Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:39391005-39391420 | Common:1; Rare:159 | ||||
chr19:39406739-39406866 | Rare:54 | ||||
chr19:39435903-39436167 | Common:5; Rare:97 | ||||
chr19:39846335-39846478 | Common:1; Rare:65 | ||||
chr19:39970908-39971200 | Common:4; Rare:83 | ||||
chr19:40056188-40056260 | Rare:10 | ||||
chr19:40090923-40090966 | Rare:9 | ||||
chr19:40285251-40285537 | Common:1; Rare:107 | ||||
chr19:40348398-40348734 | Common:4; Rare:109 | ||||
chr19:40751076-40751304 | Common:3; Rare:70 | ||||
chr19:41219275-41219403 | Common:1; Rare:43 | ||||
chr19:41220512-41220756 | Common:1; Rare:76 | ||||
chr19:41262381-41262554 | Rare:30 | ||||
chr19:41860103-41860281 | Common:1; Rare:73; Clinvar:3; Clinvar (benign):1 | ||||
chr19:43465601-43465766 | Common:1; Rare:42 |