| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:24123253-24123514 | Common:1; Rare:69 | ||||
| chr2:24793018-24793161 | Rare:60 | ||||
| chr2:24971700-24971842 | Common:1; Rare:51 | ||||
| chr2:24971900-24972153 | Common:1; Rare:83 | ||||
| chr2:25041954-25042293 | Common:4; Rare:89 | ||||
| chr2:25252228-25252529 | Rare:66 | ||||
| chr2:25342456-25342773 | Common:1; Rare:68 | ||||
| chr2:25878435-25878648 | Common:1; Rare:61 | ||||
| chr2:26033725-26034146 | Common:4; Rare:157 | ||||
| chr2:26194582-26194798 | Common:1; Rare:49; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr2:26244580-26244975 | Common:2; Rare:145; Clinvar:5; Clinvar (benign):9 | ||||
| chr2:26345781-26346189 | Common:1; Rare:123 | ||||
| chr2:26764193-26764325 | Common:1; Rare:52 | ||||
| chr2:27032862-27032995 | Rare:50 | ||||
| chr2:27071413-27072024 | Common:3; Rare:179 |