| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:117929568-117929802 | Not yet | Common:3; Rare:69 | 198 | ||
| chr1:119140645-119140748 | Not yet | Rare:29 | 114 | ||
| chr1:120176432-120176535 | Not yet | Rare:28 | 131 | ||
| chr1:145823922-145824238 | Not yet | Rare:109 | 174 | ||
| chr1:145918700-145919013 | Not yet | Common:2; Rare:64 | 228 | ||
| chr1:145927415-145927657 | Not yet | Common:1; Rare:68; Clinvar (pathogenic):1 | 176 | ||
| chr1:145964587-145964748 | Not yet | Rare:38 | 95 | ||
| chr1:147172427-147172744 | Not yet | Common:1; Rare:85 | 153 | ||
| chr1:147225256-147225530 | Not yet | Common:3; Rare:58 | 201 | ||
| chr1:147541205-147541518 | Not yet | Common:2; Rare:48 | 204 | ||
| chr1:149886663-149886959 | Not yet | Rare:100 | 198 | ||
| chr1:149887952-149888178 | Not yet | Rare:52 | 195 | ||
| chr1:149927760-149927906 | Not yet | Common:1; Rare:59; Clinvar (benign):4 | 145 | ||
| chr1:150067633-150067873 | Not yet | Rare:71 | 174 | ||
| chr1:150293730-150293903 | Not yet | Rare:60 | 182 |