| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:4867613-4867814 | Common:3; Rare:61 | ||||
| chr19:4909415-4909502 | Rare:23 | ||||
| chr19:5293211-5293447 | Common:1; Rare:102 | ||||
| chr19:5622537-5622569 | Rare:11 | ||||
| chr19:5622573-5623388 | Common:6; Rare:315 | ||||
| chr19:5680468-5681055 | Rare:168 | ||||
| chr19:5694883-5694919 | Common:1; Rare:13; Clinvar (pathogenic):1 | ||||
| chr19:5847246-5847590 | Common:4; Rare:68 | ||||
| chr19:5848479-5848555 | Rare:15 | ||||
| chr19:5848686-5848919 | Rare:50 | ||||
| chr19:5848938-5848995 | Rare:7 | ||||
| chr19:5849049-5849354 | Rare:60 | ||||
| chr19:5851380-5851579 | Common:1; Rare:35 | ||||
| chr19:5903704-5903848 | Common:1; Rare:72; Clinvar:2; Clinvar (benign):3 | ||||
| chr19:5978078-5978415 | Common:3; Rare:130 |