Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr15:40382813-40383022 | Common:1; Rare:103 | ||||
chr15:40405620-40405827 | Common:2; Rare:59; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
chr15:40695076-40695214 | Rare:39 | ||||
chr15:40755227-40755424 | Common:2; Rare:62 | ||||
chr15:40807450-40807761 | Common:4; Rare:104 | ||||
chr15:40953213-40953476 | Common:1; Rare:71 | ||||
chr15:41115982-41116148 | Rare:48 | ||||
chr15:41416989-41417193 | Common:2; Rare:89 | ||||
chr15:41827927-41828127 | Common:3; Rare:66 | ||||
chr15:41972512-41972771 | Common:1; Rare:72 | ||||
chr15:42208261-42208363 | Rare:32 | ||||
chr15:42273060-42273224 | Common:1; Rare:61 | ||||
chr15:42273402-42273487 | Rare:33 | ||||
chr15:42491089-42491196 | Rare:28 | ||||
chr15:42548733-42548890 | Common:1; Rare:91 |