Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:132659672-132660079 | Common:3; Rare:89; Clinvar:1 | ||||
chr3:133661886-133662011 | Rare:30 | ||||
chr3:134485718-134486062 | Common:4; Rare:117 | ||||
chr3:136862017-136862286 | Common:1; Rare:81 | ||||
chr3:138946931-138947234 | Common:3; Rare:71; Clinvar (benign):1 | ||||
chr3:139359160-139359329 | Rare:61 | ||||
chr3:139389608-139389855 | Common:1; Rare:78 | ||||
chr3:143001436-143001626 | Common:3; Rare:70 | ||||
chr3:143971751-143971860 | Common:2; Rare:47 | ||||
chr3:146161036-146161085 | Rare:19; Clinvar:3 | ||||
chr3:150603157-150603299 | Common:1; Rare:43 | ||||
chr3:152268677-152268965 | Rare:114 | ||||
chr3:152269486-152269676 | Rare:62 | ||||
chr3:155854374-155854746 | Rare:104 | ||||
chr3:156674373-156674599 | Common:3; Rare:60 |