| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:40751076-40751345 | Common:3; Rare:75 | ||||
| chr19:40777910-40778280 | Common:1; Rare:101 | ||||
| chr19:41218697-41218973 | Common:7; Rare:60 | ||||
| chr19:41219047-41219421 | Common:1; Rare:94 | ||||
| chr19:41262346-41262571 | Rare:42 | ||||
| chr19:41264985-41265109 | Common:1; Rare:26 | ||||
| chr19:41310138-41310308 | Rare:73 | ||||
| chr19:41363795-41363992 | Common:1; Rare:70; Clinvar:1 | ||||
| chr19:41364080-41364181 | Common:1; Rare:30; Clinvar:2 | ||||
| chr19:41397321-41397617 | Common:4; Rare:78 | ||||
| chr19:41439531-41439715 | Common:1; Rare:50 | ||||
| chr19:41860012-41860285 | Common:1; Rare:98; Clinvar:3; Clinvar (benign):3 | ||||
| chr19:41884253-41884444 | Rare:50 | ||||
| chr19:42075816-42076199 | Rare:105 | ||||
| chr19:42132416-42132528 | Rare:19 |