| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:15034213-15034392 | Rare:36 | ||||
| chr4:15043756-15043909 | Rare:25 | ||||
| chr4:15044865-15044955 | Rare:22 | ||||
| chr4:15418877-15418965 | Rare:13 | ||||
| chr4:15475850-15475971 | Rare:24; Clinvar:2 | ||||
| chr4:15509972-15510207 | Common:1; Rare:46; Clinvar (benign):1 | ||||
| chr4:15605774-15605976 | Common:1; Rare:43 | ||||
| chr4:15612258-15612563 | Common:1; Rare:53 | ||||
| chr4:16744897-16745202 | Common:2; Rare:58 | ||||
| chr4:22491856-22491913 | Common:1; Rare:11 | ||||
| chr4:30719316-30719732 | Common:2; Rare:100 | ||||
| chr4:37458712-37458974 | Common:1; Rare:39 | ||||
| chr4:37464417-37464860 | Common:6; Rare:72 | ||||
| chr4:37469186-37469436 | Common:1; Rare:41 | ||||
| chr4:37494908-37495001 | Rare:17 |