Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:153633985-153634177 | Common:1; Rare:58 | ||||
chr1:153634331-153634412 | Common:1; Rare:23 | ||||
chr1:153775201-153775436 | Rare:122 | ||||
chr1:153932725-153932942 | Common:1; Rare:53 | ||||
chr1:153941997-153942220 | Common:2; Rare:55 | ||||
chr1:153945190-153945317 | Rare:20 | ||||
chr1:153958192-153958418 | Common:2; Rare:63 | ||||
chr1:153962755-153962920 | Rare:30 | ||||
chr1:153963495-153963744 | Common:2; Rare:68 | ||||
chr1:153967623-153967939 | Common:1; Rare:57 | ||||
chr1:153990583-153990775 | Common:1; Rare:65 | ||||
chr1:154170393-154170688 | Rare:61; Clinvar (benign):1 | ||||
chr1:154172911-154173185 | Common:1; Rare:49; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
chr1:154182988-154183114 | Rare:32 | ||||
chr1:154183141-154183308 | Rare:58 |