| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:42469490-42469850 | Common:3; Rare:67; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:43337680-43338143 | Common:3; Rare:183 | ||||
| chr12:44021472-44021716 | Rare:48 | ||||
| chr12:44445043-44445443 | Common:1; Rare:95 | ||||
| chr12:44445628-44446028 | Common:1; Rare:75 | ||||
| chr12:44847851-44848794 | Common:14; Rare:249 | ||||
| chr12:45186679-45187079 | Common:5; Rare:86 | ||||
| chr12:45216678-45216783 | Common:2; Rare:31 | ||||
| chr12:45216803-45217056 | Common:2; Rare:77 | ||||
| chr12:45232449-45233321 | Common:4; Rare:247 | ||||
| chr12:45244560-45244870 | Rare:55 | ||||
| chr12:45269070-45269430 | Rare:72 | ||||
| chr12:45576161-45576278 | Common:1; Rare:22 | ||||
| chr12:45726465-45727044 | Common:3; Rare:208 | ||||
| chr12:45727258-45727950 | Common:2; Rare:612 |