Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:93184828-93185371 | Rare:164 | ||||
chr14:93206977-93207288 | Common:2; Rare:152 | ||||
chr14:93976559-93976860 | Rare:59 | ||||
chr14:94026190-94026499 | Common:1; Rare:75 | ||||
chr14:94081133-94081356 | Common:4; Rare:73 | ||||
chr14:95157422-95157711 | Common:4; Rare:102 | ||||
chr14:95319795-95320155 | Common:5; Rare:91 | ||||
chr14:95533550-95533659 | Rare:46 | ||||
chr14:95534539-95534705 | Common:2; Rare:66 | ||||
chr14:95535345-95535357 | Rare:7 | ||||
chr14:95535368-95535406 | Rare:19; Clinvar (pathogenic):1 | ||||
chr14:96363295-96363552 | Common:1; Rare:87 | ||||
chr14:96391799-96392152 | Common:2; Rare:101 | ||||
chr14:96502232-96502595 | Common:2; Rare:153 | ||||
chr14:96502775-96502871 | Common:1; Rare:30 |