| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:4320910-4321267 | Common:10; Rare:246 | ||||
| chr12:4538431-4538930 | Common:6; Rare:224 | ||||
| chr12:4648994-4649178 | Common:4; Rare:116; Clinvar (benign):4 | ||||
| chr12:6309880-6310360 | Common:3; Rare:103 | ||||
| chr12:6310527-6310738 | Common:8; Rare:92 | ||||
| chr12:6341953-6342274 | Common:1; Rare:112; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:6363600-6364090 | Common:4; Rare:212 | ||||
| chr12:6374660-6375180 | Common:5; Rare:280; Clinvar:5; Clinvar (benign):5 | ||||
| chr12:6375197-6375326 | Common:4; Rare:58 | ||||
| chr12:6383961-6384252 | Common:2; Rare:133 | ||||
| chr12:6451750-6452170 | Common:8; Rare:139 | ||||
| chr12:6470644-6470859 | Common:1; Rare:107 | ||||
| chr12:6493212-6493399 | Common:12; Rare:100 | ||||
| chr12:6493763-6494145 | Common:4; Rare:221 | ||||
| chr12:6533340-6533830 | Common:1; Rare:120 |