| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:1971884-1972167 | Common:3; Rare:82 | ||||
| chr16:2009637-2009980 | Common:16; Rare:143 | ||||
| chr16:2047770-2048038 | Rare:124; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:2155292-2155500 | Rare:90 | ||||
| chr16:2155519-2155857 | Common:2; Rare:98 | ||||
| chr16:2205670-2205889 | Common:4; Rare:103 | ||||
| chr16:2215176-2215333 | Common:1; Rare:51 | ||||
| chr16:2223303-2223688 | Rare:155 | ||||
| chr16:2267772-2267863 | Common:3; Rare:32 | ||||
| chr16:2268055-2268193 | Common:1; Rare:69 | ||||
| chr16:2268351-2268506 | Common:1; Rare:55 | ||||
| chr16:2340772-2341104 | Common:2; Rare:92 | ||||
| chr16:2429121-2429484 | Common:3; Rare:119 | ||||
| chr16:2459945-2460161 | Common:2; Rare:64 | ||||
| chr16:2474987-2475151 | Rare:53 |