| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7686646-7687489 | Common:3; Rare:304; Clinvar:4; Clinvar (benign):3 | ||||
| chr17:7687410-7688622 | Common:21; Rare:753; Clinvar:20; Clinvar (benign):9 | ||||
| chr17:7688615-7689015 | Common:2; Rare:123; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:7717173-7718436 | Common:12; Rare:354 | ||||
| chr17:7843600-7843769 | Rare:189 | ||||
| chr17:7843846-7844270 | Common:17; Rare:347 | ||||
| chr17:7844710-7845201 | Common:8; Rare:532 | ||||
| chr17:7856549-7857368 | Common:7; Rare:764 | ||||
| chr17:7857383-7857820 | Common:18; Rare:723 | ||||
| chr17:7857840-7858160 | Common:3; Rare:557 | ||||
| chr17:7884708-7885780 | Common:24; Rare:1065 | ||||
| chr17:7885705-7886105 | Common:7; Rare:84 | ||||
| chr17:7930864-7931264 | Common:2; Rare:88 | ||||
| chr17:7931732-7932363 | Common:36; Rare:858 | ||||
| chr17:7933020-7933360 | Rare:209 |