| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:34172351-34172733 | Common:1; Rare:136 | ||||
| chr19:34254485-34254608 | Rare:39 | ||||
| chr19:34347732-34347999 | Rare:69 | ||||
| chr19:34359402-34359525 | Common:1; Rare:48 | ||||
| chr19:34365103-34365381 | Common:1; Rare:114; Clinvar (pathogenic):1 | ||||
| chr19:34404277-34404433 | Common:2; Rare:62 | ||||
| chr19:34428305-34428580 | Common:1; Rare:91 | ||||
| chr19:34675693-34675834 | Common:1; Rare:29 | ||||
| chr19:34676004-34676215 | Common:5; Rare:68 | ||||
| chr19:34677215-34677833 | Common:8; Rare:163 | ||||
| chr19:34734077-34734273 | Common:1; Rare:61 | ||||
| chr19:34734467-34734579 | Rare:25 | ||||
| chr19:34773142-34773307 | Common:2; Rare:61 | ||||
| chr19:34926800-34927072 | Common:1; Rare:86 | ||||
| chr19:35000185-35000475 | Common:4; Rare:72 |