Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:231421059-231421118 | Rare:17 | ||||
chr1:231421175-231421382 | Rare:70; Clinvar:2; Clinvar (benign):1 | ||||
chr1:231828271-231828444 | Rare:17 | ||||
chr1:232629057-232629344 | Common:1; Rare:72 | ||||
chr1:232869151-232869211 | Rare:10 | ||||
chr1:233113002-233113271 | Common:1; Rare:43 | ||||
chr1:233113514-233113835 | Common:3; Rare:51 | ||||
chr1:234356930-234357068 | Common:2; Rare:52 | ||||
chr1:234369205-234369271 | Common:1; Rare:10 | ||||
chr1:234369716-234370046 | Rare:44 | ||||
chr1:234372428-234372547 | Rare:22 | ||||
chr1:234403005-234403159 | Rare:28 | ||||
chr1:234600053-234600337 | Common:7; Rare:119 | ||||
chr1:234610176-234610338 | Common:2; Rare:70 | ||||
chr1:234611362-234611494 | Common:1; Rare:44 |