Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:28863498-28863552 | Rare:12 | ||||
chr16:28925162-28925251 | Rare:23 | ||||
chr16:29805335-29805762 | Common:2; Rare:201 | ||||
chr16:29807973-29808184 | Rare:117 | ||||
chr16:29926193-29926316 | Common:2; Rare:44 | ||||
chr16:29995606-29995729 | Rare:55 | ||||
chr16:29996067-29996296 | Common:2; Rare:81 | ||||
chr16:30065721-30065912 | Rare:70 | ||||
chr16:30069543-30070013 | Common:1; Rare:171; Clinvar:6; Clinvar (benign):7 | ||||
chr16:30355207-30355488 | Common:2; Rare:92 | ||||
chr16:30407473-30407655 | Rare:62 | ||||
chr16:30534913-30535113 | Common:2; Rare:70 | ||||
chr16:30698058-30698196 | Rare:69 | ||||
chr16:31074238-31074454 | Common:1; Rare:62 | ||||
chr16:31459331-31459517 | Common:1; Rare:76 |