| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:1771521-1771623 | Rare:42 | ||||
| chr16:1782509-1782767 | Common:4; Rare:84 | ||||
| chr16:1943169-1943497 | Common:1; Rare:102 | ||||
| chr16:1964511-1965074 | Common:18; Rare:241 | ||||
| chr16:1971938-1972113 | Common:1; Rare:50 | ||||
| chr16:2047795-2048050 | Rare:121; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:2205687-2205894 | Common:4; Rare:97 | ||||
| chr16:2268072-2268482 | Common:4; Rare:138 | ||||
| chr16:2429155-2429472 | Common:2; Rare:100 | ||||
| chr16:2459976-2460109 | Rare:33 | ||||
| chr16:2474993-2475151 | Rare:51 | ||||
| chr16:2537705-2538066 | Common:4; Rare:139 | ||||
| chr16:2776997-2777353 | Common:2; Rare:124 | ||||
| chr16:2911746-2912048 | Common:5; Rare:98 | ||||
| chr16:2980436-2980621 | Common:2; Rare:63 |