| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:11419280-11419450 | Common:1; Rare:33 | ||||
| chr19:11435180-11435699 | Common:7; Rare:162; Clinvar:2; Clinvar (benign):5 | ||||
| chr19:11446859-11447106 | Common:2; Rare:72; Clinvar:1 | ||||
| chr19:11559195-11559407 | Common:1; Rare:66 | ||||
| chr19:11738860-11739203 | Common:4; Rare:97 | ||||
| chr19:11848635-11848787 | Common:1; Rare:43 | ||||
| chr19:11887676-11887888 | Common:1; Rare:65 | ||||
| chr19:11964910-11965082 | Common:1; Rare:44 | ||||
| chr19:12035635-12035825 | Common:2; Rare:68 | ||||
| chr19:12140309-12140593 | Rare:74 | ||||
| chr19:12237501-12237623 | Common:2; Rare:24 | ||||
| chr19:12365612-12365784 | Common:3; Rare:47 | ||||
| chr19:12484725-12484923 | Rare:49 | ||||
| chr19:12551385-12551732 | Common:2; Rare:94 | ||||
| chr19:12610688-12611007 | Rare:102 |