Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:82278323-82278692 | Common:4; Rare:120 | ||||
chr5:83077339-83077602 | Common:1; Rare:78 | ||||
chr5:84384378-84384529 | Rare:44 | ||||
chr5:88883162-88883324 | Rare:55; Clinvar:3; Clinvar (benign):1 | ||||
chr5:90409728-90410057 | Common:8; Rare:109 | ||||
chr5:94618599-94618696 | Rare:22 | ||||
chr5:95554964-95555122 | Rare:44 | ||||
chr5:103120116-103120386 | Common:1; Rare:65 | ||||
chr5:108748702-108748970 | Common:2; Rare:86 | ||||
chr5:110738929-110739063 | Common:2; Rare:47 | ||||
chr5:115841529-115841602 | Common:1; Rare:49 | ||||
chr5:115841851-115842016 | Common:3; Rare:56 | ||||
chr5:122845516-122845621 | Common:3; Rare:40 | ||||
chr5:129460104-129460314 | Common:4; Rare:32 | ||||
chr5:131635194-131635424 | Common:1; Rare:86 |