| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:123436418-123436550 | Rare:23 | ||||
| chr12:123436600-123436991 | Common:2; Rare:81 | ||||
| chr12:123457868-123458235 | Common:1; Rare:78 | ||||
| chr12:123458253-123458616 | Common:5; Rare:85 | ||||
| chr12:123533902-123534044 | Common:2; Rare:39 | ||||
| chr12:123584317-123584634 | Common:6; Rare:115 | ||||
| chr12:123601769-123602213 | Common:6; Rare:122 | ||||
| chr12:123633571-123633913 | Common:2; Rare:162; Clinvar:8; Clinvar (benign):1 | ||||
| chr12:123670975-123671211 | Common:5; Rare:58; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:123712105-123712478 | Common:8; Rare:136; Clinvar:3; Clinvar (benign):2 | ||||
| chr12:123972960-123973337 | Common:2; Rare:119 | ||||
| chr12:124389321-124389610 | Rare:75 | ||||
| chr12:124566950-124567238 | Rare:66 | ||||
| chr12:124567874-124568154 | Common:2; Rare:66 | ||||
| chr12:124863814-124864162 | Common:1; Rare:96 |