Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:153634283-153634340 | Rare:19 | ||||
chr1:153634343-153634378 | Common:1; Rare:11 | ||||
chr1:153634384-153634445 | Rare:20 | ||||
chr1:153766810-153766985 | Rare:37 | ||||
chr1:153952192-153952434 | Common:1; Rare:70 | ||||
chr1:153963265-153963716 | Common:2; Rare:107 | ||||
chr1:153964072-153964298 | Common:1; Rare:47 | ||||
chr1:153967309-153967536 | Common:1; Rare:45 | ||||
chr1:153967710-153967948 | Rare:45 | ||||
chr1:153968182-153968253 | Rare:12 | ||||
chr1:153990706-153990829 | Common:2; Rare:74 | ||||
chr1:154172904-154173173 | Common:1; Rare:49; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
chr1:154183141-154183318 | Rare:63 | ||||
chr1:154219837-154220251 | Common:5; Rare:116 | ||||
chr1:154220340-154221043 | Common:1; Rare:232 |