| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:92136630-92136689 | Rare:9 | ||||
| chr12:92466571-92466828 | Common:2; Rare:44 | ||||
| chr12:93412418-93412470 | Rare:12 | ||||
| chr12:93737717-93738015 | Rare:52 | ||||
| chr12:93738591-93738755 | Rare:24 | ||||
| chr12:94586831-94587115 | Rare:39 | ||||
| chr12:96239810-96239931 | Rare:26 | ||||
| chr12:98503848-98503975 | Common:2; Rare:38 | ||||
| chr12:101616037-101616359 | Common:2; Rare:54 | ||||
| chr12:101748187-101748611 | Common:1; Rare:71 | ||||
| chr12:101771110-101771373 | Common:1; Rare:69 | ||||
| chr12:101773360-101773651 | Rare:56 | ||||
| chr12:101796681-101796858 | Common:1; Rare:44; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr12:103942339-103942629 | Common:1; Rare:62 | ||||
| chr12:103946620-103946936 | Rare:79 |