| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:4320947-4321260 | Common:5; Rare:118 | ||||
| chr12:4538440-4538932 | Common:3; Rare:111 | ||||
| chr12:4648994-4649178 | Common:2; Rare:60; Clinvar (benign):2 | ||||
| chr12:6124514-6124764 | Rare:35; Clinvar:2 | ||||
| chr12:6124887-6124941 | Rare:16 | ||||
| chr12:6200005-6200364 | Common:3; Rare:97 | ||||
| chr12:6383988-6384243 | Common:1; Rare:55 | ||||
| chr12:6452028-6452120 | Common:1; Rare:20 | ||||
| chr12:6461002-6461255 | Rare:54 | ||||
| chr12:6470665-6470791 | Rare:38 | ||||
| chr12:6493107-6493502 | Common:8; Rare:124 | ||||
| chr12:6493746-6494146 | Common:2; Rare:117 | ||||
| chr12:6534316-6534593 | Common:5; Rare:115 | ||||
| chr12:6534651-6534860 | Common:3; Rare:86 | ||||
| chr12:6556052-6556222 | Common:3; Rare:59 |