| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:69643616-69643834 | Rare:79 | ||||
| chr2:69829501-69829769 | Common:1; Rare:102 | ||||
| chr2:69914571-69915185 | Common:2; Rare:149 | ||||
| chr2:70086931-70087118 | Common:1; Rare:93 | ||||
| chr2:70087292-70087758 | Common:3; Rare:177 | ||||
| chr2:70087760-70088588 | Common:1; Rare:215 | ||||
| chr2:70257978-70258182 | Common:1; Rare:73 | ||||
| chr2:70274857-70275067 | Common:1; Rare:56 | ||||
| chr2:70293645-70293862 | Common:3; Rare:74 | ||||
| chr2:71068526-71068678 | Rare:73 | ||||
| chr2:71070427-71070566 | Common:3; Rare:47 | ||||
| chr2:71130215-71130367 | Common:2; Rare:55; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:71130581-71130697 | Common:2; Rare:44 | ||||
| chr2:71130738-71130782 | Rare:16 | ||||
| chr2:71453458-71453878 | Common:3; Rare:76 |