| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:71895254-71895578 | Common:3; Rare:123 | ||||
| chr16:72093579-72093934 | Rare:89 | ||||
| chr16:73059080-73059104 | Rare:1 | ||||
| chr16:74296458-74296938 | Common:1; Rare:160 | ||||
| chr16:74607074-74607192 | Rare:65 | ||||
| chr16:74666857-74667091 | Common:1; Rare:78 | ||||
| chr16:75116726-75116799 | Common:2; Rare:24 | ||||
| chr16:75433330-75433869 | Common:4; Rare:180 | ||||
| chr16:75556212-75556369 | Common:2; Rare:57; Clinvar (benign):4 | ||||
| chr16:75566242-75566439 | Common:1; Rare:102 | ||||
| chr16:75623208-75623378 | Common:4; Rare:65 | ||||
| chr16:75647605-75647837 | Common:2; Rare:114; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr16:77190702-77191010 | Common:10; Rare:101 | ||||
| chr16:77191133-77191221 | Common:1; Rare:39 | ||||
| chr16:79600732-79600958 | Common:1; Rare:65 |