| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:184805525-184805832 | Common:1; Rare:56 | ||||
| chr4:184808508-184808625 | Rare:21 | ||||
| chr4:185143136-185143392 | Common:3; Rare:84; Clinvar:1; Clinvar (benign):5 | ||||
| chr4:185203857-185204173 | Common:5; Rare:102 | ||||
| chr4:185210652-185210832 | Common:2; Rare:26 | ||||
| chr4:185395898-185396080 | Rare:58 | ||||
| chr4:185396569-185396851 | Rare:91 | ||||
| chr4:185425864-185426272 | Common:4; Rare:126 | ||||
| chr4:185471049-185471533 | Common:11; Rare:98 | ||||
| chr4:185656659-185656832 | Rare:33 | ||||
| chr4:185656955-185657556 | Common:3; Rare:140 | ||||
| chr4:185775249-185775533 | Common:3; Rare:48 | ||||
| chr4:186069141-186069206 | Common:2; Rare:11 | ||||
| chr4:186191466-186191826 | Common:6; Rare:121; Clinvar:2; Clinvar (benign):5 | ||||
| chr4:186723695-186723903 | Common:4; Rare:81 |