| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:75271094-75271442 | Common:8; Rare:123 | ||||
| chr17:75289358-75289671 | Common:6; Rare:191; Clinvar:2; Clinvar (benign):4 | ||||
| chr17:75393530-75394220 | Common:2; Rare:270 | ||||
| chr17:75405505-75406150 | Common:3; Rare:248 | ||||
| chr17:75456436-75456671 | Common:1; Rare:117 | ||||
| chr17:75515451-75515767 | Common:6; Rare:176 | ||||
| chr17:75516391-75516615 | Common:4; Rare:121; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr17:75525474-75525754 | Common:5; Rare:179 | ||||
| chr17:75532130-75532480 | Common:3; Rare:138 | ||||
| chr17:75667106-75667439 | Common:8; Rare:194 | ||||
| chr17:75721159-75721564 | Common:6; Rare:240; Clinvar:4 | ||||
| chr17:75727230-75727800 | Common:2; Rare:198; Clinvar:3; Clinvar (pathogenic):2 | ||||
| chr17:75765141-75765291 | Common:2; Rare:87; Clinvar:2 | ||||
| chr17:75779131-75779538 | Common:2; Rare:266 | ||||
| chr17:75779746-75780068 | Rare:118 |