| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:39412170-39413066 | Common:8; Rare:738 | ||||
| chr19:39413336-39413537 | Common:1; Rare:58 | ||||
| chr19:39413864-39414056 | Common:2; Rare:33 | ||||
| chr19:39435901-39436212 | Common:7; Rare:124 | ||||
| chr19:39445374-39445693 | Common:5; Rare:108 | ||||
| chr19:39480593-39480913 | Common:3; Rare:155; Clinvar (pathogenic):1 | ||||
| chr19:39498630-39498960 | Common:2; Rare:81 | ||||
| chr19:39532782-39532949 | Rare:75 | ||||
| chr19:39540086-39540318 | Common:2; Rare:68 | ||||
| chr19:39833533-39833864 | Common:2; Rare:109 | ||||
| chr19:39834074-39834339 | Rare:74 | ||||
| chr19:39846298-39846545 | Common:1; Rare:118 | ||||
| chr19:39970820-39971210 | Common:6; Rare:109 | ||||
| chr19:39996885-39997132 | Common:5; Rare:69 | ||||
| chr19:40056127-40056369 | Rare:40 |