| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:42798661-42798792 | Rare:44 | ||||
| chr17:42832900-42833200 | Common:4; Rare:119 | ||||
| chr17:42833260-42833512 | Rare:153 | ||||
| chr17:42854010-42854135 | Common:1; Rare:16 | ||||
| chr17:42900490-42900802 | Common:2; Rare:112 | ||||
| chr17:42964406-42964579 | Common:1; Rare:121 | ||||
| chr17:42979860-42980333 | Common:4; Rare:182 | ||||
| chr17:42980473-42980614 | Common:2; Rare:117 | ||||
| chr17:42980780-42981040 | Rare:107 | ||||
| chr17:42998211-42998564 | Common:4; Rare:96 | ||||
| chr17:43022275-43022630 | Rare:132 | ||||
| chr17:43024902-43025446 | Common:2; Rare:189 | ||||
| chr17:43125294-43125738 | Rare:227; Clinvar:10; Clinvar (benign):8 | ||||
| chr17:43169748-43170148 | Common:7; Rare:109 | ||||
| chr17:43170195-43170557 | Common:6; Rare:139 |