Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:40418783-40418943 | Common:1; Rare:18 | ||||
chr1:42924280-42924461 | Common:1; Rare:55 | ||||
chr1:44048386-44048464 | Rare:9 | ||||
chr1:45205844-45205950 | Common:1; Rare:33 | ||||
chr1:45303634-45303859 | Common:1; Rare:61 | ||||
chr1:45647511-45647653 | Common:1; Rare:27 | ||||
chr1:45651978-45652025 | Rare:6 | ||||
chr1:45692991-45693128 | Rare:24 | ||||
chr1:46195846-46195992 | Rare:40; Clinvar:6; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
chr1:46580570-46580876 | Common:2; Rare:62 | ||||
chr1:46592499-46592596 | Common:1; Rare:13 | ||||
chr1:46592795-46592936 | Rare:22 | ||||
chr1:46718271-46718540 | Common:2; Rare:59 | ||||
chr1:47437648-47437764 | Common:1; Rare:30 | ||||
chr1:51518138-51518308 | Rare:37 |