| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:69339548-69339821 | Common:1; Rare:110; Clinvar (benign):1 | ||||
| chr16:69726435-69726734 | Common:4; Rare:80 | ||||
| chr16:69762185-69762381 | Common:1; Rare:57 | ||||
| chr16:70346751-70346940 | Common:1; Rare:95 | ||||
| chr16:70523532-70523844 | Common:3; Rare:100; Clinvar (pathogenic):1 | ||||
| chr16:71845877-71846023 | Common:2; Rare:50 | ||||
| chr16:71895315-71895540 | Common:2; Rare:74 | ||||
| chr16:72093587-72093934 | Rare:86 | ||||
| chr16:74296719-74296894 | Rare:72 | ||||
| chr16:74607093-74607232 | Rare:73 | ||||
| chr16:74701133-74701343 | Common:1; Rare:47 | ||||
| chr16:75647635-75647809 | Common:2; Rare:82; Clinvar:3 | ||||
| chr16:75648086-75648242 | Rare:67 | ||||
| chr16:77190686-77191010 | Common:10; Rare:107 | ||||
| chr16:78099512-78099715 | Common:1; Rare:83 |