Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:74949086-74949282 | Common:6; Rare:47 | ||||
chr11:76444660-76444796 | Rare:33 | ||||
chr11:76783066-76783357 | Common:8; Rare:94 | ||||
chr11:77637739-77637877 | Common:1; Rare:49 | ||||
chr11:77820989-77821164 | Common:1; Rare:49 | ||||
chr11:78079800-78079934 | Common:2; Rare:45 | ||||
chr11:78139590-78139751 | Rare:61; Clinvar:2 | ||||
chr11:83071866-83072088 | Common:3; Rare:63 | ||||
chr11:83193645-83193786 | Common:1; Rare:62 | ||||
chr11:85628339-85628645 | Common:6; Rare:103 | ||||
chr11:85647904-85648047 | Common:1; Rare:41; Clinvar:2; Clinvar (benign):1 | ||||
chr11:86244970-86245268 | Common:1; Rare:132 | ||||
chr11:88337721-88337811 | Common:3; Rare:53; Clinvar:1; Clinvar (benign):2 | ||||
chr11:90223021-90223211 | Common:1; Rare:77 | ||||
chr11:93741393-93741702 | Common:7; Rare:127 |