Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:88337706-88337888 | Common:3; Rare:83; Clinvar:3; Clinvar (benign):2 | ||||
chr11:90222999-90223120 | Common:1; Rare:48 | ||||
chr11:93741474-93741708 | Common:5; Rare:84 | ||||
chr11:93784194-93784342 | Common:2; Rare:53 | ||||
chr11:94493795-94494012 | Common:3; Rare:63; Clinvar (benign):1 | ||||
chr11:94973528-94973728 | Rare:61 | ||||
chr11:95790359-95790584 | Common:1; Rare:88 | ||||
chr11:95924108-95924161 | Rare:18 | ||||
chr11:96389860-96390028 | Common:1; Rare:61 | ||||
chr11:102110228-102110448 | Rare:88 | ||||
chr11:102317297-102317499 | Rare:42 | ||||
chr11:102347120-102347260 | Common:1; Rare:38 | ||||
chr11:103092044-103092261 | Common:1; Rare:69 | ||||
chr11:106077317-106077687 | Common:2; Rare:105 | ||||
chr11:108008888-108008948 | Rare:19 |