| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:88650860-88651330 | Common:7; Rare:442; Clinvar (benign):8; Clinvar (pathogenic):4 | ||||
| chr16:88651350-88651850 | Common:9; Rare:232 | ||||
| chr16:88662204-88662604 | Common:5; Rare:85 | ||||
| chr16:88662985-88663436 | Common:67; Rare:1138 | ||||
| chr16:88663571-88663971 | Common:4; Rare:107 | ||||
| chr16:88686036-88686436 | Common:2; Rare:143 | ||||
| chr16:88686376-88686813 | Common:20; Rare:678 | ||||
| chr16:88700880-88701333 | Common:8; Rare:407 | ||||
| chr16:88706203-88706724 | Common:29; Rare:913 | ||||
| chr16:88784380-88784977 | Common:7; Rare:274; Clinvar (benign):1 | ||||
| chr16:88784970-88785304 | Common:11; Rare:399 | ||||
| chr16:88785413-88785813 | Rare:242 | ||||
| chr16:88802720-88803301 | Common:28; Rare:248 | ||||
| chr16:88803464-88803905 | Common:36; Rare:873 | ||||
| chr16:88804403-88804830 | Common:4; Rare:364; Clinvar (benign):6 |