| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:101431299-101431411 | Common:1; Rare:20 | ||||
| chr12:101796681-101796841 | Common:1; Rare:40; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr12:101931810-101932086 | Common:2; Rare:49 | ||||
| chr12:103706612-103707047 | Common:2; Rare:123 | ||||
| chr12:103925350-103925377 | Rare:5 | ||||
| chr12:103946531-103946941 | Common:1; Rare:108 | ||||
| chr12:104637801-104637957 | Common:1; Rare:30 | ||||
| chr12:104644118-104644204 | Common:1; Rare:23 | ||||
| chr12:104648934-104648965 | Rare:2 | ||||
| chr12:105199442-105199697 | Rare:70 | ||||
| chr12:106248948-106249147 | Common:1; Rare:39 | ||||
| chr12:108536719-108536939 | Rare:54 | ||||
| chr12:108634546-108634737 | Common:1; Rare:33 | ||||
| chr12:108635728-108635897 | Rare:26 | ||||
| chr12:108655802-108655915 | Common:2; Rare:19 |