| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:84145105-84145325 | Common:2; Rare:106; Clinvar:4 | ||||
| chr16:84368391-84368599 | Common:3; Rare:81 | ||||
| chr16:84504616-84504853 | Common:8; Rare:101 | ||||
| chr16:85027618-85027801 | Common:1; Rare:95 | ||||
| chr16:85613061-85613339 | Common:1; Rare:102 | ||||
| chr16:85799574-85799748 | Common:2; Rare:53 | ||||
| chr16:85898998-85899183 | Common:3; Rare:51 | ||||
| chr16:86555174-86555306 | Rare:68 | ||||
| chr16:87765919-87766017 | Rare:41 | ||||
| chr16:88570208-88570482 | Common:1; Rare:113 | ||||
| chr16:88663070-88663374 | Common:8; Rare:125 | ||||
| chr16:88856810-88857166 | Common:4; Rare:168; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:89217619-89217712 | Common:1; Rare:42 | ||||
| chr16:89560535-89560710 | Rare:74 | ||||
| chr16:89657647-89658113 | Common:3; Rare:243 |