| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:22494624-22494902 | Not yet | Common:1; Rare:35 | 278 | ||
| chr15:22944633-22944892 | Not yet | Common:1; Rare:74 | 328 | ||
| chr15:23303479-23303775 | Not yet | Rare:25 | 273 | ||
| chr15:25056561-25056860 | Not yet | Common:3; Rare:94 | 365 | ||
| chr15:31215842-31215929 | Not yet | Common:2; Rare:21 | 136 | ||
| chr15:32536440-32536819 | Not yet | Common:2; Rare:40 | 238 | ||
| chr15:37102003-37102235 | Not yet | Common:1; Rare:59 | 267 | ||
| chr15:39580312-39580434 | Not yet | Common:1; Rare:32 | 163 | ||
| chr15:39583878-39584422 | Not yet | Common:1; Rare:140 | 424 | ||
| chr15:39585672-39585980 | Not yet | Common:3; Rare:39 | 373 | ||
| chr15:43876251-43876393 | Not yet | Common:1; Rare:20 | 154 | ||
| chr15:45279224-45279463 | Not yet | Common:1; Rare:91 | 272 | ||
| chr15:48474253-48474559 | Not yet | Common:1; Rare:68; Clinvar:7; Clinvar (benign):4; Clinvar (pathogenic):3 | 402 | ||
| chr15:48490212-48490473 | Not yet | Common:3; Rare:40; Clinvar (benign):1 | 349 | ||
| chr15:51094627-51095003 | Not yet | Common:8; Rare:100 | 229 |