Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:108215502-108215703 | Common:1; Rare:53 | ||||
chr13:108218296-108218520 | Common:1; Rare:83 | ||||
chr13:110307155-110307442 | Common:5; Rare:92; Clinvar (benign):5 | ||||
chr13:111153622-111153714 | Common:2; Rare:40 | ||||
chr13:113208641-113208706 | Rare:36 | ||||
chr13:114281480-114281644 | Common:2; Rare:80 | ||||
chr13:114281804-114282073 | Common:6; Rare:136 | ||||
chr14:20343219-20343648 | Common:12; Rare:244 | ||||
chr14:20413425-20413531 | Common:3; Rare:30 | ||||
chr14:20454852-20455259 | Common:4; Rare:97 | ||||
chr14:21456041-21456134 | Common:2; Rare:23 | ||||
chr14:21476942-21477258 | Common:1; Rare:90 | ||||
chr14:22871651-22871986 | Rare:84 | ||||
chr14:22919089-22919455 | Common:8; Rare:98 | ||||
chr14:22982508-22982900 | Common:2; Rare:137 |