Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:155129065-155129375 | Rare:70 | ||||
chr1:155135129-155135465 | Rare:67 | ||||
chr1:155135718-155135892 | Common:2; Rare:72 | ||||
chr1:155172880-155172986 | Common:1; Rare:41 | ||||
chr1:155209143-155209263 | Rare:53 | ||||
chr1:155236408-155236631 | Common:1; Rare:70; Clinvar (pathogenic):2 | ||||
chr1:155308365-155308572 | Rare:30 | ||||
chr1:155308643-155308954 | Common:1; Rare:69 | ||||
chr1:155562731-155562970 | Common:1; Rare:131 | ||||
chr1:155563090-155563260 | Rare:72 | ||||
chr1:155688635-155689113 | Common:2; Rare:150 | ||||
chr1:155859328-155859544 | Common:2; Rare:53 | ||||
chr1:155934349-155934587 | Common:1; Rare:94 | ||||
chr1:155978525-155978636 | Rare:29 | ||||
chr1:156054632-156054910 | Common:3; Rare:75 |