| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:89508280-89508451 | Common:1; Rare:99; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:89560504-89560717 | Rare:96 | ||||
| chr16:89657647-89658089 | Common:3; Rare:233 | ||||
| chr16:89686567-89686707 | Common:6; Rare:63 | ||||
| chr16:89720865-89720993 | Common:1; Rare:34 | ||||
| chr16:89816625-89816823 | Common:5; Rare:101; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:89873474-89873797 | Common:2; Rare:148 | ||||
| chr16:89972478-89972614 | Common:1; Rare:47 | ||||
| chr16:90022533-90022716 | Common:1; Rare:73 | ||||
| chr17:336203-336323 | Rare:33 | ||||
| chr17:386216-386405 | Common:3; Rare:45 | ||||
| chr17:714794-714870 | Common:2; Rare:29 | ||||
| chr17:752253-752379 | Common:1; Rare:42 | ||||
| chr17:752787-752891 | Rare:27 | ||||
| chr17:996793-997158 | Common:2; Rare:109 |