Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:36492767-36493078 | Common:2; Rare:65 | ||||
chr19:37928542-37928705 | Common:1; Rare:35 | ||||
chr19:39402629-39402864 | Rare:61 | ||||
chr19:41352492-41352730 | Common:2; Rare:68 | ||||
chr19:41531561-41531772 | Common:1; Rare:46 | ||||
chr19:41546462-41546532 | Rare:14 | ||||
chr19:41880667-41880938 | Rare:74; Clinvar:1; Clinvar (benign):1 | ||||
chr19:41887921-41888078 | Common:1; Rare:39 | ||||
chr19:41945548-41945704 | Rare:20 | ||||
chr19:42114530-42114663 | Rare:26 | ||||
chr19:42129525-42129817 | Rare:61 | ||||
chr19:42396902-42397184 | Common:1; Rare:67 | ||||
chr19:43755594-43755717 | Common:1; Rare:42 | ||||
chr19:43765953-43766061 | Rare:16 | ||||
chr19:43784334-43784388 | Common:2; Rare:8 |