| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:101282447-101282811 | Common:4; Rare:60 | ||||
| chr4:101345370-101345466 | Common:1; Rare:22 | ||||
| chr4:101345721-101345951 | Common:2; Rare:49 | ||||
| chr4:101346215-101346286 | Common:1; Rare:12 | ||||
| chr4:101650224-101650286 | Rare:6 | ||||
| chr4:101730572-101730756 | Common:1; Rare:40 | ||||
| chr4:101961332-101961420 | Rare:11 | ||||
| chr4:102344512-102344601 | Rare:31; Clinvar (pathogenic):2 | ||||
| chr4:102438913-102439009 | Common:2; Rare:16 | ||||
| chr4:102439019-102439116 | Common:1; Rare:11 | ||||
| chr4:102439272-102439621 | Common:1; Rare:61 | ||||
| chr4:102440010-102440060 | Rare:5 | ||||
| chr4:102500473-102500594 | Rare:16 | ||||
| chr4:103887326-103887478 | Rare:29 | ||||
| chr4:103996319-103996365 | Rare:10 |