| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:75271139-75271346 | Common:1; Rare:39 | ||||
| chr17:75289387-75289692 | Common:2; Rare:93; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:75393794-75394117 | Common:1; Rare:73 | ||||
| chr17:75515427-75515647 | Common:3; Rare:65 | ||||
| chr17:75667131-75667429 | Common:4; Rare:100 | ||||
| chr17:75721159-75721577 | Common:3; Rare:130; Clinvar:2 | ||||
| chr17:75779183-75779421 | Common:1; Rare:124 | ||||
| chr17:75779659-75780087 | Common:1; Rare:172 | ||||
| chr17:75784564-75784894 | Common:2; Rare:150 | ||||
| chr17:75875935-75876267 | Rare:90 | ||||
| chr17:75904871-75904982 | Common:1; Rare:41 | ||||
| chr17:75979003-75979283 | Rare:80; Clinvar:4 | ||||
| chr17:75979381-75979470 | Common:1; Rare:26; Clinvar (benign):1 | ||||
| chr17:76072497-76072587 | Rare:29 | ||||
| chr17:76103712-76103867 | Common:4; Rare:49 |