Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:21526378-21526568 | Common:1; Rare:61 | ||||
chr10:21533955-21534375 | Common:3; Rare:172 | ||||
chr10:22316255-22316452 | Rare:89 | ||||
chr10:24208854-24209184 | Rare:95 | ||||
chr10:24238401-24238705 | Common:1; Rare:44 | ||||
chr10:24239278-24239382 | Rare:23 | ||||
chr10:24466435-24466560 | Rare:22 | ||||
chr10:24722709-24722832 | Rare:36 | ||||
chr10:27100419-27100582 | Common:3; Rare:50; Clinvar:4; Clinvar (benign):2 | ||||
chr10:27154315-27154446 | Rare:33 | ||||
chr10:27240763-27240897 | Rare:31 | ||||
chr10:27242058-27242207 | Common:1; Rare:64 | ||||
chr10:28532454-28532826 | Common:5; Rare:143 | ||||
chr10:28532990-28533200 | Rare:85 | ||||
chr10:30059501-30059689 | Common:1; Rare:70 |