Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:153986232-153986426 | Rare:49 | ||||
chr1:153990638-153990814 | Common:2; Rare:78 | ||||
chr1:154182916-154183305 | Rare:123 | ||||
chr1:154219929-154220220 | Common:5; Rare:81 | ||||
chr1:154220489-154221007 | Common:1; Rare:174 | ||||
chr1:154221248-154221372 | Rare:30 | ||||
chr1:154272490-154272785 | Common:4; Rare:77; Clinvar:3; Clinvar (benign):3 | ||||
chr1:154558908-154559104 | Common:1; Rare:71 | ||||
chr1:154567641-154567807 | Common:1; Rare:37 | ||||
chr1:154627870-154628082 | Common:5; Rare:96 | ||||
chr1:154936501-154936598 | Rare:18 | ||||
chr1:154936659-154936762 | Common:2; Rare:33 | ||||
chr1:154936861-154937012 | Rare:31 | ||||
chr1:154956085-154956276 | Common:1; Rare:56 | ||||
chr1:154961742-154962051 | Common:1; Rare:106 |