Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:41925151-41925301 | Common:1; Rare:61 | ||||
chr5:43067419-43067559 | Rare:25 | ||||
chr5:43121416-43121648 | Common:1; Rare:87 | ||||
chr5:43483837-43483967 | Common:1; Rare:45 | ||||
chr5:43602907-43603204 | Rare:72 | ||||
chr5:44808777-44808955 | Common:2; Rare:56 | ||||
chr5:52989043-52989369 | Common:5; Rare:92; Clinvar (benign):1 | ||||
chr5:53109716-53109899 | Common:1; Rare:95; Clinvar:3 | ||||
chr5:55307657-55308009 | Common:4; Rare:113 | ||||
chr5:57173548-57173858 | Common:2; Rare:109 | ||||
chr5:60488077-60488180 | Rare:14 | ||||
chr5:60700102-60700204 | Rare:42 | ||||
chr5:60945026-60945246 | Common:5; Rare:84; Clinvar:3; Clinvar (benign):5 | ||||
chr5:61162415-61162684 | Common:1; Rare:75 | ||||
chr5:62403833-62404030 | Common:3; Rare:67 |