| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:84504608-84504847 | Common:6; Rare:104 | ||||
| chr16:85027603-85027819 | Common:1; Rare:118 | ||||
| chr16:85613037-85613327 | Common:1; Rare:110 | ||||
| chr16:85799526-85799748 | Common:2; Rare:64 | ||||
| chr16:85898974-85899179 | Common:4; Rare:62 | ||||
| chr16:86555180-86555329 | Rare:77 | ||||
| chr16:87317394-87317523 | Common:2; Rare:49 | ||||
| chr16:87765911-87766033 | Rare:48 | ||||
| chr16:88570179-88570482 | Common:1; Rare:117 | ||||
| chr16:88663076-88663374 | Common:8; Rare:122 | ||||
| chr16:88706251-88706522 | Common:4; Rare:125 | ||||
| chr16:88811895-88811970 | Common:1; Rare:45; Clinvar (benign):1 | ||||
| chr16:88856932-88857153 | Common:4; Rare:97; Clinvar (benign):2 | ||||
| chr16:89217627-89217738 | Common:1; Rare:49 | ||||
| chr16:89508316-89508432 | Common:1; Rare:61; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 |