Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:89632896-89633189 | Common:1; Rare:81 | ||||
chr1:89994973-89995151 | Common:2; Rare:70 | ||||
chr1:92298945-92299067 | Common:1; Rare:57; Clinvar:1; Clinvar (benign):1 | ||||
chr1:93079094-93079290 | Common:2; Rare:84 | ||||
chr1:93180224-93180764 | Common:2; Rare:216 | ||||
chr1:93345807-93345946 | Common:2; Rare:52 | ||||
chr1:93879144-93879263 | Common:1; Rare:37 | ||||
chr1:94418108-94418455 | Common:3; Rare:123 | ||||
chr1:94541736-94541991 | Rare:74 | ||||
chr1:94926922-94927179 | Common:3; Rare:83 | ||||
chr1:95072876-95073008 | Rare:52 | ||||
chr1:95233955-95234228 | Common:5; Rare:81 | ||||
chr1:96721690-96721818 | Common:1; Rare:43 | ||||
chr1:98661602-98661885 | Common:2; Rare:99 | ||||
chr1:99969922-99970046 | Rare:34 |