Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:102596810-102597035 | Common:1; Rare:108 | ||||
chr13:102773736-102773865 | Rare:55 | ||||
chr13:102845754-102846078 | Common:8; Rare:84; Clinvar:2; Clinvar (benign):4 | ||||
chr13:106567849-106568267 | Rare:116 | ||||
chr13:108218294-108218532 | Common:1; Rare:87 | ||||
chr13:110561664-110561889 | Common:5; Rare:81 | ||||
chr13:111153620-111153721 | Common:2; Rare:44 | ||||
chr13:113208630-113208741 | Rare:64 | ||||
chr13:114281526-114281654 | Common:1; Rare:70 | ||||
chr14:20343294-20343635 | Common:9; Rare:193 | ||||
chr14:20413425-20413537 | Common:3; Rare:33 | ||||
chr14:20455051-20455287 | Common:2; Rare:72 | ||||
chr14:20684438-20684682 | Common:2; Rare:45; Clinvar:1; Clinvar (benign):2 | ||||
chr14:21456041-21456221 | Common:3; Rare:48 | ||||
chr14:21476950-21477262 | Common:1; Rare:89 |