Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:207529722-207530166 | Common:3; Rare:125 | ||||
chr2:207769865-207770194 | Common:1; Rare:103 | ||||
chr2:208124371-208124536 | Common:2; Rare:76; Clinvar:1; Clinvar (benign):3 | ||||
chr2:208124574-208124665 | Rare:29 | ||||
chr2:208254209-208254484 | Rare:68 | ||||
chr2:208254959-208255239 | Common:2; Rare:70 | ||||
chr2:208266036-208266418 | Common:9; Rare:129; Clinvar:1; Clinvar (benign):2 | ||||
chr2:209661203-209661525 | Common:3; Rare:57 | ||||
chr2:210171310-210171574 | Common:4; Rare:99 | ||||
chr2:210476677-210476867 | Rare:58 | ||||
chr2:210477535-210477720 | Rare:53 | ||||
chr2:212539250-212539457 | Common:5; Rare:38 | ||||
chr2:213150445-213150530 | Common:2; Rare:21 | ||||
chr2:213151570-213151941 | Common:1; Rare:139 | ||||
chr2:213284198-213284481 | Rare:90 |