| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:231707011-231707201 | Rare:44 | ||||
| chr2:231710278-231710527 | Common:2; Rare:124 | ||||
| chr2:231961648-231961745 | Rare:26; Clinvar:1 | ||||
| chr2:232550544-232550721 | Rare:70 | ||||
| chr2:232550970-232551110 | Common:1; Rare:27 | ||||
| chr2:233854528-233854720 | Common:4; Rare:44 | ||||
| chr2:237085761-237085982 | Common:2; Rare:82 | ||||
| chr2:237414327-237414620 | Common:1; Rare:52 | ||||
| chr2:237487179-237487294 | Common:1; Rare:34 | ||||
| chr2:237966728-237967074 | Common:3; Rare:107 | ||||
| chr2:238060738-238061029 | Common:4; Rare:88 | ||||
| chr2:238203583-238203821 | Common:3; Rare:101 | ||||
| chr2:238426895-238427067 | Common:1; Rare:63 | ||||
| chr2:239401641-239401739 | Rare:45 | ||||
| chr2:240025253-240025417 | Common:2; Rare:60; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 |