| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:24123253-24123512 | Common:1; Rare:68 | ||||
| chr2:24360315-24360508 | Common:2; Rare:46 | ||||
| chr2:24971603-24971842 | Common:2; Rare:86 | ||||
| chr2:24971900-24972189 | Common:1; Rare:95 | ||||
| chr2:25041925-25042295 | Common:4; Rare:97 | ||||
| chr2:25252218-25252552 | Rare:76 | ||||
| chr2:25673386-25673722 | Common:1; Rare:113 | ||||
| chr2:25878450-25878659 | Common:1; Rare:62 | ||||
| chr2:26033736-26034142 | Common:4; Rare:149 | ||||
| chr2:26244586-26244990 | Common:2; Rare:147; Clinvar:5; Clinvar (benign):8 | ||||
| chr2:26345750-26346187 | Common:2; Rare:131 | ||||
| chr2:26764215-26764332 | Rare:47 | ||||
| chr2:27032831-27033011 | Rare:74 | ||||
| chr2:27051546-27051735 | Rare:59 | ||||
| chr2:27071543-27071898 | Common:1; Rare:106 |