Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:36356115-36356127 | |||||
chr2:36966498-36966846 | Common:4; Rare:149 | ||||
chr2:37084269-37084559 | Common:4; Rare:108 | ||||
chr2:37156912-37157047 | Common:1; Rare:43 | ||||
chr2:37196394-37196524 | Rare:48 | ||||
chr2:37211841-37212384 | Common:3; Rare:163 | ||||
chr2:37231132-37231350 | Rare:62 | ||||
chr2:37231391-37231790 | Common:6; Rare:200; Clinvar:1; Clinvar (benign):5 | ||||
chr2:37231946-37232245 | Common:3; Rare:101; Clinvar (benign):1 | ||||
chr2:37247321-37247555 | Common:1; Rare:69; Clinvar (benign):2 | ||||
chr2:37324703-37324961 | Common:1; Rare:102 | ||||
chr2:37344604-37344737 | Common:1; Rare:55 | ||||
chr2:37671566-37671723 | Common:1; Rare:76 | ||||
chr2:37925224-37925406 | Common:3; Rare:79 | ||||
chr2:38076149-38076265 | Rare:28 |