| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:14643631-14643810 | Common:1; Rare:68 | ||||
| chr11:14891599-14891832 | Rare:69 | ||||
| chr11:16607390-16607528 | Rare:22 | ||||
| chr11:16607617-16607971 | Common:1; Rare:52 | ||||
| chr11:16738420-16738895 | Common:3; Rare:126 | ||||
| chr11:17014255-17014330 | Rare:28 | ||||
| chr11:17077500-17077979 | Common:4; Rare:197 | ||||
| chr11:17207916-17208143 | Common:2; Rare:86 | ||||
| chr11:17208370-17208583 | Rare:40 | ||||
| chr11:17276532-17276828 | Common:5; Rare:85; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr11:17276932-17277053 | Rare:23 | ||||
| chr11:17351930-17352022 | Rare:23 | ||||
| chr11:18012896-18013061 | Common:5; Rare:62 | ||||
| chr11:18105973-18106308 | Common:4; Rare:115 | ||||
| chr11:18322108-18322300 | Common:3; Rare:73; Clinvar:2; Clinvar (benign):2 |