| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:46701003-46701074 | Common:1; Rare:29 | ||||
| chr11:46846204-46846421 | Common:1; Rare:64 | ||||
| chr11:47214328-47214496 | Common:1; Rare:18 | ||||
| chr11:47214833-47215115 | Common:2; Rare:71; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:47248785-47248925 | Rare:56 | ||||
| chr11:47257624-47257745 | Rare:14 | ||||
| chr11:47269981-47270231 | Common:2; Rare:88 | ||||
| chr11:47378369-47378640 | Rare:73 | ||||
| chr11:47553071-47553341 | Common:2; Rare:99 | ||||
| chr11:47565483-47565620 | Common:3; Rare:27 | ||||
| chr11:47578959-47579128 | Rare:90; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr11:47642467-47642805 | Rare:125 | ||||
| chr11:47767201-47767411 | Common:1; Rare:101 | ||||
| chr11:57324880-57325148 | Common:1; Rare:87 | ||||
| chr11:57426451-57426581 | Common:1; Rare:20 |