Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:132866428-132866688 | Common:1; Rare:85; Clinvar:1; Clinvar (benign):1 | ||||
chr5:133051851-133052152 | Rare:107 | ||||
chr5:133968582-133968688 | Rare:47 | ||||
chr5:134004647-134004850 | Common:1; Rare:75 | ||||
chr5:134226022-134226421 | Common:1; Rare:127 | ||||
chr5:134371157-134371520 | Common:2; Rare:111 | ||||
chr5:134411843-134411981 | Rare:47 | ||||
chr5:134648689-134648859 | Rare:55 | ||||
chr5:134738338-134738616 | Rare:104 | ||||
chr5:134845853-134846113 | Rare:120 | ||||
chr5:134874224-134874418 | Common:1; Rare:97 | ||||
chr5:135399105-135399346 | Rare:63 | ||||
chr5:136132765-136132944 | Common:1; Rare:55 | ||||
chr5:138178615-138178767 | Rare:35 | ||||
chr5:138178946-138179181 | Common:3; Rare:48 |