| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:96489471-96489610 | Common:1; Rare:33 | ||||
| chr12:96907139-96907285 | Common:1; Rare:52 | ||||
| chr12:98515435-98515725 | Rare:95; Clinvar:1 | ||||
| chr12:98593423-98593771 | Common:2; Rare:123; Clinvar:4; Clinvar (benign):4 | ||||
| chr12:98644621-98644843 | Common:3; Rare:78 | ||||
| chr12:98644930-98645301 | Common:2; Rare:109 | ||||
| chr12:100200717-100200851 | Rare:44 | ||||
| chr12:100267060-100267287 | Common:1; Rare:106 | ||||
| chr12:100794714-100795027 | Common:1; Rare:65 | ||||
| chr12:101407641-101408061 | Common:3; Rare:107 | ||||
| chr12:101877437-101877755 | Common:3; Rare:84 | ||||
| chr12:102120048-102120266 | Rare:90 | ||||
| chr12:103930051-103930557 | Common:8; Rare:172 | ||||
| chr12:103957125-103957353 | Common:7; Rare:62 | ||||
| chr12:103965674-103965960 | Common:2; Rare:72 |