| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:16913883-16914115 | Not yet | Common:8; Rare:47 | 174 | ||
| chr1:17588408-17588472 | Not yet | Rare:21 | 78 | ||
| chr1:19076778-19077192 | Not yet | Rare:96 | 432 | ||
| chr1:25875492-25875731 | Not yet | Rare:66 | 191 | ||
| chr1:26863732-26864248 | Not yet | Common:1; Rare:125 | 328 | ||
| chr1:36180053-36180355 | Not yet | Common:2; Rare:75 | 291 | ||
| chr1:39956888-39957170 | Not yet | Rare:60 | 293 | ||
| chr1:42929761-42930018 | Not yet | Common:2; Rare:65; Clinvar:5; Clinvar (benign):10; Clinvar (pathogenic):5 | 291 | ||
| chr1:43609122-43609426 | Not yet | Common:2; Rare:79 | 300 | ||
| chr1:44644732-44645008 | Not yet | Common:1; Rare:58 | 254 | ||
| chr1:51518031-51518305 | Not yet | Rare:56 | 435 | ||
| chr1:58575778-58576202 | Not yet | Common:5; Rare:78; Clinvar:3; Clinvar (benign):6 | 419 | ||
| chr1:58576204-58577133 | Not yet | Common:5; Rare:358; Clinvar:4; Clinvar (benign):5 | 424 | ||
| chr1:58782299-58782785 | Not yet | Common:2; Rare:167; Clinvar:1 | 287 | ||
| chr1:58783054-58783125 | Not yet | Rare:21 | 107 |