Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:44808761-44809068 | Common:4; Rare:113 | ||||
chr5:52787823-52787987 | Common:1; Rare:31 | ||||
chr5:52989171-52989365 | Common:4; Rare:56; Clinvar (benign):1 | ||||
chr5:53109716-53109909 | Common:1; Rare:98; Clinvar:3 | ||||
chr5:54310518-54310711 | Rare:61 | ||||
chr5:55160087-55160280 | Rare:59 | ||||
chr5:55307604-55308073 | Common:5; Rare:172 | ||||
chr5:55994797-55995196 | Rare:135 | ||||
chr5:56952100-56952368 | Rare:105 | ||||
chr5:57173550-57173871 | Common:2; Rare:112 | ||||
chr5:58459964-58460246 | Common:6; Rare:117 | ||||
chr5:59768478-59768586 | Rare:31 | ||||
chr5:59768632-59768892 | Rare:62 | ||||
chr5:60700067-60700237 | Common:1; Rare:67 | ||||
chr5:60945026-60945253 | Common:5; Rare:85; Clinvar:3; Clinvar (benign):5 |