Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:50189685-50189913 | Common:3; Rare:50; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
chr17:50190000-50190356 | Common:1; Rare:100; Clinvar:4; Clinvar (benign):3 | ||||
chr17:64975551-64975695 | Common:1; Rare:46 | ||||
chr17:76557631-76557806 | Common:1; Rare:61 | ||||
chr18:5238030-5238125 | Common:1; Rare:40 | ||||
chr19:6712383-6712627 | Rare:80; Clinvar (benign):3 | ||||
chr19:27793376-27793467 | Common:1; Rare:26 | ||||
chr19:27793891-27794064 | Common:1; Rare:36 | ||||
chr19:36797259-36797545 | Rare:60 | ||||
chr19:42287190-42287398 | Common:1; Rare:63; Clinvar:1 | ||||
chr19:46860778-46861121 | Common:3; Rare:112 | ||||
chr19:48966400-48966702 | Rare:100; Clinvar:1 | ||||
chr2:45192245-45192404 | Common:2; Rare:32 | ||||
chr2:55923040-55923157 | Rare:21 | ||||
chr2:70088209-70088358 | Common:1; Rare:41 |