Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr18:76491497-76491651 | Common:3; Rare:65 | ||||
chr19:3977206-3977612 | Common:4; Rare:133; Clinvar (benign):8 | ||||
chr19:10284610-10284950 | Common:3; Rare:101 | ||||
chr19:11143422-11143644 | Rare:43 | ||||
chr19:12793500-12793749 | Common:3; Rare:68 | ||||
chr19:12954482-12954683 | Rare:58 | ||||
chr19:14565950-14566082 | Common:1; Rare:53 | ||||
chr19:19776370-19776586 | Common:2; Rare:60 | ||||
chr19:27793256-27793480 | Common:4; Rare:50 | ||||
chr19:27793891-27794066 | Common:1; Rare:36 | ||||
chr19:36797259-36797542 | Rare:60 | ||||
chr19:38004576-38004702 | Rare:30 | ||||
chr19:38845730-38845912 | Common:1; Rare:63 | ||||
chr19:41352902-41353290 | Common:5; Rare:103; Clinvar (benign):3 | ||||
chr19:42396916-42397184 | Common:1; Rare:63 |