| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:106247348-106247748 | Common:10; Rare:205 | ||||
| chr12:106247892-106248370 | Common:3; Rare:216 | ||||
| chr12:106302252-106303014 | Common:41; Rare:414 | ||||
| chr12:106357677-106357826 | Common:3; Rare:35; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:106357937-106358177 | Common:7; Rare:196 | ||||
| chr12:106774030-106774390 | Common:6; Rare:162 | ||||
| chr12:106774410-106774725 | Common:2; Rare:114 | ||||
| chr12:106955496-106956054 | Common:4; Rare:360 | ||||
| chr12:106956657-106957117 | Common:1; Rare:132 | ||||
| chr12:106987046-106987281 | Common:4; Rare:68 | ||||
| chr12:107093503-107093645 | Rare:95 | ||||
| chr12:107093784-107094087 | Common:4; Rare:133 | ||||
| chr12:107685628-107685965 | Common:4; Rare:202 | ||||
| chr12:108515002-108515329 | Common:2; Rare:193 | ||||
| chr12:108560830-108561050 | Common:1; Rare:126 |