Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:67429989-67430439 | Rare:172 | ||||
chr1:67430443-67430550 | Rare:29 | ||||
chr1:67685000-67685218 | Common:1; Rare:54 | ||||
chr1:67685761-67686118 | Common:1; Rare:111 | ||||
chr1:67833332-67833549 | Common:2; Rare:86 | ||||
chr1:68232429-68232666 | Common:1; Rare:52 | ||||
chr1:68497040-68497320 | Common:3; Rare:93 | ||||
chr1:69568202-69568328 | Rare:41 | ||||
chr1:70205527-70205775 | Rare:85 | ||||
chr1:70221290-70221735 | Rare:180 | ||||
chr1:70354664-70354862 | Rare:66 | ||||
chr1:70411069-70411295 | Common:2; Rare:58; Clinvar:1; Clinvar (benign):1 | ||||
chr1:71080938-71081383 | Rare:118 | ||||
chr1:74198117-74198350 | Common:3; Rare:126 | ||||
chr1:74732960-74733359 | Common:6; Rare:138 |