| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:832854-833018 | Common:7; Rare:60 | ||||
| chr11:842522-842832 | Common:7; Rare:128 | ||||
| chr11:4094748-4094832 | Rare:24 | ||||
| chr11:6481321-6481519 | Common:3; Rare:79 | ||||
| chr11:6603553-6603795 | Common:4; Rare:71 | ||||
| chr11:8682721-8682803 | Common:1; Rare:42 | ||||
| chr11:10304973-10305078 | Rare:25 | ||||
| chr11:27506758-27506842 | Common:1; Rare:37 | ||||
| chr11:28108110-28108402 | Common:1; Rare:87 | ||||
| chr11:31509611-31509784 | Common:1; Rare:53 | ||||
| chr11:33161449-33161653 | Common:6; Rare:53 | ||||
| chr11:33736391-33736513 | Common:2; Rare:39 | ||||
| chr11:34916311-34916646 | Common:9; Rare:137; Clinvar:3; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
| chr11:36510249-36510350 | Rare:26 | ||||
| chr11:47214843-47214979 | Common:1; Rare:34 |