| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:107720165-107720504 | Common:7; Rare:137 | ||||
| chr4:107824617-107824735 | Rare:26 | ||||
| chr4:107989690-107989930 | Common:5; Rare:109; Clinvar:4; Clinvar (benign):5 | ||||
| chr4:108168842-108168870 | Rare:5 | ||||
| chr4:108620388-108620647 | Common:6; Rare:131 | ||||
| chr4:109302657-109302754 | Rare:35 | ||||
| chr4:109433750-109433998 | Common:1; Rare:86 | ||||
| chr4:109815461-109815553 | Rare:28 | ||||
| chr4:110198514-110198847 | Rare:98 | ||||
| chr4:112231582-112231852 | Common:2; Rare:85 | ||||
| chr4:112636867-112637197 | Common:1; Rare:92 | ||||
| chr4:112637384-112637570 | Common:3; Rare:52 | ||||
| chr4:112817977-112818244 | Rare:44 | ||||
| chr4:113116719-113117049 | Common:1; Rare:49 | ||||
| chr4:113292583-113292861 | Common:2; Rare:54 |