| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:53492850-53493290 | Common:10; Rare:212 | ||||
| chr12:53500655-53500968 | Common:5; Rare:119 | ||||
| chr12:53501165-53501370 | Rare:86 | ||||
| chr12:53501483-53501661 | Rare:84 | ||||
| chr12:53625898-53626020 | Rare:35 | ||||
| chr12:53626322-53626541 | Common:6; Rare:103 | ||||
| chr12:53676027-53676167 | Common:1; Rare:78 | ||||
| chr12:53727419-53727771 | Rare:155 | ||||
| chr12:54188922-54189171 | Rare:105 | ||||
| chr12:54280070-54280303 | Rare:80 | ||||
| chr12:54280537-54280744 | Common:1; Rare:48 | ||||
| chr12:54282971-54283922 | Common:9; Rare:658; Clinvar:6; Clinvar (pathogenic):5 | ||||
| chr12:55715996-55716178 | Common:3; Rare:142 | ||||
| chr12:55728932-55729331 | Rare:141 | ||||
| chr12:55729655-55730006 | Rare:137 |