| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:23503308-23503621 | Common:4; Rare:133 | ||||
| chr18:23586335-23586547 | Common:4; Rare:90; Clinvar:7; Clinvar (benign):3 | ||||
| chr18:23872905-23873110 | Rare:63; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr18:23898793-23899065 | Rare:75; Clinvar:1 | ||||
| chr18:23949766-23950154 | Rare:107; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr18:24397784-24397986 | Common:2; Rare:83 | ||||
| chr18:26091128-26091491 | Common:2; Rare:82 | ||||
| chr18:26226259-26226481 | Common:3; Rare:78 | ||||
| chr18:26226892-26227089 | Common:1; Rare:59 | ||||
| chr18:26546902-26547094 | Rare:63 | ||||
| chr18:31042576-31042980 | Common:1; Rare:99 | ||||
| chr18:31102408-31102712 | Common:1; Rare:67 | ||||
| chr18:31162520-31163054 | Common:1; Rare:132 | ||||
| chr18:31343232-31343608 | Rare:90 | ||||
| chr18:31498063-31498259 | Common:1; Rare:63; Clinvar:4; Clinvar (benign):5 |