| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:121802940-121803091 | Rare:35 | ||||
| chr12:122526887-122527262 | Common:3; Rare:126 | ||||
| chr12:122716794-122716811 | Rare:5 | ||||
| chr12:122980571-122980732 | Common:1; Rare:51 | ||||
| chr12:123233096-123233493 | Common:2; Rare:133; Clinvar:1 | ||||
| chr12:123364816-123364974 | Common:2; Rare:61 | ||||
| chr12:123584278-123584681 | Common:8; Rare:141 | ||||
| chr12:123633640-123633851 | Common:1; Rare:93; Clinvar:8; Clinvar (benign):1 | ||||
| chr12:123972575-123972903 | Common:6; Rare:115 | ||||
| chr12:132887553-132887798 | Rare:74 | ||||
| chr12:132956280-132956426 | Common:1; Rare:29 | ||||
| chr12:133080730-133080941 | Rare:65 | ||||
| chr12:133130261-133130602 | Common:7; Rare:105 | ||||
| chr13:19633493-19633746 | Common:1; Rare:99 | ||||
| chr13:20773931-20773991 | Rare:19 |