| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:8138125-8138214 | Rare:9 | ||||
| chr17:8138962-8139131 | Common:6; Rare:74 | ||||
| chr17:8173359-8173592 | Common:12; Rare:317; Clinvar:3; Clinvar (pathogenic):4 | ||||
| chr17:8186233-8186354 | Common:1; Rare:40 | ||||
| chr17:8186364-8186395 | Rare:16 | ||||
| chr17:8186825-8187158 | Common:4; Rare:178 | ||||
| chr17:8187421-8187591 | Common:5; Rare:54 | ||||
| chr17:8189890-8189922 | Rare:10 | ||||
| chr17:8192204-8192490 | Common:3; Rare:56 | ||||
| chr17:8196056-8196292 | Rare:42 | ||||
| chr17:8220938-8221041 | Common:3; Rare:46 | ||||
| chr17:8221338-8221567 | Common:3; Rare:98 | ||||
| chr17:8221926-8222649 | Common:4; Rare:264 | ||||
| chr17:8222904-8223241 | Common:2; Rare:108 | ||||
| chr17:8223525-8223654 | Rare:23 |