| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:40285243-40285497 | Common:1; Rare:96 | ||||
| chr19:40348510-40348724 | Common:3; Rare:68 | ||||
| chr19:40425989-40426147 | Common:1; Rare:46 | ||||
| chr19:40465713-40466011 | Common:2; Rare:93 | ||||
| chr19:40576719-40576902 | Common:3; Rare:56 | ||||
| chr19:40716880-40716993 | Common:1; Rare:34 | ||||
| chr19:40750472-40750641 | Common:2; Rare:48 | ||||
| chr19:40751033-40751311 | Common:3; Rare:87 | ||||
| chr19:40777910-40778280 | Common:1; Rare:101 | ||||
| chr19:40798638-40798665 | Rare:7 | ||||
| chr19:41262350-41262604 | Rare:47 | ||||
| chr19:41363771-41363992 | Common:1; Rare:74; Clinvar:1 | ||||
| chr19:41397324-41397477 | Common:3; Rare:44 | ||||
| chr19:41397580-41397824 | Common:7; Rare:86; Clinvar (benign):4 | ||||
| chr19:41439875-41439925 | Rare:27 |