| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6568235-6568388 | Rare:59 | ||||
| chr12:6606422-6606710 | Common:3; Rare:98 | ||||
| chr12:6688887-6688973 | Rare:20 | ||||
| chr12:6689448-6689782 | Common:2; Rare:85 | ||||
| chr12:6723830-6724291 | Common:1; Rare:103 | ||||
| chr12:6752937-6753191 | Common:6; Rare:78 | ||||
| chr12:6765253-6765516 | Common:1; Rare:38 | ||||
| chr12:6766395-6766748 | Rare:102 | ||||
| chr12:6829658-6829904 | Common:2; Rare:63 | ||||
| chr12:6851236-6851429 | Rare:47 | ||||
| chr12:6851902-6852182 | Rare:73 | ||||
| chr12:6867355-6867680 | Common:2; Rare:152; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:6868882-6869181 | Rare:89; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:6873311-6873541 | Common:1; Rare:66 | ||||
| chr12:6904721-6904890 | Rare:41 |