Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:111913148-111913270 | Rare:37 | ||||
chr11:112073995-112074345 | Common:1; Rare:72 | ||||
chr11:112086720-112086941 | Rare:95; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):4 | ||||
chr11:112226310-112226657 | Common:1; Rare:144; Clinvar:1; Clinvar (pathogenic):3 | ||||
chr11:113314408-113314602 | Rare:67 | ||||
chr11:113875493-113875781 | Common:4; Rare:106 | ||||
chr11:114059385-114059734 | Rare:77 | ||||
chr11:114296229-114296559 | Rare:64 | ||||
chr11:114400450-114400753 | Common:2; Rare:122 | ||||
chr11:117144191-117144418 | Common:2; Rare:104 | ||||
chr11:117199008-117199428 | Common:6; Rare:132 | ||||
chr11:117232036-117232186 | Rare:40 | ||||
chr11:117232533-117232753 | Common:2; Rare:75 | ||||
chr11:118359410-118359650 | Common:3; Rare:101 | ||||
chr11:118401340-118401678 | Rare:113 |