Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:93207055-93207294 | Common:2; Rare:120 | ||||
chr14:94081154-94081376 | Common:3; Rare:71 | ||||
chr14:96363333-96363550 | Common:1; Rare:69 | ||||
chr14:100375371-100375753 | Common:3; Rare:63 | ||||
chr14:100376259-100376485 | Common:3; Rare:74 | ||||
chr14:102139697-102139916 | Rare:73 | ||||
chr14:102362856-102363110 | Rare:109 | ||||
chr14:103528985-103529235 | Common:1; Rare:69 | ||||
chr14:103562636-103563002 | Common:5; Rare:127; Clinvar (benign):1 | ||||
chr14:103715409-103715860 | Common:1; Rare:155 | ||||
chr14:105248457-105248614 | Common:4; Rare:80 | ||||
chr14:105419791-105419885 | Rare:18 | ||||
chr15:34101849-34102080 | Common:1; Rare:45 | ||||
chr15:35546151-35546258 | Common:1; Rare:38 | ||||
chr15:37100523-37100768 | Common:1; Rare:81 |