| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:16264885-16265243 | Common:2; Rare:116 | ||||
| chr3:16513492-16513807 | Common:4; Rare:73 | ||||
| chr3:16884947-16885208 | Common:7; Rare:81 | ||||
| chr3:17742596-17742913 | Common:3; Rare:108 | ||||
| chr3:19946974-19947438 | Common:7; Rare:173 | ||||
| chr3:20186139-20186415 | Common:4; Rare:90 | ||||
| chr3:21751067-21751413 | Common:4; Rare:109 | ||||
| chr3:23202926-23203214 | Common:1; Rare:101 | ||||
| chr3:23805771-23806066 | Common:2; Rare:55 | ||||
| chr3:23916878-23917181 | Rare:116 | ||||
| chr3:25428106-25428391 | Rare:64 | ||||
| chr3:25664889-25665092 | Common:2; Rare:65 | ||||
| chr3:25783371-25783627 | Common:2; Rare:89; Clinvar (benign):3 | ||||
| chr3:25789993-25790118 | Common:3; Rare:48 | ||||
| chr3:26623289-26623603 | Common:1; Rare:55 |