| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:56387414-56387524 | Rare:36 | ||||
| chr4:56435473-56435973 | Common:6; Rare:164 | ||||
| chr4:56467542-56467692 | Common:2; Rare:63; Clinvar (benign):4 | ||||
| chr4:56977597-56977727 | Common:1; Rare:47 | ||||
| chr4:67545442-67545742 | Common:2; Rare:76 | ||||
| chr4:67701117-67701368 | Common:4; Rare:117 | ||||
| chr4:68349945-68350209 | Common:1; Rare:96 | ||||
| chr4:70688214-70688574 | Common:2; Rare:94 | ||||
| chr4:70902185-70902450 | Common:6; Rare:93 | ||||
| chr4:70993470-70993815 | Common:6; Rare:108 | ||||
| chr4:73069682-73069944 | Common:1; Rare:112 | ||||
| chr4:73259124-73259247 | Rare:26 | ||||
| chr4:74157878-74158179 | Common:2; Rare:134 | ||||
| chr4:75514268-75514489 | Common:1; Rare:74 | ||||
| chr4:75673307-75673692 | Common:1; Rare:154 |