Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:95066905-95066994 | Rare:15 | ||||
chr11:95067460-95067758 | Common:3; Rare:134 | ||||
chr11:95089715-95089930 | Common:3; Rare:93 | ||||
chr11:95789465-95789895 | Common:4; Rare:199 | ||||
chr11:95790346-95790694 | Common:3; Rare:138 | ||||
chr11:95923829-95924164 | Common:2; Rare:147; Clinvar:5; Clinvar (benign):5 | ||||
chr11:96389854-96390076 | Common:2; Rare:91 | ||||
chr11:101914904-101915266 | Common:6; Rare:99 | ||||
chr11:102110201-102110470 | Common:1; Rare:104 | ||||
chr11:102347101-102347354 | Common:2; Rare:82 | ||||
chr11:102452526-102452944 | Common:2; Rare:137 | ||||
chr11:103092027-103092259 | Common:1; Rare:69 | ||||
chr11:103109307-103109576 | Common:1; Rare:79; Clinvar:1; Clinvar (benign):1 | ||||
chr11:106022162-106022546 | Common:3; Rare:113 | ||||
chr11:106077317-106077728 | Common:2; Rare:128 |