| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:72686122-72686234 | Common:2; Rare:43; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr15:72783497-72783775 | Common:1; Rare:109 | ||||
| chr15:73926322-73926471 | Rare:43 | ||||
| chr15:73994581-73994801 | Common:1; Rare:46 | ||||
| chr15:74461100-74461323 | Rare:67 | ||||
| chr15:74540966-74541276 | Common:4; Rare:109 | ||||
| chr15:74614696-74614904 | Common:1; Rare:68 | ||||
| chr15:74615622-74615898 | Common:3; Rare:92 | ||||
| chr15:74843113-74843318 | Common:1; Rare:62 | ||||
| chr15:74937997-74938265 | Common:2; Rare:93 | ||||
| chr15:74995329-74995608 | Common:5; Rare:102 | ||||
| chr15:75201767-75201908 | Rare:43 | ||||
| chr15:75347531-75347899 | Common:2; Rare:91 | ||||
| chr15:75368585-75368909 | Rare:87 | ||||
| chr15:75451656-75451983 | Common:1; Rare:90 |