| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:125111731-125112011 | Common:3; Rare:57 | ||||
| chr11:125164528-125164759 | Rare:44 | ||||
| chr11:125496169-125496506 | Rare:74 | ||||
| chr11:125592506-125592933 | Common:6; Rare:138 | ||||
| chr11:125625864-125626003 | Rare:45 | ||||
| chr11:125887484-125887737 | Common:2; Rare:81 | ||||
| chr11:125903183-125903362 | Rare:46 | ||||
| chr11:126062627-126062921 | Common:6; Rare:89 | ||||
| chr11:126211620-126211819 | Rare:91 | ||||
| chr11:126264521-126264843 | Common:3; Rare:78 | ||||
| chr11:126265994-126266158 | Common:1; Rare:58 | ||||
| chr11:126266608-126266746 | Rare:46 | ||||
| chr11:126268356-126268613 | Common:3; Rare:58 | ||||
| chr11:126268689-126269207 | Common:2; Rare:199; Clinvar:2; Clinvar (benign):4 | ||||
| chr11:126282764-126283131 | Common:2; Rare:107 |