| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:70853229-70853420 | Rare:23 | ||||
| chr15:70853893-70854289 | Common:1; Rare:113 | ||||
| chr15:70892338-70892855 | Common:1; Rare:115 | ||||
| chr15:71547260-71547287 | Rare:7 | ||||
| chr15:72117798-72118435 | Common:5; Rare:214 | ||||
| chr15:72230190-72230488 | Rare:78 | ||||
| chr15:72231107-72231309 | Common:1; Rare:73 | ||||
| chr15:72231362-72231520 | Common:1; Rare:46 | ||||
| chr15:72231589-72231649 | Rare:10 | ||||
| chr15:72272514-72272826 | Common:1; Rare:96 | ||||
| chr15:72375919-72376124 | Common:2; Rare:83; Clinvar:7; Clinvar (benign):2; Clinvar (pathogenic):5 | ||||
| chr15:72474178-72474630 | Rare:164 | ||||
| chr15:72475153-72475246 | Common:1; Rare:25 | ||||
| chr15:72686144-72686431 | Common:2; Rare:95; Clinvar:3; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr15:72783508-72783821 | Common:2; Rare:127 |