| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:84116801-84117072 | Common:3; Rare:109 | ||||
| chr16:84617824-84618030 | Common:1; Rare:85 | ||||
| chr16:85027579-85027813 | Common:2; Rare:129 | ||||
| chr16:85799508-85799774 | Common:2; Rare:83 | ||||
| chr16:86555182-86555306 | Rare:63 | ||||
| chr16:87317363-87317516 | Common:4; Rare:58 | ||||
| chr16:88570179-88570424 | Common:1; Rare:88 | ||||
| chr16:88663044-88663374 | Common:8; Rare:138 | ||||
| chr16:88706343-88706587 | Common:4; Rare:121 | ||||
| chr16:88856900-88857192 | Common:4; Rare:149; Clinvar:1; Clinvar (benign):2 | ||||
| chr16:89217627-89217746 | Common:1; Rare:52 | ||||
| chr16:89508258-89508452 | Common:2; Rare:113; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:89657583-89658133 | Common:4; Rare:275; Clinvar (benign):1 | ||||
| chr16:89816626-89816767 | Common:2; Rare:64; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:89873475-89873665 | Common:1; Rare:91 |