| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:95217386-95217746 | Common:4; Rare:99 | ||||
| chr12:95474039-95474192 | Common:2; Rare:71 | ||||
| chr12:96907162-96907290 | Common:1; Rare:45 | ||||
| chr12:98515271-98515795 | Common:1; Rare:174; Clinvar:2 | ||||
| chr12:98593474-98593743 | Common:2; Rare:91; Clinvar:4; Clinvar (benign):2 | ||||
| chr12:100200707-100200814 | Rare:29 | ||||
| chr12:100267065-100267264 | Common:1; Rare:95 | ||||
| chr12:101407697-101408056 | Common:3; Rare:85 | ||||
| chr12:102120065-102120256 | Rare:75 | ||||
| chr12:103930068-103930529 | Common:8; Rare:155 | ||||
| chr12:103965710-103965960 | Common:2; Rare:54 | ||||
| chr12:104138158-104138426 | Common:1; Rare:78 | ||||
| chr12:104286935-104287087 | Common:2; Rare:39 | ||||
| chr12:104287204-104287268 | Rare:10 | ||||
| chr12:105236065-105236296 | Common:2; Rare:105 |