| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:63422370-63422677 | Common:2; Rare:85 | ||||
| chr18:63970008-63970147 | Common:1; Rare:29 | ||||
| chr18:68714969-68715262 | Common:6; Rare:129 | ||||
| chr18:74148358-74148552 | Common:1; Rare:60 | ||||
| chr18:74291872-74292242 | Common:3; Rare:105 | ||||
| chr18:74496131-74496435 | Common:4; Rare:100 | ||||
| chr18:74499776-74499965 | Common:2; Rare:44 | ||||
| chr18:74597334-74597484 | Common:1; Rare:33 | ||||
| chr18:74597606-74597929 | Common:2; Rare:87 | ||||
| chr18:77087440-77087503 | Common:4; Rare:17 | ||||
| chr18:79988280-79988661 | Common:4; Rare:126; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr19:344786-344955 | Common:3; Rare:61 | ||||
| chr19:507218-507524 | Common:3; Rare:102 | ||||
| chr19:572322-572693 | Common:1; Rare:186 | ||||
| chr19:633520-633749 | Common:8; Rare:100 |