| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:54000450-54001020 | Common:9; Rare:370 | ||||
| chr12:54017166-54017928 | Common:3; Rare:224 | ||||
| chr12:54028177-54028713 | Common:8; Rare:226 | ||||
| chr12:54188816-54189241 | Rare:447 | ||||
| chr12:54259256-54259372 | Rare:16 | ||||
| chr12:54259368-54260030 | Common:1; Rare:269 | ||||
| chr12:54279549-54279978 | Common:8; Rare:580 | ||||
| chr12:54279978-54280780 | Common:7; Rare:887 | ||||
| chr12:54280965-54281502 | Common:16; Rare:559 | ||||
| chr12:54283060-54284101 | Common:12; Rare:670; Clinvar:8; Clinvar (pathogenic):12 | ||||
| chr12:54285130-54285530 | Common:3; Rare:93 | ||||
| chr12:54286004-54286225 | Rare:85 | ||||
| chr12:54286160-54286560 | Common:1; Rare:83 | ||||
| chr12:54295687-54296126 | Rare:294 | ||||
| chr12:54297851-54298353 | Common:2; Rare:323 |