Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:88337708-88337888 | Common:3; Rare:83; Clinvar:3; Clinvar (benign):2 | ||||
chr11:93741481-93741695 | Common:5; Rare:79 | ||||
chr11:94493792-94494011 | Common:3; Rare:63; Clinvar (benign):1 | ||||
chr11:94768049-94768390 | Common:2; Rare:86 | ||||
chr11:94973535-94973719 | Rare:54 | ||||
chr11:95089731-95089872 | Common:3; Rare:57 | ||||
chr11:95790359-95790557 | Rare:79 | ||||
chr11:96389863-96390033 | Common:1; Rare:63 | ||||
chr11:102798046-102798055 | Rare:5 | ||||
chr11:103091839-103091944 | Rare:38 | ||||
chr11:106077344-106077706 | Common:2; Rare:109 | ||||
chr11:108009254-108009349 | Rare:48 | ||||
chr11:112074008-112074343 | Common:1; Rare:68 | ||||
chr11:112086692-112086891 | Rare:88 | ||||
chr11:114296251-114296579 | Rare:61 |