| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:39413190-39413603 | Common:3; Rare:108 | ||||
| chr19:39413633-39413827 | Rare:38 | ||||
| chr19:39413830-39413918 | Rare:13 | ||||
| chr19:39434916-39435209 | Common:1; Rare:63 | ||||
| chr19:39435293-39435583 | Common:4; Rare:91 | ||||
| chr19:39435823-39436223 | Common:9; Rare:159 | ||||
| chr19:39445330-39445722 | Common:5; Rare:125 | ||||
| chr19:39445906-39445948 | Rare:11 | ||||
| chr19:39480004-39480284 | Common:2; Rare:46 | ||||
| chr19:39480647-39481039 | Common:6; Rare:174; Clinvar (pathogenic):1 | ||||
| chr19:39532770-39532974 | Rare:86 | ||||
| chr19:39539947-39540367 | Common:5; Rare:117 | ||||
| chr19:39833597-39833948 | Common:2; Rare:112 | ||||
| chr19:39834011-39834196 | Rare:54 | ||||
| chr19:39845445-39845838 | Common:3; Rare:90 |