| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:77140661-77141059 | Common:2; Rare:137 | ||||
| chr17:77319348-77319602 | Common:3; Rare:68; Clinvar (benign):3 | ||||
| chr17:77320077-77320329 | Common:1; Rare:66; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr17:77373277-77373531 | Common:1; Rare:100; Clinvar (benign):1 | ||||
| chr17:77450409-77450729 | Common:1; Rare:74 | ||||
| chr17:78187029-78187386 | Common:3; Rare:117 | ||||
| chr17:78360160-78360461 | Common:2; Rare:85 | ||||
| chr17:78782219-78782577 | Common:9; Rare:116 | ||||
| chr17:78840751-78841047 | Common:2; Rare:106 | ||||
| chr17:78924960-78925026 | Rare:9 | ||||
| chr17:79009727-79009917 | Common:8; Rare:60; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:79023854-79024290 | Common:1; Rare:94 | ||||
| chr17:80035843-80036037 | Common:1; Rare:68 | ||||
| chr17:80147003-80147331 | Common:8; Rare:138 | ||||
| chr17:80220309-80220468 | Common:1; Rare:61; Clinvar:1; Clinvar (pathogenic):2 |