| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:87317293-87317594 | Common:8; Rare:122 | ||||
| chr16:87765886-87766062 | Common:1; Rare:72 | ||||
| chr16:87951213-87951506 | Common:2; Rare:109 | ||||
| chr16:88570159-88570467 | Common:2; Rare:115 | ||||
| chr16:88663034-88663382 | Common:9; Rare:149 | ||||
| chr16:88706251-88706555 | Common:4; Rare:143 | ||||
| chr16:88728115-88728281 | Common:1; Rare:61 | ||||
| chr16:88811891-88812052 | Common:2; Rare:71; Clinvar (benign):1 | ||||
| chr16:88856873-88857178 | Common:4; Rare:144; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:89093763-89093936 | Common:3; Rare:76 | ||||
| chr16:89217565-89217738 | Common:1; Rare:84 | ||||
| chr16:89508296-89508516 | Common:1; Rare:116; Clinvar:5; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr16:89560513-89560712 | Rare:87 | ||||
| chr16:89657637-89658130 | Common:3; Rare:249 | ||||
| chr16:89686585-89686706 | Common:6; Rare:58 |