Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:184851027-184851450 | Common:2; Rare:81 | ||||
chr5:1479570-1479890 | Rare:88 | ||||
chr5:14757943-14758113 | Common:1; Rare:20 | ||||
chr5:17118587-17119002 | Common:2; Rare:78 | ||||
chr5:34586254-34586412 | Rare:34 | ||||
chr5:40406836-40407054 | Common:5; Rare:38 | ||||
chr5:42950744-42950935 | Rare:55 | ||||
chr5:43017982-43018145 | Common:1; Rare:35 | ||||
chr5:54519297-54519573 | Common:2; Rare:89 | ||||
chr5:56816849-56817006 | Common:1; Rare:40 | ||||
chr5:61541915-61542096 | Rare:35 | ||||
chr5:78175694-78175839 | Common:2; Rare:44; Clinvar (benign):1 | ||||
chr5:80146230-80146293 | Rare:18 | ||||
chr5:83490881-83491152 | Common:1; Rare:41 | ||||
chr5:91314373-91314600 | Common:3; Rare:42 |