| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:11704067-11704253 | Common:1; Rare:53 | ||||
| chr8:11802440-11802831 | Common:6; Rare:215 | ||||
| chr8:11821479-11821830 | Common:3; Rare:140 | ||||
| chr8:13133212-13133568 | Common:14; Rare:101 | ||||
| chr8:13566735-13566898 | Common:6; Rare:61 | ||||
| chr8:17246578-17247063 | Common:5; Rare:202 | ||||
| chr8:17496868-17497158 | Common:5; Rare:117 | ||||
| chr8:17801075-17801344 | Common:7; Rare:101 | ||||
| chr8:17922616-17923039 | Common:5; Rare:167 | ||||
| chr8:17923234-17923323 | Rare:30 | ||||
| chr8:18084771-18085038 | Common:2; Rare:92; Clinvar (benign):1 | ||||
| chr8:19817085-19817515 | Common:8; Rare:146 | ||||
| chr8:21919423-21919773 | Common:2; Rare:132 | ||||
| chr8:21966038-21966313 | Rare:68 | ||||
| chr8:22056744-22057001 | Rare:58 |