Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr8:23336052-23336237 | Common:1; Rare:35 | ||||
chr8:25509102-25509190 | Rare:12 | ||||
chr8:26408002-26408326 | Rare:86 | ||||
chr8:37748020-37748060 | Rare:20 | ||||
chr8:43130532-43130850 | Common:3; Rare:54 | ||||
chr8:43197738-43197931 | Common:1; Rare:57; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
chr8:47736974-47737008 | Rare:10 | ||||
chr8:48420489-48420747 | Common:2; Rare:39 | ||||
chr8:66922324-66922385 | Rare:16 | ||||
chr8:68760004-68760123 | Rare:14 | ||||
chr8:69523157-69523274 | Common:1; Rare:21 | ||||
chr8:69620811-69621080 | Common:1; Rare:53 | ||||
chr8:69646258-69646409 | Common:1; Rare:32 | ||||
chr8:70633848-70633967 | Rare:23 | ||||
chr8:106272182-106272268 | Rare:17 |