| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:42659231-42659304 | Rare:19 | ||||
| chr17:42761065-42761254 | Rare:52 | ||||
| chr17:42773369-42773470 | Rare:27 | ||||
| chr17:42798681-42798767 | Rare:24 | ||||
| chr17:42833093-42833471 | Rare:108 | ||||
| chr17:42964422-42964537 | Rare:54 | ||||
| chr17:42998378-42998486 | Common:3; Rare:40 | ||||
| chr17:43125359-43125590 | Rare:39; Clinvar:3; Clinvar (benign):2 | ||||
| chr17:43171030-43171245 | Rare:66 | ||||
| chr17:43398876-43398996 | Common:1; Rare:36 | ||||
| chr17:43483661-43484034 | Rare:103 | ||||
| chr17:43778911-43779073 | Rare:36 | ||||
| chr17:44070570-44070925 | Common:3; Rare:117; Clinvar:4; Clinvar (benign):2 | ||||
| chr17:44186666-44187002 | Common:1; Rare:121 | ||||
| chr17:44221211-44221478 | Rare:76 |