| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:71564930-71564986 | Rare:22 | ||||
| chr16:71808774-71808875 | Common:1; Rare:58 | ||||
| chr16:71809034-71809308 | Common:3; Rare:88 | ||||
| chr16:71845895-71846038 | Common:2; Rare:45 | ||||
| chr16:71895306-71895578 | Common:3; Rare:99 | ||||
| chr16:72008517-72008773 | Common:5; Rare:94; Clinvar (benign):1 | ||||
| chr16:72093571-72093957 | Rare:97 | ||||
| chr16:74296460-74296909 | Common:1; Rare:149 | ||||
| chr16:74607074-74607195 | Rare:65 | ||||
| chr16:74666857-74667169 | Common:4; Rare:99 | ||||
| chr16:74701076-74701345 | Common:2; Rare:52 | ||||
| chr16:75433416-75433812 | Common:4; Rare:119 | ||||
| chr16:75566242-75566431 | Common:1; Rare:97 | ||||
| chr16:75623229-75623415 | Common:3; Rare:63 | ||||
| chr16:75647614-75647794 | Common:1; Rare:91; Clinvar:4; Clinvar (pathogenic):1 |