| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:9003996-9004117 | Rare:44 | ||||
| chr11:9460697-9461060 | Common:3; Rare:98 | ||||
| chr11:9575466-9575669 | Common:1; Rare:34 | ||||
| chr11:9663893-9664241 | Common:4; Rare:116 | ||||
| chr11:10304866-10305099 | Common:1; Rare:53 | ||||
| chr11:10455137-10455414 | Common:5; Rare:50; Clinvar:2; Clinvar (benign):6 | ||||
| chr11:10541145-10541331 | Rare:70 | ||||
| chr11:10568446-10568931 | Common:1; Rare:104 | ||||
| chr11:10693470-10693702 | Common:1; Rare:70 | ||||
| chr11:10751144-10751289 | Rare:44 | ||||
| chr11:10799042-10799388 | Common:3; Rare:126 | ||||
| chr11:10800430-10801092 | Common:2; Rare:204 | ||||
| chr11:10808704-10808811 | Rare:27 | ||||
| chr11:10808834-10809014 | Common:1; Rare:75 | ||||
| chr11:10858007-10858260 | Common:3; Rare:83 |