| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:69106152-69106321 | Common:2; Rare:45 | ||||
| chr16:69132057-69132385 | Common:1; Rare:164 | ||||
| chr16:69132507-69132721 | Rare:201 | ||||
| chr16:69186946-69187295 | Rare:269 | ||||
| chr16:69187490-69188088 | Common:5; Rare:292 | ||||
| chr16:69311027-69311504 | Common:2; Rare:364 | ||||
| chr16:69329910-69330440 | Common:9; Rare:386 | ||||
| chr16:69330458-69330911 | Common:9; Rare:496; Clinvar (benign):3 | ||||
| chr16:69339427-69339871 | Common:6; Rare:525; Clinvar:3; Clinvar (benign):12 | ||||
| chr16:69385774-69386064 | Rare:199 | ||||
| chr16:69424304-69424789 | Common:8; Rare:361 | ||||
| chr16:69565609-69566190 | Common:14; Rare:501 | ||||
| chr16:69566307-69566777 | Common:4; Rare:203 | ||||
| chr16:69566817-69566995 | Rare:43 | ||||
| chr16:69726264-69727110 | Common:16; Rare:613 |