| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:15427471-15427629 | Common:1; Rare:57 | ||||
| chr3:15601512-15601810 | Common:4; Rare:127; Clinvar:2 | ||||
| chr3:16264872-16265243 | Common:2; Rare:124 | ||||
| chr3:16513641-16513775 | Common:4; Rare:34 | ||||
| chr3:17742596-17742767 | Common:3; Rare:53 | ||||
| chr3:19946974-19947439 | Common:7; Rare:173 | ||||
| chr3:20186176-20186415 | Common:2; Rare:77 | ||||
| chr3:23805812-23806061 | Common:1; Rare:51 | ||||
| chr3:23916911-23917359 | Rare:150 | ||||
| chr3:24494784-24494883 | Rare:25 | ||||
| chr3:25428102-25428391 | Rare:65 | ||||
| chr3:25783391-25783634 | Common:2; Rare:77; Clinvar (benign):3 | ||||
| chr3:28241439-28241659 | Common:1; Rare:72 | ||||
| chr3:28348592-28349196 | Common:4; Rare:180 | ||||
| chr3:29280837-29281358 | Common:14; Rare:104 |