| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:40358102-40358314 | Common:6; Rare:91 | ||||
| chr15:40382791-40383069 | Common:1; Rare:140 | ||||
| chr15:40405539-40405868 | Common:2; Rare:100; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
| chr15:40440781-40441000 | Rare:57 | ||||
| chr15:40441130-40441221 | Rare:27 | ||||
| chr15:40470905-40471059 | Rare:52 | ||||
| chr15:40471341-40471366 | Common:1; Rare:9; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr15:40564909-40565275 | Common:3; Rare:73 | ||||
| chr15:40569119-40569387 | Common:3; Rare:64 | ||||
| chr15:40569897-40569935 | Rare:12 | ||||
| chr15:40593864-40594096 | Common:1; Rare:114 | ||||
| chr15:40594206-40594407 | Common:1; Rare:47; Clinvar (benign):1 | ||||
| chr15:40594651-40594829 | Common:1; Rare:47 | ||||
| chr15:40694593-40694835 | Rare:71 | ||||
| chr15:40694896-40695354 | Common:3; Rare:131; Clinvar:1 |