Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:93180162-93180751 | Common:2; Rare:231 | ||||
chr1:93345766-93345953 | Common:4; Rare:74 | ||||
chr1:93448002-93448211 | Common:2; Rare:71 | ||||
chr1:93845865-93846177 | Common:4; Rare:61 | ||||
chr1:93847208-93847292 | Common:1; Rare:19 | ||||
chr1:93879096-93879279 | Common:1; Rare:71 | ||||
chr1:94237514-94237770 | Rare:96 | ||||
chr1:94418119-94418476 | Common:2; Rare:127 | ||||
chr1:94541730-94542000 | Rare:78 | ||||
chr1:94926923-94927043 | Common:3; Rare:32 | ||||
chr1:94927048-94927464 | Common:1; Rare:137 | ||||
chr1:95072855-95073008 | Common:1; Rare:64; Clinvar (benign):2 | ||||
chr1:95233955-95234229 | Common:5; Rare:81 | ||||
chr1:96721603-96721822 | Common:2; Rare:93 | ||||
chr1:97920930-97921148 | Rare:93; Clinvar:3 |