| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:49851814-49851921 | Rare:34 | ||||
| chr19:49865321-49865567 | Rare:83; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr19:49866929-49867096 | Rare:46; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr19:49867255-49867415 | Common:2; Rare:39 | ||||
| chr19:49867452-49867702 | Common:3; Rare:70; Clinvar:1; Clinvar (benign):5 | ||||
| chr19:49876180-49876346 | Rare:55 | ||||
| chr19:49876531-49876888 | Common:1; Rare:122 | ||||
| chr19:49876982-49877145 | Rare:38 | ||||
| chr19:49877197-49877780 | Common:2; Rare:156 | ||||
| chr19:49877810-49878336 | Common:5; Rare:165 | ||||
| chr19:49913197-49913447 | Rare:68 | ||||
| chr19:49928588-49928790 | Common:2; Rare:45 | ||||
| chr19:49929014-49929255 | Common:3; Rare:79 | ||||
| chr19:49929330-49929858 | Common:7; Rare:176 | ||||
| chr19:49929881-49930276 | Common:2; Rare:99 |