| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:5033920-5033955 | Rare:14 | ||||
| chr16:5097726-5098025 | Common:4; Rare:106 | ||||
| chr16:8797610-8797905 | Common:1; Rare:119; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:10385886-10386071 | Rare:65 | ||||
| chr16:10580569-10580853 | Common:2; Rare:96 | ||||
| chr16:10878654-10878999 | Rare:76 | ||||
| chr16:10944326-10944681 | Common:1; Rare:113 | ||||
| chr16:11586891-11587027 | Common:1; Rare:39 | ||||
| chr16:11797181-11797568 | Common:4; Rare:152 | ||||
| chr16:11846502-11846761 | Common:1; Rare:88 | ||||
| chr16:11851499-11851681 | Rare:93 | ||||
| chr16:11915372-11915725 | Common:5; Rare:134 | ||||
| chr16:11915868-11916202 | Common:2; Rare:135 | ||||
| chr16:11976624-11976776 | Common:2; Rare:60 | ||||
| chr16:14186576-14186912 | Rare:65 |