| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:72206855-72207279 | Common:2; Rare:87 | ||||
| chr15:72231083-72231504 | Common:3; Rare:129 | ||||
| chr15:72231586-72231881 | Common:2; Rare:58 | ||||
| chr15:72375944-72376146 | Common:3; Rare:81; Clinvar:7; Clinvar (benign):2; Clinvar (pathogenic):5 | ||||
| chr15:73633189-73633561 | Common:1; Rare:144 | ||||
| chr15:73994583-73994801 | Common:1; Rare:46 | ||||
| chr15:74461107-74461319 | Rare:65 | ||||
| chr15:74540964-74541283 | Common:4; Rare:112 | ||||
| chr15:74615594-74615898 | Common:4; Rare:99 | ||||
| chr15:74695948-74696098 | Rare:52 | ||||
| chr15:74781908-74782114 | Common:3; Rare:66 | ||||
| chr15:74842650-74842849 | Rare:40 | ||||
| chr15:74843014-74843318 | Common:2; Rare:94 | ||||
| chr15:74906760-74906856 | Common:1; Rare:42 | ||||
| chr15:74937925-74938227 | Common:3; Rare:96 |