Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:102798920-102799180 | Common:1; Rare:53 | ||||
chr13:102845644-102846080 | Common:9; Rare:118; Clinvar:2; Clinvar (benign):4 | ||||
chr13:106567574-106567751 | Rare:58 | ||||
chr13:106567841-106568273 | Rare:117 | ||||
chr13:108218307-108218508 | Rare:77 | ||||
chr13:110914974-110915296 | Common:3; Rare:133 | ||||
chr13:111153599-111153753 | Common:2; Rare:72 | ||||
chr13:112588093-112588283 | Rare:49 | ||||
chr13:112689761-112690080 | Common:5; Rare:100 | ||||
chr13:113208632-113208741 | Rare:63 | ||||
chr13:113297037-113297287 | Common:1; Rare:100 | ||||
chr13:113490683-113491085 | Common:2; Rare:146 | ||||
chr13:114281505-114281690 | Common:2; Rare:105 | ||||
chr14:20343412-20343647 | Common:7; Rare:110 | ||||
chr14:20454700-20455287 | Common:7; Rare:164 |