Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:1876170-1876293 | Common:1; Rare:42 | ||||
chr19:2065040-2065160 | Rare:25 | ||||
chr19:3409559-3409736 | Rare:49 | ||||
chr19:3951353-3951391 | Rare:13 | ||||
chr19:5212215-5212415 | Common:3; Rare:71 | ||||
chr19:6071004-6071277 | Rare:42 | ||||
chr19:6707139-6707541 | Common:2; Rare:123; Clinvar:1; Clinvar (benign):2 | ||||
chr19:6709688-6710061 | Common:5; Rare:91; Clinvar:4; Clinvar (benign):2 | ||||
chr19:6718095-6718413 | Common:1; Rare:80; Clinvar:2; Clinvar (benign):1 | ||||
chr19:9010368-9010564 | Rare:36 | ||||
chr19:12194882-12195024 | Rare:48 | ||||
chr19:12643953-12644044 | Rare:18 | ||||
chr19:12796584-12796883 | Rare:67 | ||||
chr19:14622046-14622289 | Common:1; Rare:14 | ||||
chr19:16283581-16283831 | Common:1; Rare:60 |