Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:102845881-102846078 | Common:3; Rare:48; Clinvar:2; Clinvar (benign):1 | ||||
chr13:102846562-102846666 | Rare:18 | ||||
chr13:106568091-106568267 | Rare:56 | ||||
chr13:108215502-108215695 | Common:1; Rare:50 | ||||
chr13:108218339-108218520 | Rare:71 | ||||
chr13:110615380-110615581 | Common:2; Rare:63 | ||||
chr13:111153619-111153720 | Common:2; Rare:43 | ||||
chr13:113208629-113208766 | Rare:80 | ||||
chr13:113449140-113449309 | Rare:37 | ||||
chr13:114281295-114281642 | Common:5; Rare:129 | ||||
chr14:20343219-20343640 | Common:12; Rare:240 | ||||
chr14:20413425-20413571 | Common:3; Rare:43 | ||||
chr14:20455042-20455259 | Common:2; Rare:62 | ||||
chr14:20989665-20990002 | Common:7; Rare:71 | ||||
chr14:21104039-21104099 | Rare:18 |