| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:34481820-34482190 | Common:5; Rare:166 | ||||
| chr19:34677300-34677801 | Common:16; Rare:246 | ||||
| chr19:34733432-34733666 | Common:1; Rare:40 | ||||
| chr19:34733764-34734346 | Common:11; Rare:457 | ||||
| chr19:34734350-34735106 | Common:2; Rare:212 | ||||
| chr19:34926795-34927098 | Common:3; Rare:227 | ||||
| chr19:34927110-34927550 | Common:9; Rare:157 | ||||
| chr19:34963990-34964190 | Rare:57 | ||||
| chr19:34964127-34964300 | Common:2; Rare:32 | ||||
| chr19:34994950-34995239 | Common:3; Rare:135 | ||||
| chr19:34999156-34999820 | Common:6; Rare:208 | ||||
| chr19:35000100-35000524 | Common:12; Rare:277 | ||||
| chr19:35001236-35001647 | Common:4; Rare:109 | ||||
| chr19:35030325-35030942 | Common:2; Rare:360; Clinvar:11; Clinvar (benign):10 | ||||
| chr19:35031060-35031370 | Common:3; Rare:131 |