| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:70097852-70098092 | Common:1; Rare:54 | ||||
| chr15:70892404-70892880 | Common:1; Rare:115 | ||||
| chr15:72118168-72118434 | Common:2; Rare:87 | ||||
| chr15:72231013-72231034 | Rare:8 | ||||
| chr15:72231107-72231560 | Common:4; Rare:151 | ||||
| chr15:72272526-72272826 | Common:1; Rare:96 | ||||
| chr15:72375958-72376118 | Common:2; Rare:71; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr15:72474210-72474325 | Rare:37 | ||||
| chr15:72686147-72686220 | Common:2; Rare:28; Clinvar:2; Clinvar (benign):2 | ||||
| chr15:73633265-73633595 | Common:2; Rare:122 | ||||
| chr15:73994581-73994716 | Common:1; Rare:20 | ||||
| chr15:74130073-74130371 | Rare:67 | ||||
| chr15:74130425-74130644 | Common:2; Rare:42 | ||||
| chr15:74130768-74131093 | Rare:56 | ||||
| chr15:74461100-74461307 | Rare:64 |