| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:43824641-43824803 | Common:2; Rare:42 | ||||
| chr15:43826884-43827028 | Rare:56 | ||||
| chr15:44536863-44537192 | Common:1; Rare:116 | ||||
| chr15:44711352-44711613 | Rare:82; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr15:48645621-48646132 | Common:3; Rare:157; Clinvar (benign):1 | ||||
| chr15:48878045-48878212 | Rare:68 | ||||
| chr15:49155558-49155811 | Common:1; Rare:84 | ||||
| chr15:49423317-49423377 | Rare:5 | ||||
| chr15:49620810-49621093 | Common:6; Rare:110 | ||||
| chr15:50354859-50354998 | Rare:20 | ||||
| chr15:50355109-50355472 | Common:3; Rare:133 | ||||
| chr15:50908595-50908765 | Common:1; Rare:70; Clinvar (benign):2 | ||||
| chr15:51971744-51971841 | Rare:44 | ||||
| chr15:55318933-55318989 | Rare:16 | ||||
| chr15:55319091-55319255 | Common:2; Rare:47 |