Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:93741388-93741693 | Common:7; Rare:127 | ||||
chr11:93784175-93784390 | Common:3; Rare:67 | ||||
chr11:94128935-94129177 | Common:1; Rare:81 | ||||
chr11:94493789-94494053 | Common:4; Rare:77; Clinvar (benign):1 | ||||
chr11:94973542-94973707 | Rare:49 | ||||
chr11:95789766-95790014 | Common:3; Rare:86 | ||||
chr11:95790350-95790587 | Common:1; Rare:94 | ||||
chr11:95924090-95924152 | Rare:24 | ||||
chr11:96389837-96390083 | Common:2; Rare:98 | ||||
chr11:101914859-101915338 | Common:8; Rare:140 | ||||
chr11:102347129-102347279 | Common:2; Rare:48 | ||||
chr11:102452596-102452943 | Common:2; Rare:111 | ||||
chr11:103092038-103092259 | Common:1; Rare:68 | ||||
chr11:105609977-105610320 | Common:1; Rare:76 | ||||
chr11:106077301-106077730 | Common:2; Rare:134 |