| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:207890217-207890389 | Common:1; Rare:31 | ||||
| chr1:208243852-208244001 | Rare:40 | ||||
| chr1:208244255-208244509 | Common:1; Rare:78 | ||||
| chr1:209806137-209806320 | Common:5; Rare:65; Clinvar:2; Clinvar (benign):2 | ||||
| chr1:209827871-209828076 | Common:1; Rare:57 | ||||
| chr1:211259094-211259399 | Common:1; Rare:101 | ||||
| chr1:212035510-212035801 | Common:2; Rare:77 | ||||
| chr1:212608472-212608761 | Common:1; Rare:75 | ||||
| chr1:212791764-212791926 | Common:3; Rare:63 | ||||
| chr1:213015421-213015628 | Rare:57 | ||||
| chr1:214280933-214281264 | Common:3; Rare:135 | ||||
| chr1:214551560-214551861 | Common:2; Rare:104 | ||||
| chr1:217631029-217631365 | Common:2; Rare:91 | ||||
| chr1:218285178-218285352 | Common:2; Rare:84 | ||||
| chr1:219173766-219173925 | Common:1; Rare:91 |