| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:2047727-2048038 | Rare:149; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:2205683-2205937 | Common:5; Rare:117 | ||||
| chr16:2459980-2460146 | Common:1; Rare:48 | ||||
| chr16:2519254-2519580 | Common:1; Rare:106 | ||||
| chr16:2682367-2682628 | Rare:119 | ||||
| chr16:2777023-2777371 | Common:2; Rare:122 | ||||
| chr16:2911739-2912018 | Common:3; Rare:97 | ||||
| chr16:2980410-2980619 | Common:2; Rare:73 | ||||
| chr16:3020064-3020476 | Rare:127 | ||||
| chr16:3065207-3065493 | Common:5; Rare:77 | ||||
| chr16:3112506-3112608 | Common:1; Rare:26 | ||||
| chr16:3134859-3135172 | Common:3; Rare:89 | ||||
| chr16:3263665-3263823 | Common:1; Rare:40 | ||||
| chr16:3282819-3282936 | Common:1; Rare:43 | ||||
| chr16:3305385-3305514 | Common:1; Rare:46 |