| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:19516155-19516287 | Rare:83; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr19:19628194-19628355 | Rare:45 | ||||
| chr19:19628525-19628667 | Rare:21 | ||||
| chr19:19668598-19668893 | Common:2; Rare:81 | ||||
| chr19:19821660-19821905 | Common:1; Rare:81 | ||||
| chr19:19865714-19865954 | Common:2; Rare:64 | ||||
| chr19:19900778-19901056 | Common:3; Rare:71 | ||||
| chr19:20167022-20167277 | Common:2; Rare:103 | ||||
| chr19:20565744-20565950 | Rare:58 | ||||
| chr19:20923003-20923342 | Rare:86 | ||||
| chr19:21141853-21142138 | Rare:74 | ||||
| chr19:21358806-21359106 | Common:6; Rare:77 | ||||
| chr19:23074929-23075326 | Common:2; Rare:81 | ||||
| chr19:23116854-23117075 | Common:6; Rare:62 | ||||
| chr19:23758808-23758909 | Common:2; Rare:31 |