Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:35389428-35389472 | Common:1; Rare:6 | ||||
chr19:35395791-35395973 | Rare:35 | ||||
chr19:35399303-35399676 | Common:1; Rare:51 | ||||
chr19:35633245-35633313 | Common:1; Rare:18 | ||||
chr19:36142654-36142942 | Rare:76 | ||||
chr19:36797283-36797554 | Common:1; Rare:59 | ||||
chr19:38693524-38693759 | Common:3; Rare:35 | ||||
chr19:39486187-39486493 | Common:2; Rare:111; Clinvar (pathogenic):1 | ||||
chr19:39974347-39974587 | Common:2; Rare:70 | ||||
chr19:40646201-40646441 | Common:3; Rare:48 | ||||
chr19:40833868-40834035 | Common:3; Rare:38 | ||||
chr19:42243130-42243347 | Common:1; Rare:81 | ||||
chr19:42244532-42244749 | Rare:47 | ||||
chr19:42396897-42397196 | Common:1; Rare:70 | ||||
chr19:42480707-42480901 | Common:1; Rare:42 |