Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:131161025-131161235 | Common:1; Rare:30 | ||||
chr5:131379787-131379937 | Rare:29 | ||||
chr5:132476734-132476863 | Common:1; Rare:21 | ||||
chr5:132487105-132487323 | Rare:44 | ||||
chr5:133930368-133930704 | Common:1; Rare:56 | ||||
chr5:134926841-134927048 | Common:5; Rare:50 | ||||
chr5:134927076-134927133 | Common:1; Rare:14 | ||||
chr5:137752761-137753060 | Rare:74 | ||||
chr5:139325501-139325793 | Rare:79; Clinvar:4; Clinvar (benign):2 | ||||
chr5:141318272-141318515 | Common:1; Rare:42 | ||||
chr5:141319116-141319175 | Rare:13 | ||||
chr5:141319454-141319678 | Common:2; Rare:37 | ||||
chr5:150402959-150403290 | Common:1; Rare:90 | ||||
chr5:150407125-150407457 | Common:2; Rare:83 | ||||
chr5:150408127-150408354 | Common:1; Rare:43 |