Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:65750916-65751085 | Common:2; Rare:68 | ||||
chr7:65770746-65770941 | Common:6; Rare:58 | ||||
chr7:66493534-66493754 | Common:4; Rare:95 | ||||
chr7:66592313-66592449 | Common:2; Rare:47 | ||||
chr7:66654430-66654567 | Common:1; Rare:54 | ||||
chr7:66844837-66845087 | Common:2; Rare:108 | ||||
chr7:67302402-67302696 | Common:5; Rare:95 | ||||
chr7:72829286-72829505 | Rare:56 | ||||
chr7:73005886-73006154 | Rare:22 | ||||
chr7:74890542-74890820 | Common:2; Rare:84 | ||||
chr7:75358962-75359246 | Common:1; Rare:9 | ||||
chr7:94409356-94409608 | Rare:70; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr7:94420438-94420649 | Rare:61; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr7:96321293-96321540 | Common:2; Rare:60 | ||||
chr7:97972254-97972372 | Common:1; Rare:29 |