| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:35240917-35241089 | Common:2; Rare:63 | ||||
| chr18:35290193-35290384 | Common:2; Rare:68 | ||||
| chr18:35972475-35972722 | Common:3; Rare:78 | ||||
| chr18:36129301-36129525 | Common:1; Rare:70 | ||||
| chr18:36129772-36129928 | Common:1; Rare:59 | ||||
| chr18:36828736-36829266 | Common:3; Rare:209 | ||||
| chr18:45967261-45967407 | Rare:48 | ||||
| chr18:46104136-46104399 | Common:3; Rare:75; Clinvar (benign):1 | ||||
| chr18:47150465-47150567 | Common:3; Rare:36 | ||||
| chr18:49487198-49487329 | Common:2; Rare:49 | ||||
| chr18:49490476-49490914 | Common:1; Rare:110 | ||||
| chr18:49813835-49814128 | Common:1; Rare:124 | ||||
| chr18:50281453-50281658 | Common:2; Rare:70 | ||||
| chr18:50374876-50375071 | Common:2; Rare:69 | ||||
| chr18:51030082-51030222 | Rare:44 |