| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:34988228-34988365 | Rare:59 | ||||
| chr15:35546141-35546412 | Common:1; Rare:74 | ||||
| chr15:37095962-37096137 | Common:2; Rare:40 | ||||
| chr15:37098168-37098251 | Common:1; Rare:28 | ||||
| chr15:37100265-37100824 | Common:1; Rare:162 | ||||
| chr15:37101280-37101439 | Common:24; Rare:66 | ||||
| chr15:37101701-37101871 | Rare:58 | ||||
| chr15:39782789-39782877 | Rare:24 | ||||
| chr15:39920888-39921060 | Common:2; Rare:66 | ||||
| chr15:40039094-40039329 | Rare:98 | ||||
| chr15:40358128-40358306 | Common:5; Rare:78 | ||||
| chr15:40405552-40405827 | Common:2; Rare:77; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr15:40569201-40569332 | Common:3; Rare:23 | ||||
| chr15:40695076-40695180 | Rare:27 | ||||
| chr15:40755220-40755397 | Common:1; Rare:57 |