| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:147684096-147684302 | Common:1; Rare:85 | ||||
| chr4:150581763-150581942 | Rare:34 | ||||
| chr4:152679898-152680112 | Rare:67 | ||||
| chr4:152779636-152780009 | Common:2; Rare:96 | ||||
| chr4:156970922-156971227 | Common:1; Rare:50 | ||||
| chr4:158671849-158672313 | Common:5; Rare:113; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:158723315-158723484 | Common:2; Rare:76 | ||||
| chr4:165112810-165113015 | Common:1; Rare:61 | ||||
| chr4:165327411-165327741 | Common:2; Rare:95 | ||||
| chr4:168631369-168631617 | Common:1; Rare:65 | ||||
| chr4:168831922-168832099 | Common:2; Rare:48 | ||||
| chr4:169620358-169620626 | Common:2; Rare:106 | ||||
| chr4:173369809-173369908 | Common:1; Rare:32 | ||||
| chr4:173370668-173370962 | Common:2; Rare:73 | ||||
| chr4:174283643-174283932 | Common:1; Rare:51 |