Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:3057369-3057544 | Rare:61 | ||||
chr11:3840921-3841097 | Rare:71 | ||||
chr11:5624894-5625033 | Rare:21 | ||||
chr11:6390254-6390494 | Common:2; Rare:69 | ||||
chr11:6481309-6481524 | Common:4; Rare:85 | ||||
chr11:6603558-6603801 | Common:4; Rare:74 | ||||
chr11:8682694-8682811 | Common:1; Rare:52 | ||||
chr11:8964378-8964531 | Common:3; Rare:45 | ||||
chr11:10541144-10541293 | Rare:53 | ||||
chr11:10858030-10858231 | Common:2; Rare:56 | ||||
chr11:14499797-14499924 | Common:2; Rare:41 | ||||
chr11:16738466-16738687 | Common:2; Rare:44 | ||||
chr11:18322406-18322619 | Common:2; Rare:77 | ||||
chr11:18394393-18394645 | Common:1; Rare:99; Clinvar (benign):1 | ||||
chr11:18634340-18634588 | Common:2; Rare:79 |