| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:88802996-88803079 | Common:2; Rare:29 | ||||
| chr16:88856932-88857147 | Common:4; Rare:93; Clinvar (benign):2 | ||||
| chr16:89093747-89093933 | Common:5; Rare:83 | ||||
| chr16:89217632-89217721 | Common:1; Rare:37 | ||||
| chr16:89508280-89508411 | Rare:72 | ||||
| chr16:89560514-89560725 | Rare:95 | ||||
| chr16:89657664-89657838 | Common:1; Rare:94 | ||||
| chr16:89686482-89686704 | Common:9; Rare:85 | ||||
| chr16:89686898-89686971 | Rare:32 | ||||
| chr16:89816584-89816752 | Common:3; Rare:87; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
| chr16:89873460-89873678 | Common:2; Rare:105 | ||||
| chr16:89923150-89923345 | Rare:74 | ||||
| chr16:89948072-89948338 | Common:7; Rare:77 | ||||
| chr16:89972509-89972861 | Common:2; Rare:131 | ||||
| chr16:90022581-90022691 | Rare:43 |