| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:46918380-46918810 | Common:5; Rare:134; Clinvar:5; Clinvar (benign):4 | ||||
| chr11:46936629-46936845 | Common:4; Rare:128 | ||||
| chr11:47175689-47176488 | Common:1; Rare:292 | ||||
| chr11:47176766-47177163 | Common:1; Rare:418 | ||||
| chr11:47185410-47185762 | Common:2; Rare:115 | ||||
| chr11:47185693-47186110 | Common:3; Rare:143 | ||||
| chr11:47186339-47186585 | Rare:119 | ||||
| chr11:47214225-47214554 | Common:3; Rare:82 | ||||
| chr11:47214784-47215182 | Common:6; Rare:288; Clinvar:9; Clinvar (benign):3 | ||||
| chr11:47215210-47216071 | Common:1; Rare:195 | ||||
| chr11:47248737-47249465 | Common:2; Rare:344 | ||||
| chr11:47269023-47269877 | Common:9; Rare:506 | ||||
| chr11:47269886-47270281 | Common:6; Rare:312 | ||||
| chr11:47408267-47408684 | Common:6; Rare:320; Clinvar:1; Clinvar (benign):5 | ||||
| chr11:47426174-47426290 | Rare:41 |