| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:46104654-46104843 | Common:3; Rare:42 | ||||
| chr18:46173335-46173636 | Common:1; Rare:66 | ||||
| chr18:46173873-46174204 | Common:2; Rare:80 | ||||
| chr18:46333632-46333723 | Rare:20 | ||||
| chr18:46916832-46916899 | Rare:17 | ||||
| chr18:46916925-46916967 | Rare:11 | ||||
| chr18:46917376-46917716 | Common:3; Rare:134 | ||||
| chr18:46947165-46947255 | Common:1; Rare:12 | ||||
| chr18:47150078-47150376 | Common:3; Rare:90 | ||||
| chr18:47150392-47150701 | Common:4; Rare:114 | ||||
| chr18:47176258-47176424 | Common:1; Rare:78; Clinvar (benign):2 | ||||
| chr18:47929783-47929990 | Common:1; Rare:42 | ||||
| chr18:47930043-47930115 | Rare:19 | ||||
| chr18:47930272-47930422 | Common:1; Rare:70 | ||||
| chr18:47930431-47930692 | Common:1; Rare:119 |