| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:63422391-63422677 | Common:2; Rare:76 | ||||
| chr18:68715030-68715262 | Common:5; Rare:104 | ||||
| chr18:70205648-70205877 | Common:3; Rare:89; Clinvar (benign):2 | ||||
| chr18:74148358-74148552 | Common:1; Rare:60 | ||||
| chr18:74291229-74291501 | Common:13; Rare:44 | ||||
| chr18:74291865-74292288 | Common:4; Rare:127 | ||||
| chr18:74496021-74496417 | Common:4; Rare:129 | ||||
| chr18:74597810-74597929 | Common:1; Rare:35 | ||||
| chr18:76822226-76822585 | Common:11; Rare:98 | ||||
| chr18:79988360-79988661 | Common:4; Rare:110; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr19:344790-344939 | Common:3; Rare:50 | ||||
| chr19:572339-572618 | Rare:149 | ||||
| chr19:804683-804934 | Rare:78 | ||||
| chr19:893165-893484 | Common:3; Rare:133 | ||||
| chr19:913153-913288 | Rare:43 |