| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:38857715-38857857 | Common:1; Rare:29 | ||||
| chr4:38857963-38857985 | Rare:3 | ||||
| chr4:38967304-38967531 | Common:2; Rare:42 | ||||
| chr4:39151248-39151356 | Common:1; Rare:7 | ||||
| chr4:39183156-39183173 | Rare:1 | ||||
| chr4:39353295-39353336 | Rare:8 | ||||
| chr4:39353543-39353633 | Rare:18 | ||||
| chr4:39353958-39354258 | Common:1; Rare:36 | ||||
| chr4:39459786-39459909 | Rare:20 | ||||
| chr4:39460132-39460196 | Rare:10 | ||||
| chr4:39465127-39465314 | Common:1; Rare:39; Clinvar:1; Clinvar (benign):2 | ||||
| chr4:39469488-39469695 | Rare:30 | ||||
| chr4:39637535-39637727 | Common:1; Rare:39 | ||||
| chr4:39697115-39697344 | Common:2; Rare:38 | ||||
| chr4:39823244-39823552 | Rare:55 |