Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:112086716-112086913 | Rare:85; Clinvar:2; Clinvar (pathogenic):2 | ||||
chr11:112226274-112226456 | Rare:78 | ||||
chr11:113314454-113314602 | Rare:51 | ||||
chr11:113875482-113875804 | Common:4; Rare:121 | ||||
chr11:114059417-114059734 | Rare:67 | ||||
chr11:114400434-114400766 | Common:2; Rare:127 | ||||
chr11:116772922-116773064 | Rare:58 | ||||
chr11:117144191-117144418 | Common:2; Rare:104 | ||||
chr11:117232034-117232185 | Rare:40 | ||||
chr11:117232517-117232725 | Common:2; Rare:70 | ||||
chr11:118252267-118252497 | Rare:62 | ||||
chr11:118264226-118264600 | Common:1; Rare:59 | ||||
chr11:118401273-118401710 | Rare:148 | ||||
chr11:118610109-118610440 | Rare:41 | ||||
chr11:118621086-118621498 | Rare:76 |