| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:123272209-123272433 | Rare:50 | ||||
| chr12:123364810-123364948 | Common:1; Rare:53 | ||||
| chr12:123383919-123384191 | Rare:63 | ||||
| chr12:123436403-123436592 | Rare:41 | ||||
| chr12:123584330-123584826 | Common:8; Rare:162 | ||||
| chr12:123602023-123602174 | Common:3; Rare:56 | ||||
| chr12:123633544-123633851 | Common:1; Rare:145; Clinvar:8; Clinvar (benign):1 | ||||
| chr12:123712216-123712622 | Common:4; Rare:145; Clinvar:4; Clinvar (benign):3 | ||||
| chr12:123972550-123972899 | Common:6; Rare:119 | ||||
| chr12:124311064-124311344 | Rare:59 | ||||
| chr12:124335264-124335561 | Common:4; Rare:83 | ||||
| chr12:124388777-124388962 | Common:3; Rare:60 | ||||
| chr12:124422503-124422828 | Common:5; Rare:92 | ||||
| chr12:124423016-124423332 | Common:2; Rare:78 | ||||
| chr12:124786473-124786789 | Common:3; Rare:85 |