Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:154961698-154961830 | Rare:56 | ||||
chr1:154966196-154966364 | Rare:45 | ||||
chr1:154970163-154970377 | Rare:69 | ||||
chr1:154970688-154970896 | Common:1; Rare:40 | ||||
chr1:154971092-154971291 | Rare:33 | ||||
chr1:154974339-154974801 | Rare:118 | ||||
chr1:154983059-154983402 | Common:2; Rare:68; Clinvar (benign):1 | ||||
chr1:155051159-155051368 | Common:1; Rare:70 | ||||
chr1:155058095-155058407 | Common:1; Rare:80 | ||||
chr1:155201676-155201755 | Rare:18 | ||||
chr1:155254972-155255239 | Common:3; Rare:55 | ||||
chr1:155255417-155255569 | Common:1; Rare:32 | ||||
chr1:155308365-155308982 | Common:1; Rare:121 | ||||
chr1:155324320-155324544 | Common:2; Rare:93 | ||||
chr1:155562794-155562970 | Common:1; Rare:99 |