| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:67404770-67404817 | Rare:6 | ||||
| chr11:67409247-67409484 | Common:2; Rare:65 | ||||
| chr11:67421117-67421401 | Common:4; Rare:99 | ||||
| chr11:67428027-67428628 | Common:1; Rare:175 | ||||
| chr11:67437587-67437821 | Rare:57 | ||||
| chr11:67443457-67443643 | Common:2; Rare:67 | ||||
| chr11:67464545-67464985 | Rare:211 | ||||
| chr11:67469124-67469502 | Common:5; Rare:130 | ||||
| chr11:67482654-67483209 | Common:2; Rare:128; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr11:67505267-67505471 | Rare:49 | ||||
| chr11:67508024-67508577 | Common:1; Rare:130 | ||||
| chr11:67508605-67508824 | Common:3; Rare:81 | ||||
| chr11:67583461-67583577 | Common:5; Rare:17 | ||||
| chr11:67583701-67583938 | Common:1; Rare:83 | ||||
| chr11:67584344-67584519 | Common:1; Rare:50 |