| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:151390890-151391210 | Common:3; Rare:160 | ||||
| chr6:151391503-151391756 | Common:6; Rare:109 | ||||
| chr6:151451999-151452548 | Common:5; Rare:193; Clinvar (benign):3 | ||||
| chr6:152983009-152983378 | Common:4; Rare:216 | ||||
| chr6:152983508-152983783 | Common:8; Rare:202 | ||||
| chr6:153002666-153002872 | Common:8; Rare:132 | ||||
| chr6:154510623-154510875 | Common:2; Rare:78 | ||||
| chr6:154733279-154733507 | Rare:157 | ||||
| chr6:154733567-154733741 | Common:2; Rare:82 | ||||
| chr6:154733806-154734325 | Common:10; Rare:238 | ||||
| chr6:155314440-155314766 | Common:15; Rare:182 | ||||
| chr6:157323020-157323420 | Common:1; Rare:154 | ||||
| chr6:157323486-157323634 | Common:4; Rare:94 | ||||
| chr6:157380910-157381547 | Common:4; Rare:269 | ||||
| chr6:157715758-157716157 | Rare:107 |