| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:69339562-69339821 | Common:1; Rare:103; Clinvar (benign):1 | ||||
| chr16:69424334-69424678 | Common:2; Rare:86 | ||||
| chr16:70289440-70289767 | Common:3; Rare:135; Clinvar:1 | ||||
| chr16:70299092-70299230 | Common:1; Rare:29 | ||||
| chr16:70346759-70346945 | Common:1; Rare:91 | ||||
| chr16:70523539-70523879 | Common:3; Rare:107 | ||||
| chr16:71808799-71809129 | Common:1; Rare:136 | ||||
| chr16:71845890-71846017 | Common:2; Rare:41 | ||||
| chr16:71895330-71895578 | Common:1; Rare:84 | ||||
| chr16:72093587-72093934 | Rare:86 | ||||
| chr16:74296498-74296882 | Common:1; Rare:125 | ||||
| chr16:74607074-74607398 | Common:2; Rare:136 | ||||
| chr16:74700845-74701015 | Common:2; Rare:31 | ||||
| chr16:75433402-75433798 | Common:4; Rare:120 | ||||
| chr16:75647605-75647794 | Common:1; Rare:94; Clinvar:4; Clinvar (pathogenic):1 |