| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:52036851-52037390 | Common:2; Rare:266 | ||||
| chr12:52041780-52042622 | Common:4; Rare:185 | ||||
| chr12:52050590-52051040 | Common:2; Rare:108 | ||||
| chr12:52051080-52051524 | Common:6; Rare:647 | ||||
| chr12:52069442-52071238 | Common:19; Rare:1122 | ||||
| chr12:52903056-52903456 | Common:11; Rare:67 | ||||
| chr12:52903421-52903686 | Common:5; Rare:91 | ||||
| chr12:52903719-52904119 | Common:18; Rare:191 | ||||
| chr12:52904325-52904725 | Common:2; Rare:84 | ||||
| chr12:52904972-52905833 | Common:24; Rare:392 | ||||
| chr12:52907116-52907520 | Common:16; Rare:258 | ||||
| chr12:52948769-52949171 | Common:9; Rare:425; Clinvar:4 | ||||
| chr12:52949158-52949686 | Common:3; Rare:226; Clinvar:6; Clinvar (pathogenic):2 | ||||
| chr12:52949746-52950146 | Rare:351 | ||||
| chr12:53005920-53006561 | Common:26; Rare:1094 |