| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:5978078-5978383 | Common:3; Rare:113 | ||||
| chr19:6056825-6057016 | Rare:34 | ||||
| chr19:6057227-6057300 | Common:2; Rare:16 | ||||
| chr19:6110426-6110854 | Common:3; Rare:128 | ||||
| chr19:6391901-6392188 | Common:2; Rare:96 | ||||
| chr19:6393366-6393756 | Common:5; Rare:114 | ||||
| chr19:6416793-6417019 | Common:1; Rare:80 | ||||
| chr19:6670143-6670261 | Common:1; Rare:27 | ||||
| chr19:6684386-6684651 | Rare:76; Clinvar:2 | ||||
| chr19:6684773-6685155 | Rare:100; Clinvar (benign):1 | ||||
| chr19:6710643-6711197 | Common:3; Rare:171; Clinvar:2; Clinvar (benign):5 | ||||
| chr19:6713994-6714443 | Common:2; Rare:141; Clinvar:2; Clinvar (benign):3 | ||||
| chr19:6720516-6720821 | Common:2; Rare:74; Clinvar (benign):2 | ||||
| chr19:6737252-6737331 | Rare:22 | ||||
| chr19:6739453-6739779 | Common:6; Rare:92 |