| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:27383927-27384180 | Common:1; Rare:50 | ||||
| chr2:27436715-27437104 | Common:1; Rare:88 | ||||
| chr2:27438201-27438249 | Rare:4 | ||||
| chr2:27441102-27441328 | Rare:62 | ||||
| chr2:27464313-27464562 | Rare:41 | ||||
| chr2:27467271-27467410 | Common:2; Rare:19 | ||||
| chr2:27478066-27478399 | Common:1; Rare:62; Clinvar (pathogenic):1 | ||||
| chr2:27481253-27481527 | Common:3; Rare:70; Clinvar (benign):1 | ||||
| chr2:27584722-27584861 | Common:1; Rare:27 | ||||
| chr2:27649469-27649698 | Rare:43 | ||||
| chr2:27688537-27688768 | Rare:44 | ||||
| chr2:27799217-27799521 | Rare:48 | ||||
| chr2:27885734-27886084 | Common:1; Rare:64 | ||||
| chr2:27948624-27948931 | Rare:61 | ||||
| chr2:28002080-28002357 | Rare:43 |