Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:111913128-111913281 | Rare:44 | ||||
chr11:111923738-111923810 | Common:1; Rare:7 | ||||
chr11:112025304-112025693 | Common:4; Rare:132; Clinvar:2; Clinvar (benign):9 | ||||
chr11:112073996-112074408 | Common:1; Rare:85 | ||||
chr11:112086638-112086939 | Rare:134; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):3 | ||||
chr11:112150723-112151041 | Common:2; Rare:39 | ||||
chr11:112226304-112226657 | Common:1; Rare:147; Clinvar:1; Clinvar (pathogenic):3 | ||||
chr11:113314454-113314615 | Rare:58 | ||||
chr11:113773628-113773778 | Rare:55 | ||||
chr11:113875486-113875771 | Common:4; Rare:102 | ||||
chr11:114059410-114059734 | Rare:71 | ||||
chr11:114059836-114059912 | Rare:14 | ||||
chr11:114400395-114400753 | Common:2; Rare:137 | ||||
chr11:114439643-114439675 | Rare:5 | ||||
chr11:116772930-116773107 | Common:1; Rare:69 |