| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:95218165-95218313 | Common:2; Rare:36 | ||||
| chr12:95473863-95474191 | Common:3; Rare:127 | ||||
| chr12:95858817-95859076 | Common:3; Rare:77 | ||||
| chr12:96194245-96194646 | Common:6; Rare:126 | ||||
| chr12:96399350-96399474 | Common:1; Rare:38 | ||||
| chr12:96400464-96400664 | Common:1; Rare:87 | ||||
| chr12:96489417-96489653 | Common:3; Rare:63 | ||||
| chr12:96907190-96907293 | Rare:39 | ||||
| chr12:98515555-98515876 | Rare:121; Clinvar:5; Clinvar (benign):1 | ||||
| chr12:98644703-98644843 | Common:3; Rare:47 | ||||
| chr12:98644982-98645307 | Common:2; Rare:96 | ||||
| chr12:100267074-100267277 | Common:1; Rare:94 | ||||
| chr12:100573551-100573770 | Rare:74 | ||||
| chr12:101407690-101408035 | Common:3; Rare:78 | ||||
| chr12:101877616-101877795 | Common:4; Rare:49 |