| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:182392130-182392344 | Common:4; Rare:62; Clinvar (benign):1 | ||||
| chr1:182588811-182588922 | Common:1; Rare:22 | ||||
| chr1:182589158-182589298 | Rare:29 | ||||
| chr1:182603971-182604026 | Common:1; Rare:5 | ||||
| chr1:182604319-182604591 | Rare:65 | ||||
| chr1:182789392-182789481 | Common:1; Rare:15 | ||||
| chr1:182789484-182789537 | Common:1; Rare:14 | ||||
| chr1:182789591-182789842 | Common:2; Rare:89 | ||||
| chr1:182839020-182839433 | Common:2; Rare:137 | ||||
| chr1:182839508-182839795 | Common:3; Rare:120 | ||||
| chr1:182839946-182840111 | Common:2; Rare:55 | ||||
| chr1:183022928-183023569 | Common:6; Rare:171 | ||||
| chr1:183186116-183186289 | Common:2; Rare:28; Clinvar (benign):2 | ||||
| chr1:183471837-183472159 | Common:1; Rare:77 | ||||
| chr1:183472193-183472638 | Common:3; Rare:135 |