| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:12812806-12813006 | Common:1; Rare:62 | ||||
| chr8:22125328-22125667 | Common:5; Rare:109; Clinvar:5; Clinvar (benign):3 | ||||
| chr8:22125831-22126067 | Common:3; Rare:43 | ||||
| chr8:22138723-22138969 | Common:2; Rare:82 | ||||
| chr8:22248244-22248577 | Rare:98 | ||||
| chr8:22525585-22525741 | Common:2; Rare:23 | ||||
| chr8:22609931-22609994 | Common:2; Rare:8 | ||||
| chr8:22618918-22619458 | Common:1; Rare:199 | ||||
| chr8:22733050-22733361 | Common:3; Rare:65 | ||||
| chr8:22739203-22739506 | Common:1; Rare:61 | ||||
| chr8:23441175-23441441 | Common:2; Rare:53 | ||||
| chr8:25278436-25278629 | Rare:47 | ||||
| chr8:25430031-25430279 | Common:3; Rare:39 | ||||
| chr8:26408080-26408375 | Rare:75 | ||||
| chr8:27309856-27309895 | Common:1; Rare:7 |