Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:16817345-16817769 | Common:4; Rare:154 | ||||
chr10:17201636-17201741 | Common:1; Rare:33 | ||||
chr10:17643898-17644265 | Common:2; Rare:109 | ||||
chr10:18651579-18651668 | Common:1; Rare:30 | ||||
chr10:18659254-18659349 | Common:1; Rare:34 | ||||
chr10:19816189-19816464 | Common:5; Rare:58 | ||||
chr10:21533996-21534324 | Common:3; Rare:131 | ||||
chr10:22316261-22316473 | Common:1; Rare:96 | ||||
chr10:22325491-22325671 | Common:1; Rare:80 | ||||
chr10:27154314-27154480 | Rare:44 | ||||
chr10:27155191-27155441 | Common:7; Rare:109; Clinvar:3; Clinvar (benign):7 | ||||
chr10:27240565-27240889 | Common:2; Rare:84 | ||||
chr10:27242079-27242218 | Common:1; Rare:58 | ||||
chr10:27504202-27504372 | Rare:101; Clinvar:3; Clinvar (benign):1 | ||||
chr10:28532466-28532862 | Common:5; Rare:156 |