Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:88337662-88337888 | Common:4; Rare:108; Clinvar:6; Clinvar (benign):3 | ||||
chr11:90223006-90223224 | Common:1; Rare:84 | ||||
chr11:93741474-93741702 | Common:5; Rare:83 | ||||
chr11:93784189-93784380 | Common:3; Rare:55 | ||||
chr11:94493780-94494038 | Common:4; Rare:77; Clinvar:1; Clinvar (benign):2 | ||||
chr11:94973537-94973833 | Rare:75 | ||||
chr11:95089731-95089930 | Common:3; Rare:87 | ||||
chr11:95789555-95789870 | Common:3; Rare:141 | ||||
chr11:95790359-95790584 | Common:1; Rare:88 | ||||
chr11:95923835-95924120 | Common:2; Rare:125; Clinvar:5; Clinvar (benign):5 | ||||
chr11:96389862-96390065 | Common:1; Rare:84 | ||||
chr11:101583906-101584091 | Rare:46; Clinvar:1 | ||||
chr11:101914859-101915054 | Common:2; Rare:54 | ||||
chr11:101915112-101915329 | Common:3; Rare:63 | ||||
chr11:102110228-102110454 | Rare:89 |