| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:96907143-96907293 | Common:1; Rare:52 | ||||
| chr12:98515494-98515648 | Rare:43; Clinvar:1 | ||||
| chr12:98515856-98515882 | Rare:11 | ||||
| chr12:98593345-98593776 | Common:2; Rare:142; Clinvar:4; Clinvar (benign):4 | ||||
| chr12:98644737-98645301 | Common:5; Rare:164 | ||||
| chr12:99154461-99154540 | Rare:20 | ||||
| chr12:100200717-100200851 | Rare:44 | ||||
| chr12:100267047-100267286 | Common:1; Rare:115 | ||||
| chr12:100573554-100573770 | Rare:74 | ||||
| chr12:101280050-101280132 | Common:1; Rare:28 | ||||
| chr12:101407675-101408035 | Common:3; Rare:84 | ||||
| chr12:102120065-102120263 | Rare:80 | ||||
| chr12:103930006-103930577 | Common:9; Rare:185 | ||||
| chr12:103965664-103965947 | Common:2; Rare:74 | ||||
| chr12:104064058-104064122 | Rare:17 |