| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:189867289-189867453 | Rare:32 | ||||
| chr2:189889507-189889757 | Common:1; Rare:48 | ||||
| chr2:190194451-190194663 | Common:2; Rare:49 | ||||
| chr2:190196133-190196349 | Rare:44 | ||||
| chr2:190208863-190208967 | Rare:31; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr2:190211008-190211092 | Rare:14 | ||||
| chr2:190211094-190211285 | Common:2; Rare:35 | ||||
| chr2:190211505-190211703 | Rare:20 | ||||
| chr2:190264389-190264720 | Common:1; Rare:48 | ||||
| chr2:190551103-190551328 | Rare:24 | ||||
| chr2:190642956-190642968 | Common:1; Rare:2 | ||||
| chr2:190760496-190760629 | Rare:34 | ||||
| chr2:190881980-190882194 | Common:2; Rare:49 | ||||
| chr2:190883095-190883357 | Rare:47 | ||||
| chr2:190884074-190884211 | Rare:27 |