| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:42609316-42609732 | Common:8; Rare:174; Clinvar (benign):2 | ||||
| chr17:42676986-42677224 | Common:1; Rare:69 | ||||
| chr17:42745023-42745151 | Common:3; Rare:46 | ||||
| chr17:42773362-42773478 | Rare:34 | ||||
| chr17:42798685-42798785 | Rare:28 | ||||
| chr17:42833093-42833514 | Rare:119 | ||||
| chr17:42964436-42964512 | Rare:36 | ||||
| chr17:42998176-42998515 | Common:4; Rare:96 | ||||
| chr17:43125313-43125680 | Rare:94; Clinvar:3; Clinvar (benign):3 | ||||
| chr17:43170292-43170554 | Common:3; Rare:51 | ||||
| chr17:43171023-43171370 | Common:1; Rare:109 | ||||
| chr17:43483691-43484028 | Rare:96 | ||||
| chr17:44070612-44070922 | Common:3; Rare:105; Clinvar:4; Clinvar (benign):2 | ||||
| chr17:44141651-44142015 | Common:2; Rare:82 | ||||
| chr17:44186666-44186998 | Common:1; Rare:120 |