| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7310968-7311017 | Rare:16 | ||||
| chr17:7311725-7311944 | Common:2; Rare:70 | ||||
| chr17:7390263-7390634 | Common:2; Rare:109 | ||||
| chr17:7836319-7836462 | Common:1; Rare:43 | ||||
| chr17:7838230-7838381 | Common:1; Rare:22 | ||||
| chr17:7885903-7886224 | Common:4; Rare:64 | ||||
| chr17:7910016-7910153 | Rare:23 | ||||
| chr17:8141098-8141565 | Rare:137 | ||||
| chr17:8200225-8200355 | Rare:37 | ||||
| chr17:8380880-8381152 | Common:3; Rare:54 | ||||
| chr17:13557198-13557339 | Common:1; Rare:27 | ||||
| chr17:15705037-15705088 | Common:1; Rare:17 | ||||
| chr17:16000340-16000623 | Common:2; Rare:56 | ||||
| chr17:16006346-16006667 | Common:1; Rare:90; Clinvar:3; Clinvar (pathogenic):2 | ||||
| chr17:16006961-16007269 | Common:2; Rare:63 |