| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:9663895-9664191 | Common:4; Rare:97 | ||||
| chr11:10304899-10305101 | Common:1; Rare:49 | ||||
| chr11:10455130-10455432 | Common:5; Rare:55; Clinvar:2; Clinvar (benign):6 | ||||
| chr11:10541128-10541314 | Common:1; Rare:71 | ||||
| chr11:10750695-10751019 | Common:4; Rare:85 | ||||
| chr11:10751163-10751302 | Rare:42 | ||||
| chr11:10808860-10809117 | Common:1; Rare:107 | ||||
| chr11:10858013-10858269 | Common:3; Rare:83 | ||||
| chr11:11841909-11842086 | Common:1; Rare:50 | ||||
| chr11:12377470-12377648 | Rare:72 | ||||
| chr11:13463150-13463596 | Common:2; Rare:138 | ||||
| chr11:14499774-14499959 | Common:3; Rare:61 | ||||
| chr11:14520297-14520526 | Rare:80 | ||||
| chr11:14891652-14891728 | Rare:18 | ||||
| chr11:15114769-15114923 | Common:3; Rare:44 |