| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:9089892-9090293 | Common:4; Rare:78 | ||||
| chr12:9115762-9116283 | Common:3; Rare:116 | ||||
| chr12:9760893-9761010 | Rare:15 | ||||
| chr12:9869328-9869538 | Common:1; Rare:34 | ||||
| chr12:10213403-10213767 | Common:3; Rare:82 | ||||
| chr12:10613459-10613636 | Rare:69 | ||||
| chr12:11170872-11171238 | Common:4; Rare:99 | ||||
| chr12:11171545-11171770 | Common:6; Rare:76 | ||||
| chr12:11649685-11650017 | Common:1; Rare:93 | ||||
| chr12:12356991-12357249 | Common:5; Rare:123 | ||||
| chr12:12560857-12560966 | Common:2; Rare:25 | ||||
| chr12:12561021-12561203 | Common:1; Rare:38 | ||||
| chr12:12611627-12612170 | Common:3; Rare:159 | ||||
| chr12:12717050-12717486 | Rare:147; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:12725649-12725971 | Common:3; Rare:73 |