| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:11154362-11154542 | Common:3; Rare:45 | ||||
| chr3:11719432-11719556 | Rare:38 | ||||
| chr3:12287733-12287970 | Common:6; Rare:47 | ||||
| chr3:12663981-12664330 | Common:2; Rare:95; Clinvar:2; Clinvar (benign):7 | ||||
| chr3:13420226-13420452 | Common:1; Rare:63 | ||||
| chr3:13480036-13480339 | Common:2; Rare:71 | ||||
| chr3:14124728-14125179 | Common:4; Rare:128; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14178564-14178869 | Common:2; Rare:160; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:14402435-14402749 | Common:3; Rare:67 | ||||
| chr3:14651486-14651807 | Rare:93 | ||||
| chr3:14947307-14947554 | Common:3; Rare:110 | ||||
| chr3:15206028-15206287 | Rare:99 | ||||
| chr3:15427478-15427623 | Common:1; Rare:51 | ||||
| chr3:15601516-15601801 | Common:4; Rare:120; Clinvar:1 | ||||
| chr3:16264866-16265227 | Common:2; Rare:121 |