| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6851902-6852180 | Rare:73 | ||||
| chr12:6867355-6867594 | Common:2; Rare:120; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:6868061-6868161 | Common:4; Rare:39 | ||||
| chr12:6873291-6873546 | Common:1; Rare:75 | ||||
| chr12:6904676-6904847 | Rare:41 | ||||
| chr12:6914395-6914636 | Rare:64 | ||||
| chr12:6943531-6944172 | Common:18; Rare:498; Clinvar:6; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:6970625-6970963 | Common:4; Rare:106; Clinvar (benign):1 | ||||
| chr12:7018773-7018927 | Rare:45 | ||||
| chr12:7107991-7108282 | Common:2; Rare:66 | ||||
| chr12:7108497-7108643 | Common:1; Rare:41 | ||||
| chr12:7130270-7130433 | Common:4; Rare:47 | ||||
| chr12:7189512-7189723 | Rare:73; Clinvar:4 | ||||
| chr12:7936147-7936347 | Common:1; Rare:37 | ||||
| chr12:8032568-8032759 | Common:4; Rare:66 |