Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:94390604-94390771 | Common:1; Rare:45 | ||||
chr14:94504275-94504403 | Rare:35 | ||||
chr14:95157434-95157685 | Common:4; Rare:91 | ||||
chr14:95534609-95534679 | Rare:19 | ||||
chr14:95535348-95535378 | Rare:15 | ||||
chr14:96204726-96204850 | Common:1; Rare:34 | ||||
chr14:96363333-96363553 | Common:1; Rare:72 | ||||
chr14:96502308-96502446 | Rare:56 | ||||
chr14:100376259-100376489 | Common:3; Rare:76 | ||||
chr14:101809686-101809890 | Rare:42 | ||||
chr14:102086994-102087429 | Common:5; Rare:189 | ||||
chr14:102139671-102139920 | Rare:85 | ||||
chr14:102362862-102363092 | Rare:103 | ||||
chr14:102928434-102928653 | Rare:78 | ||||
chr14:103562624-103563053 | Common:8; Rare:170; Clinvar (benign):5 |