| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:44218460-44219222 | Rare:436 | ||||
| chr17:44219466-44220032 | Common:6; Rare:532 | ||||
| chr17:44220793-44221039 | Rare:135 | ||||
| chr17:44221219-44221498 | Common:1; Rare:194 | ||||
| chr17:44222005-44222390 | Rare:178 | ||||
| chr17:44308320-44308920 | Common:4; Rare:232 | ||||
| chr17:44314870-44315215 | Common:4; Rare:124 | ||||
| chr17:44315230-44315710 | Common:4; Rare:155 | ||||
| chr17:44324706-44325034 | Common:11; Rare:321 | ||||
| chr17:44325240-44325754 | Common:7; Rare:156 | ||||
| chr17:44344987-44345424 | Common:5; Rare:227; Clinvar:15; Clinvar (benign):12 | ||||
| chr17:44345690-44346090 | Common:1; Rare:87 | ||||
| chr17:44351801-44352350 | Rare:275; Clinvar:18; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
| chr17:44385285-44385620 | Common:12; Rare:303; Clinvar:3 | ||||
| chr17:44503219-44503806 | Common:1; Rare:477 |