Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:107563888-107564021 | Common:2; Rare:79; Clinvar (benign):3 | ||||
chr7:107580144-107580285 | Common:2; Rare:56 | ||||
chr7:107743582-107743801 | Common:3; Rare:83 | ||||
chr7:107744053-107744171 | Rare:37 | ||||
chr7:107929510-107929842 | Common:2; Rare:68; Clinvar:2; Clinvar (benign):1 | ||||
chr7:107932500-107932549 | Rare:8 | ||||
chr7:107937167-107937467 | Rare:76; Clinvar (benign):1 | ||||
chr7:108002390-108002448 | Rare:23 | ||||
chr7:108526095-108526475 | Common:5; Rare:116 | ||||
chr7:108569572-108570006 | Common:3; Rare:158 | ||||
chr7:111091114-111091135 | |||||
chr7:112206297-112206751 | Common:2; Rare:149 | ||||
chr7:116499434-116499790 | Common:3; Rare:119 | ||||
chr7:116499947-116500234 | Common:3; Rare:62 | ||||
chr7:116525680-116525775 | Rare:27 |