| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:34396276-34396652 | Common:1; Rare:99; Clinvar (pathogenic):1 | ||||
| chr19:34428312-34428535 | Rare:81 | ||||
| chr19:34677032-34677319 | Common:7; Rare:44 | ||||
| chr19:34677563-34677754 | Common:4; Rare:57 | ||||
| chr19:34733955-34734356 | Common:3; Rare:111 | ||||
| chr19:34734475-34734588 | Rare:24 | ||||
| chr19:34926823-34927061 | Common:1; Rare:77 | ||||
| chr19:35000166-35000470 | Common:4; Rare:75 | ||||
| chr19:35009939-35010177 | Common:6; Rare:86 | ||||
| chr19:35154541-35154987 | Common:2; Rare:79 | ||||
| chr19:35545446-35545777 | Common:4; Rare:106 | ||||
| chr19:35612713-35612792 | Common:1; Rare:32 | ||||
| chr19:35740385-35740808 | Common:6; Rare:158 | ||||
| chr19:35745347-35745729 | Rare:110 | ||||
| chr19:35748286-35748625 | Common:3; Rare:98 |