| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:129376021-129376196 | Rare:58 | ||||
| chr11:129815748-129815898 | Common:1; Rare:37 | ||||
| chr11:129895535-129895695 | Common:2; Rare:59 | ||||
| chr11:130002760-130002905 | Common:2; Rare:27 | ||||
| chr11:130314395-130314520 | Common:1; Rare:42 | ||||
| chr11:134224533-134224695 | Rare:61 | ||||
| chr11:134225448-134225514 | Rare:21 | ||||
| chr11:134253278-134253617 | Common:2; Rare:125; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:389230-389358 | Rare:48 | ||||
| chr12:401446-401664 | Rare:58 | ||||
| chr12:643616-643681 | Rare:10 | ||||
| chr12:752306-752602 | Common:1; Rare:88 | ||||
| chr12:990452-990562 | Common:1; Rare:31 | ||||
| chr12:991093-991322 | Common:3; Rare:105 | ||||
| chr12:1690873-1691053 | Common:1; Rare:56 |