Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:51323561-51323739 | Common:1; Rare:60 | ||||
chr19:51346836-51346909 | Common:1; Rare:23; Clinvar (benign):3 | ||||
chr19:52923393-52923532 | Common:3; Rare:59 | ||||
chr19:52942563-52942782 | Common:7; Rare:78 | ||||
chr19:54210876-54211162 | Common:1; Rare:74 | ||||
chr19:55230527-55230640 | Common:3; Rare:54 | ||||
chr19:55241009-55241251 | Common:1; Rare:82 | ||||
chr19:58599275-58599340 | Rare:4 | ||||
chr2:8119046-8119174 | Common:1; Rare:29 | ||||
chr2:8119602-8119941 | Rare:54 | ||||
chr2:8139115-8139356 | Common:1; Rare:48 | ||||
chr2:8412214-8412467 | Common:2; Rare:44 | ||||
chr2:8583790-8584073 | Common:3; Rare:86 | ||||
chr2:10009967-10010289 | Common:3; Rare:63 | ||||
chr2:10045729-10045945 | Common:1; Rare:61 |