Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:160222628-160222899 | Common:1; Rare:52 | ||||
chr1:160237115-160237157 | Rare:11; Clinvar (pathogenic):1 | ||||
chr1:160292121-160292303 | Rare:37 | ||||
chr1:160294814-160294997 | Common:1; Rare:38 | ||||
chr1:160297729-160297994 | Common:1; Rare:49 | ||||
chr1:160934327-160934428 | Rare:20 | ||||
chr1:160947982-160948151 | Common:1; Rare:29 | ||||
chr1:160999874-161000180 | Common:1; Rare:66 | ||||
chr1:161020184-161020270 | Rare:15 | ||||
chr1:161120222-161120554 | Common:1; Rare:80 | ||||
chr1:161123183-161123329 | Rare:39 | ||||
chr1:161216974-161217283 | Rare:50 | ||||
chr1:161389892-161390198 | Common:4; Rare:64 | ||||
chr1:161399314-161399414 | Rare:27 | ||||
chr1:161399597-161399882 | Common:6; Rare:165 |