Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:65525495-65525792 | Common:1; Rare:75 | ||||
chr1:65525800-65526077 | Common:1; Rare:56 | ||||
chr1:66924845-66925050 | Rare:83 | ||||
chr1:66925193-66925503 | Common:2; Rare:97 | ||||
chr1:67053925-67054229 | Common:2; Rare:106 | ||||
chr1:67429989-67430531 | Rare:196 | ||||
chr1:70205490-70205759 | Rare:101 | ||||
chr1:70221316-70221639 | Rare:124 | ||||
chr1:70354697-70354862 | Rare:58 | ||||
chr1:70411069-70411583 | Common:2; Rare:144; Clinvar:2; Clinvar (benign):1 | ||||
chr1:71080992-71081367 | Rare:100 | ||||
chr1:74198148-74198292 | Common:1; Rare:79 | ||||
chr1:74732814-74733367 | Common:6; Rare:173 | ||||
chr1:77219334-77219482 | Common:1; Rare:73 | ||||
chr1:77979006-77979298 | Common:2; Rare:103 |