| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7627718-7628016 | Common:3; Rare:99 | ||||
| chr17:7686413-7686677 | Rare:65 | ||||
| chr17:7843686-7843746 | Rare:21 | ||||
| chr17:7857096-7857353 | Common:1; Rare:129 | ||||
| chr17:7857382-7858095 | Common:5; Rare:231 | ||||
| chr17:7858172-7858299 | Common:1; Rare:43 | ||||
| chr17:7885194-7885351 | Rare:51 | ||||
| chr17:7885519-7885565 | Rare:9 | ||||
| chr17:7931810-7932258 | Common:5; Rare:125 | ||||
| chr17:8087526-8087592 | Rare:14 | ||||
| chr17:8087698-8088077 | Common:1; Rare:79 | ||||
| chr17:8103688-8103832 | Rare:29 | ||||
| chr17:8152348-8152611 | Common:2; Rare:62 | ||||
| chr17:8176313-8176441 | Rare:44 | ||||
| chr17:8248021-8248129 | Common:2; Rare:54; Clinvar:3; Clinvar (benign):3 |