| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:39445485-39445849 | Common:2; Rare:96 | ||||
| chr19:39480561-39480948 | Common:3; Rare:175; Clinvar (pathogenic):1 | ||||
| chr19:39846308-39846493 | Common:1; Rare:89 | ||||
| chr19:39970918-39971200 | Common:4; Rare:78 | ||||
| chr19:40056157-40056277 | Rare:18 | ||||
| chr19:40090873-40090979 | Common:1; Rare:30 | ||||
| chr19:40285216-40285537 | Common:1; Rare:114 | ||||
| chr19:40348388-40348739 | Common:4; Rare:117 | ||||
| chr19:40377835-40378144 | Common:2; Rare:106; Clinvar (benign):1 | ||||
| chr19:40425964-40426147 | Common:1; Rare:60 | ||||
| chr19:40715074-40715145 | Rare:24 | ||||
| chr19:40750659-40750913 | Common:1; Rare:48 | ||||
| chr19:40751076-40751322 | Common:3; Rare:71 | ||||
| chr19:41219107-41219411 | Common:1; Rare:79 | ||||
| chr19:41264985-41265172 | Common:1; Rare:41 |