| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:118061044-118061271 | Common:1; Rare:66 | ||||
| chr12:118103709-118104113 | Common:1; Rare:99 | ||||
| chr12:118135938-118136232 | Common:2; Rare:93 | ||||
| chr12:118372820-118373199 | Common:2; Rare:104 | ||||
| chr12:119668100-119668192 | Common:1; Rare:18 | ||||
| chr12:119672230-119672251 | Rare:6 | ||||
| chr12:119674161-119674366 | Common:1; Rare:30 | ||||
| chr12:120116705-120116955 | Common:3; Rare:86 | ||||
| chr12:120194683-120194798 | Rare:42 | ||||
| chr12:120201084-120201366 | Common:2; Rare:89 | ||||
| chr12:120224708-120224823 | Common:1; Rare:38 | ||||
| chr12:120225947-120226091 | Common:1; Rare:25 | ||||
| chr12:120437859-120438241 | Common:2; Rare:142; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr12:120446353-120446489 | Common:2; Rare:63 | ||||
| chr12:120469597-120469873 | Common:2; Rare:99 |