Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:14264712-14264885 | Common:1; Rare:54 | ||||
chr5:14769147-14769365 | Rare:48; Clinvar (benign):1 | ||||
chr5:18437730-18437897 | Common:1; Rare:24 | ||||
chr5:18518031-18518325 | Common:2; Rare:48 | ||||
chr5:20463507-20463652 | Rare:25 | ||||
chr5:21341260-21341456 | Common:2; Rare:41 | ||||
chr5:23951253-23951693 | Common:2; Rare:174 | ||||
chr5:23952039-23952198 | Common:1; Rare:41 | ||||
chr5:27472103-27472321 | Common:1; Rare:43 | ||||
chr5:28670502-28670575 | Rare:16 | ||||
chr5:28670579-28670733 | Common:2; Rare:31 | ||||
chr5:32505315-32505483 | Rare:28 | ||||
chr5:34244387-34244574 | Rare:40 | ||||
chr5:36875907-36876040 | Rare:31 | ||||
chr5:37777621-37777830 | Common:3; Rare:49 |