Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:108218321-108218520 | Rare:78 | ||||
chr13:111153569-111153715 | Common:2; Rare:67 | ||||
chr13:113208638-113208723 | Rare:46 | ||||
chr13:114281501-114281657 | Common:2; Rare:83 | ||||
chr13:114281787-114282065 | Common:6; Rare:145 | ||||
chr14:20343230-20343647 | Common:11; Rare:238 | ||||
chr14:20413413-20413521 | Common:2; Rare:31 | ||||
chr14:20454793-20455287 | Common:7; Rare:130 | ||||
chr14:20684479-20684629 | Common:1; Rare:24; Clinvar (benign):1 | ||||
chr14:20989663-20990003 | Common:7; Rare:73 | ||||
chr14:21476925-21477258 | Common:1; Rare:93 | ||||
chr14:22766524-22766704 | Common:1; Rare:89 | ||||
chr14:22871669-22871861 | Rare:45 | ||||
chr14:22929363-22929609 | Rare:56 | ||||
chr14:22957078-22957204 | Rare:40 |