| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:51166318-51166552 | Common:2; Rare:56 | ||||
| chr17:51166684-51166938 | Rare:71 | ||||
| chr17:51259988-51260587 | Common:3; Rare:214 | ||||
| chr17:54968608-54968799 | Common:3; Rare:91 | ||||
| chr17:55421867-55422182 | Common:2; Rare:111 | ||||
| chr17:55751041-55751091 | Rare:17 | ||||
| chr17:56961015-56961071 | Common:1; Rare:27 | ||||
| chr17:56978042-56978182 | Common:3; Rare:74 | ||||
| chr17:57084980-57085329 | Rare:117 | ||||
| chr17:57257007-57257024 | Rare:9 | ||||
| chr17:57850006-57850274 | Common:1; Rare:86 | ||||
| chr17:57988180-57988535 | Common:5; Rare:103 | ||||
| chr17:58007210-58007390 | Common:1; Rare:78 | ||||
| chr17:58007609-58007756 | Rare:34 | ||||
| chr17:58219234-58219372 | Common:1; Rare:57; Clinvar:2; Clinvar (benign):3 |