| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:68679307-68679609 | Common:4; Rare:100 | ||||
| chr2:69013288-69013412 | Rare:24 | ||||
| chr2:69387113-69387384 | Common:1; Rare:73; Clinvar:2 | ||||
| chr2:69437387-69437534 | Rare:68; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:69643611-69643829 | Rare:78 | ||||
| chr2:69742005-69742136 | Rare:31 | ||||
| chr2:69829468-69829737 | Common:1; Rare:109 | ||||
| chr2:69893892-69894006 | Rare:33 | ||||
| chr2:70086931-70087116 | Common:1; Rare:93 | ||||
| chr2:70087310-70087762 | Common:2; Rare:176 | ||||
| chr2:70087810-70087873 | Rare:13 | ||||
| chr2:70190973-70191131 | Common:1; Rare:37 | ||||
| chr2:70248503-70248766 | Common:4; Rare:112 | ||||
| chr2:70257902-70258177 | Common:1; Rare:89 | ||||
| chr2:70293645-70293912 | Common:3; Rare:87 |