| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:19787043-19787314 | Not yet | Common:3; Rare:45 | 295 | ||
| chr1:20650293-20650517 | Not yet | Common:3; Rare:61; Clinvar (benign):1 | 289 | ||
| chr1:20654345-20654633 | Not yet | Common:4; Rare:86; Clinvar (benign):2; Clinvar (pathogenic):1 | 374 | ||
| chr1:20779823-20779980 | Not yet | Common:1; Rare:48 | 219 | ||
| chr1:21013060-21013196 | Not yet | Common:2; Rare:23 | 210 | ||
| chr1:21603811-21604081 | Not yet | Common:3; Rare:76 | 297 | ||
| chr1:21619032-21619329 | Not yet | Common:2; Rare:78 | 275 | ||
| chr1:21638778-21639001 | Not yet | Common:1; Rare:46 | 318 | ||
| chr1:21672179-21672463 | Not yet | Common:4; Rare:54 | 332 | ||
| chr1:21831461-21831672 | Not yet | Common:2; Rare:62; Clinvar:2; Clinvar (benign):1 | 267 | ||
| chr1:21880434-21880715 | Not yet | Common:3; Rare:88; Clinvar:6; Clinvar (benign):3 | 260 | ||
| chr1:21884811-21885151 | Not yet | Common:1; Rare:100; Clinvar:1; Clinvar (benign):1 | 372 | ||
| chr1:23562236-23562332 | Not yet | Rare:14 | 278 | ||
| chr1:24110871-24111145 | Not yet | Common:2; Rare:52 | 336 | ||
| chr1:24515820-24515863 | Not yet | Rare:6 | 78 |