| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:34583578-34583708 | Common:2; Rare:46 | ||||
| chr15:34588447-34588505 | Rare:20 | ||||
| chr15:34988236-34988409 | Common:1; Rare:70 | ||||
| chr15:35546122-35546278 | Common:1; Rare:57 | ||||
| chr15:36579518-36579737 | Common:3; Rare:60 | ||||
| chr15:37100325-37100793 | Common:1; Rare:138 | ||||
| chr15:37101280-37101407 | Common:23; Rare:56 | ||||
| chr15:37101711-37101851 | Rare:47 | ||||
| chr15:39580813-39581084 | Common:1; Rare:76 | ||||
| chr15:39588812-39589100 | Rare:93 | ||||
| chr15:39933991-39934220 | Common:4; Rare:85 | ||||
| chr15:40038851-40039349 | Common:1; Rare:175 | ||||
| chr15:40405646-40405827 | Common:2; Rare:54; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr15:40569138-40569332 | Common:3; Rare:33 | ||||
| chr15:40695070-40695200 | Rare:35 |