Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:631391-631700 | Common:5; Rare:36 | ||||
chr1:778608-778819 | Common:3; Rare:89 | ||||
chr1:827500-827821 | Common:2; Rare:105 | ||||
chr1:8025123-8025436 | Common:2; Rare:70 | ||||
chr1:8121353-8121605 | Common:3; Rare:44 | ||||
chr1:9244749-9244959 | Common:2; Rare:52; Clinvar (benign):1 | ||||
chr1:9687517-9687640 | Common:1; Rare:33 | ||||
chr1:9731759-9732187 | Common:1; Rare:121 | ||||
chr1:12619027-12619236 | Rare:42 | ||||
chr1:12619946-12620007 | Rare:11 | ||||
chr1:15807678-15807888 | Rare:38 | ||||
chr1:15834846-15835133 | Common:2; Rare:130 | ||||
chr1:15835791-15836134 | Common:6; Rare:166 | ||||
chr1:16217372-16217676 | Common:1; Rare:48 | ||||
chr1:16499212-16499354 | Rare:59 |