| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:24971907-24972159 | Common:1; Rare:80 | ||||
| chr2:25041969-25042263 | Common:1; Rare:80 | ||||
| chr2:26033725-26034167 | Common:4; Rare:167 | ||||
| chr2:26034339-26034644 | Common:2; Rare:85 | ||||
| chr2:26194568-26194705 | Common:1; Rare:40; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr2:26244530-26245152 | Common:2; Rare:208; Clinvar:7; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
| chr2:26345791-26346172 | Common:1; Rare:114 | ||||
| chr2:26692438-26693333 | Common:3; Rare:206; Clinvar:2 | ||||
| chr2:26764213-26764413 | Common:2; Rare:65 | ||||
| chr2:27032848-27033039 | Rare:74 | ||||
| chr2:27050770-27050778 | Common:1; Rare:6 | ||||
| chr2:27051546-27051734 | Rare:59 | ||||
| chr2:27071324-27071888 | Common:2; Rare:176 | ||||
| chr2:27078968-27079053 | Common:1; Rare:20 | ||||
| chr2:27086548-27086797 | Common:2; Rare:69; Clinvar (benign):1 |