| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:47930347-47930765 | Common:1; Rare:173 | ||||
| chr18:47930787-47931032 | Rare:76 | ||||
| chr18:47931103-47931426 | Common:2; Rare:116 | ||||
| chr18:48137708-48137791 | Rare:15 | ||||
| chr18:48538844-48539205 | Common:1; Rare:78 | ||||
| chr18:48930174-48930460 | Common:1; Rare:60 | ||||
| chr18:48942693-48942826 | Rare:29 | ||||
| chr18:48948591-48948871 | Rare:81 | ||||
| chr18:48949884-48950038 | Rare:57 | ||||
| chr18:49460447-49460826 | Common:2; Rare:102; Clinvar:8; Clinvar (benign):1 | ||||
| chr18:49487129-49487388 | Common:4; Rare:107 | ||||
| chr18:49491345-49491507 | Common:1; Rare:45 | ||||
| chr18:49491727-49491966 | Common:1; Rare:77 | ||||
| chr18:49492385-49492547 | Common:1; Rare:73 | ||||
| chr18:49560438-49560780 | Common:7; Rare:65 |