| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7843944-7844197 | Common:3; Rare:70 | ||||
| chr17:7854912-7855111 | Common:1; Rare:81 | ||||
| chr17:7857163-7857296 | Common:1; Rare:73 | ||||
| chr17:7857431-7857735 | Common:2; Rare:96 | ||||
| chr17:7857869-7858074 | Rare:71 | ||||
| chr17:7885187-7885351 | Rare:51 | ||||
| chr17:7931890-7932258 | Common:5; Rare:99 | ||||
| chr17:8146450-8146692 | Rare:90 | ||||
| chr17:8147743-8148022 | Rare:92 | ||||
| chr17:8152348-8152549 | Common:2; Rare:44 | ||||
| chr17:8156589-8156869 | Common:3; Rare:77 | ||||
| chr17:8162881-8163079 | Common:1; Rare:65 | ||||
| chr17:8176297-8176483 | Rare:61 | ||||
| chr17:8190009-8190492 | Common:1; Rare:146 | ||||
| chr17:8248025-8248142 | Common:2; Rare:57; Clinvar:3; Clinvar (benign):2 |