| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:23940363-23940529 | Common:3; Rare:60 | ||||
| chr2:24049560-24049858 | Common:2; Rare:92 | ||||
| chr2:24076219-24076594 | Rare:102 | ||||
| chr2:24123313-24123494 | Common:1; Rare:49 | ||||
| chr2:24792984-24793171 | Rare:73 | ||||
| chr2:25252194-25252550 | Rare:81 | ||||
| chr2:25878445-25878741 | Common:3; Rare:88 | ||||
| chr2:25982462-25982630 | Common:1; Rare:41 | ||||
| chr2:26033767-26034159 | Common:4; Rare:146 | ||||
| chr2:26034390-26034611 | Common:2; Rare:58 | ||||
| chr2:26195096-26195340 | Rare:83; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr2:26244592-26244984 | Common:2; Rare:143; Clinvar:5; Clinvar (benign):8 | ||||
| chr2:26345785-26346210 | Common:1; Rare:130 | ||||
| chr2:26764221-26764321 | Rare:37 | ||||
| chr2:27032862-27033004 | Rare:55 |