| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:36067397-36067708 | Common:2; Rare:110 | ||||
| chr18:36129270-36129538 | Common:3; Rare:87 | ||||
| chr18:36129772-36129934 | Common:1; Rare:64 | ||||
| chr18:36187439-36187521 | Common:2; Rare:33 | ||||
| chr18:36297829-36297998 | Rare:45 | ||||
| chr18:36828742-36829169 | Common:3; Rare:174 | ||||
| chr18:41954980-41955283 | Common:2; Rare:105 | ||||
| chr18:45739377-45739607 | Common:2; Rare:59; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr18:45967235-45967495 | Rare:97; Clinvar (pathogenic):1 | ||||
| chr18:46098175-46098592 | Common:11; Rare:129; Clinvar (benign):8 | ||||
| chr18:46104135-46104408 | Common:4; Rare:80; Clinvar (benign):1 | ||||
| chr18:46756834-46756950 | Common:2; Rare:32 | ||||
| chr18:46917385-46917652 | Common:2; Rare:113 | ||||
| chr18:47150450-47150554 | Common:3; Rare:37 | ||||
| chr18:48538905-48539292 | Common:2; Rare:85 |