Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:154942638-154942762 | Rare:34 | ||||
chr1:154947465-154947673 | Common:2; Rare:63 | ||||
chr1:155008041-155008151 | Rare:29 | ||||
chr1:155008488-155008875 | Rare:70 | ||||
chr1:155178798-155179111 | Common:1; Rare:77 | ||||
chr1:155227415-155227733 | Common:3; Rare:93 | ||||
chr1:155561831-155562030 | Common:1; Rare:43 | ||||
chr1:155637507-155637684 | Common:1; Rare:36 | ||||
chr1:155977128-155977315 | Rare:29 | ||||
chr1:156130320-156130629 | Common:2; Rare:77; Clinvar:1; Clinvar (benign):2 | ||||
chr1:156218097-156218316 | Rare:29 | ||||
chr1:156480939-156481214 | Common:2; Rare:77 | ||||
chr1:156661385-156661580 | Common:1; Rare:37 | ||||
chr1:156800227-156800473 | Common:1; Rare:51 | ||||
chr1:157839370-157839504 | Common:1; Rare:37 |