Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:26565845-26566020 | Common:2; Rare:47 | ||||
chr11:26996472-26996663 | Common:1; Rare:39 | ||||
chr11:33891267-33891523 | Common:10; Rare:51 | ||||
chr11:34086151-34086360 | Common:1; Rare:47 | ||||
chr11:34651559-34651802 | Common:1; Rare:68 | ||||
chr11:34909994-34910346 | Common:4; Rare:67 | ||||
chr11:35193059-35193328 | Common:1; Rare:50 | ||||
chr11:43471386-43471547 | Rare:36 | ||||
chr11:45180958-45181092 | Common:1; Rare:28 | ||||
chr11:45355391-45355495 | Rare:27 | ||||
chr11:47165472-47165539 | Common:8; Rare:30 | ||||
chr11:47290044-47290299 | Rare:70 | ||||
chr11:47376590-47376857 | Common:1; Rare:56 | ||||
chr11:47413415-47413648 | Common:2; Rare:79; Clinvar:4; Clinvar (benign):6 | ||||
chr11:57332458-57332690 | Rare:55 |