| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:151452029-151452578 | Common:4; Rare:196 | ||||
| chr6:151807077-151807270 | Rare:36 | ||||
| chr6:152982960-152983358 | Common:2; Rare:122 | ||||
| chr6:152983516-152983774 | Common:4; Rare:98 | ||||
| chr6:153002643-153002881 | Common:4; Rare:88 | ||||
| chr6:153131225-153131470 | Rare:108 | ||||
| chr6:154733182-154733425 | Rare:99 | ||||
| chr6:155314447-155314798 | Common:10; Rare:122 | ||||
| chr6:157323465-157323597 | Common:2; Rare:57 | ||||
| chr6:158168166-158168402 | Common:3; Rare:89; Clinvar:1 | ||||
| chr6:158536600-158536728 | Rare:69 | ||||
| chr6:158644692-158645005 | Common:3; Rare:111 | ||||
| chr6:158818101-158818358 | Common:5; Rare:103 | ||||
| chr6:158819316-158819537 | Common:2; Rare:86 | ||||
| chr6:158999702-158999991 | Common:1; Rare:122; Clinvar:4; Clinvar (benign):2 |