| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:89524748-89524869 | Common:1; Rare:22 | ||||
| chr12:89709273-89709548 | Common:3; Rare:113 | ||||
| chr12:92145843-92146133 | Common:1; Rare:87 | ||||
| chr12:93570834-93571012 | Rare:51 | ||||
| chr12:95003642-95003821 | Common:3; Rare:69; Clinvar (benign):3 | ||||
| chr12:96035511-96035778 | Common:2; Rare:62 | ||||
| chr12:98515435-98515682 | Rare:81; Clinvar:1 | ||||
| chr12:98601255-98601379 | Rare:37; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:100200717-100200843 | Rare:41 | ||||
| chr12:100267061-100267424 | Common:1; Rare:148 | ||||
| chr12:101407652-101407815 | Common:2; Rare:50 | ||||
| chr12:102120065-102120262 | Rare:79 | ||||
| chr12:103841192-103841444 | Common:4; Rare:94 | ||||
| chr12:103930101-103930490 | Common:8; Rare:133 | ||||
| chr12:103965705-103965910 | Common:2; Rare:53 |