| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:113904813-113905392 | Not yet | Common:7; Rare:169; Clinvar (benign):1 | 394 | ||
| chr1:114716737-114716828 | Not yet | Rare:44; Clinvar:3 | 241 | ||
| chr1:114757942-114758078 | Not yet | Common:2; Rare:41 | 172 | ||
| chr1:114780628-114780841 | Not yet | Common:1; Rare:71 | 265 | ||
| chr1:117929578-117929827 | Not yet | Common:4; Rare:77 | 336 | ||
| chr1:119140634-119140743 | Not yet | Rare:33 | 167 | ||
| chr1:145823937-145824260 | Not yet | Rare:114 | 245 | ||
| chr1:145845542-145845636 | Not yet | Common:3; Rare:24 | 98 | ||
| chr1:145918689-145919022 | Not yet | Common:2; Rare:74 | 388 | ||
| chr1:145927422-145927644 | Not yet | Common:1; Rare:65; Clinvar (pathogenic):1 | 304 | ||
| chr1:145957961-145958195 | Not yet | Rare:57 | 287 | ||
| chr1:145964567-145964755 | Not yet | Rare:47 | 151 | ||
| chr1:146938297-146938331 | Not yet | Rare:15 | 74 | ||
| chr1:147172457-147172744 | Not yet | Common:1; Rare:76 | 260 | ||
| chr1:149842746-149842954 | Not yet | Rare:3 | 272 |