| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:31074184-31074452 | Common:1; Rare:74 | ||||
| chr16:31202686-31203049 | Common:2; Rare:120 | ||||
| chr16:31427813-31428023 | Common:18; Rare:78 | ||||
| chr16:31442763-31443059 | Common:1; Rare:48 | ||||
| chr16:31459091-31459161 | Rare:23 | ||||
| chr16:31459299-31459517 | Common:1; Rare:88 | ||||
| chr16:31472109-31472191 | Rare:23 | ||||
| chr16:31508374-31508484 | Common:2; Rare:43 | ||||
| chr16:46689134-46689435 | Common:1; Rare:106; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:46747864-46748107 | Rare:79 | ||||
| chr16:46748111-46748548 | Rare:94 | ||||
| chr16:46763040-46763343 | Common:1; Rare:48 | ||||
| chr16:46789924-46790066 | Common:4; Rare:30 | ||||
| chr16:46973523-46973757 | Rare:90 | ||||
| chr16:47461027-47461372 | Common:2; Rare:133; Clinvar (benign):2 |