| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:24360423-24360668 | Common:3; Rare:86 | ||||
| chr2:24793025-24793161 | Rare:58 | ||||
| chr2:24971603-24971830 | Common:2; Rare:79 | ||||
| chr2:24971907-24972153 | Common:1; Rare:79 | ||||
| chr2:25878446-25878746 | Common:3; Rare:92 | ||||
| chr2:26033771-26034159 | Common:4; Rare:143 | ||||
| chr2:26034339-26034732 | Common:2; Rare:93 | ||||
| chr2:26195090-26195402 | Rare:98; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr2:26244573-26245017 | Common:2; Rare:159; Clinvar:7; Clinvar (benign):9 | ||||
| chr2:26345825-26346165 | Common:1; Rare:101 | ||||
| chr2:26764212-26764352 | Common:1; Rare:54 | ||||
| chr2:27032815-27033011 | Rare:76 | ||||
| chr2:27051536-27051706 | Rare:51 | ||||
| chr2:27071513-27071882 | Common:1; Rare:110 | ||||
| chr2:27078353-27078753 | Common:3; Rare:99 |