Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:2634631-2634846 | Common:1; Rare:53 | ||||
chr19:3369517-3369617 | Common:1; Rare:30 | ||||
chr19:3409418-3409946 | Common:4; Rare:130 | ||||
chr19:3977213-3977535 | Common:4; Rare:101; Clinvar (benign):5 | ||||
chr19:4171378-4171672 | Rare:84 | ||||
chr19:6675029-6675192 | Rare:32 | ||||
chr19:6707029-6707436 | Common:2; Rare:134; Clinvar:1; Clinvar (benign):5 | ||||
chr19:6709805-6710027 | Common:4; Rare:50; Clinvar (benign):1 | ||||
chr19:6717533-6718018 | Common:10; Rare:111 | ||||
chr19:6718020-6718430 | Common:3; Rare:110; Clinvar:2; Clinvar (benign):1 | ||||
chr19:8376518-8376713 | Common:4; Rare:45 | ||||
chr19:8388408-8388481 | Rare:16 | ||||
chr19:10037457-10037623 | Common:1; Rare:35 | ||||
chr19:10070852-10071008 | Common:2; Rare:26 | ||||
chr19:10071157-10071520 | Common:2; Rare:80 |