Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:122845293-122845625 | Common:3; Rare:112 | ||||
chr5:123423313-123423599 | Rare:97 | ||||
chr5:123511990-123512268 | Rare:73 | ||||
chr5:124746782-124747002 | Common:5; Rare:41 | ||||
chr5:124748753-124749019 | Common:3; Rare:59 | ||||
chr5:126423439-126423544 | Rare:26 | ||||
chr5:126595185-126595370 | Common:4; Rare:82; Clinvar:3; Clinvar (benign):9 | ||||
chr5:127517506-127517757 | Common:5; Rare:108 | ||||
chr5:131165190-131165364 | Rare:69; Clinvar (benign):1 | ||||
chr5:131170692-131170996 | Common:1; Rare:62; Clinvar (benign):1 | ||||
chr5:131635160-131635446 | Common:1; Rare:109 | ||||
chr5:131796928-131797215 | Rare:82 | ||||
chr5:132257517-132257779 | Common:7; Rare:64 | ||||
chr5:132369598-132369890 | Common:6; Rare:91; Clinvar:3; Clinvar (benign):3 | ||||
chr5:132490743-132490989 | Rare:60 |