| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:14499748-14500008 | Common:3; Rare:81 | ||||
| chr11:14520240-14520673 | Rare:127 | ||||
| chr11:14643577-14644076 | Common:2; Rare:170 | ||||
| chr11:14644720-14644740 | Rare:9 | ||||
| chr11:14891123-14891305 | Rare:46 | ||||
| chr11:14891589-14892009 | Rare:119 | ||||
| chr11:14892121-14892412 | Rare:111 | ||||
| chr11:16738192-16738771 | Common:6; Rare:159 | ||||
| chr11:17077614-17078172 | Common:4; Rare:195 | ||||
| chr11:17207876-17208251 | Common:2; Rare:126 | ||||
| chr11:17208448-17208597 | Rare:34 | ||||
| chr11:17276423-17276809 | Common:4; Rare:110; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr11:17389359-17389492 | Common:2; Rare:18 | ||||
| chr11:18012864-18013317 | Common:6; Rare:160 | ||||
| chr11:18105986-18106179 | Common:2; Rare:87 |