| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:101407650-101407841 | Common:2; Rare:56 | ||||
| chr12:101408003-101408278 | Rare:67 | ||||
| chr12:101408282-101408332 | Rare:11 | ||||
| chr12:101697378-101697883 | Common:4; Rare:150 | ||||
| chr12:101698004-101698313 | Common:1; Rare:91 | ||||
| chr12:101830683-101830921 | Common:4; Rare:104; Clinvar:1; Clinvar (benign):3 | ||||
| chr12:101830925-101831149 | Rare:52 | ||||
| chr12:101877100-101877787 | Common:9; Rare:161 | ||||
| chr12:101877969-101878067 | Rare:21 | ||||
| chr12:101908496-101908770 | Common:1; Rare:43 | ||||
| chr12:102061782-102061831 | Rare:14 | ||||
| chr12:102061859-102062216 | Common:1; Rare:102 | ||||
| chr12:102119773-102119797 | Rare:2 | ||||
| chr12:102119809-102119885 | Rare:25 | ||||
| chr12:102119966-102120322 | Common:1; Rare:131 |