| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:130181538-130181714 | Common:2; Rare:70 | ||||
| chr2:130182077-130182346 | Common:2; Rare:103 | ||||
| chr2:130342104-130342279 | Rare:76; Clinvar:1 | ||||
| chr2:130342645-130342931 | Common:5; Rare:90 | ||||
| chr2:131105214-131105356 | Common:1; Rare:60 | ||||
| chr2:134918597-134918857 | Common:1; Rare:102 | ||||
| chr2:135531195-135531514 | Common:1; Rare:59 | ||||
| chr2:135985398-135985720 | Common:4; Rare:134; Clinvar (benign):1 | ||||
| chr2:138501664-138502005 | Common:2; Rare:120 | ||||
| chr2:142877511-142877694 | Common:1; Rare:28 | ||||
| chr2:144517422-144517767 | Common:5; Rare:93 | ||||
| chr2:144518134-144518203 | Common:1; Rare:14 | ||||
| chr2:144520068-144520547 | Common:4; Rare:86; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:148020688-148021109 | Common:2; Rare:97; Clinvar (benign):2 | ||||
| chr2:148021318-148021462 | Rare:29 |