| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:119178614-119179024 | Common:1; Rare:72; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:119179339-119179423 | Rare:29; Clinvar:3 | ||||
| chr12:119877230-119877565 | Common:3; Rare:79 | ||||
| chr12:120116652-120116974 | Common:6; Rare:107 | ||||
| chr12:120194690-120194774 | Rare:29 | ||||
| chr12:120201061-120201372 | Common:2; Rare:101 | ||||
| chr12:120265684-120265966 | Common:1; Rare:106 | ||||
| chr12:120437867-120438229 | Common:2; Rare:137; Clinvar (benign):2 | ||||
| chr12:120446338-120446495 | Common:2; Rare:72 | ||||
| chr12:120469542-120469880 | Common:3; Rare:119 | ||||
| chr12:120495830-120496550 | Common:8; Rare:234 | ||||
| chr12:120529111-120529270 | Common:2; Rare:53 | ||||
| chr12:120581344-120581577 | Common:1; Rare:79 | ||||
| chr12:120686960-120687164 | Common:1; Rare:70 | ||||
| chr12:120725725-120725875 | Rare:47; Clinvar:1 |