| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:58703059-58703284 | Common:1; Rare:38 | ||||
| chr15:58772090-58772120 | Rare:12 | ||||
| chr15:58847170-58847385 | Common:1; Rare:55 | ||||
| chr15:59051625-59051894 | Common:5; Rare:52 | ||||
| chr15:59138355-59138411 | Rare:24 | ||||
| chr15:59174125-59174340 | Common:1; Rare:57; Clinvar (pathogenic):1 | ||||
| chr15:59214640-59214950 | Common:1; Rare:82 | ||||
| chr15:59222176-59222388 | Rare:36 | ||||
| chr15:59222785-59222985 | Common:3; Rare:48 | ||||
| chr15:59223052-59223306 | Common:2; Rare:82 | ||||
| chr15:59235809-59235892 | Common:1; Rare:16 | ||||
| chr15:59246731-59246947 | Common:2; Rare:47 | ||||
| chr15:59342887-59342976 | Common:2; Rare:17 | ||||
| chr15:59371576-59371621 | Common:1; Rare:13 | ||||
| chr15:59371663-59371989 | Common:1; Rare:91 |