| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:76353596-76353692 | Rare:39 | ||||
| chr17:76353796-76354236 | Common:2; Rare:138 | ||||
| chr17:76384468-76384650 | Common:1; Rare:51 | ||||
| chr17:76537811-76537898 | Rare:20 | ||||
| chr17:76537904-76537960 | Rare:18 | ||||
| chr17:76710997-76711212 | Common:2; Rare:54 | ||||
| chr17:76725811-76726051 | Rare:66 | ||||
| chr17:76726424-76727161 | Common:7; Rare:290 | ||||
| chr17:76737316-76737704 | Common:4; Rare:139 | ||||
| chr17:76737826-76738131 | Common:4; Rare:89 | ||||
| chr17:77140661-77141089 | Common:2; Rare:147 | ||||
| chr17:77287762-77287993 | Rare:32 | ||||
| chr17:77319355-77319562 | Common:3; Rare:58; Clinvar (benign):3 | ||||
| chr17:77450606-77450789 | Rare:36 | ||||
| chr17:78186968-78187430 | Common:3; Rare:169 |