| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:14948435-14948637 | Common:2; Rare:60 | ||||
| chr3:15205976-15206279 | Rare:111 | ||||
| chr3:15427486-15427718 | Common:1; Rare:77 | ||||
| chr3:15601138-15601338 | Common:2; Rare:54 | ||||
| chr3:15601498-15601804 | Common:4; Rare:127; Clinvar:1 | ||||
| chr3:15859784-15860127 | Common:4; Rare:111 | ||||
| chr3:16174541-16174861 | Common:1; Rare:77 | ||||
| chr3:16264859-16265224 | Common:2; Rare:124 | ||||
| chr3:18424389-18424568 | Common:1; Rare:34 | ||||
| chr3:19946974-19947497 | Common:7; Rare:192 | ||||
| chr3:20186183-20186365 | Common:1; Rare:51 | ||||
| chr3:23916898-23917231 | Rare:127 | ||||
| chr3:23917608-23918031 | Common:2; Rare:113; Clinvar (benign):1 | ||||
| chr3:24494722-24494917 | Rare:54 | ||||
| chr3:25428107-25428284 | Rare:33 |