| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:37977133-37977447 | Rare:82 | ||||
| chr4:38867707-38867830 | Common:1; Rare:46 | ||||
| chr4:39182256-39182548 | Rare:65; Clinvar:2 | ||||
| chr4:39366311-39366431 | Rare:36 | ||||
| chr4:39458849-39459109 | Common:3; Rare:147; Clinvar (benign):5 | ||||
| chr4:39527383-39527761 | Common:2; Rare:94 | ||||
| chr4:39527952-39527987 | Rare:9 | ||||
| chr4:39638834-39639140 | Common:1; Rare:112 | ||||
| chr4:39697936-39698174 | Common:2; Rare:103 | ||||
| chr4:40056662-40056935 | Common:4; Rare:90 | ||||
| chr4:40629762-40629917 | Common:1; Rare:45 | ||||
| chr4:41359515-41359669 | Rare:25 | ||||
| chr4:41990389-41990566 | Common:1; Rare:65 | ||||
| chr4:44678573-44678680 | Rare:46 | ||||
| chr4:44726523-44726642 | Rare:46 |