Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:92835677-92835781 | Rare:24 | ||||
chr1:92841460-92841802 | Common:3; Rare:76; Clinvar:1; Clinvar (benign):1 | ||||
chr1:92845316-92845506 | Common:1; Rare:33 | ||||
chr1:93133740-93134198 | Rare:133 | ||||
chr1:93261924-93261978 | Rare:12 | ||||
chr1:93324077-93324206 | Rare:24 | ||||
chr1:93338487-93338543 | Rare:8 | ||||
chr1:93338711-93338943 | Rare:37 | ||||
chr1:93574421-93574499 | Rare:16 | ||||
chr1:93586164-93586258 | Common:1; Rare:13 | ||||
chr1:93595079-93595295 | Common:2; Rare:31 | ||||
chr1:93619347-93619431 | Rare:13 | ||||
chr1:93657738-93657916 | Common:1; Rare:32 | ||||
chr1:93659816-93660015 | Common:2; Rare:32 | ||||
chr1:93660190-93660223 | Common:1; Rare:7 |