Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:40425984-40426147 | Common:1; Rare:46 | ||||
chr19:40444271-40444476 | Common:3; Rare:64 | ||||
chr19:40444728-40444907 | Common:2; Rare:52 | ||||
chr19:40465693-40465869 | Common:1; Rare:68 | ||||
chr19:40576708-40576994 | Common:4; Rare:91 | ||||
chr19:40580614-40580807 | Rare:67 | ||||
chr19:40613758-40613963 | Common:1; Rare:63; Clinvar (benign):1 | ||||
chr19:40690632-40690935 | Common:3; Rare:69 | ||||
chr19:40714864-40715210 | Rare:78 | ||||
chr19:40716718-40717124 | Common:2; Rare:118 | ||||
chr19:40750386-40750950 | Common:7; Rare:148 | ||||
chr19:40751067-40751481 | Common:3; Rare:130 | ||||
chr19:40751792-40751866 | Rare:17 | ||||
chr19:40777910-40778391 | Common:1; Rare:135 | ||||
chr19:40798876-40799262 | Common:6; Rare:143 |