| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:77129847-77130127 | Common:1; Rare:44 | ||||
| chr17:78187052-78187382 | Common:3; Rare:104 | ||||
| chr17:78782233-78782577 | Common:9; Rare:116 | ||||
| chr17:78840758-78841035 | Common:2; Rare:102 | ||||
| chr17:79022904-79022989 | Common:1; Rare:21 | ||||
| chr17:79025356-79025774 | Common:8; Rare:75 | ||||
| chr17:80035831-80035989 | Common:1; Rare:54 | ||||
| chr17:80220289-80220468 | Common:1; Rare:72; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr17:80415114-80415189 | Common:1; Rare:49 | ||||
| chr17:81239038-81239321 | Common:2; Rare:93 | ||||
| chr17:81666554-81666763 | Common:1; Rare:91 | ||||
| chr17:81683713-81684069 | Common:4; Rare:180 | ||||
| chr17:81703294-81703517 | Common:2; Rare:62; Clinvar (benign):2 | ||||
| chr17:81833242-81833335 | Rare:39 | ||||
| chr17:81937261-81937415 | Rare:56 |