Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:50783581-50783903 | Common:2; Rare:106 | ||||
chr3:196292-196614 | Common:1; Rare:80 | ||||
chr3:196707-197072 | Common:2; Rare:118 | ||||
chr3:197086-197334 | Common:3; Rare:83 | ||||
chr3:197358-198061 | Common:10; Rare:244 | ||||
chr3:2098592-2098975 | Common:4; Rare:151 | ||||
chr3:3126813-3126990 | Common:4; Rare:78; Clinvar (benign):2 | ||||
chr3:3799303-3799529 | Common:3; Rare:90 | ||||
chr3:3799761-3799877 | Common:1; Rare:42 | ||||
chr3:4303252-4303642 | Common:3; Rare:148 | ||||
chr3:5122419-5122515 | Common:1; Rare:33 | ||||
chr3:6860822-6861134 | Common:2; Rare:82 | ||||
chr3:6862644-6862798 | Common:3; Rare:52 | ||||
chr3:8501620-8501854 | Rare:85 | ||||
chr3:9249308-9249750 | Common:2; Rare:97 |