| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:229921939-229922150 | Common:2; Rare:87 | ||||
| chr2:229922406-229922511 | Rare:32 | ||||
| chr2:230327049-230327204 | Rare:32 | ||||
| chr2:232550494-232550719 | Rare:90 | ||||
| chr2:232550953-232551098 | Common:1; Rare:28 | ||||
| chr2:237085809-237085976 | Common:1; Rare:68 | ||||
| chr2:237487165-237487287 | Common:2; Rare:35 | ||||
| chr2:238060712-238061029 | Common:4; Rare:99 | ||||
| chr2:240025263-240025455 | Common:2; Rare:72; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr2:240560765-240560851 | Rare:35 | ||||
| chr2:240561022-240561295 | Common:4; Rare:129 | ||||
| chr2:241149434-241149682 | Common:4; Rare:85 | ||||
| chr2:241239601-241239979 | Common:2; Rare:123 | ||||
| chr2:241315120-241315398 | Common:5; Rare:91 | ||||
| chr2:241315646-241315986 | Common:5; Rare:133 |