| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:38899813-38900020 | Rare:68 | ||||
| chr19:38930726-38930992 | Common:3; Rare:76; Clinvar:2; Clinvar (benign):3 | ||||
| chr19:39156526-39156697 | Common:2; Rare:35 | ||||
| chr19:39390990-39391418 | Common:1; Rare:163 | ||||
| chr19:39406684-39406852 | Rare:58 | ||||
| chr19:39435884-39436154 | Common:4; Rare:102 | ||||
| chr19:39480716-39480931 | Common:3; Rare:114; Clinvar (pathogenic):1 | ||||
| chr19:39846316-39846532 | Common:1; Rare:105 | ||||
| chr19:39970854-39971215 | Common:5; Rare:103 | ||||
| chr19:40056188-40056260 | Rare:10 | ||||
| chr19:40348513-40348715 | Common:3; Rare:60 | ||||
| chr19:40444290-40444517 | Common:3; Rare:68 | ||||
| chr19:40751096-40751220 | Common:1; Rare:28 | ||||
| chr19:41364123-41364294 | Rare:56; Clinvar:1 | ||||
| chr19:41860070-41860285 | Common:1; Rare:84; Clinvar:3; Clinvar (benign):1 |