| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:2843699-2844016 | Common:3; Rare:115 | ||||
| chr4:2867719-2867879 | Rare:31 | ||||
| chr4:2934767-2934923 | Common:3; Rare:71 | ||||
| chr4:2963299-2963595 | Common:2; Rare:111 | ||||
| chr4:2963957-2964067 | Common:1; Rare:55 | ||||
| chr4:3074516-3074714 | Common:4; Rare:67 | ||||
| chr4:3292729-3293079 | Common:3; Rare:133 | ||||
| chr4:3532208-3532485 | Rare:146; Clinvar (pathogenic):2 | ||||
| chr4:4248147-4248266 | Common:4; Rare:62 | ||||
| chr4:4290110-4290312 | Common:3; Rare:81 | ||||
| chr4:4541936-4542338 | Common:2; Rare:143 | ||||
| chr4:5019423-5019568 | Common:1; Rare:48 | ||||
| chr4:6640518-6641084 | Common:4; Rare:195 | ||||
| chr4:6693704-6693880 | Rare:40 | ||||
| chr4:6709231-6709376 | Rare:54 |