| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:152779811-152780021 | Common:1; Rare:55 | ||||
| chr4:156971071-156971279 | Common:1; Rare:36 | ||||
| chr4:158172354-158172711 | Rare:60 | ||||
| chr4:158671830-158672377 | Common:5; Rare:136; Clinvar:3; Clinvar (benign):1 | ||||
| chr4:163166856-163166981 | Common:2; Rare:42 | ||||
| chr4:164956873-164957021 | Common:2; Rare:48 | ||||
| chr4:165327411-165327776 | Common:2; Rare:106 | ||||
| chr4:168831958-168832097 | Common:2; Rare:41 | ||||
| chr4:169010236-169010459 | Common:1; Rare:64 | ||||
| chr4:169620391-169620702 | Common:2; Rare:107 | ||||
| chr4:169660036-169660257 | Common:1; Rare:41 | ||||
| chr4:173369744-173369965 | Common:1; Rare:74 | ||||
| chr4:173370772-173370976 | Common:1; Rare:56 | ||||
| chr4:173530195-173530353 | Rare:33 | ||||
| chr4:174283599-174283938 | Common:1; Rare:66 |