| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:158968516-158968755 | Rare:72 | ||||
| chr2:159286653-159286926 | Common:5; Rare:105 | ||||
| chr2:159615225-159615343 | Common:2; Rare:28 | ||||
| chr2:159615469-159615702 | Common:2; Rare:79 | ||||
| chr2:159616421-159616689 | Common:2; Rare:53 | ||||
| chr2:159712345-159712611 | Common:2; Rare:97 | ||||
| chr2:160062474-160062740 | Common:5; Rare:66 | ||||
| chr2:160493432-160493575 | Common:1; Rare:47 | ||||
| chr2:161308351-161308533 | Common:2; Rare:48 | ||||
| chr2:164955538-164955596 | Rare:16 | ||||
| chr2:165953733-165954083 | Common:3; Rare:118; Clinvar:6; Clinvar (benign):1 | ||||
| chr2:166375867-166376094 | Common:4; Rare:66; Clinvar:1; Clinvar (benign):5 | ||||
| chr2:166493980-166494171 | Rare:27 | ||||
| chr2:166494173-166494380 | Common:1; Rare:37 | ||||
| chr2:166494381-166494468 | Rare:23 |