| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:16644644-16644773 | Not yet | Common:1; Rare:2 | 163 | ||
| chr1:16913896-16914121 | Not yet | Common:8; Rare:48 | 180 | ||
| chr1:16978852-16978994 | Not yet | Common:2; Rare:35 | 167 | ||
| chr1:20644241-20644540 | Not yet | Common:1; Rare:77; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | 388 | ||
| chr1:20654360-20654629 | Not yet | Common:3; Rare:78; Clinvar (benign):1; Clinvar (pathogenic):1 | 352 | ||
| chr1:20656124-20656276 | Not yet | Common:1; Rare:39; Clinvar (benign):1 | 228 | ||
| chr1:21855521-21855913 | Not yet | Common:4; Rare:132; Clinvar:9; Clinvar (benign):5 | 330 | ||
| chr1:21857147-21857372 | Not yet | Common:1; Rare:68; Clinvar:4; Clinvar (benign):1 | 297 | ||
| chr1:21907947-21908057 | Not yet | Rare:13 | 247 | ||
| chr1:22025185-22025544 | Not yet | Common:7; Rare:95 | 422 | ||
| chr1:22509954-22510157 | Not yet | Common:1; Rare:33 | 302 | ||
| chr1:24151290-24151505 | Not yet | Common:1; Rare:42 | 349 | ||
| chr1:25875508-25875765 | Not yet | Rare:69 | 248 | ||
| chr1:27428768-27429134 | Not yet | Common:2; Rare:77 | 403 | ||
| chr1:27525603-27525746 | Not yet | Common:1; Rare:25 | 192 |