| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:149608223-149608370 | Common:1; Rare:33 | ||||
| chr7:149624565-149624870 | Common:3; Rare:95 | ||||
| chr7:150377945-150378458 | Common:2; Rare:103 | ||||
| chr7:150379960-150380006 | Rare:14 | ||||
| chr7:150380033-150380107 | Rare:22 | ||||
| chr7:150380188-150380310 | Rare:14 | ||||
| chr7:150380497-150380673 | Common:1; Rare:32 | ||||
| chr7:150406735-150406838 | Common:1; Rare:18 | ||||
| chr7:150406844-150407234 | Rare:57 | ||||
| chr7:150433440-150433500 | Rare:8 | ||||
| chr7:150433656-150433768 | Common:1; Rare:12 | ||||
| chr7:150435697-150435994 | Common:5; Rare:54 | ||||
| chr7:150451505-150451657 | Common:1; Rare:35 | ||||
| chr7:150755526-150755711 | Common:7; Rare:38 | ||||
| chr7:150974624-150974877 | Common:1; Rare:68; Clinvar:7; Clinvar (benign):8; Clinvar (pathogenic):3 |