| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:51238661-51238914 | Common:8; Rare:113 | ||||
| chr12:51239121-51239338 | Common:2; Rare:64 | ||||
| chr12:51324017-51324196 | Rare:62 | ||||
| chr12:51391613-51391780 | Common:2; Rare:55 | ||||
| chr12:51391802-51391876 | Rare:17 | ||||
| chr12:52007414-52007691 | Common:2; Rare:58 | ||||
| chr12:52036939-52037263 | Rare:103 | ||||
| chr12:52051152-52051454 | Common:1; Rare:99 | ||||
| chr12:52948994-52949159 | Rare:48 | ||||
| chr12:52949826-52949923 | Rare:22 | ||||
| chr12:53079344-53079537 | Common:2; Rare:68 | ||||
| chr12:53180605-53180735 | Common:1; Rare:44 | ||||
| chr12:53299411-53299710 | Common:2; Rare:78 | ||||
| chr12:53321197-53321418 | Common:2; Rare:74; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr12:53441471-53441787 | Common:1; Rare:89 |