| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:113124060-113124359 | Common:2; Rare:65 | ||||
| chr10:113125574-113125791 | Rare:38 | ||||
| chr10:113126520-113126844 | Common:3; Rare:73 | ||||
| chr10:113129115-113129467 | Common:1; Rare:62 | ||||
| chr10:114631995-114632146 | Rare:42 | ||||
| chr10:120355215-120355232 | Common:1; Rare:2 | ||||
| chr10:127999459-127999550 | Rare:19 | ||||
| chr10:132947155-132947368 | Rare:22 | ||||
| chr11:373103-373285 | Common:2; Rare:59 | ||||
| chr11:792183-792429 | Common:1; Rare:83; Clinvar:6; Clinvar (benign):16; Clinvar (pathogenic):1 | ||||
| chr11:840479-840645 | Common:4; Rare:59 | ||||
| chr11:1445653-1445785 | Common:2; Rare:48 | ||||
| chr11:1598867-1599015 | Rare:31 | ||||
| chr11:2591512-2591642 | Common:1; Rare:40 | ||||
| chr11:3512144-3512264 | Common:2; Rare:21 |