| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:39390850-39390957 | Rare:39 | ||||
| chr19:39390968-39391495 | Common:1; Rare:203 | ||||
| chr19:39412261-39412731 | Common:3; Rare:184 | ||||
| chr19:39412795-39412926 | Common:1; Rare:22 | ||||
| chr19:39413290-39413580 | Common:2; Rare:80 | ||||
| chr19:39435854-39436188 | Common:8; Rare:128 | ||||
| chr19:39445426-39445965 | Common:3; Rare:162 | ||||
| chr19:39466555-39466745 | Common:2; Rare:54 | ||||
| chr19:39480701-39480955 | Common:3; Rare:126; Clinvar (pathogenic):1 | ||||
| chr19:39540123-39540322 | Common:2; Rare:54 | ||||
| chr19:39833635-39833865 | Common:1; Rare:80 | ||||
| chr19:39834085-39834357 | Rare:72 | ||||
| chr19:39846306-39846532 | Common:1; Rare:110 | ||||
| chr19:39970918-39971223 | Common:4; Rare:87 | ||||
| chr19:39996925-39997144 | Common:5; Rare:66 |