| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:52713593-52713780 | Rare:27 | ||||
| chr4:52722392-52722421 | Rare:7 | ||||
| chr4:52945604-52945729 | Rare:17 | ||||
| chr4:54010123-54010405 | Common:1; Rare:56 | ||||
| chr4:54231865-54232100 | Common:2; Rare:53 | ||||
| chr4:54267286-54267645 | Common:3; Rare:100; Clinvar:28; Clinvar (benign):17 | ||||
| chr4:55382645-55382945 | Common:2; Rare:43 | ||||
| chr4:55947920-55948139 | Common:2; Rare:39 | ||||
| chr4:57032429-57032734 | Common:1; Rare:74 | ||||
| chr4:57051943-57052124 | Common:5; Rare:29 | ||||
| chr4:57102318-57102455 | Rare:26 | ||||
| chr4:57109809-57109842 | Rare:11 | ||||
| chr4:70678502-70678694 | Rare:27 | ||||
| chr4:70689449-70689605 | Rare:35 | ||||
| chr4:75971390-75971593 | Common:1; Rare:47 |