| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6689418-6689700 | Common:2; Rare:76 | ||||
| chr12:6724196-6724296 | Rare:21 | ||||
| chr12:6753063-6753189 | Common:4; Rare:47 | ||||
| chr12:6851902-6852191 | Rare:76 | ||||
| chr12:6873263-6873500 | Common:2; Rare:68 | ||||
| chr12:6943979-6944161 | Common:3; Rare:179; Clinvar:5; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:6970612-6970936 | Common:2; Rare:94 | ||||
| chr12:7108481-7108681 | Common:1; Rare:58 | ||||
| chr12:8032520-8032794 | Common:5; Rare:88 | ||||
| chr12:8949972-8950056 | Common:1; Rare:20 | ||||
| chr12:10212565-10212752 | Common:3; Rare:33 | ||||
| chr12:10718092-10718389 | Common:2; Rare:52 | ||||
| chr12:10721979-10722103 | Rare:27 | ||||
| chr12:10722711-10723022 | Common:3; Rare:98 | ||||
| chr12:10723324-10723452 | Common:2; Rare:36 |