| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:42496730-42496971 | Common:1; Rare:34 | ||||
| chr15:42503978-42505742 | Common:11; Rare:429 | ||||
| chr15:42605280-42605570 | Rare:64 | ||||
| chr15:42606738-42607138 | Rare:149 | ||||
| chr15:42608025-42608660 | Common:3; Rare:259 | ||||
| chr15:42608720-42609417 | Common:4; Rare:178 | ||||
| chr15:42734303-42734703 | Common:5; Rare:139 | ||||
| chr15:42872503-42872919 | Rare:107; Clinvar (benign):1 | ||||
| chr15:42921583-42921698 | Rare:21 | ||||
| chr15:43237840-43238270 | Common:10; Rare:99 | ||||
| chr15:43249752-43250051 | Common:1; Rare:69 | ||||
| chr15:43251960-43252190 | Common:1; Rare:37 | ||||
| chr15:43253380-43254380 | Common:20; Rare:640; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr15:43268790-43269100 | Common:1; Rare:52 | ||||
| chr15:43363748-43364170 | Common:2; Rare:147 |