| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:18280387-18280486 | Rare:40 | ||||
| chr19:18919344-18919763 | Common:3; Rare:154 | ||||
| chr19:19033461-19033664 | Common:2; Rare:69 | ||||
| chr19:19033798-19033930 | Common:1; Rare:36 | ||||
| chr19:19192096-19192262 | Common:1; Rare:54 | ||||
| chr19:19192607-19192978 | Common:2; Rare:90 | ||||
| chr19:19320496-19320850 | Common:4; Rare:125 | ||||
| chr19:19516167-19516331 | Rare:95; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr19:20776120-20776304 | Common:1; Rare:44 | ||||
| chr19:29212907-29213213 | Common:3; Rare:82 | ||||
| chr19:29665252-29665532 | Common:4; Rare:101 | ||||
| chr19:29715160-29715296 | Common:1; Rare:53 | ||||
| chr19:32406015-32406138 | Rare:35 | ||||
| chr19:32675094-32675422 | Common:4; Rare:109 | ||||
| chr19:32675710-32675905 | Common:2; Rare:52 |