| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:47214357-47214490 | Common:1; Rare:12 | ||||
| chr11:47214823-47215127 | Common:2; Rare:81; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:47248794-47248957 | Rare:66 | ||||
| chr11:47269074-47269382 | Common:1; Rare:62 | ||||
| chr11:47269587-47269714 | Common:1; Rare:46 | ||||
| chr11:47269966-47270202 | Common:1; Rare:83 | ||||
| chr11:47426402-47426653 | Common:1; Rare:62 | ||||
| chr11:47553031-47553184 | Common:2; Rare:61 | ||||
| chr11:47565478-47565643 | Common:3; Rare:32 | ||||
| chr11:47578940-47579097 | Rare:82; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr11:47642454-47642779 | Rare:122 | ||||
| chr11:47767270-47767411 | Rare:69 | ||||
| chr11:47848317-47848404 | Rare:45 | ||||
| chr11:57324896-57325183 | Common:1; Rare:90 | ||||
| chr11:57530649-57530824 | Common:2; Rare:38 |