| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:102827439-102827622 | Rare:65 | ||||
| chr4:102827702-102828137 | Common:3; Rare:136 | ||||
| chr4:102868850-102869083 | Common:2; Rare:83 | ||||
| chr4:103076217-103076243 | Rare:6 | ||||
| chr4:104494725-104495045 | Common:1; Rare:65 | ||||
| chr4:105147476-105147616 | Common:3; Rare:28 | ||||
| chr4:105708641-105708845 | Common:1; Rare:66 | ||||
| chr4:106315979-106316625 | Common:5; Rare:194 | ||||
| chr4:106316638-106316676 | Rare:4 | ||||
| chr4:107720183-107720511 | Common:7; Rare:130 | ||||
| chr4:107989675-107989915 | Common:6; Rare:113; Clinvar:4; Clinvar (benign):5 | ||||
| chr4:108620393-108620647 | Common:6; Rare:128 | ||||
| chr4:109433750-109433954 | Common:1; Rare:66 | ||||
| chr4:109560096-109560363 | Rare:76 | ||||
| chr4:109730045-109730226 | Common:2; Rare:41 |