Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:65148903-65149075 | Common:2; Rare:53 | ||||
chr1:65420340-65420750 | Common:5; Rare:108; Clinvar:2; Clinvar (benign):1 | ||||
chr1:66332166-66332475 | Rare:80 | ||||
chr1:66533368-66533652 | Common:2; Rare:40 | ||||
chr1:66533667-66534196 | Common:2; Rare:129 | ||||
chr1:66924800-66925041 | Rare:101 | ||||
chr1:66925182-66925518 | Common:2; Rare:107 | ||||
chr1:66930070-66930393 | Rare:104 | ||||
chr1:67429989-67430062 | Rare:31 | ||||
chr1:67430137-67430585 | Rare:164 | ||||
chr1:67684929-67685273 | Common:3; Rare:94 | ||||
chr1:68232446-68232643 | Common:1; Rare:46 | ||||
chr1:70205534-70205771 | Rare:78 | ||||
chr1:70221290-70221537 | Rare:107 | ||||
chr1:70354659-70354844 | Rare:63 |