Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:94768889-94769015 | Rare:32 | ||||
chr11:96341709-96342107 | Common:1; Rare:95 | ||||
chr11:102401608-102401936 | Common:2; Rare:94 | ||||
chr11:104918135-104918203 | Common:1; Rare:12 | ||||
chr11:108143915-108144047 | Common:3; Rare:48; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr11:111720792-111721009 | Common:1; Rare:59 | ||||
chr11:112151763-112151942 | Rare:24 | ||||
chr11:112152308-112152537 | Rare:37 | ||||
chr11:114058651-114058899 | Common:4; Rare:57 | ||||
chr11:114066177-114066460 | Common:2; Rare:56 | ||||
chr11:114074887-114074990 | Rare:24 | ||||
chr11:114078920-114079011 | Common:1; Rare:23 | ||||
chr11:114109439-114109780 | Common:3; Rare:58 | ||||
chr11:114120655-114120860 | Rare:37 | ||||
chr11:114130594-114130848 | Rare:38 |