| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:35581527-35581761 | Common:21; Rare:44 | ||||
| chr18:35581948-35581981 | Rare:6 | ||||
| chr18:35582052-35582108 | Common:2; Rare:12 | ||||
| chr18:35972217-35972796 | Common:6; Rare:187 | ||||
| chr18:35972803-35972900 | Common:1; Rare:38 | ||||
| chr18:36067331-36067741 | Common:2; Rare:140 | ||||
| chr18:36129190-36129557 | Common:4; Rare:117 | ||||
| chr18:36129720-36130027 | Common:3; Rare:109 | ||||
| chr18:36187387-36187557 | Common:4; Rare:61 | ||||
| chr18:36297543-36297799 | Common:4; Rare:96 | ||||
| chr18:36828183-36828264 | Rare:13 | ||||
| chr18:36828713-36829344 | Common:3; Rare:236 | ||||
| chr18:36829369-36829436 | Rare:20 | ||||
| chr18:41955012-41955286 | Common:1; Rare:101 | ||||
| chr18:45967163-45967577 | Common:1; Rare:149; Clinvar (benign):1; Clinvar (pathogenic):1 |