| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:18322467-18322645 | Common:2; Rare:73 | ||||
| chr11:18394340-18394633 | Common:1; Rare:120; Clinvar (benign):1 | ||||
| chr11:18526841-18526987 | Rare:72 | ||||
| chr11:18588667-18588815 | Rare:53 | ||||
| chr11:18634326-18634575 | Common:2; Rare:79 | ||||
| chr11:22625530-22625603 | Rare:36; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr11:22829322-22829422 | Common:1; Rare:25 | ||||
| chr11:27506738-27506857 | Common:1; Rare:51 | ||||
| chr11:28108104-28108414 | Common:1; Rare:92 | ||||
| chr11:30322930-30323175 | Common:2; Rare:73 | ||||
| chr11:31369737-31369908 | Rare:53 | ||||
| chr11:31509561-31509784 | Common:1; Rare:70 | ||||
| chr11:32583663-32583929 | Rare:95 | ||||
| chr11:33015784-33015935 | Common:1; Rare:59 | ||||
| chr11:33161440-33161682 | Common:6; Rare:68 |