Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:96363251-96363552 | Common:1; Rare:99 | ||||
chr14:96502235-96502592 | Common:2; Rare:153 | ||||
chr14:100065270-100065466 | Rare:32 | ||||
chr14:100306448-100306702 | Common:3; Rare:92 | ||||
chr14:100376264-100376514 | Common:3; Rare:81 | ||||
chr14:101809742-101809905 | Rare:33 | ||||
chr14:102085245-102085342 | Rare:45 | ||||
chr14:102086885-102087184 | Common:6; Rare:127 | ||||
chr14:102139678-102139914 | Rare:80 | ||||
chr14:102362849-102363103 | Rare:113 | ||||
chr14:103123347-103123483 | Rare:19 | ||||
chr14:103333910-103334210 | Common:3; Rare:122 | ||||
chr14:103529071-103529258 | Common:1; Rare:58 | ||||
chr14:103562620-103563007 | Common:5; Rare:138; Clinvar (benign):1 | ||||
chr14:103629133-103629211 | Rare:37 |