| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:99950258-99950477 | Rare:40 | ||||
| chr4:102826779-102826986 | Rare:61 | ||||
| chr4:102827439-102827637 | Rare:72 | ||||
| chr4:102827675-102827980 | Common:3; Rare:91 | ||||
| chr4:102827993-102828299 | Common:3; Rare:104 | ||||
| chr4:102868850-102869063 | Common:2; Rare:72 | ||||
| chr4:103019676-103019776 | Common:1; Rare:31 | ||||
| chr4:105708641-105708849 | Common:1; Rare:69 | ||||
| chr4:106316163-106316613 | Common:5; Rare:145 | ||||
| chr4:107036301-107036542 | Common:2; Rare:50 | ||||
| chr4:107720181-107720522 | Common:7; Rare:137 | ||||
| chr4:107824480-107824735 | Common:1; Rare:52 | ||||
| chr4:107989679-107989941 | Common:6; Rare:117; Clinvar:4; Clinvar (benign):5 | ||||
| chr4:108620401-108620640 | Common:6; Rare:121 | ||||
| chr4:109433757-109433998 | Common:1; Rare:85 |