| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:13463141-13463341 | Common:1; Rare:71 | ||||
| chr11:14520297-14520561 | Rare:92 | ||||
| chr11:14643619-14643862 | Common:1; Rare:91 | ||||
| chr11:14644668-14644725 | Rare:19 | ||||
| chr11:16606064-16606110 | Rare:13 | ||||
| chr11:16606112-16606267 | Common:3; Rare:29 | ||||
| chr11:16607702-16607840 | Common:1; Rare:21 | ||||
| chr11:16738466-16738862 | Common:3; Rare:96 | ||||
| chr11:17014243-17014318 | Rare:27 | ||||
| chr11:17077618-17077868 | Common:2; Rare:104 | ||||
| chr11:17207916-17208112 | Common:2; Rare:73 | ||||
| chr11:17276451-17276828 | Common:5; Rare:108; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr11:18248591-18248861 | Common:1; Rare:66 | ||||
| chr11:18322094-18322332 | Common:5; Rare:91; Clinvar:2; Clinvar (benign):2 | ||||
| chr11:18322447-18322610 | Common:2; Rare:64 |