| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:10717462-10718309 | Common:2; Rare:362; Clinvar:4; Clinvar (benign):1 | ||||
| chr19:10836117-10836597 | Common:6; Rare:246 | ||||
| chr19:10928520-10928885 | Common:4; Rare:228 | ||||
| chr19:10960654-10961178 | Common:6; Rare:199; Clinvar (benign):2 | ||||
| chr19:10983851-10984391 | Common:1; Rare:222; Clinvar:42; Clinvar (benign):23 | ||||
| chr19:11089287-11089580 | Rare:116; Clinvar:26; Clinvar (pathogenic):7 | ||||
| chr19:11090312-11090613 | Common:4; Rare:157 | ||||
| chr19:11155729-11156088 | Common:6; Rare:168 | ||||
| chr19:11197488-11197718 | Common:2; Rare:130 | ||||
| chr19:11197740-11198090 | Common:4; Rare:182 | ||||
| chr19:11262451-11262572 | Common:1; Rare:48 | ||||
| chr19:11339555-11339830 | Common:7; Rare:107 | ||||
| chr19:11344389-11344789 | Common:2; Rare:104 | ||||
| chr19:11346170-11346780 | Rare:259 | ||||
| chr19:11374536-11374737 | Common:1; Rare:70 |