Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:69926032-69926122 | Common:1; Rare:14 | ||||
chr3:69926173-69926187 | |||||
chr3:69926295-69926360 | Rare:11 | ||||
chr3:69926417-69926842 | Rare:107 | ||||
chr3:69928801-69928918 | Rare:23 | ||||
chr3:69928919-69929439 | Common:4; Rare:91 | ||||
chr3:69937746-69938150 | Rare:102; Clinvar:3; Clinvar (benign):1 | ||||
chr3:69940577-69940634 | Rare:12 | ||||
chr3:69941966-69942262 | Rare:55 | ||||
chr3:69945032-69945234 | Common:1; Rare:38 | ||||
chr3:69997740-69998001 | Rare:50 | ||||
chr3:69999499-69999798 | Common:1; Rare:95 | ||||
chr3:70000087-70000181 | Rare:27 | ||||
chr3:70000970-70001047 | Rare:18 | ||||
chr3:70038778-70038929 | Rare:26 |