| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:40405561-40405835 | Common:2; Rare:79; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):3 | ||||
| chr15:40569201-40569346 | Common:3; Rare:29 | ||||
| chr15:40695076-40695180 | Rare:27 | ||||
| chr15:40755205-40755394 | Common:2; Rare:63 | ||||
| chr15:40763917-40764120 | Rare:52 | ||||
| chr15:40807050-40807125 | Rare:20 | ||||
| chr15:40807409-40807765 | Common:4; Rare:120 | ||||
| chr15:40894210-40894483 | Rare:84 | ||||
| chr15:41115987-41116261 | Common:2; Rare:77 | ||||
| chr15:41402435-41402558 | Common:4; Rare:41; Clinvar:1; Clinvar (benign):1 | ||||
| chr15:41416958-41417313 | Common:4; Rare:129 | ||||
| chr15:41544243-41544359 | Rare:49 | ||||
| chr15:41621442-41621564 | Common:1; Rare:28 | ||||
| chr15:41660302-41660535 | Rare:74 | ||||
| chr15:41972523-41972776 | Common:1; Rare:67 |