Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:151266488-151266525 | Rare:5 | ||||
chr1:151281241-151281554 | Common:4; Rare:101 | ||||
chr1:151281957-151282327 | Rare:106 | ||||
chr1:151327351-151327443 | Common:1; Rare:29 | ||||
chr1:151327621-151327808 | Common:2; Rare:38 | ||||
chr1:151346814-151347037 | Rare:63 | ||||
chr1:151347201-151347350 | Rare:29 | ||||
chr1:151399361-151399596 | Common:2; Rare:64; Clinvar (pathogenic):1 | ||||
chr1:151540137-151540319 | Rare:51 | ||||
chr1:151612128-151612211 | Rare:23 | ||||
chr1:151763366-151763574 | Common:2; Rare:86 | ||||
chr1:151790422-151790863 | Common:3; Rare:107 | ||||
chr1:151909375-151909709 | Common:4; Rare:120 | ||||
chr1:153535962-153536153 | Common:1; Rare:44 | ||||
chr1:153545100-153545299 | Rare:25 |