| chr8:17697394-17697468 | Rare:27 | ||||
| chr8:17800920-17801344 | Common:8; Rare:137 | ||||
| chr8:17922606-17923375 | Common:5; Rare:282 | ||||
| chr8:17923474-17923731 | Common:7; Rare:92 | ||||
| chr8:18083516-18083792 | Common:3; Rare:66 | ||||
| chr8:18084773-18084912 | Common:1; Rare:62; Clinvar (benign):1 | ||||
| chr8:18084915-18085057 | Common:1; Rare:31 | ||||
| chr8:19013589-19013976 | Common:6; Rare:115 | ||||
| chr8:19602193-19602259 | Rare:18 |