| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:75979103-75979274 | Rare:48; Clinvar:4 | ||||
| chr17:75979386-75979415 | Common:1; Rare:8; Clinvar (benign):1 | ||||
| chr17:76103712-76103867 | Common:4; Rare:49 | ||||
| chr17:76726487-76726865 | Common:5; Rare:132 | ||||
| chr17:76737329-76737525 | Common:2; Rare:72 | ||||
| chr17:78187042-78187365 | Common:3; Rare:102 | ||||
| chr17:78782278-78782587 | Common:9; Rare:97 | ||||
| chr17:79777896-79778198 | Common:1; Rare:136 | ||||
| chr17:80035861-80036012 | Common:1; Rare:53 | ||||
| chr17:80220304-80220468 | Common:1; Rare:64; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr17:81295278-81295433 | Common:2; Rare:37 | ||||
| chr17:81512720-81513094 | Common:7; Rare:197; Clinvar (benign):14 | ||||
| chr17:81666544-81666763 | Common:1; Rare:98 | ||||
| chr17:81683681-81684052 | Common:4; Rare:188 | ||||
| chr17:81703286-81703488 | Common:2; Rare:55; Clinvar (benign):2 |