| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:17207924-17208030 | Common:1; Rare:43 | ||||
| chr11:17276443-17276837 | Common:5; Rare:109; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr11:17310990-17311281 | Rare:58 | ||||
| chr11:18105929-18106307 | Common:4; Rare:127 | ||||
| chr11:18322102-18322574 | Common:8; Rare:167; Clinvar:2; Clinvar (benign):2 | ||||
| chr11:18394456-18394612 | Common:1; Rare:63; Clinvar (benign):1 | ||||
| chr11:18526855-18526992 | Rare:66 | ||||
| chr11:18588671-18588782 | Rare:43 | ||||
| chr11:18634278-18634596 | Common:3; Rare:115 | ||||
| chr11:18634780-18634921 | Common:2; Rare:31 | ||||
| chr11:20387470-20387771 | Common:5; Rare:98 | ||||
| chr11:22625016-22625251 | Common:2; Rare:92; Clinvar:4; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr11:22625801-22626002 | Common:2; Rare:70; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr11:22829354-22829447 | Common:1; Rare:28 | ||||
| chr11:27362843-27362961 | Common:1; Rare:52 |