| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:36129709-36130052 | Common:3; Rare:124 | ||||
| chr18:36130164-36130318 | Common:3; Rare:36 | ||||
| chr18:36187332-36187577 | Common:4; Rare:78 | ||||
| chr18:36297600-36297775 | Common:3; Rare:75 | ||||
| chr18:36828127-36828282 | Common:2; Rare:23 | ||||
| chr18:36828700-36829315 | Common:3; Rare:231 | ||||
| chr18:41954987-41955322 | Common:2; Rare:119 | ||||
| chr18:44680028-44680161 | Rare:24 | ||||
| chr18:44680615-44680765 | Rare:43 | ||||
| chr18:45825614-45825891 | Common:1; Rare:78 | ||||
| chr18:45967201-45967591 | Common:1; Rare:142; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr18:46072209-46072294 | Common:1; Rare:28 | ||||
| chr18:46097790-46098095 | Common:4; Rare:100 | ||||
| chr18:46098227-46098641 | Common:11; Rare:117; Clinvar (benign):6 | ||||
| chr18:46104172-46104459 | Common:3; Rare:89 |