| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:28176973-28177072 | Rare:46 | ||||
| chr18:28177103-28177320 | Common:1; Rare:96 | ||||
| chr18:35290162-35290384 | Common:2; Rare:74 | ||||
| chr18:36067400-36067722 | Common:2; Rare:112 | ||||
| chr18:36129307-36129501 | Common:1; Rare:54 | ||||
| chr18:36129786-36129990 | Common:2; Rare:86 | ||||
| chr18:36187408-36187557 | Common:4; Rare:56 | ||||
| chr18:36828713-36829131 | Common:3; Rare:154 | ||||
| chr18:41955018-41955294 | Common:1; Rare:103 | ||||
| chr18:45967237-45967531 | Common:1; Rare:110; Clinvar (pathogenic):1 | ||||
| chr18:46104213-46104408 | Common:3; Rare:54 | ||||
| chr18:46917409-46917630 | Common:2; Rare:90 | ||||
| chr18:48539102-48539213 | Rare:23 | ||||
| chr18:49813765-49814055 | Common:1; Rare:112 | ||||
| chr18:51030060-51030241 | Rare:60 |