| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:46700941-46701082 | Common:1; Rare:44 | ||||
| chr11:46846214-46846483 | Common:1; Rare:76 | ||||
| chr11:46918530-46918693 | Common:2; Rare:36; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:46936592-46936806 | Common:2; Rare:63 | ||||
| chr11:47176827-47177161 | Common:1; Rare:143 | ||||
| chr11:47185534-47185699 | Rare:26 | ||||
| chr11:47185831-47185957 | Rare:28 | ||||
| chr11:47186388-47186567 | Rare:48 | ||||
| chr11:47214290-47214505 | Common:1; Rare:24 | ||||
| chr11:47214816-47215125 | Common:2; Rare:81; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:47215407-47215520 | Rare:22 | ||||
| chr11:47248569-47249198 | Common:2; Rare:172; Clinvar (benign):1 | ||||
| chr11:47269107-47269385 | Common:1; Rare:58 | ||||
| chr11:47269501-47269698 | Common:1; Rare:63 | ||||
| chr11:47269953-47270231 | Common:2; Rare:99 |