| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:79625208-79625517 | Common:2; Rare:54 | ||||
| chr18:79678934-79678973 | Common:1; Rare:10 | ||||
| chr18:79678983-79679268 | Common:6; Rare:82 | ||||
| chr18:79856664-79856900 | Common:1; Rare:46 | ||||
| chr18:80105451-80105523 | Rare:15 | ||||
| chr18:80147248-80147461 | Common:1; Rare:45 | ||||
| chr18:80147752-80148072 | Common:2; Rare:82 | ||||
| chr18:80194919-80195214 | Common:3; Rare:57 | ||||
| chr18:80213308-80213455 | Rare:22 | ||||
| chr19:267143-267319 | Common:4; Rare:34 | ||||
| chr19:506742-506930 | Common:4; Rare:43 | ||||
| chr19:610803-611025 | Common:5; Rare:92 | ||||
| chr19:632689-632806 | Common:1; Rare:35 | ||||
| chr19:662213-662438 | Common:2; Rare:63 | ||||
| chr19:860567-860690 | Rare:49; Clinvar (pathogenic):1 |