Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:25232444-25232666 | Rare:91 | ||||
chr1:25247040-25247139 | Rare:30 | ||||
chr1:25247428-25247638 | Common:2; Rare:78 | ||||
chr1:25430193-25430278 | Common:2; Rare:29 | ||||
chr1:25800066-25800244 | Rare:73; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
chr1:25819880-25820208 | Common:4; Rare:99 | ||||
chr1:25859270-25859558 | Common:3; Rare:117 | ||||
chr1:25892572-25892681 | Common:1; Rare:19 | ||||
chr1:25906384-25906595 | Rare:80 | ||||
chr1:26021638-26021809 | Common:1; Rare:28 | ||||
chr1:26111653-26111863 | Common:1; Rare:74 | ||||
chr1:26177223-26177559 | Common:5; Rare:94 | ||||
chr1:26279964-26280201 | Rare:131 | ||||
chr1:26280587-26280931 | Common:1; Rare:90 | ||||
chr1:26306581-26306860 | Common:13; Rare:86 |