| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:50686632-50686996 | Common:5; Rare:136 | ||||
| chr15:50687168-50687216 | Rare:13 | ||||
| chr15:50765175-50765585 | Common:3; Rare:131 | ||||
| chr15:50765658-50765820 | Common:2; Rare:59 | ||||
| chr15:50765821-50765857 | Rare:12 | ||||
| chr15:50765880-50766043 | Rare:24 | ||||
| chr15:50908005-50908831 | Common:5; Rare:283; Clinvar (benign):4 | ||||
| chr15:51622567-51622844 | Common:1; Rare:89 | ||||
| chr15:51622952-51623167 | Common:3; Rare:69 | ||||
| chr15:51737635-51737783 | Common:1; Rare:52 | ||||
| chr15:51829412-51829801 | Common:1; Rare:95 | ||||
| chr15:51830003-51830356 | Common:2; Rare:78 | ||||
| chr15:51971268-51971331 | Common:1; Rare:7 | ||||
| chr15:51971421-51971570 | Rare:36 | ||||
| chr15:51971662-51972064 | Common:1; Rare:143 |