| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:125625864-125625941 | Rare:26 | ||||
| chr11:126211644-126211806 | Rare:75 | ||||
| chr11:126268808-126269192 | Common:1; Rare:148; Clinvar:2; Clinvar (benign):2 | ||||
| chr11:129279491-129279741 | Common:3; Rare:107 | ||||
| chr11:129815748-129815881 | Common:1; Rare:34 | ||||
| chr11:130314395-130314520 | Common:1; Rare:42 | ||||
| chr11:134224541-134224680 | Rare:48 | ||||
| chr11:134225441-134225504 | Rare:21 | ||||
| chr11:134253286-134253620 | Common:2; Rare:126; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr11:134276362-134276688 | Common:4; Rare:85 | ||||
| chr12:389023-389383 | Common:5; Rare:175 | ||||
| chr12:401446-401645 | Rare:53 | ||||
| chr12:643620-643961 | Common:2; Rare:71 | ||||
| chr12:752291-752602 | Common:1; Rare:91 | ||||
| chr12:2004439-2004669 | Common:2; Rare:67 |