| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:38825172-38825408 | Common:2; Rare:71 | ||||
| chr17:38853698-38853889 | Common:3; Rare:77 | ||||
| chr17:39200009-39200358 | Common:2; Rare:110 | ||||
| chr17:39461910-39462078 | Common:3; Rare:41 | ||||
| chr17:39637008-39637174 | Common:3; Rare:52 | ||||
| chr17:39688018-39688094 | Rare:24 | ||||
| chr17:40140202-40140544 | Common:5; Rare:175 | ||||
| chr17:40318079-40318360 | Common:1; Rare:61 | ||||
| chr17:40322466-40322777 | Rare:75 | ||||
| chr17:40341181-40341425 | Rare:68 | ||||
| chr17:40342034-40342426 | Common:1; Rare:83 | ||||
| chr17:41688670-41688956 | Common:1; Rare:118 | ||||
| chr17:41689295-41689755 | Common:4; Rare:162 | ||||
| chr17:42017402-42017576 | Common:1; Rare:59 | ||||
| chr17:42536124-42536262 | Common:1; Rare:46; Clinvar:3; Clinvar (benign):1 |