| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:89560479-89560756 | Common:1; Rare:133 | ||||
| chr16:89657657-89657881 | Common:2; Rare:122 | ||||
| chr16:89686560-89686766 | Common:8; Rare:104 | ||||
| chr16:89686916-89687049 | Common:2; Rare:57 | ||||
| chr16:89701634-89701808 | Common:1; Rare:62 | ||||
| chr16:89702024-89702266 | Common:9; Rare:78 | ||||
| chr16:89720590-89721150 | Common:6; Rare:176 | ||||
| chr16:89721340-89721690 | Common:3; Rare:152 | ||||
| chr16:89816602-89816854 | Common:5; Rare:140; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):3 | ||||
| chr16:89828340-89828539 | Rare:81 | ||||
| chr16:89873419-89873658 | Common:4; Rare:118 | ||||
| chr16:89874229-89874460 | Common:2; Rare:72 | ||||
| chr16:89921727-89922147 | Rare:111 | ||||
| chr16:89922817-89923372 | Common:3; Rare:185 | ||||
| chr16:89947938-89948338 | Common:7; Rare:120 |