| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:44066628-44066800 | Common:1; Rare:57 | ||||
| chr17:44070168-44070301 | Common:1; Rare:31 | ||||
| chr17:44070601-44070985 | Common:3; Rare:132; Clinvar:4; Clinvar (benign):2 | ||||
| chr17:44071063-44071194 | Rare:51; Clinvar:2; Clinvar (pathogenic):4 | ||||
| chr17:44086890-44087199 | Common:2; Rare:92 | ||||
| chr17:44111204-44111319 | Rare:37 | ||||
| chr17:44123569-44123895 | Common:3; Rare:92 | ||||
| chr17:44123969-44124107 | Rare:33 | ||||
| chr17:44141775-44142044 | Common:1; Rare:68 | ||||
| chr17:44142142-44142149 | |||||
| chr17:44186473-44187050 | Common:3; Rare:177 | ||||
| chr17:44199355-44199509 | Common:1; Rare:44 | ||||
| chr17:44199731-44200553 | Common:4; Rare:300 | ||||
| chr17:44210427-44210587 | Rare:67 | ||||
| chr17:44218562-44218810 | Rare:89 |