| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:18039018-18039527 | Common:15; Rare:365; Clinvar:2; Clinvar (benign):3 | ||||
| chr17:18087693-18088026 | Rare:217 | ||||
| chr17:18088242-18088948 | Rare:271 | ||||
| chr17:18158020-18158390 | Common:3; Rare:185 | ||||
| chr17:18182916-18183624 | Common:2; Rare:455 | ||||
| chr17:18183625-18183988 | Common:2; Rare:386 | ||||
| chr17:18225200-18225750 | Common:7; Rare:151 | ||||
| chr17:18257707-18258057 | Common:2; Rare:89 | ||||
| chr17:18258633-18258868 | Common:2; Rare:112 | ||||
| chr17:18260393-18260722 | Rare:262 | ||||
| chr17:18260710-18261050 | Common:4; Rare:108 | ||||
| chr17:18261280-18261881 | Common:6; Rare:188 | ||||
| chr17:18314883-18315479 | Common:7; Rare:464 | ||||
| chr17:18363310-18363753 | Common:16; Rare:373 | ||||
| chr17:18377410-18377791 | Common:4; Rare:160 |