| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:103076291-103076385 | Rare:29 | ||||
| chr4:105146602-105146911 | Common:1; Rare:98 | ||||
| chr4:105147470-105147604 | Common:3; Rare:29 | ||||
| chr4:105708622-105708877 | Common:3; Rare:83 | ||||
| chr4:106315493-106315646 | Rare:24 | ||||
| chr4:106316151-106316910 | Common:6; Rare:207 | ||||
| chr4:107035686-107035977 | Common:3; Rare:70 | ||||
| chr4:107036203-107036353 | Common:1; Rare:39 | ||||
| chr4:107036430-107036486 | Rare:15 | ||||
| chr4:107283656-107283825 | Rare:34 | ||||
| chr4:107720104-107720522 | Common:9; Rare:168 | ||||
| chr4:107989694-107989874 | Common:4; Rare:81; Clinvar:2; Clinvar (benign):4 | ||||
| chr4:108620388-108620726 | Common:6; Rare:148 | ||||
| chr4:108621947-108622204 | Common:1; Rare:62 | ||||
| chr4:108650567-108650791 | Rare:78 |