Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:28799384-28799528 | Rare:29 | ||||
chr22:37747277-37747550 | Rare:64 | ||||
chr22:39521464-39521834 | Common:2; Rare:168 | ||||
chr22:40107964-40108069 | Rare:25 | ||||
chr22:45448526-45448786 | Common:2; Rare:52 | ||||
chr22:46069865-46070060 | Rare:43 | ||||
chr3:14125710-14125783 | Rare:13 | ||||
chr3:28347645-28347882 | Common:1; Rare:38 | ||||
chr3:39411647-39411960 | Common:1; Rare:83; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr3:40453171-40453411 | Common:5; Rare:51 | ||||
chr3:42654377-42654642 | Rare:77 | ||||
chr3:57952318-57952484 | Rare:30 | ||||
chr3:61560670-61560812 | Common:1; Rare:43 | ||||
chr3:75435060-75435378 | Common:3; Rare:112 | ||||
chr3:75641108-75641421 | Common:1; Rare:51 |