| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:172750380-172750794 | Common:4; Rare:93 | ||||
| chr3:173397461-173397792 | Common:4; Rare:105 | ||||
| chr3:174440806-174441006 | Common:2; Rare:54 | ||||
| chr3:179347608-179347768 | Common:1; Rare:39 | ||||
| chr3:179451373-179451711 | Common:1; Rare:118 | ||||
| chr3:179604610-179604855 | Common:2; Rare:93 | ||||
| chr3:180602020-180602235 | Common:1; Rare:70 | ||||
| chr3:180989619-180989838 | Rare:90; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:183697982-183698112 | Common:1; Rare:47 | ||||
| chr3:183884842-183885071 | Common:2; Rare:75 | ||||
| chr3:184135248-184135388 | Common:2; Rare:37; Clinvar:2 | ||||
| chr3:184248877-184249021 | Rare:75; Clinvar:5; Clinvar (benign):2 | ||||
| chr3:184249531-184249733 | Common:1; Rare:63 | ||||
| chr3:184298946-184299338 | Common:5; Rare:119 | ||||
| chr3:184711953-184712243 | Common:1; Rare:97 |