| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:40613903-40614068 | Common:1; Rare:51; Clinvar:2; Clinvar (benign):2 | ||||
| chr19:40614669-40614822 | Common:1; Rare:39 | ||||
| chr19:40690569-40690965 | Common:3; Rare:87 | ||||
| chr19:40691062-40691152 | Rare:25 | ||||
| chr19:40715048-40715279 | Rare:61 | ||||
| chr19:40715605-40715735 | Common:1; Rare:29 | ||||
| chr19:40715736-40716027 | Common:4; Rare:55 | ||||
| chr19:40716084-40716426 | Common:3; Rare:47 | ||||
| chr19:40716636-40717576 | Common:5; Rare:293 | ||||
| chr19:40717596-40717691 | Rare:23 | ||||
| chr19:40717979-40718050 | Rare:28 | ||||
| chr19:40718206-40718311 | Common:1; Rare:29; Clinvar:1 | ||||
| chr19:40718600-40718673 | Common:1; Rare:18 | ||||
| chr19:40750203-40750335 | Common:2; Rare:39 | ||||
| chr19:40750371-40750984 | Common:7; Rare:157 |