Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:10541174-10541265 | Rare:30 | ||||
chr11:18526887-18526969 | Rare:37 | ||||
chr11:27506757-27506840 | Common:1; Rare:36 | ||||
chr11:31509523-31509782 | Common:2; Rare:81 | ||||
chr11:32435356-32435721 | Common:1; Rare:81; Clinvar:4 | ||||
chr11:34916373-34916448 | Common:1; Rare:25; Clinvar:1; Clinvar (benign):1 | ||||
chr11:47578966-47579085 | Rare:61; Clinvar:2 | ||||
chr11:61333044-61333253 | Rare:69 | ||||
chr11:61361830-61361971 | Common:1; Rare:37 | ||||
chr11:61362158-61362397 | Common:2; Rare:73; Clinvar:7; Clinvar (benign):1 | ||||
chr11:61429920-61430141 | Common:1; Rare:99; Clinvar (benign):2 | ||||
chr11:61792562-61792927 | Common:5; Rare:100 | ||||
chr11:62665150-62665312 | Common:3; Rare:69 | ||||
chr11:62728418-62728538 | Common:1; Rare:70 | ||||
chr11:62832022-62832229 | Rare:76 |