| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:197297840-197298083 | Rare:94 | ||||
| chr3:197736847-197737251 | Common:3; Rare:129 | ||||
| chr3:197749329-197749490 | Common:1; Rare:36 | ||||
| chr3:197749815-197750037 | Rare:85 | ||||
| chr3:197949864-197950270 | Common:4; Rare:119; Clinvar (benign):2 | ||||
| chr3:197950934-197951312 | Rare:113; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:197959971-197960264 | Common:1; Rare:105 | ||||
| chr4:337539-337861 | Common:1; Rare:87 | ||||
| chr4:499136-499324 | Common:3; Rare:70 | ||||
| chr4:663407-663725 | Common:1; Rare:95 | ||||
| chr4:673814-674038 | Common:1; Rare:93 | ||||
| chr4:674211-674679 | Common:4; Rare:205 | ||||
| chr4:705579-705974 | Common:1; Rare:130 | ||||
| chr4:932131-932511 | Common:2; Rare:148 | ||||
| chr4:986919-987235 | Common:4; Rare:103; Clinvar:4; Clinvar (benign):3 |