| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:70432056-70432929 | Rare:297 | ||||
| chr16:70433343-70433677 | Rare:89 | ||||
| chr16:70433676-70434116 | Common:3; Rare:146 | ||||
| chr16:70434395-70434795 | Common:4; Rare:114 | ||||
| chr16:70437051-70437451 | Common:1; Rare:167 | ||||
| chr16:70437541-70438311 | Common:2; Rare:278 | ||||
| chr16:70476590-70476836 | Common:1; Rare:42 | ||||
| chr16:70483420-70483890 | Common:1; Rare:117; Clinvar:1; Clinvar (benign):1 | ||||
| chr16:70520687-70521680 | Common:10; Rare:233 | ||||
| chr16:70522387-70522582 | Common:1; Rare:50 | ||||
| chr16:70525127-70525317 | Common:4; Rare:87 | ||||
| chr16:70737129-70737904 | Common:33; Rare:627 | ||||
| chr16:70792004-70792404 | Rare:95 | ||||
| chr16:71369390-71369970 | Common:5; Rare:123 | ||||
| chr16:71426389-71426577 | Common:3; Rare:124 |