Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:62653268-62653504 | Common:1; Rare:67 | ||||
chr11:62665139-62665317 | Common:4; Rare:81 | ||||
chr11:62671834-62672027 | Common:1; Rare:69; Clinvar (benign):1 | ||||
chr11:62679032-62679162 | Rare:41 | ||||
chr11:62706257-62706463 | Common:2; Rare:94; Clinvar (benign):3 | ||||
chr11:62728446-62728522 | Common:1; Rare:49 | ||||
chr11:62761371-62761654 | Common:1; Rare:84 | ||||
chr11:62771273-62771393 | Rare:30 | ||||
chr11:62855882-62856143 | Rare:102 | ||||
chr11:63614385-63614587 | Common:5; Rare:40 | ||||
chr11:64226106-64226304 | Common:2; Rare:57 | ||||
chr11:64240891-64241139 | Rare:67 | ||||
chr11:64241313-64241655 | Rare:72 | ||||
chr11:64242060-64242179 | Common:1; Rare:20 | ||||
chr11:64284547-64284851 | Common:1; Rare:125 |