Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:68471887-68471999 | Common:1; Rare:55; Clinvar (benign):1 | ||||
chr10:68900940-68901361 | Common:3; Rare:164 | ||||
chr10:68956116-68956441 | Common:3; Rare:108 | ||||
chr10:69179918-69180323 | Common:3; Rare:131 | ||||
chr10:70146652-70146984 | Common:2; Rare:72 | ||||
chr10:70170449-70170721 | Common:3; Rare:86 | ||||
chr10:70233331-70233547 | Common:6; Rare:79; Clinvar (benign):1 | ||||
chr10:70403983-70404155 | Rare:63 | ||||
chr10:70815865-70816021 | Rare:69 | ||||
chr10:71773508-71773693 | Common:3; Rare:55 | ||||
chr10:72273588-72273658 | Rare:18 | ||||
chr10:72273709-72273942 | Rare:63 | ||||
chr10:72354898-72355196 | Common:2; Rare:108 | ||||
chr10:73096764-73097187 | Common:4; Rare:125 | ||||
chr10:73167965-73168125 | Rare:37 |