| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:102827985-102828324 | Common:3; Rare:114 | ||||
| chr4:102868796-102869082 | Common:2; Rare:96 | ||||
| chr4:102869229-102869403 | Rare:71 | ||||
| chr4:103019638-103019764 | Rare:34 | ||||
| chr4:103076291-103076577 | Common:1; Rare:88 | ||||
| chr4:103099798-103099969 | Rare:29 | ||||
| chr4:103198315-103198469 | Common:2; Rare:37 | ||||
| chr4:104494848-104495219 | Common:3; Rare:83 | ||||
| chr4:105147788-105147844 | Rare:5 | ||||
| chr4:105708636-105708896 | Common:3; Rare:82 | ||||
| chr4:106316173-106316683 | Common:5; Rare:156 | ||||
| chr4:107720169-107720432 | Common:6; Rare:107 | ||||
| chr4:107989656-107989935 | Common:6; Rare:123; Clinvar:4; Clinvar (benign):5 | ||||
| chr4:108167774-108167831 | Rare:18 | ||||
| chr4:108168842-108168864 | Rare:4 |