Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:95924088-95924164 | Rare:31 | ||||
chr11:96389853-96390060 | Common:1; Rare:87 | ||||
chr11:102317254-102317565 | Rare:65 | ||||
chr11:102347115-102347298 | Common:2; Rare:61 | ||||
chr11:102452525-102452588 | Rare:23 | ||||
chr11:102452668-102452949 | Common:1; Rare:88 | ||||
chr11:106077311-106077706 | Common:2; Rare:118 | ||||
chr11:108008882-108008955 | Rare:25 | ||||
chr11:108009284-108009351 | Rare:34 | ||||
chr11:108222636-108222924 | Rare:86; Clinvar:2 | ||||
chr11:108467488-108467654 | Common:3; Rare:64 | ||||
chr11:108664802-108665114 | Common:5; Rare:119 | ||||
chr11:111871494-111871630 | Rare:59; Clinvar:2; Clinvar (benign):1 | ||||
chr11:111879161-111879471 | Rare:86 | ||||
chr11:112025344-112025495 | Rare:39; Clinvar:1; Clinvar (benign):1 |