Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:18140938-18141165 | Common:2; Rare:49 | ||||
chr10:18141570-18141716 | Common:2; Rare:28 | ||||
chr10:18651548-18651754 | Common:1; Rare:89 | ||||
chr10:18659048-18659646 | Common:4; Rare:192 | ||||
chr10:19816279-19816448 | Common:5; Rare:32 | ||||
chr10:21533943-21534330 | Common:3; Rare:164 | ||||
chr10:22316234-22316478 | Common:2; Rare:113 | ||||
chr10:24208780-24209221 | Common:1; Rare:127 | ||||
chr10:24466428-24466574 | Rare:28 | ||||
chr10:24722704-24722836 | Rare:37 | ||||
chr10:27154314-27154480 | Rare:44 | ||||
chr10:27155179-27155448 | Common:7; Rare:116; Clinvar:4; Clinvar (benign):7 | ||||
chr10:27240498-27240560 | Rare:28 | ||||
chr10:27240571-27240897 | Common:2; Rare:85 | ||||
chr10:27242058-27242241 | Common:1; Rare:78 |