| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:48716673-48716929 | Common:4; Rare:83 | ||||
| chr12:48815379-48815620 | Common:1; Rare:55 | ||||
| chr12:48818583-48818897 | Common:1; Rare:114 | ||||
| chr12:48852102-48852387 | Common:2; Rare:80 | ||||
| chr12:48939653-48940071 | Common:2; Rare:91 | ||||
| chr12:48957000-48957131 | Common:1; Rare:20 | ||||
| chr12:48957297-48957678 | Common:4; Rare:104 | ||||
| chr12:49018736-49018933 | Common:1; Rare:83 | ||||
| chr12:49069988-49070160 | Common:2; Rare:39 | ||||
| chr12:49110808-49111058 | Rare:59 | ||||
| chr12:49131296-49131685 | Common:2; Rare:151 | ||||
| chr12:49188455-49188644 | Common:2; Rare:25 | ||||
| chr12:49188965-49189288 | Rare:86; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:49227966-49228141 | Common:1; Rare:33 | ||||
| chr12:49264774-49265082 | Common:4; Rare:106 |