| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:47269553-47269811 | Common:1; Rare:90 | ||||
| chr11:47269966-47270242 | Common:2; Rare:93 | ||||
| chr11:47272110-47272248 | Common:2; Rare:27 | ||||
| chr11:47378466-47378528 | Rare:14 | ||||
| chr11:47378531-47378760 | Common:1; Rare:42 | ||||
| chr11:47407044-47407299 | Common:1; Rare:44 | ||||
| chr11:47553012-47553356 | Common:3; Rare:121 | ||||
| chr11:47565483-47565643 | Common:3; Rare:31 | ||||
| chr11:47578653-47579106 | Common:1; Rare:153; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr11:47628953-47629148 | Rare:43 | ||||
| chr11:47642444-47642747 | Rare:120 | ||||
| chr11:47710279-47710406 | Common:1; Rare:37 | ||||
| chr11:47715316-47715441 | Common:1; Rare:36 | ||||
| chr11:47848240-47848406 | Common:1; Rare:84 | ||||
| chr11:47848531-47848653 | Common:3; Rare:23 |