Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:290218-290504 | Common:4; Rare:54 | ||||
chr19:3977213-3977610 | Common:4; Rare:130; Clinvar (benign):8 | ||||
chr19:5718713-5718891 | Rare:28 | ||||
chr19:10284637-10284901 | Common:3; Rare:78 | ||||
chr19:12793565-12793777 | Common:2; Rare:52 | ||||
chr19:13037336-13037430 | Rare:18 | ||||
chr19:14622000-14622323 | Common:1; Rare:16 | ||||
chr19:15828805-15829110 | Common:3; Rare:48 | ||||
chr19:19776391-19776586 | Common:2; Rare:52 | ||||
chr19:21569219-21569416 | Common:7; Rare:56 | ||||
chr19:23762904-23763011 | Common:1; Rare:40 | ||||
chr19:27793121-27793479 | Common:5; Rare:86 | ||||
chr19:27793888-27794059 | Common:1; Rare:37 | ||||
chr19:36142725-36142953 | Rare:53 | ||||
chr19:36331628-36331934 | Common:2; Rare:80 |