| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7479675-7479829 | Common:4; Rare:32 | ||||
| chr17:7483787-7484010 | Common:3; Rare:56 | ||||
| chr17:7484238-7484628 | Common:3; Rare:170 | ||||
| chr17:7484646-7484993 | Common:1; Rare:143 | ||||
| chr17:7548346-7548529 | Common:2; Rare:23 | ||||
| chr17:7548846-7549013 | Rare:49 | ||||
| chr17:7549020-7549048 | Rare:4 | ||||
| chr17:7558097-7558340 | Common:1; Rare:48 | ||||
| chr17:7561693-7561923 | Rare:67 | ||||
| chr17:7562420-7562474 | Rare:6 | ||||
| chr17:7572380-7572508 | Rare:30 | ||||
| chr17:7572535-7572932 | Common:1; Rare:195 | ||||
| chr17:7573460-7573884 | Common:2; Rare:148 | ||||
| chr17:7579409-7579675 | Common:1; Rare:87 | ||||
| chr17:7583632-7583952 | Common:1; Rare:126; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):1 |