Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:87671164-87671401 | Common:1; Rare:66 | ||||
chr13:87673121-87673234 | Common:1; Rare:25 | ||||
chr13:87673978-87674098 | Common:2; Rare:33 | ||||
chr13:99015648-99015854 | Common:3; Rare:34 | ||||
chr13:99016027-99016376 | Rare:58 | ||||
chr14:24006996-24007094 | Common:1; Rare:33 | ||||
chr14:28761986-28762172 | Common:1; Rare:53 | ||||
chr14:28764365-28764565 | Common:1; Rare:46 | ||||
chr14:28766552-28766779 | Common:2; Rare:68 | ||||
chr14:28768162-28768501 | Rare:75; Clinvar:2; Clinvar (benign):10; Clinvar (pathogenic):2 | ||||
chr14:28772692-28772845 | Rare:38 | ||||
chr14:32203267-32203578 | Common:12; Rare:131 | ||||
chr14:49633956-49634064 | Common:1; Rare:43; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr14:49862639-49862989 | Common:1; Rare:165 | ||||
chr14:75981846-75982117 | Common:3; Rare:61 |