| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:37244052-37244187 | Common:2; Rare:26 | ||||
| chr4:37826571-37826729 | Common:1; Rare:57 | ||||
| chr4:37977208-37977459 | Rare:57 | ||||
| chr4:38664211-38664291 | Rare:26 | ||||
| chr4:38867700-38867833 | Common:1; Rare:52 | ||||
| chr4:38868167-38868465 | Rare:62 | ||||
| chr4:39182202-39182560 | Common:1; Rare:81; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:39366324-39366394 | Rare:22 | ||||
| chr4:39406965-39407248 | Common:2; Rare:88 | ||||
| chr4:39458849-39459112 | Common:3; Rare:149; Clinvar (benign):5 | ||||
| chr4:39527405-39527754 | Common:2; Rare:85 | ||||
| chr4:39638823-39639170 | Common:1; Rare:124 | ||||
| chr4:39697936-39698185 | Common:2; Rare:108 | ||||
| chr4:40629762-40629932 | Common:1; Rare:49 | ||||
| chr4:41256753-41257000 | Common:2; Rare:82; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 |