| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:96907187-96907295 | Rare:41 | ||||
| chr12:98515395-98515886 | Common:1; Rare:179; Clinvar:5; Clinvar (benign):1 | ||||
| chr12:98593494-98593771 | Common:1; Rare:93; Clinvar:4; Clinvar (benign):4 | ||||
| chr12:98644703-98645305 | Common:7; Rare:175 | ||||
| chr12:100142842-100142971 | Common:1; Rare:49 | ||||
| chr12:100200707-100200854 | Rare:48 | ||||
| chr12:100267032-100267385 | Common:1; Rare:154 | ||||
| chr12:100573486-100573770 | Rare:84 | ||||
| chr12:100593669-100593978 | Common:1; Rare:56 | ||||
| chr12:101280034-101280186 | Common:1; Rare:44 | ||||
| chr12:101407641-101408110 | Common:3; Rare:127 | ||||
| chr12:101757229-101757423 | Common:1; Rare:39; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr12:101877524-101877797 | Common:5; Rare:69 | ||||
| chr12:102120048-102120269 | Common:1; Rare:90 | ||||
| chr12:102917281-102917356 | Common:1; Rare:24 |