| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:89560532-89560902 | Rare:153 | ||||
| chr16:89616734-89616891 | Common:2; Rare:66 | ||||
| chr16:89657584-89658329 | Common:7; Rare:369; Clinvar (benign):1 | ||||
| chr16:89686520-89686982 | Common:11; Rare:226 | ||||
| chr16:89687332-89687528 | Rare:63 | ||||
| chr16:89720865-89720970 | Common:1; Rare:29 | ||||
| chr16:89816568-89816782 | Common:4; Rare:117; Clinvar:6; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
| chr16:89817675-89817784 | Common:1; Rare:47 | ||||
| chr16:89873475-89873858 | Common:3; Rare:172 | ||||
| chr16:89923171-89923372 | Rare:85 | ||||
| chr16:89971651-89971868 | Common:1; Rare:80 | ||||
| chr16:89972462-89972712 | Common:1; Rare:88 | ||||
| chr16:89972810-89972896 | Common:1; Rare:30 | ||||
| chr16:90022551-90022721 | Common:1; Rare:70 | ||||
| chr17:331023-331540 | Common:16; Rare:115 |