| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:50356095-50356260 | Common:2; Rare:39 | ||||
| chr15:50367512-50367578 | Rare:11 | ||||
| chr15:50370831-50371124 | Common:4; Rare:36 | ||||
| chr15:50465081-50465363 | Common:1; Rare:58; Clinvar (benign):1 | ||||
| chr15:50570036-50570135 | Rare:23 | ||||
| chr15:50613536-50613735 | Common:1; Rare:51 | ||||
| chr15:50639510-50639723 | Rare:63 | ||||
| chr15:50712468-50712673 | Common:3; Rare:35 | ||||
| chr15:51106455-51106674 | Common:2; Rare:33 | ||||
| chr15:51484814-51485025 | Common:1; Rare:32 | ||||
| chr15:51828640-51828914 | Rare:49 | ||||
| chr15:51842749-51843152 | Common:3; Rare:76 | ||||
| chr15:51849982-51850029 | Rare:8 | ||||
| chr15:51907064-51907116 | Rare:8 | ||||
| chr15:51938159-51938510 | Common:5; Rare:77 |