Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:96740036-96740354 | Common:5; Rare:72 | ||||
chr2:96816147-96816270 | Common:1; Rare:44 | ||||
chr2:97645808-97646110 | Common:3; Rare:92 | ||||
chr2:97663980-97664272 | Rare:82 | ||||
chr2:97713486-97713582 | Rare:13 | ||||
chr2:98608431-98608637 | Common:1; Rare:90 | ||||
chr2:98731060-98731262 | Common:3; Rare:78 | ||||
chr2:99154877-99155037 | Common:1; Rare:67; Clinvar (benign):1 | ||||
chr2:99180984-99181226 | Common:2; Rare:71 | ||||
chr2:99337319-99337577 | Rare:97 | ||||
chr2:100562719-100563052 | Common:3; Rare:106 | ||||
chr2:101253242-101253310 | Common:1; Rare:16 | ||||
chr2:102736828-102736941 | Common:1; Rare:54 | ||||
chr2:105329661-105329804 | Common:2; Rare:48 | ||||
chr2:108378027-108378155 | Common:1; Rare:23 |