Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:151165850-151166162 | Common:3; Rare:87 | ||||
chr1:151254500-151254803 | Rare:73 | ||||
chr1:151281957-151282327 | Rare:106 | ||||
chr1:151327358-151327473 | Common:2; Rare:34 | ||||
chr1:151346852-151347059 | Rare:55 | ||||
chr1:151347220-151347492 | Rare:64 | ||||
chr1:151399339-151399615 | Common:3; Rare:75; Clinvar (pathogenic):1 | ||||
chr1:151511129-151511436 | Common:4; Rare:68 | ||||
chr1:151540137-151540319 | Rare:51 | ||||
chr1:151763457-151763586 | Common:1; Rare:51 | ||||
chr1:151790426-151790863 | Common:3; Rare:106 | ||||
chr1:151909397-151909593 | Common:1; Rare:76 | ||||
chr1:153535971-153536275 | Common:2; Rare:62 | ||||
chr1:153633862-153634123 | Common:4; Rare:80 | ||||
chr1:153634357-153634528 | Common:1; Rare:53 |