| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:70205648-70205755 | Common:2; Rare:49; Clinvar (benign):2 | ||||
| chr18:74148358-74148589 | Common:1; Rare:67 | ||||
| chr18:74291847-74292224 | Common:2; Rare:107; Clinvar:1 | ||||
| chr18:74496021-74496434 | Common:4; Rare:132 | ||||
| chr18:74499393-74499481 | Rare:14 | ||||
| chr18:74597584-74597675 | Common:1; Rare:26 | ||||
| chr18:74597801-74597929 | Common:1; Rare:37 | ||||
| chr18:75209045-75209260 | Common:1; Rare:73 | ||||
| chr19:344790-344947 | Common:3; Rare:55 | ||||
| chr19:572328-572670 | Rare:181 | ||||
| chr19:633520-633764 | Common:8; Rare:106 | ||||
| chr19:821930-822119 | Rare:54 | ||||
| chr19:893158-893484 | Common:3; Rare:139 | ||||
| chr19:984225-984348 | Common:1; Rare:46 | ||||
| chr19:1026494-1026683 | Rare:74 |