Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:197627840-197628017 | Common:6; Rare:66 | ||||
chr3:197850987-197851085 | Rare:17 | ||||
chr4:868633-868829 | Common:1; Rare:67 | ||||
chr4:3955407-3955615 | Common:6; Rare:64 | ||||
chr4:5825536-5825778 | Common:5; Rare:72 | ||||
chr4:6673441-6673447 | Common:1; Rare:2 | ||||
chr4:6673835-6673948 | Common:6; Rare:59 | ||||
chr4:6709265-6709318 | Rare:19 | ||||
chr4:7768998-7769181 | Rare:69 | ||||
chr4:30719347-30719709 | Common:1; Rare:82 | ||||
chr4:38664853-38665022 | Rare:51 | ||||
chr4:38868329-38868454 | Rare:26 | ||||
chr4:38908479-38908726 | Rare:68; Clinvar:1 | ||||
chr4:54231870-54232080 | Common:2; Rare:47 | ||||
chr4:54260886-54261242 | Rare:85; Clinvar:10; Clinvar (benign):4 |