Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:38009281-38009347 | Rare:13 | ||||
chr1:38012414-38012805 | Common:1; Rare:117 | ||||
chr1:38873301-38873554 | Common:3; Rare:87 | ||||
chr1:39026246-39026398 | Common:1; Rare:41 | ||||
chr1:39738749-39738898 | Common:2; Rare:30 | ||||
chr1:39883467-39883575 | Rare:42; Clinvar (pathogenic):1 | ||||
chr1:40040432-40040806 | Common:3; Rare:115 | ||||
chr1:40161247-40161415 | Rare:46 | ||||
chr1:40257886-40258303 | Common:4; Rare:116; Clinvar:8; Clinvar (benign):1 | ||||
chr1:40450058-40450145 | Common:1; Rare:34 | ||||
chr1:40508674-40508789 | Common:3; Rare:31 | ||||
chr1:40531514-40531721 | Common:1; Rare:53 | ||||
chr1:40691495-40691805 | Common:3; Rare:153 | ||||
chr1:40692033-40692079 | Rare:19 | ||||
chr1:40979627-40979806 | Common:1; Rare:61 |