| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:26090573-26090959 | Common:4; Rare:150 | ||||
| chr18:26091169-26091367 | Common:2; Rare:49 | ||||
| chr18:28177009-28177339 | Common:3; Rare:162 | ||||
| chr18:31498118-31498254 | Common:1; Rare:45; Clinvar:3; Clinvar (benign):4 | ||||
| chr18:32092381-32092706 | Common:4; Rare:147 | ||||
| chr18:35290193-35290377 | Common:2; Rare:67 | ||||
| chr18:35344406-35344552 | Common:2; Rare:49 | ||||
| chr18:36129223-36129469 | Common:4; Rare:76 | ||||
| chr18:36129788-36129928 | Common:1; Rare:54 | ||||
| chr18:36828728-36829138 | Common:3; Rare:153 | ||||
| chr18:45967265-45967492 | Rare:79 | ||||
| chr18:46098246-46098571 | Common:11; Rare:89; Clinvar (benign):5 | ||||
| chr18:46104136-46104412 | Common:4; Rare:80; Clinvar (benign):1 | ||||
| chr18:49561879-49562098 | Rare:56 | ||||
| chr18:49813826-49814080 | Common:1; Rare:109 |