| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:82540421-82540632 | Common:1; Rare:62 | ||||
| chr15:82809486-82809669 | Common:1; Rare:47 | ||||
| chr15:82986151-82986221 | Rare:16 | ||||
| chr15:83011564-83011755 | Common:4; Rare:82 | ||||
| chr15:83066757-83066794 | Rare:7 | ||||
| chr15:83207741-83208142 | Common:2; Rare:118 | ||||
| chr15:84716062-84716204 | Rare:49 | ||||
| chr15:84716418-84716543 | Rare:26 | ||||
| chr15:84748266-84748614 | Rare:95 | ||||
| chr15:85619116-85619465 | Common:4; Rare:76 | ||||
| chr15:88467323-88467736 | Common:4; Rare:131 | ||||
| chr15:88546584-88546786 | Rare:72 | ||||
| chr15:89328743-89328948 | Common:1; Rare:66; Clinvar:3; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr15:89655408-89655602 | Common:1; Rare:68; Clinvar (benign):2 | ||||
| chr15:89690703-89690811 | Common:2; Rare:33 |