| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:31506343-31506465 | Rare:23 | ||||
| chr4:31997265-31997379 | Common:2; Rare:24 | ||||
| chr4:33891666-33891973 | Rare:57 | ||||
| chr4:33892715-33892826 | Rare:20 | ||||
| chr4:34039884-34039954 | Common:1; Rare:20 | ||||
| chr4:34315472-34315493 | Rare:5 | ||||
| chr4:34335345-34335649 | Common:3; Rare:82 | ||||
| chr4:38279872-38279979 | Rare:17 | ||||
| chr4:38286893-38287008 | Common:1; Rare:22 | ||||
| chr4:38532141-38532243 | Common:1; Rare:19 | ||||
| chr4:38627390-38627686 | Rare:59 | ||||
| chr4:38905603-38905771 | Rare:57 | ||||
| chr4:39460687-39460844 | Rare:35; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr4:39641541-39641681 | Common:1; Rare:21 | ||||
| chr4:40056090-40056177 | Rare:26 |