| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:10096010-10096456 | Common:3; Rare:188 | ||||
| chr19:10102002-10102275 | Common:2; Rare:40 | ||||
| chr19:10102283-10102344 | Rare:12 | ||||
| chr19:10102651-10103016 | Common:1; Rare:82 | ||||
| chr19:10106030-10106484 | Common:4; Rare:136 | ||||
| chr19:10111389-10111694 | Common:2; Rare:80; Clinvar:1 | ||||
| chr19:10119819-10120054 | Common:1; Rare:92 | ||||
| chr19:10194672-10194752 | Common:1; Rare:16 | ||||
| chr19:10194862-10195257 | Common:2; Rare:156; Clinvar (benign):2 | ||||
| chr19:10230989-10231078 | Common:1; Rare:24 | ||||
| chr19:10231222-10231458 | Common:1; Rare:54 | ||||
| chr19:10251771-10252028 | Common:1; Rare:63 | ||||
| chr19:10252096-10252297 | Common:2; Rare:87 | ||||
| chr19:10270390-10270604 | Rare:44 | ||||
| chr19:10270876-10271202 | Common:1; Rare:104 |