| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:63367114-63367330 | Common:1; Rare:76 | ||||
| chr18:63422299-63422747 | Common:2; Rare:131 | ||||
| chr18:63476729-63476988 | Common:2; Rare:61 | ||||
| chr18:63702099-63702540 | Common:2; Rare:90 | ||||
| chr18:63887428-63887759 | Common:2; Rare:67 | ||||
| chr18:63949144-63949376 | Common:1; Rare:79 | ||||
| chr18:63970008-63970142 | Rare:28 | ||||
| chr18:63971001-63971067 | Rare:14 | ||||
| chr18:65750779-65751059 | Common:2; Rare:89 | ||||
| chr18:66603963-66604383 | Common:5; Rare:88 | ||||
| chr18:68714971-68715296 | Common:7; Rare:138 | ||||
| chr18:69895685-69896283 | Common:4; Rare:177 | ||||
| chr18:69896290-69896362 | Common:1; Rare:26 | ||||
| chr18:69947851-69947981 | Common:1; Rare:25 | ||||
| chr18:70205644-70205803 | Common:3; Rare:65; Clinvar (benign):2 |