| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:52191969-52192049 | Common:1; Rare:16 | ||||
| chr12:52232599-52232721 | Rare:21 | ||||
| chr12:52232953-52233003 | Rare:9 | ||||
| chr12:52233016-52233354 | Common:4; Rare:79 | ||||
| chr12:52233630-52233874 | Common:2; Rare:51 | ||||
| chr12:52248177-52248273 | Rare:27 | ||||
| chr12:52492752-52493078 | Common:1; Rare:107 | ||||
| chr12:52493205-52493485 | Rare:58 | ||||
| chr12:52519445-52519507 | Rare:14 | ||||
| chr12:52520187-52520447 | Common:2; Rare:92; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr12:52847839-52847947 | Common:1; Rare:35 | ||||
| chr12:52903455-52903671 | Common:2; Rare:48 | ||||
| chr12:52903903-52904271 | Common:2; Rare:79 | ||||
| chr12:52904983-52905030 | Common:2; Rare:17 | ||||
| chr12:52905037-52905347 | Common:3; Rare:68 |