| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:10456239-10456275 | Rare:7 | ||||
| chr11:10541134-10541268 | Rare:49 | ||||
| chr11:10568542-10568868 | Common:1; Rare:64 | ||||
| chr11:10751144-10751345 | Rare:61 | ||||
| chr11:10808709-10808770 | Rare:16 | ||||
| chr11:10808882-10809145 | Common:3; Rare:113 | ||||
| chr11:10858013-10858266 | Common:3; Rare:83 | ||||
| chr11:11841920-11842079 | Common:1; Rare:44 | ||||
| chr11:13009134-13009327 | Common:1; Rare:70 | ||||
| chr11:13463109-13463366 | Common:1; Rare:92 | ||||
| chr11:16738466-16738854 | Common:3; Rare:92 | ||||
| chr11:17207910-17208082 | Common:2; Rare:66 | ||||
| chr11:17276557-17276829 | Common:4; Rare:74; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr11:18266248-18266270 | Common:2; Rare:7 | ||||
| chr11:18322113-18322321 | Common:4; Rare:78; Clinvar:1; Clinvar (benign):2 |