| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:32964617-32964665 | Not yet | Rare:13 | 28 | ||
| chr1:32964712-32965091 | Not yet | Common:2; Rare:137 | 140 | ||
| chr1:33036791-33037184 | Not yet | Rare:141; Clinvar (pathogenic):2 | 163 | ||
| chr1:33080936-33081196 | Not yet | Common:2; Rare:73 | 110 | ||
| chr1:33182012-33182181 | Not yet | Rare:38 | 83 | ||
| chr1:33256224-33256584 | Not yet | Common:1; Rare:90 | 109 | ||
| chr1:33348982-33349235 | Not yet | Rare:52 | 114 | ||
| chr1:33349753-33350197 | Not yet | Common:3; Rare:144 | 133 | ||
| chr1:33472278-33472749 | Not yet | Common:1; Rare:93 | 182 | ||
| chr1:34859655-34860003 | Not yet | Common:1; Rare:88 | 183 | ||
| chr1:34985252-34985636 | Not yet | Common:4; Rare:99 | 157 | ||
| chr1:35031181-35031294 | Not yet | Rare:28 | 95 | ||
| chr1:35031587-35031845 | Not yet | Common:1; Rare:81 | 143 | ||
| chr1:35031912-35032069 | Not yet | Common:1; Rare:43 | 88 | ||
| chr1:35079271-35079605 | Not yet | Common:3; Rare:80 | 133 |