Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr8:124539042-124539198 | Common:2; Rare:87; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
chr8:125091710-125091914 | Common:2; Rare:71; Clinvar (benign):3 | ||||
chr8:127735884-127736076 | Rare:41 | ||||
chr8:133297185-133297476 | Common:3; Rare:117; Clinvar:3; Clinvar (benign):1 | ||||
chr8:141391854-141392073 | Common:2; Rare:87 | ||||
chr8:142777218-142777596 | Common:4; Rare:69 | ||||
chr8:143018408-143018558 | Common:1; Rare:43 | ||||
chr8:143541430-143541636 | Common:2; Rare:69 | ||||
chr8:143558236-143558401 | Common:1; Rare:60 | ||||
chr8:143635873-143636079 | Common:2; Rare:93 | ||||
chr8:143829306-143829488 | Rare:69 | ||||
chr8:144078512-144078722 | Common:1; Rare:64 | ||||
chr8:144082503-144082670 | Common:2; Rare:58 | ||||
chr8:144104215-144104465 | Common:1; Rare:71 | ||||
chr8:144413548-144413674 | Rare:42; Clinvar:1 |