| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:5433745-5433910 | Common:1; Rare:33 | ||||
| chr12:5468858-5469050 | Rare:34 | ||||
| chr12:5474600-5474991 | Common:1; Rare:67 | ||||
| chr12:5515154-5515161 | Rare:1 | ||||
| chr12:5522495-5522752 | Common:2; Rare:47 | ||||
| chr12:6330045-6330275 | Common:3; Rare:48; Clinvar (benign):2 | ||||
| chr12:6569948-6570125 | Rare:42 | ||||
| chr12:6575989-6576027 | Common:1; Rare:6 | ||||
| chr12:6602035-6602434 | Common:1; Rare:124 | ||||
| chr12:6769572-6769999 | Common:1; Rare:116 | ||||
| chr12:6827378-6827652 | Common:2; Rare:80 | ||||
| chr12:6877133-6877225 | Rare:21 | ||||
| chr12:6966343-6966506 | Common:1; Rare:39 | ||||
| chr12:7089293-7089729 | Common:3; Rare:139 | ||||
| chr12:7107414-7107607 | Common:1; Rare:28 |