Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:103789713-103790011 | Common:6; Rare:36 | ||||
chr10:103890259-103890569 | Rare:50 | ||||
chr10:103892312-103892437 | Rare:23 | ||||
chr10:103967807-103967893 | Rare:15 | ||||
chr10:104039462-104039642 | Common:1; Rare:60; Clinvar (benign):1 | ||||
chr10:104047760-104048057 | Rare:78 | ||||
chr10:110872558-110872640 | Common:1; Rare:29 | ||||
chr10:114515716-114515830 | Rare:22 | ||||
chr10:114576106-114576292 | Rare:28 | ||||
chr10:119840849-119841117 | Common:1; Rare:60 | ||||
chr10:122338959-122339187 | Rare:45 | ||||
chr10:123157841-123157962 | Rare:29 | ||||
chr10:130110466-130110597 | Common:3; Rare:49 | ||||
chr10:131970932-131971010 | Rare:25 | ||||
chr10:132902736-132903017 | Common:1; Rare:44 |