Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:88104361-88104508 | Rare:19 | ||||
chr10:88131829-88132207 | Common:4; Rare:68 | ||||
chr10:88254222-88254396 | Common:2; Rare:36 | ||||
chr10:88939550-88939904 | Common:1; Rare:57; Clinvar:1; Clinvar (benign):3 | ||||
chr10:88941772-88941982 | Common:1; Rare:43; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
chr10:88951820-88952015 | Common:1; Rare:34 | ||||
chr10:89415207-89415368 | Common:2; Rare:35 | ||||
chr10:89494845-89494922 | Rare:13 | ||||
chr10:89837771-89837905 | Common:4; Rare:32 | ||||
chr10:91807506-91807566 | Rare:18 | ||||
chr10:92591626-92591789 | Common:1; Rare:51 | ||||
chr10:92699750-92700041 | Common:3; Rare:49 | ||||
chr10:93417388-93417538 | Rare:25 | ||||
chr10:93420898-93421192 | Common:1; Rare:49 | ||||
chr10:93600454-93600696 | Common:3; Rare:71 |