Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:95534609-95534679 | Rare:19 | ||||
chr14:95535352-95535379 | Rare:12 | ||||
chr14:96363271-96363550 | Common:1; Rare:91 | ||||
chr14:96502300-96502586 | Common:1; Rare:123 | ||||
chr14:99480728-99481013 | Common:2; Rare:110 | ||||
chr14:100375438-100375755 | Common:2; Rare:49 | ||||
chr14:100376269-100376521 | Common:3; Rare:83 | ||||
chr14:102139671-102139932 | Rare:91 | ||||
chr14:102362847-102363092 | Rare:112 | ||||
chr14:103333957-103334252 | Common:1; Rare:121 | ||||
chr14:103529069-103529243 | Common:1; Rare:53 | ||||
chr14:103562303-103562392 | Rare:31 | ||||
chr14:103562622-103563019 | Common:6; Rare:143; Clinvar (benign):2 | ||||
chr14:103673158-103673388 | Common:1; Rare:53 | ||||
chr14:103715452-103715844 | Common:1; Rare:127 |