| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:224585451-224585797 | Common:4; Rare:93 | ||||
| chr2:226799174-226799332 | Common:1; Rare:38 | ||||
| chr2:226799734-226799944 | Rare:76 | ||||
| chr2:226835895-226836136 | Common:1; Rare:97 | ||||
| chr2:227325203-227325382 | Common:4; Rare:60 | ||||
| chr2:227714524-227714888 | Common:9; Rare:49 | ||||
| chr2:227717897-227718126 | Common:1; Rare:61; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:227871571-227871666 | Common:4; Rare:36 | ||||
| chr2:229271220-229271389 | Common:1; Rare:53 | ||||
| chr2:229921308-229921726 | Common:3; Rare:99 | ||||
| chr2:229921890-229922121 | Common:2; Rare:90 | ||||
| chr2:229922182-229922510 | Common:1; Rare:97 | ||||
| chr2:229922897-229923129 | Rare:55 | ||||
| chr2:229923167-229923256 | Rare:21 | ||||
| chr2:230219917-230220009 | Rare:14 |