| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:44219475-44220040 | Common:6; Rare:260 | ||||
| chr17:44220867-44221052 | Rare:60 | ||||
| chr17:44221208-44221402 | Rare:93 | ||||
| chr17:44324130-44324530 | Common:6; Rare:139 | ||||
| chr17:44324718-44325025 | Common:6; Rare:203 | ||||
| chr17:44325362-44325495 | Common:1; Rare:27 | ||||
| chr17:44345072-44345339 | Rare:113; Clinvar:10; Clinvar (benign):8 | ||||
| chr17:44385330-44385730 | Common:9; Rare:208; Clinvar:5 | ||||
| chr17:44503359-44503751 | Rare:283 | ||||
| chr17:44557065-44557437 | Common:2; Rare:93 | ||||
| chr17:44708559-44708923 | Common:8; Rare:185 | ||||
| chr17:44775590-44775820 | Common:1; Rare:85 | ||||
| chr17:44898820-44899260 | Common:8; Rare:155 | ||||
| chr17:44899341-44899801 | Common:6; Rare:263; Clinvar:6; Clinvar (benign):2 | ||||
| chr17:44947584-44947911 | Common:2; Rare:146 |