Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:31207471-31207839 | Common:2; Rare:123 | ||||
chr14:31420497-31420760 | Common:4; Rare:88 | ||||
chr14:31561322-31561503 | Common:2; Rare:69; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr14:32075670-32075723 | Common:1; Rare:14 | ||||
chr14:32076583-32077086 | Common:3; Rare:142 | ||||
chr14:32077506-32077562 | Rare:18 | ||||
chr14:33950448-33950565 | Rare:36 | ||||
chr14:33950941-33951249 | Common:1; Rare:100 | ||||
chr14:34461887-34462124 | Common:1; Rare:54 | ||||
chr14:34462177-34462566 | Common:1; Rare:142 | ||||
chr14:34629916-34630249 | Common:5; Rare:131 | ||||
chr14:34874864-34875025 | Common:1; Rare:54 | ||||
chr14:34875257-34875495 | Rare:91 | ||||
chr14:34982346-34982730 | Common:1; Rare:152 | ||||
chr14:35046126-35046554 | Common:1; Rare:145 |