| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:17972378-17972639 | Common:1; Rare:78 | ||||
| chr17:18039095-18039371 | Common:3; Rare:70; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:18087793-18088027 | Rare:62 | ||||
| chr17:18183023-18183111 | Rare:30 | ||||
| chr17:18183317-18183504 | Rare:47 | ||||
| chr17:18183723-18183925 | Rare:89 | ||||
| chr17:18225354-18225682 | Common:4; Rare:111 | ||||
| chr17:18314903-18315339 | Common:1; Rare:124 | ||||
| chr17:18363487-18363705 | Common:4; Rare:74 | ||||
| chr17:18682216-18682465 | Common:8; Rare:25 | ||||
| chr17:18697970-18698039 | Common:1; Rare:17 | ||||
| chr17:18781083-18781318 | Common:5; Rare:66 | ||||
| chr17:18856184-18856391 | Common:1; Rare:39 | ||||
| chr17:19362570-19362773 | Common:2; Rare:94; Clinvar:1; Clinvar (benign):2 | ||||
| chr17:19377638-19377774 | Common:2; Rare:36 |