| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:26121222-26121414 | Common:1; Rare:35 | ||||
| chr2:26122653-26122912 | Common:2; Rare:42 | ||||
| chr2:26122969-26123073 | Rare:23 | ||||
| chr2:26123973-26124257 | Common:1; Rare:42 | ||||
| chr2:26284112-26284400 | Common:2; Rare:58; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:26289732-26289918 | Common:2; Rare:33; Clinvar:1 | ||||
| chr2:26383189-26383315 | Common:1; Rare:29 | ||||
| chr2:26387845-26387955 | Common:1; Rare:20 | ||||
| chr2:27057089-27057402 | Common:4; Rare:85 | ||||
| chr2:27319969-27320103 | Common:1; Rare:25 | ||||
| chr2:27333701-27333856 | Common:1; Rare:37 | ||||
| chr2:27352685-27352768 | Rare:18 | ||||
| chr2:27375586-27375911 | Common:1; Rare:134 | ||||
| chr2:27393181-27393298 | Rare:30 | ||||
| chr2:27444401-27444637 | Common:1; Rare:55; Clinvar (benign):1; Clinvar (pathogenic):1 |