Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:46069860-46070067 | Rare:46 | ||||
chr3:14945779-14946033 | Rare:69 | ||||
chr3:23947551-23947836 | Common:8; Rare:67 | ||||
chr3:28347652-28347846 | Common:1; Rare:35 | ||||
chr3:40453171-40453417 | Common:5; Rare:53 | ||||
chr3:41225503-41225687 | Rare:36; Clinvar (pathogenic):1 | ||||
chr3:51991276-51991357 | Rare:26 | ||||
chr3:54967961-54968218 | Common:1; Rare:37 | ||||
chr3:55485148-55485324 | Rare:35 | ||||
chr3:55488478-55488677 | Common:2; Rare:48 | ||||
chr3:57952311-57952463 | Rare:28 | ||||
chr3:64685092-64685136 | Rare:11 | ||||
chr3:75434291-75434390 | Common:2; Rare:15 | ||||
chr3:75434964-75435372 | Common:5; Rare:139 | ||||
chr3:75670144-75670313 |