Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:39491370-39491790 | Common:17; Rare:314 | ||||
chr1:39575006-39575406 | Common:2; Rare:92 | ||||
chr1:39575727-39576137 | Common:6; Rare:224 | ||||
chr1:39576285-39576685 | Rare:196 | ||||
chr1:39576760-39577120 | Rare:251 | ||||
chr1:39639511-39639911 | Rare:302 | ||||
chr1:39738619-39739058 | Common:12; Rare:344 | ||||
chr1:39788701-39789154 | Common:10; Rare:381 | ||||
chr1:39883350-39883750 | Common:11; Rare:440; Clinvar (pathogenic):5 | ||||
chr1:39901097-39901497 | Rare:209 | ||||
chr1:39901821-39902614 | Common:29; Rare:401 | ||||
chr1:40039550-40039780 | Rare:82 | ||||
chr1:40039741-40040248 | Common:14; Rare:479 | ||||
chr1:40040315-40040910 | Common:25; Rare:1009 | ||||
chr1:40041316-40041716 | Common:4; Rare:61 |