| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:23641223-23641530 | Common:2; Rare:86; Clinvar:1; Clinvar (benign):3 | ||||
| chr16:24729604-24729844 | Common:7; Rare:101 | ||||
| chr16:25015262-25015461 | Common:2; Rare:68 | ||||
| chr16:25111472-25111829 | Common:2; Rare:102 | ||||
| chr16:27268712-27268872 | Common:1; Rare:57 | ||||
| chr16:27313239-27313635 | Common:3; Rare:79 | ||||
| chr16:27549861-27550167 | Common:2; Rare:119 | ||||
| chr16:28491933-28492127 | Common:2; Rare:46; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:28494340-28494679 | Rare:68 | ||||
| chr16:28538795-28539192 | Common:2; Rare:92 | ||||
| chr16:28822591-28822752 | Rare:64 | ||||
| chr16:28823975-28824091 | Rare:27 | ||||
| chr16:28846249-28846696 | Common:2; Rare:150; Clinvar:6; Clinvar (benign):6 | ||||
| chr16:28863504-28863875 | Common:1; Rare:99 | ||||
| chr16:28863918-28863979 | Rare:13 |