Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:155001650-155001778 | Rare:30 | ||||
chr1:155003644-155003929 | Common:1; Rare:55 | ||||
chr1:155019055-155019239 | Rare:26 | ||||
chr1:155357660-155357834 | Common:1; Rare:29 | ||||
chr1:155745733-155745805 | Common:2; Rare:22 | ||||
chr1:156130334-156130643 | Common:2; Rare:80; Clinvar:2; Clinvar (benign):2 | ||||
chr1:156508384-156508641 | Rare:45 | ||||
chr1:156508978-156509134 | Rare:24 | ||||
chr1:156800161-156800522 | Common:1; Rare:70 | ||||
chr1:158177898-158178050 | Common:2; Rare:36 | ||||
chr1:160208290-160208478 | Rare:34 | ||||
chr1:160260553-160260608 | Common:2; Rare:10 | ||||
chr1:160309099-160309307 | Rare:37 | ||||
chr1:160317002-160317307 | Common:2; Rare:55 | ||||
chr1:161389928-161390214 | Common:4; Rare:56 |