| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:209652367-209652571 | Common:1; Rare:50; Clinvar:2; Clinvar (benign):1 | ||||
| chr1:209675264-209675885 | Common:4; Rare:168 | ||||
| chr1:209756022-209756157 | Common:1; Rare:23 | ||||
| chr1:209806044-209806269 | Common:4; Rare:59; Clinvar:2; Clinvar (benign):2 | ||||
| chr1:209827835-209828066 | Common:1; Rare:61 | ||||
| chr1:211259088-211259399 | Common:1; Rare:102 | ||||
| chr1:211326550-211326874 | Common:5; Rare:83 | ||||
| chr1:211579186-211579499 | Rare:101 | ||||
| chr1:212035486-212035793 | Common:2; Rare:84 | ||||
| chr1:212285038-212285445 | Common:5; Rare:132 | ||||
| chr1:212285855-212286113 | Common:1; Rare:67 | ||||
| chr1:212608289-212608377 | Common:2; Rare:21 | ||||
| chr1:212608495-212608773 | Rare:66 | ||||
| chr1:212791760-212791964 | Common:4; Rare:91 | ||||
| chr1:212858074-212858336 | Common:4; Rare:69; Clinvar:2 |