Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:35628751-35629094 | Common:4; Rare:103 | ||||
chr19:35745397-35745681 | Rare:87 | ||||
chr19:36014201-36014522 | Common:2; Rare:87 | ||||
chr19:36114852-36114978 | Common:2; Rare:55 | ||||
chr19:36215070-36215180 | Rare:34 | ||||
chr19:36573247-36573379 | Common:3; Rare:35 | ||||
chr19:36687385-36687602 | Common:2; Rare:64 | ||||
chr19:38264296-38264659 | Common:6; Rare:96 | ||||
chr19:38618808-38619256 | Common:4; Rare:130 | ||||
chr19:38647372-38647713 | Common:3; Rare:120 | ||||
chr19:38831780-38832026 | Common:3; Rare:71 | ||||
chr19:38852319-38852433 | Rare:31 | ||||
chr19:38899566-38899686 | Rare:39 | ||||
chr19:38930742-38931013 | Common:3; Rare:71; Clinvar:2; Clinvar (benign):3 | ||||
chr19:39084105-39084247 | Rare:38 |