| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:91965983-91966176 | Common:1; Rare:41 | ||||
| chr15:92775171-92775237 | Rare:20 | ||||
| chr15:92891886-92892075 | Common:1; Rare:37 | ||||
| chr15:92893150-92893328 | Common:2; Rare:38 | ||||
| chr15:92897889-92898063 | Common:1; Rare:37 | ||||
| chr15:92901012-92901346 | Rare:82; Clinvar (benign):2 | ||||
| chr15:92981382-92981736 | Common:2; Rare:82; Clinvar:1; Clinvar (benign):1 | ||||
| chr15:92981853-92981921 | Rare:11 | ||||
| chr15:93000385-93000667 | Rare:69; Clinvar:2; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr15:93001987-93002100 | Common:1; Rare:16 | ||||
| chr15:93002142-93002577 | Common:4; Rare:99; Clinvar (benign):9; Clinvar (pathogenic):2 | ||||
| chr15:93346295-93346499 | Common:1; Rare:36 | ||||
| chr15:94487353-94487642 | Common:4; Rare:67 | ||||
| chr15:94764998-94765078 | Rare:16 | ||||
| chr15:94790857-94791042 | Common:3; Rare:37 |