| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:264517-264975 | Common:4; Rare:169 | ||||
| chr2:677342-677557 | Common:1; Rare:92 | ||||
| chr2:1413277-1413461 | Common:2; Rare:48 | ||||
| chr2:1744389-1744570 | Common:1; Rare:66 | ||||
| chr2:3377794-3378009 | Common:1; Rare:61 | ||||
| chr2:3379619-3379754 | Common:1; Rare:53 | ||||
| chr2:3519467-3519674 | Common:3; Rare:61 | ||||
| chr2:3558269-3558571 | Common:6; Rare:110 | ||||
| chr2:3575107-3575447 | Common:2; Rare:98; Clinvar:3; Clinvar (benign):6 | ||||
| chr2:9423143-9423685 | Common:1; Rare:144 | ||||
| chr2:9474493-9474630 | Common:6; Rare:63 | ||||
| chr2:9555621-9555992 | Common:2; Rare:122 | ||||
| chr2:9630255-9630811 | Common:6; Rare:221 | ||||
| chr2:9630944-9631316 | Common:3; Rare:119 | ||||
| chr2:9843413-9843539 | Common:3; Rare:34 |