| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:1827171-1827232 | Common:1; Rare:31 | ||||
| chr16:1943183-1943518 | Common:1; Rare:105 | ||||
| chr16:1964572-1965074 | Common:17; Rare:224 | ||||
| chr16:1971878-1972153 | Common:3; Rare:80 | ||||
| chr16:2009674-2009965 | Common:15; Rare:125 | ||||
| chr16:2047737-2048038 | Rare:142; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:2155670-2155815 | Common:1; Rare:44 | ||||
| chr16:2268071-2268468 | Common:4; Rare:137 | ||||
| chr16:2429126-2429478 | Common:2; Rare:116 | ||||
| chr16:2459963-2460150 | Common:1; Rare:57 | ||||
| chr16:2474982-2475151 | Rare:53 | ||||
| chr16:2537697-2538071 | Common:4; Rare:142 | ||||
| chr16:2682343-2682628 | Rare:136 | ||||
| chr16:2777235-2777392 | Common:1; Rare:65 | ||||
| chr16:2911763-2912018 | Common:3; Rare:88 |