| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:5622531-5623359 | Common:6; Rare:328 | ||||
| chr19:5680464-5681169 | Rare:209 | ||||
| chr19:5694883-5695157 | Common:2; Rare:87; Clinvar (pathogenic):1 | ||||
| chr19:5775114-5775202 | Rare:18 | ||||
| chr19:5978062-5978393 | Common:3; Rare:124 | ||||
| chr19:6110412-6110854 | Common:3; Rare:135 | ||||
| chr19:6216997-6217175 | Rare:34 | ||||
| chr19:6361716-6361847 | Rare:53; Clinvar:1; Clinvar (benign):1 | ||||
| chr19:6381123-6381479 | Common:3; Rare:147 | ||||
| chr19:6393397-6393544 | Common:1; Rare:43 | ||||
| chr19:6424514-6424680 | Common:2; Rare:45 | ||||
| chr19:6469586-6469607 | Rare:7 | ||||
| chr19:6684793-6685101 | Rare:86; Clinvar (benign):1 | ||||
| chr19:6710748-6711065 | Common:3; Rare:95; Clinvar:1; Clinvar (benign):2 | ||||
| chr19:6714164-6714442 | Common:1; Rare:78; Clinvar:1; Clinvar (benign):2 |