Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:93846510-93846840 | Common:3; Rare:274 | ||||
chr1:93847064-93847502 | Common:7; Rare:209 | ||||
chr1:93847452-93847641 | Common:1; Rare:124 | ||||
chr1:93879107-93879349 | Common:7; Rare:199 | ||||
chr1:93908670-93909150 | Common:6; Rare:226 | ||||
chr1:93909378-93909840 | Common:6; Rare:329 | ||||
chr1:94237499-94237786 | Rare:234 | ||||
chr1:94418078-94418509 | Common:6; Rare:312 | ||||
chr1:94541710-94542070 | Rare:252 | ||||
chr1:94820130-94820460 | Common:11; Rare:202 | ||||
chr1:94820400-94820810 | Common:6; Rare:119 | ||||
chr1:95072575-95072793 | Rare:66; Clinvar (benign):1 | ||||
chr1:95072862-95073390 | Common:11; Rare:312; Clinvar (benign):2 | ||||
chr1:95116851-95117840 | Common:3; Rare:437 | ||||
chr1:95233901-95234284 | Common:16; Rare:301 |