| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:49851042-49851232 | Common:2; Rare:141 | ||||
| chr19:49866940-49867692 | Common:11; Rare:331; Clinvar:9; Clinvar (benign):21; Clinvar (pathogenic):1 | ||||
| chr19:49876540-49876733 | Common:1; Rare:126 | ||||
| chr19:49877219-49877720 | Common:3; Rare:196 | ||||
| chr19:49877836-49878174 | Common:5; Rare:107 | ||||
| chr19:49878260-49878660 | Common:2; Rare:208 | ||||
| chr19:49928270-49928790 | Common:8; Rare:170 | ||||
| chr19:49928891-49929239 | Common:7; Rare:134 | ||||
| chr19:49929381-49929573 | Common:8; Rare:127 | ||||
| chr19:50025335-50025539 | Common:5; Rare:63 | ||||
| chr19:50025580-50025810 | Common:3; Rare:68 | ||||
| chr19:50376610-50377120 | Common:12; Rare:182 | ||||
| chr19:50384007-50384412 | Common:5; Rare:306; Clinvar:4; Clinvar (benign):10 | ||||
| chr19:50398402-50399216 | Common:17; Rare:350; Clinvar:68; Clinvar (benign):42 | ||||
| chr19:50476328-50476658 | Rare:230 |