Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:16817342-16817734 | Common:4; Rare:139 | ||||
chr10:17228458-17228675 | Common:1; Rare:58 | ||||
chr10:17228923-17229247 | Common:3; Rare:67 | ||||
chr10:17643898-17644276 | Common:2; Rare:112 | ||||
chr10:18651578-18651748 | Common:1; Rare:70 | ||||
chr10:22316259-22316459 | Rare:89 | ||||
chr10:24208814-24208935 | Rare:37 | ||||
chr10:24722742-24722842 | Rare:33 | ||||
chr10:25016413-25016666 | Common:8; Rare:90 | ||||
chr10:27100427-27100609 | Common:3; Rare:52; Clinvar:4; Clinvar (benign):2 | ||||
chr10:27154323-27154495 | Rare:48 | ||||
chr10:27155170-27155429 | Common:7; Rare:112; Clinvar:5; Clinvar (benign):7 | ||||
chr10:27240466-27240667 | Common:2; Rare:63 | ||||
chr10:27242058-27242237 | Common:1; Rare:76 | ||||
chr10:28532426-28532856 | Common:5; Rare:160 |