| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:85799283-85799795 | Common:6; Rare:306 | ||||
| chr16:85800033-85800441 | Common:2; Rare:243 | ||||
| chr16:86555127-86555327 | Rare:191 | ||||
| chr16:87317301-87317560 | Common:13; Rare:180 | ||||
| chr16:87383634-87383964 | Common:3; Rare:237 | ||||
| chr16:87765867-87766085 | Common:2; Rare:157 | ||||
| chr16:87869438-87869802 | Common:11; Rare:187 | ||||
| chr16:87936422-87936798 | Common:2; Rare:166 | ||||
| chr16:87949320-87949513 | Common:2; Rare:81 | ||||
| chr16:87950845-87951210 | Common:6; Rare:126 | ||||
| chr16:87951315-87951537 | Common:2; Rare:166 | ||||
| chr16:88570122-88570482 | Common:4; Rare:260 | ||||
| chr16:88570656-88571132 | Common:3; Rare:266 | ||||
| chr16:88650453-88651824 | Common:20; Rare:795; Clinvar (benign):5; Clinvar (pathogenic):3 | ||||
| chr16:88662963-88663449 | Common:22; Rare:431 |