Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:58519761-58520030 | Rare:71 | ||||
chr19:58554921-58555210 | Common:2; Rare:92 | ||||
chr19:58573282-58573661 | Common:2; Rare:95 | ||||
chr2:677364-677518 | Common:1; Rare:59 | ||||
chr2:1744397-1744573 | Common:1; Rare:63 | ||||
chr2:3377811-3377856 | Rare:12 | ||||
chr2:3379625-3379813 | Common:2; Rare:74 | ||||
chr2:3519449-3519649 | Common:2; Rare:63 | ||||
chr2:3558269-3558481 | Common:5; Rare:89 | ||||
chr2:3575107-3575358 | Common:2; Rare:73; Clinvar:3; Clinvar (benign):5 | ||||
chr2:9003957-9004046 | Rare:25 | ||||
chr2:9422796-9422850 | Rare:6 | ||||
chr2:9423033-9423677 | Common:2; Rare:156 | ||||
chr2:9474455-9474642 | Common:7; Rare:78 | ||||
chr2:9555630-9555901 | Common:2; Rare:85 |