| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:49641895-49642237 | Rare:99 | ||||
| chr19:49665588-49666047 | Common:6; Rare:211; Clinvar (pathogenic):1 | ||||
| chr19:49685858-49686084 | Common:2; Rare:47 | ||||
| chr19:49690980-49691140 | Rare:36 | ||||
| chr19:49763200-49763396 | Rare:42 | ||||
| chr19:49766699-49767159 | Common:2; Rare:163 | ||||
| chr19:49767315-49767417 | Rare:18 | ||||
| chr19:49800846-49801052 | Rare:42 | ||||
| chr19:49801460-49801889 | Common:1; Rare:123 | ||||
| chr19:49808726-49809046 | Common:3; Rare:99; Clinvar:1 | ||||
| chr19:49809162-49809407 | Common:1; Rare:63 | ||||
| chr19:49813249-49813338 | Rare:36 | ||||
| chr19:49817405-49817599 | Common:3; Rare:39 | ||||
| chr19:49817886-49818039 | Rare:34 | ||||
| chr19:49818239-49818408 | Common:3; Rare:75; Clinvar:3; Clinvar (benign):1 |