Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:208662-208865 | Rare:79 | ||||
chr11:236324-236559 | Common:8; Rare:81 | ||||
chr11:236895-237064 | Common:1; Rare:64 | ||||
chr11:375476-375718 | Common:1; Rare:91 | ||||
chr11:506732-507001 | Common:3; Rare:92 | ||||
chr11:507180-507297 | Rare:39 | ||||
chr11:535426-535743 | Common:5; Rare:131; Clinvar (benign):1 | ||||
chr11:560718-561024 | Common:5; Rare:137 | ||||
chr11:576412-576569 | Rare:66 | ||||
chr11:695724-695841 | Rare:44 | ||||
chr11:747279-747578 | Rare:128; Clinvar:5; Clinvar (benign):1 | ||||
chr11:777452-777623 | Common:1; Rare:75 | ||||
chr11:797943-798025 | Rare:22 | ||||
chr11:798224-798317 | Common:1; Rare:43 | ||||
chr11:809492-809595 | Rare:33 |