| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:23503243-23503601 | Common:4; Rare:148 | ||||
| chr18:23503946-23504017 | Rare:14 | ||||
| chr18:23586340-23586660 | Common:5; Rare:133; Clinvar:7; Clinvar (benign):4 | ||||
| chr18:23586727-23587126 | Common:3; Rare:118 | ||||
| chr18:23662775-23662964 | Common:4; Rare:61 | ||||
| chr18:23689404-23689659 | Rare:52 | ||||
| chr18:24014509-24014730 | Common:3; Rare:48 | ||||
| chr18:24014842-24014921 | Common:1; Rare:20 | ||||
| chr18:24015076-24015302 | Common:1; Rare:55 | ||||
| chr18:24138852-24139110 | Common:2; Rare:77 | ||||
| chr18:24271237-24271352 | Common:2; Rare:13 | ||||
| chr18:24271664-24271738 | Common:2; Rare:18 | ||||
| chr18:24271940-24271984 | Rare:9 | ||||
| chr18:24272131-24272321 | Rare:42 | ||||
| chr18:24397202-24397315 | Rare:30 |