| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:5978062-5978401 | Common:3; Rare:127 | ||||
| chr19:6110426-6110834 | Common:2; Rare:121 | ||||
| chr19:6381539-6381853 | Common:4; Rare:130 | ||||
| chr19:6393371-6393580 | Common:2; Rare:61 | ||||
| chr19:6415123-6415666 | Common:4; Rare:196 | ||||
| chr19:6424757-6424840 | Rare:31 | ||||
| chr19:6530889-6531036 | Common:3; Rare:66 | ||||
| chr19:6590647-6591217 | Common:3; Rare:155 | ||||
| chr19:6737205-6737471 | Common:4; Rare:77 | ||||
| chr19:7069552-7069748 | Common:1; Rare:58 | ||||
| chr19:7394890-7395208 | Common:6; Rare:89 | ||||
| chr19:7441670-7441999 | Common:6; Rare:109 | ||||
| chr19:7489011-7489123 | Rare:51 | ||||
| chr19:7515946-7516047 | Rare:23 | ||||
| chr19:7533838-7534225 | Common:4; Rare:108; Clinvar (benign):2 |