| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:46637266-46637405 | Rare:25 | ||||
| chr22:46649588-46649925 | Common:1; Rare:67 | ||||
| chr22:50197719-50197947 | Common:1; Rare:79 | ||||
| chr22:50205102-50205323 | Common:3; Rare:45 | ||||
| chr22:50314502-50314599 | Common:1; Rare:46 | ||||
| chr22:50387360-50387690 | Common:1; Rare:63 | ||||
| chr3:10508656-10508876 | Common:3; Rare:36 | ||||
| chr3:32491731-32492078 | Common:4; Rare:59 | ||||
| chr3:37055134-37055186 | Rare:16 | ||||
| chr3:39384249-39384466 | Common:7; Rare:51 | ||||
| chr3:39387689-39387837 | Rare:23 | ||||
| chr3:39388790-39388943 | Common:1; Rare:27 | ||||
| chr3:39411647-39411993 | Common:1; Rare:88; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:40453163-40453417 | Common:6; Rare:56 | ||||
| chr3:42770571-42770628 | Common:2; Rare:32 |