| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:88706325-88706563 | Common:5; Rare:120 | ||||
| chr16:88811891-88812022 | Common:2; Rare:65; Clinvar (benign):1 | ||||
| chr16:88856893-88857178 | Common:4; Rare:139; Clinvar:1; Clinvar (benign):2 | ||||
| chr16:89217619-89217738 | Common:1; Rare:56 | ||||
| chr16:89508296-89508424 | Rare:72; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr16:89560535-89560732 | Rare:88 | ||||
| chr16:89657644-89658095 | Common:3; Rare:236 | ||||
| chr16:89686504-89686716 | Common:7; Rare:89 | ||||
| chr16:89720838-89721003 | Common:1; Rare:46 | ||||
| chr16:89816619-89816767 | Common:2; Rare:71; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:89873471-89873773 | Common:2; Rare:138 | ||||
| chr16:89948560-89948803 | Common:3; Rare:72 | ||||
| chr16:89972478-89972658 | Common:1; Rare:66 | ||||
| chr16:90019348-90019691 | Common:6; Rare:104 | ||||
| chr16:90022544-90022709 | Rare:64 |