| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:55709893-55710132 | Common:4; Rare:49 | ||||
| chr12:57195770-57195904 | Common:1; Rare:41 | ||||
| chr12:57244314-57244619 | Common:1; Rare:81; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr12:80700357-80700654 | Common:1; Rare:53 | ||||
| chr12:92466742-92466941 | Common:3; Rare:36 | ||||
| chr12:101619108-101619160 | Rare:7 | ||||
| chr12:101627733-101627804 | Rare:28 | ||||
| chr12:101631567-101632143 | Common:1; Rare:150; Clinvar:1; Clinvar (benign):2 | ||||
| chr12:102351109-102351245 | Common:2; Rare:16 | ||||
| chr12:109233756-109234053 | Common:2; Rare:100 | ||||
| chr12:109265095-109265524 | Common:2; Rare:167; Clinvar:1 | ||||
| chr12:109266203-109266273 | Rare:23 | ||||
| chr12:110249922-110250209 | Common:1; Rare:39 | ||||
| chr12:110339251-110339721 | Common:1; Rare:91; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:119195511-119195749 | Common:3; Rare:39 |