| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:5097726-5098030 | Common:4; Rare:106 | ||||
| chr16:8797618-8797889 | Rare:106; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:8868982-8869310 | Common:6; Rare:146 | ||||
| chr16:10428610-10428937 | Common:2; Rare:69 | ||||
| chr16:10580563-10580781 | Rare:68 | ||||
| chr16:10743726-10743880 | Rare:65 | ||||
| chr16:10944326-10944637 | Common:1; Rare:97 | ||||
| chr16:11586891-11587036 | Common:1; Rare:44 | ||||
| chr16:11587161-11587313 | Common:1; Rare:35 | ||||
| chr16:11668195-11668522 | Common:3; Rare:138 | ||||
| chr16:11742805-11743108 | Common:2; Rare:120 | ||||
| chr16:11851406-11851657 | Common:1; Rare:129 | ||||
| chr16:11886911-11886977 | Rare:18 | ||||
| chr16:11894952-11895045 | Rare:15 | ||||
| chr16:11897992-11898231 | Common:2; Rare:52 |