| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:126282796-126283140 | Common:2; Rare:96 | ||||
| chr11:126304023-126304125 | Rare:65 | ||||
| chr11:126355526-126355771 | Common:2; Rare:69 | ||||
| chr11:128522263-128522551 | Common:1; Rare:91 | ||||
| chr11:128693801-128694153 | Common:2; Rare:64 | ||||
| chr11:129815748-129815881 | Common:1; Rare:34 | ||||
| chr11:130314395-130314521 | Common:1; Rare:42 | ||||
| chr11:134224533-134224584 | Rare:17 | ||||
| chr11:134253236-134253628 | Common:3; Rare:136; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr12:213590-213764 | Rare:31 | ||||
| chr12:237559-237580 | Rare:3 | ||||
| chr12:389230-389398 | Common:1; Rare:66 | ||||
| chr12:401436-401664 | Rare:63 | ||||
| chr12:610367-610510 | Common:1; Rare:15 | ||||
| chr12:643616-643681 | Rare:10 |