| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:183504533-183504803 | Common:1; Rare:87 | ||||
| chr4:183505972-183506110 | Rare:54 | ||||
| chr4:183659105-183659417 | Common:1; Rare:104 | ||||
| chr4:184474454-184474801 | Rare:74 | ||||
| chr4:184649434-184649796 | Common:4; Rare:115 | ||||
| chr4:184825931-184826265 | Common:7; Rare:106 | ||||
| chr4:185143163-185143453 | Common:3; Rare:96; Clinvar:1; Clinvar (benign):6 | ||||
| chr4:185395919-185396011 | Rare:28 | ||||
| chr4:185396574-185396694 | Rare:38 | ||||
| chr4:185425870-185426252 | Common:3; Rare:115 | ||||
| chr4:185471060-185471412 | Common:10; Rare:43 | ||||
| chr4:185535341-185535655 | Common:2; Rare:115; Clinvar:1; Clinvar (benign):9 | ||||
| chr4:185656638-185656794 | Rare:35 | ||||
| chr4:185657271-185657374 | Common:1; Rare:26 | ||||
| chr4:185811731-185811829 | Rare:19 |