Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:92792408-92792529 | Common:1; Rare:26 | ||||
chr1:93179842-93179948 | Common:1; Rare:22 | ||||
chr1:93180053-93180532 | Rare:172 | ||||
chr1:93345807-93345919 | Common:2; Rare:43 | ||||
chr1:93847220-93847279 | Common:1; Rare:14 | ||||
chr1:93879124-93879274 | Common:1; Rare:55 | ||||
chr1:94418236-94418470 | Common:2; Rare:83 | ||||
chr1:94541632-94541994 | Common:1; Rare:107 | ||||
chr1:94820186-94820404 | Common:3; Rare:57 | ||||
chr1:94927047-94927456 | Common:1; Rare:137 | ||||
chr1:95072870-95073018 | Rare:57 | ||||
chr1:95233945-95234248 | Common:5; Rare:94 | ||||
chr1:98661598-98661879 | Common:2; Rare:99 | ||||
chr1:99646013-99646358 | Rare:69 | ||||
chr1:99850274-99850418 | Rare:36; Clinvar:3; Clinvar (benign):1 |