Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:99200668-99200894 | Common:6; Rare:104 | ||||
chr13:100088955-100089117 | Rare:57; Clinvar:1; Clinvar (benign):2 | ||||
chr13:102596807-102597024 | Common:1; Rare:99 | ||||
chr13:106568085-106568267 | Rare:58 | ||||
chr13:108218293-108218526 | Common:1; Rare:84 | ||||
chr13:110615382-110615581 | Common:2; Rare:62 | ||||
chr13:110712995-110713261 | Common:2; Rare:117 | ||||
chr13:111153573-111153706 | Common:2; Rare:59 | ||||
chr13:113208641-113208707 | Rare:36 | ||||
chr13:114281480-114281651 | Common:2; Rare:87 | ||||
chr14:20343240-20343635 | Common:11; Rare:227 | ||||
chr14:20455051-20455245 | Common:1; Rare:58 | ||||
chr14:22766506-22766721 | Common:1; Rare:114 | ||||
chr14:22919077-22919455 | Common:8; Rare:100 | ||||
chr14:23095104-23095324 | Common:1; Rare:115 |