| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:42566994-42567120 | Common:3; Rare:38 | ||||
| chr17:42577671-42577864 | Common:1; Rare:96 | ||||
| chr17:42609328-42609732 | Common:8; Rare:170; Clinvar (benign):2 | ||||
| chr17:42659381-42659421 | Rare:10 | ||||
| chr17:42760650-42760916 | Common:5; Rare:88 | ||||
| chr17:42760963-42761058 | Rare:21 | ||||
| chr17:42761083-42761264 | Rare:51 | ||||
| chr17:42773369-42773470 | Rare:27 | ||||
| chr17:42798685-42798767 | Rare:21 | ||||
| chr17:42833333-42833488 | Rare:59 | ||||
| chr17:42964436-42964537 | Rare:49 | ||||
| chr17:42980444-42980552 | Rare:34 | ||||
| chr17:42998241-42998475 | Common:3; Rare:69 | ||||
| chr17:43125345-43125643 | Rare:72; Clinvar:3; Clinvar (benign):2 | ||||
| chr17:43170271-43170407 | Rare:27 |