| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:31728916-31729457 | Common:1; Rare:160 | ||||
| chr12:31959066-31959112 | Rare:13 | ||||
| chr12:31959119-31959666 | Common:4; Rare:158 | ||||
| chr12:31959752-31959927 | Common:1; Rare:47 | ||||
| chr12:31960050-31960106 | Rare:12 | ||||
| chr12:31962180-31962509 | Common:4; Rare:71 | ||||
| chr12:32106538-32107051 | Common:6; Rare:144 | ||||
| chr12:32399136-32399976 | Common:9; Rare:221 | ||||
| chr12:32400031-32400163 | Common:1; Rare:28 | ||||
| chr12:32501986-32502225 | Common:2; Rare:49; Clinvar:3; Clinvar (benign):2 | ||||
| chr12:32534252-32534307 | Common:2; Rare:7 | ||||
| chr12:32679034-32679975 | Common:7; Rare:276; Clinvar:1; Clinvar (benign):4 | ||||
| chr12:32755243-32755576 | Common:1; Rare:120; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr12:32755838-32756058 | Common:1; Rare:78 | ||||
| chr12:32756332-32756489 | Rare:35 |