Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:32222323-32222488 | Rare:71 | ||||
chr1:32273790-32274190 | Rare:137 | ||||
chr1:32291812-32292159 | Common:1; Rare:97 | ||||
chr1:32351126-32351253 | Common:2; Rare:30 | ||||
chr1:32351407-32351715 | Common:1; Rare:95 | ||||
chr1:32394378-32394906 | Common:1; Rare:149 | ||||
chr1:32464921-32465124 | Rare:58 | ||||
chr1:32539240-32539492 | Rare:50 | ||||
chr1:32650415-32650673 | Common:1; Rare:107 | ||||
chr1:32650989-32651241 | Common:1; Rare:85 | ||||
chr1:32703181-32703311 | Rare:24 | ||||
chr1:32741437-32741548 | Rare:22 | ||||
chr1:32816820-32816963 | Rare:25 | ||||
chr1:32817292-32817682 | Rare:98; Clinvar:5; Clinvar (benign):1 | ||||
chr1:32818066-32818332 | Common:1; Rare:79 |