| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:68539029-68539681 | Common:13; Rare:501 | ||||
| chr16:68764895-68765295 | Rare:74 | ||||
| chr16:68843315-68843715 | Rare:336 | ||||
| chr16:68843900-68844220 | Rare:127 | ||||
| chr16:69105320-69105750 | Common:2; Rare:119 | ||||
| chr16:69105930-69106540 | Common:4; Rare:225 | ||||
| chr16:69131300-69132796 | Common:8; Rare:1267 | ||||
| chr16:69133391-69133567 | Rare:59 | ||||
| chr16:69186809-69187296 | Common:1; Rare:507 | ||||
| chr16:69187419-69188085 | Common:4; Rare:288 | ||||
| chr16:69310976-69311411 | Common:3; Rare:299 | ||||
| chr16:69319030-69319430 | Common:2; Rare:122 | ||||
| chr16:69328535-69329048 | Common:5; Rare:180; Clinvar:2; Clinvar (benign):4 | ||||
| chr16:69329047-69330322 | Common:8; Rare:612; Clinvar (benign):2 | ||||
| chr16:69330471-69330871 | Common:15; Rare:726; Clinvar (benign):4 |