| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7479545-7479774 | Common:1; Rare:36 | ||||
| chr17:7484226-7484370 | Common:1; Rare:59 | ||||
| chr17:7561803-7561996 | Common:2; Rare:52 | ||||
| chr17:7583510-7583858 | Common:1; Rare:139; Clinvar:3; Clinvar (benign):3 | ||||
| chr17:7627444-7627583 | Common:1; Rare:40 | ||||
| chr17:7687476-7687625 | Rare:31 | ||||
| chr17:7854853-7855080 | Common:1; Rare:74 | ||||
| chr17:7857198-7857371 | Common:1; Rare:90 | ||||
| chr17:7931876-7932208 | Common:5; Rare:89 | ||||
| chr17:8162936-8163082 | Rare:41 | ||||
| chr17:8176333-8176455 | Rare:41 | ||||
| chr17:8210555-8210710 | Common:2; Rare:30 | ||||
| chr17:8248042-8248159 | Common:3; Rare:51; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:8435650-8435971 | Common:4; Rare:136 | ||||
| chr17:10697503-10697653 | Common:3; Rare:59; Clinvar:2; Clinvar (benign):2 |