| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:1974943-1975216 | Common:2; Rare:123 | ||||
| chr16:2009639-2009891 | Common:15; Rare:101 | ||||
| chr16:2026766-2027054 | Common:2; Rare:93 | ||||
| chr16:2033500-2033636 | Common:1; Rare:35 | ||||
| chr16:2035769-2035969 | Common:3; Rare:82 | ||||
| chr16:2047389-2047427 | Rare:9 | ||||
| chr16:2047764-2048056 | Rare:144; Clinvar:2; Clinvar (benign):4 | ||||
| chr16:2205683-2205875 | Common:4; Rare:91 | ||||
| chr16:2267780-2267902 | Rare:44 | ||||
| chr16:2268060-2268171 | Rare:56 | ||||
| chr16:2268358-2268497 | Common:1; Rare:52 | ||||
| chr16:2340577-2340936 | Common:3; Rare:128; Clinvar:5; Clinvar (benign):3 | ||||
| chr16:2459976-2460109 | Rare:33 | ||||
| chr16:2474970-2475157 | Rare:60; Clinvar (benign):2 | ||||
| chr16:2513667-2514179 | Common:1; Rare:198 |