| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:241272811-241273030 | Rare:76 | ||||
| chr2:241314811-241315503 | Common:7; Rare:228 | ||||
| chr2:241315578-241316220 | Common:5; Rare:231 | ||||
| chr2:241316344-241316446 | Common:2; Rare:29 | ||||
| chr2:241356063-241356369 | Common:4; Rare:119 | ||||
| chr2:241508536-241509013 | Common:4; Rare:143 | ||||
| chr2:241617460-241617755 | Common:2; Rare:65 | ||||
| chr2:241636964-241637154 | Rare:74 | ||||
| chr2:241637260-241637748 | Common:2; Rare:230 | ||||
| chr2:241686171-241686371 | Common:1; Rare:39 | ||||
| chr2:241686692-241687222 | Common:4; Rare:161 | ||||
| chr2:241687251-241687380 | Common:1; Rare:30 | ||||
| chr2:241701362-241701550 | Common:2; Rare:52 | ||||
| chr2:241701807-241702122 | Common:1; Rare:117 | ||||
| chr2:241702313-241702502 | Common:1; Rare:75 |