Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:23633518-23633709 | Common:2; Rare:42 | ||||
chr20:25854008-25854118 | Common:3; Rare:42 | ||||
chr20:30579939-30580228 | Common:1; Rare:53 | ||||
chr20:31604251-31604423 | Common:1; Rare:69 | ||||
chr20:35267884-35268061 | Common:2; Rare:42 | ||||
chr20:35490964-35491051 | Rare:17 | ||||
chr20:36049891-36050224 | Common:1; Rare:76 | ||||
chr20:36050238-36050786 | Common:2; Rare:177 | ||||
chr20:38985754-38985993 | Rare:50 | ||||
chr20:40687634-40687894 | Rare:61; Clinvar:2; Clinvar (benign):3 | ||||
chr20:44137633-44137839 | Common:2; Rare:32 | ||||
chr20:44180886-44181087 | Rare:29 | ||||
chr20:44188926-44189124 | Rare:39 | ||||
chr20:44208884-44209133 | Common:1; Rare:34 | ||||
chr20:44532467-44532620 | Rare:30 |