| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:162023309-162023393 | Not yet | Rare:28; Clinvar (pathogenic):1 | 119 | ||
| chr1:162023611-162023958 | Not yet | Common:1; Rare:100 | 236 | ||
| chr1:162790447-162790765 | Not yet | Common:3; Rare:79 | 364 | ||
| chr1:163202908-163203066 | Not yet | Rare:29 | 165 | ||
| chr1:163321752-163322057 | Not yet | Common:1; Rare:81 | 334 | ||
| chr1:165768777-165768933 | Not yet | Common:1; Rare:69 | 148 | ||
| chr1:166839322-166839522 | Not yet | Rare:57 | 219 | ||
| chr1:167935943-167936327 | Not yet | Common:2; Rare:116 | 399 | ||
| chr1:167936544-167936994 | Not yet | Common:1; Rare:163 | 304 | ||
| chr1:168225714-168226091 | Not yet | Common:4; Rare:126 | 347 | ||
| chr1:169367773-169368250 | Not yet | Common:3; Rare:91 | 477 | ||
| chr1:169485941-169486139 | Not yet | Rare:48; Clinvar:1 | 285 | ||
| chr1:169794889-169795094 | Not yet | Common:3; Rare:53 | 157 | ||
| chr1:170532074-170532210 | Not yet | Rare:76; Clinvar:1 | 203 | ||
| chr1:170663031-170663209 | Not yet | Rare:48 | 235 |