| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:231961680-231961748 | Rare:16; Clinvar:1 | ||||
| chr2:232539679-232539692 | Rare:1 | ||||
| chr2:232550497-232550723 | Rare:92 | ||||
| chr2:232697101-232697379 | Common:2; Rare:92 | ||||
| chr2:233251520-233251703 | Common:3; Rare:64 | ||||
| chr2:233854472-233854779 | Common:5; Rare:88 | ||||
| chr2:234951797-234952109 | Common:1; Rare:82 | ||||
| chr2:237085742-237085951 | Common:2; Rare:74 | ||||
| chr2:237487150-237487287 | Common:2; Rare:36 | ||||
| chr2:237966728-237967039 | Common:3; Rare:91 | ||||
| chr2:238203616-238203821 | Common:3; Rare:89 | ||||
| chr2:239401641-239401750 | Rare:52 | ||||
| chr2:240025289-240025428 | Common:1; Rare:57; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr2:240560766-240560982 | Common:3; Rare:109 | ||||
| chr2:241102270-241102395 | Common:2; Rare:44 |