| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:69437415-69437568 | Rare:68; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:69643611-69643825 | Rare:76 | ||||
| chr2:69829517-69829726 | Rare:86 | ||||
| chr2:69914746-69915082 | Common:2; Rare:75 | ||||
| chr2:70086877-70087071 | Common:1; Rare:98 | ||||
| chr2:70087310-70087758 | Common:2; Rare:174 | ||||
| chr2:70191002-70191134 | Common:1; Rare:31 | ||||
| chr2:70257978-70258174 | Common:1; Rare:69 | ||||
| chr2:70293645-70293841 | Common:2; Rare:68 | ||||
| chr2:70978996-70979238 | Common:3; Rare:84 | ||||
| chr2:71068537-71068686 | Rare:64 | ||||
| chr2:71130227-71130662 | Common:6; Rare:120; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:71227049-71227417 | Common:2; Rare:89 | ||||
| chr2:71276440-71276643 | Rare:77 | ||||
| chr2:72144371-72144715 | Common:4; Rare:78 |