| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:8158697-8159110 | Common:4; Rare:154 | ||||
| chr4:8440717-8440785 | Rare:26 | ||||
| chr4:11428886-11429066 | Common:1; Rare:54 | ||||
| chr4:15655232-15655481 | Common:2; Rare:101 | ||||
| chr4:15681459-15681875 | Common:4; Rare:145 | ||||
| chr4:15703011-15703101 | Common:1; Rare:19 | ||||
| chr4:17614527-17614722 | Common:3; Rare:111 | ||||
| chr4:17810649-17810988 | Common:1; Rare:105 | ||||
| chr4:18021732-18021911 | Common:2; Rare:69 | ||||
| chr4:23889904-23890134 | Rare:42 | ||||
| chr4:25160344-25160728 | Common:3; Rare:117; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:25914051-25914347 | Common:3; Rare:128 | ||||
| chr4:37826588-37826729 | Common:1; Rare:54 | ||||
| chr4:37977168-37977447 | Rare:68 | ||||
| chr4:38664194-38664391 | Common:2; Rare:60 |