| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:2135453-2135802 | Common:1; Rare:84; Clinvar (pathogenic):1 | ||||
| chr11:2138230-2138472 | Common:1; Rare:49 | ||||
| chr11:2631866-2631954 | Rare:15 | ||||
| chr11:2645138-2645182 | Rare:6 | ||||
| chr11:2646006-2646362 | Common:2; Rare:58 | ||||
| chr11:2669577-2669782 | Common:1; Rare:30 | ||||
| chr11:2682581-2682759 | Rare:33 | ||||
| chr11:3477036-3477197 | Common:2; Rare:44 | ||||
| chr11:7906251-7906574 | Common:4; Rare:57 | ||||
| chr11:9758122-9758320 | Rare:53 | ||||
| chr11:10803092-10803280 | Common:1; Rare:46 | ||||
| chr11:46312644-46312915 | Common:1; Rare:53 | ||||
| chr11:59212363-59212421 | Rare:21 | ||||
| chr11:62574966-62575108 | Rare:42 | ||||
| chr11:65420014-65420187 | Rare:41 |