| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:48966035-48966314 | Common:2; Rare:75; Clinvar:1 | ||||
| chr19:48988415-48988596 | Common:1; Rare:33 | ||||
| chr19:48990544-48990736 | Rare:44 | ||||
| chr19:49009810-49010000 | Rare:72 | ||||
| chr19:49061108-49061238 | Common:1; Rare:27 | ||||
| chr19:49090286-49090521 | Rare:52 | ||||
| chr19:49098422-49098711 | Rare:69 | ||||
| chr19:49103494-49103712 | Rare:63 | ||||
| chr19:49104292-49104585 | Common:1; Rare:93 | ||||
| chr19:49105961-49106234 | Common:2; Rare:59 | ||||
| chr19:49107589-49108005 | Rare:131 | ||||
| chr19:49521595-49521632 | Rare:5 | ||||
| chr19:49592743-49592832 | Rare:18 | ||||
| chr19:49636700-49636999 | Common:4; Rare:102; Clinvar:1; Clinvar (benign):4 | ||||
| chr19:49719439-49719574 | Rare:33 |