Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:28108134-28108414 | Common:1; Rare:82 | ||||
chr11:30322971-30323164 | Common:1; Rare:55 | ||||
chr11:30584045-30584136 | Rare:26 | ||||
chr11:30584197-30584358 | Common:3; Rare:19 | ||||
chr11:31369735-31369888 | Rare:47 | ||||
chr11:31509566-31509893 | Common:1; Rare:118 | ||||
chr11:32583663-32583906 | Rare:91 | ||||
chr11:33039685-33039746 | Rare:11 | ||||
chr11:33161425-33161657 | Common:6; Rare:63 | ||||
chr11:33257204-33257427 | Common:3; Rare:74 | ||||
chr11:33736404-33736605 | Common:1; Rare:64 | ||||
chr11:34051622-34051731 | Rare:46 | ||||
chr11:34105523-34105724 | Common:2; Rare:69 | ||||
chr11:34438763-34439007 | Common:2; Rare:80; Clinvar (benign):1 | ||||
chr11:34916287-34916676 | Common:10; Rare:158; Clinvar:5; Clinvar (benign):11; Clinvar (pathogenic):1 |