Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:65333624-65333896 | Common:1; Rare:117 | ||||
chr11:65386480-65386674 | Common:1; Rare:61 | ||||
chr11:65524821-65525166 | Rare:63 | ||||
chr11:65570359-65570504 | Rare:64 | ||||
chr11:65614199-65614393 | Rare:40 | ||||
chr11:65662828-65663084 | Common:1; Rare:66 | ||||
chr11:65663297-65663477 | Common:2; Rare:42 | ||||
chr11:65712156-65712270 | Rare:44 | ||||
chr11:65720482-65720588 | Common:1; Rare:58 | ||||
chr11:65860172-65860436 | Common:1; Rare:86 | ||||
chr11:65860487-65860769 | Common:1; Rare:89 | ||||
chr11:65872682-65872937 | Common:2; Rare:66; Clinvar:2; Clinvar (benign):2 | ||||
chr11:65873570-65873748 | Common:2; Rare:63 | ||||
chr11:65888374-65888670 | Common:1; Rare:102 | ||||
chr11:65900381-65900546 | Common:1; Rare:31 |