Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:14499782-14499918 | Common:2; Rare:47 | ||||
chr11:16738466-16738707 | Common:3; Rare:52 | ||||
chr11:17077618-17077963 | Common:2; Rare:142 | ||||
chr11:17207922-17208082 | Common:1; Rare:60 | ||||
chr11:18322131-18322321 | Common:4; Rare:67; Clinvar:1; Clinvar (benign):2 | ||||
chr11:18322474-18322582 | Common:2; Rare:44 | ||||
chr11:18526889-18526971 | Rare:37 | ||||
chr11:18588679-18588769 | Rare:32 | ||||
chr11:22625796-22626016 | Common:3; Rare:75; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr11:27363135-27363306 | Rare:71 | ||||
chr11:27506748-27506857 | Common:1; Rare:45 | ||||
chr11:28108134-28108406 | Common:1; Rare:79 | ||||
chr11:31509600-31509784 | Common:1; Rare:56 | ||||
chr11:33015784-33015923 | Common:1; Rare:53 | ||||
chr11:33258075-33258346 | Rare:97 |