| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:203626684-203626832 | Common:1; Rare:38 | ||||
| chr1:206003411-206003534 | Common:1; Rare:20 | ||||
| chr1:206865374-206865552 | Rare:23 | ||||
| chr1:206909353-206909665 | Common:4; Rare:68 | ||||
| chr1:207032673-207032926 | Common:3; Rare:42 | ||||
| chr1:207053109-207053281 | Common:1; Rare:45 | ||||
| chr1:207751854-207752132 | Common:1; Rare:97 | ||||
| chr1:209652371-209652609 | Common:3; Rare:54; Clinvar:2; Clinvar (benign):1 | ||||
| chr1:209675275-209675476 | Common:1; Rare:49 | ||||
| chr1:209806064-209806291 | Common:5; Rare:75; Clinvar:2; Clinvar (benign):2 | ||||
| chr1:209827853-209828000 | Common:1; Rare:36 | ||||
| chr1:212035521-212035784 | Common:2; Rare:64 | ||||
| chr1:212791760-212791926 | Common:3; Rare:65 | ||||
| chr1:214280963-214281266 | Common:2; Rare:128 | ||||
| chr1:217631045-217631379 | Common:2; Rare:90 |