| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:236032507-236032830 | Not yet | Common:1; Rare:82; Clinvar:1 | 366 | ||
| chr1:242001523-242001755 | Not yet | Common:3; Rare:34 | 329 | ||
| chr1:244451132-244451263 | Not yet | Common:2; Rare:37 | 166 | ||
| chr1:244863715-244863833 | Not yet | Rare:37; Clinvar:1; Clinvar (benign):2 | 109 | ||
| chr1:244970954-244971054 | Not yet | Rare:24 | 105 | ||
| chr10:246578-246843 | Not yet | Rare:65 | 355 | ||
| chr10:388048-388193 | Not yet | Rare:41 | 238 | ||
| chr10:633555-633878 | Not yet | Common:2; Rare:70 | 355 | ||
| chr10:4995767-4995949 | Not yet | Common:1; Rare:59; Clinvar (pathogenic):1 | 246 | ||
| chr10:5766518-5766738 | Not yet | Rare:44 | 290 | ||
| chr10:17010854-17010992 | Not yet | Common:1; Rare:23 | 241 | ||
| chr10:19768008-19768266 | Not yet | Common:1; Rare:55 | 434 | ||
| chr10:19839318-19839397 | Not yet | Common:1; Rare:23 | 182 | ||
| chr10:22251821-22252088 | Not yet | Rare:59 | 310 | ||
| chr10:29409497-29409606 | Not yet | Common:1; Rare:32 | 129 |