| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:66130719-66130854 | Rare:44 | ||||
| chr12:68686794-68687000 | Common:5; Rare:60 | ||||
| chr12:71686040-71686099 | Common:1; Rare:14 | ||||
| chr12:82358372-82358549 | Rare:74 | ||||
| chr12:82358731-82358869 | Common:3; Rare:72 | ||||
| chr12:88142043-88142368 | Rare:89; Clinvar:3 | ||||
| chr12:93441895-93442139 | Common:2; Rare:80 | ||||
| chr12:98644974-98645293 | Common:2; Rare:95 | ||||
| chr12:101407731-101408056 | Common:2; Rare:81 | ||||
| chr12:102120061-102120219 | Rare:60 | ||||
| chr12:103930063-103930367 | Common:4; Rare:80 | ||||
| chr12:103965705-103965927 | Common:2; Rare:53 | ||||
| chr12:109477328-109477644 | Common:3; Rare:62 | ||||
| chr12:109573450-109573813 | Common:3; Rare:116; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr12:110468671-110468873 | Rare:47 |