| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:151760957-151761239 | Rare:99 | ||||
| chr4:152779728-152780005 | Common:1; Rare:76 | ||||
| chr4:153152910-153153147 | Rare:46 | ||||
| chr4:153204261-153204463 | Common:1; Rare:38 | ||||
| chr4:153344514-153344740 | Common:4; Rare:67 | ||||
| chr4:153345361-153345409 | Rare:8 | ||||
| chr4:153466104-153466395 | Common:3; Rare:114 | ||||
| chr4:154550359-154550519 | Rare:50 | ||||
| chr4:158671825-158672339 | Common:5; Rare:130; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:158723311-158723463 | Common:2; Rare:69 | ||||
| chr4:163494481-163494725 | Common:2; Rare:98 | ||||
| chr4:164956907-164957018 | Common:1; Rare:36 | ||||
| chr4:165112825-165113011 | Common:1; Rare:55 | ||||
| chr4:165327383-165327737 | Common:3; Rare:106 | ||||
| chr4:167234450-167234723 | Rare:70 |