| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:12411858-12411960 | Common:1; Rare:18 | ||||
| chr11:12513106-12513359 | Common:2; Rare:76 | ||||
| chr11:14888102-14888360 | Common:3; Rare:33 | ||||
| chr11:16988585-16988722 | Common:4; Rare:32 | ||||
| chr11:16996402-16996655 | Rare:48 | ||||
| chr11:17091547-17091807 | Common:1; Rare:55 | ||||
| chr11:19714580-19714723 | Rare:28 | ||||
| chr11:27392590-27392917 | Common:1; Rare:56 | ||||
| chr11:27459521-27459666 | Rare:31 | ||||
| chr11:27470688-27470769 | Common:1; Rare:12 | ||||
| chr11:27471193-27471239 | Rare:6 | ||||
| chr11:34137022-34137184 | Common:1; Rare:36 | ||||
| chr11:34651550-34651802 | Common:1; Rare:71 | ||||
| chr11:35663532-35663747 | Rare:66; Clinvar (pathogenic):1 | ||||
| chr11:35704250-35704545 | Common:2; Rare:60 |