| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:124800397-124800481 | Rare:34 | ||||
| chr11:125063168-125063305 | Common:2; Rare:40 | ||||
| chr11:125164541-125164759 | Rare:41 | ||||
| chr11:125496205-125496506 | Rare:67 | ||||
| chr11:125592508-125592913 | Common:6; Rare:131 | ||||
| chr11:125625842-125625980 | Common:2; Rare:48 | ||||
| chr11:125903188-125903337 | Rare:35 | ||||
| chr11:126211641-126211804 | Rare:75 | ||||
| chr11:126268814-126269192 | Common:1; Rare:145; Clinvar:2; Clinvar (benign):2 | ||||
| chr11:126304009-126304075 | Rare:35 | ||||
| chr11:126355532-126355738 | Common:1; Rare:54 | ||||
| chr11:128693797-128694120 | Common:2; Rare:57 | ||||
| chr11:129815714-129815881 | Common:1; Rare:42 | ||||
| chr11:129895535-129895666 | Common:2; Rare:48 | ||||
| chr11:130069630-130069980 | Common:2; Rare:128 |