| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:9663984-9664191 | Common:4; Rare:78 | ||||
| chr11:10304818-10305080 | Common:1; Rare:57 | ||||
| chr11:10455125-10455445 | Common:5; Rare:56; Clinvar:2; Clinvar (benign):6 | ||||
| chr11:10541134-10541250 | Rare:44 | ||||
| chr11:10751183-10751302 | Rare:37 | ||||
| chr11:10798996-10799388 | Common:3; Rare:135 | ||||
| chr11:10808703-10808790 | Rare:22 | ||||
| chr11:10808836-10809119 | Common:1; Rare:117 | ||||
| chr11:10857298-10857383 | Rare:20 | ||||
| chr11:10858023-10858269 | Common:2; Rare:78 | ||||
| chr11:11841687-11842095 | Common:4; Rare:120 | ||||
| chr11:13463109-13463392 | Common:1; Rare:104 | ||||
| chr11:14337155-14337434 | Common:2; Rare:49 | ||||
| chr11:14499776-14499951 | Common:2; Rare:55 | ||||
| chr11:14520318-14520428 | Rare:36 |