| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:49340615-49340917 | Common:5; Rare:155 | ||||
| chr3:49411874-49412453 | Common:12; Rare:1174 | ||||
| chr3:49429200-49429540 | Common:4; Rare:281 | ||||
| chr3:49429560-49429910 | Common:4; Rare:146 | ||||
| chr3:49468904-49470343 | Common:13; Rare:1005 | ||||
| chr3:49470347-49470879 | Common:1; Rare:230; Clinvar (benign):2 | ||||
| chr3:49554239-49554639 | Common:2; Rare:401 | ||||
| chr3:49673161-49674035 | Common:21; Rare:471 | ||||
| chr3:49674107-49674605 | Common:9; Rare:714 | ||||
| chr3:49674954-49675354 | Rare:136 | ||||
| chr3:49688959-49689710 | Common:2; Rare:441 | ||||
| chr3:49689970-49690400 | Rare:133 | ||||
| chr3:49723228-49723645 | Common:3; Rare:265; Clinvar:4; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
| chr3:49723760-49724303 | Common:64; Rare:893 | ||||
| chr3:49724380-49724543 | Rare:59 |