Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:6603553-6603834 | Common:4; Rare:85; Clinvar (benign):3 | ||||
chr11:6926411-6926436 | Common:1; Rare:5 | ||||
chr11:6926496-6926545 | Common:1; Rare:12 | ||||
chr11:7513632-7513796 | Common:2; Rare:52 | ||||
chr11:8682641-8682814 | Common:2; Rare:78 | ||||
chr11:8964378-8964510 | Common:3; Rare:40 | ||||
chr11:8964931-8964987 | Common:1; Rare:11 | ||||
chr11:9460687-9461029 | Common:3; Rare:93 | ||||
chr11:10541143-10541331 | Rare:71 | ||||
chr11:10799037-10799288 | Common:3; Rare:94 | ||||
chr11:10800202-10800650 | Rare:121 | ||||
chr11:10802049-10802357 | Common:1; Rare:89 | ||||
chr11:10858010-10858275 | Common:3; Rare:86 | ||||
chr11:14513567-14513866 | Rare:66 | ||||
chr11:14643658-14643854 | Common:1; Rare:68 |