| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:14644059-14644880 | Common:1; Rare:431 | ||||
| chr11:16738435-16738837 | Common:6; Rare:162 | ||||
| chr11:17014377-17014478 | Common:1; Rare:58 | ||||
| chr11:17077580-17077990 | Common:4; Rare:308 | ||||
| chr11:17207851-17208167 | Common:4; Rare:215 | ||||
| chr11:17208270-17208640 | Rare:110 | ||||
| chr11:17276484-17276831 | Common:8; Rare:167; Clinvar:6; Clinvar (pathogenic):2 | ||||
| chr11:17351920-17352298 | Rare:122 | ||||
| chr11:17389190-17389720 | Common:6; Rare:132 | ||||
| chr11:17533836-17534127 | Common:4; Rare:87 | ||||
| chr11:18012911-18013237 | Common:11; Rare:188 | ||||
| chr11:18322094-18322381 | Common:9; Rare:177; Clinvar:3; Clinvar (benign):4 | ||||
| chr11:18322444-18322640 | Common:4; Rare:142 | ||||
| chr11:18394331-18394658 | Common:2; Rare:232; Clinvar (benign):2 | ||||
| chr11:18396060-18396600 | Common:4; Rare:305 |