| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:11539639-11539972 | Common:3; Rare:75 | ||||
| chr19:11540861-11541172 | Common:3; Rare:89 | ||||
| chr19:11559195-11559448 | Common:3; Rare:79 | ||||
| chr19:11597310-11597521 | Rare:66 | ||||
| chr19:11738872-11739230 | Common:4; Rare:98 | ||||
| chr19:11766697-11767057 | Rare:80 | ||||
| chr19:11887707-11887829 | Common:1; Rare:33 | ||||
| chr19:11924961-11925131 | Common:6; Rare:46 | ||||
| chr19:12162814-12163112 | Rare:75 | ||||
| chr19:12365620-12365787 | Common:3; Rare:43 | ||||
| chr19:12441074-12441251 | Common:4; Rare:55 | ||||
| chr19:12551402-12551733 | Common:2; Rare:90 | ||||
| chr19:12610699-12610994 | Rare:97 | ||||
| chr19:12658104-12658280 | Common:1; Rare:58; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr19:12666674-12666864 | Rare:79; Clinvar:4 |