| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:154627916-154628138 | Common:4; Rare:79 | ||||
| chr1:154870260-154870445 | Rare:39 | ||||
| chr1:154936484-154936807 | Common:3; Rare:89 | ||||
| chr1:154936850-154937050 | Rare:39 | ||||
| chr1:154937192-154937448 | Common:1; Rare:60 | ||||
| chr1:154955827-154955900 | Rare:9 | ||||
| chr1:154956027-154956289 | Common:1; Rare:76 | ||||
| chr1:154961641-154962066 | Common:1; Rare:144 | ||||
| chr1:154962210-154962278 | Rare:14 | ||||
| chr1:154970663-154970962 | Common:1; Rare:57 | ||||
| chr1:154973702-154974268 | Common:3; Rare:146 | ||||
| chr1:154974270-154974714 | Rare:103 | ||||
| chr1:154974857-154975176 | Common:3; Rare:104 | ||||
| chr1:154975212-154975531 | Common:1; Rare:54 | ||||
| chr1:154982895-154983592 | Common:4; Rare:143; Clinvar (benign):2 |