Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:17643904-17644301 | Common:2; Rare:122 | ||||
chr10:18651564-18651675 | Common:1; Rare:43 | ||||
chr10:18659259-18659403 | Common:2; Rare:46 | ||||
chr10:24722704-24722836 | Rare:37 | ||||
chr10:27154316-27154474 | Rare:42 | ||||
chr10:27155203-27155391 | Common:4; Rare:67; Clinvar:2; Clinvar (benign):4 | ||||
chr10:27242058-27242211 | Common:1; Rare:66 | ||||
chr10:28532463-28532890 | Common:5; Rare:160 | ||||
chr10:28533002-28533206 | Rare:82 | ||||
chr10:28677245-28677526 | Common:5; Rare:130 | ||||
chr10:29634863-29635037 | Rare:43 | ||||
chr10:29735772-29735976 | Common:3; Rare:40 | ||||
chr10:29736936-29737105 | Common:2; Rare:48 | ||||
chr10:30059501-30059774 | Common:2; Rare:87 | ||||
chr10:30433879-30434188 | Common:3; Rare:80 |