Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:204411741-204412295 | Common:13; Rare:158 | ||||
chr1:204494056-204494276 | Rare:45 | ||||
chr1:204494429-204494484 | Rare:12 | ||||
chr1:204494510-204495003 | Common:1; Rare:137 | ||||
chr1:204495086-204495262 | Rare:37 | ||||
chr1:204515759-204515881 | Rare:28 | ||||
chr1:204516137-204516764 | Common:2; Rare:160 | ||||
chr1:204525164-204525322 | Common:1; Rare:40 | ||||
chr1:205121875-205122486 | Common:5; Rare:176 | ||||
chr1:205211184-205211510 | Common:2; Rare:139; Clinvar:1; Clinvar (pathogenic):1 | ||||
chr1:205211518-205211853 | Rare:83 | ||||
chr1:205591867-205592067 | Rare:53 | ||||
chr1:205592075-205592140 | Rare:15 | ||||
chr1:205631377-205631665 | Common:5; Rare:104 | ||||
chr1:205631799-205632180 | Common:4; Rare:141 |