| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:7109166-7109564 | Common:2; Rare:94 | ||||
| chr12:7128778-7129038 | Common:1; Rare:42 | ||||
| chr12:7130256-7130423 | Common:4; Rare:45 | ||||
| chr12:7189576-7189748 | Common:1; Rare:66; Clinvar:4; Clinvar (benign):1 | ||||
| chr12:8227606-8227691 | Rare:24 | ||||
| chr12:8697814-8698102 | Common:1; Rare:104 | ||||
| chr12:8914146-8914214 | Rare:14 | ||||
| chr12:8914344-8914789 | Common:6; Rare:130 | ||||
| chr12:8949408-8949495 | Rare:9 | ||||
| chr12:8949955-8950099 | Common:1; Rare:39 | ||||
| chr12:9079737-9080003 | Rare:56 | ||||
| chr12:9115835-9116325 | Common:3; Rare:94 | ||||
| chr12:9607884-9607989 | Common:1; Rare:22 | ||||
| chr12:10178902-10179228 | Common:1; Rare:49 | ||||
| chr12:10613485-10613634 | Rare:59 |