| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:42396458-42396675 | Rare:38 | ||||
| chr19:42396828-42397253 | Common:3; Rare:257 | ||||
| chr19:42397800-42398590 | Common:15; Rare:186 | ||||
| chr19:42401891-42402062 | Rare:64; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr19:42421560-42422100 | Rare:149 | ||||
| chr19:42441190-42441550 | Common:1; Rare:53 | ||||
| chr19:42443601-42443796 | Common:1; Rare:25 | ||||
| chr19:42471900-42472270 | Rare:56 | ||||
| chr19:42480887-42481071 | Common:1; Rare:27 | ||||
| chr19:43439250-43439540 | Common:10; Rare:71 | ||||
| chr19:43455211-43455943 | Common:5; Rare:253 | ||||
| chr19:43755586-43755720 | Common:1; Rare:46 | ||||
| chr19:44260438-44260674 | Common:2; Rare:42 | ||||
| chr19:44435460-44435940 | Common:2; Rare:86 | ||||
| chr19:44575165-44575692 | Common:12; Rare:242 |