| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:23882100-23882224 | Common:1; Rare:16 | ||||
| chr4:23889963-23890179 | Rare:39 | ||||
| chr4:24584248-24584654 | Rare:139 | ||||
| chr4:24795249-24795637 | Common:1; Rare:83 | ||||
| chr4:24979676-24979718 | Rare:11 | ||||
| chr4:25160301-25160740 | Common:3; Rare:140; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:25233817-25234058 | Rare:96 | ||||
| chr4:25376939-25377349 | Common:4; Rare:122 | ||||
| chr4:25914051-25914335 | Common:2; Rare:122 | ||||
| chr4:26319354-26319753 | Rare:109 | ||||
| chr4:26320514-26320745 | Common:1; Rare:60 | ||||
| chr4:26320748-26321059 | Rare:131; Clinvar (benign):1 | ||||
| chr4:26359665-26359750 | Common:1; Rare:20 | ||||
| chr4:26583892-26584131 | Rare:51 | ||||
| chr4:26857555-26857739 | Common:3; Rare:56 |