| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:39413240-39413576 | Common:1; Rare:89 | ||||
| chr19:39413584-39413829 | Common:1; Rare:53 | ||||
| chr19:39414176-39414470 | Rare:61 | ||||
| chr19:39415187-39415448 | Common:1; Rare:87; Clinvar:1 | ||||
| chr19:39420964-39421300 | Rare:98 | ||||
| chr19:39435842-39436201 | Common:9; Rare:137 | ||||
| chr19:39445436-39445986 | Common:3; Rare:162 | ||||
| chr19:39458839-39459249 | Common:2; Rare:95 | ||||
| chr19:39480606-39480956 | Common:3; Rare:165; Clinvar (pathogenic):1 | ||||
| chr19:39540098-39540342 | Common:2; Rare:66 | ||||
| chr19:39834068-39834561 | Common:3; Rare:145 | ||||
| chr19:39846159-39846470 | Common:1; Rare:122 | ||||
| chr19:39970951-39971238 | Common:3; Rare:78 | ||||
| chr19:39996925-39997142 | Common:5; Rare:66 | ||||
| chr19:40056148-40056293 | Rare:19 |