Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:58578847-58579192 | Common:4; Rare:104 | ||||
chr11:58905318-58905597 | Common:2; Rare:75 | ||||
chr11:59142736-59142945 | Common:1; Rare:39 | ||||
chr11:59668999-59669312 | Rare:107 | ||||
chr11:60906532-60906666 | Rare:34 | ||||
chr11:60952138-60952290 | Rare:33 | ||||
chr11:61161408-61161737 | Common:1; Rare:91 | ||||
chr11:61333038-61333257 | Rare:72 | ||||
chr11:61361835-61361972 | Common:1; Rare:35 | ||||
chr11:61362249-61362404 | Common:2; Rare:45; Clinvar:8; Clinvar (benign):1 | ||||
chr11:61392507-61392649 | Common:2; Rare:48; Clinvar:3; Clinvar (benign):2 | ||||
chr11:61429912-61430173 | Common:1; Rare:119; Clinvar:3; Clinvar (benign):6 | ||||
chr11:61792564-61792946 | Common:5; Rare:105 | ||||
chr11:61816755-61816813 | Rare:18 | ||||
chr11:61967311-61967778 | Common:3; Rare:176; Clinvar:4 |