Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:85530030-85530176 | Common:1; Rare:32 | ||||
chr14:90396887-90397145 | Common:3; Rare:129 | ||||
chr14:92040031-92040170 | Common:2; Rare:33; Clinvar (benign):1 | ||||
chr14:92121667-92121985 | Common:4; Rare:105 | ||||
chr14:92794004-92794370 | Rare:110 | ||||
chr14:93184882-93185001 | Rare:37 | ||||
chr14:93207038-93207277 | Common:2; Rare:115 | ||||
chr14:94081150-94081366 | Common:3; Rare:71 | ||||
chr14:96363369-96363552 | Common:1; Rare:62 | ||||
chr14:96502286-96502446 | Rare:61 | ||||
chr14:100376269-100376485 | Common:3; Rare:73 | ||||
chr14:102139684-102139914 | Rare:79 | ||||
chr14:102362862-102363075 | Rare:100 | ||||
chr14:103562624-103563013 | Common:6; Rare:139; Clinvar (benign):2 | ||||
chr15:30903732-30903938 | Common:1; Rare:54 |