| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:92890515-92890572 | Rare:20 | ||||
| chr15:92891354-92891404 | Common:1; Rare:8 | ||||
| chr15:92893058-92893327 | Common:4; Rare:62 | ||||
| chr15:92895632-92895987 | Common:1; Rare:59 | ||||
| chr15:93000324-93000658 | Rare:77; Clinvar:2; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr15:93002140-93002563 | Common:4; Rare:93; Clinvar (benign):9; Clinvar (pathogenic):2 | ||||
| chr15:96331491-96331688 | Common:1; Rare:61 | ||||
| chr15:98647322-98647511 | Common:3; Rare:70 | ||||
| chr15:98651336-98651517 | Common:1; Rare:45 | ||||
| chr15:98653292-98653311 | Rare:1 | ||||
| chr15:98763665-98763964 | Common:1; Rare:55 | ||||
| chr15:98766381-98766623 | Common:1; Rare:40 | ||||
| chr15:98804055-98804337 | Common:1; Rare:53 | ||||
| chr15:98843910-98843954 | Rare:5 | ||||
| chr15:98853810-98853938 | Common:3; Rare:36 |