Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:151165830-151166177 | Common:3; Rare:95 | ||||
chr1:151190048-151190288 | Rare:68 | ||||
chr1:151198394-151198613 | Common:1; Rare:78 | ||||
chr1:151254611-151254905 | Common:3; Rare:76 | ||||
chr1:151281241-151281640 | Common:6; Rare:126 | ||||
chr1:151281876-151282337 | Rare:126 | ||||
chr1:151327645-151327829 | Common:2; Rare:38 | ||||
chr1:151346823-151347037 | Rare:61 | ||||
chr1:151347220-151347545 | Rare:75 | ||||
chr1:151399478-151399635 | Common:2; Rare:60; Clinvar (pathogenic):2 | ||||
chr1:151511139-151511406 | Common:3; Rare:62 | ||||
chr1:151540137-151540319 | Rare:51 | ||||
chr1:151715965-151716290 | Common:3; Rare:63 | ||||
chr1:151716761-151717144 | Common:2; Rare:112 | ||||
chr1:151721278-151721599 | Common:2; Rare:92 |