Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:78595154-78595451 | Rare:37 | ||||
chr5:93600558-93600658 | Rare:16 | ||||
chr5:93621458-93621611 | Common:3; Rare:38 | ||||
chr5:95752158-95752292 | Rare:34 | ||||
chr5:98109661-98109947 | Common:1; Rare:42 | ||||
chr5:108727770-108727939 | Common:1; Rare:34 | ||||
chr5:108728265-108728421 | Rare:52 | ||||
chr5:112006833-112007039 | Common:3; Rare:31 | ||||
chr5:136054503-136054825 | Common:3; Rare:84; Clinvar (benign):2 | ||||
chr5:150138825-150138966 | Common:1; Rare:22 | ||||
chr5:150778644-150778849 | Common:1; Rare:83 | ||||
chr5:150946540-150946826 | Common:1; Rare:59 | ||||
chr5:173454369-173454644 | Rare:46 | ||||
chr5:176348295-176348407 | Rare:27 | ||||
chr5:177489537-177489809 | Common:1; Rare:93 |