| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:17277209-17277329 | Common:2; Rare:22 | ||||
| chr11:17351570-17351628 | Rare:15 | ||||
| chr11:17351643-17351836 | Rare:37 | ||||
| chr11:17351851-17352092 | Common:2; Rare:65 | ||||
| chr11:17352231-17352300 | Rare:12 | ||||
| chr11:17389118-17389492 | Common:2; Rare:76 | ||||
| chr11:18012311-18012659 | Common:2; Rare:74 | ||||
| chr11:18012865-18013310 | Common:6; Rare:155 | ||||
| chr11:18105989-18106312 | Common:3; Rare:109 | ||||
| chr11:18321805-18321854 | Rare:8 | ||||
| chr11:18322028-18322359 | Common:7; Rare:114; Clinvar:2; Clinvar (benign):3 | ||||
| chr11:18322482-18322752 | Common:2; Rare:96 | ||||
| chr11:18394003-18394224 | Common:1; Rare:29 | ||||
| chr11:18394260-18394682 | Common:2; Rare:150; Clinvar (benign):1 | ||||
| chr11:18394686-18395069 | Common:4; Rare:79 |