| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:74361843-74362060 | Common:1; Rare:43 | ||||
| chr17:74430650-74431150 | Common:5; Rare:115 | ||||
| chr17:74431271-74431464 | Common:1; Rare:56 | ||||
| chr17:74431826-74432128 | Common:2; Rare:100 | ||||
| chr17:74433780-74434180 | Common:5; Rare:127 | ||||
| chr17:74748423-74748691 | Common:4; Rare:100 | ||||
| chr17:74763883-74764170 | Common:3; Rare:54 | ||||
| chr17:74776261-74776562 | Common:5; Rare:101 | ||||
| chr17:74872525-74872994 | Common:5; Rare:202; Clinvar (pathogenic):1 | ||||
| chr17:74873240-74873527 | Common:5; Rare:96 | ||||
| chr17:74971941-74972304 | Common:2; Rare:96 | ||||
| chr17:74972303-74973008 | Common:3; Rare:207 | ||||
| chr17:74987482-74987670 | Rare:54 | ||||
| chr17:74987802-74988557 | Common:1; Rare:175 | ||||
| chr17:75012518-75012696 | Common:1; Rare:42 |