| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:235328491-235328584 | Common:1; Rare:30 | ||||
| chr1:235328788-235329044 | Common:1; Rare:86 | ||||
| chr1:235504420-235504762 | Common:4; Rare:103 | ||||
| chr1:235866893-235867152 | Common:2; Rare:76 | ||||
| chr1:236281943-236282193 | Common:5; Rare:69 | ||||
| chr1:236604453-236604657 | Common:4; Rare:62 | ||||
| chr1:236795042-236795513 | Common:7; Rare:189; Clinvar:5; Clinvar (benign):1 | ||||
| chr1:240091705-240091995 | Common:3; Rare:110 | ||||
| chr1:241519654-241519988 | Common:2; Rare:106; Clinvar:12; Clinvar (benign):10; Clinvar (pathogenic):4 | ||||
| chr1:241847785-241848016 | Common:1; Rare:65 | ||||
| chr1:241848070-241848461 | Common:2; Rare:86 | ||||
| chr1:243255047-243255433 | Common:1; Rare:92 | ||||
| chr1:243255762-243256140 | Common:1; Rare:110; Clinvar:4; Clinvar (benign):1 | ||||
| chr1:243851115-243851186 | Rare:26 | ||||
| chr1:244048221-244048551 | Rare:106 |