| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:6110467-6110834 | Common:2; Rare:110 | ||||
| chr19:6361714-6361801 | Rare:37; Clinvar:1; Clinvar (benign):1 | ||||
| chr19:6372479-6372860 | Common:5; Rare:129 | ||||
| chr19:6381123-6381379 | Common:3; Rare:101 | ||||
| chr19:6393110-6393235 | Common:2; Rare:28 | ||||
| chr19:6459784-6459930 | Common:3; Rare:34 | ||||
| chr19:6710807-6711073 | Common:2; Rare:85; Clinvar:1; Clinvar (benign):1 | ||||
| chr19:6740678-6741163 | Common:1; Rare:133 | ||||
| chr19:6745897-6746152 | Common:6; Rare:101 | ||||
| chr19:7348922-7348942 | Rare:3 | ||||
| chr19:7395014-7395247 | Common:6; Rare:65 | ||||
| chr19:7488993-7489116 | Rare:57 | ||||
| chr19:7535543-7535791 | Common:3; Rare:91; Clinvar:2 | ||||
| chr19:7629520-7629848 | Common:5; Rare:119; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr19:7636997-7637170 | Common:2; Rare:54; Clinvar (benign):1 |