| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:126355532-126355790 | Common:1; Rare:72 | ||||
| chr11:129895535-129895698 | Common:2; Rare:59 | ||||
| chr11:134253306-134253592 | Common:2; Rare:93; Clinvar (benign):1 | ||||
| chr11:134276307-134276376 | Common:1; Rare:22 | ||||
| chr12:389261-389347 | Rare:31 | ||||
| chr12:401446-401677 | Rare:61 | ||||
| chr12:991109-991245 | Common:1; Rare:50 | ||||
| chr12:2794949-2795208 | Rare:105 | ||||
| chr12:2877031-2877254 | Rare:68 | ||||
| chr12:3873355-3873529 | Common:1; Rare:39 | ||||
| chr12:4320991-4321274 | Common:4; Rare:108 | ||||
| chr12:4538506-4538900 | Common:1; Rare:85 | ||||
| chr12:4649016-4649154 | Common:2; Rare:49; Clinvar (benign):1 | ||||
| chr12:6493199-6493386 | Common:7; Rare:50 | ||||
| chr12:6493778-6494135 | Common:2; Rare:107 |