Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:99015662-99015854 | Common:3; Rare:32 | ||||
chr13:101917477-101917697 | Rare:57 | ||||
chr13:102394493-102394654 | Common:1; Rare:60 | ||||
chr13:107719568-107719784 | Common:1; Rare:38 | ||||
chr13:107867989-107868244 | Common:1; Rare:55 | ||||
chr13:112056306-112056517 | Common:1; Rare:69 | ||||
chr13:112106665-112106957 | Common:1; Rare:59 | ||||
chr14:21192072-21192214 | Rare:31 | ||||
chr14:23430817-23430906 | Common:1; Rare:21; Clinvar (benign):4 | ||||
chr14:23487285-23487584 | Common:1; Rare:54 | ||||
chr14:23512408-23512566 | Rare:24 | ||||
chr14:23512952-23513160 | Common:1; Rare:41 | ||||
chr14:23513212-23513374 | Common:1; Rare:37 | ||||
chr14:27833149-27833329 | Common:2; Rare:36 | ||||
chr14:28764365-28764564 | Common:1; Rare:45 |