| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:2392656-2392996 | Common:7; Rare:157 | ||||
| chr17:2511844-2512022 | Common:2; Rare:55 | ||||
| chr17:2593858-2593996 | Common:1; Rare:37; Clinvar:3; Clinvar (benign):3 | ||||
| chr17:3636231-3636508 | Common:4; Rare:84; Clinvar (benign):1 | ||||
| chr17:3668552-3668837 | Common:2; Rare:112 | ||||
| chr17:3723764-3723932 | Common:1; Rare:96 | ||||
| chr17:4143013-4143246 | Rare:76 | ||||
| chr17:4143638-4143745 | Common:3; Rare:59 | ||||
| chr17:4263943-4264065 | Rare:49 | ||||
| chr17:4433875-4433955 | Rare:19 | ||||
| chr17:4555293-4555570 | Common:4; Rare:129 | ||||
| chr17:4704104-4704280 | Rare:86 | ||||
| chr17:4807007-4807192 | Common:4; Rare:62 | ||||
| chr17:4833088-4833537 | Common:1; Rare:115 | ||||
| chr17:4939892-4940367 | Common:2; Rare:139 |