| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:15339835-15339988 | Rare:36 | ||||
| chr4:15479036-15479251 | Common:2; Rare:45 | ||||
| chr4:15655291-15655466 | Common:1; Rare:82 | ||||
| chr4:15681553-15681854 | Common:3; Rare:108 | ||||
| chr4:17614577-17614651 | Common:1; Rare:34 | ||||
| chr4:17810701-17811012 | Common:2; Rare:96 | ||||
| chr4:25914051-25914283 | Common:2; Rare:100 | ||||
| chr4:26320914-26321041 | Rare:44; Clinvar (benign):1 | ||||
| chr4:37826538-37826729 | Common:6; Rare:68 | ||||
| chr4:39458889-39459093 | Common:2; Rare:108; Clinvar (benign):4 | ||||
| chr4:39527383-39527755 | Common:2; Rare:91 | ||||
| chr4:39638847-39639149 | Common:1; Rare:112 | ||||
| chr4:39697936-39698174 | Common:2; Rare:103 | ||||
| chr4:41360700-41360819 | Common:1; Rare:37 | ||||
| chr4:41990401-41990580 | Common:1; Rare:65 |