| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:123062064-123062382 | Common:5; Rare:135 | ||||
| chr11:123062393-123062672 | Common:4; Rare:131 | ||||
| chr11:124673715-124673926 | Common:4; Rare:63 | ||||
| chr11:124762256-124762417 | Rare:41 | ||||
| chr11:124800406-124800461 | Rare:18 | ||||
| chr11:124954023-124954149 | Common:3; Rare:30 | ||||
| chr11:125164516-125164769 | Rare:47 | ||||
| chr11:125592592-125592909 | Common:6; Rare:102 | ||||
| chr11:125625867-125625959 | Rare:32 | ||||
| chr11:125887480-125887727 | Common:2; Rare:78 | ||||
| chr11:126211641-126211819 | Rare:82 | ||||
| chr11:126266023-126266147 | Common:1; Rare:40 | ||||
| chr11:126268784-126269198 | Common:1; Rare:158; Clinvar:2; Clinvar (benign):3 | ||||
| chr11:126283019-126283120 | Rare:40 | ||||
| chr11:126303974-126304090 | Rare:68 |