Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:69269732-69270132 | Common:4; Rare:129 | ||||
chr10:69314960-69315904 | Common:5; Rare:333 | ||||
chr10:69316090-69316600 | Common:12; Rare:196 | ||||
chr10:69317709-69318596 | Common:12; Rare:467 | ||||
chr10:69318501-69320047 | Common:33; Rare:978 | ||||
chr10:69408612-69409048 | Common:56; Rare:363 | ||||
chr10:69629951-69630380 | Common:5; Rare:190 | ||||
chr10:70132627-70133408 | Common:19; Rare:599 | ||||
chr10:70146658-70147058 | Common:2; Rare:98 | ||||
chr10:70169834-70170255 | Common:4; Rare:164 | ||||
chr10:70170374-70170857 | Common:21; Rare:620 | ||||
chr10:70233293-70233700 | Common:36; Rare:632; Clinvar (benign):6 | ||||
chr10:70233775-70234175 | Common:5; Rare:96 | ||||
chr10:70381638-70382373 | Common:1; Rare:204 | ||||
chr10:70382489-70382937 | Common:19; Rare:517 |