Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:100088827-100089117 | Rare:110; Clinvar:1; Clinvar (benign):2 | ||||
chr13:102596785-102597021 | Common:1; Rare:107 | ||||
chr13:102798915-102799144 | Common:1; Rare:49 | ||||
chr13:106568103-106568267 | Rare:52 | ||||
chr13:108218313-108218508 | Rare:75 | ||||
chr13:110307091-110307491 | Common:6; Rare:130; Clinvar:1; Clinvar (benign):8 | ||||
chr13:113208638-113208721 | Rare:45 | ||||
chr13:113297167-113297294 | Rare:51 | ||||
chr13:113490688-113490995 | Common:1; Rare:113 | ||||
chr13:113759152-113759232 | Rare:20 | ||||
chr13:113863945-113864195 | Common:2; Rare:64 | ||||
chr13:114314281-114314542 | Rare:74 | ||||
chr14:20343415-20343635 | Common:6; Rare:102 | ||||
chr14:20454843-20455342 | Common:5; Rare:122 | ||||
chr14:20455425-20455701 | Rare:81 |