| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:2155289-2155856 | Common:4; Rare:361 | ||||
| chr16:2163500-2164234 | Common:17; Rare:478 | ||||
| chr16:2189522-2189842 | Common:1; Rare:88 | ||||
| chr16:2196540-2196960 | Common:1; Rare:123 | ||||
| chr16:2205683-2205892 | Common:8; Rare:184 | ||||
| chr16:2214767-2215104 | Common:4; Rare:245 | ||||
| chr16:2223304-2223688 | Rare:308 | ||||
| chr16:2251542-2251736 | Rare:71 | ||||
| chr16:2267766-2268610 | Common:13; Rare:598 | ||||
| chr16:2340658-2340936 | Common:2; Rare:106; Clinvar:3; Clinvar (benign):2 | ||||
| chr16:2429084-2429494 | Common:5; Rare:253 | ||||
| chr16:2459963-2460145 | Common:1; Rare:102 | ||||
| chr16:2474961-2475186 | Rare:126; Clinvar (benign):7 | ||||
| chr16:2513520-2514064 | Rare:266 | ||||
| chr16:2537676-2538098 | Common:8; Rare:312 |