| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:101345918-101346262 | Common:2; Rare:103 | ||||
| chr4:102344157-102344279 | Common:1; Rare:17 | ||||
| chr4:102344422-102344582 | Rare:54; Clinvar (pathogenic):2 | ||||
| chr4:102500369-102500520 | Rare:28 | ||||
| chr4:102500548-102500583 | Rare:7 | ||||
| chr4:102687439-102687557 | Common:1; Rare:21 | ||||
| chr4:102687814-102687928 | Rare:18 | ||||
| chr4:102829225-102829377 | Rare:32 | ||||
| chr4:102867660-102867991 | Common:3; Rare:66 | ||||
| chr4:102868216-102868329 | Rare:17 | ||||
| chr4:103075066-103075225 | Common:2; Rare:23 | ||||
| chr4:104490556-104490732 | Rare:50 | ||||
| chr4:104491050-104491094 | Rare:10 | ||||
| chr4:104491149-104491733 | Common:3; Rare:182 | ||||
| chr4:104492417-104492608 | Rare:28 |