| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:88856896-88857163 | Common:4; Rare:127; Clinvar:1; Clinvar (benign):2 | ||||
| chr16:89508258-89508403 | Common:1; Rare:81 | ||||
| chr16:89657634-89658082 | Common:3; Rare:238 | ||||
| chr16:89686634-89686739 | Common:7; Rare:69 | ||||
| chr16:89816628-89816772 | Common:2; Rare:65; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:714807-714955 | Common:2; Rare:48 | ||||
| chr17:732345-732621 | Common:2; Rare:91 | ||||
| chr17:1491615-1491775 | Common:1; Rare:48 | ||||
| chr17:1516542-1516931 | Common:2; Rare:132 | ||||
| chr17:1716192-1716536 | Common:3; Rare:106 | ||||
| chr17:1829780-1830073 | Common:8; Rare:125 | ||||
| chr17:2303771-2303993 | Common:2; Rare:81 | ||||
| chr17:2336420-2336528 | Rare:41 | ||||
| chr17:3636241-3636496 | Common:4; Rare:71; Clinvar (benign):1 | ||||
| chr17:3668502-3668821 | Common:3; Rare:129 |