Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:9933507-9933857 | Common:2; Rare:140; Clinvar:3 | ||||
chr3:9933993-9934065 | Rare:19 | ||||
chr3:10026334-10026434 | Rare:30 | ||||
chr3:11643610-11643731 | Common:1; Rare:19 | ||||
chr3:11719427-11719589 | Rare:49 | ||||
chr3:12664087-12664300 | Common:1; Rare:58; Clinvar:1; Clinvar (benign):2 | ||||
chr3:14124746-14125167 | Common:4; Rare:123; Clinvar:4; Clinvar (benign):1 | ||||
chr3:14178573-14178861 | Common:2; Rare:148; Clinvar:3; Clinvar (benign):1 | ||||
chr3:14402441-14402628 | Rare:47 | ||||
chr3:14651468-14651788 | Rare:88 | ||||
chr3:14947233-14947554 | Common:4; Rare:147 | ||||
chr3:15206028-15206248 | Rare:75 | ||||
chr3:15427510-15427629 | Rare:37 | ||||
chr3:15601550-15601769 | Common:3; Rare:81; Clinvar:1 | ||||
chr3:16264881-16265220 | Common:2; Rare:109 |