| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:14651486-14651802 | Rare:91 | ||||
| chr3:14947402-14947569 | Common:2; Rare:84 | ||||
| chr3:15427471-15427623 | Common:1; Rare:57 | ||||
| chr3:15601507-15601804 | Common:4; Rare:124; Clinvar:1 | ||||
| chr3:16264885-16265229 | Common:2; Rare:109 | ||||
| chr3:16513475-16513802 | Common:4; Rare:84 | ||||
| chr3:19946974-19947433 | Common:7; Rare:169 | ||||
| chr3:20186182-20186415 | Common:2; Rare:75 | ||||
| chr3:23202971-23203191 | Rare:74 | ||||
| chr3:23916911-23917181 | Rare:102 | ||||
| chr3:25428107-25428289 | Rare:34 | ||||
| chr3:25783392-25783640 | Common:2; Rare:77; Clinvar (benign):3 | ||||
| chr3:25789904-25790118 | Common:4; Rare:77 | ||||
| chr3:27369338-27369586 | Rare:54 | ||||
| chr3:28348779-28348888 | Common:1; Rare:29 |