| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:86555174-86555352 | Common:1; Rare:101 | ||||
| chr16:87317348-87317545 | Common:6; Rare:80 | ||||
| chr16:87765908-87766082 | Common:1; Rare:68 | ||||
| chr16:87868977-87869036 | Rare:12 | ||||
| chr16:87951264-87951495 | Common:1; Rare:82 | ||||
| chr16:88570116-88570476 | Common:2; Rare:140 | ||||
| chr16:88663078-88663374 | Common:8; Rare:121 | ||||
| chr16:88706203-88706555 | Common:4; Rare:156 | ||||
| chr16:88856873-88857178 | Common:4; Rare:144; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:88857893-88858142 | Common:2; Rare:50 | ||||
| chr16:89093794-89093933 | Common:3; Rare:64 | ||||
| chr16:89217593-89217749 | Common:1; Rare:75 | ||||
| chr16:89508285-89508424 | Rare:78; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr16:89560506-89561063 | Common:1; Rare:237 | ||||
| chr16:89657637-89658145 | Common:4; Rare:251 |