| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:15659831-15660127 | Common:1; Rare:61 | ||||
| chr4:15681554-15681869 | Common:3; Rare:110 | ||||
| chr4:15703036-15703134 | Common:1; Rare:22 | ||||
| chr4:17577316-17577539 | Rare:106 | ||||
| chr4:17614572-17614660 | Common:2; Rare:41 | ||||
| chr4:17810687-17811061 | Common:4; Rare:119 | ||||
| chr4:18021732-18022045 | Common:2; Rare:101 | ||||
| chr4:20253425-20253778 | Common:3; Rare:82 | ||||
| chr4:25160388-25160727 | Common:3; Rare:96; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:25655568-25655887 | Common:1; Rare:82 | ||||
| chr4:25914051-25914301 | Common:2; Rare:106 | ||||
| chr4:26320715-26321028 | Rare:129; Clinvar (benign):1 | ||||
| chr4:30720240-30720422 | Common:1; Rare:46 | ||||
| chr4:36281503-36281645 | Rare:24 | ||||
| chr4:37826577-37826729 | Common:1; Rare:56 |