| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:65133794-65133923 | Common:1; Rare:37 | ||||
| chr15:65185122-65185167 | Rare:21 | ||||
| chr15:65185303-65185713 | Common:2; Rare:159 | ||||
| chr15:65286838-65287098 | Rare:78 | ||||
| chr15:65517220-65517343 | Common:1; Rare:44 | ||||
| chr15:65517581-65517735 | Common:1; Rare:60 | ||||
| chr15:65530341-65530724 | Common:3; Rare:136 | ||||
| chr15:65611089-65611421 | Common:3; Rare:110 | ||||
| chr15:65792027-65792501 | Common:4; Rare:135 | ||||
| chr15:65869397-65869622 | Rare:89 | ||||
| chr15:65912506-65912634 | Common:2; Rare:22 | ||||
| chr15:65971241-65971360 | Common:1; Rare:17 | ||||
| chr15:66293449-66293880 | Common:6; Rare:135 | ||||
| chr15:66356630-66356801 | Common:1; Rare:51 | ||||
| chr15:66386653-66386944 | Common:2; Rare:111; Clinvar:3; Clinvar (benign):4 |