| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:6736572-6736773 | Common:1; Rare:55 | ||||
| chr19:6737347-6738210 | Common:23; Rare:454 | ||||
| chr19:6739430-6739780 | Common:11; Rare:175 | ||||
| chr19:6767202-6767959 | Common:13; Rare:229 | ||||
| chr19:7069137-7069505 | Common:2; Rare:145 | ||||
| chr19:7069599-7069816 | Common:2; Rare:103 | ||||
| chr19:7294227-7294625 | Common:15; Rare:215 | ||||
| chr19:7394965-7395233 | Common:16; Rare:200 | ||||
| chr19:7488923-7489150 | Common:2; Rare:199 | ||||
| chr19:7515730-7516210 | Common:4; Rare:197 | ||||
| chr19:7522420-7522710 | Common:3; Rare:235; Clinvar:4 | ||||
| chr19:7534029-7534223 | Common:9; Rare:118; Clinvar (benign):3 | ||||
| chr19:7535220-7535870 | Common:11; Rare:348; Clinvar:3 | ||||
| chr19:7595737-7596019 | Common:8; Rare:224 | ||||
| chr19:7629486-7629873 | Common:19; Rare:400; Clinvar (benign):6; Clinvar (pathogenic):3 |