Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:181699184-181699465 | Rare:41 | ||||
chr3:181699484-181699719 | Rare:36 | ||||
chr3:181699724-181699800 | Common:1; Rare:15 | ||||
chr3:181702201-181702286 | Rare:14 | ||||
chr3:181712562-181713095 | Common:1; Rare:128; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):7 | ||||
chr3:181717764-181718037 | Common:3; Rare:57 | ||||
chr3:181724696-181724902 | Common:2; Rare:37 | ||||
chr3:181728950-181729069 | Rare:14 | ||||
chr3:183447414-183447843 | Common:3; Rare:101 | ||||
chr3:184183991-184184233 | Common:2; Rare:50 | ||||
chr3:184259006-184259306 | Common:1; Rare:42 | ||||
chr3:184710913-184711093 | Common:1; Rare:66 | ||||
chr3:191425395-191425541 | Common:1; Rare:36 | ||||
chr3:192514743-192514955 | Rare:48 | ||||
chr3:194381667-194381819 | Common:1; Rare:42 |