Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:88691495-88691673 | Common:2; Rare:56 | ||||
chr2:95165651-95165847 | Rare:63 | ||||
chr2:95402633-95402750 | Rare:36 | ||||
chr2:96208230-96208418 | Rare:100 | ||||
chr2:96208816-96208942 | Common:3; Rare:42 | ||||
chr2:96265970-96266343 | Common:2; Rare:111; Clinvar:1 | ||||
chr2:97645808-97646097 | Common:2; Rare:89 | ||||
chr2:97663907-97664261 | Common:1; Rare:108 | ||||
chr2:98608420-98608636 | Common:1; Rare:93; Clinvar (benign):1 | ||||
chr2:99180978-99181227 | Common:2; Rare:72 | ||||
chr2:100562687-100563046 | Common:4; Rare:110 | ||||
chr2:101002142-101002313 | Rare:67 | ||||
chr2:102070289-102070476 | Common:2; Rare:32 | ||||
chr2:102104556-102104805 | Common:6; Rare:65 | ||||
chr2:102142671-102142925 | Common:4; Rare:82 |