| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:3636712-3636814 | Common:1; Rare:28; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:3667853-3668253 | Rare:142 | ||||
| chr17:3668348-3668920 | Common:10; Rare:571 | ||||
| chr17:3723749-3724119 | Common:3; Rare:415 | ||||
| chr17:3754560-3755464 | Common:22; Rare:351 | ||||
| chr17:3845512-3846130 | Common:1; Rare:228 | ||||
| chr17:3846180-3846511 | Common:2; Rare:103 | ||||
| chr17:3892880-3893350 | Common:8; Rare:340 | ||||
| chr17:3963478-3964276 | Common:6; Rare:273 | ||||
| chr17:3964281-3964664 | Common:8; Rare:275 | ||||
| chr17:4142890-4143250 | Common:9; Rare:360 | ||||
| chr17:4143576-4143833 | Common:15; Rare:397 | ||||
| chr17:4143930-4144440 | Common:8; Rare:246 | ||||
| chr17:4187070-4187470 | Common:1; Rare:72 | ||||
| chr17:4263782-4264136 | Common:2; Rare:291 |