| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:120265675-120265804 | Rare:71 | ||||
| chr12:120437755-120438228 | Common:2; Rare:158; Clinvar (benign):2 | ||||
| chr12:120446266-120446687 | Common:3; Rare:159 | ||||
| chr12:120469618-120469926 | Common:3; Rare:109 | ||||
| chr12:120495838-120496197 | Common:8; Rare:122 | ||||
| chr12:120528907-120529009 | Rare:34 | ||||
| chr12:120529079-120529303 | Common:2; Rare:78 | ||||
| chr12:120529420-120529478 | Rare:11 | ||||
| chr12:120534176-120534445 | Common:1; Rare:72 | ||||
| chr12:120534909-120535102 | Common:1; Rare:70 | ||||
| chr12:120535211-120535264 | Rare:13 | ||||
| chr12:120581287-120581677 | Common:2; Rare:138 | ||||
| chr12:120650114-120650283 | Rare:34 | ||||
| chr12:120686266-120686624 | Common:3; Rare:96 | ||||
| chr12:120686787-120686819 | Rare:8 |