| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:35290150-35290391 | Common:2; Rare:78 | ||||
| chr18:35344388-35344655 | Common:2; Rare:84 | ||||
| chr18:35972449-35972756 | Common:4; Rare:107 | ||||
| chr18:36067425-36067722 | Common:2; Rare:103 | ||||
| chr18:36129177-36129548 | Common:4; Rare:117 | ||||
| chr18:36129812-36129934 | Rare:51 | ||||
| chr18:36187413-36187525 | Common:2; Rare:43 | ||||
| chr18:36828706-36829244 | Common:3; Rare:208 | ||||
| chr18:44680792-44680996 | Common:1; Rare:54; Clinvar:2; Clinvar (benign):1 | ||||
| chr18:45967243-45967531 | Common:1; Rare:108 | ||||
| chr18:46098175-46098386 | Common:11; Rare:94; Clinvar (benign):8 | ||||
| chr18:46104135-46104426 | Common:4; Rare:90; Clinvar (benign):1 | ||||
| chr18:46917355-46917652 | Common:3; Rare:130 | ||||
| chr18:47150425-47150525 | Common:3; Rare:42 | ||||
| chr18:48539002-48539287 | Common:2; Rare:61 |