| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:230186095-230186219 | Not yet | Rare:31 | 191 | ||
| chr2:231393687-231393804 | Not yet | Rare:21 | 297 | ||
| chr2:231482884-231482978 | Not yet | Rare:23 | 146 | ||
| chr2:234495922-234496080 | Not yet | Rare:46 | 178 | ||
| chr2:237689518-237689784 | Not yet | Rare:46 | 250 | ||
| chr2:241741199-241741379 | Not yet | Rare:31 | 313 | ||
| chr2:241804756-241804991 | Not yet | Rare:70 | 261 | ||
| chr2:241842972-241842990 | Not yet | Rare:6 | 20 | ||
| chr2:241881275-241881423 | Not yet | Rare:36 | 196 | ||
| chr20:326236-326324 | Not yet | Common:1; Rare:23 | 110 | ||
| chr20:327327-327448 | Not yet | Rare:51 | 160 | ||
| chr20:2837040-2837374 | Not yet | Rare:58 | 418 | ||
| chr20:3082794-3083062 | Not yet | Common:3; Rare:80; Clinvar (pathogenic):1 | 182 | ||
| chr20:3083421-3083669 | Not yet | Common:2; Rare:57 | 245 | ||
| chr20:3083879-3084005 | Not yet | Rare:22 | 200 |