| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6363200-6363540 | Common:2; Rare:115; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:6363786-6363945 | Common:2; Rare:53 | ||||
| chr12:6375347-6375699 | Common:3; Rare:88; Clinvar:1; Clinvar (benign):6 | ||||
| chr12:6376116-6376278 | Common:2; Rare:37 | ||||
| chr12:6377784-6377937 | Common:1; Rare:30 | ||||
| chr12:6383959-6384207 | Common:1; Rare:62 | ||||
| chr12:6470657-6471162 | Common:7; Rare:144 | ||||
| chr12:6493210-6493433 | Common:6; Rare:68 | ||||
| chr12:6493763-6494144 | Common:2; Rare:112 | ||||
| chr12:6533493-6533643 | Rare:32 | ||||
| chr12:6534203-6534570 | Common:6; Rare:140 | ||||
| chr12:6568230-6568531 | Common:1; Rare:107 | ||||
| chr12:6606593-6606872 | Rare:100 | ||||
| chr12:6635938-6636125 | Common:2; Rare:48 | ||||
| chr12:6636129-6636327 | Common:1; Rare:34 |