Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:132985180-132985346 | Common:2; Rare:36 | ||||
chr10:133369007-133369124 | Rare:32; Clinvar (benign):1 | ||||
chr11:310163-310246 | Rare:22 | ||||
chr11:319955-320130 | Common:1; Rare:54 | ||||
chr11:459918-460025 | Rare:23 | ||||
chr11:760002-760253 | Rare:70; Clinvar:1 | ||||
chr11:2699994-2700267 | Common:2; Rare:105 | ||||
chr11:9758122-9758366 | Rare:66 | ||||
chr11:9759504-9759574 | Rare:7 | ||||
chr11:10303817-10304008 | Rare:32 | ||||
chr11:10803098-10803270 | Common:1; Rare:44 | ||||
chr11:12693668-12693919 | Rare:46 | ||||
chr11:14644947-14644950 | Rare:1 | ||||
chr11:14852695-14852953 | Rare:34 | ||||
chr11:16356399-16356741 | Rare:52 |