| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:78002830-78003300 | Common:5; Rare:118 | ||||
| chr16:78796310-78796510 | Common:1; Rare:91 | ||||
| chr16:78957770-78958060 | Common:4; Rare:97 | ||||
| chr16:79001076-79001476 | Common:5; Rare:197 | ||||
| chr16:79124003-79125252 | Common:28; Rare:518 | ||||
| chr16:79165590-79165870 | Common:4; Rare:109 | ||||
| chr16:79597973-79598801 | Common:27; Rare:310 | ||||
| chr16:79598947-79599106 | Rare:38; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:79723860-79724170 | Common:1; Rare:87 | ||||
| chr16:79770450-79770990 | Common:8; Rare:198 | ||||
| chr16:80931997-80932497 | Common:5; Rare:187 | ||||
| chr16:81415838-81416018 | Common:1; Rare:51 | ||||
| chr16:81730361-81730761 | Common:1; Rare:166 | ||||
| chr16:82138952-82139251 | Common:2; Rare:97 | ||||
| chr16:83058006-83059089 | Common:28; Rare:440 |