| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:72475060-72475660 | Common:7; Rare:263 | ||||
| chr15:72686099-72686500 | Common:4; Rare:228; Clinvar:5; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
| chr15:72783310-72783965 | Common:6; Rare:361 | ||||
| chr15:73052120-73052569 | Common:8; Rare:238 | ||||
| chr15:73633208-73633633 | Common:5; Rare:322 | ||||
| chr15:73684043-73684470 | Rare:190 | ||||
| chr15:73992221-73992446 | Common:1; Rare:150 | ||||
| chr15:73994568-73994819 | Common:2; Rare:101 | ||||
| chr15:74202442-74202619 | Common:2; Rare:38 | ||||
| chr15:74202660-74203070 | Common:1; Rare:163; Clinvar:4 | ||||
| chr15:74208900-74209380 | Common:2; Rare:147 | ||||
| chr15:74365663-74365808 | Common:1; Rare:28 | ||||
| chr15:74366038-74366271 | Rare:83 | ||||
| chr15:74461103-74461509 | Rare:188 | ||||
| chr15:74540911-74541310 | Common:9; Rare:269 |