| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:2460283-2460476 | Common:1; Rare:69 | ||||
| chr16:2474903-2475155 | Rare:80; Clinvar (benign):2 | ||||
| chr16:2513543-2514061 | Rare:203 | ||||
| chr16:2520192-2520459 | Common:8; Rare:155 | ||||
| chr16:2520878-2520999 | Rare:54 | ||||
| chr16:2537481-2538119 | Common:5; Rare:218 | ||||
| chr16:2682260-2682654 | Rare:176 | ||||
| chr16:2720973-2721221 | Common:1; Rare:73 | ||||
| chr16:2751767-2752064 | Rare:107 | ||||
| chr16:2752090-2752390 | Common:2; Rare:106 | ||||
| chr16:2752535-2752752 | Common:1; Rare:90 | ||||
| chr16:2752911-2753210 | Common:3; Rare:167 | ||||
| chr16:2777243-2777636 | Common:4; Rare:124 | ||||
| chr16:2830128-2830308 | Common:3; Rare:62 | ||||
| chr16:2882564-2882898 | Common:4; Rare:85 |