| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:31296759-31297032 | Common:4; Rare:82 | ||||
| chr10:12195887-12196219 | Rare:78 | ||||
| chr11:66480247-66480438 | Common:1; Rare:50 | ||||
| chr16:56451320-56451535 | Common:1; Rare:49 | ||||
| chr16:75647643-75647822 | Common:2; Rare:81; Clinvar:2 | ||||
| chr19:18919352-18919691 | Common:2; Rare:102 | ||||
| chr19:39391121-39391387 | Common:1; Rare:101 | ||||
| chr19:43670163-43670365 | Common:2; Rare:44 | ||||
| chr2:74529672-74529975 | Rare:91; Clinvar:3; Clinvar (benign):1 | ||||
| chr22:49918421-49918694 | Common:1; Rare:100 | ||||
| chr5:74685127-74685234 | Common:2; Rare:37; Clinvar:1; Clinvar (benign):2 | ||||
| chr8:124539076-124539132 | Common:1; Rare:22 | ||||
| chrM:12122-12337 |