| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:17246441-17246569 | Common:2; Rare:46 | ||||
| chr8:17246798-17247012 | Common:2; Rare:91 | ||||
| chr8:17413180-17413700 | Common:14; Rare:263 | ||||
| chr8:17496877-17497124 | Common:4; Rare:103 | ||||
| chr8:17721935-17722256 | Common:6; Rare:75 | ||||
| chr8:17722483-17722680 | Rare:52 | ||||
| chr8:17922489-17923076 | Common:8; Rare:231 | ||||
| chr8:18084043-18084458 | Common:4; Rare:186; Clinvar:9; Clinvar (benign):2 | ||||
| chr8:18084792-18085003 | Common:2; Rare:71; Clinvar (benign):1 | ||||
| chr8:18886780-18887247 | Rare:148 | ||||
| chr8:19013174-19013586 | Common:6; Rare:148 | ||||
| chr8:19013593-19014000 | Common:6; Rare:123 | ||||
| chr8:19817006-19817156 | Common:3; Rare:50 | ||||
| chr8:19817167-19817514 | Common:6; Rare:120 | ||||
| chr8:20182960-20183360 | Common:2; Rare:140 |