| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:19516079-19516313 | Rare:142; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr19:19618671-19618949 | Rare:92 | ||||
| chr19:19627702-19627819 | Common:1; Rare:22 | ||||
| chr19:19628410-19628760 | Rare:69 | ||||
| chr19:19643560-19643900 | Common:4; Rare:93 | ||||
| chr19:19663664-19664178 | Common:2; Rare:132 | ||||
| chr19:19668606-19668889 | Common:2; Rare:80 | ||||
| chr19:19733073-19733278 | Common:2; Rare:53 | ||||
| chr19:19821678-19821906 | Common:1; Rare:77 | ||||
| chr19:19865722-19865930 | Common:1; Rare:53 | ||||
| chr19:19900734-19901008 | Common:2; Rare:83 | ||||
| chr19:19901191-19901309 | Common:1; Rare:25 | ||||
| chr19:20039217-20039337 | Common:2; Rare:35 | ||||
| chr19:20039415-20039640 | Common:2; Rare:53 | ||||
| chr19:20077812-20078037 | Common:2; Rare:64 |