| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:49818254-49818384 | Common:1; Rare:68; Clinvar:3; Clinvar (benign):1 | ||||
| chr19:49850564-49850864 | Rare:87 | ||||
| chr19:49850880-49851319 | Common:2; Rare:171 | ||||
| chr19:49851433-49851783 | Common:1; Rare:108 | ||||
| chr19:49851809-49851849 | Rare:11 | ||||
| chr19:49865230-49865571 | Rare:118; Clinvar:6; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr19:49866403-49866561 | Common:1; Rare:55; Clinvar:2; Clinvar (benign):1 | ||||
| chr19:49867200-49867467 | Common:2; Rare:73; Clinvar (benign):5 | ||||
| chr19:49867516-49867713 | Common:3; Rare:61; Clinvar:1 | ||||
| chr19:49867838-49868038 | Common:2; Rare:46 | ||||
| chr19:49876166-49876286 | Rare:44 | ||||
| chr19:49876539-49876900 | Common:1; Rare:122 | ||||
| chr19:49876975-49877359 | Common:2; Rare:94 | ||||
| chr19:49877367-49877801 | Common:2; Rare:124 | ||||
| chr19:49877820-49878141 | Common:5; Rare:99 |